重组DNA
毒素
微生物学
产气荚膜梭菌
维罗细胞
中和抗体
病毒学
生物
灭活疫苗
抗体
病毒
免疫学
生物化学
细菌
基因
遗传学
作者
Jige Du,Bo Liu,Tuanjie Wang,Zhen Zhu,Chunsheng Yin,Yufeng Luo,Ying Liu,Xiaoyun Chen
出处
期刊:Vaccine
[Elsevier]
日期:2023-01-10
卷期号:41 (6): 1232-1238
被引量:2
标识
DOI:10.1016/j.vaccine.2022.11.021
摘要
Clostridium perfringens epsilon toxin (ETX) and Clostridium septicum alpha toxin (CSA) are lethal and necrotizing toxins, which play key roles in enterotoxemia and braxy of ruminants, respectively. In the present study, we synthesized a bivalent chimeric protein rETXm3CSAm4/TMD comprising ETXm3 (Y30A/H106P/Y196A) and CSAm4/TMD (C86L/N296A/H301A/W342A and a deletion of residues 212 to 222). Compared with recombinant ETX and recombinant CSA, rETXm3CSAm4/TMD showed no cytotoxicity in Madin-Darby Canine Kidney cells and was not fatal to mice. Moreover, rETXm3CSAm4/TMD could protect immunized mice against 10 × mouse LD100 of crude ETX or 3 × mouse LD100 of crude CSA without obvious histopathologic difference. Most importantly, both rabbits and sheep immunized with rETXm3CSAm4/TMD produced high titers of neutralizing antibody which protected the animals against the challenge with crude ETX or crude CSA. These data suggest that genetically detoxified rETXm3CSAm4/TMD is a potential subunit vaccine candidate against enterotoxemia and braxy.
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