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Resolution of habitat-associated ecogenomic signatures in bacteriophage genomes and application to microbial source tracking

Just as the expansion in genome sequencing has revealed and permitted the exploitation of phylogenetic signals embedded in bacterial genomes, the application of metagenomics has begun to provide similar insights at the ecosystem level for microbial communities. However, little is known regarding thi...

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Autores principales: Ogilvie, Lesley A., Nzakizwanayo, Jonathan, Guppy, Fergus M., Dedi, Cinzia, Diston, David, Taylor, Huw, Ebdon, James, Jones, Brian V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864186/
https://www.ncbi.nlm.nih.gov/pubmed/29259289
http://dx.doi.org/10.1038/s41396-017-0015-7
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author Ogilvie, Lesley A.
Nzakizwanayo, Jonathan
Guppy, Fergus M.
Dedi, Cinzia
Diston, David
Taylor, Huw
Ebdon, James
Jones, Brian V.
author_facet Ogilvie, Lesley A.
Nzakizwanayo, Jonathan
Guppy, Fergus M.
Dedi, Cinzia
Diston, David
Taylor, Huw
Ebdon, James
Jones, Brian V.
author_sort Ogilvie, Lesley A.
collection PubMed
description Just as the expansion in genome sequencing has revealed and permitted the exploitation of phylogenetic signals embedded in bacterial genomes, the application of metagenomics has begun to provide similar insights at the ecosystem level for microbial communities. However, little is known regarding this aspect of bacteriophage associated with microbial ecosystems, and if phage encode discernible habitat-associated signals diagnostic of underlying microbiomes. Here we demonstrate that individual phage can encode clear habitat-related 'ecogenomic signatures', based on relative representation of phage-encoded gene homologues in metagenomic data sets. Furthermore, we show the ecogenomic signature encoded by the gut-associated ɸB124-14 can be used to segregate metagenomes according to environmental origin, and distinguish 'contaminated' environmental metagenomes (subject to simulated in silico human faecal pollution) from uncontaminated data sets. This indicates phage-encoded ecological signals likely possess sufficient discriminatory power for use in biotechnological applications, such as development of microbial source tracking tools for monitoring water quality.
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spelling pubmed-58641862018-03-23 Resolution of habitat-associated ecogenomic signatures in bacteriophage genomes and application to microbial source tracking Ogilvie, Lesley A. Nzakizwanayo, Jonathan Guppy, Fergus M. Dedi, Cinzia Diston, David Taylor, Huw Ebdon, James Jones, Brian V. ISME J Article Just as the expansion in genome sequencing has revealed and permitted the exploitation of phylogenetic signals embedded in bacterial genomes, the application of metagenomics has begun to provide similar insights at the ecosystem level for microbial communities. However, little is known regarding this aspect of bacteriophage associated with microbial ecosystems, and if phage encode discernible habitat-associated signals diagnostic of underlying microbiomes. Here we demonstrate that individual phage can encode clear habitat-related 'ecogenomic signatures', based on relative representation of phage-encoded gene homologues in metagenomic data sets. Furthermore, we show the ecogenomic signature encoded by the gut-associated ɸB124-14 can be used to segregate metagenomes according to environmental origin, and distinguish 'contaminated' environmental metagenomes (subject to simulated in silico human faecal pollution) from uncontaminated data sets. This indicates phage-encoded ecological signals likely possess sufficient discriminatory power for use in biotechnological applications, such as development of microbial source tracking tools for monitoring water quality. Nature Publishing Group UK 2017-12-19 2018-04 /pmc/articles/PMC5864186/ /pubmed/29259289 http://dx.doi.org/10.1038/s41396-017-0015-7 Text en © The Author(s) 2017 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ogilvie, Lesley A.
Nzakizwanayo, Jonathan
Guppy, Fergus M.
Dedi, Cinzia
Diston, David
Taylor, Huw
Ebdon, James
Jones, Brian V.
Resolution of habitat-associated ecogenomic signatures in bacteriophage genomes and application to microbial source tracking
title Resolution of habitat-associated ecogenomic signatures in bacteriophage genomes and application to microbial source tracking
title_full Resolution of habitat-associated ecogenomic signatures in bacteriophage genomes and application to microbial source tracking
title_fullStr Resolution of habitat-associated ecogenomic signatures in bacteriophage genomes and application to microbial source tracking
title_full_unstemmed Resolution of habitat-associated ecogenomic signatures in bacteriophage genomes and application to microbial source tracking
title_short Resolution of habitat-associated ecogenomic signatures in bacteriophage genomes and application to microbial source tracking
title_sort resolution of habitat-associated ecogenomic signatures in bacteriophage genomes and application to microbial source tracking
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864186/
https://www.ncbi.nlm.nih.gov/pubmed/29259289
http://dx.doi.org/10.1038/s41396-017-0015-7
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