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Tetherin antagonism by SARS-CoV-2 ORF3a and spike protein enhances virus release

Stewart, Hazel; Palmulli, Roberta; Johansen, Kristoffer H; McGovern, Naomi; Shehata, Ola M; Carnell, George W; Jackson, Hannah K; Lee, Jin S; Brown, Jonathan C; Burgoyne, Thomas; Heeney, Jonathan L; Okkenhaug, Klaus; Firth, Andrew E; Peden, Andrew A; Edgar, James R

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Authors

Hazel Stewart

Roberta Palmulli

Kristoffer H Johansen

Naomi McGovern

Ola M Shehata

George W Carnell

Jin S Lee

Jonathan C Brown

Thomas Burgoyne

Jonathan L Heeney

Klaus Okkenhaug

Andrew E Firth

Andrew A Peden

James R Edgar



Abstract

The antiviral restriction factor, tetherin, blocks the release of several different families of enveloped viruses, including the Coronaviridae. Tetherin is an interferon-induced protein that forms parallel homodimers between the host cell and viral particles, linking viruses to the surface of infected cells and inhibiting their release. We demonstrate that SARS-CoV-2 infection causes tetherin downregulation and that tetherin depletion from cells enhances SARS-CoV-2 viral titres. We investigate the potential viral proteins involved in abrogating tetherin function and find that SARS-CoV-2 ORF3a reduces tetherin localisation within biosynthetic organelles where Coronaviruses bud, and increases tetherin localisation to late endocytic organelles via reduced retrograde recycling. We also find that expression of Spike protein causes a reduction in cellular tetherin levels. Our results confirm that tetherin acts as a host restriction factor for SARS-CoV-2 and highlight the multiple distinct mechanisms by which SARS-CoV-2 subverts tetherin function.

Journal Article Type Article
Acceptance Date Dec 1, 2023
Online Publication Date Oct 11, 2023
Publication Date Dec 6, 2023
Deposit Date May 28, 2024
Publicly Available Date May 29, 2024
Journal EMBO Reports
Print ISSN 1469-221X
Electronic ISSN 1469-3178
Publisher EMBO Press
Peer Reviewed Peer Reviewed
Volume 24
Issue 12
Article Number e57224
DOI https://doi.org/10.15252/embr.202357224
Public URL https://nottingham-repository.worktribe.com/output/35432130
Publisher URL https://www.embopress.org/doi/full/10.15252/embr.202357224
Additional Information Received: 2023-03-21; Accepted: 2023-09-21; Published: 2023-10-11

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