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Effects of hypervariable regions in spike protein on pathogenicity, tropism, and serotypes of infectious bronchitis virus
To study the roles of hypervariable regions (HVRs) in receptor-binding subunit S1 of the spike protein, we manipulated the genome of the IBV Beaudette strain using a reverse genetics system to construct seven recombinant strains by separately or simultaneously replacing the three HVRs of the Beaudet...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114591/ https://www.ncbi.nlm.nih.gov/pubmed/29684409 http://dx.doi.org/10.1016/j.virusres.2018.04.013 |
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author | Shan, Dan Fang, Shouguo Han, Zongxi Ai, Hui Zhao, Wenjun Chen, Yuqiu Jiang, Lei Liu, Shengwang |
author_facet | Shan, Dan Fang, Shouguo Han, Zongxi Ai, Hui Zhao, Wenjun Chen, Yuqiu Jiang, Lei Liu, Shengwang |
author_sort | Shan, Dan |
collection | PubMed |
description | To study the roles of hypervariable regions (HVRs) in receptor-binding subunit S1 of the spike protein, we manipulated the genome of the IBV Beaudette strain using a reverse genetics system to construct seven recombinant strains by separately or simultaneously replacing the three HVRs of the Beaudette strain with the corresponding fragments from a QX-like nephropathogenic isolate ck/CH/LDL/091022 from China. We characterized the growth properties of these recombinant IBVs in Vero cells and embryonated eggs, and their pathogenicity, tropism, and serotypes in specific pathogen-free (SPF) chickens. All seven recombinant IBVs proliferated in Vero cells, but the heterogenous HVRs could reduce their capacity for adsorption during in vitro infection. The recombinant IBVs did not significantly increase the pathogenicity compared with the Beaudette strain in SPF chickens, and they still shared the same serotype as the Beaudette strain, but the antigenic relatedness values between the recombinant strain and Beaudette strain generally decreased with the increase in the number of the HVRs exchanged. The results of this study demonstrate the functions of HVRs and they may help to develop a vaccine candidate, as well as providing insights into the prevention and control of IBV. |
format | Online Article Text |
id | pubmed-7114591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71145912020-04-02 Effects of hypervariable regions in spike protein on pathogenicity, tropism, and serotypes of infectious bronchitis virus Shan, Dan Fang, Shouguo Han, Zongxi Ai, Hui Zhao, Wenjun Chen, Yuqiu Jiang, Lei Liu, Shengwang Virus Res Article To study the roles of hypervariable regions (HVRs) in receptor-binding subunit S1 of the spike protein, we manipulated the genome of the IBV Beaudette strain using a reverse genetics system to construct seven recombinant strains by separately or simultaneously replacing the three HVRs of the Beaudette strain with the corresponding fragments from a QX-like nephropathogenic isolate ck/CH/LDL/091022 from China. We characterized the growth properties of these recombinant IBVs in Vero cells and embryonated eggs, and their pathogenicity, tropism, and serotypes in specific pathogen-free (SPF) chickens. All seven recombinant IBVs proliferated in Vero cells, but the heterogenous HVRs could reduce their capacity for adsorption during in vitro infection. The recombinant IBVs did not significantly increase the pathogenicity compared with the Beaudette strain in SPF chickens, and they still shared the same serotype as the Beaudette strain, but the antigenic relatedness values between the recombinant strain and Beaudette strain generally decreased with the increase in the number of the HVRs exchanged. The results of this study demonstrate the functions of HVRs and they may help to develop a vaccine candidate, as well as providing insights into the prevention and control of IBV. Elsevier B.V. 2018-05-02 2018-04-21 /pmc/articles/PMC7114591/ /pubmed/29684409 http://dx.doi.org/10.1016/j.virusres.2018.04.013 Text en © 2018 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 Shan, Dan Fang, Shouguo Han, Zongxi Ai, Hui Zhao, Wenjun Chen, Yuqiu Jiang, Lei Liu, Shengwang Effects of hypervariable regions in spike protein on pathogenicity, tropism, and serotypes of infectious bronchitis virus |
title | Effects of hypervariable regions in spike protein on pathogenicity, tropism, and serotypes of infectious bronchitis virus |
title_full | Effects of hypervariable regions in spike protein on pathogenicity, tropism, and serotypes of infectious bronchitis virus |
title_fullStr | Effects of hypervariable regions in spike protein on pathogenicity, tropism, and serotypes of infectious bronchitis virus |
title_full_unstemmed | Effects of hypervariable regions in spike protein on pathogenicity, tropism, and serotypes of infectious bronchitis virus |
title_short | Effects of hypervariable regions in spike protein on pathogenicity, tropism, and serotypes of infectious bronchitis virus |
title_sort | effects of hypervariable regions in spike protein on pathogenicity, tropism, and serotypes of infectious bronchitis virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114591/ https://www.ncbi.nlm.nih.gov/pubmed/29684409 http://dx.doi.org/10.1016/j.virusres.2018.04.013 |
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