Suppr超能文献

利用免疫信息学方法针对越橘病毒结构蛋白进行多表位疫苗设计。

Targeting Yezo Virus Structural Proteins for Multi-Epitope Vaccine Design Using Immunoinformatics Approach.

机构信息

Department of Zoology, Abdul Wali Khan University, Mardan 23200, Khyber Pakhtunkhwa, Pakistan.

Department of Dermatology, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi 600, Taiwan.

出版信息

Viruses. 2024 Sep 3;16(9):1408. doi: 10.3390/v16091408.

Abstract

A novel tick-borne orthonairovirus called the Yezo virus (YEZV), primarily transmitted by the tick, has been recently discovered and poses significant threats to human health. The YEZV is considered endemic in Japan and China. Clinical symptoms associated with this virus include thrombocytopenia, fatigue, headache, leukopenia, fever, depression, and neurological complications ranging from mild febrile illness to severe outcomes like meningitis and encephalitis. At present, there is no treatment or vaccine readily accessible for this pathogenic virus. Therefore, this research employed an immunoinformatics approach to pinpoint potential vaccine targets within the YEZV through an extensive examination of its structural proteins. Three structural proteins were chosen using specific criteria to pinpoint T-cell and B-cell epitopes, which were subsequently validated through interferon-gamma induction. Six overlapping epitopes for cytotoxic T-lymphocytes (CTL), helper T-lymphocytes (HTL), and linear B-lymphocytes (LBL) were selected to construct a multi-epitope vaccine, achieving a 92.29% coverage of the global population. These epitopes were then fused with the 50S ribosomal protein L7/L12 adjuvant to improve protection against international strains. The three-dimensional structure of the designed vaccine construct underwent an extensive evaluation through structural analysis. Following molecular docking studies, the YEZV vaccine construct emerged as a candidate for further investigation, showing the lowest binding energy (-78.7 kcal/mol) along with favorable physiochemical and immunological properties. Immune simulation and molecular dynamics studies demonstrated its stability and potential to induce a strong immune response within the host cells. This comprehensive analysis indicates that the designed vaccine construct could offer protection against the YEZV. It is crucial to conduct additional in vitro and in vivo experiments to verify its safety and effectiveness.

摘要

一种新型蜱传正呼肠孤病毒,即越诺病毒(YEZV),主要通过蜱传播,最近被发现,对人类健康构成重大威胁。YEZV 被认为在日本和中国流行。与该病毒相关的临床症状包括血小板减少、疲劳、头痛、白细胞减少、发热、抑郁以及从轻度发热疾病到脑膜炎和脑炎等严重后果的神经并发症。目前,这种致病病毒没有现成的治疗或疫苗。因此,本研究采用免疫信息学方法,通过对其结构蛋白进行广泛研究,确定 YEZV 中的潜在疫苗靶点。使用特定标准选择三种结构蛋白,以确定 T 细胞和 B 细胞表位,然后通过干扰素-γ诱导进行验证。选择六个重叠的细胞毒性 T 淋巴细胞(CTL)、辅助 T 淋巴细胞(HTL)和线性 B 淋巴细胞(LBL)表位,构建多表位疫苗,覆盖全球 92.29%的人口。然后将这些表位与 50S 核糖体蛋白 L7/L12 佐剂融合,以提高对国际株的保护作用。设计的疫苗构建体的三维结构通过结构分析进行了广泛评估。在进行分子对接研究后,YEZV 疫苗构建体被确定为进一步研究的候选物,其结合能最低(-78.7 kcal/mol),同时具有良好的理化和免疫学特性。免疫模拟和分子动力学研究表明其在宿主细胞内具有稳定性和诱导强烈免疫反应的潜力。这项综合分析表明,设计的疫苗构建体可能对 YEZV 提供保护。有必要进行更多的体外和体内实验来验证其安全性和有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9273/11437474/4ed7fe5d6795/viruses-16-01408-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验