Chicken miR-126-5p negatively regulates antiviral innate immunity by targeting TRAF3

Vet Res. 2022 Oct 12;53(1):82. doi: 10.1186/s13567-022-01098-x.

Abstract

Innate immunity plays an essential role in preventing the invasion of pathogenic microorganisms. However, innate immunity is a double-edged sword, whose excessive activation is detrimental to immune homeostasis and even leads to a "cytokine storm" of the infected host. The host develops a series of negative regulatory mechanisms to balance the immune response. Here, we report a negative regulatory mechanism of chicken innate immunity mediated by miRNA. In the GEO database, we found that miR-126-5p was markedly up-regulated in chickens infected by RNA viruses. Upregulation of miR-126-5p by RNA virus was then further shown via both a cell model and in vivo tests. Overexpression of miR-126-5p significantly inhibited the expression of interferon and inflammatory cytokine-related genes induced by RNA viruses. The opposite result was achieved after the knockdown of miR-126-5p expression. Bioinformatics analysis identified TRAF3 as candidate target gene of miR-126-5p. Experimentally, miR-126-5p can target TRAF3, as shown by the effects of miR-126-5p on the endogenous expression of TRAF3, and by the TRAF3 3'UTR driven luciferase reporter assay. Furthermore, we demonstrated that miR-126-5p negatively regulated innate immunity by blocking the MAVS-TRAF3-TBK1 axis, with a co-expression assay. Overall, our results suggest that miR-126-5p is involved in the negative regulation of chicken innate immunity, which might contribute to maintaining immune balance.

Keywords: Chicken; RNA viruses; TRAF3; innate immunity; miR-126-5p.

MeSH terms

  • 3' Untranslated Regions
  • Animals
  • Antiviral Agents
  • Chickens / genetics
  • Chickens / metabolism
  • Cytokines / metabolism
  • Immunity, Innate / genetics
  • Interferons / metabolism
  • Luciferases / genetics
  • Luciferases / metabolism
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • TNF Receptor-Associated Factor 3* / genetics
  • TNF Receptor-Associated Factor 3* / metabolism

Substances

  • 3' Untranslated Regions
  • Antiviral Agents
  • Cytokines
  • MicroRNAs
  • TNF Receptor-Associated Factor 3
  • Interferons
  • Luciferases