Cargando…

Genome sequence and origin analyses of the recombinant novel IBV virulent isolate SAIBK2

Recombination between infectious bronchitis viruses (IBVs), together with point mutations, insertions, and deletions, is thought to be responsible for the emergence of new IBV variants. SAIBK2 is a nephropathogenic strain isolated from layer flocks vaccinated with live attenuated H120 vaccine in Sic...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Xuan, Yang, Xin, Xu, Pengwei, Zhou, Long, Zhang, Zhikun, Wang, Hongning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088859/
https://www.ncbi.nlm.nih.gov/pubmed/27108998
http://dx.doi.org/10.1007/s11262-016-1337-7
_version_ 1783509626453491712
author Wu, Xuan
Yang, Xin
Xu, Pengwei
Zhou, Long
Zhang, Zhikun
Wang, Hongning
author_facet Wu, Xuan
Yang, Xin
Xu, Pengwei
Zhou, Long
Zhang, Zhikun
Wang, Hongning
author_sort Wu, Xuan
collection PubMed
description Recombination between infectious bronchitis viruses (IBVs), together with point mutations, insertions, and deletions, is thought to be responsible for the emergence of new IBV variants. SAIBK2 is a nephropathogenic strain isolated from layer flocks vaccinated with live attenuated H120 vaccine in Sichuan province, China in 2011. SAIBK2 causes severe kidney lesions and results in 50 % mortality in 30-day-old specific-pathogen-free chickens (with a dose of 10(5) EID(50)/0.1 mL SAIBK2 per chicken). The complete genome of SAIBK2 consists of 27669 nucleotides, excluding the poly-A tail at the 3′ end. SAIBK2 has the highest identity to YX10 in terms of complete genome. Phylogenetic analysis of complete sequence showed that SAIBK2 belongs to the most dominant genotype in China. Comparison and recombination analyses with other IBV strains revealed that SAIBK2 may originate from recombination events among a YX10-, a YN-, and a Mass-like strain. Furthermore, whole gene 5 and parts of nsp 3, nsp 4, nsp 16, and N genes are involved in the recombination events, and the uptake of these regions from YN and Mass strains by SAIBK2 may increase its replication efficiency and be responsible for its increased virulence in specific-pathogen-free chickens.
format Online
Article
Text
id pubmed-7088859
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-70888592020-03-23 Genome sequence and origin analyses of the recombinant novel IBV virulent isolate SAIBK2 Wu, Xuan Yang, Xin Xu, Pengwei Zhou, Long Zhang, Zhikun Wang, Hongning Virus Genes Article Recombination between infectious bronchitis viruses (IBVs), together with point mutations, insertions, and deletions, is thought to be responsible for the emergence of new IBV variants. SAIBK2 is a nephropathogenic strain isolated from layer flocks vaccinated with live attenuated H120 vaccine in Sichuan province, China in 2011. SAIBK2 causes severe kidney lesions and results in 50 % mortality in 30-day-old specific-pathogen-free chickens (with a dose of 10(5) EID(50)/0.1 mL SAIBK2 per chicken). The complete genome of SAIBK2 consists of 27669 nucleotides, excluding the poly-A tail at the 3′ end. SAIBK2 has the highest identity to YX10 in terms of complete genome. Phylogenetic analysis of complete sequence showed that SAIBK2 belongs to the most dominant genotype in China. Comparison and recombination analyses with other IBV strains revealed that SAIBK2 may originate from recombination events among a YX10-, a YN-, and a Mass-like strain. Furthermore, whole gene 5 and parts of nsp 3, nsp 4, nsp 16, and N genes are involved in the recombination events, and the uptake of these regions from YN and Mass strains by SAIBK2 may increase its replication efficiency and be responsible for its increased virulence in specific-pathogen-free chickens. Springer US 2016-04-25 2016 /pmc/articles/PMC7088859/ /pubmed/27108998 http://dx.doi.org/10.1007/s11262-016-1337-7 Text en © Springer Science+Business Media New York 2016 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
Wu, Xuan
Yang, Xin
Xu, Pengwei
Zhou, Long
Zhang, Zhikun
Wang, Hongning
Genome sequence and origin analyses of the recombinant novel IBV virulent isolate SAIBK2
title Genome sequence and origin analyses of the recombinant novel IBV virulent isolate SAIBK2
title_full Genome sequence and origin analyses of the recombinant novel IBV virulent isolate SAIBK2
title_fullStr Genome sequence and origin analyses of the recombinant novel IBV virulent isolate SAIBK2
title_full_unstemmed Genome sequence and origin analyses of the recombinant novel IBV virulent isolate SAIBK2
title_short Genome sequence and origin analyses of the recombinant novel IBV virulent isolate SAIBK2
title_sort genome sequence and origin analyses of the recombinant novel ibv virulent isolate saibk2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088859/
https://www.ncbi.nlm.nih.gov/pubmed/27108998
http://dx.doi.org/10.1007/s11262-016-1337-7
work_keys_str_mv AT wuxuan genomesequenceandoriginanalysesoftherecombinantnovelibvvirulentisolatesaibk2
AT yangxin genomesequenceandoriginanalysesoftherecombinantnovelibvvirulentisolatesaibk2
AT xupengwei genomesequenceandoriginanalysesoftherecombinantnovelibvvirulentisolatesaibk2
AT zhoulong genomesequenceandoriginanalysesoftherecombinantnovelibvvirulentisolatesaibk2
AT zhangzhikun genomesequenceandoriginanalysesoftherecombinantnovelibvvirulentisolatesaibk2
AT wanghongning genomesequenceandoriginanalysesoftherecombinantnovelibvvirulentisolatesaibk2