Long-read genome sequence assembly provides insight into ongoing retroviral invasion of the koala germline

• Published in: Scientific reports 2017-11, Vol.7 (1), p.15838-9, Article 15838
• Main Authors: Hobbs, Matthew, King, Andrew, Salinas, Ryan, Chen, Zhiliang, Tsangaras, Kyriakos, Greenwood, Alex D., Johnson, Rebecca N., Belov, Katherine, Wilkins, Marc R., Timms, Peter
• Format: Article
• Language: English
• Subjects: 45; 45/23; 631/181/735; 631/326/596/1787; Animals; Disease transmission; Evolution, Molecular; Gammaretrovirus; Genomes; Germ Cells; Humanities and Social Sciences; Integration; multidisciplinary; Nucleotide sequence; Phascolarctidae - genetics; Phascolarctidae - virology; Phascolarctos cinereus; Retroviridae - genetics; Retroviridae - pathogenicity; Retroviridae Infections - genetics; Retroviridae Infections - virology; Science; Science (multidisciplinary); Sequence Analysis, DNA; Whole Genome Sequencing
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-16171-1

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.