Toward shotgun metagenomic approaches for microbial source tracking sewage spills based on laboratory mesocosms. (15th February 2022)

• Record Type: Journal Article
• Authors: Lindner, Blake G.; Suttner, Brittany; Zhu, Kevin J.; Conrad, Roth E.; Rodriguez-R, Luis M.; Hatt, Janet K.; Brown, Joe; Konstantinidis, Konstantinos T.
• Is Part Of: Water research. Volume 210(2022)
• Publication Date: 2022-02-15
• Subjects: Source tracking -- Metagenomics -- Sewage collection systems -- Wastewater -- Microbial ecology -- Water quality; Water -- Pollution -- Research -- Periodicals; 363.7394
• DOI: 10.1016/j.watres.2021.117993
• Languages: English
• ISSNs: 0043-1354

Abstract

Highlights: Sewage microbiomes harbor populations discrete from those of both the human gut and aquatic environments. Multiple source specific libraries were generated and curated for monitoring use. Metagenomic workflow with analytical limits of detection developed for MST. Sewage spills show depletion of traditional and metagenomic markers after 4 days. Metagenomics can inform questions of virulence, ARGs, and source attribution. Abstract: Little is known about the genomic diversity of the microbial communities associated with raw municipal wastewater (sewage), including whether microbial populations specific to sewage exist and how such populations could be used to improve source attribution and apportioning in contaminated waters. Herein, we used the influent of three wastewater treatment plants in Atlanta, Georgia (USA) to perturb laboratory freshwater mesocosms, simulating sewage contamination events, and followed these mesocosms with shotgun metagenomics over a 7-day observational period. We describe 15 abundant non-redundant bacterial metagenome-assembled genomes (MAGs) ubiquitous within all sewage inocula yet absent from the unperturbed freshwater control at our analytical limit of detection. Tracking the dynamics of the populations represented by these MAGs revealed varied decay kinetics, depending on (inferred) phenotypes, e.g., anaerobes decayed faster than aerobes under the well-aerated incubation conditions. Notably, a portion of these populations showed decay patterns similar to those of common markers, Enterococcus and HF183. Despite the apparent decay of these populations, the abundance of β-lactamase encoding genes remained high throughout incubation relative to the control. Lastly, we constructed genomic libraries representing several different fecal sources and outline a bioinformatic approach which leverages these libraries for identifying and apportioning contamination signal among multiple probable sources using shotgun metagenomic data. Graphical abstract: Image, graphical abstract