Oshiro L S, Levy J A, Riggs J L, Lennette E H
J Gen Virol. 1977 May;35(2):317-23. doi: 10.1099/0022-1317-35-2-317.
The indirect ferritin-labelled antibody technique was used to determine the reactivity of an antiserum prepared against the NZB xenotropic virus with three murine xenotropic viruses, a feline xenotropic virus and a murine ecotropic virus. The envelope antigens of the xenotropic type C viruses isolated from the NZB, NIH Swiss and C57L mice were tagged with ferritin. The feline RD114 virus was not. Gross murine leukaemia virus was tagged, but only at high serum concentrations. The cross-reactivity titre of Gross virus to anti-NZB serum was removed by a serum dilution which was still reactive to xenotropic viruses. This difference in reactivity titres between a xenotropic and an ecotropic virus was sufficient to distinguish one from the other in doubly infected cultures. Specific tagging of membrances of cells infected by xenotropic virus was also observed.
采用间接铁蛋白标记抗体技术,测定针对NZB嗜异性病毒制备的抗血清与三种鼠嗜异性病毒、一种猫嗜异性病毒和一种鼠亲嗜性病毒的反应性。从NZB、NIH瑞士小鼠和C57L小鼠分离出的嗜异性C型病毒的包膜抗原用铁蛋白进行标记。猫RD114病毒未被标记。鼠白血病病毒被标记,但仅在高血清浓度下。嗜异性病毒的交叉反应滴度在仍对嗜异性病毒有反应的血清稀释度下被消除。嗜异性病毒和亲嗜性病毒在反应滴度上的这种差异足以在双重感染培养物中区分彼此。还观察到受嗜异性病毒感染的细胞膜的特异性标记。