并以甲病毒属的基孔肯亚病毒和黄病毒属的黄热病毒细胞培养物为检测模型，摸索了合适的病毒基因处理与扩增方法。
Taking the cell culture of Chikungunya virus and Yellow fever virus as experimental models, appropriate method for purification and amplification the virus genes were developed.
甲病毒属的东部马脑炎病毒和西部马脑炎病毒之间，及与黄病毒属的黄热病毒均无交叉反应，表明建立的RT _ PCR检测方法特异性强。
No cross reactions were observed between eastern equine encephalitis virus, western equine encephalitis and yellow fever virus strains, which suggested a high specificity of established RT_PCR method.
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