4.1 Article

Liver virome of a Little Corella (Cacatua sanguinea) reveals coinfection with a novel parvovirus and two beak and feather disease viruses

Journal

AUSTRALIAN VETERINARY JOURNAL
Volume 101, Issue 9, Pages 366-372

Publisher

WILEY
DOI: 10.1111/avj.13271

Keywords

Avian; beak and feather disease virus; circovirus; co-infection; next-generation sequencing; parvovirus

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This study identified a novel psittaciform chaphamaparvovirus 3 (PsChV-3) in an Australian free-ranging little corella, as well as two complete novel beak and feather disease (BFDV) genomes. Phylogenetic analysis showed that the sequenced novel BFDV genomes clustered with other BFDVs isolated from Australian cockatoos. This study contributes to the understanding of chaphamaparvoviruses and BFDV in Australian parrots, highlighting the need for ongoing monitoring and molecular studies.
Emerging diseases are acknowledged as a growing threat to wildlife, with the continued identification of pathogenic and potentially pathogenic viruses in avian species resulting from ongoing advances in molecular diagnostic techniques. Parvoviruses under the genus Chaphamaparvovirus (subfamily Hamaparvovirinae) are highly divergent. The detection and characterisation of parvoviruses in psittacine birds is limited. This study reports a novel parvovirus, tentatively named psittaciform chaphamaparvovirus 3 (PsChV-3) under the genus Chaphamaparvovirus, identified in an Australian free-ranging little corella (Cacatua sanguinea). The PsChV-3 genome is 4277 bp in length and encompasses four predicted open-reading frames, including two major genes, a nonstructural replicase gene (NS1), and a structural capsid gene (VP1). The NS1 and VP1 genes showed the closest amino acid identities of 78.8% and 69.7%, respectively, with a recently sequenced psittaciform chaphamaparvovirus 2 from Australian Neophema species grass parrots. In addition, the presence of two complete novel beak and feather disease (BFDV) genomes, 1993 and 1868 nt in length, respectively, were detected from the same bird. Both these BFDV genomes contained two bidirectional ORFs encoding the putative Rep and Cap proteins. Phylogenetic analysis showed that the sequenced novel BFDV genomes clustered in a distinct subclade with other BFDVs isolated from Australian cockatoos. This study contributes to the characterisation chaphamaparvoviruses and BFDV in Australian parrots and supports the need for ongoing monitoring and molecular studies into the avian virome in native Australian psittacine bird species.

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