Routine monitoring of foodborne pathogens such as Listeria monocytogenes in food processing environments are time-consuming necessities to ensure food safety. Alternative rapid diagnostic methods for pathogen detection are increasingly used, but often demand specialized equipment, making them unsuitable for on-site testing. This short communication describes the successful demonstration of combining the sample preparation method Matrix-Lysis with a chemiluminescent based detection platform (AquaSpark™) for detection of L. monocytogenes in milk and yogurt. The proposed method was evaluated against qPCR resulting in 100% relative specificity for both foodstuffs and a relative sensitivity of 100% for milk as well as 96% for yogurt for bacterial levels >1 CFU/ml. Only at very low initial bacterial concentrations (<1 CFU/ml) diverging results were found highlighting the advantages and limitations of both methods. While being less susceptible to contamination and false positive results from non-growing or dead cells, qPCR had a slightly lower overall detection limit. However, it has to be pointed out that qPCR has an increased analytical cost and also requires an additional 24 h analysis time. This study demonstrates the first successful application of a chemilumonogenic detection approach for L. monocytogenes in food that has a high potential for on-site testing.
Keywords: AquaSpark; Listeria monocytogenes; Rapid methods; Sample preparation; qPCR.
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