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与质粒介导的AmpCβ-内酰胺酶或碳青霉烯酶从肠杆菌科细菌扩散相关的可移动遗传元件:西班牙一项多中心研究的结果

Mobile genetic elements related to the diffusion of plasmid-mediated AmpC β-lactamases or carbapenemases from Enterobacteriaceae: findings from a multicenter study in Spain.

作者信息

Zamorano L, Miró E, Juan C, Gómez L, Bou G, González-López J J, Martínez-Martínez L, Aracil B, Conejo M C, Oliver A, Navarro F

机构信息

Servicio de Microbiología and Unidad de Investigación, Hospital Universitario Son Espases, Instituto de Investigación Sanitaria de Palma (IdISPa), Palma de Mallorca, Spain.

Servei de Microbiologia, Hospital de la Santa Creu i Sant Pau, Institut d'Investigació Biomèdica Sant Pau, Barcelona, Spain.

出版信息

Antimicrob Agents Chemother. 2015 Sep;59(9):5260-6. doi: 10.1128/AAC.00562-15. Epub 2015 Jun 15.

Abstract

We examined the genetic context of 74 acquired ampC genes and 17 carbapenemase genes from 85 of 640 Enterobacteriaceae isolates collected in 2009. Using S1 pulsed-field gel electrophoresis and Southern hybridization, 37 of 74 bla AmpC genes were located on large plasmids of different sizes belonging to six incompatibility groups. We used sequencing and PCR mapping to investigate the regions flanking the acquired ampC genes. The bla CMY-2-like genes were associated with ISEcp1; the surrounding bla DHA genes were similar to Klebsiella pneumoniae plasmid pTN60013 associated with IS26 and the psp and sap operons; and the bla ACC-1 genes were associated with IS26 elements inserted into ISEcp1. All of the carbapenemase genes (bla VIM-1, bla IMP-22, and bla IMP-28) were located in class 1 integrons. Therefore, although plasmids are the main cause of the rapid dissemination of ampC genes among Enterobacteriaceae, we need to be aware that other mobile genetic elements, such as insertion sequences, transposons, or integrons, can be involved in the mobilization of these genes of chromosomal origin. Additionally, three new integrons (In846 to In848) are described in this study.

摘要

我们研究了2009年收集的640株肠杆菌科细菌分离株中85株的74个获得性ampC基因和17个碳青霉烯酶基因的遗传背景。使用S1脉冲场凝胶电泳和Southern杂交,74个bla AmpC基因中的37个位于属于六个不相容群的不同大小的大质粒上。我们使用测序和PCR定位来研究获得性ampC基因侧翼区域。bla CMY-2样基因与ISEcp1相关;周围的bla DHA基因与肺炎克雷伯菌质粒pTN60013相似,该质粒与IS26以及psp和sap操纵子相关;bla ACC-1基因与插入ISEcp1的IS26元件相关。所有碳青霉烯酶基因(bla VIM-1、bla IMP-22和bla IMP-28)都位于1类整合子中。因此,虽然质粒是ampC基因在肠杆菌科细菌中快速传播的主要原因,但我们需要意识到其他移动遗传元件,如插入序列、转座子或整合子,可能参与这些染色体来源基因的移动。此外,本研究描述了三个新的整合子(In846至In848)。

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