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首页> 外文期刊>Molecular Microbiology >PhoP-PhoQ homologues in Pseudomonas aeruginosa regulate expression of the outer-membrane protein OprH and polymyxin B resistance.
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PhoP-PhoQ homologues in Pseudomonas aeruginosa regulate expression of the outer-membrane protein OprH and polymyxin B resistance.

机译:铜绿假单胞菌中的PhoP-PhoQ同源物调节外膜蛋白OprH和多粘菌素B抵抗的表达。

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摘要

Rapid adaptation to environmental challenge is essential for the survival of many bacterial species, and is often effectively mediated by two-component regulatory systems. Part of the adaptive response of Pseudomonas aeruginosa to Mg2+ starvation is overexpression of the outer-membrane protein OprH and increased resistance to the polycationic antibiotic polymyxin B. Two overlapping open reading frames that encoded proteins with high similarities to the PhoP-PhoQ two-component regulatory system of Salmonella typhimurium were identified downstream of the oprH gene. A P. aeruginosa PhoP-null mutant, H851, was constructed by means of a phoP:xylE-GmR transcriptional fusion, and shown to be deficient in OprH expression. In contrast, an analogous PhoQ-null mutant, H854 (phoQ:xylE-GmR), exhibited constitutive overexpression of OprH. Normal Mg2+-regulated OprH expression could be restored in both mutants by complementation with a plasmid carrying the phoP and phoQ genes. Measurement of the catechol-2,3-dioxygenase activity, expressed from the xylE transcriptional fusion in strains H851 and H854, indicated that PhoP-PhoQ is involved in the regulation of phoP-phoQ as well as oprH. Reverse transcription polymerase chain reaction experiments and Northern blot analysis revealed linkage of oprH, phoP and phoQ into an operon that was demonstrated to be under the joint control of PhoP-PhoQ and Mg2+ ion concentration. In addition, studies of the polymyxin B resistance of the two mutant strains, H851 and H854, indicated that PhoP-PhoQ is involved in regulating P. aeruginosa polymyxin resistance in response to external Mg2+ concentrations.
机译:快速适应环境挑战对于许多细菌物种的生存至关重要,并且通常由两组分调节系统有效介导。铜绿假单胞菌对Mg2 +饥饿的适应性反应的一部分是外膜蛋白OprH的过表达和对多阳离子抗生素多粘菌素B的抗性增加。两个重叠的开放阅读框,其编码与PhoP-PhoQ两组分调节蛋白高度相似的蛋白鼠伤寒沙门氏菌系统在oprH基因的下游被确定。铜绿假单胞菌PhoP-null突变体H851是通过phoP:xylE-GmR转录融合构建的,显示OprH表达不足。相反,类似的PhoQ-null突变体H854(phoQ:xylE-GmR)表现出OprH的组成型过表达。通过与携带phoP和phoQ基因的质粒互补,可以在两个突变体中恢复正常的Mg2 +调节的OprH表达。测量菌株H851和H854中xylE转录融合表达的儿茶酚2,3-二加氧酶活性表明PhoP-PhoQ参与了phoP-phoQ和oprH的调控。逆转录聚合酶链反应实验和Northern印迹分析表明oprH,phoP和phoQ连接到操纵子中,该操纵子被证明受PhoP-PhoQ和Mg2 +离子浓度的共同控制。此外,对两个突变株H851和H854的多粘菌素B抗性的研究表明,PhoP-PhoQ参与响应外部Mg2 +浓度而调节的铜绿假单胞菌多粘菌素抗性。

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