Tannock G A, Romanova J R, Paul J A
Faculty of Medicine, University of Newcastle, Callaghan, New South Wales, Australia.
Arch Virol. 1995;140(1):201-9. doi: 10.1007/BF01309736.
Two surface antigen segregants were prepared by co-infection of chicken embryo kidney cell cultures with reassortants of the cold-adapted influenza A master strain A/Ann Arbor/6/60-ca (H2N2) possessing the surface antigens of A/Queensland/6/72 (H3N2) and A/Hong Kong/123/77 (H1N1) and other genes that were common to the master strain. The segregants were shown by serological tests to possess H3N1 and H1N2 surface antigens but it was not possible to determine the presence of H1 or N1 genes by single-stranded RNA polyacrylamide gel electrophoresis. The immunogenic properties of A/Queensland/6/72-ca and H3N1 segregant CR6/35/2/9 were compared by immunising mice intranasally with graded doses of each virus twice at an interval of 3 weeks and then challenging with the wild-type A/Queensland/6/72 (H3N2). Clearance of the challenge virus occurred in mice immunised with the same vaccinating dose, indicating that the immunogenicity of both the ca H3N2 and H3N1 viruses was identical and similar findings were obtained for mice immunised with A/Hong Kong/123/77-ca and the H1N2 segregant CR6/35/1/19 and challenged with the wild-type A/Hong Kong/123/77. Therefore, there appears to be a good correlation between immunogenicity and the inheritance of the haemagglutinin gene.
通过将具有A/昆士兰/6/72(H3N2)表面抗原和A/香港/123/77(H1N1)表面抗原以及与主毒株共有的其他基因的冷适应甲型流感主毒株A/安阿伯/6/60 - ca(H2N2)的重配体与鸡胚肾细胞培养物共同感染,制备了两种表面抗原分离株。血清学检测显示,这些分离株具有H3N1和H1N2表面抗原,但通过单链RNA聚丙烯酰胺凝胶电泳无法确定H1或N1基因的存在。通过以分级剂量分别对小鼠进行鼻内免疫,每隔3周免疫两次,然后用野生型A/昆士兰/6/72(H3N2)进行攻击,比较了A/昆士兰/6/72 - ca和H3N1分离株CR6/35/2/9的免疫原性。在用相同接种剂量免疫的小鼠中,攻击病毒被清除,这表明冷适应H3N2和H3N1病毒具有相同的免疫原性,在用A/香港/123/77 - ca和H1N2分离株CR6/35/1/19免疫并用野生型A/香港/123/77攻击的小鼠中也获得了类似的结果。因此,免疫原性与血凝素基因的遗传之间似乎存在良好的相关性。