σ 抑制 聚-N-乙酰葡糖胺多糖的生物合成和生物膜形成。

σ Inhibits Poly--Acetylglucosamine Exopolysaccharide Synthesis and Biofilm Formation in .

机构信息

Laboratory of Microbial Pathogenesis, Navarrabiomed-Universidad Pública de Navarra (UPNA)-Complejo Hospitalario de Navarra (CHN), Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Navarra, Spain.

Laboratory of Microbial Pathogenesis, Navarrabiomed-Universidad Pública de Navarra (UPNA)-Complejo Hospitalario de Navarra (CHN), Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Navarra, Spain

出版信息

J Bacteriol. 2019 May 8;201(11). doi: 10.1128/JB.00098-19. Print 2019 Jun 1.

Abstract

clinical strains are able to produce at least two distinct types of biofilm matrixes: biofilm matrixes made of the polysaccharide intercellular adhesin (PIA) or poly--acetylglucosamine (PNAG), whose synthesis is mediated by the locus, and biofilm matrixes built of proteins (polysaccharide independent). σ is a conserved alternative sigma factor that regulates the expression of more than 100 genes in response to changes in environmental conditions. While numerous studies agree that σ is required for polysaccharide-independent biofilms, controversy persists over the role of σ in the regulation of PIA/PNAG-dependent biofilm development. Here, we show that genetically unrelated σ-deficient strains produced stronger biofilms under both static and flow conditions and accumulated higher levels of PIA/PNAG exopolysaccharide than their corresponding wild-type strains. The increased accumulation of PIA/PNAG in the σ mutants correlated with a greater accumulation of the IcaC protein showed that it was not due to adjustments in operon transcription and/or mRNA stability. Overall, our results reveal that in the presence of active σ, the turnover of Ica proteins is accelerated, reducing the synthesis of PIA/PNAG exopolysaccharide and consequently the PIA/PNAG-dependent biofilm formation capacity. Due to its multifaceted lifestyle, needs a complex regulatory network to connect environmental signals with cellular physiology. One particular transcription factor, named σ (SigB), is involved in the general stress response and the expression of virulence factors. For many years, great confusion has existed about the role of σ in the regulation of the biofilm lifestyle in Our study demonstrated that σ is not necessary for exopolysaccharide-dependent biofilms and, even more, that produces stronger biofilms in the absence of σ The increased accumulation of exopolysaccharide correlates with higher stability of the proteins responsible for its synthesis. The present findings reveal an additional regulatory layer to control biofilm exopolysaccharide synthesis under stress conditions.

摘要

临床株至少能产生两种不同类型的生物膜基质

由胞间多糖黏附素(PIA)或聚-N-乙酰葡糖胺(PNAG)组成的生物膜基质,其合成由 基因座介导,以及由蛋白质组成的生物膜基质(多糖非依赖性)。σ 是一种保守的替代 σ 因子,可响应环境条件的变化调节超过 100 个基因的表达。虽然许多研究都认为 σ 是多糖非依赖性生物膜所必需的,但 σ 在调节 PIA/PNAG 依赖性生物膜发育中的作用仍存在争议。在这里,我们表明,遗传上不相关的 σ 缺陷菌株在静态和流动条件下产生更强的生物膜,并比相应的野生型菌株积累更高水平的 PIA/PNAG 胞外多糖。σ 突变体中 PIA/PNAG 的积累增加与 IcaC 蛋白的积累增加相关,表明这不是由于 操纵子转录和/或 mRNA 稳定性的调整。总的来说,我们的结果表明,在活性 σ 的存在下,Ica 蛋白的周转加速,减少 PIA/PNAG 胞外多糖的合成,从而降低 PIA/PNAG 依赖性生物膜形成能力。由于其多方面的生活方式, 需要一个复杂的调控网络将环境信号与细胞生理学联系起来。一种特殊的转录因子,命名为 σ(SigB),参与一般应激反应和毒力因子的表达。多年来,σ 在调节 生物膜生活方式中的作用一直存在很大的混淆。我们的研究表明,σ 对于依赖胞外多糖的生物膜不是必需的,甚至更多的是,在没有 σ 的情况下, 产生更强的生物膜。胞外多糖的积累增加与负责其合成的蛋白质更高的稳定性相关。这些发现揭示了在应激条件下控制生物膜胞外多糖合成的另一个调控层。

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