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Visual DNA microarrays for simultaneous detection of human immunodeficiency virus type-1 and Treponema pallidum coupled with multiplex asymmetric polymerase chain reaction.

机译:视觉DNA芯片,用于同时检测人类1型免疫缺陷病毒和苍白螺旋体,并进行多重不对称聚合酶链反应。

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摘要

Based on gold label silver stain and coupled with multiplex asymmetric polymerase chain reaction (PCR) analysis, we developed the visual DNA microarray for simultaneous, sensitive, and specific detection of human immunodeficiency virus type-1 (HIV-1) and Treponema pallidum. The 5'-end amino-modified oligonucleotides were immobilized on glass surface, which were used as the capturing probes to bind the complement biotinylated target DNA. The gold-conjugated streptavidins were introduced to the microarray for specific binding to biotin. The black image of microarray spots, which were the result from the precipitation of silver onto nanogold particles and bound to streptavidins, was visualized and accounted as the detection of biotinylated target DNA. Multiplex asymmetric PCR products of HIV-1 and T. pallidum and Bacillus subtilis (used as positive control) were performed for preparing the abundant biotinylated single-stranded target DNA of which could affect detection efficiency and sensitivity of hybridization on microarray. One hundred sixty-nine clinical samples of HIV-1 and T. pallidum from infected patients were tested using the homemade DNA microarrays. The results were identical to those shown in the assays of ELISA and fluorescence quantitative real-time PCR. Our results demonstrate that we have developed the visual gene detection technique, which is of high sensitivity and specificity; it may have potential in clinical applications.
机译:基于金标银染剂,并结合多重不对称聚合酶链反应(PCR)分析,我们开发了视觉DNA芯片,用于同时,敏感和特异地检测人类1型免疫缺陷病毒(HIV-1)和梅毒螺旋体。将5'端氨基修饰的寡核苷酸固定在玻璃表面上,将其用作捕获探针以结合补体生物素化的靶DNA。将金缀合的链霉亲和素引入微阵列以特异性结合生物素。可视化的微阵列斑点的黑色图像是银沉淀到纳米金颗粒上并与链霉亲和素结合的结果,可视为生物素化靶DNA的检测。进行HIV-1,苍白螺旋体和枯草芽孢杆菌(用作阳性对照)的多重不对称PCR产物,以制备丰富的生物素化单链靶DNA,其可能影响检测效率和在微阵列上杂交的敏感性。使用自制的DNA芯片对来自感染患者的169份HIV-1和苍白螺旋体临床样本进行了测试。结果与ELISA和荧光定量实时PCR的测定结果相同。我们的结果表明,我们已经开发了具有高灵敏度和特异性的视觉基因检测技术。它可能在临床应用中具有潜力。

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