首页|禽脑脊髓炎病毒VP1蛋白抗体间接ELISA检测方法的建立与临床应用

禽脑脊髓炎病毒VP1蛋白抗体间接ELISA检测方法的建立与临床应用

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为建立1种禽脑脊髓炎病毒(avian encephalomyelitis virus,AEV)抗体检测方法,试验对AEV VP1蛋白进行截短表达,以表达蛋白为包被抗原建立检测AEV抗体的间接ELISA方法.结果显示,重组VP1蛋白以包涵体形式表达,大小为34 kDa;可与AEV阳性血清发生特异性反应;以VP1蛋白为包被抗原建立的间接ELISA方法检测ALV、IBDV、IBV、ILTV、NDV、AIV-H9阳性血清均为阴性;检测AEV抗体的最低检出效价为1:51 200;与IDEXX试剂盒的符合率为95.24%;检测新疆地区1 127份AEV疫苗免疫鸡血清样品和879份未免疫鸡血清样品的免疫抗体阳性率和感染抗体阳性率分别为88.91%和8.19%.结果表明,建立的间接ELISA方法特异、敏感、准确,可用于临床中免疫抗体和野毒感染抗体的检测和筛查.
Establishment and clinical application of an indirect ELISA method for detecting VP1 protein antibody of avian encephalomyelitis virus
To establish a method for detecting antibodies against avian encephalomyelitis virus(AEV),the truncated VP1 protein of AEV was expressed and used as the coating antigen to estab-lish an indirect ELISA method for detecting AEV antibodies.The results showed that the recombi-nant VP1 protein was expressed in the form of an inclusion body with a size of 34 kDa and reacted specifically with AEV positive serum.The indirect ELISA method established was negative for de-tecting serum of ALV,IBDV,IBV,ILTV,NDV,AIV-H9.The lowest detectable titer for AEV an-tibodies was 1:51 200,with a coincidence rate of 95.24%with IDEXX reagent kit.The antibody positive rates were 88.91%and 8.19%for 1 127 chicken serum samples immunized with AEV vac-cine and 879 chicken serum samples with no vaccination,respectively in Xinjiang region.The indi-rect ELISA method established in this study was specific,sensitive,and accurate,and can be used for the detection and screening of AEV infection.

avian encephalomyelitis virusVP1 proteinindirect ELISAclinical application

吕转平、苏晓月、唐思静、王艳萍、张多明

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新疆巴音郭楞职业技术学院,新疆库尔勒 841000

新疆羌都畜牧科技有限公司,新疆巴音郭楞 841801

禽脑脊髓炎病毒 VP1蛋白 间接ELISA 临床应用

新疆维吾尔自治区科技特派员基金(2022)

2022KF044

2024

中国兽医学报
吉林大学

中国兽医学报

CSTPCD北大核心
影响因子:0.702
ISSN:1005-4545
年,卷(期):2024.44(5)
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