Development of a novel multi-epitope vaccine for brucellosis prevention

• Published in: Heliyon 2024-07, Vol.10 (14), p.e34721, Article e34721
• Main Authors: Shang, Kaiyu, Zhu, Yuejie, Tian, Tingting, Shi, Huidong, Yin, Zhengwei, He, Yueyue, Shi, Juan, Ding, Jianbing, Zhang, Fengbo
• Format: Article
• Language: English
• Subjects: Brucella; Epitope prediction; Molecular docking; Molecular modeling; Multi-epitope vaccine
• ISSN: 2405-8440; 2405-8440
• DOI: 10.1016/j.heliyon.2024.e34721

Brucellosis, a zoonotic disease caused by Brucella, presents a significant threat to both animal and human health. In animals, the disease can lead to infertility, miscarriage, and high fever, while in humans, symptoms may include recurrent fever, fatigue, sweating, hepatosplenomegaly, and joint and muscle pain following infection. Treatment often involves long-term antibiotic therapy, placing a substantial psychological and financial burden on patients. While vaccination is crucial for prevention, current animal vaccines have drawbacks such as residual virulence, and a safe and effective human vaccine is lacking. Hence, the development of a vaccine for brucellosis is imperative. In this study, we utilized bioinformatics methods to design a multi-epitope vaccine targeting Brucella. Targeting Heme transporter BhuA and polysaccharide export protein, we identified antigenic epitopes, including six cytotoxic T lymphocyte (CTL) dominant epitopes, six helper T lymphocyte (HTL) dominant epitopes, one conformation B cell dominant epitope, and three linear B cell dominant epitopes. By linking these epitopes with appropriate linkers and incorporating a Toll-like receptor (TLR) agonist (human beta-defensin-2) and an auxiliary peptide (Pan HLA-DR epitopes), we constructed the multi-epitope vaccine (MEV). The MEV demonstrated high antigenicity, non-toxicity, non-allergenicity, non-human homology, stability, and solubility. Molecular docking analysis and molecular dynamics simulations confirmed the interaction and stability of the MEV with receptors (MHCI, MHCII, TLR4). Codon optimization and in silico cloning validated the translation efficiency and successful expression of MEV in Escherichia coli. Immunological simulations further demonstrated the efficacy of MEV in inducing robust immune responses. In conclusion, our findings suggest that the engineered MEVs have the potential to stimulate both humoral and cellular immune responses, offering valuable insights for the future development of safe and efficient Brucella vaccines. [Display omitted] •Our selection of two proteins as candidates for a Brucella multi-epitope vaccine.•Two candidate proteins are associated with intracellular infection and virulence in Brucella.•Constructed multi-epitope vaccines are candidates for Brucella vaccines.