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Oral Administration of a Salmonella enterica-Based Vaccine Expressing Bacillus anthracis Protective Antigen Confers Protection against Aerosolized B. anthracis▿

机译:口服沙门氏菌表达的炭疽芽孢杆菌保护性抗原疫苗可赋予对气溶胶炭疽芽孢杆菌的保护作用▿

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摘要

Bacillus anthracis is the causative agent of anthrax, a disease that affects wildlife, livestock, and humans. Protection against anthrax is primarily afforded by immunity to the B. anthracis protective antigen (PA), particularly PA domains 4 and 1. To further the development of an orally delivered human vaccine for mass vaccination against anthrax, we produced Salmonella enterica serovar Typhimurium expressing full-length PA, PA domains 1 and 4, or PA domain 4 using codon-optimized PA DNA fused to the S. enterica serovar Typhi ClyA and under the control of the ompC promoter. Oral immunization of A/J mice with Salmonella expressing full-length PA protected five of six mice against a challenge with 105 CFU of aerosolized B. anthracis STI spores, whereas Salmonella expressing PA domains 1 and 4 provided only 25% protection (two of eight mice), and Salmonella expressing PA domain 4 or a Salmonella-only control afforded no measurable protection. However, a purified recombinant fusion protein of domains 1 and 4 provided 100% protection, and purified recombinant 4 provided protection in three of eight immunized mice. Thus, we demonstrate for the first time the efficacy of an oral S. enterica-based vaccine against aerosolized B. anthracis spores.
机译:炭疽杆菌是炭疽的病原体,炭疽杆菌是一种影响野生动植物,牲畜和人类的疾病。对炭疽的保护主要是通过对炭疽芽孢杆菌保护性抗原(PA)(特别是PA结构域4和1)的免疫力来提供的。为了进一步开发用于大规模接种炭疽疫苗的口服人类疫苗,我们生产了表达完整的小肠沙门氏菌血清型鼠伤寒沙门氏菌。使用融合到链球菌血清型鼠伤寒沙门氏菌ClyA上的密码子优化的PA DNA并在ompC启动子的控制下,对PA,PA域1和4或PA域4进行全长克隆。用表达全长PA的沙门氏菌对A / J小鼠进行口服免疫可保护六只小鼠中的五只免受105 CFU气雾化炭疽杆菌STI孢子的攻击,而表达PA结构域1和4的沙门氏菌仅提供25%的保护(八分之二)小鼠)和表达PA结构域4的沙门氏菌或仅沙门氏菌的对照无法提供可测量的保护。但是,结构域1和4的纯化的重组融合蛋白可提供100%的保护,而纯化的重组4可在八只免疫小鼠中的三只中提供保护。因此,我们首次证明了口服的基于肠炎链球菌的疫苗对雾化的炭疽芽孢杆菌孢子的功效。

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