{"title":"横向流动免疫层析法快速检测酵母中的圣弗朗西施乳杆菌。","authors":"Kyoka Aiki , Tatsuya Tominaga","doi":"10.1016/j.mimet.2025.107256","DOIUrl":null,"url":null,"abstract":"<div><div>When maintaining sourdough by backslopping, there is a risk that the desired lactic acid bacteria (LAB) strain may be replaced by another. To rapidly monitor the proliferative status of the desired LAB, we developed a lateral flow immunochromatographic assay (LFIA) targeting <em>Fructilactobacillus sanfranciscensis</em>. We investigated the detection sensitivity of LFIA for 13 strains of <em>F. sanfranciscensis</em>. The limit of detection was 5–6 Log (cells/test). No positive result was obtained when the newly developed LFIA was applied against 51 strains other than <em>F. sanfranciscensis</em>, suggesting that it can specifically detect <em>F. sanfranciscensis</em>. To verify the practicality of LFIA, sourdough supplemented with <em>F. sanfranciscensis</em> and <em>Saccharomyces cerevisiae</em> as starters was passaged for 10 days at three different temperatures (23 °C, 30 °C, and 37 °C) with daily backslopping. The condition of these sourdoughs was monitored by pH measurements, yeast and LAB count surveys, amplicon analysis, and LFIA, and the methods were compared for their effectiveness as a management tool. Compared to the 23 °C-incubated samples, fewer <em>F. sanfranciscensis</em> cells were seen in the 30 °C-incubated samples, and the major LAB was replaced by putative <em>Pediococcus acidilactici</em> in the 37 °C-incubated samples. LFIA was successful in detecting both of these sourdough abnormalities. Lateral flow immunochromatographic assay could detect <em>F. sanfranciscensis</em> within 30 min, including the pretreatment step. The newly developed LFIA is expected to be a useful tool for artisan bakeries that want to provide customers with consistent quality sourdough bread every day.</div></div>","PeriodicalId":16409,"journal":{"name":"Journal of microbiological methods","volume":"238 ","pages":"Article 107256"},"PeriodicalIF":1.9000,"publicationDate":"2025-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rapid detection of Fructilactobacillus sanfranciscensis in sourdough by lateral flow immunochromatographic assay\",\"authors\":\"Kyoka Aiki , Tatsuya Tominaga\",\"doi\":\"10.1016/j.mimet.2025.107256\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>When maintaining sourdough by backslopping, there is a risk that the desired lactic acid bacteria (LAB) strain may be replaced by another. To rapidly monitor the proliferative status of the desired LAB, we developed a lateral flow immunochromatographic assay (LFIA) targeting <em>Fructilactobacillus sanfranciscensis</em>. We investigated the detection sensitivity of LFIA for 13 strains of <em>F. sanfranciscensis</em>. The limit of detection was 5–6 Log (cells/test). No positive result was obtained when the newly developed LFIA was applied against 51 strains other than <em>F. sanfranciscensis</em>, suggesting that it can specifically detect <em>F. sanfranciscensis</em>. To verify the practicality of LFIA, sourdough supplemented with <em>F. sanfranciscensis</em> and <em>Saccharomyces cerevisiae</em> as starters was passaged for 10 days at three different temperatures (23 °C, 30 °C, and 37 °C) with daily backslopping. The condition of these sourdoughs was monitored by pH measurements, yeast and LAB count surveys, amplicon analysis, and LFIA, and the methods were compared for their effectiveness as a management tool. Compared to the 23 °C-incubated samples, fewer <em>F. sanfranciscensis</em> cells were seen in the 30 °C-incubated samples, and the major LAB was replaced by putative <em>Pediococcus acidilactici</em> in the 37 °C-incubated samples. LFIA was successful in detecting both of these sourdough abnormalities. Lateral flow immunochromatographic assay could detect <em>F. sanfranciscensis</em> within 30 min, including the pretreatment step. The newly developed LFIA is expected to be a useful tool for artisan bakeries that want to provide customers with consistent quality sourdough bread every day.</div></div>\",\"PeriodicalId\":16409,\"journal\":{\"name\":\"Journal of microbiological methods\",\"volume\":\"238 \",\"pages\":\"Article 107256\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-09-14\",\"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/S0167701225001721\",\"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/S0167701225001721","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}
Rapid detection of Fructilactobacillus sanfranciscensis in sourdough by lateral flow immunochromatographic assay
When maintaining sourdough by backslopping, there is a risk that the desired lactic acid bacteria (LAB) strain may be replaced by another. To rapidly monitor the proliferative status of the desired LAB, we developed a lateral flow immunochromatographic assay (LFIA) targeting Fructilactobacillus sanfranciscensis. We investigated the detection sensitivity of LFIA for 13 strains of F. sanfranciscensis. The limit of detection was 5–6 Log (cells/test). No positive result was obtained when the newly developed LFIA was applied against 51 strains other than F. sanfranciscensis, suggesting that it can specifically detect F. sanfranciscensis. To verify the practicality of LFIA, sourdough supplemented with F. sanfranciscensis and Saccharomyces cerevisiae as starters was passaged for 10 days at three different temperatures (23 °C, 30 °C, and 37 °C) with daily backslopping. The condition of these sourdoughs was monitored by pH measurements, yeast and LAB count surveys, amplicon analysis, and LFIA, and the methods were compared for their effectiveness as a management tool. Compared to the 23 °C-incubated samples, fewer F. sanfranciscensis cells were seen in the 30 °C-incubated samples, and the major LAB was replaced by putative Pediococcus acidilactici in the 37 °C-incubated samples. LFIA was successful in detecting both of these sourdough abnormalities. Lateral flow immunochromatographic assay could detect F. sanfranciscensis within 30 min, including the pretreatment step. The newly developed LFIA is expected to be a useful tool for artisan bakeries that want to provide customers with consistent quality sourdough bread every day.
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.