RNA/DNA Parasites
Alpha-Proteo Microbes
Endosymbiont
Symbiogenesis

Algae
Plastid
Protist
Amoeba
Amoeboid
Amoebozoa
Plasmodium
Myxosporea
Mycoplasma
Slime Mold
Nanobe
Prion

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viruses are the carboxysome (exosome mimicking) spores of alga-plastid intercellular endosymbiont parasites, that misfold telomere stem cells.

mycoplasma has the ability to morph depending upon its environment, requires powerful antibiotics to extract a sample, hidden dormant in cells, bone marrow and brain.

the idea is to use mycoplasma as vector to DNA endosymbionts.

symbiont maleria apicoplast plastid algae, may have evolved into the west African Chimpanzee kidneys.

Proto-HIV as an endosymbiont of Maleria.

weaponized chronic diseases, GWS, Lyme, HIV ect.. gain of function research (government flu) all seem to degenerate the Telomere Stem Cell regeneration process, and have similarity to endosymbiont parasites, not viruses.

suspect all proteo-bacteria & proto-archaea symbiogenesis have an alga-plastid element, and something to do with Nanobe.

i think.. weaponized mycoplasma with extremophiles components is for the survival (endurance) of very delicate endosymbionts, that can only survive inside a host body cells, organs, bone marrow, brain ect.. once introduced to the elements, instantly oxide by the oxygen, mycoplasma inserts or enhancements create a transport environment to act as a vector.

thinking about how only a handful of HIV envelopes can be found (transferred) in both Mycoplasma Incognitus & SARS-CoV-2.

this makes me think how infinite Frankenstein combinations can be assembled or accumulate into apparently different yet similar diseases.

it almost seems if endosymbionts act as mimicking printing press for cell RNA/DNA forgery data causing misfolding & disease.

the misfolded data is packaged in what would appear natural exosome, or viruses, but more resemble carboxysome full of Protist spores.

this is a clue, Garth learned from his teacher, how to shake out mycoplasma from deep tissue & cells, using very powerful antibiotics then immediately blood testing for mycoplasma.

but at that time they had no way to go into the mycoplasma, to see what artifacts were inside, Craig Venter has rhat technology, he can put GIF files & code transcription inside them, and make them smaller then ever possible by removing genomes, called minimal genome, then program them to very specific tasks, exactly like an endosymbiont, such as mimicking.

my suspension is they can hyjack the cell nucleolus clamp & press assembly of data code RNA/DNA.

my suspension is HIV is a endosymbiont of Maleria.

yet Malaria is is a blood parasite, so Ivermectin Quinine are water based.

if HIV is hidden in the Kidney, or Liver, that requires oil based.

Fenbendazole is oil based, but not reported to cure HIV.

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G6PD looks to me a rare genetic disease, that looks like Maleria and acts like HIV.. DNA Chromosome parasites, Maleria Endosymbiont.

HIV is a variant of Malaria, and so is all similar autoimmune diseases, and genetic diseases.

https://en.m.wikipedia.org/wiki/Importin

https://en.m.wikipedia.org/wiki/G_protein-coupled_receptor

Importin disease states and pathologies that are associated with mutations or changes in expression of importin-α and importin-β.

Importins are vital regulatory proteins during the processes of gametogenesis and embryogenesis. As a result, a disruption in the expression patterns of importin-α has been shown to cause fertility defects in Drosophila melanogaster (whitefly).

https://en.m.wikipedia.org/wiki/Cryptotope

Cryptotopes are becoming important for HIV vaccine research as a number of studies have shown that cryptic epitopes can be revealed or exposed when HIV gp120 binds to CD4.

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what they say vaccine research may reveal the actual problem.

almost like T Cells are hyjacked.

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Epitope, also known as antigenic determinant, is the part of an antigen that is recognized by the immune system, specifically by antibodies, B cells, or T cells. 

T cells are born from Hematopoietic stem cells, found in the bone marrow.

B cells mature in the bone marrow, which is at the core of most bones.

B cells develop from hematopoietic stem cells (HSCs) that originate from bone marrow.

High-sensitivity virus and mycoplasma screening test reveals high prevalence of parvovirus B19 infection in human synovial tissues and bone marrow.

The coding portion of Parvoviridae genome is flanked by telomeres at each end that form into hairpin loops that are important during replication.

Viral messenger RNA (mRNA) is then transcribed and translated, resulting in NS1 initiating replication.