Prelog M, Fille M, Prodinger W, Grif K, Brunner A, Würzner R, Zimmerhackl L B
Dept. of Pediatrics, Medical University Innsbruck, Anichstr. 35, A-6020, Innsbruck, Austria.
Infection. 2008 Aug;36(4):362-7. doi: 10.1007/s15010-008-7309-7. Epub 2008 Jun 21.
The present study was aimed to searching for CTX-M-type extended-spectrum beta-lactamases in community- and hospital-acquired Escherichia coli (E. coli) collected in western Austria and to investigate their clonal relatedness and their ability to spread.
All patients with E. coli positive cultures collected from a catchment population of 186,000 between January and July 2006 were enrolled into the study. CTX-M-producing E. coli were identified by antibiotic susceptibility testing and blaCTX-M multiplex PCR. Clonal relatedness was analyzed by pulsed-field gel electrophoresis (PFGE).
In 2,042 E. coli isolates, 20 isolates (16 from urine, 4 from blood cultures) demonstrated CTX-M-1-related genes and no CTX-M-2- or CTX-M-9-related enzymes or CTX-M-15-producing strains were identified. We did not find clonal relatedness among CTX-M-1 producers isolated from the same referring center. E. coli were investigated for plasmid transfer ability of CTX-M-1-encoding genes. Plasmid digest patterns were not consistent with episomal spread of resistance loci. Transfection of CTX-M-encoding plasmids failed.
Our data suggest that the emergence of CTX-M-1-producing E. coli in western Austria may be attributed to multiple independent events.
本研究旨在寻找奥地利西部社区获得性和医院获得性大肠杆菌中CTX-M型超广谱β-内酰胺酶,调查其克隆相关性及其传播能力。
纳入2006年1月至7月间从186,000人群中收集的所有大肠杆菌阳性培养患者。通过药敏试验和blaCTX-M多重PCR鉴定产CTX-M的大肠杆菌。通过脉冲场凝胶电泳(PFGE)分析克隆相关性。
在2042株大肠杆菌分离株中,20株(16株来自尿液,4株来自血培养)显示出与CTX-M-1相关的基因,未鉴定出与CTX-M-2或CTX-M-9相关的酶或产CTX-M-15的菌株。我们未在从同一转诊中心分离的CTX-M-1生产者中发现克隆相关性。对大肠杆菌进行了CTX-M-1编码基因的质粒转移能力研究。质粒消化模式与抗性位点的游离传播不一致。CTX-M编码质粒的转染失败。
我们的数据表明,奥地利西部产CTX-M-1大肠杆菌的出现可能归因于多个独立事件。