Human DNA alone does not produce a positive result on the RT-PCR test for SARS-CoV-2 – Health Feedback

Posted: August 31, 2020 at 8:09 pm

CLAIM

WHO coronavirus PCR test primer sequence is found in all human DNA; this means that the WHO test kits should find a positive result in all humans

DETAILS

Fails to grasp significance of observation: In order for the PCR amplification process to begin, it is essential for both primers to flank the same target sequence. Having only a single primer that binds to a sequence does not lead to amplification and produces a negative test result.Flawed reasoning: If the SARS-CoV-2 RT-PCR test detected human DNA, then all tests would return a positive result. This is clearly contradicted by the fact that only about 9% of all tests administered in the U.S. have been positive.

KEY TAKE AWAY

The reverse-transcription PCR (RT-PCR) test is the method of choice for detecting SARS-CoV-2 in samples and is highly specific for the virus. For a PCR test to successfully amplify nucleic acids (DNA or RNA) in a sample, it is necessary for a pair of primers, which are short sequences of single-stranded nucleic acids that recognize and bind to a specific region of the genome, to flank the same target sequence. If only one primer in the pair is able to do so, amplification does not take place and the test would produce a negative result. Therefore, an RT-PCR test for SARS-CoV-2 which uses a primer that matches a human gene sequence would produce a negative result if only human DNA alone were present.

REVIEW A blog post claiming that the SARS-CoV-2 nucleic acid test would give positive results for every test because it also identifies human DNA was published in April 2020 and has received more than 13,000 interactions on Facebook and other social media platforms like Reddit, according to social media analytics tool CrowdTangle. While it was published several months ago, the article has seen a resurgence of interest on social media in August 2020.

Claims calling into question the nucleic acid tests used to detect SARS-CoV-2 are not new; Health Feedback also reviewed a related claim that the PCR test would detect other coronaviruses and found it to be false, as the test is highly specific and does not detect genetic material from other coronaviruses.

The Piece of Mindful blog post takes a different tack from the earlier claim by citing the protocol of a SARS-CoV-2 nucleic acid test developed at the Pasteur Institute in Paris, which is available on the website of the World Health Organization. The protocol lists the nucleotide sequences of various primers used in the test. According to the blog post, the sequence of one primer matches that of a sequence found on the human chromosome 8 and because of this, the post claims that the test would also detect human DNA, thereby giving false-positive results. As we explain below, this claim stems from a fundamental misunderstanding of how PCR works.

The laboratory technique known as PCR, or polymerase chain reaction, is a widely-used technique in laboratories worldwide that was invented by Kary Mullis, who received the 1993 Nobel Prize in Chemistry for this work. PCR is used to make many copies of a particular segment of nucleic acid (DNA/RNA), a process known as amplification, which enables scientists to detect tiny amounts of nucleic acid in a sample (see animation video by Cold Spring Harbor Laboratorys DNA Learning Center below).

The method of choice for detecting SARS-CoV-2 in most countries is a variant of PCR which detects RNA, called reverse transcription PCR (RT-PCR) (SARS-CoV-2 is an RNA virus).

Our knowledge of the SARS-CoV-2 genetic sequence allows us to design primers that specifically bind to sequences that are unique to the virus, based on the principle of complementary base pairing. These primers are required to start the amplification process. In the protocol, the primers in question detect the presence of the gene sequence for RNA-dependent RNA polymerase (RdRp), which encodes an enzyme that is needed to make more copies of the viral genome[1].

However, primers act in pairs. In order to begin the amplification process, it is essential for both the forward and reverse primers to bind/anneal and flank the same target sequence. Although the sequence CTCCCTTTGTTGTGTTGT which matches the reverse primer also exists on the human chromosome 8, the forward primer listed in the protocol (ATGAGCTTAGTCCTGTTG) does not bind to any sequence on chromosome 8. We demonstrate this below by using the Basic Local Alignment Search Tool (BLAST), developed by the U.S. National Center for Biotechnology Information, to align the forward primer listed in the protocol with the human genome.

As we can see from the alignment results, none of the sequences among the top matches in the list, which are partial matches, can be found on chromosome 8:

In summary, although the sequence CTCCCTTTGTTGTGTTGT is present in the human chromosome 8, only one of the primers is able to recognize this sequence, which would produce a negative result if only human DNA was present. Therefore the claim that the PCR test would produce a false-positive result due to human DNAand the implication that the number of positive SARS-CoV-2 test results is artificially inflatedis incorrect and misleading. Furthermore, it is evident from testing statistics that not all tests produce positive results; according to the U.S. Centers for Disease Control and Preventions COVID Data Tracker, only 9% of all tests conducted in the U.S. are positive as of 30 August 2020, as Lead Stories pointed out in their fact-check of the same blog post:

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Human DNA alone does not produce a positive result on the RT-PCR test for SARS-CoV-2 - Health Feedback

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