Danner K, Heubeck D, Mayr A
Arch Virol. 1978;57(1):63-75. doi: 10.1007/BF01315638.
Borna virus produces non-lytic infections in a wide spectrum of primary cell cultures and cell lines. The sensitivity and virus yields vary with the different cell systems. Accurate virus titrations can be performed in the RK 13 cell line by counting immunoflourescent microfoci between the 5th and 10th day after infection. Since the virus is not released from the cells and does not spread via the culture medium, the use of a semisolid overlay in unnecessary in virus titrations. The cell line most productive for Borna virus is the CV 1 line. The conditions for optimum virus production include a prolonged cultivation period of at least two weeks with regular changes of medium, and an incubation temperature of 35 degrees C. Harvest of the virus requires thorough disruption of the infected cells, preferably by ultrasonication, since Borna virus seems to be closely associated with cellular structures.
博尔纳病毒在多种原代细胞培养物和细胞系中产生非裂解性感染。其敏感性和病毒产量因不同的细胞系统而异。通过在感染后第5天至第10天之间计数免疫荧光微集落,可在RK 13细胞系中进行准确的病毒滴定。由于病毒不会从细胞中释放出来,也不会通过培养基传播,因此在病毒滴定中无需使用半固体覆盖层。对博尔纳病毒最具生产性的细胞系是CV 1细胞系。最佳病毒生产条件包括至少两周的延长培养期,定期更换培养基,以及35摄氏度的孵育温度。收获病毒需要彻底破坏受感染的细胞,最好通过超声处理,因为博尔纳病毒似乎与细胞结构密切相关。