Predicting the Antigenic Relationship of Foot-and-Mouth Disease Virus for Vaccine Selection Through a Computational Model

被引:5
作者
Qiu, Jingxuan [1 ]
Qiu, Tianyi [2 ,3 ]
Dong, Qingli [1 ]
Xu, Dongpo [1 ]
Wang, Xiang [1 ]
Zhang, Qi [1 ]
Pan, Jing [1 ]
Liu, Qing [3 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Med Instrument & Food Engn, Shanghai 200093, Peoples R China
[2] Fudan Univ, Shanghai Med Sch, Shanghai Publ Hlth Clin Ctr, Shanghai 200032, Peoples R China
[3] Fudan Univ, Shanghai Med Sch, Inst Biomed Sci, Shanghai 200032, Peoples R China
基金
中国博士后科学基金; 国家重点研发计划; 美国国家科学基金会; 中国国家自然科学基金;
关键词
Vaccines; Proteins; Viruses (medical); Amino acids; Computational modeling; Biological system modeling; Foot-and-mouth disease virus; antigenicity; vaccine; computational model; bioinformatics; MIDDLE-EAST; SEROTYPE; BANK;
D O I
10.1109/TCBB.2019.2923396
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Foot-and-mouth disease virus (FMDV) is an antigenic-variable RNA virus that is responsible for the recurrence of foot-and-mouth disease in livestock and can be prevented and controlled using a vaccine with broad-spectrum protection. Current anti-genicity evaluation methods, which involve animal immunity experiments and serum preparation, are unable to fulfill the needs of high-throughput antigenicity measurements. This study designed an antigenicity scoring model to rapidly predict the antigenicity of FMDV. Antigenic-dominant sites were initially determined on the VP1 protein, a position-specific scoring matrix and physical chemical indexes were integrated to generate antigenicity descriptors. Independent tests showed a high accuracy of 0.848 and an AUC value of 0.889, indicating the good performance of the model in antigenicity measurement. When applying this model to historical data, annual antigenicity coverage of widely used vaccine strains was successfully evaluated, this was also supported by previous experiments. Furthermore, the utility of this model was extended to select potential broad-spectrum vaccines among 1,201 historical non-redundant strains to recommend potential univalent, bivalent and trivalent vaccine candidates. The results suggested that the computational model designed in this study could be used for the high-throughput antigenicity measurement of FMDV and could aid in vaccine development for preventing FMDV epidemics.
引用
收藏
页码:677 / 685
页数:9
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