Cytoplasmic Listeria monocytogenes stimulates IFN-beta synthesis without requiring the adapter protein MAVS

FEBS Lett. 2006 Apr 17;580(9):2341-2346. doi: 10.1016/j.febslet.2006.03.057.

Abstract

The mitochondria-associated adapter protein MAVS (also called IPS-1, VISA or CARDIF, designated MAVS for reasons of simplicity in our manuscript) relays signals from cytoplasmic sensors of viral RNA to the IRF3 kinase complex and the interferon-beta (IFN-beta) gene. Using siRNA-mediated knock-down in macrophages we show that IFN-beta synthesis in response to transfected, intracellular double-stranded RNA (dsRNA), a pathogen-associated molecular pattern of viruses, is decreased in absence of MAVS. By contrast, the Gram-positive bacterium Listeria monocytogenes targets the IFN-beta gene without detectable MAVS requirement. The data show that MAVS is not a central adapter protein for all cytoplasmic pathogen sensors that stimulate IFN-beta synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / immunology*
  • Animals
  • Cell Line
  • Cytoplasm / genetics
  • Cytoplasm / immunology
  • Cytoplasm / metabolism
  • Cytoplasm / microbiology
  • Interferon-beta / biosynthesis
  • Interferon-beta / genetics
  • Interferon-beta / immunology*
  • Listeria monocytogenes / immunology*
  • Listeriosis / genetics
  • Listeriosis / immunology*
  • Listeriosis / metabolism
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Macrophages / microbiology
  • Mice
  • RNA, Double-Stranded / genetics
  • RNA, Double-Stranded / immunology
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / immunology
  • Signal Transduction / genetics
  • Signal Transduction / immunology*

Substances

  • Adaptor Proteins, Signal Transducing
  • RNA, Double-Stranded
  • RNA, Small Interfering
  • VISA protein, mouse
  • Interferon-beta