Development of multi-epitope subunit vaccine for protection against the norovirus' infections based on computational vaccinology

被引:25
作者
Ahmad, Irfan [1 ]
Ali, Syed Shujait [1 ]
Zafar, Bisma [2 ]
Hashmi, Huma Farooque [3 ]
Shah, Ismail [1 ]
Khan, Shahzeb [1 ]
Suleman, Muhammad [1 ]
Khan, Mazhar [4 ]
Ullah, Saif [1 ]
Ali, Shahid [1 ]
Khan, Jafar [1 ]
Ali, Mohammad [1 ]
Khan, Abbas [5 ]
Wei, Dong-Qing [5 ,6 ,7 ,8 ]
机构
[1] Univ Swat, Ctr Biotechnol & Microbiol, Swat, Pakistan
[2] Univ Okara, Dept Biotechnol, Punjab, Pakistan
[3] Shandong Univ, Sch Life Sci, Jinan, Shandong, Peoples R China
[4] Univ Sci & Technol China USTC, CAS Key Lab Innate Immun & Chron Dis, Hefei Natl Lab Phys Sci Microscale,Sch Life Sci, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, Hefei, Peoples R China
[5] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Dept Bioinformat & Biol Stat, Shanghai 200240, Peoples R China
[6] Shanghai Jiao Tong Univ, Shanghai Islamabad Belgrade Joint Innovat Ctr Ant, Joint Lab Int Cooperat Metab & Dev Sci, State Key Lab Microbial Metab,Minist Educ, Shanghai, Peoples R China
[7] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Shanghai, Peoples R China
[8] Peng Cheng Lab, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
Norovirus; epitopes; docking; MD simulation; in-silico cloning; ROUND-STRUCTURED VIRUSES; NORWALK-LIKE VIRUSES; FREE-ENERGY CALCULATIONS; MOLECULAR-DYNAMICS; GENOMIC DIVERSITY; PROTEIN-STRUCTURE; GASTROENTERITIS; EPIDEMIOLOGY; PREDICTION; OUTBREAKS;
D O I
10.1080/07391102.2020.1845799
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human Norovirus belongs to a family Calciviridae, and was identified in the outbreak of gastroenteritis in Norwalk, due to its seasonal prevalence known as "winter vomiting disease." Treatment of Norovirus infection is still mysterious because there is no effective antiviral drugs or vaccine developed to protect against the infection, to eradicate the infection an effective vaccine should be developed. In this study, capsid protein (A7YK10), small protein (A7YK11), and polyprotein (A7YK09) were utilized. These proteins were subjected to B and T cell epitopes prediction by using reliable immunoinformatics tools. The antigenic and non-allergenic epitopes were selected for the subunit vaccine, which can activate cellular and humoral immune responses. Linkers joined these epitopes together. The vaccine structure was modelled and validated by using Errat, ProSA, and rampage servers. The modelled vaccine was docked with TLR-7. The stability of the docked complex was evaluated by MD simulation. To apply the concept in a wet lab, the reverse translated vaccine sequence was cloned in pET28a (+). The vaccine developed in this study requires experimental validation to ensure its effectiveness against the disease. Communicated by Ramaswamy H. Sarma
引用
收藏
页码:3098 / 3109
页数:12
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