» Articles » PMID: 20219910

Avian Bornavirus Associated with Fatal Disease in Psittacine Birds

Overview
Journal J Virol
Date 2010 Mar 12
PMID 20219910
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Thanks to new technologies which enable rapid and unbiased screening for viral nucleic acids in clinical specimens, an impressive number of previously unknown viruses have recently been discovered. Two research groups independently identified a novel negative-strand RNA virus, now designated avian bornavirus (ABV), in parrots with proventricular dilatation disease (PDD), a severe lymphoplasmacytic ganglioneuritis of the gastrointestinal tract of psittacine birds that is frequently accompanied by encephalomyelitis. Since its discovery, ABV has been detected worldwide in many captive parrots and in one canary with PDD. ABV induced a PDD-like disease in experimentally infected cockatiels, strongly suggesting that ABV is highly pathogenic in psittacine birds. Until the discovery of ABV, the Bornaviridae family consisted of a single species, classical Borna disease virus (BDV), which is the causative agent of a progressive neurological disorder that affects primarily horses, sheep, and some other farm animals in central Europe. Although ABV and BDV share many biological features, there exist several interesting differences, which are discussed in this review.

Citing Articles

Evolutionary Analysis of a Parrot Bornavirus 2 Detected in a Sulphur-Crested Cockatoo () Suggests a South American Ancestor.

Chacon R, Sanchez-Llatas C, Diaz Forero A, Guimaraes M, L Pajuelo S, Astolfi-Ferreira C Animals (Basel). 2024; 14(1).

PMID: 38200778 PMC: 10778322. DOI: 10.3390/ani14010047.


Genetic trends in parrot Bornavirus: a clinical analysis.

Hong S, Kim S, Seo M, Han M, Kim J, Lee S J Vet Med Sci. 2024; 86(2):239-246.

PMID: 38171882 PMC: 10898989. DOI: 10.1292/jvms.23-0312.


Cannabinoid receptor 2 evolutionary gene loss makes parrots more susceptible to neuroinflammation.

Divin D, Samblas M, Veetil N, Voukali E, Swiderska Z, Krajzingrova T Proc Biol Sci. 2022; 289(1988):20221941.

PMID: 36475439 PMC: 9727682. DOI: 10.1098/rspb.2022.1941.


Canary Bornavirus () Infections Are Associated with Clinical Symptoms in Common Canaries ( dom.).

Rinder M, Baas N, Hagen E, Drasch K, Korbel R Viruses. 2022; 14(10).

PMID: 36298742 PMC: 9607494. DOI: 10.3390/v14102187.


Avian Bornavirus Research-A Comprehensive Review.

Rubbenstroth D Viruses. 2022; 14(7).

PMID: 35891493 PMC: 9321243. DOI: 10.3390/v14071513.


References
1.
Henkel M, Planz O, Fischer T, Stitz L, Rziha H . Prevention of virus persistence and protection against immunopathology after Borna disease virus infection of the brain by a novel Orf virus recombinant. J Virol. 2004; 79(1):314-25. PMC: 538698. DOI: 10.1128/JVI.79.1.314-325.2005. View

2.
Villanueva I, Gray P, Mirhosseini N, Payne S, Hoppes S, Honkavuori K . The diagnosis of proventricular dilatation disease: use of a Western blot assay to detect antibodies against avian Borna virus. Vet Microbiol. 2009; 143(2-4):196-201. DOI: 10.1016/j.vetmic.2009.11.041. View

3.
Schneider U, Schwemmle M, Staeheli P . Genome trimming: a unique strategy for replication control employed by Borna disease virus. Proc Natl Acad Sci U S A. 2005; 102(9):3441-6. PMC: 552903. DOI: 10.1073/pnas.0405965102. View

4.
Gough R, Drury S, Culver F, Britton P, Cavanagh D . Isolation of a coronavirus from a green-cheeked Amazon parrot (Amazon viridigenalis Cassin). Avian Pathol. 2006; 35(2):122-6. DOI: 10.1080/03079450600597733. View

5.
Durrwald R, Kolodziejek J, Muluneh A, Herzog S, Nowotny N . Epidemiological pattern of classical Borna disease and regional genetic clustering of Borna disease viruses point towards the existence of to-date unknown endemic reservoir host populations. Microbes Infect. 2006; 8(3):917-29. DOI: 10.1016/j.micinf.2005.08.013. View