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Recombinant Green Fluorescent Protein-Expressing Human Cytomegalovirus as a Tool for Screening Antiviral Agents

机译:重组绿色荧光蛋白表达人类巨细胞病毒作为筛选抗病毒药物的工具

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摘要

A recombinant human cytomegalovirus (AD169-GFP) expressing green fluorescent protein was generated by homologous recombination. Infection of human fibroblast cultures with AD169-GFP virus produced stable and readily detectable amounts of GFP signals which were quantitated by automated fluorometry. Hereby, high levels of sensitivity and reproducibility could be achieved, compared to those with the conventional plaque reduction assay. Antiviral activities were determined for four reference compounds as well as a set of putative novel cytomegalovirus inhibitors. The results obtained were exactly in line with the known characteristics of reference compounds and furthermore revealed distinct antiviral activities of novel in vitro inhibitors. The fluorometric data could be confirmed by GFP-based flow cytometry and fluorescence microscopy. In addition, laboratory virus variants derived from the recombinant AD169-GFP virus provided further possibilities for study of the characteristics of drug resistance. The GFP-based antiviral assay appeared to be very reliable for measuring virus-inhibitory effects in concentration- and time-dependent fashions and might also be adaptable for high-throughput screenings of cytomegalovirus-specific antiviral agents.
机译:通过同源重组产生表达绿色荧光蛋白的重组人巨细胞病毒(AD169-GFP)。用AD169-GFP病毒感染人成纤维细胞培养物产生稳定且易于检测的GFP信号量,其通过自动荧光法定量。因此,与常规噬菌斑减少测定法相比,可以实现高水平的灵敏度和重现性。确定了四种参考化合物以及一组推定的新型巨细胞病毒抑制剂的抗病毒活性。获得的结果与参考化合物的已知特征完全一致,而且还揭示了新型体外抑制剂的独特抗病毒活性。荧光数据可以通过基于GFP的流式细胞仪和荧光显微镜确认。另外,衍生自重组AD169-GFP病毒的实验室病毒变体为研究耐药性提供了进一步的可能性。基于GFP的抗病毒测定似乎非常可靠,可以以浓度和时间依赖性的方式测量病毒抑制作用,也可能适用于高通量筛选巨细胞病毒特异性抗病毒剂。

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