A Novel Cre Recombinase-Mediated In Vivo Minicircle DNA (CRIM) Vaccine Provides Partial Protection against Newcastle Disease Virus

被引:14
作者
Jiang, Yanlong [1 ]
Gao, Xing [1 ]
Xu, Ke [1 ]
Wang, Jianzhong [1 ]
Huang, Haibin [1 ]
Shi, Chunwei [1 ]
Yang, Wentao [1 ]
Kang, Yuanhuan [1 ]
Curtiss, Roy, III [2 ]
Yang, Guilian [1 ]
Wang, Chunfeng [1 ]
机构
[1] Jilin Agr Univ, Key Lab Anim Prod Prod Qual & Secur, Jilin Prov Engn Res Ctr Anim Probiot, Minist Educ,Coll Anim Sci & Technol, Changchun, Jilin, Peoples R China
[2] Univ Florida, Coll Vet Med, Dept Infect Dis & Immunol, Gainesville, FL USA
基金
中国国家自然科学基金;
关键词
DNA vaccines; Salmonella-delivered vaccines; minicircle DNA; CO-DELIVERY; TRANSGENE EXPRESSION; PLASMID DNA; SALMONELLA; SYSTEM; INFECTION; CHICKENS; REPORTER; IMMUNITY; MICELLES;
D O I
10.1128/AEM.00407-19
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Minicircle DNA (mcDNA), which contains only the necessary components for eukaryotic expression and is thus smaller than traditional plasmids, has been designed for application in genetic manipulation. In this study, we constructed a novel plasmid containing both the Cre recombinase under the phosphoglycerate kinase (PGK) promoter and recombinant lox66 and lox71 sites located outside the cytomegalovirus (CMV) expression cassette. The strictly controlled synthesis of Cre recombinase in vivo maintained the complete form of the plasmid in vitro, whereas the in vivo production of Cre transformed the parental plasmid to mcDNA after transfection. The newly designed Cre recombinase-mediated in vivo mcDNA platform, named CRIM, significantly increased the nuclear entry of mcDNA, followed by increased production of mRNA and protein, using enhanced green fluorescent protein (EGFP) as a model. Similar results were also observed in chickens when the vaccine was delivered by the regulated-delayed-lysis Salmonella strain chi 11218, where significantly increased production of EGFP was observed in chicken livers. Then, we used the HN gene of genotype VII Newcastle disease virus as an antigen model to construct the traditional plasmid pYL43 and the novel mcDNA plasmid pYL47. After immunization, our CRIM vaccine provided significantly increased protection against challenge compared with that of the traditional plasmid, providing us with a novel mcDNA vaccine platform. IMPORTANCE Minicircle DNA (mcDNA) has been considered an attractive alternative to DNA vaccines; however, the relatively high cost and complicated process of purifying mcDNA dramatically restricts the application of mcDNA in the veterinary field. We designed a novel in vivo mcDNA platform in which the complete plasmid could spontaneously transform into mcDNA in vivo. In combination with the regulated-delayed-lysis Salmonella strain, the newly designed mcDNA vaccine provides us with an elegant platform for veterinary vaccine development.
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页码:1 / 17
页数:17
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