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Colorimetric method for rapid detection of Oxacillin resistance in Staphylococcus aureus and its comparison with PCR for mec A gene

机译:比色法快速检测金黄色葡萄球菌对奥沙西林的耐药性及其与mec A基因PCR的比较

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摘要

Rapid and accurate detection of Methicillin Resistant Staphylococcus aureus (MRSA) is an important role of clinical microbiology laboratories to avoid treatment failure. The detection of MRSA is based on phenotypic assays which require at least 24 h to perform. Detection of the mecA gene or of PBP 2a is the “gold standard”, but not always available. The aim of this study was to evaluate a rapid method for detection of MRSA by using 3 (4, 5 dimethyl thiazole -2-yl) -2, 5 diphenyl tetrazolium bromide (MTT). Total 126 isolates of MRSA were collected from tertiary healthcare center and were confirmed by oxacillin screening agar test as per CLSI guidelines. Amplification of mecA gene was performed by using PCR. MTT assay was carried out for all the isolates in 96 well Microtitre plate and compared with standard methods of CLSI. Out of 126 isolates, 98 were found to be mecA positive. MTT method was found to be 98.98% sensitive and 96.43% specific. The MTT based colorimetric method is rapid and simple test for screening of oxacillin resistance in Staphylococcus aureus. It significantly shortens the time to just >7 h required to obtained a drug susceptibility test and could be useful to screen MRSA.
机译:快速准确地检测耐甲氧西林金黄色葡萄球菌(MRSA)是临床微生物学实验室避免治疗失败的重要作用。 MRSA的检测基于至少需要24小时才能进行的表型分析。 mecA基因或PBP 2a的检测是“黄金标准”,但并非始终可用。这项研究的目的是评估通过使用3(4,5二甲基噻唑-2-基)-2,5二苯基四唑溴化物(MTT)快速检测MRSA的方法。从三级医疗中心收集了126株MRSA分离株,并根据CLSI指南通过奥沙西林筛选琼脂试验进行了确认。通过使用PCR进行mecA基因的扩增。在96孔微量滴定板中对所有分离物进行MTT测定,并与CLSI的标准方法进行比较。在126个分离株中,发现98个是mecA阳性。发现MTT方法灵敏度为98.98%,特异性为96.43%。基于MTT的比色法是快速,简便的测试方法,用于筛选金黄色葡萄球菌对奥沙西林的耐药性。它大大缩短了获得药敏测试所需的时间,只需> 7 h ,对于筛选MRSA可能很有用。

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