Skip Navigation


MBE Advance Access originally published online on March 6, 2007
Molecular Biology and Evolution 2007 24(5):1242-1258; doi:10.1093/molbev/msm039
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
24/5/1242    most recent
msm039v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Gottschling, M.
Right arrow Articles by Bravo, I. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gottschling, M.
Right arrow Articles by Bravo, I. G.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2007. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Research Articles

Multiple Evolutionary Mechanisms Drive Papillomavirus Diversification

Marc Gottschling*, Alexandros Stamatakis{dagger}, Ingo Nindl*, Eggert Stockfleth*, Ángel Alonso{ddagger} and Ignacio G. Bravo{ddagger}

* Skin Cancer Center Charité, University Hospital of Berlin, Berlin, Germany
{dagger} École Polytechnique Fédérale de Lausanne, School of Computer & Communication Sciences, Laboratory for Computational Biology and Bioinformatics, Lausanne, Switzerland
{ddagger} Deutsches Krebsforschungszentrum/German Cancer Research Centre, Infection and Cancer, Heidelberg, Germany

E-mail: i.bravo{at}dkfz.de.

Accepted for publication February 28, 2007.

The circular, double-stranded 8-kb DNA genome of papillomaviruses (PVes) consists mainly of 4 large genes, E1, E2, L2, and L1. Approximately 150 papillomavirus genomes have been sequenced to date. We analyzed a representative sample of 53 PVes genomes using maximum likelihood, Bayesian inference, maximum parsimony, and distance-based methods both on nucleotide (nt) and on amino acid (aa) alignments. When the 4 genes were analyzed separately, aa-inferred phylogenies contradicted each other less than nt-inferred trees (judged by partition homogeneity tests). In particular, gene combinations including the L2 gene generated significant incongruence (P < 0.001). Combined analyses of the remaining genes E1–E2–L1 produced a well-supported phylogeny including supertaxon ß + {gamma} + {pi} + {xi}-PVes (infecting Artiodactyla, Carnivora, Primates, and Rodentia) and supertaxon {kappa} + {lambda} + µ + {nu} + {sigma}-PVes (infecting Carnivora, Lagomorpha, Primates, and Rodentia). Based on the tree topology, host-linked evolution appears plausible at shallow, rather than deeper, taxonomic levels. Diversification within PVes may also involve adaptive radiation establishing different niches (within a single-host species) and recombination events (within single-host cells). Heterogeneous groups of closely related PVes infecting, for example, humans and domestic animals such as hamster, dog, and cattle suggest multiple infections across species borders. Additional evolutionary phenomena such as strong codon usage preferences, and computational biases including reconstruction artifacts and insufficient taxon sampling, may contribute to the incomplete resolution of deep phylogenetic nodes. The molecular data globally supports a complex evolutionary scenario for PVes, which is driven by multiple mechanisms but not exclusively by coevolution with corresponding hosts.

Key Words: adaptive radiation • coevolution • high performance computing • host • interspecies transmission • recombination • virology • zoonosis


Aoife McLysaght, Associate Editor


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Gen. Virol.Home page
E. Schulz, M. Gottschling, G. Wibbelt, E. Stockfleth, and I. Nindl
Isolation and genomic characterization of the first Norway rat (Rattus norvegicus) papillomavirus and its phylogenetic position within Pipapillomavirus, primarily infecting rodents
J. Gen. Virol., November 1, 2009; 90(11): 2609 - 2614.
[Abstract] [Full Text] [PDF]


Home page
Microbiol. Mol. Biol. Rev.Home page
M. Lazarczyk, P. Cassonnet, C. Pons, Y. Jacob, and M. Favre
The EVER Proteins as a Natural Barrier against Papillomaviruses: a New Insight into the Pathogenesis of Human Papillomavirus Infections
Microbiol. Mol. Biol. Rev., June 1, 2009; 73(2): 348 - 370.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
E. Schulz, M. Gottschling, I. G. Bravo, U. Wittstatt, E. Stockfleth, and I. Nindl
Genomic characterization of the first insectivoran papillomavirus reveals an unusually long, second non-coding region and indicates a close relationship to Betapapillomavirus
J. Gen. Virol., March 1, 2009; 90(3): 626 - 633.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.