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Novel municipal sewage-associated bacterial genomes and their potential in source tracking

View ORCID ProfileBlake G. Lindner, View ORCID ProfileBrittany Suttner, View ORCID ProfileRoth E. Conrad, View ORCID ProfileLuis M. Rodriguez-R, View ORCID ProfileJanet K. Hatt, Kevin J. Zhu, View ORCID ProfileJoe Brown, Konstantinos T. Konstantinidis
doi: https://doi.org/10.1101/2021.07.15.452399
Blake G. Lindner
1School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
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Brittany Suttner
1School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
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  • ORCID record for Brittany Suttner
Roth E. Conrad
2Ocean Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
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Luis M. Rodriguez-R
1School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
3Department of Microbiology and Digital Science Center (DiSC), University of Innsbruck, 6020 Innsbruck, Tyrol, Austria
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Janet K. Hatt
1School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
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  • ORCID record for Janet K. Hatt
Kevin J. Zhu
1School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
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Joe Brown
1School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
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Konstantinos T. Konstantinidis
1School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
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  • For correspondence: kostas@ce.gatech.edu
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Abstract

Little is known about the genomic diversity of raw municipal wastewater (sewage) microbial communities, including to what extent sewage-specific populations exist and how they can be used to improve source attribution and partitioning in sewage-contaminated waters. Herein, we used the influent of three wastewater treatment plants in Atlanta, Georgia (USA) as inoculum in multiple controlled laboratory mesocosms to simulate sewage contamination events and followed these perturbed freshwater microbial communities with metagenomics over a 7-day observational period. We describe 15 abundant non-redundant bacterial metagenome-assembled genomes (MAGs) ubiquitous within all sewage inoculum yet absent from the unperturbed freshwater control at our analytical limit of detection. Tracking the dynamics of populations represented by these MAGs revealed varied decay kinetics, depending on (inferred) phenotypes, e.g., anaerobes decayed faster under the well-aerated incubation conditions. Notably, a portion of these populations show decay patterns similar to common markers, Enterococcus and HF183. Comparisons against MAGs from different sources such as human and animal feces, revealed low cross-reactivity, indicating how genomic collections could be used to sensitively identify sewage contamination and partition signal among multiple sources. Overall, our results indicate the usefulness of metagenomic approaches for assessing sewage contamination in waterbodies and provides needed methodologies for doing so.

Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted July 15, 2021.
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Novel municipal sewage-associated bacterial genomes and their potential in source tracking
Blake G. Lindner, Brittany Suttner, Roth E. Conrad, Luis M. Rodriguez-R, Janet K. Hatt, Kevin J. Zhu, Joe Brown, Konstantinos T. Konstantinidis
bioRxiv 2021.07.15.452399; doi: https://doi.org/10.1101/2021.07.15.452399
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Novel municipal sewage-associated bacterial genomes and their potential in source tracking
Blake G. Lindner, Brittany Suttner, Roth E. Conrad, Luis M. Rodriguez-R, Janet K. Hatt, Kevin J. Zhu, Joe Brown, Konstantinos T. Konstantinidis
bioRxiv 2021.07.15.452399; doi: https://doi.org/10.1101/2021.07.15.452399

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