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Completion of the Porcine Epidemic Diarrhoea Coronavirus (PEDV) Genome Sequence

The sequence of the replicase gene of porcine epidemic diarrhoea virus (PEDV) has been determined. This completes the sequence of the entire genome of strain CV777, which was found to be 28,033 nucleotides (nt) in length (excluding the poly A-tail). A cloning strategy, which involves primers based o...

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Autores principales: Kocherhans, Rolf, Bridgen, Anne, Ackermann, Mathias, Tobler, Kurt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kluwer Academic Publishers 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089135/
https://www.ncbi.nlm.nih.gov/pubmed/11724265
http://dx.doi.org/10.1023/A:1011831902219
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author Kocherhans, Rolf
Bridgen, Anne
Ackermann, Mathias
Tobler, Kurt
author_facet Kocherhans, Rolf
Bridgen, Anne
Ackermann, Mathias
Tobler, Kurt
author_sort Kocherhans, Rolf
collection PubMed
description The sequence of the replicase gene of porcine epidemic diarrhoea virus (PEDV) has been determined. This completes the sequence of the entire genome of strain CV777, which was found to be 28,033 nucleotides (nt) in length (excluding the poly A-tail). A cloning strategy, which involves primers based on conserved regions in the predicted ORF1 products from other coronaviruses whose genome sequence has been determined, was used to amplify the equivalent, but as yet unknown, sequence of PEDV. Primary sequences derived from these products were used to design additional primers resulting in the amplification and sequencing of the entire ORF1 of PEDV. Analysis of the nucleotide sequences revealed a small open reading frame (ORF) located near the 5′ end (no 99–137), and two large, slightly overlapping ORFs, ORF1a (nt 297–12650) and ORF1b (nt 12605–20641). The ORF1a and ORF1b sequences overlapped at a potential ribosomal frame shift site. The amino acid sequence analysis suggested the presence of several functional motifs within the putative ORF1 protein. By analogy to other coronavirus replicase gene products, three protease and one growth factor-like motif were seen in ORF1a, and one polymerase domain, one metal ion-binding domain, and one helicase motif could be assigned within ORF1b. Comparative amino acid sequence alignments revealed that PEDV is most closely related to human coronavirus (HCoV)-229E and transmissible gastroenteritis virus (TGEV) and less related to murine hepatitis virus (MHV) and infectious bronchitis virus (IBV). These results thus confirm and extend the findings from sequence analysis of the structural genes of PEDV.
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spelling pubmed-70891352020-03-23 Completion of the Porcine Epidemic Diarrhoea Coronavirus (PEDV) Genome Sequence Kocherhans, Rolf Bridgen, Anne Ackermann, Mathias Tobler, Kurt Virus Genes Article The sequence of the replicase gene of porcine epidemic diarrhoea virus (PEDV) has been determined. This completes the sequence of the entire genome of strain CV777, which was found to be 28,033 nucleotides (nt) in length (excluding the poly A-tail). A cloning strategy, which involves primers based on conserved regions in the predicted ORF1 products from other coronaviruses whose genome sequence has been determined, was used to amplify the equivalent, but as yet unknown, sequence of PEDV. Primary sequences derived from these products were used to design additional primers resulting in the amplification and sequencing of the entire ORF1 of PEDV. Analysis of the nucleotide sequences revealed a small open reading frame (ORF) located near the 5′ end (no 99–137), and two large, slightly overlapping ORFs, ORF1a (nt 297–12650) and ORF1b (nt 12605–20641). The ORF1a and ORF1b sequences overlapped at a potential ribosomal frame shift site. The amino acid sequence analysis suggested the presence of several functional motifs within the putative ORF1 protein. By analogy to other coronavirus replicase gene products, three protease and one growth factor-like motif were seen in ORF1a, and one polymerase domain, one metal ion-binding domain, and one helicase motif could be assigned within ORF1b. Comparative amino acid sequence alignments revealed that PEDV is most closely related to human coronavirus (HCoV)-229E and transmissible gastroenteritis virus (TGEV) and less related to murine hepatitis virus (MHV) and infectious bronchitis virus (IBV). These results thus confirm and extend the findings from sequence analysis of the structural genes of PEDV. Kluwer Academic Publishers 2001 /pmc/articles/PMC7089135/ /pubmed/11724265 http://dx.doi.org/10.1023/A:1011831902219 Text en © Kluwer Academic Publishers 2001 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
Kocherhans, Rolf
Bridgen, Anne
Ackermann, Mathias
Tobler, Kurt
Completion of the Porcine Epidemic Diarrhoea Coronavirus (PEDV) Genome Sequence
title Completion of the Porcine Epidemic Diarrhoea Coronavirus (PEDV) Genome Sequence
title_full Completion of the Porcine Epidemic Diarrhoea Coronavirus (PEDV) Genome Sequence
title_fullStr Completion of the Porcine Epidemic Diarrhoea Coronavirus (PEDV) Genome Sequence
title_full_unstemmed Completion of the Porcine Epidemic Diarrhoea Coronavirus (PEDV) Genome Sequence
title_short Completion of the Porcine Epidemic Diarrhoea Coronavirus (PEDV) Genome Sequence
title_sort completion of the porcine epidemic diarrhoea coronavirus (pedv) genome sequence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089135/
https://www.ncbi.nlm.nih.gov/pubmed/11724265
http://dx.doi.org/10.1023/A:1011831902219
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