Key result
In silico analysis of RVB VP7 from infected pigs identified 9 completely conserved antigenic sites driven by negative selection, highlighting potential targets for subunit vaccine design.
Population
Rotavirus B (RVB) strains from clinically infected pigs in the United States and Canada
Design
Preclinical
Authors
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May inform swine RVB vaccine antigen selection; leaves open human translation pending in vivo validation.
Identified highly conserved, negatively selected antigenic residues on RVB VP7 that may serve as candidate regions for a subunit vaccine design.
Shepherd et al. (2017) studied Rotavirus B (RVB) infection. Amino acid sequence variability and predicted antigenicity analysis of RVB VP7 was evaluated on Identification of genotype-specific antigenic sites and nucleotide substitution rates (dN/dS). In silico analysis of RVB VP7 from infected pigs identified 9 completely conserved antigenic sites driven by negative selection, highlighting potential targets for subunit vaccine design.
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