La Trobe

Germline viral "fossils" guide in silico Ereconstruction of a mid-Cenozoic era marsupial adeno-associated virus

Download (5.61 MB)
journal contribution
posted on 2023-03-29, 04:49 authored by RH Smith, CV Hallwirth, Michael WestermanMichael Westerman, NA Hetherington, Y-S Tseng, S Cecchini, T Virag, M-L Ziegler, IB Rogozin, EV Koonin, M Agbandje-McKenna, RM Kotin, IE Alexander
Germline endogenous viral elements (EVEs) genetically preserve viral nucleotide sequences useful to the study of viral evolution, gene mutation, and the phylogenetic relationships among host organisms. Here, we describe a lineage-specific, adeno-associated virus (AAV)-derived endogenous viral element (mAAV-EVE1) found within the germline of numerous closely related marsupial species. Molecular screening of a marsupial DNA panel indicated that mAAV-EVE1 occurs specifically within the marsupial suborder Macropodiformes (present-day kangaroos, wallabies, and related macropodoids), to the exclusion of other Diprotodontian lineages. Orthologous mAAV-EVE1 locus sequences from sixteen macropodoid species, representing a speciation history spanning an estimated 30 million years, facilitated compilation of an inferred ancestral sequence that recapitulates the genome of an ancient marsupial AAV that circulated among Australian metatherian fauna sometime during the late Eocene to early Oligocene. In silico gene reconstruction and molecular modelling indicate remarkable conservation of viral structure over a geologic timescale. Characterisation of AAV-EVE loci among disparate species affords insight into AAV evolution and, in the case of macropodoid species, may offer an additional genetic basis for assignment of phylogenetic relationships among the Macropodoidea. From an applied perspective, the identified AAV "fossils" provide novel capsid sequences for use in translational research and clinical applications.

Funding

IBR and EVK were supported by the Intramural Research Program of the National Library of Medicine (National Institutes of Health, US Department of Health and Human Services). CVH and NAH are supported by a Discovery Project grant (DP150101253) from the Australian Research Council. MA-M was supported by NIH R01 GM082946. RHS, SC, TV, and RMK were supported by the Intramural Research Program of the National Heart, Lung, and Blood Institute, of the National Institutes of Health.

History

Publication Date

2016-07-05

Journal

Scientific Reports

Volume

6

Article Number

28965

Pagination

17p.

Publisher

Nature Publishing Group

ISSN

2045-2322

Rights Statement

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Usage metrics

    Journal Articles

    Licence

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC