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Plasmids Shaped the Recent Emergence of the Major Nosocomial Pathogen Enterococcus faecium

Enterococcus faecium is a gut commensal of humans and animals but is also listed on the WHO global priority list of multidrug-resistant pathogens. Many of its antibiotic resistance traits reside on plasmids and have the potential to be disseminated by horizontal gene transfer. Here, we present the f...

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Autores principales: Arredondo-Alonso, S., Top, J., McNally, A., Puranen, S., Pesonen, M., Pensar, J., Marttinen, P., Braat, J. C., Rogers, M. R. C., van Schaik, W., Kaski, S., Willems, R. J. L., Corander, J., Schürch, A. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018651/
https://www.ncbi.nlm.nih.gov/pubmed/32047136
http://dx.doi.org/10.1128/mBio.03284-19
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author Arredondo-Alonso, S.
Top, J.
McNally, A.
Puranen, S.
Pesonen, M.
Pensar, J.
Marttinen, P.
Braat, J. C.
Rogers, M. R. C.
van Schaik, W.
Kaski, S.
Willems, R. J. L.
Corander, J.
Schürch, A. C.
author_facet Arredondo-Alonso, S.
Top, J.
McNally, A.
Puranen, S.
Pesonen, M.
Pensar, J.
Marttinen, P.
Braat, J. C.
Rogers, M. R. C.
van Schaik, W.
Kaski, S.
Willems, R. J. L.
Corander, J.
Schürch, A. C.
author_sort Arredondo-Alonso, S.
collection PubMed
description Enterococcus faecium is a gut commensal of humans and animals but is also listed on the WHO global priority list of multidrug-resistant pathogens. Many of its antibiotic resistance traits reside on plasmids and have the potential to be disseminated by horizontal gene transfer. Here, we present the first comprehensive population-wide analysis of the pan-plasmidome of a clinically important bacterium, by whole-genome sequence analysis of 1,644 isolates from hospital, commensal, and animal sources of E. faecium. Long-read sequencing on a selection of isolates resulted in the completion of 305 plasmids that exhibited high levels of sequence modularity. We further investigated the entirety of all plasmids of each isolate (plasmidome) using a combination of short-read sequencing and machine-learning classifiers. Clustering of the plasmid sequences unraveled different E. faecium populations with a clear association with hospitalized patient isolates, suggesting different optimal configurations of plasmids in the hospital environment. The characterization of these populations allowed us to identify common mechanisms of plasmid stabilization such as toxin-antitoxin systems and genes exclusively present in particular plasmidome populations exemplified by copper resistance, phosphotransferase systems, or bacteriocin genes potentially involved in niche adaptation. Based on the distribution of k-mer distances between isolates, we concluded that plasmidomes rather than chromosomes are most informative for source specificity of E. faecium.
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spelling pubmed-70186512020-02-26 Plasmids Shaped the Recent Emergence of the Major Nosocomial Pathogen Enterococcus faecium Arredondo-Alonso, S. Top, J. McNally, A. Puranen, S. Pesonen, M. Pensar, J. Marttinen, P. Braat, J. C. Rogers, M. R. C. van Schaik, W. Kaski, S. Willems, R. J. L. Corander, J. Schürch, A. C. mBio Research Article Enterococcus faecium is a gut commensal of humans and animals but is also listed on the WHO global priority list of multidrug-resistant pathogens. Many of its antibiotic resistance traits reside on plasmids and have the potential to be disseminated by horizontal gene transfer. Here, we present the first comprehensive population-wide analysis of the pan-plasmidome of a clinically important bacterium, by whole-genome sequence analysis of 1,644 isolates from hospital, commensal, and animal sources of E. faecium. Long-read sequencing on a selection of isolates resulted in the completion of 305 plasmids that exhibited high levels of sequence modularity. We further investigated the entirety of all plasmids of each isolate (plasmidome) using a combination of short-read sequencing and machine-learning classifiers. Clustering of the plasmid sequences unraveled different E. faecium populations with a clear association with hospitalized patient isolates, suggesting different optimal configurations of plasmids in the hospital environment. The characterization of these populations allowed us to identify common mechanisms of plasmid stabilization such as toxin-antitoxin systems and genes exclusively present in particular plasmidome populations exemplified by copper resistance, phosphotransferase systems, or bacteriocin genes potentially involved in niche adaptation. Based on the distribution of k-mer distances between isolates, we concluded that plasmidomes rather than chromosomes are most informative for source specificity of E. faecium. American Society for Microbiology 2020-02-11 /pmc/articles/PMC7018651/ /pubmed/32047136 http://dx.doi.org/10.1128/mBio.03284-19 Text en Copyright © 2020 Arredondo-Alonso et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Arredondo-Alonso, S.
Top, J.
McNally, A.
Puranen, S.
Pesonen, M.
Pensar, J.
Marttinen, P.
Braat, J. C.
Rogers, M. R. C.
van Schaik, W.
Kaski, S.
Willems, R. J. L.
Corander, J.
Schürch, A. C.
Plasmids Shaped the Recent Emergence of the Major Nosocomial Pathogen Enterococcus faecium
title Plasmids Shaped the Recent Emergence of the Major Nosocomial Pathogen Enterococcus faecium
title_full Plasmids Shaped the Recent Emergence of the Major Nosocomial Pathogen Enterococcus faecium
title_fullStr Plasmids Shaped the Recent Emergence of the Major Nosocomial Pathogen Enterococcus faecium
title_full_unstemmed Plasmids Shaped the Recent Emergence of the Major Nosocomial Pathogen Enterococcus faecium
title_short Plasmids Shaped the Recent Emergence of the Major Nosocomial Pathogen Enterococcus faecium
title_sort plasmids shaped the recent emergence of the major nosocomial pathogen enterococcus faecium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018651/
https://www.ncbi.nlm.nih.gov/pubmed/32047136
http://dx.doi.org/10.1128/mBio.03284-19
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