结合传统培养方法、基因图谱和单叠氮丙啶定量PCR对即食沙拉中单核增生李斯特菌的评估

Rita Bernardo, A. Duarte, L. Tavares, A. Barreto, A. Henriques
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引用次数: 0

摘要

单核细胞增生李斯特菌仍然是食源性疾病的一个重要原因。李斯特菌病几乎完全通过食物传播。几项研究证实,即食食品是单核细胞增生乳杆菌传播给消费者的媒介。本研究旨在利用传统的基于培养和分子的方法来评估即食沙拉的保质期。利用多重PCR对分离的单核增生乳杆菌进行鉴定和血清分型,并利用脉冲场凝胶电泳(PFGE)进行遗传分型。pmax - qpcr是L.食品科学进展3 www.videleaf.com食品中单核增生基因定量的替代方法。沙拉样品分别在4°C、12°C和16°C下保存8天并进行分析。在4°C时,考虑到整个研究过程中的卫生指标,即肠杆菌科(范围为3.55±0.15 log cfu/g至5.39±0.21 log cfu/g)和好氧嗜中菌菌落计数(范围为5.91±0.90 log cfu/g至9.41±0.58 log cfu/g),获得了可接受的结果,但在12°C和16°C时,情况并非如此。与传统的基于培养的方法相比,基于培养的单核增生乳杆菌定量显示出较低的数量(3 log cfu/g),表明有活力但不可培养的形式。本研究结果强调,在即食食品的货架期研究中,需要将传统方法与更敏感、更特异、更快速的单核细胞增生乳杆菌评估方法相结合,以降低消费者的潜在风险。
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Combined Use of Conventional Culture-Based Methods, Genetic Profiling, and Propidium Monoazide Quantitative PCR for Listeria monocytogenes Assessment in a Ready-to-Eat Salad Shelf-Life Study
Listeria monocytogenes remains a significant cause of foodborne illness. Listeriosis is almost exclusively transmitted through food consumption. Ready-to-eat foods have been confirmed as vehicles for transmission of L. monocytogenes to consumers in several studies. This study aimed to assess the shelf-life of a ready-to-eat salad using conventional culture-based and molecular methods. L. monocytogenes isolates were confirmed and serogrouped using multiplex PCR, and genetic subtyping was performed by pulsed-field gel electrophoresis (PFGE). PMAxx-qPCR was used as an alternative method for L. Advances in Food Science 3 www.videleaf.com monocytogenes quantification in foods. Salad samples were kept at 4 °C, 12 °C, and 16 °C for eight days and analysed. At 4 °C, acceptable results were obtained considering hygiene indicators, i.e., Enterobacteriaceae (ranging from 3.55 ± 0.15 log cfu/g to 5.39 ± 0.21 log cfu/g) and aerobic mesophilic colony counts (5.91 ± 0.90 log cfu/g to 9.41 ± 0.58 log cfu/g) throughout the study, but the same did not happen at 12 °C and 16 °C. L. monocytogenes culture-based quantification exhibited low numbers (<1 log cfu/g) for all temperatures. From 30 presumptive isolates, 10 (33.3%) were confirmed as L. monocytogenes with the majority belonging to serogroup IVb. PFGE subtyping showed that 7 of the 10 L. monocytogenes isolates had 100% of pulsotype similarity, suggesting a possible common contamination source. PMAxx-qPCR revealed a statistically higher L. monocytogenes quantification (>3 log cfu/g) when compared to the conventional culture-based method, suggesting viable but non-culturable forms. This study results emphasize the need to combine conventional methods with more sensitive, specific, and rapid ones for L. monocytogenes assessment in ready-to-eat foods shelf-life studies to reduce the potential risk for consumers.
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