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Assessing genetic diversity and similarity of 435 KPC-carrying plasmids
The global spread and diversification of multidrug-resistant Gram-negative (MRGN) bacteria poses major challenges to healthcare. In particular, carbapenem-resistant Klebsiella pneumoniae strains have been frequently identified in infections and hospital-wide outbreaks. The most frequently underlying...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6677891/ https://www.ncbi.nlm.nih.gov/pubmed/31375735 http://dx.doi.org/10.1038/s41598-019-47758-5 |
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author | Brandt, Christian Viehweger, Adrian Singh, Abhijeet Pletz, Mathias W. Wibberg, Daniel Kalinowski, Jörn Lerch, Sandrina Müller, Bettina Makarewicz, Oliwia |
author_facet | Brandt, Christian Viehweger, Adrian Singh, Abhijeet Pletz, Mathias W. Wibberg, Daniel Kalinowski, Jörn Lerch, Sandrina Müller, Bettina Makarewicz, Oliwia |
author_sort | Brandt, Christian |
collection | PubMed |
description | The global spread and diversification of multidrug-resistant Gram-negative (MRGN) bacteria poses major challenges to healthcare. In particular, carbapenem-resistant Klebsiella pneumoniae strains have been frequently identified in infections and hospital-wide outbreaks. The most frequently underlying resistance gene (bla(KPC)) has been spreading over the last decade in the health care setting. bla(KPC) seems to have rapidly diversified and has been found in various species and on different plasmid types. To review the progress and dynamics of this diversification, all currently available KPC plasmids in the NCBI database were analysed in this work. Plasmids were grouped into 257 different representative KPC plasmids, of which 79.4% could be clearly assigned to incompatibility (Inc) group or groups. In almost half of all representative plasmids, the KPC gene is located on Tn4401 variants, emphasizing the importance of this transposon type for the transmission of KPC genes to other plasmids. The transposons also seem to be responsible for the occurrence of altered or uncommon fused plasmid types probably due to incomplete transposition. Moreover, many KPC plasmids contain genes that encode proteins promoting recombinant processes and mutagenesis; in consequence accelerating the diversification of KPC genes and other colocalized resistance genes. |
format | Online Article Text |
id | pubmed-6677891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66778912019-08-08 Assessing genetic diversity and similarity of 435 KPC-carrying plasmids Brandt, Christian Viehweger, Adrian Singh, Abhijeet Pletz, Mathias W. Wibberg, Daniel Kalinowski, Jörn Lerch, Sandrina Müller, Bettina Makarewicz, Oliwia Sci Rep Article The global spread and diversification of multidrug-resistant Gram-negative (MRGN) bacteria poses major challenges to healthcare. In particular, carbapenem-resistant Klebsiella pneumoniae strains have been frequently identified in infections and hospital-wide outbreaks. The most frequently underlying resistance gene (bla(KPC)) has been spreading over the last decade in the health care setting. bla(KPC) seems to have rapidly diversified and has been found in various species and on different plasmid types. To review the progress and dynamics of this diversification, all currently available KPC plasmids in the NCBI database were analysed in this work. Plasmids were grouped into 257 different representative KPC plasmids, of which 79.4% could be clearly assigned to incompatibility (Inc) group or groups. In almost half of all representative plasmids, the KPC gene is located on Tn4401 variants, emphasizing the importance of this transposon type for the transmission of KPC genes to other plasmids. The transposons also seem to be responsible for the occurrence of altered or uncommon fused plasmid types probably due to incomplete transposition. Moreover, many KPC plasmids contain genes that encode proteins promoting recombinant processes and mutagenesis; in consequence accelerating the diversification of KPC genes and other colocalized resistance genes. Nature Publishing Group UK 2019-08-02 /pmc/articles/PMC6677891/ /pubmed/31375735 http://dx.doi.org/10.1038/s41598-019-47758-5 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Brandt, Christian Viehweger, Adrian Singh, Abhijeet Pletz, Mathias W. Wibberg, Daniel Kalinowski, Jörn Lerch, Sandrina Müller, Bettina Makarewicz, Oliwia Assessing genetic diversity and similarity of 435 KPC-carrying plasmids |
title | Assessing genetic diversity and similarity of 435 KPC-carrying plasmids |
title_full | Assessing genetic diversity and similarity of 435 KPC-carrying plasmids |
title_fullStr | Assessing genetic diversity and similarity of 435 KPC-carrying plasmids |
title_full_unstemmed | Assessing genetic diversity and similarity of 435 KPC-carrying plasmids |
title_short | Assessing genetic diversity and similarity of 435 KPC-carrying plasmids |
title_sort | assessing genetic diversity and similarity of 435 kpc-carrying plasmids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6677891/ https://www.ncbi.nlm.nih.gov/pubmed/31375735 http://dx.doi.org/10.1038/s41598-019-47758-5 |
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