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Many years ago low grade folk demon Jenny Greenteeth found her natural habitat was shrinking due to modern agricultural methods. It is a fallacy that folk demons are stupid creatures made of fear and superstition, they are actually highly intelligent and Jenny discovered a new habitat for herself in electricity, which is as fluid as water though not as substantial. Living in the electricity system she could do mischief but had no way of making herself known. Then came the internet. Now CEO (Chief Ectoplasmic Officer,) of Greenteeth Digital Publishing, she would loves to cause trouble by spreading the information The Powers That Be would rather you remained unaware of.

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Coronavirus Contains “HIV Insertions”: Claim Stokes Fears Over Genetically Modified Bioweapon

For the past two weeks mainstream media reporting of the epidemic of a new strain of coronavirus in China has been getting more and more hysterical. However, reports have pushed back against one "conspiracy theory" about the origins of the virus that has now infected as many as 70,000+ people in the central China city of Wuhan alone (depending on whom you believe).


A coronavirus variant Picture source: anonymous

The theory that China obtained the coronavirus via a Canadian research program, and started molding it into a bioweapon at the Institute of Virology in Wuhan before it somehow escaped could be an attempt by the establishment (the Davosocracy,) to spread fear and panic as they see resurgent nationalism across the developed world and growing scepticism about the Greta Thunberg fronted campaign to reignite fear and panic about runaway climate change causing millions of deaths and widespread destruction. Establishment controlled news media such as The New York Times, The Guardian, CNN and the BBC have dismissed the claim as 'fake news', though the story was widely shared across independent-leaning media.

According to the weaponised virus theory the virus, which was developed by infectious disease experts may have originated in the Wuhan-based lab of Dr. Peng Zhou, China's preeminent researcher of bat immune systems, specifically in how their immune systems adapt to the presence of viruses like coronavirus and other destructive viruses. Somehow, the virus escaped from the lab, and found its way to stalls in the Hunan fish market. Claims that the fish market is where the virus supposedly originated have been dismissed as a public relations exercise.

Now, a respected researcher into how epidemics spread, and who recently came in for a lot of criticism by tweeting that the virus appeared to be much more contagious than initially believed is pointing out irregularities in the virus's genome that suggests it might have been genetically engineered for the purposes of a weapon, and not just any weapon but the deadliest one of all.

In "Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag", Indian researchers are baffled by segments of the virus's RNA that have no relation to other coronaviruses like SARS, and instead appear to be closer to HIV. The virus even responds to treatment by HIV medications.

A link to the full paper (.pdf) is provided below, those with the patience to read it will find the first part focuses on the unique nature of 2019-nCoV, and observes that four amino acid sequences in the Wuhan Coronavirus which are homologous to amino acid sequences in HIV1.

Why do the authors think the virus may be man-made? Because, they say, when looking at the above insertions which are not present in any of the closest coronavirus families, "it is quite unlikely for a virus to have acquired such unique insertions naturally in a short duration of time." Instead, they can be found in cell identification and membrane binding proteins located in the HIV genome.

READ THE FULL REPORT in .pdf format

For other readers, here are a few key points:

... To further investigate if these inserts are present in any other corona virus, we performed a multiple sequence alignment of the spike glycoprotein amino acid sequences of all available coronaviruses (n=55) [refer Table S.File1] in NCBI refseq (ncbi.nlm.nih.gov) this includes one sequence of 2019-nCoV[Fig.S1]. We found that these 4 insertions [inserts 1, 2, 3 and 4] are unique to 2019-nCoV and are not present in other coronaviruses analyzed. Another group from China had documented three insertions comparing fewer spike glycoprotein sequences of coronaviruses .

We then translated the aligned genome and found that these inserts are present in all Wuhan 2019-nCoV viruses except the 2019-nCoV virus of Bat as a host [Fig.S4]. Intrigued by the 4 highly conserved inserts unique to 2019-nCoV we wanted to understand their origin. For this purpose, we used the 2019-nCoV local alignment with each insert as query against all virus genomes and considered hits with 100% sequence coverage.

Surprisingly, each of the four inserts aligned with short segments of the Human immunodeficiency Virus-1 (HIV-1) proteins. The amino acid positions of the inserts in 2019-nCoV and the corresponding residues in HIV-1 gp120 and HIV-1 Gag are shown in Table 1.

When looking at the above insertions which are not present in any of the closest coronavirus families, "it is quite unlikely for a virus to have acquired such unique insertions naturally in a short duration of time." Instead, they can be found in cell identification and membrane binding proteins located in the HIV genome.

Since the S protein of 2019-nCoV shares closest ancestry with SARS GZ02, the sequence coding for spike proteins of these two viruses were compared using MultiAlin software. We found four new insertions in the protein of 2019-nCoV- “GTNGTKR” (IS1), “HKNNKS” (IS2), “GDSSSG” (IS3) and “QTNSPRRA” (IS4) (Figure 2). To our surprise, these sequence insertions were not only absent in S protein of SARS but were also not observed in any other member of the Coronaviridae family (Supplementary figure). This is startling as it is quite unlikely for a virus to have acquired such unique insertions naturally in a short duration of time.

The insertions were observed to be present in all the genomic sequences of 2019-nCoV virus available from the recent clinical isolates. To know the source of these insertions in 2019-nCoV a local alignment was done with BLASTp using these insertions as query with all virus genome. Unexpectedly, all the insertions got aligned with Human immunodeficiency Virus-1 (HIV-1). Further analysis revealed that aligned sequences of HIV-1 with 2019-nCoV were derived from surface glycoprotein gp120 (amino acid sequence positions: 404-409, 462-467, 136-150) and from Gag protein (366-384 amino acid) (Table 1). Gag protein of HIV is involved in host membrane binding, packaging of the virus and for the formation of virus-like particles. Gp120 plays crucial role in recognizing the host cell by binding to the primary receptor CD4.This binding induces structural rearrangements in GP120, creating a high affinity binding site for a chemokine co-receptor like CXCR4 and/or CCR5.

We are not qualified to comment on the quality of this work beyond saying that evidence is stacking up that points to there being something extremely dodgy about the origins of the coronavirus currently running wild in China. Because us old farts have surprisingly good memories we are reminded of the Ebola outbreak in west Africa a few years ago, which again was reported to be a previously unknown strain of the virus, much more infectious than those identified in previous outbreaks.

More Evidence Deadly Ebola Strain Was Created By US Biological Weapons Research Scientists

from Russ Winter

‘I presented the case for the Kemena bio-lab as the source of spreading the Ebola outbreak in Saturday’s post, and I had to circle back and debunk the debunkers. It states on the hospital consortium’s own website that it is involved in research on lethal diseases at Kenema.

Indeed, starting in January, the consortium running the Kenema lab inked a $140 million deal with Department of Defense and a pharma company called Tekmira to conduct Phase I Ebola vaccine trails at Kenema on humans [see "Tekmira Doses First Subject in Human Clinical Trial of TKM-Ebola" press release].

The information provided begs the question: Where did they get the human subjects? There was no outbreak as of the end of March in Sierra Leone. Seems the DoD/pharma goon squads were recruiting Ebola trial participants from nearby Guinea, where there was a small outbreak underway.’

Top Scientist: This Version Of Ebola Looks Like ‘A Very Different Bug’ In another iteration of the old "The Science Is Settled" bollocks, President Obama and his senior advisers on medical science have been saying we know exactly how Ebola spreads. The case is however that there is much about this strain of the virus currently raging in West Africa that we simply do not know and the propaganda coming from the usual suspects who claim the science is settled looks very dubious.
READ ALL: Top Scientist: This Version Of Ebola Looks Like ‘A Very Different Bug’

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