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首页> 外文期刊>Journal of bacteriology >The Pseudomonas aeruginosa Vfr Regulator Controls Global Virulence Factor Expression through Cyclic AMP-Dependent and -Independent Mechanisms
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The Pseudomonas aeruginosa Vfr Regulator Controls Global Virulence Factor Expression through Cyclic AMP-Dependent and -Independent Mechanisms

机译:铜绿假单胞菌Vfr调节剂通过循环AMP依赖和独立机制控制全局毒力因子表达

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Vfr is a global regulator of virulence factor expression in the human pathogen Pseudomonas aeruginosa. Although indirect evidence suggests that Vfr activity is controlled by cyclic AMP (cAMP), it has been hypothesized that the putative cAMP binding pocket of Vfr may accommodate additional cyclic nucleotides. In this study, we used two different approaches to generate apo-Vfr and examined its ability to bind a representative set of virulence gene promoters in the absence and presence of different allosteric effectors. Of the cyclic nucleotides tested, only cAMP was able to restore DNA binding activity to apo-Vfr. In contrast, cGMP was capable of inhibiting cAMP-Vfr DNA binding. Further, we demonstrate that vfr expression is autoregulated and cAMP dependent and involves Vfr binding to a previously unidentified site within the vfr promoter region. Using a combination of in vitro and in vivo approaches, we show that cAMP is required for Vfr-dependent regulation of a specific subset of virulence genes. In contrast, we discovered that Vfr controls expression of the lasR promoter in a cAMP-independent manner. In summary, our data support a model in which Vfr controls virulence gene expression by distinct (cAMP-dependent and -independent) mechanisms, which may allow P. aeruginosa to fine-tune its virulence program in response to specific host cues or environments.
机译:Vfr是铜绿假单胞菌(Pseudomonas aeruginosa)病原体中毒力因子表达的全球调节因子。尽管间接证据表明Vfr的活性受环AMP(cAMP)的控制,但已经假设Vfr的cAMP结合口袋可能会容纳其他环核苷酸。在这项研究中,我们使用了两种不同的方法来生成载脂蛋白Vfr,并在不存在和存在不同的变构效应子的情况下,研究了其结合代表性毒力基因启动子的能力。在测试的环状核苷酸中,只有cAMP能够恢复DNA与apo-Vfr的结合活性。相反,cGMP能够抑制cAMP-Vfr DNA结合。此外,我们证明了 vfr 表达是自动调节的,并且依赖于cAMP,并且涉及Vfr与 vfr 启动子区域内以前未鉴定的位点的结合。结合使用体外体内方法,我们证明了cAMP是毒力基因特定子集的Vfr依赖性调节所必需的。相反,我们发现Vfr以不依赖cAMP的方式控制 lasR 启动子的表达。总而言之,我们的数据支持一个模型,其中Vfr通过独特的(依赖cAMP和不依赖cAMP)机制控制毒力基因表达,这可能允许 P。铜绿假单胞菌,以根据特定宿主线索或环境微调其毒力程序。

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