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A deletion defining a common Asian lineage of Mycobacterium tuberculosis associates with immune subversion

机译:定义亚洲结核分枝杆菌常见谱系的缺失与免疫颠覆有关

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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 H_2O_2-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.
机译:结核分枝杆菌的六个主要谱系似乎在不同种族之间优先传播。我们在CH中发现了一个影响Rv1519的缺失,这是从英国莱斯特的一次大暴发中分离出来的一种菌株,该菌株恰好定义了与该城市主要种族相匹配的东非-印度血统。在肉汤培养基中,与参考测序菌株(CDC1551和H37Rv)相比,CH的生长速度较慢,酸性较低,对H_2O_2的耐受性较低。尽管如此,CH在人类单核细胞衍生的巨噬细胞中的生长能力并未受到损害。与CDC1551和H37Rv相比,CH诱导的保护性IL-12p40较少,而抗炎性IL-10和IL-6基因的转录和分泌来自单核细胞巨噬细胞。因此看来,CH通过偏向吞噬细胞失活的先天反应来补偿微生物的衰减。 Rv1519的互补,但与类型株H37Rv相比,CH中不存在9个其他基因,这些基因均不能逆转CH引起巨噬细胞产生抗炎性IL-10的能力。结核分枝杆菌中的Rv1519多态性赋予免疫颠覆表型,有助于这种谱系的持久性和爆发潜力。

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