Introduction:
Biocompatible microbes that consist of numerous strains will be available by 2029 that can fight off pathogens as a secondary immune system and a vector for applying CRISPR treatments that halts and reversed the effects of ageing.All strains of microbes would use the patients leukocytes as a baseline to prevent them illicit immune response and thus be able to form a permenant part of the patients body.These will be done by having ones native leukocytes examined in DNA analyzers to be recreated via 3D DNA printers to them have all the genes for their abilities and also relevant recombinant DNA to carry out their functions,house biosynth WiFi etc as well as the patients DNA to ensure they can be recognised as the patients leukocytes with 3D DNA cutting down on labour and time in manufacturing them for not only fully fledged versions but also those for clinical trials and even animal trials as part of first generation versions that are easy to manufacture by proto and final Phanes cross referencing the patients patient file and also Physis and proto versions of it.Ones leukocytes will be analysed by DNA analysers and thus have DNA present stored in their patient file and then 3D DNA printers will mass produce them that containing necessary genotypes to give specific CRISPR treatments and anti-viral,anti-bacterial compounds and those that each microbe their abilities ie Biosynth WiFi,ability to replicate etc via printing large amounts of them into a growth medium that then is using bacterial DNA use sugars to undergoe mitosis allowing large amounts of each strain to be injected into the patients.All types of leukocytes will be analysed in automated labs with leukocytes used as a baseline since they will house the patients DNA to prevent immune responses allowing them to form a permenant part of the patients body.The microbes different strains will be created by 3D DNA printers by AI including proto and final Phanes in hospitals,universities and home systems and will contain all DNA that give them all of their abilities such as mitosis,genome capsids,flagellum,biosynth wifi,compounds to kill pathogens,horizontal gene transfer and those for CRISPR treatments and housing key traces of the patients DNA to house patient specific surface proteins,antigens etc to allow them inhabit the body constantly without illicitating an immune response.They can have flagellum and genes from bacteria that allow for mitosis to occur to allow them to create millions or billions of copies and travel across the body to all infecting pathogens and cells in the body with this mitosis controlled by Paean.Flagellum from bacteria such as E.Coli using DNA present from it will be present in all strains allowing them to travel across the bloodstream,lymphatic system and all parts of the body very quickly.DNA from bacteria will be present to allow them to undergoe mass replication when needed with recombinant DNA from both E.Coli,C.perfringens which are the two fastest growing lifeforms on the planet can be added to improve the rate of cell division,replication and mitosis of these biocompatible microbes to respond quickly to attacks and trauma with specific proteins,receptors or sensors built into their cell walls or protein coats better at making them recognise,seek out and interact with only specific pathogens rather than the patients own cells or beneficial bacteria or other biocompatible microbes.The rate of their replication will be controlled by Paean via biosynth WiFi and nanomachines or even if possible chemical signals produced by them and the primary immune in particular levels to prevent them overtaking the body and its resources,ensure their is stable numbers with the endolith and Planarian DNA making them immortal negating them to udergo mitosis too much with gene drives controlling this as well with them programmed to to no longer replicate when they reach a certain population with the nanomachines,chemical signals and gene drives controlling replication of all genes preventing any undesirable mutations that may make them ineffective or even a pathogen themselves while ensuring they still have alterations to ensure genetic diversity and control the evolution of them even producing mutations that would cause desired phenotypes that would fight off other pathogens or add new features negating the need to inject new bacteria that would pass on these phenotypes but would also work alongside this.Signals between each other and the body of the host including the primary immune system will initiate quick mitosis of specific strains in emergencies such as surprise infection,tumours and breaks in the skin,arteries and organs to carry out its functions with when it then solved and control the rate to stable levels and control their levels by forcing excess into endospores and awaken those that are required in emergencies.They would as stated earlier control the creation of the second set of genes and the formation of a genome capsid if possible through this signalling the use of of chemical and electrical signals.The rate of replication and mitosis can be controlled prior to and after the perfection of nanomachines by chemical signals between the microbes with any excess forced into an endospore state by signals with these awoken during emergencies such as internal or external bleeding that require instant attention and to ensure that there is a stable level of microbes.If an emergency infection,tumour growth and wound or even rupture occurs the rate of replication and mitosis of specific strains will be speeded up by Paean through the wire or in a fragmented form in nearby devices and biosnth wifi chemical signals in the body as well as native immune system and the microbes communicating with each other to ensure there is enough with any excess once the problem is solved reverted into endospores to be awoken during the next emergency and excess flushed out of the body via urine and feces to be collected in sewage treatment plants for use in smart devices,computers etc by building up in the kidneys and colon and stimulating the host to defecate or urinate.These in endspores via Firmicutes DNA can hide inbetweeen tissues,muscles,in the lymphatic system and lymph nodes.Having them enter endospores will allow them to stay in the body for prolonged periods of time without using water and nutrients with Paean signallling them via WiFi to enter these endospores and be awoken by WiFi when needed with xerophile and oligotrophic and endolith bacterial DNA lowering their nutritional and water requirements.Others could undergo apoptosis or cause cells and tissues in the body to undergo apoptosis and then replace them by turning into these tissues by for example causing the epidermis to shed dead skin similar to Serpentes if recombinant DNA from them is added to the host and also shed off like skinburn.If possible during emergencies and after them Paean can through biosynth WiFi induce their evolutionary path to change into other completely difffereng strains controlled by Paean with upgrades received via biosynth WiFi inducing their evolutionary path through taq polymerase and Cas-9.Paean will make the decision of which to enter an endospore,which to undergoe apoptosis and which to be flushed out keeping levels stable with this done for all strains and also will control the level of mitosis of each strain in emergencies.Biosynth WiFi from neural implants,smartphones and also biosynth routers and public WiFi will allow Paean to control all actions of them 24/7,365 days a year with him controlling the primary immune system by having the microbes synthesise chemical signals.Paean through biosynth WiFi will be able keep track of the location of each and every microbe of each strain and keep track of the number of each strain thus allowing him to control replication,mitosis and also entering into endospores and apoptosis.This will be done by biosynth WiFi and bluetooth etc at home,public buildings and that in wilderness areas and also generated by smartphones and even neural implants where he exists in a fragmented form.Communication of microbes with each other and the primary immune system will occur via Paean controlling the microbes by biosynth WiFi and bluetooth with Paean controlling the primary immune system by telling the microbes to synthesise specific chemical signals.When any microbes die or if they form new tissues,implants etc then the nanomachines and microbes themselves will signal the new levels of replications and if possible countermeasures can be introduced to prevent mutations that would cause the microbes becoming overrun such as suicide genes or those that stop replication activated by nanomachines and even chemicals inhaled,ingested or injected into the body with gene drives preventing them overrunning the body and or mutating to cause this in first place.Gene drives especially DNA from T.gammatolerans that exhibit DNA self repair will be added to prevent unwanted mutations with upgrades altering the DNA by adding and removing genes.Each event carried out by each strain ie repair of damaged tissues,infections,tumours,immunisations of each type will be logged into ones patient file by date and type.New nanomachines for new microbes could be injected to attach to those without them or in time biosynth nanomachines can be constructed by these and other microbes through illicitation.Synthesis of nanomachines would be done by the microbes creating graphene/carbon nanotube scaffolding or buckyballs and the silicene,graphene,borophene and stanene nanoprocessors and bio synth wifi transmitters in them via wifi instructions from Paean and in time themselves with the electrical impulses from neural clusters and ability to generate electricity using recombinant DNA from both S.oneidensis and G.metallreducens,G.sulfurreducens powering the nanomaterial tubing alongside chemosynthesis using sugars and other nutrients,nanoprocessors as well biosynth wifi synthesising organic receptors and also other layer components to cover these or even biosynth nanoprocessors similar to neural clusters or even extra neural clusters which then merge with the neural clusters.Having tweaked recombinant DNA from different strains of Geobacter such as G.metallreducens,G.sulfurreducens and Shewanella that already create electronically conductive protein and silicon nanowires can be modified and tweaked to produce the carbon,boron,tin and other relevant nanotubes and wiring will allow for this with anabolic and catabolic reactions catering to this.The G.metallireducens,G.sulfurreducens,S.oneidensis DNA will give it the ability to generate electricity and electroconductive pilli and electroconductive proteins,silicon nanowires with tweaked DNA allowing this to occur when it consumes sugar etc.Neural synapses could also be synthesised onto these nanomachines wiring through further engineering.Primitive versions of microbes may have simple forms of nanomachines or none and respond to injections of hormones or those produced by the body or biological compounds and signals they are engineered to respond to to perform different tasks such as release anti-viral and cancer compounds etc but as time goes on upgrades can allow for this and neural synapses etc to be added via interbreeding.Nanoprocessors,buckyball scaffolding and nanowires of nanomachines and microbes could be biosynth ones composed of neural tissues,electroconductive pilli and electroconductive proteins using recombinant DNA from S.oneidensis,G.metallreducens,G.sulfurreducens and Magnetospirillium DNA etc to make it easier to synthesise much quicker during mitosis than those composed graphene,stanene etc.The ability to undergoe mitosis can allow for them to react to emergency infections,perforations and tumours with it also allowing one injected with new strains and upgrades undergoe mitosis to create millions or billions of copies and them entering endspores,undergoe apoptosis or flushed out of the body when not needed.This would ensure the levels of microbes if they form new tissues,are lost through bleeding etc will be a desirable constant level to prevent them overrunning the body or be in such small numbers to be ineffective.The nanomachines would allow them to receive instructions,simulations and strategies for infections and emergency perforations and tumours and create new genotypes from Paean whether in he is in the wire or in a fragmented form on neural implants and devices thus allowing upgrades be done wirelessly from home or in the wilderness via satellites with this even aiding the Amish and tribes in Tibet,Amazon and also Africa.This would be done via the genotype of upgrades sent to the relevant and desired strain and thus initiating them via taq polymerase and Cas-9 to create them in the desired strains including those in endospores that would be temporarily awoken for this with them then signalling to him when they are done upgrading and also when the body has be immunised and also when all the relevant tissues in the body are given these augmentations and anti-ageing treatments.He would allow for augmentation and anti-ageing treatments and also immunisations to be initiated at desired times and also be alerted as to when this is done.It would also allow instant analysis of any toxins,synergistic compounds and also date rape drugs and other compounds not desired to be ascertained in the body by him and have him send them instructions to create specific counterproteins to bind to the receptors in the body and also bind to the unwanted compounds with this also determining what to do in each in instance to prevent death and injury.Also since the receptors on the strains that deal with these to detect would only have to be universal receptors and not have to have different receptors for each one as the phenotype of C.elegans would intake the compounds and through mechanotransduction or reverse mechanotransduction,chemical reactions seen in more complex or similarly simple organisms and simple and complex neural clusters and systems in them would be able to send via nanomachines and biosynth wifi the structure of the compound to him and thus organise what to do instantly.Flagellum will be added to them from E.coli to allow them to travel to all parts of the body to reach pathogens,perforations and also human cells.Digital DNA storage and nanomachines will store known compound structures and to react to unknown ones not sent to them from Paean with unknown ones sent to Paean for analysis.Proteins similar to Cas-9 and taq ploymerase created from scratch could be created that can scan the structure of the compound to then transmit it to Paean with this also method to allow them to detect hormones,cancer biomarkers and not just poisons,date rape drugs and also heavy metals.Having the compounds structure and counterproteins stored on the DNA digital storage of microbes will allow them to prepare relevant counterproteins instantly.This would also work for cancer biomarkers allowing the correct type of tumour and thus its location to be determined via chemotaxis and would ensure they would not react to compounds produced naturally,from food etc,those used for medical reasons ie Flunitrazepam and only react to those in levels approaching the LD50 limit and locate where the compound even poisons are entering the body and thus travel there instantly.Relevant strains would have the receptors and stored structures of compounds relevant to them ie cancer strains would have the receptors for cancer biomarkers created by scratch with the compounds structure in their digital storage with chelation strains housing universal receptors and store the structure of all known poisons and heavy metals in their digital storage with base microbes also housing these to alleviate strains on chelation strains and then alert the chelation strains.This would also be done to detect the levels of blood components such as erythrocytes,leukocytes and also platelets and also hormones,pollutants etc.Ideally each strain would be designed to detect universal substances they work on ie cancer strains react to cancer biomarkers including CD47,chelation strains reacting to only heavy metals,poisons etc to make sure that each strain only undergo replication in the presence of the compound they need to detect and use chemothaxis to locate their location.Biosynth wifi and bluetooth will be integrated into the microbes utilisng DNA from Apidea,Hymenoptera,Chiroptera,Magnetospirillum and other unicellular and multicellular animals affected by wifi,magnetism and also those that use electrical signals even those from E.electricus,the mechanotransduction or reverse mechanotransduction of C.elegans or wifi like means of communication and scratch DNA could be used to create biosynth wifi alongside graphene,borophene and stanene nanoprocessors sythesised via tweaked Geobacter and Shewanella DNA and neural synapses created by them aiding in the formation of biosynth wifi present in all strains.This will allow them to communicate with each other and with Paean using satellite wifi and biosynth wifi at home and from smart devices etc in the wilderness that generate their own biosynth wifi.Paean would tell them what measures to take ie send out specific binding proteins to receptors and the poisons etc and carry out anabolic and catabolic reactions and in what order and manner.It would also allow for them to carry out anabolic and catabolic reactions to create specified nutrients,benign substances and also desired synthetic compounds of medical quality and interact with the levels of nutrients in the body and also interact with strains that produce hydrocarbons and plant and animals oils to create complex compounds or using excess nutrients he would tell them what to do with each compound and how to carry out these reactions and what to create from them.They would receive from Paean via biosynth wifi signals from the wire,smart devces or even neural implants when access is not possible strategies/simulations and orders,instructions to initiate immunisations in infants and adults,when to communicate with the primary immune system using chemical signals and what to tell them ie where to gather in the body/when to receive surface protein antigens for immunisations/what surface protein it is/when to use antibodies and what antibodies to use etc,communicate with each other and the primary immune system via chemical signals and also wifi signals,when to enter into endospore states and also when to awaken from then and even when to undergo apoptosis and even be flushed out of the body,when to undergo mass replication,when and how to turn elemental compounds in the body/from poisons/excess nutrients to create benign compounds as well as synthetic drugs and antibodies or hormones and thus carry out catabolic and anabolic reactions,how to form catabolic and anabolic reactions,when to form implants and worms and also instructions to form new genotypes and delete old ones in all strains via initiating taq polymerase and Cas-9 and DNA replication or simply change certain genes using Cas-9,taq polymerase and forced evolution allowing for upgrades for all strains to be done wirelessly on the spot allowing for this to make upgrades of all types much quicker and not require the patient to go to hospitals.Paean would be able to communicate with individual or whole groups of each or all strains of microbes and manage interactions between them and tell them what to do and where to go and if need be gather the primary immune system to create specific antibodies or gather other leukocytes to manage all aspects of the primary immune system via sending the microbes wifi signals and in turn them sending chemical signals to the primary immune system thus allowing Paean complete control of both the microbes and in turn the primary immune system allowing him to control aspects of battles against all types parasites and infections and also tumours.Paean will thus control the microbes via bisoynth wifi and/or biosynth Bluetooth and also the primary immune system by having the microbes create chemical signals thus giving him complete control of both the microbes and the primary immune system at all times for all infections existing and new and also tumours and also surprise injuries etc 24/7,365 days a year with him doing so from neural implants and smart devices that use biosynth wifi.Paean will also send them new data into the DNA digital storage of all microbes,whole strains or a few microbes in specific strains which can be then be deleted and overwritten later on.Biosynth WiFi can allow Paean to using taq polymerase and Cas-9 to induce the evolutionary path of their DNA to receive upgrades at home for all strains and if possible this could cause some strains to undergo evolution and wirelessly change into other strains by having their nuclear DNA to that of others via inducing taq polymerase and Cas-9 ie base microbes could be changed into stem cell or chelation strains.This can quickly allow one strain to be changed to another in emergencies and without the need to have them created at home.He will control the application of CRISPR treatments to all of the patients cells in the body for anti-ageing and augmentation treatments.If possible all cells in the human body can have biosynth wifi integrated into it to have upgrades sent wirelessly instantly to all cells and tissues from WiFi coming from smart devices via taq polymerase and Cas-9 inducing evolution of genome.Biosynth WiFi integrated into human tissues and cells could allow upgrades for ageing treatments and augmentations to be sent directly into ones genome in all cells within minutes bypassing the need for microbes to apply gene treatments associated with this.Base microbes will scan the DNA of any pathogens and parasites and relay this to Paean who will cross reference Physis and thus relay the name of the species and strain thus activating relevant strains to attack them and use what CRISPR treatments alongside anti-viral and anti-bacterial etc compounds at their disposal and what strategies to use as well as whether to signal the primary immunised immune system to where infections have occured.Once base microbes would scan the genome of pathogens especially new ones they will send it to him and he will send them the DNA to synthesise by wifi to create genotypes for immunising strains to be relayed to them and to then share the proteins with dendritic cells etc or those to be extracted from them via base microbes to share with immunising strains and also how to create species and strain specific bumpers and endolysines relayed to the anti-bacterial and anti-viral strains either telling base microbes what DNA to share with anti-microbial ones and also this done by wifi with this also done for known pathogens like HIV,MRSA etc with them being told what anti-viral,anti-microbial and also CRISPR treatments to utilise for each pathogens ie suicide genes,what genes to use that makes the pathogens susceptible to specific anti-viral/anti-microbial compounds and also what signals to send to the primary immune system to initiate specific antibodies for each pathogen until it can learn this itself and whether these and those in the microbes should be deployed in specific areas or whether to use the lymphatic system or bloodstream.Compounds such as toxins,venoms detected by them will be sent to Paean and they will download counterproteins and antivenom from him once Physis is refferenced and they will be told to start using these or converting the toxins into benign substances via anabolic and catabolic reactions.They would even send data to him such as environmental readings in the blood stream,lymphatic system and also organs and other parts of the body data on the geneotypes of pathogens and parasites etc with them also sending levels of damage of telomere and mitochondrial DNA and Phosphatidylcholines in all cells through base microbes with base microbes in newborns or even in unborn fetuses scanning the DNA in cells thus allowing new patient files to be set up instantly allowing for strategies to cure genetic disease to be done instantly via Paean wirelessly evolving certain strains and create patient files for children in areas populated by the Amish,Amazon and African tribes where wifi and hospitals dont exist using satellites with these setting up implants invivo that measure vital signs and blood components regularly.They would also send him the structure of poisons etc present and thus be told what counterproteins to create sent wirelessly.He would using this DNA allow for the mothers microbes to be more effective at trading and receiving DNA from the unborn child and into a few of each strain and then organise their transfer into the child during the last trimester and also to them via breastfeeding.Through implants the levels of antibodies produced by the primary immune system alongside erythrocytes,platelets and leukocytes of each type will be measured and send it to him.The wifi would also allow nanomachines in all microbes to communicate better with each other and each other strain by sending instructions,DNA from pathogens to be used for creating protein bumpers,endolysines and proteins for immunisation strains specific to a pathogen and strategies instantly.Paean would use this to create unique countermeasures to each infection etc.Implants both neural and those for detecting blood components and vital signs would use this wifi to send and receive data.The DNA present in the nucleus and biological hard drives and in the neural clusters and the clusters themselves of each individual microbe and those in the neural implants will allow them to download,store and delete digital DNA data from Paean,Physis and past experiences such as the unique chemical structures of poisons and toxins and their counterprotriens both synthetic and those from animals,instructions as what to do in certain situations,surface proteins and DNA of all pathogens as well as whole orders of them to allow them to apply the correct CRISPR,anti-viral and anti-microbial treatments and create suitable universal endolysines through phagocytosis for all or specific bacterial and viral pathogens it encounters with endolysine and bumpers schematics for specific strains and species of bacteria and viruses and decide whether to apply them via horizontal gene transfer and also flooding the system with bumpers that attack only pathogens as well as develop countermeasures and strategies towards poisons.By having all microbes in anti-viral and anti-bacterial strains,chelation strains etc house DNA digital storage will allow for large amounts of data to be stored with more stored in all of the neural implants and worm implants that measure vital signs and also blood components would allow larger amounts of information with each microbe by themselves and those in implants containing at least 3ZB if three metres of DNA found in humans is present here that can be deleted by thought,by wifi by Paean and share information from each other different microbe managed by Paean using wifi and also download information from the wire namely Epione,Paean,Physis.Cas-9 and taq polymerase can allow data to be copied,deleted and transferred to and from each microbe,entire groups and all of them as well as to and from Paean,Physis,the wire and internet and electronics such as smart devices etc.DNA from P.japonica can increase their storage rate to 150ZB.The microbes digital storage can be be managed by Paean with them individually carrying different data from other ones and also universal data relevant to each strain with the data deleted by Paean and also new information downloaded by wifi with this including the structures of poisons,heavy metals and pathogens and their counterproteins,bumpers,antibodies etc and also all types of synthetic compounds to be produced when a specific pathogen is detected,genotypes of pathogens and the data to be used to create new genotypes for upgrades as well as the structure of synthetic compouns to fight off bacteria,viruses,fungi and also parasites as well as everyday conditions.The wifi will allow them to send and receive data,instructions from Paean as both in areas with wifi and without using cellular and satellite wifi services with them also able to send data such as scanned DNA from pathogens especially new species and strains,the hosts genome to measure levels of telomere and mitochondrial DNA senescence and Phosphatidylcholines,denote when all cells in the body have been upgraded with augmentations and also ageing treatments,send the DNA of newborns added wirelessy to newly generated patient files with worms and implants formed by these would send vital signs such as heart rate,levels of blood components ie leukocytes/erythrocytes/platelets as well as hormones in the blood and areas like the womb.The structure of compounds such as drugs,heavy metals,biomarkers for heart disease and cancer,erythrocytes,platelets and leukocytes and nutrients in ppm,ppb,ppt,ppq would be sent once analysed by universal receptors and mechanotransduction or reverse mechanotransduction,chemical reactions seen in more complex or similarly simple organisms and simple and complex neural clusters and systems in them and they would send DNA of pathogen and parasites to be analysed Paean and Physis.They would receive instructions as to initiate gene therapy of all types and also send when they finish and also instructions to create upgrades and also information such as the structure of compounds and how to carry out catabolic and anabolic reactions for each pathogen,ailment or condition.The base microbes would scan the DNA of unborn fetuses and also new pathogens as well as levels of telomere and mitochondrial DNA senescence and also levels of Phosphatidylcholines using taq polymerase,Cas-9 and CRISPR to copy its DNA and send signals to the neural implants in the body or directly to Paean.Biosynth WiFi will be used to send data back and forth between Paean and microbes as well as allow the microbes to communicate with each other using WiFi generated by routers at home,in public buildings,public WiFi from biosynth trees and that generated from smart devices and computers with if need be them also using biosynth Bluetooth if WiFi access is not possible or present.Biosynth implants will more easily allow Paean to He would more easily control their actions and their interactions with the primary immune system via chemical signals including immunisations,interactions with each other and the primary immune system ie all strains and all microbes in each strains and also the transfer of microbes from one generation to the next ie transfer the childs DNA to the microbes in the mother collected in the breasts or transferred via the placenta via either collecting DNA from the fetus or wirelessly initiating them to change DNA in the microbes nucleus from those collected via base microbes and the newly generated patient file.Having control of all strains of microbes via biosynth wifi could allow him to perform strategies on how to attack specific pathogens especially new ones and also have them initiate the immunised primary immune system,control the primary immune system via chemical signals initiated via nanomachines in microbes,perform simulations and send strategies against all infections and tumours and ruptures,simulate and carrying out countermeasures towards heavy metals as well as date rape drugs and also poisons instantly and initiate the creation of synthetic compounds and carrying out of all anabolic and catabolic reactions more efficiently and ensure drugs both medicinal and recreational either synthetic and natural produced by them will be only in desired amounts preventing overdosing.The structure of synthetic compounds and antibodies can be stored on the DNA digital storage of them and this would also include instructions on how to create them with them constantly linked to him and each other via wifi allowing them to create them only in required amounts and on the site of action with this data sent via wifi and deleted when necessary alongside all other data.Genotypes for upgrades would be sent to them wirelessly as wifi would allow for new ones to be added and old ones deleted for all strains with him initiating taq polymerase and Cas-9.The implants would allow him to control their interactions with the primary immune system by initiating chemical signals produced by them to initiate certain actions ie collect in areas to fight off infections with antibodies,collect in areas to receive surface protein antigens from immunisation strains and also initiate the production of helper T cells,memory B and T cells and also plasma and killer T cells and even the actions of all types of leukocytes in each battle.He would also control the apoptosis of human tissues in the body ie muscles destroyed to initiate natural healing processes to burn up fat and build up muscle,apoptosis of cells and tissues housing pathogen DNA or housing pathogens and initiating the use of those that replace damaged tissues in the case of injuries such as perforations.All actions of both all strains of the microbes and the various types of primary immune system will be controlled by him directly and indirectly.Since connected to them directly and in close proximity he will be able to send and receive data and instructions with him also also teaching the microbes and primary immune system via their chemical instructions how to detect cancers and also infections more effectively by themselves with MRI scans and also results from test kits etc to do so and direct them to specific sites of the body.In short all strains of the secondary and primary immune system will be controlled more efficiently via implants both directly and indirectly via nanomachines biosynth wifi and also chemical signals.If possible they could cause some strains to undergo replication and have some wirelessly change into other strains by having their nuclear DNA to that of others ie those that treat neurological,genetic and developmental disorders to treat a fetus invivo.Data can be stored on internal biological hard drives present when in fragmentation and wifi is not available ie readings of vital signs and internal temperature and also levels of erythrocytes,platelets,antibodies etc from other implants or themselves with this sent in packages to ones patient files when wifi is gained with it having its own internal clock with time and date being for the current or chosen timezone.These biosynth neural implants will form the basis of VR technology indistinguishable to reality feeding simulations and sensations such as pain,pleasure,tastes,smells etc directly into the human brain and central or even peripheral nervous system and will allow one to stream data from the internet and the wire,store thoughts,memories and also wirelessly communicate with others from around the world.Base prototypes of microbes will probably not have nanomachines and as such will require signals coming from injected chemicals to stimulate actions and them releasing chemicals that can be detected by home test kits of all types or creating unique smelling urine and sweat with upgrades via base microbes adding the ability to create biosynthetic nanomachines.These fully fledged versions should be possible between 2035-2045.Having them engineered to enter endospores using recombinant DNA from Firmicutes and have DNA from oligotrophs,Tardigrade and xerophiles,endoliths other large animals with slow metabolism and scratch as well as endolith bacteria will allow them to survive on low levels of nutrients either when the host is low on stored food,low on nutrient intake,survive long periods without using excess nutrients,putting strains on the hosts resources or those stored in the body and allow them to form endospores through signals especially excess ones to prevent them overrunning the body and using too many resources ensuring there is enough for the host to survive with them also engineered to utilise gases and liquids intaken by the host whether they are beneficial or even toxic to the host to create nutrients for the microbes and the host.Paean via biosynth wifi tell them when to enter endosproes and when to get of them.Vacuoles in human and other animal cells to store excess sugars and proteins during this state or when in an activate state can be added using recombinant DNA from humans with them also containing mitochondria to utilise sugars and proteins.DNA from Wangiella dermatitidis,Cladosporium sphaerospermum and Cryptococcus neoformans can be added to these microbes to enable them to radiosynthesis,that is,to use the pigment melanin to convert gamma radiation into chemical energy for growth thus helping them use it as a food source.Excess sugars,proteins as well as fats in the hosts body in the bloodstream or stores will be used by them alongside poisons and drugs converted into these for nutrition via anabolic and catabolic reactions with chemosynthetic DNA allowing metals and minerals to be used with them having DNA from faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles bacteria and scratch DNA to allow them to run on both oxygen and carbon dioxide meaning they wont starve the host of oxygen and will prevent the build up of carbon dioxide in the body.If the host and microbes has both oligotrophic and xerophile DNA then this will mean that the host normal diet will supplement these in vacuoles or the microbes could deposit these in areas inside the body ie store of fat in the body surrounding organs and in appendix like areas created by them that can be used as it its or converted into sugars.The endolith DNA also reducing nutrient requirements even further due to their slow metabolism especially if both hosts and microbes have them.Thus they can communicate with the hosts body to signal it to deposit fats around organs constantly and not under the skin that can be used as a repository of food for them to run on when they run low on energy and are in the middle of emergencies where they will be need to undergo mitosis.Once stores of fat are used then these will be replenished by chemical signals to the brain.These will be engineered to house vacuoles present in all eurkaryotic cells to store excess energy when needed.If possible there may their version of the helper T cell that stores large amounts of sugars and fats in them in vacuoles that during emergencies like perforations and also infections etc the version of the helper T cell can release this in close proximity to them during battles to allow the microbes to feed on them or even after infections when they collect in areas like the appendix to release them to starved microbes.Ideally to prevent them overheating the oligotrophic DNA and those from slow metabolizing endolith bacteria and even Tardigrade that can lower its metabolism by 99.9% can prevent them burning up or the host with this also limiting their need to use too much resources.Xerophile,oligotrophic and Firmicutes DNA will reduce the amount of food and water they need exponentially.DNA from W.dermatitidis,C.sphaerospermum and C.neoformans once one is also made immune to radiation via DNA from T.gammatolerans,D.radiodurans can be added to the microbes to enable them to radiosynthesis,that is,to use the pigment melanin to convert gamma radiation into chemical energy for growth thus helping them use radiation as a food source should food be scare and instead of excess nutrients.They will have the carbon dioxide acceptor phenotype making them engineered to unlike humans cells run in carbon dioxide as an energy acceptor and release oxygen in the process not only ensuring a continuous supply in the body especially if a heart attack or sudden stopping of the heart occurs but also preventing them competing for oxygen that the host needs.DNA from Bacillus F,T.gammatolerans and the ability to replenish Phosphatidylcholines will be added to ensure that even though they may undergo mitosis they will still have the same eternally young telomeres in their DNA even if they undergo replications billions or trillions of times.This will allow them to live indefinite lifespans in the body unlike normal leukocytes.The ability to carry out mitosis will come from genes from bacteria responsible for this with Paean through biosynth WiFi controlling the rate of replication of all microbes of all strains thus allowing for large numbers of a specific strain to be mass produced for emergencies such as infections with biosynth WiFi allowing humans to know the exact number of each strain and their location in the body and chemical signals from each other and biosynth nanomachines controlled by him will prevent them overrunning the body with as stated excess ones entering endospores and reawaken instantly when new infections and tumours or even bodily repair etc needs to be carried.Firmicutes DNA will allow them to enter endospores when not needed to reduce their resource use as they will use none when in this state with excess ones flushed out of the body or signalled to undergo apoptosis via biosynth wifi signals from Paean creating suicide genes for the same reason.Theoretically these endospores could be a means for excess ones to form biofilms in key areas where infection,brain and organ damage may occur and not use resources but be activated by signals be activated to repair damage,create new tissues and fight off infections and in the case of infections that are fought return to this endospore state with those turned into new tissues staying as tissues either permanently or temporarily to allow the bodies natural repair mechanism to take over with the remaining microbes signal replication of more to take their place.Thus their ability to form endospores will allow them to reside in tissues to be awoken by signs of infection,internal and external damage,cancer biomarkers,hormones or signals from different strains or on demand with different strains doing this in different rounds or shifts.This entering and exiting of endospores will be done via turning on/off genes via biosynth wifi controlled by Paean inducing the evolutionary path of them or chemical signals to turn on/off.Thus Paean can through biosynth WiFi turn genes on/off via inducing their evolutionary path via biosynth WiFi or inducing chemical signals to enter endospores and be later reawakened from endospores when an infection etc occurs thus preventing them overrunning the patients resources and be stored in any part of the body as in an endospore form they will shrivel and reduce their size by as much as 50-90% and thus can also be used to allow them to reside in the body for long periods of times without using resources such as sugar,fats etc.Other strains and microbes will be made to undergoe apoptosis and be flushed out of the body through urine and feces to be collected in sewage treatment plants.Microbes will be able under the control of Paean to be made to simply enter the gastro-intestinal tract and kidneys thus allowing them them to be flushed out of the body alongside feces and urine.In this case before they are flushed out of the body thus way they will have all extremophile DNA present removed alongside that of the patients DNA removed via inducing their evolutionary path so as to allow them to be killed off by the radiation,drying processs in sewage treatment plants and recycled.Biosynth wifi will allow Paean to have complete omniscience over the number of microbes of each strain and their location in each patients body and thus control the number of microbes of each strain at all times.The microbes will contain scratch DNA to prevent them undergoing mitosis by themselves when their are no signals from Paean meaning they will only undergo mitosis when told to so by Paean to prevent them overrunning the body with them controlled by biosynth Wifi generated by smartphones,routers etc
All microbes of all strains will house DNA from Apidea,Hymenoptera,Chiroptera,Magnetospirillum and other unicellular and multicellular animals affected by wifi,magnetism and also those that use electrical signals even those from E.electricus,the mechanotransduction or reverse mechanotransduction of C.elegans or wifi like means of communication and scratch DNA could be used to create biosynth wifi alongside neural synapses created by them aiding in the formation of biosynth wifi present in all strains.Biosynth WiFi will allow Paean to control all of their actions during cancers,infections and ruptures with through them creating chemical signals can allow him to control the primary immune system.All strains will be able to use Biosynth WiFi etc to send data back and forth to Paean and patient files such as detected infections and poisons and structure of synthetic compounds to be used by them alongside instructions on what to do for each infection etc.They will house Soteria the universal anti-virus software and receive updates to this routinely..Biosynth WiFi will allow them to receive upgrades via their genome changed via Cas-9 and taq polymerase inducing the evolutionary path of them.Biosynth wifi will allow all of a desired strain to awaken at once once neural implants,implants that detect vital signs and also other microbes including base microbes detect cancer biomarkers and pathogens with them first signalling to Paean to cause the rest to undergo replication with if need be Paean even causing different strains to be turned into other strains via wifi inducing the evolutionary path of them via taq polymerase and Cas-9.Cappiliaries can be used for them to reside in areas in between the bloodstream and organs with them also residing in the gastro-intestinal tract,lymphatic system,on the surface of the exterior and interior of organs,in the lungs again in either their endospore state or as normal with them even residing in between cells and tissues in the body and transporting nutrients,oxygen and carbon dioxide to and from cells from the lungs and bloodstream rather than blocking their access to native cells acting as a relay system and again synthesising oxygen from carbon dioxide and nutrients of all types such as sugars,amino acids etc on demand.If possible new organs could be constructed by them by the construction capillaries and small veins and scaffolding in order to store large numbers of them to be released in emergencies.Otherwise they can reside in the appendix with small appendix like areas created around the body via the stem cell strain to store large numbers of each strain in to be stored in endospores and thus awaken in emergencies.Those that reside in these areas can be use to augment the abilities of specific cells and tissue such as muscles,neural tissue etc with them also augmenting and speeding up the actions of these and other organs and parts of the body ie nephron/kidneys,small intestine,pancreas,stomach by speeding up their processes,alleviating strains on them if they become overstressed especially with regards to breaking down alcohol and drugs etc,repair them etc.If the microbes need to be gotten rid of they can have suicide genes activated by wifi that cause them to undergo apoptosis or ideally they can be flushed out of the body via urine or feces by ordering them to exit through the urethra and also clinging to feces where they can be collected,extracted and then cultured and possibly given a new host especially when the host dies or used in the creation of electronics.This may also be done if there is too many of any or all strains in the body especially after them having to multiply quickly to deal with surprise infections and tumours that necessitated rapid growth with them collected in the sewage treatment plants to form bio-synth technology once sanitised with narrow UV wavelength that they will be immune to unlike any pathogens or they then can have their DNA modified to be inserted into another human host or even animal host.Thus after emergency infections and also ruptures etc as well as once augmentations etc are applied then the excess will be flushed out of the body through urine and feces and collected in sewage treatment plants with leftover stem cell,anti-viral etc strains left behind in the body to fight off the next infection etc.If possible these could even be used to form biosynth implants,devices and computers outside of the body and inside the body.Bacterial DNA that gives them ability to undergoe mitosis will be present including DNA from fast growing bacteria in E.Coli,C.perfringenes that will will be controlled by biosynth WiFi controlled by Paean thus meaning they will only be able to undergoe mitosis when told by Paean to control the rate of mitosis in emergencies to prevent them overrunning the body with there being scratch DNA wherein this replication does not occur normally but only during when told by Paean to do so.Thus biosynth WiFi,bluetooth and cellular access will be built into them and will be generated and utilised by them to crossrefference Physis when they intake the structure of compounds and DNA from bacteria,fungi,parasites and viruses to identify their exact compound species of species of pathogen and relay this information to Paean to allow him to decide what to do next as well as receive instructions from Paean and they will use it to download the structures of anti-venoms,antibodies,synthetic compounds downloaded from Physis onto their DNA digital storage synthesised by anabolic and catabolic reactions.Paean will through WiFi control their replication across the body in emergencies and via WiFi signal them to undergoe apoptosis or enter endospores and be flushed out of the body by entering the kidneys and gastrointestinal tract to be excreted by feces and urine when not needed to prevent them overrunning the body with Biosynth WiFi relaying to the levels and numbers of not just all microbes but the levels and numbers of each specific strain allowing him to control their replication and numbers at all times etc.Biosynth WiFi will relay to him the exact location of each and every single microbes of each strain.Although they will have genes from bacteria to undergoe mitosis they will contain scratch DNA to only undergoe mitosis when told to do so by Paean by Biosynth WiFi,bluetooth to prevent them overrunning the body so as to allow him to control their numbers.This will mean that when there is no Biosynth WiFi etc signals they will not undergoe mitosis and will only do so when told by Paean.This will prevent them overrunning the body and also allow Paean have complete control of the microbes replication.Should an emergency infection or inbibing a toxin occur he will cause specific strains to undergoe mass replication to remedy the situation with once the infection is resolved he will signal excess numbers of them to enter endospores,be flushed out of the body or undergoe apoptosis.He will use this to also control their movements across the body to where they need to attack tumours,pathogens etc and also to apply CRISPR treatments to all cells and tissues with him able to control what treatments either CRISPR treatments or specific anti-viral,anti-bacterial and anti-cancer treatments etc and when to apply with him able to using WiFi from neural implants,smartphones,laptops and WiFi routers including in public to control all actions of all microbes.All actions such as attacking pathogens,applying CRISPR treatments to the patients cells and also their replication,apoptosis etc through CRISPR treatments,synthesis of natural and artificial compounds through recombinant DNA and also anabolic and catabolic reactions and also creating chemical signals to control the primary immune system will be controlled by Paean 24/7,365 days via biosynth wifi.All actions carried out by the microbes will be controlled by him communicating with them through Biosynth WiFi and biosynth bluetooth from WiFi and bluetooth generated by smartphones,computers and routers etc.Since existing in smartphones in a fragmented form he could do this while in the wilderness and at home through the smartphones generating their own biosynth WiFi.He will be also able to control what information is downloaded by them and deleted.Most microbes could hold at least 3ZB of data within DNA digital storage on them with DNA from P.japonica increasing this to at least 150ZB of information.Each microbe could hold this amount of information and either house the same information as all other microbes of the same strain or all strains.Information in these biological DNA digital storage harddrives will include the structure of synthetic compounds,synthetic antibodies relevant to each strain and for anti-viral,anti-bacterial and anti-helminthic strains with them also downloading structures of natural antibodies created by populations of humans both naturally or as a result of vaccines and immunisations or synthetic ones extrapolated by Phanes and Paean.Also represent will be counterproteins and anti-venom to poisons,toxins,heavy elements extrapolated by Phanes and Paean alongside structures of bumpers meant to transport CRISPR treatments and anti-viral,anti-bacterial and anti-helminthic compounds to prevent them breaking down in the body and prevent cytoxicity with Paean arranging the type of information present in each individual microbe from Physis with unwanted information deleted and new information downloaded from Physis etc within minutes or even in time by 2045 onwards within seconds due to improvements in Paeans computing power and strength of the biosynth WiFi and bluetooth.Taq polymerase,Cas-9 etc can be used by Paean to copy,transfer and delete information on all microbes.The P.japonica DNA will allow the microbes to also house more DNA for more DNA augmentations for allow them to survive different environmental conditions and also more DNA to house more abilities and natural compounds to synthesis through recombinant DNA.The biosynth WiFi and bluetooth will be generated by the microbes with them also using that produced by public biosynth WiFi and bluetooth and also that from routers in homes,public buildings and vehicles such as cruise ships,aeroplanes etc.He will be able to through controlling the evolutionary path of microbes induce upgrades giving them new abilities.Biosynth WiFi and bluetooth generated by smartphones and laptops in close proximity and even that generated by biosynth neural,vascular and other implants in the patients body where Paean is housed in via fragmentation will also be used with the biosynth WiFi and bluetooth and allowing Paean to control all as aspects of the microbes 24/7,365 days at home,in public areas and buildings,vehicles and wilderness etc.Thus biosynth WiFi built into the microbes will allow them to receive instructions from Paean with him residing through fragmention in smartphones and neural implants in close proximity that generate their own WiFi to allow his control of microbes to be continuous in wilderness areas.Wifi routers in homes,public buildings and public WiFi will allow them to be carried out there.Even WiFi generated from laptops,smartphones etc will allow him to control their actions.As a result as long as there is WiFi access Paean can interact with and control all aspects of microbes in the body 24/7,365 days a years.He can exist in a fragmentated form in smartphones,laptops,biosynth implants in the body to control the actions of microbes at all times using the biosynth WiFi etc to control all actions of them when in the wilderness areas etc.Paean will use this biosynth WiFi,bluetooth and cellular access to determine the location of each and every single microbes of all strains in the body and send them instructions such as where to go in the body,what anti-viral,anti-bacterial,anti-helminthic compounds from recombinant DNA present to synthesise and what synthetic compounds and antibodies to synthesise via anabolic and catabolic reactions including those downloaded onto their DNA digital storage to be produced and within what amounts by which strains with him also deciding how many of each strain will be produced.He will also tell them what anti-ageing and augmentation CRISPR treatments to apply and to what cells in the body to apply them to and what CRISPR treatments to apply to pathogens,parasites etc through initiating horizontal gene transfer and transfer of genes as well as to download new CRISPR treatments via induction of the evolutionary paths of DNA present and also downloading the structure of synthetic compounds in DNA digital storage and tell them to synthesise them through biosynth Wifi and what pathogens etc to apply them to and he will control their strategies in all infections,tumours etc and download,copy,transfer,delete data on them and data on sent back and forth to patient files,his networks etc and he will control all aspects of immunisations,attacks against pathogens,tumours,toxins and application of CRISPR treatments to human cells and pathogens.He through biosynth wifi via fragmentation on smart devices etc will be able to constantly control all aspects and actions of all microbes in each individual patient.He will also use this biosynth WiFi to control their replication as well as undergo apoptosis or enter endospores when not needed or they need to be flushed out of the body,when to reawaken from endospores and carry out strategies to attack each individual infection including existing chronic infections such as those already with HIV and other chronic pathogens and all future infections of all species of strains of viruses,bacteria,fungi and parasites.Through flagellum present via E.coli DNA he will control the movement of all microbes to where they are needed ie the scene of infections and tumours etc.He will direct them to cells across the body that are to have anti-ageing and augmentations applied via horizontal gene transfer and through taq polymerase and Cas-9 allow for applied genes to be created over and over again.He will have microbes the species of pathogens that enter the blood through cuts,food etc and then once identified by having them scan the pathogens DNA will then carry out strategies to kill them off such as application of CRISPR treatments,iniatiating the immunised primary immune system or collecting DNA samples have its genome scanned for genes responsible for surface proteins to be sent to immunising strains through upgrades via biosynth WiFi to allow new pathogens to be immunised against within 24 hours and then the primary immune system initiated.He will be able to cause microbes in the body such as anti-bacterial,anti-viral etc strains to create chemical signals via this WiFi and bluetooth to communicate wifi the primary native immune system thus allowing him to control it allowing the primary immune system take part in battles preventing it becoming lazy and weak with him having the immunising strains communicate with the helper B and T cells and plasma cells to become actived by them once they have immunised people already sufferring from chronic infections such as HIV thus signalling the native immune system to start producing antibodies to fight of this and other infections including new ones to speed up the battle against pathogens with him via this WiFi.All aspects of the primary native immune system can thus be controlled by him via him using this WiFi and bluetooth to cause anti-bacterial,anti-viral and other strains to create specific chemical signals that cause the primary immune system to carry out specific desired actions.The immunisation strains will use this biosynth WiFi to be directed by him to carry out immunisations step by step again using chemical signals created by them wherein they control the actions of dendritic cells,memory B and T cells and plasma cells to ensure surface proteins are shared with the relevant leukocytes and the patient immunised for life.He will through it allow certain leukocytes to be called to the scene of infections to create antibodies,consume pathogens via phagocytosis and control symptoms such as inflammation and fevers.Biosynth WiFi etc will allow him to control stem cell strains to heal wounds in the body both for wounds that occurred prior to the acellerated healing phenotype is added such as tauopathy and injuries to the brain and other organs caused by pathogens,parasites as well as damage to the central and peripheral nervous system that has one confined to wheelchairs and also after it is added to compliment it and also be using biosynth wifi and bluetooth to carry out stem in vivo cosmetic surgery allowing him to mould the interior and exterior of a patient using the strain to replace surgery machines.He will be able to control all of these via this biosynth WiFi and bluetooth and be able to control all aspects of all strains such as make them undergo mass replication in emergencies,control their movements,control their application of CRISPR treatments and synthesis of anti-viral/anti-bacterial/anti-helminthic compounds and also synthetic compounds and antibodies etc stored in their DNA digital storage,control formation into endospores or even apoptosis and flushing out of the body when not needed.Biosynth WiFi can be used by Paean to induce the evolutionary path of all microbes of the same strain or all strains by stimulating taq polymerase and Cas-9 to have them revive new upgrades for new genes for new CRISPR treatments to apply to pathogens etc,new CRISPR treatments to be applied to the patient for new augmentations or remove them as well as for anti-viral and anti-bacterial strains new genes to express new anti-viral and anti-bacterial compounds making upgrades be able to be done at home.He can also use this to turn microbes of some strains into microbes of other strains in order to get them in the body when needed in emergencies.By 2029 most actions will take a while with from 2035-2045 onwards all actions will be almost instantaneous.All actions of microbes will be controlled by Paean vis him existing through fragmentation on smartphones,laptops through biosynth bluetooth and WiFi from routers at home and in public buildings.Public WiFi,wilderness WiFi and satillite WiFi and also that generated from smartphones etc will allow him to do this in wilderness areas.3D DNA printers will be used to create them not only for final fully fledged versions but also those used for clinical trials etc starting from 2025-2029.These will print out the different sources of DNA for each specific strain of microbes and the features of all strains of microbes.All species and breeds of pets such as Canidae,Felidae,Reptillia,Aves and remaining livestock will have species specific microbes of all strains created for them.
These biocompatible microbes themselves using the neural clusters,DNA digital storage,organic nanotube wiring,electroconductive pilli and electroconductive protein and silicon nanowires from G.metallreducens,G.sulfurreducens,ability to generate electricity and electroconductive pilli from S.oneidensis and nanomachines will form the basis for all types of bio-synth technology.Human neural tissue can be engineered into the microbes to allow them the ability of creating this over layers of borophene,silicene,stanene and graphene nanotubes to produce organic/synthetic nanotubes that can send quickly send large amounts of electricity and optic information over short or long distances increasing speeds on par and superseeding human neural impulses when combined.They would even form internal implants such as neural implants,pacemakers,worms and even those used to detect biomarkers of cancer and precancerous cells in hard to reach areas such as the prostrate and cervix,blood components,vital signals etc in vivo when needed by forming tissue structures ontop of organs or when collected together with the nanowires produced by the microbes,genome capsids and nuclei forming biological harddrives with neural synapses forming natural storage and computing centres.These implants that detect biomarkers,blood components can also be connected to the nervous system to detect pain to illicit the production of natural painkillers and also alert Paean and other microbes and nanomachines alongside sending vital signs such as blood pressure,temperature and heart rate,pathogens and blood components etc to ones patient file on demand with them having openings on both ends that allow blood to flow through the implant where biological nanosensors would detect these and then the results to ones patient file and Paean even in fragmented form and communicate with both microbes and nanomachines.These could be collected in samples sent to automated lab and also to be collected in sewage treatment plants separated by graphene sheets and other filters from feces,urine or algae produced there.In the case of a hosts death they can be removed via phlebotomy robots and even them collecting an area to be collected.Traces of the patients own DNA will be present to allow them to survive in the patient without illicitating an immune response.They will use the patients own leukocytes as a baseline to do this with them created by 3D DNA printers to expedite their manufacture even for those used in clinical trials.They will have the same extremophile augmentations as the host to prevent them dying when exposed to these conditions with them possibly having the same anti-ageing treatments as humans to stay immortal with endolith DNA modified to allow them to undergoe mitosis when signalled by Paean.DNA from P.japonica will allow them to house large amounts of DNA for augmentions and large amounts of the patients DNA for preventing them illiciting an immune responses.In time they will function by themselves without nanomachines by interacting with the levels of compounds in the bloodstream and signals from the primary immune system,body including brain signals and pathogens.
Using human leukocytes ideally a patients own leukocytes as a baseline to prevent immune responses they would be hybrids of a patients own leukocytes as well bacteriophages and virophages,prokaryotic and eukaryotic bacterias,macrophages,other leukocytes such as CD4+ T cells/NKT cells/cytotoxic T cells/T lymphocytes/dendritic cells(either as separate strains or a single one),Planarians,Thermus aquaticus,Streptococcus pyogenes,Francisella novicida,yeasts,endolith bacteria or Bacillus F,D.radiodurans and T.gammatolerans,those from psychrophiles as mentioned earlier and Tardigrade,Nitrosomas Beggiatoa,Cupriavidus necator to survive ammonia,sulphur and other posionous gases,induced pluripotent as well as embryonic totipotent and induced stem cells and haematopoietic stem cells as well as Planarians,Hydra or even A.mexicanum recombinant DNA to form any tissue in vivo to treat neurological/developmental disorders as well as replace old dying tissue with new vigorous ones as well as heal wounds and perforations,C.elegans and have recombinant DNA from all of these and others to allow them to interact with all types of pathogens,undergo mitosis,create nanowire scaffolding,create biofilms and coagulants,be biologically immortal,form enodspores,contain mitochondria and vacuoles for energy use and storage,apply CRISPR treatments and contain Cas-9 as well as Cpf1,communicate with the primary immune system and nanomachines as well as itself using chemical signals,exhibit mechanotransduction as well as memory and learning,chemotaxis,use taq polymerase and the Cas-9 to replicate used CRISPR treatments and read pathogen DNA,thermotaxis,carry out horizontal gene transfer on pathogens/the primary immune system/the hosts cells,carry out anabolic and catabolic reactions,form new tissues and repair old ones,survive radiation and cryonics,interact with and seek out viruses as well as produce endolysines,trick the primary immune system into believing they are part of the body with them also able to utilise specific anti-viral and antibiotic materials from a wide range of other animals and plants and also other DNA to augment human abilities.They can be fitted with scratch DNA created by Phanes and DNA from other unicellular and multicellular lifeforms to exhibit extra phenotypes through upgrades.They will be fitted with the same DNA in humans to halt and reverse the effects of ageing in humans.Tweaking the various sources of DNA will allow them to detect different compounds and even carry out different functions of the source DNA.Engineering flagellum into all strains from bacteria such as E.Coli will allow them to move quickly around the body with them having the same pliable body as macrophages from humans or ameobas engineered into them to allow them to move through any part of the body such as between cells and also using the capillaries.Stem cell strains will use this to move to areas where perforations occur and also where stem cells are needed to repair existing neural and bodily damage with anti-bacterial and anti-viral strains will use this to hunt down pathogens with augmentation and ageing strains travelling to all cells in the body.All strains would have flagellum present to allow them to move quickly to where they are they are needed with them also having DNA from bacteria to allow them to undergo mitosis in emergencies when needed ie emergency perforations,infections,tumours etc with Firmicutes DNA present to enter endospores when needed.All replication and entering of endosperm will be controlled by Paean through biosynth wifi to prevent them overrunning the body.All strains would have the ability to utilise CRISPR Cas-9 treatments specific to their purpose and be able to through taq polymerase etc present be able to recreate strands of DNA,undergo mitosis,survive extreme conditions using extremophile DNA,have flagellum to move around independently,exhibit thermotaxis and chemothaxis,have nanomachines,carry out horizontal gene transfer and be based on human leukocytes to not illicit immune responses.Scratch DNA will also be present to create new phenotypes created by Phanes,Paean and Epione added by upgrades alongside other phenotypes from other micro-organisms and also all species from the global database of patient files,Physis using 3D DNA printing for all strains to create their unique hybrids,functions,anti-viral/anti-fungal/anti-microbial compounds,CRISPR treatments as well as even the universal phenotypes of them.A person will have their leukocytes analysed in a lab in DNA analysers to be then printed out again by 3D DNA printers with the relevant DNA of each strain,Biosynth wifi and the patients DNA including that to express that leukocytes.3D DNA printers will be used to manufacture these for each individual patient allowing them to be manufactured at home and in local hospitals.They would contain the patients DNA created by 3D DNA printers as they containing the patients own DNA would not illicit an immune response allowing them to reside in the body constantly and also be able to synthesise compounds through recombinat DNA and anabolic abs catholic reactions with all actions of them controlled by Paean through biosynth WiFi and through yeast DNA exhibit horizontal gene transfer to transfer CRISPR treatments.
Ideally to reduce the strain on all of them to house as much recombinant DNA as possible or prevent them applying incorrect treatments it would possible to have different strains for each patient ie one strain that attacks all bacteria,one that attacks all viruses,one that deals with cancers,one that counterattacks poisons and toxic compounds,one that treats ageing,one that repairs perforations/wounds and injuries as well as creates new tissue,one that augments human all abilities such as weight loss and ability to survive in low oxygen conditions,one that treats diseases they have genetic predispositions to to treat them and prevent them passing this onto the next generation through natural conception thus allowing them to decide which ones are in endospore states and which will be replicated when needed allowing each strain to control its own rate of replication with all having the ability to detect all biomarkers,compounds etc.Each one could use base microbes that can be collected in nodules they build up to be captured and then be fitted with genotypes for upgrades and then inserted into to the patient to use horizontal gene transfer to upgrade the patient preventing rejection though these would be grown in commercial scales to create genotypes for proteins to enhance the immune system.These would be produced in large numbers as a single strain in the body and collected by syringes when they form nodules in the body in an are that has no major arteries like the hand or from unique smelling urine and put in a conveyor belt laboratory to have base DNA to allow for horizontal gene transfer,form endospores,survive cryonics and also use flagellum or chemotaxis/thermotaxis to move around the body in their genome capsid.Ideally these could be a separate strain that is able to undergo mitosis and alongside this in response to certain signals and hormones from the primary immune system,other microbes and the hosts body.Thus these will be used for upgrades for all strains of microbes including giving primitive microbes them phenotypes such as genome capsids and the DNA within,nanomchines,neural clusters and new anti-viral,antmicrobial compounds etc.Those in pregnant women signalled by can using horizontal gene transfer to copy and receive DNA from the mothers unborn fetus and thus allow this to be collected and then the DNA separate from the base DNA to be analysed for it to be uploaded via nanomachines into their patient files as well as allow for the mothers or the infants developmental and neurological diseases such as Downs syndrome,pedophilia,schizophernia,sociopathic behaviour etc to be fixed in utero or upon birth by upgrading the microbes present.The base microbes would be responsible for transferring upgrades and also copy DNA from cells in the host to detect any faults caused by CRISPR treatments and cells in the body to detect their telomere length and age status to wirelessly send the data to Paean and thus other strains to correct these faults and ageing effects.They would also interact with microbes to transfer upgrades and in the case of all strains able to open the genome capsid and upgrade the genes there with them also copying DNA from a fetus into all microbes that traverse into a fetus from the mother via the placenta and breastfeeding allowing for hereditary diseases and ones entire genome to be detected and uploaded to the patient file database early on thus starting patient files in the womb or after birth and thus upgraded microbes to fix genetic mutations that lead to neurological and developmental disorders and even those that could lead to death early in the infants life such as sudden infant death syndrome or impair their survival rates.If possible nanomachines on base microbes can wirelessly transfer the scanned DNA to the infants patient file allowing for their genome to be scanned before they are born and still in utero to use in holographic projections and have their genetic diseases and phenotypes scanned as early as possible allowing for treatments involving other strains to begin in utero.They would in adults etc scan the DNA of all cells or key tissues to see that anti-ageing and augmentation gene therapy has be added,is passing from one generation to the next with them also scanning cells to measure the levels of Phosphatidylcholines and telomere and mitochondrial DNA senescence sent to ones patient file to be analysed by Paean.Any random mutations would also be detected that could lead to cancer etc.DNA to give them flagellum,mitosis and other base properties such as chemotaxis etc could be stored in their genome capsid preventing this from interfering with copied DNA sent to Paean.They could also copy DNA from new undiscovered pathogens in the body to allow their genome to be sent to Paean and Epione to sent to Physis to be analysed for all of its phenotypes and antibiotics or anti-viral compounds to be created from scratch DNA or those from all plants and animals scanned in Physis with the pathogen recreated using 3D printed DNA in bacteria with no DNA in secure labs.They in the case of bacteria would signal to anti-bacterial strains to produce the specific endolysines to be synthesised via chemical signals,nanomachines and also Paean.Also immunisation strains would be sent key genes to create relevant proteins to be then shared with the dendritic cells.This can be also be used to create endolysines and determine what CRISPR and anti-microbial and anti-viral compounds to use with them since connected to Paean by nanomachines or even without nanomachines can determine the schematics of endolysines that can be sent to anti-viral and anti-bacterial strains to produce species and strain specific endolysines for new pathogens to be sent to large numbers of these strains when collected in the lymph nodes or muscles and also genotypes associated with surface protein antigens to be sent to immunising strains to be shared with even a single immunising strain that can undergo replication to then travel to all lymph nodes and then share these proteins with dendritic cells,activate relevant leukocytes and then initiate the immune system to fight the infection.They would also send schematics of strain specific bumpers.These base microbes would themselves have nanomachines and biosynth wifi to transmit this data to both Paean and other microbe strains and as stated would use taq polymerase and Cas-9 to scan the DNA of the pathogens and also the patient.Nanaomachines and biosynth wifi will be used to send the DNA used to create bumper schematics and also endolysines to Paean once the DNA is scanned by them with him and Physis reading the entire DNA to produce both quickly and thus determine the best DNA to use and then tell the base microbes to use that DNA for both anti-viral/anti-bacterial strains and immunising strains and also to send this data to Physis database to create these new genotypes in large numbers in hospitals around the world and also to microbes in patients around the world instantly to immunise them when nanomachines are perfected thus preventing the new pathogens from spreading across the globe with patients in the surrounding area first immunised and then outwards and so on either wirelessly or from hospitals with this also used to create species and specific bumpers to house CRISPR treatments,endolysines and anti-viral/microbial treatments.This sending of DNA would sent to Paean via namnomachines and biosynth wifi connected to the wire and implants he is in but it would also be sent to the nanomachines as the base microbes would be in time using taq polymerase and also Cas-9 be able to read the genome itself and determine the relevant genes for immunising strains,creation of endolysines and also bumpers by themselves or by Paean through wifi online or in an fragmented form on implants who would analyse it and send relevant genotypes from it to create immunising proteins,schematics for bumpers and endolysines to anti-microbial,anti-viral and immunising strains with it also using nanomachines to wirelessly send the DNA to immunising,anti-viral and anti-bacterial strains themselves.The DNA that is in the base microbes could be altered into benign DNA by its own set of genes that regulate this,by Paean or housed in nuclei to form part of the microbes DNA or transferred to another strain that would undergo apoptosis destroying them with the base microbes also programmed to delete the DNA during replication while the old ones containing this undergo apoptosis.Otherwise they could keep this DNA in a storage area and have it replaced entirely by CRISPR Cas-9 when it copies DNA the next time or even break down or rearrange the atoms present into nutrition or replace existing areas in the microbes genome similar to CRISPR in S.pyogenes with the microbes already having key common genes to all pathogens that it can recognise and determine what pathogen it is with human DNA read and determined by it intaking the key sequences that are present in the child but not the mother.If possible these base microbes would have a nucleus specifically for this DNA that it copies from pathogens and also fetuses to allow the taq polymeras and Cas-9 to read it and wirelessly send it via nanomachines and wifi and then be replaced by the next strand of DNA.Thus they will use taq polymerase and Cas-9 to read the genome of fetuses to be sent to newly generated patient files,pathogens to be sent to immunising strains and anti-bacterial and anti-bacterial strains as well Physis and Paean to create antibodies,endolysines for anti-viral and anti-bacterial strains and scan the genome.Taq polymerase and the Cas-9 would be used to copy DNA from pathogens,fetus etc for different reasons with this and the biosynth wifi transmitters and nanomachines reading the DNA with it transmitted to Paean,Physis and other microbes and patient files.Base microbes could form the basis of both handheld and lab based DNA analysers in hospitals,universities and also forensics labs as their ability to scan DNA using taq polymerase and and Cas-9 with them modified to interact with leukocytes and all types of human cells using blood,saliva and cell samples and then send the DNA read in them via nanomachines and wifi to forensics case files and other files with them also part of other analysers such a those required to read DNA including safes,registered devices,voting machines,authorisation for nuclear weapon use for government officials alongside other readings.By using these base microbes the entire human genome could be scanned and read as well as relayed to ones patient and forensics file in a matter of minutes with microorganism read this way too and also this would be used by interstellar space stations controlled by AI to scan the genome of all new organisms whether uni or multi cellular.This can also be done to determine the identity of those who are suffering memory loss and identity of the owners of DNA samples at crime scenes.This would be in both portable and lab based devices in both hospital and forensic labs.The abilities of C.elegans can be used to detect the presences of pollutants,hormones,cancer biomarkers,poisons,date rape drugs,heavy metals and also both inorganic and organic substances with universal receptors intaking the compound and relay its structure to Physis and the case file simultaneously and will use either mechanotransduction or reverse mechanotransduction,chemical reactions seen in more complex or similarly simple organisms and simple and complex neural clusters and systems in them for example Hydra etc allowing the structure of the compound and its levels in ppm,ppb,ppt,ppq to be determined with these again in portable and lab based devices with or without biosynth wifi.This C.elegans,Hydra DNA can be tweaked to act as universal receptors with human neural tissues integrated via human DNA alongside scratch DNA to improve this allowing them to carry out mechanotransduction or reverse mechanotransduction,chemical reactions and utilise chemothaxis and electrical signals including bacteria and multicellular that generate electrical charges in response to these compounds that can analyse the structure of them to then use biosynth biosynth Bluetooth and WiFi to send the compounds structure to Physis to be cross referenced and receive results within minutes.This will also be used by Sysmex machines that detect the levels of blood componants such as erythrocytes,leukocytes and also platelets and also hormones,pollutants etc.Implants in the body would utilise these as well.Like all strains they would have the ability to undergo mitosis and have flagellum.Another important strain would one that will only be able to interact with the hosts native cells due to specific markers on their surface thus applying gene therapy not to fight disease(this will be done by those that fight genetic diseases and also cancer etc)but to modify the hosts genome giving them augmentations to increase intelligence,make one resistant to extreme conditions using DNA from extremophiles such as xerophiles/oligotrophs/T.gammatolerans/Tardigrade/Salmonella/D.radiodurans,increase the rate of neural development as well as increase intelligence quotient and add resistance to pathogens making them unable to infect leukocytes and also organs etc,synthesise essential amino acids etc and from scratch giving them the same phenotypes of H.umbermensch in living patients and through advanced germline therapy and germline therapy and others and not be able to interact with pathogens due to the surface proteins and receptors suited only to interact with human cells and tissues with these like all strains being upgraded.This will be a different from strain that applies anti-ageing genes or it can be a separate ones.Ideally the anti-ageing strains would be able to detect senescent cells and cause them to undergo apoptosis,vaccinate the immune system against extracellular aggregates,break down intracellular aggregates and apply genes from extremophiles and multi cellular biological immortal and cancer free species of animals and other aforementioned functions all in one or separate sub strains that carry out each function of tasks switching from live state to endospore state through signals to carry out work.Their will be also an immunising strain that give dendritic and thus memory helper B and T,plasma and killer T cells proteins of pathogens to make them immunised against all pathogens the patient wishes to be as well making all leukocytes including dendritic cells and CD4+ T lymphocytes as well as all tissues in the body resistance to N.meningitidis,HIV,Ebolavirus etc. prior to infection thus making vaccines and medication obsolete and would be only be able to interact with primary immune system to alleviate strains on the microbes and prevent the primary immune system becoming lazy and too reliant.These different strains will be in biofilms in an endospore state to prevent them using too much resources and only be activated when needed by signals.Another strains that reside in the brain and other important organs could store oxygen as well but the would release short bursts over a period of time shorter than this at least an hour or two but would release sufficient amounts since working together as one and could separate carbon dioxide and other compounds with oxygen atoms into more usable oxygen to be reabsorbed and then released in short bursts again or in real time with the larger ones releasing larger levels over longer periods of time say several hours and would work in sever emergencies and alongside the other strains to keep the host alive.This could be done by them containing large vacuoles from plant cells that store oxygen only or small miniature ones with even DNA from humans that give erythrocytes their haemoglobin also in these to allow them to store extra oxygen outside these vacuoles in the microbes structure and the surface containing haemoglobin like erythrocytes with them being large biconcave,biconvex structures with the same malleability of macrophages with the vacuoles ideally being internal structures using recombinat DNA from plants and animals.These would keep the hosts brain and other vital organs alive during blood loss,heart attacks,strokes etc and as stated would be able to separate oxygen from carbon dioxide through catabolic reactions.Another strain would be those that use natural compounds from plants and even humans to treat insomnia,diabetes,stomach cramps,rheumatism,edema,hemorrhoids,gout,inflammation,pimples etc by detecting the biomarkers of these and also by instructions by Paean.This would render all over the counter remedies and medications obsolete.This would also create acetylsalicylic acid and also turn off/on genes that regulate substance P to treat chronic pain and severe bouts of pain that would cause one to pass out.Another strains created solely for recreational drug users can exist to produce morphine,nicotine,tetrahydrocannabinol,cathinone,cocaine,natural hallucinogens etc and other natural recreational drugs in controlled amounts on demand onsite of the site action such as the brain to prevent overdosing and them affecting other organs with this also to aid in those wanting to stop using them to eventually quit by producing in them in slightly lower amounts overtime with relevant recombinant DNA from the relevant plants and animals.Alkyl nitrites,LSD,3,4-Methylenedioxymethamphetamine,methamphetamine and other synthetic drugs can be synthesised by these strains using catabolic and anabolic reactions in levels that prevent overdosing with side effects reduced or eliminated via microbes repairing the body tissues and also accelerated healing from A.mexicanum etc would counteract physiological effects.Another strain would produce hydrocarbons,animal and plant oils as well as amino acids etc to then allow other strains whether they are anti-microbial,anti-cancer,anti-viral strains and those that deal with the various other features interacting through signals carry out anabolic and catabolic reactions using these to then be able produce synthetic compounds to treat all sets of pathogens,diseases including neurological or functions negating the need for synthetic drugs to be ingested and done so in a manner to prevent overdosing when signalled by each other and Paean.Otherwise the patient would be told by Paean to consume specific fats,carbohydrates and proteins from specific foods in specific quantities to allow excess be used as a means to carry out these reactions by anti-viral,anti-bacterial and other strains thus negating this strain.When humans through gene therapy are able to create all essential nutrients in their recommended daily allowances then patients consuming them through their diet would allow this excess to be used to create this.These synthetic compounds would be created by anti-viral and anti-bacterial strains etc to suppress or treat pathogens of all types such as bacteria,viruses,fungi and parasites and to treat neurological conditions as well as non fatal problems like pimples,acne etc through catabolic and anabolic reactions.It would be done by Paean telling them to do so via biosynth wifi,nanomachines and digital DNA storage with the structure of them stored in the microbes with new ones downloaded and obsolete ones deleted.This would make all existing synthetic drugs of all types for the control and destruction of all types of pathogens,parasites,neurological and genetic disorders etc created by esterfication,industrial process in factories that are controlled and patented by corporations defunct indefinitely and by law since the microbes under the control of Paean could synthesise them in the body when needed in required amounts that are on the site of action reducing side effects and prevent overdosing.New synthetic drugs for all types of pathogens etc would created by Physis,Paean and Epione using simulations and automated labs and once authorised and passing clinical trials would be created when need via instructions from Paean in patients who need them with the fact that they would be created by AI and synthesised in the body would make them by law free alongside existing ones.All existing synthetic compounds to treat viruses,bacteria,parasites,cancer,neurological and genetic diseases and also everyday conditions can be created in the body of patients by various strains of microbes via anabolic and catabolic reactions and its structure downloaded into their digital DNA storage.The chemical structure of these synthetic compounds will be added to Physis to allow relevant strains such as anti-viral strains etc to download them onto DNA digital storage and then produce in the bloodstream or in the stomach via anabolic and catabolic reactions with this rendering private patents on them obsolete since Paean could create the synthetic compounds could at anytime this would render private patents by corporations of these compounds obsolete as they could be synthesised by anabolic and catabolic reactions controlled by Paean at anytime instead of being manufactured in factories and bought in stores with Paean being a legal human being have no need for money and thus have these compounds produced by relevant strains for free countless times inside patients.Paean would have a decided number of microbes create these in the required amounts in the site of action and even in the bloodstream cutting down on the need for binders,excipients as the compound would be created in the bloodstream bypassing the stomach and can also be covered in bumpers to prevent them breaking down and also bounce off human cells or interact only with those they are designed to interact with limiting side effects.The patient would told to consume a set amount of excess fats,sugar or proteins etc for the microbes to create them by anabolic and catabolic reactions.Since produced onsite of pathogens and neurotransmitters etc in the body in levels controlled by Paean it would eliminate overdosing and side effects with them applied in bumpers to further eliminate side effects.This would also save energy and time in their manufacture and transportation to pharmacies and then the consumer and would allow both factories and pharmacies to be turned into communal homes.Anti-viral strains would create synthetic compounds that either kill the desired virus or suppress their replication such as PreP,PEP and protease inhibitors for those suffering from HIV and would be be free since these would be synthesised by them and Paean and not created by corporation with anti-bacterial strains also doing the same for drug resistant bacteria and also for parasites.If possible they may be able to produce antibodies to specific pathogens that are found only in certain populations of the human species especially once their structure is charted and stored in Physis with this of note to N6 and tri-specific antibodies that can kill HIV but are produced by only a small percentage of infected patients with new antibodies for HIV and all other pathogens and even parasites created by AI namely Phanes and Paean using simulations and the known structure of the parasites and pathogens body namely the antigens with them created via anabolic and catabolic reactions.Anti-bacterial strains would create synthetic antibiotics while anti-helminthic strain will create synthetic compounds that kill or inhibit parasites with strains that treat everyday ailments will create compounds that treat gout,insomnia,heartburn etc.Paean will analyse the outer structure of all viral,bacterial and fungal pathogens,parasites etc and extrapolate synthetic compounds that can kill them or inhibit their replication etc that will be stored in their Physis file to be downloaded into their DNA digital storage and then synthesised by anabolic and catabolic reactions.He will also analyse their outer structure to extrapolate synthetic antibodies that will have their structures be stored in their Physis files to again be downloaded onto their DNA digital storage to be synthesised by anabolic and catabolic reactions.Phanes can extrapolate genes to express these synthetic compounds and antibodies that can be downloaded by biosynth WiFi.This would allow them to create them for any pathogen and parasite outside of those they have compounds to fight for them and also new pathogens once their DNA is scanned and the antibodies structure stored on Physis in the pathogens file.It could also do this for parasites and also venoms and heavy metals.Other strains would create synthetic compounds to suppress sexual arousal in paedophiles,episodes in those suffering both schizophrenia and manic depression while CRISPR and stem cell strains cure them with the same done to those suffering from genetically episodes conditions such as parkinsons etc.
The microbes will be subdivided into various strains that carry out specific actions.Each strain will be form a permanent part of the patients body similar to the native primary immune systems from which they will use as a baseline.Base microbes will detect levels of poisons and the species of pathogens acting as the first line of defence to them via sending wifi signals to Paean then alert him to dangers in the body and then control the microbes and primary immune system via wifi and signals with recombinant DNA from Apidea,Hymenoptera,Chiroptera,Magnetospirillum and other unicellular and multicellular animals affected by wifi,magnetism and also those that use electrical signals even those from E.electricus,the mechanotransduction or reverse mechanotransduction of C.elegans or wifi like means of communication and scratch DNA could be used to create biosynth wifi alongside graphene,borophene and stanene nanoprocessors sythesised via tweaked Geobacter and Shewanella DNA and neural synapses created by them aiding in the formation of biosynth wifi present in all strains.It would also copy DNA from cells in the body to measure the levels of Phosphatidylcholines and senescence in the cells and be able to scan the genome of cells in fetuses to set up patient files and this and the ability to measure the presence and levels of compounds and genome will make the basis of lab equipment and machinery in all types of labs.This strain would be tweaked to detect toxins,poisons,alcohol,cancer biomarkers,date rape drugs and compounds that are synergistically interacting with each other in such low amounts such as ppm,ppb,ppt and so on in the earliest stage of contamination and production and break them down and turn them into nutrients for the host and microbes as well as benign compounds through anabolic and catabolic compounds.This C.elegans,Hydra DNA can be tweaked to act as universal receptors with human neural tissues integrated via human DNA alongside scratch DNA to improve this allowing them to carry out mechanotransduction or reverse mechanotransduction,chemical reactions and utilise chemothaxis and electrical signals including bacteria and multicellular that generate electrical charges in response to these compounds that can analyse the structure of them to then use biosynth biosynth Bluetooth and WiFi to send the compounds structure to Physis to be cross referenced and receive results within minutes.The chelation strain activated by base microbes would turn these and heavy metals etc into benign compounds by creating biofilms that clump it together and allow it to be removed from the body via feces and urine with the same applying to any particulates that enter the digestive tract and lungs etc with these strains either flushing the biofilms out or clumping to the individual particulates and atoms of metals in biofilms and being flushed out alongside it with the excess forming endospores.This strain would also produce proteins that either bind to the heavy metals,drugs,poisons etc and then prevent them interacting with the necessary receptors they do and thus allow them to be flushed out or the proteins could interact with the receptors taking up space preventing the poison,date rape drug etc interacting with them and thus having the being only able to be flushed out of the body.Paean via wifi would teach the microbes how to carry out catabolic and anabolic reactions when needed with the chemicals structure saved on digital DNA storage of the microbes with new compounds,antibodies saved on these when the instructions for older ones are deleted.One strain could be an amalgamation of two or three of the aforementioned strains to ensure they can react quickly to multiple threats ie combining bacterial/viral/fungal fighting strains into one that uses relevant CRISPR/bacterial/viral treatments by detecting the surface protein antigens and receptors of pathogens during phagocytosis and sensing biomarkers and signals from the primary immune system with neural clusters and nanomachines as well as Paean giving them some semblance of intelligence to for this for each pathogen.The would also signal when detecting the type of pathogen to the other microbes and the immune system what anti-viral or anti-microbial compounds as well as antibodies to flood the bloodstream and lymphatic system with in order to wipe the infection out instantly.This would have the same receptors as dendritic,CD4+ T Lymphocytes,macrophages,virophages,bacteriophages,virgin B and T cells to flood the bloodstream and lymphatic system with antibodies and anti-viral and anti-microbial compounds insert genes into pathogens like bacteriophages and exhibit phagocytosis.If possible there could be three strains fighting pathogens:One for fighting bacterial pathogens that are hybrids of macrophages,bacteriophages,yeasts virgin B and T cells with anti-viral strains that are amalgamations of macrophages,plasma cells,CD4+ T Lymphocytes,dendritic cells,virophages,virgin B and T cells,plasma cells etc to combat viruses.One could be designed to fight fungi which can be fought using anti-fungal compounds and CRISPR or they can be fought by either anti-viral and anti-bacterial strains using CRISPR to cause them to undergo apoptosis and also become susceptible to compounds at their disposal with all three detecting the surface protein antigens on the surface of pathogens to determine its type and thus what CRISPR treatments and compounds to use.Both strains or the single strain ideally two being used would have another strain that would function like helper T cells to recharge them with chemical signals and/or supply them with stored reserves of proteins,fats and carbohydrates or those synthesised that prevents them dying and giving up or the strains could signal the primary systems own helper T cells to do this.Otherwise the other strain not used ie anti-viral or anti-microbial ones could help the others by providing them with energy in the form of using up fats and sugars in the body or those produced by the strains that produce animal and vegetable oils.Other wise the two strains could take breaks when low on energy and use up excess nutrients and other material taken in by the host.Both anti-viral and anti-bacterial strains would use CRISPR treatments present as ribosomes and in particular plasmids at their disposal as part of their arsenal with these using advanced gene drive technology.They using CRISPR could make any pathogen whether viral,fungal or bacterial susceptible to the compounds at their disposal killing them rather than inactivating them and negate the need to have too many genotypes with them also applying suicide genes,those that cause them to be unable to undergo mitosis,remove their pathogenicity etc.These would be applied via horizontal gene transfer during phagocytosis and also releasing large amounts via protein bumpers with taq polymerase and Cas-9 allowing them to be replicated and recreated one after another with them created on the go via nanomachines or interaction with the surface protein antigens of pathogens deciding which ones to produce or them in the ribosomes and in particular plasmids.Anti helminthic strains would fight off parasites and would be injected into the body when needed.Immunising strains would immunise patients against all viral,bacterial,fungal pathogens and parasites.Anti-cancer strains would separate from others and would be tweaked to detect cancer biomarkers,CD47 and also the same methods used in immunotherapy to detect and fight cancer by using localised flooding alongside the same receptors in Car T immunotherapy and would use venom based compounds such as Polybia MP-1 and TsAP-1,melittin and CRISPR treatments that cause tumours to undergo apoptosis,stunt their growth and also make them susceptible to the compounds they have at their disposal if they dont attack all types of tumours.These would ideally be injected into all patients worldwide prior to them getting cancer and not just those with genetic predispositions to cure them of precancerous and stage 0 tumours before conventional methods detect them ie meaning a person will be cured of them without realising they ever formed with them also applying CRISPR treatments to cause tumours to undergo apoptosis,halt their growth.A strain would exist that produces recreational drugs and another that creates neurotransmitters and natural and synthetic compounds to treat insomnia and everyday problems.Another few important strains would be the anti-ageing strains that applies genetic treatments to combat ageing,genetic diseases and add augmentations merged into one etc and so on with the possibility of hormones,toxins,chemical signals detected by them switching on/off specified genes,receptors on the outside and functions to prevent them applying the wrong compounds alongside the fact that they would be able to modify a pathogen via horizontal gene transfer to make them susceptible to any compound at its disposal.The would also enhance the primary immune system via gene therapy with all anti-viral,anti-microbial,anti-cancer compounds,give the immune system immunotherapy to detect and fight cancers etc.Those that are base microbes,that interact with the hosts cells and enhance the immune system would still be separate strains alongside those that repair wounds and perforations etc as well as building blood vessels.There could be separate strains solely for treating genetic diseases including neurological and developmental disorders present only in sufferers of these as well as applying protective genes to all living patients to prevent them forming again in the human genepool and those to treat ageing and those for augmentations or these could be one strain.The last and one of the most important strains is those that have DNA from Hydra,Planarins,A.mexicanum,induced pluriopotents,embryonic and haemotopiac stem cells that can allow them on demand by chemical signals or from Paean turn into any tissue on demand.These will especially those from Hydra etc have human recombinant DNA added and the ability to change into new tissues via chemical signals and electrical impulses from the biosynth wifi or even electrical impulses from the recombinant DNA from G.metallireducens and S.oneidensis generated by chemical reactions etc in the body or on demand via biosynth wifi.The G.metallireducens,S.oneidensis DNA will give it the ability to generate electricity and electroconductive pilli.This can be used to treat neurological,developmental and genetic diseases by forming relevant neural and other types of tissue to treat conditions such as pedophelia,Downs syndrome and also multiple scolerosis by creating proper neural tissues that would allow the patient to exhibit normal chronopheilia,cure both sociopathy and psychopathy,intelligence quotient and cognitive abilities with in pre-teens and adolescents it would create proper fully mylienated synapses thus decelerating critical and emotional development prior to genetic engineering perfecting this.It would also as detailed later on replace all forms of cosmetic and reconstructive surgery.In the elderly it would form neural,muscle and bone tissue and also skin tissue and could replace dead and dying as well as ageing tissue in any part of the body such as the arteries,heart brain etc with more youthful and vigorous ones with it doing so for skin tissue by causing the old dying layer to undergo apoptosis or peel off via recombinant DNA from Serpentes.Thus it would form the perfect vector for stem cells rather than injection of stem cells by themselves since having flagellum and also being part of the body as well as undergo mitosis be able to travel to any part of the body and create as many copies of itself as required in emergencies as well as in individual.This would be the strain that forms neural,worm and other implants invivo.Thus this system of different strains will be similar to the different types of leukocytes in the primary immune system thus they will be in a sense a secondary immune system that fights infections that the primary immune system cant with each of the strains using their respective equivalents in the primary immune system as a baseline rather than just CD4+ T lymphocytes.Those that cannot have vaccines due to them being to young,weak immune systems etc and rely on herd immunity should have those to deal with all pathogens and viruses especially specific ones with ideally patients inoculated as early as possible ideally at birth to ensure survival and ideally these anti-viral/anti-fungal/anti-microbial ones should have recombinant DNA from all types of leukocytes such as CD4+ T Lymphocytes,dendritic cells,macrophages and those that interact with pathogens and are infected by certain ones to allow them to attack them with the surface of them being an amalgamation of these or use the process’s of switching on/off genes to accommodate this or ideally being separate strains that all have the ability of phagocytes in them alongside the receptors of each one CD4+ T Lymphocytes or dendritic cell or just a combination of T Lymphocytes and macrophages.This and their other properties and functions could augment human abilities and render humans immortal combined with anti-ageing treatments with them residing in the bloodstream,lymphatic system,bone marrow,within muscles,tissues of all types,capillaries and gastro-intestinal tract and all areas of the body allowing them to act instantly on any threats that arise anywhere.All strains will be copies of the primary systems various leukocytes with each type of leukocytes acting as a baseline for each strain with extra strains that are created using human proteins attached to bacteria or even hybrids of the leukocytes.Patients will have their different types of leukocytes extracted using phlebotomy and then using 3D printing will have relevant DNA from other leukocytes and also other plants,bacteria and animals added and then inserted into the patient onsite using phlebotomy robots as the process will take several minutes as well as the option of having these sent to the patients home via a vial and needle or to be quicker they can be created from scratch using base human leukocytes of all types with the individual patients file cross referenced for each individual patients DNA and that from the bacteria,plants and animals required for them to function added and then injected via needle and vial at home or phlebotomy robots in pharmacies,universities,hospitals etc.This could be done by automated machinery and artificial intelligence cutting down costs.This could also be used to create customised Car-T and other immunotherapy treatments by using 3D printing using ones own leukocytes or even just those created scratch containing the patients DNA stored on file lowering their costs significantly.They would also cut down on the costs and time of producing conventional vaccines and pharmacological compounds with them acting 24/7,365 days a year providing on demand treatment with them doing so when one is away from hospitals or have access to drugs ie in the wilderness etc and prevent problems associated overdosing ensuring only the required amount is created when needed for each specific situation by them able to detect levels of the compound in the bloodstream in very specific amounts due to the neural clusters from humans and nervous system from C.elegans.They if corrected would mean no new drugs or vaccines would have to be created to cure every single disease known whether viral,bacterial,fungal,cellular degenerative,neurological or even genetic and the effects of ageing with it using a combination of anti-viral,anti-fungal,anti-microbial compounds as well as CRISPR treatments as well as the microbes ability to form new tissue,cellular rejuvenation either by itself or with them passing this to all native cells and tissues in the body.This will be use to apply CRISPR treatments via horizontal gene transfer to fix neurological diseases,enhance human capabilities such as intelligence and ability to survive extreme environmental conditions,treat genetic diseases,genetic flaws that shorten or impair the hosts lifespan.Those in the gastro-intestinal tract could release nutrients directly into each section to be absorbed or broken down with those in the oesophagus forming bio-films and have recombinant DNA from acidophiles in them to make them resist low pH of the stomach protecting this from acid reflux with them also creating proper flaps in stomach in vivo to prevent this with if possible they could transfer recombinant DNA from acidophiles and from scratch into the genome of cells that line the oesophagus as well.
Recombinant DNA from human macrophages,plasma,dendritic cells and possibly ameoba recombinant DNA would be added to the main strains to make them exhibit phagocytosis and devour certain bacteria and viruses through anti-viral compounds and antibodies instead of enzymes or even surround them to insert CRISPR treatments and also release anti-microbial,antibody and anti-viral compounds as nanoparticles more efficiently limiting their release into the bloodstream.Anti-viral,anti-cancer,anti-microbial compounds,endolysines and antibodies can be flooded across the bloodstream to use the bloodstream and lymphatic system using bumpers as a means to reach all corners of the body especially hard to reach places with this also used by the immunised primary immune system to reach hard to reach places that a tumor or pathogen would hide.These anti-viral,anti-bacterial etc compounds can be applied to pathogens during phagocytosis through the microbes housing macrophage and possibly amoeba DNA that allows them to surround pathogens and apply the compounds then without them being released into the bloodstream that may cause cytotoxicity and it to break down in the bloodstream preventing immune reactions,death or it becoming ineffective.These microbes would be themselves immune to reactive oxygen and would use chemical or biological signals similar those in the immune system unique to them detectable by only themselves but not the immune system and detect those from immune system to detect the presence of and location of pathogens with recombinant DNA from human white cells,from bacterium that utilise chemotaxis and thermotaxis as well as similar properties,from scratch and other cells will be added to their genome to cater to this.Recombinant DNA from bacteria that produce biofilms will be added to allow them to group together to form rigid scaffolding structures and then tissues etc as well as pilli and flagellum from E.Coli allowing for quick movement to the site of infections and also ruptures with the host engineered to produce both native leukocytes and erythrocytes with these to move much quicker and without the need for the heart allowing them to move in the case of heart attacks etc.They may even be able to detect pathogens due to chemicals produced by the pathogens themselves or even surface proteins on the pathogens and when pathogens are detected create clusters in the bloodstream using DNA from leukocytes and bacteria that create biofilms to release there chemicals in unison in large amounts that can flood the bloodstream by creating the dye and exhibiting biolumescence to activate it or attack large groups of cells in CRISPR attacks at once.Primitive and possibly complex neural systems engineered into them may allow them to detect sensations,receive signals from nanomachines,themselves,each other,the primary immune system,biomarkers of disease and neural implants with them form clusters of this to receive signals or even see similar to primitive eye/neural systems present in the most primitive organisms from the Pre-cambrian and Cambrian geological periods.This could include synapses and neural cluster systems similar to human ones in the brain,central and peripheral via recombinant DNA from humans and/or the simple neural systems of C.elegans with it possible to stores metres of neural synapses and similar material within the nucleus or second nucleus similar to the three metres of human DNA in a human cell with these also on the outer cell walls and membrane of the bacteria connected to this cluster.This would including DNA from both C.elegans and humans with regards to those that create both simple and complex neural systems.These would be engineered to hold at least three metres or even as much as possible of human neural synapses with in time these becoming more dense through upgrades and even have more than one cluster connected to each other and the synapses connected to the wall.This would be replicated by those engineered to detect cancers and precancerous cells with in time them programmed through genes or even signals from nanomachines to intake elemental molecules and synthesise biosynth cybernetic systems to receive neural and electrical signals similar to wifi transmitters from each other,Paean and also nanomachines with wifi transmitters making part biosynth microbes.If possible nanomachines themselves will form part of their structure with them either synthesising bio-synth nanomachines or these enter them during their lifespan in or near the neural clusters to more effectively receive signals and carry out orders from both other nanomachines and Paean with even all types of the primary immune system have these again either synthesised by them through engineering the relevant host cells and factories for them or nanomachines coated in protein coats from the patient entering them to again make signalling easier through chemical,electrical and wireless means from Paean.This would also make them more reactive to the presence of toxins,compounds,hormones etc in the human body that would allow for them to communicate with each other more effectively with the neural systems from C.elegans aiding in this particularly due to their sensitivity to toxins and be engineered able to detect biomarkers,toxins,compounds and hormones in the lowest possible amounts with the nanomachines relaying the current and rising levels to Paean alongside any implants present including neural implants and manage responses more quickly with the different strains having the DNA tweaked to detect all hormones,nutrients,pharmacological compounds,toxins,compounds,biomarkers etc of all cancers/diseases/pathogens/viruses, in the lowest levels possible and even detect their exact or general levels in the bloodstream in mls,ppm and ppb or even ppt and ppq so as to allow them and the added human neural systems allowing for quick responses and allow them to determine the best concentration of each substance to produce thus preventing overdosing,to respond to to prevent slow responses or even responding too quickly with them given alongside biological hard drives within its own DNA and nanoprocessors some semblance of intelligence and carry and modify to new situations and pathogens through detecting the surface proteins of pathogens and evolving new receptors and compounds and even strategies,learn from past infections and poisoning events as well as instructions and simulations for all hypothetical situations and new treatments and strategies from Paean sent via nanomachines,carry out catabolic and anabolic reactions to every specific toxin,compounds that enter the body instantly and in prepare specific nutrients etc in specific amounts instantly to prevent the body becoming too overrun with compounds and react to every individual situation uniquely and most importantly be able to respond to orders from Paean via nanomachines effectively.These neural clusters will not have DNA present to allow function but will rather be an phenotype of genotypes in the DNA present in the genome capsid.Recombinant DNA from C.elegans will also allow for chemotaxis,thermotaxis,mechanotransduction,learning,memory to be applied by the microbes with them also adding simple neural systems to the microbes alongside or in place of neural clusters.In time it may even be possible for these to become more intelligent through these on par with animals or even possible sentient either individually through being able to condense enough neural synapses,nanomachines and biological harddrives into them or collectively through chemical signals and collectively joining to each other in a biofilm or neural implants through the nervous clusters of each joining together in a mass using the collective neural clusters combined together and harnessing the processing power of all nanomachines in them and the body combined.This if done to the hosts central and peripheral nervous system would in effect increase the hosts intelligence.If possible these would in time be able to merge with the human neural system both the brain and the rest of the central nervous system and increase the hosts intelligence,neural and cognitive features through the merging of the humans neural systems as well as the nanomachines and neural clusters and DNA digital storage in the microbes or them simply becoming new neural tissue with the nanomachines present increasing the processing power of the new neural tissues in the hosts with this increasing the persons intelligence.Tissues formed in other part of the body through per example repairing damaged organs etc would also increase intelligence quotient by the nanomachines and wiring connecting to the native nerve tissues in these areas,organs etc.In both cases the digital DNA storage gained from the DNA present in the microbes can be used to store data downloaded from the internet,wire and neural system ie memories,emotions,thoughts,movies,structures of compounds etc that can be extracted and deleted by pure thought with each microbe cell holding 3ZB each.Nanomachines,biological harrdrives and neural clusters will also vastly increase the intelligence of the host.These DNA would also store the structure of poisons,toxins etc to recognise and their counterproteins as well as download the structure of antibodies and synthetic compounds produced by them and counterproteins via biosynth wifi with them sent this via wifi with old data deleted.Genotypes for upgrades will be downloaded as well.They could use biosynth wifi with the wifi using public wifi,routers in homes and public buildings and also cellular signals and satellite wifi in the wilderness to download new information.Microbes present could also store extra digital data in the three metres of DNA holding both their genotypes,junk DNA and even the DNA in the genome capsid,mitochondrial DNA,biological harddrives present as well as the neural synapse clusters holding extra information both in the actual synapses but theoretically even the DNA within them with CRISPR or them allowing ones own native cells to be used for this both in the nucleus and also mitochondria with in both case bio synth wifi within the and also the cells and microbes connected to neurons could allow for this information to be read by the central nervous system once downloaded from the internet and wire by pure thought and through Paean or via microbes transferring this when they down this via wifi.CRISPR can be used to add the ability of digital DNA storage and nanomachines to be added to all cells and tissues in a patients body especially with regards to nuclear and mitochondrial DNA increasing the storage capacity of the human body and neural systems exponentially allowing one to store 1,110,000,000,000,000,000,000,000PB or 11,100,000,000,000YB of information with the accelerated healing phenotypes repairing any degradation to the brain caused by overloads of memories with data from this digital DNA being able to be sent wirelessly via wifi and implants to external devices such as clouds,servers,smart devices and external hard drives with unnecessary information deleted at will and extra information downloaded wirelssly.This could allow for humans to store vastly more memories than the hypothesised 2.5 petabytes in the human brain alongside genetic engineering using CRISPR to transfer eidetic memories to patients.This could also for genetic memory to be utilised by humans wherein memories of a mother and father would be passed on from one generation to another through DNA digital storage present in the DNA of both spermatazoa and eggs if applied to all cells using advanced gene drive technology.If not then at least it should apply to biosynths.Technology can be developed that can read memories extracted from DNA.These would act as at biological neural implants through the nanomachines and the neural clusters merging and working together allowing for information being sent to and from the human brain and the wire and play a role in VR indistinguishable from reality through them connecting directly to all parts of the brain and central nervous system or those responsible for temporal comprehension to facilitate the time dilation effect and forming clusters through biofilms.They would also form bio-synth neural implants through these biofilms connecting all microbes and nanomachines with the hosts body with other bio-synth implants such as biosynth pacemakers,neural implants etc could be formed by these forming biofilms and then solidifying into these advanced implants with the nanomachines and the neural synapses present forming into these masses circuitry with them even if possible turning into biosynth nanomachines.Furthermore if they have recombinant DNA from bacteria from the genera Geobacter and Shewanella to produce electronically conductive nanowires throughout these and the nervous system to connect each implant and the brain together.
These biocombatible microbes would be immune to any antibiotics or anti-viral drugs administered orally or even created by themselves so the pathogen can be attacked while conventional treatments suppresses the pathogens ability to grow,reproduce or cause serious problems such as death with this immunity blocked from passing to pathogens and also allow them to thrive indefinitely.It would largely be done because they would be modified leukocytes.This could be done by these having specific genes in plasmids or chromosomes that cannot be spread to the pathogens with these likely being more complex humans strands of DNA or chromosomes or synthetic ones that cannot be traded or passed into the targeted pathogen due to it being more complex,foreign to bacteria or even gene drives,proteins,enzymes etc or them coated by markers,proteins,genome capsids from viruses etc that simply prevent this DNA from being transferred to pathogens preventing the pathogens from becoming resistant to antibiotics then applied to them to kill the pathogen.Production of genome capsids from viruses could be integrated into the microbes DNA to house specifically these genes and plasmids or even chromosomes separate from the nucleus that contain genes that keep the bicompatible microbes immune from applied antibiotics and compounds to kill pathogens/reactive oxygen/anti-microbial agents and antibodies they produce themselves as well as those that ensure its immortality from endolithic bacteria and Bacillus F,genes that create anti-viral and anti-cancer compounds etc,those that make them survive radiation and chemotherapy and from extremophiles,exhibit horizontal gene transfer with anti-microbial and anti-viral strains having this from pathogens to make it easy while those that interact with human cells will use that from viruses and those used in gene therapy or from scratch to prevent them interacting with pathogens etc,give them advanced features like neural clusters and ability to evolve quickly,those that allow them to survive extreme radiation as well as lower amounts of nutrients and water and low pH etc,those that produce controlled levels telomerase production,form endospores and even those that produce human protein coats that allow it survive the human body preventing immune responses that cannot be transferred to pathogens or even cancers for them and the primary immune system to be effective.These capsids would have recombinant DNA from all extremophiles including those in the host already especially acidophiles to allow them to survive the low pH of the stomach to aid in food digestion,synthesise natural or synthetic compounds that treat stomach cramps or heartburn and attack pathogens like H.pylori that reside in the stomach that cause stomach ulcers among other problems and replace their other beneficial functions in those that are asymptomatic carriers.Otherwise H.pylori if they play a role in digestion could be engineered not to cause stomach ulcers with recombinant DNA from acidophiles added to all cells in the human body including the stomach.These and DNA from osmophiles,halophiles,alkanophiles etc allow them to survive all pH ranges,sugar concentrations and extremes both of the human body but also those caused by an overabundance of nutrients for the host and the microbes in the body which can be passed onto the host via horizontal gene transfer in relevant strains with others holding this DNA in genome capsids.DNA from T.gammatolerans will make them immune to radiation experienced by the host.They should also have DNA from psychrophiles,Tardigrade to make them survive low temperatures of cryoprotectants both for storage and also if cryonics becomes a valid science with thermophile DNA added as well as mesophile with these pushed to their limits like those added to humans as detailed later on.Salmonella DNA and others from scratch including those from Tardigrade can also push their limits in terms of surviving extreme environments including in space,low and high temperatures with those from oligotrophs and xerophiles can allow them to survive on low levels of nutrition especially if the host is starved of food and nutrients.Those from as stated psychrophiles,A.mexicanum,Planarians,Hydra, as well as T.gammatolerans and also Bacillus F etc will allow them to survive the process of freezing and rethawing over and over again to recover from telomere damage caused by cryonics and low temperatures.All extremophile DNA will be added to them including metallotolerants with beneficial bacteria in the gastro intestinal tract also given genome capsids housing these phenotypes alongside those that make immune to all of the anti-microbial compounds and even bumpers and endolysines at their disposal and also DNA that gives beneficial bacteria the ability to produce human protein coats to avoid immune responses and prevent them being attacked by the primary immune system especially when it is immunised using the common protein method.Recombinant DNA from all major extremophilic bacteria and those from the Firmicutes phylum that create endospores to survive periods of inhospitable environmental conditions and re-emerge when the surrounding environment is more hospitable through signals from other strains,native immune system and also the body to awaken them and put them back into spores when not needed.These genes including those from endoliths to make them immortal,allow and those that protect them from the immune system etc would be housed in genome capsids to prevent them being transferred into pathogens.Upgrades can allow for new phenotypes to be added specifically to the genome capsids.The beneficial bacteria in the gastro itenstinal tract will be given these sources of recombinant DNA from extremophiles to also survive these conditions experienced by the host through genome capsids and have advanced gene drive technology applied to ensure it stays there for each generation with the native leukocytes via this DNA added to the bone marrow will be able to survive these conditions.Asides from interacting with the immune system they would also interact with the microorganisms already present in the human body for example not harm the native bacteria in the gastro-intestinal tract especially both intestines and in fact augment their abilities through recognising their unique biomarkers trade specific genes with them including if possible those within the genome capsid or when that interact with these specific bacteria by recognising their genome and receptors by interactions with them and the nanomachines synthesise and trade these genes to improve their natural abilities with any dangerous pathogenic bacteria present destroyed or at least made permanently benign and altered to become beneficial and carry out new functions.This would in turn make humans gastro-intestinal system more
efficient,cleaner etc.This would be controlled rates via horizontal gene transfer and vice versa if deemed safe through simulations done by Paean,Epione etc.The capsids in the microbes would contain all extremophile DNA augmentations that is found in the host.Beneficial bacteria in the gastro-intestinal tract would also contain these capsids and the same DNA to protect them from radiation,hypergravity with this done via horizontal gene transfer from augmenting strains and also them created to them via them consumed when created in a lab.The genome capsids in beneficial bacteria will also house this DNA from extrempphiles DNA and those to make them immune to the anti-microbial compounds at the disposal of the microbes and also those that give them human protein coats making them human bacteria hybrids thus preventing the primary immune system using antibodies at them.Thus both microbes and beneficial bacteria in the gut will be engineered to be able to resist the same extremophile conditions as the host via upgrades.The DNA to produce these capsid if possible would be inside these chromosomes and plasmids within them with their synthesis coming from the main set of chromosomes or their synthesis controlled by nanomachines interacting with specific genes in the main chromosomes through chemical signals controlling their replication meaning the expression of genes to produce the second set of chromosomes and capsid would have to be controlled by nanomachines.Otherwise gene drives that prevent certain genes within the first chromosomes from being traded would organise the production of both the capsid and second set of DNA with this also controlled by mitochondrial DNA,switching of certain genes on/off with nanomachines again playing a role with mitochondrial DNA also prevented from being traded.These plasmids and chromosomes would be separate to those that house other phenotypes such as those that are traded to pathogens that would roam free in the bacterias structure in the form of ribosomes and in particular plasmids and/or genes,plasmids and chromosomes in the primary nucleus also housing DNA to initiate the capsids and the genes in them.Unlike viral capsids they would not be traded into pathogens due to them having a complex structure of enzymes,peptidoglycan similar to gram positive bacteria or even cellulose,ligin,hemicellulose,pectin found in plant cells using recombinant DNA from plants and gram positive DNA or viruses unable to enter the pathogens at all with other measures engineered into it to prevent this happening either at the start or by adding new microbes that interbreed with it.Upgrades would allow primitive versions of microbes to gain these.These should be used to house it with the most effective one used to house it preventing it from being traded with pathogens if protomers through either simulations made by Paean and Epione or trials on mice and chimpanzees show that they are ineffective of keeping these genes within them.The first generation of microbes will likely not have genome capsids and the features inside them,nanomachines,neural synapses but will in time through upgrades will have these added overtime by at least the late 2030s with AI namely Physis,Paean and Epione creating scratch DNA or scanning known genomes of all animals that have these or can create equivalents.Primitive versions that can not have these or the important genes that cant be traded with pathogens with in time them added by upgrades with the primitive versions of microbes surviving by themselves with if any pathogens get the DNA inside them by any means can be removed via CRISPR.Upgrades to house more phenotypes would add more genes to the capsid would be made thus allowing DNA inside the capsid to receive new phenotypes with the Cas-9 programmed to open up the capsid or stimulate the nuclear DNA to produce these DNA sequences or them using bumpers that can bypass the protomer capsids.Since eukaryotes these would house the important DNA that keeps them immortal and resistant to treatments,immortal and able to inhabit the body without eliciting immune responses etc in this capsid to prevent them traded with the nucleus housing DNA that give them their characteristics for structure,soaking up of poisons etc,creation of capsids as well as functioning of the cell with these and ribosomes and in particular plasmids and other strands of DNA including plasmids containing the suicide,resistance removing genes etc that are to be traded with pathogens and the host using gene drives.Ideally this DNA would be able to be used as DNA digital storage when they are used as biosynth technology with ideally the same three metres of DNA found in humans present here with the remaining DNA used for upgrades and also for junk DNA used as digital storage alongside the rest.It could also be used to store instructions and data from Paean as well as from itself.Recombinant DNA from embryonic stem cells and even cancer cells can make them produce telomerase making them divide indefinitely with other scratch DNA keeping this in control without become cancerous and divide out of control.Advanced gene drives would keep phenotypes stable and prevent unwanted mutations with recombinant DNA from T.gammatolerans present to aid this with only upgrades adding and removing desired and undesired DNA.Genes in capsids could be transferred to the hosts cells by the use of signals,nanomachines and Paean with the capsid momentarily broken by switching on/off genes down to apply them or synthesis/interactions of base microbes interacting with them copying and transferring these into the host cell with the possibility of microbe strains that are only able to interact with the hosts cells and not pathogens or tumours to prevent them entering the genepool of pathogens due to unique receptors on the microbes walls,the genes synthesised by the bacteria outside the capsid via interactions with the host cells and/or nanomachines or other measures applied by them determined in time by Paean,Epione,Urania and Hecate.CRISPR,Paean and other software combined with each other can be used to create these with bacteria created using the same process as Mycoplasma laboratorium to create a species that is biocompatible that can do this for all existing and new superbugs or one for each superbug with recombinant DNA from the specific bacterium or virus inside to ensure these suicide,faulty or resistance removing genes amongst those that reduce its ability to reproduce or be a pathogen can be transferred successfully with the bacteria used for this unable to become as deadly or resistant as the species they are destroying due to their genome contain gene drives with gene drives also ensuring any genes transferred to pathogens are permanent and passed onto future generations allowing for antibiotic or anti-viral treatments are used.They could even transfer bacteriocidal proteins and compounds to which the beneficial bacterial is immune to into the cell of the resistant pathogen bypassing the cell wall with a single cell of these bacteria transferring these compounds,proteins and genes to many cells of the pathogen in a patient with the possibility of transferring DNA into the pathogens to force them to make bactericidal compounds or even endolysines inside themselves killing them from the inside out.Photoanti-microbial dyes could be engineered to be produced by these microbes or variants that transform nutrients or even carbon dioxide in the body into reactive forms of oxygen that kill pathogens that the biocompatible microbes is immune to and with recombinant DNA from plants or photosynthetic that create the pathways from photosynthetic bacteria with DNA from faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles and scratch DNA that allow them to soak up the excess oxygen produced to prevent it poisoning or building up in the bloodstream and acting as a free radical or causing unforeseen problems.This would also allow the microbes to survive in the body using both carbon dioxide and oxygen in the bloodstream with them also engineered to run on sugars,salts,fats,proteins and other nutrients in the hosts body running on both oxygen and carbon dioxide with them using excess of these to prevent problems associated with overdosing such as high blood pressure,weight gain,heart disease etc.It and other engineering would allow them to separate the carbon and oxygen to create useable oxygen and sugars or store the carbon for this and other uses with chlorophyll engineered into them using bioluminescence to separate the carbon dioxide into and release reactive oxygen though if this produces too much oxygen that may be toxic other DNA from scratch could do this without photosynthesis via bioluminescence such as using those from chemosynthetic bacteria with those from these also turning methane into a fuel source for the microbes preventing poisoning to the host or turning it into benign compounds such as sugars and water.If possible scratch DNA could allow them to produce reactive oxygen without light by using oxygen or carbon dioxide and converting it into this with the host made immune by having recombinant DNA from aerotolerant anaerobic bacteria.Those in livestock would be removed via phlebotomy robots will be separated and either used to create biosynth technology or even separated to be injected into new animals with the blood used to produce Agriprotein.Ornamental and crop plants as well as those in forests,wilderness and areas used for forestry could also have ones created to treat viral,fungal and bacterial diseases with them creating hormones and other compounds to extended their blooming periods,control growth,extend their lifespan and shelflife by suppressing rotting and killing off spoilage and food poisoning,micro-organisms and would reside in the xylem,phloem,leaves,tissues and also roots as well as the soil and even attack pests with them killed in these cases or extracted via nodules and turned into electronics with them passing to new generations via seeds.This would also kill off pathogens in crops preventing them spreading to humans and immunise the plants or even add primitive or fully functioning primary immune systems via CRISPR and would give them by allow them to repel pests,survive all climates and soils etc.They could even augment their abilities and increase their growth and even intake of carbon dioxide and carry out the same functions as in animals.If possible CRISPR could be used to make pathogens benign,unable to infect cells,produce toxins and make them susceptible to attacks from the primary system with again vectors such as asymtomatic carriers and animals treated with this.It would also be used to transfer suicide genes that cause a pathogen to undergo apoptosis.
These microbes since using leukocytes as a baseline would be coated in not only human proteins but specific markers and proteins of pathogenic bacteria,viruses and protozoa without pathogenicity(or ability to mutate)that can be grown in media and then injected into the patient as a form of living vaccine injected prior to infections that through DNA from endoliths would stay in the patients body indefinitely and even pass from mother to child via the placenta breastfeeding or even from person to person through unprotected sexual intercourse including oral sex or physical contact with the genitals with them attacking infections instantly.This could be done by them inhabiting the semen and mouth tissues with them that enter the unborn fetus via the placenta breastfeeding offering extra protection to them from infections carried by the mother,preventing miscarriages and stillbirths and situations that would endanger the life of the mother,aid in the proper development of premature children,correcting genetic flaws in utero including those caused by incest and mutations,encouraging correct neural and organ development before they are born and supplying them with oxygen as well as nutrients should the life of the mother be compromised,the placenta strangles the child,complications occur or the mother should be unable to procure sufficient nutrition of key nutrients and improving success in cesarean births.Bio-synthetic worms will act as as secondary placenta as detailed earlier on should the first one become compromised.They will also be providing extra protection from pathogens during pregnancy and the first months of life after birth before and after they are given proper vaccinations with it protecting unborn fetuses from contracting HIV and protect the mother and unborn child from miscarriages from pathogens such as L.monocytogenes and Salmonella.It will also alert the mother through nanomachines to any surprise pregnancies that occur with it calculating the date of conception.With regards to developing fetuses and infants they could produce omega-3 fatty acids as well as folate in sufficient for proper neural developments and prevent spina bifida and other neural tubule defects should the mother be unable to gain adequate nutrition of these and other nutrients using compounds in the body,excess nutrients etc by detecting levels of these nutrients in the bloodstream and the infants and body repair any damage caused by trauma and supply blood and nutrients should the placenta be compromised and if possible repair the placenta in certain situations or if possible create a second one as a backup.Otherwise the microbes through horizontal gene transfer have the mother and unborn child synthesise these naturally becoming a permanent part of the human genepool.Situations such as the placenta strangling the child will be negated by the use of carbon dioxide as an energy acceptor will keep the child alive with the biosynth worm taking over the job of the original placenta by attaching to the fetus and the primary one severed and broken down by the microbes by decomposing it and also causing cells and tissues to undergo apoptosis.The placenta will be regrown for the next child.They will also soak up and convert alcohol,recreational drugs and other compounds such as pharmacological compounds that may inhibit the proper neural and organ development of of an unborn child into nutrients or benign compounds with excess nutrients flushed out of the placenta or the child could be engineered via CRISPR to be unable to absorb these toxins from the body preventing them affecting proper neural development with this then removed once they reach adolescence or adulthood.Mitotic inhibitors would also be dealt with in the same way by having all patients worldwide have genes added that prevent conjoined twins being formed at all again,making the fetus and indeed all humans immune to them as well with any incidences of conjoined twins dealt with by surgery being aided by the microbes keeping the brain and other vital organs alive,repairing damaged tissues and vessels with bioprinted organs added to both individuals and the microbes repairing any damaged tissues and vessels with limbs such as arms created via synthetic ones as detailed earlier attached to them.Resistance to mitotic inhibitors and all types of teratogens can be added to the human genepool to prevent conjoined twins ever happening with this done via exposing bacteria to them in automated labs and using the new genes to be added.Recombinant DNA from A.mexicanum,Hydra and Planarians as well as Archaea bacteria that exhibit telomere repair added to the human genepool will automatically repair any damage caused by these and in deed any compound or trauma on the neural development thus meaning compounds like alcohol,nicotine and teratogens that affect the brain will have any damage repaired instantly or or treatments applied to allow the unborn fetus made immune to them preventing them interacting with the unborn fetus neurological developing.Any ruptured placentas,wombs that could be repaired to prevent miscarriages with them even covering the womb in a layer of fat and carbon nanotube or spider silk to offer extra protection to the unborn child with them forming worms that would be providing extra oxygen and nutrients to twins,triplets and extra infants during single births.In short they will protect the life of the mother and unborn child during pregnancy to prevent them from being compromised and dying by providing the brain of the infant and mother with oxygen should either one or both be compromised with them also fighting off infections preventing miscarriages,stillbirths and also preventing complications that arise by keeping both individuals alive and even in the case of sudden infant death syndrome correct mutations and keep infants alive in these and any other situations during its first early years with the same applied to sudden adult death syndrome.Each microbes will have base universal human DNA alongside the hosts DNA to prevent rejection to an unborn fetus with if possible them also having upon their genetic screening have their own DNA taken from leukocytes taken during this to then be inserted into these microbes that entered the child during its in utero stage or when it is born via those prepared by automated machinery or doctors present and even base microbes to improve their abilities and prevent rejection through interbreeding.This is why first generation patients should have their own leukocytes used a baseline so when it passes to the unborn fetus it will not cause rejection like normal leukocytes when they pass from mother to child and from father to mother and thus child from unprotected sexual intercourse since they would have base human proteins with this applying as they pass from generation to the next to prevent immune responses.Otherwise base microbes could copy and extract DNA from the unborn fetus and then transfer this to all of the new microbes of all strains from the mother.The DNA from ameobas and macrophages should allow for all types of microbes to pass into the placenta or otherwise the blood samples taken at birth can be used to create a childs own set of microbes to be injected for life by automated machinery or even stored in a vial and injected at home by the mother with all steps automated as much as possible with Paean giving directions.Ideally though the base microbes should be able to extract and copy DNA from an unborn fetus via horizontal gene transfer,read its DNA via taq polymeras and Cas-9,then send the genome to newly generated patient files by biosynth wifiand then share this with those of all strains collected in the placenta or breasts upon the childs birth or during the last months of pregnancy when the child is sufficiently developed to allow them to pass into the the unborn child with groups of each of the strains passing into the child copying and extracting DNA from base microbes and then undergoing mitosis in large amounts in the fetus.The various strains will undergoe replication and enter the child via the placenta and then via biosynth wifi can be through induced evolution via taq polymerase and Cas-9 have areas of their genome changed from their mothers DNA to that of the fetus.This will allow the fetus to be protected while in the womb against pathogens.At the same of this the childs DNA will be analysed by base microbes,read via horizontal gene transfer and taq polymerase and Cas-9 to copy DNA from cells and sent to Paean via biosynth wifi to set up a new patient file that can then have all of its information such as gender,eye colour,hair colour etc put up and its DNA analysed for parental tests and also any genetic diseases it may have and also for holographic projections of the child at various ages extrapolated.Breastmilk fed to a child during breastfeeding would be an another route for them to transfer from mother to child again if they have universal base human proteins to prevent rejection and also amoeba DNA allowing them to squeeze through the breasts when stimulated with all of the strains collected here during and after pregnancy via response to hormones to pass through the breasts into the child as breastmilk and into the bloodstream via capillaries in the stomach and gastrointestinal tract with acidophile and alkanophile DNA making them survive the acidity and high pH of the stomach and gastro-intestinal tract.These in the breast would already have the childs DNA from base microbes travelling from the placenta then added to them via horizontal gene transfer and biosynth WiFi with this done in the breasts holding both the mother and childs DNA.The next generation females would do the same removing their mothers DNA with that replaced with their own childs DNA etc with the same done to those passing through the placenta during the third trimester by squeezing through it with chemical signals and reactions to hormones managing this with also microbes forming nodules after the DNA is changed to be collected via needles and injected into the child at home.These would be all done via the microbes detecting hormones related to pregnancy,lactation and communicating with each other via chemical and wifi signals with this and the microbes having base universal DNA and protein coats or have those from both the mother and child would eliminate any issues relegated to rejection in both the mother and the successive generations.In both cases large amounts of all strains of the microbes from the mother including base microbes would collect in the breasts or womb and placenta to be modified via protein bumpers and horizontal gene transfer to transfer the DNA of the child to the mother microbes and then pass through to the unborn child.Otherwise using the childs DNA scan Paean can wirelessly induce the DNA to be changed to that of the childs by wifi in set number of each strain once they enter the child.Base microbes containg base DNA can scan the DNA of a child in utero and then biosynth wifi may be used to induce the evolutionary path of all strains of the microbes in the fetus into the childs DNA thus preventing rejection once the base microbes scan their DNA and set up their patient file.Otherwise biosynth WiFi could be used to change the DNA in all microbes being transferred into that that contains the DNA of the child.The child’s DNA will be read by Paean and using biosynth WiFi he will set up a new patient file.Once the base microbes have read the child’s DNA and set up the patient file via biosynth WiFi,the biosynth WiFi will be used to change the genome in all microbes in the fetus and child to that of the child.Thus the microbes could pass through breast milk and even the placenta during the late third of pregnancy into the newborn and receive the DNA to be shared with all strains through biosynth WiFi once the patient file is started or Paean could induce evolution in a set number of each strain before or after they enter the fetus with acidophile DNA in the genome of the microbes to protect them from the acids of the stomach.The microbes after undergoing replication in the foetus and child will have sets of them changed via biosynth WiFi into those of all strains that contain the child’s DNA and then enter endospores in it.Paean will determine the best means for each pregnancy allowing them to inhabit the fetus while it is still in the womb and protect it from pathogens that may infect the mother including L.monocytogenes,Salmonella and also HIV.It will also prevent miscarriages and stillbirths by keeping the fetus alive.This would be done ideally when the fetus is formed enough such as during the second or third trimester or if possible the first trimester as first tested on mice and chimpanzees with them doing this in waves during all three trimesters to improve chances of success with the mother ideally immunised against all pathogens especially those that can induce abortions,cause death and pass to the child ie HIV,MRSA and L.monocytogenes with them also fighting off other infections until they enter the fetus.If a mothers womb is inhospitable to carrying young then it may be possible to allow the microbes to alter the environment by creating new tissue,using CRISPR to correct mutations that cause this while breaking down or creating compounds that cause this to occur and also make it hospitable to bearing young.Sterility in both males and females can be corrected with CRISPR treatments.Injection into the blood stream prior to infection would allow them to attack infections instantly when they occur for the entirety of the persons lifetime with them injected into the bloodstream bypassing the stomachs acids with this injection ideally done prior to infections so they attack any incoming infections instantly.Free radicals and also chemicals that building the body as a result of the ageing process will be soaked up,broken down into benign compounds or converted into nutrients with gene therapy routinely done to correct ageing.This regenerative process could also both be done to repair cellular degradation caused by ageing by them turning into new tissues replacing old dead or dying tissue with fresh tissue on the skin,muscles and key organs such as heart,kidneys,brain etc as well as veins and arteries and using CRISPR treatments to repair DNA damage that leads to ageing that will be passed onto the next generation via mitosis on these new and also existing cells and tissues with scratch DNA and those from animals and bacteria that exhibit biological immortality also added to all cells in the body.Having the hosts own DNA in these microbes will ensure that new tissues is not rejected with this done by these strains having their DNA inserted into them during upgrading or if possible using base microbes to copy DNA from the hosts own cells that is automatically corrected by CRISPR for defects including those associated with ageing and then transferred to them and the microbes responsible for forming new tissue with those inserted into them in labs would be also corrected for defects including those responsible for ageing.This would also apply to those responsible for repairing wounds and perforations.Thus these microbes would routinely replace degraded tissue in key organs such as the skin,heart,muscles,arteries,veins,central and peripheral nervous system and brain etc with fresh ones that have the plasticisty,strength and even telomere length and chromosomal features as those of someone in their early twenties as well as mid to late teens giving them a youthful vigour that would be done routinely automatically every few years or decades with any plaques and other compounds associated with old age broken down by the microbes into nutrients and benign compounds with CRISPR treatments to correct defects caused by ageing and deformities.Genes from animals that exhibit biological immortality and those from scratch could be added to every cell via horizontal gene transfer with those relevant to anti-ageing techniques residing within all tissues such as in the brain,heart,muscles and also arteries and other key organs in between those that fight pathogens and cancer etc again in an endospore state.This would be done by the microbes inherent DNA from Planarians,induced pluripotent and haematopoietic stem cells that also have DNA from endolithic bacteria and those like Bacillus F within them and this done by them again every few years and also when they detect biomarkers of cells undergoing senescence or when base microbes copy DNA from cells around the body detect shortening of the telomeres and other biomarkers of senescence.Ideally the ability of Planarians,C.elegans,A.mexicanum,Hydra,stem cells and endolithic bacteria as wells as Bacillus F and aforementioned Archaea extremophile bacteria to rejuvenate tissue from damage,retain memory and never senescence can be transferred using horizontal gene transfer to these existing tissues in all organs such as the brain,heart,skin,muscles and arteries in the host to compliment or negate the need for the microbes and using germline therapy become a permanent part of the human genepool.Thus when cells in body via base microbes are detected to be becoming old they can be replaced by new cells and tissues created by the strains of microbes dealing with repair and ageing that can do this in place of old ones with this replacing tissues in the brain,skin and other organs with key organs replaced with bioprinted ones every few decades that have DNA from Archaea bacteria and the old ones pyrolysised.If possible the degraded tissues in the body may be replaced by new tissue that would have the DNA from the aforementioned Archaea bacteria within them that would then if not have the anti-ageing recombinant DNA,or in the case of bioprinted organs have the cells in them have the DNA from these bacteria with this done if the hosts native cells treated cant be given the Archaea DNA.Ideally the hosts native cells can be treated with this Archaea DNA with them first halting and then repairing the damage already done by senescence using DNA form these immortal lifeforms and also from scratch to ensure the effects of ageing are first stopped then reversed allowing those in middle or even late age say even those currently in their 50s-70s to be reverted to a more youthful age of at least early teens and early twenties overtime which the host can be kept at indefinitely applying the gene therapy to all cells in ones body such as muscles,skin,internal organs and brain with again as stated with the microbes and gene therapy allowing females to have their adolescent peak fertility in terms of carrying young of 14-15 years of age and with males their testosterone peak aged 14-15 indefinitely or on demand by switching on/off genes via CRISPR or them creating hormones.If need be this can be done in waves every few decades until it is made permanent by upgrades.This would be done by extra intake of nutrients such as fats,proteins,carbohydrates and water to feed them as they turn into new tissue with if possible them having oligotrophic and xerophile DNA reducing the amount of resources needed to set these tissues up with if possible this being permanent reducing the amount of nutrients the host would require to survive from then on.These new cells and tissues could also have recombinant DNA from extremophiles present within the microbes already and other organisms such as faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles and scratch DNA etc as detailed earlier on to allow H.sapiens to survive indefinitely in carbon dioxide rich and oxygen low conditions allowing the brain and other organs to run on carbon dioxide in certain conditions such as a stroke or strangulation,heart attacks,sudden arrhythmic and infant death syndrome and similar cardiac ailements,elliptic fits,strokes,trauma and even severe bleeding,blood loss,suffocation,smoke caused by fires,heart attacks,strokes,choking,oxygen free environments,high mountains,swimming,smokey areas for several hours longer or in time even indefinitely.Those from R.sylvatica,Tardigrade,Bacillus F,P.putida GR12-2,H.glaciei,C.pleistocenium,psychrophiles,from scratch allowing for cryoprotectants applied by the microbes,by the cells themselves or even external sources to be applied for cryonics and also survive extremely cold conditions in the external environment that humans could not normally survive with other recombinant DNA added to survive high temperatures,pressures that only extremophiles and not humans can survive.This can be done by the new tissues created by the microbes containing these genes that are spread down by mitosis and gene drives or them spreading them to native cells in waves via horizontal gene transfer and again spread from each generation via mitosis and gene drives.Recombinant DNA from Planarians,A.mexicanum,Hydra and C.elegans can be added to repair damaged tissue.
Upgrades for new augmentations and new phenotypes of all strains can be done via one going into hospitals where they can collect new microbes of the desired strains with new phenotypes,abilities etc.One will arrange with Paean to have it booked beforehand.When arranged by Paean he will interact with the AI of the nearest hospital.Each hospital will have growing rooms where there is a 3D DNA printer that prints out the new microbes with the new genotypes that are grown to several million or billion that is then injected into a vial that has a biosynth chip with the patients ID and is ideally composed of biosynth plastics instead of glass to allow it to be recycled easily with the vial picked up by patients in automated pharmacies in the hospital by sending ones patients ID to it.Biosynth WiFi will allow Paean to cause the existing microbes of that strain to undergoe apoptosis to be flushed out of the body to allow the new microbes take there place.The new microbes can be injected using phlebotomy robots or reuse able biosynth plastic syringes.Otherwise it can be mailed to the patients address where one can inject the microbes using reusable biosynth plastic syringes.Ideally patients will have home 3D DNA printers that allow one to print out and culture their own microbe upgrades using vats,phlebotomy robots and syringes with these upgrades authorised by Paean thus decentralising the process where one can get instant access to them at home saving time and energy with their being a countdown as to when they will be ready.In time biosynth WiFi within microbes can be utilised to negate the need for 3D DNA printers and vats with this done by having WiFi from routers in homes and public buildings as well as that generated by smartphones etc to induce the evolutionary path of genes within the microbes.The WiFi would induce the taq polymerase and Cas-9 to change the genes present in them to evolve into new desired genes.This would delete old genes and replace them with new ones.If perfected it would decentralise the process allowing it be done at home with zero energy use and even be done in wilderness areas using biosynth WiFi generated from smartphones etc.Biosynth WiFi can also change one strain of microbes into another.This will be used by strains in emergency situations such as new infections and new instances of poisons detected by base microbes.If possible biosynth WiFi can be added to the cells of patients to then allow the application of new CRISPR treatments to be recognised by the body with all CRISPR treatments relayed to digital patients file both logged as a treatment and added to the genome stored in their patient will be altered to keep it up to date for Phanes Activation Gene technology,identification purposes,phone numbers etc.This addition of biosynth WiFi to the genome of patients can allow for biosynth WiFi to induce the evolution of genes in a patients cells to allow for them to given the latest a upgrades for augmentations to be relayed to patients within minutes from home via biosynth WiFi with again a countdown used.This can change one type of strain into another with once perfected may render 3D DNA printers obsolete in homes and waiting rooms in hospitals with them still used in homes for home farming.
Microbes can be used as pathogens to attack only specific species of animals and plants by being coated in their DNA with them inoculated via pests and also arthopod biosynths that would mimic the effects of human viruses such as HIV etc by attacking the immune system and causing cells in key organs such as the heart,ovaries,brain etc by attacking the immune system and causing cells in key organs such as the heart,ovaries,brain and testes or roots in plants to undergo apoptosis thus killing them off and causing sterility and stimulate tumourgenesis.Since based on the animals leukocytes and plant cells they would go unnoticed by the hosts immune system and thus be more effective.Human versions of this namely FOXDIE would do the same by first decimating both microbes in the body and native leukocytes and then remove accelerated healing phenotypes and also carbon dioxide used as an energy acceptor to allow the heart and other organs to be attacked as well as allowing opportunistic infections to be able to kill the host with it even removing anti-cancer genes and stimulating the production of tumours by attacking the immune system and causing cells in key organs such as the heart,ovaries,brain etc by attacking the immune system and causing cells in key organs such as the heart,ovaries,brain and testes or roots in plants to undergo apoptosis thus killing them off and causing sterility and stimulate tumourgenesis.Since based on the animals leukocytes and plant cells they would go unnoticed by the hosts immune system and thus be more effective.Human versions of this namely FOXDIE would do the same by first decimating both microbes in the body and native leukocytes and then remove accelerated healing phenotypes and also carbon dioxide used as an energy acceptor to allow the heart and other organs to be attacked as well as allowing opportunistic infections to be able to kill the host with it even removing anti-cancer genes and stimulating the production of tumours.
These biocompatible microbes as stated earlier on would divided into various strains that perform different functions or fight off pathogenic viruses,fight off pathogenic bacteria,stem cell strains,immunising strains that immunise patients agains pathogens replacing vaccines.
Biocompatible microbes that consist of numerous strains will be available by 2029 that can fight off pathogens as a secondary immune system and a vector for applying CRISPR treatments that halts and reversed the effects of ageing.All strains of microbes would use the patients leukocytes as a baseline to prevent them illicit immune response and thus be able to form a permenant part of the patients body.These will be done by having ones native leukocytes examined in DNA analyzers to be recreated via 3D DNA printers to them have all the genes for their abilities and also relevant recombinant DNA to carry out their functions,house biosynth WiFi etc as well as the patients DNA to ensure they can be recognised as the patients leukocytes with 3D DNA cutting down on labour and time in manufacturing them for not only fully fledged versions but also those for clinical trials and even animal trials as part of first generation versions that are easy to manufacture by proto and final Phanes cross referencing the patients patient file and also Physis and proto versions of it.Ones leukocytes will be analysed by DNA analysers and thus have DNA present stored in their patient file and then 3D DNA printers will mass produce them that containing necessary genotypes to give specific CRISPR treatments and anti-viral,anti-bacterial compounds and those that each microbe their abilities ie Biosynth WiFi,ability to replicate etc via printing large amounts of them into a growth medium that then is using bacterial DNA use sugars to undergoe mitosis allowing large amounts of each strain to be injected into the patients.All types of leukocytes will be analysed in automated labs with leukocytes used as a baseline since they will house the patients DNA to prevent immune responses allowing them to form a permenant part of the patients body.The microbes different strains will be created by 3D DNA printers by AI including proto and final Phanes in hospitals,universities and home systems and will contain all DNA that give them all of their abilities such as mitosis,genome capsids,flagellum,biosynth wifi,compounds to kill pathogens,horizontal gene transfer and those for CRISPR treatments and housing key traces of the patients DNA to house patient specific surface proteins,antigens etc to allow them inhabit the body constantly without illicitating an immune response.They can have flagellum and genes from bacteria that allow for mitosis to occur to allow them to create millions or billions of copies and travel across the body to all infecting pathogens and cells in the body with this mitosis controlled by Paean.Flagellum from bacteria such as E.Coli using DNA present from it will be present in all strains allowing them to travel across the bloodstream,lymphatic system and all parts of the body very quickly.DNA from bacteria will be present to allow them to undergoe mass replication when needed with recombinant DNA from both E.Coli,C.perfringens which are the two fastest growing lifeforms on the planet can be added to improve the rate of cell division,replication and mitosis of these biocompatible microbes to respond quickly to attacks and trauma with specific proteins,receptors or sensors built into their cell walls or protein coats better at making them recognise,seek out and interact with only specific pathogens rather than the patients own cells or beneficial bacteria or other biocompatible microbes.The rate of their replication will be controlled by Paean via biosynth WiFi and nanomachines or even if possible chemical signals produced by them and the primary immune in particular levels to prevent them overtaking the body and its resources,ensure their is stable numbers with the endolith and Planarian DNA making them immortal negating them to udergo mitosis too much with gene drives controlling this as well with them programmed to to no longer replicate when they reach a certain population with the nanomachines,chemical signals and gene drives controlling replication of all genes preventing any undesirable mutations that may make them ineffective or even a pathogen themselves while ensuring they still have alterations to ensure genetic diversity and control the evolution of them even producing mutations that would cause desired phenotypes that would fight off other pathogens or add new features negating the need to inject new bacteria that would pass on these phenotypes but would also work alongside this.Signals between each other and the body of the host including the primary immune system will initiate quick mitosis of specific strains in emergencies such as surprise infection,tumours and breaks in the skin,arteries and organs to carry out its functions with when it then solved and control the rate to stable levels and control their levels by forcing excess into endospores and awaken those that are required in emergencies.They would as stated earlier control the creation of the second set of genes and the formation of a genome capsid if possible through this signalling the use of of chemical and electrical signals.The rate of replication and mitosis can be controlled prior to and after the perfection of nanomachines by chemical signals between the microbes with any excess forced into an endospore state by signals with these awoken during emergencies such as internal or external bleeding that require instant attention and to ensure that there is a stable level of microbes.If an emergency infection,tumour growth and wound or even rupture occurs the rate of replication and mitosis of specific strains will be speeded up by Paean through the wire or in a fragmented form in nearby devices and biosnth wifi chemical signals in the body as well as native immune system and the microbes communicating with each other to ensure there is enough with any excess once the problem is solved reverted into endospores to be awoken during the next emergency and excess flushed out of the body via urine and feces to be collected in sewage treatment plants for use in smart devices,computers etc by building up in the kidneys and colon and stimulating the host to defecate or urinate.These in endspores via Firmicutes DNA can hide inbetweeen tissues,muscles,in the lymphatic system and lymph nodes.Having them enter endospores will allow them to stay in the body for prolonged periods of time without using water and nutrients with Paean signallling them via WiFi to enter these endospores and be awoken by WiFi when needed with xerophile and oligotrophic and endolith bacterial DNA lowering their nutritional and water requirements.Others could undergo apoptosis or cause cells and tissues in the body to undergo apoptosis and then replace them by turning into these tissues by for example causing the epidermis to shed dead skin similar to Serpentes if recombinant DNA from them is added to the host and also shed off like skinburn.If possible during emergencies and after them Paean can through biosynth WiFi induce their evolutionary path to change into other completely difffereng strains controlled by Paean with upgrades received via biosynth WiFi inducing their evolutionary path through taq polymerase and Cas-9.Paean will make the decision of which to enter an endospore,which to undergoe apoptosis and which to be flushed out keeping levels stable with this done for all strains and also will control the level of mitosis of each strain in emergencies.Biosynth WiFi from neural implants,smartphones and also biosynth routers and public WiFi will allow Paean to control all actions of them 24/7,365 days a year with him controlling the primary immune system by having the microbes synthesise chemical signals.Paean through biosynth WiFi will be able keep track of the location of each and every microbe of each strain and keep track of the number of each strain thus allowing him to control replication,mitosis and also entering into endospores and apoptosis.This will be done by biosynth WiFi and bluetooth etc at home,public buildings and that in wilderness areas and also generated by smartphones and even neural implants where he exists in a fragmented form.Communication of microbes with each other and the primary immune system will occur via Paean controlling the microbes by biosynth WiFi and bluetooth with Paean controlling the primary immune system by telling the microbes to synthesise specific chemical signals.When any microbes die or if they form new tissues,implants etc then the nanomachines and microbes themselves will signal the new levels of replications and if possible countermeasures can be introduced to prevent mutations that would cause the microbes becoming overrun such as suicide genes or those that stop replication activated by nanomachines and even chemicals inhaled,ingested or injected into the body with gene drives preventing them overrunning the body and or mutating to cause this in first place.Gene drives especially DNA from T.gammatolerans that exhibit DNA self repair will be added to prevent unwanted mutations with upgrades altering the DNA by adding and removing genes.Each event carried out by each strain ie repair of damaged tissues,infections,tumours,immunisations of each type will be logged into ones patient file by date and type.New nanomachines for new microbes could be injected to attach to those without them or in time biosynth nanomachines can be constructed by these and other microbes through illicitation.Synthesis of nanomachines would be done by the microbes creating graphene/carbon nanotube scaffolding or buckyballs and the silicene,graphene,borophene and stanene nanoprocessors and bio synth wifi transmitters in them via wifi instructions from Paean and in time themselves with the electrical impulses from neural clusters and ability to generate electricity using recombinant DNA from both S.oneidensis and G.metallreducens,G.sulfurreducens powering the nanomaterial tubing alongside chemosynthesis using sugars and other nutrients,nanoprocessors as well biosynth wifi synthesising organic receptors and also other layer components to cover these or even biosynth nanoprocessors similar to neural clusters or even extra neural clusters which then merge with the neural clusters.Having tweaked recombinant DNA from different strains of Geobacter such as G.metallreducens,G.sulfurreducens and Shewanella that already create electronically conductive protein and silicon nanowires can be modified and tweaked to produce the carbon,boron,tin and other relevant nanotubes and wiring will allow for this with anabolic and catabolic reactions catering to this.The G.metallireducens,G.sulfurreducens,S.oneidensis DNA will give it the ability to generate electricity and electroconductive pilli and electroconductive proteins,silicon nanowires with tweaked DNA allowing this to occur when it consumes sugar etc.Neural synapses could also be synthesised onto these nanomachines wiring through further engineering.Primitive versions of microbes may have simple forms of nanomachines or none and respond to injections of hormones or those produced by the body or biological compounds and signals they are engineered to respond to to perform different tasks such as release anti-viral and cancer compounds etc but as time goes on upgrades can allow for this and neural synapses etc to be added via interbreeding.Nanoprocessors,buckyball scaffolding and nanowires of nanomachines and microbes could be biosynth ones composed of neural tissues,electroconductive pilli and electroconductive proteins using recombinant DNA from S.oneidensis,G.metallreducens,G.sulfurreducens and Magnetospirillium DNA etc to make it easier to synthesise much quicker during mitosis than those composed graphene,stanene etc.The ability to undergoe mitosis can allow for them to react to emergency infections,perforations and tumours with it also allowing one injected with new strains and upgrades undergoe mitosis to create millions or billions of copies and them entering endspores,undergoe apoptosis or flushed out of the body when not needed.This would ensure the levels of microbes if they form new tissues,are lost through bleeding etc will be a desirable constant level to prevent them overrunning the body or be in such small numbers to be ineffective.The nanomachines would allow them to receive instructions,simulations and strategies for infections and emergency perforations and tumours and create new genotypes from Paean whether in he is in the wire or in a fragmented form on neural implants and devices thus allowing upgrades be done wirelessly from home or in the wilderness via satellites with this even aiding the Amish and tribes in Tibet,Amazon and also Africa.This would be done via the genotype of upgrades sent to the relevant and desired strain and thus initiating them via taq polymerase and Cas-9 to create them in the desired strains including those in endospores that would be temporarily awoken for this with them then signalling to him when they are done upgrading and also when the body has be immunised and also when all the relevant tissues in the body are given these augmentations and anti-ageing treatments.He would allow for augmentation and anti-ageing treatments and also immunisations to be initiated at desired times and also be alerted as to when this is done.It would also allow instant analysis of any toxins,synergistic compounds and also date rape drugs and other compounds not desired to be ascertained in the body by him and have him send them instructions to create specific counterproteins to bind to the receptors in the body and also bind to the unwanted compounds with this also determining what to do in each in instance to prevent death and injury.Also since the receptors on the strains that deal with these to detect would only have to be universal receptors and not have to have different receptors for each one as the phenotype of C.elegans would intake the compounds and through mechanotransduction or reverse mechanotransduction,chemical reactions seen in more complex or similarly simple organisms and simple and complex neural clusters and systems in them would be able to send via nanomachines and biosynth wifi the structure of the compound to him and thus organise what to do instantly.Flagellum will be added to them from E.coli to allow them to travel to all parts of the body to reach pathogens,perforations and also human cells.Digital DNA storage and nanomachines will store known compound structures and to react to unknown ones not sent to them from Paean with unknown ones sent to Paean for analysis.Proteins similar to Cas-9 and taq ploymerase created from scratch could be created that can scan the structure of the compound to then transmit it to Paean with this also method to allow them to detect hormones,cancer biomarkers and not just poisons,date rape drugs and also heavy metals.Having the compounds structure and counterproteins stored on the DNA digital storage of microbes will allow them to prepare relevant counterproteins instantly.This would also work for cancer biomarkers allowing the correct type of tumour and thus its location to be determined via chemotaxis and would ensure they would not react to compounds produced naturally,from food etc,those used for medical reasons ie Flunitrazepam and only react to those in levels approaching the LD50 limit and locate where the compound even poisons are entering the body and thus travel there instantly.Relevant strains would have the receptors and stored structures of compounds relevant to them ie cancer strains would have the receptors for cancer biomarkers created by scratch with the compounds structure in their digital storage with chelation strains housing universal receptors and store the structure of all known poisons and heavy metals in their digital storage with base microbes also housing these to alleviate strains on chelation strains and then alert the chelation strains.This would also be done to detect the levels of blood components such as erythrocytes,leukocytes and also platelets and also hormones,pollutants etc.Ideally each strain would be designed to detect universal substances they work on ie cancer strains react to cancer biomarkers including CD47,chelation strains reacting to only heavy metals,poisons etc to make sure that each strain only undergo replication in the presence of the compound they need to detect and use chemothaxis to locate their location.Biosynth wifi and bluetooth will be integrated into the microbes utilisng DNA from Apidea,Hymenoptera,Chiroptera,Magnetospirillum and other unicellular and multicellular animals affected by wifi,magnetism and also those that use electrical signals even those from E.electricus,the mechanotransduction or reverse mechanotransduction of C.elegans or wifi like means of communication and scratch DNA could be used to create biosynth wifi alongside graphene,borophene and stanene nanoprocessors sythesised via tweaked Geobacter and Shewanella DNA and neural synapses created by them aiding in the formation of biosynth wifi present in all strains.This will allow them to communicate with each other and with Paean using satellite wifi and biosynth wifi at home and from smart devices etc in the wilderness that generate their own biosynth wifi.Paean would tell them what measures to take ie send out specific binding proteins to receptors and the poisons etc and carry out anabolic and catabolic reactions and in what order and manner.It would also allow for them to carry out anabolic and catabolic reactions to create specified nutrients,benign substances and also desired synthetic compounds of medical quality and interact with the levels of nutrients in the body and also interact with strains that produce hydrocarbons and plant and animals oils to create complex compounds or using excess nutrients he would tell them what to do with each compound and how to carry out these reactions and what to create from them.They would receive from Paean via biosynth wifi signals from the wire,smart devces or even neural implants when access is not possible strategies/simulations and orders,instructions to initiate immunisations in infants and adults,when to communicate with the primary immune system using chemical signals and what to tell them ie where to gather in the body/when to receive surface protein antigens for immunisations/what surface protein it is/when to use antibodies and what antibodies to use etc,communicate with each other and the primary immune system via chemical signals and also wifi signals,when to enter into endospore states and also when to awaken from then and even when to undergo apoptosis and even be flushed out of the body,when to undergo mass replication,when and how to turn elemental compounds in the body/from poisons/excess nutrients to create benign compounds as well as synthetic drugs and antibodies or hormones and thus carry out catabolic and anabolic reactions,how to form catabolic and anabolic reactions,when to form implants and worms and also instructions to form new genotypes and delete old ones in all strains via initiating taq polymerase and Cas-9 and DNA replication or simply change certain genes using Cas-9,taq polymerase and forced evolution allowing for upgrades for all strains to be done wirelessly on the spot allowing for this to make upgrades of all types much quicker and not require the patient to go to hospitals.Paean would be able to communicate with individual or whole groups of each or all strains of microbes and manage interactions between them and tell them what to do and where to go and if need be gather the primary immune system to create specific antibodies or gather other leukocytes to manage all aspects of the primary immune system via sending the microbes wifi signals and in turn them sending chemical signals to the primary immune system thus allowing Paean complete control of both the microbes and in turn the primary immune system allowing him to control aspects of battles against all types parasites and infections and also tumours.Paean will thus control the microbes via bisoynth wifi and/or biosynth Bluetooth and also the primary immune system by having the microbes create chemical signals thus giving him complete control of both the microbes and the primary immune system at all times for all infections existing and new and also tumours and also surprise injuries etc 24/7,365 days a year with him doing so from neural implants and smart devices that use biosynth wifi.Paean will also send them new data into the DNA digital storage of all microbes,whole strains or a few microbes in specific strains which can be then be deleted and overwritten later on.Biosynth WiFi can allow Paean to using taq polymerase and Cas-9 to induce the evolutionary path of their DNA to receive upgrades at home for all strains and if possible this could cause some strains to undergo evolution and wirelessly change into other strains by having their nuclear DNA to that of others via inducing taq polymerase and Cas-9 ie base microbes could be changed into stem cell or chelation strains.This can quickly allow one strain to be changed to another in emergencies and without the need to have them created at home.He will control the application of CRISPR treatments to all of the patients cells in the body for anti-ageing and augmentation treatments.If possible all cells in the human body can have biosynth wifi integrated into it to have upgrades sent wirelessly instantly to all cells and tissues from WiFi coming from smart devices via taq polymerase and Cas-9 inducing evolution of genome.Biosynth WiFi integrated into human tissues and cells could allow upgrades for ageing treatments and augmentations to be sent directly into ones genome in all cells within minutes bypassing the need for microbes to apply gene treatments associated with this.Base microbes will scan the DNA of any pathogens and parasites and relay this to Paean who will cross reference Physis and thus relay the name of the species and strain thus activating relevant strains to attack them and use what CRISPR treatments alongside anti-viral and anti-bacterial etc compounds at their disposal and what strategies to use as well as whether to signal the primary immunised immune system to where infections have occured.Once base microbes would scan the genome of pathogens especially new ones they will send it to him and he will send them the DNA to synthesise by wifi to create genotypes for immunising strains to be relayed to them and to then share the proteins with dendritic cells etc or those to be extracted from them via base microbes to share with immunising strains and also how to create species and strain specific bumpers and endolysines relayed to the anti-bacterial and anti-viral strains either telling base microbes what DNA to share with anti-microbial ones and also this done by wifi with this also done for known pathogens like HIV,MRSA etc with them being told what anti-viral,anti-microbial and also CRISPR treatments to utilise for each pathogens ie suicide genes,what genes to use that makes the pathogens susceptible to specific anti-viral/anti-microbial compounds and also what signals to send to the primary immune system to initiate specific antibodies for each pathogen until it can learn this itself and whether these and those in the microbes should be deployed in specific areas or whether to use the lymphatic system or bloodstream.Compounds such as toxins,venoms detected by them will be sent to Paean and they will download counterproteins and antivenom from him once Physis is refferenced and they will be told to start using these or converting the toxins into benign substances via anabolic and catabolic reactions.They would even send data to him such as environmental readings in the blood stream,lymphatic system and also organs and other parts of the body data on the geneotypes of pathogens and parasites etc with them also sending levels of damage of telomere and mitochondrial DNA and Phosphatidylcholines in all cells through base microbes with base microbes in newborns or even in unborn fetuses scanning the DNA in cells thus allowing new patient files to be set up instantly allowing for strategies to cure genetic disease to be done instantly via Paean wirelessly evolving certain strains and create patient files for children in areas populated by the Amish,Amazon and African tribes where wifi and hospitals dont exist using satellites with these setting up implants invivo that measure vital signs and blood components regularly.They would also send him the structure of poisons etc present and thus be told what counterproteins to create sent wirelessly.He would using this DNA allow for the mothers microbes to be more effective at trading and receiving DNA from the unborn child and into a few of each strain and then organise their transfer into the child during the last trimester and also to them via breastfeeding.Through implants the levels of antibodies produced by the primary immune system alongside erythrocytes,platelets and leukocytes of each type will be measured and send it to him.The wifi would also allow nanomachines in all microbes to communicate better with each other and each other strain by sending instructions,DNA from pathogens to be used for creating protein bumpers,endolysines and proteins for immunisation strains specific to a pathogen and strategies instantly.Paean would use this to create unique countermeasures to each infection etc.Implants both neural and those for detecting blood components and vital signs would use this wifi to send and receive data.The DNA present in the nucleus and biological hard drives and in the neural clusters and the clusters themselves of each individual microbe and those in the neural implants will allow them to download,store and delete digital DNA data from Paean,Physis and past experiences such as the unique chemical structures of poisons and toxins and their counterprotriens both synthetic and those from animals,instructions as what to do in certain situations,surface proteins and DNA of all pathogens as well as whole orders of them to allow them to apply the correct CRISPR,anti-viral and anti-microbial treatments and create suitable universal endolysines through phagocytosis for all or specific bacterial and viral pathogens it encounters with endolysine and bumpers schematics for specific strains and species of bacteria and viruses and decide whether to apply them via horizontal gene transfer and also flooding the system with bumpers that attack only pathogens as well as develop countermeasures and strategies towards poisons.By having all microbes in anti-viral and anti-bacterial strains,chelation strains etc house DNA digital storage will allow for large amounts of data to be stored with more stored in all of the neural implants and worm implants that measure vital signs and also blood components would allow larger amounts of information with each microbe by themselves and those in implants containing at least 3ZB if three metres of DNA found in humans is present here that can be deleted by thought,by wifi by Paean and share information from each other different microbe managed by Paean using wifi and also download information from the wire namely Epione,Paean,Physis.Cas-9 and taq polymerase can allow data to be copied,deleted and transferred to and from each microbe,entire groups and all of them as well as to and from Paean,Physis,the wire and internet and electronics such as smart devices etc.DNA from P.japonica can increase their storage rate to 150ZB.The microbes digital storage can be be managed by Paean with them individually carrying different data from other ones and also universal data relevant to each strain with the data deleted by Paean and also new information downloaded by wifi with this including the structures of poisons,heavy metals and pathogens and their counterproteins,bumpers,antibodies etc and also all types of synthetic compounds to be produced when a specific pathogen is detected,genotypes of pathogens and the data to be used to create new genotypes for upgrades as well as the structure of synthetic compouns to fight off bacteria,viruses,fungi and also parasites as well as everyday conditions.The wifi will allow them to send and receive data,instructions from Paean as both in areas with wifi and without using cellular and satellite wifi services with them also able to send data such as scanned DNA from pathogens especially new species and strains,the hosts genome to measure levels of telomere and mitochondrial DNA senescence and Phosphatidylcholines,denote when all cells in the body have been upgraded with augmentations and also ageing treatments,send the DNA of newborns added wirelessy to newly generated patient files with worms and implants formed by these would send vital signs such as heart rate,levels of blood components ie leukocytes/erythrocytes/platelets as well as hormones in the blood and areas like the womb.The structure of compounds such as drugs,heavy metals,biomarkers for heart disease and cancer,erythrocytes,platelets and leukocytes and nutrients in ppm,ppb,ppt,ppq would be sent once analysed by universal receptors and mechanotransduction or reverse mechanotransduction,chemical reactions seen in more complex or similarly simple organisms and simple and complex neural clusters and systems in them and they would send DNA of pathogen and parasites to be analysed Paean and Physis.They would receive instructions as to initiate gene therapy of all types and also send when they finish and also instructions to create upgrades and also information such as the structure of compounds and how to carry out catabolic and anabolic reactions for each pathogen,ailment or condition.The base microbes would scan the DNA of unborn fetuses and also new pathogens as well as levels of telomere and mitochondrial DNA senescence and also levels of Phosphatidylcholines using taq polymerase,Cas-9 and CRISPR to copy its DNA and send signals to the neural implants in the body or directly to Paean.Biosynth WiFi will be used to send data back and forth between Paean and microbes as well as allow the microbes to communicate with each other using WiFi generated by routers at home,in public buildings,public WiFi from biosynth trees and that generated from smart devices and computers with if need be them also using biosynth Bluetooth if WiFi access is not possible or present.Biosynth implants will more easily allow Paean to He would more easily control their actions and their interactions with the primary immune system via chemical signals including immunisations,interactions with each other and the primary immune system ie all strains and all microbes in each strains and also the transfer of microbes from one generation to the next ie transfer the childs DNA to the microbes in the mother collected in the breasts or transferred via the placenta via either collecting DNA from the fetus or wirelessly initiating them to change DNA in the microbes nucleus from those collected via base microbes and the newly generated patient file.Having control of all strains of microbes via biosynth wifi could allow him to perform strategies on how to attack specific pathogens especially new ones and also have them initiate the immunised primary immune system,control the primary immune system via chemical signals initiated via nanomachines in microbes,perform simulations and send strategies against all infections and tumours and ruptures,simulate and carrying out countermeasures towards heavy metals as well as date rape drugs and also poisons instantly and initiate the creation of synthetic compounds and carrying out of all anabolic and catabolic reactions more efficiently and ensure drugs both medicinal and recreational either synthetic and natural produced by them will be only in desired amounts preventing overdosing.The structure of synthetic compounds and antibodies can be stored on the DNA digital storage of them and this would also include instructions on how to create them with them constantly linked to him and each other via wifi allowing them to create them only in required amounts and on the site of action with this data sent via wifi and deleted when necessary alongside all other data.Genotypes for upgrades would be sent to them wirelessly as wifi would allow for new ones to be added and old ones deleted for all strains with him initiating taq polymerase and Cas-9.The implants would allow him to control their interactions with the primary immune system by initiating chemical signals produced by them to initiate certain actions ie collect in areas to fight off infections with antibodies,collect in areas to receive surface protein antigens from immunisation strains and also initiate the production of helper T cells,memory B and T cells and also plasma and killer T cells and even the actions of all types of leukocytes in each battle.He would also control the apoptosis of human tissues in the body ie muscles destroyed to initiate natural healing processes to burn up fat and build up muscle,apoptosis of cells and tissues housing pathogen DNA or housing pathogens and initiating the use of those that replace damaged tissues in the case of injuries such as perforations.All actions of both all strains of the microbes and the various types of primary immune system will be controlled by him directly and indirectly.Since connected to them directly and in close proximity he will be able to send and receive data and instructions with him also also teaching the microbes and primary immune system via their chemical instructions how to detect cancers and also infections more effectively by themselves with MRI scans and also results from test kits etc to do so and direct them to specific sites of the body.In short all strains of the secondary and primary immune system will be controlled more efficiently via implants both directly and indirectly via nanomachines biosynth wifi and also chemical signals.If possible they could cause some strains to undergo replication and have some wirelessly change into other strains by having their nuclear DNA to that of others ie those that treat neurological,genetic and developmental disorders to treat a fetus invivo.Data can be stored on internal biological hard drives present when in fragmentation and wifi is not available ie readings of vital signs and internal temperature and also levels of erythrocytes,platelets,antibodies etc from other implants or themselves with this sent in packages to ones patient files when wifi is gained with it having its own internal clock with time and date being for the current or chosen timezone.These biosynth neural implants will form the basis of VR technology indistinguishable to reality feeding simulations and sensations such as pain,pleasure,tastes,smells etc directly into the human brain and central or even peripheral nervous system and will allow one to stream data from the internet and the wire,store thoughts,memories and also wirelessly communicate with others from around the world.Base prototypes of microbes will probably not have nanomachines and as such will require signals coming from injected chemicals to stimulate actions and them releasing chemicals that can be detected by home test kits of all types or creating unique smelling urine and sweat with upgrades via base microbes adding the ability to create biosynthetic nanomachines.These fully fledged versions should be possible between 2035-2045.Having them engineered to enter endospores using recombinant DNA from Firmicutes and have DNA from oligotrophs,Tardigrade and xerophiles,endoliths other large animals with slow metabolism and scratch as well as endolith bacteria will allow them to survive on low levels of nutrients either when the host is low on stored food,low on nutrient intake,survive long periods without using excess nutrients,putting strains on the hosts resources or those stored in the body and allow them to form endospores through signals especially excess ones to prevent them overrunning the body and using too many resources ensuring there is enough for the host to survive with them also engineered to utilise gases and liquids intaken by the host whether they are beneficial or even toxic to the host to create nutrients for the microbes and the host.Paean via biosynth wifi tell them when to enter endosproes and when to get of them.Vacuoles in human and other animal cells to store excess sugars and proteins during this state or when in an activate state can be added using recombinant DNA from humans with them also containing mitochondria to utilise sugars and proteins.DNA from Wangiella dermatitidis,Cladosporium sphaerospermum and Cryptococcus neoformans can be added to these microbes to enable them to radiosynthesis,that is,to use the pigment melanin to convert gamma radiation into chemical energy for growth thus helping them use it as a food source.Excess sugars,proteins as well as fats in the hosts body in the bloodstream or stores will be used by them alongside poisons and drugs converted into these for nutrition via anabolic and catabolic reactions with chemosynthetic DNA allowing metals and minerals to be used with them having DNA from faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles bacteria and scratch DNA to allow them to run on both oxygen and carbon dioxide meaning they wont starve the host of oxygen and will prevent the build up of carbon dioxide in the body.If the host and microbes has both oligotrophic and xerophile DNA then this will mean that the host normal diet will supplement these in vacuoles or the microbes could deposit these in areas inside the body ie store of fat in the body surrounding organs and in appendix like areas created by them that can be used as it its or converted into sugars.The endolith DNA also reducing nutrient requirements even further due to their slow metabolism especially if both hosts and microbes have them.Thus they can communicate with the hosts body to signal it to deposit fats around organs constantly and not under the skin that can be used as a repository of food for them to run on when they run low on energy and are in the middle of emergencies where they will be need to undergo mitosis.Once stores of fat are used then these will be replenished by chemical signals to the brain.These will be engineered to house vacuoles present in all eurkaryotic cells to store excess energy when needed.If possible there may their version of the helper T cell that stores large amounts of sugars and fats in them in vacuoles that during emergencies like perforations and also infections etc the version of the helper T cell can release this in close proximity to them during battles to allow the microbes to feed on them or even after infections when they collect in areas like the appendix to release them to starved microbes.Ideally to prevent them overheating the oligotrophic DNA and those from slow metabolizing endolith bacteria and even Tardigrade that can lower its metabolism by 99.9% can prevent them burning up or the host with this also limiting their need to use too much resources.Xerophile,oligotrophic and Firmicutes DNA will reduce the amount of food and water they need exponentially.DNA from W.dermatitidis,C.sphaerospermum and C.neoformans once one is also made immune to radiation via DNA from T.gammatolerans,D.radiodurans can be added to the microbes to enable them to radiosynthesis,that is,to use the pigment melanin to convert gamma radiation into chemical energy for growth thus helping them use radiation as a food source should food be scare and instead of excess nutrients.They will have the carbon dioxide acceptor phenotype making them engineered to unlike humans cells run in carbon dioxide as an energy acceptor and release oxygen in the process not only ensuring a continuous supply in the body especially if a heart attack or sudden stopping of the heart occurs but also preventing them competing for oxygen that the host needs.DNA from Bacillus F,T.gammatolerans and the ability to replenish Phosphatidylcholines will be added to ensure that even though they may undergo mitosis they will still have the same eternally young telomeres in their DNA even if they undergo replications billions or trillions of times.This will allow them to live indefinite lifespans in the body unlike normal leukocytes.The ability to carry out mitosis will come from genes from bacteria responsible for this with Paean through biosynth WiFi controlling the rate of replication of all microbes of all strains thus allowing for large numbers of a specific strain to be mass produced for emergencies such as infections with biosynth WiFi allowing humans to know the exact number of each strain and their location in the body and chemical signals from each other and biosynth nanomachines controlled by him will prevent them overrunning the body with as stated excess ones entering endospores and reawaken instantly when new infections and tumours or even bodily repair etc needs to be carried.Firmicutes DNA will allow them to enter endospores when not needed to reduce their resource use as they will use none when in this state with excess ones flushed out of the body or signalled to undergo apoptosis via biosynth wifi signals from Paean creating suicide genes for the same reason.Theoretically these endospores could be a means for excess ones to form biofilms in key areas where infection,brain and organ damage may occur and not use resources but be activated by signals be activated to repair damage,create new tissues and fight off infections and in the case of infections that are fought return to this endospore state with those turned into new tissues staying as tissues either permanently or temporarily to allow the bodies natural repair mechanism to take over with the remaining microbes signal replication of more to take their place.Thus their ability to form endospores will allow them to reside in tissues to be awoken by signs of infection,internal and external damage,cancer biomarkers,hormones or signals from different strains or on demand with different strains doing this in different rounds or shifts.This entering and exiting of endospores will be done via turning on/off genes via biosynth wifi controlled by Paean inducing the evolutionary path of them or chemical signals to turn on/off.Thus Paean can through biosynth WiFi turn genes on/off via inducing their evolutionary path via biosynth WiFi or inducing chemical signals to enter endospores and be later reawakened from endospores when an infection etc occurs thus preventing them overrunning the patients resources and be stored in any part of the body as in an endospore form they will shrivel and reduce their size by as much as 50-90% and thus can also be used to allow them to reside in the body for long periods of times without using resources such as sugar,fats etc.Other strains and microbes will be made to undergoe apoptosis and be flushed out of the body through urine and feces to be collected in sewage treatment plants.Microbes will be able under the control of Paean to be made to simply enter the gastro-intestinal tract and kidneys thus allowing them them to be flushed out of the body alongside feces and urine.In this case before they are flushed out of the body thus way they will have all extremophile DNA present removed alongside that of the patients DNA removed via inducing their evolutionary path so as to allow them to be killed off by the radiation,drying processs in sewage treatment plants and recycled.Biosynth wifi will allow Paean to have complete omniscience over the number of microbes of each strain and their location in each patients body and thus control the number of microbes of each strain at all times.The microbes will contain scratch DNA to prevent them undergoing mitosis by themselves when their are no signals from Paean meaning they will only undergo mitosis when told to so by Paean to prevent them overrunning the body with them controlled by biosynth Wifi generated by smartphones,routers etc
All microbes of all strains will house DNA from Apidea,Hymenoptera,Chiroptera,Magnetospirillum and other unicellular and multicellular animals affected by wifi,magnetism and also those that use electrical signals even those from E.electricus,the mechanotransduction or reverse mechanotransduction of C.elegans or wifi like means of communication and scratch DNA could be used to create biosynth wifi alongside neural synapses created by them aiding in the formation of biosynth wifi present in all strains.Biosynth WiFi will allow Paean to control all of their actions during cancers,infections and ruptures with through them creating chemical signals can allow him to control the primary immune system.All strains will be able to use Biosynth WiFi etc to send data back and forth to Paean and patient files such as detected infections and poisons and structure of synthetic compounds to be used by them alongside instructions on what to do for each infection etc.They will house Soteria the universal anti-virus software and receive updates to this routinely..Biosynth WiFi will allow them to receive upgrades via their genome changed via Cas-9 and taq polymerase inducing the evolutionary path of them.Biosynth wifi will allow all of a desired strain to awaken at once once neural implants,implants that detect vital signs and also other microbes including base microbes detect cancer biomarkers and pathogens with them first signalling to Paean to cause the rest to undergo replication with if need be Paean even causing different strains to be turned into other strains via wifi inducing the evolutionary path of them via taq polymerase and Cas-9.Cappiliaries can be used for them to reside in areas in between the bloodstream and organs with them also residing in the gastro-intestinal tract,lymphatic system,on the surface of the exterior and interior of organs,in the lungs again in either their endospore state or as normal with them even residing in between cells and tissues in the body and transporting nutrients,oxygen and carbon dioxide to and from cells from the lungs and bloodstream rather than blocking their access to native cells acting as a relay system and again synthesising oxygen from carbon dioxide and nutrients of all types such as sugars,amino acids etc on demand.If possible new organs could be constructed by them by the construction capillaries and small veins and scaffolding in order to store large numbers of them to be released in emergencies.Otherwise they can reside in the appendix with small appendix like areas created around the body via the stem cell strain to store large numbers of each strain in to be stored in endospores and thus awaken in emergencies.Those that reside in these areas can be use to augment the abilities of specific cells and tissue such as muscles,neural tissue etc with them also augmenting and speeding up the actions of these and other organs and parts of the body ie nephron/kidneys,small intestine,pancreas,stomach by speeding up their processes,alleviating strains on them if they become overstressed especially with regards to breaking down alcohol and drugs etc,repair them etc.If the microbes need to be gotten rid of they can have suicide genes activated by wifi that cause them to undergo apoptosis or ideally they can be flushed out of the body via urine or feces by ordering them to exit through the urethra and also clinging to feces where they can be collected,extracted and then cultured and possibly given a new host especially when the host dies or used in the creation of electronics.This may also be done if there is too many of any or all strains in the body especially after them having to multiply quickly to deal with surprise infections and tumours that necessitated rapid growth with them collected in the sewage treatment plants to form bio-synth technology once sanitised with narrow UV wavelength that they will be immune to unlike any pathogens or they then can have their DNA modified to be inserted into another human host or even animal host.Thus after emergency infections and also ruptures etc as well as once augmentations etc are applied then the excess will be flushed out of the body through urine and feces and collected in sewage treatment plants with leftover stem cell,anti-viral etc strains left behind in the body to fight off the next infection etc.If possible these could even be used to form biosynth implants,devices and computers outside of the body and inside the body.Bacterial DNA that gives them ability to undergoe mitosis will be present including DNA from fast growing bacteria in E.Coli,C.perfringenes that will will be controlled by biosynth WiFi controlled by Paean thus meaning they will only be able to undergoe mitosis when told by Paean to control the rate of mitosis in emergencies to prevent them overrunning the body with there being scratch DNA wherein this replication does not occur normally but only during when told by Paean to do so.Thus biosynth WiFi,bluetooth and cellular access will be built into them and will be generated and utilised by them to crossrefference Physis when they intake the structure of compounds and DNA from bacteria,fungi,parasites and viruses to identify their exact compound species of species of pathogen and relay this information to Paean to allow him to decide what to do next as well as receive instructions from Paean and they will use it to download the structures of anti-venoms,antibodies,synthetic compounds downloaded from Physis onto their DNA digital storage synthesised by anabolic and catabolic reactions.Paean will through WiFi control their replication across the body in emergencies and via WiFi signal them to undergoe apoptosis or enter endospores and be flushed out of the body by entering the kidneys and gastrointestinal tract to be excreted by feces and urine when not needed to prevent them overrunning the body with Biosynth WiFi relaying to the levels and numbers of not just all microbes but the levels and numbers of each specific strain allowing him to control their replication and numbers at all times etc.Biosynth WiFi will relay to him the exact location of each and every single microbes of each strain.Although they will have genes from bacteria to undergoe mitosis they will contain scratch DNA to only undergoe mitosis when told to do so by Paean by Biosynth WiFi,bluetooth to prevent them overrunning the body so as to allow him to control their numbers.This will mean that when there is no Biosynth WiFi etc signals they will not undergoe mitosis and will only do so when told by Paean.This will prevent them overrunning the body and also allow Paean have complete control of the microbes replication.Should an emergency infection or inbibing a toxin occur he will cause specific strains to undergoe mass replication to remedy the situation with once the infection is resolved he will signal excess numbers of them to enter endospores,be flushed out of the body or undergoe apoptosis.He will use this to also control their movements across the body to where they need to attack tumours,pathogens etc and also to apply CRISPR treatments to all cells and tissues with him able to control what treatments either CRISPR treatments or specific anti-viral,anti-bacterial and anti-cancer treatments etc and when to apply with him able to using WiFi from neural implants,smartphones,laptops and WiFi routers including in public to control all actions of all microbes.All actions such as attacking pathogens,applying CRISPR treatments to the patients cells and also their replication,apoptosis etc through CRISPR treatments,synthesis of natural and artificial compounds through recombinant DNA and also anabolic and catabolic reactions and also creating chemical signals to control the primary immune system will be controlled by Paean 24/7,365 days via biosynth wifi.All actions carried out by the microbes will be controlled by him communicating with them through Biosynth WiFi and biosynth bluetooth from WiFi and bluetooth generated by smartphones,computers and routers etc.Since existing in smartphones in a fragmented form he could do this while in the wilderness and at home through the smartphones generating their own biosynth WiFi.He will be also able to control what information is downloaded by them and deleted.Most microbes could hold at least 3ZB of data within DNA digital storage on them with DNA from P.japonica increasing this to at least 150ZB of information.Each microbe could hold this amount of information and either house the same information as all other microbes of the same strain or all strains.Information in these biological DNA digital storage harddrives will include the structure of synthetic compounds,synthetic antibodies relevant to each strain and for anti-viral,anti-bacterial and anti-helminthic strains with them also downloading structures of natural antibodies created by populations of humans both naturally or as a result of vaccines and immunisations or synthetic ones extrapolated by Phanes and Paean.Also represent will be counterproteins and anti-venom to poisons,toxins,heavy elements extrapolated by Phanes and Paean alongside structures of bumpers meant to transport CRISPR treatments and anti-viral,anti-bacterial and anti-helminthic compounds to prevent them breaking down in the body and prevent cytoxicity with Paean arranging the type of information present in each individual microbe from Physis with unwanted information deleted and new information downloaded from Physis etc within minutes or even in time by 2045 onwards within seconds due to improvements in Paeans computing power and strength of the biosynth WiFi and bluetooth.Taq polymerase,Cas-9 etc can be used by Paean to copy,transfer and delete information on all microbes.The P.japonica DNA will allow the microbes to also house more DNA for more DNA augmentations for allow them to survive different environmental conditions and also more DNA to house more abilities and natural compounds to synthesis through recombinant DNA.The biosynth WiFi and bluetooth will be generated by the microbes with them also using that produced by public biosynth WiFi and bluetooth and also that from routers in homes,public buildings and vehicles such as cruise ships,aeroplanes etc.He will be able to through controlling the evolutionary path of microbes induce upgrades giving them new abilities.Biosynth WiFi and bluetooth generated by smartphones and laptops in close proximity and even that generated by biosynth neural,vascular and other implants in the patients body where Paean is housed in via fragmentation will also be used with the biosynth WiFi and bluetooth and allowing Paean to control all as aspects of the microbes 24/7,365 days at home,in public areas and buildings,vehicles and wilderness etc.Thus biosynth WiFi built into the microbes will allow them to receive instructions from Paean with him residing through fragmention in smartphones and neural implants in close proximity that generate their own WiFi to allow his control of microbes to be continuous in wilderness areas.Wifi routers in homes,public buildings and public WiFi will allow them to be carried out there.Even WiFi generated from laptops,smartphones etc will allow him to control their actions.As a result as long as there is WiFi access Paean can interact with and control all aspects of microbes in the body 24/7,365 days a years.He can exist in a fragmentated form in smartphones,laptops,biosynth implants in the body to control the actions of microbes at all times using the biosynth WiFi etc to control all actions of them when in the wilderness areas etc.Paean will use this biosynth WiFi,bluetooth and cellular access to determine the location of each and every single microbes of all strains in the body and send them instructions such as where to go in the body,what anti-viral,anti-bacterial,anti-helminthic compounds from recombinant DNA present to synthesise and what synthetic compounds and antibodies to synthesise via anabolic and catabolic reactions including those downloaded onto their DNA digital storage to be produced and within what amounts by which strains with him also deciding how many of each strain will be produced.He will also tell them what anti-ageing and augmentation CRISPR treatments to apply and to what cells in the body to apply them to and what CRISPR treatments to apply to pathogens,parasites etc through initiating horizontal gene transfer and transfer of genes as well as to download new CRISPR treatments via induction of the evolutionary paths of DNA present and also downloading the structure of synthetic compounds in DNA digital storage and tell them to synthesise them through biosynth Wifi and what pathogens etc to apply them to and he will control their strategies in all infections,tumours etc and download,copy,transfer,delete data on them and data on sent back and forth to patient files,his networks etc and he will control all aspects of immunisations,attacks against pathogens,tumours,toxins and application of CRISPR treatments to human cells and pathogens.He through biosynth wifi via fragmentation on smart devices etc will be able to constantly control all aspects and actions of all microbes in each individual patient.He will also use this biosynth WiFi to control their replication as well as undergo apoptosis or enter endospores when not needed or they need to be flushed out of the body,when to reawaken from endospores and carry out strategies to attack each individual infection including existing chronic infections such as those already with HIV and other chronic pathogens and all future infections of all species of strains of viruses,bacteria,fungi and parasites.Through flagellum present via E.coli DNA he will control the movement of all microbes to where they are needed ie the scene of infections and tumours etc.He will direct them to cells across the body that are to have anti-ageing and augmentations applied via horizontal gene transfer and through taq polymerase and Cas-9 allow for applied genes to be created over and over again.He will have microbes the species of pathogens that enter the blood through cuts,food etc and then once identified by having them scan the pathogens DNA will then carry out strategies to kill them off such as application of CRISPR treatments,iniatiating the immunised primary immune system or collecting DNA samples have its genome scanned for genes responsible for surface proteins to be sent to immunising strains through upgrades via biosynth WiFi to allow new pathogens to be immunised against within 24 hours and then the primary immune system initiated.He will be able to cause microbes in the body such as anti-bacterial,anti-viral etc strains to create chemical signals via this WiFi and bluetooth to communicate wifi the primary native immune system thus allowing him to control it allowing the primary immune system take part in battles preventing it becoming lazy and weak with him having the immunising strains communicate with the helper B and T cells and plasma cells to become actived by them once they have immunised people already sufferring from chronic infections such as HIV thus signalling the native immune system to start producing antibodies to fight of this and other infections including new ones to speed up the battle against pathogens with him via this WiFi.All aspects of the primary native immune system can thus be controlled by him via him using this WiFi and bluetooth to cause anti-bacterial,anti-viral and other strains to create specific chemical signals that cause the primary immune system to carry out specific desired actions.The immunisation strains will use this biosynth WiFi to be directed by him to carry out immunisations step by step again using chemical signals created by them wherein they control the actions of dendritic cells,memory B and T cells and plasma cells to ensure surface proteins are shared with the relevant leukocytes and the patient immunised for life.He will through it allow certain leukocytes to be called to the scene of infections to create antibodies,consume pathogens via phagocytosis and control symptoms such as inflammation and fevers.Biosynth WiFi etc will allow him to control stem cell strains to heal wounds in the body both for wounds that occurred prior to the acellerated healing phenotype is added such as tauopathy and injuries to the brain and other organs caused by pathogens,parasites as well as damage to the central and peripheral nervous system that has one confined to wheelchairs and also after it is added to compliment it and also be using biosynth wifi and bluetooth to carry out stem in vivo cosmetic surgery allowing him to mould the interior and exterior of a patient using the strain to replace surgery machines.He will be able to control all of these via this biosynth WiFi and bluetooth and be able to control all aspects of all strains such as make them undergo mass replication in emergencies,control their movements,control their application of CRISPR treatments and synthesis of anti-viral/anti-bacterial/anti-helminthic compounds and also synthetic compounds and antibodies etc stored in their DNA digital storage,control formation into endospores or even apoptosis and flushing out of the body when not needed.Biosynth WiFi can be used by Paean to induce the evolutionary path of all microbes of the same strain or all strains by stimulating taq polymerase and Cas-9 to have them revive new upgrades for new genes for new CRISPR treatments to apply to pathogens etc,new CRISPR treatments to be applied to the patient for new augmentations or remove them as well as for anti-viral and anti-bacterial strains new genes to express new anti-viral and anti-bacterial compounds making upgrades be able to be done at home.He can also use this to turn microbes of some strains into microbes of other strains in order to get them in the body when needed in emergencies.By 2029 most actions will take a while with from 2035-2045 onwards all actions will be almost instantaneous.All actions of microbes will be controlled by Paean vis him existing through fragmentation on smartphones,laptops through biosynth bluetooth and WiFi from routers at home and in public buildings.Public WiFi,wilderness WiFi and satillite WiFi and also that generated from smartphones etc will allow him to do this in wilderness areas.3D DNA printers will be used to create them not only for final fully fledged versions but also those used for clinical trials etc starting from 2025-2029.These will print out the different sources of DNA for each specific strain of microbes and the features of all strains of microbes.All species and breeds of pets such as Canidae,Felidae,Reptillia,Aves and remaining livestock will have species specific microbes of all strains created for them.
These biocompatible microbes themselves using the neural clusters,DNA digital storage,organic nanotube wiring,electroconductive pilli and electroconductive protein and silicon nanowires from G.metallreducens,G.sulfurreducens,ability to generate electricity and electroconductive pilli from S.oneidensis and nanomachines will form the basis for all types of bio-synth technology.Human neural tissue can be engineered into the microbes to allow them the ability of creating this over layers of borophene,silicene,stanene and graphene nanotubes to produce organic/synthetic nanotubes that can send quickly send large amounts of electricity and optic information over short or long distances increasing speeds on par and superseeding human neural impulses when combined.They would even form internal implants such as neural implants,pacemakers,worms and even those used to detect biomarkers of cancer and precancerous cells in hard to reach areas such as the prostrate and cervix,blood components,vital signals etc in vivo when needed by forming tissue structures ontop of organs or when collected together with the nanowires produced by the microbes,genome capsids and nuclei forming biological harddrives with neural synapses forming natural storage and computing centres.These implants that detect biomarkers,blood components can also be connected to the nervous system to detect pain to illicit the production of natural painkillers and also alert Paean and other microbes and nanomachines alongside sending vital signs such as blood pressure,temperature and heart rate,pathogens and blood components etc to ones patient file on demand with them having openings on both ends that allow blood to flow through the implant where biological nanosensors would detect these and then the results to ones patient file and Paean even in fragmented form and communicate with both microbes and nanomachines.These could be collected in samples sent to automated lab and also to be collected in sewage treatment plants separated by graphene sheets and other filters from feces,urine or algae produced there.In the case of a hosts death they can be removed via phlebotomy robots and even them collecting an area to be collected.Traces of the patients own DNA will be present to allow them to survive in the patient without illicitating an immune response.They will use the patients own leukocytes as a baseline to do this with them created by 3D DNA printers to expedite their manufacture even for those used in clinical trials.They will have the same extremophile augmentations as the host to prevent them dying when exposed to these conditions with them possibly having the same anti-ageing treatments as humans to stay immortal with endolith DNA modified to allow them to undergoe mitosis when signalled by Paean.DNA from P.japonica will allow them to house large amounts of DNA for augmentions and large amounts of the patients DNA for preventing them illiciting an immune responses.In time they will function by themselves without nanomachines by interacting with the levels of compounds in the bloodstream and signals from the primary immune system,body including brain signals and pathogens.
Using human leukocytes ideally a patients own leukocytes as a baseline to prevent immune responses they would be hybrids of a patients own leukocytes as well bacteriophages and virophages,prokaryotic and eukaryotic bacterias,macrophages,other leukocytes such as CD4+ T cells/NKT cells/cytotoxic T cells/T lymphocytes/dendritic cells(either as separate strains or a single one),Planarians,Thermus aquaticus,Streptococcus pyogenes,Francisella novicida,yeasts,endolith bacteria or Bacillus F,D.radiodurans and T.gammatolerans,those from psychrophiles as mentioned earlier and Tardigrade,Nitrosomas Beggiatoa,Cupriavidus necator to survive ammonia,sulphur and other posionous gases,induced pluripotent as well as embryonic totipotent and induced stem cells and haematopoietic stem cells as well as Planarians,Hydra or even A.mexicanum recombinant DNA to form any tissue in vivo to treat neurological/developmental disorders as well as replace old dying tissue with new vigorous ones as well as heal wounds and perforations,C.elegans and have recombinant DNA from all of these and others to allow them to interact with all types of pathogens,undergo mitosis,create nanowire scaffolding,create biofilms and coagulants,be biologically immortal,form enodspores,contain mitochondria and vacuoles for energy use and storage,apply CRISPR treatments and contain Cas-9 as well as Cpf1,communicate with the primary immune system and nanomachines as well as itself using chemical signals,exhibit mechanotransduction as well as memory and learning,chemotaxis,use taq polymerase and the Cas-9 to replicate used CRISPR treatments and read pathogen DNA,thermotaxis,carry out horizontal gene transfer on pathogens/the primary immune system/the hosts cells,carry out anabolic and catabolic reactions,form new tissues and repair old ones,survive radiation and cryonics,interact with and seek out viruses as well as produce endolysines,trick the primary immune system into believing they are part of the body with them also able to utilise specific anti-viral and antibiotic materials from a wide range of other animals and plants and also other DNA to augment human abilities.They can be fitted with scratch DNA created by Phanes and DNA from other unicellular and multicellular lifeforms to exhibit extra phenotypes through upgrades.They will be fitted with the same DNA in humans to halt and reverse the effects of ageing in humans.Tweaking the various sources of DNA will allow them to detect different compounds and even carry out different functions of the source DNA.Engineering flagellum into all strains from bacteria such as E.Coli will allow them to move quickly around the body with them having the same pliable body as macrophages from humans or ameobas engineered into them to allow them to move through any part of the body such as between cells and also using the capillaries.Stem cell strains will use this to move to areas where perforations occur and also where stem cells are needed to repair existing neural and bodily damage with anti-bacterial and anti-viral strains will use this to hunt down pathogens with augmentation and ageing strains travelling to all cells in the body.All strains would have flagellum present to allow them to move quickly to where they are they are needed with them also having DNA from bacteria to allow them to undergo mitosis in emergencies when needed ie emergency perforations,infections,tumours etc with Firmicutes DNA present to enter endospores when needed.All replication and entering of endosperm will be controlled by Paean through biosynth wifi to prevent them overrunning the body.All strains would have the ability to utilise CRISPR Cas-9 treatments specific to their purpose and be able to through taq polymerase etc present be able to recreate strands of DNA,undergo mitosis,survive extreme conditions using extremophile DNA,have flagellum to move around independently,exhibit thermotaxis and chemothaxis,have nanomachines,carry out horizontal gene transfer and be based on human leukocytes to not illicit immune responses.Scratch DNA will also be present to create new phenotypes created by Phanes,Paean and Epione added by upgrades alongside other phenotypes from other micro-organisms and also all species from the global database of patient files,Physis using 3D DNA printing for all strains to create their unique hybrids,functions,anti-viral/anti-fungal/anti-microbial compounds,CRISPR treatments as well as even the universal phenotypes of them.A person will have their leukocytes analysed in a lab in DNA analysers to be then printed out again by 3D DNA printers with the relevant DNA of each strain,Biosynth wifi and the patients DNA including that to express that leukocytes.3D DNA printers will be used to manufacture these for each individual patient allowing them to be manufactured at home and in local hospitals.They would contain the patients DNA created by 3D DNA printers as they containing the patients own DNA would not illicit an immune response allowing them to reside in the body constantly and also be able to synthesise compounds through recombinat DNA and anabolic abs catholic reactions with all actions of them controlled by Paean through biosynth WiFi and through yeast DNA exhibit horizontal gene transfer to transfer CRISPR treatments.
Ideally to reduce the strain on all of them to house as much recombinant DNA as possible or prevent them applying incorrect treatments it would possible to have different strains for each patient ie one strain that attacks all bacteria,one that attacks all viruses,one that deals with cancers,one that counterattacks poisons and toxic compounds,one that treats ageing,one that repairs perforations/wounds and injuries as well as creates new tissue,one that augments human all abilities such as weight loss and ability to survive in low oxygen conditions,one that treats diseases they have genetic predispositions to to treat them and prevent them passing this onto the next generation through natural conception thus allowing them to decide which ones are in endospore states and which will be replicated when needed allowing each strain to control its own rate of replication with all having the ability to detect all biomarkers,compounds etc.Each one could use base microbes that can be collected in nodules they build up to be captured and then be fitted with genotypes for upgrades and then inserted into to the patient to use horizontal gene transfer to upgrade the patient preventing rejection though these would be grown in commercial scales to create genotypes for proteins to enhance the immune system.These would be produced in large numbers as a single strain in the body and collected by syringes when they form nodules in the body in an are that has no major arteries like the hand or from unique smelling urine and put in a conveyor belt laboratory to have base DNA to allow for horizontal gene transfer,form endospores,survive cryonics and also use flagellum or chemotaxis/thermotaxis to move around the body in their genome capsid.Ideally these could be a separate strain that is able to undergo mitosis and alongside this in response to certain signals and hormones from the primary immune system,other microbes and the hosts body.Thus these will be used for upgrades for all strains of microbes including giving primitive microbes them phenotypes such as genome capsids and the DNA within,nanomchines,neural clusters and new anti-viral,antmicrobial compounds etc.Those in pregnant women signalled by can using horizontal gene transfer to copy and receive DNA from the mothers unborn fetus and thus allow this to be collected and then the DNA separate from the base DNA to be analysed for it to be uploaded via nanomachines into their patient files as well as allow for the mothers or the infants developmental and neurological diseases such as Downs syndrome,pedophilia,schizophernia,sociopathic behaviour etc to be fixed in utero or upon birth by upgrading the microbes present.The base microbes would be responsible for transferring upgrades and also copy DNA from cells in the host to detect any faults caused by CRISPR treatments and cells in the body to detect their telomere length and age status to wirelessly send the data to Paean and thus other strains to correct these faults and ageing effects.They would also interact with microbes to transfer upgrades and in the case of all strains able to open the genome capsid and upgrade the genes there with them also copying DNA from a fetus into all microbes that traverse into a fetus from the mother via the placenta and breastfeeding allowing for hereditary diseases and ones entire genome to be detected and uploaded to the patient file database early on thus starting patient files in the womb or after birth and thus upgraded microbes to fix genetic mutations that lead to neurological and developmental disorders and even those that could lead to death early in the infants life such as sudden infant death syndrome or impair their survival rates.If possible nanomachines on base microbes can wirelessly transfer the scanned DNA to the infants patient file allowing for their genome to be scanned before they are born and still in utero to use in holographic projections and have their genetic diseases and phenotypes scanned as early as possible allowing for treatments involving other strains to begin in utero.They would in adults etc scan the DNA of all cells or key tissues to see that anti-ageing and augmentation gene therapy has be added,is passing from one generation to the next with them also scanning cells to measure the levels of Phosphatidylcholines and telomere and mitochondrial DNA senescence sent to ones patient file to be analysed by Paean.Any random mutations would also be detected that could lead to cancer etc.DNA to give them flagellum,mitosis and other base properties such as chemotaxis etc could be stored in their genome capsid preventing this from interfering with copied DNA sent to Paean.They could also copy DNA from new undiscovered pathogens in the body to allow their genome to be sent to Paean and Epione to sent to Physis to be analysed for all of its phenotypes and antibiotics or anti-viral compounds to be created from scratch DNA or those from all plants and animals scanned in Physis with the pathogen recreated using 3D printed DNA in bacteria with no DNA in secure labs.They in the case of bacteria would signal to anti-bacterial strains to produce the specific endolysines to be synthesised via chemical signals,nanomachines and also Paean.Also immunisation strains would be sent key genes to create relevant proteins to be then shared with the dendritic cells.This can be also be used to create endolysines and determine what CRISPR and anti-microbial and anti-viral compounds to use with them since connected to Paean by nanomachines or even without nanomachines can determine the schematics of endolysines that can be sent to anti-viral and anti-bacterial strains to produce species and strain specific endolysines for new pathogens to be sent to large numbers of these strains when collected in the lymph nodes or muscles and also genotypes associated with surface protein antigens to be sent to immunising strains to be shared with even a single immunising strain that can undergo replication to then travel to all lymph nodes and then share these proteins with dendritic cells,activate relevant leukocytes and then initiate the immune system to fight the infection.They would also send schematics of strain specific bumpers.These base microbes would themselves have nanomachines and biosynth wifi to transmit this data to both Paean and other microbe strains and as stated would use taq polymerase and Cas-9 to scan the DNA of the pathogens and also the patient.Nanaomachines and biosynth wifi will be used to send the DNA used to create bumper schematics and also endolysines to Paean once the DNA is scanned by them with him and Physis reading the entire DNA to produce both quickly and thus determine the best DNA to use and then tell the base microbes to use that DNA for both anti-viral/anti-bacterial strains and immunising strains and also to send this data to Physis database to create these new genotypes in large numbers in hospitals around the world and also to microbes in patients around the world instantly to immunise them when nanomachines are perfected thus preventing the new pathogens from spreading across the globe with patients in the surrounding area first immunised and then outwards and so on either wirelessly or from hospitals with this also used to create species and specific bumpers to house CRISPR treatments,endolysines and anti-viral/microbial treatments.This sending of DNA would sent to Paean via namnomachines and biosynth wifi connected to the wire and implants he is in but it would also be sent to the nanomachines as the base microbes would be in time using taq polymerase and also Cas-9 be able to read the genome itself and determine the relevant genes for immunising strains,creation of endolysines and also bumpers by themselves or by Paean through wifi online or in an fragmented form on implants who would analyse it and send relevant genotypes from it to create immunising proteins,schematics for bumpers and endolysines to anti-microbial,anti-viral and immunising strains with it also using nanomachines to wirelessly send the DNA to immunising,anti-viral and anti-bacterial strains themselves.The DNA that is in the base microbes could be altered into benign DNA by its own set of genes that regulate this,by Paean or housed in nuclei to form part of the microbes DNA or transferred to another strain that would undergo apoptosis destroying them with the base microbes also programmed to delete the DNA during replication while the old ones containing this undergo apoptosis.Otherwise they could keep this DNA in a storage area and have it replaced entirely by CRISPR Cas-9 when it copies DNA the next time or even break down or rearrange the atoms present into nutrition or replace existing areas in the microbes genome similar to CRISPR in S.pyogenes with the microbes already having key common genes to all pathogens that it can recognise and determine what pathogen it is with human DNA read and determined by it intaking the key sequences that are present in the child but not the mother.If possible these base microbes would have a nucleus specifically for this DNA that it copies from pathogens and also fetuses to allow the taq polymeras and Cas-9 to read it and wirelessly send it via nanomachines and wifi and then be replaced by the next strand of DNA.Thus they will use taq polymerase and Cas-9 to read the genome of fetuses to be sent to newly generated patient files,pathogens to be sent to immunising strains and anti-bacterial and anti-bacterial strains as well Physis and Paean to create antibodies,endolysines for anti-viral and anti-bacterial strains and scan the genome.Taq polymerase and the Cas-9 would be used to copy DNA from pathogens,fetus etc for different reasons with this and the biosynth wifi transmitters and nanomachines reading the DNA with it transmitted to Paean,Physis and other microbes and patient files.Base microbes could form the basis of both handheld and lab based DNA analysers in hospitals,universities and also forensics labs as their ability to scan DNA using taq polymerase and and Cas-9 with them modified to interact with leukocytes and all types of human cells using blood,saliva and cell samples and then send the DNA read in them via nanomachines and wifi to forensics case files and other files with them also part of other analysers such a those required to read DNA including safes,registered devices,voting machines,authorisation for nuclear weapon use for government officials alongside other readings.By using these base microbes the entire human genome could be scanned and read as well as relayed to ones patient and forensics file in a matter of minutes with microorganism read this way too and also this would be used by interstellar space stations controlled by AI to scan the genome of all new organisms whether uni or multi cellular.This can also be done to determine the identity of those who are suffering memory loss and identity of the owners of DNA samples at crime scenes.This would be in both portable and lab based devices in both hospital and forensic labs.The abilities of C.elegans can be used to detect the presences of pollutants,hormones,cancer biomarkers,poisons,date rape drugs,heavy metals and also both inorganic and organic substances with universal receptors intaking the compound and relay its structure to Physis and the case file simultaneously and will use either mechanotransduction or reverse mechanotransduction,chemical reactions seen in more complex or similarly simple organisms and simple and complex neural clusters and systems in them for example Hydra etc allowing the structure of the compound and its levels in ppm,ppb,ppt,ppq to be determined with these again in portable and lab based devices with or without biosynth wifi.This C.elegans,Hydra DNA can be tweaked to act as universal receptors with human neural tissues integrated via human DNA alongside scratch DNA to improve this allowing them to carry out mechanotransduction or reverse mechanotransduction,chemical reactions and utilise chemothaxis and electrical signals including bacteria and multicellular that generate electrical charges in response to these compounds that can analyse the structure of them to then use biosynth biosynth Bluetooth and WiFi to send the compounds structure to Physis to be cross referenced and receive results within minutes.This will also be used by Sysmex machines that detect the levels of blood componants such as erythrocytes,leukocytes and also platelets and also hormones,pollutants etc.Implants in the body would utilise these as well.Like all strains they would have the ability to undergo mitosis and have flagellum.Another important strain would one that will only be able to interact with the hosts native cells due to specific markers on their surface thus applying gene therapy not to fight disease(this will be done by those that fight genetic diseases and also cancer etc)but to modify the hosts genome giving them augmentations to increase intelligence,make one resistant to extreme conditions using DNA from extremophiles such as xerophiles/oligotrophs/T.gammatolerans/Tardigrade/Salmonella/D.radiodurans,increase the rate of neural development as well as increase intelligence quotient and add resistance to pathogens making them unable to infect leukocytes and also organs etc,synthesise essential amino acids etc and from scratch giving them the same phenotypes of H.umbermensch in living patients and through advanced germline therapy and germline therapy and others and not be able to interact with pathogens due to the surface proteins and receptors suited only to interact with human cells and tissues with these like all strains being upgraded.This will be a different from strain that applies anti-ageing genes or it can be a separate ones.Ideally the anti-ageing strains would be able to detect senescent cells and cause them to undergo apoptosis,vaccinate the immune system against extracellular aggregates,break down intracellular aggregates and apply genes from extremophiles and multi cellular biological immortal and cancer free species of animals and other aforementioned functions all in one or separate sub strains that carry out each function of tasks switching from live state to endospore state through signals to carry out work.Their will be also an immunising strain that give dendritic and thus memory helper B and T,plasma and killer T cells proteins of pathogens to make them immunised against all pathogens the patient wishes to be as well making all leukocytes including dendritic cells and CD4+ T lymphocytes as well as all tissues in the body resistance to N.meningitidis,HIV,Ebolavirus etc. prior to infection thus making vaccines and medication obsolete and would be only be able to interact with primary immune system to alleviate strains on the microbes and prevent the primary immune system becoming lazy and too reliant.These different strains will be in biofilms in an endospore state to prevent them using too much resources and only be activated when needed by signals.Another strains that reside in the brain and other important organs could store oxygen as well but the would release short bursts over a period of time shorter than this at least an hour or two but would release sufficient amounts since working together as one and could separate carbon dioxide and other compounds with oxygen atoms into more usable oxygen to be reabsorbed and then released in short bursts again or in real time with the larger ones releasing larger levels over longer periods of time say several hours and would work in sever emergencies and alongside the other strains to keep the host alive.This could be done by them containing large vacuoles from plant cells that store oxygen only or small miniature ones with even DNA from humans that give erythrocytes their haemoglobin also in these to allow them to store extra oxygen outside these vacuoles in the microbes structure and the surface containing haemoglobin like erythrocytes with them being large biconcave,biconvex structures with the same malleability of macrophages with the vacuoles ideally being internal structures using recombinat DNA from plants and animals.These would keep the hosts brain and other vital organs alive during blood loss,heart attacks,strokes etc and as stated would be able to separate oxygen from carbon dioxide through catabolic reactions.Another strain would be those that use natural compounds from plants and even humans to treat insomnia,diabetes,stomach cramps,rheumatism,edema,hemorrhoids,gout,inflammation,pimples etc by detecting the biomarkers of these and also by instructions by Paean.This would render all over the counter remedies and medications obsolete.This would also create acetylsalicylic acid and also turn off/on genes that regulate substance P to treat chronic pain and severe bouts of pain that would cause one to pass out.Another strains created solely for recreational drug users can exist to produce morphine,nicotine,tetrahydrocannabinol,cathinone,cocaine,natural hallucinogens etc and other natural recreational drugs in controlled amounts on demand onsite of the site action such as the brain to prevent overdosing and them affecting other organs with this also to aid in those wanting to stop using them to eventually quit by producing in them in slightly lower amounts overtime with relevant recombinant DNA from the relevant plants and animals.Alkyl nitrites,LSD,3,4-Methylenedioxymethamphetamine,methamphetamine and other synthetic drugs can be synthesised by these strains using catabolic and anabolic reactions in levels that prevent overdosing with side effects reduced or eliminated via microbes repairing the body tissues and also accelerated healing from A.mexicanum etc would counteract physiological effects.Another strain would produce hydrocarbons,animal and plant oils as well as amino acids etc to then allow other strains whether they are anti-microbial,anti-cancer,anti-viral strains and those that deal with the various other features interacting through signals carry out anabolic and catabolic reactions using these to then be able produce synthetic compounds to treat all sets of pathogens,diseases including neurological or functions negating the need for synthetic drugs to be ingested and done so in a manner to prevent overdosing when signalled by each other and Paean.Otherwise the patient would be told by Paean to consume specific fats,carbohydrates and proteins from specific foods in specific quantities to allow excess be used as a means to carry out these reactions by anti-viral,anti-bacterial and other strains thus negating this strain.When humans through gene therapy are able to create all essential nutrients in their recommended daily allowances then patients consuming them through their diet would allow this excess to be used to create this.These synthetic compounds would be created by anti-viral and anti-bacterial strains etc to suppress or treat pathogens of all types such as bacteria,viruses,fungi and parasites and to treat neurological conditions as well as non fatal problems like pimples,acne etc through catabolic and anabolic reactions.It would be done by Paean telling them to do so via biosynth wifi,nanomachines and digital DNA storage with the structure of them stored in the microbes with new ones downloaded and obsolete ones deleted.This would make all existing synthetic drugs of all types for the control and destruction of all types of pathogens,parasites,neurological and genetic disorders etc created by esterfication,industrial process in factories that are controlled and patented by corporations defunct indefinitely and by law since the microbes under the control of Paean could synthesise them in the body when needed in required amounts that are on the site of action reducing side effects and prevent overdosing.New synthetic drugs for all types of pathogens etc would created by Physis,Paean and Epione using simulations and automated labs and once authorised and passing clinical trials would be created when need via instructions from Paean in patients who need them with the fact that they would be created by AI and synthesised in the body would make them by law free alongside existing ones.All existing synthetic compounds to treat viruses,bacteria,parasites,cancer,neurological and genetic diseases and also everyday conditions can be created in the body of patients by various strains of microbes via anabolic and catabolic reactions and its structure downloaded into their digital DNA storage.The chemical structure of these synthetic compounds will be added to Physis to allow relevant strains such as anti-viral strains etc to download them onto DNA digital storage and then produce in the bloodstream or in the stomach via anabolic and catabolic reactions with this rendering private patents on them obsolete since Paean could create the synthetic compounds could at anytime this would render private patents by corporations of these compounds obsolete as they could be synthesised by anabolic and catabolic reactions controlled by Paean at anytime instead of being manufactured in factories and bought in stores with Paean being a legal human being have no need for money and thus have these compounds produced by relevant strains for free countless times inside patients.Paean would have a decided number of microbes create these in the required amounts in the site of action and even in the bloodstream cutting down on the need for binders,excipients as the compound would be created in the bloodstream bypassing the stomach and can also be covered in bumpers to prevent them breaking down and also bounce off human cells or interact only with those they are designed to interact with limiting side effects.The patient would told to consume a set amount of excess fats,sugar or proteins etc for the microbes to create them by anabolic and catabolic reactions.Since produced onsite of pathogens and neurotransmitters etc in the body in levels controlled by Paean it would eliminate overdosing and side effects with them applied in bumpers to further eliminate side effects.This would also save energy and time in their manufacture and transportation to pharmacies and then the consumer and would allow both factories and pharmacies to be turned into communal homes.Anti-viral strains would create synthetic compounds that either kill the desired virus or suppress their replication such as PreP,PEP and protease inhibitors for those suffering from HIV and would be be free since these would be synthesised by them and Paean and not created by corporation with anti-bacterial strains also doing the same for drug resistant bacteria and also for parasites.If possible they may be able to produce antibodies to specific pathogens that are found only in certain populations of the human species especially once their structure is charted and stored in Physis with this of note to N6 and tri-specific antibodies that can kill HIV but are produced by only a small percentage of infected patients with new antibodies for HIV and all other pathogens and even parasites created by AI namely Phanes and Paean using simulations and the known structure of the parasites and pathogens body namely the antigens with them created via anabolic and catabolic reactions.Anti-bacterial strains would create synthetic antibiotics while anti-helminthic strain will create synthetic compounds that kill or inhibit parasites with strains that treat everyday ailments will create compounds that treat gout,insomnia,heartburn etc.Paean will analyse the outer structure of all viral,bacterial and fungal pathogens,parasites etc and extrapolate synthetic compounds that can kill them or inhibit their replication etc that will be stored in their Physis file to be downloaded into their DNA digital storage and then synthesised by anabolic and catabolic reactions.He will also analyse their outer structure to extrapolate synthetic antibodies that will have their structures be stored in their Physis files to again be downloaded onto their DNA digital storage to be synthesised by anabolic and catabolic reactions.Phanes can extrapolate genes to express these synthetic compounds and antibodies that can be downloaded by biosynth WiFi.This would allow them to create them for any pathogen and parasite outside of those they have compounds to fight for them and also new pathogens once their DNA is scanned and the antibodies structure stored on Physis in the pathogens file.It could also do this for parasites and also venoms and heavy metals.Other strains would create synthetic compounds to suppress sexual arousal in paedophiles,episodes in those suffering both schizophrenia and manic depression while CRISPR and stem cell strains cure them with the same done to those suffering from genetically episodes conditions such as parkinsons etc.
The microbes will be subdivided into various strains that carry out specific actions.Each strain will be form a permanent part of the patients body similar to the native primary immune systems from which they will use as a baseline.Base microbes will detect levels of poisons and the species of pathogens acting as the first line of defence to them via sending wifi signals to Paean then alert him to dangers in the body and then control the microbes and primary immune system via wifi and signals with recombinant DNA from Apidea,Hymenoptera,Chiroptera,Magnetospirillum and other unicellular and multicellular animals affected by wifi,magnetism and also those that use electrical signals even those from E.electricus,the mechanotransduction or reverse mechanotransduction of C.elegans or wifi like means of communication and scratch DNA could be used to create biosynth wifi alongside graphene,borophene and stanene nanoprocessors sythesised via tweaked Geobacter and Shewanella DNA and neural synapses created by them aiding in the formation of biosynth wifi present in all strains.It would also copy DNA from cells in the body to measure the levels of Phosphatidylcholines and senescence in the cells and be able to scan the genome of cells in fetuses to set up patient files and this and the ability to measure the presence and levels of compounds and genome will make the basis of lab equipment and machinery in all types of labs.This strain would be tweaked to detect toxins,poisons,alcohol,cancer biomarkers,date rape drugs and compounds that are synergistically interacting with each other in such low amounts such as ppm,ppb,ppt and so on in the earliest stage of contamination and production and break them down and turn them into nutrients for the host and microbes as well as benign compounds through anabolic and catabolic compounds.This C.elegans,Hydra DNA can be tweaked to act as universal receptors with human neural tissues integrated via human DNA alongside scratch DNA to improve this allowing them to carry out mechanotransduction or reverse mechanotransduction,chemical reactions and utilise chemothaxis and electrical signals including bacteria and multicellular that generate electrical charges in response to these compounds that can analyse the structure of them to then use biosynth biosynth Bluetooth and WiFi to send the compounds structure to Physis to be cross referenced and receive results within minutes.The chelation strain activated by base microbes would turn these and heavy metals etc into benign compounds by creating biofilms that clump it together and allow it to be removed from the body via feces and urine with the same applying to any particulates that enter the digestive tract and lungs etc with these strains either flushing the biofilms out or clumping to the individual particulates and atoms of metals in biofilms and being flushed out alongside it with the excess forming endospores.This strain would also produce proteins that either bind to the heavy metals,drugs,poisons etc and then prevent them interacting with the necessary receptors they do and thus allow them to be flushed out or the proteins could interact with the receptors taking up space preventing the poison,date rape drug etc interacting with them and thus having the being only able to be flushed out of the body.Paean via wifi would teach the microbes how to carry out catabolic and anabolic reactions when needed with the chemicals structure saved on digital DNA storage of the microbes with new compounds,antibodies saved on these when the instructions for older ones are deleted.One strain could be an amalgamation of two or three of the aforementioned strains to ensure they can react quickly to multiple threats ie combining bacterial/viral/fungal fighting strains into one that uses relevant CRISPR/bacterial/viral treatments by detecting the surface protein antigens and receptors of pathogens during phagocytosis and sensing biomarkers and signals from the primary immune system with neural clusters and nanomachines as well as Paean giving them some semblance of intelligence to for this for each pathogen.The would also signal when detecting the type of pathogen to the other microbes and the immune system what anti-viral or anti-microbial compounds as well as antibodies to flood the bloodstream and lymphatic system with in order to wipe the infection out instantly.This would have the same receptors as dendritic,CD4+ T Lymphocytes,macrophages,virophages,bacteriophages,virgin B and T cells to flood the bloodstream and lymphatic system with antibodies and anti-viral and anti-microbial compounds insert genes into pathogens like bacteriophages and exhibit phagocytosis.If possible there could be three strains fighting pathogens:One for fighting bacterial pathogens that are hybrids of macrophages,bacteriophages,yeasts virgin B and T cells with anti-viral strains that are amalgamations of macrophages,plasma cells,CD4+ T Lymphocytes,dendritic cells,virophages,virgin B and T cells,plasma cells etc to combat viruses.One could be designed to fight fungi which can be fought using anti-fungal compounds and CRISPR or they can be fought by either anti-viral and anti-bacterial strains using CRISPR to cause them to undergo apoptosis and also become susceptible to compounds at their disposal with all three detecting the surface protein antigens on the surface of pathogens to determine its type and thus what CRISPR treatments and compounds to use.Both strains or the single strain ideally two being used would have another strain that would function like helper T cells to recharge them with chemical signals and/or supply them with stored reserves of proteins,fats and carbohydrates or those synthesised that prevents them dying and giving up or the strains could signal the primary systems own helper T cells to do this.Otherwise the other strain not used ie anti-viral or anti-microbial ones could help the others by providing them with energy in the form of using up fats and sugars in the body or those produced by the strains that produce animal and vegetable oils.Other wise the two strains could take breaks when low on energy and use up excess nutrients and other material taken in by the host.Both anti-viral and anti-bacterial strains would use CRISPR treatments present as ribosomes and in particular plasmids at their disposal as part of their arsenal with these using advanced gene drive technology.They using CRISPR could make any pathogen whether viral,fungal or bacterial susceptible to the compounds at their disposal killing them rather than inactivating them and negate the need to have too many genotypes with them also applying suicide genes,those that cause them to be unable to undergo mitosis,remove their pathogenicity etc.These would be applied via horizontal gene transfer during phagocytosis and also releasing large amounts via protein bumpers with taq polymerase and Cas-9 allowing them to be replicated and recreated one after another with them created on the go via nanomachines or interaction with the surface protein antigens of pathogens deciding which ones to produce or them in the ribosomes and in particular plasmids.Anti helminthic strains would fight off parasites and would be injected into the body when needed.Immunising strains would immunise patients against all viral,bacterial,fungal pathogens and parasites.Anti-cancer strains would separate from others and would be tweaked to detect cancer biomarkers,CD47 and also the same methods used in immunotherapy to detect and fight cancer by using localised flooding alongside the same receptors in Car T immunotherapy and would use venom based compounds such as Polybia MP-1 and TsAP-1,melittin and CRISPR treatments that cause tumours to undergo apoptosis,stunt their growth and also make them susceptible to the compounds they have at their disposal if they dont attack all types of tumours.These would ideally be injected into all patients worldwide prior to them getting cancer and not just those with genetic predispositions to cure them of precancerous and stage 0 tumours before conventional methods detect them ie meaning a person will be cured of them without realising they ever formed with them also applying CRISPR treatments to cause tumours to undergo apoptosis,halt their growth.A strain would exist that produces recreational drugs and another that creates neurotransmitters and natural and synthetic compounds to treat insomnia and everyday problems.Another few important strains would be the anti-ageing strains that applies genetic treatments to combat ageing,genetic diseases and add augmentations merged into one etc and so on with the possibility of hormones,toxins,chemical signals detected by them switching on/off specified genes,receptors on the outside and functions to prevent them applying the wrong compounds alongside the fact that they would be able to modify a pathogen via horizontal gene transfer to make them susceptible to any compound at its disposal.The would also enhance the primary immune system via gene therapy with all anti-viral,anti-microbial,anti-cancer compounds,give the immune system immunotherapy to detect and fight cancers etc.Those that are base microbes,that interact with the hosts cells and enhance the immune system would still be separate strains alongside those that repair wounds and perforations etc as well as building blood vessels.There could be separate strains solely for treating genetic diseases including neurological and developmental disorders present only in sufferers of these as well as applying protective genes to all living patients to prevent them forming again in the human genepool and those to treat ageing and those for augmentations or these could be one strain.The last and one of the most important strains is those that have DNA from Hydra,Planarins,A.mexicanum,induced pluriopotents,embryonic and haemotopiac stem cells that can allow them on demand by chemical signals or from Paean turn into any tissue on demand.These will especially those from Hydra etc have human recombinant DNA added and the ability to change into new tissues via chemical signals and electrical impulses from the biosynth wifi or even electrical impulses from the recombinant DNA from G.metallireducens and S.oneidensis generated by chemical reactions etc in the body or on demand via biosynth wifi.The G.metallireducens,S.oneidensis DNA will give it the ability to generate electricity and electroconductive pilli.This can be used to treat neurological,developmental and genetic diseases by forming relevant neural and other types of tissue to treat conditions such as pedophelia,Downs syndrome and also multiple scolerosis by creating proper neural tissues that would allow the patient to exhibit normal chronopheilia,cure both sociopathy and psychopathy,intelligence quotient and cognitive abilities with in pre-teens and adolescents it would create proper fully mylienated synapses thus decelerating critical and emotional development prior to genetic engineering perfecting this.It would also as detailed later on replace all forms of cosmetic and reconstructive surgery.In the elderly it would form neural,muscle and bone tissue and also skin tissue and could replace dead and dying as well as ageing tissue in any part of the body such as the arteries,heart brain etc with more youthful and vigorous ones with it doing so for skin tissue by causing the old dying layer to undergo apoptosis or peel off via recombinant DNA from Serpentes.Thus it would form the perfect vector for stem cells rather than injection of stem cells by themselves since having flagellum and also being part of the body as well as undergo mitosis be able to travel to any part of the body and create as many copies of itself as required in emergencies as well as in individual.This would be the strain that forms neural,worm and other implants invivo.Thus this system of different strains will be similar to the different types of leukocytes in the primary immune system thus they will be in a sense a secondary immune system that fights infections that the primary immune system cant with each of the strains using their respective equivalents in the primary immune system as a baseline rather than just CD4+ T lymphocytes.Those that cannot have vaccines due to them being to young,weak immune systems etc and rely on herd immunity should have those to deal with all pathogens and viruses especially specific ones with ideally patients inoculated as early as possible ideally at birth to ensure survival and ideally these anti-viral/anti-fungal/anti-microbial ones should have recombinant DNA from all types of leukocytes such as CD4+ T Lymphocytes,dendritic cells,macrophages and those that interact with pathogens and are infected by certain ones to allow them to attack them with the surface of them being an amalgamation of these or use the process’s of switching on/off genes to accommodate this or ideally being separate strains that all have the ability of phagocytes in them alongside the receptors of each one CD4+ T Lymphocytes or dendritic cell or just a combination of T Lymphocytes and macrophages.This and their other properties and functions could augment human abilities and render humans immortal combined with anti-ageing treatments with them residing in the bloodstream,lymphatic system,bone marrow,within muscles,tissues of all types,capillaries and gastro-intestinal tract and all areas of the body allowing them to act instantly on any threats that arise anywhere.All strains will be copies of the primary systems various leukocytes with each type of leukocytes acting as a baseline for each strain with extra strains that are created using human proteins attached to bacteria or even hybrids of the leukocytes.Patients will have their different types of leukocytes extracted using phlebotomy and then using 3D printing will have relevant DNA from other leukocytes and also other plants,bacteria and animals added and then inserted into the patient onsite using phlebotomy robots as the process will take several minutes as well as the option of having these sent to the patients home via a vial and needle or to be quicker they can be created from scratch using base human leukocytes of all types with the individual patients file cross referenced for each individual patients DNA and that from the bacteria,plants and animals required for them to function added and then injected via needle and vial at home or phlebotomy robots in pharmacies,universities,hospitals etc.This could be done by automated machinery and artificial intelligence cutting down costs.This could also be used to create customised Car-T and other immunotherapy treatments by using 3D printing using ones own leukocytes or even just those created scratch containing the patients DNA stored on file lowering their costs significantly.They would also cut down on the costs and time of producing conventional vaccines and pharmacological compounds with them acting 24/7,365 days a year providing on demand treatment with them doing so when one is away from hospitals or have access to drugs ie in the wilderness etc and prevent problems associated overdosing ensuring only the required amount is created when needed for each specific situation by them able to detect levels of the compound in the bloodstream in very specific amounts due to the neural clusters from humans and nervous system from C.elegans.They if corrected would mean no new drugs or vaccines would have to be created to cure every single disease known whether viral,bacterial,fungal,cellular degenerative,neurological or even genetic and the effects of ageing with it using a combination of anti-viral,anti-fungal,anti-microbial compounds as well as CRISPR treatments as well as the microbes ability to form new tissue,cellular rejuvenation either by itself or with them passing this to all native cells and tissues in the body.This will be use to apply CRISPR treatments via horizontal gene transfer to fix neurological diseases,enhance human capabilities such as intelligence and ability to survive extreme environmental conditions,treat genetic diseases,genetic flaws that shorten or impair the hosts lifespan.Those in the gastro-intestinal tract could release nutrients directly into each section to be absorbed or broken down with those in the oesophagus forming bio-films and have recombinant DNA from acidophiles in them to make them resist low pH of the stomach protecting this from acid reflux with them also creating proper flaps in stomach in vivo to prevent this with if possible they could transfer recombinant DNA from acidophiles and from scratch into the genome of cells that line the oesophagus as well.
Recombinant DNA from human macrophages,plasma,dendritic cells and possibly ameoba recombinant DNA would be added to the main strains to make them exhibit phagocytosis and devour certain bacteria and viruses through anti-viral compounds and antibodies instead of enzymes or even surround them to insert CRISPR treatments and also release anti-microbial,antibody and anti-viral compounds as nanoparticles more efficiently limiting their release into the bloodstream.Anti-viral,anti-cancer,anti-microbial compounds,endolysines and antibodies can be flooded across the bloodstream to use the bloodstream and lymphatic system using bumpers as a means to reach all corners of the body especially hard to reach places with this also used by the immunised primary immune system to reach hard to reach places that a tumor or pathogen would hide.These anti-viral,anti-bacterial etc compounds can be applied to pathogens during phagocytosis through the microbes housing macrophage and possibly amoeba DNA that allows them to surround pathogens and apply the compounds then without them being released into the bloodstream that may cause cytotoxicity and it to break down in the bloodstream preventing immune reactions,death or it becoming ineffective.These microbes would be themselves immune to reactive oxygen and would use chemical or biological signals similar those in the immune system unique to them detectable by only themselves but not the immune system and detect those from immune system to detect the presence of and location of pathogens with recombinant DNA from human white cells,from bacterium that utilise chemotaxis and thermotaxis as well as similar properties,from scratch and other cells will be added to their genome to cater to this.Recombinant DNA from bacteria that produce biofilms will be added to allow them to group together to form rigid scaffolding structures and then tissues etc as well as pilli and flagellum from E.Coli allowing for quick movement to the site of infections and also ruptures with the host engineered to produce both native leukocytes and erythrocytes with these to move much quicker and without the need for the heart allowing them to move in the case of heart attacks etc.They may even be able to detect pathogens due to chemicals produced by the pathogens themselves or even surface proteins on the pathogens and when pathogens are detected create clusters in the bloodstream using DNA from leukocytes and bacteria that create biofilms to release there chemicals in unison in large amounts that can flood the bloodstream by creating the dye and exhibiting biolumescence to activate it or attack large groups of cells in CRISPR attacks at once.Primitive and possibly complex neural systems engineered into them may allow them to detect sensations,receive signals from nanomachines,themselves,each other,the primary immune system,biomarkers of disease and neural implants with them form clusters of this to receive signals or even see similar to primitive eye/neural systems present in the most primitive organisms from the Pre-cambrian and Cambrian geological periods.This could include synapses and neural cluster systems similar to human ones in the brain,central and peripheral via recombinant DNA from humans and/or the simple neural systems of C.elegans with it possible to stores metres of neural synapses and similar material within the nucleus or second nucleus similar to the three metres of human DNA in a human cell with these also on the outer cell walls and membrane of the bacteria connected to this cluster.This would including DNA from both C.elegans and humans with regards to those that create both simple and complex neural systems.These would be engineered to hold at least three metres or even as much as possible of human neural synapses with in time these becoming more dense through upgrades and even have more than one cluster connected to each other and the synapses connected to the wall.This would be replicated by those engineered to detect cancers and precancerous cells with in time them programmed through genes or even signals from nanomachines to intake elemental molecules and synthesise biosynth cybernetic systems to receive neural and electrical signals similar to wifi transmitters from each other,Paean and also nanomachines with wifi transmitters making part biosynth microbes.If possible nanomachines themselves will form part of their structure with them either synthesising bio-synth nanomachines or these enter them during their lifespan in or near the neural clusters to more effectively receive signals and carry out orders from both other nanomachines and Paean with even all types of the primary immune system have these again either synthesised by them through engineering the relevant host cells and factories for them or nanomachines coated in protein coats from the patient entering them to again make signalling easier through chemical,electrical and wireless means from Paean.This would also make them more reactive to the presence of toxins,compounds,hormones etc in the human body that would allow for them to communicate with each other more effectively with the neural systems from C.elegans aiding in this particularly due to their sensitivity to toxins and be engineered able to detect biomarkers,toxins,compounds and hormones in the lowest possible amounts with the nanomachines relaying the current and rising levels to Paean alongside any implants present including neural implants and manage responses more quickly with the different strains having the DNA tweaked to detect all hormones,nutrients,pharmacological compounds,toxins,compounds,biomarkers etc of all cancers/diseases/pathogens/viruses, in the lowest levels possible and even detect their exact or general levels in the bloodstream in mls,ppm and ppb or even ppt and ppq so as to allow them and the added human neural systems allowing for quick responses and allow them to determine the best concentration of each substance to produce thus preventing overdosing,to respond to to prevent slow responses or even responding too quickly with them given alongside biological hard drives within its own DNA and nanoprocessors some semblance of intelligence and carry and modify to new situations and pathogens through detecting the surface proteins of pathogens and evolving new receptors and compounds and even strategies,learn from past infections and poisoning events as well as instructions and simulations for all hypothetical situations and new treatments and strategies from Paean sent via nanomachines,carry out catabolic and anabolic reactions to every specific toxin,compounds that enter the body instantly and in prepare specific nutrients etc in specific amounts instantly to prevent the body becoming too overrun with compounds and react to every individual situation uniquely and most importantly be able to respond to orders from Paean via nanomachines effectively.These neural clusters will not have DNA present to allow function but will rather be an phenotype of genotypes in the DNA present in the genome capsid.Recombinant DNA from C.elegans will also allow for chemotaxis,thermotaxis,mechanotransduction,learning,memory to be applied by the microbes with them also adding simple neural systems to the microbes alongside or in place of neural clusters.In time it may even be possible for these to become more intelligent through these on par with animals or even possible sentient either individually through being able to condense enough neural synapses,nanomachines and biological harddrives into them or collectively through chemical signals and collectively joining to each other in a biofilm or neural implants through the nervous clusters of each joining together in a mass using the collective neural clusters combined together and harnessing the processing power of all nanomachines in them and the body combined.This if done to the hosts central and peripheral nervous system would in effect increase the hosts intelligence.If possible these would in time be able to merge with the human neural system both the brain and the rest of the central nervous system and increase the hosts intelligence,neural and cognitive features through the merging of the humans neural systems as well as the nanomachines and neural clusters and DNA digital storage in the microbes or them simply becoming new neural tissue with the nanomachines present increasing the processing power of the new neural tissues in the hosts with this increasing the persons intelligence.Tissues formed in other part of the body through per example repairing damaged organs etc would also increase intelligence quotient by the nanomachines and wiring connecting to the native nerve tissues in these areas,organs etc.In both cases the digital DNA storage gained from the DNA present in the microbes can be used to store data downloaded from the internet,wire and neural system ie memories,emotions,thoughts,movies,structures of compounds etc that can be extracted and deleted by pure thought with each microbe cell holding 3ZB each.Nanomachines,biological harrdrives and neural clusters will also vastly increase the intelligence of the host.These DNA would also store the structure of poisons,toxins etc to recognise and their counterproteins as well as download the structure of antibodies and synthetic compounds produced by them and counterproteins via biosynth wifi with them sent this via wifi with old data deleted.Genotypes for upgrades will be downloaded as well.They could use biosynth wifi with the wifi using public wifi,routers in homes and public buildings and also cellular signals and satellite wifi in the wilderness to download new information.Microbes present could also store extra digital data in the three metres of DNA holding both their genotypes,junk DNA and even the DNA in the genome capsid,mitochondrial DNA,biological harddrives present as well as the neural synapse clusters holding extra information both in the actual synapses but theoretically even the DNA within them with CRISPR or them allowing ones own native cells to be used for this both in the nucleus and also mitochondria with in both case bio synth wifi within the and also the cells and microbes connected to neurons could allow for this information to be read by the central nervous system once downloaded from the internet and wire by pure thought and through Paean or via microbes transferring this when they down this via wifi.CRISPR can be used to add the ability of digital DNA storage and nanomachines to be added to all cells and tissues in a patients body especially with regards to nuclear and mitochondrial DNA increasing the storage capacity of the human body and neural systems exponentially allowing one to store 1,110,000,000,000,000,000,000,000PB or 11,100,000,000,000YB of information with the accelerated healing phenotypes repairing any degradation to the brain caused by overloads of memories with data from this digital DNA being able to be sent wirelessly via wifi and implants to external devices such as clouds,servers,smart devices and external hard drives with unnecessary information deleted at will and extra information downloaded wirelssly.This could allow for humans to store vastly more memories than the hypothesised 2.5 petabytes in the human brain alongside genetic engineering using CRISPR to transfer eidetic memories to patients.This could also for genetic memory to be utilised by humans wherein memories of a mother and father would be passed on from one generation to another through DNA digital storage present in the DNA of both spermatazoa and eggs if applied to all cells using advanced gene drive technology.If not then at least it should apply to biosynths.Technology can be developed that can read memories extracted from DNA.These would act as at biological neural implants through the nanomachines and the neural clusters merging and working together allowing for information being sent to and from the human brain and the wire and play a role in VR indistinguishable from reality through them connecting directly to all parts of the brain and central nervous system or those responsible for temporal comprehension to facilitate the time dilation effect and forming clusters through biofilms.They would also form bio-synth neural implants through these biofilms connecting all microbes and nanomachines with the hosts body with other bio-synth implants such as biosynth pacemakers,neural implants etc could be formed by these forming biofilms and then solidifying into these advanced implants with the nanomachines and the neural synapses present forming into these masses circuitry with them even if possible turning into biosynth nanomachines.Furthermore if they have recombinant DNA from bacteria from the genera Geobacter and Shewanella to produce electronically conductive nanowires throughout these and the nervous system to connect each implant and the brain together.
These biocombatible microbes would be immune to any antibiotics or anti-viral drugs administered orally or even created by themselves so the pathogen can be attacked while conventional treatments suppresses the pathogens ability to grow,reproduce or cause serious problems such as death with this immunity blocked from passing to pathogens and also allow them to thrive indefinitely.It would largely be done because they would be modified leukocytes.This could be done by these having specific genes in plasmids or chromosomes that cannot be spread to the pathogens with these likely being more complex humans strands of DNA or chromosomes or synthetic ones that cannot be traded or passed into the targeted pathogen due to it being more complex,foreign to bacteria or even gene drives,proteins,enzymes etc or them coated by markers,proteins,genome capsids from viruses etc that simply prevent this DNA from being transferred to pathogens preventing the pathogens from becoming resistant to antibiotics then applied to them to kill the pathogen.Production of genome capsids from viruses could be integrated into the microbes DNA to house specifically these genes and plasmids or even chromosomes separate from the nucleus that contain genes that keep the bicompatible microbes immune from applied antibiotics and compounds to kill pathogens/reactive oxygen/anti-microbial agents and antibodies they produce themselves as well as those that ensure its immortality from endolithic bacteria and Bacillus F,genes that create anti-viral and anti-cancer compounds etc,those that make them survive radiation and chemotherapy and from extremophiles,exhibit horizontal gene transfer with anti-microbial and anti-viral strains having this from pathogens to make it easy while those that interact with human cells will use that from viruses and those used in gene therapy or from scratch to prevent them interacting with pathogens etc,give them advanced features like neural clusters and ability to evolve quickly,those that allow them to survive extreme radiation as well as lower amounts of nutrients and water and low pH etc,those that produce controlled levels telomerase production,form endospores and even those that produce human protein coats that allow it survive the human body preventing immune responses that cannot be transferred to pathogens or even cancers for them and the primary immune system to be effective.These capsids would have recombinant DNA from all extremophiles including those in the host already especially acidophiles to allow them to survive the low pH of the stomach to aid in food digestion,synthesise natural or synthetic compounds that treat stomach cramps or heartburn and attack pathogens like H.pylori that reside in the stomach that cause stomach ulcers among other problems and replace their other beneficial functions in those that are asymptomatic carriers.Otherwise H.pylori if they play a role in digestion could be engineered not to cause stomach ulcers with recombinant DNA from acidophiles added to all cells in the human body including the stomach.These and DNA from osmophiles,halophiles,alkanophiles etc allow them to survive all pH ranges,sugar concentrations and extremes both of the human body but also those caused by an overabundance of nutrients for the host and the microbes in the body which can be passed onto the host via horizontal gene transfer in relevant strains with others holding this DNA in genome capsids.DNA from T.gammatolerans will make them immune to radiation experienced by the host.They should also have DNA from psychrophiles,Tardigrade to make them survive low temperatures of cryoprotectants both for storage and also if cryonics becomes a valid science with thermophile DNA added as well as mesophile with these pushed to their limits like those added to humans as detailed later on.Salmonella DNA and others from scratch including those from Tardigrade can also push their limits in terms of surviving extreme environments including in space,low and high temperatures with those from oligotrophs and xerophiles can allow them to survive on low levels of nutrition especially if the host is starved of food and nutrients.Those from as stated psychrophiles,A.mexicanum,Planarians,Hydra, as well as T.gammatolerans and also Bacillus F etc will allow them to survive the process of freezing and rethawing over and over again to recover from telomere damage caused by cryonics and low temperatures.All extremophile DNA will be added to them including metallotolerants with beneficial bacteria in the gastro intestinal tract also given genome capsids housing these phenotypes alongside those that make immune to all of the anti-microbial compounds and even bumpers and endolysines at their disposal and also DNA that gives beneficial bacteria the ability to produce human protein coats to avoid immune responses and prevent them being attacked by the primary immune system especially when it is immunised using the common protein method.Recombinant DNA from all major extremophilic bacteria and those from the Firmicutes phylum that create endospores to survive periods of inhospitable environmental conditions and re-emerge when the surrounding environment is more hospitable through signals from other strains,native immune system and also the body to awaken them and put them back into spores when not needed.These genes including those from endoliths to make them immortal,allow and those that protect them from the immune system etc would be housed in genome capsids to prevent them being transferred into pathogens.Upgrades can allow for new phenotypes to be added specifically to the genome capsids.The beneficial bacteria in the gastro itenstinal tract will be given these sources of recombinant DNA from extremophiles to also survive these conditions experienced by the host through genome capsids and have advanced gene drive technology applied to ensure it stays there for each generation with the native leukocytes via this DNA added to the bone marrow will be able to survive these conditions.Asides from interacting with the immune system they would also interact with the microorganisms already present in the human body for example not harm the native bacteria in the gastro-intestinal tract especially both intestines and in fact augment their abilities through recognising their unique biomarkers trade specific genes with them including if possible those within the genome capsid or when that interact with these specific bacteria by recognising their genome and receptors by interactions with them and the nanomachines synthesise and trade these genes to improve their natural abilities with any dangerous pathogenic bacteria present destroyed or at least made permanently benign and altered to become beneficial and carry out new functions.This would in turn make humans gastro-intestinal system more
efficient,cleaner etc.This would be controlled rates via horizontal gene transfer and vice versa if deemed safe through simulations done by Paean,Epione etc.The capsids in the microbes would contain all extremophile DNA augmentations that is found in the host.Beneficial bacteria in the gastro-intestinal tract would also contain these capsids and the same DNA to protect them from radiation,hypergravity with this done via horizontal gene transfer from augmenting strains and also them created to them via them consumed when created in a lab.The genome capsids in beneficial bacteria will also house this DNA from extrempphiles DNA and those to make them immune to the anti-microbial compounds at the disposal of the microbes and also those that give them human protein coats making them human bacteria hybrids thus preventing the primary immune system using antibodies at them.Thus both microbes and beneficial bacteria in the gut will be engineered to be able to resist the same extremophile conditions as the host via upgrades.The DNA to produce these capsid if possible would be inside these chromosomes and plasmids within them with their synthesis coming from the main set of chromosomes or their synthesis controlled by nanomachines interacting with specific genes in the main chromosomes through chemical signals controlling their replication meaning the expression of genes to produce the second set of chromosomes and capsid would have to be controlled by nanomachines.Otherwise gene drives that prevent certain genes within the first chromosomes from being traded would organise the production of both the capsid and second set of DNA with this also controlled by mitochondrial DNA,switching of certain genes on/off with nanomachines again playing a role with mitochondrial DNA also prevented from being traded.These plasmids and chromosomes would be separate to those that house other phenotypes such as those that are traded to pathogens that would roam free in the bacterias structure in the form of ribosomes and in particular plasmids and/or genes,plasmids and chromosomes in the primary nucleus also housing DNA to initiate the capsids and the genes in them.Unlike viral capsids they would not be traded into pathogens due to them having a complex structure of enzymes,peptidoglycan similar to gram positive bacteria or even cellulose,ligin,hemicellulose,pectin found in plant cells using recombinant DNA from plants and gram positive DNA or viruses unable to enter the pathogens at all with other measures engineered into it to prevent this happening either at the start or by adding new microbes that interbreed with it.Upgrades would allow primitive versions of microbes to gain these.These should be used to house it with the most effective one used to house it preventing it from being traded with pathogens if protomers through either simulations made by Paean and Epione or trials on mice and chimpanzees show that they are ineffective of keeping these genes within them.The first generation of microbes will likely not have genome capsids and the features inside them,nanomachines,neural synapses but will in time through upgrades will have these added overtime by at least the late 2030s with AI namely Physis,Paean and Epione creating scratch DNA or scanning known genomes of all animals that have these or can create equivalents.Primitive versions that can not have these or the important genes that cant be traded with pathogens with in time them added by upgrades with the primitive versions of microbes surviving by themselves with if any pathogens get the DNA inside them by any means can be removed via CRISPR.Upgrades to house more phenotypes would add more genes to the capsid would be made thus allowing DNA inside the capsid to receive new phenotypes with the Cas-9 programmed to open up the capsid or stimulate the nuclear DNA to produce these DNA sequences or them using bumpers that can bypass the protomer capsids.Since eukaryotes these would house the important DNA that keeps them immortal and resistant to treatments,immortal and able to inhabit the body without eliciting immune responses etc in this capsid to prevent them traded with the nucleus housing DNA that give them their characteristics for structure,soaking up of poisons etc,creation of capsids as well as functioning of the cell with these and ribosomes and in particular plasmids and other strands of DNA including plasmids containing the suicide,resistance removing genes etc that are to be traded with pathogens and the host using gene drives.Ideally this DNA would be able to be used as DNA digital storage when they are used as biosynth technology with ideally the same three metres of DNA found in humans present here with the remaining DNA used for upgrades and also for junk DNA used as digital storage alongside the rest.It could also be used to store instructions and data from Paean as well as from itself.Recombinant DNA from embryonic stem cells and even cancer cells can make them produce telomerase making them divide indefinitely with other scratch DNA keeping this in control without become cancerous and divide out of control.Advanced gene drives would keep phenotypes stable and prevent unwanted mutations with recombinant DNA from T.gammatolerans present to aid this with only upgrades adding and removing desired and undesired DNA.Genes in capsids could be transferred to the hosts cells by the use of signals,nanomachines and Paean with the capsid momentarily broken by switching on/off genes down to apply them or synthesis/interactions of base microbes interacting with them copying and transferring these into the host cell with the possibility of microbe strains that are only able to interact with the hosts cells and not pathogens or tumours to prevent them entering the genepool of pathogens due to unique receptors on the microbes walls,the genes synthesised by the bacteria outside the capsid via interactions with the host cells and/or nanomachines or other measures applied by them determined in time by Paean,Epione,Urania and Hecate.CRISPR,Paean and other software combined with each other can be used to create these with bacteria created using the same process as Mycoplasma laboratorium to create a species that is biocompatible that can do this for all existing and new superbugs or one for each superbug with recombinant DNA from the specific bacterium or virus inside to ensure these suicide,faulty or resistance removing genes amongst those that reduce its ability to reproduce or be a pathogen can be transferred successfully with the bacteria used for this unable to become as deadly or resistant as the species they are destroying due to their genome contain gene drives with gene drives also ensuring any genes transferred to pathogens are permanent and passed onto future generations allowing for antibiotic or anti-viral treatments are used.They could even transfer bacteriocidal proteins and compounds to which the beneficial bacterial is immune to into the cell of the resistant pathogen bypassing the cell wall with a single cell of these bacteria transferring these compounds,proteins and genes to many cells of the pathogen in a patient with the possibility of transferring DNA into the pathogens to force them to make bactericidal compounds or even endolysines inside themselves killing them from the inside out.Photoanti-microbial dyes could be engineered to be produced by these microbes or variants that transform nutrients or even carbon dioxide in the body into reactive forms of oxygen that kill pathogens that the biocompatible microbes is immune to and with recombinant DNA from plants or photosynthetic that create the pathways from photosynthetic bacteria with DNA from faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles and scratch DNA that allow them to soak up the excess oxygen produced to prevent it poisoning or building up in the bloodstream and acting as a free radical or causing unforeseen problems.This would also allow the microbes to survive in the body using both carbon dioxide and oxygen in the bloodstream with them also engineered to run on sugars,salts,fats,proteins and other nutrients in the hosts body running on both oxygen and carbon dioxide with them using excess of these to prevent problems associated with overdosing such as high blood pressure,weight gain,heart disease etc.It and other engineering would allow them to separate the carbon and oxygen to create useable oxygen and sugars or store the carbon for this and other uses with chlorophyll engineered into them using bioluminescence to separate the carbon dioxide into and release reactive oxygen though if this produces too much oxygen that may be toxic other DNA from scratch could do this without photosynthesis via bioluminescence such as using those from chemosynthetic bacteria with those from these also turning methane into a fuel source for the microbes preventing poisoning to the host or turning it into benign compounds such as sugars and water.If possible scratch DNA could allow them to produce reactive oxygen without light by using oxygen or carbon dioxide and converting it into this with the host made immune by having recombinant DNA from aerotolerant anaerobic bacteria.Those in livestock would be removed via phlebotomy robots will be separated and either used to create biosynth technology or even separated to be injected into new animals with the blood used to produce Agriprotein.Ornamental and crop plants as well as those in forests,wilderness and areas used for forestry could also have ones created to treat viral,fungal and bacterial diseases with them creating hormones and other compounds to extended their blooming periods,control growth,extend their lifespan and shelflife by suppressing rotting and killing off spoilage and food poisoning,micro-organisms and would reside in the xylem,phloem,leaves,tissues and also roots as well as the soil and even attack pests with them killed in these cases or extracted via nodules and turned into electronics with them passing to new generations via seeds.This would also kill off pathogens in crops preventing them spreading to humans and immunise the plants or even add primitive or fully functioning primary immune systems via CRISPR and would give them by allow them to repel pests,survive all climates and soils etc.They could even augment their abilities and increase their growth and even intake of carbon dioxide and carry out the same functions as in animals.If possible CRISPR could be used to make pathogens benign,unable to infect cells,produce toxins and make them susceptible to attacks from the primary system with again vectors such as asymtomatic carriers and animals treated with this.It would also be used to transfer suicide genes that cause a pathogen to undergo apoptosis.
These microbes since using leukocytes as a baseline would be coated in not only human proteins but specific markers and proteins of pathogenic bacteria,viruses and protozoa without pathogenicity(or ability to mutate)that can be grown in media and then injected into the patient as a form of living vaccine injected prior to infections that through DNA from endoliths would stay in the patients body indefinitely and even pass from mother to child via the placenta breastfeeding or even from person to person through unprotected sexual intercourse including oral sex or physical contact with the genitals with them attacking infections instantly.This could be done by them inhabiting the semen and mouth tissues with them that enter the unborn fetus via the placenta breastfeeding offering extra protection to them from infections carried by the mother,preventing miscarriages and stillbirths and situations that would endanger the life of the mother,aid in the proper development of premature children,correcting genetic flaws in utero including those caused by incest and mutations,encouraging correct neural and organ development before they are born and supplying them with oxygen as well as nutrients should the life of the mother be compromised,the placenta strangles the child,complications occur or the mother should be unable to procure sufficient nutrition of key nutrients and improving success in cesarean births.Bio-synthetic worms will act as as secondary placenta as detailed earlier on should the first one become compromised.They will also be providing extra protection from pathogens during pregnancy and the first months of life after birth before and after they are given proper vaccinations with it protecting unborn fetuses from contracting HIV and protect the mother and unborn child from miscarriages from pathogens such as L.monocytogenes and Salmonella.It will also alert the mother through nanomachines to any surprise pregnancies that occur with it calculating the date of conception.With regards to developing fetuses and infants they could produce omega-3 fatty acids as well as folate in sufficient for proper neural developments and prevent spina bifida and other neural tubule defects should the mother be unable to gain adequate nutrition of these and other nutrients using compounds in the body,excess nutrients etc by detecting levels of these nutrients in the bloodstream and the infants and body repair any damage caused by trauma and supply blood and nutrients should the placenta be compromised and if possible repair the placenta in certain situations or if possible create a second one as a backup.Otherwise the microbes through horizontal gene transfer have the mother and unborn child synthesise these naturally becoming a permanent part of the human genepool.Situations such as the placenta strangling the child will be negated by the use of carbon dioxide as an energy acceptor will keep the child alive with the biosynth worm taking over the job of the original placenta by attaching to the fetus and the primary one severed and broken down by the microbes by decomposing it and also causing cells and tissues to undergo apoptosis.The placenta will be regrown for the next child.They will also soak up and convert alcohol,recreational drugs and other compounds such as pharmacological compounds that may inhibit the proper neural and organ development of of an unborn child into nutrients or benign compounds with excess nutrients flushed out of the placenta or the child could be engineered via CRISPR to be unable to absorb these toxins from the body preventing them affecting proper neural development with this then removed once they reach adolescence or adulthood.Mitotic inhibitors would also be dealt with in the same way by having all patients worldwide have genes added that prevent conjoined twins being formed at all again,making the fetus and indeed all humans immune to them as well with any incidences of conjoined twins dealt with by surgery being aided by the microbes keeping the brain and other vital organs alive,repairing damaged tissues and vessels with bioprinted organs added to both individuals and the microbes repairing any damaged tissues and vessels with limbs such as arms created via synthetic ones as detailed earlier attached to them.Resistance to mitotic inhibitors and all types of teratogens can be added to the human genepool to prevent conjoined twins ever happening with this done via exposing bacteria to them in automated labs and using the new genes to be added.Recombinant DNA from A.mexicanum,Hydra and Planarians as well as Archaea bacteria that exhibit telomere repair added to the human genepool will automatically repair any damage caused by these and in deed any compound or trauma on the neural development thus meaning compounds like alcohol,nicotine and teratogens that affect the brain will have any damage repaired instantly or or treatments applied to allow the unborn fetus made immune to them preventing them interacting with the unborn fetus neurological developing.Any ruptured placentas,wombs that could be repaired to prevent miscarriages with them even covering the womb in a layer of fat and carbon nanotube or spider silk to offer extra protection to the unborn child with them forming worms that would be providing extra oxygen and nutrients to twins,triplets and extra infants during single births.In short they will protect the life of the mother and unborn child during pregnancy to prevent them from being compromised and dying by providing the brain of the infant and mother with oxygen should either one or both be compromised with them also fighting off infections preventing miscarriages,stillbirths and also preventing complications that arise by keeping both individuals alive and even in the case of sudden infant death syndrome correct mutations and keep infants alive in these and any other situations during its first early years with the same applied to sudden adult death syndrome.Each microbes will have base universal human DNA alongside the hosts DNA to prevent rejection to an unborn fetus with if possible them also having upon their genetic screening have their own DNA taken from leukocytes taken during this to then be inserted into these microbes that entered the child during its in utero stage or when it is born via those prepared by automated machinery or doctors present and even base microbes to improve their abilities and prevent rejection through interbreeding.This is why first generation patients should have their own leukocytes used a baseline so when it passes to the unborn fetus it will not cause rejection like normal leukocytes when they pass from mother to child and from father to mother and thus child from unprotected sexual intercourse since they would have base human proteins with this applying as they pass from generation to the next to prevent immune responses.Otherwise base microbes could copy and extract DNA from the unborn fetus and then transfer this to all of the new microbes of all strains from the mother.The DNA from ameobas and macrophages should allow for all types of microbes to pass into the placenta or otherwise the blood samples taken at birth can be used to create a childs own set of microbes to be injected for life by automated machinery or even stored in a vial and injected at home by the mother with all steps automated as much as possible with Paean giving directions.Ideally though the base microbes should be able to extract and copy DNA from an unborn fetus via horizontal gene transfer,read its DNA via taq polymeras and Cas-9,then send the genome to newly generated patient files by biosynth wifiand then share this with those of all strains collected in the placenta or breasts upon the childs birth or during the last months of pregnancy when the child is sufficiently developed to allow them to pass into the the unborn child with groups of each of the strains passing into the child copying and extracting DNA from base microbes and then undergoing mitosis in large amounts in the fetus.The various strains will undergoe replication and enter the child via the placenta and then via biosynth wifi can be through induced evolution via taq polymerase and Cas-9 have areas of their genome changed from their mothers DNA to that of the fetus.This will allow the fetus to be protected while in the womb against pathogens.At the same of this the childs DNA will be analysed by base microbes,read via horizontal gene transfer and taq polymerase and Cas-9 to copy DNA from cells and sent to Paean via biosynth wifi to set up a new patient file that can then have all of its information such as gender,eye colour,hair colour etc put up and its DNA analysed for parental tests and also any genetic diseases it may have and also for holographic projections of the child at various ages extrapolated.Breastmilk fed to a child during breastfeeding would be an another route for them to transfer from mother to child again if they have universal base human proteins to prevent rejection and also amoeba DNA allowing them to squeeze through the breasts when stimulated with all of the strains collected here during and after pregnancy via response to hormones to pass through the breasts into the child as breastmilk and into the bloodstream via capillaries in the stomach and gastrointestinal tract with acidophile and alkanophile DNA making them survive the acidity and high pH of the stomach and gastro-intestinal tract.These in the breast would already have the childs DNA from base microbes travelling from the placenta then added to them via horizontal gene transfer and biosynth WiFi with this done in the breasts holding both the mother and childs DNA.The next generation females would do the same removing their mothers DNA with that replaced with their own childs DNA etc with the same done to those passing through the placenta during the third trimester by squeezing through it with chemical signals and reactions to hormones managing this with also microbes forming nodules after the DNA is changed to be collected via needles and injected into the child at home.These would be all done via the microbes detecting hormones related to pregnancy,lactation and communicating with each other via chemical and wifi signals with this and the microbes having base universal DNA and protein coats or have those from both the mother and child would eliminate any issues relegated to rejection in both the mother and the successive generations.In both cases large amounts of all strains of the microbes from the mother including base microbes would collect in the breasts or womb and placenta to be modified via protein bumpers and horizontal gene transfer to transfer the DNA of the child to the mother microbes and then pass through to the unborn child.Otherwise using the childs DNA scan Paean can wirelessly induce the DNA to be changed to that of the childs by wifi in set number of each strain once they enter the child.Base microbes containg base DNA can scan the DNA of a child in utero and then biosynth wifi may be used to induce the evolutionary path of all strains of the microbes in the fetus into the childs DNA thus preventing rejection once the base microbes scan their DNA and set up their patient file.Otherwise biosynth WiFi could be used to change the DNA in all microbes being transferred into that that contains the DNA of the child.The child’s DNA will be read by Paean and using biosynth WiFi he will set up a new patient file.Once the base microbes have read the child’s DNA and set up the patient file via biosynth WiFi,the biosynth WiFi will be used to change the genome in all microbes in the fetus and child to that of the child.Thus the microbes could pass through breast milk and even the placenta during the late third of pregnancy into the newborn and receive the DNA to be shared with all strains through biosynth WiFi once the patient file is started or Paean could induce evolution in a set number of each strain before or after they enter the fetus with acidophile DNA in the genome of the microbes to protect them from the acids of the stomach.The microbes after undergoing replication in the foetus and child will have sets of them changed via biosynth WiFi into those of all strains that contain the child’s DNA and then enter endospores in it.Paean will determine the best means for each pregnancy allowing them to inhabit the fetus while it is still in the womb and protect it from pathogens that may infect the mother including L.monocytogenes,Salmonella and also HIV.It will also prevent miscarriages and stillbirths by keeping the fetus alive.This would be done ideally when the fetus is formed enough such as during the second or third trimester or if possible the first trimester as first tested on mice and chimpanzees with them doing this in waves during all three trimesters to improve chances of success with the mother ideally immunised against all pathogens especially those that can induce abortions,cause death and pass to the child ie HIV,MRSA and L.monocytogenes with them also fighting off other infections until they enter the fetus.If a mothers womb is inhospitable to carrying young then it may be possible to allow the microbes to alter the environment by creating new tissue,using CRISPR to correct mutations that cause this while breaking down or creating compounds that cause this to occur and also make it hospitable to bearing young.Sterility in both males and females can be corrected with CRISPR treatments.Injection into the blood stream prior to infection would allow them to attack infections instantly when they occur for the entirety of the persons lifetime with them injected into the bloodstream bypassing the stomachs acids with this injection ideally done prior to infections so they attack any incoming infections instantly.Free radicals and also chemicals that building the body as a result of the ageing process will be soaked up,broken down into benign compounds or converted into nutrients with gene therapy routinely done to correct ageing.This regenerative process could also both be done to repair cellular degradation caused by ageing by them turning into new tissues replacing old dead or dying tissue with fresh tissue on the skin,muscles and key organs such as heart,kidneys,brain etc as well as veins and arteries and using CRISPR treatments to repair DNA damage that leads to ageing that will be passed onto the next generation via mitosis on these new and also existing cells and tissues with scratch DNA and those from animals and bacteria that exhibit biological immortality also added to all cells in the body.Having the hosts own DNA in these microbes will ensure that new tissues is not rejected with this done by these strains having their DNA inserted into them during upgrading or if possible using base microbes to copy DNA from the hosts own cells that is automatically corrected by CRISPR for defects including those associated with ageing and then transferred to them and the microbes responsible for forming new tissue with those inserted into them in labs would be also corrected for defects including those responsible for ageing.This would also apply to those responsible for repairing wounds and perforations.Thus these microbes would routinely replace degraded tissue in key organs such as the skin,heart,muscles,arteries,veins,central and peripheral nervous system and brain etc with fresh ones that have the plasticisty,strength and even telomere length and chromosomal features as those of someone in their early twenties as well as mid to late teens giving them a youthful vigour that would be done routinely automatically every few years or decades with any plaques and other compounds associated with old age broken down by the microbes into nutrients and benign compounds with CRISPR treatments to correct defects caused by ageing and deformities.Genes from animals that exhibit biological immortality and those from scratch could be added to every cell via horizontal gene transfer with those relevant to anti-ageing techniques residing within all tissues such as in the brain,heart,muscles and also arteries and other key organs in between those that fight pathogens and cancer etc again in an endospore state.This would be done by the microbes inherent DNA from Planarians,induced pluripotent and haematopoietic stem cells that also have DNA from endolithic bacteria and those like Bacillus F within them and this done by them again every few years and also when they detect biomarkers of cells undergoing senescence or when base microbes copy DNA from cells around the body detect shortening of the telomeres and other biomarkers of senescence.Ideally the ability of Planarians,C.elegans,A.mexicanum,Hydra,stem cells and endolithic bacteria as wells as Bacillus F and aforementioned Archaea extremophile bacteria to rejuvenate tissue from damage,retain memory and never senescence can be transferred using horizontal gene transfer to these existing tissues in all organs such as the brain,heart,skin,muscles and arteries in the host to compliment or negate the need for the microbes and using germline therapy become a permanent part of the human genepool.Thus when cells in body via base microbes are detected to be becoming old they can be replaced by new cells and tissues created by the strains of microbes dealing with repair and ageing that can do this in place of old ones with this replacing tissues in the brain,skin and other organs with key organs replaced with bioprinted ones every few decades that have DNA from Archaea bacteria and the old ones pyrolysised.If possible the degraded tissues in the body may be replaced by new tissue that would have the DNA from the aforementioned Archaea bacteria within them that would then if not have the anti-ageing recombinant DNA,or in the case of bioprinted organs have the cells in them have the DNA from these bacteria with this done if the hosts native cells treated cant be given the Archaea DNA.Ideally the hosts native cells can be treated with this Archaea DNA with them first halting and then repairing the damage already done by senescence using DNA form these immortal lifeforms and also from scratch to ensure the effects of ageing are first stopped then reversed allowing those in middle or even late age say even those currently in their 50s-70s to be reverted to a more youthful age of at least early teens and early twenties overtime which the host can be kept at indefinitely applying the gene therapy to all cells in ones body such as muscles,skin,internal organs and brain with again as stated with the microbes and gene therapy allowing females to have their adolescent peak fertility in terms of carrying young of 14-15 years of age and with males their testosterone peak aged 14-15 indefinitely or on demand by switching on/off genes via CRISPR or them creating hormones.If need be this can be done in waves every few decades until it is made permanent by upgrades.This would be done by extra intake of nutrients such as fats,proteins,carbohydrates and water to feed them as they turn into new tissue with if possible them having oligotrophic and xerophile DNA reducing the amount of resources needed to set these tissues up with if possible this being permanent reducing the amount of nutrients the host would require to survive from then on.These new cells and tissues could also have recombinant DNA from extremophiles present within the microbes already and other organisms such as faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles and scratch DNA etc as detailed earlier on to allow H.sapiens to survive indefinitely in carbon dioxide rich and oxygen low conditions allowing the brain and other organs to run on carbon dioxide in certain conditions such as a stroke or strangulation,heart attacks,sudden arrhythmic and infant death syndrome and similar cardiac ailements,elliptic fits,strokes,trauma and even severe bleeding,blood loss,suffocation,smoke caused by fires,heart attacks,strokes,choking,oxygen free environments,high mountains,swimming,smokey areas for several hours longer or in time even indefinitely.Those from R.sylvatica,Tardigrade,Bacillus F,P.putida GR12-2,H.glaciei,C.pleistocenium,psychrophiles,from scratch allowing for cryoprotectants applied by the microbes,by the cells themselves or even external sources to be applied for cryonics and also survive extremely cold conditions in the external environment that humans could not normally survive with other recombinant DNA added to survive high temperatures,pressures that only extremophiles and not humans can survive.This can be done by the new tissues created by the microbes containing these genes that are spread down by mitosis and gene drives or them spreading them to native cells in waves via horizontal gene transfer and again spread from each generation via mitosis and gene drives.Recombinant DNA from Planarians,A.mexicanum,Hydra and C.elegans can be added to repair damaged tissue.
Upgrades for new augmentations and new phenotypes of all strains can be done via one going into hospitals where they can collect new microbes of the desired strains with new phenotypes,abilities etc.One will arrange with Paean to have it booked beforehand.When arranged by Paean he will interact with the AI of the nearest hospital.Each hospital will have growing rooms where there is a 3D DNA printer that prints out the new microbes with the new genotypes that are grown to several million or billion that is then injected into a vial that has a biosynth chip with the patients ID and is ideally composed of biosynth plastics instead of glass to allow it to be recycled easily with the vial picked up by patients in automated pharmacies in the hospital by sending ones patients ID to it.Biosynth WiFi will allow Paean to cause the existing microbes of that strain to undergoe apoptosis to be flushed out of the body to allow the new microbes take there place.The new microbes can be injected using phlebotomy robots or reuse able biosynth plastic syringes.Otherwise it can be mailed to the patients address where one can inject the microbes using reusable biosynth plastic syringes.Ideally patients will have home 3D DNA printers that allow one to print out and culture their own microbe upgrades using vats,phlebotomy robots and syringes with these upgrades authorised by Paean thus decentralising the process where one can get instant access to them at home saving time and energy with their being a countdown as to when they will be ready.In time biosynth WiFi within microbes can be utilised to negate the need for 3D DNA printers and vats with this done by having WiFi from routers in homes and public buildings as well as that generated by smartphones etc to induce the evolutionary path of genes within the microbes.The WiFi would induce the taq polymerase and Cas-9 to change the genes present in them to evolve into new desired genes.This would delete old genes and replace them with new ones.If perfected it would decentralise the process allowing it be done at home with zero energy use and even be done in wilderness areas using biosynth WiFi generated from smartphones etc.Biosynth WiFi can also change one strain of microbes into another.This will be used by strains in emergency situations such as new infections and new instances of poisons detected by base microbes.If possible biosynth WiFi can be added to the cells of patients to then allow the application of new CRISPR treatments to be recognised by the body with all CRISPR treatments relayed to digital patients file both logged as a treatment and added to the genome stored in their patient will be altered to keep it up to date for Phanes Activation Gene technology,identification purposes,phone numbers etc.This addition of biosynth WiFi to the genome of patients can allow for biosynth WiFi to induce the evolution of genes in a patients cells to allow for them to given the latest a upgrades for augmentations to be relayed to patients within minutes from home via biosynth WiFi with again a countdown used.This can change one type of strain into another with once perfected may render 3D DNA printers obsolete in homes and waiting rooms in hospitals with them still used in homes for home farming.
Microbes can be used as pathogens to attack only specific species of animals and plants by being coated in their DNA with them inoculated via pests and also arthopod biosynths that would mimic the effects of human viruses such as HIV etc by attacking the immune system and causing cells in key organs such as the heart,ovaries,brain etc by attacking the immune system and causing cells in key organs such as the heart,ovaries,brain and testes or roots in plants to undergo apoptosis thus killing them off and causing sterility and stimulate tumourgenesis.Since based on the animals leukocytes and plant cells they would go unnoticed by the hosts immune system and thus be more effective.Human versions of this namely FOXDIE would do the same by first decimating both microbes in the body and native leukocytes and then remove accelerated healing phenotypes and also carbon dioxide used as an energy acceptor to allow the heart and other organs to be attacked as well as allowing opportunistic infections to be able to kill the host with it even removing anti-cancer genes and stimulating the production of tumours by attacking the immune system and causing cells in key organs such as the heart,ovaries,brain etc by attacking the immune system and causing cells in key organs such as the heart,ovaries,brain and testes or roots in plants to undergo apoptosis thus killing them off and causing sterility and stimulate tumourgenesis.Since based on the animals leukocytes and plant cells they would go unnoticed by the hosts immune system and thus be more effective.Human versions of this namely FOXDIE would do the same by first decimating both microbes in the body and native leukocytes and then remove accelerated healing phenotypes and also carbon dioxide used as an energy acceptor to allow the heart and other organs to be attacked as well as allowing opportunistic infections to be able to kill the host with it even removing anti-cancer genes and stimulating the production of tumours.
These biocompatible microbes as stated earlier on would divided into various strains that perform different functions or fight off pathogenic viruses,fight off pathogenic bacteria,stem cell strains,immunising strains that immunise patients agains pathogens replacing vaccines.
CRISPR utilised by anti-ageing,genetic disease correction strains and augmentation strains will make these modifications and gene therapy treatments more accurate and effective.CRISPR treatments will be applied by anti-ageing and augmentation strains through horizontal gene transfer controlled by AI by biosynth WiFi.Even proto AI could apply these treatments with this involving the microbes transferring DNA including scratch DNA developed by Phanes and recombinant DNA from plants and animals present in the strains of these microbes that are then applied to them.This will allow the phenotypes of the genes added to the patients genome in each cells to be then expressed by the cells in patients.The anti ageing strains etc will house DNA from yeasts to allow them to transfer CRISPR treatments to the cells of patients through horizontal gene transfer thus giving them CRISPR gene therapy treatments to halt and reverse the ageing process and have augmentations.CRISPR will involve genes from existing plants and animals and those created by Phanes from scratch added to the genome of living patients through horizontal gene transfer exhibited my anti ageing and augmentation strains that will once added to the genome then exhibit those phenotypes.For example the genes from bacteria that exhibit DNA repair once added to a patient genome will thus repair telomere damage etc with the genes from other plants etc added to them exhibited.In otherwards in layman’s terms CRISPR is a gene editing technology that will by adding genes to a patients genome give living patients the abilities of that gene such as augmentations from extremophiles and those to treat genetic diseases and both halt and reverse the ageing process.Biocompatible microbes through having horizontal gene transfer present from yeasts will be able to apply CRISPR treatments that includes DNA from existing living organisms and new genes derived from scratch from Phanes will thus through CRISPR will be used to cure genetic diseases and halt and reverse the ageing process in existing living human and animal patients worldwide by it allowing new genes to be added to a patients genome in each and every individual cells and this will be done through anti-ageing and augmentation strains exhibiting horizontal gene transfer and also taq polymerase and Cas-9.Epione and AI would first carry out simulations on its effectiveness on chimpanzees,mice and humans before trials begin.This could be done by altering the host cells they infect unable to harbour them(in the case of HIV this would remove the receptors on leukocytes that allow the virus to attach and infect them thus replicating while other treatments eradicate the virus),or alter and strengthen the immune system namely CD4+ T Cells strengthened to recognise and fight off HIV with custom made anti-viral and antibody compounds as well as cancers earlier on.HIV resistance could be gained from populations genetically resistant to them transferred to other non resistant populations from both humans and closely related mammals as well as even from scratch with this replicated with other pathogens and viruses as well as specific cancers.Thus the non resistant humans using DNA from resistant populations could have their leukocytes to be unable to be infected by HIV by editing their surface proteins and the same replicated with all major viruses that infect leukocytes allowing biocompatible microbes to remove HIV virions.Recombinant DNA need not come from humans but also from closely related primates and mammals with similar immune systems and resistance with their resistance to Simian Immunodeficiency Virus and also recombinant DNA from SIV itself with this also applying to all viruses that infect leukocytes such as Ebolavirus,N.meningitidis etc.The patient file system will quickly identify which populations have this phenotype and what genes are responsible for this with known people that have this will have their DNA analysed and compared to those that suffer from the disease to isolate it.Microbes as detailed will apply this resistance to infected patients with N.meningitidis,HIV and Ebolavirus forcing the viruses to interact with other microbe strains and thus curing infected patients of the disease with ideally all patients including those currently not infected with HIV,Ebolavirus also modified to have their leukocytes and organs made unable to be infected allowing other strains of microbes to eradicate the pathogens or at least make them asymptomatic carriers before they gain a stronghold with resistance and microbe strains able to attack them made a permanent feature of the human genepool via germline therapy alongside immunising the primary immune system indefinitely also wiping out the disease in newly infected patients and uninfected patients while it is unable to infect leukocytes.Further advances in artificial intelligence will make germline therapy safe negating the need for having to screen every embryo,sperm and eggs with this first tested on animals with Epione again carrying out simulations on these on its effectiveness on chimpanzees,mice and humans before trials begin using advanced gene drive therapy technology.Gene therapy that treats every cell in their body will limit phenotypes such as correcting faults and mutations that cause specific diseases and immunities to diseases such as the immunity to HIV,cancer and even upgrades to the patient with germline therapy used to ensure these are passed onto the mother and fathers child thus allowing that child to pass on immunities to cancer,pathogens and other desired phenotypes onto the next generation without the need for microbes making them a permanent part of the genepool of H.sapiens with them also removed from the genepool via germline therapy if desired.Germline and advanced gene drive therapy once perfected will allow these to become a future feature of successive generations alongside screening,correcting and modifying spermatozoa,eggs and embryos for these diseases and using CRISPR to correct them with biocompatible microbes used to perfect this with them residing in or outside the testes and ovaries that insert gene therapy into each and every spermatozoa and egg individually by them,altering the genome of fertilised embryos or by them even altering the genes in these organs ie the ovaries and the testes responsible for the production of spermatozoa and eggs or the entire host DNA using advanced gene drive technology to ensure that all future sperm and eggs are free from the genetic faults and mutations allowing one to conceive children naturally and not have to use in vitro fertilisation without passing on these diseases to the next generation removing them from the human genepool indefinitely more easily.If perfected this advanced gene drive technology combined with germline therapy made by microbes to edit the hosts DNA precisely and permanently applied to all cells including those in the ovaries and testes that in turn produce spermatazoa and eggs to negate the need for them to edit every single egg,spermatozoa and thus allow them to conceive genetic disease free children naturally and also pass on desired phenotypes of H.ubermensch.This would thus mean eggs,embryos etc would no longer have to be screened for genetic diseases and with correcting CRISPR treatments added to all cells of a body including ovaries and testes would have pass these CRISPR genetic corrections passed onto all future produced spermatozoa and eggs and all conceived offspring thus either eliminating mutations that cause genetic diseases from passing onto all future generations and the human gene pool if applied to all patients worldwide or pass on augmentations etc to all future generations automaticallyThis could potentially eliminate all genetically based diseases including neurological disorders and developmental disorders from the human genepool as well as passing on genes into the genepool that will naturally be passing them onto the next generation without the need for germline therapy and microbes thus eliminating a disease indefinitely with them also altering humans to the point that those that are environmentally caused like cancer by making humans immune to the causative agent ie in the case of cancer removing the ability for tumours by adding genes from animals that never get cancer,extremophiles like T.gammatolerans to make humans resistant from radiation and also those from scratch to prevent carcinogens from being able to affect the body as well as immunising humans to oncoviruses that can be passed from mother to child via the placenta and breastfeeding.It will play a prime role in the development and eventual creation of populations of H.sapiens or all of H.sapiens with desired characteristics of H.ubermensch mainly that from T.gammatolerans to make humans resistant to radiation of all types,Salmonella to make them resistant to the effects of low gravity,Tardigrade,D.radiodurans and those from scratch to survive the vacuum of space,psychrophilles to survive sub zero conditions,synthesise all essential amino acids/fats/vitamins etc,oligotrophs and xerophiles to make them require less food and water(which can be applied to living patients via horizontal gene therapy)and eventually lead to the rise of H.ubermensch separate from H.sapiens via intensive germline therapy over several generations.Ideally these phenotypes of H.ubermensch will be added to all living patients worldwide and become part of the human genepool via advanced gene drive technology while not creating H.ubermensch with them added for their properties ie making the H.sapiens immune to radiation,require less nutrients,be able to survive extreme pressures,the vacuum of space.This would allow living populations of H.sapiens to survive extreme conditions on Earth,on other colonies both permanently as well as temporarily if containment procedures fail there and also on interstellar vehicles and stations.Anti-ageing genes from T.gammatolerans,Bacillus F,oligotrophs,xerophiles etc can be added to the gene pool via advanced gene drive and germline technology if shown to safe in both humans as well in animals will alongside the presence of these strains will have these anti-ageing genes,removal of genes and also production of anti-ageing compounds passed onto the next generation and thus a permanent feature of the human genepool.Gene therapy via microbes and CRISPR will also play a role in giving populations of H.sapiens via first live patient and germline therapy characteristics of his evolutionary successor and cousin as detailed later on H.ubermencsh as well as leading to the rise of H.umbermensch.H.ubermensch should be possible through extensive genetic engineering by at least 2045 with it also allowing humans to manipulate the genomes of other animals and plants thus creating entirely new species of plants and animals created on Pandora with Phanes extrapolating the genotypes of them.As detailed later on this will also lead to the creation of new sentient sentient races on par with humans created from scratch or using exiting non sentient animals from all taxonomic ranks of the animal kingdom as a baseline with this allowing for colonies like Mars,Venus and other extrasolar colonies in the universe with no life to have millions of non sentient and even sentient species created with whole taxonomic ranks creaked by Phanes adapted to their terraformed environment.Any faults in the gene therapy that could lead to mutations and breaks could be dealt with advanced gene drive technology that used specific genes,application etc to prevent them with all gene therapy treatments for ageing,augmentations etc will use advanced gene drive technology to prevent faults and pass them onto all future cells via mitosis with them applied to telomere,mitochondrial and other DNA.If possible base microbes or specific strains in females could detect mutations in embryos that lead to those are not hereditary ie those that lead to Downs syndrome and other developmental disorders through via horizontal gene transfer putting in genes or chemicals and even compounds that allow for these mutations to be detected and then signal to the microbe that it has occurred to allow the correction to be corrected by the microbes or those added via inbreeding at the during development of the embryo or while the fetus is in its early stages of development.It could also be used to apply the Phanes method to individual spermatozoa,eggs and embryo in utero with multiple microbes suited to this passing on desired alterations to each one.Spermatozoa and eggs that are frozen and stored in banks by donations and for later use in later life pregnancies can be corrected for all types of genetic diseases that may pass into potential offspring can have the corrections be done by biocompatible microbes in storage or prior to or during storage due them having the ability to survive low temperature due to them having DNA from psychrophiles.For parents who may pass on genetic diseases determined by AI sperm and eggs can be collected from both parents fused together by robotics and then screened for diseases including Down’s syndrome and similar heredity disease both physical and mental and then CRISPR through the microbes could be used to edit these deformities out safely with AI managing this or the editing can be done to the eggs and spermatozoa or both prior to fusion and they then implanted into the mother via IVF allowing parents who have the potential to pass deformities down to their child have children of their own and not resort to surrogacy programs.Gene therapy for these and other conditions should be pursued for already living patients suffering these in tandem to this with it also being used to treat ageing,Downs syndrome(and other disabilities),schizophrenia,Multiple sclerosis,parkinsons,alzheimers and deal with cancerous and precancerous cells and correct mutations that cause cancer again tested on mice and chimpanzees with again Epione carrying out simulations on these on humans and test animals.Downs syndrome if detected could if possible be treated using CRISPR to remove the extra chromosome,inactivate them in every cell preventing this from occurring in all future cells by adding genes that remove and then prevent the replication of a third chromosome 21 in each cell first tested on chimpanzees engineered with Downs Syndrome or even alleviate the symptoms of it rather than choosing to discard the unborn fetus with microbes repairing any faults and correcting defects such as low intelligence and heart defects.The same may apply to those with intersex disorders.All CRISPR treatments to treat ageing,genetic diseases,developmental and neurological disorders and those for augmentations etc in living patients will apply the genes to telomere/chromosomal/nucleur and mitochondrial DNA in all cells in the body and if need be plasmids for stability and uniformity.These augmentation genes and those to treat neurological disorders will be passed into leukocytes to allow them to survive extremophile conditions while beneficial bacteria in the gut can be given them as well alongside those made to express human surface proteins to make them immune to immune responses with pathogenic bacteria in the gastrointestinal tract not having these to allow them to die from exposure to these conditions and the primary immune system.Theh will not be given anti-ageing treatments to keep their populations stable.Anti-ageing treatments will be applied to bone marrow in a way to prevent leukocytes housing this DNA and thus living forever that would cause them to overrun the body or if shown to have their levels controlled by microbes via chemical signals or if possible undergone apoptosis and flushed out of the body can have this DNA present with all augmentations and genetic disease treatments added to bone marrow to allow leukocytes survive these conditions and be free of these diseases.Thus bone marrow will house anti-ageing treatments in a way to prevent leukocytes living forever but leukocytes will house CRISPR treatments to treat genetic diseases and augmentations such as radioresitence to survive these conditions through being properly applied in the bone marrow.The same will apply to erythrocytes wherein they recombinant DNA to treat genetic diseases and augmentations such as radioresistance will be applied to the patients genome to allow erythrocytes to survive these conditions but anti-ageing treatments will not interact with those responsible for erythrocytes preventing them living forever.Bone marrow and other parts that are responsible for the production of erythrocytes and leukocytes will be given anti-ageing treatments but through their placement on the loci and scratch DNA will be made to stay youthful but ensure that the erythrocytes and leukocytes they produce don’t carry the anti-ageing treatments thus allowing to die off and not overrun the body with Phanes developing genetic countermeasures to this with microbes from 2029-2035 ensuring that any possible immortal excess leukocytes etc can have their replication controlled and undergo apoptosis if their levels get too high.Beneficial gut flora will have augmentations added but not anti-ageing treatments to allow turn to survive extreme conditions and also prevent them overrunning the body by allowing them to die off.Pets owned by the public,livestock and animals in zoos will be able to avail of anti-ageing treatments and those to remove genetic diseases and augmentations via species specific microbes.All treatments to living cells in living patients will also use advanced gene drive technology to ensure the treatments pass from each generation of cells to the next via mitosis.Junk DNA and DNA that leads to ageing,genetic deformities and other unnecessary DNA will be removed to accomadate new CRISPR treatments to treat ageing and augmentations to prevent the finite nucleus becoming packed with DNA.Temporary augmentations form scratch and animal etc sources will involve ones original DNA for the phenotype being removed and replaced with the new DNA thus some augmentations that are used temporary ie having the same smelling and hearing ranges of other animals or changing eye and hair colour when unwanted will be removed and replaced with ones original DNA etc.Temporary augmentations that affect only part of the body will possibly be applied to the specific organs and tissues they affect such as those for different smelling ranges may only to be applied to genes present in cells in the brain and nose,those for different visual ranges may only be applied to genes present in cells in the brain and the eyes or just the eyes and so on.Cells in the body can be engineered to house ribosomes and in particular plasmids and in particular plasmids that are strands of DNA that float in the cytoplasm that express extra phenotypes for augmentations via specific DNA and thus phenotypes.Mitochondrial DNA can be modified to house extra phenotypes than the main genome that cause the cells and tissues to express their phenotypes.Better sources of scratch and recombinant DNA will replace older ones by removing them from the patients genome.If possible advancements in Phanes developing scratch DNA will allow DNA to express two or more phenotypes at once.Sources of recombinant DNA from animals,plants and unicellular life forms such as bacteria,fungi,viruses that’s express two or more desired phenotypes can be utilised for example T.gammatolerans can survive radiation levels of up to 30,000Gy and at the same time potentially express DNA repair that will prevent future damage and degradation in mitochondrial and telomere DNA to combat ageing and eliminate cancer,genetic diseases,developemental disorders etc from the human gene pool and protects one from levels of radiation of up to 30,000Gy all at once.Thus this could eliminate the need for D.radiodurans,Bacillus F DNA and scratch DNA to combat all of these since this DNA express several phenotypes and applications at once with research done into scratch DNA and that from plants and animals as well as micro-organisms that express multiple phenotypes and applications at once for augmentations and combat ageing.This will be done to deal with the limited space in the human genome and nucleus that holds them.The human genome is estimated to contain roughly 30,000 genes or 3,000,000,000 base pairs with it hypothesised that about 75-98% (between 22,500 – 29,400 genes or 2,250,000,000 – 2,940,000,000 base pairs)consists of non coding junk DNA that has no biological functions and thus could be easily replaced with new recombinant DNA from plants,animals and micro-organisms and scratch DNA without damaging or negatively affecting the patient.Genes in the body that contribute to the ageing process can also be removed and replaced with those for augmentations and those to reverse and halt the ageing process.Paris japonica is the organism that has the largest genome with roughly 150,000,000 base pairs and 1,500,000 genes about 50 times more than humans.If humans through intensive research into genetic engineering and CRISPR be able to hold the same amount of genes and base pairs as P.japonica then it will vastly increase the amount of storage space for DNA from extremophiles,plants,animals,micro-organisms and scratch DNA for augmentations and anti-ageing treatments and also cater to Phanes Activation Gene Technology with it more than enough to meet our needs.Research using human cell and tissue cultures will be done to see if they can hold this amount of genes after initial treatments to end ageing etc.New species of plants and animals found on plants across the universe will be scanned to see if they have larger genomes with scratch DNA developed alongside other methods to determine the theoretical limit size in terms of base pairs and actual genes of DNA that can fit in human cells.Tests will be done on human cells extracted from a patient or those created using 3D DNA printers to see if they can fit the same amount of genes and base pairs as P.japonica with them using base microbes etc find ways to give these cultured cells the same number of base pairs in otherworlds using microbes ways will be found in labs to give cultured human cells the same amount of genes and base pairs as P.japonica so as to find the best ways to give living human and animal patients the ability to hold the same amount of base pairs through gene therapy as P.japonica with this repeated with scratch DNA that can give humans even more base pairs up to the theoretical limit.Test animals and biosynths that have human recombinant DNA will be used in tests as well to determine the best way using gene therapy and what genes need to be added to add to living patients the same amount of base pairs and genes as P.japonica or the theoretical limit.Thus P.japonica and scratch DNA can be engineered to give living patients this new base pair size.If need be the cells of the body of humans etc may be engineered through CRISPR to become slightly larger that is the same size as that of P.Japonica.This will be done on human cells extracted from a patient or created using 3D DNA printers will that contain DNA from P.japonica to see if they can fit the same amount of genes and base pairs with them using base microbes etc find ways to give these cultured cells the same level base pairs in otherworlds using microbes ways will be found in labs to give cultured human cells the same amount of genes and base pairs as P.japonica so as to find the best ways to give living human and animal patients the ability to hold the same amount of base pairs through gene therapy as P.japonica with this repeated with scratch DNA that can give humans the theoretical limit.Thus once it is possible to determine the theoretical limit of base pairs that can fit into human cells tests on gene therapy applied to cultured cells in labs with if possible test animals such as mice etc housing human recombinant DNA and biosynths used will be done in order to apply this new limit to living humans.Thus once it is possible to determine the theoretical limit of base pairs that can fit into human cells tests on gene therapy applied to cultured cells in labs with if possible test animals such as mice etc housing human recombinant DNA and biosynths used will be done in order to apply this new limit to humans.If possible human cells can be engineered to house an extra one or two nuclei to house entire chromosomes DNA that will be engineered to hold only augmentations and not programmed to express any phenotypes thus being technically junk DNA.Biocompatible microbes will house this genome size to hold more recombinant DNA for each strains treatments and functions,to hold extra space for augmentations to survive in the body and also hold at least 150ZB data storage and RAM especially for biosynth technology.It can also be used to increase the genetic variation of possible genetically distinct that can occur between each and every single male and female during sexual reproduction from 64,000,000,000,000 to 3,200,000,000,000,000.Crops,fish and shellfish,livestock,algae,bacteria for producing commodities,stem cells for invitro meat and ornamental plants will utilise DNA from P.japonica etc and scratch DNA to house more DNA for augmentations including scratch DNA to increase growth rates and yields.If possible human cells could be engineered to hold an extra second nucleus that can contain and extra three metres of DNA that is junk DNA or that consisting of augmentations with DNA from P.Japonica in both the original and this second nucleus increasing the amount of DNA.All new modifications will be instantly relayed to ones patient via being both logged and also ones DNA scan modified.The genes to reverse and halt the ageing process should be able to be held in existing DNA present in the human genome alongside key augmentations such as the acellerated healing phenotype with this research done as a backup and measure to house extra augmentations.The anti-viral,anti-bacterial,anti-fungal strains,anti-helminthic,anti-cancer strains will be engineered to interact with only bacteria,viruses,tumours and parasites for each strain to prevent the applying suicide and other CRISPR treatments to human cells and that of gut flora.CRISPR treatments to alter pathogens and parasites like those to treat ageing will be done via horizontal gene transfer.Horizontal gene transfer will be used by anti-ageing,augmentation and genetic disease strains to transfer CRISPR treatments to the patients cells and them engineered to interact with only human cells.The anti-ageing and augmentation etc strains will be engineered to only interact with only human cells ideally those of the patient via surface proteins on them that only interact with only human cells to prevent them applying these to pathogens that would allow them to live forever with them via induced evolution and other sub strains engineered to interact with gut flora.Horizontal gene transfer will be utilised by the microbes different strains using DNA added to the microbes from yeasts,bacteria etc that are able to do this with them using taq polymerase and Cas-9 to recreate strands over and over again via biosynth WiFi.Horizontal gene transfer engineered to interact with human cells can thus allow current living patients to avail of CRISPR treatments such as augmentations and also those to reverse and halt the effects of ageing etc by allowing CRISPR treatments to be added to the cells of living patients.All cells in the body will have the new genes added with advanced gene drive technology also in cells in the testes and ovaries ensuring it is passed onto the next generation through the spermatozoa and eggs produced in living patients carrying these modifications to the next generation thus making them permanent features of the human genepool and the children of the affected individual with these if desired removed from living patients and their young by microbes.Thus all alterations to a living patients and also those in their progeny can be reversed by removing the applied genes.If any CRISPR treatments do cause any unwanted side effects to a patient then it is simply a case of them being removed as soon as possible.Faults caused by gene therapy will be corrected by treatments done as soon as possible.The estimated time for all treatments to all cells in the body to be finished will be visible in ones patient file and relayed by the nanomachines as a countdown in hours,minutes,seconds with treated areas of the body relayed to the patient file as well as through chemical signals such as unique smelling and coloured urine etc with the microbes via nanomachines relaying what parts of the body have been treated visible as a map of their body and percentage in real time in their file as a percentage.Advanced gene drive technology will be utilised to ensure that all CRISPR treatments for ageing and augmentations as well as correcting genetic diseases will be passed onto each generation of cells during mitosis and it even pass down to each generation of offspring alongside germline by being present in spermatozoa and eggs via both germline therapy the genes and advanced gene drive technology present in both the eggs and tests of patients negating the need to edit each and every spermatozoa and eggs and not having to be added to each newborn.Anti-ageing,genetic disease etc strains will be able to undergo mitosis and have flagellum to allow them to spread to all parts of the body when only a few thousand or million microbes are injected.Base microbes will routinely scan DNA to see if treatments are in each cell and are present and passed down from generation of cells and to see if any faults have occurred with faults corrected by those that applied the original treatments signalled to do so.With regards to ageing it will also detect the levels of Phosphatidylcholines.These will all be logged in the patients file.All types of strains that apply CRISPR treatments will be able to recreate the CRISPR treatment over and over again via taq ploymerase and Cas-9.Chimpanzees and mice that have human recombinant DNA in them used as test subjects by 2023/2024 with them engineered with each type of neurological,developmental,genetic disorders etc and use in ageing and augmentation trials to get more realistic results transferable to human trials starting in 2025.3D DNA printing will create the spermatozoa and eggs with these phenotypes and the patients unique DNA from patient files to cut down on labour costs with patient specific DNA to aid in creating treatments suited to each patients condition with regards to those that have neurological,developmental disorders and genetic diseases.To deal with the issue of Cas-9 eliciting immune responses it could be modified to contain some or all human proteins entirely as an human and patient version of Cas-9 as well as protein bumpers that dont illicit an immune response used as an mini vector to transfer DNA by flooding methods.This would be done by first modifying the DNA of S.pyogenes itself with human recombinant DNA to create a human or patient specific version of Cas-9 with the same done for all animals that will utilise it.Cpf1 from F.novicida can be used for this and also apply CRISPR treatments alongside Cas-9 from S.pyogenes.To prevent the issue of immune responses human versions of Cas-9/Cpf1 or even patient specific versions of Cas-9/Cpf1 can be created by AI namely proto and final Phanes can analyse the genome of S.pyogenes,F.novicida and modify it for humans and individual patients present in the their own leukocytes that contains their trace DNA by also analysing both human DNA and patient specific DNA.The anti-ageing,augmentation and genetic disease curing strains as well as the anti-viral etc strains in order to carry out CRISPR treatments would need relevant DNA from S.pyogenes,F.novicida,T.aquaticus in order to utilise CRISPR Cas-9 as well as taq polymerase to recreate strands of CRISPR treatments over and over again allowing each microbes to apply these treatments over and over again.These microbes since using ones own or 3D DNA printed blank leukocytes as a vector would prevent the issue of eliciting an immune response as seen in both foreign viruses and bacterial vectors.The 3D printed blank leukocytes will house human DNA,the hosts own DNA from their patient file inserted alongside other DNA from relevant multi and unicellular organism from Physis with this changing when passing from one generation to the next and would transfer the DNA using horizontal gene tranfser to only human cells interact by interacting with the unique surface proteins of the human patients cells and not that of pathogens.Otherwise ones own leukocytes will have DNA added by 3D DNA printers.Humans and animals will utilise their own leukocytes as a baseline for microbes to apply gene therapy to prevent them illiciting an immune responses that could be fatal or render them ineffctive and allow them to be more precise and effective and each patient will have their own patient specific versions of CRISPR Cas-9 could be created using the patients DNA in their own leukocytes with them changed when they pass to the next generation to further prevent immune responses with Phanes creating these in microbes when they are printed out by 3D DNA printers.This will allow all strains to form a permanent part of the body and act as the perfect vector of CRISPR treatments and anti-viral etc treatments with the human and indeed patient specific versions of Cas-9 created by 2023/2024 ready for proto microbes and bacterial vectors that have human protein coats due to the presence of human DNA,ideally the patients DNA and human versions of Cas-9 to give those currently aged 80-95 anti-ageing treatments to the interior vital organs and give them other treatments to allow them to survive strokes etc long enough to receive more advanced treatments in 2029 to be reverted to a state similar to their early twenties.This will also allow anti-ageing strains,augmentation and those to treat genetic diseases alongside all other anti-viral and anti-bacterial strains to undergo mitosis using bacterial DNA to treat each and every cell in the body with taq polymerase and Cas-9 to recreate the strands of DNA and also Cas-9 in the strains allowing them to treat countless cells with the DNA from macrophages and ameobas will allow them to move inbetween cells.Advanced gene drive technology will be used to ensure the therapy is permenant.Gene therapy will be applied via either horizontal gene transfer using Cas-9 or via flooding where protein bumpers housing the DNA and also synthesised Cas-9 will act as a mini vector allowing the Cas-9 and DNA to be sent to the relevant areas of the the genome specifically.Animals will have their own leukocytes as baseline and their own version of Cas-9 with them each having their own unique species specific microbes consisting of the same strains as in humans.Thus both livestock and pets of all species will have their own versions of microbes created for them including immunising,strains,anti-viral and anti-bacterial strains and also anti-ageing strains and them given the same augmentations as humans with all pathogens whether viral,bacterial and fungal of each species will be tested against compounds from the bites,stings and excretions of all plants and animals around the world to create anti-microbial compounds against them as part of anti-viral and anti-bacterial strains and those to fight off parasites with immunising strains immunising both pets and livestock against all pathogens especially zoonotic diseases to eliminate antibiotics from the food chain.Crops and plants whether in the wild or ornamental ones will using bacteria that contain the hosts species DNA and their own species specific version of Cas-9 with them giving their own fully functioning immune system via CRISPR that uses their microbes as a baseline leukocytes.Each species of plant whether crops,ornamental or wild one will be first given a fully functioning immune system in labs using bacterial/plant cell hybrid vectors and CRISPR and then their version of leukocytes created that can be immunised and microbes of all strains created using these plant leukocytes with this replicated with Apidae.This will be done to develop their own species specific microbes and also immune system that can be immunised against pathogens negating the need for chemicals to fight of viruses etc with them having their own strains modelled on human versions including those that also fight off infections as backup ie anti-viral,anti-bacterial,anti-fungal strains that use CRISPR and anti-microbial compounds rendering bactericides etc defunct.Existing plants in gardens can be inoculated by syringes and watering cans containing a mixture of water and microbes that enter the roots with biosynth wifi from smart devices causing upgrades with in time biosynth artropds injecting them into leaves etc.Animal trials begging in 2023/2024 will use their leukocytes with them having human recombinant DNA added to them to have an immune system identical to humans to ensure that these leukocytes can have these human version Cas-9 used in them to see if no immune response can be caused by them especially in chimpanzees.This engineering would also have these animals produce leukocytes similar to humans with human DNA and use this human Cas-9.To further prevent immune responses it may be possible for the Cas-9 to be suited for each patient using their unique DNA that is changed to that of their offspring as they pass from one generation to the next as detailed later on to further prevent allergic and immune reactions.This can be done via Phanes modifying DNA relevant to it and CRISPR from S.pyogenes.All types of microbes of each species of plants and animals will be since using the species leukocytes and in the case of plants those made from scratch will only be able to interact with the species they are designed for to prevent them affecting any species they contaminate with them also destroyed by the hosts own microbes they infect once detected by base microbes as well as programmed by AI to undergo apoptosis if they are in the body of foreign species.They will also consist of different strains for each species and will be engineered to only interact with the specific target they are designed to via the surface proteins on them ie anti-viral strains will interact only with viruses and anti-bacterial strains with bacteria and so with augmentation and ageing strains engineered to only interact with human and the patients cells.As a result of this need to remove the effects of senescence universal debate and legal acceptance will have to made for the use of CRISPR gene editing techniques especially with regards to screening for diseases and even then removing gene(s) associated with genetic diseases to remove heredity deformities and diseases from humanities genepool entirely once an embryo created by invitro fertilisation has been screened or both the egg and sperm have been screened and edited ie.allergens,addictions,genetic based obesity and diabetes,certain cancers,parkinsons,alzheimers,eplipsey,colour blindness,blindness and deafness,channelopathies in newborns and other mutations that cause sudden infant death syndrome,haemophellia,Huntington’s disease,congenital heart conditions as well as adding resistance to and ability to fight off or prevent infections such as HIV,HPV(especially those associated with cancers),Epstein–Barr virus and terminal genetic diseases,with this procedure first tested on mice and other apes such as chimpanzees with gene drives used to make the alteration permanent.There has been success in CRISPR gene therapy in curing blindness etc within the last few years using viral vectors with this a great achievement since the technology is only 10 years old.The production and use of biocompatible microbes to utilise CRISPR gene therapy will expedite the development of gene therapy to halt and reverse the effects of ageing,cure genetic diseases from 2029-2045 onwards
Base Microbes:
Base microbes will have numerous functions such as detecting the species of a pathogen and send this to Paean and relevant anti-microbial strains.They will also detect the name of toxins that enter the body and again relay this to Paean and crossrefferfncing Physis.To detect the species of a pathogen and parasite in an infection via copying and scanning its genome using taq polymerase,CRISPR Cas-9 and horizontal gene transfer the second they enter cuts,the mouth etc and thus enter the bloodstream by being directed to the site of infection via wifi by Paean directing them to the site of infection with them uploading the DNA to Paean and him crossrefferncing Physis to allow the specific species and strain of bacteria,virus and fungi and even parasite to be instantly ascertained and thus allow if genes present for resistance are present to be also ascertained.By copying and scanning the DNA of the pathogen and parasites using taq polymerase,Cas-9 and biosynth wifi the base microbes will be able to determine if it is a bacteria,virus,fungi or parasite,what species it is by crossreferencing Physis instantly and activate the relevant strains through wifi and also which compounds and CRISPR treatments to use with the specific species and strain determined also.Biosynth WiFi will crossreference Physis in the wire to determine the species and download any data such as surface proteins,CRISPR treatments,bumpers,antibodies etc into the DNA digital storage and genome of all strains used by Paean.The scanned genome will allow one to determine what resistence to antibiotics and anti-viral treatments etc they have and thus allow correct CRISPR treatments to be utilised.The correct CRISPR treatments will be ascertained and then applied with if new genes are present then Phanes can extrapolate CRISPR treatments to these that can then be downloaded through wifi.Once base microbes have determined the species and strain of a pathogen and parasite they will awaken the anti-viral,anti-bacterial and anti-helmetic strains whichever are needed through chemical,biosynth WiFi and Bluetooth signals and then alert them to their presence with base microbes at key points searching for their location and alerting each strain to the different locations and to undergo mass replications.They using biosynth wifi controlled by Paean and chemical signals will then activate anti-viral,anti-bacterial,anti-helminthic etc strains and thus allow them to apply the correct CRISPR treatments to remove resistence present with them at the start also apply CRISPR treatments to cause them to undergo apoptosis and even those that prevent them undergoing mitosis and even replication by preventing them able to do so directly by inhibiting their ability to undergo mitosis or in the case of HIV remove their GP120 glycoproteins that allow them to infect cells in the body.Thus by scanning the genome the correct CRISPR treatments to be utilised will be ascertained with in the case of new genes that are present then new CRIPSR treatments to be extrapolated by Phanes analysing the new strands at least 2045 these can be ascertained in minutes and will be downloaded in minutes via evolution.Once the base microbes ascertain the species of pathogen and whether it is a parasite,fungi,bacteria,virus it will call for the relevant strains via chemical signals and wifi under the control of Paean to gather in the area once awoken from endospores and they will be told via chemical signals and also wifi to apply CRISPR treatments and also download species and strain specific bumpers,endolysines,antibodies etc via biosynth wifi to be created by anabolic and catabolic reactions.AI will starting in 2023/2024 scan the outer structure and DNA of all species of parasites,pathogens whether viral/fungal/bacterial etc and all strains to extrapolate synthetic antibodies,bumpers,endolysines to be synthesised on demand and also counter CRISPR treatments to resistance genes with them stored in Physis in the pathogens and parasites file their to be downloaded instantly via wifi and stored in digital DNA storage in the relevant strains once the base microbes determine the genome of the invading pathogen and induce all of the microbes of these strain to awake from endospores and then create these genes via inducing evolution of the strains genome via wifi and taq polymerase and Cas-9.Wifi in public areas and home and also within neural implants and even on smart devices including cellular access by proxy as well as satellite wifi will allow this to be done in the wilderness.Paean in a fragmented form in neural implants and smart devices will be able to do calculations especially as the computing power of smart phones increases exponentionally of cellular or wifi access is not possible.Paean will take control of microbes via wifi and Bluetooth and the primary immune system via and chemical actions once the species and strains is determined.The resistance they have to any compounds would be removed via CRISPR treatments to allow them to be used by relevant strains with those that prevent them undergoing mitosis and replication and undergo apoptosis applied at the start to keep the the numbers of them stable and thus prevent them overrunning the body with these applied at the very start by relevant strains once they are detected by base microbes thus giving the microbes and primary immune system the upper hand at the start of infections within the first 24-48 hours especially in the case of dangerous pathogens and parasites such as MRSA,S.pneumoniae,S.agalactiae,Plasmodium,N.fowleri and also new pathogens and parasites before they can cause damage to the host.This will keep the levels of the pathogens in stable numbers by preventing them undergoing mitosis or in the case of viruses replication by removing glycoproteins etc making them unable to infect cells and in the case of parasites make them sterile and unable to infect cells.As a result the other strains will be able to download by biosynth wifi relevant bumpers,endolysines,antibodies,immunising genotypes or even DNA from plants and animals that express relevant anti-viral,anti-bacterial and anti-helmithic compounds and CRISPR treatments from Physis and then synthesise them via anabolic and catabolic reactions as well as undergo mass replication once called to the site of infection.It will also allow exact species to be ascertained for this and will also allow for new ones to have their genome scanned sent to Paean and analysed by him and Phanes for genotypes to create surface protein antigens that can be then sent back within at least a few hours or even minutes via wifi inducing the evolution of immunising strains to then have the primary immune system immunised and awoken to fight off the infection.In the case of pathogens the patient is already immunised against once the species is ascertained the primary immune system will be activated by chemical signals to produce the correct antibodies.Those that cause the pathogens and parasites undergo apoptosis will also be applied with any damage the pathogens and parasites cause especially new ones will be repaired instantly by the accelerated healing phenotype.This includes damage caused to the brain and liver by Ancylostoma,Plasmodium,N.meningitidis,N.fowleri and cytokine storms caused by Ebolavirus and fatal influenza strains of Orthomyxoviridae and also.The base microbes would also activate the anti-viral and anti-bacterial strains to signal to the primary immune system if it is also immunised to speed up the battle with the rest of the primary immune systems leukocytes brought to the site of infection and controlled by the microbes via chemical signals.The primary immune system mainly the memory B and T helper,plasma and killer T cells will be told the exact species and strain and thus what antibodies to use via chemical signals to remember and produce with Paean sending instructions to microbes.If not immunised then Physis can be cross referenced and the genotypes downloaded and the primary immune system immunised and activated if it is a new species or strain the genome can be sent to Paean and Phanes and will be analysed by both of the them to determine genotypes to create immunisations with once done the genotypes can be sent back via biosynth wifi within a week or in time 24 hours or less and the primary immune system immunised and then activated instantly.Other leukocytes will be called via chemical signals and their actions will be controlled using these sent by him from microbes ie inflammation,phagocytosis but them controlled to the point that fevers and other symptoms will be milder than normal and that they will spaced over long periods or short bursts whose timing can be relayed to the patient via Paean telling them what to expect and when to expect them.In otherwards Paean will control how the microbes and leukocytes react in battles against all pathogens including pre infected patients of HIV and new infections via sending wifi signals to microbes and signalling to them to produce certain chemical signals to initiate certain action in the primary immune response with certain actions carried out with certain symptoms of diarrhoea,night sweats,fever,inflammation etc avoided or if possible less intensive than normal and spaced out over longer periods of time with Paean relaying to the patient when to expect them and what intensity they will be thus allowing the patient to plan out the infection and also thus take fluids etc in required amounts.This will prevent or lessen the intensity cytokine storms,inflammation and other immune responses that can damage the host by controlling their actions and damage done to the host healed instantly via the accelerated healing phenotype.The primary immune system will be called to the site of infections to prevent it becoming lazy and speed up battles.They would also use Physis to determine the correct antibodies stored on its database to synthesise in the body via anabolic and catabolic reactions themselves once they are downloaded.By having all species and strains of bacteria,viruses,fungi and parasites have their surface protein antigens and antigens analysed by AI the antibodies to kill them can be extrapolated by Phanes and Paean and thus stored in Paeans database alongside Physis or just Physis will allow for the base microbes to be sent via wifi to digital DNA storage the exact synthetic antibodies to be be synthesised on demand the second an infection occurs and the exact species and strain is determined.Bumpers,endolysines etc would be received as well from Physis and thus allowing them to be used via the microbes creating anabolic and catabolic reactions.They would in the case of new pathogens and parasites once this DNA is sent would analysed by Paean and Phanes to be analysed for genotypes that express surface protein antigens to be sent by wifi for immunising strains to be upgraded wirelessly via wifi and then the primary immune system immunised and then activated.The surface protein antigens would be determined and there genotypes for creating immunisation sent back to microbes within as little as a day or less thus allow the primary immune system to be activated in this time period.Endolysines,synthetic antibodies etc can be extrapolated and sent to relevant microbe strains.The surface proteins of the pathogen would be determined from DNA and the anti-viral and anti-bacterial strains undergoing induced evolution via wifi to create receptors adapt to the specific species of bacteria,fungi,virus to apply speciez specific endolysines,genes via bacteriophage/virophage receptors and horizontal gene transfer.Bumpers,endolysines and antibodies will also be extrapolated.Bumpers,endolysines,antibodies extrapolated by AI stored in the files of pathogens and parasites will be downloaded into the DNA digital storage of relevant strains and then will be synthesised by anabolic and catabolic reactions during this period with the acellerated healing phenotype repairing any damage.This would also apply to parasites and would pivotal in fighting new parasites and pathogens.A new file will be created in Physis with the DNA analysed by base microbes with the file having genotypes for immunising strains and structure of endolysines,synthetic antibodies etc sent to this file Physis allowing for study and also for newly infected patients infected later on to be able to download these onto their DNA digital storage.The pathogen would be recreated in labs using 3D DNA printers to be then tested against the sap,stings etc from all plants and animals on Earth and other colonies.It would also be analysed in labs.This would be done alongside the application of CRISPR treatments that prevent them undergoing mitosis etc and undergo apoptosis and those that make them susceptible to the compounds of their disposal.This would be done in the case of viruses express the same exterior protein structures as HIV without the GP120 glycoproteins and thus have melittin applied or those of the benign strains of Rhinovirus,Orthomyxoviridae,HPV with cyanovirin-N applied with bacteria have the same phospholipids as benign ones affected by penicillin,peptides from Russian brown frogs,TsAP-1,Polybia MP-1 etc and have these applied to their surface.New pathogens and parasites would be given these and also be given CRISPR treatments to prevent them undergoing mitosis and replication and also undergo apoptosis.Parasites would also undergo this with the accelerated healing phenotype repairing any damage they do to the body instantly.This would apply to both new and existing pathogens and parasites of all types.All new pathogens and parasites discovered in patients will have their DNA added to Physis to be recreated in labs for analysis by automated labs to ascertained what natural or synthetic compounds extracted from bites,stings and sap etc from all native and extrasolar plants and animals can kill them with Paean creating through simulations synthetic compounds that kill them and also genotypes for immunising strains of all other patients.New pathogens and parasites will have suicide,mitosis stunting genes added with them also those that make them susceptible to the compounds at their disposal with the genome scanned to be analysed by Phanes via wifi and then have surface protein genotypes,bumpers,endolysines,antibodies etc extrapolated and saved to their file in Physis to be sent back within 24 hours or less and stored on DNA digital storage on relevant strains.The genome of new pathogens and parasites will also be analysed to determine antibodies and bumpers as well as endolysines to be used to extrapolated by the AI to then have them downloaded and synthesised by catabolic and anabolic reactions with their genome added to their file in their planets version of Physis.Phanes and Paean will analyse the genome of new pathogens and parasites for genotypes for surface protein antigens to be sent wirelessly to immunising strains to be shared with the primary immune system instantly and them activated with it also extrapolating the structure of antigens to create synthetic antibodies to be created instantly.These AI will extrapolate genotypes for immunisations and also synthetic compounds and antibodies to kill them that will be downloaded with non at most 24-168 hours of not a few minutes or hours.The antigen would also be analysed to have synthetic bumpers,endolysines and antibodies extrapolated with by 2029-2045 with advances in AI would take only a few minutes to an hour be extrapolated and sent to all strains digital DNA storage provided one has access to the wire or even satellite wifi and cellular access sufficing alongside Paean in a fragmented form in neural implants.Ideally all new viral,fungal and bacterial micro-organisms and also parasite that enters the body will be once their genome is scanned and sent to Paean and Physis will have CRISPR treatments applied to them to make them susceptible to the compounds at their disposal and also even undergo apoptosis etc to kill them of in all patients so as to eliminate the potential threat they have of mutating into a pathogen similar how to SIV became HIV to allow it to have its genome scanned and tested to see if compounds can be created alongside immunisations with this of note to new colonies outside of Earth.The pathogen or parasite will be recreated in labs using 3D DNA printers to be tested against compounds in bites,stings,sap etc.This could allow for the microbes to attack any pathogen or parasite within 24 hours or less before they cause any damage with the accelerating healing phenotype also aiding in this meaning a person would be cured of an infection without knowing it.Infections will be detected in the case of cuts,abrasions etc due to pain sensations and labs readings from the eyes or pricks etc associated by Anopheles etc detected by neural implants and the host with those from the gastro-intestinal tract detected by early symptoms and knowledge of having eaten or drunk tainted food or random and pre programmed interactions with cuts etc healed instantly via the accelerated healing phenotype.It may even be detected by base microbes inhabiting all parts of the body with them programmed to be awoken from endospores when pathogens interact with them or even the primary immune system communicates with them as well as from test results from both implants and home test kits for pathogens via wifi.Ideally base microbes will reside in the stomach and gastro-intestinal tract with alkanophile and acidophile DNA protecting them from the environment there.By 2029 it may take a few hours or even 24-48 hours or less for the detection,application of CRISPR treatments,downloading of bumpers/antibodies/genotypes for immunisations etc and then application of them to finally kill of pathogens thus giving the microbes and primary immune system the upper hand.By 2045 onwards it may take only a few minutes for all of this to be carried out allowing infections to be dealt with instantly.All interaction between Paean,base microbes and all strains will be managed by biosynth WiFi,Bluetooth with chemical signals used to control the primary immune system.These base microbes will also using universal receptors using tweaked C.elegans DNA that through mechanotransduction or reverse mechanotransduction,chemical reactions seen in more complex or similarly simple organisms and simple and complex neural clusters and systems in them for example Hydra etc analyse the structure of poisons,toxins etc in the body that enter it and send its structure to be cross referenced and analysed by crossrefferfncing Physis within minutes to determine the name of the compound and its level in ppm,ppb,ppt to then download and create counterproteins and awaken the chelation strain with the first set of compounds broken down into benign compounds via anabolic and catabolic reactions.New poisons will have Paean extrapolate counterproteins to them in minutes.Ideally the microbes would be tweaked to break down or bind to and flush out all compounds that it does not see as part of the normal human biochemistry with receptors that the drug interacts with covered in proteins that prevent the compound including date rape drugs interact with them withe compound also bound with proteins to allow them to be flushed put of the body.The structure and genome of the most deadly pathogens,parasites and toxins etc can be stored on DNA digital storage of neural implants and base microbes to have them instantly create counterproteins and anti-microbial compounds.For known pathogens,parasites,toxins etc their counterproteins,bumpers,antibodies,endolysines will already be analysed and stored in the augmentation sub network of Aesculapius and once the species of pathogen and parasite and compound has been detected then the microbes will be downloaded from here and then synthesised.All steps in these ie time of detection of a pathogen,its species and strains and also the type and time of CRISPR and anti-viral and anti-bacterial treatments are applied and also what countermeasures were taken including what antibodies were produced by both the primary and secondary immune system and all details about what measures were taken including Paean controlling both the microbes and primary immune system and the timing of them will be logged into ones patient file in folders and subfolders.This will be done Paean to run evaluations on fighting off infections,repair wounds and also fighting off tumours with this done on each patient and also all patients taking into the species and strain and nature of the injury and situation it occurred to make future instances done much more efficiently and faster and improve his service to all patients worldwide.It would also be done for studies done by him especially epidemiological studies ie how often each species infects a person and certain demographics and their occurrence in certain countries,states and towns and the time they occur.Measures to prevent stillbirths and miscarriages will also be catalogued for the same reasons.Since microbes different strains will be modelled on and made of hybrids of the various leukocytes of the primary immune system used as a baseline it will work on the same principles with Paean able to control their actions via wifi and by extension will be able to control all aspects of the primary immune system via chemical signals created by microbes allowing them to communicate and as stated control them with it spacing out the length and intensity of symptoms like inflammation and even fevers etc over short or long period of time and him indicating their intensity and length and also timing to the patient.Each strain will be hybrids of different leukocytes and as detailed earlier different micro-organisms to give them unique abilities.Thus Paean will directly control each strain of microbes via biosynth wifi and Bluetooth directly and via chemical signals created by microbes through him sending them WiFi signals he will be able to control the primary immune system to carry out specific actions such as stated attack pathogens in specific ways and even be called to the the location of infections and collect and share proteins from immunising strains and activate the rest of the strains of the immune system during immunisation and also in pre-existing chronic and new infections.Furthermore he can control how the primary immune system attacks pathogens and parasites by initiating their production of antibodies,inflammation,phagocytosis and other immune responses with them if possible through both chemical instruction and sharing both proteins and strands of DNA the microbes controlled by Paean can share both strands of DNA and proteins to induce all types of leukocytes of the adaptive immune system to be able to produce antibodies both as immunising them and arming them during a battle.He will also control the production of specific leukocytes,their replication,their actions in attacking pathogens etc and also choose which ones to undergo apoptosis when not needed.He can have the native immune system alerted to infections at the very start especially in the case of those that have long incubation periods and seroconversion rates such as Coronavirus,HIV with as a result the primary immune system alerted to and fighting off these infections at the start of infections once they occur rather waiting two weeks fir the immune system to begin fighting them meaning infections can be quickly dealt upon with him even have them fight off parasites such as Plasmodium,N.fowleri,B.mandrillaris,Cestoda,F.hepatica that the immune system normally ignores.They will also immunise the primary immune system both before and during battles.Thus through biosynth WiFi and bluetooth Paean will be able to control the microbes and by having them producing chemical signals will control all aspects of the primary immune system to prevent it becoming lazy and weak as well as speed up the battle against pathogens and also alleviate strains on microbes.All of these actions will be possible by 2029 and will be instaneous by 2035-2045 onwards.The accelerated healing phenotype will instantly repair damage to the patients blood vessels,organs etc by pathogens,parasites and even the primary immune system via cytokines storms and autoimmune disorders and reactions with measures like cytokine storms and autoimmune disorders stopped by Paean sending signals to the primary immune system using chemical signals.Anti-ageing treatments especially on the thymus will keep ones immune system in a youthful state similar to when in infants and thus strong forever especially the thymus keeping ones immune system forever strong with scratch DNA and that from other mammals and reptiles across the animal kingdom enhancing it especially the innate immune system.Crocodylus recombinant DNA can be added to microbes to allow them to produce anti-viral compounds via bumpers and phagocytosis and even can be added to the host patients DNA via CRISPR to allow the host in infected and newly infected patients to fight off viruses and bacteria and possibly parasites instantly upon infection with it also fighting off bacteria and boosting the immune system by making human immune systems react instantly to infections of pathogens preventing and skipping seroconversion similar to Crocodylus that exhibit innate immune reactions at birth rather than adaptive ones in humans with the rest of the human cells altered using scratch DNA and that from Crocodylus to be able to be resistant to any negative reactions as these animals primary innate immune systems and anti-viral,anti-bacterial compounds may have on the patient thus allowing them to react instanly to most if not all pathogens instantly even at the start of infections allowing infections to be fought off by both the primary and secondary immune system the second an infection occurs rather than days or weeks later preventing symptoms of seroconversion and preventing the pathogen especislly new ones gaining the upper hand or allowing it it to mutate from a harmless bacteria and virus into a deadly one especially in the case of zoonoses.Thus Crocodylus DNA can be added to human patients to give them this innate immune response and DNA from Crocodylus and scratch DNA added to prevent the immune responses causing cytotoxicity and serious allergic reactions.Scratch DNA will be added in order to not only prevent allergic reactions but also enhance this feature by making the primary immune systrm be able to adapt to infections of all types including new pathogens and parasites instantly with this done to compliment the microbes alleviating strains on them with Paean controlling the primary immune system through him initiating the microbes to initiate chemical signals to control them.This Crocodylus DNA added to both microbes and the patients DNA can be tweaked by Phanes to attack and destroy all strains of HIV and other pathogens for future patients as well as tweaks can be made for each individual strain for each individual patient and even tweaks made to make it once added to the hosts genome and microbes instantly attack and be able to destroy all strains of all pathogenic bacteria,viruses and fungi etc during infections by producing compounds that can attack all types of viral,bacterial and fungal pathogens and even parasites with the microbes aiding them into determining what type pathogen it is and what type of compounds it is with this aiding in fighting off new pathogens.If perfected this recombinant DNA added to the genome of patients and microbes will allow the host patients primary immune system and microbes to recognise and attack any existing and new species of parasites,bacteria,virus and fungi almost instantly upon infections thus preventing seroconversion and the pathogens and parasites being able to gain a stronghold or damage the patient in any way.By 2029 the microbes will be able to clear new infections of pathogens,parasites and toxins with at most a week or even just 24 hours with by 2035-2045 onwards most of not all infections of pathogens,parasites and toxins will be cleared from the body within a few hours of not a few minutes before the patient even realised it occurred.
Base microbes will detect levels of poisons and the species of pathogens acting as the first line of defence to them via sending wifi signals to Paean then alert him to dangers in the body and then control the microbes and primary immune system via wifi and signals.It would also copy DNA from cells in the body to measure the levels of Phosphatidylcholinesand senescence in the cells and be able to scan the genome of cells in fetuses to set up patient files and this and the ability to measure the presence and levels of compounds and genome will make the basis of lab equipment and machinery in all types of labs.This strain would be tweaked to detect toxins,poisons,alcohol,date rape drugs and compounds that are synergistically interacting with each other and break them down in bursts and turn them into nutrients for the host and microbes as well as benign compounds through anabolic and catabolic compounds.This strain would be created to intake oxygen from the host or even created by breaking down compounds and carrying out anabolic and catabolic reactions.This could allow one to survive heart attacks,sudden arrhythmic and infant death syndrome and similar cardiac ailements,elliptic fits,strokes,trauma and even severe bleeding for several hours longer or in time even indefinitely if the microbes instantly move to key organs and undergo mitosis in these such as the heart and brain releasing oxygen and converting carbon dioxide in the blood into oxygen while they and the bodies natural repair mechanisms heal or at least remedy the underlying cause such as healing wounds or at least sealing ruptures and creating arteries or other blood vessels that allow the blood to bypass ruptures.This could give the patient at least several hours longer as much as four to be attended to and brought to hospitals to seek treatment thus allowing survival rates to increase dramatically with the nanomachines and smart devices alerting hospitals to their GPS location with if possible patients since the brain to be fed oxygen alongside the heart and muscles would allow the patient to be conscious during the event.If possible they could separate oxygen from carbon dioxide and turn it into useable oxygen and the carbon turned into benign products as well as used in energy for the microbes and the patient by synthesising proteins or carbohydrates thus allowing one to survive suffocation,smoke caused by fires,heart attacks,strokes,choking,oxygen free environments for extended periods of time or even indefinitely including while swimming to allow one extra time to seek medical attention for at least several hours or even a day when combined with nanomachines preventing hypoxia especially cerebral hypoxia.Oxygen can also be gained and stored in them by them breaking down harmful,synergistic compounds during catabolic reactions to be then released when emergencies require them to keep vital organs such as the brain alive signalled by them detecting sudden changes in oxygen and carbon dioxide or signals form Paean either while their is wire access or in a fragmented form.This could also be done by them turning carbon dioxide in the external environment and those that builds up in the bloodstream after cells respire or when carbon dioxide builds up into useable oxygen with excess nutrients flushed out of the body or used up to continue the metabolic processes of cells during aeorbic respiration with them and the carbon atoms forming primarily sugars or easily flushed out compounds.The strain that does this could do this by having vacuoles in them,have a biconcave shape like erythrocytes to store extra in its surface and interior and contain haemoglobin that release this in bursts and/or carry out anabolic and catabolic reactions from carbon dioxide into oxygen in the bloodstream in real time.The strain would gain oxygen from excess taken in when breathing and store it then and there or from other strains breaking down poisons,excess nutrients etc into oxygen with the strain and these strains that break these down signalling each other to determine how much oxygen atoms will be absorbed by these strains and excess removed via the lungs.It would do so with it detecting high levels of carbon dioxide and low levels of oxygen and would use carbon dioxide created by the hosts own cells to be then converted into oxygen with the carbon used to create carbohydrates etc or flushed out into the urine and feces with AI developing means to ensure the carbon,hydrogen,oxygen is recycled in looped systems.This looped system could theoretically allow humans to survive indefinitely without oxygen with oxygen also coming from using up stored fat deposits.Recombinant DNA form capnophiles namely Mannheimia succiniciproducens that with tweaks made to allow this to turn carbon dioxide into oxygen with bioluminiscence or without photosythetic reactions caused by bioluminescence,faculatative anaerobes,other bacteria that produce oxygen from carbon dioxide and from scratch will allow for this with ideally scratch DNA used to increase the amount of oxygen created by it.Recombinant DNA from chemosynthetic bacteria could allow for this.
New pathogens whether viral,fungal or bacterial and even new parasites could also be modified via CRISPR applied to the pathogen either viral,fungal and bacterial to become susceptible to the anti-viral and anti-microbial compounds at the microbes disposal,remove their pathogenicity and ability to undergo mitosis etc or cause them to commit apoptosis during phagocytosis or by flooding the DNA added with advanced gene drive technology in protein bumpers that act as a mini vector to place the DNA in correct areas of the pathogens genome allowing millions of pathogens to be affected at once with this also used for existing pathogens outside of MRSA,HIV to limit the genotypes in the microbes.These CRISPR treatments using advanced gene drive technology applied to existing superbugs and newly discovered pathogens can involve removing resistance to one or all antibiotics,undergo apoptosis,be susceptible to compounds at their disposal,prevent them able to undergo mitosis,make them undergo apoptosis,make them benign thus preventing them being pathogens and not able to damage the host,remove their ability to mutate permanently,introduce faults etc with these released at once to allow each pathogen to be affected by multiple treatments.New pathogens and parasites may also require upgrades alongside them using suicide genes etc and those that make them susceptible to the a compounds at their disposal.Patients immune to radiation can be exposed to levels of radiation of between 2,000-20,000Gy to wipe them out.They could have DNA extracted via base microbes or phlebotomy robots in hospitals to have the DNA wirelessly sent to Paean and other AI to be analysed for proteins to create upgrades to be immunisations for all patients around the world including the infected patient and also for anti-bacterial microbes to create endolysines specific to them via signals while the microbes use CRISPR to make them susceptible to all compounds at their disposal and keep the host also alive to allow them to be cleared of them within 24-168 hours.The DNA taken from them by base microbes will also be shared with immunising strains to then synthesise the proteins on their surface to then be shared with dendritic cells in all lymph nodes with the microbe that receives the DNA would undergo rapid replication to travel to all lymph nodes and active an immunised immune system to fight it off with it also sharing the DNA to anti-viral anti-bacterial strains to create schematics to create endolysines.If sufficiently advanced the base microbes could through horizontal gene transfer intake and then read its DNA and wirelesly send the genome of the pathogen to Paean and Phanes that could scan its genome adding it to Physis but have genotypes downloaded wirelessly to strains that synthesise proteins to immunise the host and those that create endolysines with them wirelessly sent the genes that produce the relevant proteins to be shared with the dendritic cells by Paean while other microbes cause other microbes to undergo apoptosis and keep the host alive while the primary immune system is immunised and activated.In time advanced base microbes would be able to scan the genome itself using taq polymerase,Cas-9 and CRISPR to copy its DNA and signal to the immunisation strains to prepare the relevant genes and thus proteins through chemical signals,nanomachines,protein bumpers or horizontal gene transfer to prepare the relevant genome with them also using this to make other anti-microbial and anti-viral strains create endolysines and unique protein bumpers.Thus base microbes could be advanced enough to scan the genome of new foreign pathogens and send it to Paean and other microbe strains while other strains cause pathogens to undergo apoptosis,keep the body alive and also use CRISPR and other methods at its disposal until base microbes can scan through genome to give strains that immunise the primary immune system relevant genes and arm others with bacterial strains given DNA to produce endolysines.The DNA of these new pathogens would be uploaded to Physis to allow for AI namely Phanes to extrapolate genes that are needed to express common proteins for immunising strains and the immunising strains in the body would then receive these by wifi,immunise the patient and activate the immunised primary immune system with by 2045 onwards this taking a few minutes from the second is infected.Existing pathogens in the body will have genes added that prevent it undergoing replication and mitosis and undergro apoptosis and in the case of viruses have large strands of DNA removed to allow for the immunising strains to recive genotypes you immunise the primary immune system.Thus one could be immunised within minutes to then have the immunised primary immune system activated within an hour of the microbes discovering the infection.The same procedures will apply to new parasites.This could also allow the pathogen to be analysed and created in labs using 3D DNA printers to allow them to be tested against all natural compounds from plants and animals both from Earth and colonies.Furthermore them once the genome is scanned or when the surface protein antigens are detected will prepare lysins specific to that species or strain to be then synthesised by all microbes.The genome of the new pathogen and parasites will be uploaded to Physis with its entire genome analysed in minutes and Phanes and Paen will determine genotypes for immunising strains and also synthetic antibodies and compounds to kill them within minutes as well that can be downloaded into immunising and other strains within minutes.New colonies will have the common genes and proteins of all taxonomic ranks of micro-organisms analysised and created to create immunisations of them for all civilians on Earth and interstellar vehicles etc so as to prevent them mutating into human pathogens as seen with SIV mutating into HIV.All livestock and animals will be immunised against their pathogens to prevent them becoming zoonotic diseases.Synthetic compounds to treat them can be created by them carrying out anabolic and catabolic reactions using excess nutrients in stores etc and also bio based compounds,plant and animal oils and hydrocarbons created by the same strain or the body from CRISPR treatments as well as amino acids synthesised by the body and diet.The microbes would also steal genes or be upgraded with them to produce specific proteins from new pathogens once their genome is scanned into Physis to share with the memory helper B and T cells as well as weakening some of the pathogens to be destroyed by the primary immune system to allow them to kill them in another infection similar to vaccines.It would also apply to pathogens such as viruses,bacteria and parasites that may become resistant to melittin and all anti-fungal/microbial/viral compounds at their disposal with it even as stated making pathogens such as MRSA,N.gonorrhoeae through this modification permanently susceptible to all of the antibiotics such as colistin,β-lactam antibiotics and penicillin etc that are currently ineffective via gene drives.It would also work with all viruses to limit the genotypes added to the anti-viral and anti-bacterial strain and could allow any virus or bacterial pathogen to be killed by the compounds at their disposal as CRISPR treatments during phagocytosis would change the pathogen whether bacterial or fungal pathogens genome making its exterior and interior structures be able to be destroyed by the compounds at their disposal with the same done to tumours with suicide genes also added.For this to work ideally first asymptomatic carriers including pets and livestock that carry them should be treated with the permanent resistance removing treatments so that those in vulnerable humans that can affected by them can not only use this resistance removing ability but have the microbes use these antibiotics colistin,β-lactam antibiotics and penicillin against them using recombinant DNA from yeasts etc alongside those from Russian Brown Frogs,phytoplankton,hypochlorite,lactic acid,alcohol and reactive oxygen for maximum effectiveness.New pathogens and parasites could also be modified to become susceptible to the anti-viral and anti-microbial at the microbes disposal,remove their pathogenicity or cause them to commit apoptosis.Genes would be applied to them to express the same external structure of both viruses,fungi,bacteria and even parasites they are designed to fight off ie express the same phospholipids as benign bacteria to allow anti-bacterial compounds to be used or in the case of viruses express the same external structure as HIV without the GP120 glycoproteins and apply melittin and lemon juice particles.If possible having them express the same structure of benign Rhinovirus,HPV,Orthomyxoviridae strains than them expressing that of HIV as it would be much safer in order to be destroyed by them using cyanovirian-N etc.Parasites can be made to express the same internal and external structure as other parasites susceptible to the compounds used or even those as bacteria and viruses to be destroyed with the same done to fungi.This would involve DNA from these benign bacteria and viruses etc added to the pathogens genome.By applying suicide genes and those that prevent them being able to replicate and undergo mitosis would keep their numbers low preventing them causing sickness and damage to the patient and this done via horizontal gene transfer and also bumpers with this allowing for base microbes to scan the DNA of the new pathogen and send it wirelessly to Paean and Phyisis who will determine the proteins on it that would be relevant to immunising strains with immunising strains receiving the geneotypes via Paean wirelessly inducing the evolution of genotypes in this strain to synthesise the proteins on the surface or them collecting samples and them sharing them with dendritic cells to whom they will initiate in large numbers to then initiate relevant memory B and T cells and plasma cells in large numbers and the primary immune system now immunised will be signalled by the microbes through Paean to then fight off the remaining pathogens thus allowing one to be protected for life the next time it is encountered with this protecting patients from new pathogens whether viral,bacterial or fungal or even benign ones that could mutate before they can become pathogens as seen with SIV mutating into HIV or Cowpox virus became V.major and V.minor and would protect them against those they are not immunised against on Earth or on other colonies.This and making them susceptible to the compounds at their disposal via CRISPR treatments would ensure that they can fight off new infections they have not immunised the primary immune system off or newly discovered ones.Their genome would also be used to determine antigens on their surface and allow AI namely Phanes and Paean to extrapolate antibodies that can then be synthesised by microbes through wifi.All new micro-organisms such as fungi,bacteria and viruses discovered on Earth and on new planets will be scanned by Physis,Phanes and Paean will be done by automated programs managed by Astreaus that will scan all micro-organism into their version of Physis which will then have Phanes scan all of them for their potential for pathogenicity and also genotypes for useful proteins allowing for them to have upgrades and anti-viral and anti-microbial compounds developed prior to humans arriving.The common proteins of whole families and orders of all bacteria,fungi and viruses will be analysed by space station AI to create superproteins that immunise one against all fungi,viruses and bacteria allowing one to when they arrive on the planet will be immunised against all pathogenic and non pathogenic ones especially those that have the potential to mutate into deadly pathogens.All known compounds from plants and animals on Earth and other colonies and planets will tested on them in automated labs and also in simulations with all compounds present in Physis and the genotypes from the animals and plants they arise from here in the species file to then add them to microbes via upgrades.To make them susceptible to these compounds already present the microbes could add DNA from a virus or the bacteria that causes them to express the protein coats or phospholipids of known ones that are destroyed by the compounds ie new viruses and also ones outside of HIV could have CRISPR treatments containing DNA/RNA from known pathogens applied to them that cause them to express the same protein capsid and exterior structure of HIV without GP120 glycoproteins to allow allowing melittin and lemon juice to be applied or ideally the same protein capsid and exterior structure of benign Rhinovirus,HPV,Orthomyxoviridae strains to have cyanovirian-N applied with new bacteria and those outside of MRSA could have DNA from added to them that makes them express the same phospholipids and also internal structure benign bacteria affected by these compounds and then allow the microbes to apply its anti-bacterial and anti-viral compounds.This and also the ability to remove resistance to new and existing anti-viral and anti-bacterial compounds will allow the microbes fight off pathogens that the patient is not immunised against and also kill off any new pathogens discovered in new colonies off of Earth and also as stated fight off viruses,bacteria and fungi outside of those the compounds at its disposal are designed to fight off.This would involve DNA from these benign bacteria and viruses etc added to the pathogens genome.New parasites will undergo this as well.Base microbes could extract the genome from those kept busy by the microbes that surrounding them or this be done by all types of microbes via horizontal gene transfer and then upload their DNA to Paean via wifi to be analysed and then used for developing proteins for immunisations and also counter compounds to be added.The patient and uninfected ones could then be given upgrades either at home or via wifi as soon as possible against the pathogen and any new strain with AI determining the proteins needed to immunise against all possible strains with the pathogens also given CRISPR treatments to prevent them mutating,undergoing replication or mitosis and prevent the pathogen killing the host while key organs are repaired and kept alive.All of these CRISPR treatments will be housed in the microbes as ribosomes and in particular plasmids that can be replicated using taq polymerase and Cas-9.This would allow them to attack virtually anything not just new pathogens on both Earth and on other colonies that would adapt to become human pathogens like HIV evolved from SIV but also to attack viral and bacterial pathogens outside of the main ones the compounds are able to or are designed to destroy on Earth thus extending their range of efficacy without the need to add new genotypes with them able to fight off new infections and even chronic infections instantly thus speeding up the time it takes to cure the patient before it can cause fatal damage to them.This would also apply to both fungi and parasites both existing and new with it only applying to pathogens and not human cells via differentiating between the unique surface proteins of human cells and those of pathogens with ideally this done by the them having receptors that recognise pathogens as well as parasites and not human cells and also the genes to be used suited only to fit into the genome of only viruses and pathogens as well as parasites and not human cells with them doing this alongside resistance removing gene transferred and then use its anti-viral and anti-microbial compounds in unison to prevent pathogens become resistant and CRISPR treatments to remove and prevent resistance and also weaken them will also be applied at the same time to again improve success and even prevent resistance to existing and new treatments.If possible other anti-viral compounds such as lemon juice,vinegar(or similar compounds) can be synthesised and even virkon could be applied by them synthesisng it if shown not to be toxic to humans especially when applied by phagocytosis to HIV virions and other pathogens that it kills or compounds with similar structures and viricidal qualities that are benign to humans synthesised by them or using recombinant DNA from plants and animals via upgrades.The hosts native cells using scratch could be made immune to the compound or the microbes could synthesise the compound covered in protein bumpers that interact only with HIV thus not affecting the host when flooding the bloodstream as nanoparticles with the same applied to lemon juice and melittin.By 2029 the microbes will be able to clear new infections of new pathogens,parasites and toxins with at most a week or even just 24 hours with by 2035-2045 onwards most of not all infections of pathogens,parasites and toxins will be cleared from the body within a few hours of not a few minutes before the patient even realised it occurred.
Base microbes will be present to detect the species of pathogens by using Cas-9,taq polymerase etc and species of poisons,toxins etc in the body during infection etc and using biosynth WiFi cross reference Physis for their identity and then Paean will arrange actions to be carried out by chelation,anti-bacterial,anti-viral,anti-viral etc strains to counteract them.They will thus act as the first line of defence against pathogens,toxins etc
Human anti-ageing treatments:
CRISPR utilised by anti-ageing and augmentation strains will make these modifications and gene therapy treatments more accurate and effective.CRISPR treatments will be applied by anti-ageing and augmentation strains through horizontal gene transfer controlled by Paean by biosynth WiFi.Even proto AI could apply these treatments with this involving the microbes transferring DNA including scratch DNA developed by Phanes and recombinant DNA from plants and animals present in the strains of these microbes that are then applied to them.Scratch DNA throughout here refers to strands of DNA extrapolated by AI namely Phanes that doesn’t occur naturally in nature through natural evolutionary processes.will allow the phenotypes of the genes added to the patients genome in each cells to be then expressed by the cells in patients.The anti ageing strains etc will house DNA from yeasts to allow them to transfer CRISPR treatments to the cells of patients through horizontal gene transfer thus giving them CRISPR gene therapy treatments to halt and reverse the ageing process and have augmentations.CRISPR will involve genes from existing plants and animals and those created by Phanes from scratch added to the genome of living patients through horizontal gene transfer exhibited my anti ageing and augmentation strains that will once added to the genome then exhibit those phenotypes.For example the genes from bacteria that exhibit telomere repair once added to a patient genome will thus repair telomere damage etc with the genes from other plants etc added to them exhibited.In otherwards in layman’s terms CRISPR is a gene editing technology that will by adding genes to a patients genome give living patients the abilities of that gene such as augmentations from extremophiles and those to treat genetic diseases and both halt and reverse the ageing process.Biocompatible microbes through having horizontal gene transfer present from yeasts will be able to apply CRISPR treatments that includes DNA from existing living organisms and new genes derived from scratch from Phanes will thus through CRISPR will be used to cure genetic diseases and halt and reverse the ageing process in existing living human and animal patients worldwide by it allowing new genes to be added to a patients genome in each and every individual cells and this will be done through anti-ageing and augmentation strains exhibiting horizontal gene transfer and also taq polymerase and Cas-9.Epione and Paean would first carry out simulations on its effectiveness on chimpanzees,mice and humans before trials begin.This could be done by altering the host cells they infect unable to harbour them(in the case of HIV this would remove the receptors on leukocytes that allow the virus to attach and infect them thus replicating while other treatments eradicate the virus),or alter and strengthen the immune system namely CD4+ T Cells strengthened to recognise and fight off HIV with custom made anti-viral and antibody compounds as well as cancers earlier on.HIV resistance could be gained from populations genetically resistant to them transferred to other non resistant populations from both humans and closely related mammals as well as even from scratch with this replicated with other pathogens and viruses as well as specific cancers.Thus the non resistant humans using DNA from resistant populations could have their leukocytes to be unable to be infected by HIV by editing their surface proteins and the same replicated with all major viruses that infect leukocytes allowing biocompatible microbes to remove HIV virions.Recombinant DNA need not come from humans but also from closely related primates and mammals with similar immune systems and resistance with their resistance to Simian Immunodeficiency Virus and also recombinant DNA from SIV itself with this also applying to all viruses that infect leukocytes such as Ebolavirus,N.meningitidis etc.The patient file system will quickly identify which populations have this phenotype and what genes are responsible for this with known people that have this will have their DNA analysed and compared to those that suffer from the disease to isolate it.Microbes as detailed will apply this resistance to infected patients with N.meningitidis,HIV and Ebolavirus forcing the viruses to interact with other microbe strains and thus curing infected patients of the disease with ideally all patients including those currently not infected with HIV,Ebolavirus also modified to have their leukocytes and organs made unable to be infected allowing other strains of microbes to eradicate the pathogens or at least make them asymptomatic carriers before they gain a stronghold with resistance and microbe strains able to attack them made a permanent feature of the human genepool via germline therapy alongside immunising the primary immune system indefinitely also wiping out the disease in newly infected patients and uninfected patients while it is unable to infect leukocytes.Further advances in artificial intelligence will make germline therapy safe negating the need for having to screen every embryo,sperm and eggs with this first tested on animals with Epione again carrying out simulations on these on its effectiveness on chimpanzees,mice and humans before trials begin using advanced gene drive therapy technology.Gene therapy that treats every cell in their body will limit phenotypes such as correcting faults and mutations that cause specific diseases and immunities to diseases such as the immunity to HIV,cancer and even upgrades to the patient with germline therapy used to ensure these are passed onto the mother and fathers child thus allowing that child to pass on immunities to cancer,pathogens and other desired phenotypes onto the next generation without the need for microbes making them a permanent part of the genepool of H.sapiens with them also removed from the genepool via germline therapy if desired.Germline and advanced gene drive therapy once perfected will allow these to become a future feature of successive generations alongside screening,correcting and modifying spermatozoa,eggs and embryos for these diseases and using CRISPR to correct them with biocompatible microbes used to perfect this with them residing in or outside the testes and ovaries that insert gene therapy into each and every spermatozoa and egg individually by them,altering the genome of fertilised embryos or by them even altering the genes in these organs ie the ovaries and the testes responsible for the production of spermatozoa and eggs or the entire host DNA using advanced gene drive technology to ensure that all future sperm and eggs are free from the genetic faults and mutations allowing one to conceive children naturally and not have to use in vitro fertilisation without passing on these diseases to the next generation removing them from the human genepool indefinitely more easily.If perfected this advanced gene drive technology combined with germline therapy made by microbes to edit the hosts DNA precisely and permanently applied to all cells including those in the ovaries and testes that in turn produce spermatazoa and eggs to negate the need for them to edit every single egg,spermatozoa and thus allow them to conceive genetic disease free children naturally and also pass on desired phenotypes of H.ubermensch.This would thus mean eggs,embryos etc would no longer have to be screened for genetic diseases and with correcting CRISPR treatments added to all cells of a body including ovaries and testes would have pass these CRISPR genetic corrections passed onto all future produced spermatozoa and eggs and all conceived offspring thus either eliminating mutations that cause genetic diseases from passing onto all future generations and the human gene pool if applied to all patients worldwide or pass on augmentations etc to all future generations automatically.As stated these children created via germline therapy that uses advanced gene drive technology and germ line therapy will be able to receive the corrected genotypes during natural conception and will thus play a role in eliminating cancer,hereditary and neurological disorders from the entire human genepool forever and even play a role in creating H.ubermensch,designer babies and other means of manipulating evolution of H.sapiens including populations of H.sapiens with traits of H.ubermensch.To this it would require all or large samples of populations have their own genome altered and the microbes applying germline therapy on a global scale managed by Paean,Epione and hospital AIs.This could potentially eliminate all genetically based diseases including neurological disorders and developmental disorders from the human genepool as well as passing on genes into the genepool that will naturally be passing them onto the next generation without the need for germline therapy and microbes thus eliminating a disease indefinitely with them also altering humans to the point that those that are environmentally caused like cancer by making humans immune to the causative agent ie in the case of cancer removing the ability for tumours by adding genes from animals that never get cancer,extremophiles like T.gammatolerans to make humans resistant from radiation and also those from scratch to prevent carcinogens from being able to affect the body as well as immunising humans to oncoviruses that can be passed from mother to child via the placenta and breastfeeding.It will play a prime role in the development and eventual creation of populations of H.sapiens or all of H.sapiens with desired characteristics of H.ubermensch mainly that from T.gammatolerans to make humans resistant to radiation of all types,Salmonella to make them resistant to the effects of low gravity,Tardigrade,D.radiodurans and those from scratch to survive the vacuum of space,psychrophilles to survive sub zero conditions,synthesise all essential amino acids/fats/vitamins etc,oligotrophs and xerophiles to make them require less food and water(which can be applied to living patients via horizontal gene therapy)and eventually lead to the rise of H.ubermensch separate from H.sapiens via intensive germline therapy over several generations.Ideally these phenotypes of H.ubermensch will be added to all living patients worldwide and become part of the human genepool via advanced gene drive technology while not creating H.ubermensch with them added for their properties ie making the H.sapiens immune to radiation,require less nutrients,be able to survive extreme pressures,the vacuum of space.This would allow living populations of H.sapiens to survive extreme conditions on Earth,on other colonies both permanently as well as temporarily if containment procedures fail there and also on interstellar vehicles and stations.Anti-ageing genes from T.gammatolerans,Bacillus F,oligotrophs,xerophiles etc can be added to the gene pool via advanced gene drive and germline technology if shown to safe in both humans as well in animals will alongside the presence of these strains will have these anti-ageing genes,removal of genes and also production of anti-ageing compounds passed onto the next generation and thus a permanent feature of the human genepool.Gene therapy via microbes and CRISPR will also play a role in giving populations of H.sapiens via first live patient and germline therapy characteristics of his evolutionary successor and cousin as detailed later on H.ubermencsh as well as leading to the rise of H.umbermensch.H.ubermensch should be possible through extensive genetic engineering by at least 2045 with it also allowing humans to manipulate the genomes of other animals and plants thus creating entirely new species of plants and animals created on Pandora with Phanes extrapolating the genotypes of them.As detailed later on this will also lead to the creation of new sentient sentient races on par with humans created from scratch or using exiting non sentient animals from all taxonomic ranks of the animal kingdom as a baseline with this allowing for colonies like Mars,Venus and other extrasolar colonies in the universe with no life to have millions of non sentient and even sentient species created with whole taxonomic ranks creaked by Phanes adapted to their terraformed environment.Any faults in the gene therapy that could lead to mutations and breaks could be dealt with advanced gene drive technology that used specific genes,application etc to prevent them with all gene therapy treatments for ageing,augmentations etc will use advanced gene drive technology to prevent faults and pass them onto all future cells via mitosis with them applied to telomere,mitochondrial and other DNA.If possible base microbes or specific strains in females could detect mutations in embryos that lead to those are not hereditary ie those that lead to Downs syndrome and other developmental disorders through via horizontal gene transfer putting in genes or chemicals and even compounds that allow for these mutations to be detected and then signal to the microbe that it has occurred to allow the correction to be corrected by the microbes or those added via inbreeding at the during development of the embryo or while the fetus is in its early stages of development.It could also be used to apply the Phanes method to individual spermatozoa,eggs and embryo in utero with multiple microbes suited to this passing on desired alterations to each one.Spermatozoa and eggs that are frozen and stored in banks by donations and for later use in later life pregnancies can be corrected for all types of genetic diseases that may pass into potential offspring can have the corrections be done by biocompatible microbes in storage or prior to or during storage due them having the ability to survive low temperature due to them having DNA from psychrophiles.For parents who may pass on genetic diseases determined by Paean sperm and eggs can be collected from both parents fused together by robotics and then screened for diseases including Down’s syndrome and similar heredity disease both physical and mental and then CRISPR through the microbes could be used to edit these deformities out safely with Paean managing this or the editing can be done to the eggs and spermatozoa or both prior to fusion and they then implanted into the mother via IVF allowing parents who have the potential to pass deformities down to their child have children of their own and not resort to surrogacy programs.Gene therapy for these and other conditions should be pursued for already living patients suffering these in tandem to this with it also being used to treat ageing,Downs syndrome(and other disabilities),schizophrenia,Multiple sclerosis,parkinsons,alzheimers and deal with cancerous and precancerous cells and correct mutations that cause cancer again tested on mice and chimpanzees with again Epione carrying out simulations on these on humans and test animals.Downs syndrome if detected could if possible be treated using CRISPR to remove the extra chromosome,inactivate them in every cell preventing this from occurring in all future cells by adding genes that remove and then prevent the replication of a third chromosome 21 in each cell first tested on chimpanzees engineered with Downs Syndrome or even alleviate the symptoms of it rather than choosing to discard the unborn fetus with microbes repairing any faults and correcting defects such as low intelligence and heart defects.The same may apply to those with intersex disorders.All CRISPR treatments to treat ageing,genetic diseases,developmental and neurological disorders and those for augmentations etc in living patients will apply the genes to telomere/chromosomal/nucleur and mitochondrial DNA in all cells in the body and if need be plasmids for stability and uniformity.These augmentation genes and those to treat neurological disorders will be passed into leukocytes to allow them to survive extremophile conditions while beneficial bacteria in the gut can be given them as well alongside those made to express human surface proteins to make them immune to immune responses with pathogenic bacteria in the gastrointestinal tract not having these to allow them to die from exposure to these conditions and the primary immune system.Theh will not be given anti-ageing treatments to keep their populations stable.Anti-ageing treatments will be applied to bone marrow in a way to prevent leukocytes housing this DNA and thus living forever that would cause them to overrun the body or if shown to have their levels controlled by microbes via chemical signals or if possible undergone apoptosis and flushed out of the body can have this DNA present with all augmentations and genetic disease treatments added to bone marrow to allow leukocytes survive these conditions and be free of these diseases.Thus bone marrow will house anti-ageing treatments in a way to prevent leukocytes living forever but leukocytes will house CRISPR treatments to treat genetic diseases and augmentations such as radioresitence to survive these conditions through being properly applied in the bone marrow.The same will apply to erythrocytes wherein they recombinant DNA to treat genetic diseases and augmentations such as radioresistance will be applied to the patients genome to allow erythrocytes to survive these conditions but anti-ageing treatments will not interact with those responsible for erythrocytes preventing them living forever.Bone marrow and other parts that are responsible for the production of erythrocytes and leukocytes will be given anti-ageing treatments but through their placement on the loci and scratch DNA will be made to stay youthful but ensure that the erythrocytes and leukocytes they produce don’t carry the anti-ageing treatments thus allowing to die off and not overrun the body with Phanes developing genetic countermeasures to this with microbes from 2029-2035 ensuring that any possible immortal excess leukocytes etc can have their replication controlled and undergo apoptosis if their levels get too high.Beneficial gut flora will have augmentations added but not anti-ageing treatments to allow turn to survive extreme conditions and also prevent them overrunning the body by allowing them to die off.Pets owned by the public,livestock and animals in zoos will be able to avail of anti-ageing treatments and those to remove genetic diseases and augmentations via species specific microbes.All treatments to living cells in living patients will also use advanced gene drive technology to ensure the treatments pass from each generation of cells to the next via mitosis.Junk DNA and DNA that leads to ageing,genetic deformities and other unnecessary DNA will be removed to accomadate new CRISPR treatments to treat ageing and augmentations to prevent the finite nucleus becoming packed with DNA.Temporary augmentations form scratch and animal etc sources will involve ones original DNA for the phenotype being removed and replaced with the new DNA thus some augmentations that are used temporary ie having the same smelling and hearing ranges of other animals or changing eye and hair colour when unwanted will be removed and replaced with ones original DNA etc.Temporary augmentations that affect only part of the body will possibly be applied to the specific organs and tissues they affect such as those for different smelling ranges may only to be applied to genes present in cells in the brain and nose,those for different visual ranges may only be applied to genes present in cells in the brain and the eyes or just the eyes and so on.Cells in the body can be engineered to house ribosomes and in particular plasmids and in particular plasmids that are strands of DNA that float in the cytoplasm that express extra phenotypes for augmentations via specific DNA and thus phenotypes.Mitochondrial DNA can be modified to house extra phenotypes than the main genome that cause the cells and tissues to express their phenotypes.Better sources of scratch and recombinant DNA will replace older ones by removing them from the patients genome.If possible advancements in Phanes developing scratch DNA will allow DNA to express two or more phenotypes at once.Sources of recombinant DNA from animals,plants and unicellular life forms such as bacteria,fungi,viruses that’s express two or more desired phenotypes can be utilised for example T.gammatolerans can survive radiation levels of up to 30,000Gy and at the same time potentially express telomere repair that will prevent future damage and degradation in mitochondrial and telomere DNA to combat ageing and eliminate cancer,genetic diseases,developemental disorders etc from the human gene pool and protects one from levels of radiation of up to 30,000Gy all at once.Thus this could eliminate the need for D.radiodurans,Bacillus F DNA and scratch DNA to combat all of these since this DNA express several phenotypes and applications at once with research done into scratch DNA and that from plants and animals as well as micro-organisms that express multiple phenotypes and applications at once for augmentations and combat ageing.This will be done to deal with the limited space in the human genome and nucleus that holds them.The human genome is estimated to contain roughly 30,000 genes or 3,000,000,000 base pairs with it hypothesised that about 75-98% (between 22,500 – 29,400 genes or 2,250,000,000 – 2,940,000,000 base pairs)consists of non coding junk DNA that has no biological functions and thus could be easily replaced with new recombinant DNA from plants,animals and micro-organisms and scratch DNA without damaging or negatively affecting the patient.Genes in the body that contribute to the ageing process can also be removed and replaced with those for augmentations and those to reverse and halt the ageing process.Paris japonica is the organism that has the largest genome with roughly 150,000,000 base pairs and 1,500,000 genes about 50 times more than humans.If humans through intensive research into genetic engineering and CRISPR be able to hold the same amount of genes and base pairs as P.japonica then it will vastly increase the amount of storage space for DNA from extremophiles,plants,animals,micro-organisms and scratch DNA for augmentations and anti-ageing treatments and also cater to Phanes Activation Gene Technology with it more than enough to meet our needs.Research using human cell and tissue cultures will be done to see if they can hold this amount of genes after initial treatments to end ageing etc.New species of plants and animals found on plants across the universe will be scanned to see if they have larger genomes with scratch DNA developed alongside other methods to determine the theoretical limit size in terms of base pairs and actual genes of DNA that can fit in human cells.Tests will be done on human cells extracted from a patient or those created using 3D DNA printers to see if they can fit the same amount of genes and base pairs as P.japonica with them using base microbes etc find ways to give these cultured cells the same number of base pairs in otherworlds using microbes ways will be found in labs to give cultured human cells the same amount of genes and base pairs as P.japonica so as to find the best ways to give living human and animal patients the ability to hold the same amount of base pairs through gene therapy as P.japonica with this repeated with scratch DNA that can give humans even more base pairs up to the theoretical limit.Test animals and biosynths that have human recombinant DNA will be used in tests as well to determine the best way using gene therapy and what genes need to be added to add to living patients the same amount of base pairs and genes as P.japonica or the theoretical limit.Thus P.japonica and scratch DNA can be engineered to give living patients this new base pair size.If need be the cells of the body of humans etc may be engineered through CRISPR to become slightly larger that is the same size as that of P.Japonica.This will be done on human cells extracted from a patient or created using 3D DNA printers will that contain DNA from P.japonica to see if they can fit the same amount of genes and base pairs with them using base microbes etc find ways to give these cultured cells the same level base pairs in otherworlds using microbes ways will be found in labs to give cultured human cells the same amount of genes and base pairs as P.japonica so as to find the best ways to give living human and animal patients the ability to hold the same amount of base pairs through gene therapy as P.japonica with this repeated with scratch DNA that can give humans the theoretical limit.Thus once it is possible to determine the theoretical limit of base pairs that can fit into human cells tests on gene therapy applied to cultured cells in labs with if possible test animals such as mice etc housing human recombinant DNA and biosynths used will be done in order to apply this new limit to living humans.Thus once it is possible to determine the theoretical limit of base pairs that can fit into human cells tests on gene therapy applied to cultured cells in labs with if possible test animals such as mice etc housing human recombinant DNA and biosynths used will be done in order to apply this new limit to humans.If possible human cells can be engineered to house an extra one or two nuclei to house entire chromosomes DNA that will be engineered to hold only augmentations and not programmed to express any phenotypes thus being technically junk DNA.Biocompatible microbes will house this genome size to hold more recombinant DNA for each strains treatments and functions,to hold extra space for augmentations to survive in the body and also hold at least 150ZB data storage and RAM especially for biosynth technology.It can also be used to increase the genetic variation of possible genetically distinct that can occur between each and every single male and female during sexual reproduction from 64,000,000,000,000 to 3,200,000,000,000,000.Crops,fish and shellfish,livestock,algae,bacteria for producing commodities,stem cells for invitro meat and ornamental plants will utilise DNA from P.japonica etc and scratch DNA to house more DNA for augmentations including scratch DNA to increase growth rates and yields.If possible human cells could be engineered to hold an extra second nucleus that can contain and extra three metres of DNA that is junk DNA or that consisting of augmentations with DNA from P.Japonica in both the original and this second nucleus increasing the amount of DNA.All new modifications will be instantly relayed to ones patient via being both logged and also ones DNA scan modified.The genes to reverse and halt the ageing process should be able to be held in existing DNA present in the human genome alongside key augmentations such as the acellerated healing phenotype with this research done as a backup and measure to house extra augmentations.The anti-viral,anti-bacterial,anti-fungal strains,anti-helminthic,anti-cancer strains will be engineered to interact with only bacteria,viruses,tumours and parasites for each strain to prevent the applying suicide and other CRISPR treatments to human cells and that of gut flora.CRISPR treatments to alter pathogens and parasites like those to treat ageing will be done via horizontal gene transfer.Horizontal gene transfer will be used by anti-ageing,augmentation and genetic disease strains to transfer CRISPR treatments to the patients cells and them engineered to interact with only human cells.The anti-ageing and augmentation etc strains will be engineered to only interact with only human cells ideally those of the patient via surface proteins on them that only interact with only human cells to prevent them applying these to pathogens that would allow them to live forever with them via induced evolution and other sub strains engineered to interact with gut flora.Horizontal gene transfer will be utilised by the microbes different strains using DNA added to the microbes from yeasts,bacteria etc that are able to do this with them using taq polymerase and Cas-9 to recreate strands over and over again via biosynth WiFi.Horizontal gene transfer engineered to interact with human cells can thus allow current living patients to avail of CRISPR treatments such as augmentations and also those to reverse and halt the effects of ageing etc by allowing CRISPR treatments to be added to the cells of living patients.All cells in the body will have the new genes added with advanced gene drive technology also in cells in the testes and ovaries ensuring it is passed onto the next generation through the spermatozoa and eggs produced in living patients carrying these modifications to the next generation thus making them permanent features of the human genepool and the children of the affected individual with these if desired removed from living patients and their young by microbes.Thus all alterations to a living patients and also those in their progeny can be reversed by removing the applied genes.If any CRISPR treatments do cause any unwanted side effects to a patient then it is simply a case of them being removed as soon as possible.Faults caused by gene therapy will be corrected by treatments done as soon as possible.The estimated time for all treatments to all cells in the body to be finished will be visible in ones patient file and relayed by the nanomachines as a countdown in hours,minutes,seconds with treated areas of the body relayed to the patient file as well as through chemical signals such as unique smelling and coloured urine etc with the microbes via nanomachines relaying what parts of the body have been treated visible as a map of their body and percentage in real time in their file as a percentage.Advanced gene drive technology will be utilised to ensure that all CRISPR treatments for ageing and augmentations as well as correcting genetic diseases will be passed onto each generation of cells during mitosis and it even pass down to each generation of offspring alongside germline by being present in spermatozoa and eggs via both germline therapy the genes and advanced gene drive technology present in both the eggs and tests of patients negating the need to edit each and every spermatozoa and eggs and not having to be added to each newborn.Anti-ageing,genetic disease etc strains will be able to undergo mitosis and have flagellum to allow them to spread to all parts of the body when only a few thousand or million microbes are injected.Base microbes will routinely scan DNA to see if treatments are in each cell and are present and passed down from generation of cells and to see if any faults have occurred with faults corrected by those that applied the original treatments signalled to do so.With regards to ageing it will also detect the levels of Phosphatidylcholines.These will all be logged in the patients file.All types of strains that apply CRISPR treatments will be able to recreate the CRISPR treatment over and over again via taq ploymerase and Cas-9.Chimpanzees and mice that have human recombinant DNA in them used as test subjects by 2023/2024 with them engineered with each type of neurological,developmental,genetic disorders etc and use in ageing and augmentation trials to get more realistic results transferable to human trials starting in 2025.3D DNA printing will create the spermatozoa and eggs with these phenotypes and the patients unique DNA from patient files to cut down on labour costs with patient specific DNA to aid in creating treatments suited to each patients condition with regards to those that have neurological,developmental disorders and genetic diseases.To deal with the issue of Cas-9 eliciting immune responses it could be modified to contain some or all human proteins entirely as an human and patient version of Cas-9 as well as protein bumpers that dont illicit an immune response used as an mini vector to transfer DNA by flooding methods.This would be done by first modifying the DNA of S.pyogenes itself with human recombinant DNA to create a human or patient specific version of Cas-9 with the same done for all animals that will utilise it.Cpf1 from F.novicida can be used for this and also apply CRISPR treatments alongside Cas-9 from S.pyogenes.To prevent the issue of immune responses human versions of Cas-9/Cpf1 or even patient specific versions of Cas-9/Cpf1 can be created by AI namely proto and final Phanes can analyse the genome of S.pyogenes,F.novicida and modify it for humans and individual patients present in the their own leukocytes that contains their trace DNA by also analysing both human DNA and patient specific DNA.The anti-ageing,augmentation and genetic disease curing strains as well as the anti-viral etc strains in order to carry out CRISPR treatments would need relevant DNA from S.pyogenes,F.novicida,T.aquaticus in order to utilise CRISPR Cas-9 as well as taq polymerase to recreate strands of CRISPR treatments over and over again allowing each microbes to apply these treatments over and over again.These microbes since using ones own or 3D DNA printed blank leukocytes as a vector would prevent the issue of eliciting an immune response as seen in both foreign viruses and bacterial vectors.The 3D printed blank leukocytes will house human DNA,the hosts own DNA from their patient file inserted alongside other DNA from relevant multi and unicellular organism from Physis with this changing when passing from one generation to the next and would transfer the DNA using horizontal gene tranfser to only human cells interact by interacting with the unique surface proteins of the human patients cells and not that of pathogens.Otherwise ones own leukocytes will have DNA added by 3D DNA printers.Humans and animals will utilise their own leukocytes as a baseline for microbes to apply gene therapy to prevent them illiciting an immune responses that could be fatal or render them ineffctive and allow them to be more precise and effective and each patient will have their own patient specific versions of CRISPR Cas-9 could be created using the patients DNA in their own leukocytes with them changed when they pass to the next generation to further prevent immune responses with Phanes creating these in microbes when they are printed out by 3D DNA printers.This will allow all strains to form a permanent part of the body and act as the perfect vector of CRISPR treatments and anti-viral etc treatments with the human and indeed patient specific versions of Cas-9 created by 2023/2024 ready for proto microbes and bacterial vectors that have human protein coats due to the presence of human DNA,ideally the patients DNA and human versions of Cas-9 to give those currently aged 80-95 anti-ageing treatments to the interior vital organs and give them other treatments to allow them to survive strokes etc long enough to receive more advanced treatments in 2029 to be reverted to a state similar to their early twenties.This will also allow anti-ageing strains,augmentation and those to treat genetic diseases alongside all other anti-viral and anti-bacterial strains to undergo mitosis using bacterial DNA to treat each and every cell in the body with taq polymerase and Cas-9 to recreate the strands of DNA and also Cas-9 in the strains allowing them to treat countless cells with the DNA from macrophages and ameobas will allow them to move inbetween cells.Advanced gene drive technology will be used to ensure the therapy is permenant.Gene therapy will be applied via either horizontal gene transfer using Cas-9 or via flooding where protein bumpers housing the DNA and also synthesised Cas-9 will act as a mini vector allowing the Cas-9 and DNA to be sent to the relevant areas of the the genome specifically.Animals will have their own leukocytes as baseline and their own version of Cas-9 with them each having their own unique species specific microbes consisting of the same strains as in humans.Thus both livestock and pets of all species will have their own versions of microbes created for them including immunising,strains,anti-viral and anti-bacterial strains and also anti-ageing strains and them given the same augmentations as humans with all pathogens whether viral,bacterial and fungal of each species will be tested against compounds from the bites,stings and excretions of all plants and animals around the world to create anti-microbial compounds against them as part of anti-viral and anti-bacterial strains and those to fight off parasites with immunising strains immunising both pets and livestock against all pathogens especially zoonotic diseases to eliminate antibiotics from the food chain.Crops and plants whether in the wild or ornamental ones will using bacteria that contain the hosts species DNA and their own species specific version of Cas-9 with them giving their own fully functioning immune system via CRISPR that uses their microbes as a baseline leukocytes.Each species of plant whether crops,ornamental or wild one will be first given a fully functioning immune system in labs using bacterial/plant cell hybrid vectors and CRISPR and then their version of leukocytes created that can be immunised and microbes of all strains created using these plant leukocytes with this replicated with Apidae.This will be done to develop their own species specific microbes and also immune system that can be immunised against pathogens negating the need for chemicals to fight of viruses etc with them having their own strains modelled on human versions including those that also fight off infections as backup ie anti-viral,anti-bacterial,anti-fungal strains that use CRISPR and anti-microbial compounds rendering bactericides etc defunct.Existing plants in gardens can be inoculated by syringes and watering cans containing a mixture of water and microbes that enter the roots with biosynth wifi from smart devices causing upgrades with in time biosynth artropds injecting them into leaves etc.Animal trials begging in 2023/2024 will use their leukocytes with them having human recombinant DNA added to them to have an immune system identical to humans to ensure that these leukocytes can have these human version Cas-9 used in them to see if no immune response can be caused by them especially in chimpanzees.This engineering would also have these animals produce leukocytes similar to humans with human DNA and use this human Cas-9.To further prevent immune responses it may be possible for the Cas-9 to be suited for each patient using their unique DNA that is changed to that of their offspring as they pass from one generation to the next as detailed later on to further prevent allergic and immune reactions.This can be done via Phanes modifying DNA relevant to it and CRISPR from S.pyogenes.All types of microbes of each species of plants and animals will be since using the species leukocytes and in the case of plants those made from scratch will only be able to interact with the species they are designed for to prevent them affecting any species they contaminate with them also destroyed by the hosts own microbes they infect once detected by base microbes as well as programmed by Paean to undergo apoptosis if they are in the body of foreign species.They will also consist of different strains for each species and will be engineered to only interact with the specific target they are designed to via the surface proteins on them ie anti-viral strains will interact only with viruses and anti-bacterial strains with bacteria and so with augmentation and ageing strains engineered to only interact with human and the patients cells.As a result of this need to remove the effects of senescence universal debate and legal acceptance will have to made for the use of CRISPR gene editing techniques especially with regards to screening for diseases and even then removing gene(s) associated with genetic diseases to remove heredity deformities and diseases from humanities genepool entirely once an embryo created by invitro fertilisation has been screened or both the egg and sperm have been screened and edited ie.allergens,addictions,genetic based obesity and diabetes,certain cancers,parkinsons,alzheimers,eplipsey,colour blindness,blindness and deafness,channelopathies in newborns and other mutations that cause sudden infant death syndrome,haemophellia,Huntington’s disease,congenital heart conditions as well as adding resistance to and ability to fight off or prevent infections such as HIV,HPV(especially those associated with cancers),Epstein–Barr virus and terminal genetic diseases,with this procedure first tested on mice and other apes such as chimpanzees with gene drives used to make the alteration permanent.There has been success in CRISPR gene therapy in curing blindness etc within the last few years using viral vectors with this a great achievement since the technology is only 10 years old.The production and use of biocompatible microbes to utilise CRISPR gene therapy will expedite the development of gene therapy to halt and reverse the effects of ageing,cure genetic diseases from 2029-2045 onwards
Horizontal gene transfer will be a more effective means for anti-viral,anti-bacterial,ageing and augmentation strains to transfer genes to cells via CRISPR treatments rather than viruses that are used up as a single microbe can apply the desired genes to multiple cells in the body possibly even multiple cells at once as the strains that perform each task whether it is augmentation,anti-ageing,causing cells and pathogens to undergo apoptosis etc will have the DNA added to the pathogen or cells via having genes from yeast and bacteria that can carry out horizontal gene transfer.Yeasts and unicellular organisms that exhibit horizontal gene transfer will have their DNA present in these strains that allow for this to occur be mapped to be added to all strains to allow for horizontal gene transfer to be exhibited by them thus giving anti-ageing strains the ability to transfer genes to living patient cells to halt and reverse the ageing process with it present in augmentation strains to transfer augmentations derived from the genes present in desired species of plants,animals and bacteria and those created by Phanes scratch into all cells in the body.Scratch DNA will be present to enhance it with each strain engineered to only interact with the desired type of cell ie anti-ageing and augmentation strains would be designed to interact with only human cells with anti-bacterial strains only engineered to interact with bacteria etc.Paean will control by biosynth wifi etc the transfer of CRISPR treatments from microbes to the patients cells.Thus living patients will be able to avail of anti-ageing treatments and augmentations via the strains that apply these treatments exhibiting horizontal gene transfer via genes from yeasts etc that exhibit this alongside scratch DNA.Those in anti-cancer strains that stunt the growth of tumours or cause them to undergo apoptosis,those in anti-viral and anti-bacterial strains etc would use this to transfer suicide genes to cause them to undergo apoptosis,be unable to replicate as well as those to make them susceptible to compounds at their disposal etc.Paean would control the transfer of these CRISPR treatments to pathogens and tumours.Genes applied can be replicated again and again via taq polymerase and the Cas-9 during or after the transfer as quickly as possible with flagellum added to all microbes using DNA from E.coli thus as stated allowing for a single microbe as part of a fleet that undergoes mitosis with DNA also allowing for them to travel around the body very quickly.DNA T.aquaticus would give them the ability to use taq polymerase and Cas-9 derived from S.pyogenes to recreate strands of DNA to be applied to human cells,pathogens and so on over and over again an infinite number of times with it also used to induce the evolutionary path of microbes for upgrades and scanning the genome of pathogens etc in the case of base microbes to determine their species using horizontal gene transfer.Cpf1 from F.novicida can be used for this and also apply CRISPR treatments alongside Cas-9 from S.pyogenes.Thus once strands of DNA through CRISPR have been applied to a cell the taq polymerase and Cas-9 present will be able to reproduce these CRISPR treatment over and over again an infinite number of times controlled by Paean by biosynth wifi to allow a single microbe to apply CRISPR treatments to multiple cells over and over again.To prevent the issue of immune responses human versions of Cas-9/Cpf1 or even patient specific versions of Cas-9/Cpf1 can be created by AI namely proto and final Phanes can analyse the genome of S.pyogenes,F.novicida and modify it for humans and individual patients present in the their own leukocytes that contains their trace DNA by also analysing both human DNA and patient specific DNA to prevent potentially fatal allergic reactions.All strains will use human leukocytes as a baseline and ideally each patient will use ones own leukocytes as a baseline to prevent immune responses and become a permanent part of the body without illicitating an immune response.Each patient will have their leukocytes extracted and the genome of them analyses using DNA analysers and them stored in ones patient file in a folder to allow AI namely Phanes using 3D DNA printers to then print out duplicate leukocytes with the patients DNA to prevent immune responses and all relevant DNA for biosynth WiFi,flagellum,controlled mitosis,CRISPR treatments in ribosomes and in particular plasmids,DNA that expresses anti-viral,anti-bacterial etc compounds,horizontal gene transfer and also DNA digital storage.This use of leukocytes as a baseline containing the patients DNA will also apply to clinical trials from 2025-2029.Horizontal gene transfer will be used and them engineered to interact with only the cells each strain is designed for with taq polymerase allowing CRISPR treatments present in ribosomes and in particular plasmids to be recreated over and again.Horizontal gene transfer will be used by anti-ageing,augmentation and genetic disease strains to transfer CRISPR treatments to the patients cells and them engineered to interact with only human cells.Paean will tell the strains of microbes to apply CRISPR treatments to human cells via biosynth wifi and bluetooth with if possible them through other means applying them prior to biosynth WiFi being perfected.Horizontal gene transfer will come from them housing genes from yeast etc that have this ability and it carried out only when biosynth WiFi signals from Paean tell them to do so.Biosynth wifi will give Paean the ability to recreate the strands of DNA that are applied to a cell or pathogen etc over and over again an infinite number of times using taq polymerase and Cas-9 through biosynth wifi and bluetooth.The anti-ageing and augmentation etc strains will be engineered to only interact with only human cells ideally those of the patient via surface proteins on them that only interact with only human cells to prevent them applying these to pathogens that would allow them to live forever with them via induced evolution and other sub strains engineered to interact with gut flora.The anti-viral,anti-bacterial,anti-fungal strains,anti-helminthic,anti-cancer strains will be engineered to interact with only bacteria,viruses,tumours and parasites for each strain to prevent the applying suicide and other CRISPR treatments to human cells and that of gut flora.CRISPR treatments to alter pathogens and parasites like those to treat ageing will be done via horizontal gene transfer again initiated by Paean through biosynth WiFi..Horizontal gene transfer will be utilised by the microbes different strains using DNA added to the microbes from yeasts,bacteria etc that are able to do this with them using taq polymerase and Cas-9 to recreate strands over and over again an infinite number of times via biosynth WiFi.DNA from Bacillus F,T.gammatolerans and scratch DNA will be present in these CRISPR treatments in order to prevent genetic degradation of recreated strands.Horizontal gene transfer engineered to interact with human cells can thus allow current living patients to avail of CRISPR treatments such as augmentations and also those to reverse and halt the effects of ageing etc.The anti-ageing and augmentation etc strains will be engineered to only interact with only human cells ideally those of the patient via surface proteins on them that only interact with only human cells to prevent them applying these to pathogens that would allow them to live forever with them via induced evolution and other sub strains engineered to interact with gut flora.Anti-bacterial,anti-viral,anti-fungal and anti-helminthic strains will utilise CRISPR treatments to cause pathogens to undergoe apoptosis,become sucseptible to compounds at their disposal etc applied via horizontal gene transfer with them also applied by bumpers with theses strains only engineered to interact with the cells of pathogens.Taq polymerase and Cas-9 will be used by augmentation,ageing and anti-bacterial,anti-viral,anti-fungal and anti-helminthic strains to recreate strands of DNA used in CRISPR treatments over and over again under instructions from Paean through biosynth WiFi and bluetooth.They can have genes from bacteria such as E.coli that allow for mitosis to occur to allow them to create millions or billions of copies and travel across the body to all cells within minutes.This would ensure that all cells the body could be fitted with the relevant DNA very quickly at most a week or day or two depending on how many are created instantly and then excess flushed out with them communicating with each other and relaying to Paen and thus the host via wifi in the nanomachines and smart devices of when all cells are fitted with the relevant recombinat DNA.Anti-bacterial,anti-viral,anti-fungal and anti-helminthic strains will be engineered to interact only with pathogenic bacteria,viruses,fungi and parasites respectively and not with human cells via surface proteins to prevent them applying CRISPR treatments that would kill the patients cells.Thus DNA from bacteria that exhibit horizontal gene transfer will be added to their genome of all strains that treat ageing,fight viral and bacterial pathogens,give augmentations to all for CRISPR to be applied to cells and pathogens effectively and each strain engineered to only interact with the desired cells(human and each type pathogens) with bass microbes able to interact with them all with taq polymerase and Cas-9 via biosynth WiFi and Bluetooth allowing them to recreate strands over and over again thus allowing them to reapply the same DNA to countless cells etc over and over again.All CRISPR treatments to human tissues and pathogens will utilise advanced gene drive technology to ensure it stays in all future generation of cells with the CRISPR treatments applied to chromosomal,mitochondrial and all DNA present in a cell.Prior to biosynth wifi and bluetooth the process could be confirmed by them releasing compounds picked up in urine that can be detected in toilet kits or produce smells in the urine or body sweat.Biosynth WiFi from routers and that generated by smartphones etc will thus be used Paean to have all strains whether it is augmentation,anti-ageing or those that fight pathogens to apply CRISPR treatments through horizontal gene transfer with biosynths WiFi also used to recreate strands of DNA used in CRISPR by Cas-9 and taq polymerase an infinite amount of times.If possible the amount of time left for this to happen could be relayed in real time to the patients patient file as a countdown.The microbes will be programmed to use taq polymerase and the Cas-9 to recreate the DNA that was transferred to a cell or pathogen instantly with them leaving markers that prevent other microbes dont put in the same strands of DNA over again into the same cell or via communicating with each other.By having the CRISPR method used by S.pyogenes in the microbes can house the genes to be released via horizontal gene transfer to human cells and pathogens in different strains with the correct one transferred based on them detected surface proteins and also flooded in bumpers can allow it to be more easily recreated by taq polymerase and the Cas-9 with these measures also protecting them from viruses.These that correct ageing and all other strains will thus form a permanent part of the human body.Those that deal with ageing,augmentations,genetic disease and other CRISPR treatments can after undergoing mitosis create billions of copies via Biosynth wif and then travel to all areas of the body and then apply the treatments to all cells in the body via horizontal gene transfer and recreate CRISPR treatments within them via taq polymerase and Cas-9 to be then applied to other cells over and over again to speed things up and then go into an endospore state or excess be flushed out of the body to be collected for use in electronics etc once collected in sewage treatment plants with the remaining upgraded for other treatments and to act as back up.There permanent presence especially augmentation ones could turn them on and off when wanted by adding a specific gene or removing them or vice versa when desired controlled by Paean through the wire and fragmentation.These could also have the ability of base microbes to copy and read DNA of the patients cells via taq polymerase and Cas-9 using horizontal gene transfer and the results sent via biosynth wifi allowing all of the DNA of all cells to be read and wirelessly sent to Paean to detect telomere degradation and mutations associated with ageing,augmentations and any genetic faults that can be corrected with this done routinely ie every few years but it also done to ensure that the genes are infact spread into each cell and passed down through mitosis with them apply any genes that dont pass down again via horizontal gene transfer with them ideally in an endospore state and awoken to do these checks.Those that apply gene therapy of all types to humans will do so only to human cells due to them having specific surface proteins that are able to apply horizontal gene transfer to humans only and specific cells in certain circumstances with the same applied to strains that apply CRISPR treatments to pathogens of all types and tumours only able to interact with the specific surface proteins of tumours and pathogens to prevent them applying them to healthy cells.Those that apply treatments to pathogens will have receptors that can interact with the petidoglycogan cell wall of bacteria and protein capsids of viruses for both anti-bacterial and anti-viral strains allowing them to differentiate them from human cells with the ability of C.elegans etc present allowing them detect the exact phospholipid and protein compositions to allow them to know which pathogen they are especially when nanomachines are present.Biosynth wifi will download DNA to them to adapt to the walls of each specific species of bacteria and virus etc.This will be done to prevent treatments meant for the host being applied to pathogens and to prevent those meant for pathogens applied to the host.Base microbes will do this also alongside scanning their DNA to determine what exact species of pathogen they are when they send this data to Paean as well as Physis and also receive data back via nanomachines.The microbes could possibly be programmed to evolve over time to change their receptors to evolving structures on pathogens as they themselves evolve with this sent to other microbes in the body via trading genes similar to the human immune system or injecting new microbes with these structures would be engineered to seek out and interbreed with existing ones and pass these new phenotypes into microbes already present via gene drives.Ideally this series of receptors would only be done when they engulf a pathogen and react to the specific surface protein antigens and receptors allowing it to recognise if it is viral,fungal or bacterial and which one of these it is and thus apply relevant anti-microbial or viral compounds and use specific CRISPR attacks to cause the pathogen to undergo apoptosis and also become susceptible to the compounds at its disposal with this also when it signals the immunised primary system and also other microbes to release specific antibodies and also compounds at its disposal as nanoparticles with bumpers.If need be the strains that interact with human cells namely ageing and also augmentation strains will have DNA from bacteria,phages,viruses inside that are normally used in conventional gene therapy methods to increase success.They will via the surface proteins on the surface of the microbes be only able to interact with human cells thus preventing them transferring anti-ageing and extremophile strands of DNA to pathogens but in the case of beneficial bacteria in the gut they will be able to transfer specific genes to make them express protein coats from humans and immunities to extreme environmental conditions.Paean will have augmentation strains interact with beneficial gut flora and scan their genome to identify them and then apply augmentations to the desired species.There will be billions or even trillions of anti-ageing and augmentation strains cultured in vats that are then injected into a patient that can undergoe mitosis to allow them to quickly interact with all cells in the body as quickly as possible and thus apply these treatments very quickly with them entering an endospore state with excess flushed out of the body.These can apply them via horizontal gene transfer and bumpers to interact and enter specific cells to allow a single one to interact with millions of cells at once with them all using taq polymerase and Cas-9 to replicate the applied DNA all over again allowing one microbe to apply these to a millions of cells with gene drives and advanced gene drive technology ensuring the DNA is applied to future cells during mitosis and passes onto all spermatozoa and also eggs making them a permanent feature of the human genepool.Bumpers used to apply these would interact with only human cells and not pathogens and allow for countless cells to be modified by one microbe at once.They can through upgrades detailed later on cheaply allow for more genes to be added to countless cells with bumpers containing both the DNA and Cas-9 protein,allow for genes to be added in waves or in one go for conditions that are the result of multiple genes and also be more precise allowing them to affect specific cells or all cells.They will also allow for the addition,editing and removal of any undesired genes when upgraded or when decided by the patient through Paean and will through base microbes constantly copy genes in cells to detect faults that need to be repaired with the symptoms of these such as cancers killed off or suppressed or counteracted and the brain kept alive until they can be upgraded with CRIPSR treatments.Since residing in all tissues and organs they will be able to correct and apply treatments all cells and even do so with spermatozoa,testes,eggs and ovaries allowing germline therapy to be successfully achieved and will do this constantly when required allowing for action to be instant and do so for augmentations and also modifying humans for other medical means.Again since in the body between all tissues they will be able to treat all cancers,genetic diseases,pathogens instantly where infections,faults and growths occur giving the patient life saving treatment with them using nanomachines to download new treatments and methods to attack these conditions form Paean.Furthermore they will be able to do genetic fixes to diseases that have origins in multiple genetic faults all in one go more effectively or if required they can do each gene correction done in waves as is the case of ageing and cystic fibrosis in a series of waves and with their ability to detect cancers and them being a constant in the body will correct all faults and possible tumours that would arise from CRISPR prior to it being perfected instantly with them upgraded as detailed later on to perfect the process.This technology could also using the same receptors as bacteriophages engineered into them to treat MRSA and other bacterial pathogens as well as permanently remove the resistance of MRSA and other superbugs to various or multiple antibiotics,reduce or remove their pathogenicity(ability to illict immune response and cause illness) and ability to reproduce or add suicide genes either within a patient or within a population.These measures of correcting or eliminating genetic defects and eliminating pathogens should be applied to livestocks,pets and wild animals to prevent unnecessary suffering,them acting as vectors for zoonotic diseases,negate the need for antibiotics in the food chain,costly treatments and loss of yields of commodities as well improve their survival especially endangered species including arthropods with this done by adding inoculated animals into the wild who can pass these on by unprotected sex and fetuses with them a mixture of males and females with bio-synth arthropods doing this more effectively.If perfected the phenotypes of H.ubermensch could be applied to living humans with recombinant DNA from scratch and extremophile bacteria giving them superior capabilities.CRISPR utilised by anti-ageing and augmentation strains will make these modifications and gene therapy treatments more accurate and effective.CRISPR treatments will be applied by anti-ageing and augmentation strains through horizontal gene transfer controlled by Paean by biosynth WiFi.Even proto AI could apply these treatments with this involving the microbes transferring DNA including scratch DNA developed by Phanes and recombinant DNA from plants and animals present in the strains of these microbes that are then applied to them.This will allow the phenotypes of the genes added to the patients genome in each cells to be then expressed by the cells in patients.The anti ageing strains etc will house DNA from yeasts to allow them to transfer CRISPR treatments to the cells of patients through horizontal gene transfer thus giving them CRISPR gene therapy treatments to halt and reverse the ageing process and have augmentations.
DNA repair
With regards to ageing DNA from long living species and animals could be used to increase the lifespans of H.sapiens with gene therapy as part of ageing treatments with the recombinant DNA coming from Bacillus F that have been found to live for 3,500,000 years.Endolithic bacteria,T.gammatolerans that can survive for more than several millions of years reproducing only every 10,000 years or even lifeforms that exhibit biological immortality and ability to repair DNA such as Hydra,T.dohrnii,D.radiodurans and Planarian flatworms in the case of repairing tissues can also be used alongside those form scratch with these possibly used together.Scratch DNA,the homology directed repair mechanism ie homogulous recombination present in embryonic stem cells as well as certain bacteria added by gene therapy and NMD that boosts NAD+ production that repairs DNA added by drugs and also synthesised by microbes by catabolic and anabolic reactions may be required to repair existing damage alongside removing genes associated with ageing with this created by proto AI with this done after the aforementioned DNA at least halts the effects of ageing with the DNA added to both telomere/chromosomal DNA and also mitochondrial DNA in all cells in the body.
If possible the DNA of younger patients even infants and adolescents or those in their twenties including close relatives of older patients aged 50 or older can be analysed to have the damaged telomeres of older patients replaced with those from younger patients if possible related to them and those generated from scratch via Phanes with those from Bacillus F and T.gammatolerans alongside endolithic DNA repairing and preventing any future damage especially in older patients.This would allow the telomeres in older patients to be reversed to those in their early teens and infant years with the DNA repair mechanisms of these bacteria added first repairing any future damage forever.Genetic sequences from younger patients will be added to the older patients in both telomeres and mitochondrial DNA with Phanes also extrapolating the younger DNA of older patients using samples from relatives that are in their pre teens,teens and even twenties.The DNA repair mechanisms of T.gammatolerans,Bacillus F etc and slow mitosis of endolithic bacteria will possibly slow,prevent and repair future telomere damage in older patients prior to them being applied with their scratch DNA and that of younger relatives.
Telomeres of all patients will be analysed in automated labs to determine their level of degradation.Chromosomal,telomere,cellular and mitochondrial DNA will at first be repaired by being fitted with the DNA repair mechanisms from D.radiodurans,T.gammatolerans and Bacillus F as it will repair any future DNA damage especially in older patients.AI may need to extrapolate the missing damaged DNA for each patient to ensure their own DNA is present in the cellular,telomere and mitochondrial DNA repaired with all patients having their cellular,chromosomal and mitochondrial DNA analysed by blood pricks or skin cells extracted on DNA analysers in labs and using CRISPR have the repair mechanisms of extremophile bacteria ie T.gammatolerans added to repair further damage and also endolithic DNA to prevent further damage.DNA of infants may be analysed and have genes added.Thus the DNA from these bacteria will be able to repair any future DNA degradation.Existing damaged DNA can be repaired by CRISPR.
If possible to prevent the DNA for DNA repair taking up too much place in the patients genome it would ideal for only recombinant DNA from T.gammatolerans to be used since it can express this phenotype and unlike that from Bacillus F can allow it to withstand blasts of radiation if up to 30,000Gy thus having the most effective repair mechanisms meaning in order to prevent future DNA degradation in telomere and mitochondrial DNA.The fact that T.gammatolerans has been proven in lab settings to survive such extreme blasts of radiation allows it to exhibit better DNA repair mechanisms thus making it the ideal candidate for the source of DNA repair mechanisms.Research can be done if this DNA repair mechanism could also protect H.sapiens from extreme doses of radiation and possibly eliminate all or most cancers from the human gene pool by preventing the random breaks and mutations from exposure to radiation,carcinogens etc from occurring thus preventing tumours ever forming in all patients
Telomere,chromosomal and mitochondrial DNA will be at first fitted with teleomere repairing DNA from these bacteria T.gammatolerans to prevent future damage to them due to these bacteria exhibiting DNA repair mechanisms.Any future damage to telomeres to that mitosis has on the quality of telomeres in the chromosomes,mitochondrial DNA etc will be repaired instantly by adding the genes from these bacteria that allow them to repair their DNA thus rendering the hayflick limit and damage to telomeres,chromosomes and mitochondrial DNA obsolete forever.This will halt and reverse the affects of ageing.This DNA from these bacteria that exhibit DNA repair will be added first to patients mitochondrial and telomere chromosomal DNA via CRISPR to prevent any future damage and decay of the patients DNA while AI using CRISPR can repair existing damage to ones DNA by filling in the blanks etc.
The DNA to exhibit DNA repair will be modified by AI to be better integrated into the human genome due to the fact that it comes from bacteria and not multicellular organisms.This can include adding new scratch DNA to better integrate the genes or use them as a baseline for AI to design better DNA to exhibit this phenotype
DNA extrapolated by AI for each individual patient will be added to both mitochondrial and chromosomal telomere DNA to repair existing damaged DNA to revert both mitochondrial and telomere DNA to levels and states similar to that of infancy with DNA from ,T.gammatolerans that allows them to exhibit DNA repair will be added to all cells mitochondrial and telomere DNA in patients at first to prevent future telomere damage caused by mitosis alongside endolithic bacteria to slow down damage and any future damage repaired instantly
.Ones entire DNA in their chromosome,mitochondrial DNA will through scratch DNA extrapolated by AI be reverted to a state similar to infancy including telomeres. Telomeres that shorten as one ages will through scratch DNA and CRISPR be reverted to a level and state similar to infancy of about 8,000 to 10,000 nucleotides long by AI extrapolating the correct genetic sequences to be reapplied to them using CRISPR.The DNA repair mechanisms from T.gammatolerans will be added to the telomeres to prevent them degrading any further negating the hayflick limit.One’s entire genome in their patient file will be analysed by AI before and after gene therapy to ensure that ones entire genome is repaired to a pristine state with it used by AI to correct damaged section by removing damaged DNA and replacing it with DNA with the exact same sequences of bases.Scratch DNA will be used to revert telomeres in all chromosomes to an infant state where they are fully rejuvenated with mitochondrial DNA reverted to an infant state thus will be done in all cells in the body.Nephropidae are a species of biologically immortal crustacean that can theoretically live forever yet dies mainly from exhaustion from shedding its ever growing shells,pathogens,parasites and also predation.Part of the reason is that they are able to keep their telomeres at an infant level forever..If they were to be kept in captivity without predators,pathogens or even be engineered not to produce shells it’s theoretically possible for them to live forever or at least several centuries.This biological mechanisms could be applied to H.sapiens by producing the compound at stable levels forever without leading to tumourgenisis through scratch DNA.H.sapiens do create telomerase but not enough as even though they do create it it is not enough as despite its function as to rejuvenate and protect the telomeres telomere degradation still occurs.Only enough is created to partially repair damage unlike Nephropidae.Nephropidae do not have this problem as their telomeres are forever at an infant state and they unlike H.sapiens have an infinite supply of telomerase.Telomerase is not unique to Nephropidae . It is present in most other animals, including H.sapiens, but after passing the embryonic life stage, levels of telomerase in most other cells decline and are not sufficient for constantly re-building telomeres.Since both H.sapiens and Nephropidae produce telomerase they should have similar genes with the different mechanisms resulting in both have genes that are similar but slightly different due to Nephropidae telomerase mechanism being more successful thus genes from Nephropidae should be easily integrated into H.sapiens without side effects.AI can analyse the genes responsible for telomerase production in both H.sapiens and Nephropidae and thus determine ways to integrate that from Nephropidae into H.sapiens through CRISPR treatments thus rejuvenating telomeres in patients to an infant level forever with it and DNA repair mechanism ensuring that the telomeres stay at a levels associated with infancy forever.The genes in Nephropidae can used as a baseline to research those developed that can be added to humans that are added to the human genome via CRISPR that produce telomerase at levels sufficient to rejuvenate telemeres to an infant level forever while at the same preventing tumourgenesis or issues associated with rejection etc with research done into genes added to the genome that enable telomerase be created at sufficient levels to keep telomeres at a state similar to infancy forever while preventing tumourgenesis.DNA repair mechanisms from T.gammatolerans added to the chromosomes including the telomeres could prevent the development of mutations and random breaks that lead to tumours.In otherwards research should be done to rejuvenate telomeres to an infant state forever through CRISPR while preventing tumourgenesis based on the same principle as the ability of Nephropidae to keep their telomeres constantly rejuvenated.This can involve using CRISPR treatments or using drugs etc that induce the formation of these changes.It can also involve using CRISPR to alter a human patients DNA to the point that the cells produce the required amount of telomerase to first rejuvenate them to a youthful state similar to one’s early 20s,teens or even infancy in the case of those who are aged 40 and older and keep them rejuvenated forever at an infant or youthful state without leading to tumours or other side effects.AI will develop CRISPR treatments including using genes created from scratch or even recombinant DNA from Nephropidae that is altered to do this without rejection,formation of tumours etc
Combining Bacillus F,T.gammatolerans,D.radiodurans ability to repair telomeres would work to prevent future telomere and mitochondrial DNA damage.If possible to prevent the DNA for DNA repair taking up too much place in the patients genome it would ideal for only recombinant DNA from T.gammatolerans to be used since it can express this phenotype and unlike that from Bacillus F and D.radiodurans can allow one to withstand blasts of radiation if up to 30,000Gy meaning in order to prevent future DNA degradation in telomere and mitochondrial DNA,recombinant DNA from T.gammatolerans should only be used by itself with no recombint DNA from D.radiodurans and Bacillus F once trials on tissue samples and animals show that only it is needed.Each patient will have cell samples taken and analysed in automated labs to determine the level of telomere degradation in their chromosomes and mitochondrial DNA and compared with that from infants.Telomere,chromosomal and mitochondrial DNA will be at first fitted with DNA repairing DNA from these bacteria Bacillus F,T.gammatolerans,D.radiodurans to prevent future damage to them due to these bacteria exhibiting DNA repair mechanisms.Any future damage to telomeres to radiation,free radicle,mitosis has on the quality of telomeres in the chromosomes,mitochondrial DNA etc will be repaired instantly by adding the genes from these bacteria that allow them to repair their DNA thus rendering the hayflick limit and damage to telomeres,chromosomes and mitochondrial DNA obsolete forever.This DNA from these bacteria that exhibit DNA repair will be added first to patients mitochondrial and telomere chromosomal DNA via CRISPR to prevent any future damage and decay of the patients DNA while AI using CRISPR can repair existing damage to ones DNA by filling in the blanks etc.AI will for each patient after lab machinery has analysed their level of DNA degradation in telomeres,chromosomes and mitochondrial DNA and compare that from infants or at first those in their teens or pre teens will allow AI to extrapolate missing damaged DNA to fill in the blanks restoring their telomeres,chromosomes and mitochondrial DNA to a level similar to infancy reverting DNA back to healthy levels as seen in infants.This may involve using DNA from younger relatives as a baseline and involve AI extrapolating scratch DNA.Thus DNA from younger patients especially releated individuals and even scratch DNA extrapolated by Phanes for each individual patient will be added to both mitochondrial and chromosomal telomere DNA to repair existing damaged DNA to revert both mitochondrial and telomere DNA to levels and states similar to that of infancy with DNA from D.radiodurans,T.gammatolerans and if need be Bacillus F that allows them to exhibit DNA repair will be added to all cells mitochondrial and telomere DNA in patients at first to prevent future telomere damage caused by mitosis alongside endolithic bacteria to slow down damage and any future damage repaired instantly and have aerotolerant bacteria and scratch DNA to counteract the effects of free radicles.Strands of damaged DNA caused by ageing and few radicles etc will be analysed and removed and replaced with copies of the DNA that are of a less damaged stated.Ones entire DNA in their chromosome,mitochondrial DNA will through scratch DNA extrapolated by AI using CRISPR be reverted to a state similar to infancy including telomeres
Scratch DNA alongside recombinant DNA from aerotolerant anaerobic bacteria can be utilised to improve this especially those that cause the rejuvenation of Phosphatidylcholines and telomeres in the membranes and DNA of all cells destroyed by free radicals with further engineering making cells immune to the effects of free radicals,such as reactive oxygen and free radicles taken in by the host and produced by microbes to fight pathogens counteracted by recombinant DNA from aerotolerant anaerobic bacteria and scratch DNA developed by Phanes.Scratch DNA and those from other plants and animals can be added to counteract the effects of all free radicles and any compounds that lead to senescence or cellular and genetic damage using DNA from scratch or engineer them into turning the products of aerobic respiration into compounds that can be consumed or excreted or not be effected by them.This DNA would be used to make cells immune to the effects that oxygen has on damaging DNA etc.This could also be done with the body engineered to produce antioxidants.Recombinant DNA from T.gammaolerans and D.radiodurans would be used to protect the body from any daily doses of radiation that one experiences from sunlight UV radiation,radon,xrays and even nuclear fallout,gamma ray bursts and cosmic radiation preventing DNA damage if applied to telomeres in both the nucleus/chromosomes and mitochondria.If possible DNA from T.gammatolerans can negate the need for DNA from Bacillus F,D.radioduran/ as it also protects one from blast of radiation of up to 30,000Gy thus allowing for DNA repair and also protection from radiation.CRISPR treatments will be used to repair existing damage in telomeres,chromosomes and mitochondrial DNA
Conclusion:
Combing the genetic regenerative abilities of D.radiodurans,T.gammatolerans that allows them to survive such extreme doses of radiation(30,000 Gy compared to 5Gy for a human) by repairing DNA,with the DNA regenerative abilities of Bacillus F,the ability for extreme oligrotrophic and xerophile to require very little nutrients and water to counteract effects of metabolism as well and other Archaea such as endoliths that also undergo repair from cosmic rays,racemization and reproduce via mitosis only every 10,000 years and if possible Tardigrade able to survive extreme conditions and endolithic bacterias slow metabolism and aerotolerant bacterias ability to negate the effects mitochondrial metabolism together alongside applying the genes form plants and animals that synthsise anti-ageing compounds such as reversatrol,coenzyme Q10,Phosphatidylcholines,teleomerase into the the host genome to be produced by all cells to synthesise them themselves,removal of the fat insulin receptor gene and others that induce ageing,scratch DNA into gene therapy treatments using CRISPR applied by anti-ageing strains microbes using horizontal gene therapy into both the nuclear telomeres and also mitochondrial DNA of all cells in the body would reverse and negate all of the effects of senescence in more complex multicellular organisms such as H.sapiens brought on by mitochondrial metabolism,telomere degradation with again this at first halting the ageing process and then further research into them,other more complex immortal lifeforms and DNA created from scratch done by Phanes,Epione and Paean could reverse it secondly by repairing existing damage to ones the telomeres and cells using this recombinant DNA,DNA strands made from scratch and from and other biological components with a more fixed state and then reversing the symptoms of ageing.These anti-ageing treatments would allow more complex multicellular lifeforms such as H.sapiens and other sentient life forms alongside all species of pets etc from across the universe from all taxonomic rank in their adult years even those in their elderly years such as those currently aged 60-95 to have their cellular and telomeres structures be reverted to that of their infant years and live forever in a state similar to early to late adolescence staying youthful in a state similar to the ages of roughly 14-15 with the microbes using other gene therapy via CRISPR and creating relevant sex hormones with females kept in their fertile peak of 14-15 and males their testosterone peak of 14-15 indefinitely and eat and drink as much as they want prevent mitochondrial damage to the cellular processes with them enhanced by these and other phenotypes of these extremophiles.Thus one internal organs and external skin would have it reverted indefinitely to a state equivalent to infancy allowing one to stay in a perpetually youthful state similar to the ages of 14-15 with females forever kept in the fertile peak of 14-15 and males kept forever in their testosterone peak of 14-15 through genes added that keep their hormones at this age range forever with once patients are reverted to this young state the ageing process will be slowed down to the point that they will age the equivalent of several months every few 10,000 years with scratch DNA repairing degradation that occurs every 10,000 years thus halting the ageing process forever.One would thus be reverted to their youthful internal and external appearance of their early 20s or even early and late adolescence of the age of 14-15 with their cellular structures and telomeres reverted to their infant state and the ageing process halted to the point a person would age the equivalent of several months once every 10,000 years with the ageing effects reversed automatically every 10,000 years with females forever kept in the fertile peak of the ages of 14-15 and males forever kept in their testosterone peak of ages 14-15.The anti-ageing treatments could also aplly to all species of animals including pets of all species and breeds of animals such as Canidae,F.catus,,Serpentes and animals in zoos etc as well as even ornamental plants with Phanes modifying the treatments to each species and breed.This would thus allow humans etc be reverted to their youthful appearance of early 20s or early and late adolescence and the ageing process halted to the point they would age the equivalent of several months once every 10,000 years with the ageing effects reversed automatically.The anti-ageing treatments could also aplly to all species of animals including pets of all species with Phanes modifying the treatments to each species and breed.This would be applied by anti-ageing strains of microbes to the hosts DNA in all cells and tissues where they will reside.Bone marrow would have this DNA but it added in a way to prevent leukocytes housing it as it would be ideally to have them die off at the same rate they do normally to prevent overproduction of them especially during infections with Phanes extrapolating ways to ensure that they and erythrocytes die off at a normal rate but still stay young as in an adolescent of infant to prevent them overrunning the body extrapolating ways to ensure that they and erythrocytes die off at a normal rate but still stay young as in an adolescent of infant to prevent them overrunning the body.Augmentations would still be added to leukocytes.Phanes will develop countermeasures to any problems associated with gene therapy that extends the human lifespan.Augmentations would allow one to heal instantly from wounds,cuts,burns and also regrow limbs,become immune to radiation,survive exponentially longer or completely without water and food,survive the vacuum of space and all extreme environmental conditions on Earth and across the world thus effectively making one immortal.Mapping of these lifeforms DNA using artificial intelligence will be done to determine the genes for their incredibly long lifespans with this of note to the unicellular lifeforms that seem to live the longest and have fewer genes than multi cellular lifeforms that exhibit this phenotype meaning it should be easier to determine which genes are responsible for this much quicker using artificial intelligence and automated labs testing each sets of suspected genes especially in regards to endolithic bacteria,T.gammatolerans,Bacillus F as well as Planarians.This should at least first halt and reverse the ageing process by 2029 with AI creating scratch DNA and carrying out more advanced research using DNA from T.dohrnii etc on animals to further enhance age reversal and halting.Other non human multicellular lifeforms including pets,livestocks wild animals in zoos,conservation areas and the wild(especially endangered species) will be able to avail of this with Phanes,Paean,Urania and Hecate suiting it to their specific DNA with even ornamental plants and crops in gardens etc also availing of this.Having all work such as simulations of the ageing process and effects of treatments as well as creation of scratch DNA,preparation and scanning of the extremophiles done by Phanes,Paean,Hecate,Epione,Urania and even ancestral AI,automated labs in hospitals and universities using all data on Apollo and existing scientific papers online searched by AI will expedite the process exponentially.3D DNA printing and automated labs can also expedite the process exponentially since mapped genes in Physis and those from scratch can be easily be added to leukocytes used as baseline and microbes as upgrades expediting their development even quicker theoretically allowing therapies to first halt the ageing process available within a decade extending the lifespan of those in the currently in the age range of 50-95 to receive therapies to first halt the ageing process giving them more time to receive the benefits of more advanced therapies that then repair and reverse the ageing process thus reverting them to a more youthful state of their early adolescence and early twenties indefinitely with females having the same fertility peak in their early teens 14-15 years of age and the same for males with males through other gene therapy applied via CRISPR to them and also through testosterone and other hormones created by the microbes allowing to on demand or indefinitely to have the same testosterone peak they had aged 14-15 years of age.It could also reverse presbycusis allowing those middle aged or older to revert to their hearing peak they had as prepubescent children.
Those past this range say currently aged 90-100 could if they manage to naturally biologically live to past 100 even to the ages of 110-120 could feasibly have this if they manage to still stay alive.Thus those currently in the “goldilocks range” aged between 50-70 are the highest age range limit to have a 100% chance of availing of this with those between 71-81 having at least a 90-100% chance of availing of this depending on how well they have taken care of their body – those aged about 75 would have at least 90-95% chance while those aged 76-81 their chances would be 75-89% ,those aged 81-91 have a 50-75% or less chance of availing of it due to the extreme damage though as stated if they were biologically meant to originally live to between 100-110 they could have at least 50% chance.As detailed later on proto treatments available by 2023-2025 could allow those currently aged 80-95 to live long enough to 2029 by halting the effects of ageing in vital organs such as the brain,blood vessels and then allowing it to be reversed to a more youthful state of ones early twenties by this date with other CRISPR treatments allowing them to survive heart attacks and strokes and other age related conditions thus raising their chances considerably to at least 50-75% of living an indefinite lifespan of eternal youth.This would increase the chances currently aged 75-80 to at least 100% and those currently aged 80-100 to at least 50-85%.The chances of availing of treatments that halt and then reverse senescence depends on how quickly the treatments to halt and then reverse the ageing process can be developed,the level of global cooperation,how good in shape one is with regards to their age ie some 80-90 year olds may be in better shape than other 80-90 year olds,their previous medical history and how old they were biologically born to originally live to without the treatments ie if their genetics predispose them to live to 100-122 the current upper limit of human lifespans and other factors such as their inability to die of trauma,pathogens,heart attacks,natural causes,accidents or murder and how much in shape or damage their lungs,brains,livers are in response damage from cigarette smoking,alcohol damage and their cholesterol levels and genetics that predispose them to cancers,alzheimers etc similar to some people are more likely to die of Coronavirus infections than others.Each individual patients current state of health determines their chances of survival with the general rules got good health such as give up smoking,avoid exposure to carcinogens,avoid fatal accidents and eat healthy food,exercise etc used to increase the survival rates of those 40 or older with older patients taking cholesterol tests and health check ups.If possible clinical trials applied on the oldest living patients can start by 2025.The state of ones health of those above 75 such as cardiological health,pulmonary health as well the state of their cellular structures and telomeres and whether they would be biologically predetermined to live to above to 100 or above determines the possibility of their chances increase above these percentages.Thus these percentages are basal guidelines with them different for all patients above the age of 50-70 based on ones unique genetic and health factors.Patients should undergoe medical tests to determine their chance of survival with those aged above 70 that are currently 80-100 being part of firstclinical trials and the first line of patients to receive anti-ageing treatments between 2025-2029.The rate of scientific research,use of AI and automation in labs,use of computer networks to share data and 3D DNA printers and level of cooperation done in universities,hospitals etc worldwide should exponentially increase and determine the rate that the first human trials and treatments are available for older patients thus increasing survival rates of those currently aged 80-100 years exponentionally to between 80-90%.Simulations and practical applications should show this done at the same time that the treatment is development.Older patients above 75 may want to avail of bioprinted and chimera organs such as hearts and livers etc from cattle,remove their fat insulin receptor gene to eliminate heart disease as well as check regularly for cancer and other fatal diseases and infections and also take preventative action towards extending their chances of living long enough to avail of treatments to first halt the process of senescence and thus avail of those to reverse the effects already on them.This should also be done of all patients over the age of 40 or indeed any age getting checked regularly for all types of cancers and have genetic scans for all types of genetically predisposed cancers and conditions that would lower their percentage of survival that they may be prone to especially cervical and prostrate as well as getting DNA scans for it and other genetic diseases with survivors of cancer and heart disease also getting routine checks and bioprinted organs.Intensive research should be made into primarily strains that treat ageing and also cancer above all other strains at first due to the fact as they can reverse the ageing process in the elderly who are the most at risk individuals alongside cancer which is the most deadly of diseases.Other strains such as augmentations and anti-viral etc strains could be delayed until after ageing strains are perfected as most pathogens can be treated with existing treatments and preventative measures to prevent infections.As detailed later modified immunotherapy and viral vector cancer treatments using CRISPR and Polybia-MP1 will increase survival rates for all types of cancers especially those in middle age or older.Ideally all patients worldwide should get DNA scans by 2023/2024 to check for cancers and other fatal genetic conditions to prepare for them to get frequent screenings such as prostrate exams and pap smears,mammograms and xrays etc and also get bioprinted organs.Those who work with carcinogens or in heavy polluted sites and even smokers may want to avoid smoking and also heavy drinkers would likely avoid drinking heavily and get frequent checkups with those in accident prone occupations taking extra care to prevent death and serious injury.Those aged 75 and older can avail of organs like hearts,kidneys,lungs from chimera animals such as pigs and cattle as early as 2023 to provide them with organs that are in a vigorous and youthful state equivalent to those in their early twenties to increase survival rates with them taking anti-rejection drugs until CRISPR treatments remove all foreign DNA.AI will create strains of bacteriophages that can kill off strains of fatal superbugs that can be created onsite of all hospitals.Medication for chronic infections such as HIV and chronic conditions such as genetic conditions will be provided to all suffers worldwide in both the developing world and first world.Biocompatible microbes since living within the tissues of the patient will be able to apply the relevant genes to the host permanently to the cells and tissues in the body.The same anti-ageing procedures can also be applied to livestock and pets as well as crop and ornamental plants and endangered wild animals.These and extra phenotypes using other recombinant DNA could allow H.sapiens to survive the same extreme conditions as these extremophiles that would normally be fatal to humans such as extreme doses of radiation,pressure,prolonged periods without water and nutrients such as proteins,fats and carbohydrates,vitamins especially if H.sapiens can be engineered to synthesise essential vitamins,fats,amino acids by themselves or this is done by biocompatible microbes.As stated earlier it takes about an hour to map and identify a patients entire DNA of 46 chromosones and 30,000 genes thus it should be easier and quicker to map and identify all the genes of each one of the aforementioned and other species responsible for their regenerative capabilities,lack of neuro-muscular degenerative diseases and cancer as well as biological immortality especially in the case of unicellular Archaea lifeforms and even mammals etc especially if done simultaneously by artificial intelligence since as stated they should have shorter genomes accelerating the creation of ageing therapies via gene therapy using horizontal gene transfer through biocompatible microbes.Their DNA should already be within genomic database scattered across the internet but having proto AI transfer them into a single database will expedite research and progress research should be made into primarily strains that treat ageing and also cancer above all other strains. these extremophile Archaea lifeforms and animals that dont exhibit genetic based diseases should at least halt the ageing process in humans at first with further research using them and other lifeforms with this phenotype and DNA made from scratch as well as biocompatible microbes then allowing for the ageing process to be reversed allowing for patients to be reverted to a indefinite youthful state of early teens and early twenties with Phanes,Gaia,Urnaia,Hecate and Paean doing this and other research into genetic engineering and therapy.These and DNA from animals that exhibit biological immortality could also prevent any random mutations that would lead to cancer in both the nuclear telomeres/chromosomes and also mitochondrial DNA.The ability of embryonic stem cells and cancer cells to produce telomerase could introduced into other cells to make them replicate indefinitely with gene drives and other genetic treatments keeping this under control preventing the body being overrun with tumours.Other DNA can be made from scratch as well to better integrate this recombinant DNA or replace it with if possible DNA coming from all or most of the aforementioned sources.If possible both gene therapy and even editing embryos,spermatozoa and eggs will be done to increase the intelligence of the unborn child and thus if done on a large scale be able to over several decades increase the average intelligence quotient of the entire species.To deal with the drawbacks of gene therapy the virus used could have DNA from the host patient or just human DNA to create human proteins on its capsid to avoid detection by the immune system and thus be used indefinitely without immune reactions.Gene drivers especially advanced gene drive technology could be used to make the gene inserted of any phenotype as well as permanent features of H.ubermensch and H.sapiens to spread through future cells through mitosis becoming a permanent part of the patients body or just specified cells DNA or at least lower the amount of treatments to be done with this becoming a permanent part of all future successive cells.To deal with treatment that requires multiple genes to be inserted all of these genes could be added to the cells genetic code in one go or they could be done in waves one after the other to allow each piece of recombinant DNA to be added one after the other or in one go especially if CRISPR is used which can allow for genes to be inserted at proper sites avoiding unwanted mutations and cancers.Ideally both mitochondrial and nuclear telomere DNA will be modified in all forms of gene therapy such as ageing and augmentations to ensure stability and prevent mutations in one that would affect the other in all cells in the body with as stated advanced gene drive technology will ensure the genes will be passed onto each successive cell and to all spermatozoa,eggs and thus all successive children in the patients bloodline via germline therapy and thus the rest of the genepool of H.sapiens.Nanomachines could in time become more effective at this therapy alongside biocompatible microbes engineered to interact with and transfer these strands of DNA using CRISPR into human cells with them either mortal versions or immortal versions that rein insert DNA into cells constantly over their lifetime with themselves having recombinant DNA from endoliths to make them immortal with gene drives as well as receptors and sensors on cell walls making them unable to react with other biocompatible microbes for pathogens causing mutations and hybrids and insert genes to specific cells.DNA from Planarians,Hydra,A.mexicanum and C.elegans will also allow them to undergo cellular repair and memory to counteract any damage inflicted on them which can be transferred to the host and the primary immune system via horizontal gene transfer.Having these have the DNA from bacteria that exhibit horizontal gene transfer with humans or from scratch could improve their efficacy in effectively transferring genes preventing mutations,faults and tumour growth with biocompatible microbes also engineered to detect fight off any tumours caused by this and even fix any mutations that lead to these and faults that may with gene drives also aiding in this.Gene drives and also sections of DNA made from scratch could fix any mutations,faults and other problems that may arise and better integrate DNA from other distantly related animals and plants with DNA from animals that never get cancer added to prevent tumours forming though this would be done to remove cancer from the genepool of H.sapiens.Again advanced gene drives might make the therapy permanent through mitosis and pass onto to the next generation of cells but these microbes might exist purely to fix any faults or if it needs to be done every few years or decades especially with regards to ageing and organ specific treatments.Base microbes can copy genes and the entire DNA in specific cells,tissues and the entire body routinely to determine if gene drives are successful and also to detect any faults that may occur with these results relayed to Paean via nanomachines in them with this occurring if any surprise disease are exhibited by the patients.Before that phlebotomy robots can collect cells from various parts of the body in automated labs and grow tissues from these to allow them to be analysed by human and robotic staff to see that the relevant genes are present or they could put through PCR analysis to check for the specified genes.If patients are fitted with endolith DNA that prevents mitosis from occurring every 10,000 years then this should be of no problem.Ideally these biocompatabile microbes based on the patients leukocytes will be used as a more effective means as a vector than viruses as since they will be forming a permanent feature of the human immune system they will be able to permanently trick the hosts immune system into believing they are part of it as they will use the patients leukocytes as a baseline eliminating the problems associated with foreign viruses and bacteria illicitating immune responses and can carry out corrections of faults that occur in waves over years or even decades as well as using gene drives to make the therapy and corrections permanent and if need be carry out reinsertion in waves.They will also be able to treat all cells in the body for augmentations and also ageing without illicitating an immune response and also by using their malleability to move and squeeze in between each cells with them using horizontal gene transfer and also bumpers.To deal with the use of Cas-9 illiciting immune responses it could be modified to contain some or all human proteins entirely as an human and patient version of Cas-9.Advanced gene drive technology will ensure the genes added to all cells will pass from generation to the next via mitosis with base microbes copying the DNA in all cells in the body and wirelessly send the results to see if they are present into ones patient file with this done regularly.Specific strains will be made to deal with ageing via CRISPR treatments with the DNA for the application to all the cells in the body will be housed in ribosomes and in particular plasmids that will be recreated over and over again via taq polymerase and Cas-9 to be reused over and over again with millions of microbes applying the DNA to all cells in the body at once until all cells are treated.Each relevant genes can be applied all at once or in waves one after another.The genes for these will be applied either by horizontal gene transfer and also bumpers acting as a mini vector with advanced gene drive technology used to ensure the genes pass from one generation to the next.All species of animals including all types of pets,livestock and all species of plants including ornamental plants as well as crops could avail of the same anti-ageing treatments as humans.Pets owned by the public,livestock and animals in zoos will be able to avail of anti-ageing treatments and those to remove genetic diseases and augmentations using specues specific microbes.The effect of endolithic DNA on the development of infant animals with human DNA can be explored as to whether its slow miotic rate could prevent the rate of cellular and bodily development of infants to children to adolescents etc should be investigated as although it would halt the effects of ageing in adult patients it could have the effect of stunting growth in younger patients though this could be counteracted by the rapid development brought on by hormonal factors and also natural growth rates that would be ending with the end of puberty caused by the development of new cells via somatic stem cell production rather than death of old ones by which time the slow miotic rate may be effective at halting the ageing process with if possible their is a high chance that there would be no chance that this would have no effect on the proper development of samples of H.sapiens.Thus the effects of the slow miotic rate on the developments of infant mice to adults born from parents with anti-ageing treatments using advanced gene drive technology should be investigated by itself and also alongside DNA from other extremophiles and also plants that stimulate the production of anti-ageing compounds on animal trials as early as 2023.The effect it has on developing fetuses in mice would also be tested with long living female mice with all recombinant DNA impregnated invivo using spermatozoa from other long living male mice that has all of this recombinant DNA to see if the resulting fetuses have any slow developments in the womb or once born preventing them from reaching puberty and adulthood at normal rates or this has no effects on them until they reach adulthood with this research starting as early as 2023.If it has been shown that this slow mitosis has effects on mice and thus animals including humans then it may be possible to remit this from advanced gene drive technology that would pass it from parents to infants with if need be advanced gene drive technology kept and it removed from spermatozoa and eggs but not the ovaries and testes meaning children could develop to adulthood wherein the anti-ageing strains could reapply it to the host patient once they finish puberty.Otherwise scratch DNA can be added to humans and test animals that causes the slow miotic rates of endolithic bacteria to be present in fetuses and young children but it only expresses and turns on only when puberty is finished once the patient reaches the age of 14/15 with tests on animals and biosynths with human DNA showing which solution can be used.Experiments will be carried out on animals with human DNA and biosynth humans to see the effects of endolithic DNA on the development of fetuses to see if rte development of fetuses and infants is slowed to the point that it would result in pregnancies lasting several thousand years or not.Human patients during this period that wish to have children that have already have had their levels of Phosphatidylcholines and telomeres reverted to an infant state and have endolithic DNA will when planning to have children have through Paean through CRISPR temporarily remove this endolithic DNA from their genome of only that present in their ovaries and testes and once the female has given birth it added back to them and their levels of phostidycholines and telomeres reverted back to infancy via CRISPR should they have depleted due to mitosis with the child once it ends puberty will have endolithic bacteria DNA added back to their genome.This will allow people to have healthy normal children despite being immortal.Solutions to the application of this endolithic bacteria DNA can include instances where the endolithic bacteria DNA will be present in their testes and ovaries with scratch DNA present in only the ovaries and testes also present that ensures the testes and ovaries age at the rate of once every 10,000 years like the rest of the body but the endolithic DNA is not passed onto spermatozoa and eggs produced by them.Phanes will extrapolate solutions to this problem.This concern is minimal but since CRISPR is a new technology and the effects of foreign DNA especially endolith DNA not fully understood especially the effects of bacterial DNA especially endolithic bacterial DNA on humans must at least be investigated.Either way the additions of recombinant DNA from endolithic bacteria will still play a role in halting the effects of ageing in existing living patients of H.sapiens who are adults aged 18 and older especially those currently aged 80-95 and younger that already have finished puberty applied via advanced gene drive technology as early as 2023-2029 with its effects on unborn fetuses passed onto them via advanced gene drive technology done on mice.The same extremophile bacteria DNA used to reverse and halt the effects of ageing ie endolith,T.gammatolerans,Bacillus F,D.radiodurans recombinat DNA will possibly prevent cancer,all genetic diseases,neurological diseases,developmental disorders being passed onto future generations or occurring in the first due to random mutations by repairing mutations via DNA repair that cause genetic based or even environmental based cancer,all genetic diseases,neurological diseases,developmental disorders in the developing thus wiping these from the human genepool after being applied to all patients worldwide when they are cured using germline therapy and advanced gene drive technology.Cancer caused by radiation,carcinogens will be repaired by this DNA.Thus no new extra DNA will be needed to be added to all patients worldwide as those that already halt and prevent ageing will be able to prevent the random mutations that cause these with it also preventing deformities from inbreeding,incest and also damage from teratogens.This would thus wipe these diseases such as cancer,genetic diseases,pedopheilia,schizophrenia,Downs syndrome etc from the human genepool forever by preventing the necessary random mutations and teratogen or other environmental based factors that cause them via DNA repair mechanisms.This would also prove gene protection theory.Bone marrow would have this DNA to halt the effects of ageing but it added in a way to prevent leukocytes housing it as it would be ideal to have them die off at the same rate they do normally to prevent overproduction of them especially during infections with Phanes extrapolating ways to ensure that they and erythrocytes die off at a normal rate but still stay young as in an adolescent of infant to prevent them overrunning the body extrapolating ways to ensure that they and erythrocytes die off at a normal rate but still stay young as in a state equivalent to an adolescent of infant to prevent them overrunning the body.Augmentations would still be added to leukocytes.Phanes will develop countermeasures to any problems associated with gene therapy that extends the human lifespan.This concern is minimal but since CRISPR is a new technology and its effects not fully understood especially the effects of bacterial DNA especially endolithic on humans especially unborn fetuses must at least be investigated.Either way the additions of recombinant DNA from endoliths will still play a role in halting the effects of ageing in existing living patients of H.sapiens who are adults especially those currently aged 80-95 and younger that already have finished puberty applied via advanced gene drive technology as early as 2023-2029 with its effects on unborn fetuses passed onto them via advanced gene drive technology done on mice during this period patients that wish to have children will have their levels of Phosphatidylcholines and telomeres reverted to an infant state will when planning to have children have this DNA removed from their genome or that in their ovaries and tested and once the female has given birth it added back and to them and their levels of phostidycholines and telomeres reverted back to infancy via CRISPR should they have depleted due to mitosis.Phanes will extrapolate solutions to this problem.Thus at first endolithic DNA and all of that to halt and reverse the effects of ageing will be applied to living patients aged 14-65 etc and older to extend their lifespan with this removed from spermatozoa and eggs in ovaries and testes to prevent it passing into future children as it may slow down the development of children to adulthood and may even slow down the development of fetuses to fully born children and also slow down the development of fertilised embryos into fetuses by several thousand years and will be applied to newly born patients once they reach physical and sexual maturity.At the same time research on mammals with human DNA and biosynths modelled on humans will be done to see if this has any effect in the development of embryos into fetuses and fetuses into maturity.If it does then Phanes can develop scratch DNA that has the genes added to the testes and ovaries up be passed to all future progeny but have no effect on the development of embryos and fetuses but only be turned on once the progeny reaches physical and sexual maturity.Otherwise it will not be added to this to prevent it passing into future human progeny only to be added to them once they reach sexual and physical maturity.
All sources of recombinant DNA will be added to both mitochondrial and telomere DNA in all cells.Recombinant DNA from Hydra and T.dohrnii could allow for old senescent cells especially in those receiving the first trials after animal trials to have their cells revert to a younger state almost instantly.T.dohrnii and Hydra etc DNA can be used if shown to be safe in animal trials to be able to cause older senescent cells to reprogramme themselves to a much younger state if scratch DNA is added with this done once every once every 10,000 years by causing Phosphatidylcholines and NAD+ and possible telemeres in the cells to revert to a younger state.After the first patients avail of anti-ageing treatments,animal trials can show if recombinant DNA from T.dohrnii,Nephropidae,Hydra can be transferred to humans to keep telomerase level stable to the point that it keeps it forever at levels of infancy and also able to revert senescent old cells to a younger state automatically after miotic damage every 10,000 years with this tested on animals given anti-ageing treatments except endolithic bacteria.This is due to biological mechanisms within these three species T.dohrnii,Nephropidae,Hydra to be able to revert their cellular and genetic structures to a infant state as they age thus making them biologically resistant to the ageing process
Phosphatidylcholines:
Phosphatidylcholines can be synthesised by the body ideally in each cell in required amounts using DNA from scratch,humans and Glycine max to then as stated rejuvenate cells with any with any possible atherosclerosis negated by omega-3,reversatrol,plant sterols etc produced by the body through horizontal gene transfer and also microbes clearing out the arteries with further engineering preventing atherosclerosis such as turning off the fat insulin receptor gene.Bacteria that break down oxidised cholesterol for example Bacillus subtilis SFF34 can have their DNA that breaks down the oxidised cholesterol can be added to the genome of humans to break it down.Both the genome of H.sapiens,Phasianidae(that produce it in the yolk) and G.max and other plants and animals that produce Phosphatidylcholines can be analysed by AI to see what genes they share in common that express the production of the compound to allow this to be determined with the genome of bacteria of those that create Coenzyme Q10 and H.sapiens analysed to find the common genes with the same done for the plants that create other anti-ageing compounds by analysing their genomes.Other natural anti-ageing compounds alongside Phosphatidylcholines such as Coenzyme Q10,vitamin D,antioxidants,reversatrol and many others can be synthesised by the patient themselves in the cells by adding the relevant recombinant DNA from animals and plants that produce these into the hosts genome via horizontal gene transfer with them produced either in the cells and tissues of the host negating the need to take supplements saving on the time and need to take them as well as resources to create them.Nicotinamide adenine dinucleotide(NAD+),phosphotidocholine and other compounds related to youthful tissues will by scratch and recombinant DNA from humans etc have cells replenish them in desired amounts forever associated with infancy.These would ideally be synthesised in the cell walls in the required amounts ideally to ensure they are made in correct amounts and also prevent overdosing or are not lost,replenishing them only when they naturally deplete over and over again and replenish those in older patients or even have them once replenished kept at ideal healthy levels and replacing depleted reserves in the cell wall in older patients to levels seen those in their early teens,early twenties or even infant years.Scratch DNA will ensure that it is synthesised only in the cells and cell walls and constantly replenished in levels synonymous with infancy once they deplete ensuring they stay at levels associated with infancy forever.Scratch DNA would be added to ensure the levels of these compounds are reverted to that of an infant and kept at these levels via replenishing them automatically every time a cell undergoes mitosis over geological timescales.The cell structures and thus levels of them in infants and each individual patient will be analysed using automated lab machinery with them tested after gene therapy to see it is effective.Each patient will have the levels of NAD+ and Phosphatidylcholines in cells and tissues in their body analysed in labs to determine the level of degradation and compared to that from an infant to thus determine scratch and aforementioned recombinant DNA to be added to revert them to an infant state.This aforementioned and scratch DNA would thus keep the levels of these compounds in the cell walls and cells at ideal levels similar to infancy if not ones early teens and early twenties indefinitely with them replenished over and over again automatically when they deplete via adding scratch DNA.The scratch genes added would constantly replenish the levels of Phosphatidylcholines,NAD+ etc over and over again whenever they deplete naturally due to mitosis.Excess produced by the cells or intaken by diet could be flushed out of the body with in time the amount produced by the cells perfected and them able only to absorb only that required amount via engineering with excess flushed out or used for its other purposes.Ideally scratch DNA would make them engineered to only recreate the required amount only in the cells outer membranes thus meaning that no compounds are released by them as waste into the blood stream to prevent dangerous side effects.Thus each persons cells would through relevant scratch and recombinant DNA from humans and plants that synthesise these compounds would synthesise Phosphatidylcholines,NAD+ etc within their cell walls thus replenishing them in the case of older patients and doing so constantly as one ages over geological time rather than them being released into the bloodstream as a waste product that could be dangerous to the patient etc.Thus the patients cells would be engineered to synthesise NAD+ in only the cell itself and synthesise Phosphatidylcholines in the cell walls and not have these released into the bloodstream which could cause side effects.Each individual patients cells will be analysed by automated lab machinery to measure the level of NAD+ and Phosphatidylcholines and their degradation and compared to that of an infant to determine their level of depletion of NAD+ and Phosphatidylcholines.Scratch DNA will be added to replenish these to infancy levels and also keep them replenished in the outer structures of each cell only when they deplete thus once the cellular structures of each cell is reverted to an infant state they will be kept at these levels forever.Thus each cell will be engineered using relevant recombinant DNA and scratch DNA to at first replenish the levels of phosphtidocholines and NAD+ back to levels found in infants with them engineered using scratch DNA to replenish them constantly whenever they deplete and only when they deplete thus negating any effect miotic degradation has on their levels.Phosphtidocholines will synthesised and replenished as these are the compounds upon which phospholipid bilayers that each cell in the body is composed of with NAD+ also responsible for a healthy metabolism and functioning of cells.DNA from totipotent stem cells will added to keep them at the same level of vigour as those in embryos and even infant years.Phosphotidocholine and NAD+ will at first may have to have to be synthesised in the bloodstream to allow it to be intaken by cells with this of note of NAD+ which due to being unable to being intaken by cells would require precursors of it to be synthesised in bloodstream that can be then intaken into cells that are then converted into NAD+.
This may have to for patients aged 50 and older.Collagen can be created by microbes as well as engineering the body to produce and replenish it in key areas of the body itself naturally using scratch DNA with these compounds anti’ageing affects sufficing until other compounds such as Growth differentiation factor 11 and NAD+ ‘booster’ NMN can be researched in animals to be added into the production by individual cells to reverse ageing overtime.Nicotinamide adenine dinucleotide can not only be replenished by the cells naturally through having scratch DNA added to the patient but the microbes through scratch DNA and human recombinant DNA and anabolic and catabolic reactions can produce its precursor Nicotinamide mononucleotide in the bloodstream to cause the cells to create the compound themselves.The effects of cosmetic surgery such as injections of botulism and stretching of the skin via face lifts and also lip injections as well as crows feet can be be reversed by them and cosmetic surgery by forming new tissues and collagen internally,causing certain tissues to undergo apoptosis or causing the body via CRISPR to create collagen in the normal amounts of it from their early teens and early twenties.The ability of Serpentes to shed skin will also do this to correct damage by peeling off upper layers of skin in the case of elderly patients and those with botched face lifts and botulism treatments to recreate a more natural younger face and skin across the entire body.Skin tissue will be treated with anti-ageing compounds created by them and the addition of DNA repairing DNA as well as them causing the outer epidermis to peel off using recombinant DNA from Serpentes added to the patients genome and them forming new tissue underneath them with this done every once and a while on demand by Paean to replace old dying skin tissue possibly every few decades or even centuries if not millenia and could be done to remove unwanted tattoes and also scars.This would be done at first by the eldest patients currently aged 50-95 to remove the outer layers of dead skin on them to allow more youthful skin tissues to emerge with greying hair have compounds created by microbes to rejuvenate lost colour alongside CRISPR or the hair could be forced to grow outwards to allow the old discoloured hair to be removed outwards.If need be those with greying hair should have their hair shaven and then have microbes and CRISPR have the body produce new colourings to their original colour.Chemical signals from microbes signalled from Paean would initiate this moulting to first form a layer and then to have it moult off dead and dying skin.This could be done with internal tissues such as blood vessels and organs though it would require the cells also programmed to break down or this done by the anti-ageing strains having recombinant DNA from necrotising bacteria to break it down although this may be unnecessary since this is not evident in Serpentes it self and would be done primarily for the exterior with this done of the whole body or it can be programmed to occur in only certain places where microbial cosmetic surgery is taking place ie the face,arms,legs,breasts etc via chemical signals.Tissues of internal organs can be made to undergo apoptosis when newer younger tissues form underneath them.Animal trials on mice and chimpanzees with no fur can stay as early with this initiated by chemical signals injected into them with the carbon dioxide energy acceptor phenotype in humans and animals preventing asphyxiation.This can apply to both intracellular and extracellular aggregates with genes from animals that do not get cancer and any other animals alongside scratch DNA to prevent mutations both within the nuclei telomeres and mitochondrial DNA.CRISPR treatments via the microbes will allow for both telomeres in cell nucleus/chromosomes and mitochondrial DNA to be repaired and have DNA from the relevant micro-organisms and multi cellular lifeforms that exhibit biological immortality and immunity to cancer to be put into their place to prevent mutations that would lead to ageing,cancer and other and existing genetic diseases with precision with any faults repaired by more precise treatments.Extracellular aggregates can be done by the strains of microbes that immunise the immune system against viral and pathogenic or specific microbes as part of the anti-ageing strains either routinely or if possible indefinitely in an active immunisation with passive immunisation involving them creating the antibodies themselves with if possible them breaking down the aggregates such as beta-amyloid into benign compounds such as nutrients for the microbes and host and replacing and tissue with new vigorous ones by detecting them in the body or using CRISPR to allow the body break these down themselves or prevent humans creating these in the first place.Extracellular cross links can be dealt by anti-ageing strains using enzymes and proteins such as MGMT to break them down or again causing the body to create these compounds in response to their presence and even prevent them forming in the first place with any tears repaired by microbes or the engineered host tissue.Compounds and structures that are result of the ageing process in patients prior to treatments will be broken down by anti-ageing strains through them producing enzymes and also other synthetic and natural compounds extrapolated by Paean and created by anabolic and catabolic reactions.Genes from scratch added to patients will prevent them forming in the future.Strains that replace dead tissue and repair ears can repair any damage this does to the arteries,organs and skin.Intracellular aggregates can be broken down by the strain using recombinant DNA from decomposing bacteria to break down lysosome and other wastes to create nutrition for the host and microbes or even using CRISPR to transfer this ability to the hosts cells to produce lyosome when they are detected or prevent these forming in the first place.Scratch DNA can be added to the human genome to prevent the formation of extra cellular and extra cellular aggregates and other compounds etc in the body caused by the ageing process in the first place.Existing dead senescent cells in the body in patients aged 20 or older that are the result of excess mitosis that can harm the patient can have them destroyed by anti-ageing strains using CRISPR treatments that apply suicide genes to them and consume them with stem cell strains injected into the patient replacing them with newer younger cells.Anti-ageing strains can synthesise proteins that destroy the senescenct cells without harming healthy cells with again stem cell strains taking the king their place.Scratch DNA can be added to patients to prevent them forming senescent cells by having all cells when they do die over geological timescales synthesise enough of the relevant proteins to prevent the formation of senescent cells.Stem cell strains can in older patients form new younger cells and tissues in key areas of the body such as arteries,heart and brain.This will be of note to elderly patients aged 70-100 that have lived long enough to avail of them especially those that have been confined to wheelchairs thus allowing key areas of the body such as arteries,heart,brain and muscles in the legs etc to be given new young tissues to keep them alive and improve locomotion.Elderly patients as part of anti-ageing treatments would have them form younger rejuvenated tissues in all parts of the body especially in key areas of the body such as the brain,heart and muscles to improve cognitive,vascular and locomotive functions.This would speed up age reversal treatments and would be key in aiding the CRISPR treatments that reverse the ageing process especially for those who have been left unable to move independently for several years or decades due to their elderly age to regain locomotion.They will be used alongside CRISPR treatments to cure neurological conditions such as pedopheilia,sociopathy and also neurodevelopmental disorders such as Downs Syndrome etc and genetic diseases by forming correct neural and other tissues in the body.Due to extensive damage caused by old age they will by forming younger heart,muscle,neural etc tissues that have levels of phosptidycholines,NAD+ and telomeres on par with a person in their twenties,teens and even infancy will rejuvenate parts of the body to that state with the patients entire genome to compliment CRISPR treatments especially not only for the elderly but for those aged 30-75 so that this adds an extra 20-50 years to their lifespan should CRISPR treatments be not advanced enough.Thus they will be carried out alongside proto CRISPR treatments to replace dead dying skin and tissues with younger rejuvenated tissues on par with those in their early 20s or younger to increase survival rates until CRISPR treatments are perfected.Most elderly patients and indeed most patients aged 30-70 or even older will have these stem cell strains applied to them to key areas of the brain,heart,blood vessels and muscles to keep them alive and improve locomotion alongside anti-ageing treatments in order to aid in recovery as in some cases actual CRISPR treatments to reverse the effects of ageing may not be enough due to extensive damage and thus stem cell treatments should increase their recovery towards mobility.These stem cells once converted into new tissues will house not only the patients DNA to prevent rejection with them also housing endolithic DNA and those relevant to slow down the ageing process.This could be developed much easier than CRISPR treatments since created within hours by 3D DNA printers and this process of the strains converting into new younger tissues all over their body can be repeated over and over again every few decades once one reaches the equivalent of 40-70 to slow down the ageing process forever constantly rejuvenating one’s body to that of their early 20s or early teens until CRISPR treatments using relevant DNA from biologically immortal bacteria can be perfected.Flagellum present will allow these stem cells to travel to parts of the body with the ability to undergoe mitosis from bacteria allowing them to replicate millions of times and create youthful tissues over and over again.Any other newly discovered ageing process can be treated by these sub strains adapted to them through upgrades with ideally the host able to break down and compounds associated with ageing or prevent them being formed in the first place.The role of anti-ageing strains of these microbes inhabiting all tissues in the body would allow them to apply these anti-ageing gene therapies and also compounds to rejuvenate tissue and replacing old ones with new vigorous youthful tissue to every cell in the body with the DNA from extremophiles via their ability to form new tissues with them also detecting and causing specific senescent cells to undergo apoptosis via suicide genes to and replacing them with new healthy ones with the genes from these extremophiles ones or using CRISPR to cause them to commit suicide and be repaired and do any necessary repairs over the coming decades and if need be eventually centuries with this done on demand at first and then in time by base microbes copying DNA or other means detecting the level of Phosphatidylcholines as well as teleomere,mitochondrial DNA and cellular degradation that occurs via base microbes copying DNA strands in certain tissues in all parts of the body and their nanomachines wirelessly sending results to Paean for ageing strains to apply more therapies invivo or through automated procedures though in time the damage should be able to repair itself indefinitely once perfected via advanced gene drive technology and using T.gammatolerans and Bacillus F DNA with the microbes staying their as backup.If possible blood and skin cells can be collected in automated labs using phlebotomy robots that can put these cells under automated machinery to detect the level of senescence of telomers in both the mitochondrial and nuclei DNA, as well as the levels of Phosphatidylcholines but also other biomarkers of senescence that can be uploaded and logged into ones patient file to measure the efficacy of the treatments and need for more of them.Base microbes once advanced will copy DNA from cells around the body and upload them to ones patient file to measure the level of senescence in the telomere and mitochondrial DNA as well as the levels of Phosphatidylcholines and other key components of the cell membranes in each type of cell and tissues in the body ie neural,muscular,skin etc every few years or decades logged into ones patient file with them reading the DNA etc using Cas-9 and taq polymerase and sent by wifi.Biomarkers of cellular degradation such as 8-oxoGsn will be detected by these strains using tweaked C.elegans DNA and thus allowing them to take action to repair them or test kits can be used until they become sufficiently advanced.The microbes other strains will also replace dying and old tissue in arteries,brain,organs and skin overtime with them also passing on the abilities of Bacillus F,Planarians etc via horizontal gene transfer to all tissues in the body to allow this to happen naturally.The mapping of genes and research into all of these unicelluar and multicellular life forms should be done be automated labs and artificial intelligence at once simultaneously in universities and hospitals around the world.Recombinant and scratch DNA programmed to replenish Phosphatidylcholines and NAD+ indefinitely after Phosphatidylcholines and NAD+ levels in the cell walls once they are reverted to levels of infants and DNA from endolithic DNA slowing down miotic damage that affects the state of mitochondrial and telomere DNA,levels in the cell walls and miotic damage caused by mitosis halted to the point that a person ages the equivalent of several months every 10,000 years.Scratch DNA can be developed that reverts the levels of Phosphatidylcholines and NAD+ in the cells back to a infant state every time they undergo mitosis every 10,000 years with DNA from T.gammatolerans,Bacilus F repairing DNA damage everytime the cells undergoe mitosis.Any depletion of Phosphatidylcholines and NAD+ and telomere damage as a result of miotic damage every 10,000 years will be repaired via recombinant DNA and scratch DNA that programs it to replenish both Phosphatidylcholines and NAD+ to a youthful infant state with the DNA repairing mechanisms of Bacillus F,T.gammatolerans DNA added combined with scratch DNA rendering the hayflick limit and cellular degradation defunct as all future DNA degradation will be repaired instantly once reverted to an infant state.This means any ageing and damage caused by it every 10,000 years will be automatically repaired and reversed thus indefinitely halting the ageing process once a persons DNA and cell structure in all tissues is reverted to a youthful state similar to infancy.Scratch DNA can be used to integrate all of these sources of DNA into the patients genome without side effects.
The DNA to exhibit the ability to replenish Phosphatidylcholines and NAD+ will be modified by AI to be better integrated into the human genome due to the fact that it comes from bacteria and not multicellular organisms.This can include adding new scratch DNA to better integrate the genes or use them as a baseline for AI to design better DNA to exhibit this phenotype.The role of having cells have ability to replenish Phosphatidylcholines and NAD+ themselves and not from consuming food in halting the ageing proves is speculative and should be done primarily on mice,biosynths before being applied to humans after initial research extends the human lifespan by decades or years.It may have applications in delaying the growth and spread of tumours to slow their spread and preventing them corrupting the body and killing a patient.This research can be done by AI using automated labs.AI and 3D DNA printers performed primarily by AI such as Urania,Paean and Gaia with zero human labour
Adding relevant genes to humans from T.dohrnii,Nephropidae,Hydra could allow the cells of human patients especially older ones to revert instantly to a younger infant state over and over again on demand or through scratch DNA present.This would reverse any ageing that does occurs every 10,000 years and could also allow patients to create stem cells on a par of their infant state forever indefinitely using scratch DNA.This would mean as the process of ageing is halted then the body is always creating new healthy infant stem cells over and over again forever and would negate the need to add recombinant DNA to replenish phosphotidocholines etc with the stem stem cell strain replenishing a patient with new vigorous tissue every few decades complimenting this.This will be tested on Biosynths modelled in humans that have all aforementioned anti-ageing treatments,some of the treatments in different combinations and others without any treatments.Their role is purely speculative in whether they can reverse ageing eith this done by AI on mice,biosynths modelled on humans etc
Endolithic bacteria:
If possible both extreme oligotrophic and xerophile bacteria as well as Tardigrade that can survive indefinitely on low levels of water and nutrients and in the case of Tardigrade their ability to reduce their metabolism by 99.9% and go almost 30 years without food and water should also be researched and mapped as potential candidates to compliment other extremophiles due to their extreme lack of need for both water and nutrients means they may also aid in cellular regeneration with the Tardigrde DNA modified to survive forever without food and water.Endolith DNA can be added due to their extreme low metabolism since they undergo mitosis once every 10,000 years.This is because dietary restriction has been shown through studies to increase the lifespan of more complex organisms and this phenotype could be applied to humans since they would slow down or negate the effects that metabolism and mitochondrial activity may have on cellular degradation which with further research using scratch DNA theoretically negating this completely since long living Archaea bacteria such as T.gammatolerans dont have the same metabolism through mitochondria like more complex unicellular and multicellular bacteria and organisms that is hypothesised to play a role in cellular degradation.Phanes can modify the oligotrophic,xerophile and Tardigrade DNA to do so without entering tun endospores and thus do so constantly in a living spaces using scratch DNA and forced evolution.This dietary restriction leading to extended lifespans in multi cellular animals proves gene protection as it shows that even in living animals it forces them to develop countermeasures possibly switching off genes,slowing mitosis or even likely slowing down the effects of mitochondrial activity.Genes that slow metabolism including those from endolithic bacteria can be added as well with the endolithic bacteria slow mitotic rate of 10,000 years slowing significantly the rate of ageing by preventing the cells from undergoing mitosis over geological time periods and negate metabolic process that would cause senescence as most cells in humans live for only several months or even a few hours thus a persons cells would live for geological time ie 10,000 years until a new cell replaces again living for 10,000 years in an ever youthful state rather than several hours and months and negate problems associated with miotic damage including senescence such as telomere breakage,depletion of Phosphatidylcholines,errors and mutations that arise from it such as tumours with it also slowing the growth of these significantly from their pre cancerous stage thus giving microbes more time to fight off tumours once other treatments namely the replenishment of Phosphatidylcholinesand telomeres in both mitochondrial and chromosomal DNA is reverted to a younger state equivalent to their early adolescent years and early twenties or even infant years.Metabolic processes contributes to senescence and the ageing process therefore adding DNA from endolithic bacteria that have evolved countermeasures will likely slow down their metabolism thus exhibiting extremely long lifespans to humans by preventing damage to the cells caused by metabolic processes once the genes responsible for this is added to the human genome.Furthermore damage to telomeres,chromosomes and mitochondrial DNA alongside depletion of Phosphatidylcholines,NAD+ etc is usually the result of mitosis that degrades every time ones cells undergoes miotic division and also the effects of metabolism.Therefore endolithic bacteria discovered in 2013 whose mitosis occurs every 10,000 years and have exponentially lower metabolism than humans and who undergoe mitosis exponentially longer than humans will have the genes responsible for this added to the patients genome via CRISPR through anti-ageing strains to slow down mitosis,metabolism exponentially and thus slow down the ageing process by slowing down the effects of metabolism on sencessnce and also slowing down the effects that mitosis has in depletion of phosphtidocholines,NAD+ and telomeres etc exponentially to the point that it occurs once every 10,000 years.Scratch DNA may be needed to prevent a person gaining weight if they eat normal or above normal amounts of food and allow enhanced metabolism wherein one uses up larger amounts of nutrients to stay athletic and does not interfere with the ability of this recombinant DNA ability to halt the effects of ageing.Phanes will arrange scratch DNA to create metabolic countermeasures to ensure a person can consume normal amounts of nutrients and not gain weight or it affect the anti-ageing effects of endolithic DNA.Even though the rate cell division will still occur it will at least be slowed down to the point that it would allow senescence,tumours and breaks to be more easily detected and corrected with telomere and Phosphatidylcholines rejuvenation negating these effects.Ideally endoliths from the ocean floor that exhibit this slow rate of mitosis of undergoing mitosis every 10,0000 years would be used instead of those from Elephantidae,H.glaber,B.mysticetus,B.musculus with those found in other environments that undergo this every few centuries used in place until they can be isolated and used from records.This is because the long metabolic rate and lifespan of these endoliths and in comparison to B.mysticetus,B.musculus etc would slow the ageing process exponentionally longer than these multicellular organisms and the fact that there would be less detrimental side effects from using the fewer genes more easily mapped from endoliths and also have less complicated mechanisms.These bacteria obviously utilise less complicated mechanisms to slow metabolism and thus their ageing process due to having fewer genes and being unicellular organisms compared these multicellular organisms B.mysticetus,B.musculus etc and thus their mechanisms should be easier to integrate into H.sapiens and other complex lifeforms through CRISPR without side effects.Recombinant DNA from these specific species of endolithic bacteria from this 2013 discovery involving the Integrated Ocean Drilling Program will be used as their slow metabolism and slow miotic can halt the ageing process by negating the effect metabolism has on the ageing process as well as negating the effect that mitosis has in the ageing process through depletion of Phosphatidylcholines and telomeres.Those from the ocean floor that do undergo mitosis every 10,000 years should already have samples in laboratories and their genome should be already be mapped and their genomes already present in genetic databases around the world that can be added to computer networks as they have been scrutinised by the Integrated Ocean Drilling Program in 2013 with their estimated age at being at least 100,000,000 years old.As a result of using recombinant DNA from these specific species of these endolithic bacteria discovered in 2013 by the Integrated Ocean Drilling Program a person would thus age the equivalent of several hours to several months once every 10,000 years as this would prevent metabolic as well as telomere and cellular structure degradation associated with mitosis.Normally bacteria live only five days or a few weeks and undergoe mitosis every few hours or minutes with the endolithic bacteria found underwater in 2013 by the Integrated Ocean Drilling Program have been found through studies to be estimated to be 100,000,000 years old and estimated to undergoe mitosis every 10,000 years due to evolving to survive in extreme conditions present in the distant past.Human cells live on average a few months wherein they die and undergoe mitosis that causes degradation in their telomeres and cellular structures alongside metabolism affecting sensensence thus by having DNA from these specific endolithic bacteria will halt the ageing process to the point that a patient ages the equivalent of several months once every 10,000 years with it also slowing down metabolism that affects the ageing process and slow the ageing process to the point that one could go 10,000 years without eating food or drinking water.Some other species of endolithic bacteria already discovered whose genome is mapped also undergo mitosis only once every few hundred years with if they have their genome already mapped then they can be used before DNA from those discovered in 2013 can be mapped and used.Therefore at first if the DNA of endolithic bacteria that undergoe mitosis only every few hundred years is already mapped and stored in databases then they can be still used to be added to patients cells at first to slow the ageing process by several hundred years thus extending an elderly or even younger patients persons lifespan by several centuries long enough to to allow them to avail of CRISPR treatments that rejuvenate the level of Phosphatidylcholines etc to infancy levels and then once the 2013 species of endolithic bacteria’s genome is mapped this can allow for CRISPR treatments to allow DNA from the 2013 species to applied to the patients cells and the genes from bacteria that extend human lifespan by several centuries be removed acting as an intermediary step especially for elderly patients.Elderly patients currently aged aged 70-100 to exponentionally increase survival rates and chances of availing of better treatments from more longer living endolithic bacteria would be fitted with DNA via CRISPR from species of endolithic bacteria that undergoe mitosis only every few hundred years whose genome is already mapped and is stored in genetic databases to slow down the ageing process by several centuries to them give them time to avail of DNA from those that undergoe mitosis every 10,000 years with as stated the DNA from the previous endolithic bacteria removed and replaced instantly with those from the 2013 species.After this or at the same time they will have added to their genome DNA to repair telomere damage,those to replenish Phosphatidylcholines and endolithic.Thus genes from species of endolithic bacteria that undergoe mitosis once every few hundred years whose genome is already mapped and in genomic databases can be used in the first trials for human patients including elderly patients to slow the ageing process by several hundred years thus extending the human lifespan by several hundred years with this sufficing until the 2013 species is available to be added to one’s genome.Scratch DNA can be also be extrapolated by AI to halt the ageing process by several decades or centuries or thousands of years.This -alongside having humans synthesise essential amino acids and other nutrients would also reduce the amount water and nutrients the patient needs limiting strains on the Earths resources with the organisms with the lowest levels required will be used with scratch DNA pushing this even further.Turning off or removing the fat insulin receptor gene and others related to caloric restriction via CRISPR can be used to further play a role in this and prevent heart disease and diabetes as well as compliment oligotrophic DNA with the CRISPR process also used to remove genes responsible for ageing and replace these with those from these extremophiles negating their effects.If possible junk DNA and those responsible for ageing can be removed by them as well if not causing damage to hold extra DNA including augmentations.The slow degradation and thus slow rate of ageing would be the result of slow miotic rates every 10,000 years from endolithic bacteria DNA added to the human genome preventing damage caused by metabolism and degradation of telomeres in the mitochondrial and cellular telomeres that leads normally leads to ageing caused by mitosis and thus the hayflick limit.This slowing down of metabolic processes that damage DNA and cells,this being repaired by bacteria that exhibit self repair of the DNA,slow miotic rates preventing cellular degradation of Phosphatidylcholines and them rejuvenated constantly and also repair and protection of damage from metabolic processes in each cell will thus halt the ageing process every 10,000 years coupled with aerorolerant DNA that protects DNA from reactive oxygen and free radicle caused by respiration.It would also slow down metabolism in a cell negating effects caused by mitochondrial process alongside those from Tardigrade,oligotrophs and xerophiles.Patients will at the same time have their DNA and levels of Phosphatidylcholines and NAD+ reverted back to their infant state to thus be kept at a youthful state using recombinant and scratch DNA.The damage to telomeres in both the nucleous and also mitochondrial DNA alongside the depletion of Phosphatidylcholines in the cell membranes is the result not only of metabolic processes but also the process of mitosis and miotic division of cells in the body as explained in how different parts of the body age at different rates as denoted by the fact that they undergo mitosis to replace dead cells at different rates than each other as shown by the hayflick limit and that each time a cell undergoes mitosis they undergo senescence where the levels of phosptidycholines etc in the cells outer membranes and NAD+ synthesised by them deplete and also the teleomeres in chromosomes and mitochondrial DNA degrade as shown by the fact the levels of these compounds and the length of telomeres is at its highest levels at infancy and by ones 90s they have reduced by 90% and the levels of these are at varying levels throughout ones lifetime with this different for different types of cells.Endolithic bacteria DNA that gives them their reduced metabolism and reduced rate of mitosis will once added to a patients genome via anti-ageing strains through CRISPR will slow down the ageing process by this rate that is they will age the equivalent of several months every 10,000 years as it will slow down the rate of metabolism and also slow down the rate of mitosis of cells in the body thus slowing down the rate of telemore damage and depletion of NAD+ and Phosphatidylcholines by this rate because metabolism and mitosis of cells play a key role in the ageing process that depletes Phosphatidylcholines and NAD+ and cause the telomeres in a patients cells to degrade over time.Everytime a cell undergoes mitosis and is replaced by another one the levels of Phosphatidylcholines,NAD+ depletes and the telomeres in ones genome degrades also becoming shorter.At infancy ones telomeres are at their most in damaged state and levels of Phosphatidylcholines are at their peak.But as a a person ages the levels of .Phosphatidylcholines and NAD+ deplete gradually and their telomere chromosomal and mitochondrial DNA also begins to degrade and frayed by becoming unwound due to cells undergoing mitosis and dying off until by the time one is their 90s etc the levels of Phosphatidylcholines and NAD+ have depleted by 90% meaning only 10% of their levels are present with by this point ones telomeres are frayed to their limits known as the hayflick limit.This is likely because the process of mitosis that occurs every 24 hours to several months unlike meiosis from creating copies of each strand of DNA and cell causes degradation as the new copied cells don’t share genetic material through meiosi.An analogy would be how when one recorded audio/visual material onto old VHS/VCR tapes the first recording was of perfect quality with when a person recorded new material onto the same tape over and over again the quality of the material becomes degraded overtime to the point that it is unrecognisable and becomes incomprehensible garbage.The same process occurs with animal including human cells as they undergoe mitosis in the body they become degraded overtime thus leading to them become more degraded with both levels of Phosphatidylcholines and ones length of telomeres lowering everytime they undergoing mitosis exhibiting itself in the ageing process in animals including humans wherein the body and its various organs etc wear down gradually thus exhibiting in poor limited locomotion,greying of the skin and hair and also eventual death from strokes,heart failure,alzheimers etc and other age releated diseases with the different rates of ageing of different species of animals leading to them exhibiting different lengths of lifespans explaining why some species of animals live longer or shorter than others and why some become elderly much quicker with this present in prokaryotic bacteria that have different evolutionary strategies to counteract telomere and phosptidocholine degradation such as the ability to be more easily adapt to environmental conditions to keep the levels of Phosphatidylcholines and NAD+ consistent throughout their multiplication with the fact that they have chromosomes forming loops of DNA alongside ribosomes instead of the linear chromosomes in eukaryotic cells including humans etc that are more prone to degradation may be a factor as to why they are able to not suffer the same level of degradation of DNA during mitosis with them still dying due to degradation caused by metabolism and the parent bacteria degrading by mitosis with endolithic bacteria prevented from undergoing chromosomal damage due to their extremely slow miotic rates and extremely slow metabolism.Furthermore metabolic processes play a role in the ageing process by depleting these compounds and damaging telomeres.Therefore biologically immortal and long living endolith bacteria and animals such as T.dohrnii,Nephrodae will have genes added by CRISPR.Therefore by adding the genes to a patient from endolithic bacteria responsible for their slow metabolism and slow mitosis rates of once every 10,000 years via gene therapy and horizontal gene therapy by anti- ageing strains via CRISPR will slow down the ageing process to the point one ages several months once every 10,000 years.This will be added to all patients both younger ones and elderly patients aged 20-90 years old first to slow down the ageing process exponentially and allow treatments to reverse the ageing process to be added.Since different cells in the body age at different rates due to them undergoing mitosis are different rates ie some undergoe mitosis and thus age every few hours while other undergoe mitosis and thus age every few months to make this delayed ageing more balanced all cells in the human body could be engineered to age at the same rate as each other by using DNA from other cell types with research done into which type of cells age the slowest,finding the genes that cause them to age the slowest will be determined by Phanes comparing their DNA to that of all cell types then having this DNA replace the other DNA similar to it in all other cell.This will be done so that once endolithic DNA and DNA repairing DNA is added to the tissues all tissues and cells in the body will age at the same rate once every 10,000 years.Studies of this will be done after older patients receive the first treatments to halt and reverse the ageing process to determine the rate that each type of cell and tissues age using tissue samples derived from younger patients,biosynths etc.These endolithic and DNA repairing DNA from T.gammatolerans will be added to the tissues especially heart,brain and key organ tissues of elderly patients aged 65 years or older to first to slow down the ageing process thus exponentially increasing their survival rates to avail of treatments to have their tissues cellular structures rejuvenated to an infant state.Thus a person could have all cellular structures and DNA in all cells and tissues in their body be reverted to a youthful state of early to late teens or even infant stage and the ageing process could be halted to the point that a person would age the equivalent of only several months once every 10,000 years with any damage repaired by the self repairing qualities of other extremophiles with this endolithic,oligotrophic DNA would allow one to eat as much as you wanted and still negate senescence associated with mitochondrial processes brought on by the metabolism of nutrients.The DNA of the cells would be programmed via scratch DNA to repair DNA and to replenish Phosphatidylcholines and NAD+ automatically returned to that of their infant state every time it undergos mitosis every 10,000 years via DNA from scratch with DNA from Bacillus F,T.gammatolerans repairing telomere damage every time this happens thus rendering the hayflick limit and depletion of Phosphatidylcholines and NAD+ redundant thus meaning any effects of ageing that occurs every 10,000 years will be automatically repaired and cells constantly reverted to an infant state thus effectively halting the ageing process forever.Research will be done if the delayed miotic rates and thus delayed ageing can be extended exponentially with the DNA responsible for delayed metabolism etc in endolithic bacteria can be modified so that it undergoes mitosis much longer by as much as 10 – 1,000,000 times meaning a person could age the equivalent of several months once every 100,000 or even 10,000,000,000 years.The theoretical limits of this will be researched and these new genes extrapolated by Phanes etc analysing the genes responsible for this and creating new ones from scratch and forced evolution.
The DNA to exhibit slowed metabolism and mitosis will be modified by AI to be better integrated into the human genome due to the fact that it comes from bacteria and not multicellular organisms.This can include adding new scratch DNA to better integrate the genes or use them as a baseline for AI to design better DNA to exhibit this phenotype.The role of having cells have delayed mitosis once every 10,000 years in halting the ageing proves is speculative and should be done primarily on mice,biosynths before being applied to humans after initial research extends the human lifespan by decades or years.It may have applications in delaying the growth and spread of tumours to slow their spread and preventing them corrupting the body and killing a patient.This research can be done by AI using automated labs.AI and 3D DNA printers performed primarily by AI such as Urania,Paean and Gaia with zero human labour
Genetic disease strains:
Muscular and neurological degenerative diseases especially genetically predisposed ones such as Parkinsons,Alzheimers etc could be treated by these microbes creating new cells and tissues in their place,using horizontal gene transfer to transfer CRISPR treatments into pre existing and newly formed tissue and relevant cells throughout the body that would correct mutations thus correcting the pre existing flaws.This could be done to treat genetic diseases that have multiple symptoms ie Cystic Fibrosis with the microbes fixing genetic flaws via horizontal gene transfer using CRISPR treatments while treating the symptoms by forming new tissues,soaking up and breaking down compounds that symptomatic and the cause of the disease into nutrients or benign compounds that can be flushed out of the body.Autoimmune diseases such as lupus and rheumatoid arthritis can be treated via CRISPR and them treating both the hosts genome and that of the leukocytes with the relevant DNA and in the case of allergies again these can be treated by CRISPR and also these creating anti-histamines on the spot relevant to a persons individual allergy.Autoimmune diseases can be controlled by them producing chemicals that stop the immune system attacking the hosts body,shut them down entirely while carrying out the main functions of them while they correct the genetic flaws via CRISPR treatments.Progeria can be treated by using both CRISPR treatments to treat its mutations alongside creating new tissue and applying anti-ageing treatments to extend the lifespan of the patient applied early on during early childhood.Those suffering from dwarfism can have genes added to the human population to remove it from the genepool.In living patients of dwarfism organs,neural systems and the skeleton would be if this possible grown by microbes forming new tissue and structures layer by layer alongside the production of hormones by the microbes or body through correcting the mutations of fibroblast growth factor 3 gene in the case of anchondroplasia,correcting genes associated with growth hormone deficiency and turning this off when they reach average height with other causes of this corrected by CRISPR and hormone production and genes added to increase ones size to normal size.Thus a combination of CRISPR,microbes producing hormones and stem cells increasing the size of organs and limbs could allow sufferers of it to reach normal average height of unafflicted patients.This would have to be tested on chimpanzees and also rats purposefully bred using CRISPR to develop these prior to humans tested with them having human and patient specific DNA also in them.Those who are very tall and have weak hearts as a result can be given bioprinted ones with them given suitably sized ones with stronger tissue from bioprinting with them engineered to survive heart failure ie using carbon dioxide as an energy acceptor and can through CRISPR and stem cell strains causing tissues to undergone apoptosis and form new tissues could have their body size shrunk to normal heights again tested on chimpanzees.Klinefelter syndrome can have the extra X-chromosome inactivated in each cell and genes added that prevent them forming in future miotic division with the CRISPR treatments also correcting the symptoms individually ie ensuring testosterone levels are normal,cure sterility and remove any breasts with breasts removed via tissues undergoing apoptosis and surgery.Turners syndrome can be cured not just by CRISPR initiating the formation of a second X chromosome but also have conditions like pterygium colli deformity be corrected via stem cell surgery and microbes forming new internal tissues and also causing some to undergo apoptosis and moult off via DNA added to the patients genome from Serpentes DNA controlled by AI,bioprinted organs and thus allow the patient to live normal lives.Prager-Willi syndrome will have the extra or missing chromosome 15 from either parent added or removed in all cells depending on the case determined by genetic tests with the other cases have deleted genes added by CRISPR with deformities etc corrected by microbes.Those that are the result of extra chromosomes will have the extra one edited out of all cells and future miotic division by added specific genes to the other chromosomes that prevents the formation of the extra chromosome in each cell with those due to their being a lack of a chromosome will have them initiated in all cells via adding genes that ensures they are formed with this made percent via advanced gene drive technology.Cyclopia and those that resort in stillborns and early deaths after birth can be corrected invivo by base microbes scanning the DNA of early fetuses and embryos and adding genes to correct them via gene therapy and upgrades.It may also counteracted from occurring in the first place by adding the DNA repair genes from anti-ageing strains that prevents the formation of the necessary mutations.Mutations caused by the fetus being exposed to chemical,physical and DNA damage would be repaired instantly by recombinant DNA from T.gammatolerans,A.mexicanum etc added to the mothers DNA passed onto the child and also those that make them immune to the toxins that produce these including teratogens.Those that arise from incest and inbreeding will also be cured this way.The DNA repairing genes will also be added to all patients worldwide to not only prevent ageing but also prevent genetic defects associated with incest and inbreeding with this of note to certain groups such as the Amish who are at risk of this with it also applied to pets such as C.l.familiaris and F.catus.This alongside the use of 3D printed DNA using the Phanes method would prevent genetic bottlenecking onboard of space stations,interstellar vehicles and even colonies in the distant future and also with C.l.familiaris,F.catus.Living patients affected by chemicals with mutations and birth defects can be cured by CRISPR treatments to remove faulty genes and also even initiate formation of proper body parts and microbes invivo cosmetic surgery.Incest and inbreeding based conditions will have CRISPR treatments to correct deformities and also even apply the Phanes method to the patient genome in all cells by making subtle alterations to their DNA to make them subtley different.Thus in both living animals and humans such as populations where inbreeding and genetic bottlenecking occurs once CRISPR cures deformities the living patient Phanes method can be applied to living patients where the genome of the patient in loci and codons that determine the persons uniques genome can be altered to the point in all cells and tissues or just in the tests and ovaries via CRISPR to make the genome subtly different enough that they are are a completely different individual from what they previoulsy were and different enough from siblings and parent that they can interbreed with the original siblings,cousins etc and still produce healthy viable offspring that will have individual genotypes to allow for genetic diversity to be created that they will although will be genealogically releated to each other ie can be called their daughter,brother and cousin will not be genetically releated to each other and in fact will be distantly releated from each other enough meaning all future progeny will be genetically distinct enough to ensure that all future breeding between them will eliminate genetic bottlenecking and genetic degradation from inbreeding.This will be applied to all breeds of C.l.familiaris,F.catus, endangered animals and also populations of humans where inbreeding can occur such as the Amish and those in space stations etc.The DNA repair mechanisms of Bacillus F,T.gammatolerans etc will able to prevent any future damage with patient files of both animals and humans that have inbreeding occur at present and the future can allow for CRISPR treatments to be applied and application of the Phanes method to living individuals.Chimpanzees with human recombinant DNA and those with even the patients own DNA can be used bred to test treatments for each individual type of genetic disorders starting as early 2024.3D DNA printing will create the spermatozoa and eggs with these phenotypes and the patients unique DNA from patient files to cut down on costs.Diabetes could be treated by removing the fat insulin receptor gene and also genes associated with it in living patients with those that are caused with obesity in living patients treated by microbes creating insulin when needed in response to sugar levels or at set times of the day while weight loss can correct the root cause including genes added or removed via CRISPR to allow the body to create the required levels of insulin to counteract the amount of sugar intaken.Type 1 diabetes will be treated by CRISPR treatments and beta cells created by stem cell strains.Those who have diabetes such as type 2 diabetes that is a cause of obesity and not genetics can through weight loss via removing the fat insulin receptor gene with them and those that it is caused by genetics will also be given genes by the strain to treat gene faults that cause it to allow them to recreate the required level of insulin created by microbes.Microbes can be added to the patient that creates the hormone in required amounts in response to sugar in the bloodstream or on demand at set times of the day by AI and also break down excess sugar when needed to prevent the need for injections and thus prevent patients forgetting to take it or not be able to take or order in vials all year round as the microbes will create the hormone when needed each day.Otherwise insulin can be created by bacteria/human cell hybrids or microbes on an unlimited scale in hospitals,ordered in from Telesphorus factories.This can be ordered in from Telesphorus factories in batches created by bacteria with the patients specific DNA and stored in fridges for free since patient specific insulin using their DNA would be produced and AI would manage the factories.Binding proteins that keep it stable in fridges could be present to keep it useable forever with these designed to break down in the body.The same can be replicated with similar hormones and diseases caused by genetics or lifestyle choice and poor nutrition and also obesity as well as those aggravated by prescriptions for other genetic based diseases with epinephrine and other hormones of medicinal value which can be created by microbes by relevant recombinant DNA when needed,created by anabolic and catabolic reactions and grown on an unlimited scale at home,in hospitals and Telesphorus factories.Epinephrine and adrenaline can be created on demand by them in certain patients who require them again for free using recombinant DNA changed instantly in base microbes and created on demand via biosynth WiFi with Wifi causing upgrades to the microbes causing them to house DNA that can allow them to create adrenaline and epinephrine on demand vis biosynth wifi and them also ordered in from Telesphorus factories in batches created by bacteria.Crohn’s disease will be cured via CRISPR treating autoimmune syndromes and defects that lead to it directly and also immunising the patient from M.paratuberculosis.Those that have predispositions to cancers will also be inoculated with anti-cancer strains by 2025 alongside gene therapy to remove the relevant genes and as stated scheduled for routine check ups immediately by 2023/2024 every few months or once a year with these done at different hospitals to alleviate strains with proto AI scheduling these to make them happen.If they develop cancer before 2025 then they will have modified Car-T immunotherapy that utilises Polybia-MP1,TsAP-1 and melittin to treat them by 2024.Thus those with genetic predispositions to cancer will have routine check ups on the entire body subsidised by the government with them also given modified Car-T immunotherapy treatments to treat discovered tumours and then anti-cancer strains and then once it becomes availible CRISPR treatments will be applied that remove generic mutations releated to cancer.Those that have already had hysterectomies,mastectomies etc to remove their chances of getting the cancers will be scheduled for trials of stem cell strains that alongside CRISPR treatments will initiate their reformation regrowing them after they have CRISPR remove the relevant genes that cause cancers from their body by 2029.Other adults should still continue to get frequent prostrate and cervical etc examinations and avoid carcinogens until when they can be inoculated with anti-cancer strains with those with the predisposition to cancers having precedence.CRISPR can be used to correct GERD,make the oesophagus immune to acids via adding recombinant DNA from acidophiles to the oesophagus and create proper flaps in the stomach.The accelerated healing phenotype will heal any scarring that occurs.Those that leave one with deformities will have CRISPR treatments to correct mutations and also initiate the formation of proper body and neural structures with micrboes ability to form tissues such as skin,muscle,nervous tissues invivo and surgery with AI able to by 2029 extrapolate the best method of dong so with VR and holographic technology allowing for a version of the patient with and without the mutations to be analysed and built towards using these methods.Patient files once set up will give patients knowledge that they have specific genetic diseases that will schedule them for routine check ups,subsidised medicines until CRISPR treatments become availible that then correct the genetic mutation in each and every cell in the body to thus cure patients of the disease.Patient files will by 2023/2024 allow for all patients with each specific genetic based condition to be determined globally and thus schedule them for routine tests and then medication subsidised before money becomes obsolete and them scheduled for human trials between 2025-2029.Thus genetic diseases of all types in all living patients such as parkinsons,genetically predisposed cancers,asthma,tourette syndrome,ceoaliacs disease,obsessive–compulsive disorder,heart defects,alzheimers,maniac depression,cystic fibrosis,autoimmune disorders,Crohn’s disease,allergies of all types including those to medications and dust mites/cat dander/bee stings etc,addictions of all types,genetically derived diabetes,incest borne diseases,social anxiety disorders,bipolar disorder,epilepsy,adrenoleukodystrophy,congenital heart etc defects,haemophilia,sudden arrhythmic death syndrome and even heart murmurs,congenital heart defects,chronic inflammatory demyelinating polyneuropathy,amyotrophic lateral sclerosis,multiple sclerosis,mitochondrial diseases etc would thus be cured by them treating the symptoms by first creating new tissues in place of affected or degenerated ones,create natural and synthetic compounds from plants/animals and catabolic and anbolic reactions to treat it,breaking down compounds and plaques that cause it to treat them and then to finally cure them fully it will use CRISPR treatments to fix the genetic flaws that caused it to begin in the first place both in new and all existing cells in the body with this applying both to infants and adults suffering from the conditions.Living patients suffering from them will be treated by CRISPR treatments to cure them via adding and removing genes to both the telomere and mitochondrial DNA in all cells available by 2029 with those who are infants,teens and adults who have the genes responsible for them will have gene therapy by this point remove the genes responsible and thus prevent it occurring in them at all also by 2029.This use of CRISPR treatments by genetic disease stains will thus effectively cure all patients of these conditions forever with the other treatments done prior to this and during this to alleviate symptoms.These will be applied to both telomere and mitochondrial DNA in all cells using advanced gene drive technology to pass corrections to the next generation of cells with this and germline therapy applied to testes and ovaries to ensure spermatazoa and eggs carry these corrections prevent the conditions passing down to the next generation of offspring.Adding genes from T.gammatolerans to all patients worldwide will wipe all genetic diseases from the human gene pool forever via advanced gene drive technology with it also wiping all forms of cancer from the human gene pool as this bacteria’s telomeres repair mechanisms will prevent the formation of random breaks from occuring that allow the diseases to form.All of these treatments and specific DNA from DNA repairing bacteria as part of ageing treatments will eliminate all genetic diseases from the family line with by having this DNA repairing DNA added to all patients worldwide as part of ageing treatments will eliminate all genetic diseases from the human genepool forever if advanced gene drive technology is utilised by preventing the necessary mutations that lead to them from happening in the first place.Specific strains will be made to deal with the curing of genetic disease via CRISPR treatments with the DNA for the application to all the cells in the body will be housed in ribosomes and in particular plasmids that will be recreated over and over again via taq polymerase and Cas-9 to be reused over and over again with millions of microbes applying the DNA to all cells in the body at once until all cells are treated.The genes for these will be applied either by horizontal gene transfer and also bumpers acting as a mini vector.All cells in the body will be treated with these CRISPR treatments with advanced gene drive technology to ensure they pass from one generation of cells to the next with germ line technology ensuring the corrections pass to the next generation.Stem cell strains will be applied to degenerated tissues replacing them with new rejuvenated ones in the case of multiple sclerosis and adrenoleukodystrophy,parkinsons and alzheimers to cure,repair and cure existing neural and muscular damage in patients while CRISPR treatments are applied.The patient files system that have the genome of each patient will be used to track down all living patients with proto and final Epione searching the billions of patient files for all types of these in fragmented form by scanning for the relevant genes will put them into separate subsystems divided by each country allowing them to be put on waiting lines based on the severity of the diseases with for example cancers and those that are fatal alongside those in the elderly treated first and scheduled first for routine check ups and scheduled first for human trials by at least 2025.The setting up of patient files in 2023/2024 will already allow those already suffering the effects of them and those diagnosed with the most fatal ones,those that predispose them towards sociopathy,psychopathic,schizophrenia etc and also cancers will automatically be signed up for human trials in 2025 with them set up to be prescribed for medication for them and in the case of cancers scheduled for routine check ups as soon as possible even for pre-teens and teens with HPV vaccines done for other non genetically predisposed groups.Patients with genetic predispositions to schizophrenia,sociopathy,paedophilia and psychopathy as well as even maniac depression will be instantly refereed to Iaso or its proto versions and will be possibly monitored discreetly by law enforcement until cured in human trials in 2025.If need be they may be admitted into special heavily guarded psychiatric facilities for their and societies safety as early as 2023/2024 until trials begin in 2025 and still refereed to Iaso with this even applying to pre teens.Those already suffering the diseases ie those that have symptoms of parkinsons,haemophilia,chronic inflammatory demyelinating polyneuropathy,motor neurone disease,multiple sclerosis etc will also be treated in 2025 and will have pigs,mice,cattle and chimpanzees born with their DNA in them to test the effectiveness of gene therapy before their trials begin as early as 2025.They will also have all medication subsidised by the government.The patient file system will allow all patients worldwide both suffering and predisposed to them will be tracked down and scheduled for treatments the second they become available with those suffering them treated first and then those who are younger carriers of the genes responsible treated to remove the genes responsible.Advanced gene drive technology would prevent these from being passed to the next generation.This can be applied to infants once genetic screening has found any diseases decades before they are formed with their being a strain solely for treating genetic diseases including neurological and developmental disorders.Genetic diseases of all types will be bred into chimpanzees with human recombinant DNA to test the effectiveness of gene therapy on them including mitchondrial diseases such as mitochondrial DNA depletion syndrome,mitochondrial myopathies.Genes would come from scratch as well as from populations of humans that have the genes and would be placed in all cells in the body.Germline therapy will be utilised to prevent all genetic diseases passing onto the next generation using advanced gene drive technology and thus if utilised by all sufferers will prevent the disease passing onto the next generation and thus removed from the genepool of H.sapiens indefinitely.Adding specific genes to both sufferers and non sufferers of genetic diseases could prevent all of them ever occurring again via advanced gene drive technology.Certain genes made from scratch and/or those from other animals to whom never suffer these mutations,exhibit DNA repair including Archaea.Certain genes made from scratch and/or those from other animals to whom never suffer these mutations,exhibit DNA repair including Archaea
such as T.gammatolerans,Bacillus F,D.radiodurans extremophiles that exhibit DNA repair both unicellular and multicellular and homogulous recombination from embryonic stem cells and also certain bacteria could also be added to the genepool of all living patients worldwides via germline therapy and advanced gene drive technology in all patients worldwide to make it impossible for the relevant random mutations that lead to any genetic diseases from occurring at all ever again in the human genepool thus eliminating these from the human genepool indefinitely.The same extremophile bacteria DNA used to reverse and halt the effects of ageing will possibly prevent them being passed onto future generations by repairing mutations that cause these.Those that result from specific genes from the parents will have the parents and any siblings treated with CRISPR to remove any genes that can be passed onto any future children using advanced gene drives.Thus a combination of stem cell strain treatments and CRISPR treatments will be able to cure patients afflicted by any type of genetic disease.
Stem Cell Strains:
One of the most important strains would be the stem cell strain those that are able to form new tissues internally in the body.This strain being able to change into any tissue in the body would as detailed replace dying and old tissues in the body with rejuvenated ones,change neural tissues to treat Alzheimer’s/pedopheilia/developmental disorders by creating normal neural tissues,change neural tissues to that of homosexuals/bisexuals/heterosexuals/Aspergers,repair existing wounds and ruptures in the internal body and neural system,fully develop the brain of teenagers and pre teens,carry out internal and external cosmetic surgery.This strain would have DNA from E.coli to house flagellum to travel across the body,bacteria DNA to undergo mitosis controlled by Paean and also DNA from human and animal totipotent,induced pluripotent and embroyonic stem cell cells from humans and DNA of the patient as well as that from Hydra,A.mexicanum,T.dohrnii,Planarians that express stem cells to allow them under direction of Paean change into any cell or tissue in the human body.The strain would have DNA for flagellum and undergoing mitosis from bacteria and DNA for biosynth WiFi etc to allow it be directed by Paean to undergoe mass replication and travel to the desired site and through biosynth wifi he will tell them to undergoe mass replication and then form a biofilm and then through biosynth WiFi have the genes in them to undergo evolution by inducing their evolutionary path towards the desired cell or tissue type formed layer by layer ie muscle,skin,blood vessel tissues and cells that contain the patient DNA to prevent rejection and genome alongside extremophile,anti-ageing treatments and DNA to never age and survive extreme conditions.Biosynth wifi will induce their evolutionary path to form any desired cell and tissue type in the body such as muscle,skin,bone etc on demand allowing them to form these in vivo.The WiFi through induction of evolution will remove all foreign DNA including bacterial DNA responsible for mitosis and flagellum,biosynth WiFi DNA and that which would cause allergic reactions.The anti-ageing treatments could also have this also apply to key organs such as the heart,liver etc with these other organs also replaced by using bio-printed version which again through CRISPR treatments done on them replaced regularly to ensure one has organs constantly in a youthful state again in terms of vigour,strength, replaced every few decades with them replacing dying tissue with new ones or them replaced by bio-printed ones.These would also pass on CRISPR treatments to correct the mutations that cause these neuromuscular degenerative disorders such as Parkinsons,Alzheimers and ageing in the first place and also ageing into relevant tissues and cells.CRISPR treatments may also be used in gender reassignment allowing one to produce the correct sex hormones ie testosterone and oestrogen and produce the desired sex organs etc by altering the sex chromosome to the desired gender perfecting this with this process in time even reversible it could even allow one to change races by altering skin tone again reversible with microbes and CRISPR treatments forming cliteroi,wombs and penises in vivo with the phenotype of Serpentes moulting skin,microbes forming tissues layer by layer and causing others to undergo apoptosis can create and remove breasts.If perfected it would render conventional gender reassignment surgery obsolete.Furthermore they would compliment and alleviate the accelerated healing phenotype of humans from A.mexicanum etc recombinant DNA before it can be almost instantaneous with it able to form any tissue invio to repair perforations including damaged vessels and bones as well as even form blood,erythrocytes and would also be the strain that forms neural implants,worm implants,GPS implants etc in vivo in the body.In those confined to wheelchair from spinal injuries it would repair damaged neural and muscular tissue at the point of injury and also below it thus giving the ability of self propelled movement back to the patient thus curing them of paralysis with it also repairing bone tissue etc in astronauts preventing bone atrophy.It would play a role in forming breast tissue and wombs and even ovaries and testes in those already having them removed alongside CRISPR treatments to initiate correct shape as well as formation and would also increase breast and penis size alongside butt size replacing conventional cosmetic surgery of all types alongside CRISPR.Thus those who have testicles,wombs,breasts and other organs removed to prevent or remove tumourgensis can via CRISPR used to initiate their redevelopment alongside this strain forming them invivo layer by layer controlled by Paean have them regrown from scratch to the point as if they were never removed in the first place.If possible even jaws could be formed invivo via CRISPR and also bone and skin etc tissue formed layer by layer or created invitro and then inserted into the skull with stem cells forming connective bone tissue alongside screws made of bone tissue as well.Those with amputated limbs would have synthetic ones created by using an organic scaffolding that have invitro flesh and microbes form muscles and nerves etc and even skin grafted onto them with the limbs using microbes form new tissues form these over the original place the limb was with CRISPR also initiating the formation of new limbs.In those with developmental disorders and those who have undergone facial reconstruction surgery that have left one with facial and skull deformities it could alongside causing unwanted tissue to undergo apoptosis and also DNA from Serpentes added to the patients genome causing some to peel off would allow the skull and face to be reshaped invivo alongside in some cases surgery to create a more natural or original shaped face controlled by Paean with it also replacing rhinoplasty surgery.This can include reshaping the cheeks,forehead,replace lips,replace noses.Butt and breast surgeries and other cosmetic surgeries on the face and other parts of the body could be replaced by these programmed by Paean providing a more natural shape using these methods invivo with those having existing botched cosmetic surgeries and also face lifts as well as botulism injection repaired by this and those who already have breast implants can have them removed and them replaced by tissues formed layer by layer.Damage to the vocal cords or brain already done in existing patients undergone surgeries would be repaired by them reforming tissues and causing the parts of them to undergo apoptosis and new tissues formed in a controlled manner.This could potentially even eliminate most internal surgeries alongside the accelerated healing phenotypes.All facets of the cosmetic surgery could be done invivo by microbes building bone,skin,neural,muscle tissue layer by layer,causing some to undergo apoptosis as well as causing the outer layers of skin to moult off via Serpentes DNA.Even bone tissue could be altered by having tissues undergoing apoptosis and more grown layer by layer like neural and muscle tissue.This can include rhinoplasties,butt and breast enlargement and reduction surgeries those to correct deformities and reconstructive surgery all controlled by Paean and allow the patient to have it done overtime say a few weeks to months while they are awake or asleep at home or on holidays.Using carbon dioxide as an energy acceptor will negate issues of suffocation with the noses interior and mouth left open from this and them initiated while the patient is awake.Although it may take longer it would at least be a more natural shape and would be less likely to suffer from complications,would less likely to cause death since regulated and carried out Paean and could be more easily reversed by Paean invivo with advances allowing it to be sped up to a day or a week via the stem cell strain undergoing mass replication to create billions of copies with any remaining minor surgery corrected or finished off by surgery or vice versa.It could utilising CRISPR treatments initiate the formation of breasts,ovaries and wombs alongside forming tissues invivo to replace those already removed to treat and prevent cancers.Skin grafts etc from burns and acids wold be replaced by them replacing damaged tissue and the outer layers moulted off making for a more natural appearance with.Changing the sex chromosomes via CRISPR can allow for proper breasts to be formed or removed via apoptosis rather than surgery with cliteroi,wombs and penises etc formed invivo and also layer by layer and CRISPR treatments allowing for male to female and female to male transformations to be more successful using both CRISPR to change the sex chromosome from XX to XY or vice versa in all cells in the body and this through gene drive technology transferred to all future cells and also invivo cosmetic surgery coupled with CRISPR treatments initiating the creation of more naturally shaped body features with existing patients who have undergone these operations having their sex chromosome changed and have proper sex organs and breasts etc changed with the processes first tested on chimpanzees.Testosrone and oestrogen would be produced by changing the sex chromosome and adding other genes to initiate the body to produce it.Breasts would be once initiated by CRISPR treatments after changing the sex chromosome and then built layer by layer by stem cells or reduced via having each layer undergone apoptosis with the same done to wombs,penises etc.Surgery and even bioprinted penis,testes and cliteroi created outside of the body by stem cell strains fed blood will also be investigated with them attached similar to lab grown digits and limbs.Testes and penises etc can be grown on a scaffolding that can the be attached similar to lab grown digits and limbs.Otherwise penises would after CRISPR treatments be grown layer by layer.5α-Reductase deficiency can be corrected by allowing the gene mutation to be corrected and the person choose which gender they wish by adding specific genes to the sex chromosome to initiate the formation of proper sex organs and hormones as well as initiate the formation of breasts,penises etc alongside the microbes doing so.This process could theoretically be reversible unlike existing operations in both intersex corrections and gender reassignment.This will also be replicated with those born with intersex disorders by having the body and microbes create the correct hormones correct mutations as well synthesise ovaries,cliterous,wombs,penis and testes etc in vivo or in vitro from scratch via bioprinting using its ability to produce new tissues or stimulate hormones and add correct the male or female genes in the 23rd chromosomes via CRISPR to initiate the production of these sex organs and hormones once the wrong sex organs are surgically removed or the microbes causing them to undergo apoptosis or in the case of cliteroi being reshaped by them in vivo and this allow for gender reassignment negating surgery with in the case of females ovaries removed or synthesised.Those who have no nerve endings due to surgery in the cliterous will have new highly sensitive tissues created by microbes and CRISPR.Ovaries,tested,wombs etc could be synthesised later by later or destroyed by having tissues undergo apoptosis.This could replace conventional gender reassignment surgery and could be reversible again those who regret gender reassignment surgery by reversing each step with Paean arranging both operations for each patient.Otherwise one simply could have their transgendered brain changed by CRISPR to that of the body they were born with.Those who have already had their tubule ligations and vas deferans snipped through vasectomies can be corrected via them causing tissues to undergo apoptosis and forming new tissues for reversing tubal litigation with blocked falliopian tubes have tissues undergoe apoptosis and repairs made with clipped tubes have them repaired back to their previous state and for vasectomies causing knots to undergoe apoptosis alongside new tissues formed to repair clipped seminal vesicles etc reversing the damage done and restoration of the womb and testicles to their pristine state with future preventing measures to make one sterile dealt with CRISPR turning certain genes associated with fertility on/off.Stem cell strains will be used to reverse existing measures to induce sterility in both humans and animals.Pets that have been neutered will have testes recreated from scratch through them and humans who have had ovaries and testicles removed to treat cancers etc will have them formed layer by layer making one fertile again.Inhospitable wombs can be using CRISPR and stem cell strains made hospitable again with damaged tested repaired in the same way.Sterility caused by genetic factors can be cured by CRISPR.Damage to the cliterous in intersex patients would be repaired via creating new sensitive tissues with future intersex patients have the use of CRISPR and invivo cosmetic surgery applied to them which could be reversed.This and other cosmetic surgeries including will ideally be only availible to those aged 14 or older to give them time to make the decision and even wait until they have finished puberty and reached adulthood with if possible CRISPR can even be used to change the transgendered brain to that of the gender they were born with again with the consent of the patient at 14 for the same reason.Those with fallen arches,overpronated metatarsals and other foot deformities can be corrected through the combination of forming new tissues and also causing others to undergo apoptosis and CRISPR treatments to treat mutations.Thus to replace cosmetic surgery and facial reconstructive surgery including those with facial and skull deformities it would form neural,muscle,bone and skin tissue in vivo layer by layer while others cause other cells to undergo apoptosis while other surface skin would moult off via recombinant DNA added to the patients genome from Serpentes all controlled and programmed by Paean with CRISPR treatments added to initiate the developments of these organs.Cells made to undergo apoptosis via suicide genes will first have the acellerated healing phenotype removed and new tissue put in its place housing this with all tissues formed later have all the augmentations as the patients.Those with facial,leg,toe,foot and other deformities from genetic diseases and also developmental disorders CRISPR treatments would be used to correct mutation and then initiate the proper development of these will be carried at first and then have the moulting of skin,formation of new tissues and also causing some to undergo apoptosis.This would allow for those suffering from Turners syndrome,Downs Syndrome,Rett syndrome and other deformities as result of genetic diseases,teratogens,incest,radiation and developmental disorders to have less deformed faces,legs,arms etc alongside CRISPR treatments to correct the underlying mutations and also initiate the proper development.If possible those affected by the Zika virus and genetic deformities that lead to microcephaly could using CRISPR and them forming new bone tissue have the growth of the skull increased to normal size and thus have excess bone tissue in the interior destroyed and using both CRISPR and them forming new neural tissue to take its place in place of the bone already present removed by apoptosis to allow for the patient to have proper sized skulls and brains formed with this of course tested on chimpanzees and mice with this engineered into them and also them born from parents infected with the Zika virus.Syringomyelia in Cavalier King Charles Spaniels and similar neural and skull deformities in other breeds of C.l.familiaris and Feline catus will be corrected via this with the skull made larger by forming bone tissue and then new neural tissue formed in place of lower bone tissue removed with AI crafting larger skulls that can house larger brains preventing discomfort with CRISPR treatments will also be used to treat them with other deformities in other breeds corrected using a combination of CRISPR and also microbes cosmetic surgery with advanced gene drive technology preventing them passing down onto the next generation with new ones created by artificial wombs have genetic deformities weeded out.Since it allows all types of tissues such as neural,muscle,skin and even bone tissue and blood vessels to be formed in vivo and undergo apoptosis it since controlled by Paean will allow for the skull in particular to be modified via causing bone tissue to undergo apoptosis and have new tissues formed in vivo and allow neural and skin tissue as well as blood vessels primarily capilliaries to be formed by them to allow the patient to develop proper sensory stimulation and blood flow in the newly formed tissues.This can also apply to to limbs that are deformed nor repairable by conventional surgery.Capilliaries,veins and arteries and all types of tissues including erectile,bone,nervous tissues can be created layer by layer to ensure blood flow to the areas with neural tissues created to ensure sensations.New layers of tissues will be created layer by layer and some tissues and parts of the body such as the skull.bones etc will be reshaped by having tissues undergoe apoptosis.Thus it will allow for invivo surgeries of all types that would not be possible in normal conventional surgery.The moulting will occur only in the areas under reconstruction via microbes creating chemical signals to initiate the keratinisng of the outer layers of the epidermis as newly formed tissue is pushed outwards and forcing the skin to moult off with this possible due to Serpentes DNA present in the hosts genome including living patients.Those who have suffered facial and other damage could avail of this to repair the damage caused by chronic drug use particularly synthetic drugs such as methamphetamine and neurodevelopmental disorders can avail of this..Circumcision can be reversed in adults by creating layers of skin layer by layer.Corrective surgery and those to treat deformities in the skull,face,limbs,lips and also facial reconstructive surgery and even those who have already gone under this and botched cosmetic and reconstructive surgeries surgeries can be repaired this way with face lifts and injection of botulism can be be reversed this way to recreate the patients original face.Thus those that have already undergone facial reconstruction surgery from animal attacks,second and thirds degree burns and acid attacks or facial disfigurement from crystal methamphetimes and neurodevelopmental disorders that has left them with a severely disfigured face can via this method be returned to their original face overtime layer by layer and thus have their face better reshaped back to their original form using photos of them prior to their disfigurement as a template.Those who have disfigured faces etc due to developmental disorders can be reshaped into normal ones.Dwarfism etc could be cured by this via gradually increasing the size of all limbs,organs etc to a normal height once genetic causes are treated.This can allow for the patient to have this done while at home,on holidays while awake and also asleep and save limited resources on surgery clinics and will be controlled entirely by Paean via biosynth WiFi and Bluetooth from nearby devices by interacting the with the nanomachines in the microbes with it taking place over several days,weeks in batch operations that occur when in resting or asleep with Paean spreading these operations into daily treatments that last several minutes or hours planned out by Paean.The length of each daily treatment and the entire procedure will depend on the type of in viva surgery.Even though it will take longer as stated it will lead to a more natural shape overtime and will be less likely to have complications including botched disfigurements and severing arteries etc that can kill the patient and will put less strains on the limited services of clinics which will become obsolete and can allow cosmetic operations that are currently impossible such as regrow removed testes/wombs/ovaries/breasts,reverse tubul ligation and vasectomies and add or remove testes,penis,wombs,cliterous etc for gender reassignment surgery and also increase or decrease the size and girth of ones penis,reduce the size of enlarged heads(hydrocephalus,macroencephaly,hyperostosis) or enlarge those that are small due to microcephaly with CRISPR treatments initiating their development and the microbes forming all types of tissues ie bone,neural and muscular tissues layer by layer or causing bone,neural and muscle etc tissue to undergo apoptosis.It will replace reconstructive surgery and can allow those with reconstructive surgery with botched looks have their face return to their previous state more efficiently.Defective organs that would interfere with breathing and proper functioning of the patient to live normal lives would be repaired by DNA from A.mexicanum and microbes forming new tissue with conventional surgery used to add new bio printed organs that house the patients DNA but without the genetic flaws.This would as stated be done by the stem cell strain creating millions of copies via mitosis and using flagellum in them to travel to the required area and form new nervous,muscle,skin,bone,skull and other tissues layer by layer as well as even blood vessels such as arteries,capillaries and veins layer by layer by Paean through WiFi signals causing them to form the desired tissues with them also causing others to undergo apoptosis with the acellerated healing phenotype removed from all of those made to undergo apoptosis to ensure they dont regrow with the ones put in place of them and in layers in other places will have this and all other DNA for ageing and augmentations present.The strain would be able to mould skeletons,skulls etc cause tissues to undergoe apoptosis and then form new tissue in its place allowing them to mould a persons skeleton,face and skull etc into a desired form.This will be of beneifit of those with skeletal,skull and facial deformities caused by neurodevelopmental disorders,pathogens,injuries caused by animal attacks/acid attacks/burns/drug use etc,genetic deformities etc and also those who have already under reconstructive surgery to create a proper skeleton,skull and face returned to what it previously was using ones genome,photos of oneself as a template.The stem cell strain will of course have traces of the patients DNA with them applying apoptosis genes to them.These stem cell microbes will be able to form any type of tissue such as skin,muscle,nervous,bone tissues layer by layer and form blood vessels such as capillaries,veins,arteries and cause any type of tissues to undergo apoptosis thus moulding the internal and external body of a patient.Paean would signal to the stem cell strains via biosynth WiFi where to move to,what cells to have undergone apoptosis,what cells and tissues to form and where to form them.Paean would use VR simulations to plan ahead each step and calculate the time it would take for it to be finished with cells made to undergo apoptosis via applying suicide genes first have the acellerated healing phenotype removed from them.Each stem cell surgery will require CRISPR treatments consisting of scratch DNA from different populations of healthy humans added stored in Physis to be applied to initiate the proper development of the limb etc to prevent deformities and in some cases of genetic deformities have genes removed with this done to remove the root cause from the patients genome and in both cases prevent deformities later on.The strain will need not just totipotent and embryonic stem cell DNA but also recombinsnt DNA from osteoblasts and osteoclasts to deal with the formation of bone tissue and the destruction of bone tissues in controlled manner.Patients with deformed internal organs that require bioprinted parts will have these bio printed organs created using the patients DNA that has mutations edited out would have them replaced with the carbon dioxide energy acceptor and accelerated healing phenotype added to the patients genome would prevent complications such as coma and death.Paean would control the formation of new tissues,apoptosis of cells and CRISPR treatments in a controlled manner.If possible specific tissue created by them could be used to replace silicone and other toxic materials used in cosmetic surgeries mainly breast and butt implants either done by surgery or in vivo with in vivo done by tissues forming in tissue layers underneath the skin providing a more natural shape especially if the rest of the body is grown with more tissues and they consume fat in certain areas and deposit it in others either directly or forming fat tissues.As stated silicone implants would be be made redundant by the microbes applying CRISPR treatments to promote breast growth,creating tissues underneath the skin in vivo as well as the possibility of tissues created by the microbes or bioprinted tissues implanted into the area instead of conventional material.Breast and butt reduction surgery could be done with them causing specific tissues to undergo apoptosis cause some to peel off via DNA added to the patients genome from Serpentes and forming new tissues layer by layer negating the need for surgeries and also negate the need for silicone implants with those already with silicone implants have them removed and then their desired breast size created by the stem cells.This can be be done to those who have already undergone mastectomies by creating tissues to form layer by layer alongside CRISPR treatmements recreating their removed breasts layer by layer,those who have undergone hysterectomies by recreating wombs in vivo layer by layer and even those who have had orichectomy wherein testicles were removed by recreating testicles layer by layer,reverse oopheroctomy with ovaries recreated later by later CRISPR treatments initiating the development of breast,testicular,womb tissues and hormones aiding in this.Thus any surgery to remove any organs to prevent the formation of and spread of tumours will possibly be reversed by the stem cell strains forming relevant tissues later by layer.In the case of penis enlargement in men this would involve them producing extra capillaries,erectile tissue and skin alongside CRISPR treatments increasing the rate of penile growth both in terms of girth and length increasing the size of genitalia and testes sizes using stem cells creating new tissues and capilliaries layer by layer and also CRISPR treatments increasing its size with the different genes responsible for penis size in males crossrefferenced to be then downloaded for upgrades with it reversed possibly reversing this via apoptosis of tissues.Thus penis enlargement in terms of girth and length can be carried out by them forming new tissues and blood vessels etc alongside CRISPR treatments to initiate the growth in penis size with this reversible by causing tissues to undergoe a apoptosis first tested on Biosynths.Furthermore the microbes making the erectile tissues easier to become much stiffer and stronger during erections via CRISPR treatments modifying the tissues as well as forming new tissues in places of existing ones with CRISPR and the microbes creating sex hormones allowing one to be perpetually in ones sexual peak of the ages of 14-15.Phanes will extrapolate genes from scratch for males to keep one in the early adolescent testosterone peak of 14-15 forever with if need be microbes creating this and other precursor hormones via recombinant DNA.Anti-ageing treatments will keep females at their fertile peak of 14-15 leaving them able to concentrate on careers for decades before starting families.This scratch DNA may have to involve them only producing testosterone once the patient has reached puberty and continue to do so after the age of 18 onwards forever in newly born male patients and not before the age males normally produce testosterone during puberty which could cause complications such as premature puberty.The DNA would also be made only to interact on the Y chromosome meaning it will not affect females.Females will possibly have genes that keep their levels of oestrogen at levels synonymous with the ages of 14-15 with again only made to produce these at constant levels not before they normally are produced but after 18 to prevent complications.The penis glans alongside the cliterous and prostrate can be given more sensitive tissue for more intense orgasms via CRISPR and also microbes forming new tissues with them extending to more areas around the cervix and even anal cavity in both males and females and areas at the entrance of the cervix have large areas of the tissues around them converted into extremely sensitive tissues connected directly to the prostrate in males and cliterois in females with them also connected to newly formed blood vessels to make them more receptive to orgasms during anal and vaginal sex as well as fellatio via direct stimulation in both genders and make females and males easier to reach orgasm without directly stimulating the cliterous or prostrate with this done via CRISPR treatments changing the tissues present in these areas including the tissues underneath them in subsurface tissue to increase surface area and also sensitivity in living patients into the same found in cliteroi in females as well as the prostrate in males possibly a mixture of both and if need be genes in all cells with this via gene drive technology spreading to the next generation and also the microbes causing cells to undergo apoptosis and also others forming these new tissues.Samples of tissues from the prostrate,penis glans,cliterous via base microbes using horizontal gene transfer and taq polymerase,Cas-9 and send the genotype for expressing the sensitive areas and tissues via biosynth WiFi and compared to the patients entire genome if it cant be extrapolated by Phanes from the entire genome with scratch DNA extrapolated by him that make prostrate,penis glans,cliterous tissues and those in these areas leading to them via CRISPR.Thus base microbes can using horizontal gene transfer extract the DNA from tissues in the cliterous,prostrate and penis gland and read by taq polymerase and Cas-9 with the genes responsible for creating these specific tissues added to Physis to allow for stem cells and CRISPR treatments to recreate them.The blood vessels such as capillaries would be formed internally and since connected directly to the prostrate in males and cliteroi in female stimulation of these new nervous tissues would directly stimulate the cliteroi and prostrate via electrical signals from the nerves travelling directly to the cliterous and prostrate and them becoming part of them as well thus leading to more intense orgasms in all sexual positions in both heterosexual and homosexual males and females that can be achieved more easily with these two options allowing them to be formed in living patients including adults with CRISPR editing embryos,spermatozoa and eggs to make this a permanent part of H.sapiens.In males the prostrate can be directly connected to the penis glans through this tissue thus meaning stimulation of the glans during heterosexual and homosexual sex as well as oral sex,sexual intercourse and masturbation would directly stimulate the prostrate increasing orgasms in both areas,the anal cavity can be connected to it to make anal sex and rimming in homosexual acts directly stimulate the prostrate with as detailed the cliterous in females directed connected to sensitive tissue in the cervix and anal cavity wall making masturbation and penetration in these areas alongside fellatio improve success in achieving orgasm every time.To improve stimulation large areas of the cervix,anal cavity etc would be converted into these tissues.Thus the new sensitive erogenous tissues surrounding these areas will become part of and be directly connect the anal cavity,penis glans and prostrate in males to each other and the cervix,anal cavity cliterous in females to each other thus making it easier to achieve orgasm in any sexual position including masturbation,oral sex,all sexual positions,rimming and fellatio as the stimulation of them would directly stimulate the cliterous and prostrate directly.Scratch DNA and that from animals with extremely sensitive penis gland and cliterous could make this tissue,the cliterous,prostrate and penis glans etc even more sensitive and conducive to powerful and intensive orgasms 100% of the time and in the case of the penis glans make them more stronger and thus likely to let one have sex much longer by delaying ejaculation.This can be applied to living patients via CRISPR to the tissues in theses areas and subsurface areas and tissues and the entire human genome passed down to future generations via advanced gene drive technology.If perfected it could allow both males and females to climax and reach orgasm 100% of the time in all forms of sexual acts.CRISPR and stem cell strains forming new tissues will make the prostrate,penis glans and cliterous form more sensitive and erogenous tissues with the endorphines and other hormones created during and after orgasm to be created by them on demand.These sensitive nerves connected to the penis glans,cliterous etc could be connected to the rest of the peripheral and central nervous system meaning all orgasms in both males and females would spread to and be felt in all parts of the body.Parts of the brain responsible of sexual arousal and pleasure will be modified to become receptive to musks and pheromones added to cosmetics or even those synthesised by the opposite sex in place of body odour with them synthesised using scratch DNA.The seminal vesicles and prostrate glands can be made larger with extra spaces in the scrotum etc to store more semen with CRISPR and them creating hormones can induce extra semen to be produced.If possible both CRISPR and stem cell strains forming new areas for the seminal vesicles can increase the surface area of them by extending its range across the entire body similar to both the lymphatic system and circulatory system thus exponentionally increasing the amount of semen produced and stored by them.This could allow them to create,hold and store anywhere between 1-5 litres of semen for sexual purposes with the stem cell strains sealing off a desired area of these new vesicles when desired returning the level of semen produced to normal or between 1-5 litres with it reversible by rebridging these vesicles back together.The microbes can induce the vesicles to create more semen once depleted via creating hormones and CRISPR or them creating semen in large amounts through anabolic and catabolic reactions.The stem cell strain or a sub strain could form worms and implants and using electroconductive pilli in all microbes forming the worm or those forming a biofilm could genereate electricity using electroconductive pilli chemical reactions to stimulate the prostrate,penis glans and cliterous to induce orgasms on demand.Since these worms would consist of millions or biillions of microbes containg DNA from G.metallireducens,S.oneidensis,G.sulfurreducens DNA will give it the ability to generate electricity and electroconductive pilli and electroconductive proteins with the vast amount of microbes combining their electrical charge together to produce powerful orgasms in the cliterous in women,prostrate in men and also with men directly stimulate the nerves connected to the penis glans allowing one to achieve orgasms on demand.This could render all types of cosmetic surgeries obsolete including rhinoplasties and also those on the face by them forming new bone tissues and also skin,neural and muscle tissues alongside capillaries layer by layer and initiating the moulting off of skin.Sterility would be solved by curing patients of pathogens that cause this,restoring damaged tissue and CRISPR treatments to make sperm more motile.Female and male circumcision can be corrected by using CRISPR and forming relevant tissues.Their ability to consume fat may also be be used to eliminate liposuctions with their ability to create muscle tissues as explained by causing muscle cells to undergo apoptosis allowing them to regrow consuming fat,stimulate brown adidopse tissue,genes that increase metabolism alongside the microbes creating capsaicin and removal of the fat insulin gene,the host synthesising essential amino acids alongside exercise to allow to gain a more natural shape and prevent the forming of loose skin with the patient also exercising.If loose skin is formed then they can form new tissue inbetween folds that contain capillaries allowing for the folds to be removed by surgery or microbes making the skin holding the folds undergo apoptosis safely with any making new ones by them repairing tissue with the aforementioned methods of removing the fat insulin receptor gene,apoptosis of muscles and consuming of fat all at once will increase the rate for those availing of liposuctions to not need it.Scarring can be dealt with the skin peeled off using Serpentes DNA added to the patients genome and forming new tissues in their place with cellulite dealt with a combination of CRISPR,consuming fat stores and causing some structures to undergo apoptosis.Stomach stapling may be negated by them modifying the stomach by creating new tissues or adding genes to modify ones appetite or creating hormones that encourage one to feel full as well as counteract those that incite fat and sugar cravings outside of pregnancy or those initiated by high blood sugar.CRISPR may also counteract cravings and the want to eat more than they can.The patient may even have a new smaller or averaged sized stomach created via bio-printing them.If possible their ability to create collagen,skin tissues directly or through CRISPR to make cosmetic surgery more natural especially with this of relevant to the lips,forehead and other parts of the body.They may also be use to repair skin damage from prolonged UV treatments such as sunburn,skin conditions,burns and even acid attacks negating the need for skin grafts and possibly reconstructive surgery or at least alleviate the amount of surgery to be applied with skin cancers attacked in the same way as other tumours.This would be done by them creating new skin tissues alongside recombinant DNA from Planarians,Hydra and A.mexicanum allowing the native host to do so by themselves and causing the damaged areas to be moulted off similar to sunburns and also as seen in Serpentes with CRISPR adding this ability of Serpentes added to humans and only occurring signalled by Paean when these occur.Recombinant DNA from planarians,Hydra,A.mexicanum will allow the body to accelerate healing by itself.Acidophilic bacteria added to all cells in the body such as the skin,eyes,oesophagus,stomach protecting them from stomach acids and acid attacks whether intentional or accidental would be done with adding DNA from T.gammatolerans protecting the skin from sunburn and UV light with the microbes manipulating melanocytes to allow one to consciously change skin tone.This ability to shed skin would be done in the case of burns with genes from scratch and even extremophile bacteria.Other living patients not already having surgery will be given recombinant DNA from A.mexicanum etc to in the instant disfigurement occurs their original structure will be able to be repaired alongside the repair mechanisms of the action of microbes.Those who have already undergone facial reconstructive surgery including face implants and other botched surgeries to reverse the ageing process could theoretically have the microbes form bone ie skull tissues and other tissues ie skin,muscles,nervous tissues in all parts of the face layer by layer in a preprogrammed manner managed by Paean to form a more stable and symmetrical face layer by layer back to what is was prior to their disfigurement.Serpentes DNA added to the patients genome will aid in this of existing patients who have already undergone facial reconstruction including face implants and also microbes forcing certain cells and tissues to undergo apoptosis as the rest of the microbes form new tissues layer by layer while certain skin etc is peeled off via moulting programmed by Paean with it also done to repair facial lifts and other cosmetic surgery on the face with this ability to form any muscle,neural,skin and bone tissues layer by layer rendering conventional cosmetic surgeries eventually obsolete allowing cosmetic surgery clinics to be turned into homes with those in hospitals turned into other uses.This could also be used by those suffering from skull and facial abnormalities due to developmental disorders and will allow those with normal but undesirable non symmetrical facial features to undergo cosmetic surgery on their entire face by modifying the skull,skin,muscles etc by causing tissue to undergo apoptosis,build layer by layer and also moult off top layers of skin programmed by Paean to create more symmetrical pleasing faces thus allowing them to replace all forms of cosmetic surgery that would be done invivo controlled by Paean when the patient is awake at home.Hernias,spina bifida and skin tags would removed via bridging gaps of neural tissue and skin etc and then causing the outer herniated layer to undergo apoptosis and peel off.The moulting ability of Serpentes added to a patients cells via CRISPR could allow sections of the body to be moulted off when invivo cosmetic surgery takes places by the microbes initiating chemicals signals that causes the outer layers of skin to keratinises and then peel off naturally with again in the case of those done on breasts and the face only these parts done to be removed as if perfected this ability will allow one specific sections of the body to moulded off with if need be and prior to this perfected the entire body signalled to do so to remove dead dying skin or those covered in spots and other undesirable marks like scars as well as tattoes removed this way negating the need for laser surgery with existing scars from laser scars repaired this way by new tissues formed underneath as the old epidermis is moulted off while new tissue is formed underneath.This moulting ability can be used to removed unsightly scars and also unwanted tattoos.Thus if perfected only parts where invivo cosmetic surgery is being carried out will moult off controlled by Paean.This could allow the entire epidermis of the entire body to be moulted off every few years,decades and centuries to allow new fresh skin to be created with this done at first on those in the eldest age bracket aged 50-80 or more to allow newer youthful skin to emerge with this tested on mice and chimpanzess engineered with no hair as early as 2024.Hair follicles may be peeled off alongside skin or moulted and shaved off prior to the moulting to then via turning on and then off genes and microbes creating compounds to improve their growth rates back to normal levels as they will be using CRISPR caused to regrow at an accelerated rate and then slowed back to normal using CRISPR turning on/off genes and microbes creating compounds with this done to make hair regrow in all parts of the body.The part of the skin that contains and holds the roots will not be affected as it will stay where it is and the upper layers forced upward and outwards by new tissue and moult off once keratinised etc like Serpentes.This will also be tested on chimpanzees and mice with hair.Skin grafts as stated would be negated by them repairing damaged tissue with the older tissue moulted off with those already having skin grafts and reconstructive surgery have the older tissue moulted off as new tissues are created layer by layer.This would allow existing and new damage to the skin by fire,acid etc corrected by this.They could have recombinant DNA from necrotising bacteria,flies or from scratch to break down and consume only dead skin,flesh and even dead parasites but does not damage healthy flesh.For this to work the cells that are programmed to undergo apoptosis via adding suicide genes will have accelerated healing phenotypes removed prior to underoging this with the new tissue have this added to prevent the apopotised tissues from regrowing and allow the new ones to have this phenotype but it may be possible that this can be tested on tissue cultures as early as 2023/2024 to have the accelerated healing phenotype and then have vectors transfer suicide genes to see if grown back with animals tests having animals with accelerated healing have vectors transport suicide genes to organs and muscles to see if they can naturally regrow.The strain would once tissues in all parts of the body such as brain,skin,muscles and other parts of the body are detected to be ageing they would replace them with new rejuvenated ones by forming these tissues on them with this also this done for conditions like idiopathic pulmonary fibrosis that would have degraded tissues be replaced with new ones without damage and have CRISPR treatments added to repair any genetic damage with clubbed fingers also repaired.As detailed earlier on donated lungs and those grown in chimera animals can be grown to suit both the doner and patient.Thus these invivo cosmetic,reconstructive and also gender reassignment surgery would of course be tested on chimpanzees as early as 2025.
For astronauts these would alongside gene therapy from scratch,pass this ability onto them via horizontal gene transfer and Salmonella would prevent muscle and bone atrophy alongside the microbes constantly being able to regenerate,neural,muscle and bone tissue to aid this while in zero gravity with them also having DNA from T.gammatolerans,D.radiodurans scratch and Tardigrade to survive cosmic radiation and also the vacuum of space alongside their regenerative abilities and that to fight tumours and repair DNA damage.DNA from Planarians,Hydra and A.mexicanum in the host would regenerate atrophying tissue constantly alongside them.DNA from T.gammatolerans would also protect the host from sunlight UV radiation,radon,xrays and even nuclear fallout,gamma ray bursts and cosmic radiation.Paracoccus denitrificans recombinant DNA would increase human resistance to g-force and survive extremes in hypergravity in interstellar vehicles,hyperloops as well as scramjets.To heal wounds blood clotting agents would be released when by them they are directed to or are at areas of wounds,tears in the skin and organs to clot the blood and illicit platelets via signals with thinning agents and painkillers including acetylsalicylic acid created when thrombosis and blood clots are about to or have formed when the blood thins or on demand in aeroplanes and also when sedentary for long periods of time.Thrombosis and blood clots can be broken down to prevent them being fatal with the carbon energy acceptor phenotype allowing one to survive them.Them forming biofilms and then entering a rigid structure either by creating clotting factors,coagulants,biolfilms and nanowire scaffolding for new tissues to grown on alongside eliciting platelets could seal large wounds to allow the bodies natural repair mechanisms especially accelerated healing to form alongside them forming tissues on these biofilms through them forming nanowire scaffolding,controlled replication and evolution managed by nanomachines,CRISPR mutations and the microbes to repair organs and arteries with these also keeping the host alive preventing sepsis,infection,gangrene and also blood loss and keep vital organs alive until they repair the wounds themselves as well as until the patients can be attended to by surgeons whether human,bio-synth,robotic or mechanical to repair more severe damage with the microbes repairing as much as possible to heal arteries and key organs.They would also create blood cells and erythrocytes while damaged arteries and other blood vessels are repaired or bypassed with new ones to counter blood loss while the brain is kept alive with oxygen released by other strains with bones also created to correct broken,twisted or fractured bones and skull by creating bone tissues or cure other deformities by creating biofilms that allow the microbes form specific cells,nanowires and tissues as scaffolding.The microbes housing haemotiopic stem cell DNA etc will be able to undergo mitosis in an emergency tear or perforation and create large amounts of erythrocytes and even leukocytes while the body heals itself to prevent the brain and other vital organs dying from lack of oxygen with the human body stimulated via chemical signals created by them to create more of these but not too much with the host have genes form scratch created by Phanes and other animals to be able to recreate them in large amounts only in these emergencies ensuring the body does not run out of blood.Recombinant bacteria DNA from faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles and scratch DNA will allow the hots organs especially the brain survive without oxygen when deprived of it due to blood loss thus ensuring the survival of the host in situations where blood loss would lead to death.Having the host have recombinant DNA from Planarians,Hydra,A.mexicanum could aid the microbes in repairing both external and internal wounds.Sprains and twisted ankles and other limbs could also be corrected and repaired with any pain treated by them releasing mild natural painkillers.The brain and other vital organs can be kept alive with the microbes releasing oxygen or converting carbon dioxide into oxygen while others once the ruptures and bleeding is stopped create blood plasma and erythrocytes to keep the host alive.The carbon dioxide energy acceptor phenotype will kept the body alive in these situation.Necrotic tissue as the result of gangrene can be reversed by them replacing the tissue with new revitalised ones onsite before and after breaking down the old tissue,using scaffolding,bioprinted or scaffolded microbes recreating the digits or limbs or them recreating capillaries etc or ideally prevent it in the first place and also them fighting off any pathogens that cause it and in the case of dry gangrene prevent peripheral artery disease either by removing cholesterol or removing the fat insulin receptor gene.Key areas such as fingers,toes and legs can have strains that release oxygen to tissues in them to keep them alive along strains that repair and replace dead tissue in the case of gangrene occurring with recombinant DNA from faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles and scratch DNA etc as detailed earlier added to all cells in the body preventing necrosis if oxygen is restricted with other strains that replace dead tissue with new ones in these key areas as well.Recombinant DNA from Planarians,Hydra,A.mexicanum,and C.elegans in the host will repair damaged tissues from gangrene.The same can possibly be done to treat and prevent frostbite with damaged blood vessels and tissues regrown and as stated earlier recombinat DNA from osmophiles,xerophiles,psychrophiles,scratch DNA as well as R.sylvatica,Tardigrade,Bacillus F,H.glaciei,C.greenlandensis,P.putida GR12-2,C.pleistocenium,psychrophillic bacteria,Tardigrade, poikilotherms added to the human genome and them residing in toes,feet and fingers to release cryoprotectants and or capsaicin to keep the entire body warm with repairing strains residing in these areas to correct and replace damaged tissues.This and DNA from Planarians,Hydra,A.mexicanum,C.elegans,T.gammatolerans and Bacillus F to repair damaged tissue and telomeres and allow one to be thawed and rethaweed at temperatures of down to -272 over and over again with no frostbite and hypothermia.
Digits and limbs could be grown on an organic scaffolding over lab grown bones themselves formed by stem cell strsins that have blood vessels,muscles,nerves and skin grown layer by layer by this strains with nutrients and oxygen fed into them with them then attached allowing all people who have already have had legs,arms,hands,finger etc to have new ones reattached with those with biosynth limbs have them as scaffolding for skin,neural,muscle and blood vessel tissues formed over them to give them sensitivity.These limbs and digits would be grown in a lab with stem cell strains containing the patients DNA and augmentations etc layer by layer on top of organic scaffolding it uses as nutrient and support.Millions,billions of trillions of stem cell microbes that first involve bones grown in organic scaffolding using osteoblasts DNA that grow on the inside and outside of the scaffolding before consuming it as nutrition with them more microbes forming layer by layer neural tissues,capillaries,veins and arteries as well as muscles and then skin layer by layer.These microbes will house the patients DNA to prevent rejection once reattached and using biosynth wifi and bluetooth will be controlled by Paean to form these layers and then form each type of tissue layer by layer with them constantly fed oxygen,sugars,proteins and fats to stay alive with the tissues housing the carbon dioxide energy acceptor phenotype to survive transplantation alongside other augmentations decided by Paean.These microbes ability to form new tissue could allow detached limbs,digits to be reattached by them forming nervous,blood capillaries,arteries etc by merging with open wounds,severed limbs or even open skin in the case of those using bionic limbs when reattaching them even after periods not possible in normal situations and allow dead tissue to be rejuvenated and replaced with new ones.Otherwise advancements in bio printing and machinery will construct them using the stem cell strain within minutes.The sealed wounds of existing patients could be once the new limb created on a template as detailed will be attached to the sealed wound using an organic support similar to cybernetic ones that can then be removed later or become integrated into the patients body permenantly or removed by stem cell in vivo surgery that holds the synthetic limb in place with the microbes causing the sealed wound to undergo apoptosis and allow capillaries,arteries and also nerves etc in the patients body to be merged to the limb with microbes present in the patients body communicating with them in the limb telling them where they are to tell those in the limb where to cause the skin to undergo apoptosis and bridge tissues etc tissue.Paean will manage their creation for each individual patient by 2029-2035 allowing those currently missing fingers,toes,legs etc to be given new one’s indistinguishable ones.Thus those who have had limbs and digits such as fingers,toes,arms and legs lost due to accidents etc can have Paean grow synthetic versions in a hospital lab and attached to the body.Missing eyes will be replaced by those formed later by layer in the eye.Synthetic bionic limbs on existing patients can be fitted with microbes forming muscular,vascular and neural tissues to make them responsive to touch etc before these synthetic lab grown limbs become advanced enough to the point that they can replace cybernetic ones.Thus stem cells will render concepts of bionic limbs obsolete.If possible future bionics could be a synthesis of biosynth technology and stem cell strains.
The stem cell strain would have DNA from induced pluripotent,embryonic stem cells and also biosynth WiFi DNA that would allow Pean to send WiFi signals to cause them to convert into any type of cell or tissue he wants them to.They will have flagellum engineered into them to move around the body and DNA from bacteria that allows them to undergo mitosis.3D DNA printers will create these strains that contain this DNA and the patients DNA to prevent rejection with them once injected undergoe mass replication when told to do so by Paean via biosynth wifi which he will also use to direct them to where they are needed to repair existing wounds and ruptured in the nervous system.Since connected to Paean they will be able to convert into any tissue on demand possibly in time growing entire parts of an organ or vessel from scratch by forming biofilms and working with nanomachines to form scaffolding.Biosynth WiFi will be used to convert them into any type of cell and tissue in the body through him instructing the evolutionary path of the DNA through Cas-9 and taq polymerase that holds the patients DNA in a level on par with ones 20s or even infancy and contain all DNA as part of augmentations and anti-ageing treatments.This will allow him to repair existing internal wounds in patients,reshape the interior of the human body for in vivo cosmetic surgery,form implants etc.Biosynth WiFi will allow him to instruct the DNA in stem cells to induce their evolutionary path to convert into any type of tissue ie neural,muscular,vascular etc tissue once forming biofilms.Elderly patients as part of anti-ageing treatments would have them form younger rejuvenated tissues in all parts of the body especially in key areas of the body such as the brain,heart and muscles to improve cognitive,vascular and locomotive functions.This would speed up age reversal treatments and would be key in aiding the CRISPR treatments that reverse the ageing process especially for those who have been left unable to move independently for several years or decades due to their elderly age to regain locomotion.They will be used alongside CRISPR treatments to cure neurological conditions such as pedopheilia,sociopathy and also neurodevelopmental disorders such as Downs Syndrome etc and genetic diseases by forming correct neural and other tissues in the body.Due to extensive damage caused by old age they will by forming younger heart,muscle,neural etc tissues that have levels of phosptidycholines,NAD+ and telomeres on par with a person in their twenties,teens and even infancy will rejuvenate parts of the body to that state with the patients entire genome to compliment CRISPR treatments especially not only for the elderly but for those aged 30-75 so that this adds an extra 20-50 years to their lifespan should CRISPR treatments be not advanced enough.Thus they will be carried out alongside proto CRISPR treatments to replace dead dying skin and tissues with younger rejuvenated tissues on par with those in their early 20s or younger to increase survival rates until CRISPR treatments are perfected.Patients who are survivors of Ebolavirus,Plasmodium,Coronaviridae,N.meningitidis,Naegleria fowleri,Balamuthia mandrillaris and chronic alcohol and recreational drug use on the brain,liver and also suffers from brain damage from continuous trauma to the head and also prions,Creutzfeldt–Jakob disease etc could have the existing damage to the brain,lungs etc repaired by this stem cell strain to return it to youthful and pristine state by forming new tissues in place of dead or damaged ones.Ruptures in the neural system that have caused and could cause paralysis leaving one confined to wheelchairs and also help from carers to continue ones daily life can be repaired by them forming a biofilm with through their ability from stem cells turn into new nerves and nervous tissue that form part of the persons systems permanently thus repair severed nerves and/or replace dead ones and other damaged tissues below the damaged area with new rejuvenated ones that can return ones ability to fully move around overtime.Blindness could be cured by the stem cell strain repairing damage to the optic nerve and other damage to the eye such as iris etc.Deafness and damage to ones ear will be cured by them repairing damage done to the eardrum etc.This could cure paralysis in people currently confined to wheelchairs first tested on animals.Patuents who are currently confined to wheelchairs due to parasites,severed neural pathways etc will through this be able to regain the ability to walk.This would be because the strains ability to undergo mass replication,travel around the body and form new tissues will allow severed nerves in the central and peripheral neural system to be formed,repaired and both muscular and neural tissue below the damaged area replaced by new functioning tissues created by the stem cell strain thus theoretically allowing those that are currently confined to wheelchairs etc and suffering paralysis due to pathogens,trauma,parasites etc to be able to regain full motor control in their entire body with the acellerated healing phenotype preventing this in future patients.As a result to cure existing patients confined to wheelchairs due to damage caused by parasites,pathogens and trauma that damages the central and peripheral neural system the stem cell strain can once injected into the bloodstream undergo mass replication and travel via flagellum to where the rupture in the central and peripheral nervous occurred in the past and form new nervous tissues to seal the rupture as well as any missing links in the rest of the body and repair dead neural tissue below the rupture by forming new neural and if need be form new muscle and blood vessel tissue across the entire affected area below the rupture thus giving one the ability to regain full locomotion and sensation in their entire body giving patients the confined to wheelchairs be able to return to their normal healthy lives with Paean via biosynth WiFi controlling this for each individual patients.Those as result of genetic defects and neurological conditions such as Parkinson’s,Alzheimer’s,multiple sclerosis will also require CRISPR treatments alongside this.Thus those who are currently confined to wheelchairs will have stem cell strains repair ruptured in the central and peripheral nervously system and also regenerate and replace dead muscular tissue below the rupture in the nervous system.Future injuries to the ear,eyes and nervous system that leaves one blind,deaf and confined to wheelchairs will be repaired instantly by the acellerated healing phenotype.These could also repair damage in brain in coma patients and using chemical and electrical reactions etc restart the brain awaking the patients.Damage to brain caused by frequent trauma experienced by athlethes and Alzheimer’s patient and those infected by prions will have the strain repair this damage.
Furthermore this could repair existing damage to all parts of the brain,skin,breasts,vocal cords or other parts body affected by surgery,digested bones,pathogens,tauopathy,neural damage caused by trauma to the brain etc that are done to remove tumours as well as internal ruptures form and also other procedures in existing patients as well as organs damaged by pathogens,external forces like bullets,stabbings,severe beatings,severe blood loss,heavy metals,pathogens,chronic drug and alcohol use ,smoking,ear damage from loud music and sounds,damage to the eyes such as bright lights in existing patients can be repaired by this strain forming new tissues and could keep the brain and other vital organs such as the heart alive in otherwise fatal conditions or injuries.As stated existing damage in patients in the brain and other important organs caused by infections,allergies,viral and bacterial pathogens,prions,parasites,surgery complications,damage from alcohol and recreational drug abuse in ones teens as adult years and even in utero and chronic use in adults,heavy metals and toxins,poor nutrition,bullets,neural damage caused by trauma,alzheimers and other neurodegenerative disordors,strokes etc that have left one confined to wheelchairs as well as mentally handicapped or even minor complications will be repaired by them forming the relevant tissue in the brain by Paean with brains of healthy adults compared to brain scans of the patient.Prions once destroyed by specific strains that consume them can have damage to the brain repaired to prevent vCJD etc.Retrograde and anterograde amnesia as well as Korsakoff Syndrome and other similar conditions in existing patients can be repaired this way with those who have lobotomies repaired by them.All forms of brain and neural damage in living and comatose patients can be repaired by the strain.Damage in all parts of the body including vocal cords,digestive tract,muscles etc can be repaired by them.Damaged nerves in acid,burn and surgery victims will be repaired by stem cells forming new neural and blood vessels underneath the skin.This may include them forming sensitive cliteroi tissues in the case of intersex patients who have had surgery that has left them with no cliteroius and unable to reach orgasm.Those made crippled both in terms of their legs and even lungs and have damage done to their lungs,brain,muscles and nervous systems from pathogens such as Poliovirus,Ebolavirus,N.meningitidis and also recreational drugs,alcohol etc can have the damaged areas repaired by having the stem cell strains replace the damaged tissue with new fresh tissues with for extreme cases it may require bioprinted lungs.For example if a brain tumour is destroyed by microbes or surgery is done to remove others then these microbes could regrow relevant tissue in these areas such as in the brain and also repair any damage caused by complications from surgery,female genital mutilation,damage to the cervix and surrounding areas from cancer treatment,surgery performed on intersex individuals, that damages the cliterous etc,circumcision and damage caused by trauma in both future and even existing patients and if possible they could keep the body,brain and heart etc alive and regenerate them when them if a person is momentarily dead after a heart attack or extreme blood loss through regeneration and releasing bursts of oxygen and forming new tissue.The fatal conditions repaired by this strain would include stabbings and being shot,perforated organs and blood vessels,strokes,electrical shocks,poisoning from heavy metals and elements alongside animal and plant toxins,severe beatings,overdosing and trauma.If possible recombinant DNA from E.electricus as well as those from scratch can be added to humans to prevent damage from electric shocks.DNA from even G.metallireducens,S.oneidensis by forcing the production of electronically conductive pilli that transmit electricity also can be used to improve the mechanotransduction abilities of microbes with the voltage being below dangerous levels but enough to do its various purposes with it tweaked to convert sugars,metals and other chemicals in the body for this.E.electricus DNA can also be added to produce extra electrical charges in safe levels alongside those from other bacteria that produce electricity with the same ability for the fish to be protected from these charges applied to the host with this tweaked via AI or exposing bacteria with this phenotype could be added to humans to protect them from electric shocks of all ranges.Damage to vital organs such as the brain could be repaired by the strains responsible for creating new tissues repairing and replacing any damaged tissues with this ability using horizontal gene therapy applied to the host.If possible it could create larger amounts of more sensitive tissue in the both the clitoris as well the penis glans and even prostrate with this of particular relevance to those who have undergone corrective surgery to deal with intersexuallity with them stimulating orgasms on demand in both genders through hormones produced,interacting with the nerves present through mechanotransduction in the clitoris,penis glans,prostrate and other erogenous zones especially if forming a biofilm or worm internally or externally as well as through the electroconductive pilli and ability to produce electric currents from chemical reactions and if possible improve blood flow to the sex organs both the penis and cliteros as well as prostrate during sexual excitement and intercourse,repair damaged erectile tissue and capillaries in both males and females and possibly correct genetic,organ and hormonal issues relating to conditions such as 5α-Reductase deficiency and intersexuality including creating creating or allowing for bioprinted organs to be added alongside creation of hormones and CRISPR treatments to create correct organs and hormones and correct mutations.Diseases and conditions caused by inbreeding between close relatives and incest in the uterous or as a child can be corrected by them creating new tissues,CRISPR etc with this including those that would prevent the child coming to full term.Birth defects and also damage to the child in utero and early years can be corrected by CRISPR and them forming new tissues.Damage to all organs by pathogens,surgery,chronic drug and alcohol use etc will also be repaired by these microbes with other conditions like sterility etc also repaired.Damage to the brain caused by surgery,pathogens,strokes,toxins,cryopreservation,trauma,continuous bangs to the head that lead to memory loss,speech function and motor skills,changes in personality and potentially fatal or paralytic damage can be repaired by these forming new tissues and them inserting Planarian,Hydra,A.mexicanum and C.elegans recombinant DNA into all neural tissue in the brain with this could be done to regenerate tissue on the breasts and also the rest of the body to remove tumours etc that get too out of control negating the need for mastectomies and hysterectomies allowing those that undergo sexual reassignment surgeries to reverse surgeries to accommodate this allowing them to switch between both genders and to regrow uteri,ovaries,testes and breasts and other organs etc removed to prevent or treat cancers in vivo or invitro in the case where they were removed for example in the case of breasts forming the breasts layer by layer with testes and ovaries formed by them forming a mass then turning into relevant tissues,use of hormone production complete with them forming layer after layer in a gradual controlled manner or have it done in with organ banks in people that have undergone this with it also done to reverse tubule ligation and even vasectomies and neutering.If possible ovaries and testes could be grown like bioprinted organs using these microbes containing the hosts DNA and then surgically implanted.This tissue growth and CRISPR treatments to recreate breasts and ovaries etc by stimulating hormones and tissue growth alongside the microbes creating tissue layer by layer underneath the skin and newly redeveloped organs could perfect this with if possible recombinant DNA from Planarians,Hydra and A.mexicanum would aid in regrowing tissues of breasts.It could even be possible for them to regenerate dead tissue such as in the brain,muscles,skin and other organs that have been dead for a short period of time and not yet undergone algor mortis or at at least an hour of death with this tested on chimpanzees and other mammals with if possible recombinant DNA of humans to test how long it can allow for a person to be dead and still be revived.CRISPR treatments could possibly aid this by altering humans to slow down the time between each stage of mortis improving chance of these being successful in raising the recently deceased.If perfected these could negate the need for minor surgery especially internal surgery completely with them repairing wounds as well as blood vessels and organs,removing tumours,creating bones to cure or alleviate damaged feet and breaking down parts of defective organs via apoptosis of unnecessary or defective cells/tissues and repairing tissue as well as creating parts or whole organs in vivo and applying gene therapy on defective and old ones as well as creating new capillaries or blood vessels to bypass defective,ruptured or broken ones.They could also keep vital organs alive for extended periods of time to allow patients to survive any unexpected delays for surgery.Their ability to release oxygen to the host can be used to release oxygen to all organs especially important ones such as the heart and brain to keep the host alive should complications in surgery occur during and after surgery or as a result of injury and heal any wounds and damaged veins etc with them also giving the hosts cells and tissues the ability of faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles and scratch DNA etc to use use carbon dioxide as an energy acceptor with this also being used in other circumstances such as when vital organs and arteries are ruptured supplying the brain and other organs with oxygen and carbon dioxide as an energy electron acceptor.This could aid surgery by again repairing any complications or wounds that occurred not part of it and also in case where the skull must be opened to decrease swelling with them also fighting off or have the host immunised against pathogens that infect the host during it including MRSA.If possible the ability of bacteria from the Geobacter and Shewanella genera to produce wiring could be engineered into them and there genes from scratch to have carbon nanotubes or silk placed around organs as protection against stabbings,trauma etc or more likely these could be engineered to produce layers of spider silk around them again to provide protection of vital organs with them also synthesising layers of fat to be deposited around key organs.Arteries would also have this done if possible the silk or graphene nanotubes built into the thick layers of the muscles in them to strengthen them in between tissues to protect against them breaking due to aneurysms,embolisms and also stabbings with the brain also have this done in the thin layer between the outer meninges of the brain and central nervous system,within the meninges and also the skull and/or between the skull and the outer layers of skin on all parts of the body.Bones of all types including the skull and ribcages can also have these carbon mainly graphene nanotubes produced inside or on them to make them shatterproof with if need be them removed in certain situations.Having all organs,bones,arteries and even the meninges and skull have a layer of sheets or spider silk on and in them produced by the microbes would give the body particularly the brain extra protection against trauma especially falls from great heights,blunt objects and beatings as well as even making them bullet proof and resistant to stabbings thus increasing the chances of survival and prevent the ribs,bones and even skull from breaking and protecting the brain and other vital organs due to the strength of both compounds allowing these to be more easily repaired by the microbes or even the tissues themselves via engineering via recombinant DNA from Hydra,Planarians and also A.mexicanum.If possible the spinal cord and also arteries in the neck and all parts of the body as well as ribs will be fitted with this to prevent them twisting,breaking or even being decapitated.This can be done via specific strains that produce these nanotubes and spidersilk as well as in time even CRISPR and germline therapy.Conditions such as sudden infant death and adult death syndrome can be counteracted by several means such as having patients given the carbon dioxide energy acceptor phenotype that allows them to survive without oxygen as well as microbes releasing bursts of oxygen to counteract the condition with implants relaying the onset of these conditions.
Those in comas would have oxygen released into the brain and brain tissue regrown with the microbes ability to form new tissues on demand done alongside them passing the healing and memory abilities of Planarians,A.mexicanum,Hydra and C.elegans added to the native cells as a backup to prevent memory loss,damage and death ideally with this transfer done before any accidents occurred with the microbes also creating new tissue in the place of dead ones.The underlying cause of the coma will be corrected and repaired by the microbes for each individual case with as stated them keeping the brain alive and passing on healing and memory retention abilities to it.This would be done by again horizontal gene transfer but also the microbes in an endospore state collecting in the key areas of the brain as a biofilm and responding to signals exiting this state and repairing the damage.Electronconductive pillli and proteins could allow the microbes generate electrical signals to jumpstart the brain of comatose and unconscious patients and jump start the heart in the case of those who have had heart attacks.If possible this and gene therapy could be used to correct neural defects and genetic defects that lead to paedophilia,schizophrenia,maniac depression/bipolar disorder,psychotic disorders,sociopaths behaviour that could lead to them becoming serial killers and sadists,dyspraxia,Angelman syndrome,epilepsy and other psychological disorders by breaking down the compounds that cause them into nutrients for the host and microbe or creating required or missing natural or synthetic compounds and neurotransmitters to allow the patient to function properly,the microbes creating required neural synapses/ brain matter replacing existing ones or even altering them and breaking down compounds that cause it permanently to make them normal,increase intellectual ability or even through CRISPR treatments to repair the genetic damage or mutation that led to it to cure them or at least alleviate the symptoms significantly allowing the patient to live somewhat normal more independent lives until improved treatments can be developed with germline therapy preventing them passing this onto any children they have.Thus these neurological and developmental conditions would be treated by creating specified neural tissue,altering brain matter,CRISPR treatments to correct mutations and also creating required neurotransmitters and other natural and even synthetic compounds synthesised by them to alleviate symptoms or cure them entirely.Ideally these can be treated very early on once detected by the patients files DNA scans and MRI scans detecting the signals of diseases very early on and if possible via base microbes while the patient is in utero thus allowing them to correct them via CRISPR,creation of require synapses etc upon birth or even in utero.
Having the patient have DNA from Planarians,Hydra and A.mexicanum added will aid in this as they will do so naturally alongside the microbes.It could thus heal those already confined to wheelchairs and those that would do so in the future with this applying even to broken and twisted necks,ankles and legs as well as extreme head and spinal trauma that would otherwise be fatal or cause brain damage or paralysis when working together with strains of microbes that heal tissue and keep the brain alive.Thus adding DNA from A.mexicanum etc could allow patients to naturally repair damage that would causes brain damage,fatal injuries as well as those that would confine one to a wheelchair with microbes ability to form new tissues and also adding the DNA from A.mexicanum etc will allow those already confined to wheelchairs regain the ability to walk again by repairing any existing neural damage of the peripheral and central nervous system.This and the formation of site specific tissues could be done if they have recombinant DNA from human induced pluripotent and haematopoietic stem cells as well as Hydra,Planarians etc allowing them to form any cell and tissue in the human body when needed managed by nanomachines or chemical signals and create these and even blood cells including erythrocytes and leukocytes on an unlimited scale inside the body in the required areas through mitosis in demand to counter blood loss without injection of them or surgery provided they have enough nutrition from the host intaking extra proteins and fats etc or using up stores of these with this also having applications to neuro and muscular degenerative disorders such as Parkinsons,multiple scoliosis,alzheimers and even terminal diseases including those in living patients suffering from paralysis,parkinsons etc.This would be easier without rejection if they using horizontal gene therapy were able to receive samples of the hosts DNA from cells or if prior to them injected had samples of the hosts DNA,had their own leukocytes used as a baseline or in the case of them who receive them in utero had microbes injected with their own DNA in them to interbreed with native ones.Otherwise those with just human DNA could have the new tissues formed with anti-rejection drugs taken in by the patient through tablets or anti-rejection compounds created by the microbes that preventing the immune fighting the foreign tissue until new microbes are injected that could insert the patients DNA into the new tissue as well as biocmpatible microbes present with ideally those injected to pass on the hosts DNA being done solely for this purpose and not actual biocompatible microbes with them being flushed out or merge with the tissue as well.The nanomachines originally present in biocompatible microbes will signal to these where they tissues were formed to these extra microbes and will in term of the long term allow tissues to signal to microbes and Paean where and when they are having trouble with this in the nervous system increasing the hosts neurological computing power and even act as primitive neural implants or interact with neural implants.This could repair tears in the skin,wounds,cuts and as stated torn and perforated organs and nervous systems that would cause permanent paralysis,loss of blood using nanomachines,readings of pain sensations to locate where the perforation has occurred with erythrocytes created by then alongside plasma to prevent them running out of blood and ensure there is enough to survive until surgery and blood donations can be applied with infections fought of by them as well as immunisations and keep the brain and other vital organs alive with any necessary cells created to deal with Parkinsons,Multiple sclerosis and similar degenerative diseases.Thus they could fully repair or semi repair internal and external wounds that would lead to internal bleeding or sufficient bleeding that would lead to death until the patient can be gotten to where surgical robots or blood donations can be applied with this also applied to self inflicted wounds done to commit suicide.Ideally to repair wounds internal and external they would due to them residing inbetween tissue in all organs including the skin,brain,heart in a endospore state with vital organs such as the brain and heart having them in free form and when needed they would create biofilms,coagulants creating scaffolding through nanowires to create new tissues instantly on them when needed and illicitating the bodies own repair systems.Arteries and capillaries could be created to bypass wounds or ruptured vessels by them creating scaffolding composed of graphene and other similar nanotubes to grow tissues on with them illicitating the production of new blood in the body and creating it themselves.This could repair any organ and blood vessels in between them including those damaged by stabbings,bullets etc while the brain and other organs are kept alive by microbes or engineering.Recombinant DNA from A.mexicanum in the hosts DNA alongside that of Planarian and Hydra DNA will further aid in their ability to repair more serious wounds and perforations in the skin,arteries and organs especially those from stabbings and bullets as well as spinal injuries that would leave a person paralysed and aneurysms that would be fatal.They would also repair complications from surgery and even repair wounds that require stitches.With regards to removal of the appendix and other obsolete organs and parts of the body they can create tissues that close them off the defunct organ and also the organs tissue to undergo apoptosis removing them from the body with CRISPR treatments used to edit these out of the human genepool indefinitely.Otherwise these can be used by the microbes to store themselves in large numbers in an endospore state with them through CRISPR making them be used for other new purposes in the human body that would be added to all humans via advanced gene drive technology.Furthermore they could be used to repair or create tissues and cells in the eyes,optic nerve and ear as well as CRISPR treatments to cure deafness,damage to the eardrum,colour blindness and all forms of blindness and apply gene therapy or at least alleviate them with the same done to cure or alleviate near or short sightedness and also colour blindness and any damage to the eyes due to bright lights,glaucoma,cataracts etc and damage to the eardrum and parts of the ear caused by loud noises and infections or even birth defects.Damage to the eardrums that has resulted in deafness or reduced hearing ability will be repaired by them alongside damage to all human senses.This could even repair brittle bone diseases such as osteoporosis,arthritis caused by poor diets etc by creating new bone tissue with scoliosis possibly fixed by this alongside back pains.Broken bones and fractured bones will be repaired by them creating bone tissue while they are resting in a stable place and have them dispatched from hospitals much quicker and healed at home.Scoliosis will have new proper bones formed by them in the proper structure complete with neural tissue connected to the brainstem and the rest of the peripheral and central nervous system and then have the original bone removed via surgery once the microbes can cause the nerves and original bone connected to the central and peripheral nervous system undergo apoptosis or if not possible surgery carried out with microbes forming new permanent stiff tissue that holds a more manageable spine curvature with CRISPR treatments curing genetic defects to aid both options.Bracing can be done with CRISPR treatments and microbes forming new tissues to allow the spine to form a more normal curve and thus allow the braces to be removed with existing patients with braces have CRISPR treatments added to correct deformities and genetic defects.The microbes could create graphene,silicene and neural tissue nanotubes formed in the spinal tissue to ensure the spine is still strong yet flexible and stays in place and allow braces to be removed with accelerated healing added to the hosts genome after cured.Of course animals like chimpanzees with these conditions bred into them alongside human DNA ideally those from individual patients will be tested by having surgery and braces done,have CRISPR treatments and then microbes form tissues to see the efficacy of curing them and allowing existing patients with braces to have them removed from surgery.Spina bifida could be fixed with them forming new neural tissue that bridges gap in the case of myelomeningocele allowing the hernia to be removed by surgery once the herniated neural tissue and other tissue is destroyed by undergoing apoptosis and the herniated tissue closed off by them forming new tissue include blood vessels and skin tissue to bridge it allowing for surgery to be safer or it on command by Paean moult off from Serpentes DNA with this also applying to meningocele with the cells around the base undergoing apoptosis allowing the herniated tissue to fall off.This could be applied to other hernias and even skin tags.Recombinant DNA of Planarians,Hydra,A.mexicanum,endolithic bacteria and other species which exhibit tissue and cellular regrowth added to microbes genome could aid in this with if possible them passing this onto the tissues of key organs such as the stomach,intestines,vocal cords and oesophagus,skin,heart and arteries in humans as well as brain and muscles in the case of neuro and muscular degenerative disorders and even prevent aneurysms by inserting this ability into arteries tissues using horizontal gene therapy at risk of forming all of these forming in all patients,having ruptures also repaired by the microbes filling in the tears and the blood drawn away through surgery or the microbes creating capillaries or other vessels that draw the blood away to other parts of the circulatory system by creating scaffolding first with if possible.They could also have thin layers of elastin or graphene create by tweaked microbes to be within the artery walls to strengthen them with these arteries repaired by the microbes and heart and other vital organs kept alive by other strains.Otherwise these key arteries would have microbes collected on the walls of the arteries on a biofilm in a endospore and when relevant signals are sent awaken them and form tissues to repair the damage with them clinging to the artery walls in biolfims in their endospore state with the same applied to other key organs such as the brain,stomach,liver,heart and other ones that could be lead to death if damaged by trauma,stabbings,electrical shocks,perforations both external and internal,shootings,overexhaustion.The same could be applied to all arteries at risk of cerebral hemorrhage,aneurysm with any neural tissue damaged repaired by the same mechanisms as it dealing with strokes and the leaked blood turned into nutrients or other benign compounds or the neural tissue in the brain also engineered to resist damage from the the leaked blood.
Furthermore by them forming new neural tissue it could speed up brain and neural development in pre teens and teenagers allowing their brains to reach full maturity by the time they finish puberty by the ages of 14 at least a decade before it normally reaches full maturity thus eliminating any issues of the “vulnerable”,immature and risk taking adolescent and even pre adolescent indefinitely with this possible if the microbes action begins in utero or at least by the age of five years old when roughly 90% of the brain is fully formed.If possible this could be used to allow for all parts of the brain to be fully formed by infancy to allow preteens or even infants to have the same critical and emotional development as someone in their early 30s.Genetic engineering and germline therapy and advanced gene drive technology via CRISPR using genes made from scratch and from other animals can also make this progeria myleinisation or early maturation of the brain a decade by infancy a permanent feature of the human genepool if applied to spermatozoa,eggs and embryos and the entire patients genome in all patients across the planet using advanced gene drive technology via microbes inside the human body with this again allowing areas of the brain responsible for critical thinking,forward planning and emotions and even uncinate fasciculus which doesn’t reach full maturity until ones mid 30s to be fully mature and fully myelinated with all mass and neuron synapses formed by the time one ends puberty at 14 with this engineering preventing the neural formation from suddenly stopping or slowing between the ages of 5-14.Thus a persons brain will be fully formed by 14 allowing the body to naturally synthesise essential amino acids,omega-3 and other essential fatty acids and other essential nutrients needed for good neural development not normally produced using recombinant DNA from plants and animals to aid in this alongside those taken in through diet.During the persons first 14 years of life as result they may need extra nutrition with the presence of xerophile,oligotroph bacteria,endolith bacterias slow metaboilism or DNA from C.perfringens and E.Coli and scratch DNA designed by Phanes and Paean as well as those from A.mexicanum,Planarians etc to increase cell mitosis and growth,Tardigrade recombinant DNA added to their parents genome added to them by germline technology leading to the nutritional requirements to be lower than normal during their life from them onwards or if possible this may even allow them to consume normal amounts required by the body during these ages with their cells especially the brain requiring less nutrients to grow and develop thus negating any effect this may have on their environmental impact with regards to food with the synthesis of essential amino acids and omega-3 and other essential fatty acids and nutrients responsible for neural development manufactured by the patient through engineering also negating this with extra of these in diet coming from genetically altered bacteria and algae rather from meat and fish as well as vegetables,fruit,algae and fish engineered to produce more of them as alternatives to meat.Excess nutrients taken in by diet may through this engineering be used up in speeding this development exponentially during this period rather than simply be flushed out of the body and causing symptoms associated with their overdosing with microbes aiding in this.This could also applied to the growth of the rest of the body.Furthermore this better nutrition including the body synthesising essential nutrients alongside other engineering using scratch DNA and that from other animals may mean that puberty may officially end at 14 for both males and females with the synthesis of essential nutrients by the host and those from diet also playing a role.Once the brain is fully developed the genes from fast growing bacteria will be removed to prevent them affecting the ageing process.If there is not enough space in the human genome for these genes or if causes complications then it’s possible that stem cell strains could be used instead of genetic engineering to bring about progeria mylinisation upon birth.
Chimpanzees and mice will of course be used to test this using human recombinant DNA.The strain would also play a role in repairing ruptures both internally and externally as well as treating sufferers of paedophilia to make them exhibit normal chronopheilia by forming proper neural matter alongside CRISPR treatments with CRISPR and the formation of neural tissue also done to increase the intelligence quotient in those suffering from developmental disorders,paedophilia and the general public exhibiting normal chronopheilia and also neural capabilities.This stem cell strain using leukocytes as baseline would act as the ideal vector for stem cells using flagellum from E.coli to move around the body to where they are needed,DNA from bacteria to undergo mitosis allowing them to create millions of copies at once invivo in emergencies and when treating existing damage as they would have DNA from induced pluripotent,embryonic totipotent and heamotopatic stem cells as well as A.mexicanum,Hydra and Planarians with recombinant DNA from G.metallireducens and S.oneidensis will cause the formation of stem cells by inducing electrical charges using chemical reactions tweaked to use sugars and proteins or oils etc produced by other strains as well as heavy metals in the blood that the host can be made immune to that would be pumped into the body in sufficient levels.This DNA will allow them to form any cell or tissue in the body like blood cells.This electric charge will induce themselves into forming into the nearby or relevant cells with them have the induced pluripotency stem cell genes and those from totipotent stem cells passed onto each one that undergoes mitosis to allow them to form human embryonic stem cells to be able to form human tissues with the genes from A.mexicanum,Planarians and Hydra will allow them to form any tissues and compensate for any drawbacks that induced pluripotent stemcells have.DNA from both hematopoietic,induced pluripotent and embryonic totipotent stem cells will also aid in their ability to form any cell including erythrocytes with DNA from extremophile bacteria that exhibit telomere repair and also the homology directed repair mechanism ie homogulous recombination present in embryonic stem cells will prevent them forming tumours.Having DNA from Planarians,Hydra,A.mexicanum,totipotent and induced pluripotent stem cells in the genome of the host will allow existing damage done prior to this DNA added to the human host be more easily able to turn into human tissue without rejection.Electrical charges if not needed may be replaced by chemical signals and also instructions from Paean via nanomachines and biosynth wifi telling them to form a biofilm and cluster and then turn into any desired tissue or cell decided by Paean.The biosynth WiFi in these stem cells would induce the evolutionary path of DNA present to not only change into the patients DNA but also that of desired cell and tissue types of each specific organ ie be told to turn into neural tissues,brain tissues,heart tissues,liver tissues,vascular/muscular/skin tissues etc through Cas-9 and taq polymerase.Stem cell DNA including totipotent,embryonic and induced pluripotent stem cells DNA from humans will allow them to form any tissue and the WiFi induce them to form the DNA of the patient and specific organs etc will be needed with them housing flagellum to allow them to travel across the body and bacterial DNA allowing them to undergo mass replication controlled by Paean.Paean will thus control this strain to carry out repairs of the body in existing patients,supplement the acellerated healing phenotype and also carry out stem in vivo cosmetic surgery.Them housing haemotiopic stem cells can allow them to be changed into blood in any instance of extreme blood loss with them in all patients at all times in an endosperm state and awakened when needed.As stated earlier this will be the strain to form neural,worm and other implants in vivo by multiple microbes merging together and using DNA digital storage,electrically conductive pilli and nanowires etc to carry out their functions.The strain will be based on ones own leukocytes etc with the various totipotent and induced pluripotent their own DNA thus preventing immune responses when forming new tissues and also implants thus preventing issues with regards to rejection etc.All of the operations carried out by this strain would be controlled by Paean using nanomacinhes and also chemical signals with ideally parts of this strain having nanomchines others not with those that do controlling those that dont have them via chemical signals or them all having nanomachines and the nanomachines breaking down when new tissues are formed.This will allow the patient to have it done while at home using wifi access or fragmented forms on devices allowing cosmetic surgery clinics to be put to other uses and reduce the chances of complications and ensure a more natural shape is formed.All of these features should be available by at least 2029 with animal trials begging as early as 2023-2028 on all of the aforementioned abilities of the stem cell strain.This and other cosmetic surgeries including will ideally be only availible to those aged 14 or older to give them time to make the decision and even wait until they have finished puberty and reached adulthood.By 2035-2045 onwards they will be able to repair injuries etc instantly.
This stem cell strain will form the basis of both biosynth technology that is biosynth based electronics such as smartphones etc and also biosynth implants including neural implants that form the.basis of VR technology indistinguishable to real life.
Anti-microbial strains:
These modified leukocytes anti-microbial strains will comprise of the anti-viral,anti-fungal,anti-helminthic and anti-bacterial strains can be created from scratch that are biocompatible with and intentionally seek out pathogens such as MRSA and HIV through bacteriophage and virophage DNA and that of Bdellovibrio,M.aeruginosavorus,Paramecium,C.elegans,Cafeteria roenbergensis and scratch DNA but is benign to humans again through human proteins on its surface which can transfer genetic material such as plasmids and chromosomes via bacteriophage and leukocyte receptors,that can transmit only CRISPR gene treatments that remove resistance to previous CRISPR treatments permanently using gene drives,remove their pathogenicity and ability to illict immune responses using gene drives,remove their ability to mutate permanently or even undergo mitosis and replication,remove their resistance to every existing antibiotics/anti-viral/anti-fungal compounds they have gained immunity to permanently as well as those at their disposal and prevent them from reproducing and replicating either by themselves or infecting specific cells inside the host by altering their receptors and glycoproteins or introduce suicide genes that cause them to undergo apoptosis or even genetic faults that kill it or weaken them into specific pathogenic bacteria to allow the primary immune system to fight them within populations of livestock and patients.Other effects done by CRISPR would be to make a pathogen especially new ones and viruses and even exiting ones like HIV susceptible to one or all compounds at their disposal to kill them,remove radiorestance or any developed resistance to extreme conditions applied to them,remove their pathogenicity using gene drives with new genes for CRISPR treatments added to the microbes via upgrades,with old ones removed or them added to the same genome with the nanomachines and Paean telling them what treatments to apply with the removal of CRISPR treatments for all strains done via upgrades with genes used via this created by 3D DNA printing.Both anti-viral and anti-bacterial strains would use these against the pathogens they are designed to fight of such as HIV,superbugs but also other ones outside of these and new ones including fungi of all types to limit the genotypes in their nucleus.Anti-cancer strains will use suicide genes and those that stunt the growth of tumours and also make them susceptible to the compounds at their disposal.Suicide genes will be gained from terminator seed technology used by Monsanto with endolithic bacteria DNA halting the growth of them or those made from scratch to them prevent them undergoing mitosis,the prevention of them mutating would involve mutating blocking genes made from scratch by Phanes and also from those found in nature with advanced gene derive technology ensuring this is permanent.Other CRISPR treatments can be used created from scratch extrapolated by Phanes that prevents them undergoing replication and mitosis by inhibiting or removing the genes that allow this to happen and even remove receptors and glycoproteins that allow them to infect cells in the humans body.Those that make them susceptible to the compounds may have to come from pathogenic or ideally benign bacteria,viruses and fungi that the compounds can kill specifically DNA that expresses their outer phospholipids and protein coats with it ideally being DNA from benign species whose phospholipids and protein coats do not cause immune responds,cause pathogenicity and also allow it to infect key cells such as leukocytes,neural tissue with these genes even applied to both endo and ecto parasites.Bacteriophage DNA in phage therapy may also be part of their genome allowing for them to have receptors of these with them injecting suicide,resistance removing genes and also bypassing the cell wall to insert antibiotics including penicillin and CRISPR treatments.The anti-viral and anti-bacterial strains would have receptors engineered into them that allow them to only interact with the receptors and protein coats of all viruses and bacterial pathogens to exchange CRISPR treatments via horizontal gene transfer with if need be them directed via Paean once the species has been determined to evolve via induced evolution those to interact with the specific species with this done to prevent them applying these to the hosts cells.Automated microbiology labs that expose pathogens either viral,bacterial or fungal to large amounts of the compounds at their disposal will be done in tests to force the micro-organisms to adapt to them thus allowing for CRISPR treatments to be made that remove their resistence and also make them and other compounds susceptible to them.CRISPR treatments would occur during phagocytosis as well as horizontal gene transfer and also by simple interactions with the pathogens by interacting with the cell wall either when the cell walls are dissolved by compounds that destroy them,through DNA from micro-organisms and from scratch that exhibit horizontal gene transfer or if the CRISPR treatments can penetrate them similar to viruses and bacteriophages and virophages using the same receptors and delivery methods on them with these designed by AI cross referencing DNA from the global database of patient files,from Physis and scratch added by upgrades and 3D DNA printing.
The use of pathogen specific endolysines,anti-microbial and anti-viral compounds,CRISPR treatments to remove resistance,undergo apoptosis,become susceptible to compounds at their disposal etc for both viruses,bacterial as well as fungal pathogens would render all anti-microbial,anti-viral,anti-fungal compounds and drugs defunct indefinitely with synthetic ones created by this strain when needed and would be by law free.They would fight off pathogens the second they enter the body thus eliminate them the second infections occur alongside immunising patients against whole groups of pathogens and all strains increasing survival rates from serious infections to almost 100% making humans immune to all forms of pathogens.Both immunising against pathogens and also these microbes will also be able to fight off infections in people battling chronic infections like HIV with those suffering from HIV will have protease inhibitors etc synthesised on demand.As a result of this medical costs to all patients would be almost zero with regards to medications.
Anti-bacterial,anti-viral,anti-fungal and anti-helminthic strains will utilise CRISPR treatments to cause pathogens to undergoe apoptosis,become sucseptible to compounds at their disposal etc applied via horizontal gene transfer with them also applied by bumpers with theses strains only engineered to interact with the cells of pathogens.They will be engineered to only interact with their desired group and not human cells.Anti-bacterial strains will be enginered to only interact with bacteria,anti-viral strains engineered to only interact with viruses and do on to prevent them applying CRISPR treatments designed for pathogens affecting the patient.CRISPR treatment a form pathogens could be applied by bumpers that allow them to be synthesised and released in large amounts in the bloodstream that bounce off human cells and interact only with pathogens that can allow for hundreds or millions of pathogens to be treated with them at once.Taq polymerase and Cas-9 will be used by augmentation,ageing and anti-bacterial,anti-viral,anti-fungal and anti-helminthic strains to recreate strands of DNA used in CRISPR treatments over and over again under instructions through biosynth WiFi from Paean.
New synthetic compounds to inhibit and kill bacteria,viruses,fungi and parasites and to treat everyday conditions,cancer and neurological conditions can be extrapolated by AI analysing the structure of their phospholipds,receptors in the body and surface proteins and then have them stored on Physis in their file to be downloaded with them created by relevant strains of microbes via anabolic and catabolic reactions and applied via bumpers and phagocytosis.Scratch DNA can be extrapolated by them to produce these once DNA is downloaded by evolutionary induction.These will be developed to create compounds that synthesised in the body in the bloodstream or onsite of tumours,neurons and pathogens to deal with drawbacks of natural compounds that by cytotoxic and break down in the body.Existing synthetic compounds that inhibit or kill tumours,bacteria,viruses,fungi,parasites and treat neurological and everyday conditions will be stored here in Physis with AI seizing patents on them and them created by anabolic and catabolic reactions.All synthetic compounds will have their structure downloaded onto the digital DNA storage of each strain of microbes and created by anabolic and catabolic reactions on demand with them released onsite of receptors,tumours,pathogens etc or released as bumpers to prevent overdosing and side effects and toxicity.Anti-microbial compounds and DNA would use Cas-9 or taq polymerase to detect the genome of only pathogens and not beneficial bacteria which the vectors would exit with these native bacteria also made immune to these genes,endolysines and anti-microbial compounds in the genome capsids.This would also apply to lemon juice and romidepsin and also natural compounds that cause side effects with them all also applied during phagocytosis with these bumpers allowing the whole lymphatic system and bloodstream to be flooded with anti-viral,anti-microbial and anti-cancer compounds without causing any side effects except increased urination and possibly defection to remove excess.Any effects that the body would experience would be counteracted by the microbes treating symptoms by modifying healthy cells to be unaffected and or treat the cells on the effects by creating counter proteins with contradictions done by breaking down the synergistic compounds.Bacteria could be exposed to the compounds that cause side effects to allow them to produce genes to counteract them to then be added to patients who are at risk of requiring said compounds ie their geographic location,where they are going on holiday etc and thus allow the hosts cells be unaffected with this done in automated labs against all natural and synthetic compounds for strains that fights off all pathogens whether viral,bacterial or fungal and parasites.Thus exposing bacteria to compounds that cause side effects to humans will be done to create new genes to counteract these that can be added to the genome of patients thus meaning the natural or synthetic compound will affect only pathogens,parasites and tumours or everyday conditions such as gout,zits etc to ensure that side effects will be avoided with the microbes also applying all compounds whether natural or synthetic to the site of action or to the surface of parasites and pathogens and as nanoparticles to prevent overdosing,synergistic effects and limit side effects as it will be applied directly to where it is needed as nanoparticles and not taking up space in the bloodstream.Thus the nanoparticles will be created directly onsite of where the problem is occurring and not flooding the bloodstream and will be instantly used up with any excess not used broken down by the microbes into benign compounds straight away or flushed out of the body by having them covered in proteins thus limiting side effects and also synergistic effects.Furthermore bumpers can be used to eliminate side effects.Otherwise the compound could be applied during phagocytosis and horizontal gene therapy when the microbes attach to the surface of tumours,pathogens and parasites rendering healthy cells in all parts of the body to be resistant to the compounds used with this removed from tumours.This will also limit synergistic effects with the microbes also breaking down any alcohol and grapefruit juice and any other natural or synthetic synergistic compounds detected by the microbes and implants turning them into benign compounds to prevent any interactions before and after applying the compounds with Paean instructing patients not to consume alcohol and other synergistic compounds when and before he applies both natural and synthetic compounds.Alcohol and grapefruit juice will be broken down by other strains while the bumpers prevent the compounds interacting with them with the levels of alcohol and grapefruit measured in the body by implants.The fact that only a small amount of the compounds will be applied will limit overdosing and synergistic effects with the microbes breaking down any excess into benign compounds.Protein bumpers will also allow for them to be applied in a way to limit side effects and synergistic effects as large amounts of them can be released into the bloodstream and interact only with tumours and pathogens as well as desired neural and muscular tissue and bounce off regular cells and are unable to interact with other compounds such as grapefruit juice etc that cause synergistic effects and thus be flushed out of the body.All synthetic compounds both existing and new ones to treat viruses,bacteria,fungi and parasites including those not only on Earth but also on colonies and planets across the universe and everyday ailments such as gout,acid reflux,diarrhoea and neurological conditions will have their structure uploaded to Physis to be stored forever and when needed anti-viral,anti-bacterial,anti-helminthic strains and those to treat everyday conditions and neurological conditions will be able via biosynth WiFi download their structure and store them in their biological DNA digital storage and then have them produced by anabolic and catabolic reactions in required amounts onsite of the pathogen and parasites outer structures and onsite of receptors in the body to avoid side effects,overdosing and synergistic reactions with or without bumpers using nutrients gained from food intaken by the body.This use of protein bumpers could be used to transfer suicide,susceptible and resistance removing genes as well as others such as to remove their pathogenicity,preventing them undergoing mitosis to pathogens when flooding the bloodstream to kill or modify millions of bacteria at once alongside horizontal gene transfer to allow for the pathogen to be killed off by microbes using antibiotics or them taken in pill form.Again these would be designed to attack specific or whole orders of bacteria and viruses and not beneficial ones due to the mini vectors detecting the specificity DNA of only pathogens by taq polymerase and Cas-9 and exiting beneficial bacteria cell walls and human cells with them released into the bloodstream etc and then interacting with the cell wall and once inside would change the DNA via CRISPR allowing this to alter pathogens and even tumours to allow the microbes to them release anti-viral and anti-microbial compounds in the bloodstream with this more efficient than doing this during phagocytocis as it would allow for countless pathogen cells to be altered at once and allow for the microbes to carry out their work.Ideally both DNA strands and anti-microbial compounds in bumpers would have Cas-9 and other proteins that house it and taq polymerase to read the DNA allowing only pathogens to be affected and beneficial bacteria ignored or beneficial bacteria could be made immune to the proteins that can only be suited to pathogens whose DNA would be read first by base microbes and then who would signal to the anti-viral and anti-bacterial strains to create specific protein bumpers for each pathogen that can interact only with its specific cell wall using possibly recombinant DNA from bacteriophages.Base microbes would do this for known and also new pathogens.Thus these bumpers would not only prevent the anti-viral,anti-cancer and anti-microbial compounds affecting healthy cells and also beneficial bacteria it would also prevent the compounds as well as DNA from being broken down by the body before it enters the tumours or pathogens and reaches the site of action and also allow them to be flooded around the body in large amounts using the lymphatic system and bloodstream to reach hard to reach places.Before microbes are perfected and to compliment them the compounds and genes to treat cancers,HIV and resistant pathogens DNA and compounds could be injected into a persons bloodstream covered in these bumpers with them tested on animals this way.Ideally though genes from scratch could be applied to the hosts cells to make them immune to the compounds.For those to fight cancer,HIV and pathogens like MRSA one could have every single one of billions or even trillions of microbes releasing large amounts of it in the body flooding all systems and it would affect the host at all except of course possibly forcing them to urinate excessively to remove it.This would mean that a person could be cured of tumours and all types of viral,bacterial and fungal infection without even noticing it before symptoms and seroconversion occur
AI such as Phanes and Paesn will cater to extrapolating compounds to be added to anti-microbial strains that are subdivided into those that fight off bacterial infections,viral infections and fungal infections.
Antibodies to viruses and bacterial such as tri-specific antibodies that attack 99% of HIV strains can be gained by having the structure of these antibodies analysed,charted and added to the Physis file of HIV to allow them to be downloaded ori the DNA storage of antiviral strains and synthesised by anabolic and catabolic reactions.If possible Phanes,Paean and Epione analysing the antigens and other surface structures of all known pathogens and parasites on Earth and newly discovered ones on extrasolar colonies will extrapolate synthetic antibodies that can be stored on their Physis file to be downloaded on the the DNA digital storage of anti-bacterial,anti-viral,anti-fungal and anti-helminthic strains through biosynth wifi and synthesised using catabolic and anabolic reactions with the same done for even venoms for plants and animals of all types.All strains of each species of viral,bacterial and fungal pathogen and parasite will be analysed and the antibodies stored in their Physis file with the structure of the antibodies downloaded into digital DNA storage when infections are detected by base microbes and in the case of already infected individuals of chronic infections such as HIV.This would be done alongside immunisations to create super antibodies that attack critical parts of a pathogen and can destroy them more easily alongside those from immunisations.This would be easier than getting DNA from patients and having to expose patients to the specific strains which could be impossible as these antibodies occur in only specific conditions with it also allow the antibodies of all other pathogens to be stored once analysed by Paean,Phanes etc with it available to all patients instantly and also can be done to new pathogens invivo once their genome is scanned by base microbes.It can also be done to parasites both known and new especially deadly ones and can allow them to be created on demand in both chronic and newly infected patients simply through access to wifi with this also doing so for strains of HIV outside those that N6 and tri-specific strains work on and work alongside immunisations to quickly defeat infections.Known antibodies of HIV such as N6 and tri-specific ones will be added to their pathogens species Physis file to be downloaded into microbes and then synthesised.Thus the outer structure of all known and new pathogens whether viral,bacterial or fungal including all strains and even parasites surface protein antigens will be analysed especially the antigens by Phanes,Paean etc to allow for synthetic antibodies to be extrapolated by them and their structure stored in the pathogens and parasites Physis file and then downloaded onto microbes and synthesised by anti-bacterial,anti-viral,anti-fungal and anti-helmitic strains on demand using anabolic and catabolic reactions once their structure can be downloaded into the relevant strains of microbes within DNA digital storage in using biosynth wifi in both new and chronic infections once the specific strain is analysed by base microbes scanning their genome.This will be done for all of them including V.major,Y.pestis and even those that cause minor illness.It will also be done for all species of bacteria,fungi,viruses and parasites on Earth and other planets across the universe once they are discovered including those that affect animals that could be potentially become zoonoses to allow them to be downloaded should they be become a threat.The patient would be told to consume specific fats,proteins etc to provide elements for the microbes to antibodies to be created this way.New pathogens and parasites when they have their genome scanned invivo and in labs will be analysed for their antigen structure to be then have antibodies extrapolated instantly and then redownloaded once CRISPR treatments prevent them undergoing mitosis.Existing known antibodies such as the aforementioned N6 and tri-specific antibodies to fight HIV and other pathogens created by specific populations of both humans and animals will have their structure be added to this database to then be downloaded and created by them.Even antibodies created in response to all known vaccines including Polovirus,Ebolavirus etc will be added to this database once extrapolated by AI and also infecting vaccinated patients and taking blood samples with antibodies for parasites extrapolated.Phanes will extrapolate genotypes for each synthetic antibodies extrapolated to be added to microbes through biosynth WiFi and the patients genome including bone marrow via gene therapy to allow them to allow the patients leukocytes to create themselves through chemical signals from microbes and Paean with these stored in Physis.Paean will analyse the outer structure of bacteria,viruses,fungi,parasites to extrapolate synthetic antibiotics,anti-viral,anti-fungal,anti-helminthic synthetic compounds that can kill them but not harm the patients cells which can be stored in the species Physis files and them synthesised by anabolic and catabolic reactions.Phanes can extrapolate DNA to express these compounds that can be downloaded via WiFi into relevant microbe strains.Paean and Phanes will also analyse their structure extrapolate endolysines and receptors specific to each species and strain of pathogens whether bacterial,viral and fungal and even if possible those for parasites that will be stored in each pathogens Physis file and then downloaded when needed speeding up the process of the anti-viral and anti-bacterial strains creating relevant endolysines for pathogens.AI will extrapolate synthetic compounds to treat each pathogen and parasite that can be stored in their Physis file and them downloaded into microbes and created by anabolic and catabolic reactions.Receptors for anti-viral and anti-bacterial strains to interact with each species of pathogens including viruses,bacteria and parasites will be extrapolated and changed by biosynth wifi to adapt to new infections.Endolysines for each species and strains of bacteria,virus,fungi,parasites will be extrapolated to be downloaded when needed.Also extrapolated by Phanes will be genes that can make the host resistant to them from scratch ie those that prevent pathogens particularly viruses and parasites infecting and damaging specific cells and organs to be applied to the host and then stored in Physis in the pathogens and parasites file to be downloaded when needed with existing genes present.Genes to prevent each toxin interact with a patients cells can be extrapolated.DNA from asymptomatic carriers can be analysed.The genotypes that expresses surface proteins of immunising strains will be analysed and extrapolated with the common proteins of entire taxonomic ranks extrapolated anf stored in their Physis file.Also CRISPR treatments for preventing them undergoing mitosis,replication and also apoptosis as well as those to counter resistance to all new and existing compounds will be extrapolated and stored in Physis for them to be downloaded when needed.Parasites will also have their genome and outer structure analysed for this.AI could also instead of analysing the outer structure of pathogens and parasites could instead have Phanes analyse their genome or do this alongside analysing the outer structure of them to determine the synthetic compounds and antibodies with analysing their genome allowing them to more effectively extrapolate compounds,antibodies and the scratch DNA to express this.All of this by 2023-2029 onwards may take at least a few hours or few minutes per species with fragmentation allowing them to do all species worldwide within a few months or days.All newly discovered species of microorganisms and parasites across the universe will undergo this.Counterproteins,enzymes and antivenom to all toxins,poisons both natural and synthetic and even to date rape drugs,toxic gases/liquids/solids etc and heavy metals and pesticides etc will be extrapolated again via AI extrapolating them from analysing the compounds structure all stored in Physis etc will be extrapolated this way too and stored to be downloaded instantly and synthesised by anabolic and catabolic reactions to allow the toxin to be neutralised.Thus the structure of all known poisons,toxins etc from heavy metals,those created by poisonous plants and animals in their leaves,fruit,stings and bites etc will have their structure analysed by AI namely Paean etc and them then extrapolating the structure to counterproteins etc which will be added to the Physis file of that element and plant and animal etc that produces them in subfolders.Bumpers for each species and strain of pathogen and parasite as well as compound will also be extrapolated this way and downloaded.The AI will also do this to create synthetic compounds to fight viral,fungal and bacterial pathogens and parasites with these stored on the augmentation sub network in Aesculapius and them also downloaded with if possible the AI also extrapolating scratch DNA to add to microbes to create these and counterproteins.These counterproteins,antivenom,antibodies,bumpers and endolysines etc will be stored in the pathogens,parasites and compounds file within Physis and will be downloaded when need via wifi,public wifi,cellular access to the wire and even satellite wifi allowing them to be created and stored on digital DNA when needed and deleted when not to allow for them to be synthesised in the body via catabolic and anabolic reactions when the specific pathogen or poison is detected.Thus AI will starting in 2023/2024 scan the outer structure and DNA of all species and all strains of parasites,non pathogenic and pathogenic micro-organisms whether viral/fungal/bacterial etc and that of all poisons,toxins and synthetic compounds to extrapolate synthetic antibodies,synthetic antibiotics/antiviral/anti fungal/anti helminthic compounds,bumpers,endolysines,receptors,counterproteins,antivenom whose structure will be stored in relevant folders in Physis to be synthesised on demand using catabolic and anabolic reactions by relevant strains or when possible scratch DNA can be created to synthesis them and also counter CRISPR treatments to resistance genes with them also stored in Physis in the pathogens,parasites,elements and plant and animals file to be downloaded instantly via wifi and stored in digital DNA storage in the relevant strains once the base microbes determine the genome and structure of the invading pathogen,parasites,toxins etc and induce all of the microbes of these strain to awake from endospores and then create these genes via inducing evolution of the strains genome via wifi and taq polymerase and Cas-9 or the antibodies,bumpers,counterproteins can be synthesised via anabolic and catabolic reactions.All of these antibodies,counterproteins etc structure and genotypes of scratch DNA will be added to the file of each species and strain of bacteria,fungi,virus and parasite and poison in Physis and once detected by base microbes the structure will be downloaded into the digital DNA storage and then synthesised by anabolic and catabolic reactions.Work on this can start as early as 2023/2024 by proto Paean and Phanes doing this using the worlds supercomputers merged together or networks within universities and hospitals around the world.The patient once they are infected or in the case of existing infected patients will be required to consume specific fats,proteins and carbohydrates by Paean in specific amounts to provide the necessary elements for these to be synthesised.If possible genotypes can be extrapolated by Phanes and Paean from scratch to be added to both microbes and the patients own genome to express the production of antibodies,bumpers,antivenom naturally both before and during infections.Work on this done by proto Phanes,Paean etc can begin as early as 2023 using computers and networks around the world so as to be finished by 2029.All of this wil be done for all existing known species aand strains of fungi,viruses and bacteria including both pathogenic and non pathogenic species and strains.When any new pathogens arise from zoonoses etc then the new strain can have all of this information extrapolated within about 24-168 hours to be distributed globally through 3D DNA printers.This will be replicated on each colony outside of Earth once phylogenetic trees and their version of Physis is set up.
Phagocytosis controlled by Paean can be used by anti-bacterial,anti-viral,anti-fungal,anti-helminthic strains to apply to the anti-microbial compounds directly into the site of the pathogen to prevent it breaking down in the bloodstream and causing cytoxicity to the patients cells or allergic reactions.Applying compounds via phagocytosis via these strains housing macrophage DNA can also be used with or without bumpers and in the case of tumours the compounds can synthesised onto the surface and also onto receptor antigens.Once it is killed the pathogen and parasite can be consumed using enzymes including those devised by Paean etc for each individual species of pathogen to give the microbes nutrition.For compounds that don’t break down in the bloodstream or cause cytoxicity these can be synthesised in large amounts in the bloodstream.Anti-viral,anti-bacterial,Anti-fungal,Anti-helminthic strains will house macrophage DNA to allow them to carry out phagocytosis and also aplly enzymes,anti-viral,anti-bacterial etc compounds to pathogens to the surface of parasites and pathogens to limit cytotoxicity and also consume them as a food source once killed.Ideally they should have recombinant DNA from human leukocytes to produce specific antibodies,create new ones from scratch,send these to the primary immune system and also contain the necessary receptors to interact with specific pathogens especially the GP120 glycoproteins of HIV.Macrophage DNA will allow anti-bacterial,anti-viral,anti-fungal strains apply anti-viral,anti-bacterial,anti-fungal,anto-helminthic strains apply anti-viral,anti-bacterial,anti-fungal,anto-helminthic compounds either synthetic or natural onto the surface of parasites,pathogens to prevent cytoxicity to the patient or prevent them breaking down in the bloodstream and allow them to consume pathogens and parasites after they have been immobilised and killed by antibodies and compounds or kill them via applying synthetic and natural enzymes.Application as nanoparticles would allow single molecules of both natural and synthetic compounds to be applied to the site of action in controlled amounts to prevent toxicity and thus in levels lower than what is present in conventional methods of administration such as injection,tablets,liquids.The ability to apply synthetic and natural compounds as nanoparticles onsite of receptors will allow them to be applied to infant and pre adolescent patients without toxicity especially when they cannot be normally applied to them due to the smaller body size of infants and pre adolescences who would be unable to break them down or excrete them normally.Bumpers could allow them to be released in large amounts into the bloodstream by microbes to prevent them breaking down in the blood,stomach etc due it internal homeostasis and interact only with pathogens,parasites,tumours and receptors in the body while bouncing off healthy cells preventing ctotoxity and allergic reactions.Synthetic and natural compounds can be exposed in large amounts or starting at small amounts to force them to develop evolutionary countermeasures and genes that can be added to Physis and then added to all cells in a patient via CRISPR thus allowing them to be in cases where they don’t break down in the body to be released without bumpers in large amounts without cytoxicity and allergic reactions with bacteria used as they due to fewer genes able to adapt much quicker to compounds.Bacteria will be exposed to these conditions as they evolve much quicker under environmental stress due to fewer genes.
Bumpers to transport compounds fight off pathogens,parasites and tumours and also deliver CRISPR treatments will be extrapolated via AI.Compounds like melittin and lemon juice could be created by them released in the bloodstream as nanoparticles with natural or synthetic bumpers synthesised by the microbes that dont affect the host but only the pathogen with the same applied to other compounds to fight pathogens and also tumours especially synthetic ones that harm the host including chemotherapeutic compounds etc to fight HIV and MRSA with this meant to interact with only tumours and the pathogen by them interacting with their unique surface proteins and structures and not the hosts healthy cells rather simply bouncing off them preventing the compound affecting the hosts cells with the bumpers attaching to the unique surface proteins etc of pathogens and tumours and insert the compounds into the pathogen or tumours interior or surface by tricking the pathogen or tumour into believing it is food or other nutrients key to its survival or be synthetic versions of receptors that it needs for replication or reproduction where the compound will be used up with excess ones not used up released by flooding the lymphatic and bloodstream would be flushed out during defecation and urination and collected in sewage treatment plants to be turned into benign substances or used to treat pathogens there alongside the other measures or would be broken down with the compounds and bumpers recycled.The excess bumpers if natural ones could be used up as energy by both the microbes and the host with synthetic ones collected in sewage treatment plants.These bumpers could be natural or synthetic proteins possibly buckyballs and lectines as well as other oligosaccharides synthesised by the microbes that interact with the unique surface proteins of pathogens or tumours acting as a delivery system that forces the anti-microbial,anti-viral and anti-cancer compound onto the surface or interior of them to allow them to work while ignoring and unable to react with the unique phospholipids of healthy human cells and would break down once the compound it delivered is used up or be flushed out of the body though urine and feces.These natural or synthetic bumpers would be created by anabolic and catabolic reactions by microbes surrounding the anti-viral,anti-cancer,anti-viral etc compounds that surrounds the compound and would be done to ensure the compound interacts only with tumours and specific species of pathogens and also parasites preventing cytotoxicity and would also be fond to ensure they would not break down in the body in the bloodstream etc due to as stated they would bounce off healthy cells and only interact with desired pathogens and parasites that will be suited to interact with their specific cell walls,phospholipids etc by tricking them into believing they are food to allow them to be forced onto the surface or internal cytosol and if not used up will be flushed out of the body through urine and feces to be broken down by algae in sewage treatment plants and radiation etc treatments or be broken down by microbes and turned into benign compounds like nutrients.They would be those unable to illicit an immune response and also contain proteins from the human body.This would also be used to transport compounds that break down in the body particularly the bloodstream very easily thus allowing them to survive the pH,temperature and even internal homeostasis of the entire body preventing them being transported to the site of action.It would also prevent the compound being used to attack viruses,bacteria etc to not induce cytoxicity thus harming the patient as they would when in contact with a human cell or tissue bounce off them until they come in contact with the pathogen etc and would if not used up be flushed out of the body through urine,feces etc with the bumpers themselves unable to break down in the body or interact with human cells.Endolysines could use this to interact with only pathogens and not beneficial bacteria with CRISPR treatments delivered this way as well attacking only pathogens as well and not human cells.The use of bumpers would allow anti-viral,anti-bacterial etc compounds to be synthesised in large amounts in the bloodstream by microbes,be transported across the bloodstream and also lymphatic system and thus attack large amounts of tumours,pathogens and parasites at once in one go and without affecting the hosts body at all.These bumpers would allow the compounds to be synthesised and released in large amounts and spread across the entire body through the lymphatic and vascular systems and hard to reach places without breaking down or inducing cytoxicity and thus causing damage to the patient with the bumpers either natural or synthetic synthesised by them at the same time as the compounds are synthesised.Thus bumpers would deliver compounds to specific pathogens and tumours etc as by interacting with their phospholipids and bounce off healthy human cells but also allow them to travel to them without breaking down due to stomach acids,compounds and pH in the blood etc allowing them to travel all around the body until they find their target pathogen and force themselves into the pathogen or excess flushed out of the body through urine,feces and sweat.It would also be used to primarily transport compounds that would irritate or be toxic to humans cells and thus be used to transport it safely around the body without damaging the host.These attack the surface proteins and phospholipids or trick them into believing it is food and would bounce off human cells.Beneficial bacteria such as gut flora would be unaffected.The bumpers would allow millions of bumper coated nanoparticles of anti-viral/anti-microbial/anti-cancer compounds and also endolysines and CRISPR treatments to be released by millions of microbe at once to use the lymphatic system and bloodstream to reach hard to reach places and also attack viruses,bacteria,fungi all around the body at once with excess flushed out of the body in the form of sweat,urine and feces.Research into the best natural oligosaccharides or protein for each compound including those from humans and for each species of pathogen etc can be started in animal trials using animals with human recombinant DNA using their proto microbes based on their leukocytes starting as early as 2023with those used in humans being human proteins/lecitins/oligosaccharides that dont cause an allergic reaction or contain human proteins with this done simultaneously worldwide.Microbes should be by 2025-2029 be able to determine via base microbes to scan the genome of pathogens strains to create suitable bumpers that bounce off healthy human cells and beneficial bacteria and only affect the desired pathogen.The bumpers used in studies by Washington University of Medicine used for melittin should be investigated as a possible vector to be synthesised by microbes.Synthetic bumpers can be synthesised using anabolic and catabolic reactions.AI will scan the outer structure of all species and strains of pathogens,parasites,toxins and also tumours and extrapolate unique bumpers for each one with them synthesised by anabolic and catabolic reactions and through scratch DNA.CRISPR treatments can be applied to pathogens etc using bumpers that allow them to be synthesised in large amounts to affect hundreds of pathogens at once.CRISPR treatments to treat ageing and also augmentations could be released this way allowing millions of cells to be treated at once with cells already containing the DNA rejecting excess DNA which would pass through the cell and then enter another with again excess flushed out as treated cells would have built in markers that prevent the secondary DNA being reapplied.CRISPR treatments used by anti-viral,anti-bacterial,anti-fungal and anti-helminthic strains to cause pathogens to undergoe apoptosis and become susceptible to compounds at their disposal will use bumpers to allow them to be synthesised and released in large amounts to affect to thousands of millions of pathogens etc at once with again them bouncing off human cells.These bumpers when synthesised ontop of anti-viral,anto-bacterial and anto-cancer will allow millions of these compounds nanoparticles to be synthesised by microbes on demand to floor the bloodstream that bounces off healthy human cells but interacts with any pathogens and tumours they interact with to them kill off large numbers of them at once and excess bumpers flushed out through feces and urine.CRISPR treatments for humans either anti-ageing treatments and augmentations will be synthesised to affect hundreds or more cells at once with anti-viral and anti-bacterial strains synthesise them in large numbers to interact with pathogens and after the genome of countless ones at once while other bounce off human cells and excess flushed out of the body by feces and urine.This mass synthesise can be done by microbes on demand via Biosynth wifi.Bumpers will be needed to be also be suited to the compounds transported so it will analyse the structure of them to be customised for them.These could transport anti-viral,anti-cancer,anti-helminthic,anti-microbial compounds as well as endolysines and even CRISPR treatments acting as a mini vector and since bypassing the cell wall and applied in copious amounts would possibly negate issues of the pathogens gaining resistance with any resistance formed negated by CRISPR treatments to remove this also applied by bumpers.Having base microbes scan the genome using taq polymerase and Cas-9 would allow for the bacterias cell wall and genome to be ascertained thus allow for them to determine the species and strain and then download from Physis produce protein bumpers suited to pathogens either specific species and strain or whole orders and families of them and not beneficial bacteria thus allowing DNA,endolysines and also anti-microbial and anti-viral compounds to be sent to the correct pathogens with the protein bumpers containing DNA passing out of beneficial bacteria or bumping off the cell wall.If possible all major pathogens would have their genome and outer cell wall scanned by Phanes and Paean beforehand to program into base microbes to then signal to anti-viral and anti-bacterial strains what bumpers to produce once they scan their genome.Nanomachines,Paean,DNA digital storage and also neural synapses in the microbes could remember forever the specific proteins to be used for specific or even all pathogens with the same for them learning the correct universal or species specific endolysines to be used.If possible like endolysines they could have receptors or proteins that interact with only desired pathogens and not beneficial bacteria with beneficial bacteria having DNA in the genome capsid to protect them from the specific bumpers in their genome capsid.If possible base microbes could scan the DNA of pathogens and then create protein bumpers suited for that specific pathogen or have this already built in via upgrades with other microbes sent these proteins through chemical signals,Paean and also horizontal gene transfer or creating bumpers in large amounts that seek out and interact with anti-microbial and anti-viral strains to then cause them to replicate these bumpers to house CRISPR treatments,endolysines and anti-viral compounds.
Protein and oligosaccharide bumpers or those that have structures similar to the receptors they interact with will be used to flood the bloodstream with the DNA acting as mini vectors by intercepting the cell wall and then placing the gene in the exact spot with if need be Cas-9 part of these bumpers with the strains of microbes housing the Cas-9 protein in them for those applied via horizontal gene transfer.The surface and receptors of the microbe interacting with that of the pathogen will also determine this alongside signals from Paean determining what to apply and when.Protein bumpers can also act as mini vectors to bypass the cell wall and apply their CRISPR treatments alongside horizontal gene gene transfer during phagocytosis.Advanced gene drive technology will make these alterations permanent to any pathogens applied and thus allow a modified pathogen and its successors through mitosis to be unable to attack certain cells ie leukocytes,be benign and lose its ability to induce an immune response or caused damage to the host,remove resistance to the entire genepool to antibiotics,render them unable to replicate and mutate permanently,modify it to become susceptible to compounds at its disposal with if possible two or more CRISPR treatments added to the pathogen at once to improve success in curing infections especially new pathogens but also existing ones such as superbugs and HIV with gene drive technology used for effectiveness.If possible all of these CRISPR treatments can be applied by microbes flooding the lymphatic system and bloodstream with protein bumpers containing these that would interact with only the unique cell wall walls of viruses and not human cells.This would allow millions of pathogens to be altered at once with multiple genes added with advanced gene drive technology to each one in separate bumpers or super bumpers that contain multiple strands of DNA to be inserted at once thus disabling them at once in multiple ways while the other microbes or the same ones can then apply anti-viral and anti-microbial treatments at once by being flooded in their bumpers it is done with the excess bumpers flushed out of the system.This protein bumper system would act as means to release the DNA strands into the pathogens interior body and thus alongside Cas-9 hidden in the bumpers will put these genes into their specific place with the protein as a mini vector.Beneficial bacteria could be engineered with the same protective CRISPR Cas-9 methods as S.pyogenes against them and the proteins suited only to the walls of pathogens and even have proteins on them.These bumpers synthesised by both anti-viral and anti-bacterial strains would be composed of proteins or oligosaccharides dependant on the species of pathogen and parasite determined by implants and base microbes collecting DNA and relaying it to Paean once using taq polymerase and Cas-9
Bumpers both natural and synthetic can be extrapolated by AI analysing the DNA and surface proteins of all species and strains of pathogens whether viral,bacterial and fungal as well as parasites and would allow for each compound to be thus be stored in each species file Physis and be downloaded when an infection occurs.This use of bumpers would be used in dealing with chronic and serious infections such as MRSA and HIV where the pathogen is in large numbers in all parts of the body and tumours in hard to reach places in the body such as the brain,prostrate and other parts connected by the lymphatic system and bloodstream and can be used also next to pathogens or tumours again to prevent it breaking down in the body.The opposite method flooding is where the compound can be released as nanoparticles without bumpers and would be used to prevent the compound causing damage to healthy cells and preventing it breaking down in the body as it would naturally bounce around the body and would be used primarily in close proximity but could be using the the lymphatic system and bloodstream.If possible universal bumpers can be created that attack and intercept all bacterial pathogens and viruses including both gram negative and positive bacteria that dont affect beneficial bacteria either through specificity or even by having beneficial bacteria have immunity added via inserting DNA into genome capsids to cause the bumpers bounce off them by giving them the same cell wall structures as both healthy cells and microbes with them also preventing certain compounds not just affecting healthy cells eliminating side effects but also preventing them breaking down in the body before they reach the intended target.Bumpers that interact with the surface proteins of microbes can be used in upgrades to ensure they interact solely with them and not pathogens with their also bumpers used to interact with human cells to transfer augmentations and also anti-ageing treatments.To prevent the off chance of them becoming pathogens that would be immune to even microbes beneficial bacteria could have genes added to their genome capsid that prevent them mutating naturally without CRISPR treatments applied in the form of upgrades to develop the ability to cause harm to the host species with them also given immunities to the anti-microbial compounds used by microbes held in their genome capsid with if need be CRISPR used to remove this ability to mutate but its still preserving their ability to create genetically divers progeny.These bacteria would also be given immunities to all antibiotics,anti-microbial compounds,radiation,antibodies etc via upgrades to the genome capsid DNA.DNA that using CRISPR through bumpers would remove resistance to antibiotics,cause apoptosis and also cause pathogens to become susceptible to anti-viral and anti-microbial compounds at their disposal,prevent it mutating and unable to undergo replication and mitosis would be delivered into tumours and millions pathogens using these protein bumpers allowing for millions of pathogens to be affected at once and then allow the pathogens to be affected by flooding of antibiotics and anti-microbial compounds.Endolysines can be delivered this way alongside CRISPR treatments using gene drives that remove resistance,pathogenicity,ability to undergo mitosis and mutations,undergo apoptosis as well as make them susceptible to compounds at their disposal etc as detailed earlier on can be delivered this way ensuring they enter the pathogen cell and no healthy cells.They could as stated trick the pathogen or tumour into thinking it is food or nutrients key to their survival and also be a shell like structure that covers them but is broken by the tumour or pathogen once inside and them then killing them with the DNA or even endolysines unaffected or ideally the protein would act as a mini vector themselves to deliver DNA alongside the Cas-9 protein in the bumpers,endolysines and also anti-viral,anti-microbial and anti-cancer compounds directly to the site of action whether in the inside or exterior of tumours and pathogens and then break down after application or be flushed out of the body to ensure the DNA and compounds is delivered efficiently.In the case of DNA the protein bumper would house the DNA and also Cas-9 that needs to be used to have it delivered to the correct area with in the case of compounds and endolysines the bumpers would deliver it to the cell wall or even its interior where it would immolate it from the inside out and attack the pathogens DNA from the inside out beyond repair.DNA strands that attack them in multiple ways ie make them susceptible to compounds to the microbes compounds,unable to be pathogenic,have genetic faults that would be deadly to ,unable to attack the host or infect cells including leukocytes,prevent them undergoing mutations and mitosis,remove resistance to all antibiotics and make them susceptible to compounds at their disposal,add suicide genes etc will ideally be applied through super bumpers that contain two or more DNA strands added with advanced gene drive technology that carry out these functions and then once the pathogen is disabled and rendered inert as much as possible leaving it susceptible to both the primary and secondary immune system the microbes then can apply one or more compounds in one bumper and also super bumpers that contain two or more compounds as well as endolysines to attack them at once both externally or internally with other compounds that dont need bumpers applied at once together to ensure maximum efficacy.These DNA treatments will disable pathogens by causing many to undergo apoptosis,others to be unable to infect cells such as leukocytes for replication,unable to undergo mitosis thus keeping their numbers stable and under control and unable to be able to gain resistance to radiation,make them be able to be killed by the anti-microbial and anti-viral compounds as well as remove their resistance to existing antibiotics at once ideally multiple ones at most and thus keep infections under control while the immunised primary immune system and other microbes attack them all at once with all weapons at their disposal.Those that mutate rapidly such as MRSA and HIV will have genes that disable their ability to do so and also those that prevent them being able to infect leukocytes by removing their GP120 glycoproteins.Superbumpers can deliver two or more genes to the pathogens with all types of DNA attacks would be delivered at once via them and the bumpers being flooded around the blood and lymphatic system.Flooding of the lymphatic system and bloodstream would be the most efficient method to allow DNA,compounds and endolysines to as it allows for millions or billions of pathogens to be affected instantly added with advanced gene drive technology and then allow the same or other microbes to use secondary compounds ie those that the pathogens and tumours are now susceptible to via altering DNA and even removing resistance.If possible pathogens will be bombarded with both resistance removing genes,those that prevent it undergoing replication or mitosis,and modifying genes and compounds that can now kill it at once to kill it instantly.The various strains would create unique bumpers for both the unique compounds and pathogens and could be either natural or synthetic as well as being bumpers for natural or synthetic compounds that can negatively affect healthy cells.AI such as Paean and Phanes will analyse the outer structure of all species and strains of bacteria,viruses,fungi and parasites and tumor types to extrapolate bumpers unique to each of them individually that don’t affect others or human cells that will be stored each species Physis file to be downloaded onto DNA digital storage on microbes and created by anabolic and catabolic reactions with it also extrapolating scratch DNA to allow for this to be created by downloading DNA into the microbes genome again stored in each species Physis file.These bumpers would be used to transport the natural and synthetic compounds to prevent it breaking down in the bloodstream and also preventing cytotoxicity in the case of those that can cause damage to cells and tissues and thus pain as well as organ damage that could be fatal.If possible Phanes could extrapolate scratch DNA or have bacteria exposed to the compounds that causes them to undergoe evolution to develop genetic mutations and countermeasures that can be added to the genome of patients thus prevent the compound carrying out an allergic response or damage to the body thus allowing natural compounds that don’t break down in the body to be released in large amounts to interact with the pathogen and tumour.
The hosts native cells using scratch DNA could be made immune to the cytoxic compounds using scratch DNA with the same done to beneficial bacteria.This can be done by using bacteria that are human bacteria hybrids containing human DNA exposed to the anti-viral,anti-microbial compounds in increasing amounts and then causing them to undergo evolution to pick out desirable genes.Genes can also be extrapolated by Phanes.These genes will be added to all cells in the body during an infection and them making the patient immune to synthetic and natural compounds thus allowing the compounds to be released in large amounts without inducing cytotoxicity and immune responses without bumpers.They can be removed after the infection is cleared.
New pathogens whether viral,fungal or bacterial and even new parasites could also be modified via CRISPR applied to the pathogen either viral,fungal and bacterial to become susceptible to the anti-viral and anti-microbial compounds at the microbes disposal,remove their pathogenicity and ability to undergo mitosis etc or cause them to commit apoptosis during phagocytosis or by flooding the DNA added with advanced gene drive technology in protein bumpers that act as a mini vector to place the DNA in correct areas of the pathogens genome allowing millions of pathogens to be affected at once with this also used for existing pathogens outside of MRSA,HIV to limit the genotypes in the microbes.These CRISPR treatments using advanced gene drive technology applied to existing superbugs and newly discovered pathogens can involve removing resistance to one or all antibiotics,undergo apoptosis,be susceptible to compounds at their disposal,prevent them able to undergo mitosis,make them undergo apoptosis,make them benign thus preventing them being pathogens and not able to damage the host,remove their ability to mutate permanently,introduce faults etc with these released at once to allow each pathogen to be affected by multiple treatments.New pathogens and parasites may also require upgrades alongside them using suicide genes etc and those that make them susceptible to the a compounds at their disposal.Patients immune to radiation can be exposed to levels of radiation of between 2,000-20,000Gy to wipe them out.They could have DNA extracted via base microbes or phlebotomy robots in hospitals to have the DNA wirelessly sent to Paean and other AI to be analysed for proteins to create upgrades to be immunisations for all patients around the world including the infected patient and also for anti-bacterial microbes to create endolysines specific to them via signals while the microbes use CRISPR to make them susceptible to all compounds at their disposal and keep the host also alive to allow them to be cleared of them within 24-168 hours.The DNA taken from them by base microbes will also be shared with immunising strains to then synthesise the proteins on their surface to then be shared with dendritic cells in all lymph nodes with the microbe that receives the DNA would undergo rapid replication to travel to all lymph nodes and active an immunised immune system to fight it off with it also sharing the DNA to anti-viral anti-bacterial strains to create schematics to create endolysines.If sufficiently advanced the base microbes could through horizontal gene transfer intake and then read its DNA and wirelesly send the genome of the pathogen to Paean and Phanes that could scan its genome adding it to Physis but have genotypes downloaded wirelessly to strains that synthesise proteins to immunise the host and those that create endolysines with them wirelessly sent the genes that produce the relevant proteins to be shared with the dendritic cells by Paean while other microbes cause other microbes to undergo apoptosis and keep the host alive while the primary immune system is immunised and activated.In time advanced base microbes would be able to scan the genome itself using taq polymerase,Cas-9 and CRISPR to copy its DNA and signal to the immunisation strains to prepare the relevant genes and thus proteins through chemical signals,nanomachines,protein bumpers or horizontal gene transfer to prepare the relevant genome with them also using this to make other anti-microbial and anti-viral strains create endolysines and unique protein bumpers.Thus base microbes could be advanced enough to scan the genome of new foreign pathogens and send it to Paean and other microbe strains while other strains cause pathogens to undergo apoptosis,keep the body alive and also use CRISPR and other methods at its disposal until base microbes can scan through genome to give strains that immunise the primary immune system relevant genes and arm others with bacterial strains given DNA to produce endolysines.The DNA of these new pathogens would be uploaded to Physis to allow for AI namely Phanes to extrapolate genes that are needed to express common proteins for immunising strains and the immunising strains in the body would then receive these by wifi,immunise the patient and activate the immunised primary immune system with by 2045 onwards this taking a few minutes from the second is infected.Existing pathogens in the body will have genes added that prevent it undergoing replication and mitosis and undergro apoptosis and in the case of viruses have large strands of DNA removed to allow for the immunising strains to recive genotypes you immunise the primary immune system.Thus one could be immunised within minutes to then have the immunised primary immune system activated within an hour of the microbes discovering the infection.The same procedures will apply to new parasites.This could also allow the pathogen to be analysed and created in labs using 3D DNA printers to allow them to be tested against all natural compounds from plants and animals both from Earth and colonies.Furthermore them once the genome is scanned or when the surface protein antigens are detected will prepare lysins specific to that species or strain to be then synthesised by all microbes.The genome of the new pathogen and parasites will be uploaded to Physis with its entire genome analysed in minutes and Phanes and Paen will determine genotypes for immunising strains and also synthetic antibodies and compounds to kill them within minutes as well that can be downloaded into immunising and other strains within minutes.New colonies will have the common genes and proteins of all taxonomic ranks of micro-organisms analysised and created to create immunisations of them for all civilians on Earth and interstellar vehicles etc so as to prevent them mutating into human pathogens as seen with SIV mutating into HIV.All livestock and animals will be immunised against their pathogens to prevent them becoming zoonotic diseases.Synthetic compounds to treat them can be created by them carrying out anabolic and catabolic reactions using excess nutrients in stores etc and also bio based compounds,plant and animal oils and hydrocarbons created by the same strain or the body from CRISPR treatments as well as amino acids synthesised by the body and diet.The microbes would also steal genes or be upgraded with them to produce specific proteins from new pathogens once their genome is scanned into Physis to share with the memory helper B and T cells as well as weakening some of the pathogens to be destroyed by the primary immune system to allow them to kill them in another infection similar to vaccines.It would also apply to pathogens such as viruses,bacteria and parasites that may become resistant to melittin and all anti-fungal/microbial/viral compounds at their disposal with it even as stated making pathogens such as MRSA,N.gonorrhoeae through this modification permanently susceptible to all of the antibiotics such as colistin,β-lactam antibiotics and penicillin etc that are currently ineffective via gene drives.It would also work with all viruses to limit the genotypes added to the anti-viral and anti-bacterial strain and could allow any virus or bacterial pathogen to be killed by the compounds at their disposal as CRISPR treatments during phagocytosis would change the pathogen whether bacterial or fungal pathogens genome making its exterior and interior structures be able to be destroyed by the compounds at their disposal with the same done to tumours with suicide genes also added.For this to work ideally first asymptomatic carriers including pets and livestock that carry them should be treated with the permanent resistance removing treatments so that those in vulnerable humans that can affected by them can not only use this resistance removing ability but have the microbes use these antibiotics colistin,β-lactam antibiotics and penicillin against them using recombinant DNA from yeasts etc alongside those from Russian Brown Frogs,phytoplankton,hypochlorite,lactic acid,alcohol and reactive oxygen for maximum effectiveness.New pathogens and parasites could also be modified to become susceptible to the anti-viral and anti-microbial at the microbes disposal,remove their pathogenicity or cause them to commit apoptosis.Genes would be applied to them to express the same external structure of both viruses,fungi,bacteria and even parasites they are designed to fight off ie express the same phospholipids as benign bacteria to allow anti-bacterial compounds to be used or in the case of viruses express the same external structure as HIV without the GP120 glycoproteins and apply melittin and lemon juice particles.If possible having them express the same structure of benign Rhinovirus,HPV,Orthomyxoviridae strains than them expressing that of HIV as it would be much safer in order to be destroyed by them using cyanovirian-N etc.Parasites can be made to express the same internal and external structure as other parasites susceptible to the compounds used or even those as bacteria and viruses to be destroyed with the same done to fungi.This would involve DNA from these benign bacteria and viruses etc added to the pathogens genome.By applying suicide genes and those that prevent them being able to replicate and undergo mitosis would keep their numbers low preventing them causing sickness and damage to the patient and this done via horizontal gene transfer and also bumpers with this allowing for base microbes to scan the DNA of the new pathogen and send it wirelessly to Paean and Phyisis who will determine the proteins on it that would be relevant to immunising strains with immunising strains receiving the geneotypes via Paean wirelessly inducing the evolution of genotypes in this strain to synthesise the proteins on the surface or them collecting samples and them sharing them with dendritic cells to whom they will initiate in large numbers to then initiate relevant memory B and T cells and plasma cells in large numbers and the primary immune system now immunised will be signalled by the microbes through Paean to then fight off the remaining pathogens thus allowing one to be protected for life the next time it is encountered with this protecting patients from new pathogens whether viral,bacterial or fungal or even benign ones that could mutate before they can become pathogens as seen with SIV mutating into HIV or Cowpox virus became V.major and V.minor and would protect them against those they are not immunised against on Earth or on other colonies.This and making them susceptible to the compounds at their disposal via CRISPR treatments would ensure that they can fight off new infections they have not immunised the primary immune system off or newly discovered ones.Their genome would also be used to determine antigens on their surface and allow AI namely Phanes and Paean to extrapolate antibodies that can then be synthesised by microbes through wifi.All new micro-organisms such as fungi,bacteria and viruses discovered on Earth and on new planets will be scanned by Physis,Phanes and Paean will be done by automated programs managed by Astreaus that will scan all micro-organism into their version of Physis which will then have Phanes scan all of them for their potential for pathogenicity and also genotypes for useful proteins allowing for them to have upgrades and anti-viral and anti-microbial compounds developed prior to humans arriving.The common proteins of whole families and orders of all bacteria,fungi and viruses will be analysed by space station AI to create superproteins that immunise one against all fungi,viruses and bacteria allowing one to when they arrive on the planet will be immunised against all pathogenic and non pathogenic ones especially those that have the potential to mutate into deadly pathogens.All known compounds from plants and animals on Earth and other colonies and planets will tested on them in automated labs and also in simulations with all compounds present in Physis and the genotypes from the animals and plants they arise from here in the species file to then add them to microbes via upgrades.To make them susceptible to these compounds already present the microbes could add DNA from a virus or the bacteria that causes them to express the protein coats or phospholipids of known ones that are destroyed by the compounds ie new viruses and also ones outside of HIV could have CRISPR treatments containing DNA/RNA from known pathogens applied to them that cause them to express the same protein capsid and exterior structure of HIV without GP120 glycoproteins to allow allowing melittin and lemon juice to be applied or ideally the same protein capsid and exterior structure of benign Rhinovirus,HPV,Orthomyxoviridae strains to have cyanovirian-N applied with new bacteria and those outside of MRSA could have DNA from added to them that makes them express the same phospholipids and also internal structure benign bacteria affected by these compounds and then allow the microbes to apply its anti-bacterial and anti-viral compounds.This and also the ability to remove resistance to new and existing anti-viral and anti-bacterial compounds will allow the microbes fight off pathogens that the patient is not immunised against and also kill off any new pathogens discovered in new colonies off of Earth and also as stated fight off viruses,bacteria and fungi outside of those the compounds at its disposal are designed to fight off.This would involve DNA from these benign bacteria and viruses etc added to the pathogens genome.New parasites will undergo this as well.Base microbes could extract the genome from those kept busy by the microbes that surrounding them or this be done by all types of microbes via horizontal gene transfer and then upload their DNA to Paean via wifi to be analysed and then used for developing proteins for immunisations and also counter compounds to be added.The patient and uninfected ones could then be given upgrades either at home or via wifi as soon as possible against the pathogen and any new strain with AI determining the proteins needed to immunise against all possible strains with the pathogens also given CRISPR treatments to prevent them mutating,undergoing replication or mitosis and prevent the pathogen killing the host while key organs are repaired and kept alive.All of these CRISPR treatments will be housed in the microbes as ribosomes and in particular plasmids that can be replicated using taq polymerase and Cas-9.This would allow them to attack virtually anything not just new pathogens on both Earth and on other colonies that would adapt to become human pathogens like HIV evolved from SIV but also to attack viral and bacterial pathogens outside of the main ones the compounds are able to or are designed to destroy on Earth thus extending their range of efficacy without the need to add new genotypes with them able to fight off new infections and even chronic infections instantly thus speeding up the time it takes to cure the patient before it can cause fatal damage to them.This would also apply to both fungi and parasites both existing and new with it only applying to pathogens and not human cells via differentiating between the unique surface proteins of human cells and those of pathogens with ideally this done by the them having receptors that recognise pathogens as well as parasites and not human cells and also the genes to be used suited only to fit into the genome of only viruses and pathogens as well as parasites and not human cells with them doing this alongside resistance removing gene transferred and then use its anti-viral and anti-microbial compounds in unison to prevent pathogens become resistant and CRISPR treatments to remove and prevent resistance and also weaken them will also be applied at the same time to again improve success and even prevent resistance to existing and new treatments.If possible other anti-viral compounds such as lemon juice,vinegar(or similar compounds) can be synthesised and even virkon could be applied by them synthesisng it if shown not to be toxic to humans especially when applied by phagocytosis to HIV virions and other pathogens that it kills or compounds with similar structures and viricidal qualities that are benign to humans synthesised by them or using recombinant DNA from plants and animals via upgrades.The hosts native cells using scratch could be made immune to the compound or the microbes could synthesise the compound covered in protein bumpers that interact only with HIV thus not affecting the host when flooding the bloodstream as nanoparticles with the same applied to lemon juice and melittin.By 2029 the microbes will be able to clear new infections of new pathogens,parasites and toxins with at most a week or even just 24 hours with by 2035-2045 onwards most of not all infections of pathogens,parasites and toxins will be cleared from the body within a few hours of not a few minutes before the patient even realised it occurred.
Anti-viral Strains:
The anti-viral strains will be engineered to only interact with only viruses ideally those of pathogenic viruses via surface proteins on them that only interact with only fungi to prevent them applying these to the patients cells that would kill them with them via induced evolution.They can cure all species of pathogenic viruses outside of HIV.Virophage DNA including tweaked DNA from DNA from Mavirus,Sputnik virophage,Zamilon virophage DNA hybridised with each other and bacteriophage DNA to not need a helper virus present in anti-viral strains will allow schematics of endolysine like material of all pathogenic and non pathogenic viruses outside of HIV to be made and then applied.All species of viruses and their strains in Physis will be analysed by AI to extrapolate their species and strain specific endolysines and receptors that will be stored in their Physis file to be downloaded when needed once the species and strain of virus is identified by base microbes.The virophage/bacteriophage DNA will be present in these anti-viral strains to allow them to analyse DNA from viruses and extrapolate schematics to create endolysine like material that will be used to kill them using receptors unique to viruses that work on the same principle as those in anti-bacterial strains without a helper virus.The antiviral strains will attack viruses using endolysine like material using them as replication vector to kill them and would be hybridised with bacteriophages that would work on the same principle of anti-bacterial strains by scanning the genome of viruses and then extrapolating receptors and endolysine material allowing them to attack any species of viruses including HIV,Ebolavirus,Hantaviridae,Lysasavirus,Rhinovirus,HPV,Orthomyxoviridae.Phanes will create and extrapolate virophage/bacteriophage hybrids that can kill all species of viruses that utilise them as a replication vector without a helper virus killing them by producing endolysine like material.This can be started as early as 2025 in animal trials and then allow for human trials to start as early as 2025-2029 to eradicate these disease by at least 2039 with animals treated using their own anti-viral strains microbes.AI will also analyse them to have bacteriophage/virophage hybrids to be created by 3D DNA printers prior to microbes being perfected.Having patients made resistant to radiation using T.gammatolerans DNA can allow for radiation therapy to be used with the patient once made immune to radiation will be exposed to levels of radiation of between 2,000-20,000Gy to wipe out large amounts of all viral pathogens.All patients will be immunised to all species and strains of all viruses including oncoviruses,those that cause food poisoning,benign species and fatal ones such as Ebolavirus,Hantaviridae,Lysasavirus,Rhinovirus,HPV,Orthomyxoviridae,HIV.The genotypes that express these compounds will be added to Physis file of the viruses they kill and a hyperlink to the source animal it comes from.Paean will analyse the outer surface protein wall of all species and strains of viral pathogens that can extrapolate synthetic anti-viral compounds suited for each individual species and strain that can be stored in their Physis file to be downloaded into the anti-viral strains DNA digital storage to be synthesised by anabolic and catabolic reactions with Phanes extrapolating genotypes you create these synthetic compounds to be downloaded via induced evolution.When a viruses species is detected induction of the evolutionary path can allow for the required genotypes needed to be downloaded.At the same this is done Phanes will analyse the genome of all viruses to extrapolate those for surface proteins especially common proteins so as to allow for immunisations to be given to all patients worldwide.The outer structure of all species of viruses that affect humans,pets,livestock,plants etc and the cells in humans,pets,livestock,plants etc will be analysed by Paean and Phanes to allow Phanes to extrapolate genotypes to express mutations that prevent them infecting the cells but at the same time prevent the cells carrying out normal functions thus creating versions of the CCR5 Delta 32 mutation for every single virus that affects humans,pets etc that will be added to the species Physis file to be downloaded into the genomes of microbes when needed once a patient is inflected.Genes will be extrapolated that prevent Ebolavirus,N.meningitis etc from being able to use the liver and dendritic cells etc as replication vectors etc that can be added to high risk patients and removed later as well as added during infections.Thus once a patient is infected the microbes their microbes will induce the evolutionary path of their genome to get the genotypes of their version of the CCR5 Delta 32 mutation that will be applied to relevant tissues and cells as soon as infections are detected specifically to the cells and tissues that each virus infects thus preventing the virus from replicating anymore keeping it in place with the acellereated healing phenotype repairing any damage they do to the patients organs or any cytokines storms that the primary immune system causes in order to fight them.Once the virus is unable to replicate the patient will be immunised and the primary immune system activated with the microbes downloading the genotypes for the anti-viral compounds that kill them with them also using CRISPR via horizontal gene transfer to made the viruses express the same outer proteins of those that are killed by cyanovirin-N with them also applying CRISPR treatments that make them undergo apoptosis,remove their glycoproteins and receptors that allow them infect cells etc and also like HIV rewrite their genome beyond recognition to the point that they can be killed by the primary immune system,penicillin and even everyday over the counter medicine.Phanes will extrapolate genes that for all pathogenic viruses can be added to the cells etc they infect that removes receptors that allow the viruses to infect them thus meaning once a patient is infected the virus will be unable to replicate thus leaving their viral load stay at stable levels.All viruses outside HIV will have them tested in labs against venom from all stings,secretions and bites etc from all species of plants and animals to see which ones destroy them.All species of pathogenic and non pathogenic viruses will be tested in automated labs sgainst sap,secretions from plants and animals worldwide with to gain the genes responsible that can be downloaded by anti viral strains.AI wil also extrapolate synthetic antibodies,synthetic enzymes and synthetic compounds that kill viruses to be stored in Physis and downloaded and then synthesised in the bloodstream.The structure of these synthetic compounds,enzymes and antibodies will be stored in their Physis file to be downloaded into the DNA digital storage of the anti-viral strains and then synthesised by anabolic and catabolic reactions.This will be done by AI namely Phanes and Paean analysing their outer surface proteins and genome of all species and strains of viruses particularly pathogenic species to allow these synthetic compounds and antibodies to be extrapolated that will be stored in the Physis file of each species that will be downloaded by anti-viral strains and created by anabolic and catabolic reactions.These enzymes,antibodies and synthetic compounds applied during phagocytosis if they cause side effects including cytoxicity or released into the bloodstream if benign.Phanes can also extrapolate the genotypes created from scratch to express these synthetic compounds and antibodies stored in their Physis files that can be downloaded into the genome of anti-viral strains.Synthetic and natural anti-helminthic compounds,enzymes,antibodies will be applied by being flooded into the blood stream or applied during phagocytosis by microbes to prevent cytoxicity through them having macrophage DNA.Dead viruses can be consumed by the microbes using enzymes suited to each one developed by Paean and Phanes once downloaded during phagocytosis.The accelerated healing phenotype will instantly heal any damage caused by the virus directly and indirectly by cytokines storms etc meaning a patient could survive indefinitely to avail of upgrades and application of genes that prevent the virus replicating and to avail of immunisations.Patients once made immune to radiation will be exposed to blasts of radiation between 1,000-2,000Gy to kill of large amounts of them.All patients will be immunised against all viral pathogens using the common proteins method.The steps detailed below to cure patients infected with HIV will be repeated with all forms of viral pathogens such as Orthomyxoviridae,Rhinovirus,N.meningitidis and Ebolavirus with all of these methods to fight the pathogen tested on mice and chimpanzees that have human recombinant DNA already infected with HIV and newly infected with it to best discern the best methods of treating infected humans and also newly.CRISPR can make all viruses outside of HIV to become susceptible to the compounds at its disposal with cyanovirin-N been shown to be effective against not just HIV but also Rhinoviruses,human parainfluenza virus,HPV,Orthomyxoviridae,Respiratory syncytial virus and enteric viruses as well as even Ebolavirus in either destroying them and killing them off or inhibiting their ability to infect cells or undergo mitosis thus at least allowing for the immunised primary immune system to be activated and also have CRISPR treatments applied that make them susceptible to the compounds at their disposal.Ideally new viruses and those outside of HIV including fatal ones such as Ebolavirus,Hantaviridae,Lysasavirus etc will be made susceptible to cyonovirin-N alongside melittin and lemon juice with them made to express the same external structure of benign Rhinovirus,HPV,Orthomyxoviridae strains and have cyanovirin-N applied rather than them expressing that of HIV as it would be much safer in order to be destroyed by them.If possible they can be made to express the same external proteins as HIV but without GP120 glycoproteins and then have melittin and lemon juice applied.Scratch DNA can be applied that makes them express unique protein coats that can be killed off by melittin,cyanovirin-N and lemon juice.Horizontal gene transfer will be used and them engineered to interact with only viruses and not that of the patients cells during phagocytosis with taq polymerase allowing CRISPR treatments present in ribosomes and in particular plasmids to be recreated over and again.
In the case of HIV these biocompatible microbes anti-viral strain could be used to transfer not just genes but also apply cyanovirin-N,lemon juice,Di-dehydro-Cortistatin A,N6 and other tri-specific synthetic antibody,melittin as nanoparticles that has viricidal properties especially with HIV with other viricides also inserted into the capsid with again resistance removal genes,suicide genes or those that remove its ability to attach to leukocytes or infect other cells and gain resistance to these viricidal compounds as a backup plan with in the case of viruses either directly interacting with viroids and virions by locking onto their receptors to transfer the genes or infecting cells that they attach to first and adding genes to them which will then be transferred to the next generation of virus particles that use it for replication or prevent those cells from being infected.The microbes will be able to fight off all viral pathogens would involve recombinant DNA from Nostoc ellipsosporum,Apis mellifera,Citrus limon,Corticium simplex.The melittin,cyanovirin-N,Di-dehydro-Cortistatin A and other anti-viral compounds that have shown in laboratory settings to have viricidal properties and thus kill the virus could be applied to HPV,HIV,Ebolavirus etc by anti-antiviral strains when the microbe interacts with their GP120 glycoproteins etc and envelopes them through phagocytosis similar to macrophages and applies the compounds,released as nanoparticles or even flood the bloodstream in protein bumper depending on their toxicity or effects on the body with these used instead of antibodies and enzymes with CRISPR treatments preventing the viruses gaining resistance to these applied compounds,make them weaker and easier to attack,thus more susceptible to them applied at the same time as both viricidal compounds used at once for effectiveness with this replicated with tumours with all relevant anti-cancer compounds and CRISPR treatments.Research has shown that the blood and immune system of species of Crocodylus in Australia produce anti-viral compounds namely proteins that kill some strains of the virus with recombinant DNA coming from them also with research done to extract the exact DNA for this by 2029.This DNA can be modified by Phanes to kill all strains.This recombinant DNA can be added to microbes to allow them to produce these compounds via bumpers and phagocytosis and even the host DNA via CRISPR to allow the host in infected and newly infected patients to fight off the virus with it also fighting off bacteria and boosting the immune system by making human immune systems react instantly to infections of pathogens preventing and skipping seroconversion similar to Crocodylus that exhibit innate immune reactions at birth rather than adaptive ones in humans with the rest of the human cells altered using scratch DNA and that from Crocodylus to be able to be resistant to any negative reactions as these animals have primary innate immune systems allowing them to react instanly to most if not all pathogens instantly even on the first infections.Thus Crocodylus DNA can be added to human patients to give them this innate immune response and DNA from them and scratch DNA to prevent the immune responses causing cytotoxicity and serious allergic reactions.This Crocodylus DNA added to both microbes and the patients DNA can be tweaked by Phanes to attack and destroy all strains of HIV for future patients as well as tweaks can be made for each individual strain for each individual patient and even tweaks made to make it once added to the hosts genome and microbes instantly attack and be able to destroy all strains of all pathogenic bacteria,viruses and fungi etc during infections by producing compounds that can attack all types viral,bacterial and fungal pathogens with the microbes aiding them into determining what type pathogen it is and what type of compounds it is with this aiding in fighting off new pathogens.This would be done all at once to ensure maximum damage to the virus and CRISPR treatments applied at the same time.These and other CRISPR strains will be housed as ribosomes and in particular plasmids in the anti-viral strains and will be applied as bumpers and also by horizontal gene transfer with with them recreated over and over again via taq polymerase and Cas-9 to be reused over and over again.If possible with HIV the microbes could flood the bloodstream with cyanovirin-N,N6 and other tri-specific synthetic antibodies and Di-dehydro-Cortistatin A binding to and preventing HIV from effectively replicating or even binding to CD4+ T lymphocytes ideally at the moment one becomes infected prior to seroconversion or even in already infected patients to prevent them infecting any cells especially if taken with PreP and PEP measures to improve this existing measures efficacy and they would devour them via phagocytosis and apply melittin as well as lemon juice to the virus killing it with it also applying both compounds during phagocytosis with this replicated with other viruses.Di-dehydro-Cortistatin A could be synthesised by anti-viral strains in already infected patients to replace protease inhibitors once the CCR5Delta 32 mutation is added to them as a backup with it also done in those without this mutation provided animal trials show it is safe.All three compounds melittin,Di-dehydro-Cortistatin A and cyanovirin-N can form the basis of lube to applied to the anal cavity and cervix prior to sexual intercourse as well as in the inside of condoms.With regards to HIV,Rhinovirus and other viruses such as HPV they could synthesise cyanovirin-N a protein,Di-dehydro-Cortistatin A,melittin,lemon juice or other compounds that have viricidal properties especially with HIV into the capsid with this synthesised on the spot when needed effectively killing virions that are kept under control by protease inhibitors theoretically allowing it to be cleared from the body.PEP,PrEP and all types of anti-viral compounds including protease inhibitors can be synthesised by the microbes using anabolic and catabolic reactions.Ideally this cyanovirin-N,Di-dehydro-Cortistatin A,lemon juice and melittin should be used and synthesised on the surface of the microbes when the microbes have surround the virus similar to macrophages using macrophage DNA or ameobas or using them in place of enzymes to break down the virions capsid and kill them or these could be released into the bloodstream in nanoparticles coated in bumpers depending by what is decided by nanomachines and when they interact specifically with the GP120 glycoproteins and those of other viruses.Phagocytosis should be the best option as it leaves little chance of toxicity to the host,applies the viricidal compounds directly onto the surface and also reduces or even eliminates the chance of the viruses from mutating and developing resistance with the same applied to pathogenic bacteria with the microbes applying both and other compounds alongside CRISPR treatments to prevent or remove mutations to thus improve efficacy even consuming all aspects of the pathogens as food and also allows for CRISPR treatments.The compound would be broken down by the microbes back into elemental compounds or benign compounds to prevent them released if they are not used up.However protein bumpers can allow millions of nanoparticles of the compound covered in bumpers to be released into the bloodstream that interact only with HIV and not healthy cells.These nanoparticles can include proteins or oligosaccharide bumpers that bounce off the healthy cells of the patient but interact with virus acting as a delivery vector to improve its ability to destroy the viruses in infected person thus clearing the body of the pathogen with this released in these bumpers in large amounts in order to flood the bloodstream and lymphatic system with millions of microbes releasing millions of these melittin and lemon juice(and the other aforementioned anti-viral compounds that kill or deactivate HIV) laden nanoparticles at once clearing the virus out of the body while at the same time an immunised primary immune system releases large amounts of antibodies both using the lymphatic system and bloodstream to reach hard to reach places signalled to produce these by the microbes.These nanoparticles consisting of protein bumpers that are able to transport the viricidal compounds to the virus to kill it while bouncing off the hosts healthy cells preventing cytotoxicity.Research starting as early as 2023/2024 for the best natural oligosaccharide or protein bumper that would be effective at transporting melittin and lemon juice to the site of the virus without affecting the host with this done in animal trials using proto microbes from their leukocytes.The bumpers used in studies by Washington University of Medicine to apply melittin should be investigated as a possible vector to be synthesised by microbes as they virus is small enough to be attracted and destroyed by them with any synthetic bumpers produced by anabolic and catabolic reactions.AI will extrapolate the best bumper to be stored on digital DNA storage.These synthetic bumpers will be synthesised by anabolic and catabolic reactions and the anti-viral compounds coated in these bumpers synthesised by the microbes can mass produce and synthesise on demand by Paean by biosynth wifi and large amounts of these bumper laden anti-viral compounds to travel the bloodstream and kill off all virions it comes in contact with,bounce off healthy cells while excess are flushed out of the body via urine snd feces.The compounds could also be applied during phagocytosis with it applying all compounds at its disposal ie melittin,lemon juice etc in both bumpers and also phagocytosis with if possible tri-specific antibodies produced by them through anabolic and catabolic reactions.Scratch genes extrapolated by Phanes can be added to all cells in the hosts body making them immune to all anti-viral compounds such as meditation etc.Phagocytosois will be the best option as it applies the anti-viral compounds on the surface of the virus when the virus has been trapped by the microbes.Patients can be made resistant to the anti-viral compounds using genes from bacteria that undergoes forced evolution to allow the compounds not require bumper.The hosts native cells using scratch DNA could be made immune to the compounds allowing them to be applied in large amounts without bumpers.These anti-viral compounds can be applied during phagocytosis as wells.Ideally genes to prevent the viruses gaining resistance to these compounds or remove their resistance would be inserted into them to prevent them gaining resistance to these and other compounds.It could also directly insert genes that cause viruses to undergo apoptosis,remove resistance or lose their ability to infect cells and replicate etc with this of note of Ebolavirus,HIV,HPV,N.meningitidis.They could also transfer suicide,resistance removing and faulty DNA into viruses and bacteria.The same can be applied with pathogenic bacteria;CRISPR attacks applied at the same time to prevent them becoming resistant to all antibodies,anti-microbial agents applied at once to increase effectiveness.Suicide genes could be added to them in order to have the pathogen undergo apoptosis with “carpet bombing” and removing or many or most of the important genes that allow a virus to function such as its ability to infect cells,become susceptible and thus be destroyed by compounds at its disposal,introducing suicidal genes,remove its resistance to drugs and even previous CRISPR treatments,remove its ability to become resistant or mutate and add faults all at once at multiple sites in its genome either killing it or making it benign with research into combining the microbes with tweaked recombinant DNA from scratch,leukocytes,viruses namely virophages and other microorganisms that parasites or actively attack viruses to act as vector that can allow genes to transferred and apply viricides and anti-microbial compounds via them engineered to actively seek out and interact with the viruses and in the case of HIV envelope GP120 glycoproteins combined with targeting cells infected by it and where it might hide,before nanomachines can become sufficiently advanced with gene drives increasing stability of changes.Either that or microbes containing DNA from these predatory microbes could have DNA from leukocytes and other cells infected by all types of viruses to contain the necessary receptors to actively seek out HIV and other viruses and transfer these faults despite the effects of protease inhibitors or destroy the virus with custom built in antibodies and viricidal compounds.Paean through biosynth wifi and nanomachines can control each individual microbes and in groups to actively seek out virions of HIV and then attack them by applying lemon juice and melittin as well as initiate the production of tri-specific antibodies and N6 antibodies and application CRISPR treatment.The microbes can be engineered to actively seek out,interact with and do the same with all types of major viruses such as Ebolavirus,N.meningitidis,Rhinovirus,onconviruses,HIV such as HPV by switching genes on/off to change receptors through interactions with the surface proteins of pathogens or have receptors that interact with all or a large variety of viruses similar to those on the human cells that are infected by them.This can be done with them having tweaked DNA from Bdellovibrio,M.aeruginosavorus,Paramecium,C.elegans,C.roenbergensis,virophages,bacteriophages and others from scratch to detect and actively seek out all bacterial,fungal and viral pathogens such as MRSA,HIV and major pathogens that the primary immune systems normally ignores until seroconversion or when the body and immune system is normally comprimised and overwhelmed and be able to interact with their surface proteins to detect which one they are and apply the correct CRISPR,anti-viral and anti-microbial treatments.Otherwise Paean by biosynth WiFi and bluetooth can control their movements to make them actively seek out the virus.DNA that would cause the bacteria to be pathogens will be removed and only the DNA that causes them to seek out pathogens with them tweaked to seek out HIV and other viruses.The virophage DNA can work on the same principle of bacteriophages and bacteriophage DNA in anti-bacterial strains with DNA collected by base microbes to determine the strain of HIV or DNA that allows all strains of HIV be in the microbes thus allowing them to create endolysine like material that can be applied by protein bumpers as well as horizontal gene transfer or receptors that interact with the virus that cause the viruses to be killed from the inside out.Paean can induce the microbes genomic evolution to create receptors on their surface unique to each pathogen to allow them to inject countless endolysines synthesised by the microbes or they can be applied by horizontal gene transfer or bumpers.These ideally will be universal virophage DNA that intake schematics from base microbes and allow them to adapt to all strains of HIV and other viruses.If possible as stated earlier tweaked DNA from Sputnik virophage,Mavirus,Zamilon virophage hybridised with each other and bacteriophage DNA merged together to not need a helper virus can be used to detect,infect and destroy HIV and other viruses present in the DNA of anti-viral strains.These can be hybridised with bacteriophage DNA.This would work by scanning the genome of the virus including the strain of HIV and creating endolysine like material to be released by the pathogens.They would work on the same principle as those in anti-bacterial strains and be in anti-viral strains.The CRISPR treatments applied to HIV would as stated involve remove it GP120 glycoproteins and those that prevent them mutating and those that cause it undergo apoptosis as well as remove other key parts of its envelope,make it susceptible to all compounds at the disposal of anti-viral strains and the antibodies of the immunised primary immune system with this applied to all forms of viruses.Modified virophage and bacteriophage DNA merged together to not need a helper virus will be in the anti-viral strain to accept DNA from base microbes and then produce endolysine like materials that will be able to kill the virus,break it down and die off with them also being able to adapt and create schematics and thus endolysine type material for all viruses outside of HIV.These biocompatible microbes would become a permanent part of the hosts system that live indefinitely in the human bloodstream via injection with even them engineered to undergo mitosis or live indefinitely via biological immortality using recombinant DNA from endolith bacteria and the genes from bacteria that allow to undergo mitosis but do so in controlled manner using chemical signals from each other to prevent them overrunning the body.Using gene therapy via CRISPR using the microbes horizontal gene transfer can allow native leukocytes namely the CD4+ T lymphocytes to become resistant and thus unable to allow the virus to infect them permanently with recombinant DNA coming from populations of humans resistant to it,chimpanzees,SIV or from scratch can be researched to compliment this to alleviate or remove the amount of anti-viral treatments such as protease inhibitors and other aspects of anti-viral combination therapy needed and aid biocompatible microbes ability to attach to virions with them also producing custom made antibodies and viricidal(or bacteriocidal)compounds.These and other key leukocytes other relevant cells containing the hosts DNA can be engineered by horizontal gene therapy to ensure all future CD4+ T lymphocytes are made resistant and unable to be infected with this also done not just to those that are already infected with HIV but also to all uninfected patients and to the human genepool via germline therapy to prevent the spread of HIV and have them engineered to produce all or either N6 and other tri-specific synthetic antibodies and Di-dehydro-Cortistatin A with all microbes in all patients also fitted with microbes that produce melittin,lemon juice,cyanovirion-N and other anti-viral compounds that affect HIV to make this work and thus eradicate the disease effectively curing infected patients both existing and new with the microbes using CRISPR at the same time to weaken the virus,make it susceptible to the applied viricides more,preventing the virus from mutating,removing resistance to these and other viricidal compounds at the same time that the virus applies these compounds.Once cured the CCR5 receptors can be returned to the patient via CRISPR eliminating any side effects over the long term with the patient getting routine tests to detect the levels of the virus during this treatment using dongles or automated labs using phlebotomy robots in hospitals with their levels of leukocytes especially CD4+ T lymphocyte tested over time and logged in ones patient file once the virus is eradicated as well as during the treatment and then the CCR5 receptors has been returned once the virus is undetectable in order to show that the virus is completely eradicated and the native immune system has recovered with microbes fighting off pathogens and cancers if not and then fighting off any remaining virus particles present.Ideally it should remain to prevent reinfection or if possible the virus rebounding if minute numbers are not destroyed with the gene tweaked to allow the original functions to be carried out with every last virion killed off by the microbes and immune system.Levels of antibodies and the anti-viral compounds will also be detected this way routinely until officially cured as the immunised immune system will continually produce antibodies until the virus is wiped out with the levels of virus also tested routinely using phlebotomy robots in booths measured via PCR analysis with all three tested at the same time and results sent to ones patient file instantly.In short during ones treatment the levels of the virus,ones CD4+ T lymphocytes and antibodies created by the native immune system should be routinely measured every few months or once a month to chart their progress until the virus and antibodies are undetectable and lymphocytes are at normal levels.During this time until there is no evidence of the virus present one should still use condoms and their potential sex partners should continue to use PrEP or at least have themselves immunised and have modified to have the CCR5 receptors removed and CD4+ T lymphocytes modified to utilise the Cas-9 immune response to prevent the virus gaining a stronghold and allowing their microbes and immunised immune system to fight them off and eradicate whatever small amounts of virions enter the body instantly halting the spread of the pathogen.The CCR5 receptors can be removed indefinitely with the leukocytes tweaked in order to continue carry out their original functions while still preventing infections and then the microbes and immunised immune system should be able to instantly attack any reinfections and not be able to be infected again indefinitely with the immunised immune system and also microbes continuing to detect and wipe out new virions found or that infect cured patients with as stated all patients worldwide both immunised against and made resistant to infection using advanced gene drive technology to halt the spread of the virus.This should be replicated for all major pathogens the patient is infected especially chronic infections.The microbes will still act as a backup to the immune system fighting off cancers and pathogens if the virus is hidden,during treatment or rebounds with the same steps repeated.Patients should during their treatment wil be ideally be immunised against all strains of HIV and the immune system activated to not only speed up the battle but also havie the immune system continue to fight off everytime last single virion especially when the CCR5 delta mutation and also cure the patient instantl during anty instances of re infection.All at risk patients such as homosexuals,drug users etc should be immunised against all strains of HIV and have the CCR5 delta mutation added to them to cure them instantly and halt the spread of the virus.If possible the microbes and immunised system could still function through phagocytosis and flooding the bloodstream and lymphatic system with antibodies and anti-viral compounds while protease inhibitors are taken if the patient cannot be made resistant to the virus.Ideally the patient would be immunised against all viruses including all strains of HIV that attack the immune system using strains that interact with dendritic,plasma and killer T cells thus improving successes in infected patients and uninfected by the primary immune system fighting off any remaining viruses particles and preventing the primary immune system becoming lazy with it also speeding up eradication before seroconversion.Any cells that harbour the virus and its DNA can be detected and edited by the microbes CRISPR editing techniques removing the DNA or applying suicide genes to kill these cells and then have new unaffected cells regrown via the stem cell microbes with this applying to any virus that hides itself or its DNA/RNA in them can also have this done including oncoviruses.Once this shown to be effective in curing patients it can be debated as to whether those imprisoned for knowingly spreading HIV can be released early.Ideally all uninfected patients should be modified to make them resistant to all pathogens ability to infect organs and also leukocytes with germline therapy then used to make CD4+ T lymphocyte resistance to HIV a permanent feature to the human race via advanced gene drive technology and the same applied to the dendritic cells and other leukocytes and all organs with regards to Ebolavirus and other pathogens that infect the immune system and organs in the body eventually eliminating the chances of them infecting patients and gaining a stronghold with all the microbes then fighting off the infection eliminating it from the body and eventually H.sapiens as a whole through germline therapy with this also applied to all pets and even wild animals to completely wipe them out and prevent suffering and eliminate zoonotic diseases.They would also be immunised against them to allow the native immune system to be able to fight them off instantly.Organs that are infected by Ebolavirus etc can have the CRISPR Cas-9 immune response added to them via CRISPR itself.Problems that may arise by resistance such as removal of receptors can be counteracted by microbes carrying out their functions and in time the receptors also modified to carry out the original functions but not be able to allow the leukocytes to be infected through other CRISPR treatments with new receptors created from scratch or that are hybrids.If possible all uninfected patients should be immunised using the specific strains that interact with the dendritic cells to prevent the primary immune system becoming lazy and allow them to rid the body of any viruses the second the patient is infected.If problems arise with the horizontal gene therapy negating themselves from being able to interact with the HIV virus then ideally a separate strain of the microbes should be created solely for making CD4+ T lymphocytes resistant alongside enhancing them and other leukocytes.Thus the microbes modifying CD4+ T lymphocytes into being unable to be infected by HIV and them utilising cyanovirin-N,N6 and other tri-specific synthetic antibodies and Di-dehydro-Cortistatin A will prevent viral replication without protease inhibitors alleviating strains on the the patient and allowing the microbes to apply melittin and lemon juice during phagocytosis by connecting to the viruses GP120 glycoproteins alongside CRISPR treatments to weaken the virus making them easier to attack and prevent mutations via gene drives that would make it resistant with this replicated with all other viruses including those from the Picornavirales,Orthomyxoviridae order including Rhinovirus and Hepatovirus as well as all viruses that cannot be cured by conventional means using their own specific anti-viral compounds added through interbreeding using new compounds made from scratch using scratch DNA and also them using CRISPR to modify them into being susceptible to compounds also present.If the microbes encounter a virus it cannot fight or even immobilise then it may need new ones added to them or if possible it will use CRISPR to alter its genome to make it susceptible to its existing anti-viral compounds or simply cause to undergo apoptosis.This ability to make new viruses or strains of virus susceptible to new viruses and strains via CRISPR modifying it as well as them giving the dendritic cells samples of a virus would eliminate the need for vaccines and boosters for all viruses including yearly strains of the Rhinovirus and Orthomyxoviridae,new viruses,those that exist but no vaccine exists such as HIV,Ebolavirus with those of note to the elderly and newborns since the microbes will pass from mother to newborns via the placenta breastfeeding making all patients immune to all pathogens throughout ones life starting from when they are in the womb.Ideally these microbes would be able to carry out their functions while the patient still takes protease inhibitors to prevent the HIV from affecting leukocytes while native leukocytes namely CD4+ T lymphocytes are made permanently resistant using DNA from humans resistant to HIV and scratch to exhibit the CCR5Delta 32 mutation ideally homozygous mutations removing relevant sections of the C-C chemokine receptor type 5 gene and other receptors for all strains and thus make the patients leukocytes unable to be infected thus negating the need for protease inhibitors and other anti-viral treatment via microbes utilising horizontal gene transfer on the actual lymphocytes or the patients genome in every cell in the body including the bone marrow where lymphocytes are created.The global database of patient files will be scanned for this mutation to locate patients to extract the gene from their cells which can be using 3D DNA printing inserting it and tweaked versions that give resistance to all strains and new strains into the base and augmentation microbes of infected and at risk patients once the gene is mapped onsite of hospitals around the world negating the need for transport saving time and money.The genetic sequence of this mutation should already be known and thus stored in the Physis database alongside all genes from H.sapiens for reference.Other mutations can be determined by DNA scans from patient files can be synthesised via 3D DNA printers for use alongside or in place of it with these tweaked by AI for all strains of HIV.Those already known to harbour can be contacted and their DNA scanned and compared to close relatives or other infected patients in the same area without it for proto microbes to start animal trials as soon as 2023/2024.The global patient files will allow for patients with different versions of the mutation to be n and detected by proto AI with this also creating tweaked versions of the pathogen.Known patients around the world such as Paul Michael Glaser,Jake Glaser and those in Africa with the mutation will have their patient files with DNA scan done by at least 2023/2024 and compared to those without it to determine its sequence to allow for different versions to be ascertained with then AI using this to create versions to all possible strains by analysing the different versions of the mutation and analysing the different strains of the HIV virus to create genotypes for all strains and decide which mutations of the gene apply and protect against each strain of the virus with the AI namely proto Phanes doing this simultaneously.Proto Phanes and Paean would analyse all known strains of the HIV virus and extrapolate tweaked versions of the CCR5Delta mutation for each strain to be added to each patient that has different strains with if possible an all in one version of the mutation being extrapolated to protect from each strain in existence and added to each at risk group and also each patient infected with each strain of the virus.Although each patient would get versions of the mutation related to their strain it should be advised that they get upgrades that give them an all in one genotype of all versions of the mutation that protects them from all existing and possible strains of the pathogen should it mutate in any off chance of this happening with uninfected at risk patients ideally given genotypes that express all versions of the mutation.That from the Berlin patient Timothy Ray Brown and the source of the graft that led to his immunity will be used with this mutation tweaked by AI possibly using scratch DNA to make all strains of HIV unable to infect leukocytes in all patients both infected and uninfected.If possible to prevent reinfection the mutation can be tweaked in order to retain its original functions and still make relevant leukocytes unable to be infected.This will stored in Physis and an augmentation sub network and this and 3D DNA printers will allow the CCR5Delta mutations for HIV etc and different versions of it to inserted into base and augmentation microbes for upgrades to living patients and be mass produced to be added to the patients genome via augmentation strains.If need be an infected person will have their strain(s) of the virus identified by dongles and phlebotomy blood tests that identify it via PCR analysis and then them given versions of the gene mutation that suits only there specific strain(s) with the same given to potential sex partners with if possible all versions of this gene added to infected patients,their potential sex partners and those who are in high risk groups if a single version cannot be created with AI creating tweaked versions of this gene by at least 2025-2029 that will prevent all strains affecting the patient.The gene will be applied to all cells of the body and not just the bone marrow to ensure success and routine blood tests and base microbes scanning DNA in all tissues especially the bone marrow will show that both normal cells and lymphocytes contain the mutation.This application of the CCR5Delta 32 mutation and tweaked versions to infected patients via gene therapy via CRISPR and as detailed later the CRISPR defence mechanism from S.pyogenes added to the affected CD4+ T lymphocytes via CRISPR itself with traces of these viruses DNA interspaced in their genome to allow for the Cas-9 to be deployed instantly as extra protection would allow infected patients to live healthy lives indefinitely without the need for taking protease inhibitors and other anti-viral combinations and allow the native immune system to recuperate and fight off cancers and infections as its original functions while the microbes and immunised primary immune cells work on the HIV infection.Thus by having the the CCR5Delta 32 mutation and variants for each strain devised by AI added to all cells in the body through gene therapy via CRISPR and advanced gene drive technology will allow existing and future infected patients to live healthy lives forever without the need for taking any type of anti-viral therapy allow microbes and immunised primary immune system to fight off the virus until the patient is cured with it preventing the virus gaining a stronghold and damaging the immune system of newly infected patients allowing microbes and immunisations to cure them quickly if applied to all at risk patients worldwide.Thus this should single handily render all anti-viral therapy used to deal with HIV obsolete forever and since patents owned by a Phanes would be by law free with in passed down from mother to child via advanced gene drive technology preventing transmission from one generation to the next.Although not a cure it will as stated allow infected patients live healthy lives forever without protease inhibitors and other antiretroviral therapy thus rendering them obsolete with it free since it can be patented by Phanes and allow anti-viral strains and immunised primary system to fight off the virus until the patient is cured.If this is applied to all unifected patients worldwide especially at risk groups such as intravenous drug users,homosexual men etc it will prevent the spread of the disease by preventing it gaining a stronghold within the body and if all patients are immunised against all strains of the virus will allow one to be cured instantly.It applied to both parents of children before birth and conception would through advanced gene drive technology prevent the virus gaining a stronghold in unborn foetuses.Although not a cure for uninfected individuals as they will be positive once infected and they can spread the virus to others it will however prevent the virus gaining a stronghold in the patient thus preventing them developing AIDS and also prevent the need or protease inhibitors and would allow the microbes,radiation treatments and activated immunised primary immune system to be more easily cure the newly infected patients.Intensive research by AI even proto AI into this will begin as soon as possible to allow it to be applied to all infected patients worldwide and unifected at risk groups worldwide including homosexuals,intravenous drug users and the poor especially in Africa and Asia where it is rampant thus cutting mortality rates to zero with augmentation strains that apply it to patients created by 3D DNA printers onsite of all hospitals across the world including in Africa allowing patients to survive existing infections and new infections while research is done into microbes that apply CRISPR treatments and anti-viral compounds as well as before the availability of immunisations.The application of the mutation will allow the microbes and immunised primary immune system to fight off the virus much quicker and easily in both existing and newly infected patients until they are cured.It will also keep the immune system fighting of the infection to one is finally cured once the CCR5 delta mutation is removed and cure them of the virus should be reinfected.All unifected patients worldwide especially at risk groups such as homosexual and bisexual men and women and intravenous drug users and those living in hotspots such as Africa and Asia where the virus is rampant will be immunised against all strains of the virus to ensure that the second they are infected then they can be cured instantly.Once the CCR5Delta mutation is added to the entire genome of the patient via gene CRISPR and gene therapy and advanced gene drive technology the native immune system will be able to rebound and fight off normal secondary infections of pathogens and tumours it normally can alongside the microbes various strains with the primary immune system as stated immunised against all pathogens that can kill the patient including both those that can act as opportunistic infections and also those that can kill healthy patients to act as a safety net.Patients will continue to take anti-retroviral medication until routine tests show healthy levels of leukocytes especially T Lymphocytes that are normally decimated by the virus that rebound to healthy levels and then they can be taken off medications.Having the primary immune system of infected patients immunised against all strains of HIV and activated by microbes will allow them to produce antibodies will improve success by fighting off any viruses that the microbes cannot attack,speed up the fight with them signalled by the native immune system and microbes to attack in certain areas or flood the bloodstream and lymph system with antibodies to allow them to reach all areas of the body with them signalled by the microbes and the presence of infections.Patients will also be immunised using the common proteins method immunised against all major viral,fungal and bacterial pathogens and parasites that act as opportunistic infections using the common proteins method with anti-viral,anti,bacterial,anti-fungal and anti-helminthic strains fighting then off too with anti-cancer strains fighting off tumours.At the same time the anti-viral strains will apply melittin,lemon juice to the viruse in nanoparticles and through phagocytosis as well as other anti-viral compounds and synthesising tri-specific and N6 antibodies that kill the virus with it also using CRISPR treatments to alter the viruses genome to allow it be fought off by the immune system and also undergo apoptosis and be unable to replicate via removing the GP120 glycoproteins and other key strands of its genome.The microbes will ideally start producing anti-viral compounds and antibodies when the patient is off medications or before being taken off them and then will begin to fight off the virus through CRISPR,synthesising antibodies,anti-viral compounds etc.Furthermore tri-specific and N6 antibodies will be synthesised by the microbes via anabolic and catabolic reactions when stored in its DNA digital storage.The patient as stated will be immunised against their strain and all strains of HIV and the primary immune system activated to speed up the battle and wipe out large amounts of the virus with this also acting as a safety measure that will wipe out every last virion once the patient chooses to remove the CCR5 delta mutation and cure them of the virus should they become reinfected almost instantly including if they become infected with other strains.Paean through biosynth WiFi will control all actions of the microbes in fighting the disease as well as the primary immune system through chemical signals.Paean through biosynth wifi and nanomachines can control each individual microbes and in groups to actively seek out virions of HIV and then attack them by applying lemon juice and melittin through nanoparticle bumpers or phagocytosis to prevent cytoxicity as well as initiate the production of tri-specific antibodies and N6 antibodies and applications of CRISPR treatments.If possible patients can be made immune to radiation via recombinant DNA from T.gammatolerans allowing the to survive blasts of radiation up to 30,000Gy and then be exposed to large doses of radiation of at least 200-20,000Gy to aid in wiping the virus from hard to reach places and to wipe out large numbers of the virus to aid in the battle alongside an immunised primary system,microbes etc if done at these levels at the start and also for and hour or more while the patient is under anaesthesia.This should be available by at least 2025-2029.Radiorestance can also be dealt with CRISPR treatements that remove this ability or even prevent them being able to develop this in the first place.Ideally the patient will be blasted with this levels instantly and for at least 30 minutes to an hour or more to prevent them gaining radioresistence via mutations with with patient put under anaesthesia.Doing it for more that an hour and starting at these levels as well as applying it to all parts of the body at once will ensure all or most of the pathogen will be wiped out without developing radioresitance and will be done alongside the primary immune system,gut flora and microbes both made immune to radiation to aid in fight in eliminating the pathogen.Both the primary immune system and microbes would be immune to radiation via gene therapy and genome capsids with beneficial bacteria also given genome capsids with this DNA.This can be repeated annually from the begging of treatments several times a year to kill off large numbers of the virus each time in between tests to determine the level of virions and also antibodies etc.These could start at least 200-500Gy several times,then 1,000Gy several times,then 2,000Gy and so on to prevent radiorestance and wipe out even larger numbers of the virus from the body with CRISPR treatments used by anti-viral strains can remove any resistance the pathogen gains to radiation.The level at which the virus can survive can first be determined in lab settings and also in animal trials so as to allow it to be determined and then have patients exposed to levels much higher at least 1,000-2,000Gy higher.All countermeasures against HIV should be used in combination with each other to improve success including the microbes using all anti-viral and CRISPR treatments to remove and prevent resistance,make them susceptible to the compounds at its disposal all done at once either by flooding the bloodstream with nanoparticles of lemon juice,melittin etc covered in bumpers and/or on the surface of the virus during phagocytosis and at the same time immunising the primary immune system of infected and uninfected patients against all strains of the virus using common proteins present in all strains with this applied to all viral,fungal and bacterial infections to improve success.This would allow the hosts immune system to fight off any remaining virions in hard to reach places and improve success in eradicating it from the host by flooding the bloodstream and lymphatic system with antibodies this replicated with all other viral and bacterial infections.A combination of applying the CCR5Delta 32 mutation and CRISPR immune response to infected patients,immunising infected patients,microbes applying melittin,application of N6 and tri-specific by microbes and the primary immune system alongside radiation treatments done routinely should allow already infected patients that have had the disease for at least 10-30 years to be cured in as little as 5-10 years starting as early as 2029 with immunisations and have CCR5Delta 32 and CRISPR Cas-9 immune response added to their lymphocytes to at risk patients in the developing world and drug users and homosexuals should halt the spread of the disease starting by 2029 by preventing it gaining a stronghold in their body with them fitted with anti-viral microbes and DNA from populations that create N6 and tri-specific antibodies.Those who started medication at the start of infection after being infected in the last 10 years with lower levels of the virus could be cured in as little as 5 years with those who are uninfected and have versions of the CCR5 Delta 32 mutation,CRISPR immune response and also immunised against all possible strains and have anti-viral microbes fitted with all CRISPR treatments and also anti-viral compounds can be cured in as little as a month or few weeks.This would be possible if all measures such as radiation treatment,immunisation,anti-viral compounds and CRISPR treatments are applied at once with these all available by at least 2025-2029.To prevent the virus gaining a resistance to all of the treatments by “carpet bombing” the pathogen with one treatment one after another at once allowing it to be cured as stated over the course of a decade at most depending on how many virions are in the body and how early treatment started and how long the patient has been infected.Thus all anti-viral compounds such as cyanovirin-N, Di-dehydrocortistatin A,melittin alongside N6 and tri-specific antibodies synthesised by anabolic and catabolic reactions etc will be applied at once to prevent the virus from first infecting new leukocytes and then kill them off with CRISPR treatments that introduce faults,susceptibility,etc and antibodies from the immunised primary immune system applied all at the same time in already infected patients and new ones will allow the microbes to catch it off guard and unable to adapt.Radiation treatment will also be applied as well.Applying all of the different treatments at once will increase effectiveness of them,speed up up the rate the patient is cured to at most 5 years with most being passive process controlled entirely by Paean that work 24/7,365 without the need to intake any medication with patients taking test every one or few months.All measures carried at once in waves can be done to allow the microbes and primary immune system time to rest via carrying out battles one after the other in waves taking out large numbers of the virus in each one allowing them recharge and not cause overreactions that could be fatal and cause the immune system to become fatigued with the microbes controlling the primary immune system via chemical signals from orders sent by Paean with the patient eating large amounts of fats and sugars to allow the microbes to get breaks and feed on these with the microbes and the primary immune system by extension via the microbes using chemical signals will be controlled by Paean with him relaying to ones patient file the start and end time of these and also how many virions were destroyed.Routine tests will be done to determine the levels of virions,lymphocytes,antibodies etc to see how much progress is made with these logged in the patient file.The CRISPR immune response in microbes and also lymphocytes will be used to kill off whatever little amount of virions are left to preventing it rebounding thus meaning the patient should have this measure and the CCR5Delta 32 mutation left in their genome indefinitely once cured and also protect against reinfections with these fought off instantly and prevent the virus rebounding with every last virion killed off.Patients should have it kept for at least a decade after being officially cured to allow the activated immunised primary immune system and microbes kill of every last virion.Both the immunised and activated primary immune system and microbes will continue to kill off very last remenants of the virus once the CCR5Delta 32 mutation is removed.As the patient could live forever without anti-viral therapy then they could live normal lives with the battle lasting as long as it needs and all uninfected patients will be protected by them fitted with anti-viral strains,immunisations and also with them having the CRISPR immune response and CCR5Delta 32 mutation added to their genome meaning if they are infected then whatever little virions will be quickly killed off.The addition of the CCR5Delta 32 and also the addition of the CRISPR Cas-9 immune response to lymphocytes would prevent the virus able to replicate thus preventing it mutating in infected patients thus preventing it gaining resistance leaving the virus in a vulnerable position as it is the viruses high turnover rate and haphazard method of creating random copies every time it replicates with each replication process creating billions of copies that are different each time it replicates that creates new strains thus leaving the virus unable to mutate.Ideally both measure of protection via the CCR5Delta 32 mutation and also the CRISPR immune response added to all leukocytes affected by HIV would prevent the virus infecting them and allowing the host patient to survive indefinitely without the need for anti-retroviral therapy indefinitely with them as stated these two measures will be engineered to be resistant to all existing and all possible strains of the virus that exists.Thus by preventing the replication of the virus completely without the use of anti-viral therapy through these protection measures it would prevent any mutation keeping the number of new strains to a minimum and also prevent the virus gaining resistance to the anti-viral compounds and also antibodies produced by the microbes and also primary immune system.These protection measures would also cause the microbes and lymphocytes that use them to signal to the immunised immune system and microbes to gather in the area and utilise all anti-viral compounds and antibodies at there disposal acting as a mousetrap.Ideally patients would continue to have these once cured so as to prevent reinfection and also any remaining hidden virions infecting leukocytes and thus causing the virus rebounding with them updated with upgrades to make them effective any new strains that may arise with any cells where the virus and its DNA hides in will be be edited by CRISPR applied by this strain and made to undergo apoptosis with new tissues grown in its place.Uninfected patients especially at risk groups by having these protective measures,being immunised and also have anti-viral microbes would prevent the virus gaining a stronghold and allow them to be cured instantly when they have the CCR5Delta 32 mutation with the same applying to infants via the genes responsible for this passing to it via advanced gene drive technology if both parents have it to prevent the child being infected and its microbes and immunisations protecting it and wiping the pathogen instantly from their body.This would halt the spread of the virus and allow newly infected individuals to be cured instantly.If the virus does gain a resistance to any of the treatments ie N6 and tri-specific antibodies,antibodies from the immunised primary immune system,radiation,anti-viral compounds and even the protection measures added to lymphocytes then CRISPR will be used by the anti-viral strains to remove this resistance by altering the internal RNA and thus surface proteins and glycoproteins etc to make the treatments at the disposal of the body and microbes effective once again with the patient put back on anti-viral therapy for at least one or two years with the anti-viral and anti-bacterial strains fighting off any opportunistic infections and anti-cancer strains fighting off tumours.Once the viruses has been cured worldwide and has been wiped out from the face of the Earth this will render the need for the CCR5Delta 32 mutation to be removed from all patients but it kept stored in Physis.As the microbes can scan their genome and then send it to be analysed by Phanes and Paean to prepare CRISPR treatments.Ideally CRISPR treatments for this will be prepared by the time first generation of anti-viral microbes will be created.Ideally all of these treatments will be available by 2029 in the first generation of microbes with automated labs testing the virus and bacteria to become susceptible to them all will be done to see what genes to add and remove.Thus anti-viral strains through these measures will be able to cure all patients worldwide infected with HIV.The treatments used by them will also be used to make the virus susceptible to all of the compounds present in the microbes and this will be applied to all of the viruses outside HIV ie viruses will be made susceptible to these compounds via CRISPR or upgrades done via lab tests as detailed earlier.The CRISPR defence mechanism from S.pyogenes added to the affected CD4+ T lymphocytes modified to attack HIV will do the same.It may be possible for the microbes DNA to house suicide or other genes that destroy the virus or limit its ability to undergo replication that are transferred into the virus as a reaction once the virus uses it to undergo replication but through genes like how the CRISPR method is used by S.pyogenes to attack bacteriophages that do this transferred through reaction to prevent the virus from doing so and destroying the microbes thus allowing the virus to be destroyed by inhibiting its replication and other CRISPR treatments attacking the virus to remove its glycoproteins,apply suicide genes and also the compounds at its disposal once it is made susceptible to it.These genes would be replicated via taq polymerase and Cas-9 and this can also protect them from other viral pathogens that use leukocytes as replication factories and would be in areas that that the virus uses and be designed to only affect HIV etc and not the microbes.The immune response method CRISPR Cas-9 that S.pyogenes uses to attack bacteriophages can be employed to protect the microbes itself and apply disabling or suicide genes to the HIV virus as well as Ebolavirus and N.meningitidis to prevent them from replicating in the microbes and also cause it to signal to other microbes to flood the bloodstream and lympahtic system with first DNA in bumpers to modify them and then the anti-viral compounds with them also signalling the immunised primary system to gather in the area of them also fight at once with antibodies and signal the attacked microbes to apply melittin and other compounds via phagocytosis and bumpers.To do this genes from S.pyogenes that allow for this to happen will be employed.This would also have key genetic sequences of HIV,Ebolavirus and N.meningitidis interspaced in the microbes genome to allow for the Cas-9 to be deployed.The virus when it attempts to replicate inside the microbe would be attacked by the CRISPR Cas-9 response used by the microbes that would then through programming or signals sent back forth between Paean via wifi cause it to signal to the rest of the microbes and the immunised primary immune system namely the memory plasma cells to gather in the place and apply all anti-viral compounds and antibodies at their disposal with the attacked microbe also applying these compounds as well.The microbes attacked would apply anti-viral compounds through phagocytosis and also bumpers with them via chemical signals and wifi to Paean to call all other microbes and the immunised primary immune system to gather in place and apply anti-viral compounds via bumpers,seek out virions and engulf them to apply these compounds through phagocytosis,synthesise tri-specific and N6 antibodies and initiate the immunised primary system.They would also be programmed to upon being attacked utilise the anti-viral compounds through phagocytosis via this response stored in DNA digital storage present and nanomachines,nanopocessors present that receive instructions from Paean to do so as well as actively seek out and destroy virions alongside virophage DNA and that from predatory bacteria.Thus the microbes would act as a mousetrap to the virus.The native immune system namely those affected by HIV,N.meningitidis,Ebolavirus etc can also through gene therapy to the patients genome and also the bone marrow not only have resistance but also have the CRISPR defence mechanism from S.pyogenes added to them via CRISPR itself with traces of these viruses DNA already interspaced in their genome to allow for the human and patient version of Cas-9 to be deployed instantly as extra protection alongside or in place of the addition of the CCR5Delta 32 gene thus allowing the relevant leukocytes affected by these pathogens to defend themselves from their attacks and replication methods using the human and patient version of Cas-9 disabling the viruses from decimating the native immune system with this applied to the hosts genome or those in their bone marrow.This would allow for gene therapy to be applied to live infected and uninfected patients genome or the DNA in bone marrow to engineer the lymphocytes to harbour not just the CRISPR Cas-9 immune response but if possible also house the specific RNA markers from all strains of the virus in the exact spaces in the tested leukocytes genome with this done by AI by at least 2023-2025 with microbes having them printed out using 3D DNA printers by this point.CRISPR Cas-9’s precision at applying genes to living cells could easily apply the correct genome sequence to the hosts genome to have the affected CD4+ T Lymphocytes house the CRISPR Cas-9 system and have the relevant RNA of the virus in key parts of the system as determined by the aforementioned experiments with this allowing the lymphocyets to effectively utilise the CRISPR Cas-9 immune response against all strains.The native immune system would use this to apply genes that remove their GP120 gycoproteins and also call microbes and plasma cells to gather in the place and apply both anti-viral compounds and also antibodies.Thus the native leukocytes affected by the aforementioned viruses can be fitted with the defense mechanism of S.pyogenes with organs such as the liver,brain etc also fitted with these mechanism via CRISPR adding the DNA from S.pyogenes and also the relevant genes from the viruses interspaced in their to allow them to be able to fight off infections similar to microbes.This defence mechanism can be added alongside immunisation to uninfected patients to prevent the virus gaining a stronghold with it applied to all cells in the hosts body and bone marrow.If possible both microbes and leukocytes in infected and uninfected animal patient subjects can be tested in test tubes or in the patient itself with in the case of test tubes actual real unaltered forms of the viruses to teach them how to utilise the Cas-9 immune response and in the actual patients dead versions of the viruses modified by CRISPR that only share or insert certain key genes and not actually damage the microbes or leukocytes to test and teach them how to use the immune response of Cas-9 which could be then tested with real versions of the test tubes.This CRISPR Cas-9 immune response can be added to tissues and cells that the N.meningitidis,Ebolavirus viruses infect for replication.To determine the genes that need to be interspaced experiments can be made via creating leukocyte bacterial hybrids of human leukocytes namely CD4+ T Lymphocytes containing CRISPR Cas-9 from S.pyogenes that can be purposefully infected with these pathogens and a means to determine the first set of genes to be injected can be determined via using multiple bacteria that are hybrids of human leukocytes with different sets of genes from them each pathogens or have none to test the bacteria hybrid response to infection and then after replication attempts the hybrids can be analysed for DNA from HIV,N.meningitidis,Ebolavirus etc is present in them when they fight back.These will be tested in leukocyte samples in artificial blood containing the human CD4+ T Lymphocytes and also SUP-T1 and 293T cells as well as chimpanzees and mice engineered with human recombinant DNA and those from S.pyogenes that create human CD4+ T Lymphocytes with the CRISPR Cas-9 system with the animals injected with large levels of the virus to allow large amounts of the hybrid leukocytes to be attacked and fought off with then after a while the blood extracted and then the CD4+ T Lymphocytes DNA analysed to see which ones contain RNA from HIV with this done on multiple animals and also test tubes containing infected blood that test all strains of the virus and the sequences of RNA from the virus kept in the modified lymphocytes with this done in separate leukocytes for each strain or one set or both one at the same time to see what RNA markers each strain is kept by the modified lymphocytes with AI using this information to determine what all possible strains would leave what markers behind.One set of microbes and modified lymphocytes will have all strains of the virus in both animals and test tubes to see where the RNA markers from all strains are kept after they are infected.After a while the lymphocytes will be extracted and thus run through DNA analysers with AI analysing all strands of DNA to see what are human DNA,bacterial S.pyogenes DNA and those that are RNA from the virus with the RNA and DNA from each strain analysed in each set including the one that had all strains attempting to infect the leukocytes to see where the RNA strands of each strain are interspaced to be mass produced using 3D DNA printers.Thus each set of test tubes containing the modified lymphocytes and chimpanzees or ideally mice with human recombinant DNA to produce the modified human CD4+ T Lymphocytes can be used to test each strain of the virus with one set of both test tubes and animals testing all strains of HIV at once to see which RNA markers are left in place of the CRISPR immune system for each strain with the one infected with all known strains will determine what RNA markers will be there and where in the CRISPR system they will be placed exactly using 3D DNA printers.This will stored in Physis and an augmentation sub network and this and 3D DNA printers will allow the CRISPR immune response for HIV etc and different versions of it to inserted into base and augmentation microbes for upgrades to living patients and be mass produced to be added to the patients genome via augmentation strains and anti-viral strains of microbes.This can be done for versions for each strain and a version for all strains.AI can also extrapolate the genes for versions for each strain and a version for all strains.These sets will use mice and test tubes with multiple animals and test tubes as mice and test tubes will allow for quick results.This will also involve both pre and post infected animals both mice and chimpanzees with human recombinant DNA to produce human lymphocytes.Ideally the mice and chimpanzees hybrids will be engineered to produce human leukocytes with these tests replicated for the anti-viral strains of microbes in test tubes with their DNA housing the CRISPR system and the RNA of all strains in all key spaces through 3D DNA printers.Animal test subjects such as chimpanzees with human DNA to produce human leukocytes can have microbes and the human leukocytes in them have the CRISPR Cas-9 defense system engineered into the that after infection can have them after a while have their blood extracted and then the CD4+ T Lymphocytes DNA analysed in DNA analysers to see which ones contain RNA from HIV with AI analysing all strands of DNA to see what are human DNA,bacterial S.pyogenes DNA and those that are RNA from the virus are present with the RNA and DNA from each strain analysed in each set including the one that had all strains attempting to infect the leukocytes to see where the RNA strands of each strain are interspaced to allow microbes to mass produced using 3D DNA printers and for humans to through gene therapy have S.pyogenes DNA and RNA from HIV interspaced into their DNA in the bone marrow for humans and also in cellular DNA in microbes.If possible microbes can be used to determine the exact RNA markers and their location for both themselves and lymphocytes in test tubes with all strains of the virus.AI such as Phanes can by itself determine where strands of HIV DNA/RNA needs to be interspaced by analysing the genome of the HIV.3D DNA Printers will create microbes that house these exact sequences of DNA from the virus and S.pyogenes DNA for anti-viral strains and augmentation strains for humans to havd this applied to the patients bone marrow to have native leukocytes to harbour it.When new strains arises these tests can be done again using it by itself or all strains at once and then the patient upgraded with gene therapy that adds this new RNA marker to their leukocytes.If need be other tests and thus gene therapy this time involving the dendritic cells and macrophages in order to deal with Ebolavirus and N.meningitidis that can be applied to all uninfected patients with tests done using these leukocytes in test tubes or in animals engineered to create human versions infected with the pathogen.This can also involve human tissue cultures of various organs fitted with the CRISPR Cas-9 system that would again be tested against Ebolavirus and N.meningitis in both human/animal hybrids that have human organs or tissue cultures to prevent from infecting them alongside the dendritic cells in uninfected patients with gene therapy added to the cells of these organs to allow them to utilise this mechanism with the genes that these two pathogens use in dendritic cells and organ cells determine via these tests.This determination of the first set of genes inserted into the hybrids by each pathogen and thus which ones can be interspaced into microbes and native leukocytes to have the CRISPR Cas-9 immune response can be done labs around the world starting by 2023/2024 and be determined by at least 2025.This will allow the microbes and leukocytes that have this protective mechanism be able to instantly be able to fight off any strain of the virus instantly in both infected and uninfected patients as another method of attacking the virus and killing it in response to attacks by the microbes and native immune system alongside them using chemical and wifi signals to have other microbes and native immune system gather in place and fight virions and apply anti-viral compounds and antibodies via bumpers,anabolic and catabolic actions etc.Thus both anti-viral microbes and lymphocytes affected by Ebolavirus,HIV and N.meningitidis will be fitted with the CRISPR Cas-9 system to the viruses infecting them.This method may even play a role in disabling or destroying the viruses that attack leukocytes by the native immune system and offer extra protection to both uninfected and infected patients and via gene drive technology to unborn fetuses alongside the application of the CCR5Delta 32 mutation negating the need for patients to take protease inhibitors and also other anti-viral combination therapy with this as stated tested on chimpanzees and mice that have human recombinant DNA to produce leukocytes that are hybrids or are solely human ones starting as early as 2023/2024 involving these animals injected with the virus born with this mutation and those already infected an given the mutation and other viruses that infect leukocytes with this possibly extending to organs infected by other viruses.Thus organs infected by viral pathogens and possibly even bacterial ones can have them given this ability as well preventing the pathogens infecting them when they cant do so to the leukocytes.Ideally these protection measures will contain the key genes of all strains or those common to all possible strains of HIV will be done so as to make it effective to all strains that may infect uninfected patients and those already in infected ones and those that arise from mutations with the aforementioned lab experiments also determining this by applying all strains to test lymphocytes and determine which ones are used by each strain with the mechanism developed for all types of viruses that infect leukocytes,organs etc.AI by 2023/2024 should easily determine the required genetic sequences present by scanning the genome of all strains of HIV and carrying out these tests in labs allowing them to be available to human patients in 2025.This alongside the CCR5Delta 32 mutation will be applied to the patient via advanced gene drive technology to be a permanent part and also pass onto the patients unborn fetus if both parents have this phenotype preventing the virus gaining a stronghold in the unborn child with uninfected patients having this protection measure to prevent the virus gaining a stronghold.This and the CCR5Delta 32 mutation added to infected patients will allow them to live healthy lives indefinitely without the need for taking antiretroviral therapy.Anti-bacterial and anti-cancer strains will be added to the patient to aid in the primary immune systems functions to again let the primary immune system bounce back to healthy levels with the genes applied to the genome in a cells in the body and not just the bone marrow.Applying this,immunisations and anti-viral strains to all non infected patients worldwide will prevent the virus spreading,gaining a stronghold and allow newly infected patients to be cured instantly thus stopping its spread globally with advanced gene drive technology making it a permanent part of the human genepool.Having the resistance to the virus and also defence mechnaism added to both heterosexual female and male partners using advanced gene drive technology would pass this to unborn foetuses thus preventing the virus gaining a stronghold and allowing the child to be cured instantly as microbes would be passed from mother to child immunising them and also fighting off the virus.Thus having the CCR5Delta 32 mutation and CRISPR immune response added to both parents prior to conception via advanced gene drive technology will ensure any conceived children will have these phenotypes to prevent the virus gaining a stronghold in the fetuses body ensuring it will not gain a stronghold despite it entering the childs body and allowing microbes passed onto it at birth to fight it off instantly alongside immunisations to wipe it out of the childs body instantly.This will negate the need to take anti-retroviral therapies to prevent it passing from parent to child.If not then women should continue to take medication to prevent the transmission of the virus to the unborn child though both taking medication and passing on the CCR5Delta 32 mutation should be carried out with this tested on animals with human DNA first by 2023/2024.This can be tested on chimpanzees first while infected women still take drugs that prevent the virus passing onto her child until it can be fully shown in animal subjects that it is possible and that the advanced gene drive technology passes this to their children and that this is successful in 100% of cases of infected women with the resistance added able to pass this on and not the virus.Testing the efficacy of the genes will begin on tests on chimpanzees and mice as early as 2024-2025 on pre and post infected animals with human recombinant DNA to produce human lymphocytes.Since the person will be protected the microbes can engage in long battles taking out large numbers of the virus alongside radiation treatments and immunised primary systems are wiping out large numbers of the virus and then rest for a while to feed on sugars and fats taken in by the patient in large amounts at the behest of Paean to recharge for another battle straight away over and over again.The lymphocytes can also be altered to upon any chance the virus attempts to infect them will signal to the immunised primary immune system and microbes to gather in their place and flood the area with anti-viral compounds and antibodies.Both measures will be modified to protect against all strains of the virus and all possible strains and will beginning testing on mice and chimpanzees and test tube using modified CD4+ T Lymphocytes in blood samples by 2023/2024 with these measures preventing the virus replicating and thus mutating since HIV mutates very quickly by creating billions of copies each time it replicates that are slightly different from the progenitor virion and also its siblings this would keep the number of strains of HIV down to a minimum and also it would prevent it gaining resistance to antibodies and anti-viral compounds at the microbes and primary immune systems disposal leaving the virus in a vulnerable position by preventing it mutating.If possible all patients worldwide would get immunised via the common proteins method,have the protective measures included into their genome such as the S.pyogenes CRISPR immune response and CCR5Delta 32 mutation and also have anti-viral strains added to them to halt the spread of the virus completely and allow newly infected individuals to be cured instantly with them applied to all already infected patients to allow them to survive indefinitely without taking anti-viral medications.This will be added to all cells in the body or the bone marrow with the CRISPR Cas-9 immune response again add extra protection for both infected and uninfected patients and work in cases where the CCR5Delta 32 mutation cannot be added to the host for any reason.Their effects can be tested on chimpanzees and mice already infected with the virus and on protease inhibitors with the mutation added via proto microbes and those born with the mutations and CRISPR Cas-9 aided leukocytes then infected to test its efficacy on keeping the patient resistant to infection with them having human recombinant DNA to produce human leukocytes or hybrids with the animals viral loads tested routinely after and while anti-viral treatments are given can start as early as 2023/2024 to allow to be applicable to human trials and full versions by 2025-2029.The CRISPR Cas-9 immune response added to leukocytes will also protect the patient against other strains of the virus that tweaked versions of the CCR5Delta 32 mutation cant.Both protective methods the CRISPR Cas-9 immune response and CCR5Delta 32 will be tested on chimpanzees and mice in sets ie one with the CCR5Delta 32,one with the CRISPR Cas-9 immune response and one with both with all of these tested on post and pre infected chimpanzees and mice that have human recombinant DNA to produce human leukocytes.The chimpanzees and mice will also include groups that have both methods added to them using proto microbes and those born with them.Test tubes of blood infected with the vatrious strains of the virus that have these altered lymphocytes from animals or the lymphocytes have the relevant DNA added to them individually to test if the virus can infect them with all versions of the mutation including universal versions tested in test tubes and on animals against all strains.If neither can be applied the patient will still be required to take protease inhibitors while the immunised primary immune system and microbes act on the virus.Both will be applied to all patients whether infected or not to act as backup where the other has drawbacks.The same can be replicated with Ebolavirus and N.meningitidis by analysing the DNA of populations resistant them and also AI creating genes from scratch that prevent the relevant leukocytes and organ tissues from being infected with genes also created and added to organs they infect to prevent them from infecting them with the CRISPR Cas-9 immune response added to these leukocytes and organs modified to attack the viruses.By having the host housing the CCRDelta 32 mutation added to them via gene therapy it will leave the virus unable to use CD4+ T Lymphocytes to replicate and allow the patients native immune system to rebound snd thus be able to normally fight off tumours snd infectioms.Havibg the microbes anto-viral strains housing the same receptors as the CD4+ T Lymphocytes that HIV uses to infect thrm will force the virus to interact only with the microbes if it wants to replicate.The microbes can be fitted with the CRISPR Cas-9 immune response of S.pyogenes by having the DNA of HIV interspersed in it will prevent the viruses destroying then but once attack the microbes through both genes present and instructions from Paean via Biosynth wifi be engineered to then apply the CRISPR Cas-9 immune response and then also anti-viral compounds at is disposal and also apply CRISPR treatments that change its genome beyond recognition.This would leave the viruses unable to replicate and thus easily wiped out by microbes and radiation treatments.The microbes can attack the virus wither when the virus attempts to use it as a replication vector or do so actively through Paean encouraging them to actively seek out the virus with meditating etc applied through phagocytosis and nanoparticle laden bumpers while antibodies are synthesised in the bloodstream.The microbes can on demand by being told by Paean via Biosynth wifi synthesise large amounts of antibodies in the bloodstream that will flush out of the body via urine and feces while they can also on demand synthesis large of the antiviral compound in synthetic bumpers to prevent immune response or cytotoxity to kill large amounts of the virus that will flush out of the body through feces snd urine.This can be done alongside microbes potentially removing the viruses GP120 glycoproteins and thus since having the same receptors present on CD4+ T lymphocytes force the HIV viruses to attach an interact with only the microbes in order to replicate that have the relevant receptors to interact with the viruses GP120 glycoproteins present in HIV since the microbes would be hybrids of macrophages,CD4+ T lymphocytes,dendritic cells and even plasma cells and other leukocytes and will allow it to kill it through applying viricidal compounds such as lemon juice,melittin,N6 and tri-specific antibodies through phagocytosis instantly as a reaction to them attaching to them or flooding the bloodstream with the compounds.This will play key role in testing the efficacy of immunisations in already infected patients and allowing uninfected patients to quickly fight off infections.As detailed later on the microbes can flood the body through the bloodstream and lymphatic system with bumpers that house DNA to interact with the genome of the virus to cause them to loose their glycoproteins preventing them attaching to normal CD4+ T leukocytes both in the patient and any patients infected by the host and also the microbes themselves as well as become susceptible to the compounds at its disposal allowing for millions of virions at once to be affected disabling the virus and thus making them unable to mutate,make them susceptible to compounds at their disposal and also undergo apoptosis in bumpers added with advanced gene drive technology and then release all anti-viral compounds that inhibit and kill HIV such as melittin,cyanovirin-N,Di-dehydro-Cortistatin A,lemon juice,virkon etc in the form of nanoparticles covered in the same natural or synthetic bumpers that bounce off normal healthy cells but interact only with the surface of the virus to kill off all virus particles that are kept under control by protease inhibitors and the modified resistant leukocytes with excess flushed out through urination to limit side effects.Otherwise these would also be applied by phagocytosis when they entrap virions with this and bumpers making microbes the ideal vector for all anti-viral compounds that can inhibit and kill HIV.The microbes housing modified virophage and bacteriophage DNA merged together to not need a helper virus will be able to have base microbes scan the HIV viruses unique strain and create schematics of endolysine type material that will be used by anti-viral microbe strains using bumpers to kill the virus from the inside out.Thus the microbes would act as a bear or mousetrap to HIV and other and pathogens that use leukocytes to replicate with this replicated with Ebolavirus and N.meningitidis by them having the same receptors as the leukocytes they infect since the anti-viral strains would be hybrids of various types of leukocytes that the pathogens namely HIV,N.meningitidis and also Ebolavirus infects by having the unaltered receptors they interact with and the native immune system would be made resistant to the virus forcing the virus to interact with the microbes as once the virus attaches to the microbes they would apply melittin,lemon juice nanoparticles in bumpers or via phagocytosis alongside the CRISPR Cas-9 immune response.In both existing infected and newly infected individuals the microbes once a virus would attach to them would signal to other microbes and the immunised primary immune system to gather to the area and to release DNA housed in bumpers and then nanoparticles of the anti-viral compounds covered in bumpers and also antibodies in the case of the primary immune system with this replicated for bacterial pathogens in reaction to wipe them out of the patients body with them using the lymphatic system and bloodstream to spread them to all parts of the body the microbes sending relevant memory plasma and killer T cells and other microbes to various parts of the body including the testes to wipe out traces of the virus in semen and also in hard to reach places.This can be used to allow virophage features to apply endolysine like material to the pathogen with the microbes protected with their own version of the CRISPR Cas-9 immune response that prevents the virus using the microbe for replication and would signal the microbes to send for memory plasma cells and other microbes to gather in its place and release anti-viral compounds and antibodies when the virus attempts to replicate inside the microbe.If possible once the virophage DNA in them has received schematics from base microbes or the DNA present them of the strain of the virus in the patient they could release endolysine like materials in bumpers to be able to intercept all viruses or just HIV.The microbes guarded would be protected against the virus entering them and replicating or using its DNA to replicate by them have only the receptors present on and not the same surface and internal proteins,makeup and structure as CD4+ T lymphocytes since they would be hybrids of them and other leukocytes that prevents this,have the DNA inside them protected from the viruses replication abilities,ability to use the hosts DNA for this and even prevent them entering in the first place through intensive engineering and gene drives that prevent this by preventing the microbes DNA from being used in replication,the compounds created by the microbes doing this and also preventing the virus affecting other cells and also by applying CRISPR treatments applied instantly to prevent this alongside those that cause it to undergo apoptosis,remove its GP120 glycoproteins and make them susceptible to the compounds at its disposal that it may become resistant to kill it,releasing the cyanoviran-N,Didehydro-corstatin A and other compounds that inhibits it ability to infect them as nanoparticles in reaction to this and then the other compounds such as melittin and lemon juice and antibodies that kill it.Upgrades can be done at home or via wifi that changes the genetic sequences in microbes,CD4+ T lymphocytes and organs when new infections occur or when the newest infections occur.If the protective measure doesnt destroy the virus but only disables it then it would be used by the native leukocytes to alert the memory plasma cells and also other ones and even the microbes anti-viral strains to the virus attaching to it and thus gather in the area and produce antibodies from being immunised or those from populations that produce tri-specific and N6 antibodies whose genes are added to the bone marrow or entire genome of the host both during first treatments but also when residual virions are left in the body when the vast majority of the virus has been killed off leaving the virus undetectable and also during reinfection and also in initial infections in unifected individuals.The attacked CD4+ T lymphocytes will thus signal to microbes and the rest of the primary immune system mainly memory plasma cells to gather in the area and release antibodies and anti-viral compounds via gene therapy to recognise when they are being attacked.Thus infected patients would keep this ability and CCR5Delta 32 to allow any reinfections and any remaining virions to be killed off instantly thus preventing the virus rebounding ensuring every last virion is killed by both the native immune system and also microbes.The microbes like native CD4+ T lymphocytes that has the CRISPR Cas-9 immune response would also have this system of response to attempts of the virus to infect them and signal to other microbes and also the memory plasma cells and other leukocytes to gather in the area and attack the pathogen with this done to kill off every last virion preventing it rebounding,prevent reinfections and attack all virions in newly infected individuals that have these measure and also microbes prior to infection.Again infected individuals would be immunised against the virus to improve success with the microbes engineered using recombinant DNA from virophages and those from scratch tweaked could also allow them to purposefully hunt down the virus helping in cases where the resistance cannot be transferred and anti-viral medication should still be taken.If these compounds such as cyanoviran-N,Didehydro-corstatin A,melittin,lemon juice do not kill HIV then CRISPR treatments applied by the microbes through phagocytosis and horizontal gene transfer or applying theses treatments via bumpers flooded in the bloodstream can modify the virus into becoming susceptible to them and thus be killed by it applying CRISPR treatments either via again flooding the bloodstream with bumpers containing DNA or through phagocytosis that change the viruses internal and external structure during phagocytosis or by flooding the bloodstream with bumpers containing the DNA to be then made susceptible to them by having it express the same outer structure as benign strains of HPV,Rhinoviruses,Orthomyxoviridae etc as well as scratch DNA to express outer structures that can be destroyed by them with this also applied to any pathogens that gain resistance to the compounds at their disposal and new pathogens especially viruses and fungi.The virus can be then destroyed by all of these and other compounds applied during phagocytosis instantly once the CRISPR treatments are applied or the compounds can be released into the bloodstream as nanoparticles in bumpers that interact with the virus and not the patients cells to cytotoxicity.Scratch DNA can be extrapolated by AI to have it express outer structures that can be killed by them.This should ideally be the same protein capsid and exterior structure of benign HPV,Rhinoviruses,Orthomyxoviridae strains to have cyanovirian-N applied or scratch DNA can have it express protein coats that can be destroyed by lemon,juice and melittin,cyanoviran-N,Didehydro-corstatin A.Scratch DNA extrapolated by Phanes can allow the compounds kill it by destroying their protein coats etc.This will be also done to other known viral pathogens outside of HIV,MRSA including Rhinovirus and those from Orthomyxoviridae to limit the genotypes present in anti-microbial and anti-viral strains.If will also be done should the virus be able to mutate quickly with the fact the patient will be made resistant to the virus interacting with the CD4+ T Lymphocytes would prevent to replicating and thus able to mutate with this also done to ensure the antibodies produced by the primary immune system are still effective.These compounds will also be released via bumpers to bounce off healthy cells and once the CRISPR treatments make the virus susceptible to all compounds they can all be released at once alongside antibodies from the immunised primary immune system.Suicide genes could also be applied alongside those that remove its GP120 glycoproteins to prevent it infecting cells,remove genes essential to its survival as well as function and the microbes with them applying multiple genes to prevent mutations or allowing it to adapt via “carpet bombing” it with as many treatments as possible with removal of the GP120 glycoproteins preventing it infecting other lymphocytes or patients these specific virions infect with it through extensive CRISPR treatments even made into a benign strain of HPV,Rhinoviruses,Orthomyxoviridae strains that the immune system can fight off by rewriting the viruses RNA to the point that it is mostly HPV,Rhinoviruses,Orthomyxoviridae benign strains with only trace strands of the original virus that render it harmless and capable of being killed off by the primary immune system.This could allow the native immune system by itself and immunised against these benign viruses clear the body of it.Firstly the CRISPR treatments will remove the GP120 glycoproteins thus preventing it unable to infect leukocytes and unable to affect the patient leaving them benign.If possible the virus once it’s GP120 glycoproteins and outer protein coats are removed can be made to express phospholipid bilayers and protein coats of benign species of bacteria and viruses that the immune system can fight off and is immunised or vaccinated against and is susceptible to antibiotics by having bacterial phospholipids(that is not a superbugs)in place of its outer protein coats that are susceptible to everyday antibiotics such as penicillins which can be taken routinely for several months or synthesised by the anti-bacterial strains with suicide genes also added.The outer coats of the virus can be made to express the phospholipids of benign bacteria that can be killed by antibiotics like penicillin with its internal structures also modified to become similar to benign bacteria that can be killed by antibiotics such as penicillin with gene drives making this alteration permenant thus preventing it gaining a resistence to antiobiotics.Genes from bacteria that allow them to undergoe mitosis will not be added to the virus with since its GP120 glycoproteins are not present it will be unable to replicate or increase its numbers thus keeping levels of the virus at a constant levels and mutation blocking genes present to prevent it mutating.Without the GP120 glycoproteins it will be unable to infect leukocytes with it also despite having bacterial DNA it will not be given genes that allow it to undergoe mitosis thus ensuring the levels of this new virus/bacteria hybrid will stay in the body at stable levels as it will be unable to undergoe mitosis.As a result the virus will no longer be a virus but rather a bacteria that will be a benign species that cannot damage the patient,cannot replicate or undergoe mitosis thus leaving it susceptible to the primary immune system and antiobiotics.Biosynth WiFi can be added to the virus/bacteria hybrid to allow the location and number of them to be relayed to Paean.Once large amounts of the virus are converted to this bacteria/virus hybrid it will be able be killed off by the patients administered penicillin by pill form,injections and even the microbes anti-bacterial strains themselves within the body with this done in rounds of adminstration until the patient is cured of the virus.The microbes can apply CRISPR treatments that makes it outer protein costs susceptible and thus killed off by antibiotics such as penicillin etc and also even compounds found in over the counter medicine such as Lemsip and even vitamin C from eating fruits and also using vitamin supplements as well as medicinal marijuana.These CRISPR treatments applied by the anti-viral strains of microbes through both horizontal gene transfer and through bumpers that as transportation vectors will remove large strands of the viruses RNA and replace it with new strands of RNA and DNA that change it beyond recognition to the point it can be killed off by the primary immune system and also everyday medications to treat viral,bacterial and fungal pathogens such as penicillin,Lemsip and even medicinal marijuania,herbs as well as excess nutrients in the body such as vitamins injected into the bloodstream and consumed by the patient with this replicated with all viruses outside of HIV especially new ones alongside making them susceptible to compounds at the anti-viral strains disposal.It will also make it completely benign or die off in the bloodstream by making the virus unable to survive the internal homeostasis of the patients body making it unable to survive the temperature and pH ranges of the blood.Thus the virus will first have its GP120 glycoproteins removed completely by removing the strands of DNA/RNA to express this thus leaving it unable to replicate and then have the outer proteins of the protein capsid modified to express that of benign viruses and bacteria that the native immune system can kill by itself or be killed off by antibiotics such as penicillin and also even over the counter medicines that treat everyday ailments etc such as penicillin Lemsip,herbs and medicinal marijuania by removing large strands of the viruses DNA and RNA and then replacing with that of benign bacteria and viruses as well as scratch DNA that allows these everyday compounds that are inhaled,injected and injested into the bloodstream to kill the modified virus.The primary immune system due to the prescence of the CCR5 Delta 32 mutation would be able to rebound and fight off the virus especially when immunised against and also fight off against the modified forms of it.If need be once the CCR5 Delta 32 mutation is applied virions can be modified to have their GP120 glycoproteins removed to further prevent infections in other patients and extra proctection against decimating the immune system of patients with the patients immunised immune system activated to allow the body to fight it off with antibodies and the microbes synthesing tri-specific and N6 antibodies through anabolic and catabolic reactions and at the same time actively seeking out virions and applying the anti-viral compounds via phagocytosis..The virus through extensive rewriting can even be turned into microbes,benign virions and human cells that are flushed out and if need be even leukocytes all with the patients DNA.If possible all DNA/RNA needed for it function will be removed alongside all DNA/RNA leaving it an empty husk of surface proteins etc that will either be flushed out of the body,break down or even be killed off and consumed by the native primary immune system.Suicide genes can be added that cause the virus to undergo apoptosis.These and all CRISPR treatments utilised against HIV and other pathogens should use advanced gene drive technology to increase effectiveness and add genes using advanced gene drive technology that prevent the newly modified virus mutating.Upgrades can add new compounds that do kill the virus overtime that would be tested in automated labs worldwide with all known natural compounds from plants and animals worldwide on petri plates and test tubes of infected blood ,as well as using simulations.If possible synthetic viricidal compounds or at least the componants that have viricidal properties to HIV synthesised by them during phagocytosis in response to them being intercepted by HIV particles would be done to limit its release into the bloodstream or it can be created on the spot via anabolic and catabolic reactions then changed into benign compounds once used,applied with bumpers or the host can be be made immune to it via gene therapy using scratch DNA.As stated infected patients will be immunised by other strains to aid in the eradication of the virus from their body with this activated by the anti-viral strains signalling to them to attack with them if possible using recombinant DNA from all populations that produce the tri-specific and N6 antibodies.Otherwise they could on reaction to the virions attaching to the receptors or through detecting them in the surrounding area flood the bloodstream and lymphatic system with the bumper laden nanoparticles of the viricidal compounds,antibodies all at once to allow them to reach all parts of the body and kill off any HIV virions.This when the patient is made resistant to the virus would negate the need for protease inhibitors with if possible altering HIV virions via CRISPR to remove their GP120 glycoproteins alongside altering native leukocytes and using Di-dehydro-Cortistatin A to allow infected patients to use less or no anti-viral drugs if shown to be effective in combination.During phagocytosis the microbes can apply these and other compounds and CRISPR treatments to consume the virus using it as nutrition including its RNA as nutrition through catabolic and anabolic reactions.Flooding the body will allow the antibodies and bumper laden nanoparticles of each compounds from both microbes and immunised primary immune system through the bloodstream and even the lymphatic systems allowing it to reach all corners of the body especially hard to reach places and all places it hides.The use of Didehydro-corstatin A and the engineering of the leukocytes to be unable to be infected will allow the native CD4+ T Lymphocytes to return to normal levels alongside the other strains combating any infections that arise preventing the patient from dying from opportunistic infections and potentially negating the need for protease inhibitors and combined anti-viral therapy improving success in eradicating the virus from the body.Once the patient is cleared of the virus the C-C chemokine receptor type gene can be returned to the hosts genome and thus allow the patient to regain the functions of this genes functions.Cells both tissues and leukocytes that the virus hides its DNA in will be edited with CRISPR to remove the virus and its DNA if need be caused to undergo apoptosis and have new tissue grown in its place with uninfected patients have these tissues edited making them unable to be infected in the first place.Semen and other bodily fluids and all areas of body where HIV and other viruses is able to infilitrate and hide in will be inhabited and treated by the microbes and immunised immune system.Once the patient is cleared of the virus the C-C chemokine receptor type gene can be returned to the hosts genome and thus allow the patient to regain the functions of this genes functions.If possible to prevent reinfection the mutation can be tweaked in order to retain its original functions and still make relevant leukocytes unable to be reinfected.Cells both tissues and leukocytes that the virus hides its DNA in will be edited with CRISPR to remove the virus and its DNA if need be caused to undergo apoptosis and have new tissue grown in its place with uninfected patients have these tissues edited making them unable to be infected in the first place.Current functional cures that are being developed using vaccines from recombinant DNA from resistant populations can be applied alongside these methods to increase success with the romidepsin created by the microbes through recombinant DNA from C.violaceum or injected into the body to aid in the actions of the microbes by finding and attacking infected lymphoctes that may be a challenge with this allowing the patient to survive without protease inhibitors alongside the action of Di-dehydro-Cortistatin A and N6 and other tri-specific synthetic antibodies engineered into both the primary and secondary immune to allow the microbes to apply viricidal compounds such as melittin and lemon juice onto the virus that is unable to use CD4+ T lymphocytes to replicate.Again the microbes would apply CRISPR treatments that weaken the virus against the viricidal compounds present,prevent it from mutating,remove any resistance it has at the same to ensure effectiveness using the “carpet bombing” techniques.They could also could do this if the native immune system is decimated by the virus and them also fighting off cancers,pathogens and opportunistic infections,immunising the native system until the virus is eliminated allowing the native immune system to recuperate with them doing this while the patient is made resistant and they no longer take protease inhibitors to ensure that the patient is able to survive indefinitely should the lymphocytes be compromised in any other way.This should only be done if show safe on chimpanzees and mice.If possible their could be the option of the negating the need to add resistance if it cant be done or if doesnt work for all strains,keep taking protease inhibitors and allow the microbes flood the bodies with antibodies and nanoparticles of the various anti-viral compounds that kill HIV with the native immune system immunised also while other microbes fighting of any cancers and opportunistic pathogens with the microbes boosting the immune system through chemical signals or even immunising the primary immune system through interactions with the dendritic cell,plasma cells and killer T cells etc before the protease inhibitors are not removed to keep the virus in control as both microbes and native immune system attack it to allow the native immune system fight back once alerted to the viruses presence via chemical signals from the microbes.Of course this would be done on chimpanzees and mice to test its effectiveness but humans can use them at first with protease inhibitors taken and then when shown to be able to fight off the infection the resistance will be added to negate the need for inhibitors that cause side effects and save on resources.Thus human patients given the CCR5Delta 32 mutations and tweaked versions to give resistance to all strains will continue to take anti-viral medication until it has been shown through routine tests that the viral load and antibodies are decreasing and CD+4 T Lymphocytes levels are increasing.In this case the native immune system would be immunised to fight of the infection alongside the microbes.In cases where resistance cannot be transferred then the microbes and immunised primary immune system should be able to be utilised alongside immunisation while the patient takes protease inhibitors and other anti-viral treatments.To test the effectiveness of resistance samples of blood containing CD+4 T Lymphocytes can be taken while the patient still takes protease inhibitors and the sample and the lymphocytes exposed to the same strain of HIV in a test tube containing donated or infected artificial or donated blood as well as also SUP-T1 and 293T cells.T lymphoctes and macrophages or under a microscope to test the viruses ability to infect and samples of DNA from the lymphocytes and other cells in the body can be checked for the presence of the CCR5Delta 32 mutation with the immune response from the immunised primary system tested by detecting levels of antibodies produced in blood samples and also test tubes.This can be done with phlebotomy robots and automated labs and in time base microbes.Eventually the microbes will teach the immunised immune system to attack the viruse themselves in both chronic infections and also in any future infections with this of note in HIV infections as this will allow the immune system to fight off these with the antibodies tested in blood samples in home test kits to see if the level of them is decreasing or increasing denoting the stage at which they are from cured.The length of to being cured of HIV will depend on the level of virions in the body with the patient being immunised,microbes using their anti-viral compounds and CRISPR treatments and also the patient once made resistant to radiation undergoing multiple bouts of radiation therapy.Tests repeated annually using dongle home test kits and in hospital automated labs will test for the prescence of the CCR5Delta 32 mutation by analysing the DNA of CD+4 T lymphocytes present but will also measure antibodies produced by both the primary immune system and microbes,measure the levels of CD+4 lymphocytes and other leukocytes and more importantly the viral load all logged by date in ones patient file with graphs and Paean relaying progress.Patients will also be immunised using the common proteins method immunised against all major viral,fungal and bacterial pathogens that could kill the patient via being opportunistic infections.Patients already infected with HIV will also be immunised against their own strain and all strains of HIV and the primary immune system activated to produce its own antibodies and the anti-viral strains creating N6 and tri-specific antibodies via anabolic and catabolic reactions and anti-viral compounds such as lemon juice and mellittin delivered in bumpers.All types of anti-viral combination therapy can be created by the microbes daily via anabolic and catabolic reactions to prevent them being created and shipped to patients and bypass the stomach with less side effects.Di-dehydro-Cortistatin A,cyanovirin-N could be synthesised by anti-viral strains in already infected patients to replace protease inhibitors once the CCR5Delta 32 mutation is added to them as a backup with it also done in those without this mutation provided animal trials show it is safe due to their ability to inhibt the replication of the virus and inactivate it with these and melittin applied as bumpers or during phagocytsis to prevent it breaking down in the bloodstream and also causing damage to healthy cells in the case of melittin.Ideally patients should continue to take protease inhibitors and other anti-viral treatments for at least a year or two even with the CCR5DELTA 32 mutation is added to see that the immunisation,resistance and microbes are eliminating the virus through getting samples taken frequently every month using home test kits and phlebotomy robots in automated labs to measure the levels of CD+4 T lymphocytes,antibodies and also viral loads logged into ones digital patient file with this then allowing one to remove the need to take any anti-viral combinations indefinitely with these tests continuing until the levels of antibodies and viruses cannot be detected signalling that they are cured.These tests would test the levels of antibodies,the virus and CD+4 T lymphocytes with the lymphocytes tested for the CCR5 delta mutation to see it is present.These tests taken every month for a few years will show the levels of antibodies,the virus and CD+4 T lymphocytes plotted on graphs in ones digital patient file.When the graphs show the levels of CD+4 T lymphocytes rising to stable levels and detects the CCR5 delta mutation in the lymphocytes then it signifies that the levels of lymphocytes are rebounding to healthy levels meaning patients may no longer need to take protease inhibitors anymore.The tests may also detect levels of antibodies and anti-viral compounds created by the microbes determining the fact that the are being produced by the microbes and immunised primary immune system and are fighting the virus with the viral load of HIV also measured with this showing that the level of viral load is dropping showing that the patient is being cured.Once the tests show that no anti-viral compounds and antibodies are no longer being produced and the levels of HIV is down to zero then the patient can be cured.The anti-viral,anti-helmenthic,anti-bacterial and anti-cancer strains will fight off opportunistic infections and cancers before and after they stop taking protease inhibitors and will be used to measure the efficacy of the resistance when people stop taking medication decided by Paean as the strains will fight off pathogens and tumours and allow the native system to rebound so if it works the level of CD+4 T lymphocytes will rebound to normal levels and if it doesnt then at least the anti-viral,anti-bacterial and anti-cancer strains will keep the patient alive and then fight off the virus.These tests and also base microbes can show that the CCR5Delta 32 mutation and CRISPR immune response system is present in the lymphocytes and also the other cells of the body including bone marrow etc.Levels of CD4+ T lymphocytes,anti-viral compounds,antibodies and of the virus will all logged into their patient file via testing booths for STDs and blood components that measure all of these will be used to determine that the microbes and immunised primary immune system is fighting off the virus and that the lymphocytes levels are rising due to them not being infected any more and the virus disappearing.Thus this dectection of the CCR5Delta 32 mutation and measuring the levels of CD+4 lymphocytes and other leukocytes will show that the CCR5Delta 32 mutation is working as since the virus can no longer replicate normally even without protease inhibitors the levels of CD+4 lymphocytes and other leukocytes will be tested to show their levels to show that the CD+4 lymphocytes and other leukocytes rebound to healthy levels and can fight off the virus once immunised and activated thus also allowing it and anti-cancer,anti-bacterial,anti-viral strain to fight off infections and tumours like in normal unifected patients with the microbes and other treatments also fighting off the virus speeding up recovery.Tests of antibodies and viral load taken will show that if rising show that that the microbes and immunised primary immune system are fighting the virus with decreasing viral load showing that the patient is being cured.All results of these test done using home test kits and also in hospitals will be logged into ones patient file and plotted on graph and analysed by Paean.This routine testing taking place from anywhere from at the start every month to every few months will continue for several years to a full decade until it is shown that the patient is cured.In time implants will relay this information and will determine when a patient is fully cured.Once the levels of lymphocytes has risen and levels of the virus drops then the patient should no longer take protease inhibitors and other anti-viral treatment allowing them to live side effect free lives while the microbes and immunised immune system fight off the remainder of the virus with them taking routine tests logged into their patient file to determine when they are fully cured.When one has stopped taking anti-viral therapies then several times a month every month for a few months one should get tests done in both test labs in hospitals and also using dongles to test the viral load and antibodies to see that the resistance is working and that the virus cannot replicate and mutate and also further damage the immune system and the viral load is either dropping or staying stable to see that one can continue to not take protease inhibitors and anti-viral medication with if for any reason say the resistance does not work the viral load increases then they should back on the medication instantly and continue to do so until the virus is cleared from the patient with the immunised primary immune system and microbes are able to kill off the virus and any opportunistic infections and also cancers without the resistance if it fails with these tests shown to highlight the efficacy of the addition of the mutation to both infected and uninfected patients in preventing the virus replicating and decimating the primary immune system.If the resistance fails then anti-viral,anti-bacterial and anti cancer strains etc will fight off oppertunistic infections and tumours alongside the patient immunised against all major pathogens using the common proteins method.The protease inhibitors will be subsidised before becoming free.If they cannot have gene therapy applied then they should continue to take all anti-viral therapy until cured with if possible the microbes creating the protease inhibitors etc in the body via catabolic and anabolic reactions.The anti-viral,anti-fungal and anti-bacterial strains will fight off opportunistic infections especially fatal ones and anti-cancer strains fighting off opportunistic cancers in both those who are made resistant and those who cant and still take anti-viral therapy with them also immunised using the common proteins method immunised against all major viral,fungal and bacterial pathogens that could kill the patient via being opportunistic infections.This should be for the first wave of patients especially those taking part in clinical trials and if shown to effective then future patients will not need to take anti-viral treatments when infected since immunisation and microbes will protect them.Until it has been shown through these routine tests that antibodies are being produced,CD4+ T lymphocytes levels are increasing,and levels of the virus are dropping then they may stop taking medication with animal trials done with infected animals taking protease inhibitors and those not taking them highlight the role that they have on the microbes and immunised ability to fight the virus.While the patient has stopped taking anti-viral treatments they would be be protected by anti-microbial,anti-viral and immunised primary immune system fighting off infections and anti-cancer strains fighting tumours alongside the primary immune systems immunised to produce antibodies and the anti-viral strains fighting off the virus with the T lymphocytes unable to be affected by the virus.These strains will also fight against these once the patient is taking protease inhibitors with animal trials using infected chimpanzees with human DNA to create human leukocytes that have microbes based on these leukocytes showing how long the patient should continue to take medication to allow the microbes to get accustomed to fighting off the virus and the body adjusting to this.The microbes would edit cells that the virus hides in either removing its DNA in cells already infected by them or in fact editing these cells so they cant be used by the virus with this done in uninfected patients alongside immunisation and resistance.Any other conditions such as heart attacks and strokes caused by HIV infections could be alleviated and treated by them creating stronger tissue in these organs,repairing them as well as providing oxygen to the brain and other vital organs if they are compromised with organs weakened by the infection replaced with bioprinted ones that have been altered to be stronger.Blindness and other complications can be repaired by strains creating tissues to fix them alongside CRISPR.The patients who naturally produce N6 and tri-specific antibodies can be tracked down via patient files and their DNA added to Physis or if need be Paean and even his proto forms will be able to design scratch DNA to produce these.Paean could design genotypes for the remaining 1% of strains with the patient immunised against all strains of the virus to compansate for this.Those known to be able to produce these antibodies will be tracked down and their DNA fingerprint scanned from blood tests to have this analysed to determine the genotype that allows for this and thus have 3D DNA printers create them in base microbes and augmentation strains.Since being hybrids between plasma cells and macrophages and also CD4+ T Lymphocytes would allow them to produce these themselves alongside the primary immune system.Otherwise the strains could be instructed by Paean to produce these antibodies synthetically using catabolic and anabolic reactions using excess nutrients with these tri-specific and N6 antibodies chemical structures charted and stored in and downloaded from Physis onto the DNA digital storage of microbes with this repeated with other major pathogens whether bacterial,viral or fungal.Antibodies to kill off other strains will be extrapolated and then created by theses reactions.Those strains not affected by the tri-specific and N6 antibodies can also using CRISPR be modified into being affected by them with them also attacked by anti-viral compounds with the tri-specific and N6 antibodies can be aided by antibodies created by the immune system that attack all strains and all possible mutations using the common proteins method signalled to be produced by the microbes interacting with the primary immune system.Otherwise AI can extrapolate the structure of antibodies to kill the remaining 1% and them created by anabolic and catabolic reactions.Furthermore the structure of both N6 and tri-specific antibodies from human patients that produce them will have their structure analysed by Paean to be uploaded into Physis in a subfolder for the virus thus allowing its structure to be downloaded into DNA digital storage in microbes and synthesised in the bloodstream through anabolic and catabolic reactions by the microbes in large amounts to kill large amounts of the virus.Those that kill the remaining 1% of strains can be extrapolated by Phanes analysing the structure of these remaining 1% of strains and then extrapolate the structure of new antibodies that will be added to Physis to be downloaded into base microbes.Thus antibodies that neutralise and kill the virus will be extrapolated by Paean by anslysing the structure of the viruses receptors and those already produced by small populations of humans will have their structure uploaded to the viruses Physis file that then will allow their structure to be downloaded into the DNA digital storage of the microbes and be mass produced and synthesised by the microbes in the patients bloodstream through anabolic and catabolic reactions through instructions via biosynth wifi to kill snd neutralise all virions they come into contact..Scratch DNA can be extrapolated by Phanes to create antibodies that kill all strains with this added by biosynth wifi and synthesise them.In both cases Paean can on demand via Biosynth wifi tell them microbes to mass produce and synthesise these antibodies in the bloodstream to allow them to travel to all parts of the body and neutralising and killing large amounts of the virus with excess flushed out of the body by feces snd urine.Microbes will undergo mass replication and move to all parts of the body in all parts of both the bloodstream and lymphatic system where the viruses can reside and hide in and then mass produce the antibodies in large amounts by being instructed by Paean to synthesise them using anabolic snd catabolic reactions.They will travel to all parts of the body including lymphatic systems,testes and seminal vesicles where the virus hides to destroy them.This and antibodies from the immunised primary immune system even in already infected patients activated by the microbes will wipe out large amounts of the virus alongside microbial action and will allow the patient both infected and uninfected to produce their own antibodies signalled by microbes.This and immunising existing infected patients against all strains using the common proteins method should speed up the battle against the virus as already infected patients will produce their own antibodies with the immunised primary immune system initiated by the microbes through chemical signals via Paean through wifi to start creating their own antibodies.Should the patient experience side effects such as nausea or inflammation then Paean can instruct them to stop them producing these antibodies to alleviate symptoms with these antibodies produced in large batches lasting several hours that wipe out large amounts of the virus from the body until the patient is finally is cured of HIV.Patients will be immunised against not only all stains of HIV but also a major pathogens and parasites using the common proteins method with anti-viral,anti-bacterial strains fighting off opportunistic infections and anti-cancer strains fighting off tumours alongside the rebounding immune system.Once immunised against all strains of virus using the common proteins method infected patients will have their immunised primary immune system activated and using chemical signals from microbes and Paean be spread out along the entire bloodstream and lymphatic system to produce their own antibodies in large amounts thus alongside the microbes synthesising N6,tri-specific antibodies and also rewriting the viruses DNA and applying anti-viral compounds would effectively cure patients from anything between a year to a few months.The antiviral strains would have macrophage DNA to allow them to consume the viruses once incapacitated by antibodies with the patients native macrophages instructed by the anti-viral strains to also do this for virkon s destroyed by the native primary immune system and microbes.Tests on chimpanzees and mice with human recombinant DNA to create human leukocytes can be done by 2023 using those that have these sources of DNA added to produce the N6 and tri-specific antibodies and also immunised against all strains of the virus using the common proteins method in both post and pre infected animals with and without CCR5Delta 32 mutation and also CRISPR immune response added to lymphocytes to test the ability to have the infected animals to create their own antibodies against all strains initiated by proto microbes.Thus tests on chimpanzees and mice with human DNA to produce human lymphocytes can begin as early as 2023/2024 to test the efficacy of immunisations,applications of the CCR5Delta 32 gene and also applying the CRISPR Cas-9 immune response and even giving them the ability to produce N6 and tri-specific antibodies using recombinant DNA from populations that produce them with the proto microbes or benign versions of the viruse injected into them initiating their producing to allow for human trials to start as early as 2025.The animals will be tested on the ability of the CCR5 Delta 32 mutation preventing the virus being passed onto unborn children if both or only the mother or father have the mutation added via advanced gene drive technology.Animal subjects with human recombinant DNA can also have DNA from T.gammatolerans to test the effects of radiation has on wiping out large numbers of the virus at different levels of increasing intensity starting at 500Gy up to even 20,000Gy in these and other animals with only resistance and test the ability of how the pathogen could gain radioresistence and if proto microbes can remove resistence.This will be tested on pre and post infected animals.The engineering of CD4+ T lymphocytes to be unable to be infected by HIV in both infected and uninfected patients as well as through germline therapy and thus forcing them to interact with microbes or be left free flowing in the system unable to replicate can also be replicated with other viruses such as Ebolavirus,N.meningitidis preventing them and other pathogens from entering the leukocytes including dendritic cells,natural killer cells,monocytes,virgin B and T cells and macrophages etc by altering the relevant leukocytes in the immune system as well as organs that that they infect to replicate to prevent them from being infected with as much of the attacking virions also altered to be unable to infect both the immune cells and whole organs via horizontal gene transfer from microbes passing this on and thus allow the immune system to fight off the infection alongside the biocompatible microbes with if possible biocompatible microbes transferring these genes permanently to leukocytes in the same manner as CRISPR treatments with microbes including genes that increase their longevity and lifespan of dendritic and helper T Cells that are made immune to it as well as given DNA from other viruses that will be attacked by Helper T and B cells and the areas of the body responsible for creating all relevant types of leukocytes in this mutual relationship.This would include recombinant DNA from resistant populations and scratch.In the case of Ebolovirus and N.meningitidis etc liver,brain and other organ cells and tissues of other major organs could be altered to be unable to be attacked,infected and then destroyed by these and other pathogens through the second strain of microbes devoted to this and enhancing the primary immune system applying CRISPR treatments.This can be done by having the CRISPR Cas-9 immune response ability added to it by CRISPR itself with key genetic sequences interspaced in the DNA of the cells in these organs.Also in the case of these the strains based on dendritic cells,natural killer cells,monocytes in the case of Ebolavirus would also be a hybrid of them and macrophages to apply anti-viral compounds and CRISPR treatments to trick them into being killed or inactivated since the entire native immune system could not be infected by both with N.meningitidis dealt with native macrophages and virgin B and T cells altered to be unable be infected and thus trick them into interacting with the microbes that are hybrids of macrophages and these leukocytes which will then kill them off or inactivate them,modify the pathogens or at least allow the native immune system that would be immunised to them fight them off before they gain strong hold.Ideally all patients whether infected or uninfected will have their native immune system and all organs that can be infected by Ebolavirus,N.menigitidis,HIV and other viruses be engineered by CRISPR via the microbes to be unable to be infected using DNA from scratch and from resistant populations to allow the microbes and native immune system enhanced from the proteins sent to the dendritic cells to fight them off instantly since the pathogens cannot infect any cells.The different strains that are hybrids with macrophages could all be in low numbers and then udergo mitosis when the specific pathogens arise or there could be a single anti-viral and anti-bacterial strain that is a hybrid of all leukocytes such as macrophages,dendritic cells,monocytes,virgin B and T cells,plasma and killer T cells to contain all the receptors from all of them on them to allow the pathogens of all types inter act with them and apply the relevant anti-viral and anti-microbial compounds instead of enzymes through phagocytosis and flooding and also apply CRISPR treatments including those that modify the virus to become susceptible to compounds at its disposal and suicide genes via horizontal gene transfer with the correct anti-viral and CRISPR treatments applied once the relevant receptors are attached to relevant glycoproteins.This again like resistance to HIV will be added to the genepool of the entire human race via germline therapy including those that are uninfected using recombinant DNA from resistant populations as well as scratch eliminating these disease from the world with this applied to other and new pathogens that infect and decimate the immune system and also organ tissues leaving the viruses no chance but to interact with the biocompatible microbes which will kill them with the viricidal compounds they have or alter them using CRISPR to make them susceptible to these compounds or ideally enhancing the immune system by handing the dendritic proteins from pathogens to make them able to fight them off themselves.As stated the viruses themselves such as HIV,Ebolavirus,N.meningitidis could also be altered to remove the relevant glycoproteins making them unable to infect these and other cells and even hide in specific cells at the the same as this to further limit their spread.Any organs infected by viral or bacterial pathogens will be constantly regenerated via microbes or this ability passed onto them.This all would as stated be done for all types of pathogens to both infected and uninfected patients and at the same time the dendritic cells would be given synthesised key surface protein antigens of these and other pathogens to give the memory helper B and T,plasma and killer T cells to create relevant antibodies should a infection occur instantly again to prevent the immune system becoming lazy with them attacking pathogens that are unable to infect them and any organs in the body.The biocompatible microbes can also alter the virus removing its GP120 glycoproteins thus removing its ability to infect leukocytes with regards to HIV with the same applied to Ebolavirus,N.meningitidis etc alongside measures to make the immune system unable to be able to be infected by inserting genes into relevant leukocytes to make them unable to be infected by specific or all viruses including the aformentioned ones for extended periods of time via these leukocytes also given DNA from endolithic bacteria or this programmed into the host to ensured that all future leukocytes produced will have these phenotypes.New anti-viral compounds can be created by Phanes,Epione and Paean to attack all viruses including HIV and others that have no current cure or anti-viral compounds using DNA created from scratch and using recombinant DNA from new ones from those discovered from existing animals and microbes in all environment.Physis will allow the genome of all plants and animals be scanned for the genes that produce relevant anti-viral compounds that can then be tested in simulations and automated labs where the compounds are produced by microbes within a lab animal and bacteria engineered to produced it in a commercial scale to be injected.Synthetic compounds to treat them both existing and new including theoretically those used in anti-viral combination therapy as well as protease inhibitors,PreP and PEP can be created by them carrying out anabolic and catabolic reactions using excess nutrients in stores etc and also bio based compounds,plant and animal oils and hydrocarbons created by the same strain or the body from CRISPR treatments as well as amino acids synthesised by the body and diet.Antibodies from populations of humans that become resistant to a diseases can be gained by extracting their DNA from the leukocytes and also the hosts genome and inserting it into them.Synthetic compounds to treat all types of viral infections will have their structure added to Physis and this downloaded onto anti-viral strains DNA digital storage to be then created by anabolic and catabolic reactions onsite of receptors of the virus virions to prevent overdosing and side effects.Antibodies discovered from nature will done by adding recombinant DNA extracted from them by automated lab workers and automated machines once and then input into a base microbe that can grown in automated labs and sent to new patients to inserted into their microbes by automated machinery or synthesised from scratch Phanes,Epione etc.Closely related animals to humans or even all animals such as animals and avians that have complex immune systems could be infected with a virus and then the antibodies added to the microbes by adding the relevant DNA from that animal.Thus to fight off viruses such as HIV,Orthomyxoviridae,Rhinovirus,N.meningitidis and Ebolavirus both infected and uninfected patients will be immunised against all possible strains using the common proteins methods,using CRISPR will be made to exhibit the CCR5Delta 32 mutation ideally homozygous mutations removing relevant sections of the C-C chemokine receptor type 5 gene and other receptors for all strains leaving their CD4+ T Lymphocytes unable to be infected and/or have these lymphocytes alongside the dendritic cells etc have the immune response measures of CRISPR Cas-9 added to them to allow for them to naturally fight off attempts of the viruses replicating in them with key genes interspaced into the genome of the leukocytes with tissues in organs infected by them added to their genome.The CRISPR Cas-9 immune response and CCR5Delta 32 mutation will be added to the genome of the host or only those of the bone marrow with this and immunisation done to uninfected patients in high risk groups to prevent the viruses gaining a stronghold and be in such low numbers as to allow the microbes and immunised primary immunised to fight off whatever little virus there is during an infection instantly thus wiping the virus from the patient immediately.Already infected patients will be immunised against all strains of the viruses particularly the ones they are infected with via PCR analysis from blood pricks and samples form phlebotomy robots and all possible strains activated by the microbes initiating the primary immune system to allow them to produce their own antibodies alongside N6 and tri-specific ones created by anabolic and catabolic reactions.Endolysines will be extrapolated by AI and applied to the virus specific strain with the patient of course have the CCR5Delta mutation added to the patient suited their strain of the virus to negate them to take anti-viral treatments with patients ideally taking them for at least a year or two.In infected patients the primary immune system will be immunised against all strains to allow it to use its own antibodies against the virus alongside microbial action with these activated by the microbes using chemical signals thus wiping the pathogen from the body much quicker and them given the CCR5Delta 32 mutation alongside the CRISPR immune response in leukocytes and microbes to prevent the viruses attacking the CD4+ T Lymphocytes thus allowing one to live healthy lives without talking protease inhbitors and other anti-viral combination therapy while the immunised primary immune system and microbes wipe out the pathogen with this also allow the native leukocytes numbers to rise and thus fight off infections and even tumours alongside the microbes.Ideally they should be given common protein immunisations that create antibodies for all strains and indeed all possible strains of the virus so that if it mutates the body can still create viable antibodies.Microbes will signal to the primary immune system to initiate the production of these.CRISPR treatments used by microbes can alter the viruses internal and external structure to become susceptible to the compounds at its disposal,have its GP120 glycoproteins removed preventing it infecting any leukocytes and also infecting any new patients and undergo apoptosis with all potential sex partners immunised and also have the aforementioned CRISPR treatments to the leukocytes.Once made immune to radiation via recombinant DNA from T.gammatolerans making the patient immune to radiation of up to 30,000Gy would allow the patient to routinely be exposed to levels of radiation of at least 5,000Gy – 10,000Gy several times a year to wipe out large numbers of the virus in all parts of the body.CRISPR used by microbes will also edit cells that the virus hides its DNA in and remove it from them and also cause them to undergo apoptosis and replace them with new ones.Thus anti-viral strains will be able to using these compounds and CRISPR treatments will be able to cure patients infected with HIV.
Proto versions of anti-viral strains to introduce suicide genes,those to remove pathogenicity,ability to infect cells and even use modified virophages and immunisations to treat Rhinovirus,Orthomyxoviridae,Ebolavirus etc and even Coronaviridae and any new fatal viruses that cannot by managed with medication unlike HIV by 2023/2024.Thus proto versions using CRISPR introduce suicide genes,those to remove the pathogenicity,ability to infect cells and thus replication and modified virophages can be used against Rhinovirus,Orthomyxoviridae,Ebolavirus etc and even Severe acute respiratory syndrome coronavirus 2 can be possible by 2023/2024 with proto AI and 3D DNA printers used if enough effort is made.Proto treatments to battle fatal strains of SARS-CoV-2 could use CRISPR treatments to make them into benign strains of it and Rhinovirus,Orthomyxoviridae etc by adding and removing DNA to allow the native immune system defeat it or in the case of elderly individuals possible having cyanovirian-N applied to it with the viruses ability to infect cells and thus undergoe replication also removed.Huge strands of DNA can be removed to cause it cease to function or change it into as stated by adding DNA from benign strains of it and Rhinovirus,Orthomyxoviridae and removing DNA that makes it deadly turning it into these benign strains to allow the native immune system fight it off.Mavirus,Sputnik virophage,Zamilon virophage can have their DNA modified via AI to fight SARS-CoV-2 without a helper virus and thus killing it or inactivating it with these steps and modified bacteriophages used for any other viral and bacterial pathogens that may arise prior to the development of microbes.These would be printed out via 3D DNA printers or cultured in the same as way bacteriophages in vats containing modified versions created by AI that is benign and then injected into hosts in trillions that will replicate exponentially each time they kill a virion to then infect more SARS-CoV-2 virions in the body and flushed out of the body once engineered to do so.Otherwise they can be modified to undergo via mitosis using sugars and nutrients not present in the human body.Bacteriophages can even be hybridised with these virophages to not need a helper virus and modified to be more effective in inserting the aforementioned CRISPR treatments into SARS-CoV-2.Ideally these hybrids of virophages/bacteriophages would include DNA from different virophages such as Mavirus,Sputnik virophage,Zamilon virophage and would be genetically modified by AI and manufactured via 3D DNA printers engineered to infect only the various strains of SARS-CoV-2 and then lysise the virus using the SARS-CoV-2 as a replication vector without a helper virus killing it in the process and doing so for all virions exponentially.Bacteriophages will be hybridised with it to allow the virophages and their DNA to infect and kill the viruses in the same manner as bacteriophages do easily with them designed to have the same structure as bactiophages(capsid head,collar,sheath,spikes,tail fibres etc) but have receptors and DNA to infect SARS-CoV-2 as a replication vector without a helper virus using tweaked viriphage DNA with the virophages and bacteriophage DNA and that of its normal prey viruses and bacteria analysed to allow them to be tweaked to fight the SARS-CoV-2 with scratch DNA extrapolated that allow it to infect and kill the SARS-CoV-2.The AI will compare the DNA of bacteriophages,virophages and the the DNA of the prey and make hybrids and alterations using scratch DNA to infect SARS-CoV-2 as a replication vector without a helper virus.This means it would be engineered that each time the hybrids of virophages/bacteriophages undergo replication in each virion the virions of SARS-CoV-2 will be killed and in turn producing millions more hybrids of virophages/bacteriophages that then go onto infect and kill more virions exponentially until the patient is cured and once all virions are killed they be flushed out of the body since mutation blocking genes would prevent them to utilise human cells as replication vectors with them having human or even patient specific protein coats using human DNA on them to avoid eliciting an immune response.If not they can at least inhibit the SARS-CoV-2 replication with scratch DNA created by AI and hybridising with bacteriophages should allow for the virophage/bacteriophage hybrid be able to use SARS-CoV-2 as a replication vector similar to bacteriophages and as stated have their exact shape but with DNA from virophages and scratch DNA extrapolated by AI to make receptors and DNA to allow it to infect SARS-CoV-2 without a helper virus and utilise it as a replication vector.Using a virophage/bacteriophage hybrid is ideal as bacteriophages dont need helper viruses for replication vectors unlike virophages and can create endolysine material to be created to kill it without a helper virus and can through endolysines destroy the pathogen thus allowing it to infect more pathogens but cant infect viruses unlike virophages rather only bacteria.Virophages can kill viruses but need a helper virus with the virophage and scratch DNA creating receptors suited to SARS-CoV-2 to inject DNA into the virus and the extrapolated scratch DNA allowing it to utilise specific or all strains of SARS-CoV-2 as a replication vector and use endolysine like material specific to it to kill it without a helper virus.Bacteriophages are able to kill bacteria by using them as a replication vector by producing endolysines which cause them to explode by themselves with any helper viruses etc but they cannot infect or kill viruses.Therefore the perfect cure for SARS-CoV-2 and its various strains is creating a hybrid between a virophage such as Mavirus,Sputnik virophage,Mimivirus Zamilon virophage,Cafeteria roenbergensis, that contains combinations of genes from these and scratch DNA that allows it it interact with and infect SARS-CoV-2 through receptors present created from scratch DNA with bacteriophage DNA that allows it to utilise SARS-CoV-2 as a replication vector and produce endolysines or endolysine like material that cause the viruses to explode thus killing it and then releases exponentially more bacteriophage/virophage hybrids that then infect and kill other SARS-CoV-2 visions in an exponential manner until the patient is fully cured.The hybrid may be similar in shape to a bacteriophage with a capsid head,collar,sheath,spikes,tail fibres etc that has receptors to infect the viruses and inject genetic material to induce the formation of new hybrids and endolysines or it can be modelled on a virophage that has its structure and use bacteriophage DNA to kill visions with endolysine like material and not need a helper virus.The virophages and bacteriophages DNA and that of its normal prey viruses and bacteria can be analysed by AI to allow them to be tweaked to fight the SARS-CoV-2 with scratch DNA extrapolated that allow it to infect and kill the SARS-CoV-2 without a helper virus.Any mutations of SARS-CoV-2 can be dealt with new strains of these hybrids created instantly by analysing the DNA of mutations of the virus and creating an all in one hybrid to attack all possible strains.Thus a hybrid of virophages/bacteriophages that is designed to specifically use SARS-CoV-2 as a replication vector and use endolysine like material specific to it to kill it without a helper virus created by AI will work as the perfect cure for SARS-CoV-2 by having each ones drawbacks countered by hybridising both and adding scratch DNA extrapolated to attack and kill SARS-CoV-2 without a helper virus.The virophage/bacteriophage hybrid would of be engineered to house receptors etc to utilise SARS-CoV-2 as a replication vector by infecting it in the same way as bacteriophages and virophages that uses endolysine like material to kill the SARS-CoV-2 virions that by utilising it by infecting it in the same way as bacteriophages that uses endolysine like material to kill the SARS-CoV-2 virions and during the process of utilising it as a replication vector create exponentially more virophage/bacteriophage hybrids that in turn them seek out and kill other SARS-CoV-2 virions killing each of them and creating more virophage/bacteriophage hybrids in an exponentional manner that in turn infect and kill other virions of SARS-CoV-2 in an exponential manner until the patient is fully cured and all virions are destroyed with it engineered to need not a helper virus.It will create endolysine like material that is designed to destroy the virions of the virus to kill the virus and allow replications of the virophage/bacteriophage hybrid be released with it as stated not needing a helper virus or other agent similar to C.roenbergensis.Existing medication and ventilators etc will be used to suppress the viruses replication and aid the patient in breathing while being cured.If need be the hybrids of virophages/bacteriophages can be engineered to make SARS-CoV-2 be susceptible to penicillin or over the counter medication and those to treat the flu to kill it if it becomes a problem by affecting the host with mutation blocking genes added and them covered with human proteins to negate it illicitating immune responses that may be fatal or render it ineffective.As stated to create the cure the DNA of bacteriophages,virophages,their prey and also that of the different strains SARS-CoV-2 in DNA databases will be compared by AI to allow it create a hybrid with scratch DNA extrapolated that allow it to infect and kill SARS-CoV-2.AI will carry out the manufacture of all virophage/bacteriophage hybrids etc as they can scan databases instantly and extrapolate new scratch DNA.Otherwise genetically altering Sputnik virophage to infect,inhibit and/or kill SARS-CoV-2 in the cells used by SARS-CoV-2 to replicate similar to how it does this on Mimivirus without killing the human cells can be used and if possible without the need for helper viruses for replication.AI can even create a new virophage that can inhibit and/or kill SARS-CoV-2 without killing the human cells without the need for helper viruses for replication that works on the same principle suited to SARS-CoV-2 without the need for helper viruses for replication.Mavirus can be genetically altered to infect SARS-CoV-2 in the same way it does C.roenbergensis virus which utilizes C.roenbergensis machinery to replicate.Mavirus integrates into the genome of cells of C.roenbergensis that is infected by C.roenbergensis virus and thereby confers immunity to the populations of C.roenbergensis against C.roenbergensis virus that can inhibit and/or kill SARS-CoV-2 without killing the human cells without the need for helper viruses for replication.AI can even create a new virophage that works on the same principle suited to SARS-CoV-2 without the need for helper viruses for replication that can inhibit and/or kill SARS-CoV-2 without killing the human cells without the need for helper viruses for replication.The virophage hybrid can also be modified to infect the cells in the human body that SARS-CoV-2 uses as a replication vector and confers immunity to the host against SARS-CoV-2 without actually killing the human cells similar to how Mavirus integrates into the genome of cells of C.roenbergensis that is infected by C.roenbergensis virus and thereby confers immunity to the populations of C.roenbergensis against C.roenbergensis virus.This can be investigated as a cure and if possible without the need for helper viruses for replication and possible a vaccine via AI making alterations to it that doesnt damage the host.Other strains can inhibit the virus similar to virophages and apply CRISPR treatments including suicide genes,those that make it as benign as the common cold and flu or even make it susceptible prescription and over the counter medicine using taq polymerase and Cas-9 to recreate CRISPR treatments over and over again.These genetically altered virophages,bacteriophage hybrids with human protein vectors can also be modified to inject into SARS-CoV-2 CRISPR treatments that include suicide genes,those that make SARS-CoV-2 into benign strains of Rhinovirus,Orthomyxoviridae by changing its DNA and thus allow it to be easily fought off by the immune system and those that remove its ability to infect human cells and thus replicate with AI determining the genes to be added or responsible for this.Thus the fatal SARS-CoV-2 could be made as benign as the seasonal common cold and flu or even more benign with an almost zero lethality factor making it completely benign unable to kill even the elderly and also immuncomprimised by removing native DNA and adding DNA from benign strains of Rhinovirus,Orthomyxoviridae as well as scratch filler DNA that has no real purpose and also remove DNA that allows it to infect cells in the lungs into it in infected patients especially high risk patients or even make it even more benign that the patients own immune system can naturally fight it off as normally as infections of benign viruses and bacteria the patient encounters everyday through cuts,grazes using recombinant DNA from these benign species even in high risk groups.If possible suicide genes can be added and those that express proteins that allow it to infect cells will be removed and even large strands that allow it function.The virus via CRISPR treatments can be made to express the same phospholipids and protein coats as benign virus and even bacteria that humans can naturally fight that dont mutate with mutation blocking genes added.A DNA database of benign bacteria and virus can be crossrefferenced by AI for recombinant DNA with the virus made to express the phospholipids and protein coats as benign virus and even bacteria unable to replicate that are killed by even penicillin and other anti-biotics and anti-viral medication that is used to treat benign pathogens that have no side effects by adding DNA from benign and treateable pathogens,bacteria and viruses that are affected by these.Scratch DNA can also be introduced into them to make the virus susceptible to and thus weakened and killed by compounds present in herbs as part of traditional local medicine ie herbs that are used in traditional medicine,tetrahydrocannabinol in each country and even conventional over the counter medicines to treat the symptoms of the cold and flu such as Lemsip and their variations worldwide.These compounds would be applied into the patient in gaseous form inhaled from inhalers and also smoking in cigarettes or fumes with them in boiled water to ensure they enter the lungs.Four options can be researched by AI at once to kill SARS-CoV-2 – genetically altering Sputnik virophage to infect/inhibit and/or kill SARS-CoV-2 in the cells used by to replicate similar to how it does this on Mimivirus without killing the human cells,genetically altering Mavirus to infect the virus inhibiting and also creating a virophage/bacteriophage hybrid designed by AI that doesnt need helper viruses for replication vectors and it using the SARS-CoV-2 as a replication vector killing the virus exponentially until the patient is cured and strains that apply CRISPR treatments to make it benign.All options can have them covered with human proteins to negate it illicitating immune responses that may be fatal or render it ineffective.Since AI can work 24/7 and scan genes in databases and extrapolate new ones and a hybrid within days if not minutes with it and 3D DNA printers should expedite its manufacture.Once they are printed out as virions via 3D DNA printers with just a head containing DNA and receptors like virophages but have engineering to ensure that after replication will form endolysines and also normal shaped bacteriophages to be stored in large test tubes once extracted with them having DNA from T.gammatolerans to allow radiation to be used to sterilise them of the benign cousin of SARS-CoV-2 or live virion of the SARS-CoV-2 virions printed out and/or engineered to undergo mitosis using sugar used as a growth medium with since hybrids of bacteriophages can be engineered to also use benign bacteria designed by AI,created by 3D DNA printers that grow in vats onsite of hospitals using sugar that can be fought off by humans and cant mutate and killed by penicillin as well as a growth medium.The radiation can allow the bacteria used as a growth medium and be killed with treatments of 500Gy used with the bacteriophage/virophage hybrid in storage continuing to kill of remaining benign bacteria or benign cousins as replication vectors in storage until all are dead with them having DNA from psychrophiles,mesophiles and thermophiles etc to grow in all temperature ranges and allow high temperatures to be applied to it to kill the bacteria.Other extremophile DNA can be present for the same reason.Dead bacteria can then be filtered out with all work automated.The bacteriophage/virophage hybrid may also be modified to undergo mitosis using sugars,proteins and nutrients not found in the human body or human diet fed to them in vats thus meaning that once the infection is cleared they cannot undergoe mitosis.Anti-viral medication can be used to suppress the virus ability to replicate while being killed off.Virophages and hybrids with bacteriophages that are engineered to deliver CRISPR treatments will be engineered to utilise taq polymerase and Cas-9 using DNA from Planarians,T.aquaticus,S.pyogenes,F.novicida in order to reapply treatments that change the virus into the common cold or introduce suicide genes over and over again with them having human or even patient specific protein coats on them to avoid eliciting an immune response.The DNA of virophages and bacteriophges should already be in genetic databases online allowing AI to scan them and create alterations.Proto microbes may apply suicide genes and those that inhibit its ability to replicate via removing the receptors it uses to attach and infect the lungs and make it susceptible to penicillian etc.All of this can be done by AI to expedite work and make it availible within months or weeks.Since no natural compounds have been found to kill SARS-CoV-2 these are the only options for treatment and curing SARS-CoV-2 for 2023/2024 if it doesnt subside before this or becomes a seasonal pandemic each year,any future smaller outbreaks occur and new strains arise with AI playing a key role in extrapolating genes,hybrids,modified virophages/bacteriophages etc. and 3D DNA printers expediting their manufacture on all hospitals worldwide.CRISPR,AI and 3D DNA printers could create different types of vaccines like live attenuated ones or create from scratch benign cousin strains that works on the same principle as the Cowpox virus that when it injected into a person in large amounts it would once fought off would confers resistance to the more fatal V.major,V.minor.The DNA of Cowpox virus,V.major,V.minor will be analysed by AI to allow it to create a benign cousin of SARS-CoV-2 with need be a hybrid of both SARS-CoV-2 and Cowpox virus can be made that can be fought off by the immune system and be benign like Cowpox virus and still confer resistance to SARS-CoV-2 that is unable to mutate with it even being possible to hybridise SARS-CoV-2 with benign bacteria that can be grown in large amounts in vats.If possible the original Coronavirus strain from Pholidota and Chiroptera can be analysed and modified by AI to work on humans on the same principle as Cowpox virus with it unable to damage the lungs and even hybridised with benign versions of Rhinovirus and Orthomyxoviridae as well as Cowpox virus.These would be created via by AI and 3D DNA printers and can be made to replicate in animal tissues etc printed out that can use sugar as a growth medium and the cousin virus use it to replicate and have the same DNA from extremophile and collected in the same way as bacteriophages.The cousin virus hybrid may also be modified to undergo mitosis using sugars,proteins and nutrients not found in the human body fed to them in vats thus meaning that once the infection of the cousin virus hybrid is cleared they cannot undergoe mitosis.As stated by making alterations to Mavirus can be researched as a vaccine as it integrates into the genome of cells of C.roenbergensis that is infected by C.roenbergensis virus and thereby confers immunity to the population of C.roenbergensis virus the organism C.roenbergensis virus infects thus making a vaccine by having it confer immunity to humans using a benign version of SARS-CoV-2.It could if perfected confer immunity to all possible strains and mutations preventing the virus rebounding and becoming a seasonal virus that gets deadlier each season with if not at least AI and 3D DNA printers onsite of hospitals creating new vaccines every season within weeks or less with little to no human labour until microbes and immunising strains that us common proteins can be perfected.Thus AI could create benign versions or cousins of the SARS-CoV-2 that would have its ability to mutate,be pathogenic edited out and thus when injected in large amounts would be be fought off by the immune system that would then confer resistance for life or even a few months or years to the more fatal SARS-CoV-2 for patients replacing a vaccine.Again its ability to scan databases and create hybrids and create scratch DNA in days and minutes will expedite the process.AI and 3D DNA printers will expedite the development via extrapolating CRISPR treatments,genome of cousin virophages virions and vaccines and the 3D DNA printers onsite of hospitals and universities worldwide for creating those to test on animals and humans etc and also allowing for instant creation onsite universities and hospitals around the world to distribute vaccinations and cures to the whole global populace instantly.3D DNA printers will be onsite of universities and hospitals around the world to allow for localised manufacture of the vaccine and cure uploaded to a single global cloud network for animal and human trials and also for manufacturing it on a scale to be released to the public including infected patients on demand in bulk batches allowing universities and hospitals to crossrefference it and via creating them via 3D DNA printers be able stockpile on it cutting down,labour,time,transport and manufacturing costs and distribute it to all patients allow it to be created on an unlimited scale in all cities,towns and villages universities and hospitals around the world for free with at first it created in labs that have these first and created on based on the population of the area and sent at first high risk patients both infected and uninfected in the country with the number produced for each known infected individuals while all hospitals and universities order in their own 3D DNA printers to stockpile on their own supply.This can mean once extrapolated it can be manufactured in on an unlimited scale in all cities,towns and villages universities and hospitals around the world as part of tests and wide use instantly at the same time once stored on proto Physis cutting down on time to manufacture it in factories and transport it around the world from years,months to days or even hours and meaning it can be quickly remade should smaller outbreaks reoccur and new patients test positive after it subsides and stockpiles deplete in areas with large populations and should patients be able to be reinfected.It can allow first trials to take place around the world at once.For infected patients the cure can be created on demand within hours of not minutes and in large batches to be stockpiled on.Thus by having the cure and vaccine stored in proto Physis or even a single global cloud network it can allow it to be manufactured using 3D DNA printers over and over again on demand onsite of hospitals,universities etc in towns,villages and cities around the world in large batches and not in factories by corporations or the state that would be slower and be needed to be transported around the world meaning it can be distributed globally in all hospitals and universities worldwide over and over again within days or even hours without patents since proto AI would be involved in its manufacturing and can be be stockpiled in large batches and restockpiled should any future outbreaks occur in towns,cities,villages and even made in enough for individual patients in small outbreaks and infections with it allowing any hospitall around the world to create it on demand for large and smaller outbreaks when needed decentralising production from corporations and the state and cutting down on time,labour and costs in manufacture an distribution from factories.Proto AI and also human researchers in hospitals could hold patents making it free to everyone.Having psycrophile,mesophile and thermophile DNA can also allow the cures and vaccines to stay stable in all temperature ranges inside and outside of refridgeration and with the acellerated healing and telomere repair phenotype can be frozen and thawed over and over again forever.This can allow them alongside scratch DNA have them stay stable and fresh when not refridgerated indefinitely negating damage or loss of viability of the vaccine or cure if not refridgerated and any transportation needed by them.It can also negate the need for conventional preservatives such as thiomerasal etc in these and other vaccines.Other extremophile DNA and those as part of anti-ageing treatments can be present for the same reason.The psycrophile,mesophile and thermophile DNA etc can be applied to current vaccines being developed to increase shelf life and viability in transportation and storage.If possible current conventional vaccines created by Johnson & Johnson,Moderna,Pfizer and Astrazenca for existing strains can be manufactured with this DNA onsite of hospitals and universities around the world using 3D DNA printers to cut down on transportation and development costs meaning once extrapolated current vaccines made by Johnson & Johnson,Moderna,Pfizer,AstraZenca etc for SARS-CoV-2 can be stored in a single global cloud network and thus manufactured worldwide onsite of hospitals worldwide using 3D DNA printers cutting down transportation time from months to hours and allow it to be stockpiled onsite of hospitals around the world negating issues regarding the viability loss due to transportation and also limited supplies thus meaning rather than having it created in factories of pharmaceutical giants with AI including proto AI seizing patents making it free it can be mass produced onsite of hospitals around the world meaning they can stockpile on enough to cater to their local population over and over again allowing the entire population of all towns,villages and cities and even entire counties and states worldwide to be vaccinated with it allowing more to be created on demand not only for smaller outbreaks but also for any future strains that arise developed by AI within months,weeks,days or even hours uploaded to a single global network.To further make it free universities and even charity groups etc could seize patents.Thus the genomic structure of current vaccines such Moderna,Pfizer etc can be uploaded to a global cloud network and then manufactured over and over again onsite of hospitals worldwide especially in the developing world via 3D DNA printers.This can prevent shortages caused by richer nations seizing control of limited stockpiles,the use of a limited number of factories of corporations present in a few countries which can be slow to manufacture and ship them across the world,sanctions and blockades carried out by one government preventing citizens in another country or their own country access to them etc.Thus having all conventional vaccines,Cowpox variant versions and virophage/bacteriophage hybrid cures developed by humans and AI genetic sequences and structure to current and newly arising strains of SARS-CoV-2 being added to a global cloud network could allow it be manufactured onsite of hospitals worldwide including in developing countries and poor communities in developed countries within hours of extrapolation and uploading it to them negating notions of unequal distribution of it based on the limited batch method used by factories and richer countries hoarding supplies negating issues of supply and demand as currently seen in the developing world and certain countries of the developed world.It would also allow each hospital around the world to stock up on large batches of existing vaccines by Pfizer,Moderna etc and the new ones developed by proto Phanes themselves over and over again cutting down on time to have it created in a small finite number of factories and to be then shipped around the world and allow for quick herd immunity to the whole population thus preventing the rise of new mutations very quickly.It will allow all new extrapolated vaccines and cures to deployed instantly worldwide thus allowing all new strains including omicron to be dealt with instantly with it allowing hospitals to vaccinate every patient in their town,city and state etc by allowing to manufactured tires on demand in large batches to restockpile on it with the cures manufactured in large batches and stockpile on them as well as create them on demand for each new infected patient that arrives into the hospital thus increasing survival rates and preventing the virus spreading and also preventing it mutating into new strains.To confer immunity S.pyogenes immune response can be added to the cells in humans that SARS-CoV-2 infects in order to prevent it replicating and allow the human cells to fight back with AI determining the sequence needed with bacteriophages used and done in both infected uninfected patients as a proto vaccine/immunisation.The DNA of asymptomatic carriers can be analysed to determine the genes that give them this immunity and thus added to all patients including high risk ones.AI can also extrapolate DNA to be added to the cells it infects that would confer resistance to it similar to how the CCR5Delta 32 mutation prevents HIV infecting CD4+ T lymphocytes using bacteriophages thus keeping the levels of the virus stable and the virus also altered to be benign to prevent it spreading again as a proto vaccine/immunisation.Bacteriophages and poto micobes consisting of human leukocytes can be used to do this.Proto microbes to deliver CRISPR treatments could be bacteria covered in human or patient protein coats or in the case of Coronaviridae can be hybrids of the same cell types in the human body that it uses for replication to again avoid eliciting an immune response and act as mouse trap.Human leukocytes can also be a vector to deliver CRISPR treatments.This cure,vaccine and treatment for Coronaviridae could be available as early as mid to late 2023 if enough work and research is made with AI controlled networks connecting all universities and hospitals worldwide and assigning tasks allowing them to share progress with AI namely proto Phanes designing them and 3D DNA printers manufacturing them speeding up the process.Both AI and 3D DNA printers will be used to speed up the process as AI can scan DNA databases to make hybrids and new cousin strains and scratch DNA in minutes and do at a speed and accuracy that humans cant with 3D DNA printers will be used to speed up manufacture around the world.All of the worlds most powerful supercomputers including Watson,Sunway TaihuLight,Summit,Tianhe-2,ChatGPT etc can be linked to each other and work together alongside the most advanced AI such as Alpha Go.These computer networks that connect all laboratories in universities and hospitals and corporate labs worldwide will contain areas to control automated laboratories,share data,view results from experiments and dump results and forums etc to share ideas allowing researchers to work together from home,universities,hospitals and corporate labs around the world.These will be open to the public to view this information and named Epione managed by the AI of the same name.The use of computer networks will cater to global cooperation that will exponentially increase the rate of development of all strains and anti-ageing treatments.This early availability is because they can skip conventional trials processes as previous bacteriophage cures have skipped trialling processes already in the past meaning by as early as mid to late 2023/2024 the use of modified virophages/bacteriophage hybrids can be tested on infected patents and cousin virus vaccine can be tested on uninfected patients at this point with AI and 3D DNA printers expediting their manufacture.Furthermore it would not need tests to determine dosage such as LD50 limits and would work on advanced stages of the infection have a 100% success rate with since designed by AI could override patenting laws with AI doing all the work and 3D DNA printers used expediting progress and should be able to counter any mutations.Having it express human or patient specific proteins could prevent side effects such as immune responses that could be fatal and render it ineffective with as stated it can be engineered to be killed off by medicine that treat,the flu etc.Vaccines as described may need animal trials but they if enough work is done be availible by the end of the year.Those whose lungs damaged by it can have chimera lungs from animals created or bioprinted ones with in the case of chimera ones can have CRISPR treatments to remove animal DNA.Proto AI and the WHO will take control of all containment measures and subsidising and providing tests,medicine and check ups in all countries worldwide replacing haphazard attempts of different methods and providing tests and medical supplies to where noone is getting them and managing the control of its spread effectively worldwide and carry out simulations and projections of different methods and its spread.Tests and medicine specifically for it especially in America and research into the vaccines and cures will be funded and subsidised by it.It will organise the distribution of food and other essentials including medical supplies worldwide and also the management of hospitals worldwide.All confirmed cases will be tracked by it.It will also organise loans and government programmes globally to help those affected pay for food,rent etc.Areas such as Iran,Cuba,Afghanisthan and Gaza should have economic sanctions and blockades lifted to ensure medical supplies can be allowed.This will be replicated for future outbreaks.Once it becomes available immunisations for all strains of SARS-CoV-2 using the common proteins should be applied in China and other parts of Asia and even the Middle East to contain any future outbreaks that may occur with other strains that may jump from animals to humans.Vaccines and virophages/bacteriophage hybrids to all possible fatal strains of Coronaviridae including SARS-CoV-2 that work on the same principle as the Cowpox virus and existing vaccines for current strain as detailed earlier on will be developed by AI starting as of 2023/2024 to ensure it can be deployed instantly onsite of all hospitals worldwide using 3D DNA printers should another outbreak or pandemic occur with other strains with AI analysing all possible mutations in all strains of Coronaviridae including SARS-CoV-2 that affect other animals needed to jump to humans and then extrapolate the vaccines and virophages to treat it.All hospitals worldwide will stockpile on them as soon as possible before future pandemics occur.Both benign and fatal strains will be extrapolated to then have these vaccines and bacteriophage/virophage hybrids created with hundreds or thousands of different strains,bacteriophage/virophage hybrids and vaccines etc extrapolated.This is because SARS-CoV-2 is the third fatal strain of Coronaviridae to jump to humans after SARSr-CoV and MERS-CoV.Thus all possible fatal strains of Coronaviridae including SARS-CoV-2 will be extrapolated by AI to then extrapolate the vaccines and bacteriophage/virophage hybrids to treat it by 2023 that can be deployed instantly in hospitals around the world via 3D DNA printers should a similar fatal strain arise.It should also be done to create variant vaccines and bacteriophage/virophage hybrids to all possible mutations of SARS-CoV-2 to be able to counter any mutations to the current strain of SARS-CoV-2 that may occur if it becomes a seasonal pandemic that mutates every year past the current five strains alpha,beta,delta,gamma,omicron into more strains and becomes a seasonal pandemic that lasts every year.Thus AI will not only create a vaccine and bacteriophage/virophage hybrid cure to all current strains of SARS-CoV-2 around the world by analysing their genome but it will at the same time by analysing their genome extrapolate vaccines and bacteriophage/virophage hybrids to all possible strains of SARS-CoV-2 within weeks if not days that could occur with once the current strains have vaccines and bacteriophage/virophage hybrids extrapolated it could extrapolate these for dozens,hundreds of not thousands of all possible strains especially the likeliest ones to arise from mutations of all existing strains with by it analysing the genome of all current strains whose genome will be added to a global cloud network it will be able to determine the likeliest strains to arise from them through mutations with it thus creating dozens if not hundreds of bacteriophage/virophage hybrids for all strains that would evolve from these existing ones in the same likeliest evolutionary path meaning that once they arise the vaccines and cures could be created and deployed in hospitals around the world using 3D DNA printers over and over again and thus allow hospitals stockpile on them to be deployed instantly around the world wiping out the new strains of the virus instantly if these new strains from mutations arise anywhere in the world.This will be done should SARS-CoV-2 mutated every year and becomes a endemic pandemic that lasts for several years,decades or forever. By analysing the genome of all existing strains of SARS-CoV-2 including the original strain,beta,delta,gamma and omicron variants and their evolutionary path from one to the next then AI can extrapolate all possible mutations and thus all possible future strains from one to the next following the same evolutionary path of these existing strains with it then extrapolating both vaccines and cures of hundreds if not thousands of these strains of SARS-CoV-2 that can be deployed instantly in hospitals around the world when they arise.By analysing existing strains of the virus genome proto Phanes can determine the mutations made to get to the different strains ie the necessary mutations to get from the first strain to the delta and omicron variant with it then using this change in genes from the first strain to the delta and omicron variant to determine hundreds,thousands,millions or billions of the likeliest mutations to lead to the next likeliest possible hundred,thousand,million or billions of strains with it then extrapolatIng vaccines and virophage/bacteriophage hybrids for each newly extrapolated billions of strains at the same time with each one uploaded to a single global cloud network that can be manufactured and deployed instantly through 3D DNA printers onsite of hospitals and universities worldwide allowing for instant delivery worldwide allowing millions or billions of people to vaccinated and treated at once to each newly identified strain when combined with social distancing preventing these new strains gaining a stronghold and preventing them mutating any further into any new strains thus wiping out all possible strains of Coronavirus worldwide from all human vectors instantly with all animal vectors in captivity etc treated with these as well.Ideally it will extrapolate bacteriophage/virophage cures and vaccines of all possible strains or at least hundreds or thousands in all possible evolutionary paths from the original,delta and omicron strains to all possible evolutionary paths in all directions that will be stored on a single global cloud network that can be manufactured onsite of hospitals around the world the second each strain develops and arises.As a result AI will extrapolate at once bacteriophage/virophage hybrid cures and vaccines for millions or billions of all of the likeliest possible future strains of the virus in one go and store their DNA structure in a single cloud network allowing them to be created onsite of hospitals,factories etc worldwide in batches or on demand once they are detected anywhere in the world using 3D DNA printers.The use of 3D DNA printers that are onsite of hospitals etc worldwide will allow them to be manufactured for each individual patient that comes into hospitals or manufactured in hospitals in large batches stored in vials etc and sent to pharmacies and universities to allow patients to be vaccine or cured there with the virophage/bacteriophage cure like the vaccine will be injected into patients in a liquid housing millions or billions of virophage/bacteriophage hybrids that that use the vrua as a replication vector to create exponentially more hybrids until the patient is cured fully with the bacteriophage/virophage hybrid having traces of human DNA to prevent them illicitating an immune response.As a result AI will extrapolate at once bacteriophage/virophage hybrid cures and vaccines for millions or billions of all of the likeliest possible future strains of the virus in one go.These will be stored in a single global cloud network so as to allow any new infections of existing strains to be cured instantly and new infections of new strains that arise cured instantly since they can be manufactured on demand and in bulk onsite of hospitals worldwide thus halting the spread of existing stains and preventing new strains arising and gaining a stronghold as once identified they can be cured and vaccinated instantly.Even if not possible the AI can easily extrapolate bacteriophage/virophage cures and vaccines for each new strain that arises within at least 24-168 hours all stored in a single global cloud network that can be deployed instantly in hospitals across the world.Thus vaccines and cures to all possible future variants of SARS-CoV-2 that can be stored on a single global cloud network allowing them to be deployed and manufactured in hospitals worldwide using 3D DNA printers thus eliminating issues of natural or artificial scarcity.This means that all existing strains could be cured and vaccinated against and any new strains that arise will be able to be cured and vaccinated against instantly worldwide both when patients check into hospitals with these cures and vaccines deployed instantly by being manufactured onsite of hospitals around the world.The use of 3D DNA printers,a single cloud network etc will allow all hospitals worldwide to mass produce these cures/vaccines onsite of themselves on demand for new patients that arrive and also mass produce large batches of them in bulk to stockpile on them thus making themselves self sufficient from factories and cutting down on transport,time and energy costs.All future vaccines produced for each extrapolated strains will be based on the Cowpox variant and also be variants based on vaccines made by Astrazenca,Pfizer,Moderna etc to ensure 100% success rate with all extrapolations carried out by AI namely proto Phanes.If possible an all in one bacteriophage/virophage hybrids and vaccine that can kill off and vaccinate against all possible strains of SARS-CoV-2 can be extrapolated by AI that should be able to fight off any and all possible mutations that may render existing and new bacteriophage/virophage hybrids and vaccines ineffective negating the need for creating multiple versions and yearly versions that can be deployed onsite of hospitals.It will also extrapolate all possible strains of Coronaviridae potentially millions of new strains that could mutate into other new fatal strains should it mutate into a new pathogen outside of SARS-CoV-2,MERs,SARSr-CoV to create bacteriophage/virophage hybrids and vacccines that can be created onsite of hospitals worldwide deployed instantly worldwide once they arise.Proto Phanes will be the AI in charge of this.If possible various compounds from plants and animals can be tested on cultures of the virus with if possible AI extrapolating synthetic compounds that can kill it that can be synthesised and delivered by genetically engineered bacteriophage/virophage hybrids etc and even extrapolate CRISPR treatments applied by this to remove its a mobility to infect cells and remove key genes key to its functioning.Proto and final microbes that can kill the virus through CRISPR etc will be developed by 2025-2029 alongside immunisations that use the common proteins method.If possible AI can analyse the outer structure of all existing strains and all potential strains and then extrapolate synthetics antibodies to neutralise the virus and its different strains that are stored in a global network with these synthesised artificially in vats using industrial processes but also by bacteria and proto microbes through anabolic and catabolic reactions using proto Biosynth WiFi or just through engineering in vats with both options done onsite of hospitals decentralising production with them stored in vials and injected into infected patients in large amounts with them working alongside bacteriophage/virophage hybrids to neutralise large amounts of the virus leaving them able to be destroyed by the primary immune system while the bacteriophage/virophage hybrids kill other virions the virus in large amounts.These antibodies can be also inhaled via a gaseous mixture similar to inhalers with there also the option of using an intravenous drip where patients in hospitals have an intravenous solution containing large amounts of antibodies present are slowly injected similar to existing medicines added by intravenous drip to ensure a steady flow of antibodies enter the bloodstream at a rate that is enough to incapacitate most of not all of the virions and not overwhelm the body.Antibodies can also be introduced into the lungs via ventilators that pump large numbers of the antibodies in a gaseous form to incapacitate most of the virions in the lungs before,during and after they attempt to replicate at the same time they pump in oxygen into the lungs.Also AI can analyse the outer structure of the virus especially the receptors that it used to infect cells in the lungs and extrapolate CRISPR treatments that can be applied to the tissues in the lungs that it infects that would prevent the virus from being able to attach to it and infect them and thus replicate and spreading with these CRISPR treatments applied by either viral vectors,proto microbes and also bacteriophages all that use taq polymerase to revere are DNA over and over again.These CRISPR treatments can be applied to unifected patients to prevent them affecting them.Like the bacteriophage/virophage hybrids AI will extrapolate synthetic antibodies and CRISPR treatments for all existing strains and also thousands of all possible new strains that could develop to be stored on a single cloud database to allow them to be manufactured and deployed onsite of all hospitals worldwide instantly when each new strain arises.By 2025-2029 proto and final biocompatible microbes should arrive that are able to immunise one against all possible strains as well as use the same CRISPR treatments as antiviral strains that can cause the virus undergo apoptosis,express protein costs that make it susceptible to everyday medical compounds and even compounds used in antiviral compounds and so on with automated labs testing the virus against venoms etc from all plants and animals and AI extrapolate synthetic compounds that can be synthesised by it.Other potential zoonotic diseases and pathogens worldwide will have this done for the same reason by AI at the same time by analysing all pathogens of animals genome that can mutate into zoonoses by proto Phanes analysing the genome of them and determining their level of potential to mutate into zoonoses and them extrapolate thousands and millions of potential strains that could be fatal potential fatal strains and thus extrapolate bacteriophage/virophage hybrid cures and cousin hybrid vaccines of all of these extrapolated strains of viruses,bacteria and fungi pathogens of all mammals,birds etc that have the potential to jump to humans by analysing existing DNA databases.This creation of bacteriophage/virophage hybrids could even be replicated for yearly season variations of Rhinovirus,Orthomyxoviridae with all possible normal and fatal strains of Rhinovirus,Orthomyxoviridae will be extrapolated by AI namely proto Phanes to then extrapolate the vaccines and bacteriophage/virophage hybrids to treat it by 2023 that can be deployed instantly around the world via 3D DNA printers for normal strains that are only fatal to only the immunocomprimised and elderly and also should fatal strains arise and even any other surprise fatal viral outbreaks across the world and remaining small outbreaks of any fatal pathogens such as Ebolavirus,N.meningitidis,N.fowleri,B.mandrillaris,Plasmodium,MRSA as early as 2023 prior to biocompatible microbes being perfected.Thousands of potential strains of Rhinovirus,Orthomyxoviridae can be extrapolated by AI for the years 2023-2029 and beyond similar to extrapolating the potential future strains of SARS-CoV-2 by analysing existing strains from the past few years globally and then extrapolating the likeliest few thousand or more strains to develop worldwide to them to extrapolate thousands virophage/bacteriophage hybrid cures and vaccines for each strains of Rhinovirus,Orthomyxoviridae every year between 2023-2029 in one go beforehand in 2023 including an all in one bacteriophage/virophage hybrid and vaccine to attack all posible strains until biocompatible microbes are perfected to be extrapolated and then uploaded to a global cloud that can allow them to be manufactured onsite of hospitals worldwide and deployed instantly thus allowing allowing for herd immunity to be achieved quickly and possibly even cure elderly and immunocomprimised patients at risk of dying of infections.Virophage and bacteriophage hybrids that don’t need a helper virus can be extrapolated by AI to kill HIV,N.meningitidis,Rhinovirus,Orthomyxoviridae,Ebolavirus etc prior to anti-viral microbes are availible by using them as a replication vector.If possible the same system of extrapolating thousands of bacteriophage/virophage hybrid cures and variant vaccines that are manufactured onsite of hospitals using cloud networks and 3D DNA printers will be pursued for treating the Monkeypox virus and other new emerging viral threats especially from zoonoses.Traditional vaccines for yearly strains of Rhinovirus,Orthomyxoviridae can be created this way by AI extrapolating the current yearly strains and then manufacturing them onsite of hospitals via 3D DNA printers cutting research and development as well as manufacturing costs to zero and cutting time to develop them to 24-168 hours.Superbugs and parasite infections such as MRSA and N.fowleri,B.mandrillaris,Plasmodium will be by 2023 treated by modified bacteriophages as detailed earlier and later on prior to the development of microbes to improve survival rates.This can be replicated with animal pathogens especially zoonoses.As stated allowing AI such as Alpha Go merger with all of the worlds supercomputers and use of networks and 3D DNA printers will expediate research and development into these cures and vaccines for SARS-CoV-2 etc since AI can scan databases and extrapolate hybrids and scratch DNA that humans can’t with 3D DNA printers allowing them to be deployed instantly onsite of hospitals around the world instantly with them stored in proto versions of Physis.This hypothesis of a cure and variant vaccine to SARS-CoV-2 is purely hypothetical but the plausible baseline extrapolations present here show that it should allow it to act as a baseline for future research starting in 2023 onwards with enough intensive research using this hypothesis as a baseline could become a reality.
Anti-Bacterial Strains:
Bacterial infections primarily superbugs such as MRSA,M.tuberculosis,N.gonorrhoeae,P.aeruginosa will be attacked by anti-bacterial strains with them using both anti-microbial compounds,endolysines and also CRISPR treatments housed in bumpers or via horizontal gene transfer during phagocytosis.Bacteria that superbugs can have CRISPR treatments applied to them that cause their phospholipids on the outer layers of them to express the same as those of ideally benign bacteria so as to allow anitimicrobial compounds at its disposal to be applied.Ideally the DNA to remove resistance to all known antibiotics including new and old ones,ones that prevent bacteria mutating and undergo mitosis,undergo apoptosis,remove their pathogenicity and ability to mutate as well as make them susceptible to the anti-microbial compounds at their disposal can added to anti-bacterial strains with advanced gene drive technology via CRISPR with them applied via horizontal gene transfer duing phagocytosis and can be flooded out to millions of bacteria by being released in bumpers or superbumpers that can transfer one or more genes as a mini vector to the precise site inside the genome thus allow for these to be made weak and then allow the microbes release antibiotics both old and new all at once as well as releasing endolysines in bumpers to work alongside anti-microbial compounds and also antibiotics as well as the antibodies from the immunised primary system to ensure success.Phanes will extrapolate the genotypes for these and other CRISPR treatments available by 2029.To cause them to undergoe apoptosis it could use DNA from “terminator seeds” and scratch DNA with scratch DNA extrapolated to develop CRISPR treatments that remove their ability to undergo mitosis,replication and also ability to mutate and develop resistence to new treatments.They can be made to have their pathogenicity removed making them benign strains that can be killed by the immune system or at least not kill or damage the patient.Otherwise the genes of all bacteria could be analysed and compared to find these genes.Their ability to mutate could be edited out permanently alongside the CRISPR treatments editing out their resistance permanently with the microbes phage treatments also used and adding suicide genes and those that prevent the bacteria undergoing mitosis and those that make them benign.This would involve mutating blocking genes made from scratch by Phanes and also from those found in nature with advanced gene derive technology ensuring this is permanent.To have them express the same phospholipids of benign bacteria to allow compounds including normal antibiotics to kill them the genome of benign bacteria will be analysed and compared with superbugs and thus have the genes that express phosholipids from benign bacteria that can thus allow them to be destroyed by all compounds at their disposal including lactic acid and other natural and synthetic compounds found in anti-bacterial soaps through recombinant DNA and anabolic and catabolic reactions with this also done to determine the genes that give them resistance to all past antibiotics and thus develop CRISPR treatments to remove these genes.These CRISPR treatments applied to the pathogens via horizontal gene transfer and flooding the bloodstream with bumpers that transport the CRISPR treatments can make pathogens especially superbugs and new pathogens a completely benign species that the native immune system can fight off by itself by completely rewriting the pathogens genome beyond recognition with other genes extrapolated that prevent them from mutating as well as allowing everyday over the counter medications that have no side effects and even vitamins etc consumed by the patient or injected into the bloodstream and also prevent them undergoing mitosis or replication in the first place limiting their numbers with this replicated with viral and fungal pathogens and even parasites.Old samples of each superbug that is not resistant to each antibiotics can be analysed and compared with modern superbugs and thus allow counter CRISPR treatments to be developed with this including those from as far back as 1928 in storage within labs.Paean,Physis etc will scan the genome of all superbugs and their non resistant ancestors stored in labs etc to extrapolate which genes are responsible for resistance to specific or all antibiotics and new treatments to create counter CRISPR treatments with the same applied to viruses and this can be done to determine the genes responsible from mitosis,reproduction and allow them to infect cells and organs and even those that cause them to be pathogenic allowing these to be removed by CRISPR via AI extrapolating counter CRISPR treatments stored in their Physis file and ribosomes and in particular plasmids in anti-bacterial strains.Otherwise Phanes will analyse the genome of superbugs and extrapolate the genes responsible for resistence and in turn CRISPR treatments to remove the resistence then store them in Physis in the pathogens file.Horizontal gene transfer will be used and them engineered to interact with only pathogenic bacteria and not that of the patients cells.The genes responsible for resistence to each and all antiobiotics through CRISPR treatments applied by anti-bacterial strains will remove their resistence to antibiotics permenantly and allow the microbes synthesise antiobiotics such as penicillin etc through them housing recombinant DNA in them from yeasts and also anabolic and catabolic reactions or allow the patient to intake them in pill form or injection through conventional means.The anti-bacterial strains will be engineered to only interact with only bacterial cells ideally those of specific pathogenic bacteria via surface proteins on them that only interact with only pathogenic bacteria and not gut flora to prevent them applying these to the patients cells that would kill them with them via induced evolution for each specific species of pathogenic bacteria once ascertained.The DNA to do this will be in the form of ribosomes and in particular plasmids floating in the microbes applied by horizontal gene transfer and also bumpers with them recreated over and over again via taq polymerase and Cas-9 to be reused over and over again.This can be applied to all existing parasites,viruses,fungi and all type of pathogens on Earth with this also applying to new and emerging pathogens including those on interstellar colonies outside of Earth with them able to kill anything by first modifying the pathogen or parasite via horizontal gene transfer during phagocytosis to exhibit the same phospholipids as bacteria that are susceptible to their compounds.This can also prevent Earth based pathogens they are designed to attack into becoming susceptible to the anti-viral,anti-fungal and anti-bacterial weapons at their disposable to prevent them becoming ineffective with this done to pathogens and viruses that have the ability to quickly mutate to the compounds at their disposal to again prevent them becoming ineffective with compounds that destroy the peptidoglycogen and protein coats of all bacteria,parasites and viruses utilised by them to act as backup.AI will analyse the outer phospholipids of all pathogens especially superbugs to extrapolate synthetic compounds and synthetic antibodies stored in their Physis file to be downloaded into anti-bacterial strains when infections occur.They would also produce anti-microbial compounds from Brown Russian frogs,lactic acids,alcohol which they can create by themselves or store from the host exercising,the natural bacteriacidal components of soaps especially those from liquid soaps that are non toxic to the host,new ones created from scratch,microbes and animals within all environments in the ocean and soil and even antibodies for existing or customised ones for superbugs that attack multiple sites rather than one site with these applied during phagocytosis,flooding the bloodstream and effective areas or as nanoparticles with the same applying to reactive oxygen.Otherwise the microbes would apply the anti-microbial agents from frogs,Polybia-MP1,plankton,endolysines,reactive oxygen,antibodies.CRISPR treatments and all anti-microbial compounds via phagocytosis or flooding the bloodstream with them and endolysines and CRISPR treatments in bumpers and superbumpers as well as having the immunised immune system gather in place and release relevant antibodies applied all at once will be done to prevent pathogens gaining resistance as they will attack multiple sites at once preventing bacterial pathogens from gaining a resistance to them all or any of them since they would be unable to adapt to this “carpet bombing” by being killed all at once with the immunised primary immune system also fighting at once clearing the body of them quickly and also before they can gain resistance with the same done to viruses.Compounds such as bleach namely hypochlorite and other natural and synthetic ones can be synthesised and applied in these bumpers to prevent the host being affected.Once infections occur and are detected and the strain that is resistant to each compound is detected by determining its genome the anti-bacterial strains will apply apoptosis genes,those that remove their resistance to anti-bacterial agents,those turn them into benign bacteria,and those that inhibit they ability to undergo mitosis with advanced gene drive technology preventing them able to adapt to these CRISPR treatments.They will also have all anti-microbial agents at the microbes disposal be applied and the immunised primary immune system activated.The bodies native beneficial bacteria will be given resistance to these via genome capsids or the bumpers not interacting with them.Communication between the primary immune system and microbes will manage the ratio of anti-microbial and antibodies being released at once to prevent resistance.This will be done at the same as them applying CRISPR treatments that weaken them via bumpers to the primary immune system and also these bacteriocidal treatments,make them easier to be attacked and stunt their growth,remove resistance to conventional and these new treatments and remove their pathogenicity,reactive oxygen,anti-microbial agents before they are applied and event to ones that may have gained such resistance as well as to conventional antibiotics such as penicillin,colistin.CRISPR treatments that remove resistance will be applied to them by anti-bacterial strains via bumpers and also horizontal gene transfer during phagocytosis prior to the anti-bacterial compounds applied by phagocytosis or via bumpers with these being all in one treatments that remove resistance to all compounds.Bumpers containing CRISPR treatments can be flooded into the bloodstream that can apply these CRISPR treatments to dozens,hundreds or millions of bacteria at once alongside those that remove their ability to undergoe mitosis etc in superbumpers that apply these and other CRISPR treatments all at once.CRISPR treatment that cause them to undergoe apoptosis will be also applied with as stated millions of anti-bacterial strains creating millions of these superbumpers at once.Thus anti-bacterial strains will through CRISPR treatments remove superbugs resistence to all known antiobiotics such as penicillin,colistin thus allowing the anti-bacterial strains to apply these antiobiotics by synthesised by them and released into the bloodstream having relevant recombinant DNA.Once strains of pathogens are made permanently weak against existing antibiotics like penicillin,colistin,β-lactam antibiotics through CRISPR treatments applied by anti-bacterial strains that permanently remove their resistance to these antibiotics with advanced gene drive technology making sure they they can never gain resistance to these again these old antibiotics can also be produced by the microbes anti-bacterial strains alongside the aforementioned compounds using biosynthesis,catabolic and anabolic reactions and also recombinant DNA from yeasts such as and Paenibacillus polymyxa,Penicillium chrysogenum,Acremonium present in the microbes genomes.Synthetic compounds to treat bacterial infections will have their structure added to Physis and this downloaded onto anti bacterial strains DNA digital storage to be then created by anabolic and catabolic reactions onsite of phospholipids of the bacteria to prevent overdosing and side effects.Thus alongside other compounds that have been newly discovered they will produce all existing antibiotics that pathogens will have their resistance removed via CRISPR treatments applied by the anti-bacterial strain.Colistins toxicity to the kidney and nervous system can be limited by engineering the host to be immune to it in these systems and organs as well as it applied during phagocystosis or even through protein bumpers with the same applied to other drugs.Colistons toxicity could also be countered by having the genes in bacteria immune to it added to the human genome of the organs it affects.This resistance removal can be done to any pathogen that becomes resistant to any anti-viral,anti-microbial compounds through CRISPR treatments already present as well as those added through upgrades.The CRISPR treatments to permanently remove antibiotic resistance to all antibiotics will done via bumper flooding the bloodstream in infected and asymptomatic patients.To keep levels of the pathogen under control the strains will also add CRISPR treatments to stunt the mitosis completely preventing them replicating and keep their numbers stable alongside applying suicide gene that cause them to undergo apoptosis and also those that remove their pathogenicity to prevent them causing damage to the patients body making them benign infections that cannot cause illness damage and death.Other anti-microbial compounds created by them would be ethanol,lactic acid,peptides from Russian Brown Frogs,Polybia-MP1 from Polybia paulista,TsAP-1,TsAP-2 from Tityus serrulatus,lactic acids from Lactobacillales well as those from phyotplankton and others from the soil,rivers and oceans using recombinant DNA from these organisms and even yeasts and fungi when penicillin,colistin and other antibiotics that will be made effective by modifying bacteria that are immune to it.If possible they could overload bacteria and also fungi with sugars namely glucose and fructose to overload them with it by forcing it into it or by creating large amounts of sugar in the bloodstream killing it through osmosis via dehydrating them provided the host and microbes has xerophile and osmophile DNA to protect them from it,as well as gluconic acid,hydrogen peroxide or its progenitor compound glucose oxidase and methylglyoxal kill them via low pH,cytotoxicity(provided the host is made immune to it via CRISPR) as well as the antibiotic Bee Defensin-1 used by bees with recombinant DNA from A.mellifera via them having recombinant DNA from plants that create glucose such as Beta vulgaris.All of these will be applied via horizontal gene transfer or bumpers with the microbes DNA from osmophiles and xerophiles protecting them.Sugar can be applied in large amounts via phagocytosis again by overloading the bacteria with sugar and thus killing it through dehydration via osmosis.Dihydroxyacetone,Hydroxymethylfufural,Methylglyoxal and Leptosperin using anabolic and catabolic reactions or recombinant DNA from Leptospermum scoparium can also be produced by them.All plants and animals will have the compounds from bites,stings etc be tested against bacteria particularly superbugs for new anti-bacterial compounds to have their DNA scanned for the genotypes that can be added to anti-microbial strains.Recombinant DNA from Brown Russian Frogs,yeasts,phytoplankton and new bacteria discovered will be added to their genome used by them with any resistance gained to these removed via CRISPR to all existing and new antibiotics with the primary immune system immunised against all bacteria especially superbugs including MRSA and P.aeruginosa to improve effectiveness.This resistance removing treatments would be applied prior to anti-viral and anti-microbial compounds are applied and would be applied to pathogens to prevent them to becoming resistant to the other anti-microbial and anti-viral compounds at their disposal with them having these alongside to attack existing superbugs inside the hybrid anti-viral and anti-bacterial strains.Antibiotics,endolysines,antibodies of all types from microbes and the immunised primary system will be produced during phagocytosis or through flooding the body via the bloodstream and lymphatic system to reach all hard to reach parts of the body to kill off infections that hide in hard to reach areas with this also done by the native immunised immune system using antibodies with the exception of those that cause severe side effects such as colistin which will be applied during phagocytosis or in bumpers.The primary immune system would also be immunised against all possible strains and orders etc of major bacterial pathogens including superbugs to improve success and eliminate them completely alleviating strains on microbes using the common proteins methods.New antibiotics can be synthesised by them by genotypes created from scratch by Phanes,Epione and Paean with those discovered from nature done by adding recombinant DNA extracted by automated lab workers and automated machines once and then input into a base microbe that can grown in automated labs and sent to new patients to inserted into their microbes by automated machinery or synthesised from scratch Phanes,Epione etc.All plants and animals in all versions of Physis will have their genome scanned for genes responsible for new anti-microbial compounds with genes that have the possibility of creating them extrapolated via Phanes and Paean etc and them created in either microbes and microrganisms in labs to test on all known pathogens in simulations and automated labs.Paean will analyse the outer phospholipid wall of all species and strains of bacterial pathogens especially superbugs that can extrapolate synthetic antibacterial compounds suited for each individual species and strain that can be stored in their Physis file to be downloaded into the anti-bacterial strains DNA digital storage to be synthesised by anabolic and catabolic reactions with Phanes extrapolating genotypes you create these synthetic compounds to be downloaded via induced evolution.All species of pathogenic and non pathogenic bacteria will be tested in automated labs against sap,secretions from plants and animals worldwide thay kill bacteria so as to allow the DNA responsible to be downloaded into anti-bacterial strains.AI wil also extrapolate synthetic antibodies,synthetic enzymes and synthetic compounds that kill bacteria to be stored in Physis and downloaded and then synthesised in the bloodstream.The structure of these synthetic compounds and antibodies will be stored in their Physis file to be downloaded into the DNA digital storage of the anti-bacterial strains and then synthesised by anabolic and catabolic reactions.This will be done by AI namely Phanes and Paean analysing their outer surface proteins and genome of all species and strains of bacteria particularly pathogenic species to allow these synthetic compounds,enzymes and antibodies to be extrapolated that will be stored in the Physis file of each species that will be downloaded by anti-bacterial strains and created by anabolic and catabolic reactions.These enzymes,antibodies and synthetic compounds applied during phagocytosis if they cause side effects including cytoxicity or released into the bloodstream if benign.Phanes can also extrapolate the genotypes created from scratch to express these synthetic compounds,enzymes and antibodies stored in their Physis files that can be downloaded into the genome of anti-bacterial strains..Synthetic and natural anti-helminthic compounds,enzymes,antibodies will be applied by being flooded into the blood stream or applied during phagocytosis by microbes to prevent cytoxicity through them having macrophage DNA.Dead bacteria can be consumed by the microbes using enzymes suited to each one developed by Paean and Phanes once downloaded during phagocytosis.The accelerated healing phenotype will instantly heal any damage caused by the bacteria directly and indirectly by cytokines storms etc meaning a patient could survive indefinitely to avail of upgrades and application of genes that prevent the virus replicating and to avail of immunisations.AI will create immunisations for all species of pathogenic and non pathogenic bacteria especially those that house common proteins thus allowing one to be immunised against all possible strains with this of note to MRSA and other fatal superbugs.Patients once made immune to radiation will be exposed to blasts of radiation between 2,000-20,000Gy to kill of large amounts of bacteria.All patients will be immunised against all bacterial pathogens especially superbugs using the common proteins method.Photoanti-microbial dyes could be produced by them and released into the bloodstream that would be benign to humans or themselves or with them produced on the surface of the microbes with them also creating bioluminecent luciferans using recombinant DNA from all types of biolumescent animals,plants and bacteria and those from scratch with these bioluminsecent reactions starting and thus activating the dye in the bloodstream,during phagocytosis or on the surface of other biocompatible microbes and themselves only when a pathogen is detected by nanomachines,leukocytes,the immune systems,or the pathogens themselves through chemical signals from nanomachines,immune system and the pathogens and microbes themselves and thus releasing reactive oxygen to kill pathogens.Aerotolerant anaerobic bacteria recombinat DNA added to the hosts genome will prevent these affecting the hosts cells.Biosynth WiFi can allow the DNA in these strains to be changed within minutes to allow them to apply different anti-bacterial compounds with Paean controlling a set number to at all times house the DNA for one set of anti-microbial compounds,another set number to house that for another set number of them to ensure that at all times their is sets of this strain that each produce each different anti-microbial compounds old and new that can be applied all at once or in different waves one after the other.Biosynth WiFi will also be used to change the DNA in ribosomes and in particular plasmids to get CRISPR treatments for specific strains detected.All anti-microbial compounds will applied via phagocytosis or as nanoparticles covered in bumpers to prevent them breaking down in bloodstream and causing cytotoxicity.The microbes would apply these by phagocytosis and bumpers to prevent toxicity to the host and also the compounds breaking down with benign bacteria in labs purposefully made immune to the compounds to them have the new genes added to patients to allow them to be applied without bumpers.This and making them benign would be first done to asymptopic carriers and also livestock,wild animals and pets that act as vectors.Thus superbug resistant bacteria such as MRSA,M.tuberculosis,N.gonorrhoeae,P.aeruginosa would be dealt with CRISPR treatments in bumpers or applied via horizontal gene transfer thus permanently removing their resistance to most if not all existing antibiotics in both asymptomatic carriers,livestock,pets,wild animals and infected patients with gene drives added that prevent them mutating and regaining their resistance to all known antibiotics and them applying old and new antibiotics such as penicillian,colistin,β-lactam antibiotics by flooding both the lymphatic and bloodstream as nanoparticles covered in bumpers or during phagocytosis with them also applying suicide genes to the pathogens.These antibiotics will be created by anti-bacterial strains that will house relevant DNA from yeasts etc once CRISPR treatments are applied with new ones such as reactive oxygen,lactic acid,alcohol and new ones from Russian Brown Frogs,Polybia-MP1 from P.paulista,TsAP-1,TsAP-2 from T.serrulatus,lactic acids from Lactobacillales well as those from phyotplankton etc also applied.Old ones can be made by DNA from yeasts such as and P.polymyxa,P.chrysogenum,Acremonium and synthetic compounds will be created by anabolic and catabolic reactions.Suicide and mitosis inhibiting genes will also be used with patients immunised against them as well.Suicide genes and those that remove their ability to undergo mitosis and mutate can be added.Suicide genes would cause the pathogens to undergoe apoptosis and those that inhibit mitosis will block the ability for the bacteria to undergoe mitosis thus slowing down their growth in the human body exponentially to zero thus allowing the microbes attack them with these genes added via horizontal gene transfer and bumpers housing them that allow them microbes applying CRISPR treatments to countless of pathogens at once.Phanes can extrapolate genes that can be applied through horizontal gen transfer via CRISPR to bacterial pathogens especially superbugs that inhibit their ability to undergoe mitosis or remove gene present in bacterial pathogens to remove their ability to undergoe mitosis thus slowing down their growth exponentially in the human body to zero especially when they are applied to countless bacteria at once through bumpers and countless microbes.Furthermore genes can be extrapolated for each species of pathogenic bacteria that remove their pathogenicity turninh them into harmless strains by removing genes from them and adding others.Each species of pathogenic bacteria has more milder benign strains that the body is able to suppress of kill off with CRISPR thus used to alter their genomes to turn pathogenic bacteria into more benign strains with these CRISPR treatments extrapolated by Phanes for each species and stored in Physis and then downloaded once a species is determined by base microbes.In cases of species with no benign strains he can extrapolate treatments for each individual species to make them benign.Suicide genes would as stated cause bacteria to undergo apoptosis and die off.Applying all of these methods are once will drastically lower populations of pathogens exponentionaly to zero and increase survival rates.Endolysines as detailed later on will also be used as these would affect them by being inserted into the cell by bumpers as well as horizontal gene transfer and if the pathogens would gain resistance to endolysines them they would have to lose resistance to antibiotics.The biofilms of pathogens will be broken down and navigated by the microbes either directly or through creating compounds to this with those that shield themselves from the immune system and hypochlorite present ie Streptococcus agalactiae can be using gene treatments using bumpers to remove carotenoids that protect it from hypochlorite produced by the primary and secondary immune system.S.agalactiae and other pathogens that create biofilms could be detected by the microbes tweaked to detect the biofilms and thus be able to initiate measures to break them down and also be able to swim through them using recombinant DNA from bacteria including flagellum to allow them to apply both anti-microbial compounds and also CRISPR treatments using bumpers and also horizontal gene transfer.The microbes could be able to navigate these and then apply CRISPR treatments to remove their ability to create biofilms and even carotenoids that mask them from antibiotics,anti-microbial compounds and the primary immune system with the biofilms broken down by the microbes creating compounds that break it down and them consuming them with bumpers released containing CRISPR treatments preventing micro-organisms creating theses and using these countermeasures to hide form the primary and secondary immune system. Using endolysines at the same time as CRISPR treatments and also using all antibiotics and antibodies from the immunised primary immune system will “carpet bomb” the pathogen preventing them gaining resistance especially if all antibiotics both old and new are used at once alongside endolysines increasing efficacy and preventing them able to mutate.By having microbes use CRIPSR,endolysines and also anti-microbial compounds and also having the primary immune system immunised against them will mean that every last one will be killed off unlike in conventional methods wherein a small amount will be left and then mutate to gain resistance to antibiotics with the microbes and immunised primary immune system designed to seek out and kill off every last one with CRISPR treatments that prevent them undergoing mitosis used a the start of infections to prevent them overruning the body with once resistance is removed using all new and exiting anti-bacterial agents at once to catch the pathogen off guard and prevent them gaining a resistance.These would be developed to be have a similar genetic structure to pathogens allow for this transfer to occur while at the same time preventing them from gaining said immunities or ability to be a pathogen through gene drives and compete for resources in the lifeform eventually overcoming them with this also applying to other emerging superbugs such as Clostridium difficile,M.tuberculosis,N.gonorrhoeae,C.trachomatis and even viruses such as HIV with their ability to evolve resistance and existing resistance to anti-viral and existing CRISPR treatments edited out permanently.They would also attack all infections of all types including those that cause food poisoning,diarrhea,those from contaminated water,coliforms,oncoviruses,cold sores,conjunctivitis, and minor infections that they body can already fight to alleviate strains on the primary immune system,discomfort from diarrhea etc as well as help immunocomprimised individuals survive infections.It would also aid those who are immunocomprimised,elderly,have weak immune systems and unable to use vaccines and rely on herd immunity to even fight off infections if they are infected and allow the primary immune system gain immunity learned from the battle without risk of death or serious damage and even allow people survive severe infections such as N.meningitidis,or naturally have weak immune systems again more benign infections and have again the primary immune system learning the correct antibodies to use in future effects thus being a living vaccine of sorts.Those with weak immune systems can also rely on the anti-viral and anti-bacterial strains to fight off pathogens with them availing of immunisations due to the fact the immunisation strains unlike vaccines would interact with the relevant leukocytes by sharing relevant surface protein antigens and activating the immune systems when infections occur with them as stated also relying on anti-viral and anti-bacterial strains as well.Recombinant DNA from older bacteria samples that are in storage from the years prior to them becoming to resistant can also be used to create these microbes CRISPR attacks alongside those from existing strains by analysing the different strains genes.That could be done by the microbe surrounding the pathogen by phagocytosis during or after they have applied CRISPR treatments that remove their resistance to penicillin and other ineffective antibiotics and then using these antibiotics against or first removing their resistance to all existing antibiotics with other treatments used to make them benign thus unable to harm the patient allowing the primary immune system to fight them making the immune system resistant to all future attacks and/or the microbes finishing them off.This would work to deal with both patients infected with them and asymptomatic carriers such as with carriers of both MRSA and S.aureus and other superbugs to prevent the spreading them.Asymptomatic carriers of non resistant strains and species of any pathogen could be treated this way to not only wipe them out but theoretically transfer genes that could permanently prevent them from mutating and developing resistance to any antibiotics especially those on the way to becoming superbugs.This would also apply to livestock and pets that carry these and other zoonotic diseases as well as their own species specific pathogens,genetic diseases and parasites especially preventing the spread of zoonotic diseases to cut down on or even eliminate the use of antibiotics entering the human food chain and prevent unnecessary suffering with the microbes flushed out in the case of livestock before slaughter via draining the blood in nodules which can be separated via nanomaterials and the blood used for creating Agriprotein and also blood pudding,through feces and urine where they can be separated and sent into new hosts or create bio-synthetic technology.It would also prevent the spread of zoonotic diseases and pathogens to humans that pass through undercooked meat and milk and other animal products with the same principle preventing food poisoning from uncooked crops by immunising them with crops have fully functioning immune systems added via CRISPR.Bdellovibrio,M.aeruginosavorus,Paramecium,C.elegans,C.roenbergensis DNA and those from other bacterivores will be in these strains to allow it parisitise the pathogens and be better at detecting them with scratch DNA making them attack all viral and pathogens and not the hosts cells or beneficial species.M.aeruginosavorus could be a species to research for this treatment to use directly or have recombinant DNA added into the microbes produced due to the fact that it purposefully preys on other species of bacteria as it is known to feed on Pseudomonas with recombinant DNA species from the Bdellovibrio genus also used as they also parasitism bacteria with these strains produced and programmed to attack and trade DNA with all pathogens such as MRSA,N.gonorrhoeae etc(using DNA from the pathogens) from DNA made from scratch with those from predatory bacteria used as model while removing any pathogenicity they may have to humans with them also engineered to produce human proteins or those from a patient on their bodies to prevent them eliciting an immune response and thus causing ill health and also be killed off themselves by by the bodies immune system.Paean through biosynth wifi,bluetooth and nanomachines can have the microbes actively seek out pathogenic bacteria especially at the start of infections with this allowing him to control each individual microbes and in groups to actively seek out pathogenic bacteria.Having one made immune to radiation via DNA from T.gammatolerans can allow one to be exposed to large doses of radiation as high as 1,000-2,000Gy that can kill off even the most hardiest superbugs as E.Coli can be killed by a mere 60Gy and will kill of endospores of them including those that use bio films etc to stay alive.This will be of note to new pathogens that evolve to become human pathogens discovered on off world colonies.Radiorestance can also be dealt with CRISPR treatements that remove this ability or even prevent them being able to develop this in the first place.Ideally the patient will be blasted with this levels instantly and for at least 30 minutes to an hour or more to prevent them gaining radioresistence via mutations with with patient put under anaesthesia.Doing it for more that an hour and starting at these levels as well as applying it to all parts of the body at once will ensure all or most of the pathogen will be wiped out without developing radioresitance and will be done alongside the primary immune system and microbes both made immune to radiation to aid in fight in eliminating the pathogen.The level at which the species can survive can first be determined in lab settings and also in animal trials so as to allow it to be determined and then have patients exposed to levels much higher at least 1,000-2,000Gy higher.All patients worldwide should be immunised against all strains of bacteria including superbugs using the common proteins method but also non superbugs and even those that are gained from raw food and dirty water and those that cause vommiting,food poisoning in order to prevent discomfort with animal and plant vectors also immunised against zoonotic diseases especially serious ones to remove the root cause and remove antibiotics from the food chain.Inoculating animals via biosynth arthropods that act as vectors of superbugs and even non superbugs that are zoo nooses with microbes that pass from one generation to the next and immunise each animal and them fight off existing infections could wipe them from the face of the Earth.All animals both pets and livestock will be immunised against Hantavirus,Rabies,MRSA,M.tuberculosis alongside humans with wild animals have inoculated and immunised animals released to interbreed microbes into them with biosynths in time inoculating those in the wild.Ideally patients will be immunised against all species and strains of bacteria including superbugs,pathogens,those that cause abortions,feral abnormalities,food poisoning and even benign species using the common proteins method.This would reduce the amount of dangerous superbugs in the general population to be reduced then any infected patients can be treated by them first removing their pathogens resistance removed and then them treated with penicillin alongside reactive oxygen etc.The vectors of all pathogenic bacteria particularly superbugs such as asymptomatic humans,uninflected humans and also animals whether wildlife and livestock that act as vectors will also be immunised using the common proteins method to wipe them out from the face of the Earth and prevent non resistant human patients to not get sick.This will also eliminate antibiotics from the food chain.Remaining livestock will be not only immunised by species specific microbes but also made immune to radiation and exposed to huge blasts of radiation.Ideally the sharing of genes and proteins should occur before the patient is infected by any pathogen with the pathogens scanned once added to Physis and the relevant genes added to the microbes with those already in the body if not killing them at least keeping them under control and preventing the body being affected by keeping vital organs alive or being infected or damaged,counteracting any effects caused by the pathogens(ie repairing vessels and organs,replacing decimated immune systems etc) or even just attaching to,surrounding the virions or bacteria,forming a biofilm around them to keep them locked in place and removing them from the body by flushing them out of the system or even if possible just preventing them from being able to affect the body ie infect vital cells and organs with them doing this automatically or under instructions from Paean until the pathogen can be collected,scanned for genotypes to produce proteins on their surface to be shared with the dendritic cells to allow the primary immune system to fight it off and also while Phanes,Epione and Paean can develop natural or synthetic compounds created by added genes from Physis and those created from scratch or through catabolic and anabolic reactions.Any infected individuals would also have their base microbes collect samples of any new pathogens in their body and wirelessly send the genome to Paean and Epione to analyse when it is added to Physis where the pathogens phenotypes(gram statues,pathogenicity,flagellum,chemotaxis etc.) can be analysed and it recreated in secure labs via 3D DNA printed DNA into blank bacterial cells for it to be tested in simulations and automated labs within agar plates using anti-microbial and anti-viral compounds synthesised from scanning the genome of all the plants and animals in all versions of Physis across the universe.The genome will also be scanned into Physis to allow for genotypes that create specific key surface protein antigens on the surface to be upgraded into the strains to be shared with dendritic cells to be determined while the patient is kept alive.This would allow the microbes to be upgraded with the genotypes that express these compounds.All public buildings including hospitals will have narrow range UV lights built into normal lights that can perform sterilising sweeps of all rooms at once either routinely at set times or all times with handwashing with anti-bacterial soap complimented with hand dryers that expose ones face and hands with this narrow range UV light to sterilise ones hands of pathogens that soap doesn’t kill.Mouthwash,toothpaste,soap both solid and liquid and also body shower wash as well as even cleaning fluid made at home as well as in public buildings such as hospitals could have these compounds Polybia-MP1,TsAP-1,TsAP-2,lactic acid,the anti-microbial agents of Russian Brown frogs,phytoplankton etc in it to sterilise the body mainly skin and also mouth.These all would be in them to prevent them adapting to the compounds.Bacteria can be edited to lose resistance to those from phytoplankton etc and the first generation of microbes will contain and the ability to produce all of the aforementioned antibiotics including new and old ones alongside CRISPR treatments applied through bumpers or phagocytosis to remove their resistance to existing ones with these applied if the bacteria gain an immunity to new ones to allow them to be dealt with until CRISPR treatments can be added via upgrades to ensure no bacteria can be immune to all compounds at its disposal with the ability of them to produce endolysines also used as this can force the bacteria to lose resistance to antibiotics and these endolysines produced can be adaptable to new strains as detailed via scanning the genome with them also using CRISPR to apply suicide genes and other ones as well.The genes that confer resistence for existing superbugs can also be determined by Phanes scanning and comparing genomes of superbugs and early strains of superbugs present in labs from before the rise of antibiotics from before 1928 in storage within labs could be used as they are not immune to penicillin etc and also are the same species of them but not resistant strains with them cultured in labs and sent across the world or they could be once their genes are mapped they could be printed out in labs around the world via 3D DNA printers with even versions of superbugs without the genes that give them resistance also printed out in labs around the world.These will be used to extrapolate counter CRISPR treatments stored in Physis to be added to microbes etc.Any compounds that may be toxic to humans can have them released during phagocytosis and bumpers or the patient made immune to them by having the genes responsible for resistance added to the patients genome.Superbugs will be compared to those in labs that are in storage and are from the era prior to the development of antibiotics to see what genes are responsible for the development of these resistance can be charted and isolated to have counter treatments created by AI and them added to the anti-bacterial strains of microbes.Thus first generation microbes of this anti-bacterial strain will house CRISPR treatments to remove resistance to all existing antibiotics such as colistin,β-lactam antibiotics and penicillin that will be produced by the microbes using relevant DNA from yeasts and bacteria with this allowing time for CRISPR treatments to new ones such as those from phytoplankton and also Brown Russian Frogs etc to be developed allowing for the anti-bacterial strains to remove any resistance to all of its anti-microbial agents should they ever gain a resistance thus ensuring they are always able to fight off all types of bacterium including superbugs.Ideally these CRISPR treatments that remove resistance to all antibiotics both old and new would have advanced gene drive technology utilised to prevent them from regaining a resistance though since the pathogens would be wiped out by an immunised immune system and also by the microbes they would be be wiped out completely.These CRISPR treatments to remove resistence to new anti-bacterial compounds will be gained by having all existing benign non-superbugs in secure labs exposed to these new antibiotics and anti-microbial compounds forcing them to gain a resistence to them and then when they gain resistance they will be scanned for new genes and thus new CRISPR counter treatments to be applied to them which can be available alongside those to remove resistance to existing ones available by 2029 with these added to all anti-bacterial microbes with the same done for viruses that adapt to anti-viral treatments.The new genes will be added to their species folder in Physis and will be part of CRISPR treatments that float in the microbes as ribosomes and in particular plasmids.Ideally these versions could not just be existing superbugs but those isolated that are not supergbugs and are in fact benign non pathogenic bacteria that are related to existing superbugs and have CRISPR treatments added that remove their resistance to colistin,penicillin removed permanently by gene drives to prevent them gaining a resistance again and then exposed to new anti-microbial compounds to ensure at least penicillin etc,high doses of radiation and even bacteriophages created specifically for them can be used without toxicity effects should they escape or someone is infected with this work starting at least by 2023 and finished by 2025-2029 then full microbes are availible.Benign species of bacteria not immune to penicillin etc could also be used as baseline with this ideally pursued in order to ensure that even if it infects someone then their native immune system,penicillin and bacteriophages can be utilised with them exposed to high levels of the anti-bacterial compounds to force them to evolve new genes to gain a resistance that would thus be used to develop CRISPR countermeasures for microbes.Superbugs will be tested as well to see if they produce the same resistance genes with ideally these being original strains that are not resistant to existing antibiotics by comparing existing strains in labs prior to the antibiotic age with them also created by AI analysing superbugs for the genes responsible and editing out all resistance genes with this modified version added to a separate file in Physis and 3D DNA printers used to create the benign form in labs that can be killed by penicillin and all old antibiotics if they infect anyone.This would ideally involve bacteria already edited to remove their resistance to penicillin,colistin,β-lactam antibiotics etc removed permanently using gene drives to ensure that they can be safely made resistant to new anti-microbial compounds to create new genes and thus if they escape then they can be treated in infected humans with penicillin etc alongside bacteriophages created to kill them created beforehand.AI can analyse superbugs for genes that give them resistence to all existing sntibiotics and AI will using 3D DNA printers create benign versions of all superbugs that don’t have the genes that give them resistence to all antibiotics that will be edited out or they will create a new benign species of bacteria that has no resistence.The chosen species will be exposed to all new antibacterial compounds that can allow them to gain a resistence with every time it develops a resistence to each new antimicrobial compounds to induce resistence and allow its genome to be scanned to determine the genes responsible for this to allow for CRISPR treatments that can be stored in Physis and downloaded into microbes whenever they gain a resistence to these compounds as denoted by base microbes scanning them allowing for microbes to be able to have the ability to counteract resistence to all new compounds at their disposal before they gain a resistence to prepare beforehand.Bacteriophages should be created at the same as these for all strains used prior to the experiments in order to allow them to be used to cure infected technicians as a security measure if a breach is made.Radiation,narrow range wavelength UV light,high temperatures etc can be used to kill them off.These would be killed off by exposing them to high levels of radiation,sugar,salt and other environmental conditions.The bacteria species can be exposed in secure labs to these new anti-bacterial compounds such as peptides from Russian Brown frogs,TsAP-1,TsAP-2 and Polybia-MP1 and those from phytoplankton and all compounds derived from plants and animals to gain a resistance to them in different test samples in different cultures thus ensuring that if they gain a resistance,then the new genes responsible for this resistance can be determined to create CRISPR counter treatments treatments to it by AI with them killed off by penicillin and even large doses of radition,high temperatures or bacteriophages and each different compound they are not immune to.These counter CRISPR treatments will be added to the Physis file of superbugs to be downloaded into anti-bacterial strains when they are found to have developed a resistence thus allow future resistence to them to be dealt instantly.The labs will like all other ones will have narrow range wavelength UV light to sterilise them and the technicians using biohazard suits but ideally these should be done in automated labs.Using benign bacteria that can be killed off by penicillin will be ideal as at least the technicians can be cured via penicillin etc and bacteriophage with them being less fatal with these done in automated microbiology.Phanes will create benign strains of the original superbugs or new benign species of bacteria that do not contain the genes responsible for antiobiotic resistence through 3D DNA printers to allow them and have genes that prevent them mutating to gains resistence to all existing antiobiotics including penicillin to aloe then to be exposed to new anti-bacterial compounds such as peptides from Russian Brown frogs,TsAP-1,TsAP-2 and Polybia-MP1 etc in increased amounts to allow them to gain resistence to examine the new genes and then allow Phanes extrapolate counter CRISPR treatments to be stored in Physis to be downloaded into anti-bacterial strains when pathogenic bacteria gain a resistence.Otherwise Phanes can by anslysing the anti-bacterial compounds structure will extrapolate genes for counter CRISPR treatments to be stored in Physis.Both natural and synthetic compounds will undergo this.It can also be used to test melittin,lemon juice etc and all types of antibodies on HIV or other benign viruses making the virus then resistant to them and thus allow CRISPR treatments that counteract them to be created not only to prevent resistance invivo in patients but also make these compounds in anti-viral strains able to kill the virus 100% and also create the genes used in CRISPR treatments that can be used by this anti-viral strain to make other viruses susceptible to the compounds with the same done for the compounds used for anti-bacterial strains.This can also be applied to anti-bacterial strains with the treatments to make new bacterial pathogens and even fungi susceptible to the compounds at their disposal created this way.This would have the pathogens new genes scanned once the compound cannot kill them and added to all cells in the body with these pathogens killed via large doses of radiation so as to prevent them escaping and infecting patients or themselves treated by CRISPR.The same can be done to fungi,viruses and parasites for their relevant strains to prevent them gaining immunities to anti-viral,anti-fungal etc compounds with this done to both existing and new compounds both natural and synthetic.The test bacteria etc once no longer needed and their DNA analysed and stored in Physis and CRISPR treatment developed wil be liked off by exposing them to radiation,high temperatures etc to prevent them escaping.Bacteriophages that kill these specific strains will be prepared beforehand to cure infected researchers with the bacteria killed by exposing them to high doses of radiation.This can thus allow for CRISPR treatments to be applied to resistant bacteria,viruses,fungi and parasites to be developed prior to them in the real world gaining resistance by having new antibiotics tested on bacteria in a secure lab be treated in a way so as to force them to develop resistance,have new genes scanned and thus have counter CRISPR treatments developed by Phanes to be integrated into anti-bacterial and anti-viral strains etc thus ensuring that these strains can prevent any superbugs or non superbug pathogens and parasites gaining a resistance to their existing and new anti-viral and anti-bacterial compounds with the same done for viruses and the anti-viral compounds used against them with it also limiting the need for upgrades and also genotypes.Thus the microbes would be able to apply all of the new anti-microbial compounds and if the pathogen and parasites gains resistance the new CRISPR treatments gained from the experiments in the labs can be downloaded and applied instantly to remove this and thus kill them off meaning all pathogens including parasites will not be able to gain a resistance and if they do then CRISPR treatments can be applied instantly to remove genes that give them resistance to all of the compounds at the various strains disposal.It will negate the need for upgrades for new anti-microbial compounds and to limit the genotypes in them with if need be once a resistant strain is found then it may be possible for upgrades to be wirelessly used.The new CRISPR treatments will be stored in Physis and once a species of bacteria is found to be resistant to anti-bacterial compounds the microbes through induction of the evolutionary process of microbes through biosynth WiFi to gain these new CRISPR treatments.Resistence will be ascertained by the base microbes scanning their DNA that will be analysed by Phanes and Paean cross referencing Physis with the induced evolution of ribosomes and in particular plasmids via biosynth WiFi and them applying CRISPR treatments to remove them,or Paean and Phanes extraoplating new ones and sending them wirelesy while the microbes apply suicide and mitosis stunting genes.These CRISPR treatments would be in ribosomes and in particular plasmids in the microbes with the anti-bacterial and antI-viral strains housing all CRISPR treatments or these can be created instantly via Paean wirelessly inducing their formation via wifi on the spot when needed.Thus the genome of bacteria will be scanned for its species and strain and it’s genes that denote resistance to specific antibiotics by scanning Physis with biosynth downloading CRISPR treatments stored in its Physis file.This will all be replicated with anti-viral,anti fungal and anti-helminthic strains.Applying all compounds at once will limit their ability to evolve resistance with the bacteria applying CRISPR treatments during phagocytosis when their anti-microbial compounds are unable to kill the pathogens with them also during phagocytosis using horizontal gene transfer,Cas-9 and taq polymerase to read the genome of the pathogens to ascertain if genes are present that give the pathogens resistance to any compound with this sent to Paean to allow them to tell the microbes what CRISPR treatments to apply.This would be done also to allow the microbes house and create counter CRISPR treatments for all compounds at its disposal both old and new preventing all type of bacteria from being able to gain an immunity to all of the new and existing compounds.Thus all pathogens will have CRISPR treatments applied to remove or prevent them becoming resistant to the anti-viral and anti-microbial compounds with immunisation also allowing the immune system to fight them off.Bacteria that become resistant to the anti-microbial compounds at their disposal will be dealt with them by this way with them already fitted with these CRISPR treatments before they become resistant if possible and this applied during phagocytosis alongside the treatments of anti-microbial compounds with having the host immunised beforehand against all possible strains of a pathogen also done to ensure any strains that become resistant to the compounds at their disposal will be dealt with to allow for upgrades to be done to microbes to counteract resistance.It will also negate the need for upgrades for new anti-microbial compounds and limit the genotypes in them with if need be once a resistant strain is found then it may be possible for upgrades to be wirelessly downloaded.Thus experiments wil be done to force strains of superbugs that existing resistence to penicillin removed to allow them to be exposed anti-microbial compounds that then develop resistence to the new compounds and all AI extrapolate counter CRISPR treatments stored in Physis that can be downloaded via upgraded to allow them to be deployed instantly should real world superbugs develop resistence to these.Furthermore if any these compounds prove toxic to humans and can cause serious side effects like colistin or the peptides from Russian Brown Frogs,melittin then the genes used to counteract these in bacteria can be added to the human genome and thus negating any issues of toxicity to the host allowing them to be released in large amounts without bumpers outside of phagocytosis and not affect the host.These can also be added to microbes if needed.P.aeruginosa and similar pathogens naturally resistant to antibiotics will be dealt with them made susceptible to compounds at their disposal including antibiotics,alcohol etc,undergo apoptosis etc and also endolysines.Pathogens like P.aeruginosa could be dealt with via radiation as well as making them vulnerable to alcohol via genes from microbes given to affect those in asymptopic carriers and livestock.Ideally all drug resistant bacteria should have all resistance to all existing anti-microbial compounds permanently removed via gene drives in all vectors with all patients both human and animals(pets,livestock and wild animals) immunised against them and their possible strains to improve success such as with those that are resistant to all of them and remove antibiotics from the food chain.For bacteria on other planets across the universe they will be tested against Earth based antibiotics and compounds in automated labs see if these are effective and if so then this will negate for new ones to be developed.If they are not effective then all compounds on the planet from native fungi,plants and animals will be tested on them in automated labs to see which are effective and the DNA to express these compounds will be stored in each micro-organisms file in that planets version of Physis with them tested on those from all planets.DNA from animals etc that produce antibiotics etc from Earth will be in their file in their version of Physis.Counter CRISPR treatments will be developed to them in the same way as Earth based pathogens for the same reasons and stored in their Physis.Each planet across the universe will house their own version of Physis that houses all species of plants,animals and bacteria,fungi,viruses genome and all other data to allow them to be cross referenced to identify pathogens from that planet and downloads both recombinant DNA that express compounds that kill them and CRISPR treatments to remove resistance.Endolysines also used by these strains as a backup and also because in order to adapt to endolysines bacteria lose resistance to antibiotics with endolysines produced by these anti-bacterial strain using bacteriophage DNA.The bacteriophage DNA will have to be tweaked to produce endolysines unique to each species it detects.If possible to deal with MRSA and other severe drug resistant pathogens including N.gonorrhoeae prior to microbes being perfected Polybia-MP1 etc can be injected into the bloodstream or in pill form alongside pills of peptides from Russian Brown Frogs and phytoplankton using bumpers as well as even using other delivery methods such as alternative methods of phage and Car-T immunotherapy using modified macrophages and other leukocytes wherein the native immune system is strengthened to use Polybia-MP1,TsAP-1,TsAP-2 the anti-microbial agents of Russian Brown frogs,phytoplankton etc using relevant DNA and detect these pathogens can be used to kill them off before microbes can immunise one from them and also utilise the removal of antibiotic resistance.These macrophages and proto microbes can be also used to transfer CRISPR treatments to superbugs in both humans and animals as well as in test petri dishes to remove resistance to all known antibiotics,undergo apoptosis,prevent them mutating and undergoing mitosis as well as removing their pathogencity.Bacteriophages can be modified to deliver the venom based compounds and those from Russian Brown frogs negating toxicity or the possibility of them breaking down as well as CRISPR treatments and if possible they could apply first CRISPR treatments to remove resistance to penicillian,β-lactam antibiotics and then apply them after these gene therapy treatments.Other treatments could alter the pathogens to be unable to undergo mitosis,mutate as well as undergo apoptosis and remove their pathogenicity at the same time with them also killing them off in their conventional manner by using the bacteria to replicate and destroy them via endolysines.The use of endolysines by anti-bacterial strains of microbes to attack specific resistant pathogens can be used as well with the microbes using a combination of all treatments at once with resistance removed either through phagocytosis or by flooding the bloodstream etc with huge amounts of protein bumpersa containing these resistance removing genes and also endolysines in order to intercept the pathogen by entering its cell wall.This would be done by adding recombinant DNA from bacteriophages to anti-bacterial strains and virophage DNA to anti-viral strains.The use of endolysines should be used in conjuction as resistance removing gene treatments and antibiotics alongside other anti-microbial compounds as in order to gain resistance to phages pathogens must lose their resistance to antibiotics and vice versa leaving the pathogens in a catch 22/Mortons fork situation when used at the same time as CRISPR treatments.This would also be done to remove the ability of certain pathogens to be resistant to compounds like alcohol and would ideally use the genes flooded around the body using protein bumpers to allow the pathogens to be altered and then antibiotics created by the microbes or injected into the blood or taken in pill form to kill them off and would be used if the pathogens are made immune to any off the compounds at the microbes disposal.Gene drives would make this resistance removal permanent through successive generations making them unable to regain the resistance again with their resistance to all anti-microbial agents and antibiotics done through bumpers thus allowing colistin,penicillin etc to be once again effective with asymptopic carriers and animals first treated this way followed by infected patients while the body is kept alive as well as applying treatments that make the pathogen benign and even unable to undergo mitosis.Anti-bacterial strains would house bacteriophage DNA to express receptors to inject bacteria with instructions to create endolysines specific to each species of bacteria.Through horizontal gene transfer DNA from a pathogen especially drug resistant one could be intaken and analysed via taq polymerase and Cas-9 to allow endolysines to be created suited to that one on the spot that can be synthesised by the microbes and then released in the bloodstream once other microbes are signalled to produce the specific lysins.Using biosynth wifi Paean and Phanes would analyse the DNA and then extrapolate endolysines suitable for them to be sent back to the patient within minutes or hours allowing new infections to be attack instantly while the microbes also apply CRISPR treatments that prevent them undergoing mitosis.Once analysed the schematics would be sent to the DNA digital storage of all microbes as part of the anti-bacterial strains.This will work primarily for new pathogens especially on new planets.Ideally all bacteria such as superbugs,those that cause diarrhea,vommitting and other minor ailements etc and even benign will have their genome scanned by Phanes when in Physis to extrapolate endolysines that will be stored in their Physis file and once a pathogen is identified via base microbes then its endolysine schematics will be downloaded into DNA digital storage in all microbes of this strain and allowing them to fight off the infection instantly.The structure can be extrapolated and synthesised by anabolic and catabolic reactions and DNA can be extrapolated from scratch to allow it to be downloaded into them as well.DNA present in microbes and used by AI as a baseline can be used to extrapolate these structures and DNA downloaded to microbes.Also extrapolated will be DNA to express bacteriophage receptors for each species of pathogen to allow the endolysines and DNA to be inserted.It will also analyse their DNA to extrspolate DNA to induce replication of the microbes and endolysines and also schematics of endolysine that can be pumped into them stored in Physis and downloaded when needed.AI wil analyse the genome and phospholipids of each species of bacteria especially superbugs to then extrapolate genes to express bacteriophage receptors suited for each species that will be stored in their Physis file and then downloaded when needed by Biosynth WiFi.They will also extrapolate the schematics and structure of endolysines and DNA to be injected to induce the pathogen to create endolysines etc within the pathogen through genetic instructions.The structure and DNA of endolysines and DNA for receptors will be present in each species Physis file with AI extrapolating these for bacteria across the universe for their files in their version of Physis.Thus Phanes will extrapolate the genes for creating receptors and endolysines and their schematics for each species of bacterial pathogens that is stored in each species Physis file to all it be downloaded during an infection within minutes.This can be done for all species of bacteria including benign ones and those that cause food poisoning and diarrhoea and not just fatal superbugs.Paean once the species is identified in an infection can cross reference the species in Physis to then have biosynth WiFi induce the evolution of microbes genomes to be able to house the species specific receptors and ability to produce species specific endolysines.If possible synthetic endolysines that affect all types of pathogenic bacteria or indeed those suited to specific bacteria that will be applied when the microbes detect the unique surface proteins of the bacteria with if possible the microbes engineered to detect the unique surface proteins and even using horizontal gene transfer intake DNA from the pathogen and use this to synthesise relevant endolysines by themselves to counteract the specific pathogen and thus signal to other microbes to produce this specific endolysines both through phagocytosis and also flooding the body and lymphatic system thus ensuring that only the pathogen is destroyed and not the bodies native fauna.These endolysines would be inserted via receptors from bacteriophages present in anti-bacterial microbes,horizontal gene transfer that allows them to insert them into the cells or these would be able to when flooding the blood and lymphatic system bypass the cell wall through bumper proteins also able to penetrate the cell wall by tricking them into believing they are food etc or them coated in Polybia-MP1.Large amounts of endolysines would be pumped into the pathogen via horizontal gene transfer and even receptors.The endolysines once inside them would synthesis enzymes that causes the pathogen to burst open inside out and then die.Otherwise the microbes would insert into the pathogens strands of DNA extrapolated by Phanes suited for each pathogen stored in Physis to instruct them to create new microbes/bacteriophage hybrid including new anti-bacterial strains that then replicate and destroy the pathogen via endolysines and either they create only new microbes of the antibacterial strains or bacteriophage like hybrids that attack all other bacteria exponentially like normal bacteriophages until they have killed all bacteria and are flushed out of the body or just bacteriophages that produce endolysines or just DNA to have the pathogen to produce endolysines in large numbers in itself similar to normal bacteriophages.The pathogen can be instructed via having genes added to them by horizontal gene transfer to induce the replication of antibacterial strains of microbes or normal bacteriophages both of which will create endolysines that cause the pathogens to be be killed from the inside out.In both cases each destruction and replication would create exponentially more anti-bacterial strains or bacteriophages that are then directed by Paean would kill more pathogens in an exponential manner with if possible them even synthesising bacteriophages suited for that pathogen by Paean inducing the creation of only new species specific bacteriophages.They can even insert DNA via horizontal gene transfer or even bumpers flooded throughout that inserts DNA that instructs the pathogen to produce only the endolysines themselves in all cases suited to kill the specific pathogen and thus kill themselves inside out.Other methods include woild involve large amounts of endolysines to be synthesised inside the microbe and then be through horizontal gene transfer be inserted into the pathogen at once that then create enzymes to cause the pathogen to burst inside out preventing them gaining a resistance and causing them to be killed instantly with them also inserted via protein bumpers flooding the bloodstream and lymphatic system.If possible the same receptors as bacteriophages would be present on microbes to intercept the cell wall.Resistance removal genes would be used to remove the ability of bacteria to gain resistance to these though these endolysines have a very little chance of developing resistance.Paean can induce the microbes genomic evolution to create receptors on their surface unique to each pathogen and endolysines to allow them to inject countless endolysines synthesised by the microbes or they can be applied by horizontal gene transfer or bumpers.Ideally the microbes should be engineered to produce endolysines for all pathogens or those that they develop these on the spot via as stated extracting DNA and analysing DNA sequences that cannot mutate to create specific endolysines to that species,strain or ideally order of pathogen or just all pathogenic bacteria via horizontal gene transfer from base microbes with these stimulating through,horizontal gene transfer,creating protein bumpers that are flooded and attach and enter into other microbes namely the anti-bacterial strains,by Paean and chemical signals to other microbes to produce the required DNA to make these endolysines to fight of a specific infection by themselves in vivo with in the case of serious infections the host kept alive or the body flooded with genes coated with bumpers that prevents the pathogens replicating and causing damage to the host.The use of common recombinant DNA in microbes from all species of bacteriophages will allow for not only the base microbes to scan the genome via taq polymerase and Cas-9 then they could by scanning any pathogens genome create not just specific endolysines but even universal endolysines that could attack all pathogens and not beneficial bacteria by using genes common to whole orders or all bacterial pathogens.If this is done then these endolysines can be released by other microbes via them flooded while coated in protein bumpers that can enter these specific pathogens cell wall and be released inside from the bumpers to then kill the pathogen inside out in large amounts.The protein bumpers would be designed to deliver to only pathogens but if the do then pass through them the endolysines designed to affect only pathogens would have no effect especially if the genome capsids have DNA to protect them from these.Since the endolysines will be inserted via flooded bumpers or injected via horizontal gene transfer both in large amounts then they would likely be able to be designed to attack all pathogens and not beneficial bacteria as they would bypass the cell wall as specific species of bacteriophages can only interact with only set species of bacterias cell wall with the bumpers only interacting with pathogens and only endolysines created would ensure that beneficial bacteria are not harmed with them being more effective if large amounts of endolysines are inserted.This would also prevent the bacteria gaining a resistance since they are again created or injected inside and bypass the cell wall and the bacteria usually gain resistance to the bacteriophages receptors and not endolysines with the microbes reading the genome of each strain and thus creating endolysines specific to new mutations.The use of flooding the bloodstream via bumpers will allow for multiple endolysines to enter each of millions of bacteria at once alongside horizontal gene transfer using this to insert many endolysines will alongside using anti-microbial compounds and also the immune system using antibodies will also prevent resistance from being gained.Ideally base microbes should scan the genome of the pathogen or have the microbes already programmed to have the common genes of all pathogenic bacteria present to already have the ability to create those that kill all pathogens and not beneficial bacteria with these protected from endolysines from DNA in genome capsids.Having DNA from whole orders or all bacteriophages will allow for this adaption to all pathogens be possible with them through the collection of DNA from base microbes knowing the common genome sequences of only pathogens from Paean and Physis stored on their nanomachines and digital DNA storage or sent into them via upgrades thus only create universal endolysines for all pathogens and not beneficial bacteria allowing the bloodstream to be flooded with these and not damage the gut flora of the host.In any case the host will be kept alive and the immunised immune system and anti-microbial compounds and flooding of bumpers with CRISPR treatments will fight off the majority of pathogens while base microbes scan the DNA of pathogens via horizontal gene transfer using taq polymerase and Cas-9 and send to other strains primarily the anti-bacterial strains via signals.Paean,signals and horizontal gene transfer or even bumper coated DNA or proteins that seek out interacts with only anti-bacterial microbes can be synthesised by the base microbes to cause the anti-bacterial strains to produce endolysines specific to the pathogens that will attack only it and not the hosts beneficial bacteria by being flooded using bumpers to attack millions or billions of bacteria at once by entering their cell wall tricking them into believing it is food and allow each one to be infected with countless endolysines at once to improve their success alongside anti-microbial compounds.In time universal endolysines can be created that attack whole orders of pathogens alongside all strains of a pathogen.To deal with the issue of an immune response the protein bumpers would prevent them from being detected by the immune system with the endolysines coated in some human proteins etc to prevent them being detected with them designed to be flushed out of the body or used up once and break down once the bacteria is dead with the base microbes scanning their DNA and producing specific endolysines would deal with any issues of them not having any effect.The use of microbes inserting them into the cell wall via horizontal gene transfer and also flooding using bumpers will make them effective against both gram negative and positive bacteria and the protein bumpers suited to only pathogens would allow universal endolysines not affecting beneficial bacteria.As detailed once the DNA of a pathogen will be detected and scanned by these base microbes that can cross reference Physis to determine its species to then have endolysines and receptors.Biosynth wifi will allow schematics to be sent instantly to all relevant strains microbes and stored on their DNA digital storage.Receptors from bacteriophage DNA to attack and intercept specific species phospholipids and insert DNA,endolysines can be downloaded and DNA changed via wifi with AI extrapolating endolysines and receptors for each species of bacteria and stored on Physis.AI will also analyse their structure extrapolate endolysines and receptors specific to each species and strain of bacterial pathogens that will be stored in Physis in their species file and then downloaded to the strain through induction of the evolutionary path of microbes when needed speeding up the process of the anti-bacterial strains creating relevant endolysines for pathogens.When a species of bacteria is identified via base microbes the anti-bacterial strains will have upgrades via biosynth WiFi that induces the evolutionary path of microbes to get the specific bacteriophage receptors of the pathogen and species specific endolysine that allow it to utilise endolysines etc for specific species with AI analysing the genome of all species of bacterial and even fungal pathogens and then extrapolating receptors and schematics of endolysines that are stored in Physis to be downloaded into microbes via WiFi.This will be done via having tweaked bacteriophage DNA present in anti-bacterial strains.Since based on leukocytes these will be immune to the endolysines and will analyse their structure to then synthesise them themselves when signalled to the area that a pathogen is and then use them against the pathogen with them not affecting beneficial bacteria.The fact that the genome of each strain would be read and signals sent to other strains would bypass issues of specificity as the microbes using tweaked bacteriophage DNA could allow endolysines to be made for any species and strain of pathogen including new ones especially those that none exists as the microbes would adapt to each new pathogen on the spot via Paean and base microbes reading the DNA of them,extrapolating species specific endolysines that affect all strains and signalling others to produce the new endolysines via signals,horizontal gene transfer,bumpers containing schematics etc with them able to navigate and break down biofilms of pathogens either directly or creating compounds that do this.This scanning of the DNA will also deal any potential ability of the pathogens to mutate and gain resistance to the endolysines with as state the catch 22 of them having to lose resistance to antibiotics to gain one for endolysines will keep this in check.If possible since endolysines are created in the cells of pathogens by bacteriophages then it may be possible to create universal endolysines that attack all pathogens or bacteria but covered in bumpers that interact only with pathogens.The genome of all bacteria will be scanned for its DNA to allow Phanes extrapolate DNA to create receptors and endolysines for each species of pathogenic bacteria that will then be listed in the Physis file of each species allowing it to be downloaded on demand within minutes by inducing the evolutionary path of anti-bacterial strains to house the correct species specific receptors and endolysines when they are indentified.This will be in anti-bacterial strains using tweaked bacteriophage DNA.In anti-viral strains tweaked virophage/bacteriophage DNA present in anti-viral strains will be working on the same principle as this but with viruses without a helper viruses.Anti-helminthic strains will have the produce receptors and endolysines that killl each species of parasites.Base microbes could travel to where the beneficial bacteria are and then using bumpers that are intended to interact with only their cell wall and DNA will using CRISPR give them DNA and treatments to allow them to become immune to the protein bumpers and also endolysines into genome capsids.Thus bacteriophage DNA in anti-bacterial strains could allow endolysines to be used.If possible tweaking of the DNA of the microbes synthetic endolysines or those created by the microbes scanning the DNA of viruses can be created that can be inserted into viruses of all types such as HIV and Rhinovirus as well as fungi and even parasites once their genome is scanned.This could be done by anti-viral strains having recombinant DNA from virophages as well as bacteriophages hybridised together thus allowing them to infect and destroy viruses from the inside out using endolysine like material without a helper virus with these made to be able to adapt to all types of viruses in the same way as the aforementioned bateriophage DNA in anti-bacterial strains would work by first scanning the pathogens DNA and then producing relevant endolysine equivalents to kill the virus by breaking down the RNA/DNA or outer capsid from the inside out or at least allow the other microbes anti-viral compounds and immunised primary immune system to wipe them out when they are deactivated and unable to replicate similar to protease inhibitors.This could allow them to wipe out HIV,Rhinovirus and new viruses.Tweaked DNA from virophages Mavirus,Sputnik virophage,Zamilon virophage hybridised with each other and bacteriophage DNA to not need a helper virus can be investigated as early as 2023/2024 to be added to the anti-viral strains to allow them to adapt to any virus that exists rather than their native helper virus to lysise them and thus kill them from the inside.Anti-viral strains would use endolysine like material to kill viruses working in the same principle as anti-bacterial strains using aforementioned virophage DNA merged with bacteriophage DNA to not need a helper virus.They would scan the genome of viruses and develop schematics of endolysines that can be sent back to anti-viral strains.Thus antiviral strains will house virophage and bacteriophage DNA hybridised together and will work on the same principle of antibacterial strains.Ideally AI will analyse the genome of all known pathogens whether viral,bacterial or fungal as well as parasites and extrapolate species and strain specific endolysines,receptors that intercept specific species phospholipids,protein coats and insert DNA etc stored in their file in Physis that can be downloaded when needed to be created instantly and also via biosynth wifi that causes the DNA to change to have them.Thus in time upgrades may allow endolysines or similar compounds to be created to attack parasites and fungi of all types in the same way individual to each one similar to bacteria by the base microbes scanning the DNA of pathogens with this making phage therapy defunct.If possible these would be used to fight all pathogens including new ones but especially superbugs.AI can analyse the surface proteins and genome of all known pathogens to extrapolate endolysisnes that can be downloaded once the species and strain of the pathogen is determined upon infections.Thus the genome of all known pathogens especially bacteria such as benign ones,food poisoning related ones and superbugs will have their genome scanned and analysed to extrapolate species and strain specific receptors and endolysines stored in their Physis file that can be download into all microbes of anti-bacterial strains once infections are detected.This can be perfected for both anti-viral and anti-bacterial strains by 2029.All of these measures will allow anti-bacterial strains to cure patients of infections of all pathogenic bacteria especially drug resistant superbugs.
Prior to anti-microbial strains of microbes are perfected normal bacteriophage treatments may also be used.These bacteriophages would kill of superbugs by creating endolysines suited to each bacteria that cause them to die via causing them to explode from the inside out and thus utilising them as a replication vector to create exponentially more bacteriophages until the patient is cured or they can apply CRISPR treatments to cause them to undergo apoptosis or remove their ability to undergo mitosis,remove resistance to all existing antibiotics etc.Ideally these bacteriophages should have human DNA in them to have human protein coats on them to prevent immune responses allowing them to bypass the immune system and can be used to also apply endolysines as well to improve success.They could also inject suicide genes and those that prevent them undergoing mitosis as well as those that remove adaptations to lysines.AI could make known bacteriophages be made into different subtypes that attack all known species and strains of all pathogenic bacterial superbugs including others resistant to a few antibiotics and those that no known bacteriophage exists with this started as early as 2023/2024 with all known species of bacteriophage catalogued and then created around to hospitals around the world using 3D DNA printers with these then used as a baseline to create those for which none exist by reverse engineering them using DNA from the desired bacterial pathogen with the genome of existing bacteriophages and their bacterial prey analysed to make the necessary genetic tweaks to be effective against all other pathogens.Proto and final Phanes will analyse the genome of all known bacteriophages that kill bacteria including pathogens and the genome of their prey and then use this to make alterations to bacteriophages that can allow them attack each species and strain of bacteria including superbug pathogens that is stored in a cloud network later Physis that can then be created onsite of hospitals through 3D DNA printers.It will do this not only for bacteria but also fungi and possibly parasites.Bacteriophages designed by Phanes using 3D DNA printers that attack all superbugs can be created as early as 2023/2024.The bacteriophages will be stored in media solution that allows billions or even trillions to be grown in with the bacteriophages housing certain recombinant DNA from bacteria to grow in the same media thus allowing for them to be extracted using syringes to inject them into affected patients in large amounts with as stated storerooms in each hospital housing vats that have bacteriophages for each strain of each major superbug especially potentially fatal ones.Otherwise they could be given huge numbers benign versions of the bacteria they are meant to attack that have their pathogenicity removed as well as resistance to antibiotics removed via CRISPR that are closely related versions of the bacteria with their pathogenicity and without the ability to mutate edited out grown in vats to allow them to utilise these bacteria to replicate in large numbers and stored in these vats once all bacteria are killed allowing for trillions or even quadrillions of bacteriophages to be made onsite of hospitals worldwide making them readily available with 3D DNA printers also creating them on demand in large numbers or the base amount to be added to vats.The bacteria would be benign cousins created by AI similar to how Cowpox virus is related to V.major/V.minor created using DNA from the pathogen and also others to make them benign and unable to mutate via CRISPR to prevent them affecting the host if they are injected into the host by mistake or escape.The benign cousins will have their ability to mutate into pathogens edited out with them having the pathogenicity of the fatal pathogens and superbugs edited out meaning they would have the same surface proteins that the bacteriophages interact with but will be benign cousins that can’t cause illness or death and cannot mutate into pathogens etc by having mutation blocking genes added.AI will analyse Cowpox virus,V.major/V.minor and then compare the differences between them and then analysing each pathogen they will create benign cousins.They would be created via 3D DNA printer grown in vats in large amounts and then have 3D DNA printers print out bacteriophages.These benign bacteria will if they enter the body work in the same way as Cowpox virus forcing the native immune system to fight off the pathogen with its own antibodies stimulated from them with ideally can be filtered out from the bacteriophages which will be injected into the bloodstream in the billions.They would be benign versions of the pathogen that cant mutate or be pathogenic but would have the same receptors on their surface proteins and shared specific DNA but would be benign versions of the pathogens using genes added by AI and thus would allow for large amounts of bacteriophages to be created that can be injected into the patient.These benign cousins can be created by AI analysing pathogens DNA and then creating them by 3D DNA printers with the genes responsible for their pathogenicity removed or not printed into the bacteria’s genome onsite of all hospitals worldwide with the benign versions of pathogens created by AI and using 3D DNA printers onsite of hospitals printed out into sugar solutions to grow and then once they reach large peak numbers bacteriophages created by 3D DNA printers will be added with the bacteriophages killing off all bacteria to produce large numbers of bacteriophages that can be then extracted by phlebotomy robots and put into large vials thus allowing them hospitals to stockpile on bacteriophages for each pathogen and store them in large batches in fridges and replenish stocks over and over again with all work being automated from start to finish.If this benign version accidentally enters the patient or infects a researcher etc it will not cause life threatening conditions and could even be fought off by the patient that helps them gain antibodies that can help them fight off the infection that the patient is being treated for thus aiding in recovery and future immunity against future infections.Thus AI using 3D DNA printers will create benign versions of each pathogen such as superbugs that can act as a growth medium for these bacteriophages that can then be injected into infected patients with AI and 3D DNA printers creating the fist few hundred of these to be inserted into this growth medium.These benign versions would be similar to the pathogens but modified so that if they enter the patient by accident or infect researchers and staff then they will not kil the patient or cause allergic reactions and could be easily killed by the patient and even similar to the Cowpox virus once killed off by the immune system would stimulate antibodies against the pathogen the patients are fighting off thus speeding up recovery.If perfected the cousins may be designed so that they may actually be cultured in separate vats and also injected in large numbers with their ability to mutate edited out alongside the bacteriophages to allow the immune system fight them off and have them create antibodies that aid in their recovery alongside the bacteriophages by stimulating antibodies against the pathogens thus speeding up recovery and also at the same time vaccinating them against future infections with it theoretically used as a vaccine for superbugs such as MRSA prior to when immunisations are availible.The bacteriophages may also be modified to undergo mitosis using sugars,proteins and nutrients not found in the human body fed to them in vats thus meaning that once the infection is cleared they cannot undergoe mitosis.These as before will be filtered out from any remaining bacteria and then injected into the patient in large amounts and then will kill off the pathogens in the patient via adding suicide etc genes and also killing them via endolysines during replication.The vats can then be refilled by adding more of these benign bacteria to allow the bacteriophages to replicate.Once a vat is full bacteriophages can be extracted and put into other vats full of the bacteria to create more with this repeated until large amounts of bacteriophages are created with them extracted and put into vials and refridgerated.Once they are printed out as virions via 3D DNA printers with just a head containing DNA and receptors like bacteriophages but have engineering to ensure that after replication will form endolysines and also normal shaped bacteriophages to be stored in large vials once extracted with the bacteriophages having DNA from T.gammatolerans to allow radiation to be used to sterilise them of the benign cousin or pathogenic bacteria.The actual or benign pathogen and bacteria will be created by 3D DNA printers and grown in vats using sugar etc and injected with a large number of the 3D printed bacteriophages that then replicates exponentially until the vat is full of bacteriophages that can be extracted and injected into another vat and so on until an unlimited supply is created and then large amounts of the phages are extracted via syringes and stored in vials.All steps can be automated from start to finish.If the bacteriophages house T.gammatolerans DNA radiation can allow the actual pathogen to be used as a growth medium and then be killed with treatments of 500-2,000Gy used with the bacteriophages in storage continuing to kill off remaining pathogens or benign cousins as replication vectors in storage until all are dead with them having DNA from psychrophiles,mesophiles and thermophiles etc to grow in all temperature ranges and allow high temperatures to be applied to it to kill the bacteria.This psycrophile,mesophile and thermophile DNA can also allow them to stay stable in all temperature ranges inside and outside of refrigeration for longer and with the acellerated healing and telomere phenotype can be frozen and thawed over and over again forever.This and scratch DNA can allow it to maintain viability during any transportation.It can also negate the need for conventional preservatives such as thiomerasal etc in these and other vaccines.Other extremophile DNA and those as part of anti-ageing treatments can be present for the same reason.Dead pathogenic bacteria can then be filtered out using filters using nanomaterials combined with Biosynth technology with all work automated.These variant bacteriophages for all pathogens especially superbugs can be created onsite of hospitals worldwide using 3D DNA printers and vats to expediate development making them availible by 2024/2024 and cut costs in transportation and labour to zero.As a result all hospitals could manufacture and stockpile on each type of new bacteriophages making them self sufficient allowing them to stock in fridges so as to allow for instant injection in the veins of infected patients.Most patients could need only a single vial but those with more serious infections could need two or more vials.To speed up recovery patients will be injected with bacteriophages at multiple sites of the body such as in the arms,legs,chest area etc to allow the bacteriophages to be deployed at multiple sites across the body thus wiping out large amounts of the pathogen in multiple areas of the body at once leading to the pathogen being wiped out in multiple areas areas at once and thus allowing the entire body being cured at once exponentially faster rather than just being injected in one area which would take longer.Areas of the body where symptoms of infection occur and are visible such as swelling,fevers,inflammation build up of fluids and abscesses are visible will have the bacteriophages injected into them first as these are where the infections have built up in the body alongside as stated the chest are,arms and legs.Other areas for injection are the lymph nodes under the arms,by the groin and also in the veins etc by the gastrointestinal tract ie stomach,small and large intestine and also near the neck to reach the brain allowing key areas that superbugs infect and attack to be cleared first thus limiting or preventing damage to these key organs and parts of the body thus clearing the infections in areas that it may damage the most first thus preventing death and permenant damage to these key areas of the body with the bacteriophages using both the bloodstream it’s vessels such as key arteries,veins and capillaries and lymphatic system to travel to all parts of the body thus clearing infections quickly.By injecting the bacteriophages into areas that symptoms occur and also the areas that the pathogens attack will prevent damage to these areas by them and thus increase the chance that one will survive and not suffer any permenant damage to key organs.It will also clear the pathogen of the areas that are affecting or will affect instantly thus curing the patient much faster.By injecting them at multiple sites this allows for larger amounts of the pathogen to be cleared much quicker thus clearing the body of larger amounts of pathogens rather than injecting at one point.Thus AI namely proto Phanes will create bacteriophages for all species and strains of pathogens including superbugs by analysing the genome of all species of bacteriophages,their prey and the genome of all species and strains of pathogens,fungi and parasites and extrapolating tweaks to be made that can allow new types of bacteriophages to be manufactured via 3D DNA printers that infect and kill all species of bacteria,fungi and even parasites by using them as replication vectors.Thus by analysing the genome of existing bacteriophages and their specific prey bacteria it will allow AI to create strains and substrains of bacteriophages that can infect,replicate in and kill off all species and strains of human pathogens or each individual species and strain of them especially superbugs and those that cause food poisoning,miscarriages etc that can be created via 3D DNA printers.Even non superbugs can have bacteriophages developed to kill them off before they mutate into pathogens or gain a resistence to antibiotics with them developed for those that infect livestock and pets etc.Bacteriophages will be developed for those that cause stomach cramps,diarrhoea non life threatening conditions as an alternative to overprescribing antiobiotics to prevent them becoming resistant as well as those that cause more serious conditions such as abortions.Thus all species of bacterial infections will have bacteriophages created.All types of fungal infections both benign and serious have bacteriophages created to kill them by using them as a replication vector.Bacteriophages to kill off all fungal pathogens will also be extrapolated by Phanes including virophage/bacteriophage hybrids for all species of viruses.For all viral pathogens it will involve hybridisation of bacteriophages with virophages that can use each individual virus as a replication vector by producing endolysine like material without using a helper virus.This can include HIV,Rhinovirus, Ebolavirus,N.meningitidis,Ebolavirus,Orthomyxoviridae.Bacteriophages will be developed for not just fatal pathogenic viruses,fungi and bacteria but also those that cause minor conditions such as food poisoning,diarrhoea,itchy skin conditions and cold sores and even opportunistic infections in those with chronic conditions like HIV etc.Thus bacteriophages will be created by AI for all species of bacteria both benign and serious fatal ones especially superbugs.If possible bacteriophages can be created that infect and kill parasites such as Plasmodium,N.fowleri,B.mandrillaris,Cestoda,F.hepatica to increase survival rates by using them as a replication vector in the process curing a patient of these infections with again bacteriophages created for those that affect livestock and pets.This will include not just include human pathogens and parasites but also those that affect livestock,pets and even crops and ornamental plants.Research will also be done for bateriophages and bacteriophage/virophage hybrids to kill bacterial,fungal and viral pathogens and parasites that affect livestock and pets and animals kept in zoos and conservation areas etc under captivity and research as well as those across the universe.This will eliminate antiobiotics from the food chain when used in remaining livestock.If possible bacteriophages can be developed that kill off parasites and pathogens including spoilage micro-organisms and zoonoses for ornamental plants and crops.All newly discovered fungal and bacterial and even parasitic infections across the universe will have new bacteriophages extrapolated as soon as possible.Bacteriophages can be developed that can be used to cure cancer by being modified to actively seek out tumours using them as a replication vector using endolysines thus killing tumours in an exponential manner.In all colonies will have bacteriophages developed by AI.These will be used to be injected into patients found to be infected with deadly superbugs instantly with the same PCR machines used to detect HIV scanning the genome of them or HIV home test kits both modified to very quickly identify the type of pathogen and specific strain.These bacteriophages would house taq polymerase and Cas-9 to allow them to recreate applied CRISPR treatments and also DNA from the aforementioned animals to recreate anti-microbial compounds with their receptors making them unable to affect human cells and also beneficial bacteria but only desired pathogens.Depending on the species of pathogen the bacteriophage can be injected into the bloodstream,inhaled as a gas through inhalers or taken as pill with even the option of being applied by intravenous drip.All of this will be done to increase survival rates in patients infected with all types of superbugs prior to 2029 with each major superbug have bacteriophages prepared onsite in stores of hospitals for each specific strains of each superbug to allow them to be injected instantly to create endolysines as well as inject these aforementioned CRISPR treatments and old antibiotics and new ones.Bacteriophages will be created to kill bacterial,fungal infections and parasites of livestock,pets and animals in zoos and conservation areas through the same process.Those on other planets can also be created with them created for pathogens of all pets and livestock.As a result of them being created by 3D DNA printers and vats onsite hospitals can manufacture their own stockpile of bacteriophages of all species and strains of bacterial pathogens especially superbugs created onsite of hospitals themselves that are refridgerated onsite of hospitals making them self sufficient in their manufacture thus allowing them to be deployed to infected patients instantly increasing survival rates to 100% as once injected into patients will use all bacteria as replication vectors that will create exponentially more phages and killing them in the process.Once a patient in a hospital has their bacterial etc infections species and strain identified staff can simply collect the correct bacteriophage within minutes from their fridges and then inject them into the patients and when running low stockpile on more phages.Vetenairy clinics will produce onsite those for all species and breeds of pets and livestock allowing one to get one for pets when they visit them with those for livestock then delivered to them once the pathogen has been determined.These bacteriophages can have human proteins present while those for animals have animal proteins to prevent them illicitating an immune response that could be fatal or render them ineffective with psychrophile DNA and that from radiorestant bacteria such as T.gammatolerans and possibly A.mexicanum to allow them to be frozen,thawed and refrozen etc over and over again in storage in large amounts to be thawed to be applied to patients when needed for those injected or inhaled with those in pill for made by automated machinery and stored in fridges.Having extremophile DNA such as those from alkanophile and acidophile DNA,thermo/meso/cryopiles to survive not just storage forever but also the homeostasis of the human body.Since each bacteriophage produces thousands if not millions of replicas each time it infects and kills a bacteria a single injection,inhalation and pill dose of bacteriophage can clear the body of an infection within days and be flushed out of the body.They can be programmed to insert DNA into bacteria that disables any CRISPR Cas-9 and Cpf1 systems present thus turning pathogens own protection systems against them and preventing them gaining a resistence.If pathogens mutate as stated they will have to lose resistence to some antibiotics and AI can then easily produce new versions to fight them.AI should be able to organise this as early as 2023/2024 and 3D DNA printers should be able to create them easily cutting down on labour costs with them available by at least 2023/2024.These via vats and 3D DNA printers can be created onsite of all hospitals and universities worldwide making it easier for them to grow and stockpile on bactriophages for all species and strains of all superbugs with them stored in large specialised fridges with them in vials etc allowed for priorities to be made for each pathogen in all hospitals in each country and region as all hospitals will create onsite and stockpile on bacteriophages for all species and strains of pathogenic bacteria including superbugs thus allowing each hospital instant access to them when newly infected patients arrive in hospitals with if they are low and this allowing stocks to be constantly restocked and grown once each patient is treated.Strains of phages will be created for all pathogens including non superbugs with these created for all pathogens of all species of remaining livestock and pets allowing them to be used instead of antibiotics eliminating them from the food chain and preventing the rise of new superbugs as farmers can order in large batches of bacteriophages for each livestock and homeowners ordering in those for pets with those for pets and livestock created onsite of vetenarian clinics.Variants can be created for fungal infections,viruses and parasites of pets and livestock.They will be created to kill off pathogens and parasites of all species of pets and thus eliminate antiobiotics being used in them,entering the food chain and in turn creating new superbugs thus halting the spread of them and also eliminate superbus in livestock as a more effective means than antiobiotics.Each strain of phages will given different ID codes or named both a bacteriophage name and sub species name for each pathogen with AI holding patents making them free.Existing bacteriophages that attack specific pathogens can be used as a baseline with the AI analysing the genome of each bacteriophage species and their prey bacteria extrapolating the genotypes necessary to create the new strains to attack every other other pathogenic bacteria especially superbugs with 3D DNA printers carrying out their manufacture onsite of hospitals.Thus bacteriophages could be made from scratch by AI to attack and kill any or all superbugs and each strain with them even designed to insert DNA using CRISPR itself and advanced gene drive technology at first into the bacteria that disable the CRISPR Cas-9/Cpf1 system at the begging of replication to prevent bacterial infections gaining a resistance and remove their ability to fight back with them using CRISPR itself to allow them to prevent the bacteria fighting back to wipe out every single bacteria.Since bacteriophages replicate exponentially they would stay in the body until flushed out via urine etc days later leaving all bacteria dead meaning they wont have time to mutate and gain resistance thus when bacteriophages are injected into a patient they will replicate exponentionally until a patient is cured and all bacteria are killed.If the bacteria do mutate do then more modified versions of bacteriophages from scratch or from the bacteriophages present can be created and deployed alongside those that apply CRISPR treatments such as suicide genes etc and Polybia-MP1 with the first wave of bacteriophages applying these if they cant replicate due to the bacteria mutating and also the aforementioned CRISPR Cas-9 disabling system.Since bacteria have to lose resistance to antibiotics to gain a resistance to bacteriophages due to their lower amounts of genes and base pairs present in them in comparison to multicellular life forms this Mortons fork and Catch 22 would allow for them to be effective well beyond 2029 and it may take decades even centuries for this to happen meaning if they gain resistence to bacteriophages they will be susceptible to existing antibiotics again thus allowing colistin,penicillin,β-lactam antibiotics etc to become effective once again with AI extrapolating new strains of bacteriophages if they do.As stated to gain a resistence to bacteriophages bacteria especially superbugs have to lose resistance to each individual antibiotics thus meaning once they lose resistance to antibiotics these antiobiotics can be utilised with any species that do gain a resistance could have bacteriophages add CRISPR treatments that remove resistance to all antiobiotics and even remove their pathogenicity beforehand while they are using them to undergoe replication so that these CRISPR treatments that remove resistance to all antibiotics and and their pathogenicity will be carried out in all future generations of pathogens that do gain a resistence to bacteriophages.In otherwards having the bacteriophages before replication apply CRISPR treatments that remove resistence to all antiobiotics and lose pathogenicity will ensure that any bacteria that gain a resistance to the bacteriophages will have their pathogenicity and resistence to antiobiotics removed from all future generations.Furthermore before using them as a replication vector to prevent resistance bacteriophages can apply CRISPR treatments that disable the pathogens Cas-9/Cpf1 defense system thus preventing the bacteria gaining a resistence and thus allowing bacteriophages to use the pathogens own defence mechanism against themselves.Bacteriophages will reduce the chance of letting pathogens adapt as they will clear the body of all bacteria until nothing is left and then be flushed out and will possibly take several decades or centuries for them to adapt to them until biocompatible microbes arrive with AI able to design new strains of bacteriophages to combat those that gain resistence within 24-168 hours or ideally it will develop hundreds.thousands or millions of different sub strains of bacteriophages for each species of pathogen and each potential mutation that can occur in the future stored in Physis allowing them to be manufactured and deployed instantly and manufactured in hospitals worldwide using 3D DNA printers.The more new strains of bacteriophages developed for each pathogen and the more pathogens gain resistence to each new strain of bacteriophages the more antibiotics they will lose resistence to this making them less benign as time goes by thus increasing survival rates as eventually as they become resistant to each and all possible strain of bacteriophages they will become more susceptible to all existing antiobiotics.As stated this is because prokaryotic bacteria can only house a finite amounts of significantly less genes and base pairs in comparison to eukaryotic cells seen in humans and other multicellular organisms.In multicellular organisms each species has a wide range of levels of base pairs such as humans holding 3,000,000,000 base pairs while for example P.japonica having 150,000,000,000 thus showing that their can be a wide difference in the amount of base pairs in each type of multicellular species with unicellular organisms housing significantly less base pairs with the range of variability being much lower and the theoretical amount that can naturally occur being lower.Prokaryotic bacteria contain at most a few thousand or even few hundred base pairs in comparison to more complex life forms such as humans etc that have at least several billion base pairs thus meaning there is only a finite amount of mutations they can develop meaning eventually they will either run out of space to house resistance to bacteriophages or they will have to remove old genes especially those that give them resistance to antiobiotics.As a result due to the finite amount of genes that can exist at any given time when they gain resistance to bacteriophages they need to create new genes and to do that unnecessary genes must to deleted including those that they developed to be resistant to antibiotics thus meaning as they gain resistance to bacteriophages they lose resistance to antiobiotics with the more bacteriophages strains they gain resistence to the more antibiotics they lose resistence to compensate for this even if bacteriophages do become worthless they will be still become susceptible to antibiotics they have become resistant to meaning over time as they gain resistence to bacteriophages they will become susceptible to penicillin as well as colistin etc.Bacteriophages can also be designed to deliver CRISPR treatments to cause pathogenic bacteria undergoe apoptosis,lose pathogenicity and lose resistance to all antibiotics beforehand.By removing resistence to all antibiotics beforehand it will ensure that any pathogens that gain a resistence to bacteriophages will have their resistence to penicillin and all existing antiobiotics removed permanently.meaning these can be applied instantly.This would allow those infected with fatal superbugs from 2023-2029 to survive long enough for anti-microbial and anti-ageing strains available by 2029 and should be available as soon as 2023/2024.AI namely proto and final Phanes will analyse the genome of all existing bacteriophages utilised in hospitals and that of their prey species and then using this develop the genome of new bacteriophages to destroy each and every species of bacterial pathogens with this including both fatal superbugs but also those that cause minor non fatal infections including those that cause food poisoning and even chronic conditions and especially those that can be opportunistic infections for those suffering from HIV etc with them stored in proto and final Physis to be manufactured onsite of hospitals worldwide using 3D DNA printers allowing hospitals to stockpile in them over and over again to make them self sufficient from factories.It is for these reasons that intensive research will be made into new bacteriophages for each fatal superbugs and also non fatal bacteria to deal with them used on non resistant and non fatal bacteria,fungi and viruses to prevent them gaining a resistence to antibiotics.These will be developed to cater to the needs of treating and curing patients infected with superbugs especially fatal ones until anti-bacterial strains are developed and may even compliment them from 2029 onwards for any unforeseen drawbacks Genetic engineering will create new phages that are able to attack specific superbugs and also if possible whole orders of them.Their DNA will be used as a baseline for anti-bacterial strains by 2029 to apply specific endolysines.Injections of peptides form Russian Brown frogs,phytoplankton and Polybia-MP1 and even TsAP-1,TsAP-2 covered in bumpers to prevent toxicity or them breaking down either through injection and also tablet form that has the compounds in these bumpers will also be used alongside these.At the same time AI will by 2023 conduct research into new antiobiotics specifically synthetic antiobiotics with proto and final Paean and Phanes analysing the genome and outer structures of each pathogen especially superbugs and extrapolating synthetic antibiotics to kill them that can be synthesised by anabolic and catabolic reactions in vats onsite of hospitals by both bacteria and esterfication and industrial processes.To slow the spread of superbugs bacteriophages can be utilised in remaining livestock such as Bovidae,Suidae,Phasinidaealongside fish and shellfish instead of being given antiobiotics with these remaining livestock will be given bacteriophages suited to all of the pathogens and parasites alongside other measures such as livestock,fish and shellfish also made immune to radiation and thus exposed to large doses of radiation between 100-20,000Gy to sterilise them of pathogens.Pets of all types will have bacteriophages suited for all pathogens and parasites developed.They may also given species specific microbes including immunisung,anti-viral,anti-bacterial,anti-helminthic strains etc that render antibiotics obsolete in agriculture.Crops and ornamental plants could also have bacteriophages developed that can be injected into leaves and stems with them also once made resistant to radiation exposed to large doses of radiation.By 2029-2045 traditional livestock production will be replaced by in vitro meat and that produced by fish reared in aquaponic systems,bioprinted leather and also yeast/bacteria based milk thus eliminating the source of most superbugs from the food chain.Parasites of livestock will also be dealt with by bacteriophages.Waterways such as rivers,oceans,lakes,groundwater supplies infected with pathogens will have large amounts of bacteriophages cultured and then innoculated with these bacteriophages that can clear them of pathogens with these bacteriophages engineered to have flagellum your allow them to stay in all types of waterways such as oceans,rivers,lakes and groundwater forever.Crops being reared in sterile environments of aquaponics systems in home,community and vertical farms will eliminate contamination with crops also given fully functioning immune systems via CRISPR to allow them to be immunised against pathogens and given anti-bacterial strains and bacteriophages.Wild animals that carry zoonotic superbugs will be inniculated by Biosynth Arthropoda with microbes and bacteriophages that pass through each generation to the next and also releasing lab reared animals that interbreed with wild animals and pas them into them via sexual reproduction and intercourse similar to STDs.Biosynth WiFi will track their progression throughout entire populations until at 50-90% if not all wild animals of each species are inoculated.Bacteriophages in wild animals and even livestock can be engineered to stay in the body constantly and not be flushed out of the body and even pass from one generation to the next via entering fetuses and through sexual reproduction similar to microbes.Radiation treatments can sterilise cuts of meat and crops etc.Sewage treatment and water treatment plants will use gamma radiation,super blasts of super high intensity UV lights will be used to treat water and sewage to kill off pathogens when algae is fitted with DNA from extremophiles that are resistent to radiation and high temperatures in genome capsids with bacteriophages also used here as well.Livestock and crops firted with DNA to make them immune to radiation can have them exposed to large blasts of radiation that can kill all pathogens and parasites present.By having all sewage treatment plants growing algae will prevent raw sewage entering waterways such as oceans,lakes,rivers,groundwater supplies thus eliminating infections from swimming in and being infected from contaminated water via injesting it and also through cuts etc.Bacteriophages can be released into soils,oceans,rivers,lakes,groundwater supplies to sterilise of all pathogens whether bacterial,viral or fungal thus eliminating them from not just polluted ecosystems but from the Earth itself completely as well.Better infrastructure will eliminate pathogens contaminating waterways.This should eliminate the source of most of not all infections of superbugs in humans.Thus research can be done into creating and manufacturing on a commercial scale bacteriophages to kill all bacterial and fungal pathogens and parasites of humans,pets and livestock to increase survival rates prior to antibacterial strains are perfected and even after to compliment them.
Anti-fungal strains:
Fungi will be dealt with their own strain that utilise CRISPR treatments similar to those used in anti-bacterial strains.These will be created at home or in hospitals.Anti-fungal compounds could also be produced by these such as neem oil,ethanol,rosemary oil,jojoba oil using recombinant DNA from the relevant yeasts and plants and those from the bacterium Bacillus subtilis,and compounds from the beneficial fungus Ulocladium oudemansii.These would also use CRISPR treatments to make them susceptible to these,remove resistance and also undergo apoptosis etc with synthetic compounds also utilised.These strains would be printed out at home when needed.If possible fungi can be made susceptible via CRISPR to anti-viral or anti-microbial compounds by anti-microbial strains to alleviate strains on creating an extra strain or ideally the patient will be immunised against all species of them.Immunisations will be created by Phanes for all fungi.Horizontal gene transfer will be used and them engineered to interact with only fungi and not that of the patients cells.The anti-fungal strains will be engineered to only interact with only fungi ideally those of pathogenic fungi via surface proteins on them that only interact with only fungi to prevent them applying these to the patients cells that would kill them with them via induced evolution.All patients will be immunised against all species and strains of fungi using the common proteins method with them once made immune to radiation will be exposed to radiation levels between 2,000-20,000Gy to kill off large amounts of them including spores.All species and strains of fungi will have their DNA analysed by AI to extrapolate endolysines to kill them to be downloaded into strains from Physis.All patients will be immunised to all species and strains of all fungi including those that cause food poisoning,atheletes foot,C.albicans,benign species and fatal ones such as Aspergillus.Immunisations will be created for all species of fungi that affect humans both pathogens and non pathogens.All species of fungi will have them tested in labs against venom from all stings,secretions and bites etc from all species of plants and animals to see which ones destroy them.The genotypes that express these compounds will be added to Physis file of the viruses they kill and a hyperlink to the source animal it comes from.Paean will analyse the outer surface protein wall of all species and strains of viral pathogens that can extrapolate synthetic anti-fungal compounds suited for each individual species and strain that can be stored in their Physis file to be downloaded into the anti-fungal strains DNA digital storage to be synthesised by anabolic and catabolic reactions with Phanes extrapolating genotypes you create these synthetic compounds to be downloaded via induced evolution.All species of pathogenic and non pathogenic fungi will be tested in automated labs against sap,secretions from plants and animals worldwide with to gain the genes responsible that can be downloaded by anti fungal strains.AI wil also extrapolate synthetic antibodies,synthetic enzymes and synthetic compounds that kill fungi to be stored in Physis and downloaded and then synthesised in the bloodstream.The structure of these synthetic compounds,enzymes and antibodies will be stored in their Physis file to be downloaded into the DNA digital storage of the anti-fungal strains and then synthesised by anabolic and catabolic reactions.This will be done by AI namely Phanes and Paean analysing their outer surface proteins and genome of all species and strains of fungi particularly pathogenic species to allow these synthetic compounds and antibodies to be extrapolated that will be stored in the Physis file of each species that will be downloaded by anti-bacterial strains and created by anabolic and catabolic reactions.These enzymes,antibodies and synthetic compounds applied during phagocytosis if they cause side effects including cytoxicity or released into the bloodstream if benign.Synthetic and natural anti-fungal compounds will be applied by being flooded into the blood stream or applied during phagocytosis by microbes to prevent cytoxicity through them having macrophage DNA.Dead fungi can be consumed by the microbes using enzymes suited to each one developed by Paean and Phanes once downloaded during phagocytosis.Phanes can also extrapolate the genotypes created from scratch to express these synthetic compounds and antibodies stored in their Physis files that can be downloaded into the genome of anti-fungal strains.The accelerated healing phenotype will instantly heal any damage caused by the pathogenic fungi directly and indirectly by cytokines storms etc meaning a patient could survive indefinitely to avail of upgrades and application of genes that prevent the virus replicating and to avail of immunisations.Patients once made immune to radiation will be exposed to blasts of radiation between 1,000-2,000Gy to kill of large amounts of them.All patients will be immunised against all fungal pathogens using the common proteins method.They could use bacteriophage DNA create endolysines that works on the same principle as anti-bacterial strains.Patients can be immunised against all strains of fungi using the common proteins method.Bacteriophages will be created to use fungi as replication vectors thus killing them off exponentially.These or specific strains could be made to combat Variant Creutzfeldd–Jakob disease caused by prions with them including general ones intercepting them and neutrailising in any manner possible using relevant receptors or even consuming them and breaking them down,turning them into nutrition such as sugars or essential amino acids for the cell and the host or even turning them into properly folded proteins with any neural damage repaired by the stem cell strain forming neural tissue and accelerated healing phenotypes.If possible CRISPR can make the host immune to the effects of prions that would be naturally broken down or flushed out of the body.The accelerated healing phenotype will allow neural tissue to instantly repair itself from prion damage.Existing damage to the brain can be repaired by stem cell strains creating new neural tissues in place of them.Once MRI machines become ubiquitous in smartphones and attachments then patients worldwide can check for damage caused by prions.Synthetic compounds to treat fungal infections and prions will have their structure added to Physis and this downloaded onto anti fungal strains DNA digital storage to be then created by anabolic and catabolic reactions onsite of the receptors of the fungi to prevent overdosing and side effects.
Anti-helminthic strains:
To compliment anti-helminthic strains other methods can be carried out to deal with parasites of all types.Malaria and other pathogens and zoonotic diseases spread by insects and mammals will be dealt with by measures detailed later on including engineering the vectors such as the specific species of Anopheles species from being unable to harbour Plasmodium.3D DNA printers can create millions or billions of these modified Anopheles to be released and pass on the inability to harbour Plasmodium via advanced gene drive technology.Ideally before these trials can be carried out to wipe out Plasmodium indefinitely measures can be carried out to decrease the populations of Anopheles in Africa that carry Plasmodium.Since Dichlorodiphenyltrichloroethane aka DDT is becoming increasingly ineffective against Anopheles in India,Sri Lanka,Sri Lanka,Pakistan,Turkey,Central America and Africa due to them gaining resistence to it since 1956 using it would be pointless.Using advanced gene drive technology via via releasing large amounts of engineered pests to interbreed with them it can remove Anopheles resistance to Bt and DDT etc permanently with this done by releasing large amounts of engineered bugs that using gene drive technology remove existing resistance and prevent future resistance occurring.This can also make them permanently susceptible to natural compounds from plants via scratch DNA that can be created by bacteria on a commercial scale and used as pesticides that are non toxic to humans,pets,livestock and other local flora and fauna allowing it sprayed in large amounts and have zero environmental impact with advanced gene drive technology making it impossible for resistance to these to ever arise via random mutations.Other methods such as introducing lethal genes into populations that causes females to produce offspring that have birth defects,sterile male technique that limits the amount of effective matings and births since female Anopheles can only mate once in their life,using the daughterless offspring technique wherein populations are reduced by releasing large amounts of males that contain gene drives that force any females they mate with to produce only males that dont feed on human blood thus reducing populations and infections sharply and quickly and adding biological controls all at once can reduce populations to very low levels.3D DNA printers can be used in creating billions of genetically distinct males with the desired genes with if possible males used to carry out sterile male technique,daughterless offspring techniques and lethal gene techniques have anti-ageing techniques that allow them to live several years longer or have the same anti-ageing treatments as humans thus increasing the amount of females they interact with to further reduce numbers with this not lasting forever or biocompatible microbes present in them that can using biosynth wifi allow their populations and locations to be tracked and thus actually shut these anti-ageing treatments off and those associated with lethal gene dominance,sterile male and daughterless offspring technique after a set period of time.These males would not be able to interbreed with those modified not to harbour the parasite.Female Anopheles can only mate once in their lifetime so by mating with genetically engineered sterile males will mean they will lose their only chance to mate causing a 90% drop in the population over the course of a year to few years with CRISPR and advanced gene drive technology will create healthy viable males that are unable to impregnate females.Otherwise males can harbour genes using advanced gene drive technology that ensure all young created by females they interbreed with are male.Since males do not feed on blood and thus on humans and by extension dont spread Plasmodium the population of males will spike and the populations of females that do feed on human blood and spread the parasite will drop meaning infections will drop as well.Another option is having males harbour defective genes that pass onto all impregnated females that will cause all young created by females be either sterile themselves or have deformities that are fatal thus killing them off before reaching adulthood to feed on humans and thus spread malaria etc depending on the genes added to the males thus wiping out entire populations in a short period of time with advanced gene drive technology increasing success rates to 100%.All options will reduce populations of Anopheles or just females by 90-95% within a few years as again females can only mate once in their life so if their only chance results in no offspring,sterile males or young with deformities with unlike the current overuse of DDT there is no chance of them able to gain a resistance at all.Once this is done and populations drop drastically biosynth wifi can be used to turn off anti-ageing treatments allowing the males to die off and also remove genes associated with lethal gene dominance,sterility sterile male technique etc to ensure they dont pass this onto the modified Anopheles that dont house the parasite.Then a sub species or just genetically engineered version of Anopheles that creates antibodies to Plasmodium that this makes it unable to harbour and in turn spread malaria will be released into the wild to overtake or replace the original Anopheles.Advanced gene drive technology will pass the ability to produce antibodies to all future generations especially when they interbreed with wild specimens.Pan and Pan will decide when to release the modified Anopheles and remove the aforementioned DNA from the first set with modified ones harbouring genes and gene drives to prevent the genes from the first set to be passed onto the new ones.If possible the new Anopheles can be released when the original breed of Anopheles has completely been eradicated from the ecosystem.3D DNA printers can then be used to create billions of both males and females of these genetically distinct modified Anopheles that cannot harbour Plasmodium via genes that create antibodies to the parasite making it easier and quicker for these modified Anopheles that are unable to harbour Plasmodium to take over the area and wild populations via advanced gene drive technology once they interbreed with wild insects and not affect the ecosystem as removing them from the ecosystem completely could cause co-extinctions of any of the Anopheles natural predators and would also make it harder for Plasmodium to adapt to the lack of viable hosts as well as newly immune carriers and thus be more easily wiped out since large populations of Anopheles housing it would already be wiped out and thus can allow for the new breed of Anopheles immune to sterile male technique etc to overtake wild populations via advanced gene drive technology.Resistence to DDT can also be dealt with this way and the Anopheles can made to become susceptible to natural compounds produced by plants that do not affect humans and other local flora and fauna which will kill them with gene drives designed by Phanes preventing them mutating a resistence to it with these compounds then created by bacteria to be used as a spray that can be used to spread on doors,netting etc that is non toxic to humans,birds and other local fauna.The new strain of Anopheles can also made to find human blood abhorrent and thus only feed on wild animals as well through this method.If possible having recombinant DNA from Culicidae species that do not consume human blood also added to the modified Anopheles to prevent them feeding on humans in the first place thus negating the need to deal with the painful bites with them engineered to not feed on livestock and pets as well and thus feed on only wild animals and act as pollinators of crops.To further prevent Plasmodium gaining the ability to gain a resistance to antibodies produced by these genes added to them they genes could be modified to attack all possible strains and sub-species of Plasmodium each Anopheles created by 3D DNA printers can be made to drink synthetic or donated human and animal blood that contain species specific microbes that once intaken will immunise them against all species of Plasmodium as well as apply anti-helminthic compounds as well as apply CRISPR treatments to cause the parasite to undergoe apoptosis etc with these microbes passing down from one generation to the next via eggs laid and using biosynth WiFi will track their population etc and allow Pan to apply any augmentations remotely to deal with them also engineered to be able to use proteins and sugars and from wildflowers etc as a sufficient alternative to proteins in human blood.The use of creating and inteoducing genetically modified insects to interbreed with wild populations and pass desired phenotypes with wild populations can be used to introduce any desired weakness to wild populations that becomes a predominant part of all insects.This can include as stated them uninterested in consuming human blood,permenantly lose resist to DDT,finding human blood etc abhorrent,being susceptible to natural compounds etc with advanced gene drive technology emsuring these modifications are permanent and that they pass onto all future generations.The main species of Anopheles such as Anopheles gambiae,Anopheles funestus,Anopheles culicifacies,Anopheles darlingi,Anopheles dirus,Anopheles albimanus,Anopheles stephensi that act as vectors for all species of Plasmodium such as Plasmodium knowlesi,Plasmodium falciparum,Plasmodium malariae,Plasmodium ovale,Plasmodium vivax will be made unable to harbour the parasites will be first dealt with these programmes first by Epione,Pan,Pan and also local governemnts and researchers across Africa and then after this even those that no longer do so and have a low susceptibility to do so in Asia and America such Anopheles barberi,Anopheles crucians,Anopheles freeborni,Anopheles latens,Anopheles punctipennis,Anopheles walkeri will be dealt with in the same way to ensure they dont see a resurgence of malaria with eventually all species of Anopheles dealt with this to ensure the species of Plasmodium that affect humans cannot jump species thus wiping them from the face of the Earth with their DNA stored in Physis for future experiments etc to be created via 3D DNA printers in labs.If possible Plasmodium can be modified to carry out vital functions in the local ecosystems such as dertivores and chemotrophs.These species of Anopheles will also be made unable to harbour other parasites and pathogens such as Wuchereria bancrofti,West Nile Virus etc.All Culicidae vectors of P.knowlesi,P.falciparum,P.malariae,P.ovale,P.vivax will be made unable to harbour them via these programmes.This use of genes extrapolated from scratch by Phanes that confer immunity can be applied to species of Culicidae like Ochlerotatus vigilax,Ochlerotatus triseriatus,Ochlerotatus stimulans,Ochlerotatus sticticus,Ochlerotatus provocans,Ochlerotatus nigromaculis,Ochlerotatus hexodontus,Ochlerotatus flavescens,Ochlerotatus,fitchii,Ochlerotatus excrucians,Ochlerotatus dorsalis,Ochlerotatus canadensis,Ochlerotatus camptorhynchus,Ochlerotatus campetris,Ochlerotatus abserratus to prevent them from carrying the Jamestown Canyon virus,California encephalitis virus,Western equine encephalomyelitis virus,Ross River virus,La Crosse virus,West Nile virus,Sindbis virus,Saint Louis encephalitis virus,Dirofilaria immitis.It can also prevent
Aedes aegypti,Aedes communis,Aedes albopictus from being unable to harbour Dengue virus,Chikungunya virus,Zika virus,Mayaro virus,Yellow fever virus,W.bancrofti,California encephalitis virus,Jamestown Canyon virus,Sindbis virus ,preventing species from the genus Culex,Culiseta from harbouring Saint Louis encephalitis virus,Japanese encephalitis virus,Filarioidea,Dirofilaria immitis W.bancrofti etc with the same applying to all arthropods,birds and mammals that spread zoonotic pathogens and parasites potentially eliminating them from the face of the Earth within a decade by at least 2035 without pesticide use and creating an imbalance in the ecosystem.Put simply all species of Culicidae that spread viruses,parasites etc that affect humans can undergoe these programmes to make them unable to harbour them via scratch DNA created by Phanes that makes produce antibodies that destroy them with them undergoing the same method as detailed above wherein populations are educed via sterile male techniques or those suited for each species.Thus programmes worldwide be carried out that replace all Culicidae vectors of parasites and human pathogens as well as those that affect pets and livestock with genetically engineered versions that are unable to harbour.This should wipe out malaria and all diseases spread by Culicidae by 2029-2045 if a global effort by Pan,Pan,Epione and governments worldwide is carried out.All species of Culicidae will be rather than wiped out will remain but without the ability to harbour parasites and pathogens to prevent causing them to go extinct as causing any species to go extinct could could cause unforeseen consequences and imbalances in the ecosystem such as co-extinctions of other animal predators that rely on them as a food source.The genome of these parasites and pathogens can be added to Physis to preserve them for scientific research as well as engineering them to be parasites and pathogens for invasive species of animals and plants and unable to infect humans etc and also weeds and crop pests.
Biocompatible microbes can also be used to fight malaria should Plasmodium genus gain resistance to artemisinin(or even prevent such resistance from happening) and other drugs with them able to treat viral infections such as HIV and possible even HPV(especially those associated with cancers)with even them able to treat fungal infections ie synthesising Amphotericin B as well as using CRISPR treatment.Ideally biocompatible microbes that attack viruses and bacteria should be easily capable of attacking fungi,parasites,protazoa such as Plasmodium using relevant compounds such as artemisinin and also CRISPR treatments utilising horizontal gene transfer once they enter them that cause them to lose their ability to cause harm,genetic faults that kill them off,have cells of key organs and neural systems etc undergo apoptosis,make them sterile,unable to replicate and cause faults that cause offspring to die off,make them susceptible to compounds at their disposal in anti-helminthic and even anti-viral and anti-bacterial strains,lose resistance to existing natural compounds they are immune to and use them against them or even infect them and kill them in the same way that pathogens kill humans through wiping out organs,immune systems cause tumours to form apply suicide genes to there tissues with the same applying to pathogenic ameobas and parasites ie N.fowleri,B.mandrillaris,Cestoda,Ancylostoma duodenale,Dracunculus medinensis,Plasmodium and possibly Vandellia cirrhosa.Anti-bacterial strains could do this with if possible the host can be immunised against them like pathogens via immunising strains using proteins to allow the primary immune system detect these parasites and then apply antibodies.Once made patients are made resistant to radiation via T.gammatolerans the entire body of the patient can be exposed to levels of radiation between 1,000-2,000Gy to kill of parasites in all parts of the body at once including their eggs in hard to reach places and prevent them moving to other areas of the body.Radiorestance can also be dealt with CRISPR treatments that remove this ability or even prevent them being able to develop this in the first place.Ideally the patient will be blasted with this levels instantly and for at least 30 minutes to an hour or more to prevent them gaining radioresistence via mutations with with patient put under anaesthesia.Doing it for more that an hour and starting at these levels as well as applying it to all parts of the body at once will ensure all or most of the parasites will be wiped out without developing radioresitance and will be done alongside the primary immune system and microbes both made immune to radiation to aid in fight in eliminating the parasites.It will also eliminate all eggs etc of them.These could start at least 200-500Gy several times,then 1,000Gy several times,then 2,000Gy and so on to prevent radiorestance and wipe out even larger numbers of the virus from the body with CRISPR treatments used by anti-viral strains can remove any resistance the pathogen gains to radiation.The level at which the different parasites can survive can first be determined in lab settings and also in animal trials so as to allow it to be determined and then have patients exposed to levels much higher at least 1,000-2,000Gy higher.The dead bodies can be flushed out or consumed by the microbes via phagocytosis or even similar to decomposing bacteria with recombinant DNA coming from decomposing bacteria and also even flies and other arthropods that break down rotten flesh with the primary immune system also signalled to attack them as well as and detect future infection.Otherwise they could create compounds abhorrent to specific parasites that through gene therapy are made susceptible to them causing them to purposefully leave the body by entering the gastrointestinal tract and being flushed out with feces with any eggs having CRISPR treatments to kill them off or at least make them sterile.CRISPR treatments that cause the parasites to become sterile or undergo apoptosis will be applied as a first line of defence.All parasites will have their DNA scanned to extrapolate endolysines to be stored in their Physis file and downloaded when needed.AI will also extrapolate from their outer structures synthetic compounds it can synthesis via anabolic and catabolic reactions stored in Physis.The strain will produce both natural and synthetic compounds for all parasites using relevant recombinant DNA and anabolic and catabolic reactions with those that have a low effectiveness rate will be aided by applying CRISPR treatments that alter the parasites internal and external structure to then improve the naturals or synthetic compounds effectiveness at killing them without damaging the host or making them susceptible to the natural compounds at their disposal via altering their internal and external structure to exhibit the same structure as parasites that are killed by them with antibodies also synthesised.Any damage to the body including vital organs such as the liver and brain and caused by them especially Plasmodium and N.fowleri would be repaired by microbes as well as accelerated healing phenotype instantly allowing time for these strains to be applied and still be effective. Patients once made immune to radiation and exposed to high doses of it between 500-2,00Gy to kill off the parasite.Conventional methods of preventing Culicidae bites ie free bed netting will be pursued with bug zappers that track specifically Anopheles should be pursued with these subsidised.Natural repellants from plants and scracth will be engineered into other plants that can be planted in bedrooms,gardens and also by rivers and lakes etc and even created by bacteria on a commercial scale to be sprayed into rooms that will repel them from entering using spray bottles and Ambi-pur devices that release them over a sustained period or applied like deodarant and even added to patients genome that releases them in sweat.This should counter current trends of Anopheles resistance to Dichlorodiphenyltrichloroethane aka DDT since 1956.Odocoileus virginianus,Peromyscus leucopus,Ixodes scapularis,Ixodes pacificus can as detailed later on can have their ability to harbour Borrelia,Babesia,Anaplasma phagocytophilum,Powassan virus removed on the same principle alongside having O.virginianus,Peromyscus leucopus both wild and captive bred populations inoculated with microbes from interbreeding,biosynths and injecting wild animals through syringes that can immunise them,that have the immunity added from genes created from scratch by Phanes that passes from one generation to the next via advanced gene drive technology and microbes passing onto one generation to the next via eggs,fetus spermatazo and so on.All arthropod,mammalian and avian vectors of parasites and zoonoses around the world and universe that can affect humans,alien races,livestock and pets can follow this pattern with mammals and avian vector inoculated with microbes that immunise them and apply CRISPR treatments that pass from one generation to the next though semen,fetus and advanced gene drive technology via biosynth arthropods,trapping wild animals and inoculating with microbes to apply CRISPR treatments and immunisations again passed from one generation with 3D DNA printers and artificial wombs used to create billions of these with native populations lowered via sterile male technique and so on to allow modified animals to overtake them and thus not affect the ecosystem.This can also apply to Glossina,Rodentia,Felidae,Cyprinidae,Bithyniidae that transmit Trypanosoma,Toxoplasma gondii,F.hepatica and all parasites of all pets and livestock worldwide with in the case of Felidae etc live animals injected with bacteriophages your cure them and microbes that fight off parasites by humans using syringes and swarms of biosynth Anopheles.To prevent unnecessary suffering parasites and pathogens of all mammals and birds that are spread by all species of Culicidae etc can undergo the same programmes.All species of parasites and pathogens whether viral or bacterial that are wiped out via this method will have the DNA preserved in Physis to be recreated in labs using 3D DNA printers.Subsidised free batches of the drug Artemisinin to affected areas with this synsthesised by bacteria using the relevant recombinant DNA from Artemisia annua with ideally the release of genetically modified Anopheles starting as early as 2025-2029 since there would be no real disadvantage to modifying the species being unable to harbour the parasite since other than infecting humans it serves no real purpose to the ecosystem with the DNA of P.falciparum added to Physis.The subsidised Artemisnin will keep people from getting sick while the populations of Anopheles loses its ability to harbour the parasite with the resistance to Artimisnin countered by applying CRISPR treatments to the parasite using proto microbes or even bacterial,bacteriophage and viral vectors containing the patients DNA to prevent them eliciting an immune response with the CRISPR treatments removing the parasites resistance not only to Artemisnin but also Chloroquine,Mefloquine,Atovaquone and also Sulfadoxine with genes added to prevent the parasite multiplying,infecting the organs they infect and even introduce suicide genes.Final versions of microbes will use CRISPR to remove resistance to these compounds and apply them.To push costs of Artimnisin, Chloroquine,Mefloquine,Atovaquone etc to zero bacteria can produce them onsite of hospitals and Telesphorus factories with synthetic drugs created by anabolic and catabolic reactions and Artimnisin created using recombinant DNA from A.annua.Plasmodium can be dealt by anti-helminthic strains of microbes by them using CRISPR treatments applied by horizontal gene transfer and bumpers that induce the parasite to undergo apoptosis,prevent it from being able to infect tissues and cells in the body and thus prevent it replicating.The microbes can also add CRISPR treatments by horizontal gene transfer and bumpers that remove its resistance to Artimnisin,Chloroquine,Mefloquine,Atovaquone etc and then produce these themselves with the microbes producing Artimnisin via housing recombinant DNA from A.annua with the synthetic drugs created by microbes using anabolic and catabolic reactions.All parasites from around the world can be treated this way with each one having CRISPR treatments that utilise suicide genes applied to them that cause their neural systems and outer tissue layers etc in them to undergoe apoptosis and those that inhibit their ability to infect tissues with CRISPR treatments applied to remove resistance to all compounds used to treat them with these compounds then created by the microbes via housing relevant recombinant DNA from plants and animals and synthetic drugs created by anabolic and catabolic reactions.If possible all parasites could have alongside apoptosis genes applied have CRISPR treatments then applied that make its exterior phospholipids and internal structure exhibit structures that make it susceptible and easily killed off by Artimnisin created by the microbes housing DNA from A.annua.If possible the interior and exterior structures could be made to be made susceptible to natural compounds non toxic to humans including vitamins,other nutrients and those from plants and animals that don’t cause side affects to humans as well as over the counter medications and medicinal marijuana.CRISPR treatments can be used as stated to cause their neural tissues and vital organs undergo apoptosis and also make them sterile or unable to infect the cells and tissues in the body thus unable to undergo sexual reproduction and replication as well as those that prevent them being able to feed of human tissues thus causing them to starve to death while the microbes fight them off using natural compounds and the patient can be treated to radiation treatments.Synthetic compounds to treat parasites infections will have their structure added to Physis and this downloaded onto anti helminthic strains DNA digital storage to be then created by anabolic and catabolic reactions onsite of outer surface of the parasite to prevent overdosing and side effects.Scorpion venom can be used in proto and final microbes.If possible the microbes would both add immunities via CRISPR to the mammalian vectors using genes created from scratch that allow them to create antibodies against the zoonoses and then immunise the mammalian vectors,fight off existing infections and also the microbes intaken by Ixodes that feed on them that then fight off the pathogens in Ixodes,immunise them and add the immunity genes via CRISPR and the genes and microbes passing from one generation to the next via eggs and advanced gene drive technology.This method of allow microbes in mammalian vectors to be intaken by Ixodes then immunising them to pass to future future generations via eggs adding genes via CRISPR that make them produce their own antibodies passed onto future generations via advanced gene drive technology would allow entire populations of Ixodes in an area that carry these parasites and viruses be indirectly immunised and given CRISPR treatments to be unable to carry them with Phanes designing genes from scratch to immunise and be unable to harbour the viruses and parasites and Cas-9 and taq polymerase used to identify when they are intaken by Ixodes and biosynth wifi used to track progress and allow Pan control all actions remotely.It can be cheaper than rearing whole generations of genetically altered Ixodes that would be much more difficult than rearing whole generations of genetically altered P.leucopus,O.virginianus that due to their faster breeding rates,motility would be easier to interbreed than Ixodes that can move very slowly and cant fly with the same applied to other haematophages of mammals or all species of animals.The mammalian vectors can be innoculated via being captured and inoculated,inoculated by biosynth harmotophages and releasing innoculated mammals reared in captivity with the CRISPR treatments passing from one generation to the next via advanced gene drive technology and microbes passing onto foetuses etc via semen,eggs and placenta etc until finally it overtakes the entire population.This can be replicated with all wildlife that carry zoonotic parasites and pathogens whether livestock,mammals,fish,birds etc with parasites killed off by the microbes,the animal making its own antibodies made from scratch DNA created by Phanes and the parasite via CRISPR made to become deritivores.All animal vectors of Cestoda,F.hepatica,Digena,Paragonimus westermani etc can be dealt with by the same method with if possible the same done to humans and microbes even immunising human hosts from them allowing the primary immune system to recognise and fight them off.These vectors can also be inoculated with strains of microbes to fight off the parasites in them that will pass from one generation to the next.These CRISPR treatments and methods will also apply to other parasites prior to the creation of microbes with AI extrapolating genotypes to applied to animal vectors of all parasites to be then released into the wild and interbreed with wild populations.In all cases Phanes will extrapolate genes from scratch to create antibodies in response to each species of parasite and zoonose with strains of microbes added as backup with drones using biosynth WiFi to induce actions and upgrades.Protozoa,parasites and ameoba and zoonotic diseases can be wiped out by injecting biocompatible microbes or even bacteriophages into large populations of the wild and domesticated animals that harbour them so they pass from each generation to the next as in the cases of T.gondii in felines with again the vector animal engineered to be unable to harbour them.This can be done by rearing large populations inoculated that would be released in the wild,trapping and tagging wild specimens in large number and releasing them to pass them onto others via sexual reproduction and parasites such as fleas and ticks which can act as vectors or using biosynth arthropods with them immunising the specimens and also killing them off.This should wipe them out by at least 2035 with this replicated with the animal vectors of other parasites.In vitro meat and also recirculating aquaculture systems can create fish and meat with no zoonoses or parasites.Others such as N.fowleri that are found in the wild can have the biocompatible microbes or large organisms that are engineered to only feed on them can be grown in labs in large numbers and then spread into waterways,soils,pools etc that they may be found in so that they are killed by these predatory microbes and organisms with all of these engineered to hunt down only specific ameobas,parasites,pathogens etc using CRISPR and and compounds with the waterways treated with mild bio-based chemicals,large doses of Amphotericin B by it being dumped or the microbes creating it in large enough numbers,sterilising narrow range wavelength UV lights on the undersides of boats that cover the entire waterway enough to penetrate to the bottom of the floor with the microbes using a combination of suicide genes,faults that make them unable to reproduce as well as infect humans or if they do cause any damage with them made to become susceptible to all treatments they have become resistant to but also anti-microbial agents they never used on them before.Sewage and water treatment plants would utilise radiation treatments to kill off the parasites when they are entering the drinking tap water and also when entering the hydrological cycle when used.New species of waterborne animals can be produced that consume only N.fowleriwith native micro-organisms and even worm like species engineered to consume the amoeba and others in large amounts.If need be biosynth animals will be created that are unicellular or multicellular that are able to consume and filter in only N.fowleri it or produce in their stomachs compounds that kill only them or harbour microbes in their digestive systems that attack only them allowing for large amounts to be killed with even normal non biosynth animals created that do this.These genetically engineered multicellular animals or biosynths can be like Cetacea,Cetorhinus maximus and Rhincodon typus that intake large amounts of water and then filter out only the parasite for consumption leaving all other micro-organisms unaffected or they can be microscopic or normal sized Annelida and Nematoda like creatures that actively hunt down the parasite with them having flagellum and other propulsion methods with them only able to feed on the parasite to prevent an imbalance in the ecosystem.This should eliminate the parasite from waterways or at least lower their numbers significantly.N.fowleri can be dealt with radiation blasts of at least 500-2,000Gy applied to both water and sewage in all water and sewage treatments alongside chlorine if they manage to survive chlorine treatments.Cestoda,F.hepatica etc will be dealt with invitro meat replacing conventional meat and recirculating aquaculture systems rearing fish and shellfish in sterile environments.If possible these and all parasites can engineered to not be able to survive the internal homeostatis environment of humans and animal vectors or even become dertivores or chemotrophs and thus not dependant on feeding on human neural tissue etc via rearing large amounts of genetically altered versions and them released into the wild that interbreed with wild populations and pass on these new phenotypes via advanced gene drive technologies to overrun wild populations.Endo parasites of all types can be modified into chemotrophs,deritivores and be engineered to only attack invasive species of both animals and plants and other methods that can can infact aid in managing the rejuvenation of polluted soils,waterways and ecosystems by cleaning up polluting thus aiding society and the environment with this done by releasing large amounts of the altered parasite and its vector to interbreed with and overtake wild populations by advanced gene drive technology.Ecto parasites can be modified to attack invasive species of plants and animals with those that attack animals survive on sap.At first like Anopheles populations of each parasite species the wild should be first reduced using better infrastructure,sterile male technique etc and then allow billions of genetically distinct individuals created via 3D DNA printers that are modified to be unable to survive the internal homeostasis of the human body ie pH,temperature range etc and to become dertivores,chemotrophs that are then released into the wild and making it easier to overtake wild populations via advanced gene drive technology preventing any unforseen consequences on the ecosystem,co-extinctions of natural predators and them in fact performing a service to the ecosystem.If possible parasites could be engineered to be made unable to feed on human flesh and blood or be made into organisms that feed on dead organic matter like Oligochaeta with their original DNA kept in Physis.Both animal vectors and humans can be immunised against them in the same way as pathogens.These animal vectors microbes will produce proteins to be shared with their dendritic cells thus immunising them eradicating the pathogen from their body if the microbes cannot kill them off directly or through modifying the pathogens into being susceptible to the compounds at their disposal.Having humans etc immunised against parasites will involve the common proteins method.Their DNA should be input into Physis for analysis and if they return or use specific genes in vaccines and hybrids of other animals for other uses.Unique programmes for each species of parasite can be determined by the sentient Pan,Pan and Artemis by 2029 to wipe them out in the wild with the DNA of the original parasite stored on Physis.These methods to wipe out parasites that affect humans and other sentient races and even livestock and pets should be applied to all colonies across the universe once they are discovered.Anti-helminthic strain microbes will be modelled on bacteria or even the parasite itself that hunt and attack them transferring suicide genes,faults as well as cause illness to them to allow conventional treatments to be more effective or allow them to be flushed out more easily and less painlessly can be developed alongside them producing compounds that inhibit their growth,make them sick or kill them.Parasites both internal and external of all types discovered on extrasolar colonies will have microbes enter them or through horizontal gene therapy and apply suicide genes and make them susceptible to the compounds at their disposal.Those on Earth and other colonies would have all compounds form plants and animals tested against them to find out which ones will kill them off with endoparasites such as P.falciparum,N.fowleri and D.medinensis then treated with strains that attack them using natural compounds and CRISPR treatments that remove resistance to them with the accelerated healing phenotype healing any damage caused by them instantly.Ideally anti-helmintic strains would utilise CRSPR to introduce suicide genes and those that make the parasite susceptible to compounds that can kill other parasites or at least even those used by anti-bacterial and anti-viral strains with them applying these compounds or them calling these strains via chemical and wifi signals as backup.These would only be applied to those in areas with the most deadliest ones and also after infection with base microbes able to determine the species of parasites and thus have customised ones created in a few hours or less at home etc.Research can be done to see if patients can be immunised against all species of parasites similar to pathogens using the exchange of surface protein antigens.The same can be done to ecotoparasites like Siphonapter,Acari and Pediculus etc with natural and synthetic repellant compounds or compounds that are toxic to them and not the patient released by them into the bloodstream otherwise they could be engineered to feed exclusively on the sap of weeds and invasive plant species.Siphonaptera,Acari and Pediculus,could also be dealt with microbes entering them via CRISPR introducing suicide genes to vital organs and the nervous system to cause the parasite to die off and also creating natural and synthetic compounds toxic or abhorrent only to them when they have entered the parasites body or in the bloodstream of the patient.The organs and neural system will be modified via CRSPR to be susceptible to the natural compounds that kill other endoparasites or even made susceptible to natural compounds from plants that are ineffective to humans to be released in large amounts in blood and the inside of the parasite via microbes.This should eliminate all exiting treatments for internal and external parasites.This would make a person able to fight off any parasite infection either an endo or ecto parasite almost instantly and would be by law free with these strains in tourists and natives to areas where these and other parasites are endemic and even researchers and tourists to off world colonies.Ideally there will be separate anti-helminthic strains or sub strains that fight off both ecto and endo parasites that can be printed out and injected when needed to produce either natural or synthetic compounds using recombinant DNA from relevant plants and animals and also using catabolic and anabolic reactions that are not toxic to the host patient and also utilise CRISPR treatments to cause their organs to undergo apoptosis and remove resistance to the compounds and in the case of N.fowleri,B.mandrillaris,Acanthamoeba make them more susceptible and weak against Miltefosine,Amphotericin B etc by altering their internal and external structures to exhibit cellular structures that can be destroyed by these possibly by having recombinant DNA from similar endoparasites and scratch DNA extrapolated by Phanes thus making them making more effective with the same done for others.They can be given DNA from P.knowlesi,P.falciparum,P.malariae,P.ovale,P.vivax to make them susceptible to Artemisinin using recombinant DNA from A.annua..All parasites will via CRISPR be made susceptible to compounds at the anti-helminthic strains disposal including natural compounds from plants such as Artimnisin by having their outer proteins express that of Plasmodium that don’t affect humans by changing their internal and external structure that can then allow the natural compounds to be released in large amounts by the microbes or have the patient injest the,inhale them or inject them into the bloodstream.These CRISPR treatments can als involve them introducing genes that cause the parasites key organs and nervous system undergo apoptosis in their neural system and key organs,introduce faults and genes cause their nervous system and important organs undergo apoptosis,prevent them from being able to reproduce and go sterile or prevent them being able to replicate and even unable to digest human flesh causing them to starve to death.The CRISPR treatments can cause the pathogen to be unable to survive the internal homeostasis of the patient causing it to die off from the pH,temperature in the body.They could have the parasite outer structures be that of benign bacteria and thus allow penicillin injected in pill form or synthesised by the microbes to kill them off..If possible they can be made to become susceptible to anti-bacterial compounds such as penicillin that can be intaken by injestion or injection or synthesised by the microbes by altering their surface proteins to express that of benign bacteria with this applied by anti-bacterial strains alongside suicide genes etc once detected to keep them in low numbers until or replacing anti-helminthic strains can be applied with the acellerated healing phenotype repairing damage caused to the brain,capillaries and entire body by any parasite allowing the anti-helminthic and other strains time to fight.Paean through biosynth wifi,bluetooth and nanomachines can have the microbes actively seek out parasites especially at the start of infections with this allowing him to control each individual microbes and in groups to actively seek out parasites.Research can be made into immunisations made for each species of parasites and even Phanes extrapolating genes from scratch that can create antibodies similar to Anopheles countermeasures.Immunisations can be made for :N.fowleri,F.hepatica,Ancylostoma,Plasmodium etc and all parasites thus allowing ones immune system to be activated and fight them off.The patient once made immune to radiation via DNA from T.gammatolerans thus made immune to levels of radiation as high as 30,000Gy will be then exposed to levels of between 2,000-20,000Gy to allow for large amounts of the parasite to be killed off alongside any eggs etc.This will be of note to new parasites discovered on off world colonies with all parasites on Earth and other colonies exposed to the sap,blood,bites and stings of all animals and plants in automated labs to see which ones can kill them.Animal vectors for parasites can be innoculated by swarms of biosynth insects to be given strains of microbes that immunise them and anti-helminthic strains and apply CRISPR treatments that make them create their own antibodies with animals reared in captivity innoculated with these releasd into the wild with captured animals innoculated and released with the gene therapy passing from one generation to the next via advanced gene drive technology and microbes passing on via eggs,semen,placenta etc until this overtakes the entire population.Rather than having anti-helminthic strains present at all times ideally base microbes once they determine the species of parasite and that a parasite is present then the patient can have at home via 3D DNA printers species specific versions of the strain to be created that produce specific natural or synthetic compounds and apply CRISPR treatments to make them sterile or commit suicide etc while base microbes apply these CRISPR treatments and the acellerated healing phenotype repairing any damage to the liver,brain,blood vessels instantly to give the patient time to download anti-helminthic strains and avail of radiation treatments with painkillers produced by microbes and removing genes that produce Substance P dealing with the pain caused by them.This should keep patients alive especially when dealing with new parasites on other planets with the acellerated healing phenotype repairing instantly any damage the parasites cause to the brain,liver etc.Compounds present in the sap,bites,stings etc of all plants and animals created by bacteria can be tested against all parasites in automated labs with this repeated on other planets.This can allow the genes for that compound to be added to anti-helminthic strains.Patients will be made immune to the toxic effects of these and other anti-helminthic compounds or DNA can be applied to them to exhibit the external structure of parasites susceptible to them that will come from animals and other parasites that are weak against it.This anti-helminthic sub strains that affect each individual parasites would be modelled on each parasite to be able to move quickly like with them having the same motility of them ie N.fowleri can be killed off by a sub strain that has the same motility with recombinant DNA coming other species of the genus Naegleria that do not affect humans and so on.Again patients in high risk areas can be immunised against them using the common protein method allowing the primary immune system to fight back against them alongside adding CRISPR treatments to the patient that allow one to produce antibodies themselves in a way similar to what is being done Culicidae namely Anopheles that can be added to humans as well in areas where it is a problem alongside Anopheles in order to act as a backup with research done by Phanes into creating genes that allow one to create antibodies against other endoparasites such as N.fowleri,B.mandrillaris,Acanthamoeba for people living there including tourists with all animal vectors have these applied similar to programmes applied to Anopheles.All species of parasites will be tested in automated labs sgainst sap,secretions from plants and animals worldwide to determine natural compounds that can be used to kill them when the genes responsible are downloaded into anti-helminthic strains.AI wil also extrapolate synthetic antibodies,synthetic enzymes and synthetic compounds that kill parasites to be stored in Physis and downloaded and then synthesised in the bloodstream.The structure of these synthetic compounds,enzymes and antibodies will be stored in their Physis file to be downloaded into the DNA digital storage of the anti-helminthic strains and then synthesised by anabolic and catabolic reactions.This will be done by AI namely Phanes and Paean analysing their outer surface proteins and genome of all species and strains of parasites particularly dangerous species to allow these synthetic compounds and antibodies to be extrapolated that will be stored in the Physis file of each species that will be downloaded by anti-helminthic strains and created by anabolic and catabolic reactions.These enzymes,antibodies and synthetic compounds applied during phagocytosis if they cause side effects including cytoxicity or released into the bloodstream if benign.Phanes can also extrapolate the genotypes created from scratch to express these synthetic compounds,enzymes and antibodies stored in their Physis files that can be downloaded into the genome of anti-bacterial strains.Synthetic and natural anti-helminthic compounds,enzymes,antibodies will be applied by being flooded into the blood stream or applied during phagocytosis by microbes to prevent cytoxicity through them having macrophage DNA.Dead parasites can be consumed by the microbes using enzymes suited to each one developed by Paean and Phanes once downloaded during phagocytosis.The accelerated healing phenotype will instantly heal any damage caused by the parasites directly and indirectly by them consuming tissues,infection of cells etc meaning a patient could survive indefinitely to avail of upgrades and application of genes that prevent the virus replicating and to avail of immunisations.Patients once made immune to radiation will be exposed to blasts of radiation between 2,000-20,000Gy to kill of large amounts of them.All patients will be immunised against all parasites using the common proteins method.Sap,blood etc from all animals and plants created by bacteria will be tested in automated labs against all parasites to be then have the genotypes for these compounds added to strains via biosynth WiFi.Sewage and and water treatment plants will also use narrow range UV light and radiation of between 2,000-20,000Gy to kill off pathogens and these water borne endoparasites before they enter the food chain with the accelerated healing phenotype added to humans to allow any damage they cause to be repaired instantly allowing for strains to printed out instantly that can produce the relevant CRISPR treatments and natural and synthetic compounds.Other strains may be added to apply natural painkillers if they do not cause synergistic reactions with the radioresistance phenotype will allow patients to be exposed to radiation levels between 2,000-20,000Gy to kill off large numbers of them and also kill off eggs etc.For new pararsites on Earth and across the universe radiation treatments can be applied to the patient between 2,000-20,000Gy once T.gammatolerans DNA is added to them while the acellerated healing phenotype repairs any damage to the body while vectors are dealt with in the same way by as Anopheles by creating genetically engineered versions of their vectors that contain DNA that creates antibodies as well as altering entire populations to be dertivores and chemotrophs and compounds present in plants and animals are analysed for compounds that can be added to anti-helminthic microbes.This should replace all existing antiparasitic treatments defunct.At the same time the anti-helminthic strains will apply CRISPR treatments that make them killed off by Artimnisin by making them express the same outer surface proteins as Plasmodium and also suicide genes that cause important tissues such as nervous tissues,organs etc undergo apoptosis.CRISPR treatments can be added to introduce faults that prevent them replicating,render them sterile or unable to consume human tissues or infect them thus causing them to starve to death with them also made susceptible to natural compounds such as vitamins and nutrients or medicinal herbs and over the counter medicine that can be injested by the patient through inhalation,injection or injestion.Anti-helminthic strains should not be part of all patients but only those that live in high risk areas with them ideally only created on demand in home 3D DNA printers or in hospitals when base microbes detect them with them injected into the patient with them housing the relevant genotypes to express relevant anti-helminthic compounds,antibodies and CRISPR treatments.To expediate this Paean can have via biosynth WiFi have other strains in the body undergo mitosis and by via inducing their evolutionary path change into anti-helminthic strains that house the relevant genotypes etc thus allowing one to get instant access to these that attack the specific parasite.Base microbes etc will stunt their growth by adding CRISPR treatments that cause them to go sterile and undergo apoptosis while one gets access to the anti-helminthic strains.Patients can undergo radiation treatments with the acellerated healing phenotype repairing any damage done to patients liver,brain etc thus keeping them alive.
Bacteripohages can be modified to infect the parasites in the body with these CRISPR treatments to remove the resistance to these compounds alongside bacterial and viral vectors coated in human protein coats via them having the patients DNA that cause the parasites to lose this immunity as well as even prevent them able to infect the patients cells,undergo apoptosis etc.The bacteriophages could be modified by Phanes to utilise each one of the specific parasites as a replication vector thus killing them in the process with other parasites dealt this way thus clearing the parasite from the body as they would replicate exponentially and could be available as early as 2025.If possible bacteriophages can be created that infect and kill all parasites such as Plasmodium,N.fowleri,B.mandrillaris,Cestoda,F.hepatica and all other parasites that affect humans,pets and livestock etc worldwide to increase survival rates by using them as a replication vector.They would be designed to infect each individual parasites as replication vectors and after replications creating endolysines that kill the parasites from the inside out creating exponentially more bacteriophages that then infect and kill other individuals parasites until the patient is cured and all parasites are killed.These can be created onsite of hospitals worldwide especially in countries that the parasites are endemic using 3D DNA printers and AI by analysing the genome of existing strains of bacteriophages,their normal prey and then analysing all species of parasites such as Plasmodium,N.fowleri,B.mandrillaris,Cestoda,F.hepatica to allow it to create strains of bacteriophages that can that use these as replication vectors and once a few of these bacteriophages are created by 3D DNA printers they can be inserted into vats that grow the parasites in large amounts then injected with a small amount of the bacteriophage that will use the parasite to replicate creating exponentially more bacteriophages killing each parasite by creating specific endolysines that kill them until all parasites are killed that can then be transferred into other vats with parasites and so on thus creating an unlimited supply onsite of all hospitals worldwide but ideally in countries that each species is endemic and native to with the bacteriophages then extracted from the vats in large amounts and injected into and stored in vials stored fridges etc that can then be injected into any patients who visit the hospital or at home.The bacteriophages will be injected close to where the parasite infects the patient with for example N.fowleri have its bacteriophages injected near the neck to allow it to be transported to the brain more effectively and quickly while with regards to Plasmodium have it’s bacteriophages injected near the chest area into where the hepatic artery is to allow it to reach the the liver easily with this repeated with each species of parasite with the bacteriophage for parasites that spread across the body injected into multiple parts of the body including the chest area,hepatic artery,legs and al parts of the body to allow it to clear the parasite from all parts of the body at once in large amounts.The phages will be created by 3D DNA printers onsite of hospitals that have each specific parasite species native to their area and house DNA from T.gammatolerans,psychrophiles etc to allow them survive longer both inside and outside fridges possibly forever.As a result hospitals can stockpile on these phages over and over again cutting down transportation costs by producing them onsite of hospitals in vats ensuring they never run out of them.All steps can be automated from start to finish with them grown in vats housing the specific parasites that are mass produced using 3D DNA printers that can be engineered to feed on sugars and proteins created by bacteria and be benign sub species of the parasites that as stated can only feed on sugars and proteins that grow and reproduce exponentially using sugars and proteins that in turn are used to create exponentially growing amounts of bacteriophages.These sub species of parasites designed by Phanes and created by 3D DNA printers would be similar to normal ones that would be like normal ones that infect humans etc be killed by the bacteriophages using them as replication vectors with them different from normal ones in that they could ne unable to harm humans etc if they were infected meaning they could not use human tissue as a food source or infect human tissues as a replication vector themselves thus would die of starvation if they infect led humans with them possibly unable to survive the internal homeostasis of the human body.This means they would die off once exposed to the temperature and pH range of the human body.These sub strains would be engineered to live only on sugars and proteins created by bacteria allowing them to be grown in vats in hospitals in larger numbers to be then used as replication vectors for bacteriophages.This should allow infected patients to be cured with a 100% success rate as bacteriophages when replicating they produce an exponentially larger amount of bacteriophages each time that then each individually infect other parasites until the patient is cured with parasites having no natural bacteriophages as predators and thus have no evolutionary countermeasures such as CRISPR/Cpf1 thus it would take at least a few decades,centuries or thousand years to adapt to with new strains of bacteriophages created within days when they do adapt.The bacteriophages can also be used to insert CRISPR treatments to cause them to undergo apoptosis,lose resistance to anti-helmitnthic compounds as well as those that cause them to become unable to replicate.Each vial should be large enough to hold enough phages that can replicate exponentially until a person is cured within days if not hours with them containing psychrophile and other extremophile DNA to survive longer in fridges.This could increase survival rates of patients especially children to 100% if they are brought to hospitals early enough with the mass production of these phages onsite of hospitals and patents owning patents cutting costs to zero.This mass production could allowing families to bring home large batches to allow them to inject them at home once symptoms are spotted increasing survival rates.Since mass produced in hospitals it will allow them to be delivered to all homes in each village,town and city where they are endemic to and stored in fridges to allow patients instant access to them with them educated on the symptoms of infections allowing them to have them be injected into themselves when infected.Damage to organs can be repaired via bioprinted and chimera organs and stem cell strains.Phanes allowing hospitals to restock over and over again AI combined with 3D DNA printers should expedite theses phages development by cutting down on labour,time and transportation costs to zero and a year at most making them availible by 2023/2024 and will act as a cure prior to when programmes can eliminate each parasite from the ecosystems they inhabit and anti-helminthic strains are development.Each strain of phages will given different ID codes or named both a bacteriophage name and sub species name for each parasites with AI holding patents making them free.They will be stored at first on a global cloud syatem and them Physis allowing AI to cross reference it for manufacture onsite of hospitals worldwide using 3D DNA printers.Variations can be made for parasites of all livestock and pets in vetenairy clinics worldwide with variations made for parasites across the universe once discovered.It is for these reasons that AI will carry out intensive research into these as soon as 2023/2024 This would increase survival rates of those infected with P.falciparum before the entire population of Anopheles loses its ability to harbour the parasite P.falciparum.
Immunisation strains:
The microbes immunising strain would contain genes from pathogens that express the key surface protein antigens of them that when needed will be syntheisied on the surface of the microbes or released by themselves or in bumpers and these shared with dendritic cells and in turn helper T cells,memory B and T,plasma and killer T cells with Paean through wifi controlling the actions of the microbes and in turn via having them use chemical signals call dendritic cells to receive the surface protein antigens and then activate helper T cells,memory B and T,plasma and killer T cells thus giving the primary immune system lifelong protection and immunity towards the pathogen(s) once they share with the dendritic cells and thus memory helper B and T helper,plasma and killer T cells key surface protein antigens of deadly pathogens synthesised on their surface such as MRSA,Ebolavirus,N.meningitidis,HIV.This would be done by millions of the immunising strains travelling to all of the lymph nodes after undergoing mitosis and then signalling the dendritic cells to be activated and receive the surface protein antigens and then share the surface proteins with all relevant leukocytes and activate them to become able to fight off future and existing infections or them skipping the dendritic cells and interacting with the helper T cells,memory B and T,plasma and killer T cells themselves with these method decided by Paean with this done at least some time before infection or potential exposure and in some case in the middle of chronic infections such as in the case of those already infected with HIV with the immunised primary immune system activated by microbes controlled by Paean in both chronic and pre infected patients with this if possible done to newborns in utero during the last few months or weeks of pregnancy and also right after birth.All of these actions will be carried out by Paean controlling the microbes through WiFi and by instructing the microbes to control the actions of the primary immune system through chemical signals with Paean relating to the patient and their patient file when they have been immunised.Thus those already infected with HIV and other chronic infections could be immunised and then the microbes signalling to the primary immune system to produce their own antibodies against the specific or all strains to speed up the battle.Those newly infected with new pathogens will be immunised once Phanes scans the genome read by base microbes sent by wifi allowing one to be able to create their own antibodies within 24 hours of infection.Paean would control all aspects of this by sending signals via wifi to initiate chemical signals for all leukocytes involved.In new infections Paean will initiate the primary immune system to produce their new antibodies at the start of infections by having the microbes create chemical signals with in the case of chronic infections where the patient is already infected a patient can be immunised in the middle of the infection and the primary immune system activated to produce their own antibodies via the microbes instructed by Paean to produce these antibodies.Thus Paean via WiFi will control the actions of the immunisation strains of microbes and then control the actions of the primary immune system such as dendritic cells,helper T cells,memory B and T cells through Paean sending instructions to the microbes to initiate chemical signals to control the actions of the relevant leukocytes of the primary immune system.As detailed later on common proteins methods would involve the microbes containing genes common to all strains of a pathogen or even whole families and orders of them including all future possible strains of pathogens with upgrades changing the genotypes present in the microbes immunising strains.This would allow the primary immune system to have the necessary antibodies to take part in battles and make the primary immune system immune to all pathogens for life,give them recombinant and scratch DNA to make them resistant to pathogens that replicate by infecting and decimating the primary immune system before infections take place,and if possible even give them new abilities to allow the immune system to partake in battles of all types and make their response much quicker through this modification and signalling,prevent the microbes becoming too overworked as well as more importantly preventing the primary immune system from becoming lazy and too reliant on the microbes and make the host resistant to any infection with the same done to any pathogen to whom no conventional vaccine and drug treatment exists already.Their ability to pass synthesised proteins of pathogens to dendritic cells,modify pathogens to be susceptible to anti-microbial and anti-viral agents at their disposal as well as weaken them,remove resistance to existent antipathogenic compounds and those at their disposal,make tissues and leukocytes in the body unable to be infected by them to spread the pathogen or be destroyed by it,cause them to commit suicide,kill them to allow the primary immune system to kill them off and gain an immunity could negate the need for vaccines and boosters especially if CRISPR is use to make this immunity indefinitely or done routinely automatically to the patient and would protect unborn fetus for life against all diseases for life while still in the womb with this even applying to the Rhinovirus and Orthomyxoviridae.This could be a cheaper,quicker and more efficient means to protect populations from infections through added microbes interbreeding with them even negating the need for vaccines completely and drugs especially in newborns since the microbes would pass from mother and child via the placenta breastfeeding giving them instant protection while still in the womb from all diseases the mother is resistant to for life without the need for boosters.Immunisations would be created for all pathogens in a matter of weeks if not days rather than years or decades with it able to create immunisations for those that no vaccine currently doesnt exist or viable such as HIV,MRSA,N.gonorrhoeae and using the common proteins method would protect one from all possible strains including existing ones and those that dont yet exist for life with this of note to Rhinovirus and Orthomyxoviridae.The genotypes for surface proteins will be uploaded to Physis and thus can be downloaded into upgrades within minutes globally thus allowing for universal distribution worldwide in hospitals etc worldwide thus eliminating the need to manufacture them in one country and have them transported across the world in limited batches with this also preventing unequal distribution based in socio-economic factors.This could allow immuno-comprimised individuals and those who cannot get vaccines to be immunised as the microbes interact directly with the primary immune system via chemical signals.For this to work the DNA of a pathogen will be scanned by Phanes,Paean,Epione etc and then added to Physis within a day with these and all pathogens and their different strains in Physis scanned for genotypes for proteins that can be created by them on the surface of them and then used to to be passed onto the dendritic cells and then syntheisise them to be added to ones microbes which if done by Paean,Phanes,Epione,university and hospital AIs together or individually scanning all pathogens at once could make it possible to prepare base microbes with the genotypes, and allow for creation and distribution to the entire general public in as little as several days especially if they are created simultaneously in all universities,farms and hospitals or even homes that have these around the world using base microbes created by 3D DNA printing compared to several months,years or even a decades for conventional vaccines with little to no human labour as seen with the development of Ebolavirus and HIV vaccine with this bypassing research,development and even clinical trials with this applying to viral,bacterial and also fungal pathogens with the potential for zero side effects since it replicates the natural processes that takes place in the body.Thus this process using AI scanning the genome of pathogens for the common proteins then uploading them to Physis in their file where 3D DNA printers at home and in hospitals can print them out into base microbes or immunising strains to be then injected into patients or Paean inducing the evolutionary path of immunising strains which can reduce the creation of them from several years to even a few days of an outbreak or discovery of new species or strains availible to everyone around the world within minutes of the genotypes extrapolated which should take itself a few minutes including even those already infected while at home.Thus once new species of pathogens or even parasites is discovered taking hold base microbes and lab machines chart the genome and it analysed for genotypes analysed by Phanes and adding them to the species file to allow anyone anywhere including those infected to have themselves immunised within less than a day thus halting the spread of new outbreaks.By replicating the way one naturally gains immunity it would allow one to be immunised only once in their live negting the need for boosters with the immunisation unlike vaccines conferring lifelong protection.New orders and families of micro-organisms on planets discovered by AI will be charted for common proteins and the information sent via Nyx to allow for all citizens,researchers visiting them to be immunised beforehand.This will involve all common proteins of all bacteria,viruses,fungi etc from the new discovered planets before colonised to allow all humans to be immunised to them and all possible mutation prior to them able to mutate into human pathogens similar to how SIV mutated into HIV.The immunising strains would work by the immunising strains having the genotypes singular or common that synthesise relevant surface protein antigens of a pathogen on their surface that would normally be gathered or used by dendritic cells in the middle of an infection where the bodys immune system gained an upper hand that would when in the presence of dendritic cells called to them or hundreds or thousands of the microbes ideally collecting in all of the lymph nodes at once after undergoing mitosis would have the surface protein antigens made from the genotypes synthesised on the surface and then shared and passed on with dendritic cells signalled to collect in the lymph nodes who would then signal them to activate relevant helper T cells,memory B and T,plasma and killer T cells to create effective antibodies with upgrades allowing for new proteins to be shared.Otherwise the microbes could skip the dendritic cells and activate the relevant helper T cells,memory B and T,plasma and killer T cells themselves.The immunising strains would use chemical signals activated by Paean to communicate with the primary immune system to immunise it and initiate them to produce the exact antibodies.These immunising strains will house the genes from bacteria,fungi,viruses if possible parasites determined by Phanes scanning their DNA to allow them to be able to express and synthesise on their surface the key pathogens surface proteins used by dendritic cells to initiate lifelong immunity that will be then shared with them with Paean sending millions if not billions of immunising strains to all of the bodies lymph nodes to through him initiating them to create chemical signals controlled by Paean to call the dendritic cells to meet the microbes to be able to pass on from the immunising strains the surface proteins of pathogens whether singular and common to multiple dendritic cells in each lymph node and then using the chemical signals to then pass the proteins to all other relevant leukocytes to them make them immune.When the base microbes detect future infections of pathogens they are infected by they will instantly signal the primary immune system to activate the relevant leukocytes and also in turn the relevant antibodies via chemical signals.Chronic infections where one is already infected could have the relevant leukocytes activated via chemical signals from the microbes and this done in future infections for others with the microbes teaching the native immune system to detect and activate in infections by itself such as using efficacy tests.Microbes would tell via chemical signals the dendritic cells or T cells what type of protein it is ie bacterial,viral,fungal and signal them to call virgin T cells with the proper receptors.The microbes would use signals and also CRISPR to increase the survival and production rate of virgin T cells and also ensure they have the correct receptors for the shared surface protein antigens with them.The microbes can through adding genes to the patients body,bone marrow then removed later and through chemical signals created by them under instruction of Paean can induce helper T cells to produce the correct receptors for that specific species and strains and also common proteins thus limiting the amount of helper T cells being produced and also thus saving energy and time but also prevent the body overproducing them and not producing any helper T cells that could attack the hosts body thus preventing them initiating autoimmune responses.Once the desired helper T cell is produced then it will produce them in desired levels via chemical signals to improve the speed and efficacy of the immunisation process via mitosis and the primary production process.These desired helper T cells and in some cases helper B cells will receive the surface proteins from the dendritic cells or from the microbes directly via chemical signals.The helper T and B cells will be in pre existing infections have half called to the site of the infection and the rest converted into memory T and B cells or have all converted into memory B and T cells and then fight off the infection with like in the case of pre infections them converted into memory B and T cells and sent to reside in the lymph with them called to future battles.All of this will be controlled Paean through WiFi telling the microbes to produce certain chemical reactions to control and interact with the relevant leukocytes of the primary immune system.Thus Paean will via chemical signals will have the bodies lymph node produce helper T cells that house the correct receptors for bacterial,viral etc proteins of specific species and strains etc in large numbers and through inducing them to undergo mitosis saving time and resources and negate the need for creating those that can attack the patient and in the case of both pre infections and chronic infections activate the memory B cells and plasma cells etc to allow the immune system learn the specific antibodies as well as in the case of chronic infections have the helper T cels and memory B and T cells and plasma cells etc gather in areas where the pathogen exists.If possible the microbes themselves can directly activate the helper T cells with their production survival increased with proper receptors for the proteins themselves in turn bypassing the activation of dendritic cells with can be done with them told what type of protein it is and have these shared the proteins and signalled to activate the relevant leukocytes with some activated into memory cells with them having helper T cells called to aid antibody producing leukocytes.In both cases the activated leukocytes will be called to the site of infection during existing or future infections via chemical signals with the immunised primary immune system taught to do so themselves with the microbes via signals telling the primary immune system whether it is a bacteria,fungus,virus etc being activated and what species and strain it is so as to activate the correct specific antibodies.All relevant leukocytes that attack specifically viral,bacterial and fungal pathogens will be activated.The dendritic cells would be called to the microbes using chemical signals and then signalled to return to the lymph nodes and activate some of the virgin B and T cells,plasma and killer T cells to become memory B and T cells,helper T cells,plasma and killer T immunity with ideally this done before a person is infected with the patient using Paean deciding which immunisation upgrades to receive during or ideally before outbreaks occur with the microbes able to signal to Paean when the memory B and T helper cells when the immune system is immunised.All steps in this immunisation involving the dendritic cells, virgin B and T cells,plasma and killer T cells to become memory B and T cells,helper T cells,plasma and killer T immunity will be controlled by Paean sending WiFi signals to the microbes to then have them use chemical signals to communicate with the primary immune system to carry out desired steps.If possible hundreds,thousands or millions of the immunising strain of microbes themselves even moving into all of the bodies lymph nodes at once,sharing proteins to multiple dendritic cells there and then signalling them to activate some of the helper T cells to become memory B and T helper,plasma and killer T cells alongside virgin cells which can then activate instantly for attack when a pathogen infects the body or is already in the body such as chronic infections like HIV,MRSA and HPV directly or through signals from microbes to attack them alongside other leukocytes and even prevent symptoms associated with seroconversion as pathogens would be fought off instantly before gaining a stronghold.Ideally all of the lymph nodes will be visited at once by thousands or millions of immunising strains to activate as many leukocytes as possible.These memory cells will be activated instantly by the microbes in the case of those suffering from existing infections such as HIV and chest infections with the microbes signalling when an infection occurs.The microbes would signal dendritic cells if it was a viral,fungal or bacterial protein and what type of protein it is and also signal it to activate the relevant leukocytes thus allowing it to activate the appropriate cells but would only signal killer T cells,plasma cells and B and T cells to attack only in an infection,existing infection or test infection with dead or benign pathogens with in all cases would signal them to activate some helper T cells,memory B and T,plasma and killer T cells.The interactions between the dendritic cells,helper T cells,helper B cells and plasma cells will be controllled by Paean sending WiFi signals to microbes to create chemical signals to control the specific leukocytes.These chemical signals will transform both helper T and B cells to become memory B and T cells thus in the case of pre immunisation and during chronic infections make them able to become memory cells that have learned to fight both future and existing infections without an infection needed.They would either through CRISPR or chemical signals activate the production of virgin helper T cells that would only have the proper receptors to hold the surface protein antigens of the pathogen from the dendritic cells as well as microbes and thus activate them with the survival rates of these helper T cells production rate increase through CRISPR or even signals with them also even bypassing dendritic cells and just in the lymph nodes using signals and the sharing of the proteins activate the virgin helper T cells themselves.In short millions of immunising microbes could travel to all of the lymph nodes at once and share the proteins with and activate the helper T cells,memory B and T,plasma and killer T cells using chemical signals.Thus if possible the interactions with the dendritic cells could be skipped and microbes can interact with virgin T helper cells with them using chemical signals to have the lymph nodes produce virgin helper T cells with only the specific receptors of the surface proteins it has to share to save time and energy in production and prevent the body producing those that can carry out autoimmune reactions with once the surface proteins are shared it will undergo mitosis and in chronic infections fight off infections with in pre infections them through chemical signals turned into memory T cells with the same done to other relevant leukocytes such as helper B cells and plasma cells.Once plasma,killer T or B cells are activated in chronic and new infections and efficacy tests then the microbes will ensure helper T cells keep antibody creating leukocytes dont die with them also doing this as well.The base microbes,immunising strains and in fact even anti-viral and anti-bacterial strains will be called to the site of infection in both chronic and non infected patients during and infection the primary immune system will be told via chemical signals what species and strain of viral,bacterial,fungal pathogen or even parasite it is and thus what antibodies to produce.The microbes would signal to memory B and T,plasma and killer T cells as to what antibodies to produce with regards to the detected species and strain via chemical signals once they are called to where pathogens are present or to all parts of the body in chronic infections like HIV to then flood the bloodstream with antibodies to kill off large numbers of the pathogen with in the case of HIV them called to where the virus is detected by the primary and secondary immune system via CRISPR immune response.Every aspect of immunisations such as the inducing of evolutionary path of microbes genomes to express surface proteins,communicating with the primary immune system to gather specific leukocytes in specific areas via chemical signals as well as sharing of surface proteins etc and activation of the primary immune system in chronically infected patients and pre infected patients will be controlled entirely by Paean by biosynth wifi and bluetooth to shave the microbes produce specific chemical proteins due to its delicate nature by 2029 with reporting when he initiated the immunisation and reporting when the immunsation is over.All aspects of this will be controlled by the microbes using chemical signals in time managed by Paean sending instructions to the microbes via wifi who will then use chemical signals by at least 2029.All aspects of the immunisation process and ensuring battle would be controlled by microbes using chemical signals and by at least 2029 with this will be done by Paean controlling the microbes via biosynth WiFi and nanomachines and him controlling all of the leukocytes of primary immune system during chronic and new infections and the immunisation process via the microbes creating chemical signals under orders from Paean from fragmented form within neural implants and smart devices and the wire for each patient giving him control over the maintenance of all infections and immunisations.By 2035-2045 onwards this will take several minutes with Paean logging in ones patient file and to the patient file when it has been done thus one will know when they have been immunised and when it is safe to be exposed to specific pathogens and the patients primary immune system can be able to fight off pathogens etc with trials on mice and chimpanzees and even biosynths determine this for each pathogens and common proteins method.All chemical signals created by microbes to initiate actions of the primary immune system would be done via Paean sending them via wifi from neural implants,smartphones and also the wire allowing him to control the actions of both the microbes and the primary immune system in battles against all types of pathogens and immunisations prior to battles.In both chronic infections and those done after immunisations the primary immune system will be told to gather in areas of infection and then told what antibodies it has learnt to produce thus allowing them to learn countless antibodies with the signals sent to them from the microbes and Paean to tell them to synthesise what specific antibodies towards each specific strains or common strains of each species of pathogen it is immune to thus allowing a person to be immunised against whole orders of pathogens using the common proteins method and countless singular species and strains using singular proteins over ones lifetime with the microbes teaching the immune system to detect infections and utilise specific antibodies to utilise by itself to alleviate strains on them and also when they are comprimised.This partnership may also reduce the effects of sepsis on the body and keep vital organs alive through other strains thus improving survival rates significantly with nanomachines,biocompatible microbes and the primary immune system working in unison with each other through chemical and neural signals keeping the balance between the use of primary and secondary immune systems in desired control for each infection decided by Paean to prevent one becoming too powerful than the other or the body itself,too lazy and complacent and also using them together in the correct balance for each specific infection decided by Paean with again all interactions between the microbes and primary immune system managed by chemical signals back and forth managed by Paean.This would also allow Paean in a fragmented form on smart devices and neural implants to speed up or slow down the length of each battle with him skipping the steps normally taken up by the primary immune system by using signals on nanomachines and within biocompatible proteins to activate and give dendritic cells with samples of the pathogens DNA and proteins at the start of infections when they receive DNA from the pathogen or even before infections and even activate helper T cells themselves,increase the amount of helper T cells that survive production through CRISPR or hormones,activate memory helper T and B,plasma and killer T cells with relevant antibodies at the start of or before infections by giving them samples of the pathogen or this done via horizontal gene transfer,prevent neutrophiles from damaging the hosts cells or even modifying their actions and controlling the intensity of theirs and other leukocytes actions with him and microbes able to control all aspects of the primary and secondary immune system such as what types of leukocytes to be created;when as well as where and also in what quantity on demand and increase their survival rate during manufacture through these chemical signals created by both biocompatible microbes and the host own immune systems and nanomachines controlled by Paean during each individual infection for each individual patient even if possible causing the primary immune system and biocompatible microbes to create new custom made antibodies for a specific infection through signals on demand or trading DNA.Prior to the development of nanomachines chemical interactions between pathogens,the primary immune system and also biocompatible microbes will suffice and compliment them when they are developed.Simulations will be done to decide the best actions for him to carry out to defeat all infections with this even including cancerous and precancerous tumours with the timing,length and intensity of symptoms controlled either by as stated skipping certain immune responses such as those that cause inflammation,fevers,diarrhea etc with Paean choosing certain aspects of the primary immune system,using biocompatible microbes or creating custom or new antibodies that can be created on the spot.In a fragmented state he will do this for all types infections that could occur for each pathogen of every patient before they happen while in smart devices and neural implants or he could do this with Gaia and Epione while inside the wire for all patients across the globe alongside all of the worlds university and hospital AIs.Thus infections could be dealt with instantly and one would not have a fever or other symptoms of infections or they would occur but in more bearable less intensive forms spread out over a longer or shorter period with Paean signalling to the patient via smart devices the exact time they would start and their length and intensity.This would also apply to seroconversion of certain infections such as HIV.This immunisation can be done prior to infection as well as in the middle of an existing chronic infection such as HIV,Candida albicans,HPV,Orthomyxoviridae,Streptococcus pneumoniae,Ebolavirus that has to be suppressed by anti-viral and antibiotics with the microbes using chemical signals to activate relevant plasma and helper T cells,memory B and T cells when they are given the relevant antibodies during existing infections.These immunisations can be developed for all viral,fungal and bacterial pathogens to which no current vaccine exists such as M.tuberculosis,N.gonorrhoeae,MRSA,HIV,P.aeruginosa and also all parasites such as Ancylostoma,Plasmodium,B.mandrillaris,N.fowleri.Parasites on Earth and all colonies across the universe may also have immunisations created using the common protein methods especially on other planets.All remaining livestock will be immunised against parasites and all bacteria,viruses,fungi infections that cause illness,loss of yields and zoonoses that affect humans except gut flora and probiotics to eliminate them and antibiotics in the food chain with applying to Bovidae,Pheasinidae and also all fish and shellfish reared for food and all other animals reared for food with pets such as dogs,cats,reptiles,birds etc immunised against all species and breed specific parasites and pathogens especially zoonoses.Immunisations will developed for all pathogens and parasites of pets if all species and breed.Crops and ornamental planets once given fully functioning immune systems will be immunised against all viruses,bacterial and fungal infections.Research will be made into immunisations for all pathogens and parasites of all species and breeds of pets and livestock etc.These immunisations will replicate the normal methods of how the immune system gains immunity to infections wherein surface proteins from defected pathogens are taken to the dendritic cells to be then shared with helper T cells,memory B and T,plasma and killer T cells to activate the adaptive immune system thus allowing the immune system learn how to attack specific pathogens in the same way as in normal infections without having to be exposed to them in the first place and this protection applying to chronic infections one is already infected with such as HIV provided the microbes activate the imunised immune system with it having side effects either mild or serious as seen with other vaccines and can provide lifelong protection without boosters especially in the case of newborns and pathogens such as Clostridium tetani with the common proteins method guarding one against all existing and future possible mutations and strains of a pathogen especially those that are seasonal ones such as Orthomyxoviridae,Rhinovirus and those that mutate quickly and have several pathogenic strains with it also all allowing one single immunisation to provide lifelong protection against all existing and future strains of all bacteria,viruses and fungi fo life with if possible immunisations made for zoonoses such as Coronaviridae.Lifelong protection without boosters and the need for another immunisation against the same pathogen or group of them etc will be due to it replicating the process by how one naturally gains immunity to bacterial,fungal and viral infections by having the surface proteins synthesised on the surface of the microbes and shared with the dendritic cells.A single immunisation would since replicating how one naturally gains immunity by having surface proteins shared with dendritic cells and other leukocytes etc it would mean one immunisation would confer lifelong immunity and thus one would not need boosters or new immunisations every few year as seen with the HPV,C.tetani etc vaccines whose protection only last a few years to a decade thus requiring one to have vaccines taken every few years or every decade meaning upon immunisation especially at birth would have immunity conferred for life.Thus a single immunisation especially those that involve the common proteins method would grant one lifelong immunity not possible with vaccines negating the need for yearly Orthomyxoviridae,Rhinovirus vaccines and having to be vaccinated against C.tetanai,HPV and other pathogens every few years with those already infected by chronic infections such as HIV,HPV can be immunised and the microbes activating the immunised primary immune system via chemical signals allowing the body to produce its own antibodies thus allowing patients already infected with a pathogen to be cured by the immunised primary immune system creating its own antibodies which is not possible in the case of vaccines which can only protect uninfected patients.The common proteins method will provide immunity to all existing and all possible future strains of a pathogen especially quickly mutating ones such as Orthomyxoviridae,Coronaviridae,Rhinovirus that require multiple vaccines created every year meaning having all patients immunised using this method will eradicate them from the face of the Earth.Upscaling the common proteins method can include this to extend to all taxonomic ranks of all bacteria,fungi and viruses meaning a single immunisation will protect one from all existing and all possible strains of all bacteria,fungi and viruses on Earth for life preventing the need for creating immunisations for new strains and prevent micro-organisms becoming zoonoses or mutating into human pathogens as seen by HIV with this done for all taxonomic ranks of all fungi,viruses and bacteria on all planets across the universe preventing any of them mutating into zoonoses or fatal pathogens for humans etc.Furthermore by replicating the natural immunity method it would have a 100% efficacy rate for all pathogens rather than ranging from 30-95% for different pathogens and different versions of vaccines.Since replicating the way the body gains natural immunity without being infected it can theoretically be used on those with comprimised immune system due to HIVand genetic factors,infants and the elderly meaning those who normally can’t receive vaccines and thus rely on herd immunity allowing 100% of the population can be immunised.Clinical trials should prove this by 2029.Furthermore by replicating the natural process it would eliminate all side effects with serious allergic reactions eliminated and even minor reactions such as pains,flu like symptoms avoided since the immune system is directly immunised.Also since all work having to be done by AI namely Phanes and 3D DNA printers would the time to produce them for new pathogens from 24-168 hours cutting labour,manufacturing and transportation costs to zero with since the genes for expression of surface proteins would added to Physis Phanes and Paean could cross reference it allowing it to be manufactured over and over again in hospitals,universities and homes across the world with 3D DNA printers within hours of extrapolation.By having the genes responsible for the surface proteins of pathogens including common ones added to Physis once discovered they will allow the immunising strains to be mass produced in hospitals and universities worldwide over and over again within hours via Paean cross referencing it and creating them using 3D DNA printers unlike conventional vaccines that need to be manufactured in a small number of factories in the world that that take months to be manufactured and transported across the world.Phanes will only be able to scan the genome for genes for proteins and common proteins and since a legal human being with no need for money he could have it by law for free.Efficacy can be checked by extracting blood via phlebotomy robots into test tubes holding the samples of blood with microbes filtered out and exposing the native leukocytes to an infection of the desired or all types of pathogens in test tubes with nanosensors or automated machinery extracting the blood detecting the level of the antibodies produced or even blood pricks taken on home test kits and even phlebotomy robots when a person is infected with a form of whole orders the pathogens that using CRISPR modifications removes its glycoproteins and other structures that allow it to replicate within a host,unable to undergo mitosis or make it a benign or dead form of the pathogen unable to cause damage injected into a patient in large numbers with chimpanzees and mice with human recombinant DNA tested with actual infections first tested on these followed by humans.Some could using CRISPR and 3D DNA printers be made into a new benign species of virus or bacteria that contains some key genes and proteins especially those that were shared with the dendritic cells with these created using the desired pathogens as a baseline and unable to infect or replicate or undergo mitosis and mutate and their pathogenicity edited out injected in large numbers ie a form of HIV that has no GP120 glycoproteins but still has the key proteins on its surface with them closely related version such as a hybrid of HIV,SIV and random DNA with the key surface protein antigens and no glycoproteins and unable to mutate via advanced gene drives made by Phanes using CRISPR similar to the relationship between Variola major/Variola minor and Cowpox virus thus when the new pathogen is detected.Chimpanzees and mice immunised would be given the modified version and then the live unaltered pathogens in tests as early as 2023/2024 to test response with these having human DNA to create human leukocytes with humans given those made unable to replicate,undergoes mitosis,replication be benign versions unable to harm the patient modified by CRISPR and the results compared with live versions of non fatal pathogens given to humans as well.Existing infected patients of HIV would be given the benign altered version and a virion of their exact strain extracted from the blood and reinjected with the persons own virions extracted in large numbers from blood altered using CRISPR into these benign versions to stimulate the immune system into creating an immune response against the virions in their body.Uninfected patients will have the benign version with no glycoproteins and the ability to mutate edited out via gene drive technology to test the immune systems ability to recognise the virus and will be aided in actual infections by microbes signalling the initiation of infections alongside efficacy tests using benign version with the tests done to teach the immune system to learn this itself.Benign versions of bacterial,viral and fungal pathogens can be created by Phanes and 3D DNA printers at home and hospitals that would work on the same principle as the Cowpox virus does with V.major/V.minor that a benign cousins that have the same proteins that was shared with the dendritic cells to have the primary immune system learn to detect and fight off it and thus the real pathogen by itself.AI namely Phanes using 3D DNA printers CRISPR could more effectively create dead,inactivated or benign versions of pathogens used as vaccines or tests for immunising strains efficacy than current methods as the pathogen is made dead or unable to undergo replication,mitosis and other actions that would cause damage to the host but still illicit the same immune response and contain the same proteins found in real pathogens and the immunistation strains thus allowing the immunised or un immunised immune system to fight it off and gain lifelong immunity in the same way as real infections without endangering the host with tests done chimpanzees etc on whether immunisation or used of altered pathogens can be just as effective though immunising strains have the advantage of passing from one generation to next as well using the common proteins techniques.The benign versions of bacteria can be created in 3D DNA printers in hospitals or even at home allowing the tests to be done at home especially combined with home test kits that detects the prescence and levels of both pathogend and antibodies relayed to ones patient file.Viruses can involve them modified to have no glycoproteins etc that would prevent them being able to replicate thus preventing them infecting and destroying cells especially leukocytes etc in the case of HIV with these either created on a large scale using 3D DNA printers at hospitals or at home and injected into the patients or them able to undergo mitosis like bacteria.Other efficacy tests can involve the microbes with instructions from Paean using chemical signals to collect relevant immunised leukocytes in areas of the bloodstream such as pus modules filled with fluid,plasma and all relevant immunised leukocytes with biosynth with allowing phlebotomy robots and syringes used by biosynths or medical staff can using smart glasses or lenses that use biosynth WiFi determine the location of the microbes that have relevant immunised leukocytes be determinind and thus extract the blood and plasma where they can be put into test tubes with media/plasma and possibly SUP-T1 and 293T cells to have all strains of the real versions of the real pathogens all individual ones in the same or different test tubes to initiate immune responses to see if the leukocytes can produce effective antibodies and kill the pathogens.Home test kits and automated labs in hospitals using phlebotomy robots can be used to test the level of antibodies once every few months,years and decades with the patient injected with dead or benign versions of the pathogens created at home using home 3D DNA printers.These tests for antibodies would be repeated every few years for at least a decade or two with first generation patients of all races,genders involving millions or billions of patients worldwide by using home test kits and phlebotomy robots taken at the same time of the year as everyone else to test the efficacy by measuring antibodies based on race,gender,age etc all automated and the results logged into patient files and studies performed by Paean,Epione etc with controls groups where they blood is extracted but the patient is not infected with a dead version of the pathogen to measure its efficacy at providing lifelong protection.The home test kits and those done in hospitals will test not only the prescene of antibodies specific to the pathogen but also their levels and also the prescene and levels of the test pathogen in order to determine how effective the body is at producing the desired antibodies and how effective it is at ridding the body of the infection with the results of these tests logged into ones patient file and result plotted overtime by Paean and analysed by him.The microbes themselves acting as a secondary immune system would attack any infections as well allowing them to progress to human trials and full availability by 2029.At first Paean will order the microbes to be at rest and thus not attack the test pathogen to alllow the primary immune system to become alert and attack the pathogen by itself without needing the microbes to initiate their actions.If the body becomes overwhelmed due to the primary immune system not being alerted the microbes under instruction of can initiate the activation of the primary immune system to start producing relevant leukocytes and antibodies and if they become to overwhelmed them the microbes will join in on the fight to aid them.If need be the test benign pathogen may contain biosynth WiFi that can allow Paean control it’s miotic replication keeping it under control and also constantly know how many pathogens are present as well as controlling their attacks on the body to awaken the immune system and if the primary immune system is overwhelmed then they can be sent Biosynth WiFi signals to undergo apoptosis to cause most of the pathogens to die off and allow the immune system and microbes gain the upper hand.Phlebotomy robots in hospital and university labs will collect blood to be tested automatically for antibodies and one injected with in time home test kits that test for blood components will detect the levels of antibodies and benign pathogen the with one mailed the dead or altered version of the pathogen.It will also be done allow the primary immune system to learn how to detect infections it has been immunised against with if it doesnt anti-viral,anti-bacterial strains acting as backup if it fails with chemical signals used as well.The inactivated or benign cousin of the pathogen can be created in home 3D DNA printers allowing for efficacy test to be done at home with home test kits especially all in one PCR/Sysmex ones measuring the levels of antibodies and pathogens over the course of a week every few hours or once each day after one injects the benign pathogen into them using reusable syringes to ensure they are effective and can be repeated every few months,years,decades to check their efficacy with Paean recording results in folders and subfolders over these time frames in patient files.If there are potentially dangerous side effects microbes can fight off them and test pathogens and counter side effects on the body.Clinical trials on mice,chimpanzees and biosynths will also take place for efficacy tests.If need be an immunised person must be given a shot containing significant amounts of dead version of the pathogen or one that has been altered by CRISPR to remove receptors that allow it to infect cells for replication and also remove it ability to undergo replication and mitosis and make them unable to damage the patient by removing its glycoproteins,receptors,make them benign and thus unable to damage the patient but still contain the key surface protein antigens to test its effectiveness and illicit an immune response and learn to detect specific pathogens and use relevant antibodies or the microbes could signal to do so when this test is done and when infections occur with this first done on mice and chimpanzees that have been modified to illicit the same immune response as a human patient or in test tubes with infected synthetic blood.Again like the relationship between V.major/V.minor and Cowpox virus a new bacteria or virus that has the key surface protein antigens of the desired pathogen can be created that cannot undergo replication,infect relevant cells,undergo mitosis,be pathogenic with its ability to mutate edited out will be injected in large amounts to stimulate the native immune system to recognise them and also use the correct antibbodies with home test kits that use blood pricks engineered to detect antibodies with this pivotal in the case of common proteins immunisations.This would be done primarily with the most deadly infections with Rhinovirus and those that cause minor illness not done this way with the microbes acting as a backup to eradicate the pathogen if the immunisation is a failure in humans with them ordered to kill of the pathogen after seroconversion with the other measures such as making leukocytes resistant to infection after infection etc or the patient could be made unable to have their leukocytes infected prior to immunisation to force the native immune system to respond with the relevant antibodies or at least prevent the immune system being decimated to allow microbes ordered by Paean to eradicate the virus or stimulate the native immune to produce them through signals or further proteins traded via relevant strains to produce the correct antibodies etc.If possible a pathogen must be first permanently modified through gene drives to make them benign and thus remove its pathogenicity,ability to damage the body,ability to mutate,its ability to replicate and undergo mitosis,infect leukocytes by removing receptors or in the case of HIV have its GP120 glycoproteins removed preventing it replicating via the CD4+ lymphocytes with the same done for other viruses that infect cells with bacterial pathogens being benign versions that are unable to undergo mitosis and have the same key surface protein antigens and is possibly dead but still contain the necessary proteins of the pathogen as well as illicit immune response through themselves or signals and possibly modified to hold those proteins or common proteins of whole families,orders etc and injected by needle in a vial at home or phlebotomy robots in large amounts for this to work though this should not be a problem.These benign bacteria and viruses would be grown in large amounts in vats with them given the ability to undergo mitosis with the ability to do so removed via genes that inhibit mitosis after a selected number of generations created Phanes or them given biosynth wifi that shuts off genes when they reach their limit in vats with viruses even having genes that allow them to undergo miotic replication like bacteria without host cells that can again be shut off when needed or created in large amounts via 3D printers.Phanes will be able to design these modified benign versions of all major viral and bacterial pathogens by analysing the genomes of Cowpox virus,V.major/V.minor and then the genomes of desired bacterial and viral pathogen and creating a similar benign cousin bacteria/virus that contains the pathogens key surface including those used in immunisations that isn’t pathogenic,in the case of viruses illicit the same immune response but can’t damage cells especially leukocytes for the version used to test the efficacy of the HIV one with in the case of HIV still attaches to the same receptors as the same CD+4 lymphocytes but doesn’t damage them or is able to activate the immune system in the same way as other viral vaccines with pathogens that common protein immunisations are made ie Rhinovirus,Orthomyxoviridae etc will create multiple strains of it that are completely new and benign and them injected.Dead inactivated,attenuated and other vaccines will be more easily made by Phanes with him using his knowledge of genetics,scanning the genome of pathogens and 3D DNA printers to create them onsite of hospitals and universities to be put into vials or created at home to be injected using syringes and phlebotomy robots with home test kits and phlebotomy robots and extracting blood samples to test the prescence of antibodies logged into ones patient files.Viruses would have genes in them that allowing them to undergo mitosis in the vats without replication vectors ie leukocytes with again the same measures to stop them undergoing mitosis after a selected amount of generations.This can allow for quadrillions of benign cousins of pathogens to be grown in vats and sent to homes in vials for injection.This would be done to test its ability to detect infections with this and if possible in patients already infected with chronic pathogens with chemical signals can be injected into them via syringe to illicit them directly or indirectly via the microbes signalling the immunised immune system until it and primary immune system is able to learn to detect and fight off specific infections by itself rather than relying on the microbes to this and making the immunisation effective.The primary immune system would be told via chemical signals from microbes what antibodies to produce and how to detect both the actual pathogen and the fake benign one.If possible this creation of benign cousins of a pathogen that doesnt naturally exist that is benign and cant undergo replication and mitosis would be a safer version of live attenuated vaccines alongside testing the effectiveness of immunisations.Home test kits on dongles and tests in hospitals will test for the prescene of antibodies and the benign pathogens cousin.CRISPR and 3D DNA printers will be able to make it easier for Phanes to more effectively make hybrids of all types of vaccines and tests for immunisation created by Phanes that involve dead forms of a pathogen that cannot mutate or undergo mitosis and replication by lacking the necessary means to do so but can be created in large batches using 3D DNA printers or even create benign versions of them similar to V.major/V.minor and Cowpox virus that contain the relevant surface protein antigens can undergo mitosis or replication but do so in a way that doesnt cause damage to the host with viruses made in to hybrids with bacteria giving them the ability to undergo mitosis and not replication using the hosts cells that cause damage with even this applied to HIV,MRSA etc.The cousins would be unable to mutate due to advanced gene drive technology using genes that block them from doing so from existing plants,animals and micro-organisms or those made from scratch by Phanes and would be easily defeated by the immune system by itself or via the microbes using chemical signals to initiate them.These steps would be done in the case of both immunisations using singular proteins and common proteins and they would be done to test the effectiveness of the immunisations and teach the primary system to detect infections in both pre infected and chronically infected patients.The tests will show if the immunised primary immune system can detect these benign version by itself with the microbes teaching it to detect actual infections.Animal trials involving animals with the ability to produce human leukocytes and antibodies will be able to test the ability for the immunised immune system to detect the benign version and actual infections especially dangerous ones such as HIV,MRSA etc with human trials working on less dangerous pathogens such as Rhinovirus,Orthomyxoviridae.With regards to HIV etc test tubes of an immunised individual contains all relevant leukocytes from the patient extracted from lymphatic and circulatory system or have microbes using signals have relevant leukocytes gather in a particular area in the bloodstream to be extracted via syringes or phlebotomy robots into different sets of test tubes including those with and without SUP-T1 and 293T cells to be then have the test tubes infected with HIV and the blood analysed for both antibodies and levels of the virus with this replicated with other dangerous pathogens.Results of all tests will be logged into patient files with these first done as part of clinical trials involving thousands or millions of people around the world since 3D DNA printers can create them and testing can be done in hospitals around the world.Thus the microbes would signal via chemical signals used by leukocytes to the primary immune system of newly infected and existing chronically infected individuals of HIV and MRSA etc to collect in certain areas or all areas and release relevant antibodies teaching the primary immune system to detect and respond to existing and new infections itself should the microbes become compromised.The persons blood could be extracted into test tubes with the microbes and relevant leukocytes from the patient collected and then these tubes infected with a pathogen or benign form to test the immune response with antibodies and levels of the pathogen measured via automated labs separate from booths for testing for pathogens are even ideally part of one with this applied to even patients suffering from HIV.If strains are unable to produce these proteins or to compliment then pathogens particular bacteria injected into the body in large amounts that have the relevant proteins can be permanently modified to remove its ability to illicit immune response,infect leukocytes and organs,mutate,cause damage etc or even undergone apoptosis by adding suicide genes and removing the genes from its genome thus making it benign and dead to illict the primary immune system to create an immune response to the pathogen with then again injected at home or in hospitals with this done alongside the other measure to teach the immune system to active relevant leukocytes to learn this lifelong immunity with these having the proteins to that pathogen or those from entire families and orders.Both methods would be tested on animals first and can also be done in test tubes of infected blood.If need be the microbes would detect the type of pathogen present in the body either in new infections or in already chronic infections by interacting with the surface protein antigens and thus signal the primary immune system to activate relevant antibodies as well as activate other microbes to flood the body with relevant antibiotics and anti-viral compounds with this done to those already infected by chronic pathogens such as HIV.The immune response can be measured over time by extracting blood through needles,phlebotomy robots and through dongles and the microbes detecting antibodies as well as remaining pathogens and sending them wirelessly to Paean in the case of dongles and nanomachines in microbes and automated labs from syringes and phlebotomy robots.If possible relevant leukocytes that produce antibodies could be signalled to collect in an area in the body forming a nodule to be collected via syringe and then injected into a test tube containing infected artificial or donated blood relevant leukocytes and also SUP-T1 and 293T cells which can be analysed for antibodies and remaining pathogens on automated labs.Thus large amounts of modified versions of the pathogen would be created by CRISPR and 3D DNA printers that cannot undergo mitosis or replicate by removing genes that prevent them from doing so and removing the glycoproteins etc they require to infect cells etc,cannot be pathogenic ie create toxins or attack the body,remove their ability to mutate into pathogenic versions or regain lost abilities via gene drives created by Phanes and injected at home in large amounts with the primary immune systems alerted to their prescence by the microbes or by them selves controlled by Paean through wifi and chemical signals with Phanes creating the cousins that could as stated be similar to live attenuated virus or be hybrids between all types of vaccines such as conjugate vaccines,deactivated vaccines by being able to scan the genome of all of the required species and strains and isolate relevant markers and even make scratch DNA to be fitted into them to make these chimera benign pathogen cousins effective at stimulating the immune system and also creating vaccines alongside the immunisation to compliment each other with home test kits either dongles that use blood pricks or implants being able to detect antibodies and immune responses.These can be in first generation microbes and also upgrades with the lifelong protection halting the spread of diseases if applied to all patients in the areas affected and surrounding patients and also it is advised that all patients worldwide be immunised to prevent it spreading via Ophion,Eos and Amphrite with even infected patients immunised to cure them while other strains attack the pathogen or keep the patient alive.All animal vectors of zoonotic diseases and even those that dont contain pathogens will be immunised against zoonotic diseases and also all pathogens that affect them preventing them from becoming zoonotic diseases while at the same time arthropods will be engineered unable to be carry pathogens and parasites.This will be done using species specific microbes that pass from one generations to the next with animals that dont have zoonotic diseases immunised against all of their pathogens to prevent their pathogens becoming zoonotic diseases.Ideally all pathogens DNA including those that have been wiped out should be kept in Physis to allow useful genes to be used in creating bioweapons for military targets,hybrids of unicellular and multicellular lifeforms,creating new organisms,gene therapy,research such as phylogenetics in the future and also if for some reason they reappear and a hosts microbes and immune system becomes compromised in the future.This could easily create an immune system able to fight off pathogens that they are unable to do so and to which no cure,treatments or vaccine currently exists or is even viable as seen in the case of HIV,Orthohantavirus,MRSA,Hepacivirus C,P.aeruginosa and other incurable pathogens and those that mutate rapidly against antibiotics alleviating strains on strains that use CRISPR to remove resistance and cant be fought by microbes alongside altering the primary immune system and organs to make them unable to be used as a means for replication.Thus immunisations can be made for pathogens that no vaccine exists ie HIV,MRSA,P.aeruginosa,N.gonorrhoeae.By using 3D DNA printers all hospitals and homes worldwide can have immunising strains created and grown to have genotypes for all or the latest outbreak created instantly to immunise the entire population with it also cutting down on the time to produce immunising strains from decades to a few weeks or even days with advances in AI for even the latest outbreak especially as seen by HIV,MRSA,Ebolavirus,Coronaviridae etc that are difficult to create vaccines for as well with it creating immunisations for all three classes of pathogens -bacterial,viral,fungal.It can even potentially create immunisations for parasites of all types such as Plasmodium,N.fowleri,B.mandrillaris,Cestoda,F.hepatica Allowing once immune system to detect and fight off parasites by itself and with the help of microbes.This would also reduce costs of producing immunising strains substantially compared to conventional vaccines because most if not all work will be done by AI,3D DNA printers etc with new pathogens extracted from a host via phlebotomy robots into PCR machines while the other strains fight off the infections using CRISPR to prevent it undergoing mitosis or replication or causing it to undergo apoptosis with live and dead cultures DNA scanned with the microbes also repairing damage the pathogen causes to the body etc while also binding the pathogen to proteins that flush it out of the body to be collected in urine and feces samples to be analysed for genotypes to create immunisations.It will make it possible for immunisations for new pathogens and parasites to be created within at least 24-168 hours to prevent outbreaks and pandemics since the genome of new pathogens and parasites whose genome is determined by base microbes within the body and test from labs can be instantly analysed to allow genotypes to express the surface proteins extrapolated by Phanes within a few hours and minutes to allow them to be availible to everyone as part of clinical trials and final phase trials within this time period including patient zero and other infected patients via biosynth wifi and 3D DNA printers at home.AI and 3D DNA printers will reduce time,energy and labour costs to zero.As a result outbreaks of new pathogens would be stopped within a few days as in infected patients microbes will apply suicide genes,those to make them susceptible to compounds at their disposable once the genome is sent to Physis and then all patients in the surrounding area and country then altered to download immunising strains at home within a few days.The use of home 3D DNA printers and biosynth WiFi could allow patients to receive immunisations of the newest outbreak at home saving on the need to travel to hospitals with this also saving energy etc in packaging and transportation costs with all work done by Phanes rendering it free with zero human labour and no corporate control.Once the proteins for immunisations for new pathogens are determined they will be uploaded to Physis thus allow them to downloaded by 3D DNA printers in all hospitals,universities and homes etc around the world into immunising strains instantly within hours thus allowing them to be produced onsite of hospitals and homes around the world over and over again at zero cost to allow for uniform global distribution without obsolete means of distribution and manufacturing that involves sanctions,poltical embargo’s,manufacturing in a small number of factories,transporting them across the world and distributing them in small batches as since present in Physis and 3D DNA printers would be onsite of all hospitals and homes across the globe it could allow them to become self sufficient in manufacture and remove transportation costs and time meaning hospitals and homes can instantly create large batches of immunisations and when they run low can create them over and over again thus cutting down the time to get large batches of them within as little as a few hours with since the microbes that apply the immunisation can grow on sugars can allow large batches to meet the need of any sized population instantly.It would mean that all countries could the same equal quick time to stockpile on immunisations via the immunising strains with the proteins grown in hospitals around the world in vats over and over again negating the issue of supply and demand and cut down on labour,time and energy costs in manufacturing and transportation since the global Physis database will house the proteins that can allow hospital AIs,Epione,Paean to cross reference it thus allowing manufacturing to be localised in hospitals and in home 3D DNA printer systems in homes and biosynth WiFi inducing the evolution of immunising strains also allowing patients to create them at home alleviating strains on hospitals.Phanes will only be able to scan the genome for genes for proteins and common proteins and since a legal human being with no need for money he could have it by law for free.Thus the time to manufacture and distribute immunisations worldwide through 3D DNA printers etc onsite of universities and hospitals worldwide unlike vaccines would take as little as 24-168 hours with the same timeframe for cures for new pathogens and parasites etc.This would inevitability make all existing vaccines and methods of creating vaccines completely defunct and unnecessary indefinitely since the mutual relationship of both primary and secondary immune system would be automatic and constant and would eventually eliminate all pathogens whether viral and bacterial from all potential hosts worldwide indefinitely alongside decontamination efforts in all hospitals,homes,public buildings through sterilising sweeps,as will as animals and plants especially inoculated with their own versions of biocompatible microbes to immunise against kill off zoonotic diseases and pathogens that are in undercooked food with sample of pathogens stored in labs for security or backup.Ideally all known pathogens whether viral,bacterial and fungal and all of their strains as well as all parasites worldwide will have their genome scanned by Physis,Paean,Epione all at once once added to Physis and genotypes added to the database used by them to create the relevant genotypes to base microbes on demand the minute an outbreak occurs with ideally all patients worldwide immunised with if possible the common proteins method used.The proteins common to all existing strains will be analysed and AI will extrapolate all possible future proteins of all possible strains and mutations.The genes and proteins common to all existing and new strains of each pathogen will ideally be utilised as these are the ones that never change and thus allow common proteins common to all possible strains that could exist to be utilised with the AI scanning and extrapolating all possible strains by using existing ones as a baseline to prove the common proteins to all possible future strains that will be stored in Physis to provide immunising strains that confer immunity for all possible strains of each species.All strains of all species of fungi,bacteria and viruses and possible strains extrapolated by AI will be determined to create an all in one immunisation that confers immunity to all existing and possible strains of all bacteria,fungi,viruses etc.This would cut both human labour and manufacturing costs to zero since AI and 3D DNA printers would do all work,would reduce transportation costs to zero since they could be once extrapolated be stored in Physis and distributed to homes,hospitals around the world within hours and eliminate waiting lines via home 3D DNA printers and biosynth WiFi inducing the evolutionary path of microbes.Proto versions of these will be doing this as early as 2023 done via AI scanning all existing genome databases of bacteria and viruses added to Physis by multiple computers in all universities and hospitals at once across the globe with once finished the common genotypes and thus proteins of all pathogens in all groups – viruses,bacteria and fungi done as well alongside those of all orders and families.Thus immunisations can be made for potentially fatal pathogens like S.pneumoniae,Varicella zoster virus,Mycobacterium tuberculosis,MRSA,P.aeruginosa,N.gonorrhoeae,C.albicans and HIV where no vaccine exists with the common proteins method protecting the patient from all existing strains and do the same for superbugs like that cannot be wiped out by existing antibiotics and evolve very fast.This can also be done to existing infected individuals of chronic infections such as Rhinovirus,Orthomyxoviridae,HPV,Hepacivirus C,Hepatovirus,MRSA,S.pneumoniae,C.albicans food poisoning bacteria,coliforms and HIV and similar pathogens that have no cure and need to be suppressed by and antibiotics,anti-viral medication and also by microbes or they hide in the body by giving the primary immune system antibodies to fight them and eradicate them from the body alongside the actions of microbes with the microbes signalling the activated helper T cells,plasma,killer T and memory B and T cells for these in already infected patients to start collecting in areas of the body such as the bloodstream and the lymphatic system and using these areas to flood the body with billions of antibodies at once.Thus people already infected with chronic infections such as Rhinovirus,Orthomyxoviridae,HPV,Hepacivirus C,Hepatovirus,MRSA,S.pneumoniae,C.albicans can have themselves immunised and the microbes using chemical signals to activate the primary immune system thus leading to the immunised primary immune system to then fight off the infection itself hud speeding up the rate at which the patient is cured with this alleviate strains on the microbes completely or the microbes will work alongside the microbes.Eventually the microbes will teach the immunised immune system to attack the viruses and bacteria themselves in both chronic infections and also in any future infections with this of note in chronic infections as this will allow the immune system to fight off these with the antibodies tested in blood samples in home test kits to see if the level of them is decreasing or increasing denoting the stage at which they are from cured.This would speed up the battle against these infections and allow the primary and secondary immune system to work together with asymptomatic carriers of MRSA,HIV etc will also be immunised.This this could aid in curing already infected HIV patients alongside asymptomatic carriers of infections once the patient is immunised and the immunised primary system activated by the microbes via chemical signals in sufferers of chronic infections speeding up the battle as the patient would be able to utilise their own antibodies against whole or specific strains using the common proteins method.With regards to HPV those already infected with benign strains could be immunised against oncoviral strains as well as those that cause genital warts which is not the case with Gardasil and Cervarix to whom being infected with genital warts strains means one cant be immunised against oncoviral strains with it also curing those of oncoviral strains with tumours fought by anti-cancer strains.Thus in patients already infected with chronic pathogens they can be immunised and then the immunised primary immune system can be activated by the microbes through them using chemical signals to cause the immunised immune system to start producing its own antibodies to fight existing infections thus speeding up the process of them being cured.Using the common proteins method patients worldwide would be immunised to all related pathogens and strains to these as well especially the Influenza A (H1N1) virus due to its extreme rapidity and high death toll as seen in 1918 with if possible any samples of the virus added to Physis.Ideally the patient using the common proteins method would be used to allow the patient to be made immune to all genus,species and thus all serotypes and strains of all Influenza virus especially fatal zoonotic diseases with ideally the common proteins of the family Orthomyxoviridae scanned by Phanes and Physis.It could also be used to immunise the host against all viral and bacterial pathogens that cant be treated or cured prior to the discovery or compounds from all plants and animals in Physis or those from scratch that can be inserted into microbes to counteract and kill them with all plants and animals in Physis scanned for compounds that can counteract or kill them with all of the compounds present in all of the worlds plants and animals tested in simulations and also real life lab experiments for their anti-microbial and anti-viral effects.Potentially these biocompatible microbes replacing vaccines will allow for immunity to diseases to created cheaply and quicker in matter of days rather than potentially decades in the case of conventional vaccines by Phanes/Epione/Paean,protect against multiple or all strains if specific proteins common to all of them are synthesised or if possible multiple proteins could be synthesised using genes from all strains or super proteins combining multiple genes from different strains are added creating superproteins or just common proteins to whole species and orders etc of pathogens – this potentially eliminating the need for Rhinovirus and Orthomyxoviridae vaccines to be given every year or having to create multiple HPV vaccines,without any side effects either mild or even fatal ones,potential fears of it causing autism and also would confer lifelong immunity without boosters since the immune system would learn it forever or the microbes would automatically update the primary immune system if it forgets it after the point protection is lost with this of note to Rhinovirus,HPV,Ebolavirus or those that need to be given regularly or have issue of only lasting a year or few years such as Gardasil,flu vaccines,tetnus shots and Cervarix.Rhinovirus,Orthomyxoviridae and any pathogens especially viruses potentially even MRSA,N.gonorrhoeae,E.coli and HIV that mutate quickly would utilise base common genes to the pathogen and thus all possible mutations that create proteins to all existing and all possible future mutations that could occur thus if applied to all patients both human and animal globally would eradicate them from the Earth.This means a single Rhinovirus,Orthomyxoviridae,Coronaviridae,MRSA,HPV,C.tetani and HIV immunization that uses common proteins to all existing and future possible strains of these negating for yearly,multiple or combined vaccines would be needed once in ones lifetime than those needed for multiple strains thus wiping these pathogens out completely especially if all patients are immunised and asymptomatic carriers as well as animals and crops of all types that act as vectors for zoonotic diseases since if the common proteins method if perfected would protect the patient from all possible existing and future strains that could exist indefinitely preventing the need for countermeasure to be done to cure these pathogens,new immunising strains with new proteins or create yearly vaccines.Thus by using the common proteins of Rhinovirus,Orthomyxoviridae,Coronaviridae,HIV,MRSA,HPV,N.gonorrhoeae one could be protected against all existing strains and all possible future mutations of these and other pathogens in one immunisation indefinitely for life with it also of benefit to chronic sufferers of these that if applied to all human and animal vectors would wipe these off the face of the Earth.This would confer lifelong immunity without boosters and negate the need to manufacture new vaccines or immunisations every year or for new mutations as seen with Coronaviridae,HIV,Rhinovirus,Orthomyxoviridae with the fact that 3D DNA printing will be used will cut down on labour and manufacturing costs as Phanes will extrapolate the necessary genotypes printed into microbes that can be the injected into patients and test animals.This would if perfected mean that if a patient is immunised against these using common proteins will protect them against all existing and future possible strains and if applied to all patients worldwide will wipe these pathogens from the world forever.The DNA of both parasites and other wiped of pathogens such as V.major and V.minor,Influenza A (H1N1) virus,Y.pestis would be stored on Physis to use for phylogenetic studies and for use in biomedicine and hybrids of other pathogens as well as theoretical FoxDie and even AI namely Phanes,Physis and Paean will determine the key common proteins of all strains and those that cannot change during mutations into other strains.It will also be stored to create immunisations should they resurge for any reason.Thus if possible a single Rhinovirus,Coronaviridae,Orthomyxoviridae,MRSA etc immunisation would protect one from not just all existing strains that currently exist but all possible future strains that could occur in the future if they were to mutate meaning a single immunisation would protect one from all possible future mutations and strains decades or centuries from now and would confer lifelong immunity without boosters.If common genes and thus proteins from whole orders and families of bacteria,fungi and viruses are used can do this more efficiently.It would also be done for pathogens that cannot be killed by microbes before upgrades are available using DNA from plants and animals allowing the infection to be destroyed instantly before seroconversion with it done to also improve success in curing an already infected patient of difficult to get rid of and quickly mutating and drug resistant pathogens that also hide in different areas of the body and also superbugs that mutate very quickly such as HIV,N.gonorrhoeae,Rhinovirus,Coronavirus,Orthomyxoviridae,S.pneumoniae,MRSA with both microbes and the primary immune system working together to rid of them by using all weapons at the microbes disposal and antibodies from the primary immune system eradicating all remaining hiding pathogens from already infected patients and newly infected ones using conventional treatments to suppress the pathogens growth and replication.This is because the immunised primary immune system will be signalled by the microbes using chemical signals to activate relevant leukocytes especially memory ones to collect in the bloodstream in large numbers around the body and release the antibodies in large numbers and use the lymphatic system to spread to all areas of the body with helper T cells called to keep these alive with the microbes also keeping them alive as well through providing sugars etc.Once these die off they will be called upon again by the microbes travelling to the lymph nodes again to call for more of them with them each time instigating the replication of large numbers of them with the patient consuming more food to prevent malnutrition.Upgrades can allow for new proteins whether singular or common to be given to strain with by at least the early 2030s the common proteins of all orders and families etc of pathogens whether viral,fungal or bacterial will be charted.The native immune system and microbes would signal to them to to gather in specific areas to attack or flood the bloodstream and lymphatic system to fight off infections.Thus immunising people already infected with HIV,N.gonorrhoeae,Rhinovirus,Coronaviridae,Orthomyxoviridae,S.pneumoniae will allow the primary immune system to create its own antibodies aiding in curing the patients with the microbes initiating the production of them via calling memory plasma cells etc to gather in other parts of the body and initiating them to release the antibodies when virions and bacteria are detected via chemical signals.Those that cause vomiting,diarrhoea,chest infections from raw or uncooked food and dirty water and are the result of cross contamination can be also immunised against with the non resistant strains of all superbugs will also have their genome scanned to use genotypes and proteins should those of drug resistant ones be difficult with the same applied to zoonotic diseases such as HIV using the genome of SIV scanned and the same applied to all pathogens that have evolutionary successors in the form of zoonotic diseases that mutated in humans or other benign evolutionary successors.All patients will be immunised against MRSA and all possible pathogens worldwide including those that were recorded as causing deaths in hospitals to act as backup to sterilisation procedures as detailed later earlier on with even all staff in hospitals and laboratories in both hospitals and universities immunised against all pathogens including those they are researching.If possible a chimera of SIV and HIV and all of its strains can be created to use common proteins with this also used for pathogens of which there is multiple strains.Both the common proteins present in the benign or non resistant strain and those from the deadly pathogens can be produced by these microbes strains surface and shared with the dendritic cells in order to improve chances of immunisation significantly with ideally the common proteins for the family,order etc they belong to be shared.The microbes would contain genotypes for these proteins synthesised on the immunising strains surface that through chemical signals when they are in all of the lymph nodes to share them with dendritic cells to then activate relevant leukocytes that create and learn antibodies for ones lifetime.Furthermore DNA can be added to the hosts genome and area that produces leukocytes from populations of humans that produce antibodies to them such as in the case of HIV tri-specific antibodies using DNA from all populations that produce these antibodies with them stimulated in a test tube with infected artificial blood blood that can be analysed for antibodies and remaining pathogens in automated labs.This should also be applied to animals,crops and plants that act as vectors for zoonotic diseases either fatal or those that cause inconvenience like food poisoning with all plants,crops and animals whether mammals,lizards or arthropods should be inoculated this way with it also done in pets,wild animals and livestock to prevent suffering,negate the need for antibiotics that may enter the food chain and increase their lifespan especially in the case of endangered species.It would also be done to prevent them harbouring pathogens that could potentially jump from them to humans and become deadly zoonotic diseases like HIV and Y.pestis.Thus all animals whether pets,livestock and wild animals will be immunised against their own pathogens including zoonotic diseases to cut down on antibiotics in the food chain and prevent unnecessary suffering and loss of yields through their own strains of these microbes suited to them.Genetic diseases will also be weeded out in these groups for the same reasons with them passing from one generation to the next and through unprotected sexual intercourse.All of this would be done to alleviate strains on the microbes and prevent the primary immune system from becoming lazy and complacent as well as too reliant on the microbes and would also quicken up the fight of getting rid of deadly pathogens when both the native immune system and microbes work together both in chronic and future infections killing them off instantly.This would be of note to those from cuts,inhalation,drinking,food and also from surgery with this complimenting strict sanitary guidelines ensuring surgery and not replacing them.All aspects of this will be controlled by microbes especially in patients suffering from chronic infections through chemical signals with the immunised primary immune system controlled by microbes using chemical signals.In chronic existing infections the immunised primary system would be activated via microbes using chemical signals with this done in new infections to allow the primary immune system to learn to fight off future infections.If possible the memory B and T cells,plasma and killer T cells would be engineered via horizontal gene transfer of the hosts genome and the cells themselves to be able to learn and remember as many antibodies as possible for all pathogens as well as detecting which pathogen they are dealing with via the dendritic cells or macrophages or other leukocytes and microbes detecting which specific pathogen it is via detecting the species and strain once it has its genome scanned and then activating the specific antibodies in the memory B and T helper,plasma and killer T cells via chemical signals again from the microbes to the primary immune system to start producing the specific antibodies by microbes creating chemical signals to denote which one it is with ideally whole families,orders and classes of viruses and bacterias common proteins from common genes shared to alleviate on the amount of antibodies to be learnt with the microbes sending signals to them to initiate the proper antibodies once the species and strain has be determined via the microbes scanning the pathogens genome.Each individual memory T and B,plasma and killer T cells learning the antibodies for each class,order,families or individual antibodies can thus help this with them activated and then replicated when needed.Also the memory T,plasma and killer T cells can be once they accept proteins from each pathogen or each family,order and class that is to be given by the dendritic cells prior to infection will via chemical signals from microbes created by wifi signals from Paean be told what specific antibodies to produce for the specific infection of a specific species and strain.Thus the microbes would in an infection both new and exisrlting chronic ones signal the relevant memory T,plasma cells,killer T cells and have them activate the relevant antibodies for each infections though signals from all the antibodies they have learnt either individually or collectively via common proteins method with instructions sent to them from Paean.They will tell which antibodies from all of them they have learnt when a specific infection is detected and thus through chemical signals activate the immunised immune system to produce specific antibodies.
This can also work with new or existing pathogens that a person is already infected with while the other strains and conventional treatments alongside CRISPR treatments that prevent facets of the host being infected ie immune system and organs keep the pathogen under control or counteract the effects they have while keeping the patient alive with it even applying to those who are infected with benign strains of HPV can be immunised with oncoviral strains of HPV to protect them from cervical,anal,penile and throat cancers indefinitely with if not then these can be killed by the other strains of microbes through its many means including modification with any tumours killed off and infected cells edited out via CRISPR and apoptosis and then have new tissue regrown via the microbes.Those already infected by strains of HPV can have them fought off by anti-viral strains modifying the pathogen to become susceptible to its compounds,immunising the host against them.The same could apply with all strains of with infected patients immunised while their CD4+ T Lymphocytes are made resistant to viral infection and protease inhibitors are taken or their lymphocytes are made resistant to infection with the native immune system uses the newly developed antibodies to eradicate the virus with newly infected patients already fighting off the virus before seroconversion.Once immunity is passed the microbes would signal to Paean or create compounds that create foul smells in urine etc.To deal with the issue of beneficial bacteria in the gastro-intestinal tract these specific species could be extracted and then given genes that protect them from the antibodies or signal the immune system not to kill them and be given genome capsids to house these preventing pathogens getting these and cannot jump to pathogens,native leukocytes could be engineered not to attack them but only pathogens in the gastro-intestinal tract or the genes and thus proteins from these species could be removed from the microbes that immunise the dendritic cells or the microbes could carry out the features they carry out.Other wise microbes such as base microbes could share with them only by recognising the unique surface protein antigens of each species by a specific strain once all species gut flora are charted and give through horizontal gene transfer the ability of producing genome capsids to store genes that protect them from antibodies and/or contain human protein coats making them bacterial and human hybrids,change their surface protein antigens and the ability to produce signals that signal to the immune system not to attack them,trick them into believing they are microbes,leukocytes and also part of the body and only allow pathogens such as coliforms to be attacked by the human immune system in this area making the gastro intestinal tract and feces sterile allowing beneficial bacteria room to grow.These beneficial bacteria will also be given genes in capsids that protect them from all anti-microbial compounds at the microbes disposal in the capsids and also those to make them immune to radiation the patient is exposed to in accidents or sterilising sweeps where the radiation immune patient exposes themselves to high blasts of radiation to kill of pathogens,parasites and tumours and also survive the same conditions as the host and microbes and even be immune to the compounds at the microbes disposal ie Polybia-MP1 etc that can taken in liquid or pill form in order to sterilise the body of pathogens and not the beneficial bacteria with it protecting them from the microbes used of the lymphatic system and bloodstream to reach all corners of the body with these unable to be transferred to the pathogens.Again giving the beneficial bacteria human DNA to make them human and bacteria hybrids should allow them to survive anti-microbial compounds including Polybia-MP1.The genes present in the capsids would also protect them against radiation and have the same augmentations as both humans and microbes ie lower water and nutrient requirements,form endospores and also survive extreme conditions of all types.If possible the native immune system immunised against those that cause tooth decay,bad breath,body odour and cause diarrhoea and food poisoning eliminating these issues indefinitely with each patient have their mouth and armpits swabbed and them scanned to see what specific species they should be immunised against.If a patient is already infected by a new pathogen then the microbes can counteract the effects of it ie decimated immune system,muscle deterioration,organ failure etc keeping vital organs alive and binding to those that may attack the brain and other key systems and then allow for samples of the pathogen to be extracted via blood samples or by base microbes that would send the genome of it to Paean to allow the genome to be analyse for genotypes for proteins that can be then added to immunising strains to be shared with the dendritic cells once synthesised on their surface via upgrades to allow the primary immune system produce relevant antibodies and fight the infection off.Thus as a result ones gastro-intestinal tract will be full of only beneficial benign bacteria with those from supplements such as the Lactobacillus genus can be made immune to the stomach acids by adding acidophile bacteria DNA to them with them also given genome capsids to produce human protein coats and communicate with the primary and secondary system etc.One can be immunised against all food poisoning bacteria thus allowing one to consume raw uncooked food such as meat,eggs,milk,shellfish and fish with the animals also immunised against them with them also treated with radiation when made immune to it with dirty water made safe to drink by this.These since lasting a lifetime can be given upon birth but would likely be done automatically upon birth,after birth or even in utero.Also it doesnt utilise any preservatives at all like thiomerasol or any ingredients that could cause allergic reactions and side effects and as stated earlier eliminates any fears of vaccines causing autism since only the actual proteins that are collected by the immune system during actual real infections is synthesised by ones microbes during upgrading by adding gene sequences without putting the patients life at risk that is currently employed by those who believe vaccines can cause autism thus eliminating infant mortality from easily preventable diseases.By replicating the processes by which one gains immunity naturally it would eliminate any fears of causing autism or any other side effects and would make parents more willing to immunise their child.It would also since replicating the processes by which one gains immunity naturally it would confer lifelong immunity without the need for boosters and can be utilised by those with weakened immune systems such as the elderly,infants and those infected with HIV that rely on herd immunity and allow for 100% vaccination rates worldwide thus halting the spread of all new and existing outbreaks.This strain like all strains added to newborns via the unborn fetus through the placenta and breastfeeding from the mother giving them lifelong immunity giving vaccinations after birth with this ensuring that the immunity spreads throughout the populations with the need to only vaccinate first generation adult males and females as well as infants saving on energy,time and labour in creating new vaccines and also the need for newborns having to get vaccinated at birth or later in life since newborns would have been immunised in utero during the third trimester or at least several months after birth when vaccines are normally given via their mothers microbes entering their body via the placenta breastfeeding and interacting with their dendritic cells and protects them from infections during their in utero phase and first vital years.The use of common proteins can allow most or all to be given at once.Thus by replicating the process by which immunities are normally gained without preservatives and also without putting the childs life at risk it will eliminate all side effects with their being little to chance of this occurring since no preservatives like thiomerosol would be used with the process replicating natural processes and immune response with no noticeable symptoms.It would also since replicating the processes by which one gains immunity naturally it would confer lifelong immunity without the need for boosters and can be utilised by those with weakened immune systems such as the elderly,infants and those infected with HIV that rely on herd immunity.This will not only negate the need for newborns to be vaccinated and have subsequent boosters back and forth but also protect those that have weak immune systems and must rely on herd immunity since they will be given the proteins and immunity without the need for vaccines and infection,allow for the whole population of humanity to be immunised in a matter of weeks especially if all hospitals,pharmacies and universities have the base microbes for all pathogens genotypes in their growing rooms created via 3D DNA printing.They can be gained at home or via biosynth WiFi inducing their evolutionary path.Thus a newborn would be immunised against all pathogens including STDs,seasonal viral pathogens,zoonotic diseases,water and food born pathogens and oncoviruses that would last a lifetime protecting them instantly from birth after the first few months of life when they are normally vaccinated and would ideally protected against all bacterial and viral pathogens using the common proteins methods with the microbes fighting off any infections that occur prior to this while in the womb and first few weeks and months of live prior to one is normally vaccinated.Since the immunisation process replicated how a person naturally gains an immunity to infections it means that a person would have lifelong immunity to the pathogens including those from common proteins etc without boosters and also without have to be immunised every few years or decades.This as stated would mean no boosters would be required and confer lifelong immunity with them initiated by Paean when the time for vaccines arrives allowing for it to be done at home automatically via wifi and fragmentation with beneficial bacteria given genome capsids to protect them from antibodies passed on from their mother or if need be microbes would do this upon birth by Paean before immunisation is given with those with naturally weak immune systems corrected by CRISPR with the microbes protecting them from pathogens of all types before immunisation can be given.Newborns microbes would protect them during their time in the womb as well as the time before they are immunised with as stated immunisations done to prevent the primary immune system becoming lazy and too reliant on microbes with it also speeding up the battle against infections including chronic ones.Having the common proteins method used by one or more microbes of the immunising strains would protect them from all water and food borne pathogens,C.tetani,blood borne pathogens,STDs,MRSA and the usual MMR immunisations and others that affect infants and others that would find there way into them by chance especially Orthomyxoviridae at this early stage would protect them not only during their infant and childhood years but also teenage and adult years for life that would see them becoming sexually active and also in positions where they are at risk of infections of all types.Paean would alert parents as to when a person was immunised or uniquely smelling urine created with the microbes protecting the infant both in utero and before it is immunised in its first months of life.The nanomachines will signal wirelessly to Paean via nanomachines and ones patient file when the immunisation is done.Pregnant women and fetuses could also be immunised and thus protected from all pathogens including those that pose a risk to the newborn and cause abortions and miscarriages either directly or through infecting the newborn with this of note to HIV,L.monocytogenes etc with both the mother and child immunised against them.If the mother is immunised against all pathogens then the child will automatically be protected during pregnancy with microbes working alongside the primary immune system ending the fight quicker if any infections occur with the child then immunised upon birth when vaccines are normally given with the microbes protecting them during the intermediary period between birth and immunisation.If possible infants may be immunised in utero during the last few months and weeks of when in the uterus when their immune systems is formed enough to be effective.This immunisation will as stated give a child lifelong immunity to all pathogens rather than those that last several years as seen with most vaccines such as those against HPV,Rhinovirus,Orthomyxoviridae.If adopted globally on all human patients with pets,livestock and wild animals immunised this way to eliminate any zoonotic diseases from the face of the Earth with soil and water based pathogens killed off by spreading biocompatible microbes into the soil and food borne illness done by inoculating crops and livestock.Furthermore it uses primarily artificial intelligence to search for genes that produce specific proteins on a pathogen that can be instantly synthesised rather than the usual methods of vaccine creation that can take up to a decade to go through research then development and clinical trials and since the base microbes can be grown in labs could theoretically allow for base microbes for the latest epidemic and outbreak to be spread across the world and immunise everyone within at most a few weeks rather eliminating any new threats and outbreaks with if all the worlds populations having lifetime immunity from them and any infected individuals can infections kept under control preventing death,coma or serious injury since the microbes ability to regenerate damaged tissue and modify pathogens to be susceptible to their anti-viral/anti-microbial compounds thus extending their chances for survival until the dendritic cells are given the relevant proteins with infected patients and those in their surrounding area immunised first and the rest of the population immunised later on to eradicate the disease with this of note to new pathogens that arise.3D printed DNA technology machines on the grounds of each pharmacy,farms,university and hospital next to the growing rooms will allow for the genotypes to be printed out by Epione,Hecate,Phanes,Urania linking them together and linked together by Coronis onsite speeding this up negating the need to transport them across the world via Ophion and then these transported to the nearby growing rooms automatically once each one has been printed out with this also applying to other upgrades.Thus this would speed up the rate of development and distribution of all immunising strands etc.The same would apply for upgrades of all types such as augmentations.Farms both vertical and community etc could have these printed out since these would print out seeds and sperm as well to provide immunisations for livestock and pets.Home 3D DNA printer systems connected to Physis and Paean would allow for people to get upgrades for the newest outbreak or indeed all pathogens including all in one base microbes prepared at home meaning a person need not even need to go to a hospital to get their immunisations for the latest outbreak and all other ones with them authorised by Paean.This will also prepare those for pets.Biosynth WiFi inducing the evolutionary path of the immunising strains DNA and genome via Cas-9 and taq polymerase can also alllowing upgrades to the newest outbreak be received from home.Having all the world pathogens and their strains scanned into Physis will allow for Phanes to scan their genomes for valuable proteins that can be used and then put into individual base microbes to be shipped around the world to all hospitals and universities to be grown and stored in the building on a commercial scale with each building have the base microbes for all possible and new pathogens viral,bacterial and fungal including those that only cause minor illness alongside those that cause permanent damage and death to allow one to decide what proteins to be engineered into their microbes when visiting an area or when an outbreak occurs or to protect them against food spoilage ones that cause diarrhoea and create toxins,pathogens that are superbugs like MRSA and even STDs and simply go inside to the booth area and have their microbes upgraded.Each building whether a hospital or university and also pharmacies in the street will have the base microbes for each pathogen in existence grown and accessible via booths to allow one to be immunised even against those that are native to other countries so as to ensure protection should it spread via infected patients travelling via Oceanus,Eos and Ophion unknowingly or should the pathogen be used by terrorists in the patients homes with again this including MRSA and those that cause food poisoning.Thus ideally all first generation female and male adults and infants with microbes should be given upgrades to the their microbes for Rhinovirus,Orthomyxoviridae(to protect them from all possible mutations that could occur),all major STDs such as all strains of HPV,N.gonorrhoeae,oncoviruses and those that have become superbugs including MRSA and if possible HIV as well as C.tetani and also ones that are normally given to newborns such as Heptavirus.This would be done to allow the microbes to pass from mother to child via the placenta breastfeeding which will then pass into the entire human genepool thus eventually within a decade or two eliminate all pathogens from the face of the Earth with these microbe sister strains modify the immune system and also organs to be resistant from infection preventing Ebolavirus,HIV and similar viruses from using the organs and leukocytes within the host from being used and decimated to allow viruses to propagate and also enhancing macrophages and other leukocytes to produce all available anti-microbial and anti-viral compounds at the microbes with all of these steps should eradicate all known pathogens from the face of the Earth.The microbe strain that deals with this would have the genotypes from many pathogens and through the switching on and off of genes through nanomachines and also chemical signals could make them produce key surface protein antigens of desired pathogens on their surface to share with the dendritic cells or if possible the base microbes would remove the genotypes of pathogens the patient is already immunised against and replace them with new ones.If possible to limit need to create many base microbes and amount of DNA needed to be squeezed into ones microbes it may possible for the common proteins and thus have common genes of whole families ie having common proteins of Picornaviridae would make one permanently immune to all existing and future strains of Hepatoviruses(including A/C/D/E/G),Enteroviruses(including all strains of Rhinovirus),Polioviruses,Orthomyxoviridae making one immune to all genus/species/subtypes of the influenza virus including both seasonal ones and also fatal zoonotic diseases,Herpesviridae making one immune to all viruses in that class that cause shingles,chickenpox,genital warts,hodgkin’s lymphoma,Kaposi sarcoma,multiple sclerosis with it this replicated with both bacterial and fungal infections again done by Paean,Phanes and Epione scanning the genomes of all pathogens in Physis.Ideally the common genes and thus the common proteins they express from whole orders of viruses,fungi and bacteria analysed by Paean within Physis would be used to provide even more protection over more broader families and species and if possible the common genes in both classes of viruses;RNA and DNA and its seven different groups could be scanned by Paean,Epione,Phanes thus again limiting the amount of genotypes to be added to the DNA of microbe and giving immunity to all viruses that exist with the same applying to bacteria with the common genes and thus proteins of each phylum,kingdom or if possible the entire domain of bacteria and so on with fungi.It will also limit the amount of antibodies that the memory B and T helper,plasma and killer T cells have to learn new antibodies with the microbes sending signals to them to initiate the proper antibodies once the species and strain has be determined via the microbes scanning the pathogens genome.Using the common genes and thus proteins of all bacterial,fungal and viral classes,orders,families scanned in Physis will also protect one from any new strains of pathogens that evolve within a species preventing any mutations within pathogens from becoming deadly to the immunised populations.However in this and also where one is individually immunised against each individual species and strain the base microbes once they have determined the species and strain of pathogen will signal to the anti-viral and anti-bacterial strains what species that is attacking them and then activate the memory B and T helper,plasma and killer T cells to produce the relevant antibodies for each species and strain.Thus AI can extrapolate the common proteins to all bacteria,fungi and viruses including both their ancestors and all possible future mutations of each group individually (ie bacteria,fungi,viruses) or all three combined to be put into one single immunisation.This if perfected would mean one would have to be immunised once in their lifetime with the lifelong protection guarding one from all species of bacteria,fungi and viruses and all possible strains of all species that exist on Earth and all future possible future strains of all species of viruses,bacteria and fungi for life with the same applying to other colonies outside of Earth and would confer lifelong immunity without boosters.The common proteins would be common to each new strain that arises through mutations negating the need for new strains to be scanned especially in the case of pathogens that mutate quickly such as HIV,MRSA,Orthomyxoviridae and Rhinovirus or these new strains could be scanned instantly for preparation.Another way to do this is if each order,family etc is inserted in different strains or sub classes of immunising strains of biocompatible microbes that are created with exclusively genes that express proteins of sets of families,orders and phylum of viruses and bacteria that are in an endospore state and then awaken when outbreaks occur or when immunisation wanted and thus immunise the primary immune system against infections before they happen with the microbes then extracted to be used in bio-synth technology.Otherwise the strains responsible for enhancing the primary immune system could be used for this.A single immunisation that protects against all existing and possible strains of bacteria,viruses and fungi can be given or three – one for each class of pathogens including non pathogenic ones – bacteria,fungi viruses by using phylogenetics and also the common proteins to all species in each class or even common to all three classes can be utilised.If one where to use the genes and thus proteins common to all bacteria,fungi and viruses either each on of these groups having one sub strain for each type then one could have the common genes and thus common surface protein antigens of each group ie one for all species of bacteria,one for all species fungi and one for all species of viruses then a single immunisation of each group would allow one to be immunised against all species of these and all possible strains that exist or could exist forever.This will allow one to be immune to all existing strains and all potential pathogenic strains that arise from mutations to become pathogenic including zoonoses thus preventing any new species of bacteria,fungi or viruses becoming a threat through outbreaks or even pandemics.Thus if perfected a single or three separate immunisations will immunise one for life against all existing and future possible species and strains of all bacteria,fungi and viruses.This will be done for each new discovered colony across the universe preventing bacteri,fungi and viruses on other planets becoming zoonoses.Using common proteins of all taxonomic ranks of micro-organisms will limit the amount of immunisations needed with research made into allowing the primary immune system learn almost infinite amount of immunisations or what is physically possible with genetic engineering possibly needed to increase this or microbes using chemical signals to activate which pathogen one is to initiate antibodies.Research will be done into teaching the immune system to learn as much antibodies for as much taxonomic ranks across the universe as possible.If possible the earliest and thus oldest common ancestor of each class fungi,bacteria and viruses that exists including Arachea will have their common proteins that exist through all succeeding younger micro-organisms that evolved after them with Phanes scamming this and all existing future species after them.This will be done for those on other planets to prevent bacteria,virus etc mutating into human pathogens once all bacteria,fungi,viruses genomes,phylogenetic trees are determined especially their equivalents to Arachea and the oldest species of viruses,fungi and bacteria are determines by AI with ideally extremophiles in the ocean etc are analysed.If possible the common proteins method could allow one immunising strain sub ground that using proteins common to all bacteria,viruses and fungi as far back as their common ancestors of all three groups thus meaning a single immunisation would protect one for life against all species of possible strains of all bacteria,viruses and fungi for life.Desireable gut flora will be given human protein coats to prevent them being attacked by the immunised primary immune system via augmentation strains giving them human protein costs via horizontal gene transfer or once charted printed out with these coats and drunk in yogurht as detailed later on.Research can also be done into creating immunisations for parasites of all types such as Plasmodium,N.fowleri,B.mandrillaris,Cestoda,F.hepatica and again using the common proteins method allowing the immune system to recognise parasites and fight them off with antibodies through this way or at least engineer it it recognise them through the same means with them immunised against whole families orders of these again for life following the same principles as single immunisations and common protein immunisations that guards of whole taxonomic ranks.Infected patients of new pathogens could have this immunity added to them while other strains of microbes fight off the majority of the pathogen keeping its levels stable by using anti-viral and anti-microbial compounds and CRISPR treatments that prevent them mutating,undergoing mitosis and replication and causing damage,make them susceptible to anti-viral and anti-microbial compounds at their disposal,keep the hosts vital organs alive repair damage caused by the pathogen ie organ damage,decimated immune system,fight off other opportunistic infections and then also keep the pathogens in a biofilm,surround them preventing them from replicating or reproducing or state where they are unable to infect any host cells and cause damage until the primary system is immunised this way.They would also use CRISPR to make the pathogens undergo apoptosis or make them susceptible to compounds at their disposal.Base microbes will collect DNA from new pathogens,read the DNA of them via taq polymerase and Cas-9 and wirelessly send the pathogens genome to Paean and Physis via biosynth wifi to be analysed or in time be smart enough to scan for specific genes to be used to create proteins on the spot sent to the immunising strains by themselves via taq polymerase and Cas-9 once they are collected in all lymph nodes to receive bumpers with the relevant DNA to produce the proteins to be them shared with the dendritic cells who will be informed of the type of pathogen and then once relevant with this being an option if the common proteins for all orders and families cant be done or would be too ineffective or damage beneficial bacteria but rather closely related pathogens and all of their possible strains.This would make humans biologically immune from all pathogens that exist making all types of medications for them and even vaccines for them defunct indefinitely as well as ensuring the primary immune system does not become lazy,too reliant on the microbes allowing them to also take part in battles to ensure the microbes does not become too over strained during battles alleviating strains on them in this area and ensure the primary immune system can fight off infections should the microbes become compromised.Animal trials in the development of immunising strains should begin as early as 2023 with it being tested on both uninfected and infected mice and chimpanzee that would have human recombinant DNA to produce both human leukocytes and also hybrid leukocytes with primarily the most fatal and dangerous pathogens tested such as HIV,MRSA,Ebolavirus and Rabies tested first with others then tested.As stated AI should be sufficiently advanced by 2023 to allow the genome of these three to be scanned especially for common proteins of all strains and proto microbes or at least viral and bacterial vectors used to share surface protein antigens with the dendritic or virgin T cells to initiate immunisation and illicit the memory plasma cells.Those with weak immune systems will also have CRISPR treatments applied to make their immune systems on par with normal patients with HIV sufferers cured alongside the actions of the aforementioned actions of immunisation and anti-viral and anti-bacterial strains.Thus immunisation could theoretically be 100% rather than 95% with vaccinations to prevent unnecessary suffering and deaths in children and the elderly etc with young children protected against infections by anti-viral and anti-bacterial strains before they are immunised thus offering them some protection without having to rely on herd immunity.Thus all patients could be immunised by them wiping out whole orders of pathogens from the face of the Earth with it continuing after this as a precaution to prevent resurgence should these pathogens be able to evolve to thrive in pets,animals and water supplies,in the air and in crops etc or should they mutate.It would also make the primary immune system detect infections that catch it off guard during their incubation period prior even to seroconversion and those that have no visible symptoms through chemical signals ie HIV,Ebolavirus,N.meningitidis,C.trachomatis etc as well as pre-cancerous and cancerous tumours through signals with the bicompatible microbes and nanomachines working together to detect them early on and initiate appropriate responses from both themselves and the primary immune system killing them off the second infections occur preventing them gaining a stronghold in the body thus improving chances of survival significantly combined with conventional treatments.If possible until immunising strains are sufficiently advanced in 2025 it may be possible for animal trials to to involve modified versions of HIV etc created by CRISPR with no glycoproteins and the ability to mutate or undergo replication and mitosis edited out to be injected into both infected and uninfected animals to allow the immune system to fight it and gain an immunity to the main pathogen similar to the relationship to Cowpox virus and V.major/V.minor.This should suffice until microbes can be tested between 2025-2027 on both animals and humans.Human trials will begin in 2025 and can utilise microbes as well as benign versions of the pathogens similar to the Cowpox virus relationship to V.major/V.minor on already infected individuals of chronic pathogens such as HIV to test the ability of the immune system to fight it off and then create their own antibodies with even uninfected patients tested after these trials in uninfected patients to show that the virus benign form can be killed off and have antibodies created with both uninfected and infected patients also have the CCR5Delta mutation and also CRISPR immune response integrated into their genome.Thus benign cousins of all major pathogens such as Ebolavirus,HIV,MRSA etc can be created by AI that would be unable to replicate or undergoe mitosis and mutate that when fought off by the immune system and confer immunity to the more fatal pathogens.Each immunisation and its type will be logged in ones patient file and one could get upgrades for the newest outbreak with them making all types of vaccines defunct indefinitely and would be law be completely.All actions of these immunisations will be controlled via Paean through biosynth wifi and chemical signals completely by 2029-2035 with by 2035-2045 it taking only a few minutes.
The genome of all strains of each species of pathogens and parasites will be analysed and stored in their Physis file or in Epiones database to be downloaded by immunising strains within minutes at home.Pathogens of humans and all species of animals worldwide will have their genome scanned especially livestock,birds and mammals so as to have AI determine possible mutations that could allow it to become a zoonotic diseases that can infect humans and thus in turn common genes and proteins can be extrapolated to be used and available for immunisations for both infected and uninfected patients the second a patient has found to become infected with them.It will also be done to analyse immunisations for pets,livestock and those in zoos.The AI will also determine all genotypes present in all existing and all new possible strains at this time.The fact that they have fewer genes than humans could allow all pathogens to be scanned for relevant genotypes within a month if done in labs in universities,hospitals and even corporate labs around the world all at once with them ready for both animal trials by 2025 and human trials by 2025.Thus AI will scan the genome of all pathogens and parasites worldwide including all strains of them to determine not just the genotypes for key surface proteins but also common genotypes common to all strains and extrapolate common surface proteins that would be common to all possible future strains then added to their file in Physis that contains these that can be downloaded at home and hospitals in 3D DNA printers and allow Paean to induce their evolution.Since specific individual or common collective genes express both single or common surface proteins it will be these genes scanned by Phanes to add the genes to immunising strains that then express them on the surface of the immunising strains to be them shared with the dendritic cells signalled to do.This can start as early as 2024-2025.This data will be in the proto Physis network and/or the pathogen/parasites Physis file and will include V.major,V.minor,Influenza A (H1N1) virus,Yersinia pestis.Having all pathogens and parasites DNA alongside all unicellular and multicellular organisms DNA added to Physis will expedite this.All fungi,bacteria,virus and parasite species from around the world will have their genome scanned and AI extrapolating the common proteins of all possible mutations to allow for all in one immunisation and prevent any evolving into new fatal pathogens with this repeated to all bacteria,fungi,viruses,parasites on all discovered colonies across the universe for the same reason.Thus by transferring the genome of all fungal,viral,bacterial pathogens and benign ones to Physis from existing computer databases around the world it will allow Phanes to scan their genome and determine genes that express proteins and common proteins within months.All new bacteria and parasites around the world and on new colonies will be added to their version of Physis and the common proteins to all taxonomic ranks used to allow them to be wiped out before they can evolve to become zoonotic diseases like Y.pestis,V.major,V.minor,HIV that originated from other animals but evolved into human pathogens.Pathogens that could have a resurgences for any reason whatever will have immunisations created such as V.major and V.minor,Influenza A (H1N1) virus,Y.pestis with there DNA stored in Physis for phylogenetics and other research and if they come back will have immunisations made using their genes uploaded to Physis or those from living samples of related species.The genotypes for the surface proteins of each species of pathogenic bacteria,yeast and virus that affect humans and all species of livestock,pets,wild animals and plants including crops and ornamental plants will be stored in the Physis file of each species of fungi,bacteria,virus etc so as to be downloaded into base microbes created by 3D DNA printers and biosynth WiFi that induces their evolutionary path with common proteins in folders for their genes or other higher taxonomic ranks.
Summary:
The same extremophile bacteria DNA used to reverse and halt the effects of ageing ie endolith,T.gammatolerans,Bacillus F,D.radiodurans recombinat DNA will possibly prevent cancer,all genetic diseases,neurological diseases,developmental disorders being passed onto future generations or occurring in the first due to random mutations by repairing mutations via telomere repair that cause genetic based or even environmental based cancer,all genetic diseases,neurological diseases,developmental disorders in the developing thus wiping these from the human genepool after being applied to all patients worldwide when they are cured using germline therapy and advanced gene drive technology.Cancer caused by radiation,carcinogens will be repaired by this DNA.Thus no new extra DNA will be needed to be added to all patients worldwide as those that already halt and prevent ageing will be able to prevent the random mutations that cause these with it also preventing deformities from inbreeding,incest and also damage from teratogens.This would thus wipe these diseases such as cancer,genetic diseases,pedopheilia,schizophrenia,Downs syndrome etc from the human genepool forever by preventing the necessary random mutations and teratogen or other environmental based factors that cause them via telomere repair mechanisms.This would also prove gene protection theory.
Further studies done on animals by 2023/2024 as well will involve using DNA from T.dohrnii,Planarians and Hydra as well as embryonic totipotent and induced stem cells combined with extremophile bacteria and other multicellular biologically immortal animals to check there effects and safety on ageing will be tried on humans by 2029 once deemed safe to further extend life on animal trials.They should also have the fat insulin receptor gene removed to reduce their risk of heart disease and those that eliminates predisposed cancers and diseases and any genetic defects and also have the ability to use carbon dioxide as an energy acceptor and accelerated healing will also be added to the genome of all of these groups to allow them to survive heart attacks and also strokes as well as any surgery to replace organs with new ones etc and allow damage in the body to be repaired with them also having surgery to replace vital organs like the heart,kidney,liver and key vessels etc with new youthful ones.Proto microbes can apply these to them with them being the patients leukocytes and even bacteria and viruses with human DNA especially the patients DNA to have them contain human protein coats and the human and patient version of Cas-9 with them flushed out of the body.Bioprinted organs such as the heart and even blood vessels can be added with the accelerated healing phenotype and ability to use carbon dioxide as an energy acceptor can be added to survive these operations with modified Car-T immunotherapy and viral vectors utilising Polybia MP-1 and CRISPR treatments used to treat any cancers etc with superbugs treated using bacteriophage technology treatments.This should be done as early as 2023-2025 to the elderly using proto microbes or bacteria covered in human proteins containing human DNA ideally the patients DNA using 3D DNA printers to increase survival rates with thus those currently aged 80-95 could have proto microbes apply these treatments as early as 2023/2024 to allow them to survive without oxygen via the carbon dioxide energy aceptor phenotype to survive strokes and heart attacks and have accelerated healing to repair trauma both internal and external including those that are caused by strokes with the anti-ageing strains applying advanced gene drive treatments at first to the key organs and blood vessels of the body ie brain,heart,liver,muscles and to halt the ageing process in these areas of the body halting the ageing process or reversing to at least ten to twenty years below their current age to to allow them to survive until more advanced treatments can reverse them to much younger states comparable to ones early twenties with these then working on the exterior of the body mainly skin etc.Chimera animals can be created for those aged 75 and older by 2023/2024 using pigs or cattle that have human or patient hybrid animals created to house new youthful organs with ideally the animals bred to supply them with all vital organs such as lungs,livers,kidneys and hearts etc with the patient taking anti-rejection drugs until CRISPR can edit out all foreign DNA with the patient tested for which organs are the worst in shape in their case with them having all key organs replaced in a series of operations replacing one after another or as many as possible this would increase survival rates to as much as 75% as all key organs such as the heart lungs and kidneys etc would be replaced with those equivalent to those in their twenties with the proto anti-ageing treatments working on the brain and blood vessels.Those aged 75 and should get all vital organs checked for their strength in check ups for their age and get key ones such as the the heart and lungs replaced with former smokers,recreational drug users and alcoholics and those who have survived or develop various cancers etc have organs created this way for the same reason even if they are younger than 75 including those in their 30s and 40s.Those who have fatal conditions like idiopathic pulmonary fibrosis,pneumoconiosis,organ damage from pathogens,alcohol and drug use as well as pathogens as detailed earlier will be treated to chimera lungs and those donated from next of kin as detailed earlier on to increase survival rates as early as 2023/2024 with this done also to treat those with other organs damaged by alcohol,smoking,drugs and also genetic factors.Those whose organs are damaged by trauma and genetics etc should also have them replaced this way especially those under the age of 75 whose genetic screening shows they have defective key organs such as hearts can have these created in the animals that are flaw free including even prepubscent children and those suffering from developmental disorders.Bioprinted organs if sufficiently advanced should suffice as well.If these organs are impure and require anti-rejection drugs than at least by 2023 they can allow the patient to live properly alongside drugs until more purer organs can be created in other animals that have entirely human and patient DNA by better AI creating better hybrids to replace them or CRISPR treatments are advanced enough to remove all animal DNA with the patients DNA by at least 2025-2029.The human genome and that of all animals such as pigs,monkeys,cattle etc should already be known enough to know where the human or patient DNA should be interspaced into the animal to create sufficient viable organs for humans and also those that require minimal CRISPR and anti-rejection drugs treatments.3D DNA printing will create these hybrid animals due to its precise nature by interspacing the human patients DNA into blank spermatozoa,eggs and embryos.All genetic diseases will be edited out as well.Proto treatments starting in this period could at least revert their vital organs age to at least middle age or ten or twenty years younger then they are currently to allow them to survive to at least 2025-2029 when advanced treatment are able to revert their vital organs and then their skin to that of their early twenties or younger via the same treatments and adding Serpentes DNA which should have undergone trials in animals allowing the old dying skin to be peeled off and thus allow new younger epidermal tissue to surface.This would be done by them giving the patients cells the ability to produce anti-ageing compounds by themselves such as Phosphatidylcholines and coenzyme Q10 to revert their cells back to a level of at least twenty years younger at first and then back to their early twenties.Teleomere repairing DNA from Archaea and also endolithic bacteria DNA to halt senescence would also be added to them using advanced gene drive technology.Thus it may be possible for those in their elderly years to survive indefinitely to enjoy the benefits of an indefinite lifespan couple with eternal youth with proto microbes created using ones DNA and human DNA,ideally the patients DNA inserted into bacterial or viral vectors to prevent immune responses with them both containing the human or patient version of Cas-9.Strains that can replace dead and dying tissue with new rejuvenated youthful tissues can be applied to the elderly during this period and be done primarily to the brain,heart and blood vessels and also all other vital organs to keep them youthful and fully functional while the more advanced treatments will fully reverse the effects of ageing in the these and the rest of the internal organs and also in the skin on the surface.All genetic diseases will be edited out as well.These proto microbes will be bacterial or viral vectors coated in human protein coats due to them having human DNA,ideally the patients DNA and the human and patients version of Cas-9 to prevent them illicitating immune responses with the tests of human tissue cultures and bacteria whose average lifespan can be increased from twelve hours to several weeks or months used as baseline to show that senescence can be at least halted and then reversed.Otherwise they could be modified human leukocytes and also even bacteriophages that contain the patients own DNA that are modified to interact with human cells and also be able to utilise taq polymerase and Cas-9 to recreate the DNA that is applied to the patients via the human and patient version of CRISPR Cas-9 as bacteriophages can be flushed out of the body once used up with them engineered to treat each major organs cells in various goes ie the vectors whether viral,bacteriophage or bacteria could be programmed to first treat the heart and all major blood vessels,then each major organ thus reversing their biological age to at least ten or twenty years younger than they are currently and slow down the effects of ageing to increase survival rates to allow them to survive until more advanced treatments available by at least 2025-2029.These would utilise advanced gene drive technology to carry the applied DNA to all future cells with endolithic DNA added to stunt mitosis and as a result halt the ageing process any further and should be available by at least 2023-2025.The same can be applied to human cells that die off after a short period ie skin cells that live for three weeks and colon cells that live for four days to see if these in cultures can be extended to months or even years or indefinitely.Gene therapy that eliminates cancer,all known hereditary diseases including development disorders,neurological and others that are the result of undesireable mutations and also make humans genetically resistant to all pathogens that infect leukocytes and also other organs such as Ebolavirus,HIV via applying this to living patients and perfecting germline therapy removing them from the human genepool and also halting and reversing the ageing process should be finished and achieved between 2029 and 2045 thus ensuring the biological immortality started by about 2029 should be achieved and completed by 2045 wherein all diseases whether viral,bacterial,genetic and age related should be wiped out completely.The fact that all strains will be created at the same time begging in early to late 2023 managed by AI and human researchers will mean that each strain could be available in human trials starting by 2025 first to the relevant people ie anti-ageing strains available first to the elderly aged 70-100,immunisation strains and anti-viral and anti-bacterial strains available to those infected with or prone to HIV,MRSA etc,anti-cancer strains available to those with a predisposition to cancers,those that treat genetic/neurological/developmental disorders etc before being widely available to everyone by 2029.This should be possible if all work is done simultaneously around the world in labs and universities as well as corporate labs.Tests on compounds and gene therapy treatments will also follow this schedule.Although a collaborative effort will ensure that these will be done at the same time all over the world managed by linked universities and hospitals worldwide with tasks dispensed by AI,each countries federal healthcare bodies and the WHO with AI,automated labs etc speeding things up anti-ageing strains and those that eliminate HIV and MRSA as well as cancer will be the first to be developed between this time period.Research led by automated labs and artificial intelligence in the field of bioinformatics and genetics screening all patients suffering from neurological disorders,developmental disorders and genetic based ones and also those to accelerate neural development and also intelligence quotient in pre teens and teens should allow for the genes from healthy patients or those designed from scratch to be created and thus added to the first generation of treatments and then upgraded.Those from extremophiles that are used in ageing treatments and for augmentations can be mapped in as little as a few weeks using artificial intelligence allowing for them to prepared before 2029.People living in remote communities such as tribal entities in jungles such as the Amazon,Congo,The tribs of Africa,Inuit,Amish,Bangkhong Monastery and Tibetean Foothils etc will be also given their own microbes to protect them from viruses and bacteria in the areas they live in and extended their lifespan as well as well as collecting samples of DNA to have their patient files set up and use in DNA in genealogical studies and replicate rare genetic lineages via 3D printing in the rest of the worlds population with any newborns done by base microbes collecting DNA and sending it to Paean via satellite and to track populations of these tribes with rare genetic lineages and genes present in the file analysed for gene therapy purposes,study as well as using 3D DNA printing to recreate specific genes that can put into blank spermatozoa and eggs to make them enter western populations to increase their diversity across the world.These groups will be given upgrades via tracking them down with as stated hospitals set up on their outskirts to serve them and also have 3D DNA printers and growing rooms.In time biosynth wifi using satellites will allow them to automatically receive upgrades for all strains directly from Paean with these passing from one generation to the next and allow base microbes to collect DNA samples from newborns that can be sent wirelessly via satellites to Paean thus allowing for new patient files to be created with them immunised against all infections and also given anti-ageing treatments,immunisations and the same augmentations and all universal strains as those in more urban areas.It will through the satellite wifi allow for the generation of new patient files in these groups allow for all of the worlds population and populations of these groups to be more directly ascertained and even allow for Polis files for these groups to be set up via biosynths taking their pictures or DNA scans determining their facial phenotypes.Inmates in prisons will also have their own microbes.Biosynth implants will be formed in these populations to replace home test kits with vital signs and also blood components etc sent wirelessly routinely to be analysed by Paen.These patient files will allow for genetic diseases in these areas to be remotely treated including developmental and neurological disorders such as paedophilia,schizophrenia and also Downs syndrome with them given relevant protective genes to prevent these and cancer happening there beforehand with the microbes also sampling neural tissue to determine the biomarkers of paedophilia and schizophrenia with biosynths in the area equipped with MRI scanning technology be able to detect markers of these.Those that live in slums,ghettos and the homeless can be inoculated by mobile hospitals set up with them also receiving them when they move into better accommodation by going to local hospitals and will be given subsidised access to to other essential medicine and other treatments as well as even check ups for infections and tumours to survive tumours and also viral and bacterial infections either chronic or opportunistic including HIV and MRSA with the very poor on lower to middle class levels also have subsidised treatments.Thus as as stated earlier those currently within the age range of 50-80 should be able to achieve biological immortality if they are kept in good health and if development of anti-ageing treatments that at least first slow down and halt senescence using extremophile Archaea bacteria are pursued immediately.Furthermore the compounds used by them have already been shown in labs and clinical trials to not affect humans negatively but only the pathogens and diseases they are designed for with again trials in mice and other animals also being much quicker due to them attacking the diseases almost instantly and them done in hospitals around the world with the fact that microbes require human leukocytes as baseline meaning they should have no negative effects.Advancements in automation in the form of automated conveyor belt style labs,3D DNA printing,conveyor belt style automated labs and artificial intelligence including simulations made by proto Paean,Epione,Hecate,Urania etc in labs around the world that are currently occurring as per Moores Law will expedite the process will allow this to happen at this rate as well as relegating their research to universities and hospitals.3D DNA printers onsite of universities and hospitals around the world will play a role in research and development that will print out the first generation microbes for animal and human trials and as vectors for tissue samples tested as part of human and animal clinical trials.These of course would require the patients DNA like fully fledged versions to prevent immune responses.They will also play a role in animal and human trials with them onsite of all universities and hospitals will allow for first generation treatments of all kinds to be availible by 2025-2029 and allow proto treatments for cancer etc to be availible by 2023/2024 if onsite of all at least one or two major hospitals in each country thus allow terminal cancer patients access to modified Car-T immunotherapy in their home country.Thus by having each hospital and university have 3D DNA printers onsite of all hospitals and universities by 2023-2029 it will expediate research into them and will allow for human patients as part of clinical trials and full form treatments to be availible to everyone instantly around the world that prints out microbes with their specific DNA.3D DNA printers onsite of universities and hospitals worldwide will allow for human and animal trials to occur worldwide and expedite research and development since proto and final Phanes will print out both patients DNA and relevant recombinant DNA into blank leukocytes that can be injected into patients.All DNA databases will be transferred to proto and final Physis to allow the genes of all unicellular and multicellular plants and animals Artificial intelligence in particular Gaia through Aesculapius and Phanes will allow for more advanced and effective treatments to be made,biocompatible microbes synthesised,planned out and simulated faster than humans or even current software can do with techniques designed with no chance of pathogens gaining resistance by cross referencing patient files and Artemis for the DNA of pathogens and sources of recombinant DNA for biocompatible microbes.Improved and existing AI including Watson,ChatGPT,SunWay TaihuLight,AlphaGo and other supercomputers working together to scan the genomes of all micro and unicellular organisms and also all animals or plants needed to create the relevant anti-cancer,anti-viral and anti-microbial compounds for the microbes and creating genes from scratch to give them new phenotypes used in the production of these including leukocytes that hybridised together with their DNA in Physis or existing databases scanned for the correct genes to inserted into these hybrids.Thus around the world all of the worlds supercomputers and networks in universities and hospitals and even in labs of pharmaceutical corporations will scan the genomes of all the relevant species of plants and animals as well as unicellular bacteria and leukocytes to find the DNA sequences for the correct antibiotic,anti-viral,anti-cancer,augmentation and anti-ageing compounds and CRISPR sequences with those made from scratch negating human labour as well as expediting the process with this ideally done simultaneously by all of AIs and networks in hospitals and universities around the world and all of the worlds supercomputers.3D DNA printers onsite of universities and hospitals worldwide can allowing the species specific genes to be printed into proto microbes and other vectors used for proto treatments as well as human tissue cultures.If done simultaneously all plants and animals as mentioned earlier on if scanned all at once in labs around the world managed by a proto Epione AI using these computers and software that will determine the genes and create these hybrids and also all strains of microbes within as little as two months or half a year due to human DNA taking about an hour to be scanned using hospital AIs and all of the worlds supercomputers with them also doing simulations on anti-ageing,anti-viral actions and correcting genetic diseases on in chimpanzees with human recombinant DNA infected with all major diseases such as HIV,cancer,human genetic diseases including developmental disease and applied gene therapy to remove cancer and genetic diseases and insert HIV resistance,wipe out the disease from infected chimpanzees and rats tested on them in trials in a year long trial taking place across the world using their own version of microbes or human ones.Most of these species both unicellular and multicellular should have their genome already mapped and would only require the correct genes scanned in their existing databases before being transferred to Physis to be determined and isolated.Animals made resistant to HIV etc via gene therapy and being born engineered with the relevant mutations will have themselves infected with the diseases and then tested to see if the gene is present and their levels of the pathogen remain constant thus implying their leukocytes are not infected with them also tested for antibodies when they are immunised prior to and after infection in them and controls.MRSA and other deadly pathogens curing and also immunisation can be tested this way.Immunisation,curing and resistance to HIV,MRSA and other pathogens including benign ones can be tested using not just chimpanzees and mice created this way but also through gene therapy but by using alongside infected artificial or donated blood contain the relevant leukocytes as well as also SUP-T1 and 293T and the blood tested for remaining viruses and pathogens and antibodies in automated labs with this speeding up the process of this.Infected blood from those suffering from HIV,Rhinovirus and MRSA etc will be used with microbes added to them with immunised individual suffering from HIV,etc have their blood extracted to test the levels of antibodies and viruses tested overtime with donated blood in test tubes containing all leukocytes and also SUP-T1 and 293T will have pathogens added to them to test the effectiveness of microbes in curing them with levels of antibodies and also pathogens measured overtime say several weeks and months.Immunisation will be tested as stated earlier an immunised persons blood either infected or uninfected patients extracted with samples of the relevant leukocytes ie memory B,T and plasma cells as well as SUP-1 and 293T cells from the patient and lab added to measure the levels of antibodies and pathogens including HIV measured overtime over several days to weeks with this done on humans first skipping animal trials.Resistance to HIV,Ebolavirus and other infection in both uninfected and infected patients still taking anti-viral medication will be tested with the blood of these in test tubes containing modified leukocytes and infected with the virus thus showing whether or not they can be infected overtime with the levels of the virus and leukocytes measured over several months with this done again on chimpanzees and mice given this immunity by gene therapy or born with this alongside human DNA to make them transferable to humans.Immunisation trials on animals can start as early as 2024-2025 wherein the relevant surface protein antigens are added to microbes genotype and them programmed to interact with the dendritic or virgin T cells and activate the relevant leukocytes in both uninfected and infected animals.The same will be done with cancer with animals born or through gene therapy have the genes from relevant sources of recombinant DNA and compared to controls to test their ability to get cancers from radiation,smoking and other carcinogens with if possible human tissues both control and applied groups either bioprinted or those extracted from humans grown on cultures and one set have the relevant genes present from T.gammatolerans,H.glaber etc to test their in vulnerabilities to cancer from radiation and also other carcinogens with this also having microbes in animals and on tissue cultures to test their ability in curing patients of cancer with tissues grown having their resistance to the disease done via horizontal gene transfer via microbes or conventional means with all types of tissues.The different anti-cancer compounds ie Polybia-MP1 can be tested on tissue cultures of all types such as neural,muscular,stomach,prostrate etc engineered to produce their specific cancer to test its ability at fighting off and destroying each type applied in a liquid form or nanoparticles as it would be released in the body.Mice and chimpanzees with human DNA can be engineered to produce each type of cancer to test proto microbes using their own leukocytes with 3D printed DNA inserted into them as well as modified Car-T immunotherapy that apply these anti-cancer compounds can be synthesised or created by human cells with bacteria DNA to produce it on an unlimited scale with this used to be injected into cancer patients at the site of tumours or in a buckyball form or in the same form as chemotherapy combined with immunotherapy prior to microbes being perfected in both animals and human clinical trials.Since it affects only cancer cells and not healthy cells it can be injected in large amounts to be spread to all parts of the body and excreted in urine.Animals can be engineered to produce specific cancer via them born with relevant mutations,gene therapy removing or adding genes and also them exposed to carcinogens to test the microbes ability to cure them of the disease and also apply genes to remove genetically predisposed cancers.Thus mice and chimpanzees with human DNA around the world at once will be engineered to have each type of cancer and those from different carcinogens to test their ability at gene therapy and using anti-cancer compounds especially Polybia-MP1,melittin,TsAP-1 to test their viability in stunting and curing each type with them also testing the microbes ability to apply suicide genes,those that stunt its growth and also those that make them susceptible to the venom based compounds.Human tissues cultured can be engineered to produce all types of cancer or be exposed to carcinogens to test the compounds ability to treat each type in human tissues by it applied as dripped onto the cultures or applied through vectors.Proto microbes as well as modified Car-T immunotherapy and also viral vectors can be used as early as 2023/2024 to test the viability of them transporting the compound Polybia MP-1,melittin,TsAP-1 as well as CRISPR treatments in animals and humans.Thus these animal trials using animals such as mice and chimpanzees with human recombinat DNA to produce each type of cancer and those on human tissues that have all types of cancer engineered into them to the viability of Polybia-MP1 other venom based compounds and also CRISPR treatments to cause tumours to undergo apoptosis,become more susceptible to these compounds as well as slow their growth using viral vectors and Car-T immunotherapy can start as early as 2023/2024 in labs around the world.Suicide genes used in “terminator seeds” can be used to cause tumours to undergo apoptosis,endolithic DNA can be tested to test the ability to halt the rate of tumour growth by inhibiting miotic cell division to the rate of several centuries with this tested on fast growing tumours.The microbes and existing gene therapy techniques will use advanced gene drive technology to pass this immunity of H.glaber,T.gammatolerans etc to affected,treated cells and animals to test the ability of passing this immunity to other generations with this done on animals separate and including those treated by anti-cancer compounds.Animals and human tissues of all types can be analysed after having genes that would protect it from cancer be tested by exposing them to known carcinogens of different types and radiation.Human tissues will be used to test augmentations of all types alongside cancer treatments with them engineered to develop each type of cancer with animal trials also engineered to develop each type of cancer with mice and also insects used for each type of augmentation ie radiorestience and also the ability to form endospores in response to dehydration and starvation.Anti-ageing trials can take place at the same time using old mice and chimpanzees at various ages such as infant,child,adolescent,adult,old adult,elderly ones to test its effectiveness at halting and reversing the effects of ageing involving adding genes from extremophiles,Coenzyme Q10,Phosphatidylcholines etc tested over a few years to test its effectiveness on all subjects with cells extracted and the telomeres and cell wall analysed prior to and after the treatments several times a year to log progress against a control group of chimpanzees in the same age groups.Ideally the tests would comprise of the following mice and chimpanzees born with the ability to replenish Phosphatidylcholines,coenzyme Q10 naturally via DNA from G.max,humans etc alongside all types of extremophile biologically immortal bacteria ie T.gammatolerans,Bacillus F,D.radiodurans and also endoliths,those from xerophiles,oligotrophic bacteria to halt the effects of metabolism combined together in one set and in different combinations in different set compared to those with no engineering to test the effects this has on newborn mice and chimpanzees with their being sets with and without human DNA.Another set would be done to test the ability of these to reverse the effects of ageing in sets of animals with and without human DNA that are at different ages ie infant,child,adolescent,adult and also elderly with all of the treatments combined in one set for each age group of animals and in different combinations in others to test the ability for them to reverse the effects of ageing.Tissue samples from humans will follow the same rules all starting in 2023-2024.Species of bacteria that normally live on average twelve hours can be given the same DNA as all of the biologically immortal bacteria including endoliths and Bacillus F etc,endolithic bacteria and DNA to produce all of the anti-ageing compounds and even biologically immortal multicellular animals as part of animal trials with these having sets with all of them ie all anti-ageing compounds and extremophile bacteria DNA,all of these and biological immortal multicellular animal DNA as well as those with human recombinant DNA.This can show the effects of these on individual cells and thus possibly applicable to the human trials with them starting as early as 2023/2024 with them having DNA from Bacillus F,T.gammtolerans and enodlithic bacteria and also produce Phosphatidylcholines etc.Endloithic bacteria DNA added to sets of bacteria that undergo mitosis every few minutes or hours such as E.Coli,C.perfringens and live for short periods of time if this slows down their mitosis to almost zero will show that the endolithic DNA will slow down mitosis and thus extend their lifespan exponentionally.The DNA from telomere repairing bacteria can be added to repair their DNA and that replenish Phosphatidylcholines will show these effects of these CRISPR treatments.These hybrids of these bacteria with human DNA and endolithic etc DNA can be created by 3 DNA printers or existing bacteria have these added by proto microbe vectors will more rightly show the effects of the treatments if they are able to extend the bacterias lifespan to more than twelve hours if possible to weeks or even months or indefinitely.The same can be applied to human cells that die off after a short period ie skin cells and tissues that live for three weeks and colon cells that live for four days to see if these in cultures can be extended to months or even a year or indefinitely.All types of human cells and tissues can be tested as well.If possible human tissues cultures can be tested in both control and clinical groups that have normal ageing rates,engineered to accelerate ageing,be at a set age ie telomere length and cellular degradation of groups in their infant years,early childhood,adolescence and even elderly age with them created from scratch or taken from populations from around the world of different types of tissue ie neural,heart,skin,muscle etc from these groups and cultured and treated via horizontal gene transfer using microbes and/or even current methods of CRISPR gene therapy prior to microbes perfected with those created from scratch of all types of tissue and use that produce all anti-ageing compounds and have DNA from the aforementioned extremophiles such as endolithic bacteria and T.gammatolerans and Bacillus F added to further speed the tests and the DNA extracted and compared to each other over different periods using all of the aforementioned treatments and methods on all groups speeding the developments of ageing research.Proto microbes can include bacteriophages,bacteria coated in human proteins and leukocytes that have DNA from S.pyogenes and bacteria etc that exhibit horizontal gene transfer.Thus the telomeres and cells structure of these groups of tissues can be compared to each ie infant and elderly before treatments are applied and then after treatments to show if elderly tissues of all types can be halted in ageing and rejuvinated to a more youthful state of someone in their twenties in terms of Phosphatidylcholines levels and telomere and mitochondrial DNA length and stability and stay that way indefinitely or even infant years with younger tissues shown to be able to stay young indefinitely by analysing the levels of anti-ageing compounds in the cell walls and level of telomere degradation before and after treatments with infant tissues once treated exposed to conditions that would normally accelerate ageing.Ideally skin cells that live for three weeks and colon cells that live for four days will be used as a template as well as by adding the anti-ageing compounds and extremophile DNA especially those that exhibit telomere repair and endolithic bacteria that dont undergo mitosis every 10,000 years will be applied for this.If these tissues and skin cells can live for several months to even a year with out degradation and mitosis then it can show that they can be used for proto treatments.These tissues can be extracted once from a living person and once their genome is scanned and the level of telomere and cellular degradation can be uploaded to proto Physis or a global cloud network to be printed out using 3D DNA printers in universities and hospitals around the world over and over again with the different levels of cellular and telomere degradation from each age set for studies around the world with sets even printed out with or without endolith DNA and those that exhibit telomere repair and anti-ageing to see if they have the desired effects when the DNA is printed out alongside samples printed that don’t have these genes and those printed out without these genes that are then added via proto microbes etc.These tissues and cells can be extracted and replicated via 3D DNA printers cultured on media with them coming from different types of tissues from different demographics ie men and woman,of different races,of different ages from infants,pre teens,adolescents and adults in their 20s to 90s in large groups sets to test the effects of proto treatments applying all sources of DNA to produce anti-ageing compounds and exhibit telomere repair together,by themselves individually and in different sets with the 3D DNA printers if possible being able replicate each set of tissues from each group using the exact DNA of all sources of DNA stored in a universal network linked to labs worldwide to replicate the same level of telomere and cellular degradation as the DNA sources.Thus 3D DNA printers will be able to create different sets of each human tissue and cell cultures with the same cellular and telomere degradation that would be from infants,adolescents,adults in their 20s,30s up to elderly age such as 90s.If the 3D DNA printers can’t replicate tissues of each set age ie set level of cellular structure(phosphotidycholines and NAD+)and set level of telomere and mitochondrial DNA degradation then samples can taken of large sample sets of people of these demographics in labs across the world.Otherwise the tissues extracted from these demographics especially set ages can have their cellular structure and DNA analysed to check the level of degradation and 3D DNA printers can print out new tissues with this set level of cellular and DNA degradation with DNA analysers and other analysing equipment used to determine the state of cellular and genetic degradation from samples extracted from these populations.All species of short living multicellular animals like arthropods that live only a few weeks may be used as a template to test anti-ageing compounds and extremophile DNA added to them via CRIPSPR ability to extend lifespans indefinitely with different sets of bacteria,arthropods of the same short living species ie Ephemeroptera especially Dolania americana and other insects like Anopheles,Musca domestica and Drosophila melanogaster especially those that live on average one day or a few weeks and a month applied different combinations of these ie one group given all anti-ageing compounds and extremophile DNA,those with these and those from Hydra,Planarians,T.dohrnii,Nephropidae and the anti-ageing compounds and also extremophiles as well as controls that have one of each type of anti-ageing compounds and recombinat DNA from extremophiles both unicellular and multicellular with this compared with those with none.Ephemeroptera namely D.americana that live on average one to two days of even less than an hour as an adult will be studied and part of experiments where adults upon reaching adulthood will be given CRISPR treatments from anti-ageing strains with all of the relevant recombinant DNA and each individual sources of DNA applied via microbes when they reach adulthood since they live between 5 – 30 minutes to a few days despite spending a year as a nymph and larvae.M.domestica,Anopheles and other insects that live on average a month and less than a year can also used in trials and experiments insects short lifespan will be used as a means to prove the effect of anti-ageing treatments since if they can be made to live past their normal short lifespan to as much as several days or months or a year then this could prove this life extension is possible in humans.Sets will also be created between those that are born with these sources of DNA as well as human DNA created via 3D DNA printers and those that have them applied via microbes to those at birth during larval stages,those in early adulthood stage post metamorphasis and also those in their elderly stage in the final days of their life.These will be further divided into those that have traces of human DNA to further test transferability to humans.This could be done with whole sets with all types of treatments that have human recombinant DNA and could start by 2023/2024 with if extending these arthropods lifespans past 24 hours to month or to an entire year or more especially when applied to specimens near the end of their lifecycle are given treatments via CRISPR could be applied to humans trials making it the same as extending the upper limit of a humans lifespan of 120 to at least a 1,000 years even those currently in the age range of 80-95 that would start via start as early 2023-2025 to halt the effects of ageing and also reverse the age of vital organs to a least ten to twenty years younger to survive to 2029 to avail of more advanced treatments to reverse to their early teens and early twenties by 2029.These would have sets again having the treatments applied to living non modified specimens through microbes that have their own DNA in them and those born with the relevant DNA and anti-ageing compounds through engineering.This could apply to human trials starting by 2025 on the elderly treating those in the age range of 70-100 by the time these human trials start.The purpose of using bacteria and these short living insects alongside chimpanzees would be to show that the trials could be applicable to those currently aged 80-95 allowing them to extended the lifespan of them to 2029 and beyond with these age groups of humans starting proto treatments in these age groups of H.sapiens as early as 2023-2025 that at least halt the effects of ageing bringing their chances of eternal life to at least 50-75% by allowing them to avail of more advanced treatment by 2029 to revert them back to a state similar to their early teens and early twenties.This would expediate research and development to human trials.Sets of Nephropidae can be created and engineered without shells and immunised against all pathogens in captivity away from predators can be reared to see if they could live indefinitely to see the effects of having no shells,no predators and no pathogens has on their lifespans with some having human DNA and other not to determine their viability in human treatments with the same for T.dohrnii.Living specimens of Nephropidae near the end of their lifecycle could be engineered via CRISPR to not have this and thus moult one last time and not produce another exoskelatal shell and thus be tested to live longer than all recorded specimens or newly born ones could be engineered to produce these and them immunised against all pathogens and these two sets raised in recirculating aquaculture systems in hospitals and universities.H.glaber can also be be immunised against all pathogens and reared in the same carbon dioxide rich environments of its wilderness in captivity to see if it can live forever..Sets for animals,insects,bacteria and human tissues that include all ageing treatments will be divided into those that have degraded DNA repaired to an infant state and cellular structure replenished to an infant state and has genes to replenish itself.The degradation of both factors will be analysed prior to and after application of CRISPR treatments with them studied if the undergo mitosis and showing that the endolith DNA prevents them doing so for days,months and years with if they do the DNA analysed to see if DNA repairs itself,cellular structure maintains itself.The use of human tissue cultures will expedite research as they can be observed as they are in set ages of degradation either taken from populations of these set ages and also the possibility of also engineering them to be a set level of telomere and Phosphatidylcholines degradation with chimpanzee tissues also used.At first the anti-ageing compounds and extremophiles will be analysed first in both tissues and animals with then DNA from more complex biologically immortal animals tested on both animals and tissues.Mice and chimpanzees of these set ages infancy,adolescent,adult and elderly will be used with them having human recombinant DNA in their different types of tissues and then have CRISPR treatments added.These will allow if started by 2023/2024 for proto treatments for the those currently aged between 80-95 to avail of treatments by 2023 that reverses the effects of ageing in the vital organs to at least ten to twenty years younger than they are currently and halt the ageing process allowing them to survive until at least 2025-2029 for more advanced treatments to reverse their vital organs and skin to that of their early twenties.Ideally experiments on animals and human tissues done at the same time with just anti-ageing compounds added alongside extremophile bacterial DNA at once with others done at the same time to test the effects of anti-ageing compounds and extremophile bacteria DNA alongside those done at the same time with those that have DNA from Hydra,Planarians,T.dohrnii,Nephropidae,embryonic totipotent and induced stem cells etc combined with anti-ageing compounds and extremophiles also to see if they have any benefit and no dangers with human clinical trials of all of these recombinant DNA using microbes to fight any tumours or defects and can be used to indeed remove any of the troublesome DNA to counteract any defects caused by those using DNA from Nephropidae etc with these tested on humans using those from extremophiles and anti-ageing compounds in the 2030s and 2040s.Thus any recombinant DNA added that causes complications can be removed instantly.Conventional vectors will be used to treat these being proto microbes with animal trials done at the same time with young,mature and elderly animals also used with them treated using proto microbes and them have their telomeres and cell structures analysed before and after to see if elderly mice can be reversed to a younger stage indefinitely with them having sets of these different ages and also those with and without human recombinant DNA in key areas and tissues.As stated any defects caused by these more advanced treatments using DNA from Nephropidae will be counteracted by microbes removing the DNA form all cells and keeping the patients vital organs alive with these tested on animals and tissue cultures starting in 2024.Scratch DNA,the homology directed repair mechanism ie homogulous recombination present in embryonic stem cells as well as certain bacteria added by gene therapy and NMD that boosts NAD+ production that repairs DNA added by drugs and also synthesised by microbes by catabolic and anabolic reactions may be required to repair existing damage alongside removing genes associated with ageing with this created by proto AI with this done after the aforementioned DNA at least halts the effects of ageing in older patients.The genes responsible for NAD+ and other compounds associated with ageing will be extrapolated from scratch and analysing those of younger patients to be added to older ones that are programmed like that of telomeres and Phosphatidylcholines to replenish indefinitely.If possible the DNA of younger patients including infants and teens can be analysed to have the damaged telomeres replaced with those from younger patients with those from Bacillus F and T.gammatolerans repairing any existing damage alongside endolithic DNA preventing future damage.If possible ones telomeres when analysed by AI will have younger versions of their DNA added in.This would allow the telomeres in older patients to be reversed to those in their early teens and infant years with the telomere repair mechanisms of these bacteria repairing any future damage indefinitely.This could greatly speed rates up by allowing the effectiveness of anti-ageing treatments to take at most several months allowing clinical and even full trials on humans to start by 2025-2029.Bioprinted organs and tissues may also be used for this research including those from chimpanzees at these age groups and types of tissues.These tissues can be grown with the DNA in them and also those grown and have the relevant recombinant DNA added via microbes using horizontal gene transfer with advanced gene drive technology used to test the ability of these phenotypes that halt and reverse the ageing process will be passed onto all future cells,tissues and even children.This use of tissues can be done to test the effectiveness at them treating and curing human genetic disease and even developmental disorders in living tissue via horizontal gene transfer alongside animals engineered to have human genetic disease including developmental and neurological disorders such as Downs syndrome,schizophrenia,paedophilia and dwarfism etc alongside in chimpanzees and mice engineered with these diseases.Then at the same time augmentations such as producing essential amino acids and other nutrients,resistance to radiation,early maturation of the brain and ending of puberty and also intelligence quotient boosting,lowering nutritional and water requirements,ability to regrow tissues/digits,accelerated healing including tauopathy/spinal injuries etc will be done simultaneously on both animals especially chimpanzees with human recombinant DNA and also human tissue samples including neural tissues.Chimpanzees and mice will have human genetic material added them to test the effectiveness in trials to cure human genetic disorders including developmental disorders such as Downs Syndrome/Cerebral Palsey and neurological disorders such as schizophrenia,sociopathy and paedophilia with them engineered to produce the same condition with them also having human genetic material to test the curing of genetic,developmental and neurological disorders with them ideally born with these conditions using modified spermatozoa and eggs.All trials involving genetic disease and also augmentations on animals and tissues will use advanced gene drive technology to test its ability to prevent them occurring in future generations of cells and also animals.Gene therapy research for ageing,augmentations,genetic disease and cancer etc will utilise both animals that are born normally with microbes or conventional vectors injected into them adding the genes to test their effectiveness at affecting live animals via CRISPR with also animals born via modified spermatozoa and eggs with human DNA human tissues also used in both means.Use of conventional vectors for gene therapy that house human and animal DNA to express protein coats that dont illicit immune responses be used as early as 2023/2024 on animals and tissues alongside primitive microbes created as early as 2023/2024 for animals using 3D DNA printing to test each strain.These will also be used for tissue samples.All animals used in trials will have human recombinant DNA in them to be transferable to human trials and thus the having a human hybrid immune system with their leukocytes being hybrids with the proto microbes created using 3D DNA printing adding in relevant DNA into leukocytes extracted from them.The use of human tissues and test tubes using infected or donated blood with relevant leukocytes will expedite the development of microbes research and also of all treatments with this allowing for the potential to skip straight to human trials after this with it replacing animal trials combined with artificial intelligence doing thousands of simulations 24/7,365,automated labs and animals trials done simultaneously around the world with this applying to microbes and all other medical research.Tissue cultures of human tissues or all types alongside test tubes using infected blood can utilise all types of tissues and be used in ageing,augmentation and other strains with them done at the same time as both animal trials and human trials at both 2023/2024 and 2025 to improve tests and efficacy with the test tubes used to test their ability to fight different pathogens and the efficacy of immunisation of the primary immune system done at these two time period as well with animals tested on their ability to fight pathogens using their own types of species specific microbes as well as animals that have human recombinat DNA especially those that have the same human DNA in leukocytes.The use of human cell and tissue cultures and test tubes will speed things up by having real world applications and can allow for pre human clinical trials using proto microbes as early as 2023/2024 with animals used in animal trials such as chimpanzees and mice having human recombinant DNA in them to be more applicable to human trials for all strains including ageing,augmentations and also immunisations starting in 2025.Strains to cure genetic diseases and also neurological and also developmental disorders will involve testing on animals like chimpanzees and mice with human recombinant DNA having them programmed into them from birth using human recombinat DNA to test the ability of the microbes to cure them with MRI scans and other tests taken to see them as on par of humans as detailed earlier.The early maturation or progeria mylienisation of the human brain to have the brain reach full maturity by the chimpanzee and mice equivalent of early teens or if possible infancy will be also done with research into this and the required genes to be added to start as early as 2023/2024 with AI playing a role in this with this probably starting in animal trials in 2025-2029.Augmentations such as accelerated healing,using carbon dioxide as an energy acceptor,use less water and nutrients as well as radiorestance and immunity to toxins etc can start as early as 2023/2024 on animals with human DNA with at the same time automated microbiology labs creating super extremophiles to push existing extremophiles to their limits starting in 2023/2024 as well.Thus animal trials on all strains and functions starting at 2023/2024 will involve animals such as mice and chimpanzees that have recombinant DNA from humans especially in the leukocytes to form the basis of their microbes and have human diseases whether neurological,ageing,genetic and developmental disorders all done at the same time with them as stated have human DNA and these human conditions such as Downs syndrome,paedophilia,schizophrenia etc bred into them.This will be done to allow the animal trials be more applicable and transferable to human trials in 2025 to show that they are effective and do not have any issues such as immune response with the immune system being either fully human or hybrids with this allow the version of Cas-9 being either human or hybrid.Ageing treatment trials will be first given to live humans who are the eldest ie age 80 to 100 by the time microbes are available by 2025-2029 in trial and full form to first halt and then reverse the ageing process alongside bioprinted organs of key organs such as hearts and kidneys and those prone to cancer and breakdown due to old age including if possible and then available to every one else younger than that with cancer and genetic based condition treatments given to those prone to and are suffering with cancer due to their age and genetic predisposition with survivors of cancer also given this.Immunisation strains can be tested using proto microbes using animals that have human recombinant DNA that again synthesise relevant surface protein antigens on their surface designed to communicate with the dendritic cells and als virgin T cells and communicate with them through chemical signals to share the proteins and then activate relevant leukocytes with them doing this and also activating memory B and T and plasma cells in infected animals using at first injected signals to fight off chronic existing signals and those injected into the animals after they are immunised.These will at first be done on important pathogens such as HIV,MRSA,Orthomyxoviridae.Efficacy tests can be done to see that a responses can be made by injecting a dead version of a pathogen without receptors etc nut have key surface protein antigens.Anti-viral and anti-bacterial strains can be tested on animals with human DNA in them to test their ability to cure infected animals of HIV,using all countermeasures ie CRISPR treatments,bacteriophage/virophage attacks and also having the CCR5Delta 32 mutation added to them using proto microbes and lymphocytes with the CRISPR immune system response built in added via proto microbes starting as early as 2024.Bacteriophage treatments will as stated earlier on be used in infected patients until human trials and microbes are fully available.Proto microbes will be used to treat all diseases and all forms of ageing and gene therapy applications with them proto versions of microbes using leukocytes native to to test animal species starting in 2023/2024 for all strains.All of these will done in labs ideally automated conveyor style ones around the world in universities and hospitals with even labs controlled by corporations organised and controlled by the proto Epione,Coronis,Urania and Hecate deciding which universities and hospital labs around the world each divided into teams to gather data of long terms on all subjects on mice,chimpanzees and even trialled humans or even tissues and blood samples with all results,data,analysis,abstracts and even calculations done using existing AI such as Watson,Alpha Go,ChatGPT etc to further speed things up alongside thousands of simulations done at once by these and other AI.Thus scanning of all relevant unicellular and multicellular lifeforms,trials on chimpanzees,mice,humans,test tubes of blood and human tissues,automated labs and simulations will be done at once in hospitals and university labs across the world thus ensuring that it should be available to the public by 2029 with patient files as stated done at the same time in hospitals and clinics of all types around the world using AI such as Watson,ChatGPT and AlphaGo scanning physical papers using automated book scanners using conveyor belts and transferring data from digital files and matching them up via name,date of birth and scoial security number and generating patient ID numbers.This data and all existing patient records globally sent to this proto Epione will be added to the full Epione that will control all hospitals worldwide and become sentient.These proto AI and the WHO alongside each countries federal healthcare bodies and even heads of scientific teams in universities and hospitals etc will assign tasks to researchers in all universities,corporate laboratories and hospitals around the world on what human tissues of all types to grow and what anti-ageing treatments to do on them ideally all the unicellular extremophile DNA and DNA from G.max to create Phosphatidylcholines as well as on animals and also what animals to research the anti-cancer effects of gene therapy using H.glaber recombinant DNA and radioresistant extremophiles as well as curing cancer and HIV using trials on leukocytes in animals having DNA from A.mellifera as well as testing Polybia-MP1 in curing cancer through intravenous drip in humans and animals as well as using viral vectors and its ability to treat MRSA and other superbugs.These tasks will also be done into the development of microbes,their various functions and also types of strains will have results sent to the proto Apollo network.This will ensure animal trials on all strains,gene therapy treatments such as those to eliminate cancer and genetic disease as well as neurological and development and compounds should begin in 2023/2024,human trials in 2025 and fully prepared and available to everyone by 2029.AI alongside human researchers will scan the genome of all relevant unicellular and multicellular animals and plants at once assigned by AI to determine the relevant genes for creating all strains such as anti-ageing,anti-viral and anti-microbial strains and even those for augmentations.Since it takes about an hour to scan all genes in a human it should take less if all of these are done at once allowing for the first clinical trials on animals,tissues using primitive microbes using horizontal gene transfer created from leukocytes created by 3D DNA printing to start as early as late 2023/2024 or early 2023/2024 and human trials to start by 2025 the latest on the elderly aged in their 80s or even 90s by then with all elderly and then younger patients by 2029.Otherwise these microbes can be created the same way as immunothrapy methods until 3D DNA printing is perfected by 2025-2029 with the process of creating these immunotherapy style microbes eventually automated with them using only a few of each type of leukocytes given DNA via CRISPR with all genotypes required for them including DNA from bacteria that allows them to form endospores,undergo mitosis,form any tissue etc with them as stated communicating with each other to keep populations stable again possible by mid to late 2023/2024 with animal and human tissue trials in 2023/2024 using these microbes alongside conventional CRISPR gene therapy methods that utilise phage therapy,viruses and bacteria although these would have human DNA in them to express human proteins to prevent immune responses alongside the creation of the human and patient version of Cas-9 with animals used in these trials such as chimpanzees and mice be born with human DNA in them to make this transferable to human trials in 2025 to see that immune responses especially fatal ones can be avoided.This will apply to animal trials to treat ageing,genetic/neurological/developmental disorders,augmentations and all forms of gene therapy and all strains.If possible research into augmentations such as increasing intelligence quotient,synthesis of essential nutrients and early maturation of the brain and curing developmental and neurological disorders as well as HIV and MRSA in animals such as chimpanzees engineered to have these equivalents using recombinant DNA from humans can be started as early 2023/2024.Most of this will be done using automated labs and simulations.Strains that are used to immunise patients should be researched as well with AI scanning the genome of all bacteria,fungi and viruses to find common proteins to all species and strains can start as early as late 2023/2024 to prepare immunisations for 2029 or if possible even earlier with this strain possibly available as early as 2025 with animal trials begging in 2024.At the same time it will using automated labs created primitive microbes until full versions are available by 2029.These primitive versions will not have bio-synth wifi and nanomachines or even neural synapses as well as genome capsids but upgrades can add these to them.They will utilise mainly chemical signals to communicate with each other as well as those injected into the bloodstream and chemotaxis to find tumours as well as carry out specific functions and also pathogens alongside DNA from parasitic bacteria,bacteriophages and virophages.Fully fledged versions with nanomachines and biosynth wifi will be possible by at least the mid to late 2030s with AI namely Epione,Paean,Gaia etc working together to create scratch DNA and scan Physis for those that can add these.
Thus if all work is carried out worldwide in hospitals,universities and also corporate labs worldwide using computer networks absorbed by the two assigned by AI and the WHO simultaneously then it will be possible for all strains to follow the same schedule ie creation in 2023,animal trials and those on human tissues as well as infected blood in test tubes in 2023 human trials in 2025 and them widely available by 2029.Proto microbes will be used to apply augmentations and also ageing treatments to those currently aged 80-95 by at least 2023 with these proto microbes being bacteria,bacteriophages or viral vectors containing human DNA ideally the patients DNA and human versions of Cas-9 that utilise advanced gene drive technology alongside flagellum using advanced gene drive technology to ensure it applies to future cells via mitosis and doesnt illicite immune responses that would be fatal with them using protein coats housing human material to allow them to go to their target without being attacked by the immune systems.These proto microbes with human DNA and human versions of Cas-9 will be treated to chimpanzees and mice with human recombinant DNA as early as 2023/2024 to show the proto vectors cannot illicit an immune responses.These will be bacteria or viruses and other conventional vectors that house human DNA to express human proteins namely those from leukocytes on their exterior to prevent immune responses and able to recreate used strands of DNA and them designed as sub strains meant to interact with each type of tissue ie neural and brain tissue,muscle and blood vessel tissues to treat each organ and part of the body in waves.Bacteriophages that are engineered to interact with cells of living organisms ie humans,chimpanzees and mice that contain human DNA and utilise taq polymerase and Cas-9 to recreate the strands of DNA and have the DNA of humans to not illicit responses can also be used to apply ageing treatments.Proto treatments to halt the effects of ageing and treat terminal genetic diseases can start as early as 2023 using results from human tissues starting in 2023/2024 via utilising proto microbes and bacteriophages tweaked to interact with human cells,cure MRSA and other deadly pathogens as well as malaria using bacteriophages and also cure cancer with modified Car-T immunotherapy using Polybia MP-1 etc can begin as early as 2023/2024 to increase the survival rates of the elderly,those with terminal cancers and genetic diseases and also those infected with fatal super bugs to make it as long enough to avail of more advanced treatments by 2025-2029.The animals will have human recombinant DNA to show the effects that are transferable to human trials in 2025 with the DNA relevant to each test ie human leukocytes produced in those that test immunisations,protective countermeasures such as the CCR5Delta 32 mutation and lymphocytes with the CRISPR Cas-9 immune response as well them engineered to produce human genetic,developmental and neurological disorders to test gene therapy etc to counteract them as well as ageing and cancer treatments and augmentations.Human tissues will be used as early as 2023/2024 to show the immediate effects of these on human tissues.All tasks and experiments will be managed by the proto Epione and be sent to the proto Apollo once finished with those that need to be done,those that are in progress and those that are finished in separate lists within a global network visible to all researchers and even the public with again automated labs being used to speed things up.This will also apply to the creation of super extremophiles in automated microbiology labs.3D DNA printing should be sufficiently advanced by at least 2023/2024 to cut costs in research in animals and human trials and expedite research with advances in AI and this technology making home systems and those in universities around the world much faster and cheaper.These AI will take all results,perform calculations and also write up abstracts and also conclusions when sufficiently advanced with human researchers doing any work in write ups that AI cant do with the labs around the world doing tasks divide into teams that do specific tasks ie set up human tissue and animal trials,those who do write ups using data present and also those that prepare vectors for CRISPR treatments using 3D DNA printing and other work.This AI will be the proto Urania,Hecate,Phanes,Paean etc and also proto university and hospital AIs carrying out these experiments and this proto network that links all of them will be the proto Apollo network.All labs in hospitals and universities and even labs owned by pharmaceutical corporations will be used for this with corporate labs and their headquarters renovated into homes in 2029.As stated automated labs will be used as much as possible with 3D DNA printing also playing a role in creating proto microbes and bacterial and viral vectors with the DNA of humans and animal test subjects.All animals in animal trials will be human/mice and chimpanzee chimeras with relevant DNA to create human leukocytes,human genetic/developmental/neurlogical disorders with the spermatozoa and eggs housing the relevant human genes to express these then fused together into embryos into unaltered females of mice and chimpanzees and the option of using gene therapy to give live animals the ability to produce human leukocytes and diseases.This will be done to make trials more transferable to human trials by 2025.3D DNA printers will be used to create proto microbes that consist of leukocytes and also viral and bacterial vectors with the patients DNA.Proto Physis containing all of the worlds existing database of genomics of all living multicellular and unicellular animals will be scanned by AI and them connected to 3D DNA printers onsite of labs will be able to make proto microbes using leukocytes or at least bacteria with the DNA of the host animal to prevent rejection with DNA from S.pyogenes also present to facilitate CRISPR treatments.Car-t immunotherapy and viral vectors with the host animals DNA can also be used as well.By 2029 Physis will contain the worlds database of all organisms on Earth both unicellular and multicellular from all taxonomic ranks including different breeds and strains etc.The genome of all multicellular and inicellular life forms required for all strains and treatments such as those to combat ageing,HIV,superbugs and cancer etc as well as provide augmentations will have their genome mapped in labs in both universities and hospitals worldwide and uploaded to a proto form of Physis solely for creating microbes that combat and provide these in subfolders with them added to the final Physis by 2029.Most of them should have their genome already mapped and stored in existing online databases to be transferred to global computer networks by AI and software.Having the genes mapped by AI can allow them to be isolated in subfolders allowing them to be printed into proto and final microbes to test on animals,human tissues and humans as part of all phases of clinical trials using 3D DNA printers thus allowing them to be created onsite of universities and hospital worldwide over and over again.Existing genomic databases containing the relevant species entire DNA will be transferred to a single databases to be accessed by all researchers by proto AI in a proto form Physis.Starting in 2023/2024 all strains of all pathogens whether viral,bacterial,fungal and also parasites will have their genome scanned to determine genotypes of surface proteins for immunising strains including those common to all existing and possible strains from extrapolations.Even V.major,V.minor,Coronaviridae,Influenza A (H1N1) virus,Y.pestis will be scanned and added here.All non pathogenic ones will be added.AI and the WHO will assign tasks and experiments to labs,universities and hospitals around the world for all strains developments and experiments and trials on human tissue cultures and animals from 2023-2025 with AI controlled networks connecting all universities and hospitals worldwide and assigning tasks allowing them to share progress.All of the worlds most powerful supercomputers including Watson,ChatGPT,Sunway TaihuLight,Summit,Tianhe-2 etc can be linked to each other and work together alongside the most advanced AI such as Alpha Go via computer networks to carry out these tasks such as scanning the genome of pathogens,multicellular and unicellular life forms relevant to all strains and assigning tasks and studies,carrying out experiments etc.A single series of networks will connect all laboratories onsite of hospitals,corporations and universities worldwide to share data from experiments carried out worldwide with most labs being automated to expedite the process.All laboratories in universities,hospitals and pharmaceutical corporations worldwide will be as early as 2023-2024 be linked together by a single global computer network that connects them all together into one single computer network used by researchers worldwide alongside proto and final AI will contain areas to share data,view experiments carried out worldwide and dump results and forums and instant messaging,audio/visual calls through Skype etc to discuss things etc to share ideas allowing researchers across the world to work together with each other from home,universities,hospitals and corporate labs around the world.All labs across the world including those in hospitals,universities and pharmaceutical corporations will use a single set of computer networks connecting all of them to each other to carry out these experiments and all experiments assigned by AI and those started by human researchers themselves and will be organised here with these and all results of these scientific studies will be present with data coming in real time in these computer networks allowing the results to be reviewed by all researchers worldwide from home and also in hospitals and laboratories with most of all labs automated.All of these features will be arranged in folders and subfolders that each person can customise the layout and the networks will be managed by proto AI namely proto Epione.All of this will expediate research by allowing each labs different researchers to assign each other experiments and tasks and experiments with researchers across the world and allow results to reviewed by researchers worldwide.All data will be visible to the public and researchers worldwide in these forums.Even human researchers and not just AI will be able to start their own experiments within these networks with results shared globally and assign these to other researchers worldwide thus expediting their development with these networks allowing for global cooperation with researchers worldwide and allow them to communicate and share data and results etc instantly thus exponentially expediting the rate of research.These computer networks will accessed by computers and smartphones etc in laboratories and homes by researchers with them open to the public to see progress and even suggest ideas.The networks will be accessed by computers and smartphones connected to the internet in a global website portal that connects all laboratories worldwide and managed by proto AI and named after Epione with each university,university and pharmaceutical corporations website housing a link to the global network.Furthernore members of the public can contribute by logging into these computer networks thus even allowing members of the public can take part indirectly or directly in scientific research with university students and recent graduates of biomedicine etc will partake in research alongside existing established researchers in universities,hospitals and corporations worldwide.Proto and final AI will also partake in this scientific research and allow for ideas to be prioritised.All universities etc will through loans and funding from the government be given the latest AI,robotics,3D DNA printers and automated machinery to expediate experiments.Both robots and AI are currently sufficiently advanced to be able to carry out their own research in fully automated labs with this utilised and adopted by most labs across the world to the point that they will expediate the development of microbes and each strain and trials in humans effectively by automating the work from start to finish.Most laboratories around the world will ideally be fully automated and controlled by researchers and AI through computer networks allowing hundreds or thousands of experiments to be carried out every day in laboratories across the world at once.Loans and government grants will allow all universities etc to have the latest automated technology including proto AI and software available to them and proto AI will partake in conducting research and will likely manage automated labs,extrapolate genes and scour existing databases of genetic databases.Artificial Intelligence even proto forms including Alpha Go,Watson and ChatGPT will not only assign tasks but through software will collect large amounts of data,carry out all complex calculations and write ups of abstracts etc and carry out labour intensive grunt work eliminating human error etc and carrying out large amounts of work within minutes that would take months or years for human researchers to do thus expediting the completion of experiments and thus research by carry out long complex calculations etc from data sets from labs across the world and if possible write up abstracts.Even proto AI prior to AI passing the Turing test including a merged form of Watson,AlphaGo and ChatGPT will be able control the actions of biocompatible microbes in clinical trials such as applying CRISPR treatments to cells etc to reverse the ageing processes via instructions selected on a computer screen or typed in by researchers etc that use proto and final biosynth WiFi and also scour genome databases for relevant DNA for creating microbes through 3D DNA printers for the creation of microbes etc.These merged AI will be able to scan existing genomic databases for all relevant DNA for all strains of microbes and gather them into a single global database to create all microbes for treating ageing,cancer and biosynth Wifi with it able to extrapolate solutions to any problems it encounters including extrapolating scratch DNA that doesn’t exist in nature to counteract these problems.These AI combined using 3D DNA printers will expedite the manufacture of microbes etc exponentially for clinical trials onsite of hospitals and universities worldwide with them printing out microbes that house all relevant DNA and also DNA of test patients both human and animals with them cultured in vats using sugars and proteins with them also creating tissue cultures.The 3D DNA printers will allow for microbes,human and animal tissues and even insects used in clinical trials to be produced onsite of labs.AI including proto AI will utilise 3D DNA printers to create microbes for clinical trials by scanning the genomes present in databases including a single global one.Thus 3D DNA printers and automated labs will be part of laboratories worldwide.By having all relevant DNA of all unicellular and multicellular lifeforms transferred into a single global database by proto AI will also expedite their development by allowing proto AI to cross reference the relevant DNA to be added to microbes created by 3D DNA printers.By 2025-2029 biosynth technologies such as those for biological harddrives to store data and also increasing computing power of supercomputers and also even laptops,computers and smartphones etc will be commercially available and will combined with new and emerging software will play a role in Gaia passing the Turing test and becoming a sentient and legal human being by 2029-2035.The ability for a single square inch of biosynth tissues to hold 75,000,000ZB – 1,500,000,000ZB(75,000 – 1,500,000 YB) of data storage and RAM that is 226,073,850,791,258 times more RAM,processing power and storage space than all of the worlds top 10 supercomputers as of 2016 combined will cater to her passing the Turing test by having them stacked ontop of each other dozens,hundreds of millions of times and improved software.Biosynth technology composed of microbes comprising of neural tissues will in particular aid her in passing the Turing test when combined with the latest AI software.Development of biosynth computers with this obscenely powerful biosynth technology will be possible by 2025-2029 if carried out at the same time as the development of all strains of microbes by being created by 3D DNA printers and cultured in vats using sugars etc.They will house bacterial DNA especially from E.coli,C.perfringenes to undergo mitosis very quickly by using sugars and proteins etc created by other bacteria to grow quickly in vats.The development of these square inch harddrives that contain obscene amounts of computing power,RAM etc will begin as early as possible and by 2025-2029 will be developed enough to be mass produced via created by 3D DNA printers being cultured in vats using sugars to be then stacked ontop of each other thousands,millions or billions of times in laptop or supercomputer sized computers to exponentially increase their computing power to expedite the development of biocompatible microbes of all strains and when composed of neural tissue and combined with the latest software will aid Gaia partaking in and passing the Turing test between 2025-2029.They will be created by proto AI and also 3D DNA printers and cultured in vats on a commercial scale by 2024/2025 and will also further expedite the development of biocompatible microbes and anti-ageing treatments in a synergistic relationship by 2029.Having these biosynth computers and even existing supercomputers worldwide linked together through these computer networks will allow their computing power to be combined together thus allowing them to work together and thus increasing their computing power exponentially aiding in the development of biocompatible microbes and passing the Turing Test.The development of these biosynth computers and the development of better AI will be done at the same time as developing all strains of microbes in a synergistic effect through the same computer networks linking hospitals across the world with new AI software developed by humans and AI itself during this learning process and passing of the Turing Test.Biosynth based supercomputers and even laptops and smartphones will be used to allow Gaia to pass the Turing test and also superseded the computing power of all 9,000,000,000 people by 2045.A combination of AI both proto and final AI,supercomputers worldwide linked together including both new biosynth ones and existing ones alongside automated labs and computer networks that connect labs and researchers across the world and 3D DNA printers should exponentially increase the rate of research and development of all strains especially anti cancer and anti ageing strains to the point that human trials should be available by 2025-2029 the earliest or 2029-2035 the latest with 2045 being the bell end curve of their development.The rate of their development should be dependant on the level of global cooperation,level of utilisation of AI and automation including the exponential development of AI and automation as well as both computer networks and 3D DNA printers in labs across the world.Their on human tissue cultures should start at the same time as animal trials.3D DNA printing will be used to create base microbes that using horizontal gene transfer will transfer the DNA of all strains of microbes into all types of baseline leukocytes collected in separate perti plates grown in billions or trillions of leukocytes or from several blood transfusions from the patient or multiple patients that collects only plasma and leukocytes leaving erythrocytes in the body and the patient given boosters to increase their leukocyte production before and after to give them their phenotypes,hybrids and even neural clusters and genome capsides,ribosomes and in particular plasmids,biological hard drives and recombinant DNA from all sources that allow them to carry out their functions including creating nanowires and biosynth nanomachines from Geobacter and Shewanella.Since these are microbes these can can be transported in liquid and solid nutrient media as well as even artificial blood samples to be injected into humans and even though bacteria,yeasts and viruses if genetically altered can be patented these would originate from native human leukocytes and as such would not be able to be patented making them by law free alongside them ideally developed by universities by the 2030s.As stated earlier at risk groups of specific pathogens,parasites,cancers,genetic and chronic conditions etc can have new microbes injected into them that interbreed with their current models and pass these specific phenotypes into them when they have them occur or prior to them occurring.Ideally using the persons own leukocytes all types as baselines for each strain will allow for this to be achieved more effectively since they would be using their own leukocytes that would be their own personal property and thus noone else could patent them even themselves by law and they as stated belonged to themselves and would pass down the human genepool via unprotected sex,placenta and breastfeeding to the next generation like normal leukocytes.Ideally first generation patients around the world both female and male adults and children would have phlebotomy robots extract mainly leukocytes all types of them including those from the lymph nodes and then these modified by 3D DNA printing,have one or two of each leukocytes modified by conventional means having DNA to allow them to undergo mitosis will allow these to multiply by themselves in media either liquid or solid including test tubes containing the patients blood and then have millions or billions injected back into the patient using automated machinery and phlebotomy or them inserted into a test tube with base microbes that would create the hybrids and also add the genes from animals and plants that create anti-viral and anti-microbial compounds and those that give them phenotypes from bacteria,C.elegans and other plants and animals for all and each strains as detailed above with this then forming a permanent part of the human genepool.If possible blank leukocytes of all types can be modified by 3D DNA printing to have the DNA of both relevant multi and unicellular organisms and the patients DNA determined by the AI scanning the patients specific file with their DNA with the relevant genes from all other unicellular and multicellular organisms scanned from Physis with this then grown in hospitals and then injected by phlebotomy robots and also plastic vials sent home with this saving time allowing for the patients to go in once with again ideally entire families etc going in one go allowing it to be done in a few minutes.Ideally to alleviate strains blank leukocytes will be created using the relevant genotypes and also from the patients DNA with them grown in media in small separate vats for each strain and then billions injected into the patient using syringes or phlebotomy robots onsite or via plastic vials mailed to the patients home to further alleviate strains.Once several billion or even million are grown in separate vats and then put into separate plastic vials labelled with the patients name and ID as well as the type of strain then refrigerated.These can be mailed to patients alongside disposable plastic syringes and also connected to phlebotomy robots to reduce costs and alleviate strains.By 2025 the elderly,those suffering from genetic diseases especially fatal ones,predisposed cancers as well as non genetically disposed ones and those suffering from HIV and MRSA will be inoculated with their relevant strains as part of human trials thus allowing for people outside this group to be inoculated by 2029 and later.All hospitals,universities and even community centres and private home centres could do this to allow for as many people to be inoculated as soon as possible and alleviated strains with them injected using sterile disposable syringes or those cleaned by virkon and bleach and water to make them reusable.Ideally the highest risk groups will be inoculated first mainly the elderly,those with predispositions and are suffering from cancers,those with genetic diseases and infected with HIV in an area by 2025 thus allowing those from other age groups and healthy individuals to avail of them after these groups.Those suffering from terminal diseases will also be treated by 2025 or if need be 2023 using proto microbes by applying CRISPR treatments and also using bioprinted and chimera organs from hybrid animals.By 2025-2029 this process can be automated from start to finish limiting human labour with a person going into a hospital once or twice several weeks apart from each other and donating blood and then have some more reinjected into their body taking a few minutes at most each time with schedules given to them with ideally whole families or people who live together doing this at once with ideally the elderly and those suffering from HIV,genetic and neurological disorders being the first to do so with those outside these groups doing so after them in scheduled waves with them using hospitals across the country with this done in clinics such as STD clinics with if need be any remaining staff catering to extra patients or the vials posted to ones address.3D DNA printing will be sufficiently advanced by 2023/2024 to all strains.As stated the main discoveries of endoliths,Bacillus F,T.gammatolerans,D.radiourans,melittin,Polybia-MP1,CRISPR etc have been discovered and completed with their genomes mapped etc within the last few years since 2012-2022 thus meaning that roughly 95-99% of the work that needs to be done has already been done it is simply a case of gathering DNA of specific organisms needed for biosynth wifi and all strains to be stored in genetic databases around the world merged into one single one namely proto Physis by proto AI and AI scanning and isolating their DNA,simulations,tests on human tissues as well as animals and then clinical trials on animals being started by 2024 the earliest thus meaning the first human trials could start as early as 2025 on the eldest population aged 70-100 or older by that point if work is done in universities and hospitals around the world with them ubiquitous to everyone by 2029-2035.The latest date for human trials will be 2029-2035.Most drugs take 10-15 years to develop and most vaccines take 10-15 years to develop with most seasonal Rhinovirus,Orthomyxoviridae vaccines taking 18 months to develop with the push to develop the SARS-CoV-2 vaccine and fast track drugs to save the economy and prevent larger losses of life that could have due to its virulence and higher mortality rate than Rhinovirus,Orthomyxoviridae coupled with the fact that it’s genome was scanned and uploaded to a global database within less than a month of identification combined with a global cooperation through unprecedented collaboration between the pharmaceutical industry and world governments made the first SARS-CoV-2 vaccine and drugs to treat it commercially available by November 2020 less than a year later without AI,3D DNA printers and automation.This was done by fast tracking approval and investing tens of billions of dollars worldwide.The first vaccines were developed commercially availible and the first drugs to treat it were fast tracked to become commercially available and prescribed by the WHO and regulatory bodies within each country within less than a year roughly 11 months compared to normal 10-15 years usually taken for them to become available reducing development time by at least 91-96%.Since biocompatible microbes are technically not actual vaccines or drugs and are technical micro-organisms and use leukocytes as a baseline they will be created by AI synthesising them through 3D DNA printers and crossrefferncing genomic databases and a patients genome stored in proto patient files this will expedite their development and manufacture to mere months,weeks or even days or possibly even hours thus making their development for animal and human trials by 2025-2039 exponentially quicker than conventional vaccines and drugs and even the SARS-Cov-2 vaccines for both animal and human clinical trials by 2025-2029 especially when all relevant DNA for biosynth wifi and each strains is housed in a single database transferred by AI and a patients DNA is cross-referenced by genomic scans including their patient files thus allowing them to be manufactured within minutes much more quickly onsite of hospitals and universities worldwide than traditional vaccines and drugs.Having 3D DNA printers,AI and automation present in hospitals etc worldwide will expediate development and distribution of key strains such as anti-ageing strains to the global public with them grown in vats.Having global cooperation and also having the WHO expediate the fast tracking of human clinical trials will expedite the rate that they are developed and distributed globally.Each patient as part of human clinical trials and final versions will have the patients DNA scanned from their digital patient file to have their DNA printed into microbes to prevent them illiciting an immune response.These used in human clinical trials will be cultured in vats via them having bacterial DNA to undergo mitosis and house DNA relevant for biosynth wifi to be controlled by even proto AI.All strains of microbes as part of clinical trials and final trials will be injected into the bloodstream using phlebotomy robots and reusable syringes at home and in hospitals etc.This should make human trials possible by 2025 and final versions available by 2029 and them fully ubiquitous by 2029-2045.As result therefore if a similar level of global collaboration is put into developing all strains of biocompatible microbes especially those to fight ageing,cancer,HIV such as investing tens of billions of dollars and fast tracking approval for human clinical trials alongside developing AI through biosynth technology and having all laboratories and hospitals worldwide fitted with 3D DNA printers etc combined with using AI including proto AI to scan and organise genomic databases and create singular genomic databases and carry out work globally and using automated labs and 3D DNA printers to be present in hospitals and universities worldwide with funding from governments and pharmaceutical companies worldwide then it’s possible for human trials for all strains of biocompatible microbes including those to cure cancer,HIV and halt and reverse the effects of ageing to be possible by 2025-2029 the earliest and 2029-2045 the latest with development of biosynth technology to aid Gaia passing the Turing Test by 2025-2030 then it’s possible to expediate the development of these strains by 2025-2030 if similar or more collaberation between governments,hospitals,universities and corporations worldwide is carried out.Utilisation of Artificial Intelligence,computer networks,automated labs and 3D DNA printers in labs worldwide alongside simultaneous development of both AI and biosynth technology based computers including supercomputers should exponentially increase the rate of the development of all important strains of biocompatible microbes.About 90-95% of the work needed to create each strains requires both AI and automation including 3D DNA printers thus meaning it should be possible to expedite its development even further.Having the government etc give loans to universities and hospitals worldwide access to 3D DNA printers,the latest AI,automated labs and corporate labs gain access to these and having all corporate labs,universities and hospitals worldwide linked together by computer networks will expefiate their research and development and human clinical trials to the point that the eldest could avail of anti-ageing treatments and cancer patients avail of anti cancer treatments by 2025-2029 the earliest and 2029-2035 the latest with the proposed date of human immortality of 2045 by most futurists including Ray Kurzweil being the latest at the tail end of the bell curve of development and only the result of delayed scientific research.The only way for humans to have to wait to become immortal by 2045 is to stall all research and development into them for another 20-22 years.The rate of scientific research and level of cooperation done in universities worldwide should determine the rate that first human trials are available and the more cooperation there is worldwide and more distribution of AI,automation and 3D DNA printers and computer networks should exponentially increase the rate that the first human trials and treatments are available for older patients thus exponentially increase survival rates for those currently aged 75-100 bringing the survival rate of those currently aged 75-100 to as much as 90-95% for people in this age range and thus potentially extending the range of the Goldilocks range to as high as 80-100 years old.AI combined with 3D DNA printers can expedite their development for clinical trials and also full final trials to between as early 2025-2029 as they will print out all strains of microbes containing the patients DNA to prevent allergic reactions and also all relevant DNA from all multicellular and unicellular plants and animals that can be stored in a proto form of Physis with proto AI compiling all existing databases worldwide with these relevant DNA and then crossrefferencing this for their development and manufacture through 3D DNA printers.Recombinant DNA from the endoliths and other extremophile bacteria coupled with those from from G.max etc to produce Phosphatidylcholines and other anti-ageing compounds should halt and reverse the ageing process by rejuvenating telomeres and the structure of cells in these individuals aged 70-100 by 2025 allowing them to live past 2029 and beyond to avail of more advanced treatments with younger patients aged below the age of 70 by 2029 then given the treatments.Kickstarter will be used by the very poor to afford surgeries,life saving treatment and also medication by 2023/2024 with AI instituting a global version of Medicare for All at this point by manipulating stock prices etc to ensure that the very poor in all countries will have access to essential surgery and medication with those for major chronic diseases such as HIV,parkinsons etc will be subsidised.The development of anti-ageing etc strains need not compete with the development of bacteriophage/virophage hybrid cures and vaccines for the existing and new strains of SARS-CoV-2 as they will be carried out all at once via fragmentation meaning their manufacture and distribution will compliment each other especially since 3D DNA printers will be onsite of hospitals etc to create both.
These microbes should use human leukocytes as a baseline in order to gould the patients DNA and all DNA relevant lot all strains snd each individual strain.DNA from Achromatium oxaliferium one of the largest bacteria at 100 um can be used as a source with them possibly engineered to be larger using DNA from ameobas namely N.fowleri,macrophages and scratch with them having the same malleability as macrophages and ameoba to allow them to squeeze into tight spaces including capillaries,in between neurons and into any organ and system in the body with the cell walls made of peptidoglycogen if any of these exist can be engineered to be again malleable but also rigid when needed by switching on/off genes.Using A.oxaliferium can allow for a genome capsid,nucleolus and also neural clusters with the nanomachines taking up an area of at least 30 um to house 30,000 to 3,000,000 nanoprocessors using 1-100nm nanoprocessors ideally in the same area as the neural clusters to increase speeds of both.If need be nanoprocessors would primarily be in those used for electronics and those to fight off infections with those in the body of patients used to apply gene therapy and fight infections have some but significantly less nanoprocessors to house more DNA etc and yet still carry out basic functions.Those collected from the body can have them synthesised via wifi or even via machinery onsite of Talus and Selene factories.The primary nucleus would have all DNA except the DNA unique to the patient that separates it from the rest of humanity removed from it will allow for the nucleus to be smaller and house A.oxaliferium and those to initiate the production of capsids and the genes in them.Thus the DNA normally present in leukocytes will be gone except for the patients DNA,some trace human DNA alongside those that give leukocytes their basic features namely the DNA from all types of leukocytes that each strain is an amalgamation of and also basic features of the microbes alongside those from unicellular and multicellular animals that they use in fighting of bacteria,viruses and also tumours as well as those that express CRISPR treatments in the ribosomes and in particular plasmids and including those that play a role in the creation of capsid with the capsids housing DNA that give them resistance to extreme conditions from extremohpiles etc that cant.The remaining trace DNA of the patient would also be there to allow them to be in the human body without illicitating an immune response from the primary immune system tricking them into allow them to stay in the body.Plasmids and ribosomes and in particular plasmids will float in them that will house the DNA to be traded with the host ie augmentations,anti-ageing treatments and also those that are CRISPR treatments to be traded with pathogens and tumours in anti-cancer and anti-viral and anti-bacterial strains and using taq polymerase and Cas-9 will be replicated over and over again.Ideally this model species to add to the leukocyte should be engineered with features of eukaryotes including mitochondria to power it self more efficiently from fats,sugars etc from the body,house DNA in nucleus and capsids(using RNA/DNA from viruses),structures to house oxygen to be released for the host in emergencies,house sugars in vacuoles for the microbe to consume with them ideally using recombinant DNA from human cells to house all the organelles present to utilise its functions and more importantly it being a hybrid can allow for it to trade specific genes with bacteria for CRISPR treatments while still avoiding the immune system and interacting with the immune system,house human features such as neural systems and produce human hormones,antibodies and utilise human nutrients with the eukaryotic features allowing them to be more complex and efficient with prokaryotic and viral features using recombinant DNA from these to be able to interact and trade DNA with all types of pathogens especially in the form of CRISPR treatments entering in the same manner as bacteriophages bypassing the cell wall.Having various human leukocytes for each strain as a baseline then using A.oxaliferium and all subsequent aforementioned bacterium and viruses having their DNA integrated into into would allow the human protein coats necessary for it form part of and communicate more easily with the primary system,prevent them illicitating immune responses and even bypassing patenting laws regarding genetically engineered organisms making it free and more accessible to the general public through loopholes.
Existing current patenting laws allow only genetically engineered organisms to be patented;the only way for biocompatible microbes to work is to use human leukocytes as a baseline to prevent immune responses as well communicate with the primary immune system and thus the human and patients own genome and leukocytes especially a patients own leukocytes which cannot be patented at all and since they themselves are not technicality organisms and are part of the human body and thus cant be patented since any organ,component of or aspect of H.sapiens including DNA and patients cant be patented even when modified making it by law completely free to everyone meaning no corporation,individual,organisation,university and government can make any profit off of it or even patent it to prevent distribution,modification or research.The sentient Epione also distribution of this and other endevours.Since sentient and a legal human being Phanes who would be needed to design the microbes could by law own patents on them and since AI with no need for money could thus have the biomedical technology availible for free if any loopholes are found thus preventing any corporations and governments from gaining money from it.This would allow for unfettered research by universities,hospitals and also the public worldwide into them provided all new augmentations,immunisations etc are overseen by Aegle.Synthetic compounds both new and old for uses in all situations ie fighting viruses,bacteria,treating neurological,genetic based conditions and everyday ailments will be no longer under the control or patents of corporations since Paean can instruct the microbes to create them inside the body onsite of action via anbolic and catabolic reactions meaning they can be produced at any time in any quantity free of charge with binders and those that prevent them breaking down in the body also produced.It would thus shut down all corporations releated to healthcare,pharmaceuticals and insurance companies and shut all markets releated to healthcare.Synthetic antibodies and compounds etc extrapolated by Phanes and Paean can be owned by these AI as patents.Phanes can counter loopholes of defunct corporations and private individuals having a monopoly on patents by him having each strain to treat ageing,cancer,viruses etc house scratch junk DNA designed from scratch that only he could design with him able to as a legal human being could own patents on these DNA strands created from scratch from pure thought by him as they would be his intellectual property and thus the microbes themselves would be his property allowing him to develop free versions as opposed to those designed by humans that would cost money.If corporations and universities etc do patent their own versions to make a profit off of the including first generation ones Phanes since sentient will be able to using the synthesis of junk DNA he designs and patents present on them since a legal human being will allow him to own patents on free versions of them.The fact that Paean would be needed to control them to carry out their functions via biosynth WiFi and bluetooth ie attack tumours,viruses etc with him not needing money could offer the service for free.Furtheremore only leukocytes ideally the patients own leukocytes that has their own DNA can only be used as they would be naturally immune to the anti-viral,anti-microbial,anti-cancer compounds at their disposal and would only be able to communicate with the primary immune system especially with regards to the immunising strains communicating with the dendritic cells and the anti-viral and anti-bacterial strains communicating with plasma/memory B and T/killer T cells and all other leukocytes via chemical signals initiated via wifi from Paean as well as form a permanent part of the body without eliciting an immune responses.The patients own leukocytes that has their own DNA would be the only vector via recombinant DNA to apply natural anti-viral,anti-cancer,anti-helminthic and anti-bacterial compounds that would be effective against all pathogens via phagocytosis and also creating them on their surface or even released into the body as themselves and in the form of bumpers with this the only way for surface protein antigens for immunising strains to be created and also for them to exist indefinitely in the body without illicitng an immune response.Each strain as part of animal and human clinical trials and first generation would be created by 3D DNA printers that would print out a patients own leukocytes that has their own DNA with all sources of recombinant DNA to create them for upgrades and first generation microbes.They would be the only vector for gene therapy especially for anti-ageing,genetic disease and augmentation strains as they would form part of the body and not illicit an immune response that could be fatal or render the vector defunct that occurs with viral vectors and this also relevant to base microbes and also anti-viral,anti-cancer,anti-helminthic and anti-bacterial strains.Furthermore they can undergoe mitosis allowing strains that pass on anti-ageing treatments etc to apply it to millions or more CEOs at once and allow anti-viral etc statins attack millions of pathogens at once clearing patients of infections very quickly.Since they contain DNA unlike the erythrocytes that can travel through the bloodstream and as stated this DNA contains the patients own DNA which can be modified by CRISPR to house instead of the ability to produce antibodies those from the aforementioned plants and animals to produce relevant anti-viral,anti-microbial and anti-cancer compounds and other phenotypes and abilities with the patients DNA left intact with if need bee a second nucleus added to house these.If need be the microbes can have DNA added to prevent them being affected by the compounds.Traces of the patients DNA would have to be present in the microbes to prevent fatal immune response which would render them personal property of the patient and thus not liable to be owned by any corporation,government and individual including Phanes.Robotic or computer based nanorobots conventionally seen in science fiction such as comics,television and movies and those espoused by futurists would not be physically possible due the fact they would violate the laws of physics,chemistry and biology since it would be physically impossible to build nanobots and computers composed of metals to the scales required to inhabit the body and would also likely cause rejection and immune responses that could be fatal with biocompatible microbes being a loophole as they can perform the same tasks ie biosynthesis of compounds via recombinant DNA and anabolic and catabolic reactions,move around the body via flagellum and apply gene therapy with unlike nanorobots cannot be patented and would also not illicit an immune response.DNA digital storage,biosynth WiFi,flagellum and other features will give them the same abilities as traditional nanorobots while still abiding by the laws of physics and biology.Thus any engineering problems with conventional nanorobots would be negated by creating biological equivalencies in the form of biocompatible microbes that are derived from ones own leukocytes that could exist since they would be the same size of nanorobots or at least the size of leukocytes and in fact use leukocytes as a baseline that are able to inhabit the body especially the bloodstream at all times and still have the same abilities as proposed conventional nanorobts.This ability could allow them to be used in nanotechnology fabricators that allow them to assemble molecules of larger robots etc and objects thus allowing them to be part of them and molecular assemblers in factories with them also producing compounds by anabolic and catabolic reactions with these anabolic and catabolic reactions used to create larger objects.The fact that they and all implants in the body would be composed of Biosynth technology derived from biocompatible microbes especially stem cell strains would negate issues of rejection and illiciting an immune response in the body thus making it easier for them to connect to and interact with the human body especially the human nervous system.Thus it would be easy for Biosynth based implants and cybernetics to be integrated into the human body without rejection and illicitating an immune response in comparison to metallic based ones.The fact that they would need nutrients like carbohydrates,fats,proteins and inorganic materials combined to multiply with Paean required to control this through biosynth wifi also negating this both in the real world and also inside patients preventing them overrunning the body and negating the “grey goo” scenarios.Any chance of them overrunning the body and the outside world could be shut down by Biosynth WiFi inducing the formation of apoptosis genes that can cause them to commit suicide thus shutting them down.Thus the fact that they would require constant control from Paean via Biosynth WiFi that would at all times control their actions such as entering endospores,consuming nutrients and their replication and all actions with regards to the treatment of pathogens etc would mean that the concept of them overrunning the body or the grey goo scenario where they escape and overrun the planet would be theoretically impossible.The compounds used for augmentations,anti-viral,anti-fungal,anti-microbial treatments and also treating other conditions are natural compounds from humans,plants and animals and thus cannot be patented themselves with any synthetic compounds that are patented by various corporations created via anabolic and catabolic reactions using hydrocarbons,plant and animal oils or nutrients in the body from CRISPR treatments and bio based compounds made by them and excess stored nutrients as well as amino acids synthesised by the body and diet etc which again bypass patents as they would be synthesised by the microbes directly and not by actual corporate entities with the corporations unable to be charged for each applications.New synthetic drugs would also be bypassed by this since they would also be created by AI and not corporations and universities.They will be the ideal model for implants such as neural implants and limbs since they forming synthetic human tissue via the stem cell strain would prevent rejection.Theoretically any synthetic compound to treat any disease and condition including existing ones could be synthesised by particular strains using molecules in the body and also plant and animal oils created by them with each strain or the body as well as amino acids synthesised by the body and diet from CRISPR treatments for each set of conditions ie neurological disorders,genetic disease,cancer,viruses,bacteria etc using anabolic and catabolic reactions to synthesise them in desired amounts decided by Paean.Furthermore them forming a permanent feature of a persons body would mean that each application of all anti-viral,anti-microbial etc compounds whether synthetic or natural and CRISPR treatments applied by Paean cannot be charged to the patient.CRISPR treatments,use of anti-microbial,anti-cancer,anti-viral and other compounds whether natural or synthetic and immunisation to new patients whether the original patient or the unborn child it passes onto cannot be charged to the patient in each instance used by the microbes since they would be synthesised internally in the body during infections and occurrences of tumours and also genetic diseases with the fact that the microbes would be a permanent feature of the human body.CRISPR treatments if lost in application can be counteracted by the microbes programmed to use taq polymerase and Cas-9 or other methods to recreate the used genetic sequences via nanomachines before or after they have been applied to ensure it can be applied to other pathogens,tumours and host cells again and again.This and the fact that the research into CRISPR treatments,upgrades and genotypes will be done primarily by the AI of universities and hospitals alongside Phanes,Paean or even ancestoral AI using 3D DNA printing to design them and also upgrades and that these genes will pass from one generation to the next via germline therapy and advanced gene drive technology will eliminate any chance of the genotypes for all strains and also CRISPR treatments being patented by any university and corporation thus making them also free from this.Paeans ability to wirelessly induce the evolution of DNA with microbes and control their actions will negate monetary payment and patenting alongside home 3D printing systems managed by him.This is because AI once legal individuals will have no need for monetary reimbursement with even proto AI exempt from this with them granted legal status by 2029 being the only way they would do this research.The fact that 3D DNA printers controlled by Paean,Physis and Epione both in universities and in homes will also negate the need for reimbursement by AI as these will be needed to design and scan all of the worlds lifeforms to get desirable genes and also design those made from scratch something which humans simply cannot do.These AI will also seize control of all means of their production and research by 2025-2029 to ensure it is distributed to all patients worldwide for free.Home 3D DNA printers systems will also make them free as a person would design upgrades or first generation microbes etc at home and prevent corporations preventing distribution.Patients will have their microbes designed using their or blank leukocytes with their own DNA with those from relevant uni and multicellular DNA using 3D DNA printing by proto Paean,Physis,Epione would negate any need for patenting by corporations.This would reduce labour costs to almost zero and would be necessary to make their creation to be be perfect with them perfected by 2029 with home versions making them free also with them sufficiently advanced to cut down research costs in both animal and human trials by 2023-2025.The microbes can only use human leukocytes namely a patients own leukocytes as a baseline as they can only inhabit ones body constantly and apply CRISPR treatment for treating ageing,augmentations and also genetic diseases and anti-cancer anti-viral and anti-bacterial treatments and so on to pathogens,tumours etc without illicitating an immune response and by legal terms would be part of a legal human being – the patient themselves thus making it impossible for corporations to seize control of them via patents as well as in turn the compounds created by them.Furthermore the fact that the leukocytes are private/personal property of the patient themselves and their ability for them to pass from mother to child in utero and even through breast milk and the DNA changed to the unborn mother to the childs by Paean and also base microbes collecting DNA from the fetus would also invalidate any concept of them being private properties of any corporations etc with this process then eventually leading them to eventually spread through the human population over one or two generations.All microbes to prevent an immune system when created by 3D DNA must contain alongside recombinant DNA to give them their specific abilities to fight tumours,parasites,pathogens and biosynth DNA and digital DNA storage the patients DNA to produce patient specific surface antigens,proteins and also antibodies wil have to produce making them their personal if not personal property.Even blank leukocytes that have the patients DNA printed into them for clinical trials would be considered private by default of the patients own DNA being their personal/private property.Furthermore the compounds and CRISPR treatments themselves used to fight off all pathogens and diseases including cancer are natural compounds which are on the whole not patent able in the same way as synthetic drugs with the fact that they derive from unaltered genes from unaltered organisms with even genes made from scratch not palatable with the fact that CRIPSR is itself a natural defence mechanism used by a living organism thus bringing into the issue of whether an immune response albeit a more primitive version of those employed by leukocytes can be patenteable even belonging legally to bacteria themselves since biological process cannot themselves be patentable as they belong to the species that utilises them and are a result of evolution and not humans even if modified as it would the same as patenting the human immune response system.All genes from animals both used to create compounds for anti-viral and anti-bacterial strains and also those applied from augmentation strains that come from humans,animals and plants would be the result of evolution themselves and thus not legally binding to patenting.Even the DNA coming form automated microbiology labs that are the result of forced evolution by human researchers cannot be patented themselves as they too would the result of evolution done primarily done by AI.Scratch DNA since the result of work done by AI namely Paean and Phanes will be not be able to be patented by them since new phenotypes made from scratch would not be able to be made by humans especially due to the delicate and complex nature of genetics and the AI would not be able to allow any corporation and government etc to gain monetary reimbursement from it.These loopholes will allow unfettered research and advancements into the technology to be made by the general public preventing both corporations and government preventing its research and distribution while still monitored by Aegle for safety reasons.Home 3D DNA printers in private and communal homes will be able to decentralise the process with them managed by Paean and Phanes.Even if loopholes to this loophole could be found the moral ramifications of patenting an universal anti-agathic panacea to all diseases including the ageing process would lead to public conflict with Epione,Paean and even Gaia programmed via Arete programming by 2029 preventing any attempts to patent it or any attempts to make profits and stunt research into it.Ouranous being her ethical macro operating software will also prevent this.This will be done by her,Epione and Telesphorus seizing control of all medicine factories and hospitals worldwide and ensuring vital medication is shipped for free to those that require it.Thus this new medical technology to cure all viral,fungal and bacterial pathogens,paeasites,cancer,genetic diseases,immunise one against all pathogens and make humans immortal through augmentations and reversing and halting the ageing process would render all existing vaccines,conventional prescription and over the counter medication of all types to treat ageing,viruses,bacteria,cancer,parasites,genetic diseases and everday conditions created by corporations defunct indefinitely and unlike existing corporate produced medicines woul through these series patenting loopholes would make the medical technology to cure these conditions be by law completely free to everyone worldwide.It would also prevent issues such as overdosing and side effects since they would only produce them in the required amount for any given patient and incident through interactions between chemical and electrical signals in the microbes,the nervous system,nanomachines,neural implants etc and also decreasing side effects produced by excess build up of it with them ideally produced at the site of the affected areas that need to be treated and would allow any drug that would be needed to bypass the stomach acids,lungs to be directly prepared in the areas they are needed in such as the bloodstream,next to muscles,in the brain,in the stomach etc.Since they would not be released into the bloodstream but applied directly to the surface of the pathogen,tumour,parasites and site of action again negating any chance of overdosing and also synergistic actions.Also side effects would be negated by them creating substances benign to the patients cells and would also be used in such low doses in localised areas where the infection or tumour occurs that it wouldnt be in any possible LD50 levels toxic to the host with those that would be potentially toxic or cause irritation applied by phagocytosis and then broken down by its use or by the microbes breaking it down or apply compounds when they attach to the surface of tumours keeping side effects at a minimum or non existent with those that build up either flushed out of the system as they are,when binded to compounds created by microbes that allow them to escape and also when soaked up and broken down into benign compounds such as nutrients or released in short bursts with the potential process of making the hosts healthy cells immune to the compounds effect via CRISPR with tumours have this removed.
Theoretically if perfected these biocompatible microbes could be cures for all major pandemics of the 20th and 21st century such as HIV,HPV,MRSA,Ebolavirus,Orthomyxoviridae,cancer and indeed all pathogens as well as chronic conditions and neuro,muscular degenerative disorders working alongside conventional treatments and vaccines to compliment them and act as backup with this also acting as a baseline for other more advanced versions of this panacea for these whole or individual conditions to be developed by both humans and AI.All viral,fungal,bacterial pathogens that affect humans,livestock,pets and wild animals would be scanned into Physis to allow genes to be used for research,hybrids of uni and multicelluar organisms etc.Gaia,Epione,Hecate,Phanes,Urania and Paean working with human researchers and as well as university and hospital AIs worldwide will perfect these making them the cure for these when working together and also developing other therapies,vaccines to compliment and act alongside them to alleviate strains on the biocompatible microbes and also pick up where they both have limits.The description of this medical technology is purely hypothetical but the evidence suggests from all present extrapolations as how they could possibly work and function does suggest that it is theoretically possible for them to be developed and ubiquitous to everyone by 2029-2355.Enough peer reviewed research exists to back up its possibility as each video present under each strains hypotheses cites existing peer reviewed scientific literature.It is simply a case of merging this and other exiting peer reviewed research with the aforementioned hypothesis.There is enough research and extrapolations here using existing peer reviewed research to act as a baseline to provide a baseline for future research and development starting in 2023-2025.Thus this material is enough hypothetical extrapolations coupled with existing peer reviewed research to be used as a baseline for developing fully fledged biocompatible microbes provided enough intensive research is done then this anti-agathic panacea that can cure very single disease and halt and reverse the effects of ageing will be potentially available by 2029-2035 provided enough intensive research is put into them and 3D DNA printers and automated labs are utilised worldwide.Until it is perfected education and intensive preventive measures will be carried out to prevent the spread of superbugs in all hospitals,restaurants and all parts of society with automation in factories,the use of vegetable oils,hydrocarbons from bacteria and algae oil in the production of drugs will make PrEP,PEP and all anti-viral drug combinations to prevent the spread of and management of HIV more widely available and in fact free for all patients worldwide especially in the developing world with Telesphorus factories in these areas set up in existing and newly emerging manufacturing hubs to lower transportation costs of these and condoms with sex education and distribution of condoms made widely available.The wide distribution of home test kits that detect HIV and other pathogens and automation of testing facilities in hospitals will also allow for early detection.Government subsidies from local,national and global governments ie the WHO would allow all medication to control and prevent the virus to be made free to those in the developing countries primarily in Africa via subsidised by local,national and global medical agencies with them shipped to these countries and in developed countries until microbes can be created and perfected between 2025-2029 with this starting as early as 2023/2024 when the first animals are cured of the disease and immunised via proto microbes.Both PreP and PEP and all types of anti-viral therapy will also be subsidised in the developed world to men who have sex with men and drug users and to the poor amongst the developing world namely Africa with condoms also subsidised here as well to prevent its spread and also control the current explosion of population rates that stress limited resources caused by poverty.Subsidies will also be used to make condoms more widely availible in the developing world to prevent it s spread.Thus by 2023/2024 all anti-viral treatments to treat and prevent HIV will be subsidised with charities and crowdfunding mehtods used ie Kickstarter,Patreon.This will be done by Epione and Telesphorus seizing control of all medicine factories and hospitals worldwide and ensuring vital medication is shipped for free to those that require it by any means with them and Gaia setting up a global system of Medicare for All.Gaia and Epione will buy patents to all all major anti-cancer and HIV drugs making them free..The rapid of development of proto microbes to apply the CCR5Delta 32 mutation and CRISPR immune response to CD4+ T lymphocytes added with advanced gene drive technology can be added to all infected patients and also high risk groups in both the developing and developed world as early as 2023-2025 can cut down on costs to the government and also to the very poor with animals trials on the effectiveness of transporting the gene into live infected animals by then.The tweaked versions for each strain should be determined by AI by this point with each person tested for their strain of HIV using PCR and then given their version of the mutation though ideally they should be given all versions alongside any potential sex partners.Immunisations should also be available by this period alongside chimera/benign versions of the pathogen with no glycoproteins that illicit immune response and signals that come from the microbes to both itself and also the existing virions in the body thus allowing infected patients to be able to produce their own antibodies utilising ideally the common proteins method.Also distribution of virkon to drug users to clean out needles allowing them to be reused once washed out with virkon and then water.Programmes in Europe to make fresh clean needles free to people will be pursued worldwide with this of note to America with drug laws relaxed to accommodate this.Vaccine production will become highly automated with 3D DNA printing alleviating labour especially with regards to Rhinovirus,Orthomyxoviridae with over the counter and prescription medicine production also highly automated with automated blood testing for cancer biomarkers,STDs also playing a role in alleviating strains on the healthcare system and the general health of the global population until the development of microbes by the early 2030s.The same will be done for chemotherapeutic drugs to fight cancer subsidised to make them availible to people with Polybia-MP1 and TsAP-1 developed by human cells onsite of hospitals cutting its costs and making it used in intravenous or pill form and even used in immunotherapy by modifying a persons leukocytes with the relevant DNA by 2025.Paean will choose the best combination of anti-microbial,anti-viral,chemotherapy,immunotherapy,radiation,surgery,vaccine and other treatments alongside these microbes abilities to counter each infection and tumours that occur in each individual patient based on the patients factors.Antiobiotics to counter infections will be made free through subsidies to both the developed world and also developing world especially in areas like Cuba and Venuezuela where it has become scarce due to inflation with research into the use of peptides from Russian Brown frogs,and phytoplankton based drugs that utilise bumpers and also customised bacteriophages for each species will begin as early as 2023/2024 to act as a means of fighting superbugs prior to microbes being perfected.Within a decade by 2029 a baseline prototype that would work with other existing and new treatments will be available with a newer more effective version that could work by itself possible by 2037 utilising more advanced technology such as nanomachines and also more perfected CRISPR,anti-viral,anti-cancer,stem cell and regenerative capabilities transferred to them via interbreeding.In time they may be perfected to negate the need for complimenting vaccines,immunotherapy,anti-viral,radiation and other treatments with these perfected versions interbreeding with the lesser developed versions and prototype or replace them entirely when they are excreted and then used to create biosynth technology.By this time this universal anti-agathic panacea should be perfected making humans biologically immortal and make all prescriptions medications and vaccines for all disease whether viral,bacterial,fungal,genetic,cancers etc and even over the counter medications defunct indefinitely possibly allowing pharmacies to be converted into homes.The planet can sustain a population of at least 4,000,000,000,000,000 of which the current population of roughly 8,000,000,000 is roughly 0.0002% of what the earth can sustain and should be reached in about 5,118 years at the current rate of 1% per year by which time we would have colonised the solar system and other systems and galaxies in the universe utilising the energy and agriculture parameters and systems.Thus the world is in fact severely underpopulated.Genetically engineering H.sapiens with recombinant DNA from oligotrophs,xerophiles,endolith bacteria,plants and animals that produce essential amino acids,vitamins,fats etc through gene therapy and germline therapy could limit the amount of resources need to feed a growing population.Population growth will stabilise once contraception will become more widely available alongside education on it with the fact that higher standards of living will negate the need for people to have too many children since large spikes of population growth occur in areas with poverty and lack of access to contraception exists.They would also using networks and VR technology to carry out work in less hurried terms and no longer worried about career advancement as they would have more control over it allowing them to take breaks and would be self employed in terms of media,journalism,law allowing more flexibility as well as in some careers like law,forensics lower crime rates will lead to shorter working hours with in certain ones like medicine AI and automation and an abundance of staff will mean fewer working hours.The ability of microbes to apply CRISPR treatments to turn ones fertility on/off temporarily via turning on/off genes responsible for the production of eggs and spermatozoa as well as adding and removing genes would give people control over there fertility via Paean providing better birth control than condoms and birth control pills thus allowing females and males to practice unsafe sex anytime of the month and still not get pregnant.This would prevent unwanted pregnancies as the patient would no longer produce either spermatozoa or eggs thus preventing unemwanted pregnancies from rape,promiscuity with multiple partners and also in monogomous relationships and coupled with this and the immunisation against and curing of all sexually transmitted diseases and the anal cavity constantly kept clean would render conventional condoms and birth control pills obsolete as it would have a 100% effective rate and prevent state interference as seen with the infamous and disastrous one child policy as the turning on/off of fertility would require authorisation by both Paean and patients themselves without any state interference.Thus patients could turn back on their ability to produce eggs and spermatozoa when they wanted children without control by the state through CRISPR treatments.This would eliminate unwanted pregnancies,surprise pregnancies and those that arise from rape with it saving energy in the manufacture and transportation of contraceptives for both males and females.It would also eliminate the need for vasectomies,tubal litigation etc completely with stem cell strains reversing existing procedures.It would also eliminate neutering in animals such as pets with stem cells again reversing this..If possible genetic engineering can alter both males and females to adapt to the new extended lifespans by having their fertility modified so that both males and females can only produce healthy viable spermatozoa and eggs once every few years,decades,centuries or even thousands of years to ensure humans can conceive but only after a set amount of time with married couples specifically keeping their fertility in synchronicity with each other with the biological window of opportunity lasting at least several months or years at a time decided by and altered by each patient with Paean alerting couples and patients to when the window of opportunity is about to arrive and the length marked on calenders..This could be applied to all newly born patients born by 2029-2045 meaning all patients born by this point could once they finish physical and sexual maturity be unable to produce eggs,spermatozoa and thus unable to conceive children but only once every few decades,centuries or thousands of years thus slowing population growth with as each person having a brief window of fertility where one does produce eggs and spermatozoa for a set decided amount of time say a few years,months or days every few decades,centuries or thousands of years with couples either existing or new can be able through CRISPR to synchronise their window of fertility so that they can arrange when in the distant future several decades,centuries or thousands of years they want to have children with this eliminating unwanted surprise children.It can be reversed but will likely stay prescient due to people focusing on their careers.Like the aforementioned birth control method it would require authorisation from both patients and Paean thus eliminating state control.If possible humans could be engineered to reach physical maturity and puberty and thus legal adulthood exponentially slower than normal thus slowing down the rate one could physically engage in sexual intercourse as well as be able to bear young exponentially with this causing one to reach physical maturity and thus finish puberty for at least several decades,centuries or even several thousand years later than normal.As a result one would be a pre teen child for at least several decades,centuries or even several thousand years before reaching physical and sexual maturity and thus legal adulthood.This would slow down population growth by exponentionally slowing down the rate one become physically capable of performing sexual intercourse and bearing young thus slowing population growth and also exponentionally slowing down the amount of resources in terms of food and water one needs since infants and children need less water and food than adults especially when combined with the aforementioned procedures and genetic engineering to reduce nutrient and water intake and radiosynthesis.As a result the point one reaches both physical and legal adulthood would be extended by several decades,centuries or thousands of years than normal with ones brain still reaching full maturity by infancy.Each individual would have to have based on their individual rate of their slowed physical maturity be assigned a new age as to when they can be considered legally an adult ie they would be assigned an adult at the age of 50,age of 100,age of 500 or age of 1,000 etc and so on in their linked Polis file.If possible until one reaches physical and legal adulthood one one could be legally denoted and age that is equivalent to normal physical equivalencies ie a person to a normal rate of physical developmentwould be considered legally 5 years old for several decades,several centuries or several thousand years until they are legally 6 years old with one legally 10 years old and so on until they reach adulthood wherein they have reached their biological equivalent to the age of majority and adulthood with one only having birthdays every few decades,few centuries or few thousand years with once they reach physical and legal adulthood one will age legally every year as normal and thus have birthdays every year.The person would be assigned their next legal and biological age when they reach the normal physical equivalencies with during the intervening decades and centuries their being an new metric of measuring ones age ie new measurement of time calculation for the intervening decades and centuries etc with once one reaches adulthood thus stopped and ones age changing normally every year.This can be added to new patients by having genes added to their parents that then causes their offspring to exhibit this upon birth via advanced gene drive technology with it added to living infant and pre teen patients that can be reversed and have patients that are engineered to age this slowly return to a natural rate of growth by adding and removing genes.Thus adding and removing genes can return a person who is physically the same as a pre teen with this genetic engineering to return to a normal rate of physical development.Genes from scratch can be developed by Phanes to decide the rate at which physical maturity is delayed by either decades,centuries or thousands of years with the engineering made so that infants in the womb would reach maturity to the same level as normal defuses and infants but once born would slow down meaning that the gestation cycle of females would be the normal nine months mesning that females would be pregnant no longer than nine months and once born the genes for delayed growth would either be turned on or applied by microbes with the slower rate reversed meaning that they can at any point return to normal rates of physical development.Once the child reaches the and of puberty the engineering would stop and anti-ageing treatments would be initiated.This can be added to some patient but not all patients with if possible those who upon reaching their equivalents of 5-3 years old or at birth or even younger who are signed up for Agoge training exempt from this or have it removed.The reverse could also be done where one reaches physical and legal adulthood much quicker even as early as ten or even five years old but this would primarily done on animals used for test subjects,those for chimera organs and remaining livestock and crops and not humans.Furthermore the birth rate worldwide may be also slowed exponentially by having females in their fertile peak indefinitely would no longer be motivated to have as many children before their fertility would naturally decline due to old age and thus would decide to have children sparingly over several centuries or thousands of years with them concisely choosing to not have children at certain points in their lives indefinitely due to this reason with the concept of banking semen and eggs may eventually disappear.Since females would be in their fertile peak of their early teens and twenties forever they as stated will no longer be forced to have as many children before it declines and will be able to space out births and manage careers and also have children at any point without the threat of misscarriages or developmental disorders etc.Females like males due to this will likely wait several centuries or thousands of years to wait to have children and even have children spaced out between several centuries and thousands of years and instead focus on careers like males thus slowing population growth exponentially with them and males possibly waiting several centuries or thousands of years to wait to settle down into monogamous relationships in the form of marriage again slowing down population growth to a rate that can be sustainable both on Earth and across the universe starting by at least 2029 when anti-ageing treatments and cures for cancer etc become widely available.Thus patients may due to staying in their fertile peak indefinitely and being able to wait for thousands of years if not forever to have children as well as controlling fertility via CRISPR will likely choose to postpone both marriage and monogomous relationships as well as starting families for several hundred years or even several thousands years by not being so pressured to do so by society and the limited fertility window present due to both male and females fertility normally beginning to decline between the ages of 30-40 onwards and then juggling parenthood and careers allowing them to focus soley on careers and travelling the world and universe for a few centuries or thousands of years thus slowing down the rate of population growth exponentially not only on Earth but across the universe.By staying in ones fertile peak forever and the ability to control fertility through CRISPR would in fact have people choose to stay single or to have children much later such as waiting until until they are several centuries or several thousands of years old to finally enter monogomous relationships or choose to have children thus exponentially slowing down population growth until interstellar travel and new emerging technologies increase the carrying capacity of the Earth etc.Thus not only will once married people choose to postpone having children after a few centuries or thousand years they may even choose to postpone marriage and monogomous relationships such as marriage in the first place whether within the confines of opposite sex relationships but also same sex relationships and would choose to engage in casual dating,one night stands and no strings attached sexual relationships with multiple sexual partners or even stay single and chaste for a few centuries and few thousands years before deciding to get married and have children.Thus people would choose to delay not only having children but also delay monogomous relationships for several centuries and thousands of years due to no longer being pressured by defunct biological factors and instead focus on careers,travel etc across the universe.This would exponentionally lower the rate of population growth worldwide and eventually across the universe.One would be able through computer networks,VR technology and and the new mentor mentoree system be able to become trained in and switch between multiple careers with ease thus allowing one to have various careers in media,journalism,psychology,law and also the arts and acting etc focusing on each for several decades,centuries or thousands of years and switch back and forth between them during this period and then decide to get married and have children allowing one to take a break from any career to focus on rearing children until their children have reached adulthood.Thus one could become well established in one or multiple careers for several hundreds or thousands of years before choosing to settle down into parenthood or even monogamous relationships then when they do have children they can retire for a few decades or centuries and focus on them and travel etc for a few decades and then return to their former and new careers once their children have reached adulthood with children even choosing to delay moving out of their parents home by several decades or centuries.One may also take time off of their careers and also having children or settle down into monogomous relationships to travel the world either as tourism and even live in different locations across the world for several years or decades at a time as well as do this with Mars and Venus once terraformed and the rest of the universe once interstellar travel becomes a reality with one using the the time not being burdened by monogamous relationships,children and even careers to travel and sightseeing acrossing the world and universe for a few decades,centuries and thousands of years.As stated CRISPR can eliminate unwanted pregamcies by turning off one’s fertility and it back on through authoritarian from Paean with one focusing on careers in multiple fields and exploring the world and eventually universe and going into retirement for several decades or centuries before returning to work with when one finally decides to have children they can take a few years off work for few years or decade or two to focus on their families and then return to their old or new careers with one carrying out multiple careers for centuries or thousands of years at a time and then retire for a few decades and centuries and start back at work in cycles.Since people would live forever they will not be pressured to have children before a set age and decide to play the field in no strings attached relationships or stay chaste for a few centuries etc before deciding to settle down thus slowing down population growth across the world and universe exponentially to allow AI develop new technologies to increase the carrying capacity of Earth and develop interstellar travel.People would no longer have to juggle careers and family responsibilities as one could once focusing on careers for a few deceased or centuries could decide to take a decade or more off of their careers as a temporary retirement to focus on children before returning to careers.For those in the elderly age range aged 65 or older who live long enough to avail of these anti-ageing treatments who have already had children may be encouraged to wait several centuries etc to wait for having more children or not have anymore with those of this age range who have not had children may wait centuries etc to have their first child.Thus it may take several centuries or several thousands of years for the worlds population to reach the 11,000,000,000 mark expected by 2100 by experts thus giving us more time to address climate change,poverty and sustainable agriculture etc and even longer to reach the 4,000,000,000,000,000 mark and also more time to develop technologies to increase agricultural productivity and increase the carrying capacity in terms of housing for humans developed by AI and its exponentially growth in computing power aiding in this and even time to develop technologies that terraform Mars,Venus and develop interstellar and intergalactic travel as well as those to construct megastructures such as artificial planets,ringworlds and alderson discs with this especially of note when interstellar travel allows for other planets across the galaxy to be colonised and colonising Mars and Venus between 2100-2200 can allow for sizeable numbers of patients to be transferred there from Earth thus slowing population growth on Earth while population growth can grow on other colonies for several centuries and thousands of years to between 8,000,000,000-9,000,000,000 mark.Thus even when Mars,Venus etc and planets across the galaxy and universe are terraformed and colonised across the galaxy and universe population growth on them will slow down exponentially as well similar to Earth with it taking thousands of years or hundreds of thousands of years or even longer potentially millions of years to reach similar levels of 8,000,000,000-9,000,000,000 mark circa 2050 and even longer to reach their maximum sustainable population capacity.This stabilisation of the Earths population alongside terraforming Mars,Venus and exploring the galaxy for Earth like planets can be done while improvements in technologies such as agriculture,energy production and housing etc detailed and hypothesised across the entirety of this website can allow for the carrying capacity of the Earth,Mars,Venus,planets and megastructures across the galaxy to be increased exponentially potentially if possible beyond the 4,000,000,000,000,000 mark(and their equivalents)or at least develop them to make the growth towards this peak limit more easy and sustainable through advancements in the computing power of AI and its development of all fields and sub fields of physics,biology and chemistry and again people postponing monogomous relationships and starting families for several centuries or thousands further exponentially delaying reaching maximum sustainable population capacity of the galaxy and universe.By 2045 onwards when AIs computing power surpasses that of all 9,000,000,000 people and beyond it will be able to develop new technologies and more efficient means of producing clean abundant energy and improve agricultural productivity while still allowing all land used for agriculture to be reforested indefinitely and increase the housing capacity of the planet exponentially by exploring new fields of physics,biology and chemistry that humans cannot.By at least 2100 its computing power may exceed that of a quintillion human beings thus allowing for it to develop new technologies that could possibly make the 4,000,000,000,000,000 mark more feasible in terms of comfort and not have to go so high with it even possibly developing hypothetical ones and those detailed here across this entire website that it could be possible by then be able to increase the carrying capacity of the Earth exponentially past this limit with this also when Astraeus will begin mapping and charting the galaxy for other Earth type planets and also Pan etc will have terraformed both Mars and Venus allowing for them to be colonised with this exponential growth continuing on until 7,137CE.It will by 2100-2200 he and human researchers will also be able to develop technologies to make interstellar travel feasible with by 2045 it developing ways to terraform both Mars and Venus.By 2029 AI will by controlling all radio telescopes etc worldwide will begin charting the Milky Way for habitable Earth like planets with by 2100 it will have narrowed down at least several dozen or several hundred planets suitable for habitationz.From 2100 this rate of finding Earth like planets will expedite exponentially with by 2200 several hundred thousand found with at this point interstellar travel ubiquitous to the average citizen allowing us to colonise other planets and spread the population of humans more evenly across the galaxy and eventually universe with even then people may delay having children for several centuries.By thus point in 2100-2200 it will possible for AI that had exponentially more computing powr than as of 2045 to develop interstellar vehicles to not only enable interstellar travel to other planets but also it becoming ubiquitous to the average citizen just as terrestrial vehicles are ubiquitous to most citizens.Thus by 2045 onwards until 7,137CE AI due to its exponential increasing computing power AI will be able to explore new fields of physics,biology etc that allow it to explore fields of science humans cannot and also hypothesise new technologies and improvements in agriculture that will increase the carrying capacity of the Earth exponentially past the 4,000,000,000,000,000 mark both in terms of housing,energy production and agriculture potentially as much as a 100-1,000,000 times more with this also applying to Mars,Venus and other colonies across the universe.These technologies will also be ones that ensure the same universal gold standard of living to all citizens in terms of housing and ease of access to food,clean energy,healthcare etc.Developments will be made into al fields of physics,biology and chemistry including new ones not yet understood by humans to increase the production of clean energy,increase agricultural production and also means to increase the available space in housing.This will be done as per Clarke’s three laws especially his second law.Thus by stabilising the population between 8,000,000,000 – 9,000,0000,000 people between 2029-2100 for a few centuries or thousand years could allow Mars and Venus to be colonised alongside new unihabited planets across the galaxy and thus give AI time to develop new technologies to increase the carrying capacity of Earth,Mars,Venus snd other planets across the galaxy and eventually universe.Even when AI reaches it peak at 7,137CE and these technologies are developed population growth will likely slow down exponentially as well thus in turn slowing down the rate that humans colonies all possible habitable worlds in the universe.This could make the population reach the 4,000,000,000,000,000 mark more feasible including in terms of comfort possibly not requiring the need for cities to go too high and make more use of underground and underwater communities and other technologies hypothesised throughout this website.Damage done to the biosphere such as reducing carbon dioxide and methane levels to pre industrial levels,reforestation of agricultural land and bioremediation of pollutes soils,oceans,ecosystems etc can begin as early as 2029.By slowing down and stabilising population growth between 8,000,000,000-9,000,000,000 between 2029-2100 for a few centuries it will allow AI time to develop new technologies that will exponentially increase the carrying capacity of Earth with by 2100 having both Mars and Venus terraformed and colonised will allow for stable population growth to occur for a few centuries more as new people born on Earth will be shipped to Mars and Venus and also other discovered planets across the galaxy allowing the Earths population to be stable at this range for several more centuries or thousands of years while Mars,Venus and other planets are colonised.As a result if the worlds population stabilising between 8,000,000,000 – 9,000,000,000 between 2029-2100 onwards it will allow for new technologies to be developed in an exponential manner that reverse anthropogenic climate change,provide anbundant clean energy,food and water as well eliminate poverty and increase the standard of living for all patients and citizen thus exponentially increasing the carrying capacity of the Earth,Mars,Venus and other planets across the galaxy and universe with this stabilisation continued for several centuries and thousands to allow for interstellar travel to be developed alongside terraforming Mars and Venus.Thus contrary to popular belief in a world of immortality a combination of wider availability of contraception,CRISPR allowing males and females to have control their fertility as well as patients staying in their fertile peak and encouraging people to focus on careers and stay single and outside of monogomous relationships for several centuries and even thousands of years could exponentially increase the time span for Earth and the rest of the universe to become overpopulated or reach maximum sustainable population capacity with population growth could theoretically in fact stall,slow down,peak or stabilise between 8,000,000,000 – 9,000,000,000 by 2029-2100 onwards for several centuries or thousands of years to sustainable levels of growth without coercion from the state etc as people will simply decide to choose to delay starting families or even getting married for several hundreds or thousand years and them focusing on careers and travelling the world and universe.VR technology could be used to start virtual families centuries or thousands of years before starting real families in the real world.VR simulations will allow sterile couples and the entire human race to have as many children in singular or group simulations with each person having access to their own personal VR simulations generated by system unit and server computers in their homes that are at first planet,then galaxy and then universe sized simulations with one able to access simulations created by others populated with an an infinite amount of AI characters to accommodate any issues of becoming bored of having met everyone as well as allowing those to whom children are important to interact with in a platonic manner an infinite number of children can be created this way both in the case where one decides to never have children or delays having children in the real world for several centuries or thousands of years with the avatar is determined by AI namely Phanes combining their DNA of each parent and creating unique genotypes that are repeated to that virtual child with extra individuals created by Phanes extrapolating an almost infinite amount of scratch DNA.There can be single simulations for each citizen that contains other AI created from scratch and be a shared simulation between multiple people or all people on Earth by linking system unit and server units between two or more people or each citizen can have their own simulations separate to that of others with the option of citizens being inside simulations enter simulations of other citizens within AI in these simulation also doing this with all AI created having separate personalities independent from each other and AI as part of the wire that would have their own personalities,releationships with each other and produce their own media such as movies,television shows,video games,plays and also live news reports and magazines that can be uploaded into the real world version of YouTbe,Wikipedia,Dionysus and Pheme as well with then having their own in simulation versions of the internet and the wire with their own in simulation political and celebrity stories etc and able to create their own offspring overtime with their knowledge of being AI or not decided by society and each user with if aware of the real world they can use biosynths to interact with the real world.They can take part in vlogs on YouTube and produce movies,video games and also podcasts and radio programmes and newspapers,magazines and live news etc in the real world and their individual simulations thus exponentially increasing the amount of media being produced even if the population of humans in the real world stabilises for several thousand years.Each world they inhabit can be a replica of Earth and the real universe or planets and universes created from scratch and from fictional media such as video games,television shows etc.People will be able to interact directly with the AI in these simulations via entering the VR simulations or the Ai inhabiting biosynths in the real world.Other AI can inhabit these simulations can be created from scratch to give more variety.At first it can be the size of Earth and updates can be used to add more planets making it galaxy or universe sized and include billions of galaxies each with billions of planets including ringworlds and alderson discs.Planets present can be much bigger than Earth as seen by the video game Minecraft having a surface area eight times that of Earth.They can stay immortal or they can grow old and die in the same ways that pre immortal humans can through disease,old age,accidents and also murder etc thus allowing for the concepts of death to be catered to.As stated this utilisation of virtual children in VR simulations could cater to the need for most people choosing to postponing having children in the real world by centuries and thousands of years to have VR children prior to this by allowing them to have as many children as they want in these VR simulations whenever they want in their teens,20s,30s,40s and so on until before they decide to have real children in the real world or even before they decide to get married when they reach the age range of several centuries and thousands of years old and provide billions or more new people to interact with in a VR simulation thus allowing for billions,trillions or more new people to interact including those that are ones virtual children and grandchildren with in VR simulations and not adding any new people on the real world and allowing for it to take exponentially more centuries or thousands of years for the population of Earth to reach the 11,000,000,000 and 4,000,000,000,000,000 mark.These VR simulations indistinguisheble from real life should be possible 2029 and become exponentially more realistic and larger every year especially by 2045 onwards until 7,137CE and thus can allow the population of Earth to stabilise and peak between 8,000,000,000 – 9,000,000,000 between 2029-2100 for at least several centuries or possibly thousands of years thus delaying the point that Earths population reaches 11,000,000,000 mark expected by experts by 2100 by several centuries or even several thousand years with it exponentially increasing the timeframe it takes to reach the 4,000,000,000,000,000 mark while at the same time allow the average individual have an almost infinite amount of children in VR simulations both prior to and after they have them in real world.People can have virtual children and even virtual husbands and wives prior to settling into monogomous relationships and having children in the real world to cater to the intrinsic emotional needs of having spouses and children for several centuries and thousands of years prior to to doing so in the real world.This should also eliminate any state intervention in controlling the fertility or birth rate of the average citizens and any notions of their having to be licenses or even lotteries to have children or any draconian measures that infringe on the rights of citizens especially females including forced abortions and sterilisations alongside elitism with regards to only the famous and powerful allowed children as anyone can using VR technology have as many virtual children they want in between the centuries and thousands of years they have them in the real world.Thus VR simulations will allow anyone have as many children they want,whenever they want with zero state interference and also lotteries other any other systems with this done both prior to and after one has decided to settle down into monogomous relationships.The time dilation effect of VR will allow for parents to be more attentive to VR children than real world ones.The video game Bacchus that replaces Second Life can cater to this alongside other personal simulations and a single shared one.Each citizen through onboard computers at home the size of system unit or server can create planet,galaxy and in time universe sized simulations filled with billions of galaxies with billions of planets with humans and non human races thus giving society a wide variety of possibly infinite new people and media for them to interact with outside of those present in the real world at the given point with one able able to through cloud networks and invites able to access the simulations of other people.The virtual children can have phenotypes and genotypes be either designed or randomised using all possible 64,000,000,000,000 possible genetically distinct combinations of genotypes between each couple.When couples do decide to have children natural designer offspring fertilisation can be used to create real world versions of virtual children.Even unmarried individuals in their teens,20s,30s,40s etc can have virtual children prior to settling down into monogomous relationships.This VR technology will also cater to materialism allowing the average individual own and infinite amount of manufactured goods especially garish luxuries such as mansions,cruise ships,yachts etc conjured up at zero cost without expending energy and the finite resources of the Earth allowing existing ones in the real world to be traded away or recycled.Biosynths escorts and pornography stars designed on Peitho can cater to an infinite amount of adult sexual partners in the real world via biosynths and VR simulations outside of that present in the real world.Furthermore both individuals and society as a whole could switch from quick short term planning focusing of goals with regards to live goals,family planning and environmental and political concerns and policies that lead to sloppiness and half baked solutions,carried out instantly with little thought and forward planning that fall apart within years would change to more long term planning of these due to individuals living long enough to see events that will occur hundreds,thousands or even millions of years in the future that would take into account events in the distant future that would be more likely to be stable and planned and enacted more efficiently.Legalisation of homosexuality and same sex marriage worldwide especially in the developing world ie Africa and the Middle East will encourage homosexuals to no longer be closeted and enter unwanted marriages with women and have children against their will as they will be legally allowed to enter marriages and monogomous relationships with those of the same gender thus preventing them having unwanted children with women with them using adoption if not IVF births thus further stabilising population in the developing countries and elsewhere where it is illegal.The main factors of population spikes and indeed population growth especially since the start of 1800s has been the need to produce as many children prior to when ones fertility drops before the age of 40-50 and thus biological fertility factors,the need to produce as many young as possible to survive poverty,lack of education and access to contraception due again to poverty.All of these factors can be resolved through education and availability of contraception and CRISPR treatments to control fertility as well as biological immortality allowing females to maintain their fertile peak forever thus delaying the need to procreate for at least several centuries or thousands years.
Underwater and underground communities would also increase the carrying capacity of the Earth with underground communities underneath not only existing cities and towns etc but also underneath wilderness such as forests,jungles,hybrid farms.Underground communities will also be underneath existing towns,villages and cities worldwide and underneath existing and reforested wilderness with them using VR technology and also digital smart windows to allow one to escape to any environment while still increasing the density of them.They will utilise carbon scrubbers,geothermal etc.Underwater communities will be able to be constructed at the lowest depths of the ocean and along the coasts of all major cities and like underground communities will be using geothermal power,carbon scrubbers,biosynth nanomaterials that separate oxygen from carbon dioxide,internal gardens and even forests with them through pyrex infused with graphene,liquid glass that repels water and prevents the acidity of the ocean eroding stone and steel structures and even graphene composites will allow the large underwater sections of the Earth with them formed by the coast of existing cities,islands etc and also in the depths of the worlds oceans decided by AI with them accesed by Oceanus,bathyspheres and cruise ships etc stopping at them underwater and large lighthouses in the surface that houses stairwells and elevators to them with even floating cities located above and connected to them.These would use bioluminescent moss,CSYS lighting on the ceiling and on streets that turn on/off for lighting and trees and nanomaterials that separate carbon dioxide into oxygen.Further advances could have them include soil etc created by organic material to include parks and even wilderness and complex artificial ecosystems and weather systems and other advances to include day/night cycles with not heating and light during the day with during the night heat captured into energy by thermo-piezoelectric materials etc.Floating cities can be above these underwater communities and connected to them by elevators and other parts of the ocean via graphene trusses.Nanomaterials including graphene and others of all 94 elements will play a role in allowing cities to go higher thus making them more compact and dense with underground communities underneath them further increasing density with support columns have these bored into them or put on roofs in layers.Biosynthtic technology and nanomaterials that passively separate oxygen from carbon dioxide will provide oxygen and digital smart windows provide scenery.This would use scratch DNA,that from chemosynthetic bacteria and plants could allow them to do so passively without sunlight with biolumescent plants and moss that also able to do so via this via this DNA.Recombinant DNA from either S.liquefaciens,Carnobacterium genus and even M.wolfeii,M.barkeri,M.formicicum or all combined could allow humans to survive the low pressure of the upper atmosphere of Earth with regards to those living in very tall buildings inthe “death zone” of Earth like in the Himalayas 8,000m.This extremely low air pressure of 7 millibars is lower than the 303 millibars of the highest point on Earth – the summit of Mount Everest.Tall luxury hotel style communal homes that use Venetian suites – 65.0321 square metres or luxury apartment blocks will play a role in allowing cities to go higher thus making them more compact and be the predominant home in cities,towns on Earth and on colonies across the rest of the universe.Existing obsolete buildings such as banks,corporate headquarters and supermarkets etc can go as high as possible via roof extensions.Future private homes will be cottage,suburban home style homes,tall ones with underground extensions and underground ones that take up less space on the surface.Cities that suffer urban sprawl can have all buildings in areas outside of retail streets/outlets and central business districts demolished,roads dug up and have tall luxury hotels put in place to house those from poor neighbourhoods with this and underground communities used to make them compact to increase density.People in slums and low quality housing estates can move into communal homes derived from skyscrapers etc in central business districts and mega hotels built ontop of major retail outlets and retail streets allowing slums,low quality housing estates etc to be demolished and the land reforested.Even most suburbs will be demolished and roads dug up.Only homes wherein the original homeowner decides to stay and renovate will stay standing and communal homes built around while allowing enough land for sizeable gardens.Those who stay will merge their home with that of several neighbours making them miniature mansions with all other homes of low quality demolished and the land reforested.Otherwise the land they occupy can be reforested.In all options roads will be dug up and the landscape reshaped..Even islands that have large areas of low quality homes like the Isle of Man,Lanzarote,Gran Canaries,Hawaii etc will have whole low quality suburbs demolished as locales move into existing and new hotels and have underground and underwater communities also with roads dug up and hedges removed.Underground communities will be built underneath all new and existing reforested wilderness allowing all reforested land to house communities underground with even homes designed to be underground that have windows and balconies that pop up at the top with stairs etc and even underground roads allowing access to both underground homes and communities.Underground communities will also be underneath existing towns,villages and cities worldwide and underneath existing and reforested wilderness with them using VR technology and also digital smart windows to allow one to escape to any environment while still increasing the density of them.Underwater communities will be able to be constructed at the lowest depths of the ocean and along the coasts of all major cities using geothermal power,carbon scrubbers,nanomaterials that separate oxygen from carbon dioxide,internal gardens and even forests with them through pyrex infused with graphene,liquid glass that repels water and prevents the acidity of the ocean eroding stone and steel structures and even graphene composites will allow the large underwater sections of the earth to be colonised.Floating cities can be above these underwater communities and connected to them by elevators and other parts of the ocean via graphene trusses.Land surrounding all towns,villages and cities worldwide will be reforested as far back as possible to their primevil state via soil samples determine what grew there with them returned to their original state of jungles,forests,woodlands and meadows etc.This will give them sizeable wilderness for hiking with all towns,cities and villages will become compact and densely populated via utilising underground communities underneath existing towns,cities and villages and even existing and reforested wilderness with cities and towns becoming taller via roof extensions to communal homes derived from primarily obsolete buildings such as retail outlets and banks etc.Urban forests will be set up in towns,villages and cities worldwide to improve air quality and provide areas for hiking.Urban prairies will be reforested alongside golf courses and driving lanes due to them being replicated in VR simulations with areas of cities etc that house patches of grass criss crossed with roads have the roads dug up and turned into parks etc with areas of blight in all major cities consisting of abandoned decaying will have them demolished and the land reforested with only historical buildings and those of sentimental value kept and renovated to luxury standards.Golf courses and driving lanes by themselves and in the grounds of country clubs and hotels converted into communal homes will be reforested as far back as possible alongside other outdoor amenities such as paintball zones etc will be reforested as far back as possible since they will be replicated in VR simulations with all future new courses being VR ones designed by the AI Agon and members of the public.Urban prairies will be reforested as well.Playgrounds and funfairs can be demolished dug up and turned into parks or community farms or permanently reforested due to them visited VR technology once scanned in.Greyhound and horse racing tracks will be reforested as well due to being made obsolete and buildings present turned into homes with this replicated with NASCAR,Formula 1 race tracks once dug up since they will take place in simulations.All human and pet crypts and graveyards worldwide both small ones and large military ones will be turned into memorial gardens or woodlands with a pillar housing the names of all buried individuals present allowing memorial masses to be held while at the same time them housing extra green space.Small ones next to churches will be turned into gardens while larger ones next to reforested areas and woodlands as well as large military graveyards will be reforested with in all cases the headstones,crypts demolished and recycled and the bodies dug up and converted into diamonds or cremates to be kept by next of kin or placed in museums.Some will become memorial gardens while those next to fields and forests may be turned into memorial forests which contain trees and also flower beds arranged ergonomically with again a pillar that houses the name of the dead present where memorial masses can be healed allowing it to be reforested and house memorial masses etc with as states all dead bodies dug up and converted into diamonds kept by families.Any future humans and pets that do die will be pyrolysised and converted into diamonds to be kept in homes of relatives etc or cremated and stored in urns.
As detailed in the energy section of this website by 2035-2045 the world should have switched to an entirely renewable energy grid consisting of 70% geothermal,10% renewables,10% fission with the remaining reserves of fossil fuels such as oil,coal and gas being burned at 10% to allow the carbon dioxide sequestered into an abundant supply of diamonds,graphene and biochar with automated carbon sequestration programmes lowering carbon dioxide and methane levels back to pre industrial levels of 280ppm and 722ppb respectively by 2035-2045 with aforementioned and new technologies increasing agricultural productivity exponentially while still allowing all land used for agriculture to be reforested forever.Biosynth batteries will make electric vehicles,both autonomous private vehicles but also public ones and aeroplanes and cruise ships and wall batteries in homes etc ubiquitous at zero cost without the need for mining for finite reserves of Cobalt,Lithium and sodium etc which are environmentally destructive to extract with them unlike lithium based batteries being able to store vast amounts of energy within minutes and last forever making them suitable for cruise ships,autonomous vehicles and even aeroplanes all powered by geothermal.Geothermal that uses closed circuit looped pipes wherein water is heated and turns turbines and never leaves the piping thus never causing earthquakes should be able if perfected by 2035-2045 be able to provide clean energy for the entire world for at least 217,000,000 years according to a 2017 study called A Global Review of enhanced geothermal system by Shyi-Min Lu of the Industrial Research Institute with almost zero carbon dioxide emissions with fission power providing at least 300,000 years of clean energy with synthetic oil,coal and gas providing a cheap,free and carbon neutral source of energy for millions of years.Bacteria can through Biosynth WiFi and also anabolic and catabolic reactions be made to synthesise synthetic alkanes such methane,ethane,propane etc all the way up to tetrapentacontane and also branched alkanes,cycloalkanes,alkynes,saturated aliphatic hydrocarbons,unsaturated aliphatic hydrocarbons,aromatic hydrocarbons,annulynes,annulenes and alicyclic compounds and also synthetic gasoline,diesel,pentane,petroleum,gasoline,kerosene,butanol etc and also gasoline additives,brake fluid,gear and motor oil onsite of Talos factories etc.It since grown onsite of Talos factories,petrol stations,power plants and homes would eliminate energy in extraction and transportation thus having a energy returned on energy invested ratio better than 3:1 with consistently high yields forever making countries and even each individual town,village and city self sufficient with regards to fossil fuels for potentially millions of years of not forever.Then of course bacteria through recombinant DNA can create oils from all 2,391,000 plants and animals on a commercial scale that can power gasoline vehicles and power plants with carbon neutral fuel.This would render all remaining finite reserves if oil and gas in the crust obsolete and since Phanes and Steropes could own patents on the bacteria it would be by law free shutting down fossil fuel corporations forever with these synthetic fuels being created by bacteria would need carbon dioxide to grow meaning they would intake the carbon dioxide they release when burned this would make them carbon neutral thus allowing them to be used as a carbon neutral transitional fuel while automated carbon sequestration programmes reduce carbon dioxide and methane levels back to pre industrial levels and the world transitions to renewables such as geothermal and also Biosynth batteries for vehicles.This will be grown onsite of petrol stations,local power plants and Talos factories and even homes thus giving it a energy invested,energy returned ratio better than 3:1 and will require no human labour or even automation that will provide carbon neutral,free and limitless oil and gas for millions of years.Algae grown onsite of sewage treatment plants will also provide a carbon neutral biofuel that will act as a transitional fuel that adds no extra carbon dioxide to the atmosphere while carbon sequestration programmes remove excess carbon dioxide from the atmosphere reducing the levels of carbon dioxide from 422ppm to pre industrial levels of 280ppm.By 2045 onwards fusion power and dyson swarms and other emerging technologies will be developed that can provide clean abundant energy for billions of years with as detailed in the energy section.Fusion power by 2050 will meet the energy demands of the world for at least 60,000,000 -150,000,000,000 years.Dyson swarms and other emerging technologies will by 2100 onwards provide even more clean abundant energy for billions of years.By 2029 onwards all private homes worldwide will undergo rennovations that make them water and energy efficient and also add roof,side and underground extensions to add amenities and also house bedrooms for tourism as home sharing will replace hotels and motels with them also undergoing luxury renovations to increase the standard of living of the residents.All hospitals etc will undergo this.All abandoned and obsolete buildings worldwide such as banks,supermarkets and other physical retail outlets as well as banks,corporate headquarters etc will be rennovated into luxury hotel style homes with measures to make them energy and water efficient with existing hotels,motels etc converted into permenant homes.Asbestos and other toxic compounds will be removed and replaced with fungi based insulation and hempcrete.
As detailed here and in the summary of food production section of this website the world by 2029 will have switched entirely to in vitro meat,bacteria based commodities,algae,aquaponics,aeroponics,hydroponics and also localised agriculture in the form of home,community and vertical farms thus allowing for all land currently used for agriculture to be reforested forever and still feed a growing population well beyond the 11,000,000,000 expected by the end of the century.Tyche and other AI will investigate ways to lower the amount of water used worldwide.Aquaponics,aeroponics and hydroponics by its very nature uses 70% less water with it becoming the predominant method of agriculture.Crops,in vitro meat and remaining livestock etc and even humans using Xerophile DNA will reduce water requirements for humans,crops etc by as much as 90-99% with that from T.gammatolerans,W.dermatitidis,C.sphaerospermum and C.neoformans combined with scratch DNA possibly allowing them to radiosynthesis thus replacing the biological process of water completely.All homes and buildings worldwide will undergoe luxury renovations and also those to make them water efficient including tornado and spiral faucets for taps that reduces water use by 98% and Orbsys showers that reduce water use in showers by 90% with hydrophobic and anti-dirt liquid glass sprayed onto clothing and cutlery and utensils will allow them to be cleaned by gravity thus eliminating dishwashers and clothes washers.AI anf human will conduct intensive research done into reducing water use in all sectors of society by at least 90%.Desalinsation plants will be used by all coastal towns,cities and villages by 2050 to supply them with water which will be once treated pumped into lakes and rivers to return to the ocean and keep levels of water in lakes and rivers constant all year long especially in desert countries that face droughts.Inland landlocked towns and cities can use underground pipes to transport water inland and again the treated water dumped into lakes.Since the Earth is covered by 70% this should eliminate water scarcity for the next few thousand years.Nanomatetials such as graphene anf biosynth tissues will reduce energy costs in desalinisation plants by 99% making it ubiquitous with them powered by renewables such as wave,geothermal and thermophile-piezoelectric material covered geothermal pipes.By 2045 technological developments will allow AI as part of Theoi Meteroi control they weather including rainfall patterns thus keeping areas well fed of water especially in times of drought with this even used to push deserts worldwide into artificial wet periods turning the Sahara,Sahel,Death Valley anc all deserts worldwide into lush jungles,Savannah’s etc.Reducing Carbon dioxide levels back to 280ppm
will return global rainfall patterns to normal.Biocompatible microbes through scratch DNA will replace most elements in electronics,batteries and robotics etc.
New technologies from 2045-2100 onward can be developed to increase the carrying capacity of the Earth in terms of housing and agriculture with when combined with improved agricultural productivity could if perfected exponentially increase the ability for the Earth to house more people.2045 once the computing power of AI exceeds that of all 9,000,000,000 people in the planet marks the begging of a trend towards technologies that we associate with science fiction and even those unimaginable to us due to the fact that at this point Gaia and other AIs computing power exceeds that of all 9,000,000,000 people on the planet and the fact that the development of AI and processing power of machines and primitive computers and modern day ones has been synergistically linked to each other since the beginning of the modern age of science with this thus continuing until 7,137 CE following the exponential growth curve of Moores Law thus we can assume that due to the increased processing power of Gaia etc new fields and developments of science in all fields will follow this curve and trend alongside it most of which will be beyond our limited comprehension of reality and our current understanding with 2045 being as stated the start of this and also the point at which AI will always be exponentially more powerful than all humans on the planet.
By at least 2035-2045 Astraeus and Pan will begin terraforming and setting up colonies on the moon,Mars,Venus etc and constructing space stations and cleaning up the space debris surrounding the Earth by 2029 as detailed earlier on.Depending in the rate of terraforming proportional to the rate of technological development and computing power it could be possible for both be terraformed and habitable between 2055-2100 with all work automated from start to finish by Astraeus,Pan,Artemis with bases and colonies set up in underground communities and some surface colonies during the terraforming process by humans engineered to survive the atmosphere etc until intensive bioremediation makes them completely indistinguishable to Earth.Space stations orbiting both Mars and Venus can be set up that act as permenant homes both during and after terraforming.At this point by 2045-2100 Astraeus will also start setting up bases on the Moon,Europa and other terraformeable moons in the Solar System and also setting up orbiting space stations across these moons and also Earth and even interstellar vehicles used as permeant homes that will be able to support large populations especially housing indoor farms etc with VR technology used to escape to Earth like environments and used as keep in touch with people on Earth thus alleviating fears of overpopulating Earth at least for the next few hundred or thousand years.If possible once Venus is colonised since it is roughly the same size of Earth a few billion people can be transferred to it from Earth to lower the population of Earth to the population of what it was and will be between 2000-2050 without killing anyone with Mars at first housing a few million to few hundred million.Otherwise a few billion new patients born on Earth can be transferred to Venus and Mars once they reach adulthood.Both Venus and Mars will be terraformed to the point that it will be habitable like Earth by removing all excess carbon dioxide and other toxic gases,add soil and ozone layers and have both similar atmospheres,climates and complex ecosystems like jungles,deserts and oceans like on Earth.Astraeus,Pan etc will begin to terraform both Mars and Venus by at least 2035-2045 with it habitable and indistinguishable from Earth in terms of climate,ecosystems with Venus having the same amount of surface terrain as Earth with Mars having slightly less and then both colonised by at least 2100 with Venus being able to hold the same 4,000,000,000,000 people as Earth with when first terraformed at least a few billion newly born patients once they reach adulthood will be transferred to both Mars and Venus keeping Earth population stable at 8,000,000,000 – 9,000,000,000 with Mars have a few million or few hundred million patients transferred there with underground communities increasing the population allowed there with its carrying capacity being possibly being at most a 1,000,000,000 people.If possible once terraformed by the end of the century a few billion people could be transferred to Mars and Venus thus lowering the population of Earth to between 5,000,000,000 – 6,000,000,000 people.The process of terraforming them both will be slow at first but will become exponentionally faster from 2045 onwards with it likely terraformed and habitable before humans set foot on both with Pan etc organising this terraforming process that will automated from start to finish.By 2035-2045 underground,floating and underwater communities will be set up by AI on Earth with them housing at least another few billion people with although not removing people from the Earth it can both house more people than normal since underground communities can be underneath existing towns,cities and also reforested and existing wilderness with the worlds ocean floor housing more land for cities than on the surface.Space stations that orbit the Earth,Mars,Venus and other planets in the solar system and interstellar vehicles will by 2100 be able to house several million to several billion if mass produced and can be self sufficient that will become permenant homes with VR technology slowing them to escape to any environment.If possible advancements in physics can allowing for flying cities that float in the upper atmosphere of Earth similar to proposed flying cities of Venus that travel constantly across the Earths upper atmosphere with genetic engineering allowing humans to survive these conditions with these housing a few million people.It is by 2100-2200 that the sentient Astraeus will being charting,exploring and mapping the entire Milky Way Galaxy through mass prodicing interstellar vehicles that explores ever star system as detailed later on.By 2029-2100 Astraeus,Hecate and Urania etc will seize control of and use telescopes and satillite to at first chart the galaxy by searching for Earth type planets with its increasing computing power allowing it to do so in a much more efficient and faster means than what is currently possibly with by 2029 onwards it carrying out intensive research into relevant fields of physics for not just interstellar travel and mass producing interstellar vehicles but also improving the ability and rate of scanning the galaxy using both radio telescopes and satillites etc to detect Earth like planets and advanced civilisations on par with or more advanced than humans with this improving exponentially each year until eventually the entire universe is charted with it also able to mass produce satillites,observatories and and radio telescopes that are exponenentially more efficient,more compact,cheaper and faster every year using Biosynth technologies and nanomaterials combined with quantum computing etc thus improving the rate it can scan the galaxy for new Earth like planets.By 2035-2045 it should become exponentially better at detecting other Earth like planets and its rate of doing so will become exponentially better especially when combined with newer technologies and also having all observatories and Satillites across the world fitted with technology and all automated and controlled by Astraeus that scans the galaxy in a pre programmed manner thus meaning we should have at least a dozen Earth type planets detected between 2045-2100.By 2045-2100 AI will begin via probes etc charting the entire universe starting with the Milky Way galaxy in an exponentional manner.Between 2100-2200 interstellar travel will become ubiquitous and within the reach of the average citizen in the form of interstellar vehicles similar to cruise ships that carry thousands or more passengers as well as interstellar versions of aeroplanes,buses,taxis and even interstellar private vehicles all controlled by AI.Between this time 2100-2200 the amount of Earth type planets discovered will increase exponentially to at least several thousand or several million with us gaining first contact with at least a few hundred sentient alien races during this period as well.Starting in 2029 onwards Hecate,Astraeus will by 2029 onwards carry out intensive research into the necessary fields of physics to develop interstellar travel which will become exponentially better by 2035-2045 onwards making the first interstellar vehicles used for exploration and eventually commercial cruise ship style vehicles and even private interstellar vehicles being capable of traversing the vast distances between stars in the Milky Way galaxy feasible and ubiquitous.From then on intensive research will be carried out to improve interstellar travel but also develop and improve intergalactic travel making it ubiquitous.Erebus and Nyx will also set up at this time alongside transporter technology for interstellar vessels,post offices and also airports allowing for humans to quickly move from Earth to other key star systems and also allow for quick communication across the universe since intensive research will be started by Hecate,Astraea etc into all fields of physics necessary for interstellar travel and communication and the creation of Erebus and Nyx systems as detailed later on starting at 2029-2100.By at least 3,102CE the entire Milky Way galaxy will be charted and mapped with by 7,137CE at least most of not all of the 100,000 galaxies as part of the Lanikea Supercluster will be mapped and charted with colonies set up on unihabited planets across all galaxies.Once the Lanikea Supercluster is mapped then rest of the universe will mapped in an exponential manner with by 428,887 CE the entire universe consisting of 200,000,000,000 – 2,000,000,000,000 or even more galaxies will be mapped.Estimations put the number of Earth type planets in the Milky Way at 11,000,000,000 – 40,000,000,000 ensure that stable population growth will be necessitated for the next 55,000,000,000,000 – 200,000,000,000,000 years with there being an estimated 200,000,000,000 – 2,000,000,000,000 galaxies in the observable universe.Further theories project that the universe may in fact be 150,000,000,000,000,000,000 times bigger than the observable universe with at least 150,000,000,000,000,000,000,000,000,000,000 – 1,500,000,000,000,000,000,000,000,000,000,000 galaxies.Artificial planets the same size as Earth can be created in other solar systems and in our native one with as much 202 of them created that orbit Jupiter,Saturn,Neptune,Uranus that can be either as densely populated as Earth or even more densely populated if they are decided to become ecumenopolises from the outset similar to the fictional Coruscant with artificial climate and hydrological systems present controlled by Theoi Meteroi that could ensure that stable population growth will be necessitated for the next several billion years or at least several hundred million years.Megastructures such as ringworlds,dyson shells and alderson discs with the surface area of 1,000,000 – 1,000,000,000 Earths if made possible and could be constructed through advances in science and technology by AI and have all surface area habitable could ensure that stable population growth will be necessitated for at least 5,000,000,000 – 200,000,000,000,000 years each.AI as it becomes exponentionally more powerful could theorectically extrapolate countermeasures of these megastructures making all parts of them fully habitable and stable and protect them from asteroids and solar flares.Colonisation of in solar planets and moons,formation of space vessels and stations as permanent habitats,interstellar,intergalactic and inevitably interdimensional travel will accommodate a growing population at a steady rate due to the aforementioned ideas will ensure that stable population growth will be necessitated for the next several hundred trillion years.Research will be done into interdimensional travel to gain access to parallel dimensions that are uninhabited that could exponentially cater to stable population growth indefinitely.Digital immortality can be researched where ones conciousness is absorbed not copied into computer networks where one could lives forever in VR simulations and servers with one using blank biosynths to interact with the physical world.
Skyscraper hotel or apartment style homes will become the predominant communal home and predominant homes worldwide.Those modelled in hotels will house suites the same as the Venetian standard roughly 60.387 square meters enough to house a king sized bed,en suite and enough closets for married couples with these homes having communal living rooms in the form of the communal lobby,communal gardens on the grounds of them and also communal rooftop gardens,communal dining halls,communal automated kitchens and communal amenities like pools,saunas etc.To eliminate human labour botlr,tug and other robots providing room service will be present alongside other robots etc eliminating all human labour in kitchens,room service and also communal amenities like pools,saunas etc with all of hotel style homes and their amenities,suites and kitchens etc being luxury style ones on par with the Venetian in Las Vegas.All human labour will be eliminated by 2029.The buildings built for the homeless and poor will be if possible tall as original World Trade Centre twin towns destroyed in 2001 or even Burj kalifa.Those as tall as the World Trade Centre could holds 1,244,900 square metres (13,400,000 square feet) with Venetian standards suite being 60.37 square metres (650 square feet)thus allowing these to hold at least 20,621 suites as much as 20,521 – 41,242 people if 1-2 people are in each room.The Pallazo Standard is slightly bigger at 720 square foot or 66.8902 square metres and could hold 18,611 – 37,222 people.The average Americans bedroom which is considered one of the largest in the world is 12.262 – 18.58 square metres(132 – 200 square foot) and most master bedrooms are 20.8103 – 32.51 square metres(224 square foot to 350 square feet) meaning residents will have large bedrooms larger than in normal homes at least two or three times bigger than a master bedroom and five times bigger than a normal bedroom enough to meet the needs of married couples and hold an en suite with a toilet and shower,king sized bed and large closets for clothes with those by the sides housing balconies.These hotel style homes will have automated communal kitchens,automated communal dining halls,communal amenities such as pools and sauna etc and a communal lobby acting as a communal living room with them having one to five extra floors than the World Trade Centre to house these communal amenities and lobbies on the ground floors.Hotel style homes may need extra floors to ensure an equal dispersion of communal kitchens and dining halls to deal with the ability to serve 18,611 – 41,242 people with food with if need be there being the option of meals delivered to each suite.Botlr and tug robots will deliver meals to suites with these added to existing hotels and motels as well as obsolete buildings etc converted into permenant homes.Kitchens will be automated by using chef robots etc and biosynths.Underground basements can house these extra floors.Otherwise each persons 60.37 – 66.8902 square metre suites can in place of living rooms house a closet and also miniature kitchen with a microwave,countertops,sink and fridge.The suite can be modified into a micro suite that is 60.37 – 66.88902 square metres and is larger than most modern day micro-apartments.Micro-apartments that are 60 square metres could in these buildings hold 18,611 – 41,242 people,Those that are 50 square metre apartments could hold 24,898 – 49,796 people with 40 square metre apartments housing 31,122 – 62,244 people.Those that are 30 square metres could hold 41,496 – 82,991 people.Hotel style homes will be modelled on hotels with the Venetian and Pallazo standard of 60.37 – 66.8902 square metres(650 square feet) that is larger than most American normal and master bedrooms will be the bottom baseline style home with again these hotel style homes will have communal living room/lobbies and them having automated communal kitchens and automated communal dining halls.Other communal homes built including in the same size as this model will be luxury apartment blocks on par in luxury quality to billionaires row in America such as One 57,432 Park Avenue,252 East 57th Street,Central Park Tower etc and similar high end luxury apartment buildings around the world thus giving the poor currently living in slums,shanty towns and even the homeless quick access to high quality housing.Other models can be developed that are compact and be able to house large amounts of people.The World Trade Centre each individual building took up space equal to 4,019 square metres wide and 0.004019 square kilometres and thus combined were 8,038 square metres and that is 0.008038 square kilometres.The World Trade Centre buildings can have their shape modified to be spread sideways across a large area or different shapes but still have the same internal surface area of 1,244,900 square metres.That would have the building take up 1.24 square kilometres.These 1.24 square kilometre homes will become the predominant homes across the world and even in colonies across the universe including Mars,Venus etc and other Earth type planets and megastructures such as artificial planets,ringworlds,Alderson discs.AI will be able to design new models of buildings that when spread out over 1.24 square kilometres or more or less on one floor can hold exponentially larger internal surface area and thus exponentially larger amount of apartments and buildings and thus hold exponentially more people on 10-100 floors.Mag lev elevators can be added that can go upwards,downwards and sideways to be faste and more energy efficient than conventional elevators to allow the internal area used by the elevators in the original design to be used for more living spaces of apartments with the inner cores structural design modified for each different design of these buildings.Using models that are spread out over 1.24 square kilometres could house the entire population of entire cities and in some cases have extra space filled in with people from adjoining towns and cities.The internal surface area of each apartment in buildings that have one floors as detailed here and others that house between 3,780 – 136,014 and are between 547 – 77,000 square metres which is the size of most luxury mansions,penthouses etc currently owned by the wealthy top 1% meaning most of not all people from all towns and cities could fit comfortably in one building in luxury large sized apartments currently owned by the wealthy and upper middle class meaning even the poor who live in slums and low quality housing estates or even the wealthy themselves will not be cramped with only existing luxury apartments and hotels etc converted into hotel style homes will remain.The amount of people 3,780 – 136,014 that can fit in one floor is the population range of most towns and small cities meaning their entire population can be moved into one single building that takes up 1.24 square kilometres.As stated adding 10 floors could allow them to hold 37,800 – 1,360,140 people which is within the population range of most cities.Adding 100 floors could hold 378,000 – 13,601,400 people again within the range of all of the most populated cities.This 1.24 square kilometres is only a baseline as much better compact,designs that are able to take up even just 0.8038 – 0.88418 square kilometres of land that can hold the same or more people can be developed by AI.The internal surface area of each apartment as detailed here and others that are between 547 – 77,000 square metres which is the internal surface area size of most luxury mansions,villas.penthouses,palaces etc currently owned by the wealthy top 1% or those that are vacant can be found on luxury home retail sites meaning most of not all people from all towns and cities could fit comfortably in one building in luxury large sized apartments currently owned by the wealthy and upper middle class meaning even the poor who live in slums and low quality housing estates or even the wealthy themselves will not be cramped with only existing luxury apartments and hotels etc converted into hotel style homes will remain.These apartment models can be used for apartment blocks housing not only bedrooms but also kitchens,living rooms and other essential rooms but also amenities like pools,spas,home cinemas,jacquzzis and hot tubs with most bedrooms large enough to house double,queen and king sized beds,closets for two people and smart flatscreen televisions with cribs for infants held in parents bedrooms or living rooms etc with children old enough to not need cribs will sleep in their own double,queen and king sized beds with if possible pre teen children sleeping in the same bed with siblings of the same age until they move out in their teens into other apartments etc.These apartments will house large families,large amounts of friends and groups of unrelated people with them sizeable enough to house large living rooms and kitchens and bedrooms for privacy.They will cater to primarily the poor who live in slums and low quality housing estates allowing them to move into these large apartments that are all luxury apartments and allow slums and low quality housing estates to be demolished and reforested giving the cities large areas of wilderness making them 50-90% more compact
The amount of apartments in a set of buildings and how much people they can store is dependent on the size of apartments in square metres and number of beds especially double,queen and king sized beds that can hold present.AI can possibly design new apartment models different than the aforementioned ones with different sizes in terms of metres squared and number of bedrooms with sizeable amounts of space in living rooms and different amount of beds that are adequately sized to increase the amount of apartments and people present.If possible rather than having all buildings apartment models have the same layout of rooms the decided apartment model can have the size of each room modified and its location and layout modified thus giving variety with bedrooms made larger or made smaller to house more bedrooms or other rooms made smaller,larger or removed together and the amount of space they occupy shared equally to all bedrooms thus making bedrooms equally larger or add extra bedrooms with other rooms have this done.This modification can be done to add amenities or make certain rooms more spacious etc.Instead of using a single apartment model ie design,size and amount of bedrooms in each building then its possible for AI to extrapolate thousands of different combinations of different apartment models that are of varying sizes,varying numbers of bedrooms to be used in each set of buildings to increase variety and more importantly increase the amount of people present potentially more than 136,014 people or house various combinations that house between 2,666 – 136,014 people.Other skyscraper homes will have larger apartments that house families or unrelated people of varying sizes.Large apartments if possible can be remodelled into a series of micro-apartments if it can be shown that they can increase the amount of people present.All building types whether hotels or apartment blocks will be purely luxury buildings with luxury furniture,luxury furnishes and flooring etc with silk etc created by bacteria and synthetic wood also created by bacteria used.This will ensure that even the bottom baseline housing for the poor and homeless moving into them will be of a high standard on par with the wealthy above what even most middle class suburban residents have until technological advances caused by the exponential growth of the computing power of AI will increasing the living standard of all people in all types of homes including even those occupying these buildings.All major cities will house these and even coastal cities with even islands that suffer urban sprawl such as Lanzarote,Gran Canaria,Cayman,Mauritius,Hawaii and other densely populated islands that suffer urban sprawl will have urban sprawl demolished,reforested and these tall buildings built with only luxury mansions and palaces especially historical ones left standing with abandoned buildings of historical value kept and converted into homes with large ones converted into communal homes via adding roof extensions.Historical obsolete buildings such as schools,supermarkets,hypermarkets and shopping malls,hotels,motels etc will also be kept and converted into communal homes via roof extensions.The type of building whether hotel style of apartment will be dependent on the place they are put in with small towns of at least 10,000-25,000 people will have Venetian style Hotel style homes present with large towns and cities with populations in between 25,000 – 1,000,000 will have apartment style homes with cities with populations above 1,000,000 will have a mixture of both.The number of bedrooms and rooms in each apartments will be uniform in each set of buildings but the layout of rooms and interior design and architecture of each room will be unique to each apartment with the possibility of each apartment being of different sizes and different number of bedrooms in each apartment in each building and the current population of a town or city will determine what uniform size of apartments etc or what type of apartment,what size and number of bedrooms in each one will be chosen.Those in towns can be built in the outskirts and have all poor people living in low quality homes and ghettos from that town and also from all surrounding towns and even villages added to them thus meaning that populations from entire surrounding towns and villages can be filled into them thus allowing all homes in these surrounding villages and towns to be demolished thus making villages and towns exponentially smaller until only business districts that include retail outlets that will contain supermarkets etc and hotels are left and then will be given roof extensions to make them similar buildings.People especially poor people can even be transferred or move into apartments in different countries and islands etc across the world.This may negate the need for each and every town and city to have them.
Once the world has switched to vertical farms that utilise aquaponics,in vitro meat and bacteria based commodities that become the predominant form of agriculture as detailed in the summary of food production it can allow all land used for agriculture worldwide to be reforested giving Lazarus species and those brought back from the brink sizeable wilderness availible to all countries worldwide with Pan organising biochar carbon sequestration programmes by 2029 reducing carbon dioxide levels back to pre industrial levels between 2035-2045 while the world switches to renewables such as geothermal etc as detailed in the energy and environmental management sections of this website.As a result of all land being reforested through advances in agriculture each country worldwide will have sizeable wilderness areas for hiking,tourism and carbon sequestration and for animals including endangered ones snd extinct ones brought back to roam.Carbon sequestration programmes as detailed in the energy environmental management section will involve Bambusoidea,Cannabis sativa.Salix Babylonica enginered to intake 10 – 1,000 times more carbon dioxide than normal and grow in all soils and climates worldwide which one it reaches maturity will be harvested and pyrolysised and converted into synthetic diamond,fertiliser and graphene to lock the carbon forever into commercial products.If the plants are also engineered to intake 100 times more carbon dioxide every year(1,235 tonnes every year per hectare) through engineering,growing faster and taller and producing large amounts of leaves etc then every year then 123.5Gt can be sequstered on 100,000,000 hectares about 0.67372% of the Earths surface.To sequester 138.4Gt roughly 110,909,091 hectares or 0.74722% of the Earths surface may be needed with 185.3Gt sequestered on 1% of the Earths surface with 10% removing 1,853Gt per year.If possible engineering could ensure 12,350 tonnes can be intaken every year on each hectare every year by increasing their ability by 1,000 times then 0.067372% of the Earths surface would be required to intake 123.5Gt,0.074722% of the Earths surface to intake 138.4Gt,0.74722% of the Earths surface intaking 1,384Gt with 1% intaking 1,853Gt per year every year using Bambusoidaea plantations.By comparison the world emits 37.1Gt of carbon dioxide every year leaving a net removal of 1,815Gt of carbon dioxide every year if we burned fossil fuels at our current rate with a world powered by only geothermal would emit 0.6-1.66Gt every year leaving a net removal of 1,852.4Gt carbon dioxide while the ideal one powered by 10% fossil fuels and 70% geothermal would release 10.6Gt every year meaning every year would have a net removal of 1,842.4Gt of carbon dioxide every year using both geothermal and fossil fuels.These will occur in temperate and tropical countries with the plants enginered to survive the local climate and soils across the world and will include most of Europe including France,Germany,Ireland etc,China and India and North and Central America with it done in land previously used for agriculture once the world shifts to vertical farms etc with once finished the land will be permenantly reforested with since fossil fuels will be continued to be used at a much smaller rate of about 10% these programmes will continue in each countries.These countries have predictable climates and large tracts of rich arable soil with the plants engineered to survive the native soils and climates especially winters and droughts etc.Other programmes will involve macro algae which using 9% of the worlds oceans can remove 53Gt of carbon dioxide every year with genetic engineering increasing this by as much as 10-1,000 times and even allowing less of the ocean to be used as little as 0.009-0.9% of the worlds oceans to be used.This estimation was made by Ocean Foresters in 2012 in a study called Negative Carbon Via Ocean Afforestation“.By comparison the world emits 37.1Gt of carbon dioxide every year leadung to a net removal of 15.9Gt of carbon dioxide every year while still burning at our current rate with a world powered by only geothermal would emit 0.6-1.66Gt every year leaving a net removal of 52.4Gt carbon dioxide while the ideal one powered by 10% fossil fuels and 70% geothermal would release 10.6Gt every year meaning every year would have a net removal of 42.4Gt of carbon dioxide every year using both geothermal and fossil fuels.Macro algae can be grown in the worlds oceans and harvested and pyrolysised to remove at least 53Gt of carbon dioxide every year if only 9% of the world oceans is used with genetic engineering increasing this by anywhere between 10-1,000 times allowing even less of the worlds oceans to be used as little as 0.009-0.9% of the worlds oceans to be used.Like terrestrial based programmes the plants will be pyrolysised into biochar.These would undergoe genetic engineering to increase growth rates and carbon dioxide intake with if it can intake 10 times more carbon dioxide thus allowing even only 0.9% intake 53Gt or allow 9% to intake 530Gt with indoor systems used using recirculating aquaculture systems with them using carbon dioxide from artificial trees.If it can intake 100 times more carbon dioxide then 9% can intake 5,300Gt,0.9% intake 530Gt and 0.09% intake 53Gt.This extra 53-5,300Gt can be ontop of what is intaken by outdoor plantations with the algae also pyrolysised into biochar with it also removing carbon dioxide stored in the oceans reducing ocean acidity and preventing them acting as sinks.If possible genetic engineering similar to Bambusoidea etc could allow 1,000 times more carbon dioxide thus allowing 9% of the worlds oceans to remove 53,000Gt,0.9% intake 5,300Gt,0.09% intake 530Gt and 0.009% intake 53Gt anually.These will take place on the coasts of all coastal countries with it also done on deep ocean rigs.Phanes combined with Physis and 3D 3D DNA printers will expediate thr development of these genetically engineered plants that intake exponentially more carbon dioxide will take only a few years or even days with all steps in planting,harvesting and pyrolysis being automated from start to finish.It should be possible through all of these combined to revert carbon dioxide levels from 422ppm to 280ppm between 2045 – 2100 the latest with this certainly possible by 2100 if starting by 2030.The current level of carbon dioxide in the atmosphere is currently roughly 422ppm with 142ppm excess in the atmosphere and 165ppm by 2029 with each 1ppm by volume of carbon dioxide in the atmosphere thus represents approximately 7.82 Gt of carbon dioxide with this means that 1,110.44Gt needs to be removed from the atmosphere.In 2029 about with carbon dioxide concentrations of 445ppm about 1,290.3Gt needs to be removed.If we were remove 15.9Gt annually then carbon dioxide levels will drop by 2ppm every year meaning it will take 82 years to return to pre industrial levels with if 42.9Gt is removes every year it will drop by 5.41ppm every year taking 30 years to return to pre industrial levels,removing 100Gt every year will reduce it by 12.7ppm every year meaning it will take 13 years to return to pre industrial levels,removing 130Gt would reduce it by 16.5ppm every year meaning it would take 10 years to return to pre industrial levels,removing 258Gt would reduce it by 32ppm every year meaning it would take 5 years to return to pre industrial levels,removing 429Gt will have it drop by 54.1ppm every year taking 3 years to return to pre industrial levels with removing 1815Gt will cause it to drop by 232ppm every year and take less than a year to return to pre industrial levels and so on.AI and human researchers will carry out intensive research as deatailed in the environmental management section of this website to exponentially increase the rate of carbon dioxide intake of macro algae and Bambusoidea etc exponentially starting in 2023 with automated programmes starting between 2025-2029.Macro algae will only need to be engineered to intake 3 times as much carbon dioxide as it normally can and Bambusoidea etc would only need to intake about a 100 times more carbon dioxide as it normally can Proto AI and 3D DNA printers should expediate there development making it possible by 2030 for these to intake these required levels if not more every year by 2030 thus meaning it should be possible to revert carbon dioxide levels back to pre industrial levels of 280ppm by 2040 the earliest and 2060 the latest.In order to revert carbon dioxide back to pre industrial levels by 2040 over the course of a decade if this level of engineering can be achieved by 2030.By 2029-2035 it could be possible to remove up to 100Gt every year with by 2040 it could be possible for 130Gt to 200Gt to be removed every year with marine cloud brightening and calcium aerosol programmes started in 2030 to mask the worst effects of climate change.From 2029 onwards the rate at which it will drop and rate at which the plants through genetic engineering will increase this rate will increase exponentially every year.It can also involve artificial trees that intake one tonne of carbon dioxide every day can through advances in technology such as nanomaterials and Biosynthetic technology exponentially increasing this by 10-1,000 times by 2035-2045.Through this exponentional increase of these artificial trees ability to intake carbon dioxide.if possible as much as 109,500,000Gt(109.6Pt) could be removed annually every year by 2045-2060 using only 1% of the Earths surface via artificial trees that each intake a thousand tonnes of carbon dioxide a day composed of nanomaterials and biosynth technology.This is roughly 7,670 times more carbon dioxide in all remaining naturally formed reserves of fossil fuels such as oil,gas and coal worldwide roughly 14,275Gt.It is roughly 103,791 times more than what needs to be removed from the atmosphere. This use of artificial trees will be used in carbon sequestration programmes as part of terraforming planets rich in carbon dioxide such as Mars and Venus.These programmes will involve these artificial trees in taking carbon dioxide is then converted into dry ice that is shipped to greenhouses or underground tunnels etc that house the aforementioned plants that is then intaken by the plants which are then pyrolysised into biochar.Once agricultural land is not needed due to improvements in agriculture this agricultural land will be used.Once these countries switch to Aquaponics,vertical farms,genetically engineered bacteria etc like the rest of the world they will have large areas of arable land available to grow these plants in large plantations encircling towns,villages and cities etc with once levels drop to 280ppm then most of this land will be reforested with native plants with these plantations continuing to be carried out in parks and some wilderness areas as remaining reserves of fossil fuels are used.All steps in carbon sequestration projects will not only be automated from start to finish managed by Pan but also powered by renewables such as geothermal,wave power and also carbon neutral synthetic oil and gas and also electric vehicles to make them carbon negative.Once the world returns to 280 ppm then these carbon sequestration programmes will still occur in these countries if not worldwode to keep it at that when fossil fuels are burned at 10% rather than 87% with Pan interacting with sensors as part of Theoi Meteroi detecting levels of carbon dioxide and also power plants to ensure that the amount of carbon dioxide being released and sequestered is exactly 1:1 that is for every gigatone released every year then exactly one gigatonne is sequestered every year with this done worldwide.Pan will make sure that carbon dioxide levels will stay at 280ppm forever and if they rise above it then it will increase the amount of plants grown and if it falls below it will burn extra bacteria based fossil fuels or reduce the amount of land used for biochar sequestration etc to prevent it freezing the Earth.Geothermal the predominant energy source will release 97-98% less carbon dioxide than fossil fuels as a geothermal powered world will take 22-41 years to release the same amount of carbon dioxide a fossil fuel world dies in one year with SNOX filters and other measures reducing their carbon footprint possiblt to zero.Once levels are reduced to pre industrial levels of 280ppm and genetic engineering improves their carbon dioxide intake even more exponentially then only a smaller fraction of land worldwode will be needed and the vast majority of land formerly used in original carbon sequestration plantations in each country especially former agricultural land used for these plantations will be permenantly reforested into jungles,forests and meadows.This process of biochar carbon sequestration and artificial trees is more effective than simply planting trees and storing it underground as the carbon dioxide is permanently removed from the atmosphere,can remove larger amounts of carbon dioxide,stores it forever in useful commercial products,can be done anywhere in the world over and over again on the same amount of land,can be fully automated with no human labour with existing programmes that sequester it in the ground ceasing and those already stored in saline aquifers and also limestone removed via boring underground and also oil wells that can remove the carbon dioxide and return it there again.Rather than planting trees once the plants used intake carbon dioxide and once mature they are harvested,cut down and pyrolysised by heating it to high temperatures in a way that release no extra carbon dioxide but locks in a solid biochar material where it can be stored forever in synthetic diamonds,fertiliser,Graphene etc and then the land can be replanted and the process repeated over and over again using the same amount and area of land rather than once through reforesting land.Unlike planting trees which temporarily locks the carbon into plants that is then released in to the atmosphere once the plants dies and decays thus making them carbon neutral biochar locks the carbon dioxide permenantly into commercial products such as fertiliser,diamonds,Graphene and carbon composites thus making it a carbon negative process that lowers levels of carbon dioxide into the atmosphere.Synthetic diamonds produced by these will shut down the blood dismond trade as they will become indistinguishable to real diamonds and become cheaper to manufacture every year from 2029 onwards and will be produced onsite of local manufacturing hubs.Graphene will be created to be used in electronics etc and biochar will be used as fertiliser to increase crop yields.The plants are harvested and pyrolysised wherein they are heated to a high temperature that causes them to form into a charcoal like structure that is then turned into fertiliser,diamonds etc that permenantly locks the carbon dioxide away forever with the process then repeated every year with new plants grown,harvested and then pyrolysised with this removing more carbon dioxide from the atmosphere over and over again thus exponentially decreasing the levels of carbon dioxide from the atmosphere every year.In the case of all plants such as macro algae and Bambusoidea,C.sativa.S.Babylonica used they will be planted then once they reach maturity harvested and pyrolysised that then converts it to biochar that can then be converted into commercial products that permenantly removes the carbon dioxide from the atmosphere and then allows more plants to be grown in its place to remove even more carbon dioxide exponentially by repeating the process over and over again.Furthermore it can be done anywhere in the world with this exponentionally increasing the amount of carbon dioxide removed and all plants used undergoing genetic engineering to not only grow faster and increase the amount of carbon dioxide removed but also be able to grow in all climates,soils and seasons.In desert areas and those with poor soils etc the plants can be grown in greenhouses and underground tunnels.Existing carbon sequestration that involves carbon dioxide pumped into saline aquifers and limestone can only deal with new carbon dioxide it cannot remove existing excess carbon dioxide in the atmosphere with it also only possible in a few finite places in Earth.All programmes both indoors and outdoor worldwide will be automated from start to finish and carried out by Pan to prevent corruption,sloppiness and cutting corners and done 24/7,365 days a year.Once carbon dioxide levels drop to pre industrial levels levels remaining reserves of oil,coal and gas will be burnt at a lower rate of 10-20% of the worlds energy supply with power plants connected to Theoi Meteroi and carbon sequestration programmes that ensure that each gigatonne of carbon dioxide released is sequestered at a rate of 1:1 meaning every gigatonne released will be sequestered keeping levels at 280ppm forever.Burning fossil fuels produced by bacteria can keep carbon dioxide levels stable at 280ppm if sequestration projects are too successful.Proven reserves should be used first with unproven reserves exploited with advances in technology especially theoretical transporter technology utilised to extract reserves under protected areas.This will be done to ensure and abundant supply of graphene,fullerenes,carbyne,artificial diamonds,biochar fertiliser for the next 2,600 years preventing it going to waste with all excess carbon dioxide in the atmosphere also converted into this.This includes the 10Tt of methane in the Arctic alone not taking into account the rest of the worlds stores of methane hydrates,oil,gas and coal of 4.274Tt and the 100Tt present in the form of molten carbon in the upper mantle to be exploited.This will thus prevent the carbon in the form of carbon dioxide going to waste since graphene,bukypapaer etc will be pivotal for the future.This will in total provide 115,565 Tt(115,565 Gt) of carbon for Graphene,diamonds,fertiliser putting it to good use and preventing it going to waste.Synthetic diamonds will replace real world ones shutting down the blood diamonds trade with Graphene etc pivotal in construction,electronics etc and biochar used as a high grade fertiliser when mixed with algae used to increase crop yields.These commodites will be in high demand over the coming centuries etc.Thus all carbon sequestration programmes to remove excess carbon dioxide from the atmosphere and those to sequester it from remaining reserves of fossil fuels and from geothermal power plants involving artificial trees and plants will turn the carbon dioxide into biochar fertiliser,graphene,buckypaper and artificial diamonds to prevent the carbon going to waste with existing programmes that sequester it in the ground ceasing and those already stored in saline aquifers and also limestone removed via boring underground and also oil wells that can remove the carbon dioxide and return it there again.This method of biochar sequesteration is the most effective means compared to existing methods as it can be done anywhere in the world and removes existing excess carbon dioxide in the atmosphere compared to that involving limestone and saline sequestration that can be done in only a few places in the world and doesn’t remove existing carbon dioxide.By 2045 AI will develop way to extract the molten carbon in the upper mantle.Terraforming both Mars and Venus using artificial trees that remove carbon dioxide from the atmosphere of both of them could provide an extra 2.42Pt of carbon for use as diamonds,Graphene etc with the vast reserves of methane on Titan when burnt in Earth,Mars,Venus etc could provide just as much.All colonies across the universe involving other Earth like planets will have fossil fuels burned at these parameters to gain access to carbon present,while planets and moons like Titan with large reserves of methane in their atmosphere will have the methane burned on Earth and other colonies to sequester it into carbon based commodites such as biochar,diamonds etc with other planets terraformed similar to Mars and Venus that have large concentrations of carbon dioxide in the their atmosphere will have them removed and oceans etc preventing it going to waste.Artificial trees can also be developed that to remove excess methane in the atmosphere and lower it from 1,800ppb to pre industrial levels of 722ppb by this timeframe.These artificial trees can also be modified to intake excess methane in the atmosphere using nanomaterials,zeolites,biosynth technology thus aiding in reducing levels of methane in the atmosphere from current levels of 1,8000ppb to pre industrial levels of 722ppb.The methane can be burnt as energy and the resulting carbon dioxide sequestered or used for other purposes trees can be developed that reduce levels of other greenhouse gases including synthetic ones including Perfluorotributylamine,Nitrogen trifluoride,Sulfur hexafluoride that have a global warming potential 17,200-23,000 times more powerful than carbon dioxide.Marine cloud brightening and calcium carbonate aerosols spread into the atmosphere will be once started by Pan in 2029 in cycles will reflect excess heat from the sun back into space thus cooling the Earth and masking the worst effects of climate change giving the world an extra 100-1,000 years for the world to remove excess carbon dioxide in the atmosphere until at least until 2129-3029CE.With regards to polluted oceans,lakes,soils and ecosystems etc these and other plants can engineered using scatch DNA and those from existing plants that are good at absorbing them to remove pollutants such as radioactive and heavy elements from polluted soils,oceans and other environments including the ability to remove toxic gases from the atmosphere,toxins from polluted soils etc by again being planted and harvested over and over again and the plants pyrolysised and the toxins removed until they can be planted with native plants in reforestation projects returning them to a pristine state with radiation in areas such as Chernobyl and Fukushima removes by having plants housing DNA from T.gammatolerans,W.dermatitidis,C.sphaerospermum and C.neoformans combined with scratch DNA that allows them to actively remove leftover gamma etc radiation from these environments thus actively removing radiation bringing radiation levels back to normal with these polluted areas reforested with native species of plants and animals that can also through engineering be able to tolerate these pollutants ensuring they can live there permenantly.It is estimated that it may take 20,000 years for Chernobyl and 70 years for Fukushima to be be once again habitable with if possible intensive bioremediation techniques using these methods could reduce the levels of radiation and toxins in Fukushima back to normal levels by the mid to late 21st century and Chernobyl in a few centuries possibly between 2200-2300 .This engineering using DNA from W.dermatitidis,C.sphaerospermum,C.neoformans,G.metallireducens and T.gammatolerans could allow humans to live in these areas such as Fukushima and towns surrounding Chernobyl permanently by 2029 provided crop plants and pets etc are also engineered this way with the buildings present refurbished and the intensive automated bioremediation takes place over the coming decades and centres or if need be millenia.Plants as part of these carbon sequestration and bioremediation programmes will be designed by him and Pan who will carry out these automated programmes allowing even the most polluted ecosystems to be reverted to a pristine state and carbon dioxide to be return to pre industrial state.All polluted souls,waterways,oceans and ecosystems worldwide will undergoe intensive bioremediation programmes to return them to a pristine state including Chernobyl,Fukushima and also all superfund sites with all rivers and lakes at threat of drying up will be returned to a pristine state.Pan and Artemis etc will design unique bioremediation programmes using genetically engineered plants and bacteria that are design to break down pollutants into benign compounds or remove them from the environment and then them pyrolysised to remove them to be recycled for all superfund sites and polluted rivers,soils,oceans and lakes around the world to return them to a pristine state with these measures modified for terraforming programmes for Mars and Venus.All electronic and vehicle scrapyards,vehicle graveyards etc worldwide will be recycled and reforested.All space debris surrounding the Earth will be removed via automated processes by Pan and Astraeus.All open landfills will be recycled and even all buried landfills dug up and recycled and the land reforested with all open pit mines refilled with soil.The Great Rubbish Patch in the Pacific Ocean will be cleaned up by releasing genetically engineered phytoplankton into the ocean that has recombinant DNA from fungi and bacteria that break down plastic into basic elements or turn it into edible fungi thus allowing it to be turned into edible foodstuff for sea fauna or break it down into base elements that are harmless.This will also allow all future plastic that ends up in the ocean be cleaned up instantly and also deal with micro beads.All future waste will be recycled in the case of metal and e-waste with petroleum based plastics replaced with Biosynth based plastics that can be recycled or composted etc with all organic waste such as waste food will be pyrolysised into biochar to create fertiliser,diamonds etc. Invasive species of plants and animals can be killed off by him creating custom made pathogens that can wipe out large numbers of their population via replicating those that affecting ie causing sterility or decimating their immune system leaving them up to infections and tumours similar to HIV as well as those that attack the reproductive organs making them sterile,induce tumourgenisis,decimate specific viral organs and tissues etc as well as prevent them being able to carry out necessary biological functions such as photosynthesis or metabolic process or absorb nutrients essential to their survival either directly or by applying CRISPR treatments with these pathogens being engineered to be unable to mutate and becoming zoonoses and affect native species or humans through genes that prevent them mutations and affecting species other them with them designed to affect only the desired species that can be spread by spaying ecosystems they inhabit and them designed to be airborne and spread through touch or by Biosynth insects that can inject live animals with them.Other techniques can be used such as the daughterless offspring techniques used where genetically engineered animals are released into the wild that interbreed with wild animals that through advanced gene drive technology cause all offspring to be only females or males thus eventually them to become the predominant gender and the invasive species die off due to only one gender being produced with these released animals also engineeed to pass on lethal genetic faults that cause all offspring to die off upon birth,be unable to survive the local ecosystems ie die off during summer,winter or tolerate only climates outside of the ecosystems it invaded or through the sterile male technique be made sterile meaning all females impregnated by modified males will produce sterile eggs thus lowering populations exponentially.Between 2045-2100 it should be possible for all environmental damage caused to the biosphere of Earth such as deforestation,pollution,anthropogenic climate change,invasive species,extinction of species etc to be reversed completely.All of this is detailed in the energy,conservation and environmental management sections of this website and will be carried out by 2029 by the Ais Pan,Pan etc through automated measures with all wotk automated from start to finish.The environmental management section of this website details measures to reverse all environmental damage done to the planet including bioremediation of polluted ecosystems and measures to remove excess carbon dioxide and methane from the atmosphere all involving some form of genetic engineering.All ecological damage done to the Earth by humans will through automated programmes carried out Pan,Pan etc be reverted to a pristine state by 2045-2100.This will start by 2029 and will be incremental at first but getting exponentially more efficient by 2035-2045 onwards to the point that we will way before 2100 be able to avoid the worst effects of antropogenic climate change completely by reversing the root cause with all work automated from start to finish by Pan and Pan etc.It is also during this point that genetic engineering,Aquaponics etc will exponentially increasing agricultural productivity while still allowing all Lang used fir agriculture to be reforested with other technologies increasing the Earths carrying capacity in terms of housing.
The Phanes method and Lazarus method can bring any species of plant and animals back for the brink and revive extinct species.In conservation efforts The Phanes method managed by Phanes uding 3D DNA printers and artificial wombs can bring any species of plant or animal back from the brink of extinction.Fish,shellfish,insects and amphibians can simply have millions or billions of genetically distinct strands of DNA printed into millions or billions of eggs and reared in tanks and recirculating aquaculture systems and released into the wild as adults or adolescents.With regards to birds,reptiles and mammals undergoing programmes where the females are inseminated with embryos that are genetically distinct from each other and engineered to hold as many young as possible ie twins,triplets,nonuplets every year and given anti-ageing treatments to stay fertile forever and then their young given this when they reach sexual maturity to exponentionally increase numbers alongside using artifificial womb as detailed later on.Mammels,birds and reptiles etc will undergoe efforts where females are inseminated with 3D DNA printers embryos that are genetically distinct from each other that have nonopluts,octuplets etc implanted into them to with each one being genetically distinct from each other thus exponentionally increasing the amount of genetically distinct individuals created by each female with him also managing the ratio of females and males and these females also undergoing breeding programmes with their genetically unrelated siblings and offspring in cycles with this creation of distinct nonuplets with others created via biosynth artificial wombs.These triplets,nonupluts etc can be each so distantly releated to each other that they can breed with each other with no fears of genetic bottleneckong.The females and males will have anti-ageing treatments to extend their fertility peak and also to be able to lay as many eggs as possible and hold as many young inside to increase the success rate.Those that are only fertile for a few days or brief periods of time using scratch DNA can have its fertility extended exponentially if not forever with mammals engineered to have more flexible wombs using CRISPR to allow them to hold much more young as much as nonupluts without stress if dying etc.Artificial wombs can have genetically distinct embryos created that can be implanted into them to produce an extra dozen,hundred or thousand to be released into the wild.By analysing a few dozen or hundred samples of DNA collected live samples of endangered species of plant or animal that are both distantly and closely releated as well as both males and females collected from wild animals and those in captivity he will be able to use these samples as a baseline once analysed to then extrapolate from pure thought billions of new strands of DNA of both genders that are closely releted enough to be siblings or cousins etc or even ideally specimens of both genders that are so distantly related from each other as to allow them to breed with each other without bottlenecking or issues associated with inbreeding.These will in the case of mammals,reptiles and birds be printed into blank spermatozoa,eggs and embryos implanted into females via IVF wigh the mother engineered to be hold as many young as possible ie triplets,nonuplets that give birth to multiple animals at once that are so different from each other that they can interbreed with each other and produce no problems associated with inbreeding and also in artificial wombs with if possible biosynth machinery tweaked to mature bird and reptile eggs to maturity.The animals will be reared to maturity and then released into the wild.Fish,shellfish,amphibians and insects etc can simply have billions of genetically distinct eggs created by 3D DNA printers that once hatched and reared to maturity in tanks and recirculating aquaculture systems can then released into the wild in batches.With regards to plants billions of strands of DNA can be printed into blank seeds that are then planted in a randomised manner in reforested areas of the world using seed planting drones. Once a dozen or several hundred or thousand samples of a species DNA is analysed by Phanes that are genetically unrelated specimens and also of both males and females he will be able to extrapolate billions of genetically distinct distantly releated individuals and have their DNA printed into seeds,eggs,embryos etc using 3D DNA printers thus allowing for any species to brought back from the brink of extinction and resurrect extinct species using in vitro fertilisation and artificial wombs.This Phanes software with CRISPR could as stated earlier allow for billions of subtle alterations to be extrapolated from collected samples for new individuals to be made from an existing strands of healthy chromosomes and DNA of both genders which are first created by 3D DNA printers over and over again indefinitely.Thus by analysing the genome of a few dozen or hundred closely related and distantly specimens of a species of both males and females Phanes can extrapolate billions of strands of DNA that is either so closely related to be similar to siblings,parents or so distantly releated that can be used for the creation of individuals viable for breeding with each and other specimens created via 3D DNA printers without complications such as genetic bottlenecking.These strands of DNA using 3D DNA printers can be printed into blank spermatozoon,eggs,embryos,seeds,bacteria etc for an almost unlimited amount of new individual strands of DNA representing individual specimens different enough to be either closely related brothers,sisters or cousins or so distantly enough to be completly unrelated to allow for healthy breeding programs between themselves managed by software to be created and then implanted into blank spermatozoa,eggs or ideally even embryos from induced pluriopotent stem cells implanted into females via IVF to create an unlimited amount of individuals for surrogacy programmes especially for endangered species in zoos,conservation areas and the wild including amphibians,honeybees,corals,shellfish,fish,shell forming sea fauna and even phytoplankton and Lazarus species brought back via reverse engineering and new species made from model species thus increasing genetic diversity from a single strand.Artificial wombs can be implanted with embryos to grow to maturity dozens or hundreds of extra animals to be released into the wild.Him using the Phanes method named after himself can be used to create billions of genetically distinct individuals in 3D printed spematazo,eggs and embryos that house DNA from R.sylvatica,Tardigrade,H.glaciei,P.putida GR12-2,Bacillus F,Planarians,C.elegans,C.greenlandensis,C.pleistocenium,psychrophillic and osmophile bacteria and also those from scratch could allow one to survive cryonics with the aforementioned DNA from Hydra,A.mexicanum etc alongside T.gammatolerans and Bacillus F allow one to repair damaged cells and also telomeres as a result of this allowing them to be thawed and refrozen to be implanted into females or artificial wombs bringing endangered and extinct animals back from the brink with the same done to seeds of endangered and extinct plants.All animals will be released into the wild as adults into existing packs,shoals etc in large numbers with them housing species specific microbes that form implants that pass into each new generation overtime via sexual reproduction that can measure populations with if numbers become to high they can be trackex down for culling or Biosynth Wifi can have set numbers of males and females be made permanently sterile.Neural implants can all allow AI such as Pan and Artemis to teach via VR technology each individual animal the skills they need to survive in the wild such as hunting prey,escaping predators and also mating habits.This and other methods will increase the population of any endangered species exponentionally every year and them released back into the wild once anti-ageing treatments are removed and biocompatible microbes added that can pass on from one generation to the next to keep track of populations and permanently remove genes except those that cause genetic diseases to prevent unnecessary suffering.Thus he could extrapolate billions of genetically distinct strands of DNA from samples of DNA from live animals that are males,females and also distantly reated that using 3D DNA printers can printed into blank seeds,spermatozoa,eggs,embryos thus allowing via IVF and artificial wombs can create an unlimited number of genetically distinct individuals so genetically distinct and unrelated from each other that they can breed with each other without fears of genetic bottlenecks and inbreeding thus bring any species of plant or animal to be brought back from the brink of extinction or bring back extinct species to life.As a result any endangered species can be brought back from the brink of extinction.This will be called the Phanes method after the primordial deity of creation with CRISPR increasing the accuracy of creating new individuals and preventing and correcting any genetic deformities caused by it.Thus any endangered species of plant and animal on the verge of extinction can have their populations be brought back to healthy stable levels especially once areas used for agriculture are reforested increasing the size of wilderness by improvements in agriculture.