DEAD-Box Helicase DDX6 Facilitated RIG-I-Mediated Type-I Interferon Response to EV71 Infection

Front Cell Infect Microbiol. 2021 Aug 13:11:725392. doi: 10.3389/fcimb.2021.725392. eCollection 2021.

Abstract

Previous studies have shown that DEAD (Glu-Asp-Ala-Glu)-box RNA helicases play important roles in viral infection, either as cytosolic sensors of pathogenic molecules or as essential host factors against viral infection. In the current study, we found that DDX6, an RNA helicase belonging to the DEAD-box family of helicase, exhibited anti-Enterovirus 71 activity through augmenting RIG-I-mediated type-I IFN response. Moreover, DDX6 binds viral RNA to form an RNA-protein complex to positively regulate the RIG-I-mediated interferon response; however, EV71 has evolved a strategy to antagonize the antiviral effect of DDX6 by proteolytic degradation of the molecule through its non-structural protein 2A, a virus-encoded protease.

Keywords: 2Apro; DDX6; EV71; Innate immune response; RIG-I.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DEAD Box Protein 58
  • DEAD-box RNA Helicases*
  • Enterovirus A, Human
  • Enterovirus Infections / immunology*
  • Humans
  • Interferon Type I* / immunology
  • Interferon-Induced Helicase, IFIH1
  • Proto-Oncogene Proteins*
  • RNA, Viral
  • Receptors, Immunologic

Substances

  • Interferon Type I
  • Proto-Oncogene Proteins
  • RNA, Viral
  • Receptors, Immunologic
  • RIGI protein, human
  • DDX6 protein, human
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases
  • Interferon-Induced Helicase, IFIH1