The dexd/H-box helicase DHX40 is a novel negative regulator during GCRV infection via targeting the host RLR helicases and viral nonstructural protein NS38

Fish Shellfish Immunol. 2024 Aug:151:109730. doi: 10.1016/j.fsi.2024.109730. Epub 2024 Jun 26.

Abstract

RLR helicases RIG-I and MDA5, which are known as pattern recognition receptors to sense cytoplasmic viral RNAs and trigger antiviral immune responses, are DExD/H-box helicases. In teleost, whether and how non-RLR helicases regulate RLR helicases to affect viral infection remains unclear. Here, we report that the non-RLR helicase DHX40 from grass carp (namely gcDHX40) is a negative regulator of grass carp reovirus (GCRV) infection and RLR-mediated type I IFN production. GcDHX40 was a cytoplasmic protein. Ectopic expression of gcDHX40 facilitated GCRV replication and suppressed type I IFN production induced by GCRV infection and by those genes involved the RLR antiviral signaling pathway. Mechanistically, gcDHX40 promoted the generation of viral inclusion bodies (VIBs) by interacting with the NS38 protein of GCRV. Additionally, gcDHX40 interacted with RLR helicase, and impaired the formation of RLR-MAVS functional complexes. Taken together, our results indicate that gcDHX40 is a novel important proviral host factor involving in promoting the generation of GCRV VIBs and inhibiting the production of RLR-mediated type I IFNs.

Keywords: DHX40; GCRV infection; Negative regulation; RLRs.

MeSH terms

  • Animals
  • Carps* / genetics
  • Carps* / immunology
  • DEAD-box RNA Helicases* / genetics
  • DEAD-box RNA Helicases* / immunology
  • DEAD-box RNA Helicases* / metabolism
  • Fish Diseases* / immunology
  • Fish Diseases* / virology
  • Fish Proteins* / genetics
  • Fish Proteins* / immunology
  • Gene Expression Regulation / immunology
  • Immunity, Innate* / genetics
  • RNA Helicases / genetics
  • RNA Helicases / immunology
  • RNA Helicases / metabolism
  • Reoviridae Infections* / immunology
  • Reoviridae Infections* / veterinary
  • Reoviridae* / physiology
  • Viral Nonstructural Proteins* / genetics
  • Viral Nonstructural Proteins* / immunology
  • Viral Nonstructural Proteins* / metabolism

Substances

  • Viral Nonstructural Proteins
  • Fish Proteins
  • DEAD-box RNA Helicases
  • RNA Helicases