Published March 19, 2021 | Version v6
Working paper Open

Sialic acids and viruses

  • 1. Politecnico di Torino

Description

Let us study viruses and the role of sialic acids in their first step of reproduction, the attachment to cells. We begin our study with the help of the "Earth's virology course", created by Vincent Racaniello, with David Tuller and Gertrud U. Rey. The first virus that we will study is that of influenza A. Actually, "Earth's virology course" is a proper starting point for learning the mechanisms the virus uses to attach and enter the host cells. In the case of the influenza virus, its spike protein is used to attach the virion to  sialic acid receptors of the host cells. Then, we will consider coronaviruses, with the help of literature about the role of sialic acids in their attachment by means of spike proteins. In fact, there are seven human coronavirus and they use sialic acid or angiotensin-converting enzyme 2 (ACE2) or other receptors or a combination of them. Let us review the literature to understand if  Sars-Cov-2 virus can use sialic acid for the attachment to cells or not. Its main target is considered the ACE2 receptor. We will see that a study exists which detected that Sars-Cov-2 protein molecules can bind to heparan sulfate glycans in a sulfation-dependent manner. 

Notes

About the role of sialic acids in Sars-Cov-2 attachment: a) the study in 10.1021/acscentsci.0c00855 used a glyco-nanoparticle platform, discovering that N-acetyl neuraminic acid has affinity toward the SARS-COV-2 spike glycoprotein, that is a glycan-binding function. b) a recent study, 10.1016/j.scib.2021.01.010, which has investigated the binding of the spikes of the virus by means of micro-arrays, tells that no binding with sialic acid residues was detected. All the tested protein molecules can bind to heparan sulfate glycans (as in 10.1016/j.cell.2020.09.033) in a sulfation-dependent manner. c) A preprint published on March 8, 2021, entitled "Sialic acid-Dependent Binding and Viral Entry of SARS-CoV-2". bioRxiv 2021.03.08.434228; doi: https://doi.org/10.1101/2021.03.08.434228, gives different results,

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