Substitution rate of the hepatitis B virus surface gene

Authors

  • H. L. Zaaijer,

    1. Academic Medical Center (AMC – CINIMA), Clinical Virology, University of Amsterdam, Amsterdam, The Netherlands
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  • S. Bouter,

    1. Academic Medical Center (AMC – CINIMA), Clinical Virology, University of Amsterdam, Amsterdam, The Netherlands
    2. Laboratory for Infectious Disease and Screening, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands
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  • H. J. Boot

    1. Laboratory for Infectious Disease and Screening, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands
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Dr. Hans L. Zaaijer, Academic Medical Center (AMC), Clinical Virology (L1-104), University of Amsterdam, P.O.Box 22660, 1100DD Amsterdam, The Netherlands.
E-mail: h.l.zaaijer@amc.uva.nl

Abstract

Summary.  Molecular epidemiology of hepatitis B virus (HBV) often relies on the comparison of HBV surface (S) gene sequences, although little is known about the substitution rate of the HBV S-gene. In this study, we compared HBV S-gene sequences in longitudinal sample pairs of 40 untreated, chronically HBV-infected patients, spanning 210 years of cumulative follow-up. The 40 patients included HBV e-antigen positive and negative persons; with HBV DNA levels ranging from 103 to 109 cps/mL and belonging to HBV genotypes A, B, C, D and E. In the 40 sample pairs, 70 nucleotide changes occurred in the HBV S-gene (0–8 per patient), resulting in an average substitution rate of 5.1 × 10−4 nucleotide changes/site/year (range: 0–1.3 × 10−2). Surprisingly, the number of substitutions was strongly associated with the inverse level of viremia; and only weakly with the duration of follow-up: in 11 highly viremic patients (HBV DNA ≥108 cps/mL), only four substitutions occurred despite a cumulative observation period of 56 years (substitution rate: 1.1 × 10−4), while in the 10 patients with viremia below 104 cps/mL, 29 substitutions occurred during 30 years of follow-up (substitution rate: 14.6 × 10−4). We conclude that in chronic hepatitis B virus infection the rate of nucleotide substitution in the HBV S-gene is inversely related to the level of viremia and thus varies widely from person to person; hampering the phylogenetic analysis of possible chains of HBV infection.

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