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A new single-tube platform of melting temperature curve analysis based on multiplex real-time PCR using EvaGreen for simultaneous screening detection of Shiga toxin-producing Escherichia coli, Salmonella spp. and Listeria monocytogenes in food

机译:基于多重实时PCR的新型熔融温度曲线分析的新单管平台,采用EVAGREEN同时筛选滋阴毒素大肠杆菌,沙门氏菌SPP。 和histeria单核细胞增生在食物中

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Shiga toxin-producing Escherichia colt (STEC), Salmonella spp. and Listeria monocytogenes are continuously reported as causative agents of great concern regarding food safety and widespread contamination in many food varieties. Therefore, their simultaneous detection may be advantageous in terms of cost, time and labor savings and simplicity. This study developed a new, simple platform of multiplex real-time polymerase chain reaction (mRT-PCR) for specific, sensitive and rapid detection of STEC, Salmonella spp. and L. monocytogenes in food. The single-tube mRT-PCR format was developed by combining an 18 h enrichment step in simultaneous enrichment broth, boiling based on DNA extraction assay and a mRT-PCR detection system based on melting curve analysis using a fluorescent dye (EvaGreen) for detection of the presence or absence of the three target bacterial pathogens in food samples. Three specific peaks were clearly detected with average melting temperatures of 84.52 +/- 0.90 degrees C, 87.51 +/- 0.54 degrees C and 79.32 degrees C 0.48 degrees C for STEC, Salmonella spp. and L. monocytogenes, respectively. The sensitivity and specificity of these newly developed mRT-PCR platforms were further investigated using artificially and naturally contaminated food samples. The relative sensitivity, relative specificity and relative accuracy were all 100%, with a detection limit of 1 cfu for each target pathogen in 25 g of food sample. The developed platform of EvaGreen-based single-tube mRT-PCR for detection of the three target pathogenic bacteria in food samples provided results of absence or presence within 20 h. The newly developed mRT-PCR platform in this study offers a promising approach for simple, rapid, sensitive, specific and accurate detection of the three target bacterial pathogens in food.
机译:Shiga毒素生产大肠杆菌(Stec),沙门氏菌SPP。并且李斯特菌单核细胞元被持续报告为对食品安全和许多食物品种的广泛污染的致病因素。因此,在成本,时间和劳动力节省和简单性方面,它们的同时检测可能是有利的。本研究开发了一种新的,简单的多重实时聚合酶链反应(MRT-PCR)平台,用于STEC,Salmonella SPP的特异性,灵敏和快速检测。和L.食物中的单核细胞元。通过将18小时富集步骤组合在同时富集肉汤中,基于DNA提取测定和使用荧光染料(EVAGREEEN)进行熔化曲线分析的MRT-PCR检测系统来开发单管MRT-PCR格式。在食物样品中存在或不存在三种靶细菌病原体。清楚地检测到三种特异性峰,平均熔化温度为84.52 +/- 0.90℃,87.51 +/- 0.54℃和79.32摄氏度,Salmonella SPP的Salmonella SPP为0.48℃。和L.单核细胞增生。通过人工和天然污染的食物样品进一步研究了这些新开发的MRT-PCR平台的敏感性和特异性。相对敏感性,相对特异性和相对精度均为100%,具有25g食物样品中的每种靶病原体的1 cfu的检出限。用于检测食物样品中的三个靶致病细菌的基于EVAGREEN的单管MRT-PCR的开发平台在20小时内提供了不存在或存在的结果。该研究的新开发的MRT-PCR平台提供了一种有希望的方法,可用于在食品中的三种靶细菌病原体的简单,快速,敏感,具体和准确地检测。

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