Human herpes virus protein in genome of SARS-CoV-2 provides evidence the virus that causes COVID-19 was developed for WHO to be used as a bioweapon

SARS-CoV-2 genome annotation revealed the presence of 10 open reading frames (ORFs). SARS-CoV-2 possesses two accessory proteins, ORF8 and ORF10, that share no homology to other coronavirus strains.

The SARS-CoV-2 accessory protein ORF10 (organism Human herpesvirus 8/HHV-8), a putative 38-amino acid viral protein encoded in the 3’ accessory region of the genome, is a highly ordered, hydrophobic (insoluble in water; repelling water) , and thermally stable protein, which contains at least one transmembrane region.

“the ORF10 protein contains high numbers of promiscuous cytotoxic T lymphocyte (CTL) epitopes, primarily on the α-helix. A recent study by Liu et al. 2020 found that in severe cases of COVID-19, the ORF10 was overexpressed when compared against ORF10 expression levels in moderate cases. If the ORF10 protein is synthesized (manufactured, man made), this may help to partially explain the nature behind severe cases of COVID-19. The large number of CTL epitopes in conjunction with the overproduction of the ORF10 protein could result in elevated immune responses towards SARS-CoV-2, leading to some potentially fatal immunopathological outcomes. … Alternatively, ORF10 may act itself or serve as a precursor for other RNAs in regulating gene expression/replication, translation efficiency, or interfering with cellular antiviral pathways.October 2020 study

ORF8, “although non-essential and the precise functions are unknown, it has been suggested that this protein assists in SARS-CoV-2 replication in the early secretory pathway and in immune evasion. … Since ORF8 is not an essential protein for the SARS-CoV-2 life cycle, ORF8 is likely to functionally associate with other SARS-CoV-2 components to assist with SARS-CoV-2 replication and assembly in host cells, but, the coordinated process of this mechanism is still unknown”

“It is also noteworthy that ORF10, exclusively found in SARS-CoV-2 (and not in SARS-CoV), has been shown to interact with the Cullin 2 (CUL2) RING E3 ligase complex, possibly hijacking its function. It is not known what the implications of this interaction is for virus replication, but a similar complex is recruited by other viral proteins, including HIV Vif, Adenovirus E4Orf6, EBV Bzlf and others (Mahon et al., 2014). In all cases, the virus exploits this to target an antiviral protein for proteasome degradation, and it is therefore likely the case also for Orf10.” Structural Characterization of SARS-CoV-2: Where We Are, and Where We Need to Be

Accessory proteins (ORF8, ORF10) were suggested to play an important role in virulence and host interaction in other coronaviruses (Liu et al., 2014).

Severe acute respiratory syndrome coronavirus 2 isolate Wuhan-Hu-1, complete genome contains

Protein ORF10

Gene

ORF10

Organism

Human herpesvirus 8 type P (isolate GK18) (HHV-8) (Kaposi’s sarcoma-associated herpesvirus)

Human herpesvirus 8 (HHV-8) is the infectious cause of Kaposi sarcoma (KS) and HIV-infection. HHV-8 infection is not very common in North America. It occurs more often in some Mediterranean countries and is widespread in Africa.

“In the United States, men who have sex with men (MSM) and persons with HIV infection are at increased risk for HHV-8 infection. Among MSM without HIV infection, the seroprevalence ranges from 13% to 20% and HHV-8 seroprevalence increases to 30% to 35% among MSM with HIV infection. Injection drug use may also be a risk factor for HHV-8 seropositivity, although this association has not been consistently observed.”

HHV-8 is etiologically associated with all forms of Kaposi sarcoma (KS) including classic, endemic (belonging or native to a particular people or country), transplant-related, and AIDS-related, as well as rare neoplastic disorders (primary effusion lymphoma [PEL] and solid organ variants) and the lymphoproliferative disorder known as multicentric Castleman’s disease (MCD). Although the precise pathogenesis for these tumors remains unclear, infection with HHV-8 precedes their development.” Guidelines for the Prevention and Treatment of Opportunistic Infections in Adults and Adolescents with HIV

The presence of two accessory proteins, ORF8 and ORF10, that share no homology to other coronaviruses strains but appear to assist with SARS-CoV-2 replication and and in immune evasion, suggests SARS-CoV-2 was developed for the strapped for cash WHO as a bioweapon.

ORF10 protein “HHV-8 mostly causes disease mainly in immunocompromised individuals” Johns Hopkins Medicine

Germany’s Pfizer-BioNTech and DARPA funded Moderna COVID-19 vaccines part of UN/WHO’s vaccine induced sterility/genocide program

Messenger RNA (mRNA) is genetic material, so in that sense, the vaccines are genetically based therapy. But the FDA classifies them as vaccines, not gene therapy. Here’s why?

Since 1972 “the WHO Task Force on Vaccines for Fertility Regulation has been supporting basic and clinical research on the development of birth control vaccines directed against the gametes or the preimplantation embryo. These studies have involved the use of advanced procedures in peptide chemistry, hybridoma technology and molecular genetics as well as the evaluation of a number of novel approaches in general vaccinology.” WHO Task Force on Vaccines for Fertility Regulation

The UN/WHO/World Bank’s strategy is for devising a nonsurgical method to induce permanent sterility. That has already been developed and tested.

a nonsurgical method to induce permanent sterility calls for the combined use of a “gene silencing” technology with a “gene therapy” delivery system that can target silencing molecules to specific regions of the brain critical for fertility, and cause long-term suppression of gene expression. Because the vector to be employed remains active for years, permanent sterility is expected to occur following a single systemic administration.

Recently published studies of a gene know as Enhanced at Puberty 1 (EAP1), evidence was provided that RNAi can be used to disrupt reproductive cyclicity in two species of animals, rats and non-human primates. These studies in rats and non-human primates clearly demonstrate that RNAi is capable of disrupting female reproductive cyclicity.Targeted Gene Silencing to Induce Permanent Sterility

“As of June 2020, two of the ten top vaccine candidates used RNAi technology for COVID-19 vaccination. These two vaccines were developed by Moderna and NIAD, and BioNTech and Pfizer.” Yahoo!Finance

The UN/WHO have been conducting vaccine medical experiments since WWII. The UN/WHO continued Nazi Germany’s Auschwitz medical experiment using vaccines. Photo below provides refutable proof – “United Nations personnel vaccinate an 11-year-old concentration camp survivor who was a victim of medical experiments at the Auschwitz camp.”

What the UN/WHO wants and is supporting under the “WHO Task Force on Vaccines for Fertility Regulation” is a very serious crime.  The UN/WHO supporting basic and clinical research on the development of birth control vaccines is defined as genocide.

Convention on the Prevention and Punishment of the Crime of Genocide

Article II

In the present Convention, genocide means any of the following acts committed with intent to destroy, in whole or in part, a national, ethnical, racial or religious group, as such:

  1. Killing members of the group;
  2. Causing serious bodily or mental harm to members of the group;
  3. Imposing measures intended to prevent births within the group;

The intended and stated purpose of the UN/WHO Task Force on Vaccines for Fertility Regulation “has been supporting basic and clinical research on the development of birth control vaccines

The UN/WHO is essentially saying it wants vaccines to be developed to commit genocide. Birth control vaccines are UN/WHO measures intended to prevent births = genocide.

“Genocide is the most heinous of crimes, encompassing all it touches in a tsunami of hate and destruction. It is an assault on our most fundamental shared values.” UN Secretary-general, December 9, 2020 New York

“The Genocide Convention establishes in Article I that the crime of genocide may take place in the context of an armed conflict, international or non-international, but also in the context of a peaceful situation. The latter is less common but still possible. The same article establishes the obligation of the contracting parties to prevent and to punish the crime of genocide” The United Nations Organization

Imperative RCMP, police or national forensic lab test Germany’s Pfizer-BioNTech vaccine

BioNTech SEC filing for Pfizer-BioNTech COVID-19 vaccine

It is imperative RCMP, police or national forensic lab(s) test Germany’s Pfizer-BioNTech vaccine. Test to determine whether or not Germany substituted the vaccine that the FDA approved with a vaccine that would and have caused Canadians to become sick. Canadians who have gotten the 2nd Pfizer-BioNTech vaccine have become ill. I personally know 3 people who became very sick immediately after getting the 2nd Pfizer-BioNTech vaccine. All three never got sick last year.

Canadians can’t trust Germany or the WHO. Germany and the WHO desperately needs $billions to avert economic collapse. Before COVID-19 both Germany’s EU and the UN publicly stated that they were insolvent.

A Europen Commission paper reported Germany’s COVID-19 vaccine manufacturer falsified data in order to obtain regulatory approval – needed to make $billions.

“DISHONEST SCIENTIFIC REPORT AND DATA FALSIFICATION WITH RESPECT TO THE EFFECTIVENESS OF THE CANDIDATE SARS-COV-2/COVID-19 VACCINES DEVELOPED BY BIONTECH/PFIZER,”

COVID-19 isn’t the first time a Germany manufacturer intentionally falsified data. Germany’s Volkswagen falsified emission reports. Volkswagen has been conspiring with Germany since WWII to form a Germany economic Empire – the EU.

A declassified three-page, US Military Intelligence report EW-Pa 128 (Red House Report), detailed how German industrialists were to work with the Nazi Party to rebuild Germany’s economy empire / the Fourth Reich EU. Volkswagen was specifically named as one of Germany’s co-conspirators.

Furthermore, Germany’s COVID-19 vaccine manufacturing partner Pfizer plead guilty and paid $2.3 billion in 2009 to settle civil and criminal charges that it had illegally marketed its painkiller Bextra. It was the largest health care fraud settlement and the largest criminal fine of any kind ever.

Pfizer “used advisory boards, consultant meetings and provided travel to lavish resorts to improperly promote Bextra to doctors and made misleading claims about the drug’s safety and efficacy” US Department of Justice

Source: https://www.reuters.com/article/us-pfizer-settlement-idUSTRE5813XB20090902

Pfizer also illegally promoted several other drugs, including antipsychotic drug Geodon, antibiotic Zyvox, and anti-epileptic drug Lyrica. Healthcare providers received payments for prescribing these drugs to patients for off-label use.

False claims were submitted to government healthcare programmes, bypassing the insurance programmes. The company had to pay approximately $1bn to Medicare, Medicaid, and other government insurance programmes under the settlement.

Source

Germany’s Pfizer-BioNTech vaccines, in every practical sense, were developed to make SARS-CoV-2 more transmissible and infectious

Coronaviruses are surrounded by a fatty membrane known as an envelope. In order to gain entry to the inside of the cell, enveloped viruses use spike proteins to fuse their own membrane to that of cells’ and take over the cell. “The spike protein is found on the surface of the virus that causes COVID-19.” the CDC

Germany’s Pfizer-BioNTech COVID-19 mRNA vaccines give instructions for our cells to make “spike protein” – lots of them.  2nd vaccine causes the making of more spike protein. The Pfizer-BioNTech COVID-19 vaccine uses modified messenger RNA (mRNA). “Specifically, the vaccine contains the mRNA of spike protein, which is located on the surface of the SARS-CoV-2 virus and is what SARS-CoV-2 uses to invade host cells.” Carlos Malvestutto, MD, MPH, who specializes in infectious disease at The Ohio State University Wexner Medical Center

The WHO, CDC and other health authorities know and have repeatedly stated that the “novel coronavirus uses spike protein like a key to gain entry to our cells; once inside, the virus is free to replicate, making us sick. The spike protein binds to a protein on the surface of our cells called ACE2, triggering uptake of the virus particle and eventually membrane fusion.”

That means Germany’s COVID-19 vaccines were developed to make spike protein and give the SARS-CoV-2 virus the means to invade cells and cause millions of healthy people to become sick. SARS-CoV-2 can’t invade cells and make us sick without spike (S) protein. Germany’s Pfizer-BioNTech vaccines, in every practical sense, is making SARS-CoV-2 more transmissible and infectious.

The WHO, CDC, Health Canada  and Germany would have you believe that Germany’s vaccines that instruct cells to make SARS-CoV-2’s spike protein is harmless yet they all know SARS-CoV-2 needs the spike protein to invade cells to replicate and make you sick. Furthermore, “mRNAs are created as an exact copy (a clone) of the segment of DNA found along the genome corresponding to a protein-coding gene.” UMass Medical School “Specifically, the Pfizer-BioNTech COVID-19 vaccine is a lipid nanoparticle-formulated, nucleoside-modified mRNA vaccine. The lipid coating of the nanoparticles binds to the cell membrane, facilitating entry of the (SARS-CoV-2) mRNA (genetic material) segment into the cell.” AMERICAN SOCIETY FOR REPRODUCTIVE MEDICINE (ASRM).