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首页> 外文期刊>Microbial drug resistance: MDR : Mechanisms, epidemiology, and disease >IncI1 plasmids carrying blaCTX-M-1or blaCMY-2genes in Escherichia coli from healthy humans and animals in Tunisia
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IncI1 plasmids carrying blaCTX-M-1or blaCMY-2genes in Escherichia coli from healthy humans and animals in Tunisia

机译:来自突尼斯健康人和动物的大肠杆菌中带有blaCTX-M-1或blaCMY-2基因的IncI1质粒

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摘要

The objective was to determine the location of blaCTX-M-1and blaCMY-2genes in 33 Escherichia coli isolates previously obtained from healthy humans, pets, and food-producing animals in Tunisia, and to characterize the genetic lineages of isolates. Molecular typing was performed by pulsed-field gel electrophoresis (PFGE)-XbaI and multilocus sequence typing (MLST). Plasmids were analyzed by S1-PFGE, polymerase chain reaction-based replicon typing, and plasmid MLST. Conjugation experiments were performed. The blaCTX-M-1and blaCMY-2genes were studied by I-Ceu1-PFGE and S1-PFGE, and subsequent hybridization with specific probes. Eighteen different sequence types (STs) were identified among the 30 CTX-M-1-producing isolates, 5 of them being detected in 17 isolates (ST/phylogroup): ST57/D, ST155/B1, ST58/B1, ST10/A, and ST398/A. Most of the blaCTX-M-1-positive isolates had different PFGE profiles, with the exception of four human and pet isolates of lineage ST57 with related PFGE profiles (80% identity). Three CMY-2-producing isolates were typed as ST58/B1, ST117/D, and ST3632/B2. The IncI1 replicon was detected in all the 33 E. coli studied isolates, in many cases in combination with other replicons: IncF, IncX, IncK, IncR, IncY, colE, or IncN. The blaCTX-M-1gene was transferred by conjugation in 22 of the 30 positive strains and was located into IncI1 plasmids (ST3-CC3); the blaCMY-2gene was located into a conjugative IncI1 plasmid (ST12) of 97 kb in one strain. One blaCTX-M-1-positive strain carried the qnrB19 gene in a 33 kb IncX plasmid. Diverse genetic lineages are detected in extended-spectrum beta-lactamase- and AmpC beta-lactamase-producing E. coli from different origins. The blaCTX-M-1and blaCMY-2genes were associated with conjugative IncI1 (ST3 and ST12, respectively) plasmids in E. coli strains from human and animal origin.
机译:目的是确定blaCTX-M-1和blaCMY-2基因在先前从突尼斯的健康人,宠物和食品生产动物中获得的33株大肠杆菌中的位置,并鉴定这些菌株的遗传谱系。分子分型是通过脉冲场凝胶电泳(PFGE)-XbaI和多位点序列分型(MLST)进行的。通过S1-PFGE,基于聚合酶链反应的复制子分型和质粒MLST分析质粒。进行缀合实验。通过I-Ceu1-PFGE和S1-PFGE研究了blaCTX-M-1和blaCMY-2基因,并随后与特定探针杂交。在30种产生CTX-M-1的菌株中鉴定出18种不同的序列类型(ST),其中5种在17种菌株(ST / phylogroup)中检测到:ST57 / D,ST155 / B1,ST58 / B1,ST10 / A ,和ST398 / A。大多数blaCTX-M-1阳性分离株具有不同的PFGE图谱,只有四个具有相关PFGE谱图(> 80%同一性)的人和宠物谱系ST57分离株除外。将三种产生CMY-2的分离株分为ST58 / B1,ST117 / D和ST3632 / B2。在所有研究的33种大肠杆菌中都检测到了IncI1复制子,在许多情况下还与其他复制子结合使用:IncF,IncX,IncK,IncR,IncY,colE或IncN。通过结合在30个阳性菌株中的22个中转移blaCTX-M-1基因,并将其置于IncI1质粒(ST3-CC3)中。 blaCMY-2基因位于一株97 kb的结合型IncI1质粒(ST12)中。一种blaCTX-M-1-阳性菌株在33 kb IncX质粒中携带qnrB19基因。在不同来源的产广谱β-内酰胺酶和AmpCβ-内酰胺酶的大肠杆菌中检测到多种遗传谱系。 blaCTX-M-1和blaCMY-2基因与人和动物来源的大肠杆菌菌株中的接合IncI1(分别为ST3和ST12)质粒相关。

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