Abstract
Activation of V gamma 9/V delta 2 T cells by small nonprotein Ags is frequently observed after infection with various viruses, bacteria, and eukaryotic parasites. We suggested earlier that compounds synthesized by the 2-C:-methyl-D-erythritol 4-phosphate (MEP) pathway of isopentenyl pyrophosphate synthesis are responsible for the V gamma 9/V delta 2 T cell reactivity of many pathogens. Using genetically engineered Escherichia coli knockout strains, we now demonstrate that the ability of E. coli extracts to stimulate gamma delta T cell proliferation is abrogated when genes coding for essential enzymes of the MEP pathway, dxr or gcpE, are disrupted or deleted from the bacterial genome.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Aldose-Ketose Isomerases / genetics
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Bacterial Proteins / genetics
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Cell Fractionation
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Enzymes*
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Erythritol / analogs & derivatives
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Erythritol / metabolism*
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Erythritol / physiology
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Escherichia coli / enzymology
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Escherichia coli / genetics
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Escherichia coli / immunology
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Gene Deletion
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Hemiterpenes*
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Humans
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Lymphocyte Activation*
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Molecular Weight
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Multienzyme Complexes / genetics
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Organophosphorus Compounds / metabolism*
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Oxidoreductases / genetics
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Protein Engineering
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Receptors, Antigen, T-Cell, gamma-delta / metabolism*
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Signal Transduction / immunology
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Sugar Phosphates / metabolism*
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Sugar Phosphates / physiology
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T-Lymphocyte Subsets / immunology*
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T-Lymphocyte Subsets / metabolism*
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T-Lymphocyte Subsets / microbiology
Substances
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2-C-methylerythritol 4-phosphate
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Bacterial Proteins
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Enzymes
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Hemiterpenes
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Multienzyme Complexes
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Organophosphorus Compounds
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Receptors, Antigen, T-Cell, gamma-delta
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Sugar Phosphates
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hydroxymethylbutenyl 4-diphosphate synthase
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isopentenyl pyrophosphate
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Oxidoreductases
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1-deoxy-D-xylulose 5-phosphate reductoisomerase
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Aldose-Ketose Isomerases
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Erythritol