Markovska Rumyana, Stoeva Temenuga, Schneider Ines, Boyanova Lyudmila, Popova Valentina, Dacheva Daniela, Kaneva Radka, Bauernfeind Adolf, Mitev Vanyo, Mitov Ivan
Department of Medical Microbiology, Medical University of Sofia, Sofia, Bulgaria.
Department of Microbiology, Medical University of Varna, Varna, Bulgaria.
APMIS. 2015 Oct;123(10):887-94. doi: 10.1111/apm.12433. Epub 2015 Aug 25.
A total of 36 consecutive clinical and two fecal-screening carbapenem-resistant Klebsiella pneumoniae isolates from two Bulgarian university hospitals (Varna and Pleven) were investigated. Susceptibility testing, conjugation experiments, and plasmid replicon typing were carried out. Beta-lactamases were characterized by isoelectric focusing, PCR, and sequencing. Clonal relatedness was investigated by RAPD and multilocus sequence typing (MLST). Most of the isolates demonstrated multidrug resistance profile. Amikacin and tigecycline retained good activity with susceptibility rates of 95 and 87%, respectively. The resistance rate to colistin was 63%. Six RAPD- and MLST-types were identified: the dominating MLST-type was ST15 (27 isolates), followed by ST76 (six isolates), and ST1350 (two isolates). ST101, ST258, and ST151 were detected once. All except one of the K. pneumoniae produced KPC-2, mostly in combination with CTX-M-15, while for one isolate (ST101) the enzymes OXA-48 and CTX-M-14 were found. All KPC-2-producing transconjugants revealed the presence of IncFII plasmid. The OXA-48- and CTX-M-14-producing isolate showed the presence of L/M replicon type. The dissemination of KPC-2-producing K.pneumoniae in Bulgaria is mainly due to the sustained spread of successful ST15 clone and to a lesser extent of ST76 clone. This is the first report of OXA-48 producing ST101 K. pneumoniae in Bulgaria.
对来自保加利亚两所大学医院(瓦尔纳和普列文)的36株连续临床分离株以及两株粪便筛查的耐碳青霉烯肺炎克雷伯菌进行了研究。进行了药敏试验、接合实验和质粒复制子分型。通过等电聚焦、PCR和测序对β-内酰胺酶进行了表征。通过RAPD和多位点序列分型(MLST)研究了克隆相关性。大多数分离株表现出多重耐药谱。阿米卡星和替加环素保持良好活性,药敏率分别为95%和87%。对黏菌素的耐药率为63%。鉴定出6种RAPD和MLST型:占主导的MLST型是ST15(27株分离株),其次是ST76(6株分离株)和ST1350(2株分离株)。ST101、ST258和ST151各检测到1次。除1株肺炎克雷伯菌外,其余均产生KPC-2,大多与CTX-M-15联合产生,而对于1株分离株(ST101),发现了OXA-48和CTX-M-14酶。所有产生KPC-2的接合子均显示存在IncFII质粒。产生OXA-48和CTX-M-14的分离株显示存在L/M复制子类型。产KPC-2肺炎克雷伯菌在保加利亚的传播主要是由于成功的ST15克隆的持续传播,以及ST76克隆在较小程度上的传播。这是保加利亚首次报道产OXA-48的ST101肺炎克雷伯菌。