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Genomic variations define divergence of water/wildlife-associated Campylobacter jejuni niche specialists from common clonal complexes

Although the major food-borne pathogen Campylobacter jejuni has been isolated from diverse animal, human and environmental sources, our knowledge of genomic diversity in C. jejuni is based exclusively on human or human food-chain-associated isolates. Studies employing multilocus sequence typing have...

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Autores principales: Hepworth, Philip J, Ashelford, Kevin E, Hinds, Jason, Gould, Katherine A, Witney, Adam A, Williams, Nicola J, Leatherbarrow, Howard, French, Nigel P, Birtles, Richard J, Mendonca, Chriselle, Dorrell, Nick, Wren, Brendan W, Wigley, Paul, Hall, Neil, Winstanley, Craig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569610/
https://www.ncbi.nlm.nih.gov/pubmed/21418497
http://dx.doi.org/10.1111/j.1462-2920.2011.02461.x
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author Hepworth, Philip J
Ashelford, Kevin E
Hinds, Jason
Gould, Katherine A
Witney, Adam A
Williams, Nicola J
Leatherbarrow, Howard
French, Nigel P
Birtles, Richard J
Mendonca, Chriselle
Dorrell, Nick
Wren, Brendan W
Wigley, Paul
Hall, Neil
Winstanley, Craig
author_facet Hepworth, Philip J
Ashelford, Kevin E
Hinds, Jason
Gould, Katherine A
Witney, Adam A
Williams, Nicola J
Leatherbarrow, Howard
French, Nigel P
Birtles, Richard J
Mendonca, Chriselle
Dorrell, Nick
Wren, Brendan W
Wigley, Paul
Hall, Neil
Winstanley, Craig
author_sort Hepworth, Philip J
collection PubMed
description Although the major food-borne pathogen Campylobacter jejuni has been isolated from diverse animal, human and environmental sources, our knowledge of genomic diversity in C. jejuni is based exclusively on human or human food-chain-associated isolates. Studies employing multilocus sequence typing have indicated that some clonal complexes are more commonly associated with particular sources. Using comparative genomic hybridization on a collection of 80 isolates representing diverse sources and clonal complexes, we identified a separate clade comprising a group of water/wildlife isolates of C. jejuni with multilocus sequence types uncharacteristic of human food-chain-associated isolates. By genome sequencing one representative of this diverse group (C. jejuni 1336), and a representative of the bank-vole niche specialist ST-3704 (C. jejuni 414), we identified deletions of genomic regions normally carried by human food-chain-associated C. jejuni. Several of the deleted regions included genes implicated in chicken colonization or in virulence. Novel genomic insertions contributing to the accessory genomes of strains 1336 and 414 were identified. Comparative analysis using PCR assays indicated that novel regions were common but not ubiquitous among the water/wildlife group of isolates, indicating further genomic diversity among this group, whereas all ST-3704 isolates carried the same novel accessory regions. While strain 1336 was able to colonize chicks, strain 414 was not, suggesting that regions specifically absent from the genome of strain 414 may play an important role in this common route of Campylobacter infection of humans. We suggest that the genomic divergence observed constitutes evidence of adaptation leading to niche specialization.
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spelling pubmed-35696102013-02-25 Genomic variations define divergence of water/wildlife-associated Campylobacter jejuni niche specialists from common clonal complexes Hepworth, Philip J Ashelford, Kevin E Hinds, Jason Gould, Katherine A Witney, Adam A Williams, Nicola J Leatherbarrow, Howard French, Nigel P Birtles, Richard J Mendonca, Chriselle Dorrell, Nick Wren, Brendan W Wigley, Paul Hall, Neil Winstanley, Craig Environ Microbiol Research Articles Although the major food-borne pathogen Campylobacter jejuni has been isolated from diverse animal, human and environmental sources, our knowledge of genomic diversity in C. jejuni is based exclusively on human or human food-chain-associated isolates. Studies employing multilocus sequence typing have indicated that some clonal complexes are more commonly associated with particular sources. Using comparative genomic hybridization on a collection of 80 isolates representing diverse sources and clonal complexes, we identified a separate clade comprising a group of water/wildlife isolates of C. jejuni with multilocus sequence types uncharacteristic of human food-chain-associated isolates. By genome sequencing one representative of this diverse group (C. jejuni 1336), and a representative of the bank-vole niche specialist ST-3704 (C. jejuni 414), we identified deletions of genomic regions normally carried by human food-chain-associated C. jejuni. Several of the deleted regions included genes implicated in chicken colonization or in virulence. Novel genomic insertions contributing to the accessory genomes of strains 1336 and 414 were identified. Comparative analysis using PCR assays indicated that novel regions were common but not ubiquitous among the water/wildlife group of isolates, indicating further genomic diversity among this group, whereas all ST-3704 isolates carried the same novel accessory regions. While strain 1336 was able to colonize chicks, strain 414 was not, suggesting that regions specifically absent from the genome of strain 414 may play an important role in this common route of Campylobacter infection of humans. We suggest that the genomic divergence observed constitutes evidence of adaptation leading to niche specialization. Blackwell Publishing Ltd 2011-06 2011-03-21 /pmc/articles/PMC3569610/ /pubmed/21418497 http://dx.doi.org/10.1111/j.1462-2920.2011.02461.x Text en © 2011 Society for Applied Microbiology and Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Hepworth, Philip J
Ashelford, Kevin E
Hinds, Jason
Gould, Katherine A
Witney, Adam A
Williams, Nicola J
Leatherbarrow, Howard
French, Nigel P
Birtles, Richard J
Mendonca, Chriselle
Dorrell, Nick
Wren, Brendan W
Wigley, Paul
Hall, Neil
Winstanley, Craig
Genomic variations define divergence of water/wildlife-associated Campylobacter jejuni niche specialists from common clonal complexes
title Genomic variations define divergence of water/wildlife-associated Campylobacter jejuni niche specialists from common clonal complexes
title_full Genomic variations define divergence of water/wildlife-associated Campylobacter jejuni niche specialists from common clonal complexes
title_fullStr Genomic variations define divergence of water/wildlife-associated Campylobacter jejuni niche specialists from common clonal complexes
title_full_unstemmed Genomic variations define divergence of water/wildlife-associated Campylobacter jejuni niche specialists from common clonal complexes
title_short Genomic variations define divergence of water/wildlife-associated Campylobacter jejuni niche specialists from common clonal complexes
title_sort genomic variations define divergence of water/wildlife-associated campylobacter jejuni niche specialists from common clonal complexes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569610/
https://www.ncbi.nlm.nih.gov/pubmed/21418497
http://dx.doi.org/10.1111/j.1462-2920.2011.02461.x
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