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Re-annotation and re-analysis of the Campylobacter jejuni NCTC11168 genome sequence

BACKGROUND: Campylobacter jejuni is the leading bacterial cause of human gastroenteritis in the developed world. To improve our understanding of this important human pathogen, the C. jejuni NCTC11168 genome was sequenced and published in 2000. The original annotation was a milestone in Campylobacter...

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Autores principales: Gundogdu, Ozan, Bentley, Stephen D, Holden, Matt T, Parkhill, Julian, Dorrell, Nick, Wren, Brendan W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1899501/
https://www.ncbi.nlm.nih.gov/pubmed/17565669
http://dx.doi.org/10.1186/1471-2164-8-162
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author Gundogdu, Ozan
Bentley, Stephen D
Holden, Matt T
Parkhill, Julian
Dorrell, Nick
Wren, Brendan W
author_facet Gundogdu, Ozan
Bentley, Stephen D
Holden, Matt T
Parkhill, Julian
Dorrell, Nick
Wren, Brendan W
author_sort Gundogdu, Ozan
collection PubMed
description BACKGROUND: Campylobacter jejuni is the leading bacterial cause of human gastroenteritis in the developed world. To improve our understanding of this important human pathogen, the C. jejuni NCTC11168 genome was sequenced and published in 2000. The original annotation was a milestone in Campylobacter research, but is outdated. We now describe the complete re-annotation and re-analysis of the C. jejuni NCTC11168 genome using current database information, novel tools and annotation techniques not used during the original annotation. RESULTS: Re-annotation was carried out using sequence database searches such as FASTA, along with programs such as TMHMM for additional support. The re-annotation also utilises sequence data from additional Campylobacter strains and species not available during the original annotation. Re-annotation was accompanied by a full literature search that was incorporated into the updated EMBL file [EMBL: AL111168]. The C. jejuni NCTC11168 re-annotation reduced the total number of coding sequences from 1654 to 1643, of which 90.0% have additional information regarding the identification of new motifs and/or relevant literature. Re-annotation has led to 18.2% of coding sequence product functions being revised. CONCLUSIONS: Major updates were made to genes involved in the biosynthesis of important surface structures such as lipooligosaccharide, capsule and both O- and N-linked glycosylation. This re-annotation will be a key resource for Campylobacter research and will also provide a prototype for the re-annotation and re-interpretation of other bacterial genomes.
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spelling pubmed-18995012007-06-27 Re-annotation and re-analysis of the Campylobacter jejuni NCTC11168 genome sequence Gundogdu, Ozan Bentley, Stephen D Holden, Matt T Parkhill, Julian Dorrell, Nick Wren, Brendan W BMC Genomics Research Article BACKGROUND: Campylobacter jejuni is the leading bacterial cause of human gastroenteritis in the developed world. To improve our understanding of this important human pathogen, the C. jejuni NCTC11168 genome was sequenced and published in 2000. The original annotation was a milestone in Campylobacter research, but is outdated. We now describe the complete re-annotation and re-analysis of the C. jejuni NCTC11168 genome using current database information, novel tools and annotation techniques not used during the original annotation. RESULTS: Re-annotation was carried out using sequence database searches such as FASTA, along with programs such as TMHMM for additional support. The re-annotation also utilises sequence data from additional Campylobacter strains and species not available during the original annotation. Re-annotation was accompanied by a full literature search that was incorporated into the updated EMBL file [EMBL: AL111168]. The C. jejuni NCTC11168 re-annotation reduced the total number of coding sequences from 1654 to 1643, of which 90.0% have additional information regarding the identification of new motifs and/or relevant literature. Re-annotation has led to 18.2% of coding sequence product functions being revised. CONCLUSIONS: Major updates were made to genes involved in the biosynthesis of important surface structures such as lipooligosaccharide, capsule and both O- and N-linked glycosylation. This re-annotation will be a key resource for Campylobacter research and will also provide a prototype for the re-annotation and re-interpretation of other bacterial genomes. BioMed Central 2007-06-12 /pmc/articles/PMC1899501/ /pubmed/17565669 http://dx.doi.org/10.1186/1471-2164-8-162 Text en Copyright © 2007 Gundogdu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gundogdu, Ozan
Bentley, Stephen D
Holden, Matt T
Parkhill, Julian
Dorrell, Nick
Wren, Brendan W
Re-annotation and re-analysis of the Campylobacter jejuni NCTC11168 genome sequence
title Re-annotation and re-analysis of the Campylobacter jejuni NCTC11168 genome sequence
title_full Re-annotation and re-analysis of the Campylobacter jejuni NCTC11168 genome sequence
title_fullStr Re-annotation and re-analysis of the Campylobacter jejuni NCTC11168 genome sequence
title_full_unstemmed Re-annotation and re-analysis of the Campylobacter jejuni NCTC11168 genome sequence
title_short Re-annotation and re-analysis of the Campylobacter jejuni NCTC11168 genome sequence
title_sort re-annotation and re-analysis of the campylobacter jejuni nctc11168 genome sequence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1899501/
https://www.ncbi.nlm.nih.gov/pubmed/17565669
http://dx.doi.org/10.1186/1471-2164-8-162
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