Evidence map›Paper›PMID 24006446›Full record

ArticleJournal of virology2013

Phylogenetic patterns of human coxsackievirus B5 arise from population dynamics between two genogroups and reveal evolutionary factors of molecular adaptation and transmission.

Cécile Henquell, Audrey Mirand, Jan Richter, Isabelle Schuffenecker, Blenda Böttiger, Sabine Diedrich, Elena Terletskaia-Ladwig, Christina Christodoulou, Hélène Peigue-Lafeuille, Jean-Luc Bailly

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Article in Journal of virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

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18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Cécile HenquellClermont-Université, Université d'Auvergne, EPIE, EA4843, Clermont-Ferrand, France.
Audrey Mirand
Jan Richter
Isabelle Schuffenecker
Blenda Böttiger
Sabine Diedrich
Elena Terletskaia-Ladwig
Christina Christodoulou
Hélène Peigue-Lafeuille
Jean-Luc Bailly

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to gain insights into the tempo and mode of the evolutionary processes that sustain genetic diversity in coxsackievirus B5 (CVB5) and into the interplay with virus transmission. We estimated phylodynamic patterns with a large sample of virus strains collected in Europe by Bayesian statistical methods, reconstructed the ancestral states of genealogical nodes, and tested for selection. The genealogies estimated with the structural one-dimensional gene encoding the VP1 protein and nonstructural 3CD locus allowed the precise description of lineages over time and cocirculating virus populations within the two CVB5 clades, genogroups A and B. Strong negative selection shaped the evolution of both loci, but compelling phylogenetic data suggested that immune selection pressure resulted in the emergence of the two genogroups with opposed evolutionary pathways. The genogroups also differed in the temporal occurrence of the amino acid changes. The virus strains of genogroup A were characterized by sequential acquisition of nonsynonymous changes in residues exposed at the virus 5-fold axis. The genogroup B viruses were marked by selection of three changes in a different domain (VP1 C terminus) during its early emergence. These external changes resulted in a selective sweep, which was followed by an evolutionary stasis that is still ongoing after 50 years. The inferred population history of CVB5 showed an alternation of the prevailing genogroup during meningitis epidemics across Europe and is interpreted to be a consequence of partial cross-immunity.

Indexed as

Adaptation, BiologicalEvolution, MolecularPhylogenyVirus ReplicationAmino Acid SequenceBayes TheoremCapsid ProteinsDNA, ViralEnterovirus B, HumanEnterovirus InfectionsGenetic VariationHumansMolecular Sequence DataPolymerase Chain ReactionPopulation DynamicsSelection, GeneticCapsid ProteinsDNA, Viral

Identifiers

PMID24006446
PMCPMC3807918

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.