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肺炎克雷伯菌中携带 bla KPC-2 的不典型 IncX3 型质粒 pKPC-NY79 的分子特征

Molecular Characterization of an Atypical IncX3 Plasmid pKPC-NY79 Carrying bla KPC-2 in a Klebsiella pneumoniae.

机构信息

Department of Microbiology, Queen Mary Hospital and Carol Yu Centre for Infection, The University of Hong Kong, China.

出版信息

Curr Microbiol. 2013 Oct;67(4):493-8. doi: 10.1007/s00284-013-0398-2. Epub 2013 Jun 1.

Abstract

The IncX family of plasmids has recently been expanded to include at least four subtypes, IncX1-IncX4. The revised classification provides an opportunity for improving our understanding of the sequence diversity of the IncX plasmids and the resistance genes they carried. We described the complete nucleotide sequence of a novel IncX3 plasmid, pKPC-NY79 (42,447 bp) from a sequence-type 258 Klebsiella pneumoniae strain that was isolated from a patient who was hospitalized in New York, United States. In pKPC-NY79, the plasmid scaffold and genetic load region were highly similar to homologous regions in pIncX-SHV (IncX3, JN247852) and the bla KPC carrying pKpQIL (IncFIIk, GU595196), respectively, indicating that it has possibly arisen through recombination of plasmids. The bla KPC-2 gene, as part of a transposon Tn4401a, was found within the genetic load region. The backbone of pKPC-NY79 differs from pIncX-SHV by a deletion involving the gene tandem hns-topB (encoding H-NS protein and topoisomerase III, respectively) and a putative ATPase gene. Unexpectedly, the impact of the hns-topB deletion on host fitness and plasmid stability was found to be small. In conclusion, the findings contribute to a better understanding of the plasmid platforms carrying bla KPC and of variations in the backbone of the IncX3 plasmids.

摘要

IncX 家族质粒最近已扩展到至少包括四个亚型,IncX1-IncX4。修订后的分类为提高我们对 IncX 质粒及其携带的耐药基因序列多样性的理解提供了机会。我们描述了一种新型 IncX3 质粒 pKPC-NY79(42447 bp)的完整核苷酸序列,该质粒来自一位住院于美国纽约的患者的序列型 258 肺炎克雷伯菌。在 pKPC-NY79 中,质粒支架和遗传负荷区与 pIncX-SHV(IncX3,JN247852)和携带 bla KPC 的 pKpQIL(IncFIIk,GU595196)的同源区域高度相似,表明它可能是通过质粒重组产生的。bla KPC-2 基因作为转座子 Tn4401a 的一部分,位于遗传负荷区内。pKPC-NY79 的骨架与 pIncX-SHV 的不同之处在于基因串联 hns-topB(分别编码 H-NS 蛋白和拓扑异构酶 III)和一个假定的 ATP 酶基因缺失。出人意料的是,hns-topB 缺失对宿主适应性和质粒稳定性的影响很小。总之,这些发现有助于更好地理解携带 bla KPC 的质粒平台以及 IncX3 质粒骨架的变异。

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