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首页> 外文期刊>Molecular biology reports >Development and evaluation of a new detection tool-visual DNA microarray for simultaneous and specific detection of human immunodeficiency virus type-1 and hepatitis C virus
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Development and evaluation of a new detection tool-visual DNA microarray for simultaneous and specific detection of human immunodeficiency virus type-1 and hepatitis C virus

机译:新型检测工具-视觉DNA芯片的开发和评估,可同时特异性检测人类1型免疫缺陷病毒和丙型肝炎病毒

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Human immunodeficiency virus type-1 (HIV-1) and hepatitis C virus (HCV) are transfusion-transmitted human pathogens that have a major impact on blood safety and public health. Based on multiplex asymmetrical PCR and coupled with gold labelled silver stain (GLSS), we developed the visual DNA microarray for sensitive and specific detection of these two viruses. Capturing probes of 5'-end-amino-modified oligonucleotides were immobilized on glass surface to bind the complement biotinylated target DNA. The Au-streptavidin probe was introduced to the microarray for specific binding to biotin. Black images of microarray spots which result from the precipitation of silver onto Au-streptavidin probes, were visualized by naked eyes. In order to improve the efficiency of microarray hybridization, triplex asymmetrical PCR of HIV-1, HCV and Human enterovirus 71 (EV-71, used as positive control) were performed to prepare abundant biotinylated single-stranded target DNA. The sensitivity of visual DNA microarray (10(3) copies/ml) was higher than conventional PCR (10(4) copies/ml) and was identical to FQ-PCR (10(3) copies/ml). Total 152 blood samples containing the two viruses were tested using the DNA microarray and fluorescence quantitative real-time PCR (FQ-PCR). The results were identical (P > 0.05). So this system has high sensitivity and may have potential in clinical applications.
机译:人类1型免疫缺陷病毒(HIV-1)和丙型肝炎病毒(HCV)是输血传播的人类病原体,对血液安全和公共卫生产生重大影响。基于多重不对称PCR并结合金标记的银染(GLSS),我们开发了视觉DNA微阵列,可对这两种病毒进行灵敏和特异的检测。将5'-末端-氨基修饰的寡核苷酸的捕获探针固定在玻璃表面上,以结合补体生物素化的靶DNA。将Au-链霉亲和素探针引入微阵列以特异性结合生物素。由银沉淀到Au-链霉亲和素探针上产生的微阵列斑点的黑色图像通过肉眼可见。为了提高微阵列杂交的效率,进行了HIV-1,HCV和人肠病毒71(EV-71,用作阳性对照)的三重不对称PCR,以制备丰富的生物素化的单链靶DNA。视觉DNA微阵列(10(3)拷贝/毫升)的灵敏度高于常规PCR(10(4)拷贝/毫升),并且与FQ-PCR(10(3)拷贝/毫升)相同。使用DNA微阵列和荧光定量实时PCR(FQ-PCR)测试了包含这两种病毒的152个血液样本。结果相同(P> 0.05)。因此,该系统具有很高的灵敏度,在临床应用中可能具有潜力。

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