Proceedings of the National Academy of Sciences · 2006 · 111 citations · 22 references
Life SciencesImmunologyMicrobiologyInflammationInnate ImmunityMedical MicrobiologyBacterial InfectionsBacterial PathogenesisInnate Immune ActivationInnate Immune ResponseInnate Immune Signaling PathwaysMacrophage BiologyBacterial Infection ImmunityInnate Immune CytokinesInnate Immune Response GeneticsInnate Immune Response VariationMonocyte-derived MacrophagesMycobacterium Tuberculosis InfectionMycobacterium Tuberculosis PathogenesisPhagocyte Defects
Six major lineages of Mycobacterium tuberculosis appear preferentially transmitted amongst distinct ethnic groups. We identified a deletion affecting Rv1519 in CH, a strain isolated from a large outbreak in Leicester U.K., that coincidentally defines the East African-Indian lineage matching a major ethnic group in this city. In broth media, CH grew less rapidly and was less acidic and H2O2-tolerant than reference sequenced strains (CDC1551 and H37Rv). Nevertheless, CH was not impaired in its ability to grow in human monocyte-derived macrophages. When compared with CDC1551 and H37Rv, CH induced less protective IL-12p40 and more antiinflammatory IL-10 and IL-6 gene transcription and secretion from monocyte-derived macrophages. It thus appears that CH compensates microbiological attenuation by skewing the innate response toward phagocyte deactivation. Complementation of Rv1519, but none of nine additional genes absent from CH compared with the type strain, H37Rv, reversed the capacity of CH to elicit antiinflammatory IL-10 production by macrophages. The Rv1519 polymorphism in M. tuberculosis confers an immune subverting phenotype that contributes to the persistence and outbreak potential of this lineage.
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Comparative Genomics of BCG Vaccines by Whole-Genome DNA Microarray
Marcel A. Behr, Michael A. Wilson, Wendy Gill et al. · Science · 1999 · 1.5K citations
A glycolipid of hypervirulent tuberculosis strains that inhibits the innate immune response
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