Giddens W E
Lab Invest. 1975 Apr;32(4):492-502.
The lymphocytes of five owl monkeys infected with Herpesvirus saimiri (HVS) and three control monkeys were studied. Lymphocytes were separated on Ficoll-Hypaque gradients, incubated in suspension cultures, and prepared for electron microscopic and immunofluorescent study at 24, 48, and 72 hours after the beginning of culture (AC). Buffy coats of whole blood immediately after bleeding were also prepared for study. At the time of the study, four of the five infected monkeys had died of malignant lymphoma and lymphocytic leukemia. HVS virions were demonstrated by electron microscopy and HVS antigens by immunofluorescence in 1 to 20 per cent of the lmyphocytes from infected monkeys in two of five cultures at 24 hours AC, four of five at 48 hours AC, and all five at 72 hours AC. There was quite good agreement between the electron microscopic and the immunofluorescent data. None of the control monkey cultures and none of the buffy coat preparations contained HVS virions or antigens. By electron microscopy the great majority of the virus particles were nucleocapsids within the nuclei of lymphocytes. Very seldom were enveloped virions observed. There was some evidence to suggest that the higher the percentage of lymphocytes containing HVS the poorer the prognosis for the monkey. HVS was isolated from all five infected monkeys by cocultivation of lymphocytes with Vero cells. Control lymphocyte cocultivations were negative.
对5只感染猴疱疹病毒(HVS)的夜猴和3只对照猴的淋巴细胞进行了研究。淋巴细胞通过Ficoll-泛影葡胺梯度分离,在悬浮培养中孵育,并在培养开始后24、48和72小时(AC)制备用于电子显微镜和免疫荧光研究。出血后立即制备全血的血沉棕黄层用于研究。在研究时,5只感染猴中有4只死于恶性淋巴瘤和淋巴细胞白血病。在培养开始后24小时,5份培养物中有2份、48小时时有5份中的4份、72小时时有所有5份培养物中,通过电子显微镜在1%至20%的感染猴淋巴细胞中检测到HVS病毒颗粒,通过免疫荧光检测到HVS抗原。电子显微镜和免疫荧光数据之间有相当好的一致性。对照猴的培养物和血沉棕黄层制剂中均未含有HVS病毒颗粒或抗原。通过电子显微镜观察,绝大多数病毒颗粒是淋巴细胞核内的核衣壳。很少观察到有包膜的病毒颗粒。有一些证据表明,含有HVS的淋巴细胞百分比越高,猴的预后越差。通过淋巴细胞与Vero细胞共培养,从所有5只感染猴中分离出了HVS。对照淋巴细胞共培养为阴性。