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首页> 外文期刊>Antimicrobial Resistance and Infection Control >Genotypic characterization of gentamicin and cephalosporin resistant Escherichia coli isolates from blood cultures in a Norwegian university hospital 2011–2015
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Genotypic characterization of gentamicin and cephalosporin resistant Escherichia coli isolates from blood cultures in a Norwegian university hospital 2011–2015

机译:2011–2015年挪威大学医院血液培养物中对庆大霉素和头孢菌素耐药的大肠杆菌分离株的基因型鉴定

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Cephalosporin resistance in clinical E. coli isolates is increasing internationally. The increase has been caused by virulent and often multidrug-resistant clones, especially the extended spectrum β-lactamase (ESBL) producing E. coli clone O25b-ST131. In Norway, recommended empirical treatment of sepsis consists of gentamicin and penicillin combined, or a broad-spectrum cephalosporin. To investigate if increased gentamicin and cephalosporins resistance rates in our hospital could be caused by specific clones, we conducted a retrospective study on E. coli blood culture isolates from 2011 through 2015. All E. coli isolates non-susceptible to gentamicin and/or third-generation cephalosporins were genotyped using multiple-locus variable-number of tandem repeat analysis (MLVA) and compared with antibiotic susceptible isolates. The frequency of the most common genes causing ESBL production (bla CTX-M, bla ampC) was examined by Real-Time PCR. A total of 158 cephalosporin and/or gentamicin resistant and 97 control isolates were differentiated into 126 unique MLVA types. Of these, 31% of the isolates belonged to a major MLVA cluster consisting of 41% of the gentamicin resistant and 35% of the cephalosporin resistant isolates. The majority (65/80 isolates) of this MLVA cluster contained MLVA types associated with the E. coli O25b-ST131 clone. Genes encoding CTX-M enzyme phylogroups 1 and 9 occurred in 65% and 19% of cephalosporin resistant isolates, respectively, whereas bla ampC-CIT was identified in 3%. No local E. coli bacteraemia clone was identified. Antibiotic resistance was dispersed over a variety of genotypes. However, association with the international E. coli O25b-ST131 clone was frequent and may be an important driver behind increased resistance rates. Monitoring and preventing dissemination of these resistant clones are important for continued optimal treatment.
机译:国际上临床大肠杆菌分离株对头孢菌素的耐药性正在增加。这种增加是由有毒力且通常具有多重耐药性的克隆引起的,特别是产生大范围β-内酰胺酶(ESBL)的大肠杆菌克隆O25b-ST131。在挪威,推荐的脓毒症经验治疗包括庆大霉素和青霉素联用或广谱头孢菌素。为了调查我们医院中庆大霉素和头孢菌素耐药率的升高是否可能由特定的克隆引起,我们对2011年至2015年的大肠杆菌血液培养分离株进行了回顾性研究。所有对庆大霉素和/或第三种不敏感的大肠杆菌分离株使用多位点可变数目的串联重复分析(MLVA)对第二代头孢菌素进行基因分型,并与易感抗生素分离株进行比较。通过实时PCR检测了导致ESBL产生的最常见基因(bla CTX-M,bla ampC)的频率。总共158头孢菌素和/或庆大霉素抗性和97的控制分离株被分为126种独特的MLVA类型。其中,31%的分离物属于主要的MLVA簇,由41%的庆大霉素抗性和35%的头孢菌素抗性分离物组成。该MLVA簇的大多数(65/80分离株)包含与大肠杆菌O25b-ST131克隆相关的MLVA类型。编码CTX-M酶系统群1和9的基因分别出现在65%和19%的头孢菌素抗性分离株中,而bla ampC-CIT的鉴定为3%。未发现本地大肠杆菌菌血症克隆。抗生素耐药性分散在多种基因型上。但是,与国际大肠杆菌O25b-ST131克隆的关联非常频繁,并且可能是耐药率增加的重要推动力。监测和防止这些抗性克隆的传播对于持续最佳治疗很重要。

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