McGill University AIDS Centre, Lady Davis Institute, Jewish General Hospital, Montréal, Québec, H3T 1E2 Canada.
J Virol. 2011 Mar;85(6):2828-36. doi: 10.1128/JVI.01854-10. Epub 2011 Jan 5.
Although transcription from unintegrated human immunodeficiency virus type 1 (HIV-1) DNA can occur inside infected cells, yielding all classes of viral mRNA transcripts, the translation of viral proteins is very limited. One of the proteins made is Nef, but it is unclear whether Nef produced in this way is able to play a role in immune evasion as occurs with integrated virus. We therefore asked whether transcription from preintegrated HIV-1 cDNAs could result in Nef-mediated modulation of cell surface major histocompatibility complex class I (MHC-I) expression. We infected a Rev-CEM green fluorescent protein (GFP) reporter cell line with virus and blocked integration though use of either an inactive integrase or the integrase inhibitor raltegravir. Infected cells were assayed by flow cytometry for cell surface expression of the HLA-A, HLA-B, and HLA-C allotypes (HLA-ABC), HLA-A31, and HLA-E. Viral RNA and DNA products were assayed via quantitative PCR (qPCR). The prevention of integration had no effect, relative to productively infected cells, on levels of expression of multiply spliced viral mRNA transcripts and Nef protein. Downregulation of HLA-ABC and HLA-A31 also occurred at levels similar to those seen in cells in which integration had occurred. Parallel experiments assaying cell surface HLA-ABC expression in infected activated primary CD4(+) T cells produced a similar pattern of results. Hence, the capacity of HIV-1 to modulate MHC-I is not linked to its ability to integrate. Thus, Nef-mediated evasion of host immune responsiveness might be attributable, in part at least, to transcription from unintegrated viral DNA.
虽然未整合的人类免疫缺陷病毒 1 型(HIV-1)DNA 可以在受感染的细胞内转录,产生所有类型的病毒 mRNA 转录本,但病毒蛋白的翻译非常有限。其中一种产生的蛋白是 Nef,但目前尚不清楚这种方式产生的 Nef 是否能够像整合病毒那样在免疫逃避中发挥作用。因此,我们询问了来自前整合 HIV-1 cDNA 的转录是否会导致 Nef 介导的细胞表面主要组织相容性复合体 I(MHC-I)表达的调节。我们用病毒感染 Rev-CEM 绿色荧光蛋白(GFP)报告细胞系,并通过使用失活的整合酶或整合酶抑制剂拉替拉韦阻断整合。通过流式细胞术检测感染细胞表面 HLA-A、HLA-B 和 HLA-C 同种型(HLA-ABC)、HLA-A31 和 HLA-E 的表达。通过定量 PCR(qPCR)检测病毒 RNA 和 DNA 产物。与有效感染细胞相比,整合的预防对多重拼接病毒 mRNA 转录本和 Nef 蛋白的表达水平没有影响。HLA-ABC 和 HLA-A31 的下调水平也与已发生整合的细胞相似。在感染的激活原代 CD4(+)T 细胞中检测细胞表面 HLA-ABC 表达的平行实验产生了类似的结果。因此,HIV-1 调节 MHC-I 的能力与其整合能力无关。因此,Nef 介导的宿主免疫反应逃避可能至少部分归因于未整合病毒 DNA 的转录。