Application of MinION Long-Read Sequencer for Semi-targeted Detection of Foodborne Pathogens.

Methods Mol Biol

International Iberian Nanotechnology Laboratory, Department of Life Sciences, Food Quality and Safety Research Group, Braga, Portugal.

Published: September 2024

AI Article Synopsis

  • * DNA-based methods like real-time PCR (qPCR) provide reliable detection but are targeted towards specific microbes, which can lead to false safety assessments if not all pathogens are tested.
  • * Next-generation sequencing (NGS) offers a nontargeted approach to identify all potential pathogens in food, and this chapter outlines a protocol for detecting and preliminary serotyping of key pathogens like Salmonella and E. coli.

Article Abstract

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.

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Source
http://dx.doi.org/10.1007/978-1-0716-4100-2_5DOI Listing

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