Abstract

The family Papillomaviridae contains more than 320 papillomavirus types, with most having been identified as infecting skin and mucosal epithelium in mammalian hosts. To date, only nine non-mammalian papillomaviruses have been described from birds (n = 5), a fish (n = 1), a snake (n = 1), and turtles (n = 2). The identification of papillomaviruses in sauropsids and a sparid fish suggests that early ancestors of papillomaviruses were already infecting the earliest Euteleostomi. The Euteleostomi clade includes more than 90 per cent of the living vertebrate species, and progeny virus could have been passed on to all members of this clade, inhabiting virtually every habitat on the planet. As part of this study, we isolated a novel papillomavirus from a 16-year-old female Adélie penguin (Pygoscelis adeliae) from Cape Crozier, Ross Island (Antarctica). The new papillomavirus shares ∼64 per cent genome-wide identity to a previously described Adélie penguin papillomavirus. Phylogenetic analyses show that the non-mammalian viruses (expect the python, Morelia spilota, associated papillomavirus) cluster near the base of the papillomavirus evolutionary tree. A papillomavirus isolated from an avian host (Northern fulmar; Fulmarus glacialis), like the two turtle papillomaviruses, lacks a putative E9 protein that is found in all other avian papillomaviruses. Furthermore, the Northern fulmar papillomavirus has an E7 more similar to the mammalian viruses than the other avian papillomaviruses. Typical E6 proteins of mammalian papillomaviruses have two Zinc finger motifs, whereas the sauropsid papillomaviruses only have one such motif. Furthermore, this motif is absent in the fish papillomavirus. Thus, it is highly likely that the most recent common ancestor of the mammalian and sauropsid papillomaviruses had a single motif E6. It appears that a motif duplication resulted in mammalian papillomaviruses having a double Zinc finger motif in E6. We estimated the divergence time between Northern fulmar-associated papillomavirus and the other Sauropsid papillomaviruses be to around 250 million years ago, during the Paleozoic-Mesozoic transition and our analysis dates the root of the papillomavirus tree between 400 and 600 million years ago. Our analysis shows evidence for niche adaptation and that these non-mammalian viruses have highly divergent E6 and E7 proteins, providing insights into the evolution of the early viral (onco-)proteins.

Highlights

  • The family of the Papillomaviridae contains more than 320 distinct viral species

  • One of the twenty-five cloacal swab samples of Adelie penguins from Cape Crozier on Ross Island (16-year-old female) was positive for a novel papillomavirus. This novel papillomavirus shares $64 per cent genome-wide sequence identity with Pygoscelis adeliae papillomavirus 1 (PaPV1), which was identified from a fecal sample retrieved at Cape Crozier (Varsani et al 2014)

  • We identified a novel papillomavirus (PaPV2) isolated from a 16-year-old female Adelie penguin

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Summary

Introduction

The family of the Papillomaviridae contains more than 320 distinct viral species. In recent years, there has been an exponential increase in the identification of non-human-associated papillomaviruses. The papillomavirus phylogeny shows evidence of initial, ancestral niche sorting events followed by virus–host linked speciation (Shah et al 2010; Gottschling et al 2011; Van Doorslaer 2013). This suggests that the acquisition of new ecological niches on the host (gain/loss of fur, the evolution of sweat glands, etc.), not host speciation per se may be driving papillomaviruses evolution (Brooks and Ferrao 2005)

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