Connor R I, Sheridan K E, Lai C, Zhang L, Ho D D
Aaron Diamond AIDS Research Center, New York 10016, USA.
J Virol. 1996 Aug;70(8):5306-11. doi: 10.1128/JVI.70.8.5306-5311.1996.
A small number of persons infected with human immunodeficiency virus type 1 (HIV-1) remain clinically and immunologically healthy for more than a decade after infection. Recent reports suggest that these individuals may be infected with an attenuated strain of HIV-1; however, a common genetic basis for viral attenuation has not been found in all cases. In the present study, we examined the functional properties of the HIV-1 env genes from six long-term survivors. env clones were generated by PCR amplification of proviral env sequences, followed by cloning of the amplified regions into expression vectors. Eight to ten clones from each subject were screened by transient transfection for expression of the envelope precursor glycoprotein, gp160. Those clones expressing gp160 were then cotransfected with an HIV-1 luciferase reporter vector, pNL4-3Env(-)LUC(+) and evaluated for their ability to mediate infection of phytohemagglutinin-activated peripheral blood mononuclear cells in single-cycle infectivity assays. Clones expressing gp160 were identified for all six long-term survivors, indicating the presence of proviral env genes with intact open reading frames. For two subjects, D and DH, the encoded envelope glycoproteins yielded high levels of luciferase activity when pseudotyped onto HIV-1 virions and tested in single-cycle infectivity assays. In contrast, envelope glycoproteins cloned from four other long-term survivors were poorly processed and failed to mediate infection. Sequencing of the gp120/41 cleavage site and conserved gp41 cysteine residues of these clones did not reveal any obvious mutations to explain the functional defects. The functional activity of env clones from long-term survivors D and DH was comparable to that seen with several primary HIV-1 env genes cloned from individuals with disease progression and AIDS. These results suggest that the long-term survival of subjects D and DH is not associated with overt functional defects in env; however, functional abnormalities in env may contribute to maintaining a long-term asymptomatic state in the other four cases we studied.
一小部分感染了1型人类免疫缺陷病毒(HIV-1)的人在感染后十多年里临床和免疫状况仍保持健康。最近的报告表明,这些个体可能感染了一种减毒的HIV-1毒株;然而,并非在所有病例中都发现了病毒减毒的共同遗传基础。在本研究中,我们检测了6名长期存活者的HIV-1 env基因的功能特性。通过对前病毒env序列进行PCR扩增,然后将扩增区域克隆到表达载体中,从而获得env克隆。通过瞬时转染筛选每个受试者的8至10个克隆,以检测包膜前体糖蛋白gp160的表达。然后将那些表达gp160的克隆与HIV-1荧光素酶报告载体pNL4-3Env(-)LUC(+)共转染,并在单周期感染性试验中评估它们介导植物血凝素激活的外周血单个核细胞感染的能力。在所有6名长期存活者中均鉴定出表达gp160的克隆,这表明存在具有完整开放阅读框的前病毒env基因。对于两名受试者D和DH,当编码的包膜糖蛋白假型化到HIV-1病毒颗粒上并在单周期感染性试验中进行检测时,产生了高水平的荧光素酶活性。相比之下,从其他4名长期存活者克隆的包膜糖蛋白加工不良,无法介导感染。对这些克隆的gp120/41裂解位点和保守的gp41半胱氨酸残基进行测序,未发现任何明显的突变来解释功能缺陷。长期存活者D和DH的env克隆的功能活性与从疾病进展者和艾滋病患者克隆的几个原发性HIV-1 env基因的功能活性相当。这些结果表明,受试者D和DH的长期存活与env中明显的功能缺陷无关;然而,env中的功能异常可能有助于维持我们研究的其他4例患者的长期无症状状态。