Abstract

BackgroundHuman papillomaviruses (HPVs) are genetically diverse, belonging to five distinct genera: Alpha, Beta, Gamma, Mu and Nu. All papillomaviruses have double stranded DNA genomes that are thought to evolve slowly because they co-opt high-fidelity host cellular DNA polymerases for their replication. Despite extensive efforts to catalogue all the HPV species that infect humans, it is likely that many still remain undiscovered. Here we use the sequences of ten novel Gammapapillomaviruses (Gamma-PVs) characterized in previous studies and related HPVs to analyse the evolutionary dynamics of these viruses at the whole genome and individual gene scales.ResultsWe found statistically significant incongruences between the phylogenetic trees of different genes which imply gene-to-gene variation in the evolutionary processes underlying the diversification of Gamma-PVs. We were, however, only able to detect convincing evidence of a single recombination event which, on its own, cannot explain the observed incongruences between gene phylogenies. The divergence times of the last common ancestor (LCA) of the Alpha, Beta, Mu, Nu and Gamma genera was predicted to have existed between 49.7–58.5 million years ago, before splitting into the five main lineages. The LCA of the Gamma-PVs at this time was predicted to have existed between 45.3 and 67.5 million years ago: approximately at the time when the simian and tarsier lineages of the primates diverged.ConclusionConsequently, we report here phylogenetic tree incongruence without strong evidence of recombination.

Highlights

  • Human papillomaviruses (HPVs) are genetically diverse, belonging to five distinct genera: Alpha, Beta, Gamma, Mu and Nu

  • We report here on the use of sequences of ten novel Gamma-PVs characterized in a previous studies [20, 21], and related HPVs to analyse the evolutionary dynamic of these viruses at the whole genome and individual gene levels

  • Phylogenetic incongruence and recombination An analysis of phylogenetic trees generated from different genes of the ten novel South African Gamma-PVs and their closest known relatives indicated differences, ranging from slight to major, between the branch lengths and branching orders of phylogenetic trees constructed from different genes

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Summary

Introduction

Human papillomaviruses (HPVs) are genetically diverse, belonging to five distinct genera: Alpha, Beta, Gamma, Mu and Nu. All papillomaviruses have double stranded DNA genomes that are thought to evolve slowly because they co-opt high-fidelity host cellular DNA polymerases for their replication. We use the sequences of ten novel Gammapapillomaviruses (Gamma-PVs) characterized in previous studies and related HPVs to analyse the evolutionary dynamics of these viruses at the whole genome and individual gene scales. HPVs are thought to evolve slowly because they replicate by co-opting high fidelity host cellular DNA polymerases that have an error rate of about 4.3 × 10− 5 substitutions per nucleotide site per year [5]. The cellular polymerases of different host species may differ in their degree of fidelity such that virus lineages infecting different hosts might display different substitution rates [9]

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