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01.01.2015 | Brief Report

Beak and feather disease virus: correlation between viral load and clinical signs in wild Cape parrots (Poicepahlus robustus) in South Africa

Erschienen in: Archives of Virology | Ausgabe 1/2015

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Abstract

Psittacine beak and feather disease (PBFD), the most prevalent viral disease affecting psittacines, is caused by beak and feather disease virus (BFDV). This study assessed viral load using qPCR in a wild Cape parrot population affected by PBFD and compared it to overall physical condition based on clinical signs attributable to PBFD. A significant inverse correlation between viral load and overall physical condition was found, which confirmed that clinical signs may confidently be used to diagnose the relative severity of BFDV infections in wild populations. This is the first assessment of BFDV viral load in a wild psittacine population.

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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(Pt 4):752–767. doi:10.1099/vir.0.028126-0 CrossRefPubMed

Todd D, Bendinelli M, Biagini P, Hino S, Mankertz A, Mishiro S, Niel C, Okamoto H, Raidal S, Ritchie BW, Teo GC (2005) Circoviridae. In: Fauquet CM, Mayo MA, Maniloff J, Desselberger U, Ball LA (eds) Virus taxonomy: VIIIth report of the international committee on taxonomy of viruses. Elsevier Academic Press, San Diego, pp 327–334

Crowther R, Berriman J, Curran W, Allan G, Todd D (2003) Comparison of the structures of three circoviruses: chicken anemia virus, porcine circovirus type 2, and beak and feather disease virus. J Virol 77(24):13036–13041PubMedCentralCrossRefPubMed

Bassami M, Ypelaar I, Berryman D, Wilcox G, Raidal S (2001) Genetic diversity of beak and feather disease virus detected in psittacine species in Australia. Virology 279(2):392–400CrossRefPubMed

Niagro F, Forsthoefel A, Lawther R, Kamalanathan L, Ritchie B, Latimer K, Lukert P (1998) Beak and feather disease virus and porcine circovirus genomes: intermediates between the geminiviruses and plant circoviruses. Arch Virol 143(9):1723–1744CrossRefPubMed

Todd D (2004) Avian circovirus diseases: lessons for the study of PMWS. Vet Microbiol 98(2):169–174CrossRefPubMed

Hsu C-M, Ko C-Y, Tsai H-J (2006) Detection and sequence analysis of avian polyomavirus and psittacine beak and feather disease virus from psittacine birds in Taiwan. Avian Dis 50(3):348–353CrossRefPubMed

Peters A, Patterson EI, Baker BG, Holdsworth M, Sarker S, Ghorashi SA, Raidal SR (2014) Evidence of psittacine beak and feather disease virus spillover into wild critically endangered orange-bellied parrots (Neophema chrysogaster). J Wildl Dis 50(2):288–296

Raidal S, Firth G, Cross G (1993) Vaccination and challenge studies with psittacine beak and feather disease virus. Aust Vet J 70(12):437–441CrossRefPubMed

10.

Sa RC, Cunningham AA, Dagleish MP, Wheelhouse N, Pocknell A, Borel N, Peck HL, Lawson B (2014) Psittacine beak and feather disease in a free-living ring-necked parakeet (Psittacula krameri) in Great Britain. Eur J Wildlife Res 60(2):395–398

11.

Rahaus M, Desloges N, Probst S, Loebbert B, Lantermann W, Wolff M (2008) Detection of beak and feather disease virus DNA in embryonated eggs of psittacine birds. Vet Med (Praha) 53(1):53

12.

Ritchie BW, Niagro FD, Latimer KS, Lukert PD, Steffens WL, Rakich PM, Pritchard N (1990) Ultrastructural, protein composition, and antigenic comparison of psittacine beak and feather disease virus purified from four genera of psittacine birds. J Wildl Dis 26(2):196–203CrossRefPubMed

13.

Raidal SR, McElnea CL, Cross GM (1993) Seroprevalence of psittacine beak and feather disease in wild psittacine birds in New South Wales. Aust Vet J 70(4):137–139CrossRefPubMed

14.

Gerlach H (1994) Circoviridae-psittacine beak and feather disease virus, Avian medicine: principles and practice. Wingers Publishing Incorporation, Lake Worth, pp 894–903

15.

Latimer KS, Niagro FD, Campagnoli RP, Ritchie BW, Pesti DA, Steffens III W (1993) Diagnosis of concurrent avian polyomavirus and psittacine beak and feather disease virus infections using DNA probes. J Assoc Avian Vet 7:141–146

16.

Pass D, Perry R (1985) Psittacine beak and feather disease: an update. Aust Vet Pract 15(2):55–60

17.

McOrist S, Black DG, Pass DA, Scott PC, Marshall J (1984) Beak and feather dystrophy in wild sulphur-crested cockatoos (Cacatua galerita). J Wildl Dis 20(2):120–124CrossRefPubMed

18.

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(8):368–371CrossRef

19.

Ledwoń A, Sapierzyński R, Augustynowicz-Kopeć E, Szeleszczuk P, Kozak M (2014) Experimental inoculation of BFDV-positive budgerigars (Melopsittacus undulatus) with two Mycobacterium avium subsp. avium isolates. Biomed Res Int 2014:1–5

20.

Hess M, Scope A, Heincz U (2004) Comparitive sensitivity of polymerase chain reaction diagnosis of psittacine beak and feather disease on feather samples, cloacal swabs and blood from budgerigars (Melopsittacus undulates, Shaw 18005). Avian Pathol 33(5):477–481. doi:10.1080/03079450400003619 CrossRefPubMed

21.

Boyes RS (2011) Red alert. Focus on endangered species: Cape parrot. Africa Birds and Birding 2011:66–67

22.

Bustin SA, Benes V, Garson JA, Hellemans J, Huggett J, Kubista M, Mueller R, Nolan T, Pfaffl MW, Shipley GL (2009) The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. Clin Chem 55(4):611–622CrossRefPubMed

23.

Wright TF, Schirtzinger EE, Matsumoto T, Eberhard JR, Graves GR, Sanchez JJ, Capelli S, Müller H, Scharpegge J, Chambers GK (2008) A multilocus molecular phylogeny of the parrots (Psittaciformes): support for a Gondwanan origin during the Cretaceous. Mol Biol Evol 25(10):2141–2156PubMedCentralCrossRefPubMed

24.

Barton D, Foellmer B, Du J, Tamm J, Derynck R, Francke U (1987) Chromosomal mapping of genes for transforming growth factors beta 2 and beta 3 in man and mouse: dispersion of TGF-beta gene family. Oncogene Res 3(4):323–331

25.

Ganapathy G, Howard JT, Ward JM, Li J, Li B, Li Y, Xiong Y, Zhang Y, Zhou S, Schwartz DC (2014) High-coverage sequencing and annotated assemblies of the budgerigar genome. GigaScience 3(1):1–9CrossRef

26.

Bert E, Tomassone L, Peccati C, Navarrete M, Sola S (2005) Detection of beak and feather disease virus (BFDV) and avian polyomavirus (APV) DNA in psittacine birds in Italy. J Vet Med Ser B 52(2):64–68CrossRef

27.

Katoh H, Ohya K, Fukushi H (2008) Development of novel real-time PCR assays for detecting DNA virus infections in psittaciform birds. J Virol Methods 154(1–2):92–98. doi:10.1016/j.jviromet.2008.08.015 CrossRefPubMed

28.

Ha HJ, Anderson IL, Alley MR, Springett BP, Gartrell BD (2007) The prevalence of beak and feather disease virus infection in wild populations of parrots and cockatoos in New Zealand. N Z Vet J 55(5):235–238. doi:10.1080/00480169.2007.36774 CrossRefPubMed

29.

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(3):244–247CrossRef

30.

Kundu S, Faulkes CG, Greenwood AG, Jones CG, Kaiser P, Lyne OD, Black SA, Chowrimootoo A, Groombridge JJ (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(9):5221–5229PubMedCentralCrossRefPubMed

31.

Shearer PL, Sharp M, Bonne N, Clark P, Raidal SR (2009) A quantitative, real-time polymerase chain reaction assay for beak and feather disease virus. J Virol Methods 159(1):98–104. doi:10.1016/j.jviromet.2009.03.009 CrossRefPubMed

32.

Bonne N, Shearer P, Sharp M, Clark P, Raidal 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(3):640–647CrossRefPubMed

33.

Brunborg IM, Moldal T, Jonassen CM (2004) Quantitation of porcine circovirus type 2 isolated from serum/plasma and tissue samples of healthy pigs and pigs with postweaning multisystemic wasting syndrome using a TaqMan-based real-time PCR. J Virol Methods 122(2):171–178CrossRefPubMed

34.

Khalesi B, Bonne N, Stewart M, Sharp M, Raidal S (2005) A comparison of haemagglutination, haemagglutination inhibition and PCR for the detection of psittacine beak and feather disease virus infection and a comparison of isolates obtained from loriids. J Gen Virol 86(Pt 11):3039–3046. doi:10.1099/vir.0.81275-0 CrossRefPubMed

Titel: Beak and feather disease virus: correlation between viral load and clinical signs in wild Cape parrots (Poicepahlus robustus) in South Africa
Publikationsdatum: 01.01.2015
Erschienen in: Archives of Virology / Ausgabe 1/2015
Print ISSN: 0304-8608
Elektronische ISSN: 1432-8798
DOI: https://doi.org/10.1007/s00705-014-2225-x

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Beak and feather disease virus: correlation between viral load and clinical signs in wild Cape parrots (Poicepahlus robustus) in South Africa

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