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. 2020 Jun 23:11:1480.
doi: 10.3389/fimmu.2020.01480. eCollection 2020.

Human Sialome and Coronavirus Disease-2019 (COVID-19) Pandemic: An Understated Correlation?

Affiliations

Human Sialome and Coronavirus Disease-2019 (COVID-19) Pandemic: An Understated Correlation?

Daniela Morniroli et al. Front Immunol. .
No abstract available

Keywords: COVID-19; SARS-CoV-2; human sialome; pathogen susceptibility; sialic acid; sialoquake; viral infection.

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Figures

Figure 1
Figure 1
(A) Sialic acid recognition as an infection facilitator for Coronavirus strains. (1) MERS-CoV binds to non-acetylated sialoside receptors on the epithelial cells of the respiratory tract, promoting clustering and facilitating its binding to its receptor DPP4. (2) SARS-CoV binds to ACE2 receptor. (3) SARS-CoV-2 binds to ACE2 receptor, but a surface region in Spike protein is very similar to MERS-CoV spike sialic acid-binding region, suggesting a possible role of sialic acid recognition in infection initiation. (B) Sialic acid recognition as a host defense mechanism for Coronavirus strains. (1) MERS-CoV can bind to sialylated O-linked glycans covering mucins on mucosal cell surfaces, thus being trapped in the mucous layer and consequently eliminated through ciliary movement. (2) SARS-CoV passes through the mucous layer without being stopped by decoy alternative binding sites. (3) SARS-CoV-2 shares with MERS-CoV the sialic acid binding region of Spike protein, and could therefore bind to sialylated O-linked glycans similarly to MERS-CoV, thus possibly being eliminated through ciliary movement.

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References

    1. Li W, Hulswit RJG, Widjaja I, Raj VS, McBride R, Peng W, et al. . Identification of sialic acid-binding function for the Middle East respiratory syndrome coronavirus spike glycoprotein. Proc Natl Acad Sci USA. (2017) 114:E8508–17. 10.1073/pnas.1712592114 - DOI - PMC - PubMed
    1. Lan J, Ge J, Yu J, Shan S, Zhou H, Fan S, et al. . Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor. Nature. (2020) 581:215–20. 10.1038/s41586-020-2180-5 - DOI - PubMed
    1. Milanetti E, Miotto M, Di Rienzo L, Monti M, Gosti G, Ruocco G. In-Silico evidence for two receptors based strategy of SARS-CoV-2. bioRxiv. [Preprint]. (2020). 10.1101/2020.03.24.006197 - DOI - PMC - PubMed
    1. Vandelli A, Monti M, Milanetti E, Ponti RD, Tartaglia GG. Structural analysis of SARS-CoV-2 and prediction of the human interactome. arXiv [Preprint]. arXiv:200313655 [q-bio] (2020). 10.1101/2020.03.28.013789 - DOI - PMC - PubMed
    1. Varki A. Multiple changes in sialic acid biology during human evolution. Glycoconj J. (2009) 26:231–45. 10.1007/s10719-008-9183-z - DOI - PMC - PubMed

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