Compelling evidence has just come to light to show that Wuhan scientists started Monkeypox virus research before its current impact in the world today, much like the COVID virus.
When we were just at the start of attempting to move forward from the deadly COVID-19 virus that plagued the world for years and kills millions of people, now a new threat to the global health shows up.
Many world leaders are expressing dread over the potential of economic destabilization that could come as a result of the Monkeypox. The Jewish TV Channel investigators were able to track and identify a scientific trail surrounding research into the new virus reaching worldwide, directly to where the COVID virus was allegedly released into the world.
Jewish TV Channel Statement: ‘We earnestly state that a world of difference exists between benign scientific research and intent to cause a biological weapon. However, what cannot be ignored is the lack of recognition about the role of Chinese scientists into the research of Monkeypox – before – its spread has become public knowledge.’
Below is the Director of the Wuhan Institute of Virology’s bio, and his name is very prominent in the Monkeypox research article. And while many of the scientists involved in this research have previously completed countless other meaningful studies to benefit man’s well-being, their present silence is what feels so concerning.
Xinwen CHEN, PhD,, Professor. He obtained his BSc and MSc from the Department of Biology, Central China Normal University in 1986 and Henan University of Technology in 1988, respectively. In 1998, he obtained his PhD from Wageningen University in 2001. He subsequently worked at the University of California at Berkeley and Wageningen University as a visiting scientist. Dr. Chen is one of the scientists in “Hundred-talent Project” CAS and one of the awardees of the “National Outstanding Youth Fund”. Dr. Chen’s current positions include Director General of WIV, a member of the institute’s Academic Committee, a member of the institute’s Academic Degree Committee. In addition, Dr. Chen is Editor- in-Chef of Virologica Sinica, a member of the Council of the Hubei Society of Microbiology and a member of the Council of the Hubei Society of Biotechnology. Dr. Chen as the chief scientists assume “national major scientific research projects”, and also assume multiple projects such as 973, the national natural science foundation and institute project. Dr. Chen has more than 130 publications, of which more than 70 are registered in the SCI index. He was also awarded second prize in the “National Innovation Award” in 2005, awarded first prize in the “Natural Science of Hubei Province” in 2011.
The Jewish TV Channel published an excerpt of the research study:
Article Title: Efficient assembly of a large fragment of monkeypox virus genome as a qPCR template using dual-selection-based transformation-associated recombination.
Abstract: Transformation-associated recombination (TAR) has been widely used to assemble large DNA constructs. One of the significant obstacles hindering assembly efficiency is the presence of error-prone DNA repair pathways in yeast, which results in vector backbone recircularization or illegitimate recombination products. To increase TAR assembly efficiency, we prepared a dual-selective TAR vector, pGFCS, by adding a P-ADH1 URA3 cassette to a previously described yeast-bacteria shuttle vector, pGF, harboring a P-HIS3 HIS3 cassette as a positive selection marker.
This new cassette works as a negative selection marker to ensure that yeast harboring a recircularized vector cannot propagate in the presence of 5-fluoroorotic acid. To prevent pGFCS bearing ura3 from recombining with endogenous ura3-52 in the yeast genome, a highly transformable Saccharomyces cerevisiae strain, VL6-48B, was prepared by chromosomal substitution of ura3-52 with a transgene conferring resistance to blasticidin. A 55-kb genomic fragment of monkeypox virus encompassing primary detection targets for quantitative PCR was assembled by TAR using pGFCS in VL6-48B. The pGFCS-mediated TAR assembly showed a zero rate of vector recircularization and an average correct assembly yield of 79% indicating that the dual-selection strategy provides an efficient approach to optimizing TAR assembly.
Article Summary:In summary, our study demonstrated that a PADH1-URA3 cassette can effectively abolish vector recirculation during TAR assembly, promoting the potential use of TAR in genomics and reverse genetics. Nevertheless, more research are still needed to be done to further optimize TAR assembly efficiency and to refine the administrative rules regarding the biosecurity issues related to DNA assembly.
Jewish TV Channel has obtained the full report together with the names of its authors. Once again, we only question the disturbing fact that this article has not been made public at the earliest possible moment as the world braces for another possible consequential pandemic. Is it possible that researchers engaged in benign studies are having their findings side channeled for something of a more sinister nature?
In bringing this important document to the public’s attention Jewish TV Channel sincerely hopes that it can either avoid a future witch hunt against scientists having the public welfare in mind, or act to curtail activities of a sinister and dark nature if that proves to be the case.
Introduction: One of the characteristic features of yeast is that exogenous DNA fragments can be efficiently taken up and recombined. Typically, two linearized DNA fragments with 60 base pairs (bp) of overlapping sequences can be readily recombined and ligated by homologous recombination (HR) in yeast (Noskov et al., 2001). Based on this feature, transformation-associated recombination (TAR) was developed.
Main Body Excerpts: Monkey poxviruses (MPXVs) are large DNA viruses with reported genome sizes ranging from 190,083 to 206,372 bp in length.
Since MPXV infection has never been associated with an outbreak in China, the viral genomic material required for qPCR detection is unavailable. In this report, we employed dual-selective TAR to assemble a 55-kb MPXV genomic fragment that encompasses E9L and C3L, two valuable qPCR targets for detecting MPXV or other orthopoxviruses. The dual-selective TAR assembly showed a zero rate of vector recircularization and an average legitimate assembly yield of 79%, demonstrating that PADH1-URA3, serving as a negative selective marker, can optimize TAR assembly by abolishing vector recircularization.
To prepare a qPCR detection template for MPXV, pGFCS was used as a TAR vector to capture and assemble the four synthesized MPXV segments into one large fragment in VL6-48B. Multiplex PCR was performed to screen the candidate assembly products.
Sources: Thegatewaypundit, Jewishtvchannel
