ArticleMolecular biology and evolution2006
Analysis of the overdispersed clock in the short-term evolution of hepatitis C virus: Using the E1/E2 gene sequences to infer infection dates in a single source outbreak.
Article in Molecular biology and evolution, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed, 14 citations in OpenAlex.
- Emergence of a Recombinant Bovine Enterovirus in China: Insights from Phylogenetic and Temporal Analysis.Animals : an open access journal from MDPI · 2025Article
- Examining the molecular clock hypothesis for the contemporary evolution of the rabies virus.PLoS pathogens · 2024Article
- Advanced molecular surveillance of hepatitis C virus.Viruses · 2015Review
- New insight into HCV E1/E2 region of genotype 4a.Virology journal · 2014Article
- Hepatitis C virus molecular evolution: transmission, disease progression and antiviral therapy.World journal of gastroenterology · 2014Review
- Viral phylogeny in court: the unusual case of the Valencian anesthetist.BMC biology · 2013Article
- Molecular evolution in court: analysis of a large hepatitis C virus outbreak from an evolving source.BMC biology · 2013Article
- Evolutionary analysis of the dynamics of viral infectious disease.Nature reviews. Genetics · 2009Review
- Complete genome of a European hepatitis C virus subtype 1g isolate: phylogenetic and genetic analyses.Virology journal · 2008Article
- Statistical measures of uncertainty for branches in phylogenetic trees inferred from molecular sequences by using model-based methods.Journal of applied genetics · 2008Review
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The assumption of a molecular clock for dating events from sequence information is often frustrated by the presence of heterogeneity among evolutionary rates due, among other factors, to positively selected sites. In this work, our goal is to explore methods to estimate infection dates from sequence analysis. One such method, based on site stripping for clock detection, was proposed to unravel the clocklike molecular evolution in sequences showing high variability of evolutionary rates and in the presence of positive selection. Other alternatives imply accommodating heterogeneity in evolutionary rates at various levels, without eliminating any information from the data. Here we present the analysis of a data set of hepatitis C virus (HCV) sequences from 24 patients infected by a single individual with known dates of infection. We first used a simple criterion of relative substitution rate for site removal prior to a regression analysis. Time was regressed on maximum likelihood pairwise evolutionary distances between the sequences sampled from the source individual and infected patients. We show that it is indeed the fastest evolving sites that disturb the molecular clock and that these sites correspond to positively selected codons. The high computational efficiency of the regression analysis allowed us to compare the site-stripping scheme with random removal of sites. We demonstrate that removing the fast-evolving sites significantly increases the accuracy of estimation of infection times based on a single substitution rate. However, the time-of-infection estimations improved substantially when a more sophisticated and computationally demanding Bayesian method was used. This method was used with the same data set but keeping all the sequence positions in the analysis. Consequently, despite the distortion introduced by positive selection on evolutionary rates, it is possible to obtain quite accurate estimates of infection dates, a result of especial relevance for molecular epidemiology studies.
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