A non-toxic recombinant Clostridium septicum α toxin induces protective immunity in mice and rabbits

• Published in: Toxicon (Oxford) 2023-09, Vol.233, p.107234-107234, Article 107234
• Main Authors: Du, Jige, Meki, Irene, Li, Qianlin, Liu, Ying, Zhu, Zhen, Pan, Chenfan, Xia, Yingju, Fu, Lizhi, Yang, Liu, Zhang, Suhui, Yin, Chunsheng, Luo, Yufeng, Wang, Tuanjie, Liu, Bo, Chen, Xiaoyun
• Format: Article
• Language: English
• Subjects: Antigenicity; Braxy; Clostridium septicum α toxin; Non-toxic; Recombinant expression
• ISSN: 0041-0101; 1879-3150
• DOI: 10.1016/j.toxicon.2023.107234

Clostridium septicum alpha toxin (CSA) plays significant roles in ruminant's braxy. Genetically engineered CSA has been shown to function as a potential vaccine candidate in the prevention of the disease caused by Clostridium septicum. In the present study, we synthesized a non-toxic recombinant, rCSAm4/TMD by introducing four amino acid substitutions (C86L/N296A/H301A/W342A) and 11-amino-acid deletion (residues 212 to 222). Compared to recombinant CSA, rCSAm4/TMD showed no cytotoxicity to MDCK cells and was not fatal to mice. Moreover, rCSAm4/TMD could protect immunized mice against 5 × mouse LD100 (100% lethal dose) of crude CSA without obvious pathological change. Most importantly, rabbits immunized with rCSAm4/TMD produced high titers of neutralizing antibodies which protected the rabbits against crude CSA challenge. These data suggest that genetically detoxified rCSAm4/TMD is a potential subunit vaccine candidate against braxy. [Display omitted] •Four mutations and the 11-amino-acid deletion in rCSAm4/TMD didn't affect the three-dimensional structure of the toxin.•rCSAm4/TMD could be expressed by E. coli BL21 (DE3) with a high expression level.•rCSAm4/TMD was non-toxic in vitro and in vivo.•rCSAm4/TMD induced protective immunity in mice and rabbits.