首页> 外文期刊>International Journal of Food Microbiology >A multiparametric PCR-based tool for fast detection and identification of spore-forming bacteria in food.
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A multiparametric PCR-based tool for fast detection and identification of spore-forming bacteria in food.

机译:一种基于多参数PCR的工具,用于快速检测和识别食品中的孢子形成细菌。

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摘要

The presence of psychrotrophic or highly thermoresistant spore-forming bacteria in food and feedstuff responsible for food poisoning and spoilage raises major safety and economical issues. The aim of this study was to evaluate the performances of a ready-to-use PCR assay (alternative method) in comparison with the standard microbiological plating method regarding spore-forming bacteria detection in food samples. An overnight sample enrichment was selected to increase sporeformer diversity recovery, spore germination, bacterial growth and favour DNA extraction. A total of 180 sporeformer isolates representing 38 different species and 8 genera were tested in the PCR assays. Inclusivity and exclusivity results ensured specific detection and identification of the majority of targeted genera and species. Validation studies carried on artificially contaminated food samples showed detection of the inoculated contaminants in most cases, with increased detection limit for the alternative method which enabled detection with 1 spore of B. cereus in 25 g food sample. Using naturally contaminated food samples, standard method comforted the alternative method. In a number of cases, the alternative method was able to identify species not detected with the standard method. In addition, identification and discrimination between the B. cereus group members was possible. Thus, associated to a key element, i.e., the enrichment step, the developed multiparametric PCR-based assays reported in this study provide a fast, sensitive and reliable detection and identification tool for mostly encountered spore-forming food contaminants.
机译:食物和饲料中存在引起食物中毒和腐败的精神营养性或高度耐热的芽孢形成细菌会引起重大的安全和经济问题。这项研究的目的是评估就食品样品中的孢子形成细菌检测而言,与标准微生物接种方法相比,即用型PCR分析(替代方法)的性能。选择过夜样品富集以增加孢子形成者的多样性恢复,孢子萌发,细菌生长并有利于DNA提取。在PCR分析中测试了代表38个不同物种和8个属的总共180个芽孢形成菌分离物。排他性和排他性结果确保了对大多数目标属和物种的特异性检测和鉴定。对人工污染的食品样品进行的验证研究表明,在大多数情况下,可以检测到所感染的污染物,而对另一种方法的检测限则提高了,该方法可以在25 g食品样品中用1株蜡状芽孢杆菌进行检测。使用自然污染的食品样品,标准方法使替代方法更加舒适。在许多情况下,替代方法能够识别标准方法未检测到的物种。另外,蜡状芽孢杆菌组成员之间的鉴定和区分是可能的。因此,与关键要素(即富集步骤)相关,本研究中报道的已开发的基于多参数PCR的检测方法为大多数常见的形成孢子的食品污染物提供了快速,灵敏和可靠的检测和鉴定工具。

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