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Clostridium perfringens epsilon toxin mutant Y30A-Y196A as a recombinant vaccine candidate against enterotoxemia

机译:产气荚膜梭菌ε毒素突变体Y30A-Y196A作为抗肠毒素血症的重组疫苗候选物

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摘要

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.
机译:Epsilon毒素(Etx)是由产气荚膜梭菌毒素B和D产生的形成β孔的毒素,并在肠毒素血症的发病中起关键作用,肠毒素血症是一种严重的,经常致命的反刍动物疾病,给全世界的农业生产造成重大经济损失。这项研究旨在确定Etx的定点突变体(Y30A-Y196A)被用作抗肠毒素血症的重组疫苗的潜力。用丙氨酸替代Y30和Y196产生了Etx的稳定变体,相对于野生型毒素(CT50增加430倍),MDCK.2细胞的细胞结合和细胞毒性活性显着降低,且腹膜内注射后Y30A-Y196A在小鼠中无活性以预期的LD50剂量(胰蛋白酶活化的野生型毒素)的1000倍施用胰蛋白酶活化的毒素。此外,在体外中和试验中,在兔中产生的针对Y30A-Y196A的多克隆抗体提供了针对野生型毒素的保护。这些数据表明,Y30A-Y196A突变体可以构成改良的抗肠毒血症重组疫苗的基础。

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