Phylogenetic analysis of the full‐length SARS‐CoV sequences: Evidence for phylogenetic discordance in three genomic regions
Open Access
- 14 September 2004
- journal article
- research article
- Published by Wiley in Journal of Medical Virology
- Vol. 74 (3) , 369-372
- https://doi.org/10.1002/jmv.20187
Abstract
The origin of the severe acute respiratory syndrome-coronavirus (SARS-CoV) remains unclear. Evidence based on Bayesian scanning plots and phylogenetic analysis using maximum likelihood (ML) and Bayesian methods indicates that SARS-CoV, for the largest part of the genome (∼80%), is more closely related to Group II coronaviruses sequences, whereas in three regions in the ORF1ab gene it shows no apparent similarity to any of the previously characterized groups of coronaviruses. There is discordant phylogenetic clustering of SARS-CoV and coronaviruses sequences, throughout the genome, compatible with either ancient recombination events or altered evolutionary rates in different lineages, or a combination of both. J. Med. Virol. 74:369–372, 2004.Keywords
This publication has 17 references indexed in Scilit:
- Mosaic Evolution of the Severe Acute Respiratory Syndrome CoronavirusJournal of Virology, 2004
- SARS associated coronavirus has a recombinant polymerase and coronaviruses have a history of host-shiftingInfection, Genetics and Evolution, 2003
- Analysis of the Evolutionary Relationships of HIV-1 and SIVcpz Sequences Using Bayesian Inference: Implications for the Origin of HIV-1Molecular Biology and Evolution, 2003
- The Genome Sequence of the SARS-Associated CoronavirusScience, 2003
- Characterization of a Novel Coronavirus Associated with Severe Acute Respiratory SyndromeScience, 2003
- A Novel Coronavirus Associated with Severe Acute Respiratory SyndromeNew England Journal of Medicine, 2003
- Identification of Severe Acute Respiratory Syndrome in CanadaNew England Journal of Medicine, 2003
- A General Empirical Model of Protein Evolution Derived from Multiple Protein Families Using a Maximum-Likelihood ApproachMolecular Biology and Evolution, 2001
- Modeling Amino Acid ReplacementJournal of Computational Biology, 2000
- Evidence for variable rates of recombination in the MHV genomeVirology, 1992