Toxoplasma gondii genotype determines MyD88-dependent signaling in infected macrophages

J Immunol. 2006 Aug 15;177(4):2584-91. doi: 10.4049/jimmunol.177.4.2584.

Abstract

Infection of mouse macrophages with Toxoplasma gondii elicits MAPK activation and IL-12 production, but host cell signaling pathways have not been clearly delineated. Here, we compared macrophage signaling in response to high virulence type I (RH) vs low virulence type II (ME49) strain infection. Tachyzoites of both strains induced p38 MAPK-dependent macrophage IL-12 release, although ME49 elicited 2- to 3-fold more cytokine than RH. IL-12 production was largely restricted to infected cells in each case. RH-induced IL-12 release did not require MyD88, whereas ME49-triggered IL-12 production was substantially dependent on this TLR/IL-1R adaptor molecule. MyD88 was also not required for RH-stimulated p38 MAPK activation, which occurred in the absence of detectable upstream p38 MAPK kinase activity. In contrast, ME49-driven p38 MAPK activation displayed an MyD88-dependent component. This parasite strain also induced MyD88-dependent activation of MKK4, an upstream activator of p38 MAPK. The results suggest that RH triggers MAPK activation and IL-12 production using MyD88-independent signaling, whereas ME49 uses these pathways as well as MyD88-dependent signaling cascades. Differences in host signaling pathways triggered by RH vs ME49 may contribute to the high and low virulence characteristics displayed by these parasite strains.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing / physiology*
  • Animals
  • Cell Line
  • Cells, Cultured
  • Enzyme Activation / immunology
  • Female
  • Genotype
  • Immunity, Innate
  • Interleukin-12 / biosynthesis
  • Macrophages / enzymology
  • Macrophages / immunology
  • Macrophages / parasitology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid Differentiation Factor 88
  • Signal Transduction / immunology*
  • Species Specificity
  • Toxoplasma / genetics*
  • Toxoplasma / isolation & purification
  • Toxoplasma / pathogenicity
  • Virulence
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • Interleukin-12
  • p38 Mitogen-Activated Protein Kinases