The Antiviral Activity of Interferon-Induced Transmembrane Proteins and Virus Evasion Strategies

Author:

Wang Jingjing1ORCID,Luo Yuhang1,Katiyar Harshita23,Liang Chen23,Liu Qian12ORCID

Affiliation:

1. Institute of Parasitology, McGill University, Ste Anne de Bellevue, QC H9X 3V9, Canada

2. McGill Center for Viral Diseases, Lady Davis Institute, Montreal, QC H3T 1E2, Canada

3. Division of Experimental Medicine, McGill University, Montreal, QC H4A 3J1, Canada

Abstract

Interferons (IFNs) are antiviral cytokines that defend against viral infections by inducing the expression of interferon-stimulated genes (ISGs). Interferon-inducible transmembrane proteins (IFITMs) 1, 2, and 3 are crucial ISG products and members of the CD225 protein family. Compelling evidence shows that IFITMs restrict the infection of many unrelated viruses by inhibiting the virus–cell membrane fusion at the virus entry step via the modulation of lipid composition and membrane properties. Meanwhile, viruses can evade IFITMs’ restrictions by either directly interacting with IFITMs via viral glycoproteins or by altering the native entry pathway. At the same time, cumulative evidence suggests context-dependent and multifaceted roles of IFITMs in modulating virus infections and cell signaling. Here, we review the diverse antiviral mechanisms of IFITMs, the viral antagonizing strategies, and the regulation of IFITM activity in host cells. The mechanisms behind the antiviral activity of IFITMs could aid the development of broad-spectrum antivirals and enhance preparedness for future pandemics.

Funder

Canadian Institute of Health Research

FRQNT Postdoctoral Research Scholarship

MI4 Pfizer Early Career Investigator Award

CIHR Coronavirus Variants Rapid Response Network

Publisher

MDPI AG

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