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Pneumococcal microbial surface components recognizing adhesive matrix molecules targeting of the extracellular matrix.

机译:肺炎球菌微生物表面成分可识别靶向细胞外基质的粘附基质分子。

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摘要

The attachment of bacteria to host cells and tissues, and their subsequent invasion and dissemination are key processes during pathogenesis. In this issue of Molecular Microbiology, Jensch and co-workers provide further molecular insight into these events during infection with the Gram positive bacterium Streptococcus pneumoniae. Their characterization of pneumococcal adherence and virulence factor B (PavB), a bacterial surface protein with orthologues in other streptococci, show that it binds to the extracellar matrix components fibronection and plasminogen by virtue of repetitive sequences-designated streptococcal surface repeats. In mice, a pavB mutant showed reduced nasopharyngeal colonization and was attenuated in a lung infection model. As discussed here in the context of the pneumococcus, the study of PavB highlights the central role during microbal pathogenesis of targetting the extracellular matrix by so-called microbial surface components recognizing adhesive matrix molecules (MSCRAMMs).
机译:细菌在宿主细胞和组织上的附着及其随后的入侵和传播是发病机理中的关键过程。在本期《分子微生物学》中,Jensch及其同事提供了有关革兰氏阳性细菌肺炎链球菌感染过程中这些事件的进一步分子洞察力。他们对肺炎球菌粘附和毒力因子B(PavB)(一种在其他链球菌中带有直向同源物的细菌表面蛋白)的表征表明,它通过重复序列指定的链球菌表面重复序列与细胞外基质成分纤溶酶和纤溶酶原结合。在小鼠中,pavB突变体显示出减少的鼻咽定植,并在肺部感染模型中减弱。如此处在肺炎球菌的讨论中所讨论的,PavB的研究突出了通过所谓的微生物表面成分识别粘附基质分子(MSCRAMM)靶向细胞外基质的微生物发病机理中的核心作用。

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