Obligate Endosymbiotic Gamma Proteobacterium (symbiont) vs free-living Orthologues (mycoplasma)
https://microbewiki.kenyon.edu/index.php/Candidatus_Carsonella_ruddii
Genome Structure C. C. ruddii has the smallest known cellular genome sequenced to date. The circular genome was finished on October 21, 2006 by groups in Japan and the University of Arizona. It was found to be only 159,662 base pairs (Tamames) compared this with the genome of Mycoplasma genitalium, the smallest free-living genome, with about 580,000 bp. An estimated 93-97% of the genome is coding, including 213 genes with 182 of these coding for protein. These genes tend to overlap (much more than is common in bacteria) and are smaller than what is expected of bacteria in general. The remaining 7% non-coding part contains no pseudogenes and no phage sequences. The C. C. ruddii genome has a 19.9% GC content, which is extremely low. This results in a significant AT bias which is not generally observed in their free living counterparts. This bias is likely due to deleterious mutations caused by genetic drift because of small population sizes and not much recombination. (Tamames) Because there are so few genes, there is debate as to whether C. C. ruddii is an actual living cell.
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Extreme genome reduction in symbiotic bacteria
E. coli genome, with approximately 4.5 thousand genes to the endosymbiotic bacterium Candidatus Carsonella ruddii, which has retained just around 150 genes.
4.5 thousand genes vs 150.
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mathematically how much smaller is this?
4.500÷150=00.03
150÷4.500=33.33
identity of a virus being a Endosymbiont bacteria & yeast, living natrual within mice, bats, cattle & insects, XMRV gain of function is mixing those Symbiont bacteria with, Brucella, Mycoplasma or Anthrax, then calling it a pathogenic virus.
i think they are pulling a stolen identity scam.
its impossible for a virus to jump species, thats a parasite, herd immunity is when the parasitic transcription is altered & molded by immunity or equilibrium between parasitic & probiotic, they must need to reactivate many of the diseases & reintroduced them, except for mycoplasmas & protozoa which contain free living genome.
snake & spider symbiont venom may be similar to ecoli bacteria chemical fermentation, but symbiont cannot replicate like normal bacteria within different species, because a symbiont not a free-living cell.
snake venom an identical symbiont manufacturers chemicals similar to e.coli.
redox medications bind onto oxidative peroxide radical unbound molecules, but dont necessary kill parasites like Mycoplasma.
graphene derivatives being put into everything with many different names, as part of the cybernetic dystopia nightmare being prepared for us.
graphene normally detoxifies in a few months, unfortunately the peptides in hydrogel lock them together more permanently, specifically if the hydrogel is a chimera symbiont-mycoplasma biofilm complex.
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Peptide Amphiphile
RE: Disease-X