实时荧光定量PCR法定量分析eb病毒上清液

Karen Fecenko-Tacka, Laura Schina, C. Beiswanger
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引用次数: 3

摘要

eb病毒(EBV)转化B细胞被科里尔医学研究所的CCR用于产生可再生细胞系和DNA,以进一步研究遗传和复杂疾病的基因组和蛋白质组学。最佳和有效的转化需要准确评估每种病毒制剂中的病毒滴度。然而,目前测定EBV滴度的方法是通过大规模的生物试验来评估转化效率,最终建立淋巴母细胞样细胞系(LCLs)。该方法确定能够产生LCL产物的病毒稀释度,但不确定病毒粒子数,最佳稀释度随制剂而变化。因此,我们开发了一种实时PCR方法来检测和定量EBV DNA。除了量化病毒上清液的滴度外,我们还评估了通过LCL生长测量的病毒稀释物的生物活性,以及使用稀释的EBV病毒库转化先前的病毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative Analysis of Epstein-Barr Virus Supernatant by Real-Time PCR Assay
ABSTRACT Transformation of B cells by Epstein-Barr Virus (EBV) is used by the CCR at Coriell Institute for Medical Research to produce renewable cell lines and DNA to further genomic and proteomic studies of inherited and complex diseases alike. Optimal and efficient transformation requires an accurate assessment of the titer of the virus in each virus preparation. However, current methods to determine EBV titer assess transformation efficiency using large-scale biological assays ending in the establishment of lymphoblastoid cell lines (LCLs). This method determines the virus dilution capable of producing LCL outgrowth but does not determine virion number and optimal dilution will vary with the preparation. Therefore, we developed a real-time PCR method to detect and quantify EBV DNA. In addition to quantifying the titer of the viral supernatants, we evaluated both the biological activity of the viral dilutions as measured by LCL outgrowth and the use of diluted EBV viral stocks to transform previously fr...
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