Molecular Biology Unit, Dairy Microbiology Division, National Dairy Research Institute, Karnal, 132001 Haryana India ; Product and Process Development Group, CALF Building, National Dairy Development Board, Anand, 388001 Gujarat India.
J Food Sci Technol. 2012 Apr;49(2):234-9. doi: 10.1007/s13197-011-0278-3. Epub 2011 Feb 8.
The present investigation reports development of post real time PCR (RTi-PCR) - melt curve analysis for simultaneous detection of Listeria monocytogenes and Salmonella spp. The optimal Sybr Green I (SG-I) concentration of 1.6 μM resulted in two specific peaks with melting temperature (Tm) of 79.90 ± 0.39 °C and 86.29 ± 0.13 °C for L. monocytogenes and Salmonella spp respectively. The detection sensitivity of the assay in reconstituted non-fat dried milk (NFDM; 11%) spiked with the target pathogens at different levels was 3 log cfu per ml of each pathogen. However, the sensitivity was improved up to 1 log cfu per ml by including pre-enrichment step of 6 h. On application of assay on 60 market samples, one sample each of raw milk and ice cream was detected positive for L. monocytogenes and Salmonella spp. Assay was quite specific as no cross reactivity with non target cultures could be observed. The developed assay can find valuable application in monitoring dairy products for the presence of L. monocytogenes and Salmonella spp. to ensure their microbiological quality and safety.
本研究报告开发了实时 PCR (RTi-PCR) - 熔解曲线分析,用于同时检测单核细胞增生李斯特菌和沙门氏菌。最佳的 Sybr Green I (SG-I) 浓度为 1.6 μM,产生两个特异性峰,单核细胞增生李斯特菌和沙门氏菌的熔解温度(Tm)分别为 79.90 ± 0.39°C 和 86.29 ± 0.13°C。该检测方法在不同水平添加目标病原体的再配制无脂干奶(NFDM;11%)中的检测灵敏度为每个病原体 3 个对数 cfu/ml。然而,通过包括 6 小时的预富集步骤,灵敏度提高了 1 个对数 cfu/ml。将该方法应用于 60 个市场样本,发现一份生奶和一份冰淇淋样本中单核细胞增生李斯特菌和沙门氏菌呈阳性。该检测方法具有很好的特异性,未观察到与非目标培养物的交叉反应。该方法可用于监测乳制品中单核细胞增生李斯特菌和沙门氏菌的存在,以确保其微生物质量和安全性。