畜牧兽医学报 ›› 2022, Vol. 53 ›› Issue (4): 1182-1191.doi: 10.11843/j.issn.0366-6964.2022.04.018

• 预防兽医 • 上一篇    下一篇

非洲猪瘟病毒全长与截短p72蛋白的抗原性比较

张文燕1, 王亚文1, 冯亚文2, 滕召剑1, 李潭清1, 董炜3, 刘涛4, 宋勤叶1*, 任玉红1*   

  1. 1. 河北农业大学动物医学院&河北省兽医生物技术创新中心, 保定 071000;
    2. 河北省兽药监察所, 石家庄 050051;
    3. 顺平县动物疫病预防与控制中心, 保定 072250;
    4. 瑞普生物药业有限公司, 保定 071000
  • 收稿日期:2021-08-03 出版日期:2022-04-23 发布日期:2022-04-25
  • 通讯作者: 宋勤叶,主要从事动物传染病与新型生物制品研究,Tel:+86-0312-7528342,E-mail:songqinye@126.com;任玉红,主要从事基础兽医学研究,E-mail:renyuhong1963@163.com
  • 作者简介:张文燕(1998-),女,河北廊坊人,硕士生,主要从事动物传染病与新型生物制品研究;王亚文(1992-),女,河北石家庄人,博士生,主要从事动物传染病与新型生物制品研究。张文燕和王亚文为同等贡献作者
  • 基金资助:
    河北省重点研发计划项目(21326613D)

Comparison of Antigenicity between Recombinant p72 and Truncated p72 Proteins of African Swine Fever Virus

ZHANG Wenyan1, WANG Yawen1, FENG Yawen2, TENG Zhaojian1, LI Tanqing1, DONG Wei3, LIU Tao4, SONG Qinye1*, REN Yuhong1*   

  1. 1. College of Veterinary Medicine, Hebei Agricultural University & Veterinary Biological Technology Innovation Center of Hebei Province, Baoding 071000, China;
    2. Hebei Provincial Institute of Veterinary Drug Control, Shijiazhuang 050051, China;
    3. Shunping County Animal Disease Prevention and Control Center, Baoding 072250, China;
    4. Ringpu biological pharmaceutical Co., LTD, Baoding 071000, China
  • Received:2021-08-03 Online:2022-04-23 Published:2022-04-25

摘要: 比较非洲猪瘟病毒(African swine fever virus,ASFV)全长p72与截短p72蛋白(p72s)的抗原性,为ASFV特异性抗体检测技术研究提供试验依据。应用大肠杆菌表达系统表达p72和p72s蛋白,应用Western blot和液相色谱-质谱联用(LC-MS/MS)技术鉴定表达的蛋白,分析蛋白的抗原表位;用纯化的重组全长和截短p72蛋白分别免疫小鼠,比较其免疫原性;通过ELISA和Western blot,评价重组p72和p72s蛋白与ASFV阳性血清的免疫反应性。结果:重组p72和p72s蛋白均以包涵体形式表达,相对分子质量分别约为76和42 ku,与预期大小相符;表达蛋白的酶解肽段对p72和p72s蛋白推测氨基酸序列的覆盖度分别为89.3%和88.39%,两者分别包含27和17个抗原表位;用p72与p72s蛋白免疫小鼠3次后,血清特异性抗体效价分别为1∶200~1∶25 600和1∶12 800~1∶409 600;基于重组p72与p72s蛋白的ELISA从108份猪血清中分别检出78份(72.2%)和85份(78.7%)阳性血清,两者的检测结果具有很好的一致性(kappa=0.826,P=0.016);经Western blot检测的10份ASFV抗体阳性血清中有7份与p72蛋白反应,全部与p72s蛋白反应。截短p72蛋白比全长p72蛋白的抗原性好,更适合用于ASFV抗体检测。

关键词: 非洲猪瘟病毒, p72蛋白, 截短p72蛋白, 原核表达, 抗原性

Abstract: The antigenicity of the p72 protein of African swine fever virus (ASFV) was compared with that of a truncated p72 protein (p72s) to provide experimental basis for ASFV specific antibody detection. The p72 and p72s proteins were expressed by Escherichia coli expression system, and the expressed protein was identified by Western blotting and Liquid chromatography mass spectrometer (LC-MS/MS), and the epitopes of the protein were analyzed. Mice were immunized with the purified intact p72 protein or p72s protein, respectively, and the immunogenicity of p72 and p72s proteins was compared. The immunoreactivity of the p72 and p72s proteins with ASFV-positive serum was evaluated by ELISA and Western blotting.Both recombinant p72 and p72s proteins were expressed as inclusion bodies with molecular weights of 76 and 42 kDa, respectively, which were consistent with the expected molecular weight. The coverage of predicted amino acid sequences of p72 and p72s by the hydrolysate peptide of the expression proteins was 89.3% and 88.39%, respectively, which included 27 and 17 epitopes. After mice were immunized with p72 or p72s for three times, the serum specific antibody titers were in the range of 1∶200 to 1∶25 600 and 1∶12 800 to 1∶409 600, respectively. Among 108 swine sera, 78 (72.2%) and 85 (78.7%) positive sera were detected by ELISA based on p72 and p72s proteins with a good consistency (kappa=0.826, P=0.016). Seven of the 10 ASFV positive sera detected by Western blotting reacted with p72 protein, and all of them reacted with the p72s protein. The truncated p72 protein has better antigenicity than the intact p72 protein, and it is more suitable for ASFV antibody detection.

Key words: African swine fever virus, intact/truncated p72 protein, prokaryotic expression, antigenicity

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