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.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 for telomerase production in both H.sapiens and Nephropidae and thus determine ways to integrate that from Nephropidae into H.sapiens this rejuvenating telomeres in patients to an infant level with it and DNA repair mechanism ensuring that the telomeres stay at a levels associated with infancy forever.
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 E