@mikewick77: From Avian Flu

Immunohistochemical studies identified Mycoplasma fermentans infection in the patients' lungs and liver. Mycoplasma-like particles could also be identified by electron microscopy. There is a previously unrecognized form of fulminant disease in humans that is associated with M. fermentans infections.

Mycoplasma-induced minimally conscious state

https://springerplus.springeropen.com/articles/10.1186/s40064-016-1832-2

its like the mycoplasmas can self assemble after death.

this is similar to hydra self assembly?

Hydra self assembly is because of plasmid DNA from self-replicating DNA found in bacteria?

seems like a connection, weaponized mycoplasma using Hydra DNA?

its strange how the DNA guts of Mycoplasma convert into a virus that can later re-assemble back into living Mycoplasma.

Anthrax & E.Coli are probably blended into this mysterious Crystalline Brucella.

Bacillus anthracis is a Gram-positive and rod-shaped bacterium that causes anthrax.

Mycoplasma lost its gram positive shell as Symbiont with an animal, like in cattle.

if their was a way to blend them together into non pathogenic, but instead a beneficial midrobe, that could potentially be a cure to the deadly strains, but thats not what dr evil is doing.

instead of killing pathogens, make them play nice.

if Virus are Mycoplasma zombie guts, train the microbes to behave like the good ones, no more cronic disease.

the exact way they manufactured them to be more deadly, can probably be done in reverse, they just wont let us identify the pathogen source & manufacturing process.

not to mention making them so small they enter our blood cells & mitochondria, making strange chemicals to effect DNA.

one part of HIV of AIDS may be the mycoplasma DNA guts.

zombie cells & dormant mycoplasma dna?

like mycoplasma playes possum?

whats causing the cells to this error?

because it is a breeding ground for thousands of Mycoplasma to be dormant in.

mycoplasma manufactures hydrogen peroxide within cells, this oxidative stress reduces P53, causing Cellular Senescence (Zombie Cells)

Highest prevalence rates of B. anthracis, Brucella, and Coxiella were observed in wildebeest (56%), dik-dik (50%), and impala (24%), respectively. Fresh samples, those collected during the rainy season, and samples from Selous or Serengeti had a greater relative risk of being positive. Microbiome characterization identified Firmicutes and Proteobacteria as the most abundant phyla. The results highlight and define potential risks of exposure to endemic wildlife diseases from bushmeat and the need for future investigations to address the public health and emerging infectious disease risks associated with bushmeat harvesting, trade, and consumption.

So we have Anthrax, Brucella, and Coxiella all in African bushmeat and then we have the Army giving Anthrax shots with a Brucella based Mycoplasma Fermentans and later testing those vets for Coxiella or Q Fever

Findings indicated that most of the differences in the microbiome are driven by the relative abundance of Firmicutes and Proteobacteria, as demonstrated by the PCoA (Supplemental Figure 2). This is expected, since B. anthracis belongs to the Firmicutes phylum and Brucella and Coxiella both belong to Proteobacteria.

We find the anthrax with the brucella and coxiella in the bushmeat from Africa

Coxiella causes Q fever which is one of the diseases they were testing for after the Gulf War

So all 3 of these diseases found in African Bushmeat were then found or given in Vaxx to Gulf War Vets

https://sites.duke.edu/superbugs/module-4/introduction/anthrax-the-cell-infiltrator/

https://www.nature.com/articles/s41598-021-94112-9

https://academic.oup.com/cid/article/48/5/558/386535

https://www.cdc.gov/qfever/index.html