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An alternative real-time PCR method to detect Bacillus cereus group in naturally contaminated food gelatine: a comparison study

机译:另一种检测天然污染食品明胶中蜡状芽孢杆菌组的实时pCR方法:对比研究

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摘要

Comparison of an internally controlled real-time PCR assay with the standard plate-based assay (ISO 21871) for the detection of Bacillus cereus group cells in gelatine.A comprehensive TaqMan probe was designed allowing the real-time PCR assay to be fully inclusive and exclusive. An internal amplification control was designed and implemented at 500 copies per reaction without impact on target detection. Specific and selective detection of target cells was achieved with a quick and simple DNA preparation procedure. No significant difference (kappa = 0.99) was observed between the performance of the real-time PCR and the standard plate-based method on naturally contaminated gelatines (n = 197). Relative accuracy, relative sensitivity and relative specificity were >= 99%.The real-time PCR assay is a valid alternative of the standard plate-based assay.The real-time PCR assay decreased the time between sample collection and result from 2 days to 2 h, while analysis cost did not increase. The gelatine-producing industry can ensure gelatine safety and quality in a much faster way.
机译:将内部控制的实时PCR分析与基于标准板的分析(ISO 21871)用于检测明胶中蜡状芽胞杆菌组细胞的比较。设计了全面的TaqMan探针,使实时PCR分析具有全面的包独家。内部扩增对照的设计和实施为每个反应500个拷贝,而不会影响靶标检测。通过快速简单的DNA制备程序可实现目标细胞的特异性和选择性检测。实时PCR和基于板的基于标准方法的自然污染明胶(n = 197)之间没有观察到显着差异(kappa = 0.99)。相对准确度,相对灵敏度和相对特异性均> = 99%。实时PCR测定法是标准板式测定法的有效替代方法。实时PCR测定法将样品收集与结果之间的时间从2天缩短至2小时,而分析成本并未增加。明胶生产行业可以以更快的方式确保明胶的安全性和质量。

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