Fish Rhbdd3 positively regulates IFN response through RIG-I signaling pathway

Fish Shellfish Immunol. 2023 Nov:142:109102. doi: 10.1016/j.fsi.2023.109102. Epub 2023 Sep 25.

Abstract

Rhomboid domain-containing protein 3 (Rhbdd3) is a member of the rhomboid family, which can modulate the innate immune response in mammals. Nonetheless, the function and regulatory mechanism of fish Rhbdd3 during viral infection have not been characterized. In this study, Rhbdd3 was firstly cloned from common carp (Cyprinus carpio) and nominated as CcRhbdd3. Phylogenetically characterization showed that CcRhbdd3 shared a relatively long evolutionary distance with its mammalian homologs. In vivo experiment demonstrated that spring viraemia of carp virus (SVCV) infection promoted the expression of CcRhbdd3 in the liver, spleen, kidney and muscle tissues. Furthermore, overexpression of CcRhbdd3 significantly inhibited SVCV propagation, whereas knockdown of CcRhbdd3 markedly promoted SVCV replication in susceptible cells. RNA-seq and following validation showed that CcRhbdd3 overexpression upregulated the expression of several RIG-I signaling related genes, including TRIM25, TRAF2, MDA5, LGP2, IFN1, IFN3, RIG-I, IRF3 and ISG15. Moreover, CcRhbdd3 promoted the expression of NF-κB, a central immune regulator. Subcellular localization experiments showed that CcRhbdd3 was primarily distributed in the cytoplasm and co-localized with Rab5 in the early endosomes. Truncation experiments further demonstrated that the C-terminus containing the ubiquitin-binding associated domain, was crucial for both the subcellular localization and antiviral activity of CcRhbdd3. The findings in this study provide new insight into the host antiviral mechanism against aquatic RNA virus infection, and will facilitate the development of therapeutic strategies for the infection of SVCV.

Keywords: Innate immunity; RIG-I; Rhbdd3; Spring viraemia of carp virus (SVCV); Ubiquitin-binding associated domain.

MeSH terms

  • Animals
  • Antiviral Agents
  • Carps* / metabolism
  • Fish Diseases*
  • Fish Proteins / chemistry
  • Immunity, Innate / genetics
  • Mammals / metabolism
  • Rhabdoviridae Infections*
  • Rhabdoviridae* / physiology
  • Signal Transduction

Substances

  • Fish Proteins
  • Antiviral Agents

Supplementary concepts

  • Carp sprivivirus