Aasted B, Bloom M E
J Clin Microbiol. 1983 Sep;18(3):637-44. doi: 10.1128/jcm.18.3.637-644.1983.
A solid-phase, one-step radioimmune assay was developed which could detect as little as 0.02 microliter of a standard Aleutian disease virus antigen preparation, approximately 3.2 ng of viral protein. Virus antigen was measured in different mink organs and cell types during experimental intraperitoneal infection. The gut and kidney were the first organs in which virus antigen could be detected (day 3 to 6 after infection). On day 6 or later virus antigen was found in spleen, liver, kidney, lymph nodes, peritoneal exudate, and bone marrow cells. With inhibition of antigen binding, a radioimmune assay was developed for antibody detection. Viral antibodies could be detected as early as 3 days after infection. Antibody titers from 1/10(5) to more than 1/10(6) were found in plasmacytotic mink. When the sensitivity of the antibody radioimmune assay was compared with that of other known methods for anti-Aleutian disease virus quantitation, the radioimmune assay was considerably more sensitive, detecting as little as 5 ng of antibody.
开发了一种固相一步放射免疫测定法,该方法能够检测低至0.02微升的标准阿留申病病毒抗原制剂,约3.2纳克病毒蛋白。在实验性腹腔感染期间,对不同水貂器官和细胞类型中的病毒抗原进行了检测。肠道和肾脏是最早能检测到病毒抗原的器官(感染后第3至6天)。在第6天或之后,在脾脏、肝脏、肾脏、淋巴结、腹腔渗出液和骨髓细胞中发现了病毒抗原。通过抑制抗原结合,开发了一种用于抗体检测的放射免疫测定法。感染后3天即可检测到病毒抗体。在浆细胞增多的水貂中发现抗体效价从1/10(5)到超过1/10(6)。当将抗体放射免疫测定法的灵敏度与其他已知的抗阿留申病病毒定量方法的灵敏度进行比较时,放射免疫测定法的灵敏度要高得多,能够检测低至5纳克的抗体。