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
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Brain / metabolism
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Brain / microbiology
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Brain / parasitology
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Cytomegalovirus / pathogenicity
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Female
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GTP Phosphohydrolases / deficiency
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GTP Phosphohydrolases / genetics*
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Gene Expression Regulation
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Gene Expression Regulation, Enzymologic
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Genetic Predisposition to Disease
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Infections / microbiology*
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Infections / mortality
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Infections / parasitology
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Interferon-gamma / metabolism
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Interferon-gamma / physiology*
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Listeria monocytogenes / pathogenicity
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Liver / metabolism
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Liver / microbiology
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Liver / parasitology
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Male
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Mice
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Mice, Inbred C57BL
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Mice, Inbred Strains
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Mice, Knockout
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Nitric Oxide Synthase / genetics
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Nitric Oxide Synthase Type II
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RNA, Messenger / genetics
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RNA, Messenger / metabolism
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Specific Pathogen-Free Organisms
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Spleen / metabolism
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Spleen / microbiology
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Spleen / parasitology
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Survival Rate
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Toxoplasma / pathogenicity
Substances
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RNA, Messenger
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Interferon-gamma
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Nitric Oxide Synthase
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Nitric Oxide Synthase Type II
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Nos2 protein, mouse
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GTP Phosphohydrolases
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Igtp protein, mouse