Davidson I, Malkinson M, Becker Y
Kimron Veterinary Institute, Bet Dagan, Israel.
Virus Genes. 1988 Oct;2(1):5-18. doi: 10.1007/BF00569733.
The antigenic profile of cell cultures infected with Marek's disease virus (MDV) was determined by the immunoblotting method using convalescent immune serum obtained from chickens that survived infection with MDV strain GA5. The MDV antigen profile in infected cell lysates could be accurately determined since this method has advantages over the immunoprecipitation method used in other studies. We studied six very virulent MDV isolates and the prototype of serotype 1 MDV, the GA5 strain. Immunoblots of NaDodSO4-polyacrylamide gel electrophoresis (PAGE) performed under reducing conditions revealed a main viral antigen (B) of 120-130 kD, which was present in all cell lysates infected with MDV isolates. Analysis of infected cell proteins by NaDodSO4-PAGE performed under nonreducing conditions, revealed a 205 kD major MDV antigen, which, under reducing conditions, was identical to the 130 kD major antigen. The unglycosylated precursors of the major MDV antigens were elucidated. Two polypeptides of 43 and 45 kD were found to be the unglycosylated precursors of MDV antigen A (the glycosylated form of which appears in 4 distinct bands). The unglycosylated precursors of the MDV major antigen B were found to be three polypeptides of 80, 110, and 125 kD.
利用从感染马立克氏病病毒(MDV)GA5株后存活的鸡中获得的恢复期免疫血清,通过免疫印迹法测定感染MDV的细胞培养物的抗原谱。由于该方法比其他研究中使用的免疫沉淀法具有优势,因此可以准确测定感染细胞裂解物中的MDV抗原谱。我们研究了6株超强毒MDV分离株以及1型MDV的原型GA5株。在还原条件下进行的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(PAGE)免疫印迹显示,存在一种120 - 130kD的主要病毒抗原(B),它存在于所有感染MDV分离株的细胞裂解物中。在非还原条件下通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(NaDodSO4-PAGE)分析感染细胞蛋白,发现一种205kD的主要MDV抗原,在还原条件下,它与130kD的主要抗原相同。阐明了主要MDV抗原的未糖基化前体。发现43kD和45kD的两种多肽是MDV抗原A的未糖基化前体(其糖基化形式出现在4条不同的条带中)。发现MDV主要抗原B的未糖基化前体是80kD、110kD和125kD的三种多肽。