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The global dissemination of hospital clones of Enterococcus faecium
BACKGROUND: The hospital-adapted A1 group of Enterococcus faecium remains an organism of significant concern in the context of drug-resistant hospital-associated infections. How this pathogen evolves and disseminates remains poorly understood. METHODS: A large, globally representative collection of...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008517/ https://www.ncbi.nlm.nih.gov/pubmed/33785076 http://dx.doi.org/10.1186/s13073-021-00868-0 |
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author | van Hal, Sebastiaan J. Willems, Rob J. L. Gouliouris, Theodore Ballard, Susan A. Coque, Teresa M. Hammerum, Anette M. Hegstad, Kristin Westh, Hendrik T. Howden, Benjamin P. Malhotra-Kumar, Surbhi Werner, Guido Yanagihara, Katsunori Earl, Ashlee M. Raven, Katherine E. Corander, Jukka Bowden, Rory |
author_facet | van Hal, Sebastiaan J. Willems, Rob J. L. Gouliouris, Theodore Ballard, Susan A. Coque, Teresa M. Hammerum, Anette M. Hegstad, Kristin Westh, Hendrik T. Howden, Benjamin P. Malhotra-Kumar, Surbhi Werner, Guido Yanagihara, Katsunori Earl, Ashlee M. Raven, Katherine E. Corander, Jukka Bowden, Rory |
author_sort | van Hal, Sebastiaan J. |
collection | PubMed |
description | BACKGROUND: The hospital-adapted A1 group of Enterococcus faecium remains an organism of significant concern in the context of drug-resistant hospital-associated infections. How this pathogen evolves and disseminates remains poorly understood. METHODS: A large, globally representative collection of short-read genomic data from the hospital-associated A1 group of Enterococcus faecium was assembled (n = 973). We analysed, using a novel analysis approach, global diversity in terms of both the dynamics of the accessory genome and homologous recombination among conserved genes. RESULTS: Two main modes of genomic evolution continue to shape E. faecium: the acquisition and loss of genes, including antimicrobial resistance genes, through mobile genetic elements including plasmids, and homologous recombination of the core genome. These events lead to new clones emerging at the local level, followed by the erosion of signals of clonality through recombination, and in some identifiable cases producing new clonal clusters. These patterns lead to new, emerging lineages which are able to spread globally over relatively short timeframes. CONCLUSIONS: The ability of A1 E. faecium to continually present new combinations of genes for potential selection suggests that controlling this pathogen will remain challenging but establishing a framework for understanding genomic evolution is likely to aid in tracking the threats posed by newly emerging lineages. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-021-00868-0. |
format | Online Article Text |
id | pubmed-8008517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80085172021-03-30 The global dissemination of hospital clones of Enterococcus faecium van Hal, Sebastiaan J. Willems, Rob J. L. Gouliouris, Theodore Ballard, Susan A. Coque, Teresa M. Hammerum, Anette M. Hegstad, Kristin Westh, Hendrik T. Howden, Benjamin P. Malhotra-Kumar, Surbhi Werner, Guido Yanagihara, Katsunori Earl, Ashlee M. Raven, Katherine E. Corander, Jukka Bowden, Rory Genome Med Research BACKGROUND: The hospital-adapted A1 group of Enterococcus faecium remains an organism of significant concern in the context of drug-resistant hospital-associated infections. How this pathogen evolves and disseminates remains poorly understood. METHODS: A large, globally representative collection of short-read genomic data from the hospital-associated A1 group of Enterococcus faecium was assembled (n = 973). We analysed, using a novel analysis approach, global diversity in terms of both the dynamics of the accessory genome and homologous recombination among conserved genes. RESULTS: Two main modes of genomic evolution continue to shape E. faecium: the acquisition and loss of genes, including antimicrobial resistance genes, through mobile genetic elements including plasmids, and homologous recombination of the core genome. These events lead to new clones emerging at the local level, followed by the erosion of signals of clonality through recombination, and in some identifiable cases producing new clonal clusters. These patterns lead to new, emerging lineages which are able to spread globally over relatively short timeframes. CONCLUSIONS: The ability of A1 E. faecium to continually present new combinations of genes for potential selection suggests that controlling this pathogen will remain challenging but establishing a framework for understanding genomic evolution is likely to aid in tracking the threats posed by newly emerging lineages. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-021-00868-0. BioMed Central 2021-03-30 /pmc/articles/PMC8008517/ /pubmed/33785076 http://dx.doi.org/10.1186/s13073-021-00868-0 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research van Hal, Sebastiaan J. Willems, Rob J. L. Gouliouris, Theodore Ballard, Susan A. Coque, Teresa M. Hammerum, Anette M. Hegstad, Kristin Westh, Hendrik T. Howden, Benjamin P. Malhotra-Kumar, Surbhi Werner, Guido Yanagihara, Katsunori Earl, Ashlee M. Raven, Katherine E. Corander, Jukka Bowden, Rory The global dissemination of hospital clones of Enterococcus faecium |
title | The global dissemination of hospital clones of Enterococcus faecium |
title_full | The global dissemination of hospital clones of Enterococcus faecium |
title_fullStr | The global dissemination of hospital clones of Enterococcus faecium |
title_full_unstemmed | The global dissemination of hospital clones of Enterococcus faecium |
title_short | The global dissemination of hospital clones of Enterococcus faecium |
title_sort | global dissemination of hospital clones of enterococcus faecium |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008517/ https://www.ncbi.nlm.nih.gov/pubmed/33785076 http://dx.doi.org/10.1186/s13073-021-00868-0 |
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