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Comparative Genomic Analysis Identifies a Campylobacter Clade Deficient in Selenium Metabolism

The nonthermotolerant Campylobacter species C. fetus, C. hyointestinalis, C. iguaniorum, and C. lanienae form a distinct phylogenetic cluster within the genus. These species are primarily isolated from foraging (swine) or grazing (e.g., cattle, sheep) animals and cause sporadic and infrequent human...

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Autores principales: Miller, William G., Yee, Emma, Lopes, Bruno S., Chapman, Mary H., Huynh, Steven, Bono, James L., Parker, Craig T., Strachan, Norval J.C., Forbes, Ken J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570042/
https://www.ncbi.nlm.nih.gov/pubmed/28854596
http://dx.doi.org/10.1093/gbe/evx093
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author Miller, William G.
Yee, Emma
Lopes, Bruno S.
Chapman, Mary H.
Huynh, Steven
Bono, James L.
Parker, Craig T.
Strachan, Norval J.C.
Forbes, Ken J.
author_facet Miller, William G.
Yee, Emma
Lopes, Bruno S.
Chapman, Mary H.
Huynh, Steven
Bono, James L.
Parker, Craig T.
Strachan, Norval J.C.
Forbes, Ken J.
author_sort Miller, William G.
collection PubMed
description The nonthermotolerant Campylobacter species C. fetus, C. hyointestinalis, C. iguaniorum, and C. lanienae form a distinct phylogenetic cluster within the genus. These species are primarily isolated from foraging (swine) or grazing (e.g., cattle, sheep) animals and cause sporadic and infrequent human illness. Previous typing studies identified three putative novel C. lanienae-related taxa, based on either MLST or atpA sequence data. To further characterize these putative novel taxa and the C. fetus group as a whole, 76 genomes were sequenced, either to completion or to draft level. These genomes represent 26 C. lanienae strains and 50 strains of the three novel taxa. C. fetus, C. hyointestinalis and C. iguaniorum genomes were previously sequenced to completion; therefore, a comparative genomic analysis across the entire C. fetus group was conducted (including average nucleotide identity analysis) that supports the initial identification of these three novel Campylobacter species. Furthermore, C. lanienae and the three putative novel species form a discrete clade within the C. fetus group, which we have termed the C. lanienae clade. This clade is distinguished from other members of the C. fetus group by a reduced genome size and distinct CRISPR/Cas systems. Moreover, there are two signature characteristics of the C. lanienae clade. C. lanienae clade genomes carry four to ten unlinked and similar, but nonidentical, flagellin genes. Additionally, all 76 C. lanienae clade genomes sequenced demonstrate a complete absence of genes related to selenium metabolism, including genes encoding the selenocysteine insertion machinery, selenoproteins, and the selenocysteinyl tRNA.
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spelling pubmed-55700422017-08-29 Comparative Genomic Analysis Identifies a Campylobacter Clade Deficient in Selenium Metabolism Miller, William G. Yee, Emma Lopes, Bruno S. Chapman, Mary H. Huynh, Steven Bono, James L. Parker, Craig T. Strachan, Norval J.C. Forbes, Ken J. Genome Biol Evol Research Article The nonthermotolerant Campylobacter species C. fetus, C. hyointestinalis, C. iguaniorum, and C. lanienae form a distinct phylogenetic cluster within the genus. These species are primarily isolated from foraging (swine) or grazing (e.g., cattle, sheep) animals and cause sporadic and infrequent human illness. Previous typing studies identified three putative novel C. lanienae-related taxa, based on either MLST or atpA sequence data. To further characterize these putative novel taxa and the C. fetus group as a whole, 76 genomes were sequenced, either to completion or to draft level. These genomes represent 26 C. lanienae strains and 50 strains of the three novel taxa. C. fetus, C. hyointestinalis and C. iguaniorum genomes were previously sequenced to completion; therefore, a comparative genomic analysis across the entire C. fetus group was conducted (including average nucleotide identity analysis) that supports the initial identification of these three novel Campylobacter species. Furthermore, C. lanienae and the three putative novel species form a discrete clade within the C. fetus group, which we have termed the C. lanienae clade. This clade is distinguished from other members of the C. fetus group by a reduced genome size and distinct CRISPR/Cas systems. Moreover, there are two signature characteristics of the C. lanienae clade. C. lanienae clade genomes carry four to ten unlinked and similar, but nonidentical, flagellin genes. Additionally, all 76 C. lanienae clade genomes sequenced demonstrate a complete absence of genes related to selenium metabolism, including genes encoding the selenocysteine insertion machinery, selenoproteins, and the selenocysteinyl tRNA. Oxford University Press 2017-05-10 /pmc/articles/PMC5570042/ /pubmed/28854596 http://dx.doi.org/10.1093/gbe/evx093 Text en Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution 2017. This work is written by US Government employees and is in the public domain in the US.
spellingShingle Research Article
Miller, William G.
Yee, Emma
Lopes, Bruno S.
Chapman, Mary H.
Huynh, Steven
Bono, James L.
Parker, Craig T.
Strachan, Norval J.C.
Forbes, Ken J.
Comparative Genomic Analysis Identifies a Campylobacter Clade Deficient in Selenium Metabolism
title Comparative Genomic Analysis Identifies a Campylobacter Clade Deficient in Selenium Metabolism
title_full Comparative Genomic Analysis Identifies a Campylobacter Clade Deficient in Selenium Metabolism
title_fullStr Comparative Genomic Analysis Identifies a Campylobacter Clade Deficient in Selenium Metabolism
title_full_unstemmed Comparative Genomic Analysis Identifies a Campylobacter Clade Deficient in Selenium Metabolism
title_short Comparative Genomic Analysis Identifies a Campylobacter Clade Deficient in Selenium Metabolism
title_sort comparative genomic analysis identifies a campylobacter clade deficient in selenium metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570042/
https://www.ncbi.nlm.nih.gov/pubmed/28854596
http://dx.doi.org/10.1093/gbe/evx093
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