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Abundance and diversity based on amoA genes of ammonia-oxidizing archaea and bacteria in ten wastewater treatment systems

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Abstract

The abundance and diversity of amoA genes of ammonia-oxidizing archaea (AOA) and bacteria (AOB) were investigated in ten wastewater treatment systems (WTSs) by polymerase chain reaction (PCR), cloning, sequencing, and quantitative real-time PCR (qPCR). The ten WTSs included four full-scale municipal WTSs, three full-scale industrial WTSs, and three lab-scale WTSs. AOB were present in all the WTSs, whereas AOA were detected in nine WTSs. QPCR data showed that AOB amoA genes (4.625 × 104–9.99 × 109 copies g−1 sludge) outnumbered AOA amoA genes (<limit of detection–1.90 × 107 copies g−1 sludge) in each WTS, indicating that AOB may play an important role than AOA in ammonia oxidization in WTSs. Interestingly, it was found that AOA and AOB coexisted with anaerobic ammonia oxidation (anammox) bacteria in three anammox WTSs with relatively higher abundance. In a full-scale industrial WTS where effluent ammonia was higher than influent ammonia, both AOA and AOB showed higher abundance. The phylogenetic analysis of AOB amoA genes showed that genera Nitrosomonas was the most dominant species in the ten WTSs; Nitrosomonas europaea cluster was the dominant major cluster, followed by Nitrosomonas-like cluster and Nitrosomonas oligotropha cluster; and AOB species showed higher diversity than AOA species. AOA were found to be affiliated with two major clusters: Nitrososphaera cluster and Nitrosopumilus cluster. Nitrososphaera cluster was the most dominant species in different samples and distributed worldwide.

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References

  • Abeliovich A, Vonshak A (1992) Anaerobic metabolism of Nitrosomonas-europaea. Arch Microbiol 158:267–270

    Google Scholar 

  • Arp D, Sayavedra-Soto L, Hommes N (2002) Molecular biology and biochemistry of ammonia oxidation by Nitrosomonas europaea. Arch Microbiol 178:250–255

    Google Scholar 

  • Bae H, Chung YC, Jung JY (2010) Microbial community structure and occurrence of diverse autotrophic ammonium oxidizing microorganisms in the anammox process. Water Sci Technol 61:2723–2732

    Article  PubMed  CAS  Google Scholar 

  • Bai Y, Sun Q, Wen D, Tang X (2012) Abundance of ammonia-oxidizing bacteria and archaea in industrial and domestic wastewater treatment systems. FEMS Microbiol Ecol 80:323–330

    Article  PubMed  CAS  Google Scholar 

  • Beman JM, Francis CA (2006) Diversity of ammonia-oxidizing archaea and bacteria in the sediments of a hypernutrified subtropical estuary: Bahía del Tóbari, Mexico. Appl Environ Microbiol 72:7767–7777

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Coolen MJL, Abbas B, Van Bleijswijk J, Hopmans EC, Kuypers MMM, Wakeham SG, Sinninghe Damsté JS (2007) Putative ammonia-oxidizing Crenarchaeota in suboxic waters of the Black Sea: a basin-wide ecological study using 16S ribosomal and functional genes and membrane lipids. Environ Microbiol 9:1001–1016

    Article  PubMed  CAS  Google Scholar 

  • Coskuner G, Curtis TP (2002) In situ characterization of nitrifiers in an activated sludge plant: detection of Nitrobacter spp. J Appl Microbiol 93:431–437

    Google Scholar 

  • de Vet WWJM, Dinkla IJT, Muyzer G, Rietveld LC, van Loosdrecht MCM (2009) Molecular characterization of microbial populations in groundwater sources and sand filters for drinking water production. Water Res 43:182–194

    Article  PubMed  CAS  Google Scholar 

  • Ducey TF, Vanotti MB, Shriner AD, Szogi AA, Ellison AQ (2010) Characterization of a microbial community capable of nitrification at cold temperature. Bioresour Technol 101:491–500

    Article  PubMed  CAS  Google Scholar 

  • Erguder TH, Boon N, Wittebolle L, Marzorati M, Verstraete W (2009) Environmental factors shaping the ecological niches of ammonia-oxidizing archaea. FEMS Microbiol Rev 33:855–869

    Article  PubMed  CAS  Google Scholar 

  • Francis CA, Roberts KJ, Beman JM, Santoro AE, Oakley BB (2005) Ubiquity and diversity of ammonia-oxidizing archaea in water columns and sediments of the ocean. Proc Natl Acad Sci U S A 102:14683–14688

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Fukushima T, Wu YJ, Whang LM (2012) The influence of salinity and ammonium levels on amoA mRNA expression of ammonia-oxidizing prokaryotes. Water Sci Technol 65:2228–2235

    Article  PubMed  CAS  Google Scholar 

  • Gao JF, Luo X, Wu GX, Li T, Peng YZ (2013) Quantitative analyses of the composition and abundance of ammonia-oxidizing archaea and ammonia-oxidizing bacteria in eight full-scale biological wastewater treatment plants. Bioresour Technol 138:285–296

    Article  PubMed  CAS  Google Scholar 

  • Gieseke A, Purkhold U, Wagner M, Amann R, Schramm A (2001) Community structure and activity dynamics of nitrifying bacteria in a phosphate-removing biofilm. Appl Environ Microbiol 67:1351–1362

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • He JZ, Shen JP, Zhang LM, Zhu YG, Zheng YM, Xu MG, Di H (2007) Quantitative analyses of the abundance and composition of ammonia-oxidizing bacteria and ammonia-oxidizing archaea of a Chinese upland red soil under long-term fertilization practices. Environ Microbiol 9:2364–2374

    Article  PubMed  CAS  Google Scholar 

  • Jetten MSM, Strous M, van de Pas-Schoonen KT, Schalk J, van Dongen U, van de Graaf AA, Logemann S, Muyzer G, van Loosdrecht MCM, Kuenen JG (1998) The anaerobic oxidation of ammonium. FEMS Microbiol Rev 22:421–437

    Article  PubMed  CAS  Google Scholar 

  • Jin T, Zhang T, Yan Q (2010) Characterization and quantification of ammonia-oxidizing archaea (AOA) and bacteria (AOB) in a nitrogen-removing reactor using T-RFLP and qPCR. Appl Microbiol Biotechnol 87:1167–1176

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Kayee P, Sonthiphand P, Rongsayamanont C, Limpiyakorn T (2011) Archaeal amoA genes outnumber bacterial amoA genes in municipal wastewater treatment plants in Bangkok. Microb Ecol 62:776–788

    Article  PubMed  Google Scholar 

  • Kindaichi T, Tsushima I, Ogasawara Y, Shimokawa M, Ozaki N, Satoh H, Okabe S (2007) In situ activity and spatial organization of anaerobic ammonium-oxidizing (Anammox) bacteria in biofilms. Appl Environ Microbiol 73:4931–4939

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Könneke M, Bernhard AE, De La Torre JR, Walker CB, Waterbury JB, Stahl DA (2005) Isolation of an autotrophic ammonia-oxidizing marine archaeon. Nature 437:543–546

    Article  PubMed  CAS  Google Scholar 

  • Koops HP, Pommerening-Röser A (2001) Distribution and ecophysiology of the nitrifying bacteria emphasizing cultured species. FEMS Microbiol Ecol 37:1–9

    Article  CAS  Google Scholar 

  • Kumar S, Nei M, Dudley J, Tamura K (2008) MEGA: a biologist-centric software for evolutionary analysis of DNA and protein sequences. Brief Bioinform 9:299–306

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Laanbroek H, Bodelier PE, Gerards S (1994) Oxygen consumption kinetics of Nitrosomonas europaea and Nitrobacter hamburgensis grown in mixed continuous cultures at different oxygen concentrations. Arch Microbiol 161:156–162

    Google Scholar 

  • Lam P, Jensen MM, Lavik G, McGinnis DF, Müller B, Schubert CJ, Amann R, Thamdrup B, Kuypers MMM (2007) Linking crenarchaeal and bacterial nitrification to anammox in the Black Sea. Proc Natl Acad Sci U S A 104:7104–7109

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Limpiyakorn T, Shinohara Y, Kurisu F, Yagi O (2005) Communities of ammonia-oxidizing bacteria in activated sludge of various sewage treatment plants in Tokyo. FEMS Microbiol Ecol 54:205–217

    Article  PubMed  CAS  Google Scholar 

  • Limpiyakorn T, Sonthiphand P, Rongsayamanont C, Polprasert C (2011) Abundance of amoA genes of ammonia-oxidizing archaea and bacteria in activated sludge of full-scale wastewater treatment plants. Bioresour Technol 102:3694–3701

    Article  PubMed  CAS  Google Scholar 

  • Limpiyakorn T, Fürhacker M, Haberl R, Chodanon T, Srithep P, Sonthiphand P (2013) amoA-encoding archaea in wastewater treatment plants: a review. Appl Microbiol Biotechnol 97:1425–1439

    Article  PubMed  CAS  Google Scholar 

  • Lydmark P, Almstrand R, Samuelsson K, Mattsson A, Sörensson F, Lindgren P-E, Hermansson M (2007) Effects of environmental conditions on the nitrifying population dynamics in a pilot wastewater treatment plant. Environ Microbiol 9:2220–2233

    Article  PubMed  CAS  Google Scholar 

  • Ma B, Peng Y, Zhang S, Wang J, Gan Y, Chang J, Wang S, Wang S, Zhu G (2013) Performance of anammox UASB reactor treating low strength wastewater under moderate and low temperatures. Bioresour Technol 129:606–611

    Article  PubMed  CAS  Google Scholar 

  • Mincer TJ, Church MJ, Taylor LT, Preston C, Karl DM, DeLong EF (2007) Quantitative distribution of presumptive archaeal and bacterial nitrifiers in Monterey Bay and the North Pacific Subtropical Gyre. Environ Microbiol 9:1162–1175

    Article  PubMed  CAS  Google Scholar 

  • Mobarry BK, Wagner M, Urbain V, Rittmann BE, Stahl DA (1996) Phylogenetic probes for analyzing abundance and spatial organization of nitrifying bacteria. Appl Environ Microbiol 62:2156–2162

    PubMed Central  PubMed  CAS  Google Scholar 

  • Mußmann M, Brito I, Pitcher A, Sinninghe Damsté JS, Hatzenpichler R, Richter A, Nielsen JL, Nielsen PH, Müller A, Daims H, Wagner M, Head IM (2011) Thaumarchaeotes abundant in refinery nitrifying sludges express amoA but are not obligate autotrophic ammonia oxidizers. Proc Natl Acad Sci U S A 108:16771–16776

    Article  PubMed Central  PubMed  Google Scholar 

  • Park HD, Noguera DR (2004) Evaluating the effect of dissolved oxygen on ammonia-oxidizing bacterial communities in activated sludge. Water Res 38:3275–3286

    Article  PubMed  CAS  Google Scholar 

  • Park HD, Wells GF, Bae H, Griddle CS, Francis CA (2006) Occurrence of ammonia-oxidizing archaea in wastewater treatment plant bioreactors. Appl Environ Microbiol 72:5643–5647

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Park BJ, Park SJ, Yoon DN, Schouten S, Sinninghe Damsté JS, Rhee SK (2010) Cultivation of autotrophic ammonia-oxidizing archaea from marine sediments in coculture with sulfur-oxidizing bacteria. Appl Environ Microbiol 76:7575–7587

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Pester M, Rattei T, Flechl S, Gröngröft A, Richter A, Overmann J, Reinhold-Hurek B, Loy A, Wagner M (2012) AmoA-based consensus phylogeny of ammonia-oxidizing archaea and deep sequencing of amoA genes from soils of four different geographic regions. Environ Microbiol 14:525–539

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Poth M (1986) Dinitrogen production from nitrite by a nitrosomonas isolate. Appl Environ Microbiol 52:957–959

    Google Scholar 

  • Purkhold U, Pommerening-Röser A, Juretschko S, Schmid MC, Koops H-P, Wagner M (2000) Phylogeny of all recognized species of ammonia oxidizers based on comparative 16S rRNA and amoA sequence analysis: implications for molecular diversity surveys. Appl Environ Microbiol 66(12):5368–5382

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Ritchie GA, Nicholas DJ (1972) Identification of the sources of nitrous oxide produced by oxidative and reductive processes in Nitrosomonas europaea. Biochem J 126:1181–1191

    Google Scholar 

  • Rodriguez-Caballero A, Hallin S, Pahlson C, Odlare M, Dahlquist E (2012) Ammonia oxidizing bacterial community composition and process performance in wastewater treatment plants under low temperature conditions. Water Sci Technol 65(2):197–204

    Article  PubMed  CAS  Google Scholar 

  • Rotthauwe JH, Witzel KP, Liesack W (1997) The ammonia monooxygenase structural gene amoA as a functional marker: molecular fine-scale analysis of natural ammonia-oxidizing populations. Appl Environ Microbiol 63:4704–4712

    PubMed Central  PubMed  CAS  Google Scholar 

  • Rowan AK, Snape JR, Fearnside D, Barer MR, Curtis TP, Head IM (2003) Composition and diversity of ammonia-oxidising bacterial communities in wastewater treatment reactors of different design treating identical wastewater. FEMS Microbiol Ecol 43:195–206

    Article  PubMed  CAS  Google Scholar 

  • Santoro AE, Buchwald C, McIlvin MR, Casciotti KL (2011) Isotopic signature of N2O produced by marine ammonia-oxidizing archaea. Science 333:1282–1285

    Article  PubMed  CAS  Google Scholar 

  • Sauder LA, Peterse F, Schouten S, Neufeld JD (2012) Low-ammonia niche of ammonia-oxidizing archaea in rotating biological contactors of a municipal wastewater treatment plant. Environ Microbiol 14:2589–2600

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Schloss PD, Westcott SL, Ryabin T, Hall JR, Hartmann M, Hollister EB, Lesniewski RA, Oakley BB, Parks DH, Robinson CJ, Sahl JW, Stres B, Thallinger GG, Van Horn DJ, Weber CF (2009) Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol 75:7537–7541

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Schmid M, Twachtmann U, Klein M, Strous M, Juretschko S, Jetten M, Metzger JW, Schleifer KH, Wagner M (2000) Molecular evidence for genus level diversity of bacteria capable of catalyzing anaerobic ammonium oxidation. Syst Appl Microbiol 23:93–106

    Article  PubMed  CAS  Google Scholar 

  • Shaw LJ, Nicol GW, Smith Z, Fear J, Prosser JI, Baggs EM (2006) Nitrosospira spp. can produce nitrous oxide via a nitrifier denitrification pathway. Environ Microbiol 8:214–222

    Google Scholar 

  • Siripong S, Rittmann BE (2007) Diversity study of nitrifying bacteria in full-scale municipal wastewater treatment plants. Water Res 41:1110–1120

    Article  PubMed  CAS  Google Scholar 

  • Sofia A, Liu WT, Ong SL, Ng WJ (2004) In-situ characterization of microbial community in an A/O submerged membrane bioreactor with nitrogen removal. Water Sci Technol 50:41–48

    PubMed  CAS  Google Scholar 

  • Sonthiphand P, Limpiyakorn T (2011) Change in ammonia-oxidizing microorganisms in enriched nitrifying activated sludge. Appl Microbiol Biotechnol 89:843–853

    Article  PubMed  CAS  Google Scholar 

  • Spang A, Hatzenpichler R, Brochier-Armanet C, Rattei T, Tischler P, Spieck E, Streit W, Stahl DA, Wagner M, Schleper C (2010) Distinct gene set in two different lineages of ammonia-oxidizing archaea supports the phylum Thaumarchaeota. Trends Microbiol 18:331–340

    Article  PubMed  CAS  Google Scholar 

  • Tourna M, Stieglmeier M, Spang A, Könneke M, Schintlmeister A, Urich T, Engel M, Schloter M, Wagner M, Richter A, Schleper C (2011) Nitrososphaera viennensis, an ammonia oxidizing archaeon from soil. Proc Natl Acad Sci U S A 108:8420–8425

  • Treusch AH, Leininger S, Kletzin A, Schuster SC, Klenk HP, Schleper C (2005) Novel genes for nitrite reductase and Amo-related proteins indicate a role of uncultivated mesophilic Crenarchaeota in nitrogen cycling. Environ Microbiol 7:1985–1995

    Article  PubMed  CAS  Google Scholar 

  • van de Graaf AA, de Bruijn P, Robertson LA, Jetten MSM, Kuenen JG (1996) Autotrophic growth of anaerobic ammonium-oxidizing micro-organisms in a fluidized bed reactor. Microbiology 142:2187–2196

    Article  Google Scholar 

  • Venter JC, Remington K, Heidelberg JF, Halpern AL, Rusch D, Eisen JA, Wu D, Paulsen I, Nelson KE, Nelson W, Fouts DE, Levy S, Knap AH, Lomas MW, Nealson K, White O, Peterson J, Hoffman J, Parsons R, Baden-Tillson H, Pfannkoch C, Rogers YH, Smith HO (2004) Environmental genome shotgun sequencing of the Sargasso Sea. Science 304:66–74

    Article  PubMed  Google Scholar 

  • Wang S, Zhu G, Peng Y, Jetten MSM, Yin C (2012) Anammox bacterial abundance, activity, and contribution in riparian sediments of the Pearl River estuary. Environ Sci Technol 46:8834–8842

    Article  PubMed  CAS  Google Scholar 

  • Wells GF, Park HD, Yeung CH, Eggleston B, Francis CA, Criddle CS (2009) Ammonia-oxidizing communities in a highly aerated full-scale activated sludge bioreactor: betaproteobacterial dynamics and low relative abundance of Crenarchaea. Environ Microbiol 11:2310–2328

    Article  PubMed  CAS  Google Scholar 

  • Woebken D, Fuchs BM, Kuypers MMM, Amann R (2007) Potential interactions of particle-associated anammox bacteria with bacterial and archaeal partners in the Namibian upwelling system. Appl Environ Microbiol 73:4648–4657

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Wrage N, Velthof GL, van Beusichem ML, Oenema O (2001) Role of nitrifier denitrification in the production of nitrous oxide. Soil Biol Biochem 33:1723–1732

    Article  CAS  Google Scholar 

  • Wu YJ, Whang LM, Fukushima T, Chang SH (2013) Responses of ammonia-oxidizing archaeal and betaproteobacterial populations to wastewater salinity in a full-scale municipal wastewater treatment plant. J Biosci Bioeng 115:424–432

    Article  PubMed  CAS  Google Scholar 

  • Ye L, Zhang T (2011) Ammonia-oxidizing bacteria dominates over ammonia-oxidizing archaea in a saline nitrification reactor under low DO and high nitrogen loading. Biotechnol Bioeng 108:2544–2552

    Article  PubMed  CAS  Google Scholar 

  • Zhang T, Jin T, Yan Q, Shao M, Wells G, Criddle C, Fang HHP (2009) Occurrence of ammonia-oxidizing Archaea in activated sludges of a laboratory scale reactor and two wastewater treatment plants. J Appl Microbiol 107:970–977

    Article  PubMed  CAS  Google Scholar 

  • Zhang T, Ye L, Tong A, Shao M-F, Lok S (2011) Ammonia-oxidizing archaea and ammonia-oxidizing bacteria in six full-scale wastewater treatment bioreactors. Appl Microbiol Biotechnol 91:1215–1225

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Zhu G, Wang S, Feng X, Fan G, Jetten MSM, Yin C (2011) Anammox bacterial abundance, biodiversity and activity in a constructed wetland. Environ Sci Technol 45:9951–9958

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

The authors wish to thank the NSFC (51078007, 51378027), BJ-NSF (8112007), PHR-IHLB (PHR20110819), and Beijing Talent Foundation of BJUT (2013-JH-L06) for the financial support of this study.

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Gao, J., Luo, X., Wu, G. et al. Abundance and diversity based on amoA genes of ammonia-oxidizing archaea and bacteria in ten wastewater treatment systems. Appl Microbiol Biotechnol 98, 3339–3354 (2014). https://doi.org/10.1007/s00253-013-5428-2

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