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Complete sequences of 3′ end coding region for structural protein genes of turkey coronavirus

Overlapping fragments of genomic RNA spanning 6963 nucleotides from 5′ end of spike (S) protein gene to 3′ end of nucleocapsid (N) protein gene of turkey coronavirus (TCoV) were amplified by reverse-transcription-polymerase chain reaction (RT-PCR). The primers were derived from the corresponding seq...

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Autores principales: Lin, Tsang Long, Loa, Chien Chang, Wu, Ching Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114097/
https://www.ncbi.nlm.nih.gov/pubmed/15522448
http://dx.doi.org/10.1016/j.virusres.2004.06.003
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author Lin, Tsang Long
Loa, Chien Chang
Wu, Ching Ching
author_facet Lin, Tsang Long
Loa, Chien Chang
Wu, Ching Ching
author_sort Lin, Tsang Long
collection PubMed
description Overlapping fragments of genomic RNA spanning 6963 nucleotides from 5′ end of spike (S) protein gene to 3′ end of nucleocapsid (N) protein gene of turkey coronavirus (TCoV) were amplified by reverse-transcription-polymerase chain reaction (RT-PCR). The primers were derived from the corresponding sequences of infectious bronchitis virus (IBV). The PCR products were cloned and sequenced and their nucleic acid structure and similarity to published sequences of other coronaviruses were analyzed. Sequencing and subsequent analysis revealed 9 open reading frames (ORFs) representing the entire S protein gene, tricistronic gene 3, membrane (M) protein gene, bicistronic gene 5, and N protein gene in the order of 5′–3′. The overall nucleic acid structures of these encoding regions of TCoV were very similar to the homologous regions of IBV. The consensus transcription-regulating sequence (TRS) of IBV, CT(T/G)AACAA, was highly conserved in TCoV genome at the levels of nucleotide sequence and location in regarding to the initiation codon of individual genes. Pair-wise comparison of gene 3, M gene, gene 5, or N gene sequences with their counterparts of IBV revealed high levels (82.1–92.0%) of similarity. Phylogenetic analysis based on the deduced amino acid sequences of S, M, or N protein demonstrated that TCoV was clustered within the same genomic lineage as the IBV strains while all the other mammalian coronaviruses were grouped into separate clusters corresponding to antigenic groups I or II. There were substantial differences of S protein sequence between TCoV and IBV with only 33.8–33.9% of similarity.
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spelling pubmed-71140972020-04-02 Complete sequences of 3′ end coding region for structural protein genes of turkey coronavirus Lin, Tsang Long Loa, Chien Chang Wu, Ching Ching Virus Res Article Overlapping fragments of genomic RNA spanning 6963 nucleotides from 5′ end of spike (S) protein gene to 3′ end of nucleocapsid (N) protein gene of turkey coronavirus (TCoV) were amplified by reverse-transcription-polymerase chain reaction (RT-PCR). The primers were derived from the corresponding sequences of infectious bronchitis virus (IBV). The PCR products were cloned and sequenced and their nucleic acid structure and similarity to published sequences of other coronaviruses were analyzed. Sequencing and subsequent analysis revealed 9 open reading frames (ORFs) representing the entire S protein gene, tricistronic gene 3, membrane (M) protein gene, bicistronic gene 5, and N protein gene in the order of 5′–3′. The overall nucleic acid structures of these encoding regions of TCoV were very similar to the homologous regions of IBV. The consensus transcription-regulating sequence (TRS) of IBV, CT(T/G)AACAA, was highly conserved in TCoV genome at the levels of nucleotide sequence and location in regarding to the initiation codon of individual genes. Pair-wise comparison of gene 3, M gene, gene 5, or N gene sequences with their counterparts of IBV revealed high levels (82.1–92.0%) of similarity. Phylogenetic analysis based on the deduced amino acid sequences of S, M, or N protein demonstrated that TCoV was clustered within the same genomic lineage as the IBV strains while all the other mammalian coronaviruses were grouped into separate clusters corresponding to antigenic groups I or II. There were substantial differences of S protein sequence between TCoV and IBV with only 33.8–33.9% of similarity. Elsevier B.V. 2004-11 2004-08-03 /pmc/articles/PMC7114097/ /pubmed/15522448 http://dx.doi.org/10.1016/j.virusres.2004.06.003 Text en Copyright © 2004 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
Lin, Tsang Long
Loa, Chien Chang
Wu, Ching Ching
Complete sequences of 3′ end coding region for structural protein genes of turkey coronavirus
title Complete sequences of 3′ end coding region for structural protein genes of turkey coronavirus
title_full Complete sequences of 3′ end coding region for structural protein genes of turkey coronavirus
title_fullStr Complete sequences of 3′ end coding region for structural protein genes of turkey coronavirus
title_full_unstemmed Complete sequences of 3′ end coding region for structural protein genes of turkey coronavirus
title_short Complete sequences of 3′ end coding region for structural protein genes of turkey coronavirus
title_sort complete sequences of 3′ end coding region for structural protein genes of turkey coronavirus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114097/
https://www.ncbi.nlm.nih.gov/pubmed/15522448
http://dx.doi.org/10.1016/j.virusres.2004.06.003
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