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A Novel Multiepitope Fusion Antigen as a Vaccine Candidate for the Prevention of Enterotoxigenic E. coli-Induced Calf Diarrhea.
Zhang, Haoyun; Yuan, Xinwei; He, Yanfei; Chen, Yingyu; Hu, Changmin; Chen, Jianguo; Zhang, Lei; Chen, Xi; Guo, Aizhen.
Afiliación
  • Zhang H; National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
  • Yuan X; Hubei Hongshan Laboratory, Wuhan 430070, China.
  • He Y; National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
  • Chen Y; Hubei Hongshan Laboratory, Wuhan 430070, China.
  • Hu C; National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
  • Chen J; Hubei Hongshan Laboratory, Wuhan 430070, China.
  • Zhang L; National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
  • Chen X; Hubei Hongshan Laboratory, Wuhan 430070, China.
  • Guo A; National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Vaccines (Basel) ; 12(5)2024 Apr 25.
Article en En | MEDLINE | ID: mdl-38793708
ABSTRACT
Calf diarrhea caused by enterotoxigenic E. coli (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 1217 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Vaccines (Basel) Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Vaccines (Basel) Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza