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从纽约市一家医院分离出的克雷伯氏菌菌株质粒上 blaKPC 碳青霉烯酶基因周围转座酶区域的基因组织。

Genetic organization of transposase regions surrounding blaKPC carbapenemase genes on plasmids from Klebsiella strains isolated in a New York City hospital.

作者信息

Gootz Thomas D, Lescoe Mary Kay, Dib-Hajj Fadia, Dougherty Brian A, He Wen, Della-Latta Phyllis, Huard Richard C

机构信息

Department of Infectious Diseases, Pfizer Global Research and Development, Groton, CT 06340, USA.

出版信息

Antimicrob Agents Chemother. 2009 May;53(5):1998-2004. doi: 10.1128/AAC.01355-08. Epub 2009 Mar 2.

Abstract

Carbapenem-resistant Klebsiella strains carrying Klebsiella pneumoniae carbapenemases (KPC) are endemic to New York City and are spreading across the United States and internationally. Recent studies have indicated that the KPC structural gene is located on a 10-kb plasmid-borne element designated Tn4401. Fourteen Klebsiella pneumoniae strains and one Klebsiella oxytoca strain isolated at a New York City hospital in 2005 carrying either bla(KPC-2) or bla(KPC-3) were examined for isoforms of Tn4401. Ten of the Klebsiella strains contained a 100-bp deletion in Tn4401, corresponding to the Tn4401a isoform. The presence of this deletion adjacent to the upstream promoter region of bla(KPC) in Tn4401a resulted in a different -35 promoter sequence of TGGAGA than that of CTGATT present in isoform Tn4401b. Complete sequencing of one plasmid carrying bla(KPC) from each of three nonclonal isolates indicated the presence of genes encoding other types of antibiotic resistance determinants. The 70.6-kb plasmid from K. pneumoniae strain S9 carrying bla(KPC-2) revealed two identical copies of Tn4401b inserted in an inverse fashion, but in this case, one of the elements disrupted a group II self-splicing intron. In K. pneumoniae strain S15, the Tn4401a element carrying bla(KPC-2) was found on both a large 120-kb plasmid and a smaller 24-kb plasmid. Pulsed-field gel electrophoresis results indicate that the isolates studied represent a heterogeneous group composed of unrelated as well as closely related Klebsiella strains. Our results suggest that endemic KPC-positive Klebsiella strains constitute a generally nonclonal population comprised of various alleles of bla(KPC) on several distinct plasmid genetic backgrounds. This study increases our understanding of the genetic composition of the evolving and expanding role of KPC-producing, healthcare-associated, gram-negative pathogens.

摘要

携带肺炎克雷伯菌碳青霉烯酶(KPC)的耐碳青霉烯类克雷伯菌菌株在纽约市呈地方性流行,并正在美国和国际上传播。最近的研究表明,KPC结构基因位于一个10kb的质粒携带元件上,命名为Tn4401。对2005年在纽约市一家医院分离出的14株肺炎克雷伯菌菌株和1株产酸克雷伯菌菌株进行了检测,这些菌株携带bla(KPC-2)或bla(KPC-3),以确定Tn4401的亚型。其中10株克雷伯菌菌株的Tn4401中存在一个100bp的缺失,对应于Tn4401a亚型。在Tn4401a中,该缺失位于bla(KPC)上游启动子区域附近,导致其-35启动子序列为TGGAGA,与Tn4401b亚型中的CTGATT不同。对来自三个非克隆分离株的携带bla(KPC)的一个质粒进行全序列分析,结果表明存在编码其他类型抗生素抗性决定簇的基因。肺炎克雷伯菌菌株S9携带bla(KPC-2)的70.6kb质粒显示有两个以反向方式插入的相同的Tn4401b拷贝,但在这种情况下,其中一个元件破坏了一个II类自我剪接内含子。在肺炎克雷伯菌菌株S15中,携带bla(KPC-2)的Tn4401a元件存在于一个120kb的大质粒和一个24kb的小质粒上。脉冲场凝胶电泳结果表明,所研究的分离株代表了一个异质群体,由不相关以及密切相关的克雷伯菌菌株组成。我们的结果表明,地方性KPC阳性克雷伯菌菌株构成了一个通常非克隆的群体,由几种不同质粒遗传背景上的bla(KPC)的各种等位基因组成。这项研究增进了我们对产生KPC的、与医疗保健相关的革兰氏阴性病原体不断演变和扩大的作用的遗传组成的理解。

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