Influenza A virus-encoded NS1 virulence factor protein inhibits innate immune response by targeting IKK

Cell Microbiol. 2012 Dec;14(12):1849-66. doi: 10.1111/cmi.12005. Epub 2012 Sep 17.

Abstract

The IKK/NF-κB pathway is an essential signalling process initiated by the cell as a defence against viral infection like influenza virus. This pathway is therefore a prime target for viruses attempting to counteract the host response to infection. Here, we report that the influenza A virus NS1 protein specifically inhibits IKK-mediated NF-κB activation and production of the NF-κB induced antiviral genes by physically interacting with IKK through the C-terminal effector domain. The interaction between NS1 and IKKα/IKKβ affects their phosphorylation function in both the cytoplasm and nucleus. In the cytoplasm, NS1 not only blocks IKKβ-mediated phosphorylation and degradation of IκBα in the classical pathway but also suppresses IKKα-mediated processing of p100 to p52 in the alternative pathway, which leads to the inhibition of nuclear translocation of NF-κB and the subsequent expression of downstream NF-κB target genes. In the nucleus, NS1 impairs IKK-mediated phosphorylation of histone H3 Ser 10 that is critical to induce rapid expression of NF-κB target genes. These results reveal a new mechanism by which influenza A virus NS1 protein counteracts host NF-κB-mediated antiviral response through the disruption of IKK function. In this way, NS1 diminishes antiviral responses to infection and, in turn, enhances viral pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Humans
  • I-kappa B Kinase / antagonists & inhibitors
  • I-kappa B Kinase / metabolism*
  • Immune Evasion*
  • Immunity, Innate*
  • Influenza A virus / immunology
  • Influenza A virus / pathogenicity*
  • NF-kappa B / metabolism
  • Phosphorylation
  • Protein Interaction Mapping
  • Protein Processing, Post-Translational
  • Protein Transport
  • Viral Nonstructural Proteins / immunology
  • Viral Nonstructural Proteins / metabolism*
  • Virulence Factors / immunology
  • Virulence Factors / metabolism*

Substances

  • INS1 protein, influenza virus
  • NF-kappa B
  • Viral Nonstructural Proteins
  • Virulence Factors
  • I-kappa B Kinase