Samalecos C
J Virol Methods. 1986 Jun;13(3):197-205. doi: 10.1016/0166-0934(86)90014-5.
Fish lymphocystis disease viruses (FLDV) were isolated directly from lymphocystis disease lesions of various flatfish species and further purified. Subunits could be identified only after the purified virus was disrupted. In combination with different types of treatment, Nonidet-P40, dithiothreitol, proteases digestion and after ultrasonication and ultracentrifugation, the inner region of FLDV was studied. The purified virus was used for isolation of the virus nucleoid and for further study of the viral genome. Contour length measurements of 20 DNA molecules gave an average length of 40.44 +/- 3.2 micron. Lines of precipitation between isolated nucleoid material and FLDV-antibodies were shown by immunoelectrophoresis.
鱼类淋巴囊肿病病毒(FLDV)直接从各种比目鱼的淋巴囊肿病损伤部位分离出来,然后进一步纯化。只有在纯化的病毒被破坏后才能鉴定出亚基。结合不同类型的处理方法,如使用Nonidet-P40、二硫苏糖醇、蛋白酶消化以及超声处理和超速离心后,对FLDV的内部区域进行了研究。纯化后的病毒用于分离病毒核质,并进一步研究病毒基因组。对20个DNA分子的轮廓长度测量得出平均长度为40.44±3.2微米。免疫电泳显示了分离出的核质材料与FLDV抗体之间的沉淀线。