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日本产超广谱β-内酰胺酶大肠埃希菌中质粒介导的AmpC β-内酰胺酶产生菌的流行情况和 ST131 克隆的传播。

Prevalence of plasmid-mediated AmpC β-lactamase-producing Escherichia coli and spread of the ST131 clone among extended-spectrum β-lactamase-producing E. coli in Japan.

机构信息

Department of Clinical Laboratory Medicine, Kyoto University Graduate School of Medicine, 54 Shogoin Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan.

出版信息

Int J Antimicrob Agents. 2012 Aug;40(2):158-62. doi: 10.1016/j.ijantimicag.2012.04.013. Epub 2012 Jun 27.

DOI:10.1016/j.ijantimicag.2012.04.013
PMID:22743014
Abstract

In 2010, a total of 1327 clinical Escherichia coli isolates from five hospitals in the Kyoto and Shiga regions of Japan were analysed by PCR. The prevalences of plasmid-mediated AmpC β-lactamase (pAmpC)-producers, extended-spectrum β-lactamase (ESBL)-producers and co-producers of pAmpC and ESBL were 1.7%, 9.7% and 0.3%, respectively. Less than one-half of the pAmpC-producers were reported to be resistant to third-generation cephalosporins, cephamycins and β-lactam/β-lactam inhibitors using the old 2009 Clinical and Laboratory Standards Institute (CLSI) breakpoints. CMY-2 was the most prevalent pAmpC type (95%), and CTX-M-14 (38%), CTX-M-15 (26%) and CTX-M-27 (19%) were the most prevalent ESBL types. The worldwide O25b-ST131-B2 clone accounted for 11% of pAmpC-producers and 41% of ESBL-producers. The O25b-ST131-B2 clone was characterised by a CTX-M-27- or CTX-M-15-type ESBL and ciprofloxacin-non-susceptibility with quadruple mutations in the quinolone resistance-determining regions (S83L and D87N in GyrA and S80I and E84V in ParC). A significant proportion of pAmpC-producers and the O25b-ST131-B2 clone were found in Japan by a recent regional surveillance programme.

摘要

2010 年,对来自日本京都和滋贺地区的五家医院的 1327 株临床大肠埃希菌进行了 PCR 分析。质粒介导的 AmpCβ-内酰胺酶(pAmpC)-生产者、超广谱β-内酰胺酶(ESBL)-生产者和 pAmpC 和 ESBL 共同生产者的流行率分别为 1.7%、9.7%和 0.3%。不到一半的 pAmpC-生产者对第三代头孢菌素、头孢菌素和β-内酰胺/β-内酰胺抑制剂具有耐药性,使用的是旧的 2009 年临床和实验室标准协会(CLSI)断点。CMY-2 是最常见的 pAmpC 型(95%),CTX-M-14(38%)、CTX-M-15(26%)和 CTX-M-27(19%)是最常见的 ESBL 型。全球 O25b-ST131-B2 克隆占 pAmpC 生产者的 11%和 ESBL 生产者的 41%。O25b-ST131-B2 克隆的特点是 CTX-M-27 或 CTX-M-15 型 ESBL 和喹诺酮类药物耐药决定区(GyrA 中的 S83L 和 D87N 和 ParC 中的 S80I 和 E84V)中的四重突变导致环丙沙星不敏感。最近的区域监测计划在日本发现了相当比例的 pAmpC 生产者和 O25b-ST131-B2 克隆。

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