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A Simple Sample Processing Protocol and Multiplex PCR for Direct Detection of MRSA from Uncultured Clinical Samples—A Pilot Study

机译:一种直接从未培养的临床样品中检测MRSA的简单样品处理方案和多重PCR-初步研究

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Phenotypic tests have limited discrimatory power to identify closely related members of genus Staphylococcus and particularly for identification of S. aureus . 157 isolates of S. aureus obtained from different clinical specimens were included in our study. To present a demonstration of our method’s sensitivity and ability to correctly detect S. aureus from uncultured clinical specimen, 30 known S. aureus positive but leftover uncultured clinical specimens from clinical microbiology laboratory were processed by our protocol and analyzed. All the 30 clinical specimens were confirmed as S. aureus among which 26 specimen were identified as MRSA and the remaining 4 as MSSA. These 30 clinical specimens used in the study showed 100% correlation with coagulase test and Cefoxitin disc diffusion method. Though commercial molecular diagnostic kits are available for detecting MRSA from swabs, this is probably the first time that multiplex PCR is being demonstrated directly on a variety of uncultured clinical specimens.
机译:表型试验鉴别葡萄球菌属密切相关成员,特别是鉴定金黄色葡萄球菌的鉴别能力有限。从不同临床标本中获得的157株金黄色葡萄球菌被包括在我们的研究中。为了说明我们的方法的敏感性和正确地从未培养的临床标本中检测金黄色葡萄球菌的能力,我们对方案处理了30份临床微生物学实验室已知的金黄色葡萄球菌阳性但残留的未培养的临床标本,并进行了分析。所有30个临床标本均被确认为金黄色葡萄球菌,其中26个标本被鉴定为MRSA,其余4个标本被鉴定为MSSA。研究中使用的这30个临床标本与凝血酶测试和头孢西丁圆盘扩散法显示100%相关。尽管可以使用商用分子诊断试剂盒检测棉签中的MRSA,但这可能是首次在多种未培养的临床标本上直接进行多重PCR的证明。

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