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Genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of Salmonella enterica

BACKGROUND: Divergence of bacterial populations into distinct subpopulations is often the result of ecological isolation. While some studies have suggested the existence of Salmonella enterica subsp. enterica subclades, evidence for these subdivisions has been ambiguous. Here we used a comparative g...

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Autores principales: den Bakker, Henk C, Moreno Switt, Andrea I, Govoni, Gregory, Cummings, Craig A, Ranieri, Matthew L, Degoricija, Lovorka, Hoelzer, Karin, Rodriguez-Rivera, Lorraine D, Brown, Stephanie, Bolchacova, Elena, Furtado, Manohar R, Wiedmann, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176500/
https://www.ncbi.nlm.nih.gov/pubmed/21859443
http://dx.doi.org/10.1186/1471-2164-12-425
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author den Bakker, Henk C
Moreno Switt, Andrea I
Govoni, Gregory
Cummings, Craig A
Ranieri, Matthew L
Degoricija, Lovorka
Hoelzer, Karin
Rodriguez-Rivera, Lorraine D
Brown, Stephanie
Bolchacova, Elena
Furtado, Manohar R
Wiedmann, Martin
author_facet den Bakker, Henk C
Moreno Switt, Andrea I
Govoni, Gregory
Cummings, Craig A
Ranieri, Matthew L
Degoricija, Lovorka
Hoelzer, Karin
Rodriguez-Rivera, Lorraine D
Brown, Stephanie
Bolchacova, Elena
Furtado, Manohar R
Wiedmann, Martin
author_sort den Bakker, Henk C
collection PubMed
description BACKGROUND: Divergence of bacterial populations into distinct subpopulations is often the result of ecological isolation. While some studies have suggested the existence of Salmonella enterica subsp. enterica subclades, evidence for these subdivisions has been ambiguous. Here we used a comparative genomics approach to define the population structure of Salmonella enterica subsp. enterica, and identify clade-specific genes that may be the result of ecological specialization. RESULTS: Multi-locus sequence analysis (MLSA) and single nucleotide polymorphisms (SNPs) data for 16 newly sequenced and 30 publicly available genomes showed an unambiguous subdivision of S. enterica subsp. enterica into at least two subpopulations, which we refer to as clade A and clade B. Clade B strains contain several clade-specific genes or operons, including a β-glucuronidase operon, a S-fimbrial operon, and cell surface related genes, which strongly suggests niche specialization of this subpopulation. An additional set of 123 isolates was assigned to clades A and B by using qPCR assays targeting subpopulation-specific SNPs and genes of interest. Among 98 serovars examined, approximately 20% belonged to clade B. All clade B isolates contained two pathogenicity related genomic islands, SPI-18 and a cytolethal distending toxin islet; a combination of these two islands was previously thought to be exclusive to serovars Typhi and Paratyphi A. Presence of β-glucuronidase in clade B isolates specifically suggests an adaptation of this clade to the vertebrate gastrointestinal environment. CONCLUSIONS: S. enterica subsp. enterica consists of at least two subpopulations that differ specifically in genes involved in host and tissue tropism, utilization of host specific carbon and nitrogen sources and are therefore likely to differ in ecology and transmission characteristics.
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spelling pubmed-31765002011-09-21 Genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of Salmonella enterica den Bakker, Henk C Moreno Switt, Andrea I Govoni, Gregory Cummings, Craig A Ranieri, Matthew L Degoricija, Lovorka Hoelzer, Karin Rodriguez-Rivera, Lorraine D Brown, Stephanie Bolchacova, Elena Furtado, Manohar R Wiedmann, Martin BMC Genomics Research Article BACKGROUND: Divergence of bacterial populations into distinct subpopulations is often the result of ecological isolation. While some studies have suggested the existence of Salmonella enterica subsp. enterica subclades, evidence for these subdivisions has been ambiguous. Here we used a comparative genomics approach to define the population structure of Salmonella enterica subsp. enterica, and identify clade-specific genes that may be the result of ecological specialization. RESULTS: Multi-locus sequence analysis (MLSA) and single nucleotide polymorphisms (SNPs) data for 16 newly sequenced and 30 publicly available genomes showed an unambiguous subdivision of S. enterica subsp. enterica into at least two subpopulations, which we refer to as clade A and clade B. Clade B strains contain several clade-specific genes or operons, including a β-glucuronidase operon, a S-fimbrial operon, and cell surface related genes, which strongly suggests niche specialization of this subpopulation. An additional set of 123 isolates was assigned to clades A and B by using qPCR assays targeting subpopulation-specific SNPs and genes of interest. Among 98 serovars examined, approximately 20% belonged to clade B. All clade B isolates contained two pathogenicity related genomic islands, SPI-18 and a cytolethal distending toxin islet; a combination of these two islands was previously thought to be exclusive to serovars Typhi and Paratyphi A. Presence of β-glucuronidase in clade B isolates specifically suggests an adaptation of this clade to the vertebrate gastrointestinal environment. CONCLUSIONS: S. enterica subsp. enterica consists of at least two subpopulations that differ specifically in genes involved in host and tissue tropism, utilization of host specific carbon and nitrogen sources and are therefore likely to differ in ecology and transmission characteristics. BioMed Central 2011-08-22 /pmc/articles/PMC3176500/ /pubmed/21859443 http://dx.doi.org/10.1186/1471-2164-12-425 Text en Copyright ©2011 den Bakker 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
den Bakker, Henk C
Moreno Switt, Andrea I
Govoni, Gregory
Cummings, Craig A
Ranieri, Matthew L
Degoricija, Lovorka
Hoelzer, Karin
Rodriguez-Rivera, Lorraine D
Brown, Stephanie
Bolchacova, Elena
Furtado, Manohar R
Wiedmann, Martin
Genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of Salmonella enterica
title Genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of Salmonella enterica
title_full Genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of Salmonella enterica
title_fullStr Genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of Salmonella enterica
title_full_unstemmed Genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of Salmonella enterica
title_short Genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of Salmonella enterica
title_sort genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of salmonella enterica
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176500/
https://www.ncbi.nlm.nih.gov/pubmed/21859443
http://dx.doi.org/10.1186/1471-2164-12-425
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