Atypical activation of the RNA sensor MDA5 by hepatitis C virus

Author:

Chakraborty Surajit1,Zhu Junji1,Gack Michaela U.1ORCID

Affiliation:

1. Florida Research and Innovation Center Cleveland Clinic Port St. Lucie FL USA

Abstract

Hepatitis C virus (HCV) is a significant human pathogen that can cause a number of serious diseases including chronic inflammation of the liver, cirrhosis, and hepatocellular carcinoma. A key enzyme in the HCV life cycle is the nonstructural protein 5B (NS5B), which functions as an RNA‐dependent RNA polymerase (RdRp) responsible for replicating the viral RNA genome. In their recent study, Dansako and colleagues showed that HCV NS5B induces type I interferon via activation of the RNA receptor MDA5, an activity that was dependent on the RdRp enzymatic activity but independent of viral RNA replication. Their data further indicated that the NS5B enzymes of HCV and the related GB virus‐B produce cellular double‐stranded RNA (dsRNA) species with potential immunostimulatory activity. These findings unveil an unconventional mechanism of activation of MDA5‐mediated host immunity by viral RdRp enzymes, which is expected to spur new research directions in viral immunology.

Funder

National Institute of Allergy and Infectious Diseases

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

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