Chronic impact of sulfamethoxazole on the metabolic activity and composition of enriched nitrifying microbial culture

Tugce Katipoglu-Yazan*, Christophe Merlin, Marie Noëlle Pons, Emine Ubay-Cokgor, Derin Orhon

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

50 Citations (Scopus)

Abstract

This study investigated the chronic impact of sulfamethoxazole (SMX) on activated sludge sustaining an enriched nitrifying biomass. For this purpose, a laboratory scale fill and draw reactor was operated with 100 mg COD/L of peptone mixture and 50 mg N/L of ammonia at a sludge age of 15 days. Additionally, the biomass was exposed to a daily SMX dose of 50 mg/L once the reactor reached steady-state conditions. The reactor performance and microbial composition were monitored for 37 days with conventional parameters and molecular techniques based on the gene for ammonia monooxygenase subunit A (amoA) and the prokaryotic 16S rRNA gene. Denaturing gradient gel electrophoresis (DGGE) and 16S rRNA gene cloning analyses suggested a microbial community change concurrent with the addition of SMX. Specifically, quantitative polymerase chain reaction analyses (qPCR/RT-qPCR) revealed a significant reduction in the levels and activity of ammonia oxidizing bacteria (AOB). However, the acclimation period ended with high amoA mRNA levels and improved nitrification efficiency. Partial degradation of SMX by heterotrophic bacteria was also observed.

Original languageEnglish
Pages (from-to)546-555
Number of pages10
JournalWater Research
Volume100
DOIs
Publication statusPublished - 1 Sept 2016

Bibliographical note

Publisher Copyright:
© 2016 Elsevier Ltd.

Funding

This study was conducted as a part of the project Evaluation of the Biodegradation Characteristics and Toxicity/Inhibition Effects of Selected Antibiotics on Nitrification Systems and supported by Scientific Research Fund of Istanbul Technical University. The authors would like to thank Dr. Xavier Bellanger and Hélène Guilloteau for their advice, assistance, and support throughout qPCR and cloning experiments. The authors also wish to thank Prof. G. Sockalingum and V. Untereiner for running the FT-IR analysis of EPS at the Faculty of Pharmacy, University of Reims-Champagne-Ardennes (France).

FundersFunder number
Istanbul Teknik Üniversitesi

    Keywords

    • Community molecular analyses
    • Enriched nitrifying culture
    • Gene activity
    • Nitrification
    • Sulfamethoxazole

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