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Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings

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 moti...

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Autores principales: Wang, Jianzhong, Cong, Yanlong, Yin, Renfu, Feng, Na, Yang, Songtao, Xia, Xianzhu, Xiao, Yueqiang, Wang, Wenxiu, Liu, Xiufan, Hu, Shunlin, Ding, Chan, Yu, Shengqing, Wang, Chunfeng, Ding, Zhuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114436/
https://www.ncbi.nlm.nih.gov/pubmed/25882914
http://dx.doi.org/10.1016/j.virusres.2015.04.006
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author Wang, Jianzhong
Cong, Yanlong
Yin, Renfu
Feng, Na
Yang, Songtao
Xia, Xianzhu
Xiao, Yueqiang
Wang, Wenxiu
Liu, Xiufan
Hu, Shunlin
Ding, Chan
Yu, Shengqing
Wang, Chunfeng
Ding, Zhuang
author_facet Wang, Jianzhong
Cong, Yanlong
Yin, Renfu
Feng, Na
Yang, Songtao
Xia, Xianzhu
Xiao, Yueqiang
Wang, Wenxiu
Liu, Xiufan
Hu, Shunlin
Ding, Chan
Yu, Shengqing
Wang, Chunfeng
Ding, Zhuang
author_sort Wang, Jianzhong
collection PubMed
description 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.
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spelling pubmed-71144362020-04-02 Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings Wang, Jianzhong Cong, Yanlong Yin, Renfu Feng, Na Yang, Songtao Xia, Xianzhu Xiao, Yueqiang Wang, Wenxiu Liu, Xiufan Hu, Shunlin Ding, Chan Yu, Shengqing Wang, Chunfeng Ding, Zhuang Virus Res Article 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. Elsevier B.V. 2015-05-04 2015-04-13 /pmc/articles/PMC7114436/ /pubmed/25882914 http://dx.doi.org/10.1016/j.virusres.2015.04.006 Text en Copyright © 2015 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Wang, Jianzhong
Cong, Yanlong
Yin, Renfu
Feng, Na
Yang, Songtao
Xia, Xianzhu
Xiao, Yueqiang
Wang, Wenxiu
Liu, Xiufan
Hu, Shunlin
Ding, Chan
Yu, Shengqing
Wang, Chunfeng
Ding, Zhuang
Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings
title Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings
title_full Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings
title_fullStr Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings
title_full_unstemmed Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings
title_short Generation and evaluation of a recombinant genotype VII Newcastle disease virus expressing VP3 protein of Goose parvovirus as a bivalent vaccine in goslings
title_sort generation and evaluation of a recombinant genotype vii newcastle disease virus expressing vp3 protein of goose parvovirus as a bivalent vaccine in goslings
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114436/
https://www.ncbi.nlm.nih.gov/pubmed/25882914
http://dx.doi.org/10.1016/j.virusres.2015.04.006
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