Baraniak Anna, Izdebski Radoslaw, Zabicka Dorota, Bojarska Katarzyna, Górska Sandra, Literacka Elzbieta, Fiett Janusz, Hryniewicz Waleria, Gniadkowski Marek
Department of Molecular Microbiology, National Medicines Institute, Warsaw 00-725, Poland.
Department of Epidemiology and Clinical Microbiology, The National Reference Center for Susceptibility Testing, National Medicines Institute, Warsaw 00-725, Poland.
J Antimicrob Chemother. 2017 Jun 1;72(6):1610-1616. doi: 10.1093/jac/dkx054.
In 2008-09, the KPC carbapenemase epidemiology in Poland was dominated by a Klebsiella pneumoniae ST258 KPC-2 outbreak in Warsaw and its administrative region. The aim of this study was to analyse the situation in 2010-14, with a focus on new outbreaks in other parts of the country.
KPCs were detected in all suspected isolates by PCR. The detailed study was performed on 173 isolates from 2010 to 2012, and included PFGE and MLST, PCR identification of K. pneumoniae clonal group CG258 clades and potential specificity markers ( pilv-1 , IS 66 and prp ), PCR mapping of Tn 4401 transposons, and plasmid analysis by nuclease S1 profiling and PCR-based replicon typing.
Six hundred and eight KPC cases were identified in Poland in 2010-14, almost half of which occurred in the Warsaw region, and another half in four other areas. The new outbreaks were caused by four K. pneumoniae CG258 genotypes, different from each other and from the organisms spreading in Warsaw. The new lineages were ST258 or ST512 of clade II, and had specific compositions of potential ST258/ST512 clonal markers. The isolates produced KPC-3 encoded by Tn 4401 a or Tn 4401 b elements on plasmids with single or multiple replicons, including I2, FII K (+/-FIB K ), 'FII Y -like', X3 and R. Of other species, Citrobacter freundii ST17 and Enterobacter cloacae ST254 with KPC-2 were identified in a Warsaw hospital.
The study showed remarkable changes in the KPC epidemiology in Poland in 2010-14, which, following the localized regional spread in the early phase, has converted into multiregional dissemination.
在2008 - 2009年期间,波兰KPC碳青霉烯酶的流行病学情况主要是华沙及其行政区出现肺炎克雷伯菌ST258 KPC - 2暴发。本研究的目的是分析2010 - 2014年的情况,重点关注该国其他地区的新暴发情况。
通过PCR在所有疑似分离株中检测KPC。对2010年至2012年的173株分离株进行了详细研究,包括脉冲场凝胶电泳(PFGE)和多位点序列分型(MLST)、肺炎克雷伯菌克隆群CG258分支及潜在特异性标志物(pilv - 1、IS66和prp)的PCR鉴定、Tn4401转座子的PCR定位,以及通过核酸酶S1图谱分析和基于PCR的复制子分型进行质粒分析。
2010 - 2014年波兰共鉴定出608例KPC病例,其中近一半发生在华沙地区,另一半发生在其他四个地区。新的暴发由四种肺炎克雷伯菌CG258基因型引起,它们彼此不同,也与在华沙传播的菌株不同。新谱系为分支II的ST258或ST512,具有潜在ST258/ST512克隆标志物的特定组成。分离株在带有单个或多个复制子(包括I2、FII K(+/-FIB K)、“FII Y样”、X3和R)的质粒上产生由Tn4401a或Tn4401b元件编码的KPC - 3。在华沙一家医院还鉴定出携带KPC - 2的弗氏柠檬酸杆菌ST17和阴沟肠杆菌ST254。
该研究表明,2010 - 2014年波兰KPC的流行病学情况发生了显著变化,在早期局部区域传播之后,已转变为多区域传播。