目的构建减毒沙门氏菌介导的H9亚型禽流感病毒黏膜DNA疫苗,并探讨黏膜DNA疫苗与灭活油乳苗联合应用的免疫效力。方法以RT-PCR法扩增H9N2亚型禽流感病毒分离株(A/Chicken/China/N/2005)的血凝素(HA)基因,然后克隆入pmcDNA3.1+载体中,获得重组质粒pmcDNA3.1-HA。通过电穿孔法将重组质粒转入减毒鼠伤寒沙门氏菌SL7207,构建沙门氏菌介导的黏膜DNA疫苗SL7207(pmcDNA3.1-HA)。重组菌与灭活油乳苗联合免疫1日龄商品代伊莎褐蛋鸡,并设立重组菌SL7207(pmcDNA3.1-HA)单独免疫组、油苗免疫组、空载体免疫组及空白对照组。用HI或ELISA测定血清和小肠黏膜抗体效价,以H9N2亚型禽流感病毒攻击,计算免疫保护力。结果联合免疫组和重组菌SL7207(pmcD-NA3.1-HA)单独免疫组能激发机体产生黏膜免疫应答,且与其他试验组之间存在显著性差异(P〈0.05)。联合免疫组和重组菌SL7207(pmcDNA3.1-HA)单独免疫组的免疫保护力均与空载体组、空白对照组有显著差异(P〈0.05),且联合免疫组的免疫保护率最高,达100%。结论成功构建H9亚型禽流感病毒黏膜DNA疫苗,DNA疫苗与灭活油乳苗联合应用具有良好的免疫协同作用。
In order to determine the synergistic immune efficacy of the DNA vaccine with the killed oil-emulsified vaccine of HgN2 subtype avian influenza virus(AIV), the mucosal DNA vaccine named SL7207 (pmcDNA-HA) was construsted, and the immunogenicity of the prime-boost strategy with the DNA vaccine and killed oil-emulsified vaccine was evaluated in chicken model. The hemagglutinin (HA) gene from the HgN2 subtype AIV was amplified with the RT-PCR and sub-cloned into vector pmcDNA3.1 +. The recombinant plasmid was transformed into the attenuated Salmonella typhimurium SL7207, and the positive recombinant was designated as SL7207(pmcDNA3.1-HA). One-day-old commercial ISA brown chickens were immunized with SL7207(pmcDNA3.1-HA) plus killed oil-emulsified vaccine of AIV,SL7207(pmcDNA3.1-HA) ,killed oil-emulsified vaccine of AIV,SL7207 (pmcDNA3.1), and PBS. It was shown that the intestinal mucosal antibody titers in combined inoculation and SL7207(pmcDNA3.1-HA) groups were significantly higher than those of other groups (P〈0.05). The result of protective immunity showed both the group of combined inoculation and SL7207 (pmcDNA3.1-HA) providing significantly protection compared with the negative control groups(P〈0.05), and the group of combined inoculation obtaining 100% protection. In conclusion, the mucosal DNA vaccine of HgN2 subtype AIV was successfully constructed, and the mucosal DNA vaccine plus killed oil-emulsified vaccine has good synergistic effect of protection.