Key Laboratory of Dairy Science, Ministry of Education, College of Food Science, Northeast Agricultural University, Harbin, China.
Crit Rev Food Sci Nutr. 2024;64(16):5398-5413. doi: 10.1080/10408398.2022.2154073. Epub 2022 Dec 8.
Milk contaminated with trace amounts of foodborne pathogens can considerably threaten food safety and public health. Therefore, rapid and accurate detection techniques for foodborne pathogens in milk are essential. Nucleic acid amplification (NAA)-based strategies are widely used to detect foodborne pathogens in milk. This review article covers the mechanisms of the NAA-based detection of foodborne pathogens in milk, including polymerase chain reaction (PCR), loop-mediated isothermal amplification (LAMP), recombinase polymerase amplification (RPA), rolling circle amplification (RCA), and enzyme-free amplification, among others. Key factors affecting detection efficiency and the advantages and disadvantages of the above techniques are analyzed. Potential on-site detection tools based on NAA are outlined. We found that NAA-based strategies were effective in detecting foodborne pathogens in milk. Among them, PCR was the most reliable. LAMP showed high specificity, whereas RPA and RCA were most suitable for on-site and in-situ detection, respectively, and enzyme-free amplification was more economical. However, factors such as sample separation, nucleic acid target conversion, and signal transduction affected efficiency of NAA-based strategies. The lack of simple and effective sample separation methods to reduce the effect of milk matrices on detection efficiency was noteworthy. Further research should focus on simplifying, integrating, and miniaturizing microfluidic on-site detection platforms.
微量食物病原体污染的牛奶会对食品安全和公共健康造成严重威胁。因此,快速准确地检测牛奶中的食源性病原体至关重要。基于核酸扩增 (NAA) 的策略被广泛用于检测牛奶中的食源性病原体。本文综述了基于 NAA 的牛奶中食源性病原体检测的机制,包括聚合酶链反应 (PCR)、环介导等温扩增 (LAMP)、重组酶聚合酶扩增 (RPA)、滚环扩增 (RCA) 和无酶扩增等。分析了影响检测效率的关键因素以及上述技术的优缺点。概述了基于 NAA 的潜在现场检测工具。我们发现,基于 NAA 的策略在检测牛奶中的食源性病原体方面非常有效。其中,PCR 是最可靠的。LAMP 表现出很高的特异性,而 RPA 和 RCA 分别最适合现场和原位检测,无酶扩增则更经济。然而,样本分离、核酸靶标转换和信号转导等因素会影响 NAA 策略的效率。需要注意的是,缺乏简单有效的样本分离方法来降低牛奶基质对检测效率的影响。未来的研究应侧重于简化、集成和微型化现场检测平台。