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BackgroundDespite recent breakthroughs in treatment of hepatitis C virus (HCV) infection, we have limited understanding of how virus diversity generated within individuals impacts the evolution and spread of HCV variants at the population scale. Addressing this gap is important for identifying the main sources of disease transmission and evaluating the risk of drug-resistance mutations emerging and disseminating in a population.MethodsWe have undertaken a high-resolution analysis of HCV within-host evolution from 4 individuals coinfected with human immunodeficiency virus 1 (HIV-1). We used long-read, deep-sequenced data of full-length HCV envelope glycoprotein, longitudinally sampled from acute to chronic HCV infection to investigate the underlying viral population and evolutionary dynamics.ResultsWe found statistical support for population structure maintaining the within-host HCV genetic diversity in 3 out of 4 individuals. We also report the first population genetic estimate of the within-host recombination rate for HCV (0.28 × 10-7 recombination/site/year), which is considerably lower than that estimated for HIV-1 and the overall nucleotide substitution rate estimated during HCV infection.ConclusionsOur findings indicate that population structure and strong genetic linkage shapes within-host HCV evolutionary dynamics. These results will guide the future investigation of potential HCV drug resistance adaptation during infection, and at the population scale.

More information Original publication

DOI

10.1093/infdis/jiy747

Type

Journal article

Publication Date

2019-05-01T00:00:00+00:00

Volume

219

Pages

1722 - 1729

Total pages

7

Addresses

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Keywords

Humans, Hepacivirus, HIV-1, Hepatitis C, Hepatitis C, Chronic, HIV Infections, Antiviral Agents, Genetics, Population, Evolution, Molecular, Drug Resistance, Viral, Virus Replication, Recombination, Genetic, Genotype, Genetic Variation, Molecular Epidemiology, High-Throughput Nucleotide Sequencing, Coinfection