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Spread of Extended-Spectrum β-Lactamase CTX-M-Producing Escherichia coli Clinical Isolates in Community and Nosocomial Environments in Portugal

机译:广谱β-内酰胺酶CTX-M生产大肠杆菌在葡萄牙社区和医院环境中的临床传播

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摘要

Of the 181 unduplicated Escherichia coli strains isolated in nine different hospitals in three Portuguese regions, 119 were extended-spectrum β-lactamase (ESBL)-CTX-M producers and were selected for phenotype and genotype characterization. CTX-M producer strains were prevalent among community-acquired infections (56%), urinary tract infections (76%), and patients ≥60 years old (76%). In MIC tests, all strains were resistant to cefotaxime, 92% were resistant to ceftazidime, 93% were resistant to quinolones, 89% were resistant to aminoglycoside, and 26% were resistant to trimethoprim-sulfamethoxazole; all strains were sensitive to carbapenems, and 92% of the strains had a multidrug resistance phenotype. Molecular methods identified 109 isolates harboring a blaCTX-M-15 gene, 1 harboring the blaCTX-M-32 gene (first identification in the country), and 9 harboring the blaCTX-M-14 gene. All isolates presented the ISEcp1 element upstream from the blaCTX-M genes; one presented the IS903 element (downstream of blaCTX-M-14 gene), and none had the IS26 element; 85% carried blaTEM-1B, and 84% also carried a blaOXA-30. Genetic relatedness analysis based on pulsed-field gel electrophoresis defined five clusters and indicated that 76% of all isolates (from cluster IV) corresponded to a single epidemic strain. Of the 47 strains from one hospital, 41 belonged to cluster IV and were disseminated in three main wards. CTX-M-producing E. coli strains are currently a problem in Portugal, with CTX-M-15 particularly common. This study suggests that the horizontal transfer of blaCTX-M genes, mediated by plasmids and/or mobile elements, contributes to the dissemination of CTX-M enzymes to community and hospital environments. The use of extended-spectrum cephalosporins, quinolones, and aminoglycosides is compromised, leaving carbapenems as the therapeutic option for severe infections caused by ESBL producers.
机译:在三个葡萄牙地区的9家不同医院中分离出的181株无重复的大肠杆菌菌株中,有119株是超谱β-内酰胺酶(ESBL)-CTX-M产生者,并被选择用于表型和基因型表征。 CTX-M生产菌株在社区获得性感染(56%),尿路感染(76%)和≥60岁的患者(76%)中普遍存在。在MIC测试中,所有菌株均对头孢噻肟具有抗性,对头孢他啶具有92%的抗性,对喹诺酮类具有93%的抗性,对氨基糖苷类具有抗性的89%,对甲氧苄啶-磺胺甲基异恶唑具有26%的抗性。所有菌株均对碳青霉烯敏感,其中92%的菌株具有多药耐药表型。分子方法鉴定了109株带有blaCTX-M-15基因的分离株,其中1株带有blaCTX-M-32基因(在国内首次鉴定),还有9株带有blaCTX-M-14基因。所有分离株均在blaCTX-M基因上游呈现ISEcp1元件。一个人提出了IS903元素(blaCTX-M-14基因的下游),而没有人提出了IS26元素。 85%的人携带blaTEM-1B,84%的人携带blaOXA-30。基于脉冲场凝胶电泳的遗传相关性分析定义了五个聚类,表明所有分离株(来自聚类IV)的76%对应于一个流行株。一家医院的47株菌株中,有41株属于IV组,并在三个主要病房中传播。产生CTX-M的大肠杆菌菌株目前在葡萄牙是一个问题,特别是CTX-M-15。这项研究表明,由质粒和/或移动元件介导的blaCTX-M基因的水平转移有助于CTX-M酶向社区和医院环境的传播。广谱头孢菌素,喹诺酮和氨基糖苷类药物的使用受到限制,碳青霉烯类药物可作为ESBL生产者引起的严重感染的治疗选择。

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