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Impact of selected non-steroidal anti-inflammatory pharmaceuticals on microbial community assembly and activity in sequencing batch reactors

This study covers three widely detected non-steroidal anti-inflammatory pharmaceuticals (NSAIDs), diclofenac (DCF), ibuprofen (IBP) and naproxen (NPX), as NSAIDs pollutants. The objective is to evaluate the impact of NSAIDs at their environmental concentrations on microbial community assembly and ac...

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Autores principales: Jiang, Cong, Geng, Jinju, Hu, Haidong, Ma, Haijun, Gao, Xingsheng, Ren, Hongqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480864/
https://www.ncbi.nlm.nih.gov/pubmed/28640897
http://dx.doi.org/10.1371/journal.pone.0179236
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author Jiang, Cong
Geng, Jinju
Hu, Haidong
Ma, Haijun
Gao, Xingsheng
Ren, Hongqiang
author_facet Jiang, Cong
Geng, Jinju
Hu, Haidong
Ma, Haijun
Gao, Xingsheng
Ren, Hongqiang
author_sort Jiang, Cong
collection PubMed
description This study covers three widely detected non-steroidal anti-inflammatory pharmaceuticals (NSAIDs), diclofenac (DCF), ibuprofen (IBP) and naproxen (NPX), as NSAIDs pollutants. The objective is to evaluate the impact of NSAIDs at their environmental concentrations on microbial community assembly and activity. The exposure experiments were conducted under three conditions (5 μg L(-1) DCF, 5 μg L(-1) DCF+5 μg L(-1) IBP and 5 μg L(-1) DCF+5 μg L(-1) IBP+ 5 μg L(-1) NPX) in sequencing batch reactors (SBRs) for 130 days. Removals of COD and NH(4)(+)-N were not affected but total nitrogen (TN) removal decreased. IBP and NPX had the high removal efficiencies (79.96% to 85.64%), whereas DCF was more persistent (57.24% to 64.12%). In addition, the decreased removals of TN remained the same under the three conditions (p > 0.05). The results of oxidizing enzyme activities, live cell percentages and extracellular polymeric substances (EPS) indicated that NSAIDs damaged the cell walls or microorganisms and the mixtures of the three NSAIDs increased the toxicity. The increased Shannon-Wiener diversity index suggested that bacterial diversity was increased with the addition of selected NSAIDs. Bacterial ribosomal RNA small subunit (16S) gene sequencing results indicated that Actinobacteria and Bacteroidetes were enriched, while Micropruina and Nakamurella decreased with the addition of NSAIDs. The enrichment of Actinobacteria and Bacteroidetes indicated that both of them might have the ability to degrade NSAIDs and thereby could adapt well with the presence of NSAIDs.
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spelling pubmed-54808642017-07-05 Impact of selected non-steroidal anti-inflammatory pharmaceuticals on microbial community assembly and activity in sequencing batch reactors Jiang, Cong Geng, Jinju Hu, Haidong Ma, Haijun Gao, Xingsheng Ren, Hongqiang PLoS One Research Article This study covers three widely detected non-steroidal anti-inflammatory pharmaceuticals (NSAIDs), diclofenac (DCF), ibuprofen (IBP) and naproxen (NPX), as NSAIDs pollutants. The objective is to evaluate the impact of NSAIDs at their environmental concentrations on microbial community assembly and activity. The exposure experiments were conducted under three conditions (5 μg L(-1) DCF, 5 μg L(-1) DCF+5 μg L(-1) IBP and 5 μg L(-1) DCF+5 μg L(-1) IBP+ 5 μg L(-1) NPX) in sequencing batch reactors (SBRs) for 130 days. Removals of COD and NH(4)(+)-N were not affected but total nitrogen (TN) removal decreased. IBP and NPX had the high removal efficiencies (79.96% to 85.64%), whereas DCF was more persistent (57.24% to 64.12%). In addition, the decreased removals of TN remained the same under the three conditions (p > 0.05). The results of oxidizing enzyme activities, live cell percentages and extracellular polymeric substances (EPS) indicated that NSAIDs damaged the cell walls or microorganisms and the mixtures of the three NSAIDs increased the toxicity. The increased Shannon-Wiener diversity index suggested that bacterial diversity was increased with the addition of selected NSAIDs. Bacterial ribosomal RNA small subunit (16S) gene sequencing results indicated that Actinobacteria and Bacteroidetes were enriched, while Micropruina and Nakamurella decreased with the addition of NSAIDs. The enrichment of Actinobacteria and Bacteroidetes indicated that both of them might have the ability to degrade NSAIDs and thereby could adapt well with the presence of NSAIDs. Public Library of Science 2017-06-22 /pmc/articles/PMC5480864/ /pubmed/28640897 http://dx.doi.org/10.1371/journal.pone.0179236 Text en © 2017 Jiang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jiang, Cong
Geng, Jinju
Hu, Haidong
Ma, Haijun
Gao, Xingsheng
Ren, Hongqiang
Impact of selected non-steroidal anti-inflammatory pharmaceuticals on microbial community assembly and activity in sequencing batch reactors
title Impact of selected non-steroidal anti-inflammatory pharmaceuticals on microbial community assembly and activity in sequencing batch reactors
title_full Impact of selected non-steroidal anti-inflammatory pharmaceuticals on microbial community assembly and activity in sequencing batch reactors
title_fullStr Impact of selected non-steroidal anti-inflammatory pharmaceuticals on microbial community assembly and activity in sequencing batch reactors
title_full_unstemmed Impact of selected non-steroidal anti-inflammatory pharmaceuticals on microbial community assembly and activity in sequencing batch reactors
title_short Impact of selected non-steroidal anti-inflammatory pharmaceuticals on microbial community assembly and activity in sequencing batch reactors
title_sort impact of selected non-steroidal anti-inflammatory pharmaceuticals on microbial community assembly and activity in sequencing batch reactors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480864/
https://www.ncbi.nlm.nih.gov/pubmed/28640897
http://dx.doi.org/10.1371/journal.pone.0179236
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