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Computational discovery and functional validation of novel fluoroquinolone resistance genes in public metagenomic data sets
BACKGROUND: Fluoroquinolones are broad-spectrum antibiotics used to prevent and treat a wide range of bacterial infections. Plasmid-mediated qnr genes provide resistance to fluoroquinolones in many bacterial species and are increasingly encountered in clinical settings. Over the last decade, several...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581476/ https://www.ncbi.nlm.nih.gov/pubmed/28865446 http://dx.doi.org/10.1186/s12864-017-4064-0 |
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author | Boulund, Fredrik Berglund, Fanny Flach, Carl-Fredrik Bengtsson-Palme, Johan Marathe, Nachiket P. Larsson, DG Joakim Kristiansson, Erik |
author_facet | Boulund, Fredrik Berglund, Fanny Flach, Carl-Fredrik Bengtsson-Palme, Johan Marathe, Nachiket P. Larsson, DG Joakim Kristiansson, Erik |
author_sort | Boulund, Fredrik |
collection | PubMed |
description | BACKGROUND: Fluoroquinolones are broad-spectrum antibiotics used to prevent and treat a wide range of bacterial infections. Plasmid-mediated qnr genes provide resistance to fluoroquinolones in many bacterial species and are increasingly encountered in clinical settings. Over the last decade, several families of qnr genes have been discovered and characterized, but their true prevalence and diversity still remain unclear. In particular, environmental and host-associated bacterial communities have been hypothesized to maintain a large and unknown collection of qnr genes that could be mobilized into pathogens. RESULTS: In this study we used computational methods to screen genomes and metagenomes for novel qnr genes. In contrast to previous studies, we analyzed an almost 20-fold larger dataset comprising almost 13 terabases of sequence data. In total, 362,843 potential qnr gene fragments were identified, from which 611 putative qnr genes were reconstructed. These gene sequences included all previously described plasmid-mediated qnr gene families. Fifty-two of the 611 identified qnr genes were reconstructed from metagenomes, and 20 of these were previously undescribed. All of the novel qnr genes were assembled from metagenomes associated with aquatic environments. Nine of the novel genes were selected for validation, and six of the tested genes conferred consistently decreased susceptibility to ciprofloxacin when expressed in Escherichia coli. CONCLUSIONS: The results presented in this study provide additional evidence for the ubiquitous presence of qnr genes in environmental microbial communities, expand the number of known qnr gene variants and further elucidate the diversity of this class of resistance genes. This study also strengthens the hypothesis that environmental bacterial communities act as sources of previously uncharacterized qnr genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-4064-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5581476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55814762017-09-06 Computational discovery and functional validation of novel fluoroquinolone resistance genes in public metagenomic data sets Boulund, Fredrik Berglund, Fanny Flach, Carl-Fredrik Bengtsson-Palme, Johan Marathe, Nachiket P. Larsson, DG Joakim Kristiansson, Erik BMC Genomics Research Article BACKGROUND: Fluoroquinolones are broad-spectrum antibiotics used to prevent and treat a wide range of bacterial infections. Plasmid-mediated qnr genes provide resistance to fluoroquinolones in many bacterial species and are increasingly encountered in clinical settings. Over the last decade, several families of qnr genes have been discovered and characterized, but their true prevalence and diversity still remain unclear. In particular, environmental and host-associated bacterial communities have been hypothesized to maintain a large and unknown collection of qnr genes that could be mobilized into pathogens. RESULTS: In this study we used computational methods to screen genomes and metagenomes for novel qnr genes. In contrast to previous studies, we analyzed an almost 20-fold larger dataset comprising almost 13 terabases of sequence data. In total, 362,843 potential qnr gene fragments were identified, from which 611 putative qnr genes were reconstructed. These gene sequences included all previously described plasmid-mediated qnr gene families. Fifty-two of the 611 identified qnr genes were reconstructed from metagenomes, and 20 of these were previously undescribed. All of the novel qnr genes were assembled from metagenomes associated with aquatic environments. Nine of the novel genes were selected for validation, and six of the tested genes conferred consistently decreased susceptibility to ciprofloxacin when expressed in Escherichia coli. CONCLUSIONS: The results presented in this study provide additional evidence for the ubiquitous presence of qnr genes in environmental microbial communities, expand the number of known qnr gene variants and further elucidate the diversity of this class of resistance genes. This study also strengthens the hypothesis that environmental bacterial communities act as sources of previously uncharacterized qnr genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-4064-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-02 /pmc/articles/PMC5581476/ /pubmed/28865446 http://dx.doi.org/10.1186/s12864-017-4064-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Boulund, Fredrik Berglund, Fanny Flach, Carl-Fredrik Bengtsson-Palme, Johan Marathe, Nachiket P. Larsson, DG Joakim Kristiansson, Erik Computational discovery and functional validation of novel fluoroquinolone resistance genes in public metagenomic data sets |
title | Computational discovery and functional validation of novel fluoroquinolone resistance genes in public metagenomic data sets |
title_full | Computational discovery and functional validation of novel fluoroquinolone resistance genes in public metagenomic data sets |
title_fullStr | Computational discovery and functional validation of novel fluoroquinolone resistance genes in public metagenomic data sets |
title_full_unstemmed | Computational discovery and functional validation of novel fluoroquinolone resistance genes in public metagenomic data sets |
title_short | Computational discovery and functional validation of novel fluoroquinolone resistance genes in public metagenomic data sets |
title_sort | computational discovery and functional validation of novel fluoroquinolone resistance genes in public metagenomic data sets |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581476/ https://www.ncbi.nlm.nih.gov/pubmed/28865446 http://dx.doi.org/10.1186/s12864-017-4064-0 |
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