Journal of Virology, March 2001, p. 3004-3009, Vol. 75, No. 6
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.6.3004-3009.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Hepatitis Branch, Division of Viral and Rickettsial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia,1 and Second Department of Medicine, Nagoya City University Medical School, Nagoya, Japan2
Received 11 September 2000/Accepted 16 December 2000
Four hepatitis C virus genome regions (the core, E1, HVR1, and
NS5b) were amplified and sequenced from yearly samples obtained from a
chronically infected chimpanzee over a 12-year span. Nucleotide substitutions were found to accumulate in the core, E1, and HVR1 regions during the course of chronic infection; substitutions within the NS5b region were not detected for the first 8 years and were
found to be minimal during the last 4 years. The rate of accumulation
of mutations in the core and E1 regions, based on a direct comparison
between the first 1979 sequence and the last 1990 sequence, was 1.120 × 10
3, while phylogenetic ancestral comparison using the
12 yearly sequences showed a rate of 0.816 × 10
3
bases per site per year. Temporal evaluation of the sequences revealed
that there appeared to be periods in which substitutions accumulated
and became fixed, followed by periods with relative stasis or random
substitutions that did not persist. Synonymous and nonsynonymous
substitutions within the core, E1, and HVR1 regions were also analyzed.
In the core and E1 regions, synonymous substitutions predominated and
gradually increased over time. However, within the HVR1 region,
nonsynonymous substitutions predominated but gradually decreased over time.
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