Comprehensive mapping of a novel NS1 epitope conserved in flaviviruses within the Japanese encephalitis virus serocomplex

被引:9
|
作者
Hua, Rong-Hong [1 ]
Liu, Li-Ke [1 ]
Huo, Hong [1 ]
Li, Ye-Nan [1 ]
Guo, Li-Peng [1 ]
Wang, Xiao-Lei [1 ]
Qin, Cheng-Feng [2 ]
Bu, Zhi-Gao [1 ]
机构
[1] Chinese Acad Agr Sci, Harbin Vet Res Inst, State Key Lab Vet Biotechnol, Harbin 150001, Peoples R China
[2] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogen & Biosecur, Beijing 100071, Peoples R China
关键词
Japanese encephalitis virus serocomplex; NS1; protein; Linear B-cell epitope; WEST-NILE-VIRUS; LINKED-IMMUNOSORBENT-ASSAY; B-CELL EPITOPES; PRM/M PROTEIN; DENGUE; IDENTIFICATION; DISTINGUISH; INFECTIONS; ANTIBODIES; AUSTRALIA;
D O I
10.1016/j.virusres.2014.03.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Nonstructural protein-1 (NS1) of the Japanese encephalitis virus (JEV) is an immunogenic protein that is a potential candidate for the development of vaccines and diagnostic reagents. NS1 is known to be more specific than the E protein in serological testing of flavivirus infections. However, NS1 exhibits crossreactivity among flaviviruses even within the same genus and more so within a serocomplex. However, the cross-reactive epitopes on JEV NS1 are poorly characterized. The present study describes the full mapping of a linear B-cell epitope that is common and specific to the JEV serocomplex of Flaviviridae. We generated an NS1-specific monoclonal antibody that cross-reacts with the West Nile virus (WNV) NS1 protein by immunizing mice with recombinant JEV NS1. For epitope mapping, 51 partially overlapping peptides spanning the entire NS1 protein were expressed with a glutathione S-transferase (GST) tag and screened using monoclonal antibodies. Two linear epitope-containing peptides were identified using enzyme-linked immunosorbent assay (ELISA). By sequentially removing amino acid residues from the carboxy and amino terminal of peptides, we successfully identified the smallest unit of the linear epitope required to react with the monoclonal antibody. The linear epitope was located in amino acids residues (ETHTLW232)-E-227. Furthermore, results of the sequence alignment revealed that the epitope was highly conserved among JEV strains. Notably, the epitope is highly conserved among viruses of the JEV serocomplex. Furthermore, the homologous regions on NS1 proteins from dengue viruses showed no cross-reactivity with the monoclonal antibodies. The epitope was recognized by antisera against the WNV but not against the dengue virus. This novel JEV serocomplex-specific linear B-cell epitope of NS1 would be helpful in the development of new vaccines and diagnostic assays. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 109
页数:7
相关论文
共 50 条
  • [41] Fine mapping of a linear epitope on EDIII of Japanese encephalitis virus using a novel neutralizing monoclonal antibody
    Deng, Wen-Lei
    Guan, Chi-Yu
    Liu, Ke
    Zhang, Xiao-Min
    Feng, Xiu-Li
    Zhou, Bin
    Su, Xiao-Dong
    Chen, Pu-Yan
    VIRUS RESEARCH, 2014, 179 : 133 - 139
  • [42] Comprehensive mapping of West Nile virus (WNV)- and Japanese encephalitis virus serocomplex-specific linear B-cell epitopes from WNV non-structural protein 1
    Sun, En-Cheng
    Zhao, Jing
    Liu, Ni-Hong
    Yang, Tao
    Ma, Jian-Nan
    Geng, Hong-Wei
    Wang, Ling-Feng
    Qin, Yong-Li
    Bu, Zhi-Gao
    Yang, Yin-Hui
    Lunt, Ross A.
    Wang, Lin-Fa
    Wu, Dong-Lai
    JOURNAL OF GENERAL VIROLOGY, 2012, 93 : 50 - 60
  • [43] Japanese Encephalitis Virus (JEV) NS1′ Enhances the Viral Infection of Dendritic Cells (DCs) and Macrophages in Pig Tonsils
    Xie, Shengda
    Pan, Junhui
    Zhang, Qiuting
    Guan, Ruting
    Yang, Xingmiao
    Yang, Xiaoxiao
    Liang, Zhenjie
    Cao, Ruibing
    MICROBIOLOGY SPECTRUM, 2022, 10 (04):
  • [44] Japanese encephalitis virus NS1′ protein depends on pseudoknot secondary structure and is cleaved by caspase during virus infection and cell apoptosis
    Sun, Jin
    Yu, Yongxin
    Deubel, Vincent
    MICROBES AND INFECTION, 2012, 14 (11) : 930 - 940
  • [45] Linear epitope identification of monoclonal antibodies against the duck Tembusu virus NS1
    Tan, Hantai
    Zhang, Senzhao
    Tan, Wangyang
    Hu, Tao
    He, Yu
    Wu, Zhen
    Wang, Mingshu
    Jia, Renyong
    Zhu, Dekang
    Liu, Mafeng
    Zhao, Xinxin
    Yang, Qiao
    Wu, Ying
    Zhang, Shaqiu
    Huang, Juan
    Ou, Xumi
    Gao, Qun
    Sun, Di
    Cheng, Anchun
    Chen, Shun
    POULTRY SCIENCE, 2023, 102 (10)
  • [46] Selective Reactivity of Anti-Japanese Encephalitis Virus NS4B Antibody Towards Different Flaviviruses
    Kaufusi, Pakieli H.
    Tseng, Alanna C.
    Kelley, James F.
    Nerurkar, Vivek R.
    VIRUSES-BASEL, 2020, 12 (02):
  • [47] Antibodies generated by immunization with the NS1 protein of West Nile virus confer partial protection against lethal Japanese encephalitis virus challenge
    Sun, EnCheng
    Zhao, Jing
    TaoYang
    Xu, QingYuan
    Qin, YongLi
    Wang, WenShi
    Wei, Peng
    Wu, DongLai
    VETERINARY MICROBIOLOGY, 2013, 166 (1-2) : 145 - 153
  • [48] Development and application of a monoclonal-antibody-based blocking ELISA for detection of Japanese encephalitis virus NS1 antibodies in swine
    Dengyuan Zhou
    Chao Pei
    Kelu Yang
    Jing Ye
    Shengfeng Wan
    Qiuyan Li
    Luping Zhang
    Huanchun Chen
    Shengbo Cao
    Yunfeng Song
    Archives of Virology, 2019, 164 : 1535 - 1542
  • [49] The Japanese encephalitis virus NS1 protein concentrates ER membranes in a cytoskeleton-independent manner to facilitate viral replication
    Xie, Shengda
    Lin, Xinxin
    Yang, Qing
    Shi, Miaolei
    Yang, Xingmiao
    Cao, Ziyu
    Cao, Ruibing
    JOURNAL OF VIROLOGY, 2025, 99 (03)
  • [50] COMPARISON OF PROTECTIVE IMMUNITY ELICITED BY RECOMBINANT VACCINIA VIRUSES THAT SYNTHESIZE-E OR NS1 OF JAPANESE ENCEPHALITIS-VIRUS
    KONISHI, E
    PINCUS, S
    FONSECA, BAL
    SHOPE, RE
    PAOLETTI, E
    MASON, PW
    VIROLOGY, 1991, 185 (01) : 401 - 410