B cell epitopes in the intrinsically disordered regions of neuraminidase and hemagglutinin proteins of H5N1 and H9N2 avian influenza viruses for peptide‐based vaccine development

摘要

Abstract Avian influenza viruses (AIV) are very active in several parts of the globe and are the cause of huge economic loss for the poultry industry and also human fatalities. Three dimensional modeling was carried out for neuraminidase (NA) and hemagglutinin (HA) proteins of AIV. The C‐score, estimated TM‐Score, and estimated root‐mean‐square deviation (RMSD) score for NA of H5N1 were ?1.18, 0.57?±?0.15, and 9.8?±?7.6, respectively. The C‐score, estimated TM‐Score, and estimated RMSD score for NA of H9N2 were ?1.43, 0.54?±?0.15, and 10.5?±?4.6, respectively. The C‐score, estimated TM‐Score, and estimated RMSD score for HA of H5N1 were ?0.03, 0.71?±?0.12, and 7.7?±?4.3, respectively. The C‐score, estimated TM‐Score, and estimated RMSD score for HA of H9N2 were ?0.57, 0.64?±?0.13, and 8.9?±?4.6, respectively. Intrinsically disordered regions were identified for the NA and HA proteins of H5N1 and H9N2 with the use of PONDR program. Linear B cell epitope was predicted using BepiPred 2 program for NA and HA of H5N1 and H9N2 avian influenza strains. Discontinuous epitopes were predicted by Discotope 2 program. The linear epitopes that were considered likely to be immunogenic and within the intrinsically disordered region for the NA of H5N1 was TKSTNSRSGFEMIWDPNGWTGTDSSFSVK, and for H9N2 it was VGDTPRNDDSSSSSNCRDPNNERGAP. In the case of HA of H5N1, it was QRLVPKIATRSKVNGQSG and ATGLRNSPQRERRRKK; for H9N2 it was INRTFKPLIGPRPLVNGLQG and SLKLAVGLRNVPARSSR. The discontinuous epitopes of NA of H5N1 and H9N2 were identified at various regions of the protein structure spanning from amino acid residue positions 90 to 449 and 107 to 469, respectively. Similarly, the discontinuous epitopes of HA of H5N1 and H9N2 were identified in the amino acid residue positions 27 to 517 and 136 to 521, respectively. This study has identified potential and highly immunogenic linear and conformational B‐cell epitopes towards developing a vaccine against AIV both for human and poultry use.