Abstract

Viruses of the family Polyomaviridae infect a wide variety of avian and mammalian hosts with a broad spectrum of outcomes including asymptomatic infection, acute systemic disease, and tumor induction. In this study a novel polyomavirus, the African elephant polyomavirus 1 (AelPyV-1) found in a protruding hyperplastic fibrous lesion on the trunk of an African elephant (Loxodonta africana) was characterized. The AelPyV-1 genome is 5722 bp in size and is one of the largest polyomaviruses characterized to date. Analysis of the AelPyV-1 genome reveals five putative open-reading frames coding for the classic small and large T antigens in the early region, and the VP1, VP2 and VP3 capsid proteins in the late region. In the area preceding the VP2 start codon three putative open-reading frames, possibly coding for an agnoprotein, could be localized. A regulatory, non-coding region separates the 2 coding regions. Unique for polyomaviruses is the presence of a second 854 bp long non-coding region between the end of the early region and the end of the late region. Based on maximum likelihood phylogenetic analyses of the large T antigen of the AelPyV-1 and 61 other polyomavirus sequences, AelPyV-1 clusters within a heterogeneous group of polyomaviruses that have been isolated from bats, new world primates and rodents.

Highlights

  • Members of the family Polyomaviridae are small viruses characterized by a non-enveloped icosahedral capsid and a circular double-stranded DNA genome of approximately 5000 base pairs

  • WU and KI virus have been found in patients with respiratory tract infections [6,7], and Merkel cell polyomavirus was found in patients with Merkel cell carcinoma, a rare aggressive skin cancer [8]

  • In this article we describe the isolation and characterization of a novel polyomavirus found in a protruding hyperplastic fibrous lesion on the trunk of an African Elephant (Loxodonta africana), the African elephant polyomavirus 1 (AelPyV-1)

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Summary

Introduction

Members of the family Polyomaviridae are small viruses characterized by a non-enveloped icosahedral capsid and a circular double-stranded DNA genome of approximately 5000 base pairs (bp). Sequencing of the library created from the whole-genome amplified sample resulted in 359 successful reads, representing 145,230 bases. After the amplification of the extracted whole-genomic DNA, the resulting products were subjected to a restriction enzyme analysis.

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