Posted on 07/15/2020 1:07:39 AM PDT by Grandpa Drudge
Indeed.
During the Quarantine, I watched a two-year old documentary on Smithsonian, and a CDC official said the same thing. She even recommended “masks” and “social distancing” so the term was in use at least as far back as 2018. (It was a 100-Year retrospective of the Spanish Flu)
The whole thing was ENGINEERED from the get-go.
The real issue here is whether Dr. Anthony Fauci had a hand in cooperating with Dr. Zhengli-Li Shi of the Wuhan Institute of Virology to create the chimeric virus from WIV1-CoV, which may actually now be SARS-CoV-2.
As stated in the paper cited in
https://gmwatch.org/en/news/latest-news/19410-chinese-and-us-scientists-genetically-engineered-bat-coronaviruses-in-dangerous-gain-of-function-research-stretching-back-years
"In the published paper reporting the risky experiment, the scientists state that they began their work before the 2014 US temporary moratorium on virus gain-of-function studies, which was prompted by several high-profile biosafety failures at US labs. But in spite of the moratorium, as stated in the paper, the NIH gave permission for the study to continue. Dr Fauci of the NIAID outsourced the research to the WIV in China, in the words of one media article."
For explanation, see:
https://www.snopes.com/fact-check/obama-fauci-gates-wuhan-lab/
and
https://www.snopes.com/fact-check/obama-admin-wuhan-lab-grant/
I am making serious charges in this thread, and do not wish my focus to be distorted with misinformation.
See my reply to Diogenesis, post#25
Yep...we can still find stuff like that...it hasn’t ALL gone into the Memory Hole yet.
Published in PNAS (Proceedings of the National Academy of Sciences of the United Strates of America) March 14, 2016
https://www.pnas.org/content/113/11/3048
Using the SARS-CoV infectious clone as a template (7), we designed and synthesized a full-length infectious clone of WIV1-CoV consisting of six plasmids that could be enzymatically cut, ligated together, and electroporated into cells to rescue replication competent progeny virions (Fig. S1A). In addition to the full-length clone, we also produced WIV1-CoV chimeric virus that replaced the SARS spike with the WIV1 spike within the mouse-adapted backbone (WIV1-MA15, Fig. S1B). WIV1-MA15 incorporates the original binding and entry capabilities of WIV1-CoV, but maintains the backbone changes to mouse-adapted SARS-CoV. Importantly, WIV1-MA15 does not incorporate the Y436H mutation in spike that is required for SARS-MA15 pathogenesis (8). Following electroporation into Vero cells, robust stock titers were recovered from both chimeric WIV1-MA15 and WIV1-CoV.
And the connection to Wuhan Labs in China is highlighted in the Acknowledgments:
We thank Dr. Zhengli-Li Shi of the Wuhan Institute of Virology for access to bat CoV sequences and plasmid of WIV1-CoV spike protein. Research was supported by the National Institute of Allergy and Infectious Disease and the National Institute of Aging of the NIH under Awards U19AI109761 and U19AI107810 (to R.S.B.), AI1085524 (to W.A.M.), and F32AI102561 and K99AG049092 (to V.D.M.). Human airway epithelial cell cultures were supported by the National Institute of Diabetes and Digestive and Kidney Disease under Award NIH DK065988 (to S.H.R.). Support for the generation of the mice expressing human ACE2 was provided by NIH Grants AI076159 and AI079521 (to A.C.S.).
JUDICIAL WATCH just filed a LAWSUIT for FRAUD an d WHO corresponded dence!!! GO JW
I can’t find that. Do you have a link?
PNAS March 15, 2016 113 (11) 3048-3053; first published March 14, 2016 https://doi.org/10.1073/pnas.1517719113
Edited by Peter Palese, Icahn School of Medicine at Mount Sinai, New York, NY, and approved January 6, 2016 (received for review September 4, 2015)
Using the SARS-CoV infectious clone as a template (7), we designed and synthesized a full-length infectious clone of WIV1-CoV consisting of six plasmids that could be enzymatically cut, ligated together, and electroporated into cells to rescue replication competent progeny virions (Fig. S1A). In addition to the full-length clone, we also produced WIV1-CoV chimeric virus that replaced the SARS spike with the WIV1 spike within the mouse-adapted backbone (WIV1-MA15, Fig. S1B). WIV1-MA15 incorporates the original binding and entry capabilities of WIV1-CoV, but maintains the backbone changes to mouse-adapted SARS-CoV. Importantly, WIV1-MA15 does not incorporate the Y436H mutation in spike that is required for SARS-MA15 pathogenesis (8). Following electroporation into Vero cells, robust stock titers were recovered from both chimeric WIV1-MA15 and WIV1-CoV.
We thank Dr. Zhengli-Li Shi of the Wuhan Institute of Virology for access to bat CoV sequences and plasmid of WIV1-CoV spike protein. Research was supported by the National Institute of Allergy and Infectious Disease and the National Institute of Aging of the NIH under Awards U19AI109761 and U19AI107810 (to R.S.B.), AI1085524 (to W.A.M.), and F32AI102561 and K99AG049092 (to V.D.M.). Human airway epithelial cell cultures were supported by the National Institute of Diabetes and Digestive and Kidney Disease under Award NIH DK065988 (to S.H.R.). Support for the generation of the mice expressing human ACE2 was provided by NIH Grants AI076159 and AI079521 (to A.C.S.).
National Institute of Allergy and Infectious Disease (NIAID), who supported this research, is managed by Dr. Anthony Fauci, so it is certain he knew about it in detail before September 4, 2015, when this paper was submitted for review.
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