2016
DOI: 10.1128/jcm.03244-15
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Identification of Goose-Origin Parvovirus as a Cause of Newly Emerging Beak Atrophy and Dwarfism Syndrome in Ducklings

Abstract: A recent epizootic outbreak, in China, of duck beak atrophy and dwarfism syndrome (BADS) was investigated using electron microscopic, genetic, and virological studies, which identified a parvovirus with a greater similarity to goose parvovirus (GPV) (97% protein homology) than to Muscovy duck parvovirus (MDPV) (90% protein homology). The new virus, provisionally designated GPV-QH15, was found to be antigenically more closely related to GPV than to MDPV in a virus neutralization assay. These findings were furth… Show more

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Cited by 50 publications
(57 citation statements)
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“…In NGPV, the amino acid mutation A140S (position 140, Ala to Ser) was located closely to the motif involved in DNA binding of the Rep protein, which might be related to virus transcription. The latest study showed that the antigenic epitopes on the GPV Rep protein were mainly located in the C‐terminal (aa 485–627) especially in the fragment Rep (aa 498–532) (Yu, Ma, Sheng et al., ; Yu, Ma, & Wang, ). Comparing to classical GPVs, we found seven coincidental amino acid mutations were located at the C‐terminal of Rep protein of NGPVs (Table ).…”
Section: Discussionmentioning
confidence: 99%
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“…In NGPV, the amino acid mutation A140S (position 140, Ala to Ser) was located closely to the motif involved in DNA binding of the Rep protein, which might be related to virus transcription. The latest study showed that the antigenic epitopes on the GPV Rep protein were mainly located in the C‐terminal (aa 485–627) especially in the fragment Rep (aa 498–532) (Yu, Ma, Sheng et al., ; Yu, Ma, & Wang, ). Comparing to classical GPVs, we found seven coincidental amino acid mutations were located at the C‐terminal of Rep protein of NGPVs (Table ).…”
Section: Discussionmentioning
confidence: 99%
“…The ducks with SBDS showed strong growth retardation with beak atrophy, enteritis and paralysis. Although the mortality rate was 2%–6% in affected flocks, the morbidity rate was 10%–30% and even 50% in some regions, which caused great economic losses to waterfowl industry in China (Li et al., ; Yu, Ma, & Wang, ; Yu, Ma, Sheng et al., ). To better elucidate the pathogenesis of the virus, a Cherry Valley duck model was established to reproduce SBDS by infecting the ducklings with a Cherry Valley duck‐origin NGPV strain (Chen, Dou et al., ; Chen, Wang et al., ).…”
Section: Introductionmentioning
confidence: 99%
“…Real-time PCR for the diagnosis of duck-origin GPV has many advantages compared to serological diagnosis such as agar diffusion method, immunohistochemistry and ELISA [1], and molecular diagnostics. Generally, serological diagnosis has the disadvantage of low sensitivity and more time consumption.…”
Section: Discussionmentioning
confidence: 99%
“…Later, the representative BADS isolates GPV-QH15 [1], SBDSV-M15 [2], AH-D15 [2], SD [7], DS15 [8], and QH-L01 [9] have been reported, respectively. The duck-origin GPV is similar to other members of the genus Dependoparvovirus of the family Parvoviridae [10, 11].…”
Section: Introductionmentioning
confidence: 99%
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