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首页> 外文期刊>Journal of Clinical Microbiology >Dot-enzyme immunoassay for visual detection of antibodies to pseudorabies virus in swine serum.
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Dot-enzyme immunoassay for visual detection of antibodies to pseudorabies virus in swine serum.

机译:点酶免疫分析法可用于猪血清中伪狂犬病病毒抗体的视觉检测。

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A modified solid-phase enzyme immunoassay (EIA) is described for the visual detection of anti-pseudorabies virus (anti-PRV) antibody in porcine serum. Dots of PRV antigens were adsorbed to nitrocellulose paper (hence the name dot-EIA), and the remaining nonspecifically reactive sites were blocked with bovine serum albumin or skim milk powder. After immersion in test serum, bound antibodies were reacted with a peroxidase-conjugated anti-porcine immunoglobulin G (H & L). Positive reactions were easily visualized as brown dots after enzyme degradation of a substrate containing hydrogen peroxide and diaminobenzidine. The dot-EIA was comparable to the serum neutralization test and the standard microtiter EIA in its ability to detect antibody in the sera of pigs 9 days after experimental infection and 12 days after contact with infected pigs. The sensitivity and specificity of the dot-EIA relative to the serum neutralization test and the standard EIA were determined from the testing of 856 field sera from the United Kingdom, the United States, and Canada. In all comparisons, both the relative sensitivity and specificity of the dot-EIA were in the order of 98 to 99%. The dot EIA appears to have potential application as a rapid and economical field test in the diagnosis of PRV infection.
机译:描述了一种改良的固相酶免疫分析(EIA),用于肉眼检测猪血清中的抗伪狂犬病病毒(PRV)抗体。 PRV抗原的点被吸附到硝酸纤维素纸上(因此命名为点EIA),其余的非特异性反应位点被牛血清白蛋白或脱脂奶粉封闭。浸入测试血清后,将结合的抗体与过氧化物酶结合的抗猪免疫球蛋白G(H&L)反应。酶降解包含过氧化氢和二氨基联苯胺的底物后,阳性反应很容易显示为棕点。 dot-EIA在实验感染后9天和与感染猪接触12天后可检测猪血清中抗体的能力与血清中和试验和标准微量滴定EIA相当。从英国,美国和加拿大的856场血清测试中确定了点EIA对血清中和试验和标准EIA的敏感性和特异性。在所有比较中,点-EIA的相对灵敏度和特异性均在98%至99%的数量级。点EIA似乎有可能作为诊断PRV感染的快速而经济的现场测试方法。

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