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Linking the resistome and plasmidome to the microbiome
The rapid spread of antibiotic resistance among bacterial pathogens is a serious human health threat. While a range of environments have been identified as reservoirs of antibiotic resistance genes (ARGs), we lack understanding of the origins of these ARGs and their spread from environment to clinic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776055/ https://www.ncbi.nlm.nih.gov/pubmed/31147603 http://dx.doi.org/10.1038/s41396-019-0446-4 |
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author | Stalder, Thibault Press, Maximilian O. Sullivan, Shawn Liachko, Ivan Top, Eva M. |
author_facet | Stalder, Thibault Press, Maximilian O. Sullivan, Shawn Liachko, Ivan Top, Eva M. |
author_sort | Stalder, Thibault |
collection | PubMed |
description | The rapid spread of antibiotic resistance among bacterial pathogens is a serious human health threat. While a range of environments have been identified as reservoirs of antibiotic resistance genes (ARGs), we lack understanding of the origins of these ARGs and their spread from environment to clinic. This is partly due to our inability to identify the natural bacterial hosts of ARGs and the mobile genetic elements that mediate this spread, such as plasmids and integrons. Here we demonstrate that the in vivo proximity-ligation method Hi-C can reconstruct a known plasmid-host association from a wastewater community, and identify the in situ host range of ARGs, plasmids, and integrons by physically linking them to their host chromosomes. Hi-C detected both previously known and novel associations between ARGs, mobile genetic elements and host genomes, thus validating this method. We showed that IncQ plasmids and class 1 integrons had the broadest host range in this wastewater, and identified bacteria belonging to Moraxellaceae, Bacteroides, and Prevotella, and especially Aeromonadaceae as the most likely reservoirs of ARGs in this community. A better identification of the natural carriers of ARGs will aid the development of strategies to limit resistance spread to pathogens. |
format | Online Article Text |
id | pubmed-6776055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67760552019-10-04 Linking the resistome and plasmidome to the microbiome Stalder, Thibault Press, Maximilian O. Sullivan, Shawn Liachko, Ivan Top, Eva M. ISME J Article The rapid spread of antibiotic resistance among bacterial pathogens is a serious human health threat. While a range of environments have been identified as reservoirs of antibiotic resistance genes (ARGs), we lack understanding of the origins of these ARGs and their spread from environment to clinic. This is partly due to our inability to identify the natural bacterial hosts of ARGs and the mobile genetic elements that mediate this spread, such as plasmids and integrons. Here we demonstrate that the in vivo proximity-ligation method Hi-C can reconstruct a known plasmid-host association from a wastewater community, and identify the in situ host range of ARGs, plasmids, and integrons by physically linking them to their host chromosomes. Hi-C detected both previously known and novel associations between ARGs, mobile genetic elements and host genomes, thus validating this method. We showed that IncQ plasmids and class 1 integrons had the broadest host range in this wastewater, and identified bacteria belonging to Moraxellaceae, Bacteroides, and Prevotella, and especially Aeromonadaceae as the most likely reservoirs of ARGs in this community. A better identification of the natural carriers of ARGs will aid the development of strategies to limit resistance spread to pathogens. Nature Publishing Group UK 2019-05-30 2019-10 /pmc/articles/PMC6776055/ /pubmed/31147603 http://dx.doi.org/10.1038/s41396-019-0446-4 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 Stalder, Thibault Press, Maximilian O. Sullivan, Shawn Liachko, Ivan Top, Eva M. Linking the resistome and plasmidome to the microbiome |
title | Linking the resistome and plasmidome to the microbiome |
title_full | Linking the resistome and plasmidome to the microbiome |
title_fullStr | Linking the resistome and plasmidome to the microbiome |
title_full_unstemmed | Linking the resistome and plasmidome to the microbiome |
title_short | Linking the resistome and plasmidome to the microbiome |
title_sort | linking the resistome and plasmidome to the microbiome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776055/ https://www.ncbi.nlm.nih.gov/pubmed/31147603 http://dx.doi.org/10.1038/s41396-019-0446-4 |
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