Recombination of Feline calicivirus within an endemically infected cat colony
1 Department of Veterinary Clinical Sciences, University of Liverpool Veterinary Teaching Hospital, Leahurst, Chester High Road, Neston, South Wirral CH64 7TE, UK 2 Department of Veterinary Pathology, University of Liverpool Veterinary Teaching Hospital, Leahurst, Chester High Road, Neston, South Wi...
Gespeichert in:
Veröffentlicht in: | Journal of general virology 2006-04, Vol.87 (4), p.921-926 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | 1 Department of Veterinary Clinical Sciences, University of Liverpool Veterinary Teaching Hospital, Leahurst, Chester High Road, Neston, South Wirral CH64 7TE, UK
2 Department of Veterinary Pathology, University of Liverpool Veterinary Teaching Hospital, Leahurst, Chester High Road, Neston, South Wirral CH64 7TE, UK
Correspondence K. P. Coyne kpcoyne{at}liv.ac.uk
To understand the evolution of the family Caliciviridae , the persistence of Feline calicivirus (FCV) was studied within an endemically infected cat colony. Polymerase and capsid sequences were analysed for 34 FCV isolates obtained over a 4 year period. Initially, the colony was infected with one strain of virus, but a second distinct strain was later identified. Subsequently, the emergence of a recombinant virus was observed, containing elements of both of the strains circulating within the colony. The recombination event mapped close to the ORF1/ORF2 junction. This is consistent with recombination in other caliciviruses, suggesting a common mechanism within this family. This is the first report of recombination within the genus Vesivirus in the family Caliciviridae and the first time that a recombination event has been observed where the parental strains have also been identified.
The GenBank/EMBL/DDBJ accession numbers for the sequences of V024, V037, W104, S298 and W112 determined in this work are DQ182628 DQ182632 , respectively. |
---|---|
ISSN: | 0022-1317 1465-2099 |
DOI: | 10.1099/vir.0.81537-0 |