期刊论文详细信息
PeerJ
A highly pathogenic porcine reproductive and respiratory syndrome virus candidate vaccine based on Japanese encephalitis virus replicon system
article
Pingsheng Hu1  Xiaoming Chen1  Lihong Huang1  Shukai Liu1  Fuyu Zang1  Jinchao Xing1  Youyue Zhang1  Jiaqi Liang1  Guihong Zhang1  Ming Liao1  Wenbao Qi1 
[1] National and Regional Joint Engineering Laboratory for Medicament of Zoonoses Prevention and Control, College of Veterinary Medicine, South China Agricultural University;Key Laboratory of Zoonoses, Key Laboratory of Animal Vaccine Development, Ministry of Agriculture;Key Laboratory of Zoonoses Prevention and Control of Guangdong Province, Ministry of Agriculture
关键词: JEV replicon;    HP-PRRSV;    Vaccine;   
DOI  :  10.7717/peerj.3514
学科分类:社会科学、人文和艺术(综合)
来源: Inra
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【 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 showed 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 a cellular immune 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 JEV DNA-based replicons may represent a useful molecular platform for various biological applications, and the JEV DNA-based replicons expressing GP5/M can be further developed into a novel, safe vaccine candidate for PRRS.

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