Food Hygiene, Inspection and Control Laboratory, Department of Analytical Chemistry, Nutrition and Bromatology, Campus Terra, University of Santiago de Compostela, Santiago de Compostela, Spain.
Food Quality and Safety Research Group, International Iberian Nanotechnology Laboratory, Braga, Portugal.
Methods Mol Biol. 2025;2852:65-81. doi: 10.1007/978-1-0716-4100-2_5.
Foodborne pathogens remain a serious health issue in developed and developing countries. Safeness of food products has been assured for years with culture-based microbiological methods; however, these present several limitations such as turnaround time and extensive hands-on work, which have been typically address taking advantage of DNA-based methods such as real-time PCR (qPCR). These, and other similar techniques, are targeted assays, meaning that they are directed for the specific detection of one specific microbe. Even though reliable, this approach suffers from an important limitation that unless specific assays are design for every single pathogen potentially present, foods may be considered erroneously safe. To address this problem, next-generation sequencing (NGS) can be used as this is a nontargeted method; thus it has the capacity to detect every potential threat present. In this chapter, a protocol for the simultaneous detection and preliminary serotyping of Salmonella enterica serovar Enteritidis, Salmonella enterica serovar Typhimurium, Listeria monocytogenes, and Escherichia coli O157:H7 is described.
食源性病原体仍然是发达国家和发展中国家的一个严重健康问题。多年来,基于培养的微生物学方法确保了食品的安全性;然而,这些方法存在一些局限性,例如周转时间和大量的手工操作,这些问题通常通过利用基于 DNA 的方法(如实时 PCR(qPCR))来解决。这些方法和其他类似的技术是靶向检测方法,这意味着它们是针对特定微生物的特定检测而设计的。尽管这种方法可靠,但它存在一个重要的局限性,即除非为可能存在的每一种病原体设计特定的检测方法,否则食品可能会被错误地认为是安全的。为了解决这个问题,可以使用下一代测序(NGS),因为这是一种非靶向方法;因此,它有能力检测到所有潜在的威胁。在本章中,描述了一种同时检测和初步血清分型肠炎沙门氏菌血清型肠炎亚种、鼠伤寒沙门氏菌、单增李斯特菌和大肠杆菌 O157:H7 的方法。