Downregulation of miR-296-3p by highly pathogenic porcine reproductive and respiratory syndrome virus activates the IRF1/TNF-α signaling axis in porcine alveolar macrophages

Arch Virol. 2021 Feb;166(2):511-519. doi: 10.1007/s00705-020-04921-y. Epub 2021 Jan 4.

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV, species Betaarterivirus suid 1 or 2) is a major pathogen affecting pigs on farms throughout the world. miR-296-3p is a multifunctional microRNA involved in the regulation of the inflammatory response in mice and humans. However, little is known about the biological functions of miR-296-3p in pigs. In this study, we used a highly pathogenic PRRSV-2 (species Betaarterivirus suid 2) strain to show that PRRSV infection robustly downregulates the expression of miR-296-3p in porcine alveolar macrophages (PAMs). Furthermore, we demonstrated that overexpression of miR-296-3p increases the replication of highly pathogenic (HP)-PRRSV in PAMs. Notably, the overexpression of miR-296-3p inhibited the induction of TNF-α, even with increased viral replication, compared with that in the HP-PRRSV-infected control group. We also demonstrated that miR-296-3p targets IRF1-facilitated viral infection and modulates the expression of TNF-α in PAMs during HP-PRRSV infection and that IRF1 regulates the expression of TNF-α by activating the TNF promoter via IRF1 response elements. In summary, these findings show that HP-PRRSV infection activates the IRF1/TNF-α signaling axis in PAMs by downregulating host miR-296-3p. This extends our understanding of the inflammatory response induced by HP-PRRSV infection.

MeSH terms

  • Animals
  • Cell Line
  • Chlorocebus aethiops
  • Down-Regulation / genetics*
  • Gene Expression Profiling / methods
  • HEK293 Cells
  • Host-Pathogen Interactions / genetics
  • Humans
  • Interferon Regulatory Factor-1 / genetics*
  • Macrophages, Alveolar / virology*
  • MicroRNAs / genetics*
  • Porcine Reproductive and Respiratory Syndrome / genetics*
  • Porcine Reproductive and Respiratory Syndrome / virology
  • Porcine respiratory and reproductive syndrome virus / physiology*
  • Signal Transduction / genetics
  • Swine / genetics
  • Swine / virology*
  • Transcriptome / genetics
  • Tumor Necrosis Factor-alpha / genetics*
  • Virus Replication / genetics

Substances

  • Interferon Regulatory Factor-1
  • MicroRNAs
  • Tumor Necrosis Factor-alpha