Correlation between efficacy and structure of recombinant epitope vaccines against bovine type O foot and mouth disease virus

被引:13
|
作者
Fang, Mingli [1 ]
Li, Jianli [2 ,3 ]
Wang, Hua [1 ]
Yang, Ming [4 ]
Zhang, Yongsheng [1 ]
Zhou, Lei [1 ]
Wei, Hongfei [1 ]
Yang, Guang [1 ]
Yu, Yue
Wei, Xuefeng [5 ]
Yu, Yongli
Wang, Liying [1 ]
Wan, Min [1 ]
机构
[1] Jilin Univ, Dept Mol Biol, Norman Bethune Coll Med, Changchun 130021, Peoples R China
[2] Nanjing Agr Univ, Coll Vet Med, Nanjing 210095, Jiangsu, Peoples R China
[3] Tianjin Ringpu Biotechnol Co Ltd, Natl Certified Enterprise Tech Ctr, Tianjin 300300, Peoples R China
[4] Jilin Univ, Dept Immunol, Norman Bethune Coll Med, Changchun 130021, Peoples R China
[5] Inner Mongolia Jinyu Grp Baoling Biopharmaceut Co, Hohhot 013300, Inner Mongolia, Peoples R China
关键词
Foot and mouth disease virus; Recombinant epitope vaccine; RGD sequence of B cell epitope; VP1 capsid protein; PEPTIDE; CATTLE; VP1; IMMUNOGENICITY; PROTECTION; RESPONSES; PROTEIN; REGION;
D O I
10.1007/s10529-012-0856-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To develop recombinant epitope vaccines against foot-and-mouth disease virus (FMDV), genes coding for six recombinant proteins (rP1-rP6) consisting of different combinations of B cell and T cell epitope from VP1 capsid protein (VP1) of type O FMDV were constructed and the 3D structure of these proteins analyzed. This revealed a surface-exposed RGD sequence of B cell epitopes in all six recombinant proteins as that in VP1 of FMDV and rP1, rP2 and rP4 globally mimicked the backbone conformation of the VP1. rP1, rP2 and rP4 stimulated guinea pigs to produce higher level of neutralizing antibodies capable of protecting suckling mice against FMDV challenge. rP1 stimulated cattle to produce FMDV-neutralizing antibody. The data suggest that an efficient recombinant epitope vaccine against FMDV should share local similarities with the natural VP1 of FMDV.
引用
收藏
页码:839 / 847
页数:9
相关论文
共 50 条
  • [21] Artificially designed hepatitis B virus core particles composed of multiple epitopes of type A and O foot-and-mouth disease virus as a bivalent vaccine candidate
    Lei, Yao
    Shao, Junjun
    Zhao, Furong
    Li, Yangfan
    Lei, Chenglin
    Ma, Feifei
    Chang, Huiyun
    Zhang, Yongguang
    JOURNAL OF MEDICAL VIROLOGY, 2019, 91 (12) : 2142 - 2152
  • [22] Efficacy of Expired Foot-and-mouth Disease O Type Vaccines in Cattle and Buffalo in Lao People's Democratic Republic
    Sakamoto, Kenichi
    Morioka, Kazuki
    Fukai, Katsuhiko
    Yamamoto, Takehisa
    Tsutsui, Toshiyuki
    Muroga, Norihiko
    Ojima, Noriyoshi
    Mago, Josuke
    Katagiri, Yoshito
    Aviso, Sharie R.
    Phouaravanh, Manivanh
    Soukvilay, Vilayvanh
    Keokhamphet, Chattouphone
    Buranathai, Chantanee
    Khounsy, Syseng
    Yamada, Manabu
    JARQ-JAPAN AGRICULTURAL RESEARCH QUARTERLY, 2016, 50 (02): : 163 - 168
  • [23] THE STRUCTURE AND ANTIGENICITY OF A TYPE-C FOOT-AND-MOUTH-DISEASE VIRUS
    LEA, S
    HERNANDEZ, J
    BLAKEMORE, W
    BROCCHI, E
    CURRY, S
    DOMINGO, E
    FRY, E
    ABUGHAZALEH, R
    KING, A
    NEWMAN, J
    STUART, D
    MATEU, MG
    STRUCTURE, 1994, 2 (02) : 123 - 139
  • [24] High potency vaccines induce protection against heterologous challenge with foot-and-mouth disease virus
    Brehm, K. E.
    Kumar, N.
    Thulke, H. -H.
    Haas, B.
    VACCINE, 2008, 26 (13) : 1681 - 1687
  • [25] Cross-protective efficacy of engineering serotype A foot-and-mouth disease virus vaccine against the two pandemic strains in swine
    Zheng, Haixue
    Lian, Kaiqi
    Yang, Fan
    Jin, Ye
    Zhu, Zixiang
    Guo, Jianhong
    Cao, Weijun
    Liu, Huanan
    He, Jijun
    Zhang, Keshan
    Li, Dan
    Liu, Xiangtao
    VACCINE, 2015, 33 (43) : 5772 - 5778
  • [26] In silico Design, Synthesis and Potency of an Epitope-based Vaccine Against Foot-and-mouth Disease Virus
    Liu, Yu-Fan
    Lin, Chai-Yen
    Hong, Hui-Mei
    INTERNATIONAL JOURNAL OF PHARMACOLOGY, 2017, 13 (02) : 122 - 133
  • [27] Comparison of different ELISA methods for the detection of antibodies against foot-and-mouth disease virus (FMDV) type O
    Niedbalski, W
    BULLETIN OF THE VETERINARY INSTITUTE IN PULAWY, 2004, 48 (01) : 5 - 9
  • [28] Implication of Broadly Neutralizing Bovine Monoclonal Antibodies in the Development of an Enzyme-Linked Immunosorbent Assay for Detecting Neutralizing Antibodies against Foot-and-Mouth Disease Virus Serotype O
    Cao, Yimei
    Li, Kun
    Wang, Sheng
    Fu, Yuanfang
    Sun, Pu
    Li, Pinghua
    Bai, Xingwen
    Zhang, Jing
    Ma, Xueqing
    Xing, Xiangchuan
    Zhou, Shasha
    Bao, Huifang
    Li, Dong
    Chen, Yingli
    Li, Zhiyong
    Lu, Zengjun
    Liu, Zaixin
    JOURNAL OF CLINICAL MICROBIOLOGY, 2019, 57 (12)
  • [29] Inhibitory Effects of Bovine Lactoferricin-Lactoferrampin on Senecavirus A and Foot-and-Mouth Disease Virus with Recombinant Lactobacillus Oral Treatment in Mice
    Zhao, Wenyue
    Zhang, Senhao
    Sui, Ling
    Wang, Xiaona
    Li, Jiaxuan
    Cui, Wen
    Jiang, Yanping
    Qiao, Xinyuan
    Tang, Lijie
    VETERINARY SCIENCES, 2025, 12 (03)
  • [30] Evaluation and Use of In-Silico Structure-Based Epitope Prediction with Foot-and-Mouth Disease Virus
    Borley, Daryl W.
    Mahapatra, Mana
    Paton, David J.
    Esnouf, Robert M.
    Stuart, David I.
    Fry, Elizabeth E.
    PLOS ONE, 2013, 8 (05):