首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Phosphorylcholine on the Lipopolysaccharide of Haemophilus influenzae Contributes to Persistence in the Respiratory Tract and Sensitivity to Serum Killing Mediated by C-reactive Protein
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Phosphorylcholine on the Lipopolysaccharide of Haemophilus influenzae Contributes to Persistence in the Respiratory Tract and Sensitivity to Serum Killing Mediated by C-reactive Protein

机译:流感嗜血杆菌脂多糖上的磷酸胆碱有助于呼吸道的持久性和对C反应蛋白介导的血清杀灭的敏感性

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摘要

Haemophilus influenzae undergoes phase variation in expression of the phosphorylcholine (ChoP) epitope, a structure present on several invasive pathogens residing in the human respiratory tract. In this study, structural analysis comparing organisms with and without this epitope confirmed that variants differ in the presence of ChoP on the cell surface–exposed outer core of the lipopolysaccharide. During nasopharyngeal carriage in infant rats, there was a gradual selection for H. influenzae variants that express ChoP. In addition, genotypic analysis of the molecular switch that controls phase variation predicted that the ChoP+ phenotype was predominant in H. influenzae in human respiratory tract secretions. However, ChoP+ variants of nontypable H. influenzae were more sensitive to the bactericidal activity of human serum unrelated to the presence of naturally acquired antibody to ChoP. Serum bactericidal activity required the binding of C-reactive protein (CRP) with subsequent activation of complement through the classical pathway. Results of this study suggested that the ability of H. influenzae to vary expression of this unusual bacterial structure may correlate with its ability both to persist on the mucosal surface (ChoP+ phenotype) and to cause invasive infection by evading innate immunity mediated by CRP (ChoP phenotype).
机译:流感嗜血杆菌在磷酸胆碱(ChoP)表位的表达中经历相变,该表位存在于人类呼吸道中的几种侵入性病原体上。在这项研究中,对具有和没有该表位的生物进行结构分析,结果表明,在暴露于细胞表面的脂多糖外核上存在ChoP时,变体有所不同。在婴儿大鼠的鼻咽运输过程中,逐渐选择表达ChoP的流感嗜血杆菌变异。此外,控制相变的分子开关的基因型分析表明,ChoP + 表型在人类呼吸道分泌物中以流感嗜血杆菌为主。但是,不可分型的流感嗜血杆菌的ChoP + 变体对人血清的杀菌活性更为敏感,而这种活性与天然获得的抗ChoP抗体无关。血清杀菌活性需要结合C反应蛋白(CRP),随后通过经典途径激活补体。这项研究的结果表明,流感嗜血杆菌改变这种异常细菌结构表达的能力可能与其在黏膜表面持续存在的能力(ChoP + 表型)以及通过感染引起侵袭性感染有关。规避CRP介导的先天免疫(ChoP -表型)。

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