Dedera D, Ratner L
Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.
J Virol. 1991 Nov;65(11):6129-36. doi: 10.1128/JVI.65.11.6129-6136.1991.
The mechanism of human immunodeficiency virus type 1 (HIV-1) cytopathicity is poorly understood and might involve formation of multinucleated giant cells (syncytia), single-cell lysis, or both. In order to determine the contributions of the fusion domain to syncytium formation, single-cell lysis, and viral infectivity and to clarify the molecular details of these events, insertion mutations were made in the portion of env encoding this sequence in the functional HIV-1 proviral clone HXB2. Viruses produced from these mutant clones were found to have a partial (F3) or complete (F6) loss of syncytium-forming ability in acutely infected CEM, Sup T1, and MT4 T-cell lines. During the early stage of acute infection by F6 virus, there was a loss of the syncytial cytopathic effect, which resulted in increased cell viability, and a 1.9- to 2.6-fold increase in virus yield in the cell lines tested. In the late stage of acute infection, the single-cell cytopathic effect of F6 virus was similar to that of the parental HXB2 virus. The F3 and F6 viruses were also found to have a 1.7- to 43-fold reduction in infectivity compared with the HXB2 virus. The mutant F3 and F6 and parental HXB2 envelope proteins were expressed in vaccinia virus, and the mutant envelope proteins were observed to be defective in their ability to form syncytia. BSC-40 cells infected with vaccinia virus recombinants revealed no differences in kinetics of cleavage, cell surface expression, or CD4 binding capacity of the mutant and parental envelope proteins. These results demonstrate that a loss of syncytium formation results in an attenuation of infectivity and a loss of the syncytial cytopathic effect without a loss of single-cell lysis. These mutants may reflect in tissue culture the changes observed in the HIV isolates in vivo during disease progression, which exhibit marked differences in syncytium production.
1型人类免疫缺陷病毒(HIV-1)的细胞病变机制目前了解甚少,可能涉及多核巨细胞(合胞体)的形成、单细胞裂解或两者兼有。为了确定融合结构域对合胞体形成、单细胞裂解和病毒感染性的作用,并阐明这些事件的分子细节,我们在功能性HIV-1前病毒克隆HXB2中env编码该序列的部分进行了插入突变。从这些突变克隆产生的病毒在急性感染的CEM、Sup T1和MT4 T细胞系中,合胞体形成能力部分丧失(F3)或完全丧失(F6)。在F6病毒急性感染的早期阶段,合胞体细胞病变效应丧失,导致细胞活力增加,并且在测试的细胞系中病毒产量增加了1.9至2.6倍。在急性感染的后期,F6病毒的单细胞病变效应与亲本HXB2病毒相似。与HXB2病毒相比,F3和F6病毒的感染性也降低了1.7至43倍。突变型F3和F6以及亲本HXB2包膜蛋白在痘苗病毒中表达,并且观察到突变型包膜蛋白形成合胞体的能力存在缺陷。感染痘苗病毒重组体的BSC-40细胞显示,突变型和亲本包膜蛋白在裂解动力学、细胞表面表达或CD4结合能力方面没有差异。这些结果表明,合胞体形成的丧失导致感染性减弱以及合胞体细胞病变效应丧失,而单细胞裂解并未丧失。这些突变体可能在组织培养中反映了疾病进展期间体内HIV分离株中观察到的变化,这些变化在合胞体产生方面表现出明显差异。