Quelle Liliana S, Corso Alejandra, Galas Marcelo, Sordelli Daniel O
Departamento de Microbiología, Parasitología e Inmunología, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina.
Diagn Microbiol Infect Dis. 2003 Nov;47(3):455-64. doi: 10.1016/s0732-8893(03)00137-8.
A method based on restriction profile analysis of the STAR repetitive element PCR (STAR-RP PCR) product obtained by digestion with AluI and Tru9I was developed for typing methicillin resistant Staphylococcus aureus (MRSA). We evaluated a well defined collection of MRSA from Argentina, previously characterized by PFGE (pulsed field gel electrophoresis) of chromosomal SmaI digests and hybridization with DNA probes for probes ClaI-mecA and ClaI-Tn554. We comparatively evaluated STAR-RP analysis with other PCR based methods such as Inter IS256-PCR, Rep-MP3 PCR and Coa-RP. The discriminatory power (D) of STAR-RP (0.86) was similar to that of PFGE (0.84) at the type level. Comparable results were obtained with Inter IS256 PCR (0.85) and Rep-MP3 PCR (0.80). A lower value (0.74) was obtained for Coa-RP. An excellent reproducibility (100%) of STAR-RP was observed. Good concordance between STAR-RP and other molecular typing methods was found for MRSA isolates (n = 39). STAR-RP typing showed 87% concordance with mecA::Tn554::PFGE, 87% with Inter IS256 PCR and 71% with Rep-MP3 typing. STAR-RP is suggested as an adequate molecular typing assay for MRSA epidemiologic assessment.
开发了一种基于对经AluI和Tru9I酶切获得的STAR重复元件PCR(STAR-RP PCR)产物进行限制性酶切图谱分析的方法,用于耐甲氧西林金黄色葡萄球菌(MRSA)分型。我们评估了一组来自阿根廷的明确界定的MRSA菌株,这些菌株先前已通过染色体SmaI酶切的脉冲场凝胶电泳(PFGE)以及与ClaI-mecA和ClaI-Tn554 DNA探针杂交进行了鉴定。我们将STAR-RP分析与其他基于PCR的方法(如Inter IS256-PCR、Rep-MP3 PCR和Coa-RP)进行了比较评估。在分型水平上,STAR-RP的鉴别力(D)(0.86)与PFGE(0.84)相似。Inter IS256 PCR(0.85)和Rep-MP3 PCR(0.80)也获得了类似结果。Coa-RP的值较低(0.74)。观察到STAR-RP具有出色的重复性(100%)。对于MRSA分离株(n = 39),发现STAR-RP与其他分子分型方法之间具有良好的一致性。STAR-RP分型与mecA::Tn554::PFGE的一致性为87%,与Inter IS256 PCR的一致性为87%,与Rep-MP3分型的一致性为71%。建议将STAR-RP作为MRSA流行病学评估的一种合适的分子分型检测方法。