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首页> 外文期刊>Antimicrobial agents and chemotherapy. >International spread and persistence of TEM-24 is caused by the confluence of highly penetrating enterobacteriaceae clones and an IncA/C2 plasmid containing Tn1696::Tn1 and IS5075-Tn21.
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International spread and persistence of TEM-24 is caused by the confluence of highly penetrating enterobacteriaceae clones and an IncA/C2 plasmid containing Tn1696::Tn1 and IS5075-Tn21.

机译:TEM-24的国际传播和持久性是由高渗透性肠杆菌科克隆与含有Tn1696 :: Tn1和IS5075-Tn21的IncA / C2质粒的融合所引起的。

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摘要

TEM-24 remains one of the most widespread TEM-type extended-spectrum beta-lactamases (ESBLs) among Enterobacteriaceae. To analyze the reasons influencing its spread and persistence, a multilevel population genetics study was carried out on 28 representative TEM-24 producers from Belgium, France, Portugal, and Spain (13 Enterobacter aerogenes isolates, 6 Escherichia coli isolates, 6 Klebsiella pneumoniae isolates, 2 Proteus mirabilis isolates, and 1 Klebsiella oxytoca isolate, from 1998 to 2004). Clonal relatedness (XbaI pulsed-field gel electrophoresis [PFGE] and E. coli phylogroups) and antibiotic susceptibility were determined by standard procedures. Plasmid analysis included determination of the incompatibility group (by PCR, hybridization, and/or sequencing) and comparison of restriction fragment length polymorphism (RFLP) patterns. Characterization of genetic elements conferring antibiotic resistance included integrons (classes 1, 2, and 3) and transposons (Tn3, Tn21, and Tn402). Similar PFGE patterns were identified among E. aerogenes, K. pneumoniae, and P. mirabilis isolates, while E. coli strains were diverse (phylogenetic groups A, B2, and D). Highly related 180-kb IncA/C2 plasmids conferring resistance to kanamycin, tobramycin, chloramphenicol, trimethoprim, and sulfonamides were identified. Each plasmid contained defective In0-Tn402 (dfrA1-aadA1, aacA4, or aacA4-aacC1-orfE-aadA2-cmlA1) and In4-Tn402 (aacA4 or dfrA1-aadA1) variants. These integrons were located within Tn21, Tn1696, or hybrids of these transposons, with IS5075 interrupting their IRtnp and IRmer. In all cases, blaTEM-24 was part of an IS5075-DeltaTn1 transposon within tnp1696, mimicking other genetic elements containing blaTEM-2 and blaTEM-3 variants. The international dissemination of TEM-24 is fuelled by an IncA/C2 plasmid acquired by different enterobacterial clones which seem to evolve by gaining diverse genetic elements. This work highlights the risks of a confluence between highly penetrating clones and highly promiscuous plasmids in the spread of antibiotic resistance, and it contributes to the elucidation of the origin and evolution of TEM-2 ESBL derivatives.
机译:TEM-24仍然是肠杆菌科中最广泛的TEM型超光谱β-内酰胺酶(ESBLs)之一。为了分析影响其传播和持久性的原因,我们对来自比利时,法国,葡萄牙和西班牙的28家代表性TEM-24生产者进行了多层次的群体遗传学研究(13株产气肠杆菌,6株大肠杆菌,6株肺炎克雷伯菌,从1998年到2004年,共有2株奇异变形杆菌和1株产酸克雷伯菌。通过标准程序确定克隆相关性(XbaI脉冲场凝胶电泳[PFGE]和大肠杆菌系统群)和抗生素敏感性。质粒分析包括确定不相容性基团(通过PCR,杂交和/或测序),并比较限制性片段长度多态性(RFLP)模式。赋予抗生素抗性的遗传元件的表征包括整合素(1、2和3类)和转座子(Tn3,Tn21和Tn402)。在产气大肠杆菌,肺炎克雷伯氏菌和奇异疟原虫的分离物中也发现了相似的PFGE模式,而大肠杆菌菌株则多种多样(系统发生组A,B2和D)。确定了高度相关的180 kb IncA / C2质粒,这些质粒赋予了对卡那霉素,妥布霉素,氯霉素,甲氧苄啶和磺酰胺类药物的抗性。每个质粒均包含有缺陷的In0-Tn402(dfrA1-aadA1,aacA4或aacA4-aacC1-orfE-aadA2-cmlA1)和In4-Tn402(aacA4或dfrA1-aadA1)变体。这些整合素位于Tn21,Tn1696或这些转座子的杂种内,IS5075中断了它们的IRtnp和IRmer。在所有情况下,blaTEM-24都是tnp1696中IS5075-DeltaTn1转座子的一部分,模仿了其他包含blaTEM-2和blaTEM-3变体的遗传元件。 TEM-24的国际传播是由不同肠道细菌克隆获得的IncA / C2质粒推动的,该克隆似乎通过获得多种遗传成分而进化。这项工作突出了高穿透力克隆和高度混杂的质粒在抗生素耐药性扩散中融合的风险,并且有助于阐明TEM-2 ESBL衍生物的起源和进化。

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