Huang Y, Zhang L, Ho D D
Aaron Diamond AIDS Research Center, New York University School of Medicine, New York 10016, USA.
J Virol. 1995 Dec;69(12):8142-6. doi: 10.1128/JVI.69.12.8142-8146.1995.
We have previously shown that there were no gross deletions or obvious sequence abnormalities within nef of human immunodeficiency virus type 1 (HIV-1) in the 10 long-term survivors studied (Y. Huang, L. Zhang, and D. D. Ho, J. Virol. 69:93-100, 1995). Here we extend our study to examine these nef alleles in a functional context. Using a new technique, termed site-directed gene replacement, we have precisely replaced the nef of an infectious molecular clone, HIV-1HXB2, with nef alleles derived from 10 long-term survivors as well as from a patient with AIDS. The replication properties of these chimeric viruses demonstrated that the nef alleles derived from long-term survivors neither significantly increased nor decreased viral replication, compared with the nef allele of Nef+ HIV-1HXB2 and that derived from a patient with AIDS. However, Nef+ viruses always replicated faster than virus lacking nef. Moreover, single-cell infection analysis by the MAGI assay showed that these chimeric viruses, as well as Nef+ HIV-1HXB2, were more infectious than Nef- HIV-1HXB2 was. Therefore, we conclude that the genotypic and phenotypic features of nef are not likely to account for the nonprogression of HIV-1 infection in the 10 cases studied, unless the function of the nef gene in vivo is not accurately reflected by the in vitro assays we used.
我们先前已表明,在所研究的10名长期存活者中,1型人类免疫缺陷病毒(HIV-1)的nef基因内不存在大片段缺失或明显的序列异常(Y. Huang、L. Zhang和D. D. Ho,《病毒学杂志》69:93 - 100,1995年)。在此,我们扩展研究以在功能背景下检查这些nef等位基因。使用一种称为定点基因置换的新技术,我们已用源自10名长期存活者以及一名艾滋病患者的nef等位基因精确替换了感染性分子克隆HIV-1HXB2的nef基因。这些嵌合病毒的复制特性表明,与Nef + HIV-1HXB2的nef等位基因以及源自一名艾滋病患者的nef等位基因相比,源自长期存活者的nef等位基因既未显著增加也未显著降低病毒复制。然而,Nef +病毒总是比缺乏nef的病毒复制得更快。此外,通过MAGI分析进行的单细胞感染分析表明,这些嵌合病毒以及Nef + HIV-1HXB2比Nef - HIV-1HXB2更具感染性。因此,我们得出结论,除非我们所使用的体外试验不能准确反映nef基因在体内的功能,否则nef的基因型和表型特征不太可能解释所研究的10例HIV-1感染不进展的情况。