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Microbial Community Response of an Organohalide Respiring Enrichment Culture to Permanganate Oxidation

While in situ chemical oxidation is often used to remediate tetrachloroethene (PCE) contaminated locations, very little is known about its influence on microbial composition and organohalide respiration (OHR) activity. Here, we investigate the impact of oxidation with permanganate on OHR rates, the...

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Autores principales: Sutton, Nora B., Atashgahi, Siavash, Saccenti, Edoardo, Grotenhuis, Tim, Smidt, Hauke, Rijnaarts, Huub H. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526698/
https://www.ncbi.nlm.nih.gov/pubmed/26244346
http://dx.doi.org/10.1371/journal.pone.0134615
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author Sutton, Nora B.
Atashgahi, Siavash
Saccenti, Edoardo
Grotenhuis, Tim
Smidt, Hauke
Rijnaarts, Huub H. M.
author_facet Sutton, Nora B.
Atashgahi, Siavash
Saccenti, Edoardo
Grotenhuis, Tim
Smidt, Hauke
Rijnaarts, Huub H. M.
author_sort Sutton, Nora B.
collection PubMed
description While in situ chemical oxidation is often used to remediate tetrachloroethene (PCE) contaminated locations, very little is known about its influence on microbial composition and organohalide respiration (OHR) activity. Here, we investigate the impact of oxidation with permanganate on OHR rates, the abundance of organohalide respiring bacteria (OHRB) and reductive dehalogenase (rdh) genes using quantitative PCR, and microbial community composition through sequencing of 16S rRNA genes. A PCE degrading enrichment was repeatedly treated with low (25 μmol), medium (50 μmol), or high (100 μmol) permanganate doses, or no oxidant treatment (biotic control). Low and medium treatments led to higher OHR rates and enrichment of several OHRB and rdh genes, as compared to the biotic control. Improved degradation rates can be attributed to enrichment of (1) OHRB able to also utilize Mn oxides as a terminal electron acceptor and (2) non-dechlorinating community members of the Clostridiales and Deltaproteobacteria possibly supporting OHRB by providing essential co-factors. In contrast, high permanganate treatment disrupted dechlorination beyond cis-dichloroethene and caused at least a 2–4 orders of magnitude reduction in the abundance of all measured OHRB and rdh genes, as compared to the biotic control. High permanganate treatments resulted in a notably divergent microbial community, with increased abundances of organisms affiliated with Campylobacterales and Oceanospirillales capable of dissimilatory Mn reduction, and decreased abundance of presumed supporters of OHRB. Although OTUs classified within the OHR-supportive order Clostridiales and OHRB increased in abundance over the course of 213 days following the final 100 μmol permanganate treatment, only limited regeneration of PCE dechlorination was observed in one of three microcosms, suggesting strong chemical oxidation treatments can irreversibly disrupt OHR. Overall, this detailed investigation into dose-dependent changes of microbial composition and activity due to permanganate treatment provides insight into the mechanisms of OHR stimulation or disruption upon chemical oxidation.
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spelling pubmed-45266982015-08-12 Microbial Community Response of an Organohalide Respiring Enrichment Culture to Permanganate Oxidation Sutton, Nora B. Atashgahi, Siavash Saccenti, Edoardo Grotenhuis, Tim Smidt, Hauke Rijnaarts, Huub H. M. PLoS One Research Article While in situ chemical oxidation is often used to remediate tetrachloroethene (PCE) contaminated locations, very little is known about its influence on microbial composition and organohalide respiration (OHR) activity. Here, we investigate the impact of oxidation with permanganate on OHR rates, the abundance of organohalide respiring bacteria (OHRB) and reductive dehalogenase (rdh) genes using quantitative PCR, and microbial community composition through sequencing of 16S rRNA genes. A PCE degrading enrichment was repeatedly treated with low (25 μmol), medium (50 μmol), or high (100 μmol) permanganate doses, or no oxidant treatment (biotic control). Low and medium treatments led to higher OHR rates and enrichment of several OHRB and rdh genes, as compared to the biotic control. Improved degradation rates can be attributed to enrichment of (1) OHRB able to also utilize Mn oxides as a terminal electron acceptor and (2) non-dechlorinating community members of the Clostridiales and Deltaproteobacteria possibly supporting OHRB by providing essential co-factors. In contrast, high permanganate treatment disrupted dechlorination beyond cis-dichloroethene and caused at least a 2–4 orders of magnitude reduction in the abundance of all measured OHRB and rdh genes, as compared to the biotic control. High permanganate treatments resulted in a notably divergent microbial community, with increased abundances of organisms affiliated with Campylobacterales and Oceanospirillales capable of dissimilatory Mn reduction, and decreased abundance of presumed supporters of OHRB. Although OTUs classified within the OHR-supportive order Clostridiales and OHRB increased in abundance over the course of 213 days following the final 100 μmol permanganate treatment, only limited regeneration of PCE dechlorination was observed in one of three microcosms, suggesting strong chemical oxidation treatments can irreversibly disrupt OHR. Overall, this detailed investigation into dose-dependent changes of microbial composition and activity due to permanganate treatment provides insight into the mechanisms of OHR stimulation or disruption upon chemical oxidation. Public Library of Science 2015-08-05 /pmc/articles/PMC4526698/ /pubmed/26244346 http://dx.doi.org/10.1371/journal.pone.0134615 Text en © 2015 Sutton 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sutton, Nora B.
Atashgahi, Siavash
Saccenti, Edoardo
Grotenhuis, Tim
Smidt, Hauke
Rijnaarts, Huub H. M.
Microbial Community Response of an Organohalide Respiring Enrichment Culture to Permanganate Oxidation
title Microbial Community Response of an Organohalide Respiring Enrichment Culture to Permanganate Oxidation
title_full Microbial Community Response of an Organohalide Respiring Enrichment Culture to Permanganate Oxidation
title_fullStr Microbial Community Response of an Organohalide Respiring Enrichment Culture to Permanganate Oxidation
title_full_unstemmed Microbial Community Response of an Organohalide Respiring Enrichment Culture to Permanganate Oxidation
title_short Microbial Community Response of an Organohalide Respiring Enrichment Culture to Permanganate Oxidation
title_sort microbial community response of an organohalide respiring enrichment culture to permanganate oxidation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526698/
https://www.ncbi.nlm.nih.gov/pubmed/26244346
http://dx.doi.org/10.1371/journal.pone.0134615
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