Rapid and accurate quantification of viable Listeria monocytogenes with clonal specificity using microfluidic droplet digital PCR based technology

Abstract

To overcome the technical bottlenecks in the precise quantification and molecular typing of viable foodborne pathogens, this study establishes a microfluidic droplet digital PCR (ddPCR) based method for rapid and accurate detection and quantification of viable Listeria monocytogenes with clonal specificity. In contrast to the time-consuming plate culture methods and unspecific rapid detection methods, the method in this study employs clonal complex (CC) specific primers and probe for strain-specificity and integrate the nucleic acid dye propidium monoazide (PMA) to effectively distinguish viable from dead bacteria. The rapid and precise quantification of viable bacteria is achieved through microdroplet counting. This method does not require DNA extraction, and the entire detection process takes only about 3 hours, with a quantitative detection limit of 3.3x102 CFU/mL, providing strong technical support for the risk monitoring of highly pathogenic specific types of L. monocytogenes.