Davies F G, Mungai J N, Taylor M
Trop Anim Health Prod. 1977 May;9(2):75-80. doi: 10.1007/BF02236383.
The laboratory methods available for the isolation and identification of Nairobi sheep disease virus have been compared. The results show that inoculation of tissue culture (BHK 21 C 13) with suspensions of infected organs or plasma followed by fluorescent antibody tests on coverslip preparations gave the quickest means of identification. This test did not depend on the production of a cytopathic effect. Primary isolation of the virus in infant mouse brain and identification either by fluorescent antibody methods or by complement fixation with antigen prepared from the mouse brain offers a slightly more sensitive isolation system and would be recommended where no tissue culture facility exists.
对用于内罗毕绵羊病病毒分离和鉴定的现有实验室方法进行了比较。结果表明,用感染器官或血浆悬液接种组织培养物(BHK 21 C 13),随后对盖玻片制备物进行荧光抗体检测,是最快速的鉴定方法。该检测不依赖于细胞病变效应的产生。在乳鼠脑内进行病毒的初次分离,并通过荧光抗体法或用从鼠脑制备的抗原进行补体结合试验来鉴定,提供了一个灵敏度稍高的分离系统,在没有组织培养设施的情况下推荐使用。