Rudensey L M, Papenhausen M D, Overbaugh J
Department of Microbiology, University of Washington, Seattle 98195.
J Virol. 1993 Mar;67(3):1727-33. doi: 10.1128/JVI.67.3.1727-1733.1993.
In lentivirus infections, there are typically few cells in the host that harbor the provirus. For this reason, molecular clones of human and simian immunodeficiency viruses (HIV and SIV) are generally derived after passage and amplification of the virus in cell culture. To determine whether SIV variants that persist in culture are similar to the variants that predominate in the host, we examined the proviral sequence of the SIV envelope (env) gene before and after cocultivation of lymphocytes from a macaque with AIDS with naive macaque lymphocytes or human cell lines. Many of the predominant variants in the monkey replicated and persisted in macaque lymphocytes and CEMx174 cells in culture, but a more limited population of variants replicated in C8166 cells. Passage of virus, harvested after 4 weeks of coculture, onto naive cells further demonstrated that the majority of proviruses detected by polymerase chain reaction were also viral variants that were expressed and packaged into infectious virions.
在慢病毒感染中,宿主中通常只有少数细胞含有前病毒。因此,人类和猿猴免疫缺陷病毒(HIV和SIV)的分子克隆一般是在病毒在细胞培养中传代和扩增后获得的。为了确定在培养物中持续存在的SIV变体是否与在宿主体内占主导地位的变体相似,我们检测了一只患艾滋病猕猴的淋巴细胞与未感染的猕猴淋巴细胞或人类细胞系共培养前后SIV包膜(env)基因的前病毒序列。猕猴中的许多主要变体在培养的猕猴淋巴细胞和CEMx174细胞中复制并持续存在,但在C8166细胞中复制的变体群体较为有限。共培养4周后收获的病毒接种到未感染的细胞上,进一步证明通过聚合酶链反应检测到的大多数前病毒也是能够表达并包装成感染性病毒粒子的病毒变体。