Skip to main content

Advertisement

Log in

Review of documented beak and feather disease virus cases in wild Cape parrots in South Africa during the last 20 years

  • Review
  • Published:
Journal of Ornithology Aims and scope Submit manuscript

Abstract

Worldwide, there is concern about the increased prevalence of infectious diseases and their effects on biodiversity. Increasing changes in the environment, particularly changes in climatic conditions as a consequence of anthropogenic-induced climate change, are some of the factors driving this increased disease prevalence. Vertebrate taxa that appear to be most affected by these diseases are amphibians and birds, though this may be a consequence of research effort. Beak and feather disease virus (BFDV) affecting psittacine bird species is the disease of concern here. Data on BFDV incidence in wild, endangered Cape parrots (Poicephalus robustus) were collected opportunistically from 1992 to 2014. Data show that the disease is prevalent naturally in the wild during extreme climatic events, including drought. This stresses the birds, which may result in the expression of pathological symptoms. Juveniles in particular appear to succumb during times of drought. This has conservation implications with the impacts of extreme climatic events associated with anthropogenic-induced climate change.

Zusammenfassung

Übersicht dokumentierter Schnabel- und Federkrankheitsfälle bei wildlebenden Kappapageien in Südafrika in den letzten 20 Jahren Weltweit besteht Besorgnis über die wachsende Verbreitung von Infektionskrankheiten und die Folgen für die Artenvielfalt. Unter anderem treiben zunehmende Veränderungen der Umwelt, besonders der klimatischen Bedingungen infolge anthropogenen Klimawandels, die Verbreitung von Krankheiten voran. Die am meisten von diesen Krankheiten betroffenen Wirbeltiertaxa sind offenbar Amphibien und Vögel, wobei dies auch eine Folge unterschiedlichen Forschungsaufwands sein könnte. Hier betrachten wir den Schnabel- und Federkrankheitsvirus (BFDV), der Papageienvögel befällt. Daten von BFDV-Fällen bei wildlebenden gefährdeten Kappapageien (Poicephalus robustus) wurden von 1992 bis 2014 opportunistisch gesammelt. Diese Daten zeigen, dass die Krankheit im Freiland naturgemäß während extremer Klimaereignisse wie Dürren auftritt. Diese belasten die Vögel, was eine Ausprägung pathologischer Symptome zur Folge haben kann. Offenbar erliegen besonders Jungvögel während Dürreperioden der Krankheit. Dies hat Folgen für den Schutz der Art, im Zusammenhang mit den Auswirkungen extremer Klimaereignisse, die mit anthropogenem Klimawandel in Zusammenhang stehen.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Albertyn J, Tajbhai K, Bragg R (2004) Psittacine beak and feather disease virus in budgerigars and ring-neck parakeets in South Africa. Onderst J Vet Res 71:29–34

    CAS  Google Scholar 

  • Bai C, Liu X, Fisher MC, Garner TWJ, Li Y (2012) Global and endemic Asian lineages of the emerging pathogenic fungus Batrachochytrium dendrobatidis widely infect amphibians in China. Divers Distrib 18:307–318

    Article  Google Scholar 

  • Bassami MR, Ypelaar I, Berryman D, Wilcox GE, Radial SR (2001) Genetic diversity of beak and feather disease virus detected in Psittacine species in Australia. Virology 279:392–400

    Article  CAS  PubMed  Google Scholar 

  • Boadella M, Gortazar C, Acevedo P, Carta T, Martin-Hernando MP, de la Fuente J, Vicente J (2011) Six recomendations for improving monitoring of diseases shared with wildlife: examples regarding mycobacterial infections in Spain. Euro J Wildl Res 57:697–706

    Article  Google Scholar 

  • Bonne N, Shearer P, Sharp M, Clark P, Radial S (2009) Assessment of recombinant beak and feather disease virus capsid protein as a vaccine for psittacine beak and feather disease. J Gen Virol 90:640–647

    Article  CAS  PubMed  Google Scholar 

  • Burgess M, Boyes S (2010) Cape parrot population stalked by killer virus. Farmers Weekly, July, pp 30–31

  • Daszak P, Berger L, Cunningham AA, Hyatt AD, Green DE, Speare R (1999) Emerging infectious diseases and amphibian population declines. Emerg Infect Dis 5:735–748

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Daszak P, Cunningham AA, Hyatt AD (2000) Wildlife ecology—emerging infectious diseases of wildlife—threats to biodiversity and human health. Science 287:443–449

    Article  CAS  PubMed  Google Scholar 

  • Deem SL, Karesh WB, Weisman W (2001) Putting theory into practice: wildlife health in conservation. Conserv Biol 15:1224–1233

    Article  Google Scholar 

  • Deem SL, Cruz MB, Higashiguchi JM, Parker PG (2011) Diseases of poultry and endemic birds in Galapagos: implications for the reintroduction of native species. Anim Conserv 15:73–82

    Article  Google Scholar 

  • Dobson A, Foufopoulos J (2001) Emerging infectious pathogens of wildlife. Phil Trans Biol Sci 356:1001–1012

    Article  CAS  Google Scholar 

  • Downs CT (2000) Cape Parrot Poicephalus robustus. In: Barnes KN (ed) The Eskom red data book of South Africa, Lesotho and Swaziland. BirdLife South Africa, Johannesburg

    Google Scholar 

  • Downs CT (2005a) Abundance of the endangered Cape parrot, Poicephalus robustus, in South Africa: implications for its survival. Afr Zool 40:15–24

    Google Scholar 

  • Downs CT (2005b) Artificial nest boxes and wild Cape parrots Poicephalus robustus: persistence pays off. Ostrich 76:222–224

    Article  Google Scholar 

  • Downs CT, Pfeiffer M, Hart L (2014) Fifteen years of annual Cape parrots (Poicephalus robustus) census: current population trends and conservation contributions. Ostrich 85:273–280

    Article  Google Scholar 

  • Eastwood JR, Berg ML, Spolding B, Buchanan KL, Bennett ATD, Walder K (2015) Prevalence of beak and feather disease virus in wild Platycercus elegans: comparison of three tissue types using a probe-based real-time qPCR test. Aust J Zool 63:1–8

    Article  Google Scholar 

  • Gaidet N, Caron A, Cappelle J, Cumming GS, Balança G, Hammoumi S, Cattoli G, Abolnik C, de Almeida RS, Gil P, Fereidouni SR, Grosbois V, Tran A, Mundava J, Fofana B, El Mamy AB, Ndlovu M, Mondain-Monval JY, Triplet P, Hagemeijer W, Karesh WB, Newman SH, Dodman T (2012) Understanding the ecological drivers of avian influenza virus infection in wildfowl: a continental-scale study across Africa. Proc Royal Soc B: Biol Sci 279:1131–1141

    Article  CAS  Google Scholar 

  • Ha H, Anderson I, Alley M, Springett B (2007) The prevalence of beak and feather disease virus infection in wild populations of parrots and cockatoos in New Zealand. N Zeal Vet J 55:235238

    Google Scholar 

  • Hampson K, Lembo T, Bessell P, Auty H, Packer C, Halliday J, Beesley CA, Fyumagwa R, Hoare R, Ernest E, Mentzel C, Metzger KL, Mlengeya T, Stamey K, Roberts K, Wilkins PP, Cleaveland S (2011) Predictability of anthrax infection in the Serengeti, Tanzania. J Appl Ecol 48:1333–1344

    Article  PubMed Central  PubMed  Google Scholar 

  • Harvell CD, Mitchell CE, Ward JR, Altizer S, Dobson AP, Ostfeld RS, Samuel MD (2002) Climate warming and disease risks for terrestrial and marine biota. Science 296:2158–2162

    Article  CAS  PubMed  Google Scholar 

  • Heard MJ, Smith KF, Ripp KJ, Berger M, Chen J, Dittmeier J, Goter M, McGarvey ST, Ryan E (2013) The threat of disease increases as species move toward extinction. Conserv Biol 27:1378–1388

    Article  PubMed Central  PubMed  Google Scholar 

  • Heath L, Martin DP, Warburton L, Perrin M, Horsfield W, Kingsley C, Rybicki EP, Williamson AL (2004) Evidence of unique genotypes of beak and feather disease virus in southern Africa. J Virol 78:9277–9284

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Horrocks NPC, Matson KD, Tieleman BI (2011) Pathogen pressure puts immune defence into perspective. Integr Comp Biol 51:563–576

    Article  CAS  PubMed  Google Scholar 

  • Jackson B, Lorenzo A, Theuerkauf J, Barnaud A, Duval T, Guichard P, Bloc H, Baouma A, Stainton D, Kraberger S, Murphy S, Clark N, Dillon C, Knight T, Varsani A (2014) Preliminary surveillance for beak and feather disease virus in wild parrots of New Caledonia: implications of a reservoir species for Ouvea Parakeets. Emu 114:283–289

    Article  Google Scholar 

  • Julian L, Lorenzo A, Chenuet JP, Bonzon M, Marchal C, Vignon L, Collings DA, Walters M, Jackson B, Varsani A (2012) Evidence of multiple introductions of beak and feather disease virus into the Pacific islands of Nouvelle-Calédonie (New Caledonia). J Gen Virol 93:2466–2472

    Article  CAS  PubMed  Google Scholar 

  • Katoh H, Ogawa H, Ohya K, Fukushi H (2010) A review of DNA viral infections in psittacine birds. Jap Soc Vet Sci 72:1099–1106

    Article  CAS  Google Scholar 

  • Kock ND (1989) An outbreak of beak and feather disease in lovebirds (Agapornis sp.) in Zimbabwe. Zim Vet J 20:97–103

    Google Scholar 

  • Kock ND (1990) Confirmation of psittacine beak and feather disease in Lillian’s lovebirds (Agapornis lillianae) in Zimbabwe. Zim Vet J 21:73

    Google Scholar 

  • Kock ND, Hangartner P, Lucke V (1993) Variation in clinical disease and species susceptibility to psittacine beak and feather disease in Zimbabwean lovebirds. Onderst J Vet Res 60:159–161

    CAS  Google Scholar 

  • Kondiah K, Albertyn J, Bragg RR (2005) Beak and feather disease virus haemagglutinating activity using erythrocytes from African grey parrots and brown-headed parrots. Onderst J Vet Res 72:263–265

    CAS  Google Scholar 

  • Kondiah K, Albertyn J, Bragg RR (2006) Genetic diversity of the rep gene of the beak and feather disease virus in South Africa. Arch Virol 151:2539–2545

    Article  CAS  PubMed  Google Scholar 

  • Kundu S, Faulkes CG, Greenwood AG, Jones CG (2012) Tracking viral evolution during a disease outbreak: the rapid and complete selective sweep of a circovirus in the endangered Echo Parakeet. J Virol 86:5221–5229

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • LaDeau SL, Kilpatrick AM, Marra PP (2007) West Nile virus emergence and large-scale declines of North American bird populations. Nature 447:710–713

    Article  CAS  PubMed  Google Scholar 

  • Lafferty KD (2009) The ecology of climate change and infectious diseases. Ecology 90:888–900

    Article  PubMed  Google Scholar 

  • Lafferty KD, Gerber LR (2002) Good medicine for conservation biology: the intersection of epidemiology and conservation theory. Conserv Biol 16:593–604

    Article  Google Scholar 

  • Loiseau C, Harrigan RJ, Bichet C, Julliard R, Garnier S, Lendvai AZ, Chastel O, Sorci G (2013) Predictions of avian Plasmodium expansion under climate change. Sci Rep 3:1126. doi:10.1038/srep01126

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • MacKellar N, New M, Jack C (2014) Observed and modelled trends in rainfall and temperature for South Africa: 1960–2010. S Afr J Sci. doi:10.1590/sajs.2014/20130353

    Google Scholar 

  • Massaro M, Ortiz-Catedral Julian L, Galbraith JA, Kurenbach B, Kearvell J, Kemp J, van Hal J, Elkington S, Taylor G, Greene T, van de Wetering J, van de Wetering M, Pryde M, Dilks P, Heber S, Steeves TE, Walters M, Shaw S, Potter J, Farrant M, Brunton DH, Hauber M, Jackson B, Bell P, Moorhouse R, McInnes K, Varsani A (2012) Molecular characterisation of beak and feather disease virus (BFDV) in New Zealand and its implications for managing an infectious disease. Arch Virol 157:1651–1663

    Article  CAS  PubMed  Google Scholar 

  • Mzumara TI (2014) The ecology and conservation biology of the Lilian’s Lovebird Agapornis lilianae in Malawi. PhD thesis, University of KwaZulu-Natal, Pietermaritzburg

  • Ortiz-Catedral L, McInnes K, Hauber ME, Brunton DH (2009) First report of beak and feather disease virus (BFDV) in wild red-fronted parakeets (Cyanoramphus novaezelandiae) in New Zealand. Emu 109:244–247

    Article  Google Scholar 

  • Pass DA, Perry RA (1984) The pathology of psittacine beak and feather disease. Aust Vet J 61:69–74

    Article  CAS  PubMed  Google Scholar 

  • Patz JA, Hulme M, Rosenzweig C, Mitchell TD, Goldberg RA, Githeko AK, Lele S, McMichael AJ, Le Sueur D (2002) Climate change (Communication arising): regional warming and malaria resurgence. Nature 420:627–628

    Article  CAS  PubMed  Google Scholar 

  • Pillay K, Dawson DA, Horsburgh GJ, Perrin MR, Burke T, Taylor TD (2010) Twenty-two polymorphic microsatellite loci aimed at detecting illegal trade in the Cape parrot, Poicephalus robustus (Psittacine, AVES). Mol Ecol Res 10:142–149

    Article  CAS  Google Scholar 

  • Radial SR, McElnea CL, Cross GM (1993) Seroprevalence of psittacine beak and feather disease in wild psittacine birds in New South Wales. Austr Vet J 70:137–139

    Article  Google Scholar 

  • Rahaus M, Wolff MH (2003) Psittacine beak and feather disease: a first survey of the distribution of beak and feather disease virus inside the population of captive psittacine birds in Germany. J Vet Med B 50:368–371

    Article  Google Scholar 

  • Raidal S, Firth G, Cross G (1993) Vaccination and challenge studies with psittacine beak and feather disease virus. Austr Vet J 70:437–441

    Article  CAS  Google Scholar 

  • Reed KD, Meece JK, Henkel JS, Shukla SK (2003) Birds, migration and emerging zoonoses: West Nile virus, Lyme disease, influenza A and enteropathogens. Clin Med Res 1:5–12

    Article  PubMed Central  PubMed  Google Scholar 

  • Regnard G, Boyes RS, Martin RO, Hitzeroth I, Rybicki EP (2014a) Beak and feather disease viruses circulating in Cape parrots (Poicephalus robustus) in South Africa. Arch Virol. doi:10.1007/s00705-014-2226-9

    Google Scholar 

  • Regnard G, Boyes RS, Martin RO, Hitzeroth I, Rybicki EP (2014b) Beak and feather disease virus: correlation between viral load and clinical signs in wild Cape parrots (Poicephalus robustus) in South Africa. Arch Virol. doi:10.1007/s00705-014-2225-x

    Google Scholar 

  • Ritchie BW, Carter K (1995) Circoviridae. In: Avian viruses: function and control. Wingers Publishing Inc, Lake Worth, pp 223–251

  • Ritchie BW, Niagro FD, Latimer KS, Steffens WL, Pesti D, Lukert PD (1991) Haemagglutination by psittacine beak and feather disease virus and use of haemagglutination inhibition for detection of antibodies against the virus. Am J Vet Res 52:1810–1815

    CAS  PubMed  Google Scholar 

  • Ritchie PA, Anderson IL, Lambert DM (2003) Evidence for specificity of psittacine beak and feather disease viruses among avian hosts. Virology 306:109–115

    Article  CAS  PubMed  Google Scholar 

  • Scheele BC, Hunter DA, Grogan LF, Berger LEE, Kolby JE, McFadden MS, Marantelli G, Skerratt LF, Driscoll DA (2014) Interventions for reducing extinction risk in chytridiomycosis-threatened amphibians. Conserv Biol 28:1195–1205

    Article  PubMed  Google Scholar 

  • Smith KF, Sax DF, Lafferty KD (2006) Evidence for the role of infectious disease in species extinction and endangerment. Conserv Biol 20:1349–1357

    Article  PubMed  Google Scholar 

  • Symes CT, Downs CT (2002) Occurrence of Cape parrot Poicephalus robustus at non-forest feeding sites in South Africa: threats to a declining population. Bull Afr Bird Club 9:27–31

    Google Scholar 

  • Symes CT, Perrin MR (2004) Breeding biology of the greyheaded parrot (Poicephalus fuscicollis suahelicus) in the wild. Emu 104:45–57

    Article  Google Scholar 

  • Varsani A, Regnard GL, Bragg R, Hitzeroth II, Rybicki EP (2011) Global genetic diversity and geographical and host species distribution of beak and feather disease virus isolates. J Gen Virol 92:752–767

  • Warburton LS, Perrin MR (2002) PBFDV bei frei lebenden Ruköpfchen in Sambia. Papageien 5:166–169

    Google Scholar 

  • Warburton L, Mpindi S, Howells B, Pienaar K, Patterson C, Mattison H, Whittington-Jones C, Hughes S, Fossey A, O’Grady J, Koekemoer J, Downs C, Perrin M, Evans SW (2002) Cape Parrot (Poicephalus robustus) action plan. Final workshop report. Birdlife South Africa, Johannesburg 5–13, 16, and 35

    Google Scholar 

  • Wirminghaus JO (1995) Colour variation and anomalies in South African parrots. Birding in South Afr 47:76–77

    Google Scholar 

  • Wirminghaus JO (1997) Cape Parrot. In: Harrison JA, Allan DG, Underhill LG, Herremans M, Tree AJ, Parker V, Brown CJ (eds) The atlas of southern African birds, vol 1. BirdLife South Africa, Johannesburg, pp 1–785

    Google Scholar 

  • Wirminghaus JO, Downs CT, Symes CT, Perrin MR (1999) Conservation of the Cape parrot in southern Africa. S Afr J Wildl Res 29:118–129

    Google Scholar 

  • Wirminghaus JO, Downs CT, Symes CT, Perrin MR (2000a) Abundance of the Cape parrot in South Africa. S Afr J Wildl Res 30:43–52

    Google Scholar 

  • Wirminghaus JO, Downs CT, Symes CT, Perrin MR, Dempster ER (2000b) Vocalisations and behaviours of the Cape parrot Poicephalus robustus (Psittaciformes: Psittacidae). Durb Mus Novit 25:12–17

    Google Scholar 

  • Wirminghaus JO, Downs CT, Symes CT, Perrin MR (2001a) Abundance and activity patterns of the Cape parrot (Poicephalus robustus) in two afromontane forests in South Africa. Afr Zool 36:71–77

    Google Scholar 

  • Wirminghaus JO, Downs CT, Symes CT, Perrin MR (2001b) Fruiting in two Afromontane forests in KwaZulu-Natal, South Africa: the habitat type of the Endangered Cape Parrot Poicephalus robustus. S Afr J Bot 67:329–336

    Google Scholar 

  • Wirminghaus JO, Downs CT, Symes CT, Perrin MR (2001c) Breeding biology of the Cape parrot Poicephalus robustus. Ostrich 72:159–164

    Article  Google Scholar 

  • Wirminghaus JO, Downs CT, Perrin MR, Symes CT (2002a) Taxonomic relationships of the subspecies of the Cape parrot Poicephalus robustus (Gmelin). J Nat Hist 36:361–378

    Article  Google Scholar 

  • Wirminghaus JO, Downs CT, Symes CT, Perrin MR (2002b) Diet of the Cape parrot, Poicephalus robustus, in Afromontane forests in KwaZulu-Natal, South Africa. Ostrich 73:20–25

    Article  Google Scholar 

  • Wobeser GA (1994) Disease Management—General Principles. In: investigation and management of disease in wild animals. Plenum Press, New York, pp 131–151

  • Wobeser GA (2007) Samples, sampling and sample collection. In: disease in wild animals: investigation and management, 2nd edn. Springer, New York, pp 123–142

  • Coetzer WR, Downs CT, Perrin MR, Willows-Munro S (In prep.) Molecular systematics of the Cape Parrot (Poicephalus robustus): implications for taxonomy and conservation. Plos One (Accepted)

  • Zamora-Vilchis I, Williams SE, Johnson CN (2012) Environmental temperature affects prevalence of blood parasites of birds on an elevation gradient: implications for disease in a warming climate. PLoS One 7:e39208. doi:10.1371/journal.pone.0039208

    Article  PubMed Central  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We are grateful to all those who shared their observations with us. D. York and Molecular Diagnostic Services, Durban, South Africa, are thanked for conducting BFDV analyses. In particular, we are grateful for the contributions of B. Gardner, W. Horsfield, L. Warburton, M. Perrin, and the late O. Wirminghaus.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Colleen T. Downs.

Additional information

Communicated by K. C. Klasing.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Downs, C.T., Brown, M., Hart, L. et al. Review of documented beak and feather disease virus cases in wild Cape parrots in South Africa during the last 20 years. J Ornithol 156, 867–875 (2015). https://doi.org/10.1007/s10336-015-1258-6

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10336-015-1258-6

Keywords

Navigation