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Differentiation of IncL and IncM Plasmids Associated with the Spread of Clinically Relevant Antimicrobial Resistance
INTRODUCTION: bla (OXA-48), bla (NDM-1) and bla (CTX-M-3) are clinically relevant resistance genes, frequently associated with the broad-host range plasmids of the IncL/M group. The L and M plasmids belong to two compatible groups, which were incorrectly classified together by molecular methods. In...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416936/ https://www.ncbi.nlm.nih.gov/pubmed/25933288 http://dx.doi.org/10.1371/journal.pone.0123063 |
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author | Carattoli, Alessandra Seiffert, Salome N. Schwendener, Sybille Perreten, Vincent Endimiani, Andrea |
author_facet | Carattoli, Alessandra Seiffert, Salome N. Schwendener, Sybille Perreten, Vincent Endimiani, Andrea |
author_sort | Carattoli, Alessandra |
collection | PubMed |
description | INTRODUCTION: bla (OXA-48), bla (NDM-1) and bla (CTX-M-3) are clinically relevant resistance genes, frequently associated with the broad-host range plasmids of the IncL/M group. The L and M plasmids belong to two compatible groups, which were incorrectly classified together by molecular methods. In order to understand their evolution, we fully sequenced four IncL/M plasmids, including the reference plasmids R471 and R69, the recently described bla (OXA-48)-carrying plasmid pKPN-El.Nr7 from a Klebsiella pneumoniae isolated in Bern (Switzerland), and the bla (SHV-5) carrying plasmid p202c from a Salmonella enterica from Tirana (Albania). METHODS: Sequencing was performed using 454 Junior Genome Sequencer (Roche). Annotation was performed using Sequin and Artemis software. Plasmid sequences were compared with 13 fully sequenced plasmids belonging to the IncL/M group available in GenBank. RESULTS: Comparative analysis of plasmid genomes revealed two distinct genetic lineages, each containing one of the R471 (IncL) and R69 (IncM) reference plasmids. Conjugation experiments demonstrated that plasmids representative of the IncL and IncM groups were compatible with each other. The IncL group is constituted by the bla (OXA-48)-carrying plasmids and R471. The IncM group contains two sub-types of plasmids named IncM1 and IncM2 that are each incompatible. CONCLUSION: This work re-defines the structure of the IncL and IncM families and ascribes a definitive designation to the fully sequenced IncL/M plasmids available in GenBank. |
format | Online Article Text |
id | pubmed-4416936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44169362015-05-07 Differentiation of IncL and IncM Plasmids Associated with the Spread of Clinically Relevant Antimicrobial Resistance Carattoli, Alessandra Seiffert, Salome N. Schwendener, Sybille Perreten, Vincent Endimiani, Andrea PLoS One Research Article INTRODUCTION: bla (OXA-48), bla (NDM-1) and bla (CTX-M-3) are clinically relevant resistance genes, frequently associated with the broad-host range plasmids of the IncL/M group. The L and M plasmids belong to two compatible groups, which were incorrectly classified together by molecular methods. In order to understand their evolution, we fully sequenced four IncL/M plasmids, including the reference plasmids R471 and R69, the recently described bla (OXA-48)-carrying plasmid pKPN-El.Nr7 from a Klebsiella pneumoniae isolated in Bern (Switzerland), and the bla (SHV-5) carrying plasmid p202c from a Salmonella enterica from Tirana (Albania). METHODS: Sequencing was performed using 454 Junior Genome Sequencer (Roche). Annotation was performed using Sequin and Artemis software. Plasmid sequences were compared with 13 fully sequenced plasmids belonging to the IncL/M group available in GenBank. RESULTS: Comparative analysis of plasmid genomes revealed two distinct genetic lineages, each containing one of the R471 (IncL) and R69 (IncM) reference plasmids. Conjugation experiments demonstrated that plasmids representative of the IncL and IncM groups were compatible with each other. The IncL group is constituted by the bla (OXA-48)-carrying plasmids and R471. The IncM group contains two sub-types of plasmids named IncM1 and IncM2 that are each incompatible. CONCLUSION: This work re-defines the structure of the IncL and IncM families and ascribes a definitive designation to the fully sequenced IncL/M plasmids available in GenBank. Public Library of Science 2015-05-01 /pmc/articles/PMC4416936/ /pubmed/25933288 http://dx.doi.org/10.1371/journal.pone.0123063 Text en © 2015 Carattoli et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Carattoli, Alessandra Seiffert, Salome N. Schwendener, Sybille Perreten, Vincent Endimiani, Andrea Differentiation of IncL and IncM Plasmids Associated with the Spread of Clinically Relevant Antimicrobial Resistance |
title | Differentiation of IncL and IncM Plasmids Associated with the Spread of Clinically Relevant Antimicrobial Resistance |
title_full | Differentiation of IncL and IncM Plasmids Associated with the Spread of Clinically Relevant Antimicrobial Resistance |
title_fullStr | Differentiation of IncL and IncM Plasmids Associated with the Spread of Clinically Relevant Antimicrobial Resistance |
title_full_unstemmed | Differentiation of IncL and IncM Plasmids Associated with the Spread of Clinically Relevant Antimicrobial Resistance |
title_short | Differentiation of IncL and IncM Plasmids Associated with the Spread of Clinically Relevant Antimicrobial Resistance |
title_sort | differentiation of incl and incm plasmids associated with the spread of clinically relevant antimicrobial resistance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416936/ https://www.ncbi.nlm.nih.gov/pubmed/25933288 http://dx.doi.org/10.1371/journal.pone.0123063 |
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