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Cell Surface-Exposed Tetanus Toxin Fragment C Produced by Recombinant Bacillus anthracis Protects against Tetanus Toxin

机译:重组炭疽芽孢杆菌产生的细胞表面暴露的破伤风毒素片段C可以预防破伤风毒素

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摘要

Bacillus anthracis, the causal agent of anthrax, synthesizes two surface layer (S-layer) proteins, EA1 and Sap, which account for 5 to 10% of total protein and are expressed in vivo. A recombinant B. anthracis strain was constructed by integrating into the chromosome a translational fusion harboring the DNA fragments encoding the cell wall-targeting domain of the S-layer protein EA1 and tetanus toxin fragment C (ToxC). This construct was expressed under the control of the promoter of the S-layer component gene. The hybrid protein was stably expressed on the cell surface of the bacterium. Mice were immunized with bacilli of the corresponding strain, and the hybrid protein elicited a humoral response to ToxC. This immune response was sufficient to protect mice against tetanus toxin challenge. Thus, the strategy developed in this study may make it possible to generate multivalent live veterinary vaccines, using the S-layer protein genes as a cell surface display system.
机译:炭疽杆菌是炭疽的病原体,它合成两个表面层(S层)蛋白EA1和Sap,它们占总蛋白的5%至10%,并在体内表达。通过将包含编码S层蛋白EA1的细胞壁靶向结构域和破伤风毒素片段C(ToxC)的DNA片段的染色体融合整合到染色体中,构建了重组炭疽杆菌菌株。该构建体在S层成分基因的启动子的控制下表达。杂合蛋白在细菌的细胞表面上稳定表达。用相应菌株的杆菌免疫小鼠,并且该杂合蛋白引起对ToxC的体液应答。这种免疫反应足以保护小鼠免受破伤风毒素的攻击。因此,本研究开发的策略可能使利用S层蛋白基因作为细胞表面展示系统来生产多价活兽疫苗成为可能。

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