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Rooting human parechovirus evolution in time

BACKGROUND: The Picornaviridae family contains a number of important pathogenic viruses, among which the recently reclassified human parechoviruses (HPeVs). These viruses are widespread and can be grouped in several types. Understanding the evolutionary history of HPeV could answer questions such as...

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Autores principales: Faria, Nuno R, de Vries, Michel, van Hemert, Formijn J, Benschop, Kimberley, van der Hoek, Lia
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723090/
https://www.ncbi.nlm.nih.gov/pubmed/19604368
http://dx.doi.org/10.1186/1471-2148-9-164
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author Faria, Nuno R
de Vries, Michel
van Hemert, Formijn J
Benschop, Kimberley
van der Hoek, Lia
author_facet Faria, Nuno R
de Vries, Michel
van Hemert, Formijn J
Benschop, Kimberley
van der Hoek, Lia
author_sort Faria, Nuno R
collection PubMed
description BACKGROUND: The Picornaviridae family contains a number of important pathogenic viruses, among which the recently reclassified human parechoviruses (HPeVs). These viruses are widespread and can be grouped in several types. Understanding the evolutionary history of HPeV could answer questions such as how long the circulating lineages last shared a common ancestor and how the evolution of this viral species is shaped by its population dynamics. Using both strict and relaxed clock Bayesian phylogenetics we investigated 1) the substitutions rates of the structural P1 and capsid VP1 regions and 2) evolutionary timescale of currently circulating HPeV lineages. RESULTS: Our estimates reveal that human parechoviruses exhibit high substitution rates for both structural P1 and capsid VP1 regions, respectively 2.21 × 10(-3 )(0.48 – 4.21 × 10(-3)) and 2.79 × 10(-3 )(2.05 – 3.66 × 10(-3)) substitutions per site per year. These are within the range estimated for other picornaviruses. By employing a constant population size coalescent prior, the date of the most recent common ancestor was estimated to be at around 1600 (1427–1733). In addition, by looking at the frequency of synonymous and non-synonymous substitutions within the VP1 gene we show that purifying selection constitutes the dominating evolutionary force leading to strong amino acid conservation. CONCLUSION: In conclusion, our estimates provide a timescale for the evolution of HPeVs and suggest that genetic diversity of current circulating HPeV types has arisen about 400 years ago.
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spelling pubmed-27230902009-08-08 Rooting human parechovirus evolution in time Faria, Nuno R de Vries, Michel van Hemert, Formijn J Benschop, Kimberley van der Hoek, Lia BMC Evol Biol Research Article BACKGROUND: The Picornaviridae family contains a number of important pathogenic viruses, among which the recently reclassified human parechoviruses (HPeVs). These viruses are widespread and can be grouped in several types. Understanding the evolutionary history of HPeV could answer questions such as how long the circulating lineages last shared a common ancestor and how the evolution of this viral species is shaped by its population dynamics. Using both strict and relaxed clock Bayesian phylogenetics we investigated 1) the substitutions rates of the structural P1 and capsid VP1 regions and 2) evolutionary timescale of currently circulating HPeV lineages. RESULTS: Our estimates reveal that human parechoviruses exhibit high substitution rates for both structural P1 and capsid VP1 regions, respectively 2.21 × 10(-3 )(0.48 – 4.21 × 10(-3)) and 2.79 × 10(-3 )(2.05 – 3.66 × 10(-3)) substitutions per site per year. These are within the range estimated for other picornaviruses. By employing a constant population size coalescent prior, the date of the most recent common ancestor was estimated to be at around 1600 (1427–1733). In addition, by looking at the frequency of synonymous and non-synonymous substitutions within the VP1 gene we show that purifying selection constitutes the dominating evolutionary force leading to strong amino acid conservation. CONCLUSION: In conclusion, our estimates provide a timescale for the evolution of HPeVs and suggest that genetic diversity of current circulating HPeV types has arisen about 400 years ago. BioMed Central 2009-07-15 /pmc/articles/PMC2723090/ /pubmed/19604368 http://dx.doi.org/10.1186/1471-2148-9-164 Text en Copyright © 2009 Faria et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Faria, Nuno R
de Vries, Michel
van Hemert, Formijn J
Benschop, Kimberley
van der Hoek, Lia
Rooting human parechovirus evolution in time
title Rooting human parechovirus evolution in time
title_full Rooting human parechovirus evolution in time
title_fullStr Rooting human parechovirus evolution in time
title_full_unstemmed Rooting human parechovirus evolution in time
title_short Rooting human parechovirus evolution in time
title_sort rooting human parechovirus evolution in time
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723090/
https://www.ncbi.nlm.nih.gov/pubmed/19604368
http://dx.doi.org/10.1186/1471-2148-9-164
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