Zhang Haoyun, Yuan Xinwei, He Yanfei, Chen Yingyu, Hu Changmin, Chen Jianguo, Zhang Lei, Chen Xi, Guo Aizhen
National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Hubei Hongshan Laboratory, Wuhan 430070, China.
Vaccines (Basel). 2024 Apr 25;12(5):457. doi: 10.3390/vaccines12050457.
Calf diarrhea caused by enterotoxigenic (ETEC) poses an enormous economic challenge in the cattle industry. Fimbriae and enterotoxin are crucial virulence factors and vaccine targets of ETEC. Since these proteins have complicated components with large molecular masses, the development of vaccines by directly expressing these potential targets is cumbersome Therefore, this study aimed to develop a multiepitope fusion antigen designated as MEFA by integrating major epitopes of FanC and Fim41a subunits and a toxoid epitope of STa into the F17G framework. The 3D modeling predicted that the MEFA protein displayed the epitopes from these four antigens on its surface, demonstrating the desired structural characteristics. Then, the MEFA protein was subsequently expressed and purified for mouse immunization. Following that, our homemade ELISA showed that the mouse antiserum had a consistent increase in polyclonal antibody levels with the highest titer of 1:2 to MEFA. Furthermore, the western blot assay demonstrated that this anti-MEFA serum could react with all four antigens. Further, this antiserum exhibited inhibition on ETEC adhesion to HCT-8 cells with inhibitory rates of 92.8%, 84.3%, and 87.9% against F17, F5, and F41 ETEC strains, respectively. Additionally, the stimulatory effect of STa toxin on HCT-8 cells was decreased by approximately 75.3% by anti-MEFA serum. This study demonstrates that the MEFA protein would be an antigen candidate for novel subunit vaccines for preventing ETEC-induced diarrhea in cattle.
由产肠毒素大肠杆菌(ETEC)引起的犊牛腹泻给养牛业带来了巨大的经济挑战。菌毛和肠毒素是ETEC的关键毒力因子和疫苗靶点。由于这些蛋白质的成分复杂且分子量较大,直接表达这些潜在靶点来开发疫苗很麻烦。因此,本研究旨在通过将FanC和Fim41a亚基的主要表位以及STa的类毒素表位整合到F17G框架中,开发一种名为MEFA的多表位融合抗原。三维建模预测MEFA蛋白在其表面展示了来自这四种抗原的表位,显示出所需的结构特征。然后,随后表达并纯化MEFA蛋白用于小鼠免疫。在此之后,我们自制的ELISA表明,小鼠抗血清的多克隆抗体水平持续升高,对MEFA的最高效价为1:2。此外,蛋白质印迹分析表明,这种抗MEFA血清可以与所有四种抗原发生反应。此外,这种抗血清对ETEC黏附HCT-8细胞具有抑制作用,对F17、F5和F41 ETEC菌株的抑制率分别为92.8%、84.3%和87.9%。此外,抗MEFA血清使STa毒素对HCT-8细胞的刺激作用降低了约75.3%。本研究表明,MEFA蛋白将是预防ETEC引起的犊牛腹泻的新型亚单位疫苗的抗原候选物。