Dehghani Houman, Brown Charles R, Plishka Ronald, Buckler-White Alicia, Hirsch Vanessa M
Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland 20852, USA.
J Virol. 2002 May;76(9):4379-89. doi: 10.1128/jvi.76.9.4379-4389.2002.
The role of the immunoreceptor tyrosine-based activation motif (ITAM) that is unique to the Nef protein of the acutely pathogenic simian immunodeficiency virus SIVsmPBj was studied in the context of two AIDS-inducing simian immunodeficiency virus molecular clones. NefY(+) variants of SIVagm9063-2 and SIVsmE543-3 replicated in and induced proliferation of unstimulated pig-tailed macaque PBMC. The pathogenesis of the NefY(+) and NefY(-) clones of SIVagm9063-2, SIVsmE543-3, and PBj6.6 were evaluated by intravenous inoculation of pig-tailed macaques (Macaca nemestrina). Introduction of the ITAM did not increase plasma viral RNA levels nor alter the kinetics of viremia compared with the NefY(-) versions of each clone. Clinical symptoms were not observed in animals inoculated with the NefY(-) variants. In contrast, characteristic PBj symptoms were observed in animals inoculated with any of the three NefY(+) clones. Blunting and fusion of intestinal villi and multifocal infiltration of mononuclear cells were observed in the gastrointestinal tracts of macaques inoculated with the NefY(+) versions. Lesions were associated with active viral replication, as demonstrated by simian immunodeficiency virus-specific in situ hybridization. However, only the macaque inoculated with wild-type NefY(+) SIVsmPBj developed fatal disease; lesions were more widespread and severe in this animal. A switch to macrophages as a viral reservoir and the presence of interleukin-6 in plasma was unique to the macaque infected with PBj6.6. Overall, these data suggest that the ITAM in SIV Nef alters the pathogenesis of simian immunodeficiency virus regardless of the viral background. The change in pathogenesis occurs without enhancement of viral replication. However, NefY(+) variants of SIVagm and SIVsm did not fully recapitulate the virulence of SIVsmPBj, implicating additional viral factors in this unique virus pathogenesis.
在两种致艾滋病的猿猴免疫缺陷病毒分子克隆的背景下,研究了急性致病性猿猴免疫缺陷病毒SIVsmPBj的Nef蛋白特有的基于免疫受体酪氨酸的激活基序(ITAM)的作用。SIVagm9063 - 2和SIVsmE543 - 3的NefY(+)变体在未刺激的猪尾猕猴外周血单核细胞(PBMC)中复制并诱导其增殖。通过静脉接种猪尾猕猴(食蟹猴)来评估SIVagm9063 - 2、SIVsmE543 - 3和PBj6.6的NefY(+)和NefY(-)克隆的发病机制。与每个克隆的NefY(-)版本相比,引入ITAM并没有增加血浆病毒RNA水平,也没有改变病毒血症的动力学。接种NefY(-)变体的动物未观察到临床症状。相反,接种三种NefY(+)克隆中的任何一种的动物都观察到了典型的PBj症状。在接种NefY(+)版本的猕猴胃肠道中观察到肠绒毛变钝和融合以及单核细胞的多灶性浸润。病变与活跃的病毒复制有关,猿猴免疫缺陷病毒特异性原位杂交证明了这一点。然而,只有接种野生型NefY(+) SIVsmPBj的猕猴发展为致命疾病;该动物的病变更广泛且严重。作为病毒储存库转向巨噬细胞以及血浆中白细胞介素 - 6的存在是感染PBj6.6的猕猴所特有的。总体而言,这些数据表明,SIV Nef中的ITAM改变了猿猴免疫缺陷病毒的发病机制,而与病毒背景无关。发病机制的改变在没有增强病毒复制的情况下发生。然而,SIVagm和SIVsm的NefY(+)变体并没有完全重现SIVsmPBj的毒力,这表明在这种独特的病毒发病机制中还有其他病毒因素。