Search National Agricultural Library (NAL) Digital Collections
Showing item 0 of
from your search.
Role of arginine-56 within the structural protein VP3 of foot-and-mouth disease virus (FMDV) O1 Campos in virus virulence
- FMDV O1 subtype undergoes antigenic variation under diverse growth conditions. Of particular interest is the amino acid variation observed at position 56 within the structural protein VP3. Selective pressures influence whether histidine (H) or arginine (R) is present at this position, ultimately influencing in vitro plaque morphology and in vivo pathogenesis in cattle. Using reverse genetics techniques, we have constructed FMDV type O1 Campos variants differing only at VP3 position 56, possessing either an H or R (O1Ca-VP3-56H and O1Ca-VP3-56R, respectively), and characterized their in vitro phenotype and virulence in the natural host. Both viruses showed similar growth kinetics in vitro. Conversely, they had distinct temperature-sensitivity (ts) and displayed significantly different pathogenic profiles in cattle and swine. O1Ca-VP3-56H was thermo stable and induced typical clinical signs of FMD, whereas O1Ca-VP3-56R presented a ts phenotype and was nonpathogenic unless VP3 position 56 reverted in vivo to either H or cysteine (C).
Borca, Manuel V. , Pacheco, Juan M. , Holinka, Lauren G. , Carrillo, Consuelo , Hartwig, Ethan , Garriga, Damià , Kramer, Edward , Rodriguez, Luis , Piccone, Maria E.
Foot-and-mouth disease virus , antigenic variation , arginine , cattle , cysteine , foot-and-mouth disease , genetic techniques and protocols , histidine , hosts , phenotype , structural proteins , structure-activity relationships , swine , viral proteins , virulence , viruses
- Includes references
- VIROLOGY 2012 Jan. 5, v. 422, no. 1
Journal Articles, USDA Authors, Peer-Reviewed
- Works produced by employees of the U.S. Government as part of their official duties are not copyrighted within the U.S. The content of this document is not copyrighted.