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Development and efficacy of a novel live-attenuated QX-like nephropathogenic infectious bronchitis virus vaccine in China
In this study, we attenuated a Chinese QX-like nephropathogenic infectious bronchitis virus (IBV) strain, YX10, by passaging through fertilized chicken eggs. The 90th passage strain (YX10p90) was selected as the live-attenuated vaccine candidate strain. YX10p90 was found to be safe in 7-day-old spec...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127481/ https://www.ncbi.nlm.nih.gov/pubmed/25636916 http://dx.doi.org/10.1016/j.vaccine.2015.01.036 |
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author | Feng, Keyu Xue, Yu Wang, Jinglan Chen, Weiguo Chen, Feng Bi, Yingzuo Xie, Qingmei |
author_facet | Feng, Keyu Xue, Yu Wang, Jinglan Chen, Weiguo Chen, Feng Bi, Yingzuo Xie, Qingmei |
author_sort | Feng, Keyu |
collection | PubMed |
description | In this study, we attenuated a Chinese QX-like nephropathogenic infectious bronchitis virus (IBV) strain, YX10, by passaging through fertilized chicken eggs. The 90th passage strain (YX10p90) was selected as the live-attenuated vaccine candidate strain. YX10p90 was found to be safe in 7-day-old specific pathogen free chickens without induction of morbidity or mortality. YX10p90 provided nearly complete protection against QX-like (CH I genotype) strains and partial protection against other two major Chinese genotype strains. YX10p90 also showed no reversion to virulence after five back passages in chickens. An IBV polyvalent vaccine containing YX10p90 was developed and showed that it could provide better protection against major Chinese IBV virulent strains than commercial polyvalent vaccines. In addition, the complete genome sequence of YX10p90 was sequenced. Multiple-sequence alignments identified 38 nucleotide substitutions in the whole genome which resulted in 26 amino acid substitutions and a 110-bp deletion in the 3′ untranslated region. In conclusion, the attenuated YX10p90 strain exhibited a fine balance between attenuation and immunogenicity, and should be considered as a candidate vaccine to prevent infection of Chinese QX-like nephropathogenic IBV. |
format | Online Article Text |
id | pubmed-7127481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71274812020-04-08 Development and efficacy of a novel live-attenuated QX-like nephropathogenic infectious bronchitis virus vaccine in China Feng, Keyu Xue, Yu Wang, Jinglan Chen, Weiguo Chen, Feng Bi, Yingzuo Xie, Qingmei Vaccine Article In this study, we attenuated a Chinese QX-like nephropathogenic infectious bronchitis virus (IBV) strain, YX10, by passaging through fertilized chicken eggs. The 90th passage strain (YX10p90) was selected as the live-attenuated vaccine candidate strain. YX10p90 was found to be safe in 7-day-old specific pathogen free chickens without induction of morbidity or mortality. YX10p90 provided nearly complete protection against QX-like (CH I genotype) strains and partial protection against other two major Chinese genotype strains. YX10p90 also showed no reversion to virulence after five back passages in chickens. An IBV polyvalent vaccine containing YX10p90 was developed and showed that it could provide better protection against major Chinese IBV virulent strains than commercial polyvalent vaccines. In addition, the complete genome sequence of YX10p90 was sequenced. Multiple-sequence alignments identified 38 nucleotide substitutions in the whole genome which resulted in 26 amino acid substitutions and a 110-bp deletion in the 3′ untranslated region. In conclusion, the attenuated YX10p90 strain exhibited a fine balance between attenuation and immunogenicity, and should be considered as a candidate vaccine to prevent infection of Chinese QX-like nephropathogenic IBV. Elsevier Ltd. 2015-02-25 2015-01-27 /pmc/articles/PMC7127481/ /pubmed/25636916 http://dx.doi.org/10.1016/j.vaccine.2015.01.036 Text en Copyright © 2015 Elsevier Ltd. 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 Feng, Keyu Xue, Yu Wang, Jinglan Chen, Weiguo Chen, Feng Bi, Yingzuo Xie, Qingmei Development and efficacy of a novel live-attenuated QX-like nephropathogenic infectious bronchitis virus vaccine in China |
title | Development and efficacy of a novel live-attenuated QX-like nephropathogenic infectious bronchitis virus vaccine in China |
title_full | Development and efficacy of a novel live-attenuated QX-like nephropathogenic infectious bronchitis virus vaccine in China |
title_fullStr | Development and efficacy of a novel live-attenuated QX-like nephropathogenic infectious bronchitis virus vaccine in China |
title_full_unstemmed | Development and efficacy of a novel live-attenuated QX-like nephropathogenic infectious bronchitis virus vaccine in China |
title_short | Development and efficacy of a novel live-attenuated QX-like nephropathogenic infectious bronchitis virus vaccine in China |
title_sort | development and efficacy of a novel live-attenuated qx-like nephropathogenic infectious bronchitis virus vaccine in china |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127481/ https://www.ncbi.nlm.nih.gov/pubmed/25636916 http://dx.doi.org/10.1016/j.vaccine.2015.01.036 |
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