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CTX-M-15 型超广谱β-内酰胺酶产生肺炎克雷伯菌在波斯尼亚和黑塞哥维那的出现。

Emergence of CTX-M-15 extended-spectrum beta-lactamase-producing Klebsiella pneumoniae isolates in Bosnia and Herzegovina.

机构信息

Institute of Clinical Microbiology, University of Sarajevo Clinics Centre, Sarajevo, Bosnia and Herzegovina.

出版信息

Clin Microbiol Infect. 2010 Feb;16(2):152-6. doi: 10.1111/j.1469-0691.2009.03018.x. Epub 2009 Aug 17.

Abstract

Fifty-seven nosocomial Klebsiella pneumoniae isolates producing extended-spectrum beta-lactamases (ESBLs) were collected between February 2007 and November 2007 in different wards of the Sarajevo (Bosnia-Herzegovina) reference hospital. These isolates comprise two major epidemic pulsed-field electrophoresis-defined clones plus two minor clones. In addition to the ESBL-mediated resistance, all strains uniformly showed resistance to ciprofloxacin, gentamicin and tobramycin. The beta-lactamases involved in this resistance phenotype were TEM-1, SHV-1, and CTX-M-15, as demonstrated by isoelectric focusing, PCR amplification, and sequencing. TEM-1 and CTX-M-15 beta-lactamases, as well as the aminoglycoside resistance determinants, were encoded in plasmids that could be transferred to Escherichia coli by conjugation. In three of the infected patients with the predominant clone, cefoxitin resistance development (MICs >128 mg/L) was documented. The analysis of the outer membrane proteins of the cefoxitin-susceptible and cefoxitin-resistant isolates revealed that the former expressed only one of the two major porins, OmpK36, whereas in the latter, the expression of Ompk36 was altered or abolished. This is the first report of CTX-M-15-producing K. pneumoniae in Bosnia-Herzegovina. Furthermore, we document and characterize for the first time cefoxitin resistance development in CTX-M-15-producing K. pneumoniae.

摘要

2007 年 2 月至 11 月期间,在萨拉热窝(波斯尼亚和黑塞哥维那)参考医院的不同病房中收集了 57 株产生超广谱β-内酰胺酶(ESBL)的医院内肺炎克雷伯菌分离株。这些分离株由两个主要的脉冲场电泳定义的克隆加上两个次要克隆组成。除了 ESBL 介导的耐药性外,所有菌株均均匀地对环丙沙星、庆大霉素和妥布霉素表现出耐药性。通过等电聚焦、PCR 扩增和测序证明,这种耐药表型涉及 TEM-1、SHV-1 和 CTX-M-15 型β-内酰胺酶。TEM-1 和 CTX-M-15 型β-内酰胺酶以及氨基糖苷类耐药决定簇均编码在质粒中,可通过接合转移到大肠杆菌。在三个主要克隆感染的患者中,有记录表明头孢西丁耐药性发展(MICs>128mg/L)。对头孢西丁敏感和头孢西丁耐药分离株的外膜蛋白分析表明,前者仅表达两种主要孔蛋白之一,即 OmpK36,而后者的 OmpK36 表达发生改变或被消除。这是波斯尼亚和黑塞哥维那首次报道 CTX-M-15 型肺炎克雷伯菌。此外,我们首次记录并描述了 CTX-M-15 型肺炎克雷伯菌头孢西丁耐药性的发展。

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