Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Willms, Inka Marie, Kamran, Aysha, Aßmann, Nils Frederik, Krone, Denis, Bolz, Simon Henning, Fiedler, Fabian, Nacke, Heiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
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
_version_ 1783403309471629312
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
work_keys_str_mv AT willmsinkamarie discoveryofnovelantibioticresistancedeterminantsinforestandgrasslandsoilmetagenomes
AT kamranaysha discoveryofnovelantibioticresistancedeterminantsinforestandgrasslandsoilmetagenomes
AT aßmannnilsfrederik discoveryofnovelantibioticresistancedeterminantsinforestandgrasslandsoilmetagenomes
AT kronedenis discoveryofnovelantibioticresistancedeterminantsinforestandgrasslandsoilmetagenomes
AT bolzsimonhenning discoveryofnovelantibioticresistancedeterminantsinforestandgrasslandsoilmetagenomes
AT fiedlerfabian discoveryofnovelantibioticresistancedeterminantsinforestandgrasslandsoilmetagenomes
AT nackeheiko discoveryofnovelantibioticresistancedeterminantsinforestandgrasslandsoilmetagenomes