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Detection of Staphylococcus aureus enterotoxin production genes from patient samples using an automated extraction platform and multiplex real-time PCR

机译:使用自动提取平台和多重实时PCR从患者样品中检测金黄色葡萄球菌肠毒素产生基因

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摘要

To minimize specimen volume, handling and testing time, we have developed two TaqMar (R) multiplex real-time PCR (rtPCR) assays to detect staphylococcal enterotoxins A-E and Toxic Shock Syndrome Toxin production genes directly from clinical patient stool specimens utilizing a novel lysis extraction process in parallel with the Roche MagNA Pure Compact. These assays are specific, sensitive and reliable for the detection of the staphylococcal enterotoxin encoding genes and the tst1 gene from known toxin producing strains of Staphylococcus aureus. Specificity was determined by testing a total of 47 microorganism strains, including 8 previously characterized staphylococcal enterotoxin producing strains against each rtPCR target. Sensitivity for these assays range from 1 to 25 cfu per rtPCR reaction for cultured isolates and 8-20 cfu per rtPCR for the clinical stool matrix. (C) 2015 Elsevier Ltd. All rights reserved.
机译:为了最大程度地减少标本量,处理和测试时间,我们开发了两种TaqMar(R)多重实时PCR(rtPCR)分析方法,可通过新型溶出提取法直接从临床患者粪便标本中检测葡萄球菌肠毒素AE和中毒性休克综合症毒素产生基因与Roche MagNA Pure Compact并行处理。这些测定对于从已知的金黄色葡萄球菌产生毒素的菌株中检测葡萄球菌肠毒素编码基因和tst1基因具有特异性,灵敏性和可靠性。通过测试总共47种微生物菌株(包括8种先前鉴定的针对每个rtPCR靶标的葡萄球菌肠毒素菌株)来确定特异性。这些分析的灵敏度范围为培养分离物每个rtPCR反应1到25 cfu,而临床粪便基质的每个rtPCR反应8-20 cfu。 (C)2015 Elsevier Ltd.保留所有权利。

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