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Identification of a c-di-GMP-Regulated Polysaccharide Locus Governing Stress Resistance and Biofilm and Rugose Colony Formation in Vibrio vulnificus▿

机译:c-di-GMP调控的多糖基因座在创伤弧菌中的抗逆性及生物膜和果糖菌落形成的鉴定▿

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摘要

As an etiological agent of bacterial sepsis and wound infections, Vibrio vulnificus is unique among the Vibrionaceae. Its continued environmental persistence and transmission are bolstered by its ability to colonize shellfish, form biofilms on various marine biotic surfaces, and generate a morphologically and physiologically distinct rugose (R) variant that yields profuse biofilms. Here, we identify a c-di-GMP-regulated locus (brp, for biofilm and rugose polysaccharide) and two transcription factors (BrpR and BrpT) that regulate these physiological responses. Disruption of glycosyltransferases within the locus or either regulator abated the inducing effect of c-di-GMP on biofilm formation, rugosity, and stress resistance. The same lesions, or depletion of intracellular c-di-GMP levels, abrogated these phenotypes in the R variant. The parental and brp mutant strains formed only scant monolayers on glass surfaces and oyster shells, and although the R variant formed expansive biofilms, these were of limited depth. Dramatic vertical expansion of the biofilm structure was observed in the parental strain and R variant, but not the brp mutants, when intracellular c-di-GMP levels were elevated. Hence, the brp-encoded polysaccharide is important for surface colonization and stress resistance in V. vulnificus, and its expression may control how the bacteria switch from a planktonic lifestyle to colonizing shellfish to invading human tissue.
机译:作为细菌性败血症和伤口感染的病原体,创伤弧菌在弧菌科中是独特的。它能够在贝类中定居,在各种海洋生物表面上形成生物膜并产生形态和生理上不同的皱纹(R)变体,从而产生持久的环境持久性和传播能力,从而产生大量的生物膜。在这里,我们确定了一个c-di-GMP调控的基因座(brp,用于生物膜和皱纹多糖)和两个调节这些生理反应的转录因子(BrpR和BrpT)。基因座中糖基转移酶或任一调节剂的破坏减弱了c-di-GMP对生物膜形成,皱纹和抗逆性的诱导作用。相同的病变或细胞内c-di-GMP水平的耗竭消除了R变体中的这些表型。亲本和brp突变菌株在玻璃表面和牡蛎壳上仅形成很少的单层,尽管R变体形成了膨胀的生物膜,但深度有限。当细胞内c-di-GMP水平升高时,在亲本菌株和R变体中观察到生物膜结构的急剧垂直扩展,而在brp突变体中未观察到。因此,Brp编码的多糖对于创伤弧菌的表面定殖和抗逆性很重要,它的表达可能控制细菌如何从浮游生活方式转变为定居贝类再侵袭人类组织。

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