Suppr超能文献

通过bla NDM-1的环介导等温扩增技术对环境和饮用水样本中新型德里金属β-内酰胺酶-1(NDM-1)阳性细菌进行分子检测。

Molecular Detection of New Delhi Metallo-Beta-Lactamase-1 (NDM-1) Positive Bacteria from Environmental and Drinking Water Samples by Loop Mediated Isothermal Amplification of bla NDM-1.

作者信息

Rathinasabapathi P, Hiremath Deepak S, Arunraj Rex, Parani M

机构信息

Genomics Laboratory, Department of Genetic Engineering, SRM University, Kattankulathur, Chennai, 603203 Tamil Nadu India.

出版信息

Indian J Microbiol. 2015 Dec;55(4):400-5. doi: 10.1007/s12088-015-0540-x. Epub 2015 Jun 24.

Abstract

New Delhi metallo-β-lactamase-1 gene (bla NDM-1 ) codes for New Delhi metallo-beta-lactamase-1 (NDM-1) enzyme that cleaves the amide bond of β-lactam ring, and provides resistance against major classes of β-lactam antibiotics. Dissemination of the plasmid borne bla NDM-1 through horizontal gene transfer is a potential threat to the society. In this study, a rapid non-culture method for detecting NDM-1 positive bacteria was developed by Loop Mediated Isothermal Amplification (LAMP) of bla NDM-1 . Sensitivity of this method was found to be one femtogram of plasmid DNA, which translates into 2.6-25.8 copies depending on the size of the plasmid DNA. This method was applied to detect NDM-1 positive bacteria in 81 water samples that were collected from environmental and drinking water sources. NDM-1 positive bacteria were detected in three drinking water samples by LAMP but not by PCR. These three samples were collected from the water sources that were treated with chlorine for decontamination before public distribution. NDM-1 positive bacteria were not detected in lake water samples or in the samples that were collected from the water sources that were purified by reverse osmosis before public distribution. Detection of NDM-1 positive bacteria using LAMP was found to be safe, sensitive and rapid for screening large number of samples from diverse sources. This method could be developed as on-field detection kit by using fluorescent dyes to visualize the amplified bla NDM-1 gene.

摘要

新德里金属β-内酰胺酶-1基因(blaNDM-1)编码新德里金属β-内酰胺酶-1(NDM-1),该酶可裂解β-内酰胺环的酰胺键,使细菌对主要种类的β-内酰胺抗生素产生耐药性。通过水平基因转移传播的携带blaNDM-1的质粒对社会构成潜在威胁。在本研究中,通过对blaNDM-1进行环介导等温扩增(LAMP),开发了一种快速非培养检测NDM-1阳性细菌的方法。该方法的灵敏度为1飞克质粒DNA,根据质粒DNA大小,相当于2.6至25.8个拷贝。将该方法应用于检测从环境水源和饮用水源采集的81份水样中的NDM-1阳性细菌。通过LAMP在3份饮用水样中检测到了NDM-1阳性细菌,但PCR未检测到。这3份水样采自公共供水前经氯消毒处理的水源。在湖水水样或公共供水前经反渗透净化的水源采集的水样中未检测到NDM-1阳性细菌。结果表明,使用LAMP检测NDM-1阳性细菌对从不同来源筛选大量样本而言安全、灵敏且快速。通过使用荧光染料可视化扩增的blaNDM-1基因,该方法可开发为现场检测试剂盒。

相似文献

引用本文的文献

3
β-Lactam Resistance Gene NDM-1 in the Aquatic Environment: A Review.β-内酰胺耐药基因 NDM-1 在水环境中的研究进展。
Curr Microbiol. 2021 Oct;78(10):3634-3643. doi: 10.1007/s00284-021-02630-6. Epub 2021 Aug 19.

本文引用的文献

4
Identification and screening of carbapenemase-producing Enterobacteriaceae.碳青霉烯酶肠杆菌科的鉴定和筛选。
Clin Microbiol Infect. 2012 May;18(5):432-8. doi: 10.1111/j.1469-0691.2012.03815.x.
8
Rapid detection of the blaNDM-1 gene by real-time PCR.通过实时聚合酶链反应快速检测blaNDM - 1基因。
J Antimicrob Chemother. 2011 Jul;66(7):1647-9. doi: 10.1093/jac/dkr184. Epub 2011 May 12.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验