Coronavirus Contains “HIV Insertions”, Stoking Fears Over Artificially Created Bioweapon

‘The virus even responds to treatment by HIV medications’ (Could certain COVID-19 vaccines leave people more vulnerable to the AIDS virus?) SEE FOOTNOTES AT BOTTOM!

Over the past few days, the mainstream press has vigorously pushed back against a theory about the origins of the coronavirus that has now infected as many as 70,000+ people in Wuhan alone (depending on whom you believe). The theory is that China obtained the coronavirus via a Canadian research program, and started molding it into a bioweapon at the Institute of Virology in Wuhan. Politifact pointed the finger at Zero Hedge, in particular, though the story was widely shared across independent-leaning media.

The theory is that the virus, which was developed by infectious disease experts to function as a bio-weapon, 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 the Hunan fish market where the virus supposedly originated is merely a ruse.

Now, a respected epidemiologist who recently caught flack for claiming in a twitter threat 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.

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For those pressed for time, here are the key findings from the paper, which first focuses on the unique nature of 2019-nCoV, and then observe four amino acid sequences in the Wuhan Coronavirus which are homologous to amino acid sequences in HIV1:

Our phylogentic tree of full-length coronaviruses suggests that 2019-nCoV is closely related to SARS CoV [Fig1].

In addition, other recent studies have linked the 2019-nCoV to SARS CoV. We therefore compared the spike glycoprotein sequences of the 2019-nCoV to that of the SARS CoV (NCBI Accession number: AY390556.1). On careful examination of the sequence alignment we found that the 2019- nCoV spike glycoprotein contains 4 insertions [Fig.2]. 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 ( 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 . Another group from China had documented three insertions comparing fewer spike glycoprotein sequences of coronaviruses (Zhou et al., 2020).

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.

The first 3 inserts (insert 1,2 and 3) aligned to short segments of amino acid residues in HIV-1 gp120. The insert 4 aligned to HIV-1 Gag. The insert 1 (6 amino acid residues) and insert 2 (6 amino acid residues) in the spike glycoprotein of 2019-nCoV are 100% identical to the residues mapped to HIV-1 gp120. The insert 3 (12 amino acid residues) in 2019- nCoV maps to HIV-1 gp120 with gaps [see Table 1]. The insert 4 (8 amino acid residues) maps to HIV-1 Gag with gaps.

Why do the authors think the virus may be man-made? Because 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.

A good recap of the findings was provided by Dr. Feigl-Ding, who started his explanatory thread by pointing out that the transmission rate outside China has surpassed the rate inside China.

But the ‘smoking gun’ in this case are pieces of the virus’s genetic code that Indian researchers, led by Prashant Pradhan at the Indian Institute of Technology, found may have been ’embedded’ from HIV, which belongs to an entirely different family of viruses.

16. UPDATE ON GENOME : a very intriguing new paper investigating the aforementioned mystery middle segment w/ “S” spike protein: likely origin from HIV. “Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag” from

— Dr. Eric Feigl-Ding (@DrEricDing) January 31, 2020

17. …WHOA- the authors said the finding was “Unexpectedly” related to genes from HIV virus. Notably there were 4 gene insertions (see figure in above post #16). And so, which HIV gene proteins were found in the new #coronarvirus? Gag protein and Gp120- key HIV proteins…

— Dr. Eric Feigl-Ding (@DrEricDing) January 31, 2020

18. Notably, in S , authors say for HIVinsertions: “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”

— Dr. Eric Feigl-Ding (@DrEricDing) January 31, 2020

19. Again, these are new express published findings and not peer reviewed yet. Let’s not draw conclusions yet. But evidence suggest that 2 different HIV genes are present in the #coronarvirus S gene region (that didn’t map to any other coronavirus, according to other studies).

— Dr. Eric Feigl-Ding (@DrEricDing) January 31, 2020

20. Further the authors add that “This indicates that these insertions have been preferably acquired by the 2019-nCoV, providing it with additional survival and infectivity advantage. Delving deeper we found that these insertions were similar to HIV-1.”

— Dr. Eric Feigl-Ding (@DrEricDing) January 31, 2020

21. Paper piles on: “these insertions are present at binding site of 2019-nCoV. Due to presence of gp120 motifs in 2019-nCoV spike glycoprotein at its binding domain, we propose that these motif insertions could have provided an enhanced affinity towards host cell receptors.”

— Dr. Eric Feigl-Ding (@DrEricDing) January 31, 2020

22. The authors dunked this final conclusion: “This uncanny similarity of novel inserts in the 2019- nCoV spike protein to HIV-1 gp120 and Gag is unlikely to be fortuitous”. Wow, they sure just went straight there! What a bold paper… I don’t know what to say

— Dr. Eric Feigl-Ding (@DrEricDing) January 31, 2020

The punchline:

To be sure, Dr. Feigl-Ding insists that he’s not trying to promote any ‘conspiracies’ about the virus being a bioweapon developed by the Chinese, although it is difficult to find a proper name for what appears to be an artificial, weaponized virus.

Another doctor chimed in with what he thought was a solid explanation for the virus’s irregularities…

…Until he realized something disturbing.

Oh my god. Indian scientists have just found HIV (AIDS) virus-like insertions in the 2019-nCov virus that are not found in any other coronavirus. They hint at the possibility that this Chinese virus was designed [“not fortuitous’]. Scary if true.

— Anand Ranganathan (@ARanganathan72) January 31, 2020

“Scary”… but relax, it’s just another ridiculous “conspiracy.”


AIDS is bio-terrorism created to kill billions some doctors and scientists say

Actually, it’s worse still: The vaccinated people are the “super-breeders” of covid variants, too

Not only are vaccinated people now the super-spreaders, it also turns out they’re the “super-breeders” of vaccine variants. As vaccine scientist Geert vanden Bossche explains: (emphasis ours)

…mass vaccination promotes natural selection of increasingly vaccine immunity (VI)-escaping variants in the vaccinated part of the population. Taken together, mass vaccination conducted on a background of high infectivity rates enables more infectious, increasingly VI-escaping variants to expand in prevalence. This evolution inevitably results in inclining morbidity rates in both, the non-vaccinated and vaccinated population and precipitates the emergence of circulating viral variants that will eventually fully resist vaccine-mediated immunity (VMI). This is why mass vaccination campaigns should not be conducted during a pandemic of a highly mutable virus, let alone during a pandemic of more infectious variants (unless transmission-blocking vaccines are used!). It is critical to understand that a rapid decline in viral infectivity rates that is not achieved by natural infection but merely results from expedited mass vaccination campaigns will only delay abrupt propagation of emerging, fully vaccine-resistant viral variants and hence, only delay the occurrence of a high wave of morbidity and mortality.

The “high wave of morbidity and mortality,” it seems, has only just begun.

Dr. Robert Malone warns of “worst case scenario” and cites first evidence showing Antibody Dependent Enhancement (ADE) now emerging

Over the next 12 months or so, we are likely going to see a wave of post-vaccine deaths that mirrors the wave of people obtaining vaccines earlier this year. Even Dr. Robert Malone, inventor of the mRNA vaccine technology, warns that the CDC’s admission is essentially a confirmation that Antibody Dependent Enhancement effects have begun.

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This amazing FDA document goes to say the Agency has granted emergency approval to 59 different PCR tests since the beginning of the (fake) pandemic. 59. And, “…it is not feasible to precisely compare the performance of various tests that used contrived specimens because each test validated performance using samples derived from different gene specific, synthetic, or genomic nucleic acid sources.”

Translation: Each of the 59 different PCR tests for SARS-CoV-2 told different lies and concocted different fabrications about the genetic makeup of the virus—the virus we didn’t have. Obviously, then, these tests would give unreliable results.

BUT, don’t worry, be happy, because NOW, the CDC and the FDA say, they really do have actual virus samples of SARS-CoV-2 from patients; they have better targets for the PCR test, and labs should start gearing up for the new and improved tests.

In other words, they were lying THEN, but they’re not lying NOW. They were “contriving,” but now they’re telling the truth.

If you believe that, I have Fountain of Youth water for sale, extracted from the lead-contaminated system of Flint, Michigan.

Here, once again, I report virology’s version of “we isolated the virus”: [[3] thru [3i]]

They have a soup they make in their labs.

This soup contains human and monkey cells, toxic chemicals and drugs, and all sorts of other random genetic material. Because the cells start to die, the researchers ASSUME a bit of mucus from a patient they dropped in the soup is doing the killing, and THE VIRUS must be the killer agent in the mucus.

This assumption is entirely unwarranted. The drugs and chemicals could be doing the cell-killing, and the researchers are also starving the cells of vital nutrients.

There is no proof that SARS-CoV-2 is in the soup, or that it is doing the cell-killing, or that it exists.

Yet the researchers call cell-death “isolation of the virus.”

To say this is a non-sequitur is a vast understatement. In their universe, “We have the virus buried in a soup in a dish in the lab” equals, “We’ve separated the virus from all surrounding material.”

Virology equals “how to spread bull for a living and scare the world.” Other than that, it’s perfect.

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Multiple sequence alignment between spike proteins of 2019-nCoV and SARSFigure 2: Multiple sequence alignment between spike proteins of 2019-nCoV and SARS. The sequences of spike proteins of 2019-nCoV (Wuhan-HU-1, Accession NC_045512) and of SARS CoV (GZ02, Accession AY390556) were aligned using MultiAlin software. The sites of difference are highlighted in boxes

SARS-CoV-2 Engineered With HIV Like Insertions

On the basis of these findings, we are concerned that use of an Ad5 vector for immunisation against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) could similarly increase the risk of HIV-1 acquisition among men who receive the vaccine. Both the HIV and COVID-19 pandemics disproportionately affect vulnerable populations globally. Roll-out of an effective SARS-CoV-2 vaccine globally could be given to populations at risk of HIV infection, which could potentially increase their risk of HIV-1 acquisition. This important safety consideration should be thoroughly evaluated before further development of Ad5 vaccines for SARS-CoV-2, and informed consent documents of these potential risks should reflect the considerable literature on HIV-1 acquisition with Ad5 vectors.

Use of adenovirus type-5 vectored vaccines: a cautionary tale

In a secret speech given to high-level Communist Party cadres nearly two decades ago, Chinese Defense Minister Gen. Chi Haotian explained a long-range plan for ensuring a Chinese national renaissance.

He said there were three vital issues that must be grasped. The first was the issue of living space—because China is severely overpopulated and China’s environment is deteriorating. The second issue, therefore, is that the Communist Party must teach the Chinese people to “go out.” By this Gen. Chi meant the conquest of new lands in which a “second China” could be built by “colonization.” From this arises the third vital issue: the “issue of America.”

Gen. Chi warned his listeners: “This appears to be shocking, but the logic is actually very simple.” China is “in fundamental conflict with the Western strategic interest.” Therefore, the United States will never allow China to seize other countries to build a second China. The United States stands in China’s way.

Chi explained the problem as follows: “Would the United States allow us to go out to gain new living space? First, if the United States is firm in blocking us, it is hard for us to do anything significant to Taiwan, Vietnam, India, or even Japan, [so] how much more living space can we get? Very trivial! Only countries like the United States, Canada, and Australia have the vast land to serve our need for mass colonization.”

“We are not as foolish as to want to perish together with America by using nuclear weapons,” said the general. “Only by using non-destructive weapons that can kill many people will we be able to reserve America for ourselves.” The answer is found in biological weapons. “Of course,” he added, “we have not been idle, in the past years we have seized the opportunity to master weapons of this kind.”

The ruling Chinese Communist Party considers biological weapons to be the most important weapons for accomplishing their goal of “cleaning up America.” Chi credits Deng Xiaoping with putting biological weapons ahead of all other weapon systems in the Chinese arsenal: “When Comrade Xiaoping was still with us, the Party Central Committee had the perspicacity to make the right decision not to develop aircraft carrier groups and focus instead on developing lethal weapons that can eliminate mass populations of the enemy country.”

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In an explosive interview Dr. Francis Boyle, who drafted the Biological Weapons Act has given a detailed statement admitting that the 2019 Wuhan Coronavirus is an offensive Biological Warfare Weapon and that the World Health Organization (WHO) already knows about it.

Dr. Francis Boyle Creator Of BioWeapons Act Says Coronavirus Is Biological Warfare Weapon

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Australia Scraps Billion Dollar Coronavirus Vaccine After Participants Test HIV Positive

This study attempts to profile China’s biological warfare programme (BWP), with special reference to biological weapons (BW) capabilities that exist in facilities affiliated with the defence establishment and the military. For that purpose, a wide variety of facilities affiliated with the defence establishment and with the military are reviewed and profiled. The outcome of that analysis points at 12 facilities affiliated with the defence establishment, plus 30 facilities affiliated with the PLA, that are involved in research, development, production, testing or storage of BW. This huge alignment might be regarded as superfluous, ostensibly; yet, considering the various factors discussed in the present study, the overall derived picture of the Chinese BW-related alignment is not at all surprising. The chances that an outstanding state like China would ignore new avenues of BW designing and deployment are a priori slim, if any. China, in all likelihood, is and will persist as a paramount BW possessor.

China’s Biological Warfare Programme: An Integrative Study with Special Reference to Biological Weapons Capabilities

Can the world stop China’s surge into biological warfare?

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