In the video above, Jessica Rose, Ph.D., interviews microbiologist Kevin McKernan on “Good Morning CHD.” McKernan’s team recently discovered1,2,3,4 simian virus 40 (SV40) promoters in Pfizer’s and Moderna’s bivalent mRNA COVID shots, which, for decades, have been suspected of causing cancer in humans.5 As explained in the abstract, posted on OSF Preprints in April 2023:6
“Several methods were deployed to assess the nucleic acid composition of four expired vials of the Moderna and Pfizer bivalent mRNA vaccines. Two vials from each vendor were evaluated ... Multiple assays support DNA contamination that exceeds the European Medicines Agency (EMA) 330ng/mg requirement and the FDAs 10ng/dose requirements ...”
Equally, if not more, troubling, these DNA contaminants also can alter the human genome. As explained by McKernan, genomic sequencing involves reading the letters of the genome, A, T, C and G, which make up the DNA code. Both DNA and RNA can be sequenced in this manner.
DNA can be likened to a copy of the hard drive of your cell, while RNA is like your task manager, dictating the software program being run in a given moment. When you sequence RNA, you get a sense of what the cell is being instructed to do, while sequencing DNA tells you everything the cell could possibly do if the proper instructions are present.
COVID Shots Contain Both RNA and DNA
It’s been assumed that the COVID shots contained only RNA, but using genomic sequencing, McKernan discovered they contain DNA fragments as well, and there really should not be any. The RNA is basically copied, or “Xeroxed” off the DNA, and only the RNA should be in the final product.
As noted by McKernan, the DNA used is proprietary. “They don’t want people to know all the tricks they put in the DNA to drive maximum amount of Xeroxing, if you will.” But what popped out during sequencing was the entire sequencing vector, “which shows us everything they’re doing to drive the expression of this RNA,” McKernan says.
So, we now know they’re using a T7 promoter, an SV40 promoter, an antibiotic-resistance gene, that the replication is bacterial in origin and more. As explained by McKernan, to get the amount of RNA required for these shots, you need very large amounts of DNA. To get the DNA required, a piece of DNA that codes for RNA in a circle, called a plasmid, was created and then reproduced inside E. coli in a huge vat.
Plasmids are unique in that they have an origin of replication that allows the DNA to copy itself several hundred times inside every cell of the E. coli, and, since bacteria double every 20 minutes, you get exponential amplification of the DNA overnight.
The DNA must then be extracted from the E. coli and purified. Once that’s done, a T7 in vitro transcription reaction is run on the purified DNA, which copies the RNA off that DNA.
The plasmid that is put in with the E. coli — the sequencing vector — is the blueprint for how the RNA is made, and this is what McKernan found, in its entirety, in the vials. It really should not be there. Only the purified RNA should be present.
Regulatory agencies have an acceptable upper limit for double-stranded DNA (dsDNA) in medical products, but the DNA McKernan found was orders of magnitude higher than those thresholds.
The arbitrary limit for dsDNA set by the European Medicines Agency (EMA) is 330 nanograms per milligram (ng/mg), but McKernan suspects that limit isn’t stringent enough, because they probably didn’t consider that it might include replicable DNA. In all likelihood, this limit was primarily based on concerns about E. coli DNA, which might get mixed in.
In a May 20, 2023, Substack article,7 McKernan also pointed out that Pfizer itself submitted evidence to the EMA showing sampled lots contained anywhere from 1 ng/mg to 815 ng/mg of DNA, so regulators knew they had quality control problems from the start. In McKernan’s testing, the highest level of DNA contamination found was 30%, which is rather astounding.
Endotoxin Concerns
McKernan also explains that one of the primary concerns when pulling plasmids out of E. coli is the fact that endotoxins frequently tag along. Lipopolysaccharide (LPS), an endotoxin, sits on the outside of gram-negative bacteria such as E. coli. When endotoxin is injected, it can cause anaphylaxis, and life-threatening anaphylaxis just so happens to be among the most commonly reported side effects of these shots. According to McKernan:8
“Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there's any E. coli endotoxin present because that creates anaphylaxis for the injected ... You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA ...”
What Is the SV40 Promoter For?
As mentioned earlier, the sequencing vector found also included an SV40 promoter. To be clear, this is not the whole virus. It’s only the promoter, meaning a specific portion of the viral DNA that is essential for gene expression. The problem is that this particular promoter is known to be problematic.
SV40 promoters have been studied for years and are known to trigger cancer when encountering an oncogene (a gene that has the potential to cause cancer). What’s more, McKernan found that one of the Pfizer vials had not just one but two SV40 promoters.
One of them had a nuclear localization sequence (NLS) that the other didn’t have — a 72 base pair insertion for a nuclear localization sequence (NLS) that makes the promoter “much more aggressive and also drives the sequence into the nucleus” of the cell. NLS is basically a sequence that tags a given protein for import into the cell nucleus, and this further heightens the risk of genome integration.
Now, this second, more aggressive promoter was only found in one of the two Pfizer vials tested, even though they were from the same lot. What might account for this remarkable quality discrepancy? At bare minimum, it suggests Pfizer is changing its manufacturing on the fly, without oversight. Changing the plasmid used is a major change in manufacturing that really should require regulatory oversight, McKernan notes.
As for why any of the SV40 promoters are in there, McKernan in certain that it was part of an intentional design, as these promoters have a long research history.
Genome Integration Can Occur in More Ways Than One
The reason NLS is so concerning is because it can drive genome integration even in the absence of LINE-1 (long interspersed nuclear elements 1), which allow for insertions, deletions and rearrangements within the genome through reverse transcription.
“If you’re injecting this much DNA, you don’t need LINE-1 at all. You can get integration off these vectors alone, and if vectors have things that localize in the nucleus, then odds go up tremendously that there could be genome integration going on,” McKernan says.
Cytoplasmic transfection can also allow for genetic manipulation because the nucleus disassembles and exchanges cellular components with the cytosol during cell division.
Even if genetic modification does not occur, the fact that you’re getting foreign DNA into your cells can pose a risk. Partial expression could occur, for example, or it might interfere with other transcription translations that are already in the cell.
How Might Cinnamycin Resistance Gene Affect Human Health?
Rose and McKernan also discuss how the cinnamycin-resistant gene found in the sequencing vector might impact human health. What happens if this gets into a patient and encounters bacteria? Will it make that bacteria resistant to cinnamycin (a tricyclic antibiotic)?
“While speculative, at the moment, we would assume yes,” McKernan says. “Plasmids get absorbed by bacteria at 37 degrees (Celsius) temperature, which is the temperature of your gut ... and if they can confer any selective advantage, then they’re going to replicate and become the dominant species in your microbiome.”
Possibly, it might require the patient to be on an antibiotic when this occurs, as this is what would give the bacteria the selective advantage. Still, antibiotic use is quite common, so this is not a concern that should be discarded off hand. Potentially, these bivalent jabs may be spreading antibiotic resistance through the injected population, which could have grave consequences.
Will Your Microbiome Produce Spike Protein?
A related question is whether your microbiome might also produce spike protein permanently. McKernan suspects the bacteria will make spike RNA, but bacterial ribosomes don’t have the right equipment to read that RNA, so they probably won’t be able to translate it.
That said, bacteria are frequently absorbed by mammalian cells in a process called bactofection, and this is a known gene transfer technique.9 So, this may result in your cells producing spike protein.
The RNA in the COVID jab is also modified to resist breakdown, so you really have two versions of the spike protein that can persist longer than anticipated, and the spike protein, of course, is the most toxic part of the virus that can cause your body to attack itself.
“The real concern is we’ve got an amplifiable piece of DNA that can replicate in bacteria,” McKernan says. “Your body is loaded with bacteria [and] it’s going to start replicating this DNA once it’s inside of them, and we don’t know what’s going to happen after that.
It could make RNA, it could get absorbed into mammalian cells, it could be killed and completely gotten rid of. But the DNA shouldn’t be there to begin with. So, we have to start monitoring how much DNA is actually in lot to lot? What is its length? Is it circular? And how much of it can we tolerate?”
McKernan Calls on Scientists to Reproduce His Results
On his Substack, McKernan has published all the details10 scientists and labs would need to rapidly and inexpensively replicate his investigation and assess the dsDNA contamination of COVID shots around the world, and he’s urging researchers to do so.
According to McKernan, one team has already contacted him saying they found sequencing vector in the original monovalent COVID shots. Their findings will hopefully be released shortly.
Resources for Those Injured by the COVID Jab
The more we learn about the COVID jabs, the worse they appear. If you got one or more jabs and are now reconsidering, first and foremost, never ever take another COVID booster, another mRNA gene therapy shot or regular vaccine.
You need to end the assault on your body. Even if you haven’t experienced any obvious side effects, your health may still be impacted long-term, so don’t take any more shots.
If you’re suffering from side effects, your first order of business is to eliminate the spike protein that your body is producing. Two remedies that can do this are hydroxychloroquine and ivermectin. Both drugs bind and facilitate the removal of spike protein.
The Front Line COVID-19 Critical Care Alliance (FLCCC) has developed a post-vaccine treatment protocol called I-RECOVER. Since the protocol is continuously updated as more data become available, your best bet is to download the latest version straight from the FLCCC website at covid19criticalcare.com11 (hyperlink to the correct page provided above).
For additional suggestions, check out the World Health Council’s spike protein detox guide,12 which focuses on natural substances like herbs, supplements and teas. To combat neurotoxic effects of spike protein, a March 2022 review paper13 suggests using luteolin and quercetin. Time-restricted eating (TRE) and/or sauna therapy can also help eliminate toxic proteins by stimulating autophagy.