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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 blaNDM-1

机译:blaNDM-1回路等温扩增从环境和饮用水样品中检测新德里金属-β-内酰胺酶-1(NDM-1)阳性细菌。

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摘要

New Delhi metallo-β-lactamase-1 gene (blaNDM-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 blaNDM-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 blaNDM-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 blaNDM-1 gene.
机译: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)酶,该酶可切割β-内酰胺环的酰胺键,并能抵抗主要类别的β-内酰胺类抗生素。通过水平基因转移传播质粒携带的blaNDM-1可能对社会造成威胁。在这项研究中,通过blaNDM-1的环介导等温扩增(LAMP),开发了一种用于检测NDM-1阳性细菌的快速非培养方法。发现该方法的敏感性是质粒DNA的飞克图,根据质粒DNA的大小,它可以转化为2.6–25.8拷贝。该方法用于检测81种从环境和饮用水源收集的水样中的NDM-1阳性细菌。通过LAMP(而非PCR)在三个饮用水样品中检测到NDM-1阳性细菌。这三个样品是从水源收集的,这些水在公共分配之前经过了氯处理以进行净化处理。在湖水样品中或在公开分发前通过反渗透纯化的水源样品中未检出NDM-1阳性细菌。发现使用LAMP检测NDM-1阳性细菌是安全,灵敏和快速的,可以筛查来自不同来源的大量样品。通过使用荧光染料可视化扩增的blaNDM-1基因,可以将该方法开发为现场检测试剂盒。

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