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Expression and Purification of Virus-like Particles for Vaccination
Published on: June 2, 2016
Immunoinformatics and structural vaccinology driven prediction of multi-epitope vaccine against Mayaro virus and
Shahzeb Khan1, Abbas Khan2, Ashfaq Ur Rehman2
1Centre for Biotechnology and Microbiology, University of Swat, Swat, Khyber Pakhtunkhwa, Pakistan.
Abstract:
The Mayaro virus (MAYV) belongs to genus "Alphavirus" and family "Togaviridae". MAYV has distribution in the Amazonia, Central and Northeastern regions of Brazil. The abundance of mosquito vector Haemagogus janthinomys has major role in the outbreaks of arthralgia disease in Brazil. Vaccination or immunization is an alternative approach for the protection against this disease. To search the effective candidate for vaccine against Mayaro virus, various immunoinformatics tools were used to predict both the B and T cell epitopes from five structural polyproteins (capsid, E2, 6K, E3and E1). A multi subunit vaccine was designed and the final sequence was modeled for docking with TLR-3. Human b defensin based on previous studies was used as linker. The docked complexes of vaccine-TLR-3 were then subjected to dynamics stability and RMSD and RMSF results suggested that the complexes are stable. Further, to validate our final vaccine construct, in silico cloning was carried out using E. coli as host. The CAI value of 0.96 suggests that the vaccine construct properly expresses in the host. The current findings will be useful for the future experimental validations to ratify the immunogenicity and safety of the supposed structure of vaccine, and ultimately to treat the Mayaro virus, associated infections.
Insights
This study designed a novel multi-subunit vaccine candidate against Mayaro virus (MAYV) using immunoinformatics. In silico analysis confirmed the vaccine
Area of Science:
- Virology
- Immunology
- Vaccine Development
Background:
- Mayaro virus (MAYV), an Alphavirus, causes arthralgia outbreaks in Brazil, transmitted by the Haemagogus janthinomys mosquito.
- Current protection strategies against MAYV are limited, highlighting the need for effective vaccines.
Purpose of the Study:
- To design and in silico validate a multi-subunit vaccine candidate against Mayaro virus (MAYV).
- To identify potential B and T cell epitopes from MAYV structural polyproteins for vaccine development.
Main Methods:
- Immunoinformatics tools were employed to predict B and T cell epitopes from MAYV structural polyproteins (capsid, E2, 6K, E3, E1).
- A multi-subunit vaccine construct was designed, docked with TLR-3, and its stability assessed using molecular dynamics simulations (RMSD, RMSF).
- In silico cloning in E. coli was performed to evaluate vaccine construct expression potential (CAI value).
Main Results:
- The immunoinformatics approach identified potential epitopes for vaccine design.
- Molecular dynamics simulations indicated stable vaccine-TLR-3 complexes.
- The vaccine construct demonstrated high expression potential (CAI=0.96) in silico.
Conclusions:
- The designed multi-subunit vaccine construct shows promise as a stable and potentially immunogenic candidate against Mayaro virus.
- Further experimental validation is warranted to confirm the immunogenicity and safety of this vaccine construct for treating MAYV infections.
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