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Digoxin, Endosymbiotic Archaea, Viral Pandemics and Human Species
Hyperdigoxinemic Neanderthal Predator and Cro-Magnon Hypodigoxinemic Victim
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Global warming leads to endosymbiotic and colonic archaeal growth and neanderthalisation of the species and activation of remnant Neanderthal matrilineal species. The endosymbiotic archaea secretes RNA viroids which can get converted using the human HERV reverse transcriptase to DNA viroids. The RNA viroids and DNA viroids generated by human archaea can hybridise with the human virobiome and human genome sequences producing emerging new viruses and pandemics. The homo neanderthalis serves as a generator and reservoir of the emerging viruses. The archaeal endosymbiont of homo neanderthalis synthesizes digoxin from the isoprenoid pathway. Digoxin is the Neanderthal evolutionary hormone. Digoxin is a small molecule that can act at the RNA level splicing, cutting and editing RNA and can destroy the RNA viroids per se. The archaea can induce stem cell transformation of the human cells via kynurenine pathway of tryptophan catabolism. Archaeal induced Warburg phenotype can generate stem cells. The stem cells are protected from immune attack & the archaea generated viruses can survive in the stem cells. Archaeal digoxin will keep the neanderthalic emerging viruses in check by killing them.
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