28 September 2021

Some may have ‘protective version of gene which resists severe Covid-19’ – study

28 September 2021

Some people possess a version of a gene which can potentially restrain the virus which causes Covid-19, a study has indicated.

The findings offer an explanation for why some people have better natural defences against serious Sars-CoV-2 infection, say scientists.

Scientists suggest antiviral responses are better in people who have a more protective “prenylated” version of the OAS1 gene, while others have a version which fails to detect the virus.

But if new variants learn to evade the protection offered by the prenylated gene they could become “substantially more pathogenic and transmissible in unvaccinated populations”, say experts.

The study, called A prenylated dsRNA sensor protects against severe Covid-19, is published in the journal Science and is the result of work led by the MRC-University of Glasgow Centre for Virus Research.

Prenylation, the attachment of a single molecule of fat to a protein, allows prenylated OAS1 to “seek out” the invading virus and “sound the alarm”, say researchers.

The study indicated that patients in hospital who expressed a prenylated version of the gene were associated with protection from severe Covid-19, suggesting it is a “major component of a protective antiviral response”.

It is likely to have afforded many people natural protection throughout the pandemic.

Researchers also noted those with the “bad” form of OAS1 experienced significantly more frequent levels of severe disease, with intensive care admission or death around 1.6 times more likely in these patients.

The scientists also say that around 55 million years ago horseshoe bats, the presumed source of Sars-CoV-2, lost this protective gene, so the virus did not have to adapt to evade the defence.

Cross-species transmission to humans exposed the virus Sars-CoV-2 to a new repertoire of antiviral defences, some of which Sars-CoV-2 may not know how to evade

Professor Sam Wilson, of the University of Glasgow’s Centre for Virus Research, said: “We know viruses adapt, and even Sars-CoV-2 has likely adapted to replicate in the animal reservoir(s) in which it circulates.

“Cross-species transmission to humans exposed the virus Sars-CoV-2 to a new repertoire of antiviral defences, some of which Sars-CoV-2 may not know how to evade.

“What our study shows us is that the coronavirus that caused the Sars outbreak in 2003 learned to evade prenylated OAS1.

“If Sars-CoV-2 variants learn the same trick, they could be substantially more pathogenic and transmissible in unvaccinated populations.

“This reinforces the need to continually monitor the emergence of new Sars-CoV-2 variants.”

The study was predominantly funded by the Medical Research Council, Wellcome, and UK Research and Innovation.

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