Oteo Jesús, Pérez-Vázquez María, Bautista Verónica, Ortega Adriana, Zamarrón Pilar, Saez David, Fernández-Romero Sara, Lara Noelia, Ramiro Raquel, Aracil Belén, Campos José
Laboratorio de Referencia e Investigación en Resistencia a Antibióticos e Infecciones Relacionadas con la Asistencia Sanitaria, Centro Nacional de Microbiología, Majadahonda, Madrid, Spain
Red Española de Investigación en Patología Infecciosa (REIPI), Spain.
J Antimicrob Chemother. 2016 Dec;71(12):3392-3399. doi: 10.1093/jac/dkw321. Epub 2016 Aug 15.
We analysed the microbiological traits and population structure of KPC-producing Enterobacteriaceae isolates collected in Spain between 2012 and 2014. We also performed a comparative WGS analysis of the three major KPC-producing Klebsiella pneumoniae clones detected.
Carbapenemase and ESBL genes were sequenced. The Institut Pasteur MLST scheme was used. WGS data were used to construct phylogenetic trees, to identify the determinants of resistance and to de novo assemble the genome of one representative isolate of each of the three major K. pneumoniae clones.
Of the 2443 carbapenemase-producing Enterobacteriaceae isolates identified during the study period, 111 (4.5%) produced KPC. Of these, 81 (73.0%) were K. pneumoniae and 13 (11.7%) were Enterobacter cloacae. Three major epidemic clones of K. pneumoniae were identified: ST11/KPC-2, ST101/KPC-2 and ST512/KPC-3. ST11/KPC-2 differed from ST101/KPC-2 and ST512/KPC-3 by 27 819 and 6924 SNPs, respectively. ST101/KPC-2 differed from ST512/KPC-3 by 28 345 SNPs. Nine acquired resistance genes were found in ST11/KPC-2, 11 in ST512/KPC-3 and 13 in ST101/KPC-2. ST101/KPC-2 had the highest number of virulence genes (20). An 11 bp deletion at the end of the mgrB sequence was the cause of colistin resistance in ST512/KPC-3.
KPC-producing Enterobacteriaceae are increasing in Spain. Most KPC-producing K. pneumoniae isolates belonged to only five clones: ST11 and ST512 caused interregional spread, ST101 caused regional spread and ST1961 and ST678 produced independent hospital outbreaks. ST101/KPC-2 had the highest number of resistance and virulence genes. ST101/KPC-2 and ST512/KPC-3 were recently implicated in the spread of KPC in Italy.
我们分析了2012年至2014年间在西班牙收集的产KPC肠杆菌科分离株的微生物学特征和种群结构。我们还对检测到的三种主要产KPC肺炎克雷伯菌克隆进行了全基因组测序(WGS)比较分析。
对碳青霉烯酶和超广谱β-内酰胺酶(ESBL)基因进行测序。采用巴斯德研究所多位点序列分型(MLST)方案。WGS数据用于构建系统发育树,确定耐药决定因素,并对三种主要肺炎克雷伯菌克隆的每一个代表性分离株的基因组进行从头组装。
在研究期间鉴定出的2443株产碳青霉烯酶肠杆菌科分离株中,111株(4.5%)产KPC。其中,81株(73.0%)为肺炎克雷伯菌,13株(11.7%)为阴沟肠杆菌。鉴定出三种主要的肺炎克雷伯菌流行克隆:ST11/KPC-2、ST101/KPC-2和ST512/KPC-3。ST11/KPC-2与ST101/KPC-2和ST512/KPC-3分别相差27819个和6924个单核苷酸多态性(SNP)。ST101/KPC-2与ST512/KPC-3相差28345个SNP。在ST11/KPC-2中发现9个获得性耐药基因,在ST512/KPC-3中发现11个,在ST101/KPC-2中发现13个。ST101/KPC-2的毒力基因数量最多(20个)。mgrB序列末端11 bp的缺失是ST512/KPC-3对黏菌素耐药的原因。
产KPC肠杆菌科细菌在西班牙呈上升趋势。大多数产KPC肺炎克雷伯菌分离株仅属于五个克隆:ST11和ST512引起区域间传播,ST101引起区域传播,ST1961和ST678导致独立的医院暴发。ST101/KPC-2的耐药和毒力基因数量最多。ST101/KPC-2和ST512/KPC-3最近与KPC在意大利的传播有关。