SARS-CoV nucleocapsid protein antagonizes IFN-β response by targeting initial step of IFN-β induction pathway, and its C-terminal region is critical for the antagonism

Virus Genes. 2011 Feb;42(1):37-45. doi: 10.1007/s11262-010-0544-x. Epub 2010 Oct 26.

Abstract

Severe acute respiratory syndrome coronavirus (SARS-CoV) encodes a highly basic nucleocapsid (N) protein which can inhibit the synthesis of type I interferon (IFN), but the molecular mechanism of this antagonism remains to be identified. In this study, we demonstrated that the N protein of SARS-CoV could inhibit IFN-beta (IFN-β) induced by poly(I:C) or Sendai virus. However, we found that N protein could not inhibit IFN-β production induced by overexpression of downstream signaling molecules of two important IFN-β induction pathways, toll-like receptor 3 (TLR3)- and RIG-I-like receptors (RLR)-dependent pathways. These results indicate that SARS-CoV N protein targets the initial step, probably the cellular PRRs (pattern recognition receptors)-RNAs-recognition step in the innate immune pathways, to suppress IFN expression responses. In addition, co-immunoprecipitation assays revealed that N protein did not interact with RIG-I or MDA5. Further, an assay using truncated mutants revealed that the C-terminal domain of N protein was critical for its antagonism of IFN induction, and the N deletion mutant impaired for RNA-binding almost completely lost the IFN-β antagonist activity. These results contribute to our further understanding of the pathogenesis of SARS-CoV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / immunology
  • Cell Line
  • Coronavirus Nucleocapsid Proteins
  • DEAD-box RNA Helicases / immunology
  • Humans
  • Interferon Regulatory Factor-3 / immunology
  • Interferon-beta / immunology
  • Interferon-beta / metabolism*
  • Nucleocapsid Proteins / immunology*
  • Poly I-C / immunology
  • Promoter Regions, Genetic
  • Protein Serine-Threonine Kinases / immunology
  • RNA, Viral / analysis
  • Sendai virus / immunology
  • Sequence Deletion
  • Severe acute respiratory syndrome-related coronavirus / immunology*
  • Severe acute respiratory syndrome-related coronavirus / pathogenicity
  • Toll-Like Receptor 3 / immunology

Substances

  • Adaptor Proteins, Signal Transducing
  • Coronavirus Nucleocapsid Proteins
  • IRF3 protein, human
  • Interferon Regulatory Factor-3
  • Nucleocapsid Proteins
  • RNA, Viral
  • TLR3 protein, human
  • Toll-Like Receptor 3
  • Interferon-beta
  • Protein Serine-Threonine Kinases
  • DEAD-box RNA Helicases
  • Poly I-C