Jianbo Feng, Ya Huang, Huixin Chen, Shujin Xie, Congzhu Yang, Weixin Zheng, Jinglin Su, Wentao Zheng, Jiajie Mo, Fei Lv
{"title":"基于橙绿可见染料的灵敏而特异的环路介导等温扩增测定,用于检测粪便和血液样本中的沙门氏菌、CTX-M-1 组基因、mph(A) 和 ermB。","authors":"Jianbo Feng, Ya Huang, Huixin Chen, Shujin Xie, Congzhu Yang, Weixin Zheng, Jinglin Su, Wentao Zheng, Jiajie Mo, Fei Lv","doi":"10.1089/fpd.2023.0094","DOIUrl":null,"url":null,"abstract":"<p><p><i>Salmonella</i> is a globally prevalent foodborne bacterium, and ceftriaxone and azithromycin have been regarded as drugs of choice for treating <i>Salmonella</i> infections, particularly in children. With the growing incidence of ceftriaxone and azithromycin resistance in <i>Salmonella</i>, there is an urgent requirement for a rapid and dependable gene testing approach to enhance the efficacy of treating <i>Salmonella</i> infections. Utilizing the orange to green visible dye approach, this study developed loop-mediated isothermal amplification (LAMP) assays for the sensitive and specific detection of <i>Salmonella</i>, ceftriaxone and azithromycin resistance genes (including CTX-M-1 group, <i>mph(A)</i>, and <i>ermB</i> genes) in stool and blood samples. The specificity and sensitivity of primers during the LAMP assays for detection of <i>Salmonella</i>, CTX-M-1 group, <i>mph(A)</i>, and <i>ermB</i> genes were determined in this study. The detection threshold for <i>Salmonella</i> was found to be 1.5 × 10<sup>3</sup> colony-forming units (CFU)/mL, while it was 1.5 × 10<sup>2</sup> CFU/mL for CTX-M-1 group genes (including <i>bla</i><sub>CTX-M-3</sub>, <i>bla</i><sub>CTX-M-15</sub>, and <i>bla</i><sub>CTX-M-55</sub>), 1.5 × 10<sup>2</sup> CFU/mL for <i>mph(A)</i>, and 1.5 × 10<sup>2</sup> CFU/mL for <i>ermB</i>, showing 10-10<sup>3</sup>-fold, 10<sup>3</sup>-fold, and 10<sup>5</sup>-fold increased sensitivity compared with the polymerase chain reaction assay, respectively. Results indicated that the LAMP primers designed for <i>Salmonella</i>, CTX-M-1 group, <i>mph(A)</i>, and <i>ermB</i> genes possess high specificity (100%) and sensitivity (over 94%). This novel approach advocates its application in detecting <i>Salmonella</i>, CTX-M-1 group, <i>mph(A)</i>, and <i>ermB</i> genes.</p>","PeriodicalId":12333,"journal":{"name":"Foodborne pathogens and disease","volume":null,"pages":null},"PeriodicalIF":1.9000,"publicationDate":"2024-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sensitive and Specific Loop-Mediated Isothermal Amplification Assays for Detection of <i>Salmonella</i>, CTX-M-1 Group Genes, <i>mph(A)</i>, and <i>ermB</i> in Stool and Blood Samples Based on Orange to Green Visible Dye.\",\"authors\":\"Jianbo Feng, Ya Huang, Huixin Chen, Shujin Xie, Congzhu Yang, Weixin Zheng, Jinglin Su, Wentao Zheng, Jiajie Mo, Fei Lv\",\"doi\":\"10.1089/fpd.2023.0094\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Salmonella</i> is a globally prevalent foodborne bacterium, and ceftriaxone and azithromycin have been regarded as drugs of choice for treating <i>Salmonella</i> infections, particularly in children. With the growing incidence of ceftriaxone and azithromycin resistance in <i>Salmonella</i>, there is an urgent requirement for a rapid and dependable gene testing approach to enhance the efficacy of treating <i>Salmonella</i> infections. Utilizing the orange to green visible dye approach, this study developed loop-mediated isothermal amplification (LAMP) assays for the sensitive and specific detection of <i>Salmonella</i>, ceftriaxone and azithromycin resistance genes (including CTX-M-1 group, <i>mph(A)</i>, and <i>ermB</i> genes) in stool and blood samples. The specificity and sensitivity of primers during the LAMP assays for detection of <i>Salmonella</i>, CTX-M-1 group, <i>mph(A)</i>, and <i>ermB</i> genes were determined in this study. The detection threshold for <i>Salmonella</i> was found to be 1.5 × 10<sup>3</sup> colony-forming units (CFU)/mL, while it was 1.5 × 10<sup>2</sup> CFU/mL for CTX-M-1 group genes (including <i>bla</i><sub>CTX-M-3</sub>, <i>bla</i><sub>CTX-M-15</sub>, and <i>bla</i><sub>CTX-M-55</sub>), 1.5 × 10<sup>2</sup> CFU/mL for <i>mph(A)</i>, and 1.5 × 10<sup>2</sup> CFU/mL for <i>ermB</i>, showing 10-10<sup>3</sup>-fold, 10<sup>3</sup>-fold, and 10<sup>5</sup>-fold increased sensitivity compared with the polymerase chain reaction assay, respectively. Results indicated that the LAMP primers designed for <i>Salmonella</i>, CTX-M-1 group, <i>mph(A)</i>, and <i>ermB</i> genes possess high specificity (100%) and sensitivity (over 94%). This novel approach advocates its application in detecting <i>Salmonella</i>, CTX-M-1 group, <i>mph(A)</i>, and <i>ermB</i> genes.</p>\",\"PeriodicalId\":12333,\"journal\":{\"name\":\"Foodborne pathogens and disease\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-03-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Foodborne pathogens and disease\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1089/fpd.2023.0094\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"FOOD SCIENCE & TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Foodborne pathogens and disease","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1089/fpd.2023.0094","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
Sensitive and Specific Loop-Mediated Isothermal Amplification Assays for Detection of Salmonella, CTX-M-1 Group Genes, mph(A), and ermB in Stool and Blood Samples Based on Orange to Green Visible Dye.
Salmonella is a globally prevalent foodborne bacterium, and ceftriaxone and azithromycin have been regarded as drugs of choice for treating Salmonella infections, particularly in children. With the growing incidence of ceftriaxone and azithromycin resistance in Salmonella, there is an urgent requirement for a rapid and dependable gene testing approach to enhance the efficacy of treating Salmonella infections. Utilizing the orange to green visible dye approach, this study developed loop-mediated isothermal amplification (LAMP) assays for the sensitive and specific detection of Salmonella, ceftriaxone and azithromycin resistance genes (including CTX-M-1 group, mph(A), and ermB genes) in stool and blood samples. The specificity and sensitivity of primers during the LAMP assays for detection of Salmonella, CTX-M-1 group, mph(A), and ermB genes were determined in this study. The detection threshold for Salmonella was found to be 1.5 × 103 colony-forming units (CFU)/mL, while it was 1.5 × 102 CFU/mL for CTX-M-1 group genes (including blaCTX-M-3, blaCTX-M-15, and blaCTX-M-55), 1.5 × 102 CFU/mL for mph(A), and 1.5 × 102 CFU/mL for ermB, showing 10-103-fold, 103-fold, and 105-fold increased sensitivity compared with the polymerase chain reaction assay, respectively. Results indicated that the LAMP primers designed for Salmonella, CTX-M-1 group, mph(A), and ermB genes possess high specificity (100%) and sensitivity (over 94%). This novel approach advocates its application in detecting Salmonella, CTX-M-1 group, mph(A), and ermB genes.
期刊介绍:
Foodborne Pathogens and Disease is one of the most inclusive scientific publications on the many disciplines that contribute to food safety. Spanning an array of issues from "farm-to-fork," the Journal bridges the gap between science and policy to reduce the burden of foodborne illness worldwide.
Foodborne Pathogens and Disease coverage includes:
Agroterrorism
Safety of organically grown and genetically modified foods
Emerging pathogens
Emergence of drug resistance
Methods and technology for rapid and accurate detection
Strategies to destroy or control foodborne pathogens
Novel strategies for the prevention and control of plant and animal diseases that impact food safety
Biosecurity issues and the implications of new regulatory guidelines
Impact of changing lifestyles and consumer demands on food safety.