Evaluation and Optimization of a Loop-Mediated Isothermal Amplification (LAMP) Assay for the Detection of Salmonella enterica serovar Typhi Isolated from Food Samples

Q4 Medicine
F. Foroohi, H. Zamani, Sajjad Yazdan setad
{"title":"Evaluation and Optimization of a Loop-Mediated Isothermal Amplification (LAMP) Assay for the Detection of Salmonella enterica serovar Typhi Isolated from Food Samples","authors":"F. Foroohi, H. Zamani, Sajjad Yazdan setad","doi":"10.29252/IEM.6.4.259","DOIUrl":null,"url":null,"abstract":"CITATION LINKS A R T I C L E I N F O Article Type Original Research Authors Fatemeh Forohi, PhD1* Hadi Zamani, PhD1 Sajjad Yazdansetad, PhD2 How to cite this article Forohi F., Zamani H., Yazdansetad S. Evaluation and Optimization of a Loop-Mediated Isothermal Amplification (LAMP) Assay for the Detection of Salmonella enterica serovar Typhi Isolated from Food Samples. Infection Epidemiology and Microbiology. 2020;6(4): 259-267 1Department of Microbiology, Shahr-e-Qods Branch, Islamic Azad University, Tehran, Iran 2Laboratory Sciences Research Center, Golestan University of Medical Sciences, Gorgan, Iran * Correspondence Address: Department of Microbiology, Faculty of Basic Sciences, Shahre-Qods-Branch, Islamic Azad University, Tehran, Iran. f_foroohi@ymail.com Article History Received: July 21 ,2020 Accepted: October 15 ,2020 Published: November 19 ,2020 [1] Bhandari DP. Characterization of flagellin antigen using a panel of ...[2] Babar A, Butt SJ, Ullah S. A review of prognostic models on diagnosis and ... [3] Olobatoke R. Public health burden of non-typhoidal Salmonella strains in sub-Saharan ... [4] Yang Q, Domesle KJ, Wang F, Ge B. Rapid detection of Salmonella in food and feed ... [5] Foddai AC, Grant IR. Methods for detection of viable foodborne pathogens: Current state-of-art ... [6] Zhai L, Liu H, Chen Q, Lu Z, Zhang C, Lv F, et al. Development of a real-time nucleic acid ... [7] Linh Quyen T, Nordentoft S, Chidambara Vinayaka A, Ngo TA, Engelsmenn P, Sun Y, et al. A sensitive, specific, and ... [8] Notomi T, Okayama H, Masubuchi H, Yonekawa T, Watanabe K, Amino N, et al. Loop-mediated ... [9] HaraKudo Y, Yoshino M, Kojima T, Ikedo M. Loop-mediated isothermal amplification for ... [10] Havelaar A, Grace D, Wu F. Foodborne diseases from dairy products in developing ...[11] Shahbazi S, Karam MRA, Habibi M, Talebi A, Bouzari S. Distribution of ... [12] Nair A, Balasaravanan T, Malik SS, Mohan V, Kumar M, Vergis J, et al. Isolation and ... [13] Köchl S, Niederstätter H, Parson W. DNA extraction and quantitation of forensic ... [14] Vickers NJ. Animal communication: When I’m calling you, will you answer ... [15] Zhang G, Brown EW, González-Escalona N. Comparison of real-time PCR, reverse transcriptase real-time PCR, loop-mediated isothermal amplification, and the FDA conventional microbiological method for ...[16] Srisawat M, Panbangred W. Efficient and specific detection of Salmonella in food ... [17] Yang Q, Domesle KJ, Ge B. Loop-mediated isothermal amplification for Salmonella detection ... [18] Ravan H, Amandadi M. A rapid and specific detection of pathogenic serovar Salmonella ... [19] Moganedi K, Goyvaerts E, Venter SN, Sibara M. Optimisation of the PCR-invA primers for ... [20] Techathuvanan C, Draughon FA, D’Souza DH. Loop-mediated isothermal amplification (LAMP) for ... [21] Zhao X, Wang L, Chu J, Li Y, Li Y, Xu Z, et al. Development and application of a rapid and simple ... [22] Zhang Y, Shan X, Shi L, Lu X, Tang S, Wang Y, et al. Development of a fimY-based loop-mediated isothermal ...[23] Wang L, Shi L, Alam M, Geng Y, Li L. Specific and rapid detection of foodborne Salmonella by loop-mediated isothermal amplification method. Food Res Int. 2008;41(1):69-74. [24] Chen Z, Zhang K, Yin H, Li Q, Wang L, Liu Z. Detection of Salmonella and several common Salmonella serotypes in food by loop-mediated isothermal amplification method. FSHW. 2015;4(2):75-9. [25] Nagamine K, Hase T, Notomi T. Accelerated reaction by loop-mediated isothermal amplification using loop primers. Mol Cell Pro Background: Foodborne diseases caused by Salmonella are considered as a global health concern, especially in low-income countries. Rapid and specific detection of this infective agent is highly important in the outbreak control. The current study aimed to design and optimize a LAMP method and to compare its sensitivity and efficiency with the PCR method in the detection of S. typhi in food. Materials & Methods: Food samples including mayonnaise and vegetable salad were inoculated with S. enterica serovar Typhi. Sensitivity and detection limit of LAMP test were investigated at different concentrations of contaminated mayonnaise and vegetable salad. invA gene was chosen as the target gene for bacterial detection by PCR and LAMP tests. Findings: The detection limit of Samonella was estimated to be 16 CFU/mL using LAMP and PCR. LAMP reaction revealed a visible turbidity, indicating the accurate amplification of the selected target gene and proper identification of Salmonella at different dilutions of the studied food samples. Conclusion: The present study indicated that LAMP is a rapid, cost-effective, and specific technique for the identification of Salmonella. This method could be used in laboratories with minimal equipment without the need for costly molecular detection methods.","PeriodicalId":34545,"journal":{"name":"Infection Epidemiology and Microbiology","volume":"98 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infection Epidemiology and Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29252/IEM.6.4.259","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

CITATION LINKS A R T I C L E I N F O Article Type Original Research Authors Fatemeh Forohi, PhD1* Hadi Zamani, PhD1 Sajjad Yazdansetad, PhD2 How to cite this article Forohi F., Zamani H., Yazdansetad S. Evaluation and Optimization of a Loop-Mediated Isothermal Amplification (LAMP) Assay for the Detection of Salmonella enterica serovar Typhi Isolated from Food Samples. Infection Epidemiology and Microbiology. 2020;6(4): 259-267 1Department of Microbiology, Shahr-e-Qods Branch, Islamic Azad University, Tehran, Iran 2Laboratory Sciences Research Center, Golestan University of Medical Sciences, Gorgan, Iran * Correspondence Address: Department of Microbiology, Faculty of Basic Sciences, Shahre-Qods-Branch, Islamic Azad University, Tehran, Iran. f_foroohi@ymail.com Article History Received: July 21 ,2020 Accepted: October 15 ,2020 Published: November 19 ,2020 [1] Bhandari DP. Characterization of flagellin antigen using a panel of ...[2] Babar A, Butt SJ, Ullah S. A review of prognostic models on diagnosis and ... [3] Olobatoke R. Public health burden of non-typhoidal Salmonella strains in sub-Saharan ... [4] Yang Q, Domesle KJ, Wang F, Ge B. Rapid detection of Salmonella in food and feed ... [5] Foddai AC, Grant IR. Methods for detection of viable foodborne pathogens: Current state-of-art ... [6] Zhai L, Liu H, Chen Q, Lu Z, Zhang C, Lv F, et al. Development of a real-time nucleic acid ... [7] Linh Quyen T, Nordentoft S, Chidambara Vinayaka A, Ngo TA, Engelsmenn P, Sun Y, et al. A sensitive, specific, and ... [8] Notomi T, Okayama H, Masubuchi H, Yonekawa T, Watanabe K, Amino N, et al. Loop-mediated ... [9] HaraKudo Y, Yoshino M, Kojima T, Ikedo M. Loop-mediated isothermal amplification for ... [10] Havelaar A, Grace D, Wu F. Foodborne diseases from dairy products in developing ...[11] Shahbazi S, Karam MRA, Habibi M, Talebi A, Bouzari S. Distribution of ... [12] Nair A, Balasaravanan T, Malik SS, Mohan V, Kumar M, Vergis J, et al. Isolation and ... [13] Köchl S, Niederstätter H, Parson W. DNA extraction and quantitation of forensic ... [14] Vickers NJ. Animal communication: When I’m calling you, will you answer ... [15] Zhang G, Brown EW, González-Escalona N. Comparison of real-time PCR, reverse transcriptase real-time PCR, loop-mediated isothermal amplification, and the FDA conventional microbiological method for ...[16] Srisawat M, Panbangred W. Efficient and specific detection of Salmonella in food ... [17] Yang Q, Domesle KJ, Ge B. Loop-mediated isothermal amplification for Salmonella detection ... [18] Ravan H, Amandadi M. A rapid and specific detection of pathogenic serovar Salmonella ... [19] Moganedi K, Goyvaerts E, Venter SN, Sibara M. Optimisation of the PCR-invA primers for ... [20] Techathuvanan C, Draughon FA, D’Souza DH. Loop-mediated isothermal amplification (LAMP) for ... [21] Zhao X, Wang L, Chu J, Li Y, Li Y, Xu Z, et al. Development and application of a rapid and simple ... [22] Zhang Y, Shan X, Shi L, Lu X, Tang S, Wang Y, et al. Development of a fimY-based loop-mediated isothermal ...[23] Wang L, Shi L, Alam M, Geng Y, Li L. Specific and rapid detection of foodborne Salmonella by loop-mediated isothermal amplification method. Food Res Int. 2008;41(1):69-74. [24] Chen Z, Zhang K, Yin H, Li Q, Wang L, Liu Z. Detection of Salmonella and several common Salmonella serotypes in food by loop-mediated isothermal amplification method. FSHW. 2015;4(2):75-9. [25] Nagamine K, Hase T, Notomi T. Accelerated reaction by loop-mediated isothermal amplification using loop primers. Mol Cell Pro Background: Foodborne diseases caused by Salmonella are considered as a global health concern, especially in low-income countries. Rapid and specific detection of this infective agent is highly important in the outbreak control. The current study aimed to design and optimize a LAMP method and to compare its sensitivity and efficiency with the PCR method in the detection of S. typhi in food. Materials & Methods: Food samples including mayonnaise and vegetable salad were inoculated with S. enterica serovar Typhi. Sensitivity and detection limit of LAMP test were investigated at different concentrations of contaminated mayonnaise and vegetable salad. invA gene was chosen as the target gene for bacterial detection by PCR and LAMP tests. Findings: The detection limit of Samonella was estimated to be 16 CFU/mL using LAMP and PCR. LAMP reaction revealed a visible turbidity, indicating the accurate amplification of the selected target gene and proper identification of Salmonella at different dilutions of the studied food samples. Conclusion: The present study indicated that LAMP is a rapid, cost-effective, and specific technique for the identification of Salmonella. This method could be used in laboratories with minimal equipment without the need for costly molecular detection methods.
环介导等温扩增(LAMP)法检测食品中伤寒沙门氏菌血清型的评价与优化
引用本文A R TI C L E IN F O文章类型主要作者Fatemeh Forohi, PhD1* Hadi Zamani, PhD1 Sajjad yazdansead, PhD2本文引用本文Forohi F, Zamani H, yazdansead S.环介导等温扩增(LAMP)方法检测食品样品中伤寒沙门氏菌血清型的评价与优化。1伊朗伊斯兰阿扎德大学Shahr-e-Qods分校微生物学系,伊朗德黑兰2伊朗戈勒斯坦医科大学实验室科学研究中心,伊朗戈尔根*通讯地址:伊朗德黑兰伊斯兰阿扎德大学Shahr-e-Qods分校基础科学学院微生物学系,伊朗德黑兰f_foroohi@ymail.com文章历史收稿日期:2020年7月21日收稿日期:2020年10月15日发布日期:2020年11月19日[1]Bhandari DP。鞭毛蛋白抗原的鉴定[2]刘建军,刘建军,刘建军,等。肿瘤预后模型的研究进展[j]。[3]王晓明,王晓明,王晓明,等。非伤寒沙门氏菌在撒哈拉以南地区的公共卫生负担。[4]杨强,王峰,葛波。食品和饲料中沙门氏菌的快速检测[j]。[5]李志强,李志强。食源性致病菌的检测方法:最新进展…[6]翟磊,刘辉,陈强,卢忠,张超,吕峰,等。研制实时核酸…[7]林春燕,孙勇,孙勇。一个敏感的,具体的,而且…[8]张建军,张建军,张建军,等。Loop-mediated……[9]张建军,张建军,张建军,等。[10]张晓明,王晓明,王晓明,等。食源性疾病的研究进展[11]Shahbazi S, Karam MRA, Habibi M, Talebi A, Bouzari S.…[12]李建军,李建军,李建军,等。隔离和…[13] Köchl S, Niederstätter H, Parson W. DNA提取与定量鉴定…[14]王志强,王志强。动物交流:当我叫你的时候,你会回答吗?[15]张刚,黄文华,González-Escalona .实时荧光定量PCR、逆转录酶实时荧光定量PCR、环介导等温扩增与FDA传统微生物学方法的比较[16]李建军,李建军。食品中沙门氏菌的高效特异性检测方法研究。[17]杨青,郭建军,葛波。环介导等温扩增检测沙门氏菌[j]。[18]王晓明,王晓明,王晓明,等。血清型沙门氏菌的快速检测方法[j]。[19]张建军,张建军,张建军,等。PCR-invA基因的克隆及克隆分析。[20]张建军,张建军,张建军。环介导等温扩增(LAMP)[21]赵旭,王磊,褚健,李勇,李勇,徐铮,等。开发和应用一种快速简便的…[22]张勇,单祥,石磊,卢鑫,唐松,王勇,等。基于纤维的环介导等温…[23]王丽,石丽,阿兰敏,耿勇,李丽。环介导等温扩增法对食源性沙门氏菌的特异性快速检测。食品科学,2008;41(1):69-74。[24]陈忠,张凯,尹慧,李强,王玲,刘铮。环介导等温扩增法检测食品中沙门氏菌及几种常见血清型。FSHW。2015; 4(2): 75 - 9。[25]王晓明,王晓明,王晓明,等。环介导等温扩增技术研究进展。背景:沙门氏菌引起的食源性疾病被认为是一个全球性的健康问题,特别是在低收入国家。快速和特异性地检测这种感染源对疫情控制非常重要。本研究旨在设计和优化一种LAMP检测方法,并与PCR法比较其检测食品中伤寒沙门氏菌的灵敏度和效率。材料与方法:将蛋黄酱、蔬菜沙拉等食品样品接种伤寒沙门氏菌。对不同浓度的污染蛋黄酱和蔬菜沙拉进行了LAMP试验的灵敏度和检出限研究。选择invA基因作为目的基因进行PCR和LAMP检测。结果:采用LAMP和PCR方法估计Samonella的检出限为16 CFU/mL。LAMP反应显示明显的浑浊,表明所选靶基因扩增准确,在所研究的食品样品中,不同稀释度下沙门氏菌的正确鉴定。结论:LAMP是一种快速、经济、特异的沙门氏菌鉴别方法。这种方法可以在实验室中使用最少的设备,而不需要昂贵的分子检测方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.50
自引率
0.00%
发文量
20
审稿时长
6 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信