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1999-2007 年西班牙某医院缺乏可诱导染色体 ampC 基因的肠杆菌科细菌中 AmpC β-内酰胺酶的质粒分型和遗传结构

Plasmid typing and genetic context of AmpC β-lactamases in Enterobacteriaceae lacking inducible chromosomal ampC genes: findings from a Spanish hospital 1999-2007.

机构信息

Servei de Microbiologia, Hospital de Santa Creu i Sant Pau, Departament de Genètica i de Microbiologia, Universitat Autònoma de Barcelona, Institut d'Investigacions Biomèdiques Sant Pau, Barcelona, Spain.

出版信息

J Antimicrob Chemother. 2012 Jan;67(1):115-22. doi: 10.1093/jac/dkr412. Epub 2011 Oct 6.

Abstract

OBJECTIVES

To gain insights into ampC transmission between bacterial strains.

METHODS

We examined the genetic context of 117 acquired ampC genes from 27119 Enterobacteriaceae collected between 1999 and 2007. Plasmid analysis was carried out by PCR-based replicon or relaxase typing, S1-PFGE and Southern hybridization. I-CeuI/PFGE was used for isolates not characterized by plasmid analysis. PCR reactions were used to map the genetic organization of the ampC genes.

RESULTS

Among the isolates studied, 81.2% of ampC genes were located on plasmids of known Inc/MOB groups, 7.7% were chromosomally located and 11.1% were not determined. A/C, I1 and K were the most commonly found replicons in plasmids carrying bla(CMY-2), while L/M replicons were associated with bla(DHA-1). bla(ACC-1) was linked to I1 and MOB(F11) plasmids; bla(CMY-27) was associated with IncF and MOB(P12) plasmids; the plasmid carrying bla(CMY-25) could not be typed, and bla(CMY-40) was chromosomally located. All 87 isolates carrying bla(CMY-2), bla(CMY-4), bla(CMY-25), bla(CMY-27), bla(CMY-40) or bla(ACC-1) displayed the transposon-like structures ISEcp1/ΔISEcp1-bla(CMY)-blc-sugE or ΔISEcp1-bla(ACC-1)-gdha. The most prevalent structure in bla(DHA-1) (93.3% of cases) was identical to that described in the Klebsiella pneumoniae pTN60013 plasmid. Remarkably, in three isolates containing chromosomal bla(CMY-2), this gene was mobilized by conjugation.

CONCLUSIONS

Although plasmids are the main cause of the rapid dissemination of ampC genes among bacteria, we need to be aware that other mobile genetic elements such as integrative and conjugative elements (ICEs) can be involved in the mobilization of these genes.

摘要

目的

深入了解细菌株之间的ampC 传递。

方法

我们研究了 1999 年至 2007 年间收集的 27119 株肠杆菌科中 117 个获得的 ampC 基因的遗传背景。通过基于 PCR 的复制子或松弛酶分型、S1-PFGE 和 Southern 杂交进行质粒分析。对于未通过质粒分析进行表征的分离株,使用 I-CeuI/PFGE。PCR 反应用于绘制 ampC 基因的遗传组织。

结果

在所研究的分离株中,81.2%的 ampC 基因位于已知 Inc/MOB 组的质粒上,7.7%位于染色体上,11.1%未确定。A/C、I1 和 K 是携带 bla(CMY-2)的质粒中最常见的复制子,而 L/M 复制子与 bla(DHA-1)相关。bla(ACC-1)与 I1 和 MOB(F11)质粒相连;bla(CMY-27)与 IncF 和 MOB(P12)质粒相关;携带 bla(CMY-25)的质粒无法分型,bla(CMY-40)位于染色体上。所有携带 bla(CMY-2)、bla(CMY-4)、bla(CMY-25)、bla(CMY-27)、bla(CMY-40)或 bla(ACC-1)的 87 株分离株均显示转座子样结构 ISEcp1/ΔISEcp1-bla(CMY)-blc-sugE 或 ΔISEcp1-bla(ACC-1)-gdha。bla(DHA-1)中最常见的结构(93.3%的病例)与 Klebsiella pneumoniae pTN60013 质粒中描述的结构相同。值得注意的是,在三个含有染色体 bla(CMY-2)的分离株中,该基因通过共轭转移。

结论

尽管质粒是 ampC 基因在细菌中快速传播的主要原因,但我们需要意识到,其他可移动遗传元件,如整合和共轭元件 (ICEs),也可能参与这些基因的转移。

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