Cargando…

Microbial Nitrogen Metabolism in Chloraminated Drinking Water Reservoirs

Ammonia availability due to chloramination can promote the growth of nitrifying organisms, which can deplete chloramine residuals and result in operational problems for drinking water utilities. In this study, we used a metagenomic approach to determine the identity and functional potential of micro...

Descripción completa

Detalles Bibliográficos
Autores principales: Potgieter, Sarah C., Dai, Zihan, Venter, Stephanus N., Sigudu, Makhosazana, Pinto, Ameet J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193043/
https://www.ncbi.nlm.nih.gov/pubmed/32350093
http://dx.doi.org/10.1128/mSphere.00274-20
_version_ 1783528113726029824
author Potgieter, Sarah C.
Dai, Zihan
Venter, Stephanus N.
Sigudu, Makhosazana
Pinto, Ameet J.
author_facet Potgieter, Sarah C.
Dai, Zihan
Venter, Stephanus N.
Sigudu, Makhosazana
Pinto, Ameet J.
author_sort Potgieter, Sarah C.
collection PubMed
description Ammonia availability due to chloramination can promote the growth of nitrifying organisms, which can deplete chloramine residuals and result in operational problems for drinking water utilities. In this study, we used a metagenomic approach to determine the identity and functional potential of microorganisms involved in nitrogen biotransformation within chloraminated drinking water reservoirs. Spatial changes in the nitrogen species included an increase in nitrate concentrations accompanied by a decrease in ammonium concentrations with increasing distance from the site of chloramination. This nitrifying activity was likely driven by canonical ammonia-oxidizing bacteria (i.e., Nitrosomonas) and nitrite-oxidizing bacteria (i.e., Nitrospira) as well as by complete-ammonia-oxidizing (i.e., comammox) Nitrospira-like bacteria. Functional annotation was used to evaluate genes associated with nitrogen metabolism, and the community gene catalogue contained mostly genes involved in nitrification, nitrate and nitrite reduction, and nitric oxide reduction. Furthermore, we assembled 47 high-quality metagenome-assembled genomes (MAGs) representing a highly diverse assemblage of bacteria. Of these, five MAGs showed high coverage across all samples, which included two Nitrosomonas, Nitrospira, Sphingomonas, and Rhizobiales-like MAGs. Systematic genome-level analyses of these MAGs in relation to nitrogen metabolism suggest that under ammonia-limited conditions, nitrate may be also reduced back to ammonia for assimilation. Alternatively, nitrate may be reduced to nitric oxide and may potentially play a role in regulating biofilm formation. Overall, this study provides insight into the microbial communities and their nitrogen metabolism and, together with the water chemistry data, improves our understanding of nitrogen biotransformation in chloraminated drinking water distribution systems. IMPORTANCE Chloramines are often used as a secondary disinfectant when free chlorine residuals are difficult to maintain. However, chloramination is often associated with the undesirable effect of nitrification, which results in operational problems for many drinking water utilities. The introduction of ammonia during chloramination provides a potential source of nitrogen either through the addition of excess ammonia or through chloramine decay. This promotes the growth of nitrifying microorganisms and provides a nitrogen source (i.e., nitrate) for the growth for other organisms. While the roles of canonical ammonia-oxidizing and nitrite-oxidizing bacteria in chloraminated drinking water systems have been extensively investigated, those studies have largely adopted a targeted gene-centered approach. Further, little is known about the potential long-term cooccurrence of complete-ammonia-oxidizing (i.e., comammox) bacteria and the potential metabolic synergies of nitrifying organisms with their heterotrophic counterparts that are capable of denitrification and nitrogen assimilation. This study leveraged data obtained for genome-resolved metagenomics over a time series to show that while nitrifying bacteria are dominant and likely to play a major role in nitrification, their cooccurrence with heterotrophic organisms suggests that nitric oxide production and nitrate reduction to ammonia may also occur in chloraminated drinking water systems.
format Online
Article
Text
id pubmed-7193043
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-71930432020-05-07 Microbial Nitrogen Metabolism in Chloraminated Drinking Water Reservoirs Potgieter, Sarah C. Dai, Zihan Venter, Stephanus N. Sigudu, Makhosazana Pinto, Ameet J. mSphere Research Article Ammonia availability due to chloramination can promote the growth of nitrifying organisms, which can deplete chloramine residuals and result in operational problems for drinking water utilities. In this study, we used a metagenomic approach to determine the identity and functional potential of microorganisms involved in nitrogen biotransformation within chloraminated drinking water reservoirs. Spatial changes in the nitrogen species included an increase in nitrate concentrations accompanied by a decrease in ammonium concentrations with increasing distance from the site of chloramination. This nitrifying activity was likely driven by canonical ammonia-oxidizing bacteria (i.e., Nitrosomonas) and nitrite-oxidizing bacteria (i.e., Nitrospira) as well as by complete-ammonia-oxidizing (i.e., comammox) Nitrospira-like bacteria. Functional annotation was used to evaluate genes associated with nitrogen metabolism, and the community gene catalogue contained mostly genes involved in nitrification, nitrate and nitrite reduction, and nitric oxide reduction. Furthermore, we assembled 47 high-quality metagenome-assembled genomes (MAGs) representing a highly diverse assemblage of bacteria. Of these, five MAGs showed high coverage across all samples, which included two Nitrosomonas, Nitrospira, Sphingomonas, and Rhizobiales-like MAGs. Systematic genome-level analyses of these MAGs in relation to nitrogen metabolism suggest that under ammonia-limited conditions, nitrate may be also reduced back to ammonia for assimilation. Alternatively, nitrate may be reduced to nitric oxide and may potentially play a role in regulating biofilm formation. Overall, this study provides insight into the microbial communities and their nitrogen metabolism and, together with the water chemistry data, improves our understanding of nitrogen biotransformation in chloraminated drinking water distribution systems. IMPORTANCE Chloramines are often used as a secondary disinfectant when free chlorine residuals are difficult to maintain. However, chloramination is often associated with the undesirable effect of nitrification, which results in operational problems for many drinking water utilities. The introduction of ammonia during chloramination provides a potential source of nitrogen either through the addition of excess ammonia or through chloramine decay. This promotes the growth of nitrifying microorganisms and provides a nitrogen source (i.e., nitrate) for the growth for other organisms. While the roles of canonical ammonia-oxidizing and nitrite-oxidizing bacteria in chloraminated drinking water systems have been extensively investigated, those studies have largely adopted a targeted gene-centered approach. Further, little is known about the potential long-term cooccurrence of complete-ammonia-oxidizing (i.e., comammox) bacteria and the potential metabolic synergies of nitrifying organisms with their heterotrophic counterparts that are capable of denitrification and nitrogen assimilation. This study leveraged data obtained for genome-resolved metagenomics over a time series to show that while nitrifying bacteria are dominant and likely to play a major role in nitrification, their cooccurrence with heterotrophic organisms suggests that nitric oxide production and nitrate reduction to ammonia may also occur in chloraminated drinking water systems. American Society for Microbiology 2020-04-29 /pmc/articles/PMC7193043/ /pubmed/32350093 http://dx.doi.org/10.1128/mSphere.00274-20 Text en Copyright © 2020 Potgieter et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Potgieter, Sarah C.
Dai, Zihan
Venter, Stephanus N.
Sigudu, Makhosazana
Pinto, Ameet J.
Microbial Nitrogen Metabolism in Chloraminated Drinking Water Reservoirs
title Microbial Nitrogen Metabolism in Chloraminated Drinking Water Reservoirs
title_full Microbial Nitrogen Metabolism in Chloraminated Drinking Water Reservoirs
title_fullStr Microbial Nitrogen Metabolism in Chloraminated Drinking Water Reservoirs
title_full_unstemmed Microbial Nitrogen Metabolism in Chloraminated Drinking Water Reservoirs
title_short Microbial Nitrogen Metabolism in Chloraminated Drinking Water Reservoirs
title_sort microbial nitrogen metabolism in chloraminated drinking water reservoirs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193043/
https://www.ncbi.nlm.nih.gov/pubmed/32350093
http://dx.doi.org/10.1128/mSphere.00274-20
work_keys_str_mv AT potgietersarahc microbialnitrogenmetabolisminchloraminateddrinkingwaterreservoirs
AT daizihan microbialnitrogenmetabolisminchloraminateddrinkingwaterreservoirs
AT venterstephanusn microbialnitrogenmetabolisminchloraminateddrinkingwaterreservoirs
AT sigudumakhosazana microbialnitrogenmetabolisminchloraminateddrinkingwaterreservoirs
AT pintoameetj microbialnitrogenmetabolisminchloraminateddrinkingwaterreservoirs