Will Covid-19 Vaccine Change Your DNA?
BY SARSTRUTH ON
Reverse transcriptase (RT) is an enzyme used to generate complementary DNA (cDNA) from an RNA template, a process termed reverse transcription.
The central dogma of molecular biology is an explanation of the flow of genetic information within a biological system. It is often stated as “DNA makes RNA, and RNA makes protein”
According to the Wikipedia page on RNA vaccines https://en.wikipedia.org/wiki/RNA_vaccine
A retrovirus has mechanisms to be imported into the nucleus, but other mRNA lack these mechanisms. Once inside the nucleus, creation of DNA from RNA cannot occur without a primer, which accompanies a retrovirus, but which would not exist for other mRNA if placed in the nucleus.
The “primer” they are referring to on this page is a sequence that the reverse transcriptase enzyme recognizes, which would be able to read the RNA. As we know, the mRNA vaccine is created from the genetic sequence of the spike protein. When the genomic code of the virus was published, they found that it actually contained 18 HIV-1 inserts (fragments) that make up the Spike proteins of the virus, so it stands to reason that the vaccine also contains those fragments of the HIV-1 inserts.
Now check out this revelation by Anthony Patch-
The 2019-nCov virus uses the HIV-1 insert as a vector to transmit HIV-1 into the cells cytosol, at this point the roles are reversed with retroviral HIV-1 fragments now acting as a vector for the delivery into the cell’s nucleus. These fragments provide a “gain of function” to promote entry into the host cells nucleus where the DNA resides.
As a side note, experts agree the presence of these 18 HIV-1 inserts in the genome of 2019-nCov, suggest that this could NOT be the result of normal mutations, that in fact they must be man made.
Take a look at this article-
The researchers found that published RNA sequencing data from SARS-CoV-2-infected cells showed a high number of LINE-1 elements, which was directly correlated with the abundance of chimeric reads. Within the Calu-3 cell line that allows efficient infection, a number of such elements were upregulated three- to four-fold following infection by the virus. PCR testing showed that these cells demonstrated RT-mediated integration of viral genomic material into the host DNA, perhaps by the activation of the LINE-1 RT. Cytokines can also upregulate endogenous LINE-1 expression two- to three-fold.
Another catastrophic failure, is the CDC has failed to acknowledge is that the reverse transcriptase enzyme does not need to be present in the vaccine, they should however inform people that RT it is already present within the cytoplasm of normal cells. This could perhaps be a grave violation of the Nuremberg Code, which is a set of ethics that describe permissible medical experiments. Any form of genetic engineering by way of a vaccine without informing the public, would most definitely be a violation of these ethics.
In cellular life reverse transcriptase is found abundantly in the genomes of plants and animals. Telomerase is another reverse transcriptase found in many eukaryotes, including humans, which carries its own RNA template; this RNA is used as a template for DNA replication.
Have a look at this video –
As she sated, Today nearly everybody accepts that reverse transcription is non-specific to retrovirus, and is present in all normal cells.
Still don’t believe me? Let’s ask a German biologist, named Rudolf Jaenisch who found out, back in the 1970s, that when you inject the DNA of a virus, you find it becomes integrated in the genome of embryos.
The report is titled, “SARS-CoV-2 RNA reverse-transcribed and integrated into the human genome” He explains that there is a non-null, but impossible to estimate at this stage, probability that SARS-CoV-2 RNA integrates your genome, via a process called reverse transcriptase.
Prolonged SARS-CoV-2 RNA shedding and recurrence of PCR-positive tests have been widely reported in patients after recovery, yet these patients most commonly are non-infectious. Here we investigated the possibility that SARS-CoV-2 RNAs can be reverse-transcribed and integrated into the human genome and that transcription of the integrated sequences might account for PCR-positive tests. In support of this hypothesis, we found chimeric transcripts consisting of viral fused to cellular sequences in published data sets of SARS-CoV-2 infected cultured cells and primary cells of patients, consistent with the transcription of viral sequences integrated into the genome. To experimentally corroborate the possibility of viral retro-integration, we describe evidence that SARS-CoV-2 RNAs can be reverse transcribed in human cells by reverse transcriptase (RT) from LINE-1 elements or by HIV-1 RT, and that these DNA sequences can be integrated into the cell genome and subsequently be transcribed. Human endogenous LINE-1 expression was induced upon SARS-CoV-2 infection or by cytokine exposure in cultured cells, suggesting a molecular mechanism for SARS-CoV-2 retro-integration in patients. This novel feature of SARS-CoV-2 infection may explain why patients can continue to produce viral RNA after recovery and suggests a new aspect of RNA virus replication.
The obvious concern here is that mRNA is a technology that has never been used on humans, and historically has been rejected due to the harm it has caused in experiments on lab animals. Currently over 1 billion people have been vaccinated world wide, and it seems these companies may not even be liable due the Emergency Use Authorization act, so there is potentially no resource for anything that might go wrong, and when your genes are modified there is no going back!
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