Synergistic interactions between anammox and dissimilatory nitrate reducing bacteria sustains reactor performance across variable nitrogen loading ratios

Anaerobic ammonium oxidizing (anammox) bacteria are utilized for high efficiency nitrogen removal from nitrogen-laden sidestreams in wastewater treatment plants. The anammox bacteria form a variety of competitive and mutualistic interactions with heterotrophic bacteria that often employ denitrification or dissimilatory nitrate reduction to ammonium (DNRA) for energy generation. These interactions can be heavily influenced by the influent ratio of ammonium to nitrite, NH4+:NO2−, where deviations from the widely acknowledged stoichiometric ratio (1:1.32) have been demonstrated to have deleterious effects on anammox efficiency. Thus, it is important to understand how variable NH4+:NO2− ratios impact the microbial ecology of anammox reactors. We observed the response of the microbial community in a lab scale anammox membrane bioreactor (MBR) to changes in the influent NH4+:NO2− ratio using both 16S rRNA gene and shotgun metagenomic sequencing. Ammonium removal efficiency decreased from 99.77 ± 0.04% when the ratio was 1:1.32 (prior to day 89) to 90.85 ± 0.29% when the ratio was decreased to 1:1.1 (day 89–202) and 90.14 ± 0.09% when the ratio was changed to 1:1.13 (day 169–200). Over this same timespan, the overall nitrogen removal efficiency (NRE) remained relatively unchanged (85.26 ± 0.01% from day 0–89, compared to 85.49 ± 0.01% from day 89–169, and 83.04 ± 0.01% from day 169–200). When the ratio was slightly increased to 1:1.17–1:1.2 (day 202–253), the ammonium removal efficiency increased to 97.28 ± 0.45% and the NRE increased to 88.21 ± 0.01%. Analysis of 16 S rRNA gene sequences demonstrated increased relative abundance of taxa belonging to Bacteroidetes, Chloroflexi, and Ignavibacteriae over the course of the experiment. The relative abundance of Planctomycetes, the phylum to which anammox bacteria belong, decreased from 77.19% at the beginning of the experiment to 12.24% by the end of the experiment. Analysis of metagenome assembled genomes (MAGs) indicated increased abundance of bacteria with nrfAH genes used for DNRA after the introduction of lower influent NH4+:NO2− ratios. The high relative abundance of DNRA bacteria coinciding with sustained bioreactor performance indicates a mutualistic relationship between the anammox and DNRA bacteria. Understanding these interactions could support more robust bioreactor operation at variable nitrogen loading ratios.

[1]  Lijie Zhou,et al.  Double-edged sword effects of dissimilatory nitrate reduction to ammonium (DNRA) bacteria on anammox bacteria performance in an MBR reactor. , 2023, Water research.

[2]  Yan Huang,et al.  Functional stability correlates with dynamic microbial networks in anammox process. , 2022, Bioresource technology.

[3]  Rui Du,et al.  Insight into the microbial interactions of Anammox and heterotrophic bacteria in different granular sludge systems: effect of size distribution and available organic carbon source. , 2022, Bioresource technology.

[4]  X. Zhan,et al.  Meta-Omics reveal the metabolic acclimation of freshwater anammox bacteria for saline wastewater treatment , 2022, Journal of Cleaner Production.

[5]  K. A. Hunt,et al.  Metagenomic Insights Into Competition Between Denitrification and Dissimilatory Nitrate Reduction to Ammonia Within One-Stage and Two-Stage Partial-Nitritation Anammox Bioreactor Configurations , 2022, Frontiers in Microbiology.

[6]  Y. Li,et al.  Response and resilience of anammox consortia to nutrient starvation , 2022, Microbiome.

[7]  Li Wang,et al.  Specific Denitrifying and Dissimilatory Nitrate Reduction to Ammonium Bacteria Assisted the Recovery of Anammox Community From Nitrite Inhibition , 2022, Frontiers in Microbiology.

[8]  Minsheng Huang,et al.  The coupling of mixotrophic denitrification, dissimilatory nitrate reduction to ammonium (DNRA) and anaerobic ammonium oxidation (anammox) promoting the start-up of anammox by addition of calcium nitrate. , 2021, Bioresource technology.

[9]  Taeho Lee,et al.  A twilight for the complete nitrogen removal via synergistic partial-denitrification, anammox, and DNRA process , 2021, npj Clean Water.

[10]  B. Ni,et al.  Impacts of organics on the microbial ecology of wastewater anammox processes: Recent advances and meta-analysis. , 2021, Water research.

[11]  Mingsheng Jia,et al.  Elucidating the Competition between Heterotrophic Denitrification and DNRA Using the Resource-Ratio Theory. , 2020, Environmental science & technology.

[12]  Guangxue Wu,et al.  Microbial physiology and interactions in anammox systems with the intermittent addition of organic carbons. , 2020, Bioresource technology.

[13]  Guangxue Wu,et al.  Autotrophic nitrogen removal and potential microbial interactions in anammox systems with different ammonia and organic carbon concentrations , 2020 .

[14]  Yan Zhou,et al.  Coupling anammox with heterotrophic denitrification for enhanced nitrogen removal: A review , 2020, Critical Reviews in Environmental Science and Technology.

[15]  F. Fang,et al.  The branched chains and branching degree of exopolysaccharides affecting the stability of anammox granular sludge. , 2020, Water research.

[16]  M. V. van Loosdrecht,et al.  Decorating the Anammox House: Sialic Acids and Sulfated Glycosaminoglycans in the Extracellular Polymeric Substances of Anammox Granular Sludge , 2020, Environmental science & technology.

[17]  Yongzhen Peng,et al.  Enhanced long-term advanced denitrogenation from nitrate wastewater by anammox consortia: Dissimilatory nitrate reduction to ammonium (DNRA) coupling with anammox in an upflow biofilter reactor equipped with EDTA-2Na/Fe(II) ratio and pH control. , 2020, Bioresource technology.

[18]  J. Banfield,et al.  Increased replication of dissimilatory nitrate-reducing bacteria leads to decreased anammox bioreactor performance , 2020, Microbiome.

[19]  Sunja Cho,et al.  Performance of Anammox Processes for Wastewater Treatment: A Critical Review on Effects of Operational Conditions and Environmental Stresses , 2019, Water.

[20]  M. F. Dias,et al.  Nitrogen removal from food waste digestate using partial nitritation-anammox process: Effect of different aeration strategies on performance and microbial community dynamics. , 2019, Journal of environmental management.

[21]  A. Arkin,et al.  Selective carbon sources influence the end products of microbial nitrate respiration , 2019, bioRxiv.

[22]  Bo Jiang,et al.  Discrepant gene functional potential and cross-feedings of anammox bacteria Ca. Jettenia caeni and Ca. Brocadia sinica in response to acetate. , 2019, Water research.

[23]  D. Figeys,et al.  Exploring the effects of operational mode and microbial interactions on bacterial community assembly in a one-stage partial-nitritation anammox reactor using integrated multi-omics , 2019, Microbiome.

[24]  Yonglong Lu,et al.  Resuscitation of anammox bacteria after >10,000 years of dormancy , 2018, The ISME Journal.

[25]  Bo Jiang,et al.  Genome-Centered Metagenomics Analysis Reveals the Symbiotic Organisms Possessing Ability to Cross-Feed with Anammox Bacteria in Anammox Consortia. , 2018, Environmental science & technology.

[26]  Jizhong Zhou,et al.  Stochastic Community Assembly: Does It Matter in Microbial Ecology? , 2017, Microbiology and Molecular Biology Reviews.

[27]  Huiyu Dong,et al.  Effect of influent substrate ratio on anammox granular sludge: performance and kinetics , 2017, Biodegradation.

[28]  J. G. Kuenen,et al.  Fermentative Bacteria Influence the Competition between Denitrifiers and DNRA Bacteria , 2017, Front. Microbiol..

[29]  M. V. van Loosdrecht,et al.  Evaluating the potential for dissimilatory nitrate reduction by anammox bacteria for municipal wastewater treatment. , 2017, Bioresource technology.

[30]  Katherine D. McMahon,et al.  Metabolic network analysis reveals microbial community interactions in anammox granules , 2017, Nature Communications.

[31]  J. G. Kuenen,et al.  Role of nitrite in the competition between denitrification and DNRA in a chemostat enrichment culture , 2017, AMB Express.

[32]  Mike S. M. Jetten,et al.  Whole-Community Metagenomics in Two Different Anammox Configurations: Process Performance and Community Structure. , 2017, Environmental science & technology.

[33]  P. Bodelier,et al.  Revisiting life strategy concepts in environmental microbial ecology. , 2017, FEMS microbiology ecology.

[34]  C. Etchebehere,et al.  Microbial communities in anammox reactors: a review , 2017 .

[35]  J. G. Kuenen,et al.  DNRA and Denitrification Coexist over a Broad Range of Acetate/N-NO3− Ratios, in a Chemostat Enrichment Culture , 2016, Front. Microbiol..

[36]  Brian C. Thomas,et al.  Measurement of bacterial replication rates in microbial communities , 2016, Nature Biotechnology.

[37]  Zhiguo Yuan,et al.  Metagenomic analysis of anammox communities in three different microbial aggregates. , 2016, Environmental microbiology.

[38]  B. Dutilh,et al.  Genome-based microbial ecology of anammox granules in a full-scale wastewater treatment system , 2016, Nature Communications.

[39]  S. Okabe,et al.  Anammox-based technologies for nitrogen removal: Advances in process start-up and remaining issues. , 2015, Chemosphere.

[40]  M. V. van Loosdrecht,et al.  Comparison of bacterial diversity in full scale anammox bioreactors operated under different conditions , 2015, Biotechnology progress.

[41]  R. Sougrat,et al.  Microbial Community Composition and Ultrastructure of Granules from a Full-Scale Anammox Reactor , 2015, Microbial Ecology.

[42]  Jizhong Zhou,et al.  Phasing amplicon sequencing on Illumina Miseq for robust environmental microbial community analysis , 2015, BMC Microbiology.

[43]  A. Konopka,et al.  Estimating and mapping ecological processes influencing microbial community assembly , 2015, Front. Microbiol..

[44]  S. Okabe,et al.  Draft Genome Sequence of an Anaerobic Ammonium-Oxidizing Bacterium, “Candidatus Brocadia sinica” , 2015, Genome Announcements.

[45]  A. Devol,et al.  Denitrification, anammox, and N₂ production in marine sediments. , 2015, Annual review of marine science.

[46]  L. Fleming,et al.  Anthropogenic nutrients and harmful algae in coastal waters. , 2014, Journal of Environmental Management.

[47]  R. Hettich,et al.  The environmental controls that govern the end product of bacterial nitrate respiration , 2014, Science.

[48]  Susanne Lackner,et al.  Full-scale partial nitritation/anammox experiences--an application survey. , 2014, Water research.

[49]  J. Field,et al.  Nitrite (not free nitrous acid) is the main inhibitor of the anammox process at common pH conditions , 2014, Biotechnology Letters.

[50]  Eberhard Morgenroth,et al.  Successful application of nitritation/anammox to wastewater with elevated organic carbon to ammonia ratios. , 2014, Water research.

[51]  H. O. D. op den Camp,et al.  How to make a living from anaerobic ammonium oxidation. , 2013, FEMS microbiology reviews.

[52]  Ren-Cun Jin,et al.  The importance of the substrate ratio in the operation of the Anammox process in upflow biofilter , 2013 .

[53]  Kees-Jan Françoijs,et al.  Metagenome Analysis of a Complex Community Reveals the Metabolic Blueprint of Anammox Bacterium “Candidatus Jettenia asiatica” , 2012, Front. Microbio..

[54]  Mike S. M. Jetten,et al.  Anaerobic Ammonium-Oxidizing Bacteria: Unique Microorganisms with Exceptional Properties , 2012, Microbiology and Molecular Reviews.

[55]  P. Zheng,et al.  The inhibition of the Anammox process: A review , 2012 .

[56]  R. Méndez,et al.  Short- and long-term effects of ammonium and nitrite on the Anammox process. , 2012, Journal of environmental management.

[57]  Jolein Gloerich,et al.  Molecular mechanism of anaerobic ammonium oxidation , 2011, Nature.

[58]  H. Siegrist,et al.  Combined nitritation-anammox: advances in understanding process stability. , 2011, Environmental science & technology.

[59]  M. Strous,et al.  Microbial nitrate respiration--genes, enzymes and environmental distribution. , 2011, Journal of biotechnology.

[60]  S. Okabe,et al.  Physiological characteristics of the anaerobic ammonium-oxidizing bacterium 'Candidatus Brocadia sinica'. , 2011, Microbiology.

[61]  C. Vannini,et al.  Nitrite inhibition and intermediates effects on Anammox bacteria: a batch-scale experimental study. , 2010 .

[62]  Chong-Jian Tang,et al.  Effect of substrate concentration on stability of anammox biofilm reactors , 2010 .

[63]  Martin Hartmann,et al.  Introducing mothur: Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities , 2009, Applied and Environmental Microbiology.

[64]  H. Siegrist,et al.  Full-scale nitrogen removal from digester liquid with partial nitritation and anammox in one SBR. , 2009, Environmental science & technology.

[65]  D. Schindler,et al.  Eutrophication science: where do we go from here? , 2009, Trends in ecology & evolution.

[66]  J. G. Kuenen,et al.  Anammox bacteria: from discovery to application , 2008, Nature Reviews Microbiology.

[67]  M C M van Loosdrecht,et al.  Full-scale granular sludge Anammox process. , 2007, Water science and technology : a journal of the International Association on Water Pollution Research.

[68]  S. Busby,et al.  The Escherichia coli K-12 NarL and NarP Proteins Insulate the nrf Promoter from the Effects of Integration Host Factor , 2006, Journal of bacteriology.

[69]  Dmitrij Frishman,et al.  Deciphering the evolution and metabolism of an anammox bacterium from a community genome , 2006, Nature.

[70]  J. G. Kuenen,et al.  Anaerobic ammonium oxidation by anammox bacteria in the Black Sea , 2003, Nature.

[71]  R. Huber,et al.  Mechanism of the six-electron reduction of nitrite to ammonia by cytochrome c nitrite reductase. , 2002, Journal of the American Chemical Society.

[72]  M. V. van Loosdrecht,et al.  Microbiology and application of the anaerobic ammonium oxidation ('anammox') process. , 2001, Current opinion in biotechnology.

[73]  J. Moir,et al.  Nitrate and nitrite transport in bacteria , 2001, Cellular and Molecular Life Sciences CMLS.

[74]  K. Schleifer,et al.  Molecular evidence for genus level diversity of bacteria capable of catalyzing anaerobic ammonium oxidation. , 2000, Systematic and applied microbiology.

[75]  J. G. Kuenen,et al.  Missing lithotroph identified as new planctomycete , 1999, Nature.

[76]  J. J. Heijnen,et al.  The sequencing batch reactor as a powerful tool for the study of slowly growing anaerobic ammonium-oxidizing microorganisms , 1998, Applied Microbiology and Biotechnology.

[77]  M. Jetten,et al.  Anaerobic oxidation of ammonium is a biologically mediated process , 1995 .

[78]  J. G. Kuenen,et al.  Anaerobic ammonium oxidation discovered in a denitrifying fluidized bed reactor , 1995 .

[79]  J. P. Grime,et al.  Evidence for the Existence of Three Primary Strategies in Plants and Its Relevance to Ecological and Evolutionary Theory , 1977, The American Naturalist.

[80]  Baikun Li,et al.  Performance and microbial community analysis of a novel DEAMOX based on partial-denitrification and anammox treating ammonia and nitrate wastewaters. , 2017, Water research.

[81]  P. Zheng,et al.  Characterization of oligotrophic AnAOB culture: morphological, physiological, and ecological features , 2017, Applied Microbiology and Biotechnology.

[82]  F. Meng,et al.  Spectroscopic characterization of extracellular polymeric substances from a mixed culture dominated by ammonia-oxidizing bacteria. , 2015, Water research.

[83]  M. V. van Loosdrecht,et al.  The effect of nitrite inhibition on the anammox process. , 2012, Water research.

[84]  H. O. D. op den Camp,et al.  Anammox--growth physiology, cell biology, and metabolism. , 2012, Advances in microbial physiology.

[85]  Wastewater Technology Fact Sheet 1 Side Stream Nutrient Removal , 2008 .

[86]  Mark C.M. van Loosdrecht,et al.  Towards a more sustainable municipal wastewater treatment system , 1997 .

[87]  J. Andrews,et al.  r- and K-Selection and Microbial Ecology , 1986 .