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禽多瘤病毒VP4蛋白单克隆抗体的制备及其间接免疫荧光检测方法的初步建立

汪溪 何后军 陈小云 毛娅卿 翟天舒 许冠龙 王嘉 孔冬妮 邓永 闫佳佳 薛青红 印春生

中国兽医科学2024,Vol.54Issue(5):584-594,11.
中国兽医科学2024,Vol.54Issue(5):584-594,11.DOI:10.16656/j.issn.1673-4696.2024.0083

禽多瘤病毒VP4蛋白单克隆抗体的制备及其间接免疫荧光检测方法的初步建立

Preparation of monoclonal antibody against avian polyomavirus VP4 protein and preliminary establishment of an indirect immunofluorescence detection method

汪溪 1何后军 2陈小云 3毛娅卿 3翟天舒 3许冠龙 3王嘉 3孔冬妮 3邓永 3闫佳佳 4薛青红 3印春生3

作者信息

  • 1. 江西农业大学 动物科学技术学院,江西 南昌 330045||中国兽医药品监察所,北京 100081
  • 2. 江西农业大学 动物科学技术学院,江西 南昌 330045
  • 3. 中国兽医药品监察所,北京 100081
  • 4. 中国兽医药品监察所,北京 100081||山西农业大学 动物医学学院,山西 太谷 030801
  • 折叠

摘要

Abstract

In order to prepare a monoclonal antibody against VP4 protein of avian polyomavirus(APV),and to initially establish an indirect immunofluorescence detection method for APV.The monoclonal antibody was prepared by prokaryotic expression of APV VP4 protein and immunising BALB/c mice after purification,and the reaction conditions were optimized with the prepared against VP4 monoclonal anti-body as the primary antibody and FITC-goat anti-mouse IgG as the secondary antibody.The results showed that 15 positive cell lines were screened and identified by subtype.The heavy chain of 2 monoclonal antibodies was IgG2b type,the heavy chain of 13 monoclonal antibodies was IgG1 type,and the light chain wasк type.Three cell strains were selected to prepare monoclonal antibodies.The concentrations of a-gainst VP4 monoclonal antibodies of the 3 strains were 2.9,2.6,and 3.2 mg/mL,respectively.The affin-ity constants were 1.06×1010,2.95×109,and 9.60×109,respectively.The titer of two strains was both 1 ∶204 800,and the titer of the other strain was 1 ∶51 200.Western-blot and indirect immunofluorescence assay(IFA)showed that all 3 monoclonal antibodies could react specifically with APV.The optimal conditions for the indirect immunofluorescence detection method established in this study were as follows:1 ∶1 000 dilu-tion of Anti-A-VP4-15,overnight incubation at 4℃,1 ∶200 dilution of secondary antibody,incubation at 37℃for 1 h.The established method was used to detect egg drop syndrome virus(EDSV),reticuloendotheliosis virus(REV),avian leukosis virus(ALV),Newcastle disease virus(NDV),avian infectious bronchitis virus(IBV)and APV in the cells.Only the results for APV were positive,and tests for other viruses were negative.The indirect immunofluorescence method established using this monoclonal antibody was able to detect at least 5 TCID50 APV infections on cells.The monoclonal antibody and the indirect immunofluores-cence method developed in this study provide a basis for epidemiological investigation and labora-tory diagnosis of APV infection.

关键词

禽多瘤病毒/VP4蛋白/原核表达/单克隆抗体/间接免疫荧光试验

Key words

avian polyomavirus/VP4 protein/prokaryotic expression/monoclonal antibody/indirect immunofluorescence assay

分类

农业科技

引用本文复制引用

汪溪,何后军,陈小云,毛娅卿,翟天舒,许冠龙,王嘉,孔冬妮,邓永,闫佳佳,薛青红,印春生..禽多瘤病毒VP4蛋白单克隆抗体的制备及其间接免疫荧光检测方法的初步建立[J].中国兽医科学,2024,54(5):584-594,11.

基金项目

国家自然科学基金项目(32002273) (32002273)

中国兽医药品监察所公益性专项(GY202105) (GY202105)

兽药行业公益性重点专项(GY202104). (GY202104)

中国兽医科学

OA北大核心CSTPCD

1673-4696

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