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Carbapenemases in Klebsiella pneumoniae and other Enterobacteriaceae: an evolving crisis of global dimensions.肺炎克雷伯菌和其他肠杆菌科细菌中的碳青霉烯酶:具有全球范围的不断演变的危机。
Clin Microbiol Rev. 2012 Oct;25(4):682-707. doi: 10.1128/CMR.05035-11.
2
Outbreak of Klebsiella pneumoniae carbapenemase-2-producing K. pneumoniae sequence type 11 in Taiwan in 2011.2011 年中国台湾地区爆发产碳青霉烯酶肺炎克雷伯菌碳青霉烯酶 2 的肺炎克雷伯菌 11 型序列。
Antimicrob Agents Chemother. 2012 Oct;56(10):5016-22. doi: 10.1128/AAC.00878-12. Epub 2012 Jul 16.
3
Features of infections due to Klebsiella pneumoniae carbapenemase-producing Escherichia coli: emergence of sequence type 131.产碳青霉烯酶肺炎克雷伯菌所致感染的特征:序列型 131 的出现。
Clin Infect Dis. 2012 Jul;55(2):224-31. doi: 10.1093/cid/cis387. Epub 2012 Apr 4.
4
Emergence of Proteus mirabilis harboring blaKPC-2 and qnrD in a Chinese Hospital.中国某医院出现产碳青霉烯酶肺炎克雷伯菌(携带 blaKPC-2 和 qnrD)。
Antimicrob Agents Chemother. 2012 May;56(5):2278-82. doi: 10.1128/AAC.05519-11. Epub 2012 Feb 21.
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Emergence of Escherichia coli sequence type 410 (ST410) with KPC-2 β-lactamase.产 KPC-2 型β-内酰胺酶的大肠杆菌序列型 410(ST410)的出现。
Int J Antimicrob Agents. 2012 Mar;39(3):247-50. doi: 10.1016/j.ijantimicag.2011.11.003. Epub 2012 Jan 9.
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Production of KPC-2 carbapenemase by an Escherichia coli clinical isolate belonging to the international ST131 clone.一株属于国际ST131克隆的大肠埃希菌临床分离株产KPC-2碳青霉烯酶。
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When carbapenem-hydrolyzing beta-lactamase Kpc meets Escherichia coli ST131 in France.当碳青霉烯水解β-内酰胺酶Kpc在法国遇上大肠杆菌ST131 。
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ST11, the dominant clone of KPC-producing Klebsiella pneumoniae in China.ST11,中国产 KPC 肺炎克雷伯菌的优势克隆。
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中国产 KPC-2 碳青霉烯酶的大肠杆菌序列型 131 分离株的出现。

Emergence of Escherichia coli sequence type 131 isolates producing KPC-2 carbapenemase in China.

机构信息

2nd Affiliated Hospital of Zhejiang University, Zhejiang University, Hangzhou, People's Republic of China.

出版信息

Antimicrob Agents Chemother. 2014;58(2):1146-52. doi: 10.1128/AAC.00912-13. Epub 2013 Dec 9.

DOI:10.1128/AAC.00912-13
PMID:24323475
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3910876/
Abstract

Twenty-two KPC-2-producing Escherichia coli isolates were obtained from three hospitals in Hangzhou, China, from 2007 to 2011. One isolate, with OmpC porin deficiency, exhibited high-level carbapenem resistance. Pulsed-field gel electrophoresis showed that few isolates were indistinguishable or closely related. Multilocus sequence typing indicated that sequence type 131 (ST131) was the predominant type (9 isolates, 40.9%), followed by ST648 (5 isolates), ST405 (2 isolates), ST38 (2 isolates), and 4 single STs, ST69, ST2003, ST2179, and ST744. Phylogenetic analysis indicated that 9 group B2 isolates belonged to ST131, and 5 of 11 group D isolates belonged to ST648. Only one group B1 isolate and one group A isolate were identified. A representative plasmid (pE1) was partially sequenced, and a 7,788-bp DNA fragment encoding Tn3 transposase, Tn3 resolvase, ISKpn8 transposase, KPC-2, and ISKpn6-like transposase was obtained. The blaKPC-2-surrounding sequence was amplified by a series of primers. The PCR results showed that 13 isolates were consistent with the genetic environment in pE1. It is the first report of rapid emergence of KPC-2-producing E. coli ST131 in China. The blaKPC-2 gene of most isolates was located on a similar genetic structure.

摘要

2007 年至 2011 年,从中国杭州的三家医院中分离到 22 株产 KPC-2 的大肠杆菌。其中一个分离株 OmpC 孔蛋白缺失,表现出高水平的碳青霉烯类耐药性。脉冲场凝胶电泳显示,少数分离株无法区分或密切相关。多位点序列分型表明,主要型别为 131 型(9 株,占 40.9%),其次是 648 型(5 株)、405 型(2 株)、38 型(2 株)和 4 个单型别,69 型、2003 型、2179 型和 744 型。系统进化分析表明,9 株 B2 组分离株属于 131 型,11 株 D 组分离株中有 5 株属于 648 型。只鉴定出 1 株 B1 组和 1 株 A 组分离株。部分测序了一个代表性质粒(pE1),获得了一个编码 Tn3 转座酶、Tn3 解旋酶、ISKpn8 转座酶、KPC-2 和 ISKpn6 样转座酶的 7788bp DNA 片段。通过一系列引物扩增 blaKPC-2 周围序列。PCR 结果表明,13 株分离株与 pE1 中的遗传环境一致。这是中国首例快速出现的产 KPC-2 的大肠杆菌 131 型。大多数分离株的 blaKPC-2 基因位于类似的遗传结构上。