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Complete genome sequence of a novel infectious bronchitis virus strain circulating in China with a distinct S gene
An avian infectious bronchitis virus (IBV) was isolated and identified from a commercial layer flock vaccinated with live attenuated H120 vaccine in China, designed as ck/CH/IBTZ/2012. To determine the origination and evolution of this isolated strain, we have carried out a complete genome sequencin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089373/ https://www.ncbi.nlm.nih.gov/pubmed/24682939 http://dx.doi.org/10.1007/s11262-014-1063-y |
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author | Zhou, Sheng Tang, Mengjun Jiang, Yi Chen, Xu Shen, Xinyue Li, Jianmei Dai, Yabin Zou, Jianmin |
author_facet | Zhou, Sheng Tang, Mengjun Jiang, Yi Chen, Xu Shen, Xinyue Li, Jianmei Dai, Yabin Zou, Jianmin |
author_sort | Zhou, Sheng |
collection | PubMed |
description | An avian infectious bronchitis virus (IBV) was isolated and identified from a commercial layer flock vaccinated with live attenuated H120 vaccine in China, designed as ck/CH/IBTZ/2012. To determine the origination and evolution of this isolated strain, we have carried out a complete genome sequencing of this strain. The genome of the ck/CH/IBTZ/2012 strain is 27,691 nucleotides in length and includes more than 10 open reading frames. Sequence comparison and phylogenetic analysis based on the full-length genomic sequences showed that ck/CH/IBTZ/2012 is mostly related to the LX4-like strains. However, sequence analysis based on the spike protein (S) gene sequences revealed that ck/CH/IBTZ/2012 possesses a distinct S gene setting it apart from the Massachusetts-type strains and LX4-type strains. The cleavage site within the spike protein (S) of ck/CH/IBTZ/2012 is HRRKR, which is different from the majority of the IBVs in China for their cleavage sits are HRRRR. Recombination analysis showed that ck/CH/IBTZ/2012 is a chimeric virus with a LX4-like backbone except S gene which might be from an unknown strain. Based on the data presented in this paper, it can be concluded that genetic changes due to adaptive evolution and recombination both contributed to the origin of strain ck/CH/IBTZ/2012, which belongs to a new genotype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11262-014-1063-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7089373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-70893732020-03-23 Complete genome sequence of a novel infectious bronchitis virus strain circulating in China with a distinct S gene Zhou, Sheng Tang, Mengjun Jiang, Yi Chen, Xu Shen, Xinyue Li, Jianmei Dai, Yabin Zou, Jianmin Virus Genes Article An avian infectious bronchitis virus (IBV) was isolated and identified from a commercial layer flock vaccinated with live attenuated H120 vaccine in China, designed as ck/CH/IBTZ/2012. To determine the origination and evolution of this isolated strain, we have carried out a complete genome sequencing of this strain. The genome of the ck/CH/IBTZ/2012 strain is 27,691 nucleotides in length and includes more than 10 open reading frames. Sequence comparison and phylogenetic analysis based on the full-length genomic sequences showed that ck/CH/IBTZ/2012 is mostly related to the LX4-like strains. However, sequence analysis based on the spike protein (S) gene sequences revealed that ck/CH/IBTZ/2012 possesses a distinct S gene setting it apart from the Massachusetts-type strains and LX4-type strains. The cleavage site within the spike protein (S) of ck/CH/IBTZ/2012 is HRRKR, which is different from the majority of the IBVs in China for their cleavage sits are HRRRR. Recombination analysis showed that ck/CH/IBTZ/2012 is a chimeric virus with a LX4-like backbone except S gene which might be from an unknown strain. Based on the data presented in this paper, it can be concluded that genetic changes due to adaptive evolution and recombination both contributed to the origin of strain ck/CH/IBTZ/2012, which belongs to a new genotype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11262-014-1063-y) contains supplementary material, which is available to authorized users. Springer US 2014-03-30 2014 /pmc/articles/PMC7089373/ /pubmed/24682939 http://dx.doi.org/10.1007/s11262-014-1063-y Text en © Springer Science+Business Media New York 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Zhou, Sheng Tang, Mengjun Jiang, Yi Chen, Xu Shen, Xinyue Li, Jianmei Dai, Yabin Zou, Jianmin Complete genome sequence of a novel infectious bronchitis virus strain circulating in China with a distinct S gene |
title | Complete genome sequence of a novel infectious bronchitis virus strain circulating in China with a distinct S gene |
title_full | Complete genome sequence of a novel infectious bronchitis virus strain circulating in China with a distinct S gene |
title_fullStr | Complete genome sequence of a novel infectious bronchitis virus strain circulating in China with a distinct S gene |
title_full_unstemmed | Complete genome sequence of a novel infectious bronchitis virus strain circulating in China with a distinct S gene |
title_short | Complete genome sequence of a novel infectious bronchitis virus strain circulating in China with a distinct S gene |
title_sort | complete genome sequence of a novel infectious bronchitis virus strain circulating in china with a distinct s gene |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089373/ https://www.ncbi.nlm.nih.gov/pubmed/24682939 http://dx.doi.org/10.1007/s11262-014-1063-y |
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