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Comparative genomics of Enterococcus faecalis from healthy Norwegian infants

BACKGROUND: Enterococcus faecalis, traditionally considered a harmless commensal of the intestinal tract, is now ranked among the leading causes of nosocomial infections. In an attempt to gain insight into the genetic make-up of commensal E. faecalis, we have studied genomic variation in a collectio...

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Autores principales: Solheim, Margrete, Aakra, Ågot, Snipen, Lars G, Brede, Dag A, Nes, Ingolf F
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680900/
https://www.ncbi.nlm.nih.gov/pubmed/19393078
http://dx.doi.org/10.1186/1471-2164-10-194
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author Solheim, Margrete
Aakra, Ågot
Snipen, Lars G
Brede, Dag A
Nes, Ingolf F
author_facet Solheim, Margrete
Aakra, Ågot
Snipen, Lars G
Brede, Dag A
Nes, Ingolf F
author_sort Solheim, Margrete
collection PubMed
description BACKGROUND: Enterococcus faecalis, traditionally considered a harmless commensal of the intestinal tract, is now ranked among the leading causes of nosocomial infections. In an attempt to gain insight into the genetic make-up of commensal E. faecalis, we have studied genomic variation in a collection of community-derived E. faecalis isolated from the feces of Norwegian infants. RESULTS: The E. faecalis isolates were first sequence typed by multilocus sequence typing (MLST) and characterized with respect to antibiotic resistance and properties associated with virulence. A subset of the isolates was compared to the vancomycin resistant strain E. faecalis V583 (V583) by whole genome microarray comparison (comparative genomic hybridization (CGH)). Several of the putative enterococcal virulence factors were found to be highly prevalent among the commensal baby isolates. The genomic variation as observed by CGH was less between isolates displaying the same MLST sequence type than between isolates belonging to different evolutionary lineages. CONCLUSION: The variations in gene content observed among the investigated commensal E. faecalis is comparable to the genetic variation previously reported among strains of various origins thought to be representative of the major E. faecalis lineages. Previous MLST analysis of E. faecalis have identified so-called high-risk enterococcal clonal complexes (HiRECC), defined as genetically distinct subpopulations, epidemiologically associated with enterococcal infections. The observed correlation between CGH and MLST presented here, may offer a method for the identification of lineage-specific genes, and may therefore add clues on how to distinguish pathogenic from commensal E. faecalis. In this work, information on the core genome of E. faecalis is also substantially extended.
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spelling pubmed-26809002009-05-13 Comparative genomics of Enterococcus faecalis from healthy Norwegian infants Solheim, Margrete Aakra, Ågot Snipen, Lars G Brede, Dag A Nes, Ingolf F BMC Genomics Research Article BACKGROUND: Enterococcus faecalis, traditionally considered a harmless commensal of the intestinal tract, is now ranked among the leading causes of nosocomial infections. In an attempt to gain insight into the genetic make-up of commensal E. faecalis, we have studied genomic variation in a collection of community-derived E. faecalis isolated from the feces of Norwegian infants. RESULTS: The E. faecalis isolates were first sequence typed by multilocus sequence typing (MLST) and characterized with respect to antibiotic resistance and properties associated with virulence. A subset of the isolates was compared to the vancomycin resistant strain E. faecalis V583 (V583) by whole genome microarray comparison (comparative genomic hybridization (CGH)). Several of the putative enterococcal virulence factors were found to be highly prevalent among the commensal baby isolates. The genomic variation as observed by CGH was less between isolates displaying the same MLST sequence type than between isolates belonging to different evolutionary lineages. CONCLUSION: The variations in gene content observed among the investigated commensal E. faecalis is comparable to the genetic variation previously reported among strains of various origins thought to be representative of the major E. faecalis lineages. Previous MLST analysis of E. faecalis have identified so-called high-risk enterococcal clonal complexes (HiRECC), defined as genetically distinct subpopulations, epidemiologically associated with enterococcal infections. The observed correlation between CGH and MLST presented here, may offer a method for the identification of lineage-specific genes, and may therefore add clues on how to distinguish pathogenic from commensal E. faecalis. In this work, information on the core genome of E. faecalis is also substantially extended. BioMed Central 2009-04-24 /pmc/articles/PMC2680900/ /pubmed/19393078 http://dx.doi.org/10.1186/1471-2164-10-194 Text en Copyright © 2009 Solheim 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
Solheim, Margrete
Aakra, Ågot
Snipen, Lars G
Brede, Dag A
Nes, Ingolf F
Comparative genomics of Enterococcus faecalis from healthy Norwegian infants
title Comparative genomics of Enterococcus faecalis from healthy Norwegian infants
title_full Comparative genomics of Enterococcus faecalis from healthy Norwegian infants
title_fullStr Comparative genomics of Enterococcus faecalis from healthy Norwegian infants
title_full_unstemmed Comparative genomics of Enterococcus faecalis from healthy Norwegian infants
title_short Comparative genomics of Enterococcus faecalis from healthy Norwegian infants
title_sort comparative genomics of enterococcus faecalis from healthy norwegian infants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680900/
https://www.ncbi.nlm.nih.gov/pubmed/19393078
http://dx.doi.org/10.1186/1471-2164-10-194
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