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Evaluation of Ammonia Oxidizing Bacterial Community Structure of a Municipal Activated Sludge Plant by 454 High-Throughput Pyrosequencing

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Abstract

The ammonia oxidizing bacteria (AOB) community structure in a municipal wastewater treatment plant (WWTP) was monitored over the winter and summer periods. The AOB distribution in the full-scale WWTP was investigated using barcoded 454-pyrosequencing targeting the ammonia monooxygenase alpha subunit (amoA) gene. Using the quantitative polymerase chain reaction (qPCR) technique, the AOB population was quantified over 237 days. The plant operational parameters and its nitrification performance were also monitored. As revealed by pyrosequencing, majority of the identified AOB during the study were related to uncultured ammonia oxidizing bacteria, and Nitrosomonas oligotropha. Furthermore, it revealed higher AOB abundance during the summer which was 6 times more compared to winter. Substantial percentages of the reads from both seasons could not be assigned to any phylum, which suggests that vast population of novel, ecologically significant AOB species still inhabit the complex activated sludge communities unexploited. A significant seasonal variation in temperature (α = 0.05; P = < 0.0001) was recorded in the reactor with maximum temperature amplitude of 10.2 °C. The average nitrification rate recorded during the summer was 0.09 ± 0.03 g N-NH4+/g MLSS/d, whereas it was 0.04 ± 0.02 g N-NH4+/g MLSS/d during the winter. The nitrification rate of the plant had significant correlation with AOB population abundance (r = 0.70; P = 0.01) and temperature (α = 0.05; P = 0.0018). This study indicates that AOB diversity and population abundance were contributory factors to efficient nitrification in activated sludge system.

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References

  • Abe T, Ushiki N, Fujitani H, Tsuneda S (2017) A rapid collection of yet unknown ammonia oxidizers in pure culture from activated sludge. Water Res 108:169–178

    Article  Google Scholar 

  • APHA (1998) Standard methods for the examination of water and wastewater, 20th edn. American Public Health Association

  • Arévalo J, Ruiz LM, Pérez J, Gómez MA (2014) Effect of temperature on membrane bioreactor performance working with high hydraulic and sludge retention time. Biochem Eng J 88:42–49. https://doi.org/10.1016/j.bej.2014.03.006

    Article  Google Scholar 

  • Awolusi OO (2016) Evaluation of seasonal impacts on nitrifiers and nitrification performance of a full-scale activated sludge system. Doctoral dissertation, Durban University of Technology

  • Awolusi OO, Kumari SKS, Bux F (2015) Ecophysiology of nitrifying communities in membrane bioreactors. Int J Environ Sci Technol 12:747–762. https://doi.org/10.1007/s13762-014-0551-x

    Article  Google Scholar 

  • Awolusi OO, Nasr M, Kumari S, Bux F (2016) Artificial intelligence for the evaluation of operational parameters influencing nitrification and nitrifiers in an activated sludge process. Microb Ecol 72:49–63

    Article  Google Scholar 

  • Aydin S, Ince B, Ince O (2015) Application of real-time PCR to determination of combined effect of antibiotics on bacteria, methanogenic archaea, archaea in anaerobic sequencing batch reactors. Water Res 76:88–98. https://doi.org/10.1016/j.watres.2015.02.043

    Article  Google Scholar 

  • Briese V (2002) DNA precipitation. http://www.protocol-online.org/cgi-bin/prot/view_cache.cgi?ID=2744. Accessed 9/15/ 2012

  • Degrange V, Bardin R (1995) Detection and counting of Nitrobacter populations in soil by PCR. Appl Environ Microbiol 61:2093–2098

    Google Scholar 

  • Faulwetter JL, Burr MD, Parker AE, Stein OR, Camper AK (2013) Influence of season and plant species on the abundance and diversity of sulfate reducing bacteria and ammonia oxidizing bacteria in constructed wetland microcosms. Microb Ecol 65:111–127. https://doi.org/10.1007/s00248-012-0114-y

    Article  Google Scholar 

  • Fitzgerald CM, Camejo P, Oshlag JZ, Noguera DR (2015) Ammonia-oxidizing microbial communities in reactors with efficient nitrification at low-dissolved oxygen. Water Res 70:38–51. https://doi.org/10.1016/j.watres.2014.11.041

    Article  Google Scholar 

  • Fulweiler RW, Emery HE, HE M, Berounsky VM (2011) Assessing the role of pH in determining water column nitrification rates in a coastal system. Estuar Coasts 34:1095–1102

    Article  Google Scholar 

  • Gomez-Silvan C, Molina-Munoz M, Poyatos JM, Ramos A, Hontoria E, Rodelas B, Gonzalez-Lopez J (2010) Structure of archaeal communities in membrane-bioreactor and submerged-biofilter wastewater treatment plants. Bioresour Technol 101:2096–2105. https://doi.org/10.1016/j.biortech.2009.10.091

    Article  Google Scholar 

  • Harms G, Layton AC, Dionisi HM, Gregory IR, Garrett VM, Hawkins SA, Robinson KG, Sayler GS (2003) Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant. Environ Sci Technol 37:343–351

    Article  Google Scholar 

  • Ju F, Zhang T (2015a) 16S rRNA gene high-throughput sequencing data mining of microbial diversity and interactions. Appl Microbiol Biotechnol 99:4119–4129. https://doi.org/10.1007/s00253-015-6536-y

    Article  Google Scholar 

  • Ju F, Zhang T (2015b) Bacterial assembly and temporal dynamics in activated sludge of a full-scale municipal wastewater treatment plant. ISME J 9:683–695. https://doi.org/10.1038/ismej.2014.162

    Article  Google Scholar 

  • Ju F, Guo F, Ye L, Xia Y, Zhang T (2014) Metagenomic analysis on seasonal microbial variations of activated sludge from a full-scale wastewater treatment plant over 4 years. Environ Microbiol 6:80–89. https://doi.org/10.1111/1758-2229.12110

    Article  Google Scholar 

  • Keuter S, Beth S, Quantz G, Schulz C, Spieck E (2017) Longterm monitoring of nitrification and nitrifying communities during biofilter activation of two marine recirculation aquaculture systems (RAS). Int J Aquac Fish Sci 3:051–061. https://doi.org/10.17352/2455-8400.000029

    Article  Google Scholar 

  • Kim YM (2013) Acclimatization of communities of ammonia oxidizing bacteria to seasonal changes in optimal conditions in a coke wastewater treatment plant. Bioresour Technol 147:627–631. https://doi.org/10.1016/j.biortech.2013.08.062

    Article  Google Scholar 

  • Kim J, Guo X, Park H (2008) Comparison study of the effects of temperature and free ammonia concentration on nitrifiers and nitrite accumulation. Process Biochem 43:154–160. https://doi.org/10.1016/j.procbio.2007.11.005

    Article  Google Scholar 

  • Kim YM, Cho HU, Lee DS, Park D, Park JM (2011) Influence of operational parameters on nitrogen removal efficiency and microbial communities in a full-scale activated sludge process. Water Res 45:5785–5795. https://doi.org/10.1016/j.watres.2011.08.063

    Article  Google Scholar 

  • Kim J, Lim J, Lee C (2013) Quantitative real-time PCR approaches for microbial community studies in wastewater treatment systems: applications and considerations. Biotechnol Adv 31:1358–1373. https://doi.org/10.1016/j.biotechadv.2013.05.010

    Article  Google Scholar 

  • Klindworth A, Pruesse E, Schweer T, Peplies J, Quast C, Horn M, Glockner FO (2013) Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies. Nucleic Acids Res 41:e1. https://doi.org/10.1093/nar/gks808

    Article  Google Scholar 

  • LaPara TM, Ghosh S (2006) Population dynamics of the ammonia-oxidizing bacteria in a full-scale municipal wastewater treatment facility. Environ Eng Sci 23:309–319

    Article  Google Scholar 

  • Lienen T, Kleybocker A, Verstraete W, Wurdemann H (2014) Moderate temperature increase leads to disintegration of floating sludge and lower abundance of the filamentous bacterium Microthrix parvicella in anaerobic digesters. Water Res 65:203–212. https://doi.org/10.1016/j.watres.2014.07.019

    Article  Google Scholar 

  • Liu G, Wang J (2013) Long-term low DO enriches and shifts nitrifier community in activated sludge. Environ Sci Technol 47:5109–5117. https://doi.org/10.1021/es304647y

    Article  Google Scholar 

  • McMahon KD, Gu AZ, Nerenberg R, Sturm BM (2009) Molecular methods in biological systems. Water Environ Res 81:986–1002. https://doi.org/10.2175/106143009X12445568399370

    Article  Google Scholar 

  • McTavish HJAF, Fuchs JA, Hooper AB (1993) Sequence of the gene coding for ammonia monooxygenase in Nitrosomonas europaea. J Bacteriol 175:2436–2444

    Article  Google Scholar 

  • Miura Y, Hiraiwa MN, Ito T, Itonaga T, Watanabe Y, Okabe S (2007) Bacterial community structures in MBRs treating municipal wastewater: relationship between community stability and reactor performance. Water Res 41:627–637. https://doi.org/10.1016/j.watres.2006.11.005

    Article  Google Scholar 

  • Morozova O, Marra MA (2008) Applications of next-generation sequencing technologies in functional genomics. Genomics 92:255–264. https://doi.org/10.1016/j.ygeno.2008.07.001

    Article  Google Scholar 

  • Mousavi SA, Ibrahim S, Aroua MK (2017) Effect of carbon source on acclimatization of nitrifying bacteria to achieve high-rate partial nitrification of wastewater with high ammonium concentration. Appl Water Sci 7:165–173. https://doi.org/10.1007/s13201-014-0229-z

    Article  Google Scholar 

  • Niu J, Kasuga I, Kurisu F, Furumai H, Shigeeda T, Takahashi K (2016) Abundance and diversity of ammonia-oxidizing archaea and bacteria on granular activated carbon and their fates during drinking water purification process. Appl Microbiol Biotechnol 100:729–742. https://doi.org/10.1007/s00253-015-6969-3

    Article  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  Google Scholar 

  • Ramond JB, Lako JDW, Stafford WHL, Tuffin MI, Cowan DA (2015) Evidence of novel plant-species specific ammonia oxidizing bacterial clades in acidic South African fynbos soils J Basic Microbiol: https://doi.org/10.1002/jobm.201400933

    Article  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  Google Scholar 

  • Ruiz G, Jeison D, Chamy R (2003) Nitrification with high nitrite accumulation for the treatment of wastewater with high ammonia concentration. Water Res 37:1371–1377

    Article  Google Scholar 

  • Sajuni NR, Ahmad AL, Vadivelu VM (2010) Effect of filter media characteristics, pH and temperature on the ammonia removal in the wastewater. J Appl Sci 10:1146–1150

    Article  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  Google Scholar 

  • Sekar S, Zintchem AAEA, Keshri J, Kamika I, Momba MNB (2014) Bacterial profiling in brine samples of the Emalahleni water reclamation plant, South Africa, using 454-pyrosequencing method. FEMS Microbiol Lett 359:1–9. https://doi.org/10.1111/1574-6968.12557

    Article  Google Scholar 

  • Shi P, Jia S, Zhang XX, Zhang T, Cheng S, Li A (2013) Metagenomic insights into chlorination effects on microbial antibiotic resistance in drinking water. Water Res 47:111–120. https://doi.org/10.1016/j.watres.2012.09.046

    Article  Google Scholar 

  • Shokralla S, Spall JL, Gibson JF, Hajibabaei M (2012) Next-generation sequencing technologies for environmental DNA research. Mol Ecol 21:1794–1805. https://doi.org/10.1111/j.1365-294X.2012.05538.x

    Article  Google Scholar 

  • Siripong S, Rittmann BE (2007) Diversity study of nitrifying bacteria in full-scale municipal wastewater treatment plants. Water Res 41:1110–1120. https://doi.org/10.1016/j.watres.2006.11.050

    Article  Google Scholar 

  • Steinberg LM, Regan JM (2009) mcrA-targeted real-time quantitative PCR method to examine methanogen communities. Appl Environ Microbiol 75:4435–4442. https://doi.org/10.1128/AEM.02858-08

    Article  Google Scholar 

  • Tamura K, Stecher G, Peterson D, Filipski A, Kumar S (2013) MEGA6: molecular evolutionary genetics analysis version 6.0 Mol Biol Evol 30:2725–2729

    Article  Google Scholar 

  • Tvrdik D, Stanek L, Skalova H, Dundr P, Velenska Z, Povysil C (2012) Comparison of the IHC, FISH, SISH and qPCR methods for the molecular diagnosis of breast cancer. Mol Med Rep 6:439–443. https://doi.org/10.3892/mmr.2012.919

    Article  Google Scholar 

  • Urakawa H, Tajima Y, Numata Y, Tsuneda S (2008) Low temperature decreases the phylogenetic diversity of ammonia-oxidizing archaea and bacteria in aquarium biofiltration systems. Appl Environ Microbiol 74:894–900

    Article  Google Scholar 

  • Wang X, Wen X, Criddle C, Wells G, Zhang J, Zhao Y (2010) Community analysis of ammonia-oxidizing bacteria in activated sludge of eight wastewater treatment systems. J Environ Sci 22:627–634

    Article  Google Scholar 

  • Xia S, Duan L, Song Y, Li J, Piceno YM, Andersen GL, Alvarez-Cohen L, Moreno-Andrade I, Huang CL, Hermanowicz SW (2010) Bacterial community structure in geographically distributed biological wastewater treatment reactors. Environ Sci Technol 44:7391–7396

    Article  Google Scholar 

  • Yan J, Hu YY (2009) Partial nitrification to nitrite for treating ammonium-rich organic wastewater by immobilized biomass system. Bioresour Technol 100:2341–2347. https://doi.org/10.1016/j.biortech.2008.11.038

    Article  Google Scholar 

  • Yang C, Zhang W, Liu R, Li Q, Li B, Wang S, Song C, Qiao C, Mulchandani A (2011) Phylogenetic diversity and metabolic potential of activated sludge microbial communities in full-scale wastewater treatment plants. Environ Sci Technol 45:7408–7415. https://doi.org/10.1021/es2010545

    Article  Google Scholar 

  • Zhang B, Sun B, Ji M, Liu H (2009) Population dynamic succession and quantification of ammonia-oxidizing bacteria in a membrane bioreactor treating municipal wastewater. J Hazard Mater 165:796–803. https://doi.org/10.1016/j.jhazmat.2008.10.116

    Article  Google Scholar 

  • Zhang Y, Chen L, Sun R, Dai T, Tian J, Wen D (2015) Ammonia-oxidizing bacteria and archaea in wastewater treatment plant sludge and nearby coastal sediment in an industrial area in China. Appl Microbiol Biotechnol 99:4495–4507. https://doi.org/10.1007/s00253-014-6352-9

    Article  Google Scholar 

  • Zheng Y, Hou L, Liu M, Lu M, Zhao H, Yin G, Zhou J (2013) Diversity, abundance, and activity of ammonia-oxidizing bacteria and archaea in Chongming eastern intertidal sediments. Appl Microbiol Biotechnol 97:8351–8363

    Article  Google Scholar 

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Acknowledgements

This work was supported financially by Durban University of Technology and the National Research Foundation SARChI Chair. An initial shorter version of the paper has been presented at the 10th World Congress of the European Water Resources Association (EWRA2017) “Panta Rhei”, Athens, Greece, 5-9 July, 2017 624 (http://ewra2017.ewra.net/).

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Correspondence to Oluyemi Olatunji Awolusi.

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Awolusi, O., Kumari, S. & Bux, F. Evaluation of Ammonia Oxidizing Bacterial Community Structure of a Municipal Activated Sludge Plant by 454 High-Throughput Pyrosequencing. Environ. Process. 5 (Suppl 1), 43–57 (2018). https://doi.org/10.1007/s40710-018-0319-2

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