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An oligonucleotide microarray for multiplex real-time PCR identification of HIV-1, HBV, and HCV.

机译:用于HIV-1,HBV和HCV多重实时PCR鉴定的寡核苷酸微阵列。

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摘要

We describe a novel microarray-based approach for simultaneous identification and quantification of human immunodeficiency virus type 1 (HIV-1) and hepatitis B and C viruses (HBV and HCV) in donor plasma specimens. The method is based on multiplex real-time RT-PCR performed within the microarray hydrogel pads. Double-stranded amplification products are simultaneously detected using nonspecific SYBR Green I dye due to the reaction run in separate pads bearing 5'-immobilized specific primers. Both the sensitivity and specificity of the assay, based on 132 blood specimens analyzed, were 100% (56, 26, and 8 specimens were seropositive to HBV HCV and HIV-1, respectively; 22 were positive to both HIV-1 and HCV and 2 positive to all three viruses; 18 samples were pathogen-negative). The dynamic range of the quantitative analysis covered a six-order interval ranging from 100 to 106 genome equivalents per assay. The 95% detection limits were 14 gEq for HIV-1, 10 gEq (1.7 IU) for HBV, and 15 gEq (7.5 IU) for HCV per assay. The proposed approach is considered to be versatile and could be adapted for simultaneous identification and quantification of numerous genetic targets.
机译:我们描述了一种新型的基于微阵列的方法,用于同时鉴定和定量供体血浆标本中的人类1型免疫缺陷病毒(HIV-1)以及乙型和丙型肝炎病毒(HBV和HCV)。该方法基于微阵列水凝胶垫中进行的实时多重RT-PCR。使用非特异性SYBR Green I染料可同时检测双链扩增产物,因为该反应在带有5'固定特异性引物的分离垫中进行。根据所分析的132份血液标本,该方法的敏感性和特异性均为100%(分别有56、26和8份标本对HBV HCV和HIV-1呈血清阳性; 22份对HIV-1和HCV呈阳性;所有三种病毒均为2阳性;病原体为阴性的18个样品。定量分析的动态范围涵盖了每个测定范围从100到106个基因组当量的六阶间隔。每次检测的95%检测限为HIV-1 14 gEq,HBV 10 gEq(1.7 IU)和HCV 15 gEq(7.5 IU)。所提出的方法被认为是通用的,并且可以适用于同时鉴定和定量众多遗传靶标。

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