Total RNA analysis of the active microbiome on moving bed biofilm reactor carriers under incrementally increasing micropollutant concentrations

Author:

Martin Joseph Donald12,Tisler Selina3,Scheel Maria1ORCID,Svendsen Sif1,Anwar Muhammad Zohaib14,Zervas Athanasios1ORCID,Ekelund Flemming12,Bester Kai1,Hansen Lars Hestbjerg3,Jacobsen Carsten Suhr1,Ellegaard-Jensen Lea1ORCID

Affiliation:

1. Department of Environmental Science, Aarhus University , Frederiksborgvej 399, 4000 Roskilde , Denmark

2. Department of Biology, University of Copenhagen, Copenhagen, Denmark, Terrestrial Ecology Section, Department of Biology, University of Copenhagen , Universitetsparken 15, 2100 Copenhagen , Denmark

3. Department of Plant and Environmental Sciences, University of Copenhagen , Thorvaldsensvej 40, Frederiksberg 1871 , Denmark

4. The Center for Infectious Disease Genomics and One Health, Faculty of Health Sciences, Simon Fraser University , 8888 University Dr. W, Burnaby, BC V5A 1S6 , Canada

Abstract

Abstract Micropollutants are increasingly prevalent in the aquatic environment. A major part of these originates from wastewater treatment plants since traditional treatment technologies do not remove micropollutants sufficiently. Moving bed biofilm reactors (MBBRs), however, have been shown to aid in micropollutant removal when applied to conventional wastewater treatment as a polishing step. Here, we used Total RNA sequencing to investigate both the active microbial community and functional dynamics of MBBR biofilms when these were exposed to increasing micropollutant concentrations over time. Concurrently, we conducted batch culture experiments using biofilm carriers from the MBBRs to assess micropollutant degradation potential. Our study showed that biofilm eukaryotes, in particular protozoa, were negatively influenced by micropollutant exposure, in contrast to prokaryotes that increased in relative abundance. Further, we found several functional genes that were differentially expressed between the MBBR with added micropollutants and the control. These include genes involved in aromatic and xenobiotic compound degradation. Moreover, the biofilm carrier batch experiment showed vastly different alterations in benzotriazole and diclofenac degradation following the increased micropollutant concentrations in the MBBR. Ultimately, this study provides essential insights into the microbial community and functional dynamics of MBBRs and how an increased load of micropollutants influences these dynamics.

Funder

Aarhus University Research Foundation

Canadian Institutes of Health Research

Michael Smith Health Research BC

Publisher

Oxford University Press (OUP)

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