Summary
Background
The
timing of the initial spread of hepatitis C virus genotype 1a in North
America is controversial. In particular, how and when hepatitis C virus
reached extraordinary prevalence in specific demographic groups remains
unclear. We quantified, using all available hepatitis C virus sequence
data and phylodynamic methods, the timing of the spread of hepatitis C
virus genotype 1a in North America.
Methods
We
screened 45 316 publicly available sequences of hepatitis C virus
genotype 1a for location and genotype, and then did phylogenetic
analyses of available North American sequences from five hepatitis C
virus genes (E1, E2, NS2, NS4B, NS5B), with an emphasis on
including as many sequences with early collection dates as possible. We
inferred the historical population dynamics of this epidemic for all
five gene regions using Bayesian skyline plots.
Findings
Most
of the spread of genotype 1a in North America occurred before 1965, and
the hepatitis C virus epidemic has undergone relatively little
expansion since then. The effective population size of the North
American epidemic stabilised around 1960. These results were robust
across all five gene regions analysed, although analyses of each gene
separately show substantial variation in estimates of the timing of the
early exponential growth, ranging roughly from 1940 for NS2, to 1965 for NS4B.
Interpretation
The
expansion of genotype 1a before 1965 suggests that nosocomial or
iatrogenic factors rather than past sporadic behavioural risk (ie,
experimentation with injection drug use, unsafe tattooing, high risk
sex, travel to high endemic areas) were key contributors to the
hepatitis C virus epidemic in North America. Our results might reduce
stigmatisation around screening and diagnosis, potentially increasing
rates of screening and treatment for hepatitis C virus.
Funding
The
Canadian Institutes of Health Research, Michael Smith Foundation for
Health Research, and BC Centre for Excellence in HIV/AIDS.
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