Kevin McKernan, a scientist known for his work in genomics, has been sounding the alarm recently on Pfizer’s controversial vaccine production process, and the failure to disclose manufacturing switches from even regulators, putting our health at risk at warp speed.
The discourse, which is centered around plasmid DNA contamination, has been significantly driven by a few researchers like McKernan, Geoffrey Norman Pain, Professor Retsef Levi, and Josh Guetzkow. The work also led to the discovery of SV40 sequences within the vaccine.
The fact that the egregious findings have not made headline news or finally halted production of these shots is beyond me. And while some on social media have recognized the gravitas of these discoveries, the mainstream remains mum.
I don’t know how anyone can still think these shots are safe and effective. They are dangerous and useless and below are more than five reasons as to exactly why.
Below we will cover:
Antibiotic Resistance Gene
Increased DNA Length
Risk of Contamination
Regulatory and Clinical Trial Concerns
Lot Numbers and Distribution
Regulatory and Manufacturing Processes
Lipid nanoparticles (LNPs)
SV40 (Simian Virus 40) Promoter
Open Reading Frames
Impact of Modifications
Plasmid DNA In Vats Of E.Coli | Warp Speed Pharmaceia
To gain warp speed and scale up production there were changes made in the manufacturing process of mRNA vaccines between the clinical trial phase and the production phase for widespread distribution. The public wasn’t told. This transition – termed “process one” and “process two” – raises several issues:
Process One: Initially, PCR (Polymerase Chain Reaction) was used to amplify the DNA segment needed for the “vaccine.” This is a standard laboratory technique for making multiple copies of a segment of DNA. The DNA is then transcribed into RNA using an enzyme called RNA polymerase, which was the method reportedly used during the clinical trials.
Process Two: For mass production, the DNA was placed into a plasmid – a small, circular piece of DNA that can replicate within bacteria like E. coli. These plasmids are grown in E. coli bacteria because they can replicate quickly, allowing for the mass production of the DNA that will then be transcribed into mRNA for vaccines. This method is more scalable than PCR because once the plasmid is introduced into the E. coli, the bacteria multiply and amplify the DNA, which can then be harvested in much larger quantities.
Antibiotic Resistance Gene: The plasmid also includes an antibiotic resistance gene which allows for the selection of bacteria that have successfully taken up the plasmid. When grown in the presence of antibiotics, only the bacteria with the plasmid (and therefore the DNA of interest) survive. The risks of just this alone are absolutely incredible.
Increased DNA Length: With this new process, the DNA used in the vaccine production grew in size due to additional components necessary for plasmid replication in bacteria, which was not the case in the original PCR process used in clinical trials.
DNA in Vaccines| Risk of Contamination: When grown in the presence of antibiotics, only the bacteria with the plasmid (and therefore the DNA of interest) survive. In theory. Extracting DNA from E. coli can introduce contaminants such as endotoxins (e.g. lipopolysaccharide, LPS), especially if the purification process doesn’t remove such impurities effectively. The levels of residual DNA may exceed regulatory limits and there is also criticism toward methods used to measure DNA and RNA, suggesting they could misrepresent the true quantities. Adverse reactions like anaphylaxis when injected. You know, like sudden death.