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Polyamines Induce Resistance to Cationic Peptide Aminoglycoside and Quinolone Antibiotics in Pseudomonas aeruginosa PAO1

机译:多胺诱导铜绿假单胞菌PAO1对阳离子肽氨基糖苷和喹诺酮类抗生素的抗性。

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摘要

Pseudomonas aeruginosa, a gram-negative bacterium of human pathogens, is noted for its environmental versatility, enormous metabolic capacity, and resistance to antibiotics. Overexpression of the outer membrane protein OprH and increased resistance to polycationic peptide antibiotics (e.g., polymyxin B) mediated by the PhoPQ two-component system on induction of a putative lipopolysaccharide (LPS) modification operon (PA3552-PA3559) have been reported as part of the adaptive responses to magnesium limitation in P. aeruginosa. Induction of the oprH-phoPQ operon and the LPS modification operon by exogenous spermidine was revealed from GeneChip analysis during studies of polyamine metabolism and was confirmed by the lacZ fusions of affected promoters. From the results of MIC measurements, it was found that addition of spermidine or other polyamines to the growth medium increased the MIC values of multiple antibiotics, including polycationic antibiotics, aminoglycosides, quinolones, and fluorescent dyes. MIC values of these compounds in the transposon insertion mutants of oprH, phoP, phoQ, and pmrB were also determined in the presence and absence of spermidine. The results showed that the spermidine effect on cationic peptide antibiotic and quinolone resistance was diminished in the phoP mutant only. The spermidine effect on antibiotics was not influenced by magnesium concentrations, as demonstrated by MICs and oprH::lacZ fusion studies in the presence of 20 μM or 2 mM magnesium. Furthermore, in spermidine uptake mutants, MICs of cationic peptide antibiotics and fluorescent dyes, but not of aminoglycosides and quinolones, were increased by spermidine. These results suggested the presence of a complicated molecular mechanism for polyamine-mediated resistance to multiple antibiotics in P. aeruginosa.
机译:铜绿假单胞菌(Pseudomonas aeruginosa)是人类病原菌的革兰氏阴性细菌,因其环境多功能性,巨大的代谢能力和对抗生素的耐药性而闻名。据报道,由PhoPQ两组分系统介导的诱导的脂多糖(LPS)修饰操纵子(PA3552-PA3559)引起的外膜蛋白OprH的过表达和对聚阳离子肽抗生素(例如,多粘菌素B)的耐药性增加是其中一部分。铜绿假单胞菌对镁限制的适应性反应。在多胺代谢研究中,通过GeneChip分析揭示了外源亚精胺对oprH-phoPQ操纵子和LPS修饰操纵子的诱导,并通过受影响启动子的lacZ融合得到证实。从MIC测量的结果发现,向生长培养基中添加亚精胺或其他多胺可增加多种抗生素的MIC值,包括聚阳离子抗生素,氨基糖苷类,喹诺酮类和荧光染料。在存在和不存在亚精胺的情况下,还确​​定了oprH,phoP,phoQ和pmrB转座子插入突变体中这些化合物的MIC值。结果表明,仅在phoP突变体中,亚精胺对阳离子肽抗生素和喹诺酮耐药性的作用减弱。在20μM或2 mM镁存在下,MIC和oprH :: lacZ融合研究证明,亚精胺对抗生素的作用不受镁浓度的影响。此外,在亚精胺摄取突变体中,亚精胺可提高阳离子肽抗生素和荧光染料的MIC,而氨基糖苷和喹诺酮的MIC不增加。这些结果表明存在复杂的分子机制,用于铜绿假单胞菌中多胺介导的对多种抗生素的抗性。

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