{"title":"Rapid detection of Salmonella and Staphylococcus aureus using a hand-held nucleic acid detection system","authors":"Zhen Wang, Wen Lu, Xiutong Li, Na Xu, Lihong Lin, Qi Song, Yiteng Liu, Zhiyang Hu, Sheng Guo, Yibo Gao, Weijia Wen","doi":"10.1111/jfs.13157","DOIUrl":null,"url":null,"abstract":"<p><i>Salmonella</i> and <i>Staphylococcus aureus</i> are common pathogens that cause foodborne illnesses. Currently, the detection of these pathogens involves time-consuming procedures, namely isolation, cultivation, and biochemical identification, making it impossible for on-site real-time testing. In this study, we developed a compact hand-held real-time fluorescent nucleic acid testing device and specific lyophilized reagents to achieve rapid detection of <i>Salmonella</i> and <i>S. aureus</i> within 30 min. The detection sensitivity was 100 colony-forming units (CFU)/mL for <i>Salmonella</i> and 125 CFU/mL for <i>S. aureus</i>. This technique significantly reduced the detection time compared with the traditional cultivation method. Even at low initial concentrations of 5 CFU/mL for <i>Salmonella</i> and 15 CFU/mL for <i>S. aureus</i>, it demonstrated superior performance compared with traditional cultivation, detecting the target bacteria more than 2 days earlier than that method. Notably, we achieved 100% in the detection of <i>Salmonella</i> and <i>S. aureus</i> using spiked pastry samples. In addition, the proposed detection system exhibited excellent specificity when tested against 27 bacterial strains. In conclusion, the proposed nucleic acid detection system provides a viable, miniaturized solution for rapid detection of bacteria.</p>","PeriodicalId":15814,"journal":{"name":"Journal of Food Safety","volume":"44 4","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jfs.13157","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Food Safety","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jfs.13157","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Salmonella and Staphylococcus aureus are common pathogens that cause foodborne illnesses. Currently, the detection of these pathogens involves time-consuming procedures, namely isolation, cultivation, and biochemical identification, making it impossible for on-site real-time testing. In this study, we developed a compact hand-held real-time fluorescent nucleic acid testing device and specific lyophilized reagents to achieve rapid detection of Salmonella and S. aureus within 30 min. The detection sensitivity was 100 colony-forming units (CFU)/mL for Salmonella and 125 CFU/mL for S. aureus. This technique significantly reduced the detection time compared with the traditional cultivation method. Even at low initial concentrations of 5 CFU/mL for Salmonella and 15 CFU/mL for S. aureus, it demonstrated superior performance compared with traditional cultivation, detecting the target bacteria more than 2 days earlier than that method. Notably, we achieved 100% in the detection of Salmonella and S. aureus using spiked pastry samples. In addition, the proposed detection system exhibited excellent specificity when tested against 27 bacterial strains. In conclusion, the proposed nucleic acid detection system provides a viable, miniaturized solution for rapid detection of bacteria.
期刊介绍:
The Journal of Food Safety emphasizes mechanistic studies involving inhibition, injury, and metabolism of food poisoning microorganisms, as well as the regulation of growth and toxin production in both model systems and complex food substrates. It also focuses on pathogens which cause food-borne illness, helping readers understand the factors affecting the initial detection of parasites, their development, transmission, and methods of control and destruction.