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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Pseudomonas aeruginosa AmpR is a global transcriptional factor that regulates expression of AmpC and PoxB beta-lactamases, proteases, quorum sensing, and other virulence factors.
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Pseudomonas aeruginosa AmpR is a global transcriptional factor that regulates expression of AmpC and PoxB beta-lactamases, proteases, quorum sensing, and other virulence factors.

机译:铜绿假单胞菌AmpR是一种全球转录因子,可调节AmpC和PoxBβ-内酰胺酶,蛋白酶,群体感应和其他毒力因子的表达。

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摘要

In members of the family Enterobacteriaceae, ampC, which encodes a beta-lactamase, is regulated by an upstream, divergently transcribed gene, ampR. However, in Pseudomonas aeruginosa, the regulation of ampC is not understood. In this study, we compared the characteristics of a P. aeruginosa ampR mutant, PAOampR, with that of an isogenic ampR+ parent. The ampR mutation greatly altered AmpC production. In the absence of antibiotic, PAOampR expressed increased basal beta-lactamase levels. However, this increase was not followed by a concomitant increase in the P(ampC) promoter activity. The discrepancy in protein and transcription analyses led us to discover the presence of another chromosomal AmpR-regulated beta-lactamase, PoxB. We found that the expression of P. aeruginosa ampR greatly altered the beta-lactamase production from ampC and poxB in Escherichia coli: it up-regulated AmpC but down-regulated PoxB activities. In addition, the constitutive P(ampR) promoter activity in PAOampR indicated that AmpRdid not autoregulate in the absence or presence of inducers. We further demonstrated that AmpR is a global regulator because the strain carrying the ampR mutation produced higher levels of pyocyanin and LasA protease and lower levels of LasB elastase than the wild-type strain. The increase in LasA levels was positively correlated with the P(lasA), P(lasI), and P(lasR) expression. The reduction in the LasB activity was positively correlated with the P(rhlR) expression. Thus, AmpR plays a dual role, positively regulating the ampC, lasB, and rhlR expression levels and negatively regulating the poxB, lasA, lasI, and lasR expression levels.
机译:在肠杆菌科的成员中,编码β-内酰胺酶的ampC受上游差异转录的基因ampR调控。然而,在铜绿假单胞菌中,对ampC的调节尚不了解。在这项研究中,我们比较了铜绿假单胞菌ampR突变体PAOampR和同基因ampR +亲本的特征。 ampR突变大大改变了AmpC的生产。在没有抗生素的情况下,PAOampR表达的基础β-内酰胺酶水平升高。但是,这种增加并不伴随着P(ampC)启动子活性的增加。蛋白质和转录分析的差异使我们发现了另一种染色体AmpR调节的β-内酰胺酶PoxB。我们发现铜绿假单胞菌ampR的表达大大改变了ampC和poxB在大肠杆菌中的β-内酰胺酶生产:它上调了AmpC,但下调了PoxB活性。此外,PAOampR中的本构P(ampR)启动子活性表明,在不存在或存在诱导剂的情况下,AmpRdid不会自动调节。我们进一步证明,AmpR是一种全局调节剂,因为与野生型菌株相比,携带ampR突变的菌株产生的花青素和LasA蛋白酶水平更高,而LasB弹性蛋白酶水平更低。 LasA水平的增加与P(lasA),P(lasI)和P(lasR)表达呈正相关。 LasB活性的降低与P(rhlR)表达正相关。因此,AmpR发挥双重作用,正向调节ampC,lasB和rhlR表达水平,而负向调节poxB,lasA,lasI和lasR表达水平。

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