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Evolutionary implications of genetic variations in the S1 gene of infectious bronchitis virus

The large number of phenotypically distinct strains of infectious bronchitis virus (IBV) provide a broad genetic background for examining naturally occurring coronavirus variation. Comparisons of the published nucleotide sequence of S1 genes of strains isolated in Europe, Japan and the USA and four...

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Autores principales: Li, Wang, Junker, Dave, Hock, Lisa, Ebiary, Elham, Collisson, Ellen W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134089/
https://www.ncbi.nlm.nih.gov/pubmed/7856318
http://dx.doi.org/10.1016/0168-1702(94)90132-5
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author Li, Wang
Junker, Dave
Hock, Lisa
Ebiary, Elham
Collisson, Ellen W.
author_facet Li, Wang
Junker, Dave
Hock, Lisa
Ebiary, Elham
Collisson, Ellen W.
author_sort Li, Wang
collection PubMed
description The large number of phenotypically distinct strains of infectious bronchitis virus (IBV) provide a broad genetic background for examining naturally occurring coronavirus variation. Comparisons of the published nucleotide sequence of S1 genes of strains isolated in Europe, Japan and the USA and four additional American strains described in this report identified 4 genetically distinct groups. The Dutch group was the most divergent sharing only about 60% identity with the American, Mass and European groups which were about 80% homologous with each other. Whereas the strains within the Mass, European and Dutch strains were at least 95% homologous, the strains within the American group were most variable, sharing about 80% identity. The hypervariable region (HVR) which tended to correlate with serotype extended from amino acid residue 53 to 148. In addition to the previously described putative recombination events in the S1 gene of PP14 and SE17, we have now described similar shifts in homology in the corresponding gene of the Gray, Holte, 6/82 (European strain), and Iowa strains. Although minor cross-over sites were identified in the more conserved 3' end at approximately nt 1000 and 1400, a frequently used hot-spot for recombination extended from nt 25 to a region immediately upstream of, but not including, the hypervariable region (HVR). In addition to point mutations, deletions, and insertions, recombination often involving Mass-like and Ark-like sequences, is a commonly used mechanism responsible for the evolution of IBV.
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spelling pubmed-71340892020-04-08 Evolutionary implications of genetic variations in the S1 gene of infectious bronchitis virus Li, Wang Junker, Dave Hock, Lisa Ebiary, Elham Collisson, Ellen W. Virus Res Article The large number of phenotypically distinct strains of infectious bronchitis virus (IBV) provide a broad genetic background for examining naturally occurring coronavirus variation. Comparisons of the published nucleotide sequence of S1 genes of strains isolated in Europe, Japan and the USA and four additional American strains described in this report identified 4 genetically distinct groups. The Dutch group was the most divergent sharing only about 60% identity with the American, Mass and European groups which were about 80% homologous with each other. Whereas the strains within the Mass, European and Dutch strains were at least 95% homologous, the strains within the American group were most variable, sharing about 80% identity. The hypervariable region (HVR) which tended to correlate with serotype extended from amino acid residue 53 to 148. In addition to the previously described putative recombination events in the S1 gene of PP14 and SE17, we have now described similar shifts in homology in the corresponding gene of the Gray, Holte, 6/82 (European strain), and Iowa strains. Although minor cross-over sites were identified in the more conserved 3' end at approximately nt 1000 and 1400, a frequently used hot-spot for recombination extended from nt 25 to a region immediately upstream of, but not including, the hypervariable region (HVR). In addition to point mutations, deletions, and insertions, recombination often involving Mass-like and Ark-like sequences, is a commonly used mechanism responsible for the evolution of IBV. Published by Elsevier B.V. 1994-12 2002-11-13 /pmc/articles/PMC7134089/ /pubmed/7856318 http://dx.doi.org/10.1016/0168-1702(94)90132-5 Text en Copyright © 1994 Published by Elsevier B.V. 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
Li, Wang
Junker, Dave
Hock, Lisa
Ebiary, Elham
Collisson, Ellen W.
Evolutionary implications of genetic variations in the S1 gene of infectious bronchitis virus
title Evolutionary implications of genetic variations in the S1 gene of infectious bronchitis virus
title_full Evolutionary implications of genetic variations in the S1 gene of infectious bronchitis virus
title_fullStr Evolutionary implications of genetic variations in the S1 gene of infectious bronchitis virus
title_full_unstemmed Evolutionary implications of genetic variations in the S1 gene of infectious bronchitis virus
title_short Evolutionary implications of genetic variations in the S1 gene of infectious bronchitis virus
title_sort evolutionary implications of genetic variations in the s1 gene of infectious bronchitis virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134089/
https://www.ncbi.nlm.nih.gov/pubmed/7856318
http://dx.doi.org/10.1016/0168-1702(94)90132-5
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