College of Life and Environmental Sciences, University of Exeter, Stocker Road, Exeter EX4 4QD, United Kingdom.
College of Life and Environmental Sciences, University of Exeter, Stocker Road, Exeter EX4 4QD, United Kingdom.
Vaccine. 2014 May 13;32(23):2682-7. doi: 10.1016/j.vaccine.2014.03.079. Epub 2014 Apr 5.
Epsilon toxin (Etx) is a β-pore-forming toxin produced by Clostridium perfringens toxinotypes B and D and plays a key role in the pathogenesis of enterotoxemia, a severe, often fatal disease of ruminants that causes significant economic losses to the farming industry worldwide. This study aimed to determine the potential of a site-directed mutant of Etx (Y30A-Y196A) to be exploited as a recombinant vaccine against enterotoxemia. Replacement of Y30 and Y196 with alanine generated a stable variant of Etx with significantly reduced cell binding and cytotoxic activities in MDCK.2 cells relative to wild type toxin (>430-fold increase in CT50) and Y30A-Y196A was inactive in mice after intraperitoneal administration of trypsin activated toxin at 1000× the expected LD50 dose of trypsin activated wild type toxin. Moreover, polyclonal antibody raised in rabbits against Y30A-Y196A provided protection against wild type toxin in an in vitro neutralisation assay. These data suggest that Y30A-Y196A mutant could form the basis of an improved recombinant vaccine against enterotoxemia.
ε 毒素(Etx)是由产气荚膜梭菌 B 型和 D 型产生的一种β 孔形成毒素,在肠毒血症的发病机制中起关键作用,肠毒血症是一种严重的、常致命的反刍动物疾病,给全球农业带来重大经济损失。本研究旨在确定ε 毒素(Y30A-Y196A)的定点突变作为抗肠毒血症重组疫苗的潜力。用丙氨酸取代 Y30 和 Y196 生成了 Etx 的稳定变异体,与野生型毒素相比,其在 MDCK.2 细胞中的细胞结合和细胞毒性活性显著降低(CT50 增加超过 430 倍),并且在腹腔内给予 1000 倍预期 LD50 剂量的胰酶激活野生型毒素的胰酶激活毒素后,Y30A-Y196A 在小鼠中失活。此外,针对 Y30A-Y196A 的兔多克隆抗体在体外中和试验中提供了针对野生型毒素的保护。这些数据表明,Y30A-Y196A 突变体可能成为抗肠毒血症改良重组疫苗的基础。