Rathinasabapathi P, Hiremath Deepak S, Arunraj Rex, Parani M
Genomics Laboratory, Department of Genetic Engineering, SRM University, Kattankulathur, Chennai, 603203 Tamil Nadu India.
Indian J Microbiol. 2015 Dec;55(4):400-5. doi: 10.1007/s12088-015-0540-x. Epub 2015 Jun 24.
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.
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。