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Discovery of Novel Antibiotic Resistance Determinants in Forest and Grassland Soil Metagenomes
Soil represents a significant reservoir of antibiotic resistance genes (ARGs), which can potentially spread across distinct ecosystems and be acquired by pathogens threatening human as well as animal health. Currently, information on the identity and diversity of these genes, enabling anticipation o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416219/ https://www.ncbi.nlm.nih.gov/pubmed/30899254 http://dx.doi.org/10.3389/fmicb.2019.00460 |
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author | Willms, Inka Marie Kamran, Aysha Aßmann, Nils Frederik Krone, Denis Bolz, Simon Henning Fiedler, Fabian Nacke, Heiko |
author_facet | Willms, Inka Marie Kamran, Aysha Aßmann, Nils Frederik Krone, Denis Bolz, Simon Henning Fiedler, Fabian Nacke, Heiko |
author_sort | Willms, Inka Marie |
collection | PubMed |
description | Soil represents a significant reservoir of antibiotic resistance genes (ARGs), which can potentially spread across distinct ecosystems and be acquired by pathogens threatening human as well as animal health. Currently, information on the identity and diversity of these genes, enabling anticipation of possible future resistance development in clinical environments and the livestock sector, is lacking. In this study, we applied functional metagenomics to discover novel sulfonamide as well as tetracycline resistance genes in soils derived from forest and grassland. Screening of soil metagenomic libraries revealed a total of eight so far unknown ARGs. The recovered genes originate from phylogenetically diverse soil bacteria (e.g., Actinobacteria, Chloroflexi, or Proteobacteria) and encode proteins with a minimum identity of 46% to other antibiotic resistance determinants. In particular forest soil ecosystems have so far been neglected in studies focusing on antibiotic resistance. Here, we detected for the first time non-mobile dihydropteroate synthase (DHPS) genes conferring resistance to sulfonamides in forest soil with no history of exposure to these synthetic drugs. In total, three sulfonamide resistant DHPSs, differing in taxonomic origin, were discovered in beech or pine forest soil. This indicates that sulfonamide resistance naturally occurs in forest-resident soil bacterial communities. Besides forest soil-derived sulfonamide resistance proteins, we also identified a DHPS affiliated to Chloroflexi in grassland soil. This enzyme and the other recovered DHPSs confer reduced susceptibility toward sulfamethazine, which is widely used in food animal production. With respect to tetracycline resistance, four efflux proteins affiliated to the major facilitator superfamily (MFS) were identified. Noteworthy, one of these proteins also conferred reduced susceptibility toward lincomycin. |
format | Online Article Text |
id | pubmed-6416219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64162192019-03-21 Discovery of Novel Antibiotic Resistance Determinants in Forest and Grassland Soil Metagenomes Willms, Inka Marie Kamran, Aysha Aßmann, Nils Frederik Krone, Denis Bolz, Simon Henning Fiedler, Fabian Nacke, Heiko Front Microbiol Microbiology Soil represents a significant reservoir of antibiotic resistance genes (ARGs), which can potentially spread across distinct ecosystems and be acquired by pathogens threatening human as well as animal health. Currently, information on the identity and diversity of these genes, enabling anticipation of possible future resistance development in clinical environments and the livestock sector, is lacking. In this study, we applied functional metagenomics to discover novel sulfonamide as well as tetracycline resistance genes in soils derived from forest and grassland. Screening of soil metagenomic libraries revealed a total of eight so far unknown ARGs. The recovered genes originate from phylogenetically diverse soil bacteria (e.g., Actinobacteria, Chloroflexi, or Proteobacteria) and encode proteins with a minimum identity of 46% to other antibiotic resistance determinants. In particular forest soil ecosystems have so far been neglected in studies focusing on antibiotic resistance. Here, we detected for the first time non-mobile dihydropteroate synthase (DHPS) genes conferring resistance to sulfonamides in forest soil with no history of exposure to these synthetic drugs. In total, three sulfonamide resistant DHPSs, differing in taxonomic origin, were discovered in beech or pine forest soil. This indicates that sulfonamide resistance naturally occurs in forest-resident soil bacterial communities. Besides forest soil-derived sulfonamide resistance proteins, we also identified a DHPS affiliated to Chloroflexi in grassland soil. This enzyme and the other recovered DHPSs confer reduced susceptibility toward sulfamethazine, which is widely used in food animal production. With respect to tetracycline resistance, four efflux proteins affiliated to the major facilitator superfamily (MFS) were identified. Noteworthy, one of these proteins also conferred reduced susceptibility toward lincomycin. Frontiers Media S.A. 2019-03-07 /pmc/articles/PMC6416219/ /pubmed/30899254 http://dx.doi.org/10.3389/fmicb.2019.00460 Text en Copyright © 2019 Willms, Kamran, Aßmann, Krone, Bolz, Fiedler and Nacke. 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 Willms, Inka Marie Kamran, Aysha Aßmann, Nils Frederik Krone, Denis Bolz, Simon Henning Fiedler, Fabian Nacke, Heiko Discovery of Novel Antibiotic Resistance Determinants in Forest and Grassland Soil Metagenomes |
title | Discovery of Novel Antibiotic Resistance Determinants in Forest and Grassland Soil Metagenomes |
title_full | Discovery of Novel Antibiotic Resistance Determinants in Forest and Grassland Soil Metagenomes |
title_fullStr | Discovery of Novel Antibiotic Resistance Determinants in Forest and Grassland Soil Metagenomes |
title_full_unstemmed | Discovery of Novel Antibiotic Resistance Determinants in Forest and Grassland Soil Metagenomes |
title_short | Discovery of Novel Antibiotic Resistance Determinants in Forest and Grassland Soil Metagenomes |
title_sort | discovery of novel antibiotic resistance determinants in forest and grassland soil metagenomes |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416219/ https://www.ncbi.nlm.nih.gov/pubmed/30899254 http://dx.doi.org/10.3389/fmicb.2019.00460 |
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