Superbugs, Emerging Virus, Retrovirus, Prions and Symbiotic Modulation
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Actinidic archaea has been related to human infections- superbugs, emerging virus infection, retroviral disease and prion disease. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in human infections- superbugs, emerging virus infection, retroviral disease and prion disease especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to metabolic sy...
Actinidic archaea has been related to human infections- superbugs, emerging virus infection, retroviral disease and prion disease. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in human infections- superbugs, emerging virus infection, retroviral disease and prion disease especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to metabolic syndrome. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these human infections. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated treatment of human infections- superbugs, emerging virus infection, retroviral disease and prion disease.
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