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对 BfT-GermVet 研究中分离的携带 bla(CTX-M)质粒的大肠杆菌进行分析。

Analysis of bla(CTX-M)-carrying plasmids from Escherichia coli isolates collected in the BfT-GermVet study.

机构信息

Institute of Farm Animal Genetics, Friedrich-Loeffler-Institut (FLI), Neustadt-Mariensee, Germany.

出版信息

Appl Environ Microbiol. 2011 Oct;77(20):7142-6. doi: 10.1128/AEM.00559-11. Epub 2011 Jun 17.

Abstract

In this study, 417 Escherichia coli isolates from defined disease conditions of companion and farm animals collected in the BfT-GermVet study were investigated for the presence of extended-spectrum β-lactamase (ESBL) genes. Three ESBL-producing E. coli isolates were identified among the 100 ampicillin-resistant isolates. The E. coli isolates 168 and 246, of canine and porcine origins, respectively, harbored bla(CTX-M-1), and the canine isolate 913 harbored bla(CTX-M-15), as confirmed by PCR and sequence analysis. The isolates 168 and 246 belonged to the novel multilocus sequence typing (MLST) types ST1576 and ST1153, respectively, while isolate 913 had the MLST type ST410. The ESBL genes were located on structurally related IncN plasmids in isolates 168 and 246 and on an IncF plasmid in isolate 913. The bla(CTX-M-1) upstream regions of plasmids pCTX168 and pCTX246 were similar, whereas the downstream regions showed structural differences. The genetic environment of the bla(CTX-M-15) gene on plasmid pCTX913 differed distinctly from that of both bla(CTX-M-1) genes. Detailed sequence analysis showed that the integration of insertion sequences, as well as interplasmid recombination events, accounted for the structural variability in the bla(CTX-M) gene regions.

摘要

在本研究中,对来自伴侣动物和农场动物特定疾病状况的 417 株大肠杆菌分离株进行了研究,以调查其是否存在扩展谱β-内酰胺酶(ESBL)基因。在 100 株氨苄青霉素耐药分离株中,鉴定出了 3 株产 ESBL 的大肠杆菌分离株。来自犬和猪的大肠杆菌分离株 168 和 246 分别携带 bla(CTX-M-1),而来自犬的分离株 913 携带 bla(CTX-M-15),这通过 PCR 和序列分析得到了证实。分离株 168 和 246 分别属于新型多位点序列分型(MLST)类型 ST1576 和 ST1153,而分离株 913 的 MLST 类型为 ST410。ESBL 基因位于分离株 168 和 246 中的结构相关 IncN 质粒上,而分离株 913 中的 ESBL 基因位于 IncF 质粒上。质粒 pCTX168 和 pCTX246 的 bla(CTX-M-1)上游区域相似,而下游区域则存在结构差异。质粒 pCTX913 上 bla(CTX-M-15)基因的遗传环境与 bla(CTX-M-1)基因明显不同。详细的序列分析表明,插入序列的整合以及质粒间重组事件导致了 bla(CTX-M)基因区域的结构变异性。

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