SARS-CoV-2 uses sugars to invade human cells, new study shows

 Posted: November 12, 2021

Understanding the process could help scientists look out for new, more infectious variants, say GlycoNet researchers.

Sugars found on the surface of human cells influence COVID-19 infection, according to a University of Alberta-led study that is one of the first to observe this relationship and suggests that cells in the brain might be particularly susceptible.

“The idea here is that the virus is leveraging or using the host glycans, or the host sugars, to gain access to the cells,” said Matthew Macauley, professor in the Department of Chemistry and Canada Research Chair in Chemical Glycoimmunology. “This mode of action of viral entry is not unprecedented,” he said. “What is a surprise, though, is that it hadn’t really been detected.”

These sugars, known as glycans, are made of sialic acid and a class of biomolecules that are essential for cell structure, energy storage and system regulation.

Macauley explained that up to 50 per cent of all viruses that infect our cells, the most well known of which is influenza, bind to sugars on cell receptors to gain access and infect the cell.

“That’s what all of our cells have on them, so why not exploit what’s there — that’s what viruses are good at,” he said.

The study was initiated by John Klassen, professor of chemistry in the Faculty of Science, whose lab developed the analytical tools to screen glycans. Specifically, Klassen and co-workers used a mass spectrometry technique, called catch-and-release, to study what sugars interact with the spike protein of SARS-CoV-2.

After that, Macauley and European collaborators started applying biological tools to see whether they could demonstrate a correlation between the viral proteins’ ability to recognize these sugars and the role it plays in the infection process.

Macauley’s lab initially ran experiments with a relatively harmless pseudovirus, incapable of replicating in the lab, armed with the spike protein of SARS-CoV-2. After obtaining promising results, professor Tom Hobman’s laboratory in the Department of Cell Biology in the Faculty of Medicine & Dentistry replicated findings on authentic SARS-CoV-2 under appropriate biosafety containment.

The researchers used chemical biology tools to modulate those sugars on the cell surface to study the ability for the viruses to get inside and infect cells.

Though researchers have shown that the virus’s ability to infect a cell drops by between two and 10 times when the production of sugars on cell receptors is blocked, Macauley suggested the process is not fully understood enough for the immediate development of a therapy.

“Because SARS-CoV-2 is constantly evolving, a variant that evolves with more sugar-dependent infection would be quite concerning, but our knowledge enables us to keep a lookout for such a variant,” he said.

The paper also proposes that the particular sugars the researchers were investigating — glycolipids, which are sugars attached to lipid (fat) — are found in the highest concentrations in an area where COVID-19 has been recently shown to infect: the brain.

Macauley said earlier this year, a number of studies showed that SARS-CoV-2 can find its way to the brain and infect cells of the nervous system, including neurons.

“We speculate that these sugar interactions could relate to what’s called a tissue tropism, which is the cells of the host that support viral infection and replication.”

The results from the study support similar work by one of the paper’s co-authors, Lori West, Canada Research Chair in Cardiac Transplantation in the Faculty of Medicine & Dentistry, who is trying to understand why people with blood type A are more susceptible to getting COVID-19 and are more susceptible to a more severe type of infection.

Now, with access to the variants of concern, Klassen said the team is exploring whether the variants all have similar sugar binding properties or whether these mutations are actually leading to changes in their ability to recognize specific structures.

This article is republished from Folio.

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