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多重聚合酶链反应快速检测耐甲氧西林葡萄球菌

Rapid detection of methicillin-resistant staphylococci by multiplex PCR.

作者信息

Kearns A M, Seiders P R, Wheeler J, Freeman R, Steward M

机构信息

Public Health Laboratory, General Hospital, Westgate Road, Newcastle upon Tyne, England, UK.

出版信息

J Hosp Infect. 1999 Sep;43(1):33-7. doi: 10.1053/jhin.1999.0631.

Abstract

A multiplex PCR was developed to detect the coagulase gene (coa; pathognomic of Staphylococcus aureus) and the mecA gene (characteristically encoding for methicillin resistance in staphylococci) in a single, rapid test. Suitable primers for the gene targets and an internal, amplification control were incorporated into a multiplex PCR assay, which was then optimized on a capillary air thermal cycler to improve the turnaround time of the test to approximately 1.5 hours. The assay was evaluated with 111 fresh clinical isolates of staphylococci. The multiplex PCR correctly distinguished between isolates of S. aureus, which were sensitive to methicillin (MSSA) and those resistant to it (MRSA). It also correctly differentiated between similar isolates of coagulase negative staphylococci (MSSE and MRSE respectively). It was concluded that this multiplex PCR was a rapid and reliable method for the detection of methicillin-resistant staphylococci.

摘要

开发了一种多重聚合酶链反应(multiplex PCR),用于在单一快速检测中检测凝固酶基因(coa;金黄色葡萄球菌的病理学特征)和mecA基因(特征性地编码葡萄球菌中的耐甲氧西林性)。将针对基因靶点的合适引物和一个内部扩增对照纳入多重PCR检测中,然后在毛细管空气热循环仪上对其进行优化,以将检测周转时间缩短至约1.5小时。用111株新鲜的葡萄球菌临床分离株对该检测方法进行了评估。多重PCR能够正确区分对甲氧西林敏感的金黄色葡萄球菌(MSSA)分离株和对其耐药的(MRSA)分离株。它还能正确区分凝固酶阴性葡萄球菌的相似分离株(分别为MSSE和MRSE)。得出的结论是,这种多重PCR是检测耐甲氧西林葡萄球菌的一种快速且可靠的方法。

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