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Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from two German hospitals

Introduction: Vancomycin-resistant Enterococcus faecium accounts for around 10–23% of nosocomial enterococcal infections and constitutes a relevant therapeutic problem due to its limited susceptibility to antibiotics. The resistance towards glycopeptide antibiotics is mediated by the so-called van g...

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Autores principales: Nürnberger, Laura, Schmidt, Dirk, Szumlanski, Tobias, Kirchhoff, Lisa, Ross, Birgit, Steinmann, Jörg, Rath, Peter-Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: German Medical Science GMS Publishing House 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983015/
https://www.ncbi.nlm.nih.gov/pubmed/33796441
http://dx.doi.org/10.3205/dgkh000384
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author Nürnberger, Laura
Schmidt, Dirk
Szumlanski, Tobias
Kirchhoff, Lisa
Ross, Birgit
Steinmann, Jörg
Rath, Peter-Michael
author_facet Nürnberger, Laura
Schmidt, Dirk
Szumlanski, Tobias
Kirchhoff, Lisa
Ross, Birgit
Steinmann, Jörg
Rath, Peter-Michael
author_sort Nürnberger, Laura
collection PubMed
description Introduction: Vancomycin-resistant Enterococcus faecium accounts for around 10–23% of nosocomial enterococcal infections and constitutes a relevant therapeutic problem due to its limited susceptibility to antibiotics. The resistance towards glycopeptide antibiotics is mediated by the so-called van genes. Currently, the most common resistance type in Germany is the vanB-type. Little data are available on the molecular epidemiology in Germany. Therefore, an epidemiological typing of Enterococcus faecium isolates with vanB-type resistance from two German hospitals in Essen and Nuremberg was performed. Two outbreaks and 104 sporadic cases were investigated. Methods: All 128 isolates with vanB-type resistance were collected between 2011–2012 and 2017–2018. They were characterized using multilocus sequence typing (MLST) and pulsed-field gel electrophoresis (PFGE). Results: ST 117 was the most common sequence type (ST) in both hospitals, especially since 2017. PFGE divided the isolates of this study into 68 PFGE types and showed a broad genetic diversity. Two epidemiologically assumed in-hospital outbreaks were genetically confirmed. Apart from that, in-hospital transmissions were rare events. Conclusion: The results obtained by MLST confirmed the previously described allocation of STs in Germany. PFGE showed a broad genetic diversity of vanB VRE between the two hospitals and also within each hospital. In-hospital transmissions were rare, but outbreaks did occur. Our data supports the strategy to screen and isolate patients in transmission events in order to detect monoclonality indicating a common source or hygiene mismanagement.
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spelling pubmed-79830152021-03-31 Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from two German hospitals Nürnberger, Laura Schmidt, Dirk Szumlanski, Tobias Kirchhoff, Lisa Ross, Birgit Steinmann, Jörg Rath, Peter-Michael GMS Hyg Infect Control Article Introduction: Vancomycin-resistant Enterococcus faecium accounts for around 10–23% of nosocomial enterococcal infections and constitutes a relevant therapeutic problem due to its limited susceptibility to antibiotics. The resistance towards glycopeptide antibiotics is mediated by the so-called van genes. Currently, the most common resistance type in Germany is the vanB-type. Little data are available on the molecular epidemiology in Germany. Therefore, an epidemiological typing of Enterococcus faecium isolates with vanB-type resistance from two German hospitals in Essen and Nuremberg was performed. Two outbreaks and 104 sporadic cases were investigated. Methods: All 128 isolates with vanB-type resistance were collected between 2011–2012 and 2017–2018. They were characterized using multilocus sequence typing (MLST) and pulsed-field gel electrophoresis (PFGE). Results: ST 117 was the most common sequence type (ST) in both hospitals, especially since 2017. PFGE divided the isolates of this study into 68 PFGE types and showed a broad genetic diversity. Two epidemiologically assumed in-hospital outbreaks were genetically confirmed. Apart from that, in-hospital transmissions were rare events. Conclusion: The results obtained by MLST confirmed the previously described allocation of STs in Germany. PFGE showed a broad genetic diversity of vanB VRE between the two hospitals and also within each hospital. In-hospital transmissions were rare, but outbreaks did occur. Our data supports the strategy to screen and isolate patients in transmission events in order to detect monoclonality indicating a common source or hygiene mismanagement. German Medical Science GMS Publishing House 2021-03-17 /pmc/articles/PMC7983015/ /pubmed/33796441 http://dx.doi.org/10.3205/dgkh000384 Text en Copyright © 2021 Nürnberger et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nürnberger, Laura
Schmidt, Dirk
Szumlanski, Tobias
Kirchhoff, Lisa
Ross, Birgit
Steinmann, Jörg
Rath, Peter-Michael
Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from two German hospitals
title Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from two German hospitals
title_full Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from two German hospitals
title_fullStr Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from two German hospitals
title_full_unstemmed Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from two German hospitals
title_short Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from two German hospitals
title_sort molecular characterization of vancomycin-resistant enterococcus faecium isolates from two german hospitals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983015/
https://www.ncbi.nlm.nih.gov/pubmed/33796441
http://dx.doi.org/10.3205/dgkh000384
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