Human Endosymbiotic Archaea, Retroviral Resistance and Emerging Viral Pandemics: The Crossing of Species Barrier and New Viruses

R. Kurup, P. A. Kurup
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The archaeal cholesterol catabolism can deplete the membrane rafts of the CD4 cell of cholesterol impeding the entry of the retrovirus into the cell. The archaea can produce permanent immune activation producing resistance to viral and bacterial infection. The archaeal cholesterol catabolism depletes tissue cholesterol producing vitamin D deficiency and immune activation. Thus archaeal overgrowth results in retroviral resistance and generation of the Neanderthal phenotype. The endosymbiotic archaea can secrete virus like RNA and DNA particles. The endosymbiotic archaea can induce uncoupling proteins inhibiting mitochondrial oxidative phosphorylation and generating ROS. The endosymbiotic archaeal magnetite can generate low level of EMF. The low level of EMF and ROS are genotoxic and produce breakages in hotspots of chromosome. It can also trigger rearrangements in hotspots of chromosome inhabited by retroviral and non-retroviral elements producing their expression. The archaeal secreted DNA and RNA viroids can recombine with the expressed retroviral, non-retroviral elements and other genomic segments of the human chromosome generating new RNA and DNA viruses. Thus the neanderthalised humans can serve as an origin for new RNA and DNA viruses as well as mutated retroviruses. The endosymbiotic archaea converts the Neanderthal cells to stem cells. The stem cells are resistant to immune attack. The stem cells can serve as a reservoir for this new RNA and DNA viruses. The stem cells and archaeal cells can also serve as a reservoir for viruses and bacteria belonging to other plants and animals. This helps to generate the species barrier jump in noted in recent emerging viral and bacterial infections. This paper studied the archaeal status in patients with recurrent viral infections and retroviral infections. The generation of RNA and DNA viroids from archaea was also studied. Materials and Methods: Blood samples were drawn from normal population, Neanderthal phenotype, retroviral infection and recurrent viral infection. There were 10 patients in each group and each patient had an age and sex matched healthy control selected randomly from the general population. The blood samples were drawn in the fasting state before treatment was initiated. Plasma from fasting heparinised blood was used and the experimental protocol was as follows (I) Plasma+phosphate buffered saline, (II) same as I+cholesterol substrate, (III) same as II+cerium 0.1 mg/ml, (IV) same as II+ciprofloxacine and doxycycline each in a concentration of 1 mg/ml. Cholesterol substrate was prepared as described by Richmond. Aliquots were withdrawn at zero time immediately after mixing and after incubation at 37oC for 1 hour. The following estimations were carried out:- Cytochrome F420, free RNA and free DNA. Cytochrome  F420 was estimated flourimetrically (excitation wavelength 420 nm and emission wavelength 520 nm). Results: Plasma of Neanderthal phenotype showed increased levels of the above mentioned parameters with after incubation for 1 hour and addition of cholesterol substrate resulted in still further significant increase in these parameters. The plasma of retroviral patients and those with recurrent viral infections showed similar results but the extent of increase was insignificant. The addition of antibiotics to the control plasma caused a decrease in all the parameters while addition of cerium increased their levels. The addition of antibiotics to the patient’s plasma caused a decrease in all the parameters while addition of cerium increased their levels but the extent of change was more in Neanderthal phenotype sera as compared to patients with retroviral infection and recurrent viral infection. The results are expressed in tables 1-2 as percentage change in the parameters after 1 hour incubation as compared to the values at zero time. Discussion: The homo neanderthalis has archaea as endosymbionts. The archaea behaves like stem cells and can induce conversion of somatic cells to stem cells. The stem cells and archaeal cells can serve as reservoirs of other species virus and bacteria like plant and animal viruses and bacteria. The plant and animal viruses and bacteria can thrive in the somatic stem cells and archaeal cells as they escape immune detection. The Neanderthals tissue system can be compared to an archaeal/stem cell colony or network which serves as a reservoir for other animal and plant species bacteria and viruses as well as a generating centre for new RNA and DNA viruses. The RNA and DNA viruses are created by recombination between expressed genetically rearranged bits of the human chromosome and virus like DNA and RNA particles secreted by the archaea. This paves way for the generation of unlimited number of new RNA and DNA viruses as well as produce conditions for viruses and bacteria to cross the species barrier. This is evidenced by the SARS virus, the nipah virus and hendra virus crossing species. The algal virus has been reported to infect human brains producing cognitive dysfunction. The generation of new RNA and DNA viruses and the creation of a stem cell/archaeal reservoir for other species bacteria and viruses, the Neanderthal resistance to infections by viruses and bacteria and the Neanderthals serving as a reservoir for infection results in widespread pandemic in the homo sapien population in Africa and their eventual wipeout. Conclusion: Global warming depends on human endosymbiotic archaeal overgrowth and methanogenesis. The archaea can induce stem cell conversion, archaeal digoxin induced RNA editing, digoxin induced magnesium deficiency & reverse transcriptase inhibition and cholesterol catabolism induced CD4 receptor produces retroviral resistance. The archaeal secreted DNA and RNA viroids can recombine with the expressed retroviral, non-retroviral elements and other genomic segments of the human chromosome generating new RNA and DNA viruses. Thus the neanderthalised humans can serve as an origin for new RNA and DNA viruses as well as mutated retroviruses. The stem cells and archaeal cells can also serve as a reservoir for viruses and bacteria belonging to other plants and animals. This helps to generate the species barrier jump in noted in recent emerging viral and bacterial infections.","PeriodicalId":7348,"journal":{"name":"Advances in Natural Science","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Natural Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3968/6031","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Introduction: Studies from our laboratory have shown that global warming and the low level EMF pollution results in increased endosymbiotic archaeal growth. The archaea can produce methanogenesis from hydrogen and carbon dioxide as well as from acetate. The human body methanogenesis can result in more global warming. Global warming is initially triggered by carbon dioxide and EMF pollution produced by homo sapien industrialization. It is carried forward by human endosymbiotic archaeal overgrowth and methanogenesis. The archaea can induce stem cell conversion and neanderthalisation of the human species. The archaea catabolises cholesterol generating digoxin which can modulate RNA editing and magnesium deficiency resulting in reverse transcriptase inhibition. The archaeal cholesterol catabolism can deplete the membrane rafts of the CD4 cell of cholesterol impeding the entry of the retrovirus into the cell. The archaea can produce permanent immune activation producing resistance to viral and bacterial infection. The archaeal cholesterol catabolism depletes tissue cholesterol producing vitamin D deficiency and immune activation. Thus archaeal overgrowth results in retroviral resistance and generation of the Neanderthal phenotype. The endosymbiotic archaea can secrete virus like RNA and DNA particles. The endosymbiotic archaea can induce uncoupling proteins inhibiting mitochondrial oxidative phosphorylation and generating ROS. The endosymbiotic archaeal magnetite can generate low level of EMF. The low level of EMF and ROS are genotoxic and produce breakages in hotspots of chromosome. It can also trigger rearrangements in hotspots of chromosome inhabited by retroviral and non-retroviral elements producing their expression. The archaeal secreted DNA and RNA viroids can recombine with the expressed retroviral, non-retroviral elements and other genomic segments of the human chromosome generating new RNA and DNA viruses. Thus the neanderthalised humans can serve as an origin for new RNA and DNA viruses as well as mutated retroviruses. The endosymbiotic archaea converts the Neanderthal cells to stem cells. The stem cells are resistant to immune attack. The stem cells can serve as a reservoir for this new RNA and DNA viruses. The stem cells and archaeal cells can also serve as a reservoir for viruses and bacteria belonging to other plants and animals. This helps to generate the species barrier jump in noted in recent emerging viral and bacterial infections. This paper studied the archaeal status in patients with recurrent viral infections and retroviral infections. The generation of RNA and DNA viroids from archaea was also studied. Materials and Methods: Blood samples were drawn from normal population, Neanderthal phenotype, retroviral infection and recurrent viral infection. There were 10 patients in each group and each patient had an age and sex matched healthy control selected randomly from the general population. The blood samples were drawn in the fasting state before treatment was initiated. Plasma from fasting heparinised blood was used and the experimental protocol was as follows (I) Plasma+phosphate buffered saline, (II) same as I+cholesterol substrate, (III) same as II+cerium 0.1 mg/ml, (IV) same as II+ciprofloxacine and doxycycline each in a concentration of 1 mg/ml. Cholesterol substrate was prepared as described by Richmond. Aliquots were withdrawn at zero time immediately after mixing and after incubation at 37oC for 1 hour. The following estimations were carried out:- Cytochrome F420, free RNA and free DNA. Cytochrome  F420 was estimated flourimetrically (excitation wavelength 420 nm and emission wavelength 520 nm). Results: Plasma of Neanderthal phenotype showed increased levels of the above mentioned parameters with after incubation for 1 hour and addition of cholesterol substrate resulted in still further significant increase in these parameters. The plasma of retroviral patients and those with recurrent viral infections showed similar results but the extent of increase was insignificant. The addition of antibiotics to the control plasma caused a decrease in all the parameters while addition of cerium increased their levels. The addition of antibiotics to the patient’s plasma caused a decrease in all the parameters while addition of cerium increased their levels but the extent of change was more in Neanderthal phenotype sera as compared to patients with retroviral infection and recurrent viral infection. The results are expressed in tables 1-2 as percentage change in the parameters after 1 hour incubation as compared to the values at zero time. Discussion: The homo neanderthalis has archaea as endosymbionts. The archaea behaves like stem cells and can induce conversion of somatic cells to stem cells. The stem cells and archaeal cells can serve as reservoirs of other species virus and bacteria like plant and animal viruses and bacteria. The plant and animal viruses and bacteria can thrive in the somatic stem cells and archaeal cells as they escape immune detection. The Neanderthals tissue system can be compared to an archaeal/stem cell colony or network which serves as a reservoir for other animal and plant species bacteria and viruses as well as a generating centre for new RNA and DNA viruses. The RNA and DNA viruses are created by recombination between expressed genetically rearranged bits of the human chromosome and virus like DNA and RNA particles secreted by the archaea. This paves way for the generation of unlimited number of new RNA and DNA viruses as well as produce conditions for viruses and bacteria to cross the species barrier. This is evidenced by the SARS virus, the nipah virus and hendra virus crossing species. The algal virus has been reported to infect human brains producing cognitive dysfunction. The generation of new RNA and DNA viruses and the creation of a stem cell/archaeal reservoir for other species bacteria and viruses, the Neanderthal resistance to infections by viruses and bacteria and the Neanderthals serving as a reservoir for infection results in widespread pandemic in the homo sapien population in Africa and their eventual wipeout. Conclusion: Global warming depends on human endosymbiotic archaeal overgrowth and methanogenesis. The archaea can induce stem cell conversion, archaeal digoxin induced RNA editing, digoxin induced magnesium deficiency & reverse transcriptase inhibition and cholesterol catabolism induced CD4 receptor produces retroviral resistance. The archaeal secreted DNA and RNA viroids can recombine with the expressed retroviral, non-retroviral elements and other genomic segments of the human chromosome generating new RNA and DNA viruses. Thus the neanderthalised humans can serve as an origin for new RNA and DNA viruses as well as mutated retroviruses. The stem cells and archaeal cells can also serve as a reservoir for viruses and bacteria belonging to other plants and animals. This helps to generate the species barrier jump in noted in recent emerging viral and bacterial infections.
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人类内共生古生菌、逆转录病毒耐药性和新出现的病毒大流行:物种屏障和新病毒的跨越
导言:我们实验室的研究表明,全球变暖和低水平EMF污染导致内共生古细菌生长增加。古细菌可以从氢和二氧化碳以及醋酸中产生甲烷。人体产甲烷会导致更多的全球变暖。全球变暖最初是由人类工业化产生的二氧化碳和电磁场污染引发的。它是由人类内共生的古细菌过度生长和甲烷生成而传播的。古细菌可以诱导干细胞转化和人类的尼安德特人化。古细菌分解代谢胆固醇产生地高辛,地高辛可以调节RNA编辑和镁缺乏,导致逆转录酶抑制。古细菌的胆固醇分解代谢可以消耗CD4细胞的膜筏中的胆固醇,阻碍逆转录病毒进入细胞。古细菌可以产生永久性的免疫激活,产生对病毒和细菌感染的抵抗力。古细菌胆固醇分解代谢消耗组织胆固醇,产生维生素D缺乏和免疫激活。因此,古细菌过度生长导致抗逆转录病毒抗性和尼安德特人表型的产生。内共生的古生菌可以分泌RNA和DNA颗粒等病毒。内共生古菌可以诱导解偶联蛋白抑制线粒体氧化磷酸化并产生ROS。内共生的古细菌磁铁矿可以产生低水平的电磁场。低水平的EMF和ROS具有遗传毒性,并在染色体热点处产生断裂。它还可以触发逆转录病毒和非逆转录病毒元素所居住的染色体热点的重排。古细菌分泌的DNA和RNA类病毒可以与表达的逆转录病毒、非逆转录病毒元件和人类染色体的其他基因组片段重组,产生新的RNA和DNA病毒。因此,尼安德特人可以作为新的RNA和DNA病毒以及变异的逆转录病毒的起源。内共生古生菌将尼安德特人细胞转化为干细胞。干细胞能抵抗免疫攻击。干细胞可以作为这种新的RNA和DNA病毒的储存库。干细胞和古细菌细胞也可以作为属于其他动植物的病毒和细菌的储存库。这有助于在最近出现的病毒和细菌感染中产生物种屏障跳跃。本文研究了复发性病毒感染和逆转录病毒感染患者的古细菌状况。还研究了从古细菌中产生RNA和DNA类病毒。材料和方法:从正常人群、尼安德特人表型、逆转录病毒感染和复发性病毒感染中抽取血样。每组有10名患者,每名患者从普通人群中随机选择年龄和性别匹配的健康对照。在治疗开始前,在禁食状态下抽取血样。使用空腹肝素化血血浆,实验方案如下:(I)血浆+磷酸盐缓冲盐水,(II)与I+胆固醇底物相同,(III)与II+cerium 0.1 mg/ml相同,(IV)与II+环丙沙星和多西环素浓度均为1mg /ml相同。按照Richmond的描述制备胆固醇底物。在混合和37℃孵育1小时后,立即在零时间取出等分。测定细胞色素F420、游离RNA和游离DNA。荧光法测定细胞色素F420(激发波长420 nm,发射波长520 nm)。结果:尼安德特人表型血浆在孵育1小时后上述参数水平升高,添加胆固醇底物导致这些参数进一步显著升高。逆转录病毒患者和复发性病毒感染患者血浆中出现了相似的结果,但增加的程度不显著。在对照血浆中添加抗生素使各参数均降低,而添加铈使各参数均升高。在患者血浆中添加抗生素导致所有参数下降,而添加铈则增加了它们的水平,但与逆转录病毒感染和复发性病毒感染患者相比,尼安德特人表型血清中的变化程度更大。结果在表1-2中表示为孵育1小时后参数与零时间值相比的百分比变化。讨论:尼安德特人以古生菌为内共生菌。古细菌的行为类似于干细胞,可以诱导体细胞转化为干细胞。干细胞和古细菌细胞可以作为其他物种病毒和细菌的储存库,如植物和动物病毒和细菌。
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