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Several concerns about the primer design in the universal molecular beacon real-time PCR assay and its application in HBV DNA detection

机译:通用分子信标实时PCR检测中引物设计及其在HBV DNA检测中的应用的几个问题

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A universal hepatitis B virus (HBV) DNA detection kit is appealing for the worldwide diagnosis and monitoring of the treatment of different mutant types of hepatitis B virus. A sensitive and reproducible real-time PCR assay based on the universal molecular beacon (U-MB) technique was developed for the detection of HBV DNA in serum. The U-MB probe used in the assay has no interaction with the HBV DNA sequence. The U-MB technique not only reduced the cost of HBV detection but also had the potential for the development of a universal detection kit for different mutant HBV types and other DNA systems. To demonstrate its clinical utility, 90 serum samples were analyzed using the U-MB real-time PCR method. In the experiments we found that several crucial factors needed to be considered in the primer design, such as the avoidance of formation of severe primer-dimer and primer self-hairpin structure. With the optimized primer sets, satisfactory results were obtained for all the tested samples. We concluded that this assay would be an excellent candidate for a universal HBV DNA detection method.
机译:一种通用的乙型肝炎病毒(HBV)DNA检测试剂盒吸引了全世界对不同突变型乙型肝炎病毒治疗的诊断和监测。开发了一种基于通用分子信标(U-MB)技术的灵敏且可重现的实时PCR分析方法,用于检测血清中的HBV DNA。分析中使用的U-MB探针与HBV DNA序列没有相互作用。 U-MB技术不仅降低了HBV检测的成本,而且具有开发针对不同突变型HBV类型和其他DNA系统的通用检测试​​剂盒的潜力。为了证明其临床实用性,使用U-MB实时PCR方法分析了90个血清样品。在实验中,我们发现引物设计中需要考虑几个关键因素,例如避免形成严重的引物二聚体和引物自发夹结构。使用优化的引物组,所有测试样品均获得满意的结果。我们得出的结论是,该测定将是通用HBV DNA检测方法的极佳候选者。

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