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Exploitation of glycosylation in enveloped virus pathobiology

Exploitation of glycosylation in enveloped virus pathobiology
Exploitation of glycosylation in enveloped virus pathobiology

Glycosylation is a ubiquitous post-translational modification responsible for a multitude of crucial biological roles. As obligate parasites, viruses exploit host-cell machinery to glycosylate their own proteins during replication. Viral envelope proteins from a variety of human pathogens including HIV-1, influenza virus, Lassa virus, SARS, Zika virus, dengue virus, and Ebola virus have evolved to be extensively glycosylated. These host-cell derived glycans facilitate diverse structural and functional roles during the viral life-cycle, ranging from immune evasion by glycan shielding to enhancement of immune cell infection. In this review, we highlight the imperative and auxiliary roles glycans play, and how specific oligosaccharide structures facilitate these functions during viral pathogenesis. We discuss the growing efforts to exploit viral glycobiology in the development of anti-viral vaccines and therapies.

0304-4165
Watanabe, Yasunori
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Bowden, Thomas A.
4b17a588-ac01-4112-807a-8b99a6c20d0f
Wilson, Ian A.
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Crispin, Max
cd980957-0943-4b89-b2b2-710f01f33bc9
Watanabe, Yasunori
8c0ee4af-a293-4de5-9036-3ce2051b380c
Bowden, Thomas A.
4b17a588-ac01-4112-807a-8b99a6c20d0f
Wilson, Ian A.
7865d500-d638-4a67-ad6d-fefad0ae83bb
Crispin, Max
cd980957-0943-4b89-b2b2-710f01f33bc9

Watanabe, Yasunori, Bowden, Thomas A., Wilson, Ian A. and Crispin, Max (2019) Exploitation of glycosylation in enveloped virus pathobiology. Biochimica et Biophysica Acta (BBA) - General Subjects. (doi:10.1016/j.bbagen.2019.05.012).

Record type: Review

Abstract

Glycosylation is a ubiquitous post-translational modification responsible for a multitude of crucial biological roles. As obligate parasites, viruses exploit host-cell machinery to glycosylate their own proteins during replication. Viral envelope proteins from a variety of human pathogens including HIV-1, influenza virus, Lassa virus, SARS, Zika virus, dengue virus, and Ebola virus have evolved to be extensively glycosylated. These host-cell derived glycans facilitate diverse structural and functional roles during the viral life-cycle, ranging from immune evasion by glycan shielding to enhancement of immune cell infection. In this review, we highlight the imperative and auxiliary roles glycans play, and how specific oligosaccharide structures facilitate these functions during viral pathogenesis. We discuss the growing efforts to exploit viral glycobiology in the development of anti-viral vaccines and therapies.

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Accepted/In Press date: 17 May 2019
e-pub ahead of print date: 20 May 2019

Identifiers

Local EPrints ID: 431749
URI: http://eprints.soton.ac.uk/id/eprint/431749
ISSN: 0304-4165
PURE UUID: 1dc91566-fdd0-4ac3-9972-b217e3e61e82
ORCID for Max Crispin: ORCID iD orcid.org/0000-0002-1072-2694

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Date deposited: 14 Jun 2019 16:30
Last modified: 16 Mar 2024 04:30

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Contributors

Author: Yasunori Watanabe
Author: Thomas A. Bowden
Author: Ian A. Wilson
Author: Max Crispin ORCID iD

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