Cargando…

Functional Repertoire of Antibiotic Resistance Genes in Antibiotic Manufacturing Effluents and Receiving Freshwater Sediments

Environments polluted by direct discharges of effluents from antibiotic manufacturing are important reservoirs for antibiotic resistance genes (ARGs), which could potentially be transferred to human pathogens. However, our knowledge about the identity and diversity of ARGs in such polluted environme...

Descripción completa

Detalles Bibliográficos
Autores principales: González-Plaza, Juan J., Šimatović, Ana, Milaković, Milena, Bielen, Ana, Wichmann, Fabienne, Udiković-Kolić, Nikolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776109/
https://www.ncbi.nlm.nih.gov/pubmed/29387045
http://dx.doi.org/10.3389/fmicb.2017.02675
_version_ 1783294016896368640
author González-Plaza, Juan J.
Šimatović, Ana
Milaković, Milena
Bielen, Ana
Wichmann, Fabienne
Udiković-Kolić, Nikolina
author_facet González-Plaza, Juan J.
Šimatović, Ana
Milaković, Milena
Bielen, Ana
Wichmann, Fabienne
Udiković-Kolić, Nikolina
author_sort González-Plaza, Juan J.
collection PubMed
description Environments polluted by direct discharges of effluents from antibiotic manufacturing are important reservoirs for antibiotic resistance genes (ARGs), which could potentially be transferred to human pathogens. However, our knowledge about the identity and diversity of ARGs in such polluted environments remains limited. We applied functional metagenomics to explore the resistome of two Croatian antibiotic manufacturing effluents and sediments collected upstream of and at the effluent discharge sites. Metagenomic libraries built from an azithromycin-production site were screened for resistance to macrolide antibiotics, whereas the libraries from a site producing veterinary antibiotics were screened for resistance to sulfonamides, tetracyclines, trimethoprim, and beta-lactams. Functional analysis of eight libraries identified a total of 82 unique, often clinically relevant ARGs, which were frequently found in clusters and flanked by mobile genetic elements. The majority of macrolide resistance genes identified from matrices exposed to high levels of macrolides were similar to known genes encoding ribosomal protection proteins, macrolide phosphotransferases, and transporters. Potentially novel macrolide resistance genes included one most similar to a 23S rRNA methyltransferase from Clostridium and another, derived from upstream unpolluted sediment, to a GTPase HflX from Emergencia. In libraries deriving from sediments exposed to lower levels of veterinary antibiotics, we found 8 potentially novel ARGs, including dihydrofolate reductases and beta-lactamases from classes A, B, and D. In addition, we detected 7 potentially novel ARGs in upstream sediment, including thymidylate synthases, dihydrofolate reductases, and class D beta-lactamase. Taken together, in addition to finding known gene types, we report the discovery of novel and diverse ARGs in antibiotic-polluted industrial effluents and sediments, providing a qualitative basis for monitoring the dispersal of ARGs from environmental hotspots such as discharge sites of pharmaceutical effluents.
format Online
Article
Text
id pubmed-5776109
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-57761092018-01-31 Functional Repertoire of Antibiotic Resistance Genes in Antibiotic Manufacturing Effluents and Receiving Freshwater Sediments González-Plaza, Juan J. Šimatović, Ana Milaković, Milena Bielen, Ana Wichmann, Fabienne Udiković-Kolić, Nikolina Front Microbiol Microbiology Environments polluted by direct discharges of effluents from antibiotic manufacturing are important reservoirs for antibiotic resistance genes (ARGs), which could potentially be transferred to human pathogens. However, our knowledge about the identity and diversity of ARGs in such polluted environments remains limited. We applied functional metagenomics to explore the resistome of two Croatian antibiotic manufacturing effluents and sediments collected upstream of and at the effluent discharge sites. Metagenomic libraries built from an azithromycin-production site were screened for resistance to macrolide antibiotics, whereas the libraries from a site producing veterinary antibiotics were screened for resistance to sulfonamides, tetracyclines, trimethoprim, and beta-lactams. Functional analysis of eight libraries identified a total of 82 unique, often clinically relevant ARGs, which were frequently found in clusters and flanked by mobile genetic elements. The majority of macrolide resistance genes identified from matrices exposed to high levels of macrolides were similar to known genes encoding ribosomal protection proteins, macrolide phosphotransferases, and transporters. Potentially novel macrolide resistance genes included one most similar to a 23S rRNA methyltransferase from Clostridium and another, derived from upstream unpolluted sediment, to a GTPase HflX from Emergencia. In libraries deriving from sediments exposed to lower levels of veterinary antibiotics, we found 8 potentially novel ARGs, including dihydrofolate reductases and beta-lactamases from classes A, B, and D. In addition, we detected 7 potentially novel ARGs in upstream sediment, including thymidylate synthases, dihydrofolate reductases, and class D beta-lactamase. Taken together, in addition to finding known gene types, we report the discovery of novel and diverse ARGs in antibiotic-polluted industrial effluents and sediments, providing a qualitative basis for monitoring the dispersal of ARGs from environmental hotspots such as discharge sites of pharmaceutical effluents. Frontiers Media S.A. 2018-01-17 /pmc/articles/PMC5776109/ /pubmed/29387045 http://dx.doi.org/10.3389/fmicb.2017.02675 Text en Copyright © 2018 González-Plaza, Šimatović, Milaković, Bielen, Wichmann and Udiković-Kolić. 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) or licensor 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
González-Plaza, Juan J.
Šimatović, Ana
Milaković, Milena
Bielen, Ana
Wichmann, Fabienne
Udiković-Kolić, Nikolina
Functional Repertoire of Antibiotic Resistance Genes in Antibiotic Manufacturing Effluents and Receiving Freshwater Sediments
title Functional Repertoire of Antibiotic Resistance Genes in Antibiotic Manufacturing Effluents and Receiving Freshwater Sediments
title_full Functional Repertoire of Antibiotic Resistance Genes in Antibiotic Manufacturing Effluents and Receiving Freshwater Sediments
title_fullStr Functional Repertoire of Antibiotic Resistance Genes in Antibiotic Manufacturing Effluents and Receiving Freshwater Sediments
title_full_unstemmed Functional Repertoire of Antibiotic Resistance Genes in Antibiotic Manufacturing Effluents and Receiving Freshwater Sediments
title_short Functional Repertoire of Antibiotic Resistance Genes in Antibiotic Manufacturing Effluents and Receiving Freshwater Sediments
title_sort functional repertoire of antibiotic resistance genes in antibiotic manufacturing effluents and receiving freshwater sediments
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776109/
https://www.ncbi.nlm.nih.gov/pubmed/29387045
http://dx.doi.org/10.3389/fmicb.2017.02675
work_keys_str_mv AT gonzalezplazajuanj functionalrepertoireofantibioticresistancegenesinantibioticmanufacturingeffluentsandreceivingfreshwatersediments
AT simatovicana functionalrepertoireofantibioticresistancegenesinantibioticmanufacturingeffluentsandreceivingfreshwatersediments
AT milakovicmilena functionalrepertoireofantibioticresistancegenesinantibioticmanufacturingeffluentsandreceivingfreshwatersediments
AT bielenana functionalrepertoireofantibioticresistancegenesinantibioticmanufacturingeffluentsandreceivingfreshwatersediments
AT wichmannfabienne functionalrepertoireofantibioticresistancegenesinantibioticmanufacturingeffluentsandreceivingfreshwatersediments
AT udikovickolicnikolina functionalrepertoireofantibioticresistancegenesinantibioticmanufacturingeffluentsandreceivingfreshwatersediments