Pathogen-specific loss of host resistance in mice lacking the IFN-gamma-inducible gene IGTP

Proc Natl Acad Sci U S A. 2000 Jan 18;97(2):751-5. doi: 10.1073/pnas.97.2.751.

Abstract

Interferon-gamma (IFN-gamma) is critical for defense against pathogens, but the molecules that mediate its antimicrobial responses are largely unknown. IGTP is the prototype for a family of IFN-gamma-regulated genes that encode 48-kDa GTP-binding proteins that localize to the endoplasmic reticulum. We have generated IGTP-deficient mice and found that, despite normal immune cell development and normal clearance of Listeria monocytogenes and cytomegalovirus infections, the mice displayed a profound loss of host resistance to acute infections of the protozoan parasite Toxoplasma gondii. By contrast, IFN-gamma receptor-deficient mice have increased susceptibility to all three pathogens. Thus, IGTP defines an IFN-gamma-regulated pathway with a specialized role in antimicrobial resistance.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Brain / metabolism
  • Brain / microbiology
  • Brain / parasitology
  • Cytomegalovirus / pathogenicity
  • Female
  • GTP Phosphohydrolases / deficiency
  • GTP Phosphohydrolases / genetics*
  • Gene Expression Regulation
  • Gene Expression Regulation, Enzymologic
  • Genetic Predisposition to Disease
  • Infections / microbiology*
  • Infections / mortality
  • Infections / parasitology
  • Interferon-gamma / metabolism
  • Interferon-gamma / physiology*
  • Listeria monocytogenes / pathogenicity
  • Liver / metabolism
  • Liver / microbiology
  • Liver / parasitology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Mice, Knockout
  • Nitric Oxide Synthase / genetics
  • Nitric Oxide Synthase Type II
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Specific Pathogen-Free Organisms
  • Spleen / metabolism
  • Spleen / microbiology
  • Spleen / parasitology
  • Survival Rate
  • Toxoplasma / pathogenicity

Substances

  • RNA, Messenger
  • Interferon-gamma
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • GTP Phosphohydrolases
  • Igtp protein, mouse