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Sequence analysis of infectious bronchitis virus isolates from the 1960s in the United States

To better understand the molecular epidemiology of infectious bronchitis virus (IBV) in the United States following the introduction of commercial IBV vaccines, we sequenced the S1 and N structural protein genes of thirteen IBV field isolates collected in the 1960s. Analysis of the S1 sequence showe...

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Autores principales: Mondal, Shankar, Chang, Yung-Fu, Balasuriya, Udeni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087199/
https://www.ncbi.nlm.nih.gov/pubmed/23065112
http://dx.doi.org/10.1007/s00705-012-1500-y
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author Mondal, Shankar
Chang, Yung-Fu
Balasuriya, Udeni
author_facet Mondal, Shankar
Chang, Yung-Fu
Balasuriya, Udeni
author_sort Mondal, Shankar
collection PubMed
description To better understand the molecular epidemiology of infectious bronchitis virus (IBV) in the United States following the introduction of commercial IBV vaccines, we sequenced the S1 and N structural protein genes of thirteen IBV field isolates collected in the 1960s. Analysis of the S1 sequence showed that seven isolates were of the Massachusetts (Mass) genotype, five were SE17, and one was of the Connecticut (Conn) genotype, suggesting that these three IBVs were circulating in commercial poultry raised in different regions in the United States during the 1960s. The S1 genes of Mass-type isolates had high levels of sequence variation, representing 81.3-81.9 % nucleotide (nt) and 77.3-78.7 % amino acid (aa) identity when compared to those of the SE17-type isolates. In contrast, the N genes from the same isolates were less variable (>92 % nt and >93 % aa identity) when compared to those of the SE17-type isolates. Phylogenetic analysis based on the S1 gene indicated that one isolate (L748) was more closely related to the Mass type. In contrast, phylogenetic analysis based on the N gene showed that L748 was more closely related to the SE17 type, indicating that there had been exchange of S1 genetic materials between Mass- and SE17-like viruses. In addition, the Mass-type isolates had high levels of sequence identity in the S1 gene compared with widely used modified live vaccines (Mass41, Ma5 and H120) and modern field strains from the USA and other countries, suggesting a common ancestor. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00705-012-1500-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-70871992020-03-23 Sequence analysis of infectious bronchitis virus isolates from the 1960s in the United States Mondal, Shankar Chang, Yung-Fu Balasuriya, Udeni Arch Virol Annotated Sequence Record To better understand the molecular epidemiology of infectious bronchitis virus (IBV) in the United States following the introduction of commercial IBV vaccines, we sequenced the S1 and N structural protein genes of thirteen IBV field isolates collected in the 1960s. Analysis of the S1 sequence showed that seven isolates were of the Massachusetts (Mass) genotype, five were SE17, and one was of the Connecticut (Conn) genotype, suggesting that these three IBVs were circulating in commercial poultry raised in different regions in the United States during the 1960s. The S1 genes of Mass-type isolates had high levels of sequence variation, representing 81.3-81.9 % nucleotide (nt) and 77.3-78.7 % amino acid (aa) identity when compared to those of the SE17-type isolates. In contrast, the N genes from the same isolates were less variable (>92 % nt and >93 % aa identity) when compared to those of the SE17-type isolates. Phylogenetic analysis based on the S1 gene indicated that one isolate (L748) was more closely related to the Mass type. In contrast, phylogenetic analysis based on the N gene showed that L748 was more closely related to the SE17 type, indicating that there had been exchange of S1 genetic materials between Mass- and SE17-like viruses. In addition, the Mass-type isolates had high levels of sequence identity in the S1 gene compared with widely used modified live vaccines (Mass41, Ma5 and H120) and modern field strains from the USA and other countries, suggesting a common ancestor. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00705-012-1500-y) contains supplementary material, which is available to authorized users. Springer Vienna 2012-10-11 2013 /pmc/articles/PMC7087199/ /pubmed/23065112 http://dx.doi.org/10.1007/s00705-012-1500-y Text en © Springer-Verlag Wien 2012 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 Annotated Sequence Record
Mondal, Shankar
Chang, Yung-Fu
Balasuriya, Udeni
Sequence analysis of infectious bronchitis virus isolates from the 1960s in the United States
title Sequence analysis of infectious bronchitis virus isolates from the 1960s in the United States
title_full Sequence analysis of infectious bronchitis virus isolates from the 1960s in the United States
title_fullStr Sequence analysis of infectious bronchitis virus isolates from the 1960s in the United States
title_full_unstemmed Sequence analysis of infectious bronchitis virus isolates from the 1960s in the United States
title_short Sequence analysis of infectious bronchitis virus isolates from the 1960s in the United States
title_sort sequence analysis of infectious bronchitis virus isolates from the 1960s in the united states
topic Annotated Sequence Record
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087199/
https://www.ncbi.nlm.nih.gov/pubmed/23065112
http://dx.doi.org/10.1007/s00705-012-1500-y
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