Abstract
Glycosylated protein 3 (GP3) of PRRSV is variable between different PRRSV strains, so it is helpful for subtype classifying by using distinct epitopes. In this study, two dominant linear GP3 epitopes that were recognized by highly dilute serum in an enzyme-linked immunosorbent assay (ELISA) were identified. Sequence alignments of 36 North American (NA) PRRSV isolates revealed that the epitope H87DELGFMV94 is well conserved, whereas the epitope T59RQAAAEILE68 differs in other low-virulence NA-type strains, which have at least one amino acid mutation in this region. A mutational analysis revealed that none of these mutations could be recognized by the purified antibodies directed against the corresponding epitope, indicating that the genetic variations altered the antigenicity of the antigenic region. Using ELISA, we also found that antibodies directed against the two epitopes were present in more than 45 of 50 HPPRRS-positive pig sera, suggesting that their antigenicity is excellent in vivo.
Original language | English |
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Pages (from-to) | 238-243 |
Number of pages | 6 |
Journal | Research in Veterinary Science |
Volume | 97 |
Issue number | 2 |
DOIs | |
State | Published - 2014 |
Externally published | Yes |
Keywords
- Antibody purification
- Epitope
- GP3
- HP-PRRSV