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首页> 外文期刊>Microbial drug resistance: MDR : Mechanisms, epidemiology, and disease >High Clonal diversity in a non-outbreak situation of clinical ESBL-producing klebsiella pneumoniae isolates in the first national surveillance program in Cuba
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High Clonal diversity in a non-outbreak situation of clinical ESBL-producing klebsiella pneumoniae isolates in the first national surveillance program in Cuba

机译:在古巴第一个国家监测计划中,临床ESBL产生的肺炎克雷伯菌分离株在非暴发情况下的高度克隆多样性

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摘要

This work summarized the results obtained in an institutional Klebsiella pneumoniae surveillance program recently implemented in Cuba. Eighteen hospitals from five regions provided a total of 228 K. pneumoniae isolates (164 from admitted patients, four from hospital environmental sources, and 60 isolates from community patients). The genetic relationship was assessed by pulsed-field gel electrophoresis and multilocus sequence typing. Antimicrobial susceptibility was determined by the agar dilution method, and blaESBL genes were sequenced. Fifty four K. pneumoniae isolates were extended-spectrum β-lactamases (ESBL)-producers (23.6%), mostly due to the CTX-M-15 enzyme (79.6%). ESBL isolates were grouped in 27 different sequence types (STs), being the most prevalent ST15 (15%), ST152 (13%), and both ST48 and ST147 (11%, respectively). Community-acquired criteria could be demonstrated in 60 patients (26%) corresponding to urological (33%), wound (27%), respiratory (27%), and otic (13%) infections. Population structure analysis showed that our isolates corresponded to a highly polyclonal population with 10 nonpreviously described STs, demonstrating the importance of local epidemiological studies. We report the first data of the population structure of ESBL-producing K. pneumoniae isolates obtained in a national multicenter surveillance Cuban program. Results showed that a highly polyclonal ESBL-producer K. pneumoniae population was mainly due to CTX-M-15 carriage, whereas carbapenemases production was not present.
机译:这项工作总结了最近在古巴实施的一项机构性肺炎克雷伯菌的监测计划所获得的结果。来自五个地区的18家医院共提供了228株肺炎克雷伯菌分离株(其中164例来自入院患者,四例来自医院环境,而60例来自社区患者)。通过脉冲场凝胶电泳和多基因座序列分型来评估遗传关系。通过琼脂稀释法确定抗菌药敏感性,并对blaESBL基因进行测序。 54例肺炎克雷伯菌分离株是广谱β-内酰胺酶(ESBL)产生者(23.6%),主要归因于CTX-M-15酶(79.6%)。 ESBL分离物分为27种不同的序列类型(ST),分别是最流行的ST15(15%),ST152(13%)和ST48和ST147(分别为11%)。社区获得性标准可在60例患者(26%)中得到证实,分别对应于泌尿科(33%),伤口(27%),呼吸道(27%)和耳部感染(13%)。种群结构分析表明,我们的分离株对应于一个高度多克隆的种群,具有10个先前未描述过的ST,表明了当地流行病学研究的重要性。我们报告了在国家多中心监测古巴计划中获得的生产ESBL的肺炎克雷伯菌分离株的种群结构的第一批数据。结果表明,高度多克隆的ESBL生产者肺炎克雷伯菌主要归因于CTX-M-15转运,而碳青霉烯酶的产生却不存在。

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