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首页> 外文期刊>Journal of Clinical Microbiology >Characterization of a Large Outbreak by CTX-M-1-Producing Klebsiella pneumoniae and Mechanisms Leading to In Vivo Carbapenem Resistance Development
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Characterization of a Large Outbreak by CTX-M-1-Producing Klebsiella pneumoniae and Mechanisms Leading to In Vivo Carbapenem Resistance Development

机译:产生CTX-M-1的肺炎克雷伯菌的大规模暴发的特征及其导致体内碳青霉烯耐药性发展的机制

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All extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae isolates from patients admitted to and adult intensive care unit were prospectively documented from 2002 to 2005, when a large outbreak (51 patients affected) of multiresistant ESBL-producing Klebsiella pneumoniae infection was detected. The involvement of a single K. pneumoniae clone was demonstrated by pulsed-field gel electrophoresis. In addition to the ESBL-mediated resistance, the epidemic strain uniformly showed cross-resistance to ciprofloxacin, gentamicin, tobramycin, trimethoprim-sulfamethoxazole, and tetracycline, whereas resistance to the β-lactam-β-lactamase inhibitor combinations was variable. The ESBL involved was CTX-M-1, as demonstrated by isoelectric focusing, PCR amplification, and sequencing. CTX-M-1 as well as the aminoglycoside resistance determinants were encoded in a 50-kb plasmid that could be transferred to Escherichia coli only by transformation. In two of the infected patients, carbapenem resistance development (MICs of 8 to 12, 16, and >32 μg/ml for imipenem, meropenem, and ertapenem, respectively) was documented, both in clinical samples and in intestinal colonization studies. The analysis of the outer membrane proteins of the carbapenem-susceptible and -resistant isolates revealed that the former expressed only one of the two major porins, OmpK36, whereas the latter did not express either of them. In one of the cases, the lack of expression of OmpK36 was demonstrated to be mediated by the interruption of the coding sequence by the insertion sequence IS26. This is the first report of a large outbreak of CTX-M-1-producing Enterobacteriaceae and, curiously, the first documented description in the literature of CTX-M-1 in K. pneumoniae, despite the fact that this enzyme has been found in multiple species. Furthermore, we document and characterize for the first time carbapenem resistance development in CTX-M-1-producing Enterobacteriaceae.
机译:从2002年至2005年,前瞻性地记录了2002年至2005年所有入院和成人重症监护病房患者的所有产生超广谱β-内酰胺酶(ESBL)的肠杆菌科菌株,当时多发抗药性ESBL大爆发(影响51例)检测到产肺炎克雷伯菌感染。单个 K的参与。脉冲场凝胶电泳证实了肺炎克雷伯菌的克隆。除了ESBL介导的抗药性外,该流行株还对环丙沙星,庆大霉素,妥布霉素,甲氧苄氨嘧啶-磺胺甲基恶唑和四环素具有交叉耐药性,而对β-内酰胺-β-内酰胺酶抑制剂的耐药性则各不相同。等电聚焦,PCR扩增和测序证实了所涉及的ESBL是CTX-M-1。 CTX-M-1以及氨基糖苷抗性决定簇被编码在一个50kb的质粒中,该质粒只能通过转化才能转移到大肠杆菌中。在两名感染患者中,在临床样本和肠道定植研究中均记录了碳青霉烯耐药性的发展(亚胺培南,美罗培南和厄他培南的MIC分别为8至12、16和> 32μg/ ml)。对碳青霉烯易感和耐药菌株的外膜蛋白的分析表明,前者仅表达两种主要孔蛋白之一,即OmpK36,而后者则不表达两种蛋白。在一种情况下,OmpK36表达的缺乏被证明是由于插入序列IS 26 中断了编码序列而引起的。这是关于大量生产CTX-M-1的肠杆菌科的首次报道,而且奇怪的是,这是Cem-K-1文献中在 K中首次记载的描述。肺炎,尽管该酶已在多种物种中发现。此外,我们首次记录并鉴定了产生CTX-M-1的肠杆菌科对碳青霉烯类药物的耐药性。

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