Emergence of a colistin-resistant KPC-2-producing Klebsiella pneumoniae ST258 clone in Hungary

被引:101
|
作者
Toth, A. [1 ]
Damjanova, I. [2 ]
Puskas, E. [3 ]
Janvari, L. [1 ]
Farkas, M. [4 ]
Dobak, A. [4 ]
Borocz, K. [5 ]
Paszti, J. [2 ]
机构
[1] Natl Ctr Epidemiol, Dept Bacteriol, H-1097 Budapest, Hungary
[2] Natl Ctr Epidemiol, Dept Phage Typing & Mol Epidemiol, H-1097 Budapest, Hungary
[3] Hungarian Natl Publ Hlth & Med Officer Serv, No Reg Inst, Microbiol Lab, H-3530 Miskolc, Hungary
[4] Corden Int Ltd, Microbiol Lab, Budapest, Hungary
[5] Natl Ctr Epidemiol, Dept Hosp Epidemiol & Hyg, H-1097 Budapest, Hungary
关键词
BETA-LACTAMASE; PSEUDOMONAS SPP; IDENTIFICATION; CARBAPENEMASE; EXPANSION; STRAINS;
D O I
10.1007/s10096-010-0921-3
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Nine Klebsiella pneumoniae isolates showing non-susceptibility to carbapenems were collected from three centres in the north-eastern region of Hungary. The minimum inhibitory concentrations (MICs) of antibiotics were determined by Etest. The putative production of a carbapenemase was tested by the modified Hodge test. The presence of bla (KPC) genes was verified by polymerase chain reaction (PCR) and sequencing. Furthermore, molecular typing was performed by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). All isolates showed extensively drug-resistant (XDR) phenotype, and of these, eight isolates were highly resistant to colistin. The isolates carried bla (KPC-2), bla (SHV-12), bla (TEM-1) and bla (SHV-11). PFGE analysis of the nine KPC-2-producing Hungarian ST258 K. pneumoniae isolates, two KPC-2-producing Norwegian ST258 isolates and 33 CTX-M-15-producing ST11 isolates revealed the existence of one genetic cluster at an 88% similarity level. The overall results of the PFGE clustering, MLST and the presence of SHV-11 in both ST11 and ST258 suggest that this is the first hyperepidemic clonal complex of multidrug-resistant K. pneumoniae, probably CC258/CC340, possibly undergoing worldwide spread.
引用
收藏
页码:765 / 769
页数:5
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