首页> 外文期刊>Microbial drug resistance: MDR : Mechanisms, epidemiology, and disease >CTX-M-15-producing Escherichia coli clinical isolates in Cairo (Egypt), including isolates of clonal complex ST10 and clones ST131, ST73, and ST405 in both community and hospital settings.
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CTX-M-15-producing Escherichia coli clinical isolates in Cairo (Egypt), including isolates of clonal complex ST10 and clones ST131, ST73, and ST405 in both community and hospital settings.

机译:开罗(埃及)生产CTX-M-15的大肠杆菌临床分离株,包括社区和医院环境中克隆复合物ST10以及克隆ST131,ST73和ST405的分离株。

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摘要

In Egypt, little is known about the genetic background of Escherichia coli isolates harboring extended-spectrum beta-lactamase (ESBL). Five hundred twenty Enterobacteriaceae were prospectively collected (May 2007-August 2008) at the Theodor Bilharz Research Institute (Cairo). Among the collected Enterobacteriaceae, 56% (n=291) were E. coli and 32% (n=165) Klebsiella pneumoniae. A total of 16% (n=3) of all isolates were ESBL, 19% (n=55) of the E. coli and 14% (n=23) of the K. pneumoniae. The proportion of E. coli ESBL producers did not differ significantly between in and outpatients (20% vs. 17%) but was significantly different for non-E. coli ESBL producers (18.5% vs. 1.2%: p=0.0001). The majority of E. coli ESBL producers (75%) was isolated from urine. All the ESBL-producing Enterobacteriaceae available for molecular study (n=74) produced CTX-M-15. Among the CTX-M-15-producing E. coli isolates; 40% belonged to phylogenetic group A, 32% to D, and 26% to B2. ERIC-2 PCR profiles were obtained for all these E. coli isolates and multilocus sequence typing for those belonging to group B2. Genotyping analyses showed strain diversity; however, some clusters had profiles indistinguishable from that of previously published clones. Multilocus sequence typing showed that 75% of E. coli group B2 belonged to clone ST131. This indicates that a new country in Africa is adversely affected by clones of E. coli-producing CTX-M-15.
机译:在埃及,对带有超广谱β-内酰胺酶(ESBL)的大肠杆菌分离株的遗传背景知之甚少。 (2007年5月至2008年8月)前瞻性在西奥多·比尔哈兹研究所(开罗)收集了520个肠杆菌科。在收集的肠杆菌科细菌中,大肠杆菌占56%(n = 291),肺炎克雷伯菌占32%(n = 165)。所有分离株中总共有16%(n = 3)是ESBL,19%(n = 55)的大肠杆菌和14%(n = 23)的肺炎克雷伯菌。大肠杆菌ESBL生产者的比例在门诊患者和门诊患者之间没有显着差异(20%比17%),但对于非大肠杆菌患者,则显着不同。大肠杆菌ESBL生产者(18.5%对1.2%:p = 0.0001)。大多数大肠杆菌ESBL生产者(75%)是从尿液中分离出来的。所有可用于分子研究的产ESBL肠杆菌科细菌(n = 74)均生产CTX-M-15。在产生CTX-M-15的大肠杆菌中; 40%属于系统发育组A,32%属于D,26%属于B2。对于所有这些大肠杆菌分离株均获得了ERIC-2 PCR谱图,对于属于B2组的分离株获得了多基因座序列分型。基因分型分析显示菌株多样性。但是,有些簇的特征与以前发表的克隆没有区别。多基因座序列分型显示,大肠杆菌B2组的75%属于克隆ST131。这表明非洲的一个新国家受到生产大肠杆菌的CTX-M-15克隆的不利影响。

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