共 36 条
A highly pathogenic porcine reproductive and respiratory syndrome virus candidate vaccine based on Japanese encephalitis virus replicon system
被引:3
作者:
Hu, Pingsheng
[1
]
Chen, Xiaoming
[1
]
Huang, Lihong
[1
]
Liu, Shukai
[1
]
Zang, Fuyu
[1
]
Xing, Jinchao
[1
]
Zhang, Youyue
[1
]
Liang, Jiaqi
[1
]
Zhang, Guihong
[1
]
Liao, Ming
[1
,2
,3
]
Qi, Wenbao
[1
,2
,3
]
机构:
[1] South China Agr Univ, Coll Vet Med, Natl & Reg Joint Engn Lab Medicament Zoonoses Pre, Guangzhou, Guangdong, Peoples R China
[2] Minist Agr, Key Lab Zoonoses, Key Lab Anim Vaccine Dev, Guangzhou, Guangdong, Peoples R China
[3] Minist Agr, Key Lab Zoonoses Prevent & Control Guangdong Prov, Guangzhou, Guangdong, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
JEV replicon;
HP-PRRSV;
Vaccine;
LIVE VACCINE;
PRRS MLV;
IN-VITRO;
CHINA;
GENE;
CONSTRUCTION;
REPLICATION;
CHALLENGES;
PROTECTION;
EMERGENCE;
D O I:
10.7717/peerj.3514
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
In the swine industry, porcine reproductive and respiratory syndrome (PRRS) is a highly contagious disease which causes heavy economic losses worldwide. Effective prevention and disease control is an important issue. In this study, we described the construction of a Japanese encephalitis virus (JEV) DNA-based replicon with a cytomegalovirus (CMV) promoter based on the genome of Japanese encephalitis live vaccine virus SA14-14-2, which is capable of offering a potentially novel way to develop and produce vaccines against a major pathogen of global health. This JEV DNA-based replicon contains a large deletion in the structural genes (C-prM-E). A PRRSV GP5/M was inserted into the deletion position of JEV DNA based replicons to develop a chimeric replicon vaccine candidate for PRRSV The results immune that BALB/c mice models with the replicon vaccines pJEV-REP-G-2A-M-IRES and pJEV-REP-G-2A-M stimulated antibody responses and induced cellular response. Analysis of ELSA data showed that vaccination with the replicon vaccine expressing GP5/M induced a better antibodies response than traditional DNA vaccines. Therefore, the results suggested that this ectopic expression system based. on DNA-based replicons may represent a useful molecular platform for various biological applications, and the DNA based replicons expressing GP5/M can be further developed into a novel, safe vaccine candidate for PRRS.
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页数:19
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