Cargando…

Long-term mercury contamination does not affect the microbial gene potential for C and N cycling in soils but enhances detoxification gene abundance

Soil microorganisms are key transformers of mercury (Hg), a toxic and widespread pollutant. It remains uncertain, however, how long-term exposure to Hg affects crucial microbial functions, such as litter decomposition and nitrogen cycling. Here, we used a metagenomic approach to investigate the stat...

Descripción completa

Detalles Bibliográficos
Autores principales: Frey, Beat, Rast, Basil M., Qi, Weihong, Stierli, Beat, Brunner, Ivano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581213/
https://www.ncbi.nlm.nih.gov/pubmed/36274742
http://dx.doi.org/10.3389/fmicb.2022.1034138
_version_ 1784812569370820608
author Frey, Beat
Rast, Basil M.
Qi, Weihong
Stierli, Beat
Brunner, Ivano
author_facet Frey, Beat
Rast, Basil M.
Qi, Weihong
Stierli, Beat
Brunner, Ivano
author_sort Frey, Beat
collection PubMed
description Soil microorganisms are key transformers of mercury (Hg), a toxic and widespread pollutant. It remains uncertain, however, how long-term exposure to Hg affects crucial microbial functions, such as litter decomposition and nitrogen cycling. Here, we used a metagenomic approach to investigate the state of soil functions in an agricultural floodplain contaminated with Hg for more than 80 years. We sampled soils along a gradient of Hg contamination (high, moderate, low). Hg concentrations at the highly contaminated site (36 mg kg(–1) dry soil on average) were approximately 10 times higher than at the moderately contaminated site (3 mg kg(–1) dry soil) and more than 100 times higher than at the site with low contamination (0.25 mg kg(–1) dry soil; corresponding to the natural background concentration in Switzerland). The analysis of the CAZy and NCyc databases showed that carbon and nitrogen cycling was not strongly affected with high Hg concentrations, although a significant change in the beta-diversity of the predicted genes was observed. The only functional classes from the CAZy database that were significantly positively overrepresented under higher Hg concentrations were genes involved in pectin degradation, and from the NCyc database dissimilatory nitrate reduction and N-fixation. When comparing between low and high Hg concentrations the genes of the EggNOG functional category of inorganic ion transport and metabolism, two genes encoding Hg transport proteins and one gene involved in heavy metal transport detoxification were among those that were highly significantly overrepresented. A look at genes specifically involved in detoxification of Hg species, such as the mer and hgc genes, showed a significant overrepresentation when Hg contamination was increased. Normalized counts of these genes revealed a dominant role for the phylum Proteobacteria. In particular, most counts for almost all mer genes were found in Betaproteobacteria. In contrast, hgc genes were most abundant in Desulfuromonadales. Overall, we conclude from this metagenomic analysis that long-term exposure to high Hg triggers shifts in the functional beta-diversity of the predicted microbial genes, but we do not see a dramatic change or breakdown in functional capabilities, but rather functional redundancy.
format Online
Article
Text
id pubmed-9581213
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-95812132022-10-20 Long-term mercury contamination does not affect the microbial gene potential for C and N cycling in soils but enhances detoxification gene abundance Frey, Beat Rast, Basil M. Qi, Weihong Stierli, Beat Brunner, Ivano Front Microbiol Microbiology Soil microorganisms are key transformers of mercury (Hg), a toxic and widespread pollutant. It remains uncertain, however, how long-term exposure to Hg affects crucial microbial functions, such as litter decomposition and nitrogen cycling. Here, we used a metagenomic approach to investigate the state of soil functions in an agricultural floodplain contaminated with Hg for more than 80 years. We sampled soils along a gradient of Hg contamination (high, moderate, low). Hg concentrations at the highly contaminated site (36 mg kg(–1) dry soil on average) were approximately 10 times higher than at the moderately contaminated site (3 mg kg(–1) dry soil) and more than 100 times higher than at the site with low contamination (0.25 mg kg(–1) dry soil; corresponding to the natural background concentration in Switzerland). The analysis of the CAZy and NCyc databases showed that carbon and nitrogen cycling was not strongly affected with high Hg concentrations, although a significant change in the beta-diversity of the predicted genes was observed. The only functional classes from the CAZy database that were significantly positively overrepresented under higher Hg concentrations were genes involved in pectin degradation, and from the NCyc database dissimilatory nitrate reduction and N-fixation. When comparing between low and high Hg concentrations the genes of the EggNOG functional category of inorganic ion transport and metabolism, two genes encoding Hg transport proteins and one gene involved in heavy metal transport detoxification were among those that were highly significantly overrepresented. A look at genes specifically involved in detoxification of Hg species, such as the mer and hgc genes, showed a significant overrepresentation when Hg contamination was increased. Normalized counts of these genes revealed a dominant role for the phylum Proteobacteria. In particular, most counts for almost all mer genes were found in Betaproteobacteria. In contrast, hgc genes were most abundant in Desulfuromonadales. Overall, we conclude from this metagenomic analysis that long-term exposure to high Hg triggers shifts in the functional beta-diversity of the predicted microbial genes, but we do not see a dramatic change or breakdown in functional capabilities, but rather functional redundancy. Frontiers Media S.A. 2022-10-05 /pmc/articles/PMC9581213/ /pubmed/36274742 http://dx.doi.org/10.3389/fmicb.2022.1034138 Text en Copyright © 2022 Frey, Rast, Qi, Stierli and Brunner. https://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
Frey, Beat
Rast, Basil M.
Qi, Weihong
Stierli, Beat
Brunner, Ivano
Long-term mercury contamination does not affect the microbial gene potential for C and N cycling in soils but enhances detoxification gene abundance
title Long-term mercury contamination does not affect the microbial gene potential for C and N cycling in soils but enhances detoxification gene abundance
title_full Long-term mercury contamination does not affect the microbial gene potential for C and N cycling in soils but enhances detoxification gene abundance
title_fullStr Long-term mercury contamination does not affect the microbial gene potential for C and N cycling in soils but enhances detoxification gene abundance
title_full_unstemmed Long-term mercury contamination does not affect the microbial gene potential for C and N cycling in soils but enhances detoxification gene abundance
title_short Long-term mercury contamination does not affect the microbial gene potential for C and N cycling in soils but enhances detoxification gene abundance
title_sort long-term mercury contamination does not affect the microbial gene potential for c and n cycling in soils but enhances detoxification gene abundance
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581213/
https://www.ncbi.nlm.nih.gov/pubmed/36274742
http://dx.doi.org/10.3389/fmicb.2022.1034138
work_keys_str_mv AT freybeat longtermmercurycontaminationdoesnotaffectthemicrobialgenepotentialforcandncyclinginsoilsbutenhancesdetoxificationgeneabundance
AT rastbasilm longtermmercurycontaminationdoesnotaffectthemicrobialgenepotentialforcandncyclinginsoilsbutenhancesdetoxificationgeneabundance
AT qiweihong longtermmercurycontaminationdoesnotaffectthemicrobialgenepotentialforcandncyclinginsoilsbutenhancesdetoxificationgeneabundance
AT stierlibeat longtermmercurycontaminationdoesnotaffectthemicrobialgenepotentialforcandncyclinginsoilsbutenhancesdetoxificationgeneabundance
AT brunnerivano longtermmercurycontaminationdoesnotaffectthemicrobialgenepotentialforcandncyclinginsoilsbutenhancesdetoxificationgeneabundance