Review of psittacine beak and feather disease and its effect on Australian endangered species

BACKGROUND: Since it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of psittacine birds in Australia. Our aim was to evaluate and review the effect of PBFD and its position as a key threatening process to Austra...

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Published inAustralian veterinary journal Vol. 93; no. 12; pp. 466 - 470
Main Authors Raidal, SR, Sarker, S, Peters, A
Format Journal Article
LanguageEnglish
Published England Australian Veterinary Association 01.12.2015
Blackwell Publishing Ltd
Wiley Subscription Services, Inc
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ISSN0005-0423
1751-0813
DOI10.1111/avj.12388

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Abstract BACKGROUND: Since it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of psittacine birds in Australia. Our aim was to evaluate and review the effect of PBFD and its position as a key threatening process to Australian psittacine bird species. We review the origin/evolutionary pathways and potential threat of PBFD to endangered psittacine bird populations and captive‐breeding flocks. CONCLUSIONS: The most recent beak and feather disease virus (BFDV) phylogenetic analyses indicate that all endangered Australian psittacine bird species are susceptible to, and equally likely to be infected by, BFDV genotypes from a range of host psittacine species. Management of the disease in captive‐breeding programs has relied on testing and culling, which has proven costly. The risk of PBFD should be considered very carefully by management teams contemplating the establishment of captive‐breeding flocks for endangered species. Alternative disease prevention tools, including vaccination, which are increasingly being used in wildlife health, should be considered more seriously for managing and preventing PBFD in captive flocks of critically endangered species.
AbstractList BACKGROUNDSince it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of psittacine birds in Australia. Our aim was to evaluate and review the effect of PBFD and its position as a key threatening process to Australian psittacine bird species. We review the origin/evolutionary pathways and potential threat of PBFD to endangered psittacine bird populations and captive-breeding flocks.CONCLUSIONSThe most recent beak and feather disease virus (BFDV) phylogenetic analyses indicate that all endangered Australian psittacine bird species are susceptible to, and equally likely to be infected by, BFDV genotypes from a range of host psittacine species. Management of the disease in captive-breeding programs has relied on testing and culling, which has proven costly. The risk of PBFD should be considered very carefully by management teams contemplating the establishment of captive-breeding flocks for endangered species. Alternative disease prevention tools, including vaccination, which are increasingly being used in wildlife health, should be considered more seriously for managing and preventing PBFD in captive flocks of critically endangered species.
Since it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of psittacine birds in Australia. Our aim was to evaluate and review the effect of PBFD and its position as a key threatening process to Australian psittacine bird species. We review the origin/evolutionary pathways and potential threat of PBFD to endangered psittacine bird populations and captive-breeding flocks. The most recent beak and feather disease virus (BFDV) phylogenetic analyses indicate that all endangered Australian psittacine bird species are susceptible to, and equally likely to be infected by, BFDV genotypes from a range of host psittacine species. Management of the disease in captive-breeding programs has relied on testing and culling, which has proven costly. The risk of PBFD should be considered very carefully by management teams contemplating the establishment of captive-breeding flocks for endangered species. Alternative disease prevention tools, including vaccination, which are increasingly being used in wildlife health, should be considered more seriously for managing and preventing PBFD in captive flocks of critically endangered species.
Background Since it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of psittacine birds in Australia. Our aim was to evaluate and review the effect of PBFD and its position as a key threatening process to Australian psittacine bird species. We review the origin/evolutionary pathways and potential threat of PBFD to endangered psittacine bird populations and captive‐breeding flocks. Conclusions The most recent beak and feather disease virus (BFDV) phylogenetic analyses indicate that all endangered Australian psittacine bird species are susceptible to, and equally likely to be infected by, BFDV genotypes from a range of host psittacine species. Management of the disease in captive‐breeding programs has relied on testing and culling, which has proven costly. The risk of PBFD should be considered very carefully by management teams contemplating the establishment of captive‐breeding flocks for endangered species. Alternative disease prevention tools, including vaccination, which are increasingly being used in wildlife health, should be considered more seriously for managing and preventing PBFD in captive flocks of critically endangered species.
Background Since it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of psittacine birds in Australia. Our aim was to evaluate and review the effect of PBFD and its position as a key threatening process to Australian psittacine bird species. We review the origin/evolutionary pathways and potential threat of PBFD to endangered psittacine bird populations and captive-breeding flocks. Conclusions The most recent beak and feather disease virus (BFDV) phylogenetic analyses indicate that all endangered Australian psittacine bird species are susceptible to, and equally likely to be infected by, BFDV genotypes from a range of host psittacine species. Management of the disease in captive-breeding programs has relied on testing and culling, which has proven costly. The risk of PBFD should be considered very carefully by management teams contemplating the establishment of captive-breeding flocks for endangered species. Alternative disease prevention tools, including vaccination, which are increasingly being used in wildlife health, should be considered more seriously for managing and preventing PBFD in captive flocks of critically endangered species.
Author Sarker, S
Raidal, SR
Peters, A
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Brown PB. A captive breeding program for Orange-bellied parrots. Aust Aviculture 1988;42:165-175.
White NE, Phillips MJ, Gilbert MTP et al. The evolutionary history of cockatoos (Aves: Psittaciformes: Cacatuidae). Mol Phylogenet Evol 2011;59:615-622.
Raidal SR, McElnea CL, Cross GM. Seroprevalence of psittacine beak and feather disease in wild psittacine birds in New South Wales. Aust Vet J 1993;70:137-139.
Ortiz-Catedral L, Kurenbach B, Massaro M et al. A new isolate of beak and feather disease virus from endemic wild red-fronted parakeets (Cyanoramphus novaezelandiae) in New Zealand. Arch Virol 2010;155:613-620.
Leichhardt L. Dr Leichhardts Lecture II. The Sydney Morning Herald 1846;21:2.
Sarker S, Forwood JK, Ghorashi SA et al. Beak and feather disease virus genotypes in Australian parrots reveal flexible host-switching. Aust Vet J 2015; 93:471-475.
Bassami MR, Berryman D, Wilcox GE et al. Psittacine beak and feather disease virus nucleotide sequence analysis and its relationship to porcine circovirus, plant circoviruses, and chicken anaemia virus. Virology 1998;249:453-459.
Massaro M, Ortiz-Catedral L, Julian L et al. Molecular characterisation of beak and feather disease virus (BFDV) in New Zealand and its implications for managing an infectious disease. Arch Virol 2012;157:1651-1663.
Patterson EI, Swarbrick CM, Roman N et al. Differential expression of two isolates of beak and feather disease virus capsid protein in Escherichia coli. J Virol Methods 2013;189:118-124.
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Varsani A, de Villiers GK, Regnard GL et al. A unique isolate of beak and feather disease virus isolated from budgerigars (Melopsittacus undulatus) in South Africa. Arch Virol 2011;155:435-439.
Steadman DW. Extinction of birds in Eastern polynesia: a review of the record, and comparisons with other Pacific Island groups. J Archaeol Sci 1989;16:177-205.
Doak DF, Bakker VJ, Vickers W. Using population viability criteria to assess strategies to minimize disease threats for an endangered carnivore. Conserv Biol 2013;27:303-314.
Raidal SR, Cross GM. Control by vaccination of psittacine beak and feather disease in a mixed flock of Agapornis spp. Aust Vet Pract 1994;24:178-180.
Lloyd-Smith JO, Cross PC, Briggs CJ et al. Should we expect population thresholds for wildlife disease? Trends Ecol Evol 2005;20:511-519.
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Ashby E. Parakeets moulting. Emu 1907;6:193-194.
Bassami MR, Ypelaar I, Berryman D et al. Genetic diversity of beak and feather disease virus detected in psittacine species in Australia. Virology 2001;279:392-400.
Sarker S, Ghorashi SA, Forwood JK et al. Phylogeny of beak and feather disease virus in cockatoos demonstrates host generalism and multiple-variant infections within Psittaciformes. Virology 2014;460-461:72-82.
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1984; 61
1984; 20
2013; 1
2013; 27
2000; 44
1907; 6
1903; 3
2005; 20
1994; 24
2011; 59
2013; 8
1936; 7
2011; 155
2006; 20
2013; 11
1993; 70
2013; 94
2009; 90
2008; 25
2010; 155
1998; 249
1988; 42
2014; 9
1993; 135
2014; 50
1998; 98
2012; 66
2005; 34
2007; 25
1996; 6
1995; 9
2004; 41
2003; 81
2015; 93
2012
2012; 3205
2011; 31
2013; 189
2008
1997
2005; 86
1995
2006
2005
2007; 51
2014; 111
2007; 55
2014; 114
1996; 10
2012; 93
2014; 460–461
2003; 306
2012; 157
1846; 21
2005; 8
1992; 26
2013
2014; 450–451
2010; 92
1989; 16
2001; 279
2012; 9
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Snippet BACKGROUND: Since it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of...
Background Since it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of...
Since it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of psittacine...
Background Since it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of...
BACKGROUNDSince it was first described in the early 1980s, psittacine beak and feather disease (PBFD) has become recognised as the dominant viral pathogen of...
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SubjectTerms Animals
Australia
beak
Beak and feather disease virus
Bird Diseases - epidemiology
Bird Diseases - prevention & control
Bird Diseases - virology
Birds
Circoviridae Infections - epidemiology
Circoviridae Infections - prevention & control
Circoviridae Infections - veterinary
circovirus
Circovirus - genetics
disease prevention
Endangered & extinct species
Endangered Species
flocks
Genotype
host generalism
host range
key threatening process
pathogens
phylogeny
Psittaciformes
psittacine beak and feather disease
risk
teams
vaccination
viral quasispecies
wildlife
Title Review of psittacine beak and feather disease and its effect on Australian endangered species
URI https://api.istex.fr/ark:/67375/WNG-3W7HNW3B-3/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Favj.12388
https://www.ncbi.nlm.nih.gov/pubmed/26769072
https://www.proquest.com/docview/1757107878
https://www.proquest.com/docview/1760896656
https://www.proquest.com/docview/1810046139
Volume 93
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