Cargando…
IS26-Mediated Transfer of bla(NDM–1) as the Main Route of Resistance Transmission During a Polyclonal, Multispecies Outbreak in a German Hospital
One of the most demanding challenges in infection control is the worldwide dissemination of multidrug-resistant (MDR) bacteria in clinical settings. Especially the increasing prevalence of carbapenemase producing Gram-negative pathogens poses an urgent threat to public health, as these enzymes confe...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929489/ https://www.ncbi.nlm.nih.gov/pubmed/31921015 http://dx.doi.org/10.3389/fmicb.2019.02817 |
_version_ | 1783482712431001600 |
---|---|
author | Weber, Robert E. Pietsch, Michael Frühauf, Andre Pfeifer, Yvonne Martin, Maria Luft, Dirk Gatermann, Sören Pfennigwerth, Niels Kaase, Martin Werner, Guido Fuchs, Stephan |
author_facet | Weber, Robert E. Pietsch, Michael Frühauf, Andre Pfeifer, Yvonne Martin, Maria Luft, Dirk Gatermann, Sören Pfennigwerth, Niels Kaase, Martin Werner, Guido Fuchs, Stephan |
author_sort | Weber, Robert E. |
collection | PubMed |
description | One of the most demanding challenges in infection control is the worldwide dissemination of multidrug-resistant (MDR) bacteria in clinical settings. Especially the increasing prevalence of carbapenemase producing Gram-negative pathogens poses an urgent threat to public health, as these enzymes confer resistance to almost all β-lactam antibiotics including carbapenems. In this study, we report a prolonged nosocomial outbreak of various NDM-1-producing Enterobacterales species due to clonal spread and cross-species exchange of plasmids and possibly transposons. Between July 2015 and September 2017, a total of 51 carbapenemase-positive isolates were collected from 38 patients and three environmental sources in a single German hospital. Combining molecular typing methods and whole genome sequencing, the metallo-β-lactamase gene bla(NDM–1) was found to be present in 35 isolates of which seven additionally carried the carbapenemase gene bla(KPC–2). Core genome MLST (cgMLST) revealed different clusters of closely related isolates of Escherichia coli, Klebsiella pneumoniae, Citrobacter freundii, Morganella morganii or Enterobacter cloacae indicating clonal spread. The detailed reconstruction of the plasmid sequences revealed that in all outbreak-associated isolates bla(NDM–1) was located on similar composite transposons, which were also very similar to Tn125 previously described for Acinetobacter baumannii. In contrast to Tn125, these structures were flanked by IS26 elements, which could facilitate horizontal gene transfer. Moreover, the identical plasmid was found to be shared by E. coli and M. morganii isolates. Our results highlight the importance of detailed genome-based analyses for complex nosocomial outbreaks, allowing the identification of causal genetic determinants and providing insights into potential mechanisms involved in the dissemination of antibiotic resistances between different bacterial species. |
format | Online Article Text |
id | pubmed-6929489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69294892020-01-09 IS26-Mediated Transfer of bla(NDM–1) as the Main Route of Resistance Transmission During a Polyclonal, Multispecies Outbreak in a German Hospital Weber, Robert E. Pietsch, Michael Frühauf, Andre Pfeifer, Yvonne Martin, Maria Luft, Dirk Gatermann, Sören Pfennigwerth, Niels Kaase, Martin Werner, Guido Fuchs, Stephan Front Microbiol Microbiology One of the most demanding challenges in infection control is the worldwide dissemination of multidrug-resistant (MDR) bacteria in clinical settings. Especially the increasing prevalence of carbapenemase producing Gram-negative pathogens poses an urgent threat to public health, as these enzymes confer resistance to almost all β-lactam antibiotics including carbapenems. In this study, we report a prolonged nosocomial outbreak of various NDM-1-producing Enterobacterales species due to clonal spread and cross-species exchange of plasmids and possibly transposons. Between July 2015 and September 2017, a total of 51 carbapenemase-positive isolates were collected from 38 patients and three environmental sources in a single German hospital. Combining molecular typing methods and whole genome sequencing, the metallo-β-lactamase gene bla(NDM–1) was found to be present in 35 isolates of which seven additionally carried the carbapenemase gene bla(KPC–2). Core genome MLST (cgMLST) revealed different clusters of closely related isolates of Escherichia coli, Klebsiella pneumoniae, Citrobacter freundii, Morganella morganii or Enterobacter cloacae indicating clonal spread. The detailed reconstruction of the plasmid sequences revealed that in all outbreak-associated isolates bla(NDM–1) was located on similar composite transposons, which were also very similar to Tn125 previously described for Acinetobacter baumannii. In contrast to Tn125, these structures were flanked by IS26 elements, which could facilitate horizontal gene transfer. Moreover, the identical plasmid was found to be shared by E. coli and M. morganii isolates. Our results highlight the importance of detailed genome-based analyses for complex nosocomial outbreaks, allowing the identification of causal genetic determinants and providing insights into potential mechanisms involved in the dissemination of antibiotic resistances between different bacterial species. Frontiers Media S.A. 2019-12-17 /pmc/articles/PMC6929489/ /pubmed/31921015 http://dx.doi.org/10.3389/fmicb.2019.02817 Text en Copyright © 2019 Weber, Pietsch, Frühauf, Pfeifer, Martin, Luft, Gatermann, Pfennigwerth, Kaase, Werner and Fuchs. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Weber, Robert E. Pietsch, Michael Frühauf, Andre Pfeifer, Yvonne Martin, Maria Luft, Dirk Gatermann, Sören Pfennigwerth, Niels Kaase, Martin Werner, Guido Fuchs, Stephan IS26-Mediated Transfer of bla(NDM–1) as the Main Route of Resistance Transmission During a Polyclonal, Multispecies Outbreak in a German Hospital |
title | IS26-Mediated Transfer of bla(NDM–1) as the Main Route of Resistance Transmission During a Polyclonal, Multispecies Outbreak in a German Hospital |
title_full | IS26-Mediated Transfer of bla(NDM–1) as the Main Route of Resistance Transmission During a Polyclonal, Multispecies Outbreak in a German Hospital |
title_fullStr | IS26-Mediated Transfer of bla(NDM–1) as the Main Route of Resistance Transmission During a Polyclonal, Multispecies Outbreak in a German Hospital |
title_full_unstemmed | IS26-Mediated Transfer of bla(NDM–1) as the Main Route of Resistance Transmission During a Polyclonal, Multispecies Outbreak in a German Hospital |
title_short | IS26-Mediated Transfer of bla(NDM–1) as the Main Route of Resistance Transmission During a Polyclonal, Multispecies Outbreak in a German Hospital |
title_sort | is26-mediated transfer of bla(ndm–1) as the main route of resistance transmission during a polyclonal, multispecies outbreak in a german hospital |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929489/ https://www.ncbi.nlm.nih.gov/pubmed/31921015 http://dx.doi.org/10.3389/fmicb.2019.02817 |
work_keys_str_mv | AT weberroberte is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT pietschmichael is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT fruhaufandre is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT pfeiferyvonne is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT martinmaria is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT luftdirk is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT gatermannsoren is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT pfennigwerthniels is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT kaasemartin is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT wernerguido is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital AT fuchsstephan is26mediatedtransferofblandm1asthemainrouteofresistancetransmissionduringapolyclonalmultispeciesoutbreakinagermanhospital |