The invasion of a host germline by infectious retroviruses has been a common evolutionary event that shaped the genomes of all vertebrates, including humans. Endogenous retroviruses (ERVs) comprise ca. 8% of the human genome, where they play a role in placentation and in a number of diseases. Despite their ubiquity, until recently all identified ERVs had entered their host germline thousands or millions of years ago. Many ERVs have undergone mutations, deletions and recombination, and many retroviruses that gave rise to ERVs may be extinct. Thus, the evolutionary events that occurred as retroviruses invaded host genomes can be difficult to infer. Recently, an emerging koala retrovirus (KoRV), linked to a high incidence of leukemia and immune system suppression in Australian koalas, was discovered to be in the midst of transitioning from being an infectious exogenous virus to becoming an endogenous part of the koala genome. To date, KoRV is the only known exogenous retrovirus that is currently in the midst of invading a host germ line. Our objective is to use KoRV to understand the process by which an infectious retrovirus invades its host germline, a process that has shaped the human genome, as it actually happens. We will determine how the genetic diversity of KoRV is evolving across loci, individuals, and populations. Museum samples of koalas will be used to determine how the genetic diversity of KoRV has evolved over time. Differences between ancient and modern KoRV will be determined, and examined for their effects on functional properties of the virus.
The specific aims are: (1) Examine the sequence diversity and insertional polymorphisms of KoRV across the geographic range of the host population, from which the origins, spread and evolution of KoRV may be inferred. (2) Use archival samples of koalas to directly determine the evolution of genetic and functional diversity of KoRV across the time period during which KoRV emerged in a new host and invaded the germline. (3) Use complete proviral genomes and known host pedigrees to examine the evolutionary events that are shaping KoRV. The complete genomes of individual KoRVs will be sequenced and analyzed to determine the degree to which KoRVs invading their host germ line are being affected by selection, recombination, open reading frame disruptions, host anti-viral mechanisms, and host population structure.
Retrovirus-like elements that comprise 8% of the human genome play a role in health and disease, yet the process by which endogenous retroviruses (ERVs) invaded and shaped the genomes of humans is difficult to study since human ERVs are millions of years old. There is only one known infectious retrovirus currently in the midst of invading the germ line of its host, a koala retrovirus (KoRV) linked to leukemias and immune suppression. Understanding the evolutionary events affecting the genetic diversity of KoRV, and how KoRV changed as it invaded the host germ line provides an opportunity for research into how ERVs evolve and affect the genomes of all vertebrates, including humans.
|Tsangaras, Kyriakos; Wales, Nathan; Sicheritz-Pontén, Thomas et al. (2014) Hybridization capture using short PCR products enriches small genomes by capturing flanking sequences (CapFlank). PLoS One 9:e109101|
|Ruiz-Rodriguez, Christina T; Ishida, Yasuko; Greenwood, Alex D et al. (2014) Development of 14 microsatellite markers in the Queensland koala (Phascolarctos cinereus adustus) using next generation sequencing technology. Conserv Genet Resour 6:429-431|
|Tsangaras, Kyriakos; Siracusa, Matthew C; Nikolaidis, Nikolas et al. (2014) Hybridization capture reveals evolution and conservation across the entire Koala retrovirus genome. PLoS One 9:e95633|
|Mayer, Jens; Tsangaras, Kyriakos; Heeger, Felix et al. (2013) A novel endogenous betaretrovirus group characterized from polar bears (Ursus maritimus) and giant pandas (Ailuropoda melanoleuca). Virology 443:1-10|
|Avila-Arcos, Maria C; Ho, Simon Y W; Ishida, Yasuko et al. (2013) One hundred twenty years of koala retrovirus evolution determined from museum skins. Mol Biol Evol 30:299-304|