It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
The koala retrovirus (KoRV) is implicated in several diseases affecting the koala (Phascolarctos cinereus). KoRV provirus can be present in the genome of koalas as an endogenous retrovirus (present in all cells via germline integration) or as exogenous retrovirus responsible for somatic integrations of proviral KoRV (present in a limited number of cells). This ongoing invasion of the koala germline by KoRV provides a powerful opportunity to assess the viral strategies used by KoRV in an individual. Analysis of a high-quality genome sequence of a single koala revealed 133 KoRV integration sites. Most integrations contain full-length, endogenous provirus; KoRV-A subtype. The second most frequent integrations contain an endogenous recombinant element (recKoRV) in which most of the KoRV protein-coding region has been replaced with an ancient, endogenous retroelement. A third set of integrations, with very low sequence coverage, may represent somatic cell integrations of KoRV-A, KoRV-B and two recently designated additional subgroups, KoRV-D and KoRV-E. KoRV-D and KoRV-E are missing several genes required for viral processing, suggesting they have been transmitted as defective viruses. Our results represent the first comprehensive analyses of KoRV integration and variation in a single animal and provide further insights into the process of retroviral-host species interactions.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details

1 Australian Museum Research Institute, Australian Museum, 1 William Street Sydney, NSW, Australia
2 Systems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, NSW, Australia
3 Department of Wildlife Diseases, Leibniz Institute for Zoo and Wildlife Research, Berlin, Germany; Department of Translational Genetics, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus
4 Department of Wildlife Diseases, Leibniz Institute for Zoo and Wildlife Research, Berlin, Germany; Department of Veterinary Medicine, Freie Universität Berlin, Berlin, Germany
5 School of Life and Environmental Sciences, University of Sydney, Sydney, Australia
6 Systems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, NSW, Australia; Ramaciotti Centre for Genomics, University of New South Wales, NSW, Australia
7 Faculty of Science, Health, Education & Engineering, University of the Sunshine Coast, Locked Bag 4, Maroochydore DC, Qld, Australia