Pellegrino F L P C, Casali N, Dos Santos K R N, Nouér S A, Scheidegger E M D, Riley L W, Moreira B M
Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, Brazil.
J Chemother. 2006 Apr;18(2):151-6. doi: 10.1179/joc.2006.18.2.151.
The present study was designed to characterize beta-lactamase genes and evaluate polymerase chain reaction (PCR) typing for multidrug-resistant Pseudomonas aeruginosa pulsed-field gel electrophoresis (PFGE) genotype A isolates from Rio de Janeiro, Brazil, collected between April 1999 and March 2000 and one additional isolate collected in June 2002. As reported previously, all of the genotype A isolates produced non-characterized metallo-beta-lactamase. These isolates (22) were screened for the bla(SPM) gene by PCR and dot-blotting. Isolates were typed by PCR fingerprinting with primers RAPD-1, 272, 208, 1290, ERIC-1 and ERIC-2. The bla(SPM) gene was detected in 18 (82%) of the 22 isolates. PCR fingerprinting gave results that correlated with PFGE, except with primer 1290. In Rio de Janeiro and other Brazilian states, nearly all SPM-producing P. aeruginosa isolates belong to a single PFGE type accounting for a large proportion of drug-resistant P. aeruginosa hospital infections. RAPD PCR fingerprinting may be a useful technique to screen for an epidemic multidrug-resistant strain in Brazil.
本研究旨在对β-内酰胺酶基因进行特征分析,并评估聚合酶链反应(PCR)分型用于检测来自巴西里约热内卢的多重耐药铜绿假单胞菌脉冲场凝胶电泳(PFGE)基因型A分离株,这些分离株于1999年4月至2000年3月期间收集,以及2002年6月收集的另外一株分离株。如先前报道,所有基因型A分离株均产生未鉴定的金属β-内酰胺酶。通过PCR和斑点杂交对这些分离株(22株)进行bla(SPM)基因筛查。使用引物RAPD-1、272、208、1290、ERIC-1和ERIC-2通过PCR指纹图谱对分离株进行分型。在22株分离株中的18株(82%)中检测到bla(SPM)基因。除引物1290外,PCR指纹图谱结果与PFGE结果相关。在里约热内卢和巴西其他州,几乎所有产SPM的铜绿假单胞菌分离株都属于单一PFGE型别,在耐药铜绿假单胞菌医院感染中占很大比例。RAPD PCR指纹图谱可能是在巴西筛查流行的多重耐药菌株的一种有用技术。