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首页> 外文期刊>Journal of Clinical Microbiology >Novel Multiplex PCR Assay for Characterization and Concomitant Subtyping of Staphylococcal Cassette Chromosome mec Types I to V in Methicillin-Resistant Staphylococcus aureus
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Novel Multiplex PCR Assay for Characterization and Concomitant Subtyping of Staphylococcal Cassette Chromosome mec Types I to V in Methicillin-Resistant Staphylococcus aureus

机译:新型多重PCR分析法鉴定和鉴定耐甲氧西林金黄色葡萄球菌的I型至V型葡萄球菌盒式染色体mec型

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Staphylococcal cassette chromosome mec (SCCmec) typing is essential for understanding the molecular epidemiology of methicillin-resistant Staphylococcus aureus (MRSA). SCCmec elements are currently classified into types I to V based on the nature of the mec and ccr gene complexes, and are further classified into subtypes according to their junkyard region DNA segments. Previously described traditional SCCmec PCR typing schemes require multiple primer sets and PCR experiments, while a previously published multiplex PCR assay is limited in its ability to detect recently discovered types and subtypes such as SCCmec type V and subtypes IVa, b, c, and d. We designed new sets of SCCmec type- and subtype-unique and specific primers and developed a novel multiplex PCR assay allowing for concomitant detection of the methicillin resistance (mecA gene) (also serving as an internal control) to facilitate detection and classification of all currently described SCCmec types and subtypes I, II, III, IVa, b, c, d, and V. Our assay demonstrated 100% sensitivity and specificity in accurately characterizing 54 MRSA strains belonging to the various known SCCmec types and subtypes, when compared with previously described typing methods. Further application of our assay in 453 randomly selected local clinical isolates confirmed its feasibility and practicality. This novel assay offers a rapid, simple, and feasible method for SCCmec typing of MRSA, and may serve as a useful tool for clinicians and epidemiologists in their efforts to prevent and control infections caused by this organism.
机译:葡萄球菌盒式染色体 mec (SCC mec )分型对于了解耐甲氧西林的金黄色葡萄球菌(MRSA)的分子流行病学至关重要。目前,SCC mec 元素根据 mec ccr 基因复合物的性质分为I至V型,并进一步分为亚型。根据他们的垃圾场区域DNA片段。先前描述的传统SCC mec PCR分型方案需要多个引物组和PCR实验,而先前发布的多重PCR分析在检测最近发现的类型和亚型(例如SCC mec < / em>类型V和子类型IVa,b,c和d。我们设计了新的SCC mec 类型和亚型独特的特异性引物,并开发了一种新型的多重PCR检测方法,可同时检测甲氧西林抗性( mecA 基因)(也可作为内部对照),以方便对所有目前描述的SCC mec 类型和亚型I,II,III,IVa,b,c,d和V进行检测和分类。我们的分析证明了100%与先前描述的分型方法相比,可以准确准确地鉴定属于各种已知SCC mec 类型和亚型的54个MRSA菌株的敏感性和特异性。我们的测定在453个随机选择的局部临床分离株中的进一步应用证实了其可行性和实用性。这种新颖的检测方法为SCC mec 的MRSA分型提供了一种快速,简单且可行的方法,并且可以作为临床医生和流行病学家预防和控制由该微生物引起的感染的有用工具。

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