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Community surveillance enhances Pseudomonas aeruginosa virulence during polymicrobial infection

机译:社区监测可提高细菌感染铜绿假单胞菌的毒力

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摘要

Most infections result from colonization by more than one microbe. Within such polymicrobial infections, microbes often display syn-ergistic interactions that result in increased disease severity. Although many clinical studies have documented the occurrence of synergy in polymicrobial infections, little is known about the underlying molecular mechanisms. A prominent pathogen in many polymicrobial infections is Pseudomonas aeruginosa, a Gram-negative bacterium that displays enhanced virulence during coculture with Gram-positive bacteria. In this study we discovered that during coinfection, P. aeruginosa uses peptidoglycan shed by Gram-positive bacteria as a cue to stimulate production of multiple extracellular factors that possess lytic activity against prokaryotic and eukaryotic cells. Consequently, P. aeruginosa displays enhanced virulence in a Dro-sophila model of infection when cocultured with Gram-positive bacteria. Inactivation of a gene (PA0601) required for peptidoglycan sensing mitigated this phenotype. Using Drosophila and mu-rine models of infection, we also show that peptidoglycan sensing results in P. aeruginosa-mediated reduction in the Gram-positive flora in the infection site. Our data suggest that P. aeruginosa has evolved a mechanism to survey the microbial community and respond to Gram-positive produced peptidoglycan through production of antimicrobials and toxins that not only modify the composition of the community but also enhance host killing. Additionally, our results suggest that therapeutic strategies targeting Gram-positive bacteria might be a viable approach for reducing the severity of P. aeruginosa polymicrobial infections.
机译:大多数感染是由一种以上的微生物定植造成的。在这种微生物感染中,微生物通常表现出协同作用,导致疾病严重程度增加。尽管许多临床研究已证明在微生物感染中协同作用的发生,但对潜在的分子机制知之甚少。铜绿假单胞菌(Pseudomonas aeruginosa)是许多细菌感染的主要病原体,它是一种革兰氏阴性细菌,在与革兰氏阳性细菌共培养期间显示出更高的毒力。在这项研究中,我们发现在共感染过程中,铜绿假单胞菌利用革兰氏阳性细菌释放的肽聚糖作为提示,以刺激多种具有抗原核和真核细胞裂解活性的细胞外因子的产生。因此,当与革兰氏阳性细菌共培养时,铜绿假单胞菌在Dro-Sophila感染模型中显示出增强的毒力。肽聚糖传感所需的基因(PA0601)失活减轻了该表型。使用果蝇和鼠科动物的感染模型,我们还显示肽聚糖感测导致铜绿假单胞菌介导的感染部位革兰氏阳性菌群减少。我们的数据表明,铜绿假单胞菌已发展出一种机制,可以调查微生物群落并通过产生抗菌素和毒素来应对革兰氏阳性产生的肽聚糖,这不仅改变了群落的组成,而且还增强了宿主的杀伤力。此外,我们的结果表明,针对革兰氏阳性细菌的治疗策略可能是降低铜绿假单胞菌多微生物感染严重程度的可行方法。

著录项

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  • 作者单位

    Section of Molecular Genetics and Microbiology, Institute of Cell and Molecular Biology, University of Texas at Austin, Austin, TX 78712;

    Department of Surgery, Texas Tech University Health Sciences Center, Lubbock, TX 79430;

    Department of Surgery, Texas Tech University Health Sciences Center, Lubbock, TX 79430;

    Section of Molecular Genetics and Microbiology, Institute of Cell and Molecular Biology, University of Texas at Austin, Austin, TX 78712;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    staphylococcus; quorum sensing; PQS; glucosamine;

    机译:葡萄球菌;群体感应;PQS;葡萄糖胺;
  • 入库时间 2022-08-18 00:39:52

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