Snijder E J, Ederveen J, Spaan W J, Weiss M, Horzinek M C
Institute of Virology, Veterinary Faculty, State University of Utrecht, The Netherlands.
J Gen Virol. 1988 Sep;69 ( Pt 9):2135-44. doi: 10.1099/0022-1317-69-9-2135.
From 380S particles of Berne virus (proposed family Toroviridae) one species of polyadenylated RNA was isolated. Using agarose gel electrophoresis its length was estimated as 20 kb or greater. When assayed under hypertonic transfection conditions genomic RNA was found to be infectious; RNase treatment destroyed the infectivity. The positive polarity of the molecule was confirmed by filter spot hybridization using cDNA prepared against poly(A)-selected RNA from infected cells. In embryonic mule skin cells infected with Berne virus the presence of five virus-specific, polyadenylated RNA species of 7.5, 2.1, 1.4, 0.8 and at least 20 kb was demonstrated. In vitro translation of the 7.5, 2.1 and 0.8 kb RNAs followed by immunoprecipitation showed that they encode a 151K product (possibly the precursor to the peplomer proteins), the envelope protein and the nucleocapsid protein, respectively.
从伯尔尼病毒(提议归入环曲病毒科)的380S颗粒中分离出一种多聚腺苷酸化RNA。通过琼脂糖凝胶电泳估计其长度为20 kb或更长。在高渗转染条件下进行检测时,发现基因组RNA具有感染性;核糖核酸酶处理会破坏其感染性。通过使用针对从感染细胞中选择的聚腺苷酸RNA制备的cDNA进行斑点杂交,证实了该分子的正极性。在感染伯尔尼病毒的胚胎骡皮肤细胞中,证明存在5种病毒特异性的多聚腺苷酸化RNA,大小分别为7.5、2.1、1.4、0.8 kb以及至少20 kb。对7.5、2.1和0.8 kb的RNA进行体外翻译,然后进行免疫沉淀,结果表明它们分别编码一种151K产物(可能是纤突蛋白的前体)、包膜蛋白和核衣壳蛋白。