数字农科院2.0

A ferritin-based nanoparticle displaying a neutralizing epitope for foot-and-mouth disease virus (FMDV) confers partial protection in guinea pigs

文献类型: 外文期刊

作者: Bingzhou Lu;Yi Ru;Rongzeng Hao;Yang Yang;Huanan Liu;Yajun Li;Yue Zhang;Yuhan Mao;Rui Yang;Yangyang Pan;Sijiu Yu;Haixue Zheng;Yan Cui

作者机构:

关键词: Ferritin-based nanoparticles (FNPs);Foot-and-mouth disease virus (FMDV);Neutralizing antibody;Neutralizing epitope;Protection efficacy

期刊名称: BMC Veterinary Research

ISSN: 1746-6148

年卷期: 2024 年 20 卷 1 期

页码:

收录情况: SCIE(2024版)

摘要: Background: Foot-and-mouth disease (FMD) is a devastating disease affecting cloven-hoofed animals, that leads to significant economic losses in affected countries and regions. Currently, there is an evident inclination towards the utilization of nanoparticles as powerful platforms for innovative vaccine development. Therefore, this study developed a ferritin-based nanoparticle (FNP) vaccine that displays a neutralizing epitope of foot-and-mouth disease virus (FMDV) VP1 (aa 140–158) on the surface of FNP, and evaluated the immunogenicity and protective efficacy of these FNPs in mouse and guinea pig models to provide a strategy for developing potential FMD vaccines. Results: This study expressed the recombinant proteins Hpf, HPF-NE and HPF-T34E via an E. coli expression system. The results showed that the recombinant proteins Hpf, Hpf-NE and Hpf-T34E could be effectively assembled into nanoparticles. Subsequently, we evaluated the immunogenicity of the Hpf, Hpf-NE and Hpf-T34E proteins in mice, as well as the immunogenicity and protectiveness of the Hpf-T34E protein in guinea pigs. The results of the mouse experiment showed that the immune efficacy in the Hpf-T34E group was greater than the Hpf-NE group. The results from guinea pigs immunized with Hpf-T34E showed that the immune efficacy was largely consistent with the immunogenicity of the FMD inactivated vaccine (IV) and could confer partial protection against FMDV challenge in guinea pigs. Conclusions: The Hpf-T34E nanoparticles stand out as a superior choice for a subunit vaccine candidate against FMD, offering effective protection in FMDV-infected model animals. FNP-based vaccines exhibit excellent safety and immunogenicity, thus representing a promising strategy for the continued development of highly efficient and safe FMD vaccines.

分类号:

  • 相关文献

[1]Mapping of foot-and-mouth disease virus antigenic sites recognized by single-domain antibodies reveals different 146S particle specific sites and particle flexibility. Harmsen M.M.,Li H.,Sun S.,van der Poel W.H.M.,Dekker A.. 2023

[2]A novel dendrimeric peptide induces high level neutralizing antibodies against classical swine fever virus in rabbits. Li, Guo-Xin,Zhou, Yan-Jun,Yu, Hai,Li, Ling,Wang, Ya-Xin,Tong, Wu,Hou, Jun-Wei,Xu, Yan-Zhao,Zhu, Jian-Ping,Xu, Ao-Tian,Tong, Guang-Zhi.

[3]A recombinant porcine circovirus type 2 expressing the VP1 epitope of the type O foot-and-mouth disease virus is infectious and induce both PCV2 and VP1 epitope antibodies. Huang, Liping,Zhang, Feiyan,Tang, Qinghai,Wei, Yanwu,Wu, Hongli,Guo, Longjun,Fu, Yujie,Liu, Changming.

[4]Recombinant infectious bursal disease virus expressing Newcastle disease virus (NDV) neutralizing epitope confers partial protection against virulent NDV challenge in chickens. Li, Kai,Gao, Li,Gao, Honglei,Qi, Xiaole,Gao, Yulong,Qin, Liting,Wang, Yongqiang,Wang, Xiaomei.

[5]Identification of a conformational neutralizing epitope on the VP1 protein of type A foot-and-mouth disease virus. Liu, Wenming,Yang, Baolin,Wang, Mingxia,Wang, Haiwei,Yang, Decheng,Zhou, Guohui,Yu, Li,Ma, Wenge.

[6]Porcine epidemic diarrhea virus virus-like particles produced in insect cells induce specific immune responses in mice. Wang, Cuiling,Wang, Cuiling,Yan, Feihu,Zheng, Xuexing,Wang, Hualei,Jin, Hongli,Wang, Chong,Zhao, Yongkun,Feng, Na,Wang, Tiecheng,Gao, Yuwei,Yang, Songtao,Xia, Xianzhu,Zheng, Xuexing,Jin, Hongli,Wang, Chong,Zheng, Xuexing,Wang, Hualei,Zhao, Yongkun,Feng, Na,Wang, Tiecheng,Gao, Yuwei,Yang, Songtao,Xia, Xianzhu.

[7]Highly pathogenic porcine reproductive and respiratory syndrome virus GP5 B antigenic region is not a neutralizing antigenic region. Leng, Chao-Liang,An, Tong-Qing,Chen, Jia-Zeng,Gong, Da-Qing,Peng, Jin-Mei,Yang, Yong-Qian,Wu, Jiang,Guo, Juan-Juan,Li, Deng-Yun,Zhang, Yi,Meng, Zhen-Xiang,Wu, Yu-Quan,Tian, Zhi-Jun,Tong, Guang-Zhi,Tong, Guang-Zhi.

[8]Evidence of VP1 of duck hepatitis A type 1 virus as a target of neutralizing antibodies and involving receptor-binding activity. Li, Xiaojun,Zhao, Ran,Li, Chenxi,Zhang, Tingting,Meng, Fanyi,Liu, Ming,Zhang, Yun,Lin, Wei.

[9]A spike-specific whole-porcine antibody isolated from a porcine B cell that neutralizes both genogroup 1 and 2 PEDV strains. Fu, Fang,Li, Lin,Shan, Lingling,Yang, Beibei,Shi, Hongyan,Zhang, Jiaoer,Feng, Li,Liu, Pinghuang,Wang, Hongfeng.

[10]Newcastle disease virus-vectored West Nile fever vaccine is immunogenic in mammals and poultry. Wang, Jinliang,Yang, Jie,Ge, Jinying,Hua, Ronghong,Liu, Renqiang,Wang, Xijun,Shao, Yu,Sun, Encheng,Wu, Donglai,Wen, Zhiyuan,Bu, Zhigao,Li, Xiaofeng,Qin, Chengfeng. 2016

[11]A Novel Conserved Linear Neutralizing Epitope on the Receptor-Binding Domain of the SARS-CoV-2 Spike Protein. Rong Hong Hua,Shu Jian Zhang,Bei Niu,Jin Ying Ge,Ting Lan,Zhi Gao Bu. 2023

[12]Two cross-protective antigen sites on foot-and-mouth disease virus serotype o structurally revealed by broadly neutralizing antibodies from cattle. Kun Li,Yong He,Li Wang,Pinghua Li,Sheng Wang,Pu Sun,Huifang Bao,Yimei Cao,Xuerong Liu,Guoqiang Zhu,Yali Song,Xingwen Bai,Xueqing Ma,Yuanfang Fu,Hong Yuan,Jing Zhang,Jian Wang,Yingli Chen,Dong Li,Zhiyong Lou,Zaixin Liu,Zengjun Lu. 2021

[13]Development and Validation of a Competitive ELISA Based on Bovine Monoclonal Antibodies for the Detection of Neutralizing Antibodies against Foot-and-Mouth Disease Virus Serotype A. Yimei Cao,Kun Li,Xiangchuan Xing,Guoqiang Zhu,Yuanfang Fu,Huifang Bao,Xingwen Bai,Pu Sun,Pinghua Li,Jing Zhang,Xueqing Ma,Jian Wang,Zhixun Zhao,Dong Li,Zaixin Liu,Zengjun Lu. 2022

[14]A method for screening CDV microneutralization activity in microvolume samples. Deng X.,Su J.,Hu B.,Bai X.. 2024

[15]Safety and immunogenicity of a SARS-CoV-2 mRNA vaccine (SYS6006) in minks, cats, blue foxes, and raccoon dogs. Hong Huo,Jinming Wang,Chan Li,Shuang Xiao,Han Wang,Jinying Ge,Gongxun Zhong,Zhiyuan Wen,Chong Wang,Qiaoling Lang,Lili Chen,Zilong Wang,Jinliang Wang,Xijun Wang,Xijun He,Yuntao Guan,Lei Shuai,Zhigao Bu. 2024

[16]Structural basis of different neutralization capabilities of monoclonal antibodies against H7N9 virus. Zhao, Bingbing,Sun, Zhenzhao,Wang, Shida,Shi, Zhibin,Jiang, Yongping,Wang, Xiurong,Deng, Guohua,Jiao, Peirong,Chen, Hualan,Wang, Jingfei. 2024

[17]Isolation and characterization of GI-19/L1148-like infectious bronchitis virus in China. Huixin Li,Jiabei Han,Bing Wang,Zongxi Han,Shengwang Liu. 2025

[18]A neutralizing nanobody-based liquid-phase blocking ELISA to assess the protective potency of Senecavirus A vaccine. Mu, Suyu,Pan, Songjia,Dong, Hu,Wu, Jinen,Zhang, Yun,Yin, Shuanghui,Wang, Jianing,Wei, Tian,Wen, Xiaobo,Guo, Huichen,Sun, Shiqi. 2025

[19]Establishment of a pseudovirus neutralization assay for TGEV. Haojie Wang,Jianxing Chen,Lihong Xue,Yue Sun,Tongqing An,Yue Wang,Hongyan Chen,Changqing Yu,Changyou Xia,He Zhang. 2025

[20]Preparation and application of porcine broadly neutralizing monoclonal antibodies in an immunoassay for efficiently detecting neutralizing antibodies against foot-and-mouth disease virus serotype O. Cao, Yimei,Li, Fengjuan,Xing, Xiangchuan,Zhang, Huiyan,Zhao, Qiongqiong,Sun, Pu,Fu, Yuanfang,Li, Pinghua,Ma, Xueqing,Zhang, Jing,Zhao, Zhixun,Yuan, Hong,Wang, Jian,Wang, Tao,Bao, Huifang,Bai, Xingwen,Li, Dong,Zhang, Qiang,Li, Kun,Lu, Zengjun. 2025

作者其他论文 更多>>