Hahn E C, Ramos L, Kenyon A J
Infect Immun. 1977 Jan;15(1):204-11. doi: 10.1128/iai.15.1.204-211.1977.
Infection of CRFK feline kidney cells with Aleutian disease vurus leads to production of virus-induced antigen(s) in the nucleus which could be demonstrated by the fluorescent-antibody technique. The number of fluorescent nuclei was lineraly dependent on the dilution of the inoculum, but rarely exceeded 20% of the cells. Aleutian disease nuclear antigen was only transiently detectable. The virus-induced antigen was detected after infection of cells of several divergent species; however, the CRFK line of feline kidney cells was the most susceptible. Inhibitor studies indicated that deoxyribonucleic acid synthesis, ribonucleic acid synthesis, and protein synthesis were required for viral antigen production. Cell growth was also a requirement for synthesis of viral antigen, An in situ radioimmune assay was used to measure binding of 125I-labeled mink anti-Aleutian disease virus to infected cells and competition with unlabeled sera. The system is suitable for quantitation of infectivity.
将阿留申病病毒感染猫肾细胞系(CRFK)会导致细胞核中产生病毒诱导抗原,这可以通过荧光抗体技术检测到。荧光细胞核的数量与接种物的稀释度呈线性关系,但很少超过细胞总数的20%。阿留申病核抗原只能短暂检测到。在感染几种不同物种的细胞后都能检测到病毒诱导抗原;然而,猫肾细胞系CRFK最为敏感。抑制剂研究表明,病毒抗原的产生需要脱氧核糖核酸合成、核糖核酸合成和蛋白质合成。细胞生长也是病毒抗原合成的必要条件。采用原位放射免疫分析法测定125I标记的水貂抗阿留申病病毒与感染细胞的结合以及与未标记血清的竞争情况。该系统适用于感染性的定量分析。