MiR-22 promotes porcine reproductive and respiratory syndrome virus replication by targeting the host factor HO-1

Vet Microbiol. 2016 Aug 30:192:226-230. doi: 10.1016/j.vetmic.2016.07.026. Epub 2016 Aug 1.

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) is one of the most economically important viruses affecting the swine industry worldwide. MicroRNAs (miRNAs) play vital roles in virus-host interactions by regulating the expression of viral or host gene at posttranscriptional level. Our previous research showed that PRRSV infection down-regulates the expression of heme oxygenase-1 (HO-1), a pivotal cytoprotective enzyme, and overexpression of HO-1 inhibits PRRSV replication. In this study, we demonstrate that host miRNA miR-22 can downregulate HO-1 expression by directly targeting its 3' untranslated region. Suppression of HO-1 expression by miR-22 facilitates PRRSV replication. This work suggests that PRRSV may utilize cellular miRNA to modify antiviral host factor expression, enabling viral replication, which not only provides new insights into virus-host interactions during PRRSV infection, but also suggests potential therapies for PRRSV infection.

Keywords: HO-1; PRRSV; Post-transcriptional regulation; Virus-cell interaction; miRNA.

MeSH terms

  • Animals
  • Cell Line
  • Gene Expression Regulation, Enzymologic / physiology*
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / metabolism*
  • Humans
  • MicroRNAs / genetics*
  • Porcine respiratory and reproductive syndrome virus / physiology*
  • Virus Replication / genetics
  • Virus Replication / physiology*

Substances

  • MicroRNAs
  • Heme Oxygenase-1