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Improved Template Preparation for PCR-Based Assays for Detection of Food-Borne Bacterial Pathogens

机译:改进的模板制备,用于基于PCR的食品中细菌病原体检测方法

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摘要

Shigella flexneri, Salmonella enterica serotype Typhimurium, and Listeria monocytogenes were applied to FTA filters, and the filters were used directly as templates to demonstrate their sensitivity and applicability in PCR-based detection assays. With pure cultures, the sensitivities of detection by FTA filter-based PCR were 30 to 50 and 200 CFU for the gram-negative enterics and Listeria, respectively. Different numbers of S. flexneri cells were used in controlled contamination experiments with several different foods (produce, beef, and apple cider). Aliquots from concentrated food washes subsequently spotted onto FTA filters and assayed by PCR gave consistently positive results and detection limits similar to those observed with pure-culture dilutions. This universal method for PCR template preparation from bacterial cells is rapid and highly sensitive and reduces interference from food-associated inhibitors of PCR. In addition, its broad applicability eliminates the need for multiple methods for analysis of food matrices.
机译:将弗氏志贺氏菌,肠炎沙门氏菌血清型鼠伤寒沙门氏菌和单核细胞增生李斯特菌应用于FTA过滤器,并将这些过滤器直接用作模板,以证明其灵敏度和在基于PCR的检测方法中的适用性。对于纯培养物,革兰氏阴性肠溶菌和李斯特菌的基于FTA过滤器的PCR检测灵敏度分别为30至50和200 CFU。在几种不同食品(农产品,牛肉和苹果酒)的受控污染实验中使用了不同数量的弗氏链球菌细胞。随后将浓缩的食品洗涤液的等分试样点样到FTA过滤器上,并通过PCR进行测定,得出的阳性结果和检出限始终与纯培养物稀释液相似。这种从细菌细胞制备PCR模板的通用方法是快速且高度敏感的,并减少了与食品相关的PCR抑制剂的干扰。此外,其广泛的适用性消除了对多种食品基质分析方法的需求。

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