Key result
In vitro immune selection identified at least two new neutralizing epitopes involving residues VP3-116 and -195 around the threefold axis of the FMDV capsid.
Why the study?
Foot-and-mouth disease virus contains unidentified epitopes beyond the five neutralizing antigenic sites, as previous substitutions did not confer complete resistance to neutralization.
Identification of new neutralizing epitopes in FMDV extends knowledge of capsid surface features and may aid rational vaccine design.
May guide FMDV vaccine epitope design; extends capsid mapping but leaves in vivo protection open.
Foot-and-mouth disease virus (FMDV) displays various epitopes on the capsid outer surface. In addition to the five neutralizing antigenic sites, there is evidence of the existence of other, yet unidentified, epitopes that are believed to play a role in antibody-mediated protection. Previous attempts to identify these epitopes revealed two additional substitutions at positions VP2-74 and -191 (5M2/5 virus) to be of antigenic significance. However, complete resistance to neutralization was not obtained in the neutralization assay, indicating the existence of other, undisclosed epitopes. Results from this study provides evidence of at least two new neutralizing epitopes involving residues VP3-116 and -195 around the threefold axis that have significant impact on the antigenic nature of the virus. These findings extend our knowledge of the surface features of the FMDV capsid known to elicit neutralizing antibodies, and should help with rational vaccine design.
No takes yet. Share an insight, caveat, or question.
Mahapatra et al. (2019) studied Foot-and-mouth disease virus (FMDV). In vitro immune selection was evaluated on Identification of new neutralizing epitopes. In vitro immune selection identified at least two new neutralizing epitopes involving residues VP3-116 and -195 around the threefold axis of the FMDV capsid.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: