Shixin Yan, Yuling Xiao, Ruijuan Shen, Jiazhe Cheng, Yuling Zhang, Nan Wu, Jinhao Chen, Jie Chen, Peng Zhang, Jia Geng
{"title":"Simultaneous detection of dual targets Escherichia coli and Salmonella enteritidis using enzyme-free strand displacement reaction","authors":"Shixin Yan, Yuling Xiao, Ruijuan Shen, Jiazhe Cheng, Yuling Zhang, Nan Wu, Jinhao Chen, Jie Chen, Peng Zhang, Jia Geng","doi":"10.1002/mba2.70002","DOIUrl":null,"url":null,"abstract":"<p><i>Escherichia coli</i> (<i>E. coli</i>) and <i>Salmonella enteritidis</i> (<i>S. enteritidis</i>) are common food-borne pathogens, which pose a very significant threat to the healthcare environment. The rapid detection of relevant bacteria can help control their rapid spread, while the traditional bacterial culture detection method is time-consuming and not conducive to the rapid detection of pathogens. Recently, new detection methods for related pathogenic bacteria have emerged, but these methods are relatively complex, and few methods can detect two bacteria at the same time. Therefore, there is an urgent need to develop multi-target, convenient, and fast pathogen detection methods. This method successfully constructed an enzyme-free fluorescent biosensor based on the adapter-mediated strand displacement reaction to detect <i>E. coli</i> ATCC25922 and <i>S. enteritidis</i> ATCC13076. This method had an ultrasensitive detection limit of 0.7 CFU/mL and 0.61 CFU/mL within 20 min, with a broad linear range of 34–10<sup>5</sup> CFU/mL of <i>E. coli</i> and 17–10<sup>6</sup> CFU/mL of <i>S. enteritidis</i>, respectively. Importantly, the spiked recovery of the three clinical fluid samples performed well, which proved that this method had the potential to detect <i>E. coli</i> and <i>S. enteritidis</i> in clinical samples. The sensor constructed by this method can detect dual targets at the same time, increasing the possibility of large-scale clinical use.</p>","PeriodicalId":100901,"journal":{"name":"MedComm – Biomaterials and Applications","volume":"4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mba2.70002","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"MedComm – Biomaterials and Applications","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/mba2.70002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Escherichia coli (E. coli) and Salmonella enteritidis (S. enteritidis) are common food-borne pathogens, which pose a very significant threat to the healthcare environment. The rapid detection of relevant bacteria can help control their rapid spread, while the traditional bacterial culture detection method is time-consuming and not conducive to the rapid detection of pathogens. Recently, new detection methods for related pathogenic bacteria have emerged, but these methods are relatively complex, and few methods can detect two bacteria at the same time. Therefore, there is an urgent need to develop multi-target, convenient, and fast pathogen detection methods. This method successfully constructed an enzyme-free fluorescent biosensor based on the adapter-mediated strand displacement reaction to detect E. coli ATCC25922 and S. enteritidis ATCC13076. This method had an ultrasensitive detection limit of 0.7 CFU/mL and 0.61 CFU/mL within 20 min, with a broad linear range of 34–105 CFU/mL of E. coli and 17–106 CFU/mL of S. enteritidis, respectively. Importantly, the spiked recovery of the three clinical fluid samples performed well, which proved that this method had the potential to detect E. coli and S. enteritidis in clinical samples. The sensor constructed by this method can detect dual targets at the same time, increasing the possibility of large-scale clinical use.