Novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach

被引:50
作者
Shantier, Shaza W. [1 ]
Mustafa, Mujahed, I [2 ]
Abdelmoneim, Abdelrahman H. [3 ]
Fadl, Hiba A. [4 ,5 ]
Elbager, Sahar G. [6 ]
Makhawi, Abdelrafie M. [2 ]
机构
[1] Univ Khartoum, Fac Pharm, Dept Pharmaceut Chem, Khartoum, Sudan
[2] Univ Bahri, Coll Ind & Appl Sci, Dept Biotechnol, Khartoum, Sudan
[3] Alneelain Univ, Fac Med, Khartoum, Sudan
[4] Al Neelain Univ, Fac Med Lab Sci, Dept Haematol, Khartoum, Sudan
[5] Sudanese Med Res Assoc, Dept Med Lab, Khartoum, Sudan
[6] Univ Med Sci & Technol, Fac Med Lab Sci, Khartoum, Sudan
关键词
PROTEIN SOLUBILITY; IMPORTED MONKEYPOX; WEST-AFRICAN; CONGO BASIN; PREDICTION; REEMERGENCE; TOOL; WEB;
D O I
10.1038/s41598-022-20397-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While mankind is still dealing with the COVID-19 pandemic, a case of monkeypox virus (MPXV) has been reported to the WHO on May 7, 2022. Monkeypox is a viral zoonotic disease that has been a public health threat, particularly in Africa. However, it has recently expanded to other parts of the world, so it may soon become a global issue. Thus, the current work was planned and then designed a multi-epitope vaccine against MPXV utilizing the cell surface-binding protein as a target in order to develop a novel and safe vaccine that can evoke the desirable immunological response. The proposed MHC-I, MHC-II, and B-cell epitopes were selected to design multi-epitope vaccine constructs linked with suitable linkers in combination with different adjuvants to enhance the immune responses for the vaccine constructs. The proposed vaccine was composed of 275 amino acids and was shown to be antigenic in Vaxijen server (0.5311) and non-allergenic in AllerTop server. The 3D structure of the designed vaccine was predicted, refined and validated by various in silico tools to assess the stability of the vaccine. Moreover, the solubility of the vaccine construct was found greater than the average solubility provided by protein-Sol server which indicating the solubility of the vaccine construct. Additionally, the most promising epitopes bound to MHC I and MHC II alleles were found having good binding affinities with low energies ranging between - 7.0 and - 8.6 kcal/mol. According to the immunological simulation research, the vaccine was found to elicit a particular immune reaction against the monkeypox virus. Finally, the molecular dynamic study shows that the designed vaccine is stable with minimum RMSF against MHC I allele. We conclude from our research that the cell surface-binding protein is one of the primary proteins involved in MPXV pathogenesis. As a result, our study will aid in the development of appropriate therapeutics and prompt the development of future vaccines against MPXV.
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页数:17
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