Webster W A, Charlton K M, Casey G A
Agriculture Canada, Animal Diseases Research Institute, NEPEAN, Ontario.
Can J Vet Res. 1989 Oct;53(4):445-8.
Rabies virus from the brain of a striped skunk (Mephitis mephitis) from Ontario was inoculated into murine neuroblastoma (NA-C1300) cell cultures. These cultures were incubated and the cells were subcultured every three to four days. The presence of viral antigen in the cell cultures was monitored by direct immunofluorescent staining and in the culture fluids by titration in either baby hamster kidney (BHK/C13) or NA cells or in experimental mice. The virus-infected NA cultures evolved from an initial high viral concentration in supernatant fluid through a period of decreasing titers of infectious virus in the supernatant fluids to a final phase where no infectious virus has been found following cell culture and animal inoculation methods attempted although the persistently infected cells remained 95-100% viral nucleocapsid antigen-positive. Possible mechanisms involved in the perpetuation of this infection are discussed. This is the first report of a persistent infection of cell cultures by a field strain of rabies virus.
将来自安大略省的一只带条纹臭鼬(北美臭鼬)大脑中的狂犬病病毒接种到小鼠神经母细胞瘤(NA-C1300)细胞培养物中。对这些培养物进行孵育,并每三到四天对细胞进行传代培养。通过直接免疫荧光染色监测细胞培养物中病毒抗原的存在情况,并通过在幼仓鼠肾(BHK/C13)细胞或NA细胞中滴定或在实验小鼠中滴定来监测培养液中的病毒抗原。病毒感染的NA培养物从最初上清液中高病毒浓度开始,经过上清液中传染性病毒滴度下降的阶段,进入最后阶段,尽管持续感染的细胞仍有95%-100%的病毒核衣壳抗原呈阳性,但采用细胞培养和动物接种方法均未发现传染性病毒。文中讨论了这种感染持续存在的可能机制。这是狂犬病病毒野毒株对细胞培养物进行持续感染的首次报道。