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.

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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