Interferon-γ-Induced Nitric Oxide Synthase-2 Contributes to Blood/Brain Barrier Dysfunction and Acute Mortality in Experimental Streptococcus pneumoniae Meningitis

J Interferon Cytokine Res. 2016 Feb;36(2):86-99. doi: 10.1089/jir.2015.0078. Epub 2015 Sep 29.

Abstract

The proinflammatory cytokine interferon-gamma (IFNγ) recently was shown to play a crucial role in experimental pneumococcal meningitis (PM) pathogenesis, and we aimed in this study to investigate IFNγ-driven nitric oxide synthase-2 (NOS2)-mediated pathogenesis of murine PM. We demonstrate that costimulation of toll-like receptors and IFNγ receptors was synergistic for NOS2 expression in cultured murine microglia. Using an experimental PM model, wild-type mice treated with anti-IFNγ antibody, as well as IFNγ and NOS2 gene knockout (GKO) mice, were inoculated intracerebroventricularly with 10(3) colony-forming units of Streptococcus pneumoniae (WU2 strain). Mice were monitored daily during a 200-h disease course to assess survival rate and blood-brain barrier (BBB) permeability measured at 48 h. IFNγ deficiency was protective in PM, with an approximate 3-fold increase in survival rates in both antibody-treated and IFNγ GKO mice compared to controls (P < 0.01). At 48 h postinoculation, brain NOS2 mRNA expression was significantly increased in an IFNγ-dependent manner. Mortality was significantly delayed in NOS2 GKO mice compared to controls (P < 0.01), and BBB dysfunction was reduced by 54% in IFNγ GKO mice and abolished in NOS2 GKO. These data suggest that IFNγ-dependent expression of NOS2 in the brain contributes to BBB breakdown and early mortality in murine PM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Brain Barrier / metabolism*
  • Brain
  • Cell Line, Tumor
  • Cytokines / metabolism
  • Disease Models, Animal
  • Inflammation Mediators / metabolism
  • Interferon-gamma / deficiency
  • Interferon-gamma / metabolism*
  • Meningitis, Pneumococcal / genetics
  • Meningitis, Pneumococcal / metabolism*
  • Meningitis, Pneumococcal / microbiology
  • Meningitis, Pneumococcal / mortality*
  • Meningitis, Pneumococcal / pathology
  • Mice
  • Mice, Knockout
  • Microglia / metabolism
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / deficiency
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / metabolism*
  • Reactive Oxygen Species
  • Streptococcus pneumoniae
  • Toll-Like Receptors / agonists

Substances

  • Cytokines
  • Inflammation Mediators
  • Reactive Oxygen Species
  • Toll-Like Receptors
  • Nitric Oxide
  • Interferon-gamma
  • Nitric Oxide Synthase Type II