Thomas F C, Trainer D O
Can J Comp Med. 1971 Jul;35(3):187-91.
Seven isolates of bluetongue virus with different isolation histories and one isolate of the virus of epizootic hemorrhagic disease of deer were cloned by three consecutive plaquings in L-929 cells. The isolates were categorized on plaque size and margin. Antisera to the bluetongue virus isolates were produced in calves and antiserum to epizootic hemorrhagic disease virus in deer. Plaque reduction neutralization tests were done using the eight isolates and antisera to six of these. The isolates could be partially categorized on plaque type. In the plaque reduction neutralization test, all of the bluetongue viruses cross reacted and although differences were frequently observed, no obvious antigenic classification was possible. Reactions between the bluetongue viruses and epizootic hemorrhagic disease virus were all within the limits of what is presently considered to be non-specific inhibition.
七株具有不同分离历史的蓝舌病毒毒株和一株鹿流行性出血病病毒毒株在L - 929细胞中通过连续三次空斑纯化进行克隆。根据空斑大小和边缘对这些毒株进行分类。用犊牛制备了针对蓝舌病毒毒株的抗血清,用鹿制备了针对鹿流行性出血病病毒的抗血清。使用这八株毒株和针对其中六株的抗血清进行了空斑减少中和试验。这些毒株可根据空斑类型进行部分分类。在空斑减少中和试验中,所有蓝舌病毒都发生交叉反应,尽管经常观察到差异,但无法进行明显的抗原分类。蓝舌病毒与鹿流行性出血病病毒之间的反应均在目前认为是非特异性抑制的范围内。