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Detection of Antibody Against Avian Leukosis Virus Subgroup A by Enzyme-linked Immunosorbent Assay with BaculovirusExpressed gp85 Protein

机译:用拟乌拉夫血管病毒抑制的GP85蛋白质通过酶联免疫吸附测定检测对禽白血病病毒亚组A的抗体

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摘要

To detect antibody against avian leukosis virus subgroup A (ALV-A), the gp85 gene of an ALV-A strain isolated in Taiwan was cloned and expressed in a baculovirus expression vector. The expressed protein confirmed by Western blotting and immunofluorescence tests with anti-ALV-A antiserum was coated in 96-well plates and was used as an antigen for antibody detection by an indirect enzyme-linked immunosorbent assay (ELISA). Neutralization test performed in chicken sera from the infected and uninfected flocks was used as the standard to evaluate the accuracy of the ELISA. The cut-off point was calculated by receiver operator characteristic (ROC) curve to be 1. The sensitivity and specificity of this ELISA were 80% (24/30) and 83.3% (35/42), respectively. In conclusion, this ELISA could be applied for the anti-ALV-A antibody detection in the field.
机译:为了检测对禽白血病病毒亚组A(ALV-A)的抗体,在台湾分离的ALV-A菌株的GP85基因被克隆并在杆状病毒表达载体中表达。 用抗ALV-A抗血清的蛋白质印迹和免疫荧光试验证实的表达蛋白质涂覆在96孔板中,用作间接酶联免疫吸附测定(ELISA)作为抗体检测的抗原。 从受感染和未感染的羊群中鸡血液中的中和试验用作评估ELISA的准确性的标准。 截止点通过接收器操作员特征(ROC)曲线计算为1.该ELISA的敏感性和特异性分别为80%(24/30)和83.3%(35/42)。 总之,该ELISA可以应用于抗ALV-A抗体检测。

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