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BREAKING: Designed Mutations And Cover Ups For Government Officials Confirmed The C-19 Origins!

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BREAKING: Designed Mutations And Cover Ups For Government Officials Confirmed The C-19 Origins!

Smoking guns, designed mutations, and the US government cover-ups of the laboratory roots of C-19. If you ask why the US intelligence can’t identify the origins of the pandemic and why the government doesn’t want to find the solution to that issue, you don’t have to anymore. We have the answer!

We found a cover-up underway because the powerful multi-national interests that control the government are invested in China’s economic success, and many US officials and scientists will be held responsible if they compromise those plans.

The recipe for the lab creation of the virus was detailed in the 2018 research grant application to the US DARPA

“Project DEFUSE: Defusing the Threat of Bat-borne Coronaviruses” submitted by Peter Daszak of the EcoHealth Alliance.

In 2018, all the applicants took part in the 8th International Symposium on Emerging Viral Diseases in Wuhan, China, October 21-22, 2018.

DARPA rejected the application due to the dangerous gain-of-function experiments of creating viruses that could serve as bioweapons.

DARPA left the door open for funding, and, likely, experiments were already happening in the labs of the principal investigators at the same time the app was submitted.

The proposal says that the bat coronavirus samples that were taken in southern China would be isolated and genetically sequenced in Wuhan. During the next experiments by Zheng-Li Shi of the WIV and Linda Wang of the Duke University-National University of Singapore, spike demonstrates high-risk for human infection would be artificially combined with other backbones creating new and potentially dangerous coronaviruses, which would be tested for human infection by Ralph Baric of the University of North Carolina.

Another smoking gun for the lab roots of the virus is in the presence of the furin polybasic cleavage site in the virus PRRA.

 

‘’ It is a four amino acid sequence, which does not exist in any of hundreds of close bat coronaviruses relatives from which COVID-19 could have evolved.

The enzyme furin is ubiquitous in the human body, and it has long been known that the presence of furin polybasic cleavage sites in viruses facilitates viral entry and replication in human cells, thereby increasing transmissibility and pathogenicity.’’ The Gateway Pundit explained.

The furin polybasic cleavage presence explains why the virus can attack the human organ system. Shibo Jiang and Shywen Liu demonstrated the artificial insertion of furin cleavage sites in 2013.

On May 18, 2021, TGP reported, ‘’ the artificial insertion of the furin polybasic cleavage site into a bat coronavirus backbone was likely done under the supervision of Shibo Jiang in coordination with his military-trained colleague Shuwen Liu and others at the School of Pharmaceutical Science, Southern Medical University, Guangzhou, China.’’

In 2018, the DEFUSE research grant app said that the applicants intended to insert furin polybasic cleavage sites into high abundance artificially.

It’s crucial to note that the furin polybasic cleavage site inserted in the C-19 virus may have been created to mutate into more contagious and pathogenic variants.

In July 2021, the virus mutated in the Delta variant, which is until now the most contagious. Arginine is a chemically essential amino acid, which provides the functional elements in furin polybasic cleavage sites.

We will analyze all SARS-CoV gene sequences for appropriately conserved proteolytic cleavage sites in S2 and for the presence of potential furin cleavage sites. SARSr-CoV S with mismatches in proteolytic cleavage sites can be activated by exogenous trypsin or cathepsin L. Where clear mismatches occur, we will introduce appropriate human specific cleavage sites and evaluate growth potential in Vero cells and HAE cultures. In SARS-CoV, we will ablate several of these sites based on pseudotyped particle studies and evaluate the impact of select SARSr-CoV S changes on virus replication and pathogenesis. We will also review deep sequence data for low abundant high risk SARSr-CoV that encode functional proteolytic cleavage sites, and if so, introduce these changes into the appropriate high abundant, low risk parental strain.”

Now we have the new variant. Omicron.

‘’Unless the true origin of COVID-19 is rapidly addressed, the world not only faces the possibility of another man-made pandemic, but the complete destruction of science as an honest and objective discipline. ’’

Content curated & edited from

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