Cell-type specificity and functional redundancy of RIG-I-like receptors in innate immune sensing of Coxsackievirus B3 and encephalomyocarditis virus

• Authors: Eesther Francisco, Columbia University; Mehul Suthar, Emory University; Michael Gale, Jr., University of Washington; Amy B. Rosenfeld, Columbia University; Vincent R. Racaniello, Columbia University
• Journal Title: Virology
• Volume: Volume 528
• Publisher: Academic Press Inc. & Elsevier Science | 2019-02-01, Pages 7-18
• Type of Work: Article | Post-print: After Peer Review
• Publisher DOI: http://doi.org/10.1016/j.virol.2018.12.003
• Subjects: Biology, Genetics; Biology, Virology; Health Sciences, Immunology
• Keywords: Science & Technology; Life Sciences & Biomedicine; Virology; Picornavirus; Innate immunity; RIG-I; MDA5; Interferon; Macrophage; Antiviral responses; RNA recognition; Interferon; Protein; Identification; Replication; Induction; Activation; Genes

Abstract

The contributions of RIG-I and MDA5 receptors to sensing viruses of the Picornaviridae family were investigated. The picornaviruses encephalomyocarditis virus (EMCV) and Coxsackievirus B3 (CVB3) are detected by both MDA5 and RIG-I in bone marrow derived macrophages. In macrophages from wild type mice, type I IFN is produced early after infection; IFNβ synthesis is reduced in the absence of each sensor, while IFNα production is reduced in the absence of MDA5. EMCV and CVB3 do not replicate in murine macrophages, and their detection is different in murine embryonic fibroblasts (MEFs), in which the viruses replicate to high titers. In MEFs RIG-I was essential for the expression of type I IFNs but contributes to increased yields of CVB3, while MDA5 inhibited CVB3 replication but in an IFN independent manner. These observations demonstrate functional redundancy within the innate immune response to picornaviruses.