{"title":"Evaluation of selective enrichment media for accurate most probable number enumeration of Listeria monocytogenes in ready-to-eat seafood products.","authors":"Kaori Komori, Yuna Kono, Ayaka Nakamura, Takashi Kuda, Hajime Takahashi","doi":"10.1016/j.mimet.2026.107527","DOIUrl":null,"url":null,"abstract":"<p><p>Listeria monocytogenes is a foodborne bacterium that can cause listeriosis. Ready-to-eat (RTE) seafood products are among the food categories associated with listeriosis. Because contamination levels of L. monocytogenes in RTE seafood products are often below 10 CFU/g, accurate enumeration of low bacterial concentrations is essential for reliable risk assessment of these products. A most probable number (MPN) method is widely used for enumerating low bacterial concentrations in food samples; however, the choice of selective enrichment medium strongly affects recovery, especially in the presence of competing microflora and injured cells. In this study, five types of RTE seafood products were inoculated with low concentrations of L. monocytogenes, and four selective enrichment media including half Fraser broth, Listeria enrichment broth (UVM and FDA formulation), and buffered Listeria enrichment broth (BLEB) were compared. When samples were incubated in BLEB for 48 h, the MPN values agreed with the inoculation levels in 93-100% across strains and food matrices. Under these conditions, MPN estimates for heat-injured inocula were accurate in 93% of cases. Among the media evaluated, incubation in BLEB for 48 h yielded the most accurate and consistent MPN estimates across strains and food matrices, supporting its suitability for quantitative analysis of low levels of L. monocytogenes.</p>","PeriodicalId":16409,"journal":{"name":"Journal of microbiological methods","volume":" ","pages":"107527"},"PeriodicalIF":1.9000,"publicationDate":"2026-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of microbiological methods","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.mimet.2026.107527","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Listeria monocytogenes is a foodborne bacterium that can cause listeriosis. Ready-to-eat (RTE) seafood products are among the food categories associated with listeriosis. Because contamination levels of L. monocytogenes in RTE seafood products are often below 10 CFU/g, accurate enumeration of low bacterial concentrations is essential for reliable risk assessment of these products. A most probable number (MPN) method is widely used for enumerating low bacterial concentrations in food samples; however, the choice of selective enrichment medium strongly affects recovery, especially in the presence of competing microflora and injured cells. In this study, five types of RTE seafood products were inoculated with low concentrations of L. monocytogenes, and four selective enrichment media including half Fraser broth, Listeria enrichment broth (UVM and FDA formulation), and buffered Listeria enrichment broth (BLEB) were compared. When samples were incubated in BLEB for 48 h, the MPN values agreed with the inoculation levels in 93-100% across strains and food matrices. Under these conditions, MPN estimates for heat-injured inocula were accurate in 93% of cases. Among the media evaluated, incubation in BLEB for 48 h yielded the most accurate and consistent MPN estimates across strains and food matrices, supporting its suitability for quantitative analysis of low levels of L. monocytogenes.
期刊介绍:
The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach.
All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.