Shan Shan, Xiaoyu Tong, Wenyu Du, Yin Chen, Long Cheng, Fang Yan, Yujie Zhai, Kui Zhao, Haiyan Ni, Xiaomei Sha, Xiaoqing Liu, Chengwei Liu, Shuanglong Wang, Daofeng Liu
{"title":"高分辨率融化分析同时检测淡水鱼中4种食源性致病菌","authors":"Shan Shan, Xiaoyu Tong, Wenyu Du, Yin Chen, Long Cheng, Fang Yan, Yujie Zhai, Kui Zhao, Haiyan Ni, Xiaomei Sha, Xiaoqing Liu, Chengwei Liu, Shuanglong Wang, Daofeng Liu","doi":"10.3390/foods14183202","DOIUrl":null,"url":null,"abstract":"<p><p>Many countries around the world feature raw fish in their cuisine, which is valued for its unique flavor. However, raw fish may be easily contaminated with foodborne pathogens including <i>Listeria monocytogenes</i>, <i>Salmonella</i>, <i>Vibrio parahaemolyticus</i>, and <i>Staphylococcus aureus</i>. Herein, a method was established that integrated a multiplex polymerase chain reaction (PCR) and high-resolution melting (HRM) curve assay for the simultaneous detection of these four foodborne pathogens. The target genes of the bacteria were amplified by PCR and subsequently analyzed using HRM. Differentiation was achieved based on the melting temperature (Tm) values of their respective amplicons. The detection limit of the PCR-HRM assay was 0.02-0.1 ng/µL. In addition, the Tm remained nearly constant across various concentrations of genomic DNA derived from the target bacteria. The assay demonstrated perfect specificity (8/8) and a sensitivity of 5/5 for <i>L. monocytogenes</i>, 2/2 for <i>Salmonella</i>, 3/3 for <i>V. parahaemolyticus</i>, and 3/3 for <i>S. aureus</i>. No significant interference occurred when genomic DNA from the four target bacteria was co-extracted with DNA from eight non-target strains. Furthermore, the assay offers advantages including operational simplicity, high efficiency, accurate results, reduced detection time, and lower costs, rendering it well-suited for food safety applications in the aquatic products processing industry.</p>","PeriodicalId":12386,"journal":{"name":"Foods","volume":"14 18","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12469668/pdf/","citationCount":"0","resultStr":"{\"title\":\"Simultaneous Detection of Four Foodborne Pathogens in Raw Freshwater Fish Using High-Resolution Melting Analysis.\",\"authors\":\"Shan Shan, Xiaoyu Tong, Wenyu Du, Yin Chen, Long Cheng, Fang Yan, Yujie Zhai, Kui Zhao, Haiyan Ni, Xiaomei Sha, Xiaoqing Liu, Chengwei Liu, Shuanglong Wang, Daofeng Liu\",\"doi\":\"10.3390/foods14183202\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Many countries around the world feature raw fish in their cuisine, which is valued for its unique flavor. However, raw fish may be easily contaminated with foodborne pathogens including <i>Listeria monocytogenes</i>, <i>Salmonella</i>, <i>Vibrio parahaemolyticus</i>, and <i>Staphylococcus aureus</i>. Herein, a method was established that integrated a multiplex polymerase chain reaction (PCR) and high-resolution melting (HRM) curve assay for the simultaneous detection of these four foodborne pathogens. The target genes of the bacteria were amplified by PCR and subsequently analyzed using HRM. Differentiation was achieved based on the melting temperature (Tm) values of their respective amplicons. The detection limit of the PCR-HRM assay was 0.02-0.1 ng/µL. In addition, the Tm remained nearly constant across various concentrations of genomic DNA derived from the target bacteria. The assay demonstrated perfect specificity (8/8) and a sensitivity of 5/5 for <i>L. monocytogenes</i>, 2/2 for <i>Salmonella</i>, 3/3 for <i>V. parahaemolyticus</i>, and 3/3 for <i>S. aureus</i>. 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Simultaneous Detection of Four Foodborne Pathogens in Raw Freshwater Fish Using High-Resolution Melting Analysis.
Many countries around the world feature raw fish in their cuisine, which is valued for its unique flavor. However, raw fish may be easily contaminated with foodborne pathogens including Listeria monocytogenes, Salmonella, Vibrio parahaemolyticus, and Staphylococcus aureus. Herein, a method was established that integrated a multiplex polymerase chain reaction (PCR) and high-resolution melting (HRM) curve assay for the simultaneous detection of these four foodborne pathogens. The target genes of the bacteria were amplified by PCR and subsequently analyzed using HRM. Differentiation was achieved based on the melting temperature (Tm) values of their respective amplicons. The detection limit of the PCR-HRM assay was 0.02-0.1 ng/µL. In addition, the Tm remained nearly constant across various concentrations of genomic DNA derived from the target bacteria. The assay demonstrated perfect specificity (8/8) and a sensitivity of 5/5 for L. monocytogenes, 2/2 for Salmonella, 3/3 for V. parahaemolyticus, and 3/3 for S. aureus. No significant interference occurred when genomic DNA from the four target bacteria was co-extracted with DNA from eight non-target strains. Furthermore, the assay offers advantages including operational simplicity, high efficiency, accurate results, reduced detection time, and lower costs, rendering it well-suited for food safety applications in the aquatic products processing industry.
期刊介绍:
Foods (ISSN 2304-8158) is an international, peer-reviewed scientific open access journal which provides an advanced forum for studies related to all aspects of food research. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists, researchers, and other food professionals to publish their experimental and theoretical results in as much detail as possible or share their knowledge with as much readers unlimitedly as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, unique features of this journal:
manuscripts regarding research proposals and research ideas will be particularly welcomed
electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material
we also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds