The Herpes Simplex Virus ICP0 RING Finger Domain Inhibits IRF3- and IRF7-Mediated Activation of Interferon-Stimulated Genes

Author:

Lin Rongtuan1,Noyce Ryan S.2,Collins Susan E.3,Everett Roger D.4,Mossman Karen L.23

Affiliation:

1. Lady Davis Research Institute, Montreal H3T 1E2, Canada

2. Departments of Biochemistry

3. Pathology & Molecular Medicine, McMaster University, Hamilton L8N 3Z5, Canada

4. MRC Virology Unit, Glasgow G11 5JR, Scotland, United Kingdom

Abstract

ABSTRACT Virus infection induces a rapid cellular response in cells characterized by the induction of interferon. While interferon itself does not induce an antiviral response, it activates a number of interferon-stimulated genes that collectively function to inhibit virus replication and spread. Previously, we and others reported that herpes simplex virus type 1 (HSV-1) induces an interferon -independent antiviral response in the absence of virus replication. Here, we report that the HSV-1 proteins ICP0 and vhs function in concert to disable the host antiviral response. In particular, we show that ICP0 blocks interferon regulatory factor IRF3- and IRF7-mediated activation of interferon-stimulated genes and that the RING finger domain of ICP0 is essential for this activity. Furthermore, we demonstrate that HSV-1 modifies the IRF3 pathway in a manner different from that of the small RNA viruses most commonly studied.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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