首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Self-produced exopolysaccharide is a signal that stimulates biofilm formation in Pseudomonas aeruginosa
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Self-produced exopolysaccharide is a signal that stimulates biofilm formation in Pseudomonas aeruginosa

机译:自我产生的胞外多糖是刺激铜绿假单胞菌生物膜形成的信号

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摘要

Bacteria have a tendency to attach to surfaces and grow as structured communities called biofilms. Chronic biofilm infections are a problem because they tend to resist antibiotic treatment and are difficult to eradicate. Bacterial biofilms have an extracellular matrix that is usually composed of a mixture of polysaccharides, proteins, and nucleic acids. This matrix has long been assumed to play a passive structural and protective role for resident biofilm cells. Here we show that this view is an oversimplification and that the biofilm matrix can play an active role in stimulating its own synthesis. Working with the model biofilm bacterium Pseudomonas aeruginosa, we found that Psl, a major biofilm matrix polysaccharide for this species, acts as a signal to stimulate two diguanylate cyclases, SiaD and SadC, to produce the intracellular secondary messenger molecule c-di-GMP. Elevated intracellular concentrations of c-di-GMP then lead to the increased production of Psl and other components of the biofilm. This mechanism represents a unique positive feedback regulatory circuit, where the expression of an extracellular polysaccharide promotes biofilm growth in a manner analogous to autocrine signaling in eukaryotes.
机译:细菌倾向于附着在表面并以称为生物膜的结构化群落生长。慢性生物膜感染是一个问题,因为它们倾向于抵抗抗生素治疗并且难以根除。细菌生物膜具有细胞外基质,通常由多糖,蛋白质和核酸的混合物组成。长期以来,人们一直认为该基质对驻留的生物膜细胞起被动的结构和保护作用。在这里,我们证明这种观点过于简单化,生物膜基质在刺激其自身合成中可以发挥积极作用。与模型生物膜细菌铜绿假单胞菌一起工作,我们发现Psl是该物种的主要生物膜基质多糖,可作为信号刺激两种双鸟苷酸环化酶SiaD和SadC,以产生细胞内次级信使分子c-di-GMP。然后,升高的细胞内c-di-GMP浓度导致Psl和生物膜其他成分的产生增加。该机制代表独特的正反馈调节电路,其中细胞外多糖的表达以类似于真核生物中自分泌信号传导的方式促进生物膜生长。

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    Department of Microbiology, University of Washington, Seattle, WA 98195;

    Department of Microbiology, University of Washington, Seattle, WA 98195,Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO 80523;

    Department of Microbiology, University of Washington, Seattle, WA 98195;

    Department of Microbial Infection and Immunity and Center for Microbial Interface Biology, The Ohio State University, Columbus, OH 43210;

    Department of Microbiology, University of Washington, Seattle, WA 98195;

    Department of Microbial Infection and Immunity and Center for Microbial Interface Biology, The Ohio State University, Columbus, OH 43210;

    Department of Microbiology, University of Washington, Seattle, WA 98195;

  • 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
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  • 入库时间 2022-08-18 00:40:35

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