Foot-and-mouth disease virus non-structural protein 2B negatively regulates the RLR-mediated IFN-β induction

Biochem Biophys Res Commun. 2018 Sep 26;504(1):238-244. doi: 10.1016/j.bbrc.2018.08.161. Epub 2018 Aug 31.

Abstract

Foot-and-mouth disease virus (FMDV) is the causative agent of Foot-and-mouth disease (FMD), which is an acute and highly contagious disease affecting pigs, cattle and other cloven-hoofed animals. Several studies have shown that FMDV has evolved multiple strategies to evade the host innate immune response, but the underlying mechanisms for immune evasion are still not fully understood. In the current research, we have demonstrated that FMDV utilizes its non-structural protein 2B to sabotage the host immune response. Over-expression of the FMDV 2B inhibited Poly(I:C)-induced or SeV-triggered up-regulation of IFN-β, IL-6 as well as ISG15. When HEK293T cells were transfected with FMDV 2B, the phosphorylation of TBK1 and IRF3 was inhibited. Co-immunoprecipitation and pull-down experiments indicated that FMDV 2B protein could interact with host RIG-I and MDA5. Moreover, FMDV 2B also inhibited the expression of the RIG-I and MDA5. Thus, FMDV 2B negatively regulates the RLR-mediated IFN-β induction by targeting RIG-I and MDA5.

Keywords: Evasion; Foot-and-mouth disease virus; Innate immune; Protein 2B; Type I IFNs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DEAD Box Protein 58 / metabolism
  • Foot-and-Mouth Disease Virus / metabolism*
  • HEK293 Cells
  • Humans
  • Immunity, Innate
  • Interferon-Induced Helicase, IFIH1 / metabolism
  • Interferon-beta / metabolism*
  • Phosphorylation
  • Receptors, Immunologic
  • Signal Transduction
  • Transfection
  • Up-Regulation
  • Viral Nonstructural Proteins / metabolism*

Substances

  • Receptors, Immunologic
  • Viral Nonstructural Proteins
  • Interferon-beta
  • RIGI protein, human
  • IFIH1 protein, human
  • DEAD Box Protein 58
  • Interferon-Induced Helicase, IFIH1