Hepatitis C virus transmission bottlenecks analyzed by deep sequencing.

Abstract:

:Hepatitis C virus (HCV) replication in infected patients produces large and diverse viral populations, which give rise to drug-resistant and immune escape variants. Here, we analyzed HCV populations during transmission and diversification in longitudinal and cross-sectional samples using 454/Roche pyrosequencing, in total analyzing 174,185 sequence reads. To sample diversity, four locations in the HCV genome were analyzed, ranging from high diversity (the envelope hypervariable region 1 [HVR1]) to almost no diversity (the 5' untranslated region [UTR]). For three longitudinal samples for which early time points were available, we found that only 1 to 4 viral variants were present, suggesting that productive infection was initiated by a very small number of HCV particles. Sequence diversity accumulated subsequently, with the 5' UTR showing almost no diversification while the envelope HVR1 showed >100 variants in some subjects. Calculation of the transmission probability for only a single variant, taking into account the measured population structure within patients, confirmed initial infection by one or a few viral particles. These findings provide the most detailed sequence-based analysis of HCV transmission bottlenecks to date. The analytical methods described here are broadly applicable to studies of viral diversity using deep sequencing.

journal_name

J Virol

journal_title

Journal of virology

authors

Wang GP,Sherrill-Mix SA,Chang KM,Quince C,Bushman FD

doi

10.1128/JVI.02271-09

subject

Has Abstract

pub_date

2010-06-01 00:00:00

pages

6218-28

issue

12

eissn

0022-538X

issn

1098-5514

pii

JVI.02271-09

journal_volume

84

pub_type

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