Mycobacterium tuberculosis detection and genotyping using molecular probe-based biosensor

M. Berezovskaya, D. Gorbenko
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Abstract

Nucleic acid analysis is one of the most promising approaches in modern diagnostics, however it usually requires expensive amplification equipment. In this study, we propose and approve a method for bacterial pathogens detection and genotyping using a molecular probe-based biosensor without amplification. The sensor consists of a molecular beacon probe as a signal reporter with a fluorophore and a quencher attached to it, and two DNA strands, which have fragments complementary to the reporter and to the analyzed nucleic acid (analyte). The M. tuberculosis HigA1 gene was detected using this sensor, and a point mutation associated with antibiotic resistance was discriminated. As an additional demonstration of the applicability of the method without amplification, E.Coli 16S rRNA was detected. Amplification-free sample detection has been further tested and achieved.
基于分子探针生物传感器的结核分枝杆菌检测及基因分型
核酸分析是现代诊断中最有前途的方法之一,但它通常需要昂贵的扩增设备。在这项研究中,我们提出并批准了一种基于分子探针的生物传感器的细菌病原体检测和基因分型方法。该传感器包括一个分子信标探针作为信号报告器,其上附有一个荧光团和一个淬灭器,以及两条DNA链,其片段与报告器和被分析的核酸(分析物)互补。利用该传感器检测结核分枝杆菌HigA1基因,并鉴定出与抗生素耐药性相关的点突变。为了进一步证明该方法无需扩增的适用性,我们检测了大肠杆菌16S rRNA。进一步测试并实现了无扩增样品检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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