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Opposing activities of IFITM proteins in SARS‐CoV‐2 infection

Authors
  • Shi, Guoli1
  • Kenney, Adam D.2, 3
  • Kudryashova, Elena3, 3
  • Zani, Ashley2, 3
  • Zhang, Lizhi2, 3
  • Lai, Kin Kui1
  • Hall‐Stoodley, Luanne2
  • Robinson, Richard T.2
  • Kudryashov, Dmitri S.3, 3
  • Compton, Alex A.1
  • Yount, Jacob S.2, 3
  • 1 National Cancer Institute, USA , (United States)
  • 2 The Ohio State University College of Medicine, USA , (United States)
  • 3 The Ohio State University, USA , (United States)
Type
Published Article
Journal
The EMBO Journal
Publisher
EMBO
Publication Date
Dec 03, 2020
Identifiers
DOI: 10.15252/embj.2020106501
PMID: 33270927
PMCID: PMC7744865
Source
PubMed Central
Keywords
License
Unknown
External links

Abstract

Interferon‐induced transmembrane proteins (IFITMs) restrict infections by many viruses, but a subset of IFITMs enhance infections by specific coronaviruses through currently unknown mechanisms. We show that SARS‐CoV‐2 Spike‐pseudotyped virus and genuine SARS‐CoV‐2 infections are generally restricted by human and mouse IFITM1, IFITM2, and IFITM3, using gain‐ and loss‐of‐function approaches. Mechanistically, SARS‐CoV‐2 restriction occurred independently of IFITM3 S ‐palmitoylation, indicating a restrictive capacity distinct from reported inhibition of other viruses. In contrast, the IFITM3 amphipathic helix and its amphipathic properties were required for virus restriction. Mutation of residues within the IFITM3 endocytosis‐promoting YxxΦ motif converted human IFITM3 into an enhancer of SARS‐CoV‐2 infection, and cell‐to‐cell fusion assays confirmed the ability of endocytic mutants to enhance Spike‐mediated fusion with the plasma membrane. Overexpression of TMPRSS2, which increases plasma membrane fusion versus endosome fusion of SARS‐CoV‐2, attenuated IFITM3 restriction and converted amphipathic helix mutants into infection enhancers. In sum, we uncover new pro‐ and anti‐viral mechanisms of IFITM3, with clear distinctions drawn between enhancement of viral infection at the plasma membrane and amphipathicity‐based mechanisms used for endosomal SARS‐CoV‐2 restriction.

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