Evolution of structural proteins of feline immunodeficiency virus: molecular epidemiology and evidence of selection for change
1 MRC Retrovirus Research Laboratory, Department of Veterinary Pathology, University of Glasgow, Glasgow G61 1QH 2 Centre for HIV Research, Division of Biological Sciences, University of Edinburgh, ICAPB-Crew Building, West Mains Road, Edinburgh EH9 3JN, U.K. and 3 Department of Biomedicine, Univers...
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Veröffentlicht in: | Journal of general virology 1993-03, Vol.74 (3), p.425-436 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 1 MRC Retrovirus Research Laboratory, Department of Veterinary Pathology, University of Glasgow, Glasgow G61 1QH
2 Centre for HIV Research, Division of Biological Sciences, University of Edinburgh, ICAPB-Crew Building, West Mains Road, Edinburgh EH9 3JN, U.K.
and 3 Department of Biomedicine, University of Pisa, 56124 Pisa, Italy
The DNA sequences of structural genes of several U.K. and European isolates of feline immunodeficiency virus (FIV) were determined and compared with those of other worldwide isolates. Phylogenetic analyses of both gag and env sequences demonstrate that a Japanese isolate represents a distinct sequence subgroup, with corrected amino acid distances to the other isolates averaging 23% in env and 8% in gag . Analysis also reveals that an evolutionary radiation of FIV occurred with many isolates diverging at approximately the same time, and that although isolates from similar geographical sources often cluster together, there is evidence of more than one origin for FIV in the U.K., The Netherlands and Italy. Estimation of the numbers of silent and replacement nucleotide substitutions indicates the presence of constraints against amino acid changes in gag and conserved regions of env but suggests that positive selection for protein sequence changes operates in variable regions of env . The possible immunological forces underlying these changes are discussed.
Received 3 September 1992;
accepted 19 October 1992. |
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ISSN: | 0022-1317 1465-2099 |
DOI: | 10.1099/0022-1317-74-3-425 |