Environmental Science and Pollution Research

, Volume 25, Issue 5, pp 4094–4104 | Cite as

(Anti-)estrogenic and (anti-)androgenic effects in wastewater during advanced treatment: comparison of three in vitro bioassays

  • Linda Gehrmann
  • Helena Bielak
  • Maximilian Behr
  • Fabian Itzel
  • Sven Lyko
  • Anne Simon
  • Gotthard Kunze
  • Elke Dopp
  • Martin Wagner
  • Jochen TuerkEmail author
Research Article


Endocrine-disrupting chemicals are mainly discharged into the environment by wastewater treatment plants (WWTPs) and are known to induce adverse effects in aquatic life. Advanced treatment with ozone successfully removes such organic micropollutants, but an increase of estrogenic effects after the ozonation of hospital wastewater was observed in previous studies. In order to investigate this effect, estrogenic and androgenic as well as anti-estrogenic and anti-androgenic activities were observed during treatment of hospital wastewater using three different effect-based reporter gene bioassays. Despite different matrix influences, sensitivities, and test-specific properties, all assays used obtained comparable results. Estrogenic and androgenic activities were mainly reduced during the biological treatment and further removed during ozonation and sand filtration, resulting in non-detectable agonistic activities in the final effluent. An increased estrogenic activity after ozonation could not be observed in this study. Antagonistic effects were removed in the biological treatment by up to 50 % without further reduction in the advanced treatment. Due to the presence of antagonistic substances within the wastewater, masking effects were probable. Therefore, this study showed the relevance of antagonistic activities at hospital WWTPs and illustrates the need for a better understanding about antagonistic effects.


Endocrine effects Advanced wastewater treatment Ozonation Antagonistic effects Reporter gene assays Effect-based analysis Micropollutant elimination 



The authors would like to thank for financial support from the “Ministry for Climate Protection, Agriculture, Nature Conservation and Consumer Protection of North Rhine-Westphalia (MKULNV)” within the program „Ressourceneffiziente Abwasserbeseitigung NRW“ (AZ 17-04.02.01-04a/2013). We would also like to acknowledge Jan Oesterbeck from the North Rhine-Westphalia State Agency for Nature, Environment and Consumer Protection (LANUV NRW) for the great guidance and support during this project. Our special thanks for the support and helping hand during the operation and sampling belong to the dedicated personnel of Emschergenossenschaft/Lippeverband.

Supplementary material

11356_2016_7165_MOESM1_ESM.pdf (1.8 mb)
ESM 1 (PDF 1.78 mb)


  1. Altmann D, Schaar H, Bartel C, Schorkopf DLP, Miller I, Kreuzinger N, Mostl E, Grillitsch B (2012) Impact of ozonation on ecotoxicity and endocrine activity of tertiary treated wastewater effluent. Water Res. 46(11):3693--3702.Google Scholar
  2. Aris AZ, Shamsuddin AS, Praveena SM (2014) Occurrence of 17 alpha-ethynylestradiol (EE2) in the environment and effect on exposed biota: a review. Environ Int 69:104–119CrossRefGoogle Scholar
  3. Bieling U (2011) Entwicklung einer Methode zum Nachweis und zur Identifikation endokrin wirksamer Substanzen mit estrogenem Potential aus Abwässern nach Anreicherung mit Hilfe des immobilisierten Estrogenrezeptors α. PhD Thesis, RWTH Aachen. Shaker Verlag, Oldenburg, ISBN. 978-3-8440-0385-7.Google Scholar
  4. BioDetection Systems (2009) Analysis of receptor mediated luciferase activity in ER CALUX cells. P-BDS-011, version i.Google Scholar
  5. Boehling E, Adamczak K, Nafo I, Evenblij H, Cornelissen A, McArdell C, Pahl O, Dagot C. 2012. Pharmaceutical input and elimination from local sources. Final report of the European cooperation project PILLS.
  6. Campbell CG, Borglin SE, Green FB, Grayson A, Wozei E, Stringfellow WT (2006) Biologically directed environmental monitoring, fate, and transport of estrogenic endocrine disrupting compounds in water: a review. Chemosphere 65:1265–1280CrossRefGoogle Scholar
  7. Connolly L, Ropstad E, Verhaegen S (2011) In vitro bioassays for the study of endocrine-disrupting food additives and contaminants. Trac-Trends Anal Chem 30:227–238CrossRefGoogle Scholar
  8. Dudley MW, Sheeler CQ, Wang H, Khan S (2000) Activation of the human estrogen receptor by the antiestrogens ICI 182,780 and tamoxifen in yeast genetic systems: implications for their mechanism of action. Proc Natl Acad Sci U S A 97:3696–3701CrossRefGoogle Scholar
  9. European Parliament and Council (2000) Directive 2000/60/EG of the European Parliament and of the Council of 23 October 2000 establishing a framework for Community action in the field of water policyGoogle Scholar
  10. European Commission, Common Implementation Strategy for the Water Framework Directive (2000/60/EC) Guidance on surface water chemical monitoring under the Water Framework Directive. Guidance Document No. 19; 2009–025Google Scholar
  11. European Parliament and Council 2013/39 (2013) Directive 2013/39/EU of the European Parliament and of the Council of 12 August 2013 amending Directives 2000/60/EC and 2008/105/EC as regards priority substances in the field of water policy.Google Scholar
  12. European Parliament and Council 2015/495 (2015) Commission implementing Decision (EU) 2015/495 of March 2015 establishing a watch list of substances for Union-wide monitoring in the field of water policy pursuant to Directive 2008/105/EC of the European Parliament and of the Council.Google Scholar
  13. Hahn T, Tag K, Riedel K, Uhlig S, Baronian K, Gellissen G, Kunze G (2006) A novel estrogen sensor based on recombinant Arxula adeninivorans cells. Biosens Bioelectron 21:2078–2085CrossRefGoogle Scholar
  14. Houtman CJ, Van Houten YK, Leonards PG, Brouwer A, Lamoree MH, Legler J (2006) Biological validation of a sample preparation method for ER-CALUX bioanalysis of estrogenic activity in sediment using mixtures of xeno-estrogens. Environ Sci Technol 40:2455–2461CrossRefGoogle Scholar
  15. Huber MM, Ternes TA, von Gunten U (2004) Removal of estrogenic activity and formation of oxidation products during ozonation of 17 alpha-ethinylestradiol. Environ Sci Technol 38:5177–5186CrossRefGoogle Scholar
  16. Huber MM, Gobel A, Joss A, Hermann N, Loffler D, McArdell CS, Ried A, Siegrist H, Ternes TA, von Gunten U (2005) Oxidation of pharmaceuticals during ozonation of municipal wastewater effluents: a pilot study. Environ Sci Technol 39:4290–4299CrossRefGoogle Scholar
  17. ISO 10993–5:2009: Biological evaluation of medical devices. Part 5: tests for in vitro cytotoxicityGoogle Scholar
  18. Jobling S, Burn RW, Thorpe K, Williams R, Tyler C (2009) Statistical modeling suggests that antiandrogens in effluents from wastewater treatment works contribute to widespread sexual disruption in fish living in English rivers. Environ Health Perspect 117:797–802CrossRefGoogle Scholar
  19. Kienle C, Vermeirssen E, Kunz P, Werner I (2015): Grobbeurteilung der Wasserqualität von abwasserbelasteten Gewässern anhand von ökotoxikologischen Biotests. Studie im Auftrag des BAFU. Schweizerisches Zentrum für angewandte Ökotoxikologie Eawag-EPFL, Dübendorf.Google Scholar
  20. Kinnberg K (2003) Evaluation of in vitro assays for determination of estrogenic activity in the environment. Danish Ministry of the Environment, Danish Environmental Protection AgencyGoogle Scholar
  21. Larcher S, Delbes G, Robaire B, Yargeau V (2012) Degradation of 17 alpha-ethinylestradiol by ozonation - Identification of the by-products and assessment of their estrogenicity and toxicity. Environ Int 39(1):66--72Google Scholar
  22. Lee Y, Escher BI, Von Gunten U (2008) Efficient removal of estrogenic activity during oxidative treatment of waters containing steroid estrogens. Environ Sci Technol 42:6333–6339CrossRefGoogle Scholar
  23. Legler J, van den Brink CE, Brouwer A, Murk AJ, van der Saag PT, Vethaak AD, van der Burg P (1999) Development of a stably transfected estrogen receptor-mediated luciferase reporter gene assay in the human T47D breast cancer cell line. Toxicol Sci 48:55–66CrossRefGoogle Scholar
  24. Legler J, Dennekamp M, Vethaak AD, Brouwer A, Koeman JH, van der Burg B, Murk AJ (2002) Detection of estrogenic activity in sediment-associated compounds using in vitro reporter gene assays. Sci Total Environ 293:69–83CrossRefGoogle Scholar
  25. Leusch FDL (2008) Tools to detect estrogenic activity in environmental waters. Global Water Research CoalitionGoogle Scholar
  26. Leusch FDL, De Jager C, Levi Y, Lim R, Puijker L, Sacher F, Tremblay LA, Wilson VS, Chapman HF (2010) Comparison of five in vitro bioassays to measure estrogenic activity in environmental waters. Environ Sci Technol 44:3853–3860CrossRefGoogle Scholar
  27. Liu ZH, Kanjo Y, Mizutani S (2009) Removal mechanisms for endocrine disrupting compounds (EDCs) in wastewater treatment—physical means, biodegradation, and chemical advanced oxidation. A review Sci Total Environ 407:731–748CrossRefGoogle Scholar
  28. Maletz S, Floehr T, Beier S, Kluemper C, Brouwer A, Behnisch P, Higley E, Giesy JP, Hecker M, Gebhardt W, Linnemann V, Pinnekamp J, Hollert H (2013) In vitro characterization of the effectiveness of enhanced sewage treatment processes to eliminate endocrine activity of hospital effluents. Water Res 47:1545–1557CrossRefGoogle Scholar
  29. Mertl J, Kirchnawy C, Osorio V, Grininger A, Richter A, Bergmair J, Pyerin M, Washuettl M, Tacker M (2014) Characterization of estrogen and androgen activity of food contact materials by different in vitro bioassays (YES, YAS, ER alpha and AR CALUX) and chromatographic analysis (GC-MS, HPLC-MS). PLoS One 9Google Scholar
  30. Mosmann T (1983) Rapid colorimetric assay for cellular growth and survival - Application to proliferation and cyto-toxicity assays. 65(1-2):55--63Google Scholar
  31. Neale PA, Escher BI, Leusch FDL (2015) Understanding the implications of dissolved organic carbon when assessing antagonism in vitro: an example with an estrogen receptor assay. Chemosphere 135:341–346CrossRefGoogle Scholar
  32. Prasse C, Stalter D, Schulte-Oehlmann U, Oehlmann J, Ternes TA (2015) Spoilt for choice: a critical review on the chemical and biological assessment of current wastewater treatment technologies. Water Res 87:237–270CrossRefGoogle Scholar
  33. Richard J (2013): Toxicological in vitro evaluation of organic micropollutants before and after oxidative waste water treatment. PhD Thesis, University of Duisburg, Essen.Google Scholar
  34. Routledge EJ, Sumpter JP (1996) Estrogenic activity of surfactants and some of their degradation products assessed using a recombinant yeast screen. Environ Toxicol Chem 15:241–248CrossRefGoogle Scholar
  35. Sajidan A, Farouk A, Greiner R, Jungblut P, Muller EC, Borriss R (2004) Molecular and physiological characterisation of a 3-phytase from soil bacterium Klebsiella sp ASR1. Appl Microbiol Biotechnol 65:110–118CrossRefGoogle Scholar
  36. Schwindt AR, Winkelman DL, Keteles K, Murphy M, Vajda AM (2014) An environmental oestrogen disrupts fish population dynamics through direct and transgenerational effects on survival and fecundity. J Appl Ecol 51:582–591CrossRefGoogle Scholar
  37. Scott PD, Bartkow M, Blockwell SJ, Coleman HM, Khan SJ, Lim R, McDonald JA, Nice H, Nugegoda D, Pettigrove V, Tremblay LA, Warne MSJ, Leusch FDL (2014) An assessment of endocrine activity in Australian rivers using chemical and in vitro analyses. Environ Sci Pollut Res 21:12951–12967CrossRefGoogle Scholar
  38. Sohoni P, Sumpter JP (1998) Several environmental oestrogens are also anti-androgens. J Endocrinol 158:327–339CrossRefGoogle Scholar
  39. Sonneveld E, Jansen HJ, Riteco JAC, Brouwer A, van der Burg B (2005) Development of androgen- and estrogen-responsive bioassays, members of a panel of human cell line-based highly selective steroid-responsive bioassays. Toxicol Sci 83:136–148CrossRefGoogle Scholar
  40. Stalter D, Magdeburg A, Wagner M, Oehlmann J (2011) Ozonation and activated carbon treatment of sewage effluents: removal of endocrine activity and cytotoxicity. Water Res 45:1015–1024CrossRefGoogle Scholar
  41. US EPA [740-C-09-006] (2009): Endocrine Disruptor Screening Program Test Guidelines - OPPTS 890.1300: Estrogen receptor transcriptional activation (human cell line (HeLa-9903)) [EPA 740-C-09-006]Google Scholar
  42. US EPA CCL-3 list (2009) Drinking Water Contaminant Candidate List 3. FinalGoogle Scholar
  43. US EPA draft CCL-4 list (2015) Drinking water contaminant candidate list 4. Draft.Google Scholar
  44. van der Burg B, Winter R, H-y M, Vangenechten C, Berckmans P, Weimer M, Witters H, van der Linden S (2010a) Optimization and prevalidation of the in vitro AR CALUX method to test androgenic and antiandrogenic activity of compounds. Reprod Toxicol 30:18–24CrossRefGoogle Scholar
  45. van der Burg B, Winter R, Weimer M, Berckmans P, Suzuki G, Gijsbers L, Jonas A, van der Linden S, Witters H, Aarts J, Legler J, Kopp-Schneider A, Bremer S (2010b) Optimization and prevalidation of the in vitro ER alpha CALUX method to test estrogenic and antiestrogenic activity of compounds. Reprod Toxicol 30:73–80CrossRefGoogle Scholar
  46. Völker J, Castronovo S, Wick A, Ternes TA, Joss A, Oehlmann J, Wagner M (2016): Advancing biological wastewater treatment: extended anaerobic conditions enhance the removal of endocrine and dioxin-like activities. Environ Sci Tech. doi:  10.1021/acs.est.5b05732
  47. Wagner M, Vermeirssen ELM, Buchinger S, Behr M, Magdeburg A, Oehlmann J (2013) Deriving bio-equivalents from in vitro bioassays: assessment of existing uncertainties and strategies to improve accuracy and reporting. Environ Toxicol Chem 32:1906–1917CrossRefGoogle Scholar
  48. Wartmann T, Boer E, Pico AH, Sieber H, Bartelsen O, Gellissen G, Kunze G (2002) High-level production and secretion of recombinant proteins by the dimorphic, yeast Arxula adeninivorans. FEMS Yeast Res 2:363–369Google Scholar
  49. Wildhaber YS, Mestankova H, Scharer M, Schirmer K, Salhi E, von Gunten U (2015) Novel test procedure to evaluate the treatability of wastewater with ozone. Water Res 75:324–335CrossRefGoogle Scholar
  50. Zhang ZY, Zhu HT, Wen XH, Si XR (2012) Degradation behavior of 17 alpha-ethinylestradiol by ozonation in the synthetic secondary effluent. J Environ Sci 24:228–233CrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2016

Authors and Affiliations

  • Linda Gehrmann
    • 1
  • Helena Bielak
    • 2
  • Maximilian Behr
    • 3
  • Fabian Itzel
    • 1
  • Sven Lyko
    • 4
  • Anne Simon
    • 2
  • Gotthard Kunze
    • 5
  • Elke Dopp
    • 2
    • 6
  • Martin Wagner
    • 3
  • Jochen Tuerk
    • 1
    • 6
    Email author
  1. 1.Institut für Energie- und Umwelttechnik e. V. (IUTA, Institute of Energy and Environmental Technology)DuisburgGermany
  2. 2.IWW Rheinisch-Westfälisches Institut für Wasserforschung gemeinnützige GmbHMuelheim an der RuhrGermany
  3. 3.Abteilung Aquatic EcotoxicologyGoethe University FrankfurtFrankfurt am MainGermany
  4. 4.Emschergenossenschaft/Lippeverband (EG/LV)EssenGermany
  5. 5.Leibniz Institute of Plant Genetics and Crop Plant Research (IPK)Stadt SeelandGermany
  6. 6.Centre for Water and Environmental Research (ZWU)University Duisburg-EssenEssenGermany

Personalised recommendations