Odindo M O, Payne C C, Crook N E, Jarrett P
J Gen Virol. 1986 Mar;67 ( Pt 3):527-36. doi: 10.1099/0022-1317-67-3-527.
Virus particles were isolated from hypertrophied salivary glands of the tsetse fly, Glossina pallidipes collected near Mombasa, Kenya. Purified virus particles were rod-shaped, 57 nm wide by 700 to 1300 nm long. Particle lengths fell into two size classes, with 'short' particles averaging 869 nm and 'long' particles 1175 nm. The virus particles morphologically resembled elongated baculovirus nucleocapsids although, unlike baculoviruses, no fully enveloped virions were found in purified preparations. The particles contained double-stranded DNA which appeared to be linear when analysed by electrophoresis in agarose gels, ethidium bromide-caesium chloride gradient centrifugation or electron microscopy (EM). There was some evidence for the DNA being heterogeneous in size from EM studies and from the observation that restriction enzyme analysis failed to provide a clear profile of DNA fragments. Protein from purified virions contained at least 12 polypeptides with a major component of 39 000 mol. wt. These results suggest that the virus cannot be placed in any of the existing taxonomic groupings of DNA viruses.
病毒粒子是从采自肯尼亚蒙巴萨附近的采采蝇(淡足舌蝇)肥大唾液腺中分离出来的。纯化后的病毒粒子呈杆状,宽57纳米,长700至1300纳米。粒子长度分为两个大小类别,“短”粒子平均长869纳米,“长”粒子平均长1175纳米。病毒粒子在形态上类似于拉长的杆状病毒核衣壳,不过与杆状病毒不同的是,在纯化制剂中未发现完全包膜的病毒粒子。这些粒子含有双链DNA,通过琼脂糖凝胶电泳、溴化乙锭-氯化铯梯度离心或电子显微镜(EM)分析时,其呈现为线性。电子显微镜研究以及限制酶分析未能提供清晰的DNA片段图谱这一观察结果表明,DNA在大小上存在一定程度的异质性。纯化病毒粒子的蛋白质含有至少12种多肽,主要成分的分子量为39000道尔顿。这些结果表明,该病毒无法归入现有的任何DNA病毒分类类别中。