Modulation of type I IFN induction by a virulence determinant within the alphavirus nsP1 protein

Virology. 2010 Mar 30;399(1):1-10. doi: 10.1016/j.virol.2009.12.031. Epub 2010 Jan 25.

Abstract

Alphaviruses are mosquito-borne viruses that cause serious human and animal diseases. Previous studies demonstrated that a determinant within the nsP1/nsP2 cleavage domain of the virulent Sindbis AR86 virus played a key role in regulating adult mouse virulence without adversely affecting viral replication. Additional characterization of this determinant demonstrated that a virus with the attenuating mutation induced more type I IFN production both in vivo and in vitro. Interestingly, this phenotype was not specific to the Sindbis AR86 virus, as a similar mutation in a distantly related alphavirus, Ross River Virus (RRV), also led to enhanced IFN induction. This effect was independent of virus-induced host shutoff, since IRF-3 phosphorylation, which occurs independently of de novo host transcription/translation, was induced more robustly in cells infected with the mutant viruses. Altogether, these results demonstrate that critical determinants within the nsP1/nsP2 cleavage domain play an important role in regulating alphavirus-induced IFN responses.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alphavirus Infections / metabolism
  • Alphavirus Infections / virology
  • Animals
  • Cell Line
  • Humans
  • Interferon Regulatory Factor-3 / metabolism
  • Interferon Type I / biosynthesis*
  • L Cells
  • Mice
  • Mutagenesis, Site-Directed
  • Phosphorylation
  • Protein Biosynthesis / physiology
  • RNA / biosynthesis
  • Ross River virus / genetics
  • Ross River virus / pathogenicity*
  • Ross River virus / physiology
  • Sindbis Virus / genetics
  • Sindbis Virus / pathogenicity*
  • Sindbis Virus / physiology
  • Transcriptional Activation
  • Viral Nonstructural Proteins / genetics
  • Viral Nonstructural Proteins / physiology*
  • Virulence Factors / metabolism
  • Virulence Factors / physiology*

Substances

  • Interferon Regulatory Factor-3
  • Interferon Type I
  • Viral Nonstructural Proteins
  • Virulence Factors
  • nsP1 protein, Sindbis virus
  • RNA