Germany included/added SARS-CoV-2’s unique COVID-19 causing viral protein ORF10 to its mRNA vaccines to prolong COVID-19. The disease causing viral protein ORF10 is the reason why Germany’s BioNTech lab uses bioweapons handling protocols for manufacturing Germany’s COVID-19 mRNA vaccines. ORF10 is a biological agent.
A 2021 published study “SARS-CoV-2 ORF10 suppresses the antiviral innate immune response by degrading MAVS through mitophagy” informs you why Germany manufactured its COVID-19 vaccines to include 2 major components of SARS-CoV-2 – it’s spike protein (a modified/variant form of spike protein) and it’s unique COVID-19 causing viral protein, ORF10:
“In this study, we showed that overexpression of ORF10 markedly suppressed the expression of type I interferon (IFN-I) genes and IFN-stimulated genes. Then, mitochondrial antiviral signaling protein (MAVS) was identified as the target via which ORF10 suppresses the IFN-I signaling pathway, and MAVS was found to be degraded through the ORF10-induced autophagy pathway. Furthermore, overexpression of ORF10 promoted the accumulation of LC3 in mitochondria and induced mitophagy. ”
… ORF10 transcripts can be detected in patients infected with SARS-CoV-2 [56]. Moreover, Liu et al. found that the expression level of ORF10 in patients with severe disease was much higher than that in patients with moderate disease; in addition, the expression ratio of ORF10 to nucleocapsid (N) in patients with severe disease was significantly higher than that in patients with moderate disease [57]. Therefore, ORF10 plays a vital role at all stages of SARS-CoV-2 infection. In our study, overexpression of ORF10 promoted the degradation of MAVS and the replication of SARS-CoV-2. Consistent with these results, when ORF10 was knocked down by shRNA, MAVS was not degraded and viral replication was weakened, suggesting that ORF10 facilitates SARS-CoV-2 replication via degradation of MAVS.
found that SARS-CoV-2 open reading frame 10 (ORF10) targets STING to antagonize IFN activation. Overexpression of ORF10 inhibits cGAS–STING‐induced interferon regulatory factor 3 phosphorylation, translocation, and subsequent IFN induction. Mechanistically, ORF10 interacts with STING, attenuates the STING–TBK1 association, and impairs STING oligomerization and aggregation and STING‐mediated autophagy; ORF10 also prevents the endoplasmic reticulum (ER)‐to‐Golgi trafficking of STING by anchoring STING in the ER. Taken together, these findings suggest that SARS‐CoV‐2 ORF10 impairs the cGAS–STING signaling by blocking the translocation of STING and the interaction between STING and TBK1 to antagonize innate antiviral immunity.
The origin of COVID-19 has never been fully investigated because an investigation would find that COVID-19 was a coordinated bioterrorism attack. The bioterrorism attack was perpetrated against the World’s civilian population, pursuant to and in furtherance of a State (Germany) and organizational (United Nations Organization) policy:
Obtain worldwide support for vaccinations
Obtain $billions by forcing World leaders to invest in vaccines
Germany’s Fourth Reich EU and the UN desperately needed $billions to avert default – bankruptcy. Italy/Vatican City reported in March 2020 that it needed a €500 to €700 billion ($572 billion to $801 billion) bailout. In October 2019 the UN very publicly declared that it was insolvent.
In a statement issue by his Spokesperson, the Secretary-General said he had written to Member States, “about the worst cash crisis facing the United Nations in nearly a decade. The Organization runs the risk of depleting its liquidity reserves by the end of the month and defaulting on payments to staff and vendors.”
The insolvent UN also stated in 2019 and again in January 2020 that it needed an extra $350 billion annually to bankroll its “Sustainable Development Goals”.
UN member states couldn’t just hand over $billions to bailout Germany’s Fourth Reich EU or Germany’s WWII envisioned Neuordnung (New Order) – the UN. So Germany and the WHO conspired in 2017 to wage a bioterrorism attack against the civilian population of the World using a lab created virus that was developed for the WHO/UN to target the Asian populations.
Germany and the WHO recruited co-conspirators at the 2017 G20 Hamburg Summit using emergency simulation exercise videos Germany produced in close cooperation with the WHO. The videos Germany produced for the WHO depicted a novel coronavirus outbreak. Germany and the WHO’s fictional SARS like coronavirus was called MARS. Embedded below is Germany’s G20 Emergency Simulation Exercise Video 9.
The World was warned by US Secretary of Defense William S. Cohen in 1997 that viroligsts were developing novel viruses that targeted specific ethnic groups and races.
“some countries have been trying to construct something like an Ebola Virus, and that would be a very dangerous phenomenon, to say the least. Alvin Toeffler has written about this in terms of some scientists in their laboratories trying to devise certain types of pathogens that would be ethnic specific so that they could just eliminate certain ethnic groups and races” DoD News Briefing, Secretary of Defense William S. Cohen Monday, April 28, 1997
Virologist Ron Fouchier of Erasmus University in the Netherlands is one such person. He’s been developing new pathogens that target 3 specific ethnic groups – Asian (SARS), Middle Eastern (MERS) and African (HIV) populations. Fouchier is accredited for causing the H5N1 to become more transmissible in mammals/humans. His research focuses on making the common/annual flu viruses more virulent and mutatious.
In October 2014, U.S. officials announced an unprecedented “pause” on funding for Fouchier’s research involving influenza or the Middle East respiratory syndrome (MERS) or severe acute respiratory syndrome (SARS) viruses.
It is very important to note that Fouchier resumed his research on making common flu viruses more virulent and mutatious in 2019, just months before the Wuhan, China SARS II outbreak.
It’s imperative Canadians and Americans know that the SARS coronavirus was made in a lab to specifically target the Asian population. The outbreak of SARS originated in southern China in 2002-2003. It wasn’t highly contagious. It led to 8273 cases and 775 deaths in multiple countries. The victims of SARS were predominantly Asian. Mainland China and Hong Kong accounted for 87% of all cases and 84% of all deaths.
So how did SARS version 2 become a global pandemic if the lab created SARS coronavirus wasn’t highly contagious and it only targeted the Asian populations? Germany and the UN desperately needed $billions so they resorted to bioterrorism to obtain $billions.
The act of bioterrorism can range from a simple hoax to the actual use of these biological weapons, also referred to as agents.
Germany and the insolvent WHO/UN recruited corrupt politicians like Justin Trudeau and Chrystia Freeland to assist them obtain $billions by misdiagnosing patient’s illnesses, falsifying medical records and death certificates. The WHO instructed their co-conspirators to record all annual respiratory illnesses and deaths such as influenza, bronchitis and TB as being caused by the lab created biological agent SARS-CoV-2. Ontario Premier Doug Ford complied with Germany and the WHO’s bioterrorism demands by instructing Ontario hospitals to suspend the reporting of influenza infections.
Public Health Ontario’s “Monthly Infectious Diseases Surveillance Reports” provides material evidence that Ontario Premier Doug Ford falsified medical records to assist Germany and the WHO/UN prolong their COVID-19 bioterrorism attack against Canada and Canadians.
Influenza infections occur annually, worldwide. Influenza infections don’t just vanish or skip a year or two. The Ontario government’s Monthly Infectious Diseases Surveillance Reports provides ample material evidence that medical records were falsified – pursuant to Germany and the WHO’s COVID-19 bioterrorism demands.
Falsifying medical records is a criminal offence.
Forgery
366(1) Every one commits forgery who makes a false document, knowing it to be false, with intent
(a) that it should in any way be used or acted on as genuine, to the prejudice of any one whether within Canada or not; or
(b) that a person should be induced, by the belief that it is genuine, to do or to refrain from doing anything, whether within Canada or not.
The WHO’s own reports provides the most compelling material evidence that medical records were falsified worldwide pursuant to Germany and the WHO’s COVID-19 bioterrorism demands.
WHO’s “The Global Impact of Respiratory Disease”:
“Respiratory diseases impose an immense worldwide health burden. Five of these diseases are among most common causes of severe illness and death worldwide.”
“For decades, acute lower respiratory tract infections have been among the top three causes of death and disability among both children and adults. Although the burden is difficult to quantify, it is estimated that lower respiratory tract infection causes nearly 4 million deaths annually“
“Altogether, more than 1 billion people suffer from either acute or chronic respiratory conditions. The stark reality is that, each year, 4 million people die prematurely from chronic respiratory disease.”
Screenshot from WHO’s 2019 report “The Global Impact of Respiratory Disease”
During the first herpes outbreak (called primary herpes), an infected person may experience flu-like symptoms. These include body aches, fever and headache. People who have been vaccinated with Germany’s Pfizer-BioNTech COVID-19 mRNA vaccines are experiencing the same flu-like symptoms as herpes because the human herpes virus protein ORF10 is encoded in SARS-CoV-2 and in mRNA vaccines.
There is more evidence that supports the assertion that mRNA vaccines are infecting the World population with herpes. On August 12, 2021 Europe’s drug regulator EMA published new updates on the safety of mRNA vaccines after it investigated a possible link between mRNA vaccines and a skin reaction called erythema multiforme. Erythema multiforme is a hypersensitivity reaction usually triggered by infections, most commonly herpes simplex virus (HSV).
The human herpes virus ORF10 protein (HHV-8) is the only protein that is present exclusively in SARS-CoV-2 and not in SARS-CoV or any other human coronaviruses.
The WHO’s COVID-19 Global literature on coronavirus disease suggested the severity of COVID-19 is enhanced by the human herpes virus protein ORF10.
“Could the severity of COVID-19 be enhanced by ORF10 accessory proteins?”
uniqueness of ORF10 and predicted intrinsic characteristics support possible involvement of ORF10 protein in giving COVID-19 its specific characteristics like spread and virulence
World Heath Organization
Since 1972 the WHO/UN has called for/recommended virologists develop the means to prolong virus/coronavirus infections:
An attempt should be made to see if viruses can in fact exert selective effects on immune function. e.g. by depressing (to diminish the activity, strength, or yield of) 7S (IgG) versus 19S (IgM) antibody, or by affecting T cell function as opposed to B cell function. The possibility should be looked into that the immune response to the virus itself may be impaired if the infecting virus damages, more or less selectively the cells responding to the viral antigens. If this proves to be the case, virus-induced immunodepression might conceivably be highly instrumental in prolonging certain virus infections, such as murine leukemia, hepatitis, …
Bulletin of the World Health Organization, Volume 47, p.259, 1972, Recommendations (3)
Virologists did that by genetically engineering/modifying the SARS coronavirus. The human herpes virus protein ORF10 was encoded into the SARS coronavirus to make SARS-CoV-2.
There is currently no cure or preventive treatment for the herpes infection. If a person gets either form of herpes virus infection, they will have it for life , whether or not they experience symptoms.
A 2003 patent informs us when the herpes virus protein ORF10 was added to the SARS virus by virologists to create SARS-CoV-2. The 2003 Patent US-2006257852-A1 assigned to CHIRON CORP (US), which was acquired by Novartis (Switzerland) on April 20, 2006 specifically names the ORF10 protein – a protein that is exclusively found in SARS-CoV-2 genome and not in SARS-CoV, being used/encoded in the fusion protein of the patented novel SARS coronavirus.
