Collins J J, Bolio L D, Denny T P, Bolognesi D P
J Virol. 1977 Jan;21(1):113-8. doi: 10.1128/JVI.21.1.113-118.1977.
The cytolytic reactivity of a complex goat anti-feline leukemia virus (FeLV) antiserum for mouse cells (Eveline) releasing large quantities of Friend leukemia virus (FLV) was analyzed by the sensitive [14C]nicotinamide release microcytotoxicity assay. Whereas this interspecies killing reactivity could be blocked by absorption of the goat anti-FeLV serum with a preparation of disrupted FLV, absorption with purified FLV gp71, the major envelope glycoprotein, had no effect. Subsequent serum absorptions with the individual FLV structural polypeptides revealed that the lysis of the Eveline cells by the goat anti-FeLV serum is mediated by antibodies recognizing the interspecies determinant of p30, the major internal capsid protein. The expression of this internal viral component at the surface of virus-producing cells is discussed further. The results also demonstrated that removal of approximately 70% of the carbohydrate portion of gp71 with a preparation of glycosidases did not affect the integrity of its interspecies determinant; these results are in agreement with an earlier study (Bolgnesi et al., 1975) that examined primarily the group- and type-specific sites.
通过灵敏的[14C]烟酰胺释放微量细胞毒性试验,分析了一种复杂的山羊抗猫白血病病毒(FeLV)抗血清对释放大量弗氏白血病病毒(FLV)的小鼠细胞(伊芙琳细胞)的细胞溶解反应性。虽然这种种间杀伤反应性可通过用破坏的FLV制剂吸收山羊抗FeLV血清来阻断,但用主要包膜糖蛋白纯化的FLV gp71吸收则无效果。随后用单个FLV结构多肽对血清进行吸收,结果显示山羊抗FeLV血清对伊芙琳细胞的裂解是由识别主要内部衣壳蛋白p30种间决定簇的抗体介导的。进一步讨论了这种病毒内部成分在病毒产生细胞表面的表达。结果还表明,用糖苷酶制剂去除gp71约70%的碳水化合物部分并不影响其种间决定簇的完整性;这些结果与一项早期研究(博尔涅西等人,1975年)一致,该研究主要检测了群特异性和型特异性位点。