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开发和评估一种新的检测工具——可视化 DNA 微阵列,用于同时特异性检测人类免疫缺陷病毒 1 型和丙型肝炎病毒。

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.

机构信息

The State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China.

出版信息

Mol Biol Rep. 2011 Nov;38(8):5341-8. doi: 10.1007/s11033-011-0685-6. Epub 2011 Feb 26.

DOI:10.1007/s11033-011-0685-6
PMID:21359643
Abstract

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.

摘要

人类免疫缺陷病毒 1 型 (HIV-1) 和丙型肝炎病毒 (HCV) 是经输血传播的人类病原体,对血液安全和公共卫生有重大影响。基于多重不对称 PCR,并结合金标记银染 (GLSS),我们开发了用于敏感和特异性检测这两种病毒的可视化 DNA 微阵列。将 5'-端氨基修饰的寡核苷酸的捕获探针固定在玻璃表面上,以结合互补生物素化的靶 DNA。Au-链霉亲和素探针被引入微阵列以与生物素特异性结合。通过肉眼可以观察到由于银沉淀到 Au-链霉亲和素探针上而导致微阵列斑点呈现黑色图像。为了提高微阵列杂交的效率,进行了 HIV-1、HCV 和人类肠道病毒 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单链靶 DNA。可视化 DNA 微阵列(10(3)拷贝/ml)的灵敏度高于常规 PCR(10(4)拷贝/ml),与荧光定量实时 PCR(FQ-PCR)相同(10(3)拷贝/ml)。使用 DNA 微阵列和荧光定量实时 PCR (FQ-PCR) 检测了包含这两种病毒的 152 份血液样本。结果相同(P > 0.05)。因此,该系统具有高灵敏度,可能具有临床应用潜力。

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