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Comparative genomics of 274 Vibrio cholerae genomes reveals mobile functions structuring three niche dimensions

BACKGROUND: Vibrio cholerae is a globally dispersed pathogen that has evolved with humans for centuries, but also includes non-pathogenic environmental strains. Here, we identify the genomic variability underlying this remarkable persistence across the three major niche dimensions space, time, and h...

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Autores principales: Dutilh, Bas E, Thompson, Cristiane C, Vicente, Ana CP, Marin, Michel A, Lee, Clarence, Silva, Genivaldo GZ, Schmieder, Robert, Andrade, Bruno GN, Chimetto, Luciane, Cuevas, Daniel, Garza, Daniel R, Okeke, Iruka N, Aboderin, Aaron Oladipo, Spangler, Jessica, Ross, Tristen, Dinsdale, Elizabeth A, Thompson, Fabiano L, Harkins, Timothy T, Edwards, Robert A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141962/
https://www.ncbi.nlm.nih.gov/pubmed/25096633
http://dx.doi.org/10.1186/1471-2164-15-654
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author Dutilh, Bas E
Thompson, Cristiane C
Vicente, Ana CP
Marin, Michel A
Lee, Clarence
Silva, Genivaldo GZ
Schmieder, Robert
Andrade, Bruno GN
Chimetto, Luciane
Cuevas, Daniel
Garza, Daniel R
Okeke, Iruka N
Aboderin, Aaron Oladipo
Spangler, Jessica
Ross, Tristen
Dinsdale, Elizabeth A
Thompson, Fabiano L
Harkins, Timothy T
Edwards, Robert A
author_facet Dutilh, Bas E
Thompson, Cristiane C
Vicente, Ana CP
Marin, Michel A
Lee, Clarence
Silva, Genivaldo GZ
Schmieder, Robert
Andrade, Bruno GN
Chimetto, Luciane
Cuevas, Daniel
Garza, Daniel R
Okeke, Iruka N
Aboderin, Aaron Oladipo
Spangler, Jessica
Ross, Tristen
Dinsdale, Elizabeth A
Thompson, Fabiano L
Harkins, Timothy T
Edwards, Robert A
author_sort Dutilh, Bas E
collection PubMed
description BACKGROUND: Vibrio cholerae is a globally dispersed pathogen that has evolved with humans for centuries, but also includes non-pathogenic environmental strains. Here, we identify the genomic variability underlying this remarkable persistence across the three major niche dimensions space, time, and habitat. RESULTS: Taking an innovative approach of genome-wide association applicable to microbial genomes (GWAS-M), we classify 274 complete V. cholerae genomes by niche, including 39 newly sequenced for this study with the Ion Torrent DNA-sequencing platform. Niche metadata were collected for each strain and analyzed together with comprehensive annotations of genetic and genomic attributes, including point mutations (single-nucleotide polymorphisms, SNPs), protein families, functions and prophages. CONCLUSIONS: Our analysis revealed that genomic variations, in particular mobile functions including phages, prophages, transposable elements, and plasmids underlie the metadata structuring in each of the three niche dimensions. This underscores the role of phages and mobile elements as the most rapidly evolving elements in bacterial genomes, creating local endemicity (space), leading to temporal divergence (time), and allowing the invasion of new habitats. Together, we take a data-driven approach for comparative functional genomics that exploits high-volume genome sequencing and annotation, in conjunction with novel statistical and machine learning analyses to identify connections between genotype and phenotype on a genome-wide scale. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-654) contains supplementary material, which is available to authorized users.
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spelling pubmed-41419622014-08-28 Comparative genomics of 274 Vibrio cholerae genomes reveals mobile functions structuring three niche dimensions Dutilh, Bas E Thompson, Cristiane C Vicente, Ana CP Marin, Michel A Lee, Clarence Silva, Genivaldo GZ Schmieder, Robert Andrade, Bruno GN Chimetto, Luciane Cuevas, Daniel Garza, Daniel R Okeke, Iruka N Aboderin, Aaron Oladipo Spangler, Jessica Ross, Tristen Dinsdale, Elizabeth A Thompson, Fabiano L Harkins, Timothy T Edwards, Robert A BMC Genomics Research Article BACKGROUND: Vibrio cholerae is a globally dispersed pathogen that has evolved with humans for centuries, but also includes non-pathogenic environmental strains. Here, we identify the genomic variability underlying this remarkable persistence across the three major niche dimensions space, time, and habitat. RESULTS: Taking an innovative approach of genome-wide association applicable to microbial genomes (GWAS-M), we classify 274 complete V. cholerae genomes by niche, including 39 newly sequenced for this study with the Ion Torrent DNA-sequencing platform. Niche metadata were collected for each strain and analyzed together with comprehensive annotations of genetic and genomic attributes, including point mutations (single-nucleotide polymorphisms, SNPs), protein families, functions and prophages. CONCLUSIONS: Our analysis revealed that genomic variations, in particular mobile functions including phages, prophages, transposable elements, and plasmids underlie the metadata structuring in each of the three niche dimensions. This underscores the role of phages and mobile elements as the most rapidly evolving elements in bacterial genomes, creating local endemicity (space), leading to temporal divergence (time), and allowing the invasion of new habitats. Together, we take a data-driven approach for comparative functional genomics that exploits high-volume genome sequencing and annotation, in conjunction with novel statistical and machine learning analyses to identify connections between genotype and phenotype on a genome-wide scale. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-654) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-05 /pmc/articles/PMC4141962/ /pubmed/25096633 http://dx.doi.org/10.1186/1471-2164-15-654 Text en © Dutilh et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Dutilh, Bas E
Thompson, Cristiane C
Vicente, Ana CP
Marin, Michel A
Lee, Clarence
Silva, Genivaldo GZ
Schmieder, Robert
Andrade, Bruno GN
Chimetto, Luciane
Cuevas, Daniel
Garza, Daniel R
Okeke, Iruka N
Aboderin, Aaron Oladipo
Spangler, Jessica
Ross, Tristen
Dinsdale, Elizabeth A
Thompson, Fabiano L
Harkins, Timothy T
Edwards, Robert A
Comparative genomics of 274 Vibrio cholerae genomes reveals mobile functions structuring three niche dimensions
title Comparative genomics of 274 Vibrio cholerae genomes reveals mobile functions structuring three niche dimensions
title_full Comparative genomics of 274 Vibrio cholerae genomes reveals mobile functions structuring three niche dimensions
title_fullStr Comparative genomics of 274 Vibrio cholerae genomes reveals mobile functions structuring three niche dimensions
title_full_unstemmed Comparative genomics of 274 Vibrio cholerae genomes reveals mobile functions structuring three niche dimensions
title_short Comparative genomics of 274 Vibrio cholerae genomes reveals mobile functions structuring three niche dimensions
title_sort comparative genomics of 274 vibrio cholerae genomes reveals mobile functions structuring three niche dimensions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141962/
https://www.ncbi.nlm.nih.gov/pubmed/25096633
http://dx.doi.org/10.1186/1471-2164-15-654
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