Charman H P, Kim N, Gilden R V
J Virol. 1974 Oct;14(4):910-7. doi: 10.1128/JVI.14.4.910-917.1974.
A radioimmunoassay for the major, group-specific antigen (p30) of hamster type C viruses was developed. The test detected approximately 5 ng of viral protein per ml and was highly specific for hamster viruses when used with homologous antibody. Comparison of three hamster viruses, two being mouse-hamster pseudotypes, in homologous and heterologous intraspecies assays, showed no evidence of type specificity for these proteins. The pseudotype viruses showed no evidence of mouse virus p30 antigenic determinants. An interspecies antigen assay employing (125)I-labeled hamster p30 and anti-feline p30 was completely inhibited by cat (feline leukemia virus), hamster, and rat viruses, to a slightly lesser degree by mouse viruses, and only poorly by RD 114 and Gibbon ape viruses. The Mason-Pfizer virus did not inhibit this assay. Hamster p30 was detected by radioimmunoassay in individual embryos from two LSH hamsters and in several adult tissues, excluding muscle at levels below that required for detection in complement-fixation tests.
开发了一种针对仓鼠C型病毒主要群特异性抗原(p30)的放射免疫测定法。该检测方法每毫升可检测到约5纳克病毒蛋白,与同源抗体一起使用时,对仓鼠病毒具有高度特异性。在同源和异源种内试验中,对三种仓鼠病毒(其中两种是小鼠-仓鼠假型病毒)进行比较,结果表明这些蛋白质不存在型特异性。假型病毒未显示出小鼠病毒p30抗原决定簇的证据。采用(125)I标记的仓鼠p30和抗猫p30的种间抗原检测试验,被猫(猫白血病病毒)、仓鼠和大鼠病毒完全抑制,被小鼠病毒抑制程度稍低,而RD 114和长臂猿病毒仅能微弱抑制。梅森-辉瑞病毒不能抑制该检测试验。通过放射免疫测定法在两只LSH仓鼠的单个胚胎以及几个成年组织中检测到了仓鼠p30,但肌肉中未检测到,肌肉中的水平低于补体结合试验检测所需水平。