ATG4B hinders porcine epidemic diarrhea virus replication through interacting with TRAF3 and activating type-I IFN signaling

Vet Microbiol. 2022 Oct:273:109544. doi: 10.1016/j.vetmic.2022.109544. Epub 2022 Aug 17.

Abstract

Autophagy-related 4B (ATG4B) is found to exert a vital function in viral replication, although the mechanism through which ATG4B activates type-I IFN signaling to hinder viral replication remains to be explained, so far. The current work revealed that ATG4B was downregulated in porcine epidemic diarrhea virus (PEDV)-infected LLC-PK1 cells. In addition, ATG4B overexpression inhibited PEDV replication in both Vero cells and LLC-PK1 cells. On the contrary, ATG4B knockdown facilitated PEDV replication. Moreover, ATG4B was observed to hinder PEDV replication by activating type-I IFN signaling. Further detailed analysis revealed that the ATG4B protein targeted and upregulated the TRAF3 protein to induce IFN expression via the TRAF3-pTBK1-pIRF3 pathway. The above data revealed a novel mechanism underlying the ATG4B-mediated viral restriction, thereby providing novel possibilities for preventing and controlling PEDV.

Keywords: ATG4B; IFN; PEDV; Replication; TRAF3.

MeSH terms

  • Animals
  • Chlorocebus aethiops
  • Coronavirus Infections* / veterinary
  • Porcine epidemic diarrhea virus* / genetics
  • Signal Transduction
  • Swine
  • Swine Diseases*
  • TNF Receptor-Associated Factor 3 / genetics
  • Vero Cells
  • Virus Replication

Substances

  • TNF Receptor-Associated Factor 3