Pancino G, Fossati I, Chappey C, Castelot S, Hurtrel B, Moraillon A, Klatzmann D, Sonigo P
Institut Cochin de Génétique Moléculaire (ICGM-CNRS UPR 0415), Paris, France.
Virology. 1993 Feb;192(2):659-62. doi: 10.1006/viro.1993.1083.
We report the characterization of the env gene of a feline immunodeficiency virus isolate from France (FIV Wo). FIV Wo gag and env genes were cloned directly from cat peripheral blood mononuclear cells, using polymerase chain reaction. The env molecular clone was shown to be functional and to express antigenically relevant envelope glycoproteins in vitro. Alignment of FIV Wo sequences with available FIV sequences and application of a regionalization algorithm resulted in delineation of variable and conserved domains of FIV Env. These data were used to build a schematic folding model of FIV envelope glycoproteins. The Env molecular clone, variability map, and structural model constitute helpful tools for future studies of FIV envelope aimed at the determination of structure-function relationships or design of diagnostics or vaccine reagents.
我们报告了一株来自法国的猫免疫缺陷病毒分离株(FIV Wo)env基因的特征。利用聚合酶链反应,直接从猫外周血单个核细胞中克隆出FIV Wo的gag和env基因。env分子克隆显示具有功能,并能在体外表达具有抗原相关性的包膜糖蛋白。将FIV Wo序列与现有的FIV序列进行比对,并应用区域化算法,从而划定了FIV Env的可变区和保守区。这些数据被用于构建FIV包膜糖蛋白的示意性折叠模型。Env分子克隆、变异性图谱和结构模型为今后针对确定结构-功能关系或设计诊断试剂或疫苗试剂的FIV包膜研究提供了有用的工具。