Construction and immunogenicity of a recombinant fowlpox vaccine coexpressing S1 glycoprotein of infectious bronchitis virus and chicken IL-18

被引:44
作者
Chen, Hong-Ying [1 ]
Yang, Ming-Fan [1 ]
Cui, Bao-An [1 ]
Cui, Pei [2 ]
Sheng, Min [2 ]
Chen, Guo [2 ]
Wang, Shu-Juan [1 ]
Geng, Jing-Wei [1 ]
机构
[1] Henan Agr Univ, Coll Anim Sci & Vet Med, Zhengzhou 450002, Henan, Peoples R China
[2] Anim Husb Bur Henan Prov, Henan Ctr Anim Dis Control & Prevent, Zhengzhou 450008, Henan, Peoples R China
关键词
Infectious bronchitis virus; S1; gene; Chicken interleukin-18 gene; Recombinant fowlpox virus; IMMUNE-RESPONSES; T-CELLS; INTERLEUKIN-18; PROTECTION; INDUCTION; ANTIBODY; PROTEIN; STRAIN; TH1;
D O I
10.1016/j.vaccine.2010.09.106
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Infectious bronchitis virus (IBV) poses a major threat to the chicken industry worldwide. In this study, we developed a recombinant fowlpox virus (rFPV) vaccine expressing the IBV S1 gene and chicken interleukin-18 gene (IL-18), rFPV-S1/IL18. Recombinant plasmid pSY-S1/IL18 was constructed by cloning chicken IL-18 into fowlpox virus transfer plasmid containing S1 gene and transfected into the chicken embryo fibroblasts cell pre-infected with S-FPV-017 to generate rFPV-S1/IL18. Expression of the recombinant proteins was confirmed by RT-PCR and IFA. We also constructed the recombinant fowlpox virus rFPV-S1 without IL-18. One-day-old chickens were vaccinated by wing-web puncture with the two rFPVs, and the induced humoral and cellular responses were evaluated. There was a significant difference in ELISA antibody levels (P < 0.05) elicited by either rFPV-S1 or rFPV-S1/IL18. The ratios of CD4(+) to CD8(+) in chickens immunized with rFPV-S1/IL18 were significantly higher (P < 0.05) than in those immunized with rFPV-S1. All chickens immunized with rFPV-S1/IL18 were completely protected (20/20) after challenge with the virulent IBV HN99 strain 43 days after immunization, while only 15 out of 20 of the chickens immunized with the rFPV-S1 were protected. Our results show that the protective efficacy of the rFPV-S1 vaccine could be enhanced significantly by simultaneous expression of IL-18. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8112 / 8119
页数:8
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