Flora Teoh - Refutation of

"Manufactured Pandemic" Paper

PCR tests for COVID-19 are specific for the novel coronavirus SARS-CoV-2 and do not detect other coronaviruses, contrary to claims in viral article and video .

CLAIM:

"There are no reliable tests for a specific COVID-19 virus".

VERDICT:

Inaccurate .

SOURCE: Jerry Day, Julian Rose, Global Research, 27 Mar. 2020.

DETAILS:

Inaccurate: COVID-19 tests are specific to the novel coronavirus. They do not detect other members of the coronavirus family. Additionally, PCR tests are capable of detecting viral load, contrary to the article’s claim.

Inadequate support: The article cites no data or information to support its claims, which are based solely on hearsay from an anonymous person on a “medical forum”.

KEY TAKE AWAY:

The PCR tests for COVID-19 are designed to be highly specific for the novel coronavirus—they can detect this virus unequivocally and differentiate it from other members of the coronavirus family. These PCR tests are also capable of measuring viral load (amount of virus) in patient samples, which is related to virus transmissibility and severity of infection.

FULL CLAIM: "Here’s the problem, we are testing people for any strain of a Coronavirus. Not specifically for COVID-19. There are no reliable tests for a specific COVID-19 virus."

SUMMARY:

This claim appeared in an article published on GlobalResearch.ca by Julian Rose, which was later propagated in a YouTube video by Jerry Day. The article has received more than 11,000 engagements on Facebook, while the video has been viewed more than 750,000 times. The claims are reported by the article as originating from “a widely respected professional scientist in the US”, which were written in a “medical forum”, although the article does not name this scientist.

The article criticizes the laboratory technique known as PCR, or polymerase chain reaction. This is a widely-used technique in laboratories worldwide and was invented by Kary Mullis, who received the 1993 Nobel Prize in Chemistry for this work. The article is correct in stating that PCR is used to make many copies of a particular segment of nucleic acid (DNA/RNA), a process known as amplification, enabling scientists to detect tiny amounts of nucleic acid in a sample.

However, the article errs in stating that “PCR basically takes a sample of your cells and amplifies any DNA to look for ‘viral sequences’.” PCR tests do not indiscriminately amplify any DNA in a sample; they are designed to target only the nucleic acid sequence from the microorganism of interest (specificity), in this case SARS-CoV-2, the virus causing COVID-19⁠.

PCR specificity is achieved through proper design of primers, which are short nucleic acid sequences designed to bind or anneal only to the target, and this is made possible through the rule of complementary base pairing. Bases, or nucleotides, are the individual building blocks of DNA and RNA sequences, and each base pairs with only one other base. In DNA for example, adenosine pairs only to thymine, and cytosine pairs only to guanine.

There are many requirements involved in designing appropriate PCR primers and this article by the Diamantina Institute of the University of Queensland outlines several of them and why they are important to consider:

“A lot of work has to go into designing the primers. Firstly, we need to know the sequence of the section of DNA we are wanting to amplify, particularly the ‘beginning’ (5’) and ‘ending’ (3’) of the sequence. The primers need to be designed so that they are complementary to a unique sequence of nucleotides ‘upstream’ and ‘downstream’ of the sequence of interest. They cannot match a sequence within the area of interest (or the PCR will start off too late and miss a portion of the area we want to amplify), and they should also not have complementary regions within themselves (or they will fold over and bind to themselves, forming a “hairpin”. Lastly, the forward and reverse primers should not be complementary, or they will anneal to each other and form a ‘primer dimer’.”

Figure—A graphic by the U.S. National Human Genome Research Institute showing how PCR works.

Thanks to the efforts of scientists, we now know the full genome of SARS-CoV-2 [1], which makes it possible to design specific primers for the virus that recognize unique segments of nucleic acid sequences and do not anneal to those found in other coronaviruses. Furthermore, primer annealing to the target sequence is necessary to start PCR amplification. If the primers do not match a nucleic acid sequence—for example in the case of a different coronavirus—then PCR amplification of that mismatched sequence cannot occur. In short, the claim that the test for COVID-19 detects “any strain of coronavirus” is false and unfounded.

The article also wrongly claims that PCR is “useless at telling you how much virus you may have”. On the contrary, variants of PCR, such as quantitative PCR, have been used for measuring viral load long before the COVID-19 pandemic occurred [2,3,4]. Viral load is generally related to transmissibility and severity of infection and therefore clinically important. For example, viral load testing is commonly done for HIV patients in order to manage their condition. In this article by the World Economic Forum, David Duong, Director of the Harvard Medical School Program in Global Primary Care and Social Change, stated that most countries—including the U.S.—are using reverse transcription PCR (RT-PCR) for COVID-19. RT-PCR is a variant of PCR that is able to detect RNA (SARS-CoV-2 is an RNA virus).

In summary, the article’s claims that PCR indiscriminately detects any coronavirus and that PCR cannot measure viral load does not hold up under scrutiny. Overall, this is yet another article propagating the unfounded conspiracy theory that COVID-19 is a pandemic “manufactured” to create panic and that it is not actually a new virus—numerous studies have recognized SARS-CoV-2 as a novel coronavirus not previously identified, showing this claim to be false [5,6].

SCIENTISTS’ FEEDBACK:

Raymond Tzer Pin Lin, Associate Professor, Yong Loo Lin School of Medicine, National University of Singapore:

It’s false. SARS-CoV-2, the agent of COVID-19, has unique sequences which are different from other coronaviruses. The PCR tests are very specific.

REFERENCES:

1 – Zhou et al. (2020) A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature.

2 – Mackay et al. (2002) Real-time PCR in virology. Nucleic Acids Research.

3 – Watzinger et al. (2004) Real-Time Quantitative PCR Assays for Detection and Monitoring of Pathogenic Human Viruses in Immunosuppressed Pediatric Patients. Journal of Clinical Microbiology.
4 – Engelmann et al. (2008) Rapid quantitative PCR assays for the simultaneous detection of herpes simplex virus, varicella zoster virus, cytomegalovirus, Epstein-Barr virus, and human herpesvirus 6 DNA in blood and other clinical specimens. Journal of Medical Virology.
5 – Zhu et al. (2020) A Novel Coronavirus from Patients with Pneumonia in China, 2019. New England Journal of Medicine.
6 – Lu et al. (2020) Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. The Lancet.

Published on: 06 Apr 2020 | Editor: Flora Teoh .

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Method :

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Reviewers :

Raymond Tzer Pin Lin

Associate Professor, Yong Loo Lin School of Medicine, National University of Singapore

Editor :

Flora Teoh

Science Editor, Health Feedback

ARTICLE SOURCE:

https://healthfeedback.org/claimreview/pcr-tests-for-covid-19-are-specific-for-the-novel-coronavirus-sars-cov-2-and-do-not-detect-other-coronaviruses-contrary-to-claims-in-viral-article-and-video/

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My verdict: (in progress)

I will analyse her so called refutations on another page.

1) I think she used a deliberate tactic of falsely accusing the writer of the "Manufactured Pandemic" article of attacking the brilliant scientific work of Kary Mullis on PCR in general instead of specifically how the PCR science was used in this one specific type of test (of which there might be 100 different manufactured test kits by different firms). Having done this she then probably correctly says a PCR Test can be developed to show viral load - who says it could not? - the issue is did the tests used in the first 1-3 million stats in real time show viral load, and those test kits ALONE? I think they never, and she has deliberately made a false accusation to go off piste from the real issue.

2) She claims that she is impartial, but both the writer Flora Teoh and the reviewer Raymond Tzer Pin Lin are Asians, and it was Asians who developed these inaccurate PCR Test Kits, which seems to put a shadow over the impartiality claim, as does the very small number of scientists or medics stepping forward to defend the Test as accurate and showing viral load.

3) The page of Raymond Tzer Pin Lin does not exist when you try to link to it. (that stops us checking on links to people like Kim Woo-joo, etc)

4) Flora Teoh did not allow a comments section, in order to criticize her work.

5) For a science paper to be legitimate (as far as I am aware) it must be checked and reviewed by her peers, that is plural. She had only one reviewer, the link to whose page/site is not there.

6) "Inadequate support: The article cites no data or information to support its claims" for instance in the article it says "the trouble is it has been shown not to work". The person is saying it is fine on paper but in practical terms it has been shown to go wrong. Flora Teoh says the person does not give proofs of that, but she does not say no such proof exists. So the question is not so much that the person offers no proof that in practical terms it has been shown not to fail, it is more is that evidence out there somewhere?

7) There was much talk as the months went by that they were trying to get primers for these tests. In other words some of the trimers were not adequate - is that not the inference?

8) She says the entire idea of use of PCR is under fire, when the "MP" article actually seems to say the primers were ar that time inadequate, as well as that for some reason tests failed for reasons that on paper they should work but in real time they never.