Aghomo H O, Rupprecht C E
Wistar Institute of Anatomy and Biology, Philadelphia, PA 19104.
Vet Microbiol. 1990 Mar;22(1):17-22. doi: 10.1016/0378-1135(90)90120-k.
Rabies viruses isolated from healthy dogs, were passaged in mice and adapted to cell culture. After 5-7 passages, isolated viruses were subjected to monoclonal antibody (Mab) characterization with a panel of 36 anti-nucleocapsid (NC) and 40 anti-glycoprotein (G) MAbs. The four viruses showed positive fluorescence with all NC hybridomas except MAb 422-5, confirming them as true rabies virus isolates. The anti-G MAb reactivity pattern was the same in the four isolates indicating that they belong to the same antigenic group, but were antigenically distinct from the Flury LEP rabies vaccine virus which is widely used throughout Nigeria for canine vaccination, and from other previously characterized street lyssaviruses from Nigeria.
从健康犬只分离出的狂犬病病毒,在小鼠体内传代并适应细胞培养。经过5至7代传代后,将分离出的病毒用一组36种抗核衣壳(NC)单克隆抗体(MAb)和40种抗糖蛋白(G)单克隆抗体进行单克隆抗体(Mab)鉴定。这四种病毒与除单克隆抗体422-5之外的所有NC杂交瘤均呈现阳性荧光,证实它们为真正的狂犬病病毒分离株。四种分离株中抗G单克隆抗体的反应模式相同,表明它们属于同一抗原组,但在抗原性上与在尼日利亚广泛用于犬类疫苗接种的弗吕里低毒力狂犬病疫苗病毒以及尼日利亚其他先前鉴定的街毒株狂犬病病毒不同。