Surface Display of Antigen Protein VP8*of Porcine Rotavirus on Bacillus Subtilis Spores Using CotB as a Fusion Partner

被引:20
作者
Li, Wanqiang [1 ]
Feng, Jie [1 ]
Li, Jiajun [1 ]
Li, Jianzhen [1 ,2 ]
Wang, Zhenhua [2 ]
Khalique, Abdul [1 ]
Yang, Miao [3 ]
Ni, Xueqin [1 ]
Zeng, Dong [1 ]
Zhang, Dongmei [1 ]
Jing, Bo [1 ]
Luo, Qihui [1 ]
Pan, Kangcheng [1 ]
机构
[1] Sichuan Agr Univ, Coll Vet Med, Chengdu 611130, Sichuan, Peoples R China
[2] Chengdu Vocat Coll Agr Sci & Technol, Chengdu 611100, Sichuan, Peoples R China
[3] Technol Ctr Chengdu Custom, Chengdu 611100, Sichuan, Peoples R China
来源
MOLECULES | 2019年 / 24卷 / 20期
关键词
porcine rotavirus; VP8*protein; Bacillus subtilis; spore surface display; oral immunization; immune responses; GROUP-A ROTAVIRUSES; IMMUNE-RESPONSES; RECOMBINANT PROTEINS; PROTECTIVE IMMUNITY; GNOTOBIOTIC PIGS; INDUCED DIARRHEA; INFECTION; VACCINES; SERUM; MICE;
D O I
10.3390/molecules24203793
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Porcine rotavirus is a major cause of acute viral gastroenteritis in suckling piglets, and vaccination is considered to be an effective measure to control these infections. The development of a live mucosal vaccine using Bacillus subtilis spores as an antigen delivery vehicle is a convenient and attractive vaccination strategy against porcine rotavirus. In this study, a shuttle vector was constructed for the spore surface display of the spike protein VP8* from porcine rotavirus (the genotype was G5P[7]). A successful display of the CotB-VP8* fusion protein on the spore surface was confirmed by Western blot and immunofluorescence microscopy analysis. The capacity for immune response generated after immunization with the recombinant strain was evaluated in a mouse model. The intestinal fecal IgA and serum IgG were detected by enzyme-linked-immunosorbent serologic assay (ELISA). Importantly, recombinant strain spores could elicit strong specific mucosal and humoral immune responses. These encouraging results suggest that recombinant B. subtilis BV could provide a strategy for a potential novel application approach to the development of a new and safe mucosal subunit vaccine against porcine rotavirus.
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页数:13
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