Bailey L, Newman J F, Porterfield J S
J Gen Virol. 1975 Jan;26(1):15-20. doi: 10.1099/0022-1317-26-1-15.
Nodamura virus multiplied in mosquito cell lines, as determined by infectivivity assays in adult honey bees (Apis mellifera) and wax moth larvae (Galleria mellonella). Titres of more than 10-7 and 10-5 bee LD50 /ml were obtained in culture fluids of Aedes albopictus and Aedes aegypti cells respectively after 10 days. Comparable titres were obtained after several months, during which the cultures were subdivided up to six times. Nodamura virus also multiplied in BHK cells and yielded titres of 10-4-8 to 10-6-6 mouse LD50/ml and 10-5-1 to 10-7-1 wax moth LD50/ml in culture fluid 1 to 4 days after infection. No c.p.e. was observed in infected cells.
通过在成年蜜蜂(意大利蜜蜂)和蜡螟幼虫(大蜡螟)中进行感染性测定,确定诺达木拉病毒能在蚊子细胞系中增殖。10天后,白纹伊蚊和埃及伊蚊细胞培养液中的病毒滴度分别超过10⁻⁷和10⁻⁵蜜蜂半数致死剂量/毫升。数月后获得了相当的滴度,在此期间培养物最多传代6次。诺达木拉病毒也能在BHK细胞中增殖,感染后1至4天,培养液中的病毒滴度为10⁻⁴·⁸至10⁻⁶·⁶小鼠半数致死剂量/毫升和10⁻⁵·¹至10⁻⁷·¹蜡螟半数致死剂量/毫升。在感染细胞中未观察到细胞病变效应。