畜牧兽医学报 ›› 2020, Vol. 51 ›› Issue (12): 3122-3132.doi: 10.11843/j.issn.0366-6964.2020.12.021

• 预防兽医 • 上一篇    下一篇

禽致病性大肠杆菌cOmpT单克隆抗体的研制及其识别抗原表位的鉴定

薛菲, 杨梓纯, 许炎辉, 王娅玲, 喻婷, 樊毛迪, 刘娟华, 高崧*, 刘秀梵   

  1. 扬州大学兽医学院, 江苏省动物重要疫病与人兽共患病防控协同创新中心, 农业部禽用生物制剂创制重点实验室, 扬州 225009
  • 收稿日期:2020-05-18 出版日期:2020-12-25 发布日期:2020-12-23
  • 通讯作者: 高崧,主要从事动物重要疫病流行病学、致病与免疫机理及防控对策研究,E-mail:gsong@yzu.edu.cn
  • 作者简介:薛菲(1995-),女,江苏扬州人,硕士生,主要从事APEC外膜蛋白的单克隆抗体研究,E-mail:1162362614@qq.com
  • 基金资助:
    国家自然科学基金(31972711;31672553;31602059);国家重点研发计划(2017YFD0500705;2017YFD0500203);扬州大学大学生创新创业训练计划项目;江苏高校优势学科建设工程资助项目(PAPD)

Development of Monoclonal Antibodies against the cOmpT Protein of Avian Pathogenic Escherichia coli and Identification of Epitopes Recognized by Monoclonal Antibodies

XUE Fei, YANG Zichun, XU Yanhui, WANG Yaling, YU Ting, FAN Maodi, LIU Juanhua, GAO Song*, LIU Xiufan   

  1. Key Laboratory of Avian Bioproducts Development of Ministry of Agriculture, Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China
  • Received:2020-05-18 Online:2020-12-25 Published:2020-12-23

摘要: 旨在制备禽致病性大肠杆菌(APEC)染色体编码外膜蛋白(cOmpT)的特异性单克隆抗体,本研究利用实验室已构建的APEC cOmpT重组表达质粒pET-28a-compT,经IPTG诱导表达后,获得以包涵体形式存在的约36 ku的重组蛋白cOmpT,利用尿素浓度梯度透析复性获得纯化蛋白cOmpT,并以此免疫BALB/c小鼠。建立间接ELISA检测方法,最适抗原包被浓度为0.625 μg·mL-1,最适血清稀释度为1:6 400。4次免疫后取小鼠脾进行细胞融合,采用有限稀释法多轮筛选后得到3株能稳定分泌针对cOmpT蛋白的单克隆抗体,分别命名为1G8、2C3和2G3,均为IgG2b亚类。3株杂交瘤细胞上清ELISA抗体效价分别为1:200、1:3 200和1:3 200。Western blot结果显示,3株单抗均能与cOmpT发生特异性反应,而不与其他受检菌发生交叉反应。运用原核表达系统对compT基因进行截短表达,对单克隆抗体针对的cOmpT抗原表位进行鉴定,结果显示单抗1G8、2C3和2G3识别的抗原表位分别是83DQDWMDS8990SNPGTW95197TFKYSGW203。本研究成功制备了3株抗cOmpT蛋白的单克隆抗体,并对其识别的抗原表位进行了鉴定,为cOmpT蛋白功能研究和APEC新型表位疫苗研发奠定了基础。

关键词: 禽致病性大肠杆菌, cOmpT, 单克隆抗体, 抗原表位

Abstract: To development monoclonal antibodies against cOmpT of avian pathogenic Escherichia coli (APEC), the recombinant cOmpT of APEC origin expression plasmid pET-28a-compT was employed, and cOmpT protein with a molecular weight about 36 kD in the form of inclusion bodies was obtained after induction with IPTG, and then renatured by urea gradient dialysis. BALB/c mice were immunized with the purified cOmpT. An indirect enzyme-linked immunosorbent assay (iELISA) was developed, the optimal coating concentration of the antigen was 0.625 μg·mL-1 and the optimal serum dilution was 1:6 400. After the fourth immunization, the spleen of immunized mice was collected for cell fusion, three monoclonal hybridomas that can secrete antibody specific to cOmpT were obtained after multiple screenings, named 1G8, 2C3 and 2G3 respectively. And all of their immunoglobulin subclasses were IgG2b. The titers of monoclonal antibodies in the cell culture supernatant were 1:200, 1:3 200 and 1:3 200 determined by iELISA, respectively. All three monoclonal antibodies were confirmed to react with cOmpT in Western blot, without cross reaction with other tested bacteria. The antigenic epitopes recognized by the three monoclonal antibodies were identified by using a series of E. coli strains harboring expression plasmids recombined with truncated fragments from compT gene. The results revealed that the antigenic epitope required for reactivity with the 1G8 was 83DQDWMDS89, and 90SNPGTW95, 197TFKYSGW203were recognized by 2C3 and 2G3, respectively. In this study, three monoclonal antibodies against cOmpT were successfully developed and the antigenic epitopes recognized by the antibodies were identified. The cOmpT specific monoclonal antibodies obtained in this study are potentially useful tools for both the functional study of cOmpT and the development of APEC epitope vaccines.

Key words: APEC, cOmpT, monoclonal antibody, antigenic epitope

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