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Expression of the MexXY-OprM efflux system in Pseudomonas aeruginosa with discordant cefepime/ceftazidime susceptibility profiles

机译:MexXY-OprM外排系统在铜绿假单胞菌中头孢吡肟/头孢他啶敏感性分布不协调

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摘要

While MIC distributions and percent susceptibility for cefepime and ceftazidime are generally similar among Pseudomonas aeruginosa, we noted an increasing discordance in susceptibility favoring ceftazidime at our hospital. Quantitative reverse transcriptase-polymerase chain reaction was utilized to explore overexpression of the MexXY-OprM efflux as the mechanism for this phenotype profile. Thirteen of 15 (87%) randomly selected isolates had mexY gene expression levels of 5.8–40.8-fold relative to the wild-type reference strain. While mexY overexpression was noted in the majority of isolates, other resistance mechanisms appear to contribute to the observed phenotypic profile of the Pseudomonas aeruginosa studied. Clinicians must understand not only the magnitude of difference in the MIC profiles between agents, but also the mechanism(s) responsible for these observations if strategies (ie, pharmacodynamic dosing) are to be designed to optimize patient care outcomes in the face of increasing resistance.
机译:虽然铜绿假单胞菌的头孢吡肟和头孢他啶的MIC分布和敏感性百分比通常相似,但我们注意到在我们医院,对头孢他啶的敏感性差异越来越大。定量逆转录酶-聚合酶链反应被用来探索MexXY-OprM外排的过表达作为这种表型概况的机制。相对于野生参考菌株,随机选择的15个菌株中有13个(87%)的mexY基因表达水平是5.8–40.8倍。尽管在大多数分离株中发现了mexY过表达,但其他耐药机制似乎也有助于观察到的铜绿假单胞菌的表型分布。如果要设计策略(即药效剂量)以在面对耐药性增加的情况下优化患者护理结果,则临床医生不仅必须了解药物之间MIC谱差异的大小,而且还必须了解引起这些观察的机制。 。

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