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使用多重聚合酶链反应快速检测耐甲氧西林金黄色葡萄球菌的方法

Rapid assay for detection of methicillin-resistant Staphylococcus aureus using multiplex PCR.

作者信息

Barski P, Piechowicz L, Galiński J, Kur J

机构信息

Department of Microbiology, Technical University of Gdańsk, Poland.

出版信息

Mol Cell Probes. 1996 Dec;10(6):471-5. doi: 10.1006/mcpr.1996.0066.

Abstract

The presence or absence of the mecA gene, the determinant of resistance to all beta-lactam antibiotics, was examined in clinical isolates of Staphylococcus aureus by multiplex polymerase chain reaction (MPCR). Two pairs of primers were used, which yielded two specific products; a 280-bp nuc- based PCR fragment (amplification product of the nuc gene encoding specific Staphylococcus aureus nuclease) and a 533-bp mecA-based PCR fragment (amplification product of the mecA gene). The MPCR system was designed to be incorporated into the work flow in clinical diagnostic laboratories as a routine analysis.

摘要

通过多重聚合酶链反应(MPCR)检测金黄色葡萄球菌临床分离株中mecA基因(对所有β-内酰胺类抗生素耐药的决定因素)的存在与否。使用了两对引物,产生了两个特异性产物;一个280 bp基于nuc的PCR片段(编码特异性金黄色葡萄球菌核酸酶的nuc基因的扩增产物)和一个533 bp基于mecA的PCR片段(mecA基因的扩增产物)。MPCR系统设计为作为常规分析纳入临床诊断实验室的工作流程。

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