Anonymous ID: 26cb34 July 25, 2021, 9:48 a.m. No.14196620   🗄️.is 🔗kun

IDENTIFICATION OF THE HIGHLY INFECTIVE GENOMIC COMPOSITION OF SARS COV 2 RNA: 👇

 

SARS COV 2 is a particular chimeric "armored" virus, consisting of external protuberances of S (Spike) coated, externally, by glycans and, inside these protuberances, the TGEV bacteria (E. Coli bacterium, of gastroenteritis) have been identified and HIV retroviruses.The outer membrane M has the TMPRSS2 protein which, associated with ACE2, allows the same protein S to enter the host cells.

This mechanism is well explained by the process of fusion of the M membrane with the plasma membrane of the cell.

(It is important to note that a TMPRSS2 inhibitor is BROMEXINE).

The inner nucleus N is instead composed of highly pathogenic viral genomes such as: MVH / HCV (Hepatitis C) an RNA virus belonging to the Flavivirus / Eie Yoelii family (malaria, such as ZIKA), and the viral sequences provided by the recombination of SARS with endogenous BaT CoV, such as: Marburg, Nipah, Hendra and Lyssavirus (rabies).

 

SARS COV 2 CONSTRUCTION PROCESS:

The fundamentals.

The construction process of SARS COV 2 makes use of 👉 "no-see-um" technology, developed by R. Baric, which allows the assembly of large DNAs, from smaller subclones, without the incorporation of unique restriction sites in the genome.👇

  • Link:

researchgate.net/publication/81…

 

This process consists of both serial passages in in-vitro cultures and the use of intermediate animals such as: humanized mice, ferrets, cats, hares, suckling pigs.

This process was carried out in the BSL2, BSL3, BSL4 Laboratories of the WIV / CAS of Whuan; where there have been several cases of environmental contamination and as many laboratory leaks caused by the use of laxive protocols.

 

  • SARS (Acute Pulmonary Syndrome) + HCV (Hepatitis C) is used to develop a first "armored virus" which is then recombined, in-vivo, with the "backbone" of some BaT CoV strains of bats which are natural carriers of highly infectious viral genomes.

 

  • The consolidated infectious genome is then inoculated into humanized, leukemic (HIV) mice to facilitate the passage of the virus into humanized T cells.

 

  • An enhanced and advanced variant of SARS COV 2 is eventually transmitted, by airborne transmission, to ferrets (ORF8) in-vivo, in ACE2.This enhanced version, obtainedusing only the ORF8 protein, makes the SARS COV ORF8 virus extremely infectious, virulent and mutable.

 

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