Lynch J, Swinton J, Pettit J, Key D
Avian Dis. 1984 Oct-Dec;28(4):1135-9.
Attempts to isolate and identify budgerigar papovavirus (BPV) were made during three separate outbreaks of disease diagnosed on pathological grounds. Direct electron microscopy was successful only when large areas of skin were extensively disrupted to release virus and then extracted with fluorocarbon to remove lipids. Direct inoculation of budgerigar tissue suspensions into chicken embryos or chicken cell cultures failed to produce detectable virus. However, when primary cultures of liver and kidney were prepared from affected budgerigars, BPV could be detected by electron microscopy and by the production of a cytopathic effect at the third or fourth passage in cell cultures. The isolated virus was pathogenic for 10-day-old but not 11- or 12-day-old chicken embryos. Inoculated 11- and 12-day-old embryos produced antibodies to BPV that were detectable 2 weeks after hatching by agar-gel-immunodiffusion tests.
在三次基于病理学诊断的疾病暴发期间,人们尝试分离和鉴定虎皮鹦鹉乳头瘤空泡病毒(BPV)。直接电子显微镜检查仅在大面积皮肤被广泛破坏以释放病毒,然后用氟碳化合物提取以去除脂质时才成功。将虎皮鹦鹉组织悬液直接接种到鸡胚或鸡细胞培养物中未能产生可检测到的病毒。然而,当从受影响的虎皮鹦鹉制备肝和肾的原代培养物时,通过电子显微镜检查以及在细胞培养物传代至第三代或第四代时产生的细胞病变效应,可以检测到BPV。分离出的病毒对10日龄鸡胚具有致病性,但对11日龄或12日龄鸡胚无致病性。接种11日龄和12日龄鸡胚产生了针对BPV的抗体,在孵化后2周通过琼脂凝胶免疫扩散试验可检测到这些抗体。