Promising vaccine models against astrovirus MLB2 using integrated vaccinomics and immunoinformatics approaches

被引:1
|
作者
Ali, Syed Luqman [1 ]
Ali, Awais [1 ]
Ullah, Waseef [1 ]
Khan, Asifullah [1 ]
Khatrawi, Elham Mohammed [2 ]
Malik, Abdul [3 ]
Abduldayeva, Aigul [4 ]
Baiduissenova, Aliya [5 ]
Althagafi, Hind Jaber [6 ]
Fallatah, Deema [7 ]
机构
[1] Abdul Wali Khan Univ Mardan AWKUM, Dept Biochem, Mardan 23200, Pakistan
[2] Taibah Univ, Coll Med, Dept Med Microbiol & Immunol, Madinah 42353, Saudi Arabia
[3] King Saud Univ, Coll Pharm, Dept Pharmaceut, Riyadh 11451, Saudi Arabia
[4] Astana Med Univ, Prevent Med, Astana 010000, Kazakhstan
[5] Astana Med Univ, Dept Microbiol & Virol, Astana 010000, Kazakhstan
[6] Princess Nourah bint Abdulrahman Univ, Coll Sci, Dept Biol, Riyadh, Saudi Arabia
[7] Prince Sattam bin Abdulaziz Univ, Coll Appl Med Sci, Dept Med Lab Sci, Riyadh, Saudi Arabia
来源
关键词
PROTEIN-STRUCTURE PREDICTION; WEB SERVER;
D O I
10.1039/d3me00192j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Astrovirus MLB2 (AstV-MLB2) is an emerging gastrointestinal virus causing meningitis and disseminated infections. Currently, there are no vaccine-based therapies available for AstV-MLB2. This study aims to develop multi-epitope vaccine models using candidate proteins from AstV-MLB2. Highly immunogenic epitopes (IC50 < 200 mu M) exhibiting conservation, antigenicity, and non-allergenicity were called from these proteins. Additionally, the selection criteria for epitopes were based on their potential to trigger immune cells and stimulate IFN-gamma-mediated immune responses. The model vaccine constructs were designed from identified lead epitopes, along with immune-enhancer adjuvants and linker sequences. The proposed vaccine models were assessed for allergenicity, antigenicity, and structural integrity to ensure their safety and effectiveness. The binding potential of the vaccine models to HLA and TLR-4 immune cell receptors was evaluated to identify their capacity to stimulate immune responses. Among several raw constructs, MLB2-V1 and MLB2-V2 were identified as potential vaccine candidates due to their non-allergenic features, enhanced antigenic properties, and structural stability. Both these constructs were extensively evaluated and predicted to effectively bind to and interact with immune cell receptors, potentially triggering cellular and innate immune responses. Additionally, the prioritized constructs were deemed suitable for cloning and expression using recombinant DNA systems. The model vaccine constructs showed promise, warranting further investigation into their immune efficacy against MLB2-mediated infections through experimental assays and clinical trials.
引用
收藏
页码:1285 / 1299
页数:15
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