Cargando…
Increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance
BACKGROUND: Anaerobic ammonium oxidation (anammox) is a biological process employed to remove reactive nitrogen from wastewater. While a substantial body of literature describes the performance of anammox bioreactors under various operational conditions and perturbations, few studies have resolved t...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982389/ https://www.ncbi.nlm.nih.gov/pubmed/31980038 http://dx.doi.org/10.1186/s40168-020-0786-3 |
_version_ | 1783491302976913408 |
---|---|
author | Keren, Ray Lawrence, Jennifer E. Zhuang, Weiqin Jenkins, David Banfield, Jillian F. Alvarez-Cohen, Lisa Zhou, Lijie Yu, Ke |
author_facet | Keren, Ray Lawrence, Jennifer E. Zhuang, Weiqin Jenkins, David Banfield, Jillian F. Alvarez-Cohen, Lisa Zhou, Lijie Yu, Ke |
author_sort | Keren, Ray |
collection | PubMed |
description | BACKGROUND: Anaerobic ammonium oxidation (anammox) is a biological process employed to remove reactive nitrogen from wastewater. While a substantial body of literature describes the performance of anammox bioreactors under various operational conditions and perturbations, few studies have resolved the metabolic roles of their core microbial community members. RESULTS: Here, we used metagenomics to study the microbial community of a laboratory-scale anammox bioreactor from inoculation, through a performance destabilization event, to robust steady-state performance. Metabolic analyses revealed that nutrient acquisition from the environment is selected for in the anammox community. Dissimilatory nitrate reduction to ammonium (DNRA) was the primary nitrogen removal pathway that competed with anammox. Increased replication of bacteria capable of DNRA led to the out-competition of anammox bacteria, and the loss of the bioreactor’s nitrogen removal capacity. These bacteria were highly associated with the anammox bacterium and considered part of the core microbial community. CONCLUSIONS: Our findings highlight the importance of metabolic interdependencies related to nitrogen- and carbon-cycling within anammox bioreactors and the potentially detrimental effects of bacteria that are otherwise considered core microbial community members. |
format | Online Article Text |
id | pubmed-6982389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69823892020-01-29 Increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance Keren, Ray Lawrence, Jennifer E. Zhuang, Weiqin Jenkins, David Banfield, Jillian F. Alvarez-Cohen, Lisa Zhou, Lijie Yu, Ke Microbiome Research BACKGROUND: Anaerobic ammonium oxidation (anammox) is a biological process employed to remove reactive nitrogen from wastewater. While a substantial body of literature describes the performance of anammox bioreactors under various operational conditions and perturbations, few studies have resolved the metabolic roles of their core microbial community members. RESULTS: Here, we used metagenomics to study the microbial community of a laboratory-scale anammox bioreactor from inoculation, through a performance destabilization event, to robust steady-state performance. Metabolic analyses revealed that nutrient acquisition from the environment is selected for in the anammox community. Dissimilatory nitrate reduction to ammonium (DNRA) was the primary nitrogen removal pathway that competed with anammox. Increased replication of bacteria capable of DNRA led to the out-competition of anammox bacteria, and the loss of the bioreactor’s nitrogen removal capacity. These bacteria were highly associated with the anammox bacterium and considered part of the core microbial community. CONCLUSIONS: Our findings highlight the importance of metabolic interdependencies related to nitrogen- and carbon-cycling within anammox bioreactors and the potentially detrimental effects of bacteria that are otherwise considered core microbial community members. BioMed Central 2020-01-24 /pmc/articles/PMC6982389/ /pubmed/31980038 http://dx.doi.org/10.1186/s40168-020-0786-3 Text en © The Author(s). 2020 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Keren, Ray Lawrence, Jennifer E. Zhuang, Weiqin Jenkins, David Banfield, Jillian F. Alvarez-Cohen, Lisa Zhou, Lijie Yu, Ke Increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance |
title | Increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance |
title_full | Increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance |
title_fullStr | Increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance |
title_full_unstemmed | Increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance |
title_short | Increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance |
title_sort | increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982389/ https://www.ncbi.nlm.nih.gov/pubmed/31980038 http://dx.doi.org/10.1186/s40168-020-0786-3 |
work_keys_str_mv | AT kerenray increasedreplicationofdissimilatorynitratereducingbacterialeadstodecreasedanammoxbioreactorperformance AT lawrencejennifere increasedreplicationofdissimilatorynitratereducingbacterialeadstodecreasedanammoxbioreactorperformance AT zhuangweiqin increasedreplicationofdissimilatorynitratereducingbacterialeadstodecreasedanammoxbioreactorperformance AT jenkinsdavid increasedreplicationofdissimilatorynitratereducingbacterialeadstodecreasedanammoxbioreactorperformance AT banfieldjillianf increasedreplicationofdissimilatorynitratereducingbacterialeadstodecreasedanammoxbioreactorperformance AT alvarezcohenlisa increasedreplicationofdissimilatorynitratereducingbacterialeadstodecreasedanammoxbioreactorperformance AT zhoulijie increasedreplicationofdissimilatorynitratereducingbacterialeadstodecreasedanammoxbioreactorperformance AT yuke increasedreplicationofdissimilatorynitratereducingbacterialeadstodecreasedanammoxbioreactorperformance |