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首页> 外文期刊>Journal of Clinical Microbiology >Detection of antibody to murine cytomegalovirus by enzyme-linked immunosorbent and indirect immunofluorescence assays.
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Detection of antibody to murine cytomegalovirus by enzyme-linked immunosorbent and indirect immunofluorescence assays.

机译:通过酶联免疫吸附法和间接免疫荧光测定法检测鼠巨细胞病毒抗体。

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We have compared murine cytomegalovirus (MCMV) antibody determination by enzyme-linked immunosorbent assay (ELISA) and indirect immunofluorescence assay. A comparison of antibody detection with 146 serum samples at a 1:20 dilution showed 100% agreement (60 negatives and 86 positives) between the assays. There was close agreement of endpoint determinations of sera by both methods. After experimental MCMV infection, antibody to MCMV was detected by both assays as early as day 7, and high titers persisted as late as 6 months. In contrast to immunocompetent littermates, athymic nude mice did not develop antibody after infection. Mice lacking antibody detectable by ELISA were susceptible to lethal MCMV challenge. In a survey of animals from five commercial sources, MCMV antibody was not detected unless mice were experimentally infected. MCMV antibody determination by ELISA is a convenient method, comparable to the indirect immunofluorescence assay in sensitivity and specificity.
机译:我们通过酶联免疫吸附测定(ELISA)和间接免疫荧光测定比较了鼠巨细胞病毒(MCMV)抗体的测定。用146:1稀释的146个血清样品进行抗体检测的比较表明,各测定之间的一致性为100%(60个阴性和86个阳性)。两种方法的血清终点测定结果均一致。在实验性MCMV感染后,最早在第7天就通过两种检测方法均检测到针对MCMV的抗体,高滴度持续至6个月。与具有免疫能力的同窝仔相比,无胸腺裸鼠在感染后没有产生抗体。缺少可通过ELISA检测到的抗体的小鼠易受致命的MCMV攻击。在一项对来自五个商业来源的动物的调查中,除非对小鼠进行了实验性感染,否则不会检测到MCMV抗体。通过ELISA测定MCMV抗体是一种简便的方法,在敏感性和特异性上可与间接免疫荧光测定相媲美。

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