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Fauci is Now Performing Gain-of-Function on the Spanish Flu

Published: August 21, 2022 | Print Friendly and PDF
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Source: Tom Renz

woman holding laboratory appratus
Photo by CDC on Unsplash

This will be short because it really does not need much comment. In fact, this is so absurd that I am just starting with the reference document because I am concerned no one will believe it. Here it is:

Yes, that is right, Fauci and crew are now actively performing gain-of-function (GoF) work and infecting primates with the Spanish Flu. For those of you that are unaware, GoF does not have a single agreed upon definition but, as it relates here, is essentially the modification of the Spanish Flu virus to make “more functional.” In this case, as with COVID, I have little doubt the GoF supporters will argue that this is not GoF but the article actually notes that this disease was created in canine kidneys with supplemental bovine serum. Here is a quote from the document:

Virus and cells. Influenza virus A/South Carolina/1918 (H1N1) was generated by reverse genetics (9) and handled in biosafety level 4 (BSL-4) containment at the National Microbiology Laboratory (NML). Sequences of the 1918 influenza viral segments were based on data reported under GenBank accession numbers DQ208309, DQ208310, DQ208311, AF117241, AY744935, AF250356, AY130766, and AF333238. 1918 influenza virus was cultured usingMadin-Darby canine kidney (MDCK; ATCC, Manassas, VA, USA) cells. MDCK cells were grown in minimum essential medium (MEM; HyClone) supplemented with 5% fetal bovine serum (FBS; HyClone) and 1 L-glutamine (L-Glu; Gibco, Life Technologies, Grand Island, NY, USA).

A passage 2 (P2) virus stock was prepared using MEM supplemented with 0.1% bovine serum albumin (BSA) (fraction V; HyClone), 1 L-glutamine, and 1 mg/mL N-tosyl-L-phenylalanine chloromethyl ketone (TPCK)-treated trypsin (Sigma-Aldrich). This stock was used for animal inoculation. The mouse 50% lethal dose (MLD50) for this stock was determined previously to be 103.2 PFU (9); this value was confirmed prior to the use of the stock for macaque infection.

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I frankly do not care to debate the nuance of whether the recreation of generally extinct virus “generated by reverse genetics” using pieces and parts of other animals qualifies as GoF; what I care about is that we have recreated the Spanish Flu and are experimenting with it on other animals. I also care that one focus of this article is the fact that scientists are frustrated that the recreated Spanish Flu is not dangerous enough. We do not have to get far in this to see this frustration. At the beginning of the article in the summary of its importance this statement is made:

Here, we demonstrate that even at the highest doses tested, 1918 influenza was not lethal in these two macaque species, suggesting that they are not ideal for the development and testing of novel pandemic influenza-specific vaccines and therapies. Therefore, other physiologically relevant nonhuman primate models of pandemic influenza are needed.

At this point I am preparing to release the results of a major investigation we have been undertaking at Renz Law that will demonstrate that SARS-COV2 was in fact created in the Wuhan labs as part of a GoF project. We believe the investigation demonstrates this in a way that far exceeds a preponderance of the evidence standard and probably exceeds reasonable doubt. With that in mind, and given the result of the the previous coronavirus GoF, can ANYONE possibly argue GoF work on the Spanish Flu is a good idea? Even the simple recreation of the disease demonstrates an incredible lack of respect for the disaster created by the coronavirus GoF.

So you may be asking, what moron could possibly be oblivious enough to support GoF work on the Spanish Flu while the world is still dealing with the nightmare that is COVID? The answer should not be surprising and is here:

Mable Chan,ᵃ Meenakshi Tiwary,ᵇ,ᶜ Helen L. Wu,ᵇ,ᶜ Nikesh Tailor,ᵃ Robert Vendramelli,ᵃ Jonathan Audet,ᵃ Bryce M. Warner,ᵃ Kevin Tierney,ᵃ Alix Albietz,ᵃ Thang Truong,ᵃ Kaylie Doan,ᵃ Alexander Bello,ᵃ Marnie Willman,ᵃ Bryan D. Griffin,ᵃ,ᵈ Patrick W. Hanley,ᵉ Jamie Lovaglio,ᵉ David Safronetz,ᵃ,ᶠ Jim Strong,ᵃ,ᶠ Jonah B. Sacha,ᵇ,ᶜ Darwyn Kobasaᵃ,ᶠ

a. Special Pathogens, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada

b. Vaccine and Gene Therapy Institute, Oregon Health & Science University, Portland,

c. Oregon, USA Oregon National Primate Research Center, Oregon Health & Science University, Portland, Oregon, USA

d. Vaccine Safety Surveillance, Immunization Branch, Public Health Agency of Canada, Ottawa, Ontario, Canada

e. Rocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA

f. Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Manitoba, Canada

So, NIH and NIAID are involved. Apparently Fauci does not mind what he did with funding the creation of COVID and is at it again. You might also note the vaccine development crew’s involvement. A foundational point in this article is that the newly recreated Spanish Flu is not dangerous enough. Here is a pull-quote:

However, 1918 influenza was uniformly nonlethal in these two species, demonstrating that this isolate is insufficiently pathogenic in rhesus and Mauritian cynomolgus macaques to support testing novel prophylactic influenza approaches where protection from severe disease combined with a lethal outcome is desired as a highly stringent indication of vaccine efficacy.

This means that these people are arguing that we need to make a more dangerous version of the Spanish Flu so they can make “better” vaccines for it… despite the fact that until they recreated it, it likely no longer existed in nature. Much like with COVID, these snake oil salesmen create the disease and then create the cure. Given the complete failure and innumerable dangers of the COVID jabs, the real question is whether the cure will be worse than the disease?

For my part I find the fact that I am even writing this article to be incredible. In this election year I sincerely hope that this article is put in front of every elected official in Washington and they are asked to explain how this is continuing on their watch.

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