| 摘要: |
| 为获得腐败梭菌α毒素和D型产气荚膜梭菌ε毒素的共表达产物，并鉴定其致死活性和反应原性，评价其免疫保护效力，利用PCR扩增腐败梭菌α毒素和产气荚膜梭菌ε毒素基因Gcsa和Gcpe并克隆至pETDuet-1质粒，转化E.coli BL21(DE3)，自诱导培养基诱导这2段基因共表达；用SDS-PAGE和Western-blot以及小鼠毒性试验、抗毒素血清中和试验对表达产物进行鉴定；将诱导后的大肠杆菌灭活，制成铝佐剂疫苗1 mL/只皮下注射免疫家兔2次，测定免疫血清中和抗体效价，用1 MLD的腐败梭菌毒素和D型产气荚膜梭菌毒素分别攻击。结果显示，所构建的E.coli BL21(pETDuet-Gcsa-Gcpe)可以同时表达Gcsa和Gcpe，表达产物能够与腐败梭菌和D型产气荚膜抗毒素血清反应；且具有小鼠致死毒性，只有用2种抗毒素一同作用，才能将其毒性中和；制成灭活疫苗免疫家兔，免疫血清对腐败梭菌毒素的中和抗体效价为2 MLD/0.1 mL，对D型产气荚膜梭菌毒素的中和抗体效价≥50 MLD/0.1 mL；用2种毒素攻击，免疫组家兔全部保护，对照组全部死亡，达到《中华人民共和国兽药典》（2015版）效力检验标准。结果表明，所构建的表达载体可以实现α毒素和ε毒素的活性共表达，本研究为腐败梭菌和产气荚膜梭菌的多联基因工程灭活疫苗的研究提供了实验基础。 |
| 关键词: 腐败梭菌 产气荚膜 α毒素 ε毒素 共表达 免疫 疫苗 |
| DOI： |
| 投稿时间：2018-09-09修订日期：2019-01-22 |
| 基金项目:国家重点研发计划 牛羊重要细菌病新型疫苗及其工艺研究（2017YFD0500905） |
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| Evaluation Immune Efficacy of Co-expression of Clostridium septium α-toxin and Clostridium perfringens ε-toxin |
|
| (China Institute of Veterinary Drug Control) |
| Abstract: |
| In order to prepare co-expression of Clostridium septium α-toxin and Clostridium perfringens(D) ε-toxin, identify its toxicity and reactionogenicity, and evaluate its immune efficacy, in this study, Gcsa encoding Clostridium septium α-toxin and Gcpe encoding Clostridium perfringens ε-toxin were amplified and cloned into the co-expression plasmid vector pETDuet-1 respectively, and transformed into E.coli BL21(DE3). Gcsa and Gcpe were induced and co-expressed in medium for auto-induction, and the co-expression was identified with SDS-PAGE and Western-blot, toxicity and neutralization test. Besides, the co-expression was inactivated and prepared into vaccine. Rabbits were immunized with 1 mL of the vaccine twice. And the immunological effect was evaluated by 1 MLD C.septium or C.perfringens(D) toxin challenge and serum neutralization tests. The results showed that E.coli BL21(pETDuet-Gcsa-Gcpe) was constructed and used to co-expressed Gcsa and Gcpe successfully. And the co-expression was toxicant for mouse and could react with C.septium and C.perfringens (D) anti-toxoid sera peculiarly. Furthermore, only the two kinds of anti-toxin sera together could neutralize its toxicity. In addition, the co-expression vaccine generated 2 MLD and ≥50 MLD of neutralizing antibodies against respective toxin after the rabbits were immunized twice. And the rabbits were completely protected from the two kinds of toxin challenge，which reached to the principle of Chinese Veterinary Pharmacopoeia (2015). The results suggested that C.septium α-toxin and C.perfringens ε-toxin can co-express in E.coli, and the co-expression may be developed into a bivalent vaccine candidate. |
| Key words: Clostridium septicum Clostridium perfringens α-toxin ε-toxin co-expression immune vaccine |
