The rescue and selection of thermally stable type O vaccine candidate strains of foot-and-mouth disease virus
文献类型: 外文期刊
作者: Gao, Ya 1 ; Li, Pinghua 1 ; Ma, Xueqing 1 ; Bai, Xingwen 1 ; Sun, Pu 1 ; Du, Ping 1 ; Yuan, Hong 1 ; Cao, Yimei 1 ; Li, Kun; 1 ;
作者机构: 1.Chinese Acad Agr Sci, Lanzhou Vet Res Inst, State Key Lab Vet Etiol Biol, Lanzhou 730046, Gansu, Peoples R China
期刊名称:ARCHIVES OF VIROLOGY ( 影响因子:2.243; 五年影响因子:2.176 )
ISSN: 0304-8608
年卷期:
页码:
收录情况: SCI
摘要: Inactivated foot-and-mouth disease virus (FMDV) vaccines have been used widely to control foot-and-mouth disease (FMD). However, the virions (146S) of this virus are easily dissociated into pentamer subunits (12S), which limits the immune protective efficacy of inactivated vaccines when the temperature is higher than 30 degrees C. A cold-chain system can maintain the quality of the vaccines, but such systems are usually not reliable in limited-resource settings. Thus, it is imperative to improve the thermostability of vaccine strains to guarantee the quality of the vaccines. In this study, four recombinant FMDV strains containing single or multiple amino acid substitutions in the structural proteins were rescued using a previously constructed FMDV type O full-length infectious clone (pO/DY-VP1). We found that single or multiple amino acid substitutions in the structural proteins affected viral replication to different degrees. Furthermore, the heat and acid stability of the recombinant viruses was significantly increased when compared with the parental virus. Three thermally stable recombinant viruses (rHN/DY-VP1(Y2098F), rHN/DY-VP1(V2090A-S2093H), and rHN/DY-VP1(V2090A-S2093H-Y2098F)) were prepared as inactivated vaccines to immunize pigs. Blood samples were collected every week to prepare sera, and a virus neutralization test showed that the substitutions S2093H and Y2098F, separately or in combination, did not affect the immunogenicity of the virus, but the Y2098F mutation increased the thermostability significantly (p < 0.05). Therefore, the rHN/DY-VP1(Y2098F) mutant should be considered for use in future vaccines.
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