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Metagenomics Reveals Bacterial and Archaeal Adaptation to Urban Land-Use: N Catabolism, Methanogenesis, and Nutrient Acquisition
Urbanization results in the systemic conversion of land-use, driving habitat and biodiversity loss. The “urban convergence hypothesis” posits that urbanization represents a merging of habitat characteristics, in turn driving physiological and functional responses within the biotic community. To test...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795690/ https://www.ncbi.nlm.nih.gov/pubmed/31649656 http://dx.doi.org/10.3389/fmicb.2019.02330 |
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author | Epp Schmidt, Dietrich J. Kotze, David Johan Hornung, Erzsébet Setälä, Heikki Yesilonis, Ian Szlavecz, Katalin Dombos, Miklós Pouyat, Richard Cilliers, Sarel Tóth, Zsolt Yarwood, Stephanie |
author_facet | Epp Schmidt, Dietrich J. Kotze, David Johan Hornung, Erzsébet Setälä, Heikki Yesilonis, Ian Szlavecz, Katalin Dombos, Miklós Pouyat, Richard Cilliers, Sarel Tóth, Zsolt Yarwood, Stephanie |
author_sort | Epp Schmidt, Dietrich J. |
collection | PubMed |
description | Urbanization results in the systemic conversion of land-use, driving habitat and biodiversity loss. The “urban convergence hypothesis” posits that urbanization represents a merging of habitat characteristics, in turn driving physiological and functional responses within the biotic community. To test this hypothesis, we sampled five cities (Baltimore, MD, United States; Helsinki and Lahti, Finland; Budapest, Hungary; Potchefstroom, South Africa) across four different biomes. Within each city, we sampled four land-use categories that represented a gradient of increasing disturbance and management (from least intervention to highest disturbance: reference, remnant, turf/lawn, and ruderal). Previously, we used amplicon sequencing that targeted bacteria/archaea (16S rRNA) and fungi (ITS) and reported convergence in the archaeal community. Here, we applied shotgun metagenomic sequencing and QPCR of functional genes to the same soil DNA extracts to test convergence in microbial function. Our results suggest that urban land-use drives changes in gene abundance related to both the soil N and C metabolism. Our updated analysis found taxonomic convergence in both the archaeal and bacterial community (16S amplicon data). Convergence of the archaea was driven by increased abundance of ammonia oxidizing archaea and genes for ammonia oxidation (QPCR and shotgun metagenomics). The proliferation of ammonia-oxidizers under turf and ruderal land-use likely also contributes to the previously documented convergence of soil mineral N pools. We also found a higher relative abundance of methanogens (amplicon sequencing), a higher relative abundance of gene sequences putatively identified as Ni-Fe hydrogenase and nickel uptake (shotgun metagenomics) under urban land-use; and a convergence of gene sequences putatively identified as contributing to the nickel transport function under urban turf sites. High levels of disturbance lead to a higher relative abundance of gene sequences putatively identified as multiple antibiotic resistance protein marA and multidrug efflux pump mexD, but did not lead to an overall convergence in antibiotic resistance gene sequences. |
format | Online Article Text |
id | pubmed-6795690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67956902019-10-24 Metagenomics Reveals Bacterial and Archaeal Adaptation to Urban Land-Use: N Catabolism, Methanogenesis, and Nutrient Acquisition Epp Schmidt, Dietrich J. Kotze, David Johan Hornung, Erzsébet Setälä, Heikki Yesilonis, Ian Szlavecz, Katalin Dombos, Miklós Pouyat, Richard Cilliers, Sarel Tóth, Zsolt Yarwood, Stephanie Front Microbiol Microbiology Urbanization results in the systemic conversion of land-use, driving habitat and biodiversity loss. The “urban convergence hypothesis” posits that urbanization represents a merging of habitat characteristics, in turn driving physiological and functional responses within the biotic community. To test this hypothesis, we sampled five cities (Baltimore, MD, United States; Helsinki and Lahti, Finland; Budapest, Hungary; Potchefstroom, South Africa) across four different biomes. Within each city, we sampled four land-use categories that represented a gradient of increasing disturbance and management (from least intervention to highest disturbance: reference, remnant, turf/lawn, and ruderal). Previously, we used amplicon sequencing that targeted bacteria/archaea (16S rRNA) and fungi (ITS) and reported convergence in the archaeal community. Here, we applied shotgun metagenomic sequencing and QPCR of functional genes to the same soil DNA extracts to test convergence in microbial function. Our results suggest that urban land-use drives changes in gene abundance related to both the soil N and C metabolism. Our updated analysis found taxonomic convergence in both the archaeal and bacterial community (16S amplicon data). Convergence of the archaea was driven by increased abundance of ammonia oxidizing archaea and genes for ammonia oxidation (QPCR and shotgun metagenomics). The proliferation of ammonia-oxidizers under turf and ruderal land-use likely also contributes to the previously documented convergence of soil mineral N pools. We also found a higher relative abundance of methanogens (amplicon sequencing), a higher relative abundance of gene sequences putatively identified as Ni-Fe hydrogenase and nickel uptake (shotgun metagenomics) under urban land-use; and a convergence of gene sequences putatively identified as contributing to the nickel transport function under urban turf sites. High levels of disturbance lead to a higher relative abundance of gene sequences putatively identified as multiple antibiotic resistance protein marA and multidrug efflux pump mexD, but did not lead to an overall convergence in antibiotic resistance gene sequences. Frontiers Media S.A. 2019-10-10 /pmc/articles/PMC6795690/ /pubmed/31649656 http://dx.doi.org/10.3389/fmicb.2019.02330 Text en Copyright © 2019 Epp Schmidt, Kotze, Hornung, Setälä, Yesilonis, Szlavecz, Dombos, Pouyat, Cilliers, Tóth and Yarwood. 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 Epp Schmidt, Dietrich J. Kotze, David Johan Hornung, Erzsébet Setälä, Heikki Yesilonis, Ian Szlavecz, Katalin Dombos, Miklós Pouyat, Richard Cilliers, Sarel Tóth, Zsolt Yarwood, Stephanie Metagenomics Reveals Bacterial and Archaeal Adaptation to Urban Land-Use: N Catabolism, Methanogenesis, and Nutrient Acquisition |
title | Metagenomics Reveals Bacterial and Archaeal Adaptation to Urban Land-Use: N Catabolism, Methanogenesis, and Nutrient Acquisition |
title_full | Metagenomics Reveals Bacterial and Archaeal Adaptation to Urban Land-Use: N Catabolism, Methanogenesis, and Nutrient Acquisition |
title_fullStr | Metagenomics Reveals Bacterial and Archaeal Adaptation to Urban Land-Use: N Catabolism, Methanogenesis, and Nutrient Acquisition |
title_full_unstemmed | Metagenomics Reveals Bacterial and Archaeal Adaptation to Urban Land-Use: N Catabolism, Methanogenesis, and Nutrient Acquisition |
title_short | Metagenomics Reveals Bacterial and Archaeal Adaptation to Urban Land-Use: N Catabolism, Methanogenesis, and Nutrient Acquisition |
title_sort | metagenomics reveals bacterial and archaeal adaptation to urban land-use: n catabolism, methanogenesis, and nutrient acquisition |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795690/ https://www.ncbi.nlm.nih.gov/pubmed/31649656 http://dx.doi.org/10.3389/fmicb.2019.02330 |
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