@Emily please stop spreading disinformation. We have the warp speed president back in power and he knows how to get things done. There will be a vaxx in a matter of weeks and we will all be saved just like the 1st time. No matter what virus nature throws at us, the supreme leader will protect us, especially since musk and JD vance are invested in producing mRNA vaxxes. (ramaswani too)
Hey Emily. I wonder how you find working in TV these days? After all that has occurred? Are you CA based? I work in London. It’s been a shit show since 2020, Covid craziness and the hyperwoke parasite that seems to have infected everyone.
"they" have had their sarscov(1) coronavirus spike "part" with exceptional binding to human ACE2 on their chinese communist party / people's liberation army (ccp/pla) boweapon lab shelves from 2017. they put it into a "backbone" from another sars-cov(1) to make sars-cov-2
That they have put it into another coronavirus is what they would do.
Or a 3ed and ongoing "red herring" trail to further stink up past and ongoing "chinese" communist party/people's liberation army (ccp/pla) bioweapon / bioweapon and pandemic countermeasure "complex"gain of function / gain of effect bioweapon lab work on coronavirus.
ccp/pla bioweapon lab work utilizing US developed bioweapon technologies.
The following from the the March 22, 2020 US bioweapon/bioweapon countermeasure "complex" "hide in plain sight" limited hangout, zoonotic origin / wet market infection epicenter, mis/dis/mal information propaganda piece "Emergence of SARS-CoV-2 through recombination and strong purifying selection" with its original, preprint server published, now deleted, "too revealing", supplementary data. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458444/ Here they carefully tell some truth, always make mention of zoonotic evolution while never actually saying sars-cov-2 was zoonotic (plausible deniability) and never mention lab origin. This article actually spelled out the lab creation of sars-cov-2 with the US created furin cleavage site,never mentioned as US developed bioweapon technology, and the ccp/pla sars-cov backbone and high ACE2 binding affinity sars-cov spike parts, known to be 2013 and 2017 additions to stock on the ccp/pla bioweapon lab shelves. The numbers of virulence increasing and "slow kill" bioweapon "inserts" added to the "spike" of sars-cov-2 are not mentioned here.
"We show evidence of strong purifying selection (my translation - bioweapon lab gain of function work) around the receptor binding motif (RBM) in the spike gene and in other genes among bat, pangolin and human coronaviruses, indicating similar strong evolutionary constraints in different host species. We also demonstrate that SARS-CoV-2’s entire RBM was introduced through recombination with coronaviruses from pangolins, possibly a critical step in the evolution of SARS-CoV-2’s ability to infect humans. " "we find significant recombination breakpoints before and after the ACE2 binding site (fig. S2A)," "Specifically, amino acid sequences of the receptor binding motif (RBM) in the C terminal of the S1 subunit are nearly identical to those in two Pan_SL-CoV_GD viruses, with only one amino acid difference (Q498H)—although the RBM region has not been fully sequenced in one of Guangdong pangolin virus (Pan_SL-CoV_GD/P2S)
"Thus, a functional RBM nearly identical to the one in SARS-CoV-2 is naturally present in Pan_SL-CoV_GD viruses. The very distinctive RaTG13 RBM suggests that this virus is unlikely to infect human cells, and that the acquisition of a complete functional RBM (my note; with exceptional human ACE 2 binding ability) by a RaTG13-like CoV through a recombination event with a Pan_SL-CoV_GD-like virus enabled it to use ACE2 for human infection.
note; As this "Research Article" was originally posted to the preprint? server, the supplementary data initially contained a Chinese research spreadsheet, subsequently removed, too revealing?, showing on the vertical, line by line, 3533 individual tissue samples taken from a number of sick pangolins. Virus types found in each tissue sample, averaging close to 10 per sample, were listed horizontally - sars-cov was found in sick pangolin #7 and more in sick pangolin #8, more likely the "guilty party" supplying the "spike" identified to have evolved to, or to have been "evolved" to, gain the human ACE 2 binding affinity enhancement in the spike identified in sars-cov-2.
"Furthermore, SARS-CoV-2 has a unique furin cleavage site insertion (PRRA) not found in any other CoVs in the Sarbecovirus group (24), although similar motifs are also found in MERS and more divergent bat CoVs (25) (Fig. S3). This PRRA motif makes the S1/S2 cleavage in SARS-CoV-2 much more efficiently than in SARS-CoV and may expand its tropism and/or enhance its transmissibility (23)"
Sars-cov backbone and sars-cov spike components were on the bioweapon lab shelves of the "chinese" communist party/people's liberation army (ccp/pla) bioweapon / bioweapon and pandemic countermeasure "complex" from 2013 - a sars-cov virus with a 50% fatality rate when transfected in aerosolized bat feces, this cov-2 supplied the "backbone" for sars-cov-2, and from 2017 a pangolin sars-cov spike component with exceptional binding to human ACE 2.
@Emily please stop spreading disinformation. We have the warp speed president back in power and he knows how to get things done. There will be a vaxx in a matter of weeks and we will all be saved just like the 1st time. No matter what virus nature throws at us, the supreme leader will protect us, especially since musk and JD vance are invested in producing mRNA vaxxes. (ramaswani too)
ha ha
Hey Emily. I wonder how you find working in TV these days? After all that has occurred? Are you CA based? I work in London. It’s been a shit show since 2020, Covid craziness and the hyperwoke parasite that seems to have infected everyone.
"they" have had their sarscov(1) coronavirus spike "part" with exceptional binding to human ACE2 on their chinese communist party / people's liberation army (ccp/pla) boweapon lab shelves from 2017. they put it into a "backbone" from another sars-cov(1) to make sars-cov-2
That they have put it into another coronavirus is what they would do.
Or a 3ed and ongoing "red herring" trail to further stink up past and ongoing "chinese" communist party/people's liberation army (ccp/pla) bioweapon / bioweapon and pandemic countermeasure "complex"gain of function / gain of effect bioweapon lab work on coronavirus.
ccp/pla bioweapon lab work utilizing US developed bioweapon technologies.
The following from the the March 22, 2020 US bioweapon/bioweapon countermeasure "complex" "hide in plain sight" limited hangout, zoonotic origin / wet market infection epicenter, mis/dis/mal information propaganda piece "Emergence of SARS-CoV-2 through recombination and strong purifying selection" with its original, preprint server published, now deleted, "too revealing", supplementary data. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458444/ Here they carefully tell some truth, always make mention of zoonotic evolution while never actually saying sars-cov-2 was zoonotic (plausible deniability) and never mention lab origin. This article actually spelled out the lab creation of sars-cov-2 with the US created furin cleavage site,never mentioned as US developed bioweapon technology, and the ccp/pla sars-cov backbone and high ACE2 binding affinity sars-cov spike parts, known to be 2013 and 2017 additions to stock on the ccp/pla bioweapon lab shelves. The numbers of virulence increasing and "slow kill" bioweapon "inserts" added to the "spike" of sars-cov-2 are not mentioned here.
"We show evidence of strong purifying selection (my translation - bioweapon lab gain of function work) around the receptor binding motif (RBM) in the spike gene and in other genes among bat, pangolin and human coronaviruses, indicating similar strong evolutionary constraints in different host species. We also demonstrate that SARS-CoV-2’s entire RBM was introduced through recombination with coronaviruses from pangolins, possibly a critical step in the evolution of SARS-CoV-2’s ability to infect humans. " "we find significant recombination breakpoints before and after the ACE2 binding site (fig. S2A)," "Specifically, amino acid sequences of the receptor binding motif (RBM) in the C terminal of the S1 subunit are nearly identical to those in two Pan_SL-CoV_GD viruses, with only one amino acid difference (Q498H)—although the RBM region has not been fully sequenced in one of Guangdong pangolin virus (Pan_SL-CoV_GD/P2S)
"Thus, a functional RBM nearly identical to the one in SARS-CoV-2 is naturally present in Pan_SL-CoV_GD viruses. The very distinctive RaTG13 RBM suggests that this virus is unlikely to infect human cells, and that the acquisition of a complete functional RBM (my note; with exceptional human ACE 2 binding ability) by a RaTG13-like CoV through a recombination event with a Pan_SL-CoV_GD-like virus enabled it to use ACE2 for human infection.
note; As this "Research Article" was originally posted to the preprint? server, the supplementary data initially contained a Chinese research spreadsheet, subsequently removed, too revealing?, showing on the vertical, line by line, 3533 individual tissue samples taken from a number of sick pangolins. Virus types found in each tissue sample, averaging close to 10 per sample, were listed horizontally - sars-cov was found in sick pangolin #7 and more in sick pangolin #8, more likely the "guilty party" supplying the "spike" identified to have evolved to, or to have been "evolved" to, gain the human ACE 2 binding affinity enhancement in the spike identified in sars-cov-2.
"Furthermore, SARS-CoV-2 has a unique furin cleavage site insertion (PRRA) not found in any other CoVs in the Sarbecovirus group (24), although similar motifs are also found in MERS and more divergent bat CoVs (25) (Fig. S3). This PRRA motif makes the S1/S2 cleavage in SARS-CoV-2 much more efficiently than in SARS-CoV and may expand its tropism and/or enhance its transmissibility (23)"
Sars-cov backbone and sars-cov spike components were on the bioweapon lab shelves of the "chinese" communist party/people's liberation army (ccp/pla) bioweapon / bioweapon and pandemic countermeasure "complex" from 2013 - a sars-cov virus with a 50% fatality rate when transfected in aerosolized bat feces, this cov-2 supplied the "backbone" for sars-cov-2, and from 2017 a pangolin sars-cov spike component with exceptional binding to human ACE 2.