Co-infection with Stealth Adapted Viruses May Explain Zika Virus Associated Microcephaly

doi:10.15406/jhvrv.2016.03.00080

Journal of

eISSN: 2373-6453

Human Virology & Retrovirology

Opinion Volume 3 Issue 1

Co-infection with Stealth Adapted Viruses May Explain Zika Virus Associated Microcephaly

W John Martin

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Institute of Progressive Medicine, USA

Correspondence: W John Martin, Institute of Progressive Medicine, 1634 Spruce Street, South Pasadena CA 91030, USA, Tel 626-616-2868

Received: February 11, 2016 | Published: February 11, 2016

Citation: Martin WJ (2016) Co-infection with Stealth Adapted Viruses May Explain Zika Virus Associated Microcephaly. J Hum Virol Retrovirol 3(1): 00080. DOI: 10.15406/jhvrv.2016.03.00080

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Abstract

The premise of this paper is that the apparent teratogenicity of Zika virus may result from co-infection of the mothers with stealth adapted viruses. Specific testing should, therefore, be performed on mothers and their affected infants for stealth adapted viruses. Even if infection is not confirmed, extended studies on stealth adapted viruses can provide important insights into many additional neuropsychiatric illnesses, including autism. These endeavors can also help expedite the development and evaluation of anti-virus therapies based upon enhancing the alternative cellular energy (ACE) pathway. Particular emphasis can be given to the potential clinical benefit of consuming water activated with KELEA (kinetic energy limiting electrostatic attraction). Indeed, urgent consideration should be given to having all pregnant women at risk for Zika virus infection to begin consuming KELEA activated water.

Keywords:Zika, ACE, Microcephaly, KELEA, Vaccine, Stealth adapted virus, Water, Autism, Cytomegalovirus, Enerceutical™, moringa oleifera

Abbreviations

ACE, Alternative Cellular Energy; KELEA, Kinetic Energy Limiting Electrostatic Attraction; HSV, Herpes Simplex Virus; HZV, Herpes Zoster Virus; HPV, Human Papillomavirus Virus; HIV, Human Immunodeficiency Virus

Introduction

The apparent association of Zika virus infection with microcephaly appears to be largely confined to Brazil. While this could be due to genetic changes in the Brazilian Zika virus, it is also consistent with a facilitating effect of co-infection with another virus. Public health authorities have been reluctant to acknowledge the presence of stealth adapted viruses.¹These viruses have deletions or mutations in the relatively few components in viruses that are normally targeted by the cellular immune system.²Consequently, stealth adapted viruses do not evoke an inflammatory response; the hallmark of an infectious process.³

The political reluctance to pursue stealth adapted viruses arose because some of the viruses were unequivocally derived from cytomegaloviruses of monkeys used to produce polio vaccines.⁴Moreover, cytomegalovirus contaminated polio vaccines tested in Africa may well explain the origin of HIV.⁵Cytomegaloviruses can infect the placenta and can promote the replication of other viruses in normally non-permissive cells.⁶Conversely, other viruses can enhance the replication of cytomegaloviruses.⁷It would be useful if public health authorities studying the Zika virus, extended their efforts to detecting stealth adapted viruses. This can most readily be accomplished using virus culture methods.¹Animals and possibly insects are also susceptible to certain stealth adapted viruses.^4,8

Discussion

Additional benefits will arise from such studies. First, more widespread testing will confirm that stealth adapted viruses can cause autism in children⁹as well as various neuropsychiatric illnesses in adults.^3,10Second, directed studies will show the potential role of routine vaccinations in provoking stealth adapted virus infections. This is relevant in view of the Brazilian government earlier decision to administer tetanus, diphtheria, and acellular pertussis vaccine (Tdap) to all pregnant women.¹¹It is reasonable to exclude those infected with stealth adapted viruses from routine vaccination programs, especially during pregnancy.¹²Third, and most importantly, it will highlight the alternative cellular energy (ACE) pathway as an effective non-immunological defense mechanism against both stealth adapted and conventional viruses. Indeed, preliminary studies have confirmed the clinical efficacy of enhancing the ACE pathway in the suppression of herpes simplex virus (HSV), herpes zoster virus (HZV), human papillomavirus (HPV) and human immunodeficiency virus (HIV) infections.^13-15ACE pathway therapy can also be used to suppress stealth adapted virus infections.¹⁶

The ACE pathway is mediated by a dynamic (kinetic) energy of the body’s fluids.¹⁷It results from the absorption of a natural environmental force termed KELEA (kinetic energy limiting electrostatic attraction). The fundamental role of this force is probably to prevent the fusion and annihilation of electrostatically attracted opposite electrical charges. KELEA leads to a loosening of intermolecular hydrogen bonding of fluid molecules,¹⁸as reflected in lower surface tension and in increased volatility. KELEA can also directly contribute kinetic activity and other forms of energy to fluid molecules.

Water can be activated by the addition of KELEA attracting compounds, including many simple dipolar compounds and enerceutical™ foods, including moringa oleifera.¹⁹The activating compounds can subsequently be removed by either zero-residue filtration or repeated dilutions, as in homeopathy. Water can also be activated by being placed in the vicinity of KELEA attracting energy fields.^20-22Consuming KELEA activated water would appear to provide a convenient means of enhancing the ACE pathway. Urgent efforts should, therefore, be undertaken to evaluate this option in the face of emerging and existing virus infections.

Conclusion

The emergence of new virus infections poses a recurring threat to mankind. Worldwide attention is currently focused on the occurrence of microcephaly in newborn infants in Brazil. The transplacental passage of Zika virus and subsequent brain damage may involve co-infection with stealth adapted viruses. Moreover, the severity of the stealth adapted virus infection may have been provoked in early pregnancy by the administration of Tdap vaccine. The opportunity exists for public health officials to evaluate published data relating to stealth adapted viruses and to a non-immunological, anti-virus defense mechanism mediated through the alternative cellular energy (ACE) pathway. Even while waiting for the results of controlled clinical, animal and laboratory studies, urgent consideration should be given to providing KELEA activated water to pregnant women in Zika endemic areas.