Zhao X L, Phillips R M, Li G D, Zhong A Q
Shenzhen Animal and Plant Quarantine Service, Guangdong, People's Republic of China.
Avian Dis. 1991 Oct-Dec;35(4):778-82.
An indirect enzyme-linked immunosorbent assay (ELISA) for the detection of antibody to duck hepatitis virus (DHV) is described. The results of ELISA were compared with those of an agar gel diffusion precipitin (AGDP) test and a serum-neutralization (SN) test. The specificity of the ELISA was in accordance with the specificity of the AGDP and SN tests, but there was a difference in sensitivity. The positive detection rates of ELISA, SN test, and AGDP test for 93 clinical samples were 68.8%, 68.8%, and 18.8%, respectively. A positive/negative (P/N) value larger than or equal to 2.1 plus an absorbance value larger than or equal to 0.4 was used as a comprehensive positive standard for the ELISA. This eliminated false-positive reactions. The results showed that the ELISA was a rapid, sensitive, and accurate method for detecting antibody to DHV.
本文描述了一种用于检测鸭肝炎病毒(DHV)抗体的间接酶联免疫吸附测定(ELISA)方法。将ELISA的结果与琼脂凝胶扩散沉淀试验(AGDP)和血清中和试验(SN)的结果进行了比较。ELISA的特异性与AGDP和SN试验的特异性一致,但在敏感性方面存在差异。93份临床样本的ELISA、SN试验和AGDP试验的阳性检出率分别为68.8%、68.8%和18.8%。ELISA的综合阳性标准为阳性/阴性(P/N)值大于或等于2.1且吸光度值大于或等于0.4。这消除了假阳性反应。结果表明,ELISA是一种检测DHV抗体的快速、灵敏且准确的方法。