Anti-apoptotic activity of Japanese encephalitis virus NS5 protein in human medulloblastoma cells treated with interferon-β

J Microbiol Immunol Infect. 2018 Aug;51(4):456-464. doi: 10.1016/j.jmii.2017.01.005. Epub 2017 May 19.

Abstract

Background: Japanese encephalitis virus (JEV) non-structural protein 5 (NS5) exhibits type I interferon (IFN) antagonists, contributing to immune escape, and even inducing viral anti-apoptosis. This study investigated the anti-apoptotic mechanism of JEV NS5 protein on type I IFN-induced apoptosis of human medulloblastoma cells.

Methods: Vector control and NS5-expressing cells were treated with IFN-β, and then harvested for analyzing apoptotic pathways with flow cytometry, Western blotting, subcellular localization, etc. RESULTS: Annexin V-FITC/PI staining indicated that IFN-β triggered apoptosis of human medulloblastoma cells, but JEV NS5 protein significantly inhibited IFN-β-induced apoptosis. Phage display technology and co-immunoprecipitation assay identified the anti-apoptotic protein Hsp70 as a NS5-interacting protein. In addition, Western blotting demonstrated that NS5 protein up-regulated the Hsp70 expression, and reduced IFN-β-induced phosphorylation of ERK2, p38 MAPK and STAT1. Hsp70 down-regulation by quercetin significantly recovered IFN-β-induced apoptosis of NS5-expressing cells, correlating with the increase in the phosphorylation of ERK2, p38 MAPK, and STAT1. Inhibiting the ATPase activity of Hsp70 by VER-155008 resulted in the elevated IFN-β-induced apoptosis in vector control and NS5-expressing cells.

Conclusions: The results indicated Hsp70 up-regulation by JEV NS5 not only involved in type I IFN antagonism, but also responded to the anti-apoptotic action of JEV NS5 protein through the blocking IFN-β-induced p38 MAPK/STAT1-mediated apoptosis.

Keywords: Anti-apoptosis; Hsp70; Interferon; Japanese encephalitis virus; NS5.

MeSH terms

  • Annexin A5 / analysis
  • Antiviral Agents / metabolism*
  • Apoptosis*
  • Cell Line, Tumor
  • Flow Cytometry
  • HSP72 Heat-Shock Proteins / metabolism
  • Host-Pathogen Interactions*
  • Humans
  • Interferon-beta / metabolism*
  • Protein Binding
  • Protein Interaction Mapping
  • Signal Transduction
  • Viral Nonstructural Proteins / metabolism*

Substances

  • Annexin A5
  • Antiviral Agents
  • HSP72 Heat-Shock Proteins
  • NS5 protein, flavivirus
  • Viral Nonstructural Proteins
  • Interferon-beta