Cargando…

Opportunistic Bacteria Dominate the Soil Microbiome Response to Phenanthrene in a Microcosm-Based Study

Bioremediation offers a sustainable approach for removal of polycyclic aromatic hydrocarbons (PAHs) from the environment; however, information regarding the microbial communities involved remains limited. In this study, microbial community dynamics and the abundance of the key gene (PAH-RHDα) encodi...

Descripción completa

Detalles Bibliográficos
Autores principales: Storey, Sean, Ashaari, Mardiana Mohd, Clipson, Nicholas, Doyle, Evelyn, de Menezes, Alexandre B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258822/
https://www.ncbi.nlm.nih.gov/pubmed/30519226
http://dx.doi.org/10.3389/fmicb.2018.02815
_version_ 1783374566449479680
author Storey, Sean
Ashaari, Mardiana Mohd
Clipson, Nicholas
Doyle, Evelyn
de Menezes, Alexandre B.
author_facet Storey, Sean
Ashaari, Mardiana Mohd
Clipson, Nicholas
Doyle, Evelyn
de Menezes, Alexandre B.
author_sort Storey, Sean
collection PubMed
description Bioremediation offers a sustainable approach for removal of polycyclic aromatic hydrocarbons (PAHs) from the environment; however, information regarding the microbial communities involved remains limited. In this study, microbial community dynamics and the abundance of the key gene (PAH-RHDα) encoding a ring hydroxylating dioxygenase involved in PAH degradation were examined during degradation of phenanthrene in a podzolic soil from the site of a former timber treatment facility. The 10,000-fold greater abundance of this gene associated with Gram-positive bacteria found in phenanthrene-amended soil compared to unamended soil indicated the likely role of Gram-positive bacteria in PAH degradation. In contrast, the abundance of the Gram-negative PAHs-RHDα gene was very low throughout the experiment. While phenanthrene induced increases in the abundance of a small number of OTUs from the Actinomycetales and Sphingomonadale, most of the remainder of the community remained stable. A single unclassified OTU from the Micrococcaceae family increased ~20-fold in relative abundance, reaching 32% of the total sequences in amended microcosms on day 7 of the experiment. The relative abundance of this same OTU increased 4.5-fold in unamended soils, and a similar pattern was observed for the second most abundant PAH-responsive OTU, classified into the Sphingomonas genus. Furthermore, the relative abundance of both of these OTUs decreased substantially between days 7 and 17 in the phenanthrene-amended and control microcosms. This suggests that their opportunistic phenotype, in addition to likely PAH-degrading ability, was determinant in the vigorous growth of dominant PAH-responsive OTUs following phenanthrene amendment. This study provides new information on the temporal response of soil microbial communities to the presence and degradation of a significant environmental pollutant, and as such has the potential to inform the design of PAH bioremediation protocols.
format Online
Article
Text
id pubmed-6258822
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-62588222018-12-05 Opportunistic Bacteria Dominate the Soil Microbiome Response to Phenanthrene in a Microcosm-Based Study Storey, Sean Ashaari, Mardiana Mohd Clipson, Nicholas Doyle, Evelyn de Menezes, Alexandre B. Front Microbiol Microbiology Bioremediation offers a sustainable approach for removal of polycyclic aromatic hydrocarbons (PAHs) from the environment; however, information regarding the microbial communities involved remains limited. In this study, microbial community dynamics and the abundance of the key gene (PAH-RHDα) encoding a ring hydroxylating dioxygenase involved in PAH degradation were examined during degradation of phenanthrene in a podzolic soil from the site of a former timber treatment facility. The 10,000-fold greater abundance of this gene associated with Gram-positive bacteria found in phenanthrene-amended soil compared to unamended soil indicated the likely role of Gram-positive bacteria in PAH degradation. In contrast, the abundance of the Gram-negative PAHs-RHDα gene was very low throughout the experiment. While phenanthrene induced increases in the abundance of a small number of OTUs from the Actinomycetales and Sphingomonadale, most of the remainder of the community remained stable. A single unclassified OTU from the Micrococcaceae family increased ~20-fold in relative abundance, reaching 32% of the total sequences in amended microcosms on day 7 of the experiment. The relative abundance of this same OTU increased 4.5-fold in unamended soils, and a similar pattern was observed for the second most abundant PAH-responsive OTU, classified into the Sphingomonas genus. Furthermore, the relative abundance of both of these OTUs decreased substantially between days 7 and 17 in the phenanthrene-amended and control microcosms. This suggests that their opportunistic phenotype, in addition to likely PAH-degrading ability, was determinant in the vigorous growth of dominant PAH-responsive OTUs following phenanthrene amendment. This study provides new information on the temporal response of soil microbial communities to the presence and degradation of a significant environmental pollutant, and as such has the potential to inform the design of PAH bioremediation protocols. Frontiers Media S.A. 2018-11-21 /pmc/articles/PMC6258822/ /pubmed/30519226 http://dx.doi.org/10.3389/fmicb.2018.02815 Text en Copyright © 2018 Storey, Ashaari, Clipson, Doyle and de Menezes. 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
Storey, Sean
Ashaari, Mardiana Mohd
Clipson, Nicholas
Doyle, Evelyn
de Menezes, Alexandre B.
Opportunistic Bacteria Dominate the Soil Microbiome Response to Phenanthrene in a Microcosm-Based Study
title Opportunistic Bacteria Dominate the Soil Microbiome Response to Phenanthrene in a Microcosm-Based Study
title_full Opportunistic Bacteria Dominate the Soil Microbiome Response to Phenanthrene in a Microcosm-Based Study
title_fullStr Opportunistic Bacteria Dominate the Soil Microbiome Response to Phenanthrene in a Microcosm-Based Study
title_full_unstemmed Opportunistic Bacteria Dominate the Soil Microbiome Response to Phenanthrene in a Microcosm-Based Study
title_short Opportunistic Bacteria Dominate the Soil Microbiome Response to Phenanthrene in a Microcosm-Based Study
title_sort opportunistic bacteria dominate the soil microbiome response to phenanthrene in a microcosm-based study
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258822/
https://www.ncbi.nlm.nih.gov/pubmed/30519226
http://dx.doi.org/10.3389/fmicb.2018.02815
work_keys_str_mv AT storeysean opportunisticbacteriadominatethesoilmicrobiomeresponsetophenanthreneinamicrocosmbasedstudy
AT ashaarimardianamohd opportunisticbacteriadominatethesoilmicrobiomeresponsetophenanthreneinamicrocosmbasedstudy
AT clipsonnicholas opportunisticbacteriadominatethesoilmicrobiomeresponsetophenanthreneinamicrocosmbasedstudy
AT doyleevelyn opportunisticbacteriadominatethesoilmicrobiomeresponsetophenanthreneinamicrocosmbasedstudy
AT demenezesalexandreb opportunisticbacteriadominatethesoilmicrobiomeresponsetophenanthreneinamicrocosmbasedstudy