TY - JOUR
T1 - Comparative phylodynamics of rabbit hemorrhagic disease virus in Australia and New Zealand
AU - Eden, J
AU - Kovaliski, John
AU - Duckworth, Janine
AU - Swain, G
AU - Mahar, J
AU - Strive, Tanja
AU - Holmes, Edward
PY - 2015
Y1 - 2015
N2 - The introduction of rabbit hemorrhagic disease virus (RHDV) into Australia and New Zealand during the 1990s as a means of controlling feral rabbits is an important case study in viral emergence. Both epidemics are exceptional in that the founder viruses share an origin and the timing of their release is known, providing a unique opportunity to compare the evolution of a single virus in distinct naive populations. We examined the evolution and spread of RHDV in Australia and New Zealand through a genome-wide evolutionary analysis, including data from 28 newly sequenced RHDV field isolates. Following the release of the Australian inoculum strain into New Zealand, no subsequent mixing of the populations occurred, with viruses from both countries forming distinct groups. Strikingly, the rate of evolution in the capsid gene was higher in the Australian viruses than in those from New Zealand, most likely due to the presence of transient deleterious mutations in the former. However, estimates of both substitution rates and population dynamics were strongly sample dependent, such that small changes in sample composition had an important impact on evolutionary parameters. Phylogeographic analysis revealed a clear spatial structure in the Australian RHDV strains, with a major division between those viruses from western and eastern states. Importantly, RHDV sequences from the state where the virus was first released, South Australia, had the greatest diversity and were diffuse throughout both geographic lineages, such that this region was likely a source population for the subsequent spread of the virus across the country.
AB - The introduction of rabbit hemorrhagic disease virus (RHDV) into Australia and New Zealand during the 1990s as a means of controlling feral rabbits is an important case study in viral emergence. Both epidemics are exceptional in that the founder viruses share an origin and the timing of their release is known, providing a unique opportunity to compare the evolution of a single virus in distinct naive populations. We examined the evolution and spread of RHDV in Australia and New Zealand through a genome-wide evolutionary analysis, including data from 28 newly sequenced RHDV field isolates. Following the release of the Australian inoculum strain into New Zealand, no subsequent mixing of the populations occurred, with viruses from both countries forming distinct groups. Strikingly, the rate of evolution in the capsid gene was higher in the Australian viruses than in those from New Zealand, most likely due to the presence of transient deleterious mutations in the former. However, estimates of both substitution rates and population dynamics were strongly sample dependent, such that small changes in sample composition had an important impact on evolutionary parameters. Phylogeographic analysis revealed a clear spatial structure in the Australian RHDV strains, with a major division between those viruses from western and eastern states. Importantly, RHDV sequences from the state where the virus was first released, South Australia, had the greatest diversity and were diffuse throughout both geographic lineages, such that this region was likely a source population for the subsequent spread of the virus across the country.
KW - Animals
KW - Australia/epidemiology
KW - Caliciviridae Infections/epidemiology
KW - Evolution, Molecular
KW - Hemorrhagic Disease Virus, Rabbit/genetics
KW - Humans
KW - New Zealand/epidemiology
KW - Phylogeny
KW - Rabbits
UR - http://www.scopus.com/inward/record.url?scp=84940542392&partnerID=8YFLogxK
UR - http://www.mendeley.com/research/comparative-phylodynamics-rabbit-hemorrhagic-disease-virus
UR - http://www.mendeley.com/research/comparative-phylodynamics-rabbit-hemorrhagic-disease-virus-australia-new-zealand
U2 - 10.1128/JVI.01100-15
DO - 10.1128/JVI.01100-15
M3 - Article
C2 - 26157125
SN - 0022-538X
VL - 89
SP - 9548
EP - 9558
JO - Journal of Virology
JF - Journal of Virology
IS - 18
ER -