Designing a Multiepitope Vaccine against the Foodborne Pathogenic Bacteria Listeria monocytogenes Using Subtractive Immunoinformatics Approaches

Tariq Aziz, M. Naveed, M. A. Shabbir, Khizra Jabeen, Ayaz Ali Khan, Ammarah Hasnain, Zhennai Yang, A. Zinedine, João Miguel Rocha, Thamer H Albekairi
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Abstract

Background : Listeria monocytogenes , a Gram-positive bacterium, is a prominent foodborne pathogen that causes listeriosis and poses substantial health hazards worldwide. The continuing risk of listeriosis outbreaks underlies the importance of designing an effective prevention strategy and developing a robust immune response by reverse vaccinology approaches. This study aimed to provide a critical approach for developing a potent multiepitope vaccine against this foodborne disease. Methods : A chimeric peptide construct containing 5 B-cell epitopes, 16 major histocompatibility complex I (MHC-I) epitopes, and 18 MHC-II epitopes were used to create a subunit vaccination against L. monocytogenes . The vaccine safety was evaluated by several online methods, and molecular docking was performed using ClusPro to determine the binding affinity. Immune simulation was performed using the C-ImmSimm server to demonstrate the immune response. Results : The results validated the antigenicity, non-allergenicity, and nontoxicity of the chimeric peptide construct, confirming its suitability as a subunit vaccine. Molecular docking showed a good score of 1276.5 and molecular dynamics simulations confirmed the construct’s efficacy, demonstrating its promise as a good candidate for listeriosis prophylaxis. The population coverage was as high as 91.04% with a good immune response, indicating good antigen presentation with dendritic cells and production of memory cells. Conclusions : The findings of this study highlight the potential of the designed chimeric peptide construct as an effective subunit vaccine against Listeria , paving the way for future advances in preventive methods and vaccine design.
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利用减法免疫信息学方法设计针对食源性致病菌李斯特菌的多位点疫苗
背景:单核细胞增生李斯特菌是一种革兰氏阳性细菌,是一种主要的食源性病原体,可引起李斯特菌病,对全球健康造成严重危害。李斯特菌病暴发的风险持续存在,因此必须设计有效的预防策略,并通过反向疫苗学方法培养强大的免疫反应。本研究旨在为开发针对这种食源性疾病的强效多位点疫苗提供一种关键方法。方法:使用包含 5 个 B 细胞表位、16 个主要组织相容性复合体 I(MHC-I)表位和 18 个 MHC-II 表位的嵌合肽构建物来创建针对单核细胞增生症的亚单位疫苗。采用多种在线方法评估了疫苗的安全性,并使用 ClusPro 进行了分子对接以确定结合亲和力。使用 C-ImmSimm 服务器进行了免疫模拟,以展示免疫反应。结果:结果验证了嵌合肽构建物的抗原性、非过敏性和无毒性,证实了其作为亚单位疫苗的适用性。分子对接显示其得分高达 1276.5,分子动力学模拟也证实了该构建物的有效性,这表明它有望成为李斯特菌病预防的理想候选药物。疫苗的群体覆盖率高达 91.04%,免疫反应良好,这表明树突状细胞能很好地呈现抗原并产生记忆细胞。结论 :本研究的结果凸显了所设计的嵌合肽构建物作为一种有效的李斯特菌亚单位疫苗的潜力,为未来预防方法和疫苗设计的进步铺平了道路。
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