首页> 美国卫生研究院文献>PLoS Clinical Trials >Analysis of Corynebacterium diphtheriae macrophage interaction: Dispensability of corynomycolic acids for inhibition of phagolysosome maturation and identification of a new gene involved in synthesis of the corynomycolic acid layer
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Analysis of Corynebacterium diphtheriae macrophage interaction: Dispensability of corynomycolic acids for inhibition of phagolysosome maturation and identification of a new gene involved in synthesis of the corynomycolic acid layer

机译:白喉棒状杆菌巨噬细胞相互作用的分析:胭脂红酸抑制吞噬溶酶体成熟的可分散性和鉴定参与胭脂红酸层合成的新基因

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摘要

Corynebacterium diphtheriae is the causative agent of diphtheria, a toxin mediated disease of upper respiratory tract, which can be fatal. As a member of the CMNR group, C. diphtheriae is closely related to members of the genera Mycobacterium, Nocardia and Rhodococcus. Almost all members of these genera comprise an outer membrane layer of mycolic acids, which is assumed to influence host-pathogen interactions. In this study, three different C. diphtheriae strains were investigated in respect to their interaction with phagocytic murine and human cells and the invertebrate infection model Caenorhabditis elegans. Our results indicate that C. diphtheriae is able to delay phagolysosome maturation after internalization in murine and human cell lines. This effect is independent of the presence of mycolic acids, as one of the strains lacked corynomycolates. In addition, analyses of NF-κB induction revealed a mycolate-independent mechanism and hint to detrimental effects of the different strains tested on the phagocytic cells. Bioinformatics analyses carried out to elucidate the reason for the lack of mycolates in one of the strains led to the identification of a new gene involved in mycomembrane formation in C. diphtheriae.
机译:白喉棒状杆菌是白喉的病原体,白喉是毒素介导的上呼吸道疾病,可能致命。作为CMNR组的成员,白喉衣原体与分枝杆菌属,诺卡氏菌和红球菌属的成员密切相关。这些属的几乎所有成员都包含霉菌酸的外膜层,据认为会影响宿主与病原体的相互作用。在这项研究中,研究了三种不同的白喉衣原体菌株与吞噬鼠和人细胞以及无脊椎动物感染模型秀丽隐杆线虫的相互作用。我们的结果表明,白喉衣原体能够在鼠和人细胞系内化后延迟吞噬溶酶体的成熟。这种作用与霉菌酸的存在无关,因为其中一种菌株缺乏胭酸菌。此外,对NF-κB诱导的分析揭示了一种不依赖霉菌酸盐的机制,并暗示了测试的不同菌株对吞噬细胞的有害作用。进行生物信息学分析以阐明其中一种菌株中缺乏霉菌酸酯的原因,导致鉴定出与白喉衣原体膜形成有关的新基因。

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