TLR-independent type I interferon induction in response to an extracellular bacterial pathogen via intracellular recognition of its DNA

Cell Host Microbe. 2008 Dec 11;4(6):543-54. doi: 10.1016/j.chom.2008.11.002.

Abstract

Type I interferon (IFN) is an important host defense cytokine against intracellular pathogens, mainly viruses. In assessing IFN production in response to group B streptococcus (GBS), we find that IFN-beta was produced by macrophages upon stimulation with both heat-killed and live GBS. Exposure of macrophages to heat-killed GBS activated a Toll-like receptor (TLR)-dependent pathway, whereas live GBS activated a TLR/NOD/RIG-like receptor (RLR)-independent pathway. This latter pathway required bacterial phagocytosis, proteolytic bacterial degradation, and phagolysosomal membrane destruction by GBS pore-forming toxins, leading to the release of bacterial DNA into the cytosol. GBS DNA in the cytosol induced IFN-beta production via a pathway dependent on the activation of the serine-threonine kinase TBK1 and phosphorylation of the transcription factor IRF3. Thus, activation of IFN-alpha/-beta production during infection with GBS, commonly considered an extracellular pathogen, appears to result from the interaction of GBS DNA with a putative intracellular DNA sensor or receptor.

Publication types

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

MeSH terms

  • Animals
  • Cells, Cultured
  • DNA, Bacterial / immunology*
  • Interferon Regulatory Factor-3 / metabolism
  • Interferon Type I / immunology*
  • Macrophages / immunology*
  • Macrophages / microbiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Protein Serine-Threonine Kinases / metabolism
  • Streptococcus agalactiae / immunology*
  • Toll-Like Receptors / immunology*

Substances

  • DNA, Bacterial
  • Interferon Regulatory Factor-3
  • Interferon Type I
  • Irf3 protein, mouse
  • Toll-Like Receptors
  • Tbk1 protein, mouse
  • Protein Serine-Threonine Kinases