{"title":"用流式细胞术分析食物中营养细胞和孢子萌发","authors":"Souichirou Kawai, Miyo Nakano","doi":"10.1016/j.mimet.2025.107137","DOIUrl":null,"url":null,"abstract":"<div><div>The detection of spore-forming bacteria in food is crucial because they potentially cause spoilage. However, traditional microbial tests are time-consuming and inefficient. Here, we report the use of flow cytometry with 5-cyano-2,3-ditolyl-2H-tetrazolium chloride (CTC) staining for the rapid detection and monitoring of spore germination. In particular, we investigated sporulation and metabolic activity in <em>Paenibacillus</em>, <em>Sporosarcina</em>, and <em>Clostridium</em> spp. and validated our method using real food samples. Our approach enabled the rapid detection of spore-forming bacteria and spore germination followed by outgrowth in food. Flow cytometry is a valuable tool for distinguishing vegetative cells and spores in food samples. In this study, we used flow cytometry with CTC staining to determine spore germination and vegetative cell populations. Our findings revealed that 0.2 % peracetic acid treatment inhibited spore germination, as indicated by decreased metabolically active spore count and increased vegetative cell count detected via flow cytometry. Additionally, flow cytometry enabled rapid and accurate differentiation of spores from vegetative cells, providing quantitative insights into bacterial viability within minutes. These findings indicate that flow cytometry is a reliable and practical tool for real-time microbial monitoring in food safety, offering advantages over conventional culture-based methods.</div></div>","PeriodicalId":16409,"journal":{"name":"Journal of microbiological methods","volume":"232 ","pages":"Article 107137"},"PeriodicalIF":1.7000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Analysis of vegetative cells and spore germination in food using flow cytometry\",\"authors\":\"Souichirou Kawai, Miyo Nakano\",\"doi\":\"10.1016/j.mimet.2025.107137\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The detection of spore-forming bacteria in food is crucial because they potentially cause spoilage. However, traditional microbial tests are time-consuming and inefficient. Here, we report the use of flow cytometry with 5-cyano-2,3-ditolyl-2H-tetrazolium chloride (CTC) staining for the rapid detection and monitoring of spore germination. In particular, we investigated sporulation and metabolic activity in <em>Paenibacillus</em>, <em>Sporosarcina</em>, and <em>Clostridium</em> spp. and validated our method using real food samples. Our approach enabled the rapid detection of spore-forming bacteria and spore germination followed by outgrowth in food. Flow cytometry is a valuable tool for distinguishing vegetative cells and spores in food samples. In this study, we used flow cytometry with CTC staining to determine spore germination and vegetative cell populations. Our findings revealed that 0.2 % peracetic acid treatment inhibited spore germination, as indicated by decreased metabolically active spore count and increased vegetative cell count detected via flow cytometry. Additionally, flow cytometry enabled rapid and accurate differentiation of spores from vegetative cells, providing quantitative insights into bacterial viability within minutes. These findings indicate that flow cytometry is a reliable and practical tool for real-time microbial monitoring in food safety, offering advantages over conventional culture-based methods.</div></div>\",\"PeriodicalId\":16409,\"journal\":{\"name\":\"Journal of microbiological methods\",\"volume\":\"232 \",\"pages\":\"Article 107137\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-04-25\",\"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://www.sciencedirect.com/science/article/pii/S0167701225000533\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of microbiological methods","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167701225000533","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}
Analysis of vegetative cells and spore germination in food using flow cytometry
The detection of spore-forming bacteria in food is crucial because they potentially cause spoilage. However, traditional microbial tests are time-consuming and inefficient. Here, we report the use of flow cytometry with 5-cyano-2,3-ditolyl-2H-tetrazolium chloride (CTC) staining for the rapid detection and monitoring of spore germination. In particular, we investigated sporulation and metabolic activity in Paenibacillus, Sporosarcina, and Clostridium spp. and validated our method using real food samples. Our approach enabled the rapid detection of spore-forming bacteria and spore germination followed by outgrowth in food. Flow cytometry is a valuable tool for distinguishing vegetative cells and spores in food samples. In this study, we used flow cytometry with CTC staining to determine spore germination and vegetative cell populations. Our findings revealed that 0.2 % peracetic acid treatment inhibited spore germination, as indicated by decreased metabolically active spore count and increased vegetative cell count detected via flow cytometry. Additionally, flow cytometry enabled rapid and accurate differentiation of spores from vegetative cells, providing quantitative insights into bacterial viability within minutes. These findings indicate that flow cytometry is a reliable and practical tool for real-time microbial monitoring in food safety, offering advantages over conventional culture-based methods.
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.