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About:
Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings
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schema:ScholarlyArticle
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings
Creator
Xia, Xianzhu
Yang, Songtao
Liu, Xiufan
Xiao, Yueqiang
Wang, Jianzhong
Ding, Zhuang
Yin, Renfu
Ding, Chan
Feng, Na
Yu, Shengqing
Hu, Shunlin
Cong, Yanlong
Wang, Chunfeng
Wang, Wenxiu
Source
Elsevier; Medline; PMC
abstract
Abstract Newcastle disease virus (NDV) and Goose parvovirus (GPV) are considered to be two of the most important and widespread viruses infecting geese. In this study, we generated a recombinant rmNA-VP3, expressing GPV VP3 using a modified goose-origin NDV NA-1 by changing the multi-basic cleavage site motif RRQKR↓F of the F protein to the dibasic motif GRQGR↓L as that of the avirulent strain LaSota as a vaccine vector. Expression of the VP3 protein in rmNA-VP3 infected cells was detected by immunofluorescence and Western blot assay. The genetic stability was examined by serially passaging 10 times in 10-day-old embryonated SPF chicken eggs. Goslings were inoculated with rmNA-VP3 showed no apparent signs of disease and developed a strong GPV and NDV neutralizing antibodies response. This is the first study demonstrating that recombinant NDV has the potential to serve as bivalent live vaccine against Goose parvovirus and Newcastle disease virus infection in birds.
has issue date
2015-05-04
(
xsd:dateTime
)
bibo:doi
10.1016/j.virusres.2015.04.006
bibo:pmid
25882914
has license
els-covid
sha1sum (hex)
5078f271f0b8d13359084747a8244563005d720a
schema:url
https://doi.org/10.1016/j.virusres.2015.04.006
resource representing a document's title
Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings
has PubMed Central identifier
PMC7114436
has PubMed identifier
25882914
schema:publication
Virus Research
resource representing a document's body
covid:5078f271f0b8d13359084747a8244563005d720a#body_text
is
schema:about
of
named entity 'changing'
named entity 'NDV'
named entity 'vaccine'
named entity 'stability'
named entity 'Newcastle disease virus'
named entity 'serially'
named entity 'protein'
covid:arg/5078f271f0b8d13359084747a8244563005d720a
named entity 'The'
named entity 'vaccine'
named entity 'dibasic'
named entity 'potential'
named entity 'assay'
named entity 'infecting'
named entity 'immunofluorescence'
named entity 'recombinant'
named entity 'NDV'
named entity 'NDV'
named entity 'VP3'
named entity 'vaccine'
named entity 'chicken'
named entity 'avirulent'
named entity 'cleavage site'
named entity 'live vaccine'
named entity 'genetic stability'
named entity 'inoculated'
named entity 'embryonated'
named entity 'Newcastle disease virus'
named entity 'dibasic'
named entity 'recombinant'
named entity 'Goose parvovirus'
named entity 'developed'
named entity 'gene'
named entity 'live vaccines'
named entity 'immunofluorescence'
named entity 'antibody'
named entity 'goslings'
named entity 'vaccine'
named entity 'antibody'
named entity 'vaccine'
named entity 'goslings'
named entity 'Serum samples'
named entity 'vaccine'
named entity 'vaccine'
named entity 'goslings'
named entity 'viruses'
named entity 'vaccine'
named entity 'PCR amplified'
named entity 'FITC'
named entity 'lysates'
named entity 'antibody'
named entity 'genotype'
named entity 'NDV'
named entity 'reverse genetics'
named entity 'virulent strain'
named entity 'NDV'
named entity 'syncytia'
named entity 'ICPI'
named entity 'poultry'
named entity 'IgG'
named entity 'panzootic'
named entity 'genome'
named entity 'pathogenicity'
named entity 'NDV'
named entity 'antigenicity'
named entity 'cDNA'
named entity 'fibroblasts'
named entity 'protein cleavage'
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