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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Plasmid typing and genetic context of AmpC β-lactamases in Enterobacteriaceae lacking inducible chromosomal ampC genes: findings from a Spanish hospital 1999-2007.
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Plasmid typing and genetic context of AmpC β-lactamases in Enterobacteriaceae lacking inducible chromosomal ampC genes: findings from a Spanish hospital 1999-2007.

机译:缺乏可诱导的染色体ampC基因的肠杆菌科细菌中AmpCβ-内酰胺酶的质粒分型和遗传背景:来自西班牙一家医院的发现1999-2007。

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摘要

To gain insights into ampC transmission between bacterial strains.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.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.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.
机译:为了深入了解细菌之间的ampC传播。我们检查了1999年至2007年间从27119肠杆菌科收集的117个ampC基因的遗传背景。质粒分析通过基于PCR的复制子或松弛酶分型,S1-PFGE和Southern杂交进行。 I-CeuI / PFGE用于未通过质粒分析表征的分离株。 PCR反应用于绘制ampC基因的遗传结构图谱。在研究的分离物中,有81.2%的ampC基因位于已知的Inc / MOB组的质粒上,有7.7%位于染色体上,未确定11.1%。 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)质粒连接; bla(CMY-27)与IncF和MOB(P12)质粒相关;携带bla(CMY-25)的质粒无法分型,并且bla(CMY-40)位于染色体上。带有bla(CMY-2),bla(CMY-4),bla(CMY-25),bla(CMY-27),bla(CMY-40)或bla(ACC-1)的所有87个分离株均表现出类似转座子的形式结构ISEcp1 /ΔISEcp1-bla(CMY)-blc-sugE或ΔISEcp1-bla(ACC-1)-gdha。 bla(DHA-1)中最普遍的结构(占病例的93.3%)与肺炎克雷伯菌pTN60013质粒中描述的结构相同。值得注意的是,在三个含有bla(CMY-2)染色体的分离株中,该基因是通过结合而动员的。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的遗传元件,例如整合接合因子(ICE)可能参与这些基因的动员。

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