Abstract

Polychlorinated biphenyls (PCBs) are widespread persistent pollutants that cause several adverse health effects. Aerobic bioremediation of PCBs involves the activity of either one bacterial species or a microbial consortium. Using multiple species will enhance the range of PCB congeners co-metabolized since different PCB-degrading microorganisms exhibit different substrate specificity. We have isolated a bacterial consortium by successive enrichment culture using biphenyl (analog of PCBs) as the sole carbon and energy source. This consortium is able to grow on biphenyl, benzoate, and protocatechuate. Whole-community DNA extracted from the consortium was used to analyze biodiversity by Illumina sequencing of a 16S rRNA gene amplicon library and to determine the metagenome by whole-genome shotgun Illumina sequencing. Biodiversity analysis shows that the consortium consists of 24 operational taxonomic units (≥97% identity). The consortium is dominated by strains belonging to the genus Pseudomonas, but also contains betaproteobacteria and Rhodococcus strains. whole-genome shotgun (WGS) analysis resulted in contigs containing 78.3 Mbp of sequenced DNA, representing around 65% of the expected DNA in the consortium. Bioinformatic analysis of this metagenome has identified the genes encoding the enzymes implicated in three pathways for the conversion of biphenyl to benzoate and five pathways from benzoate to tricarboxylic acid (TCA) cycle intermediates, allowing us to model the whole biodegradation network. By genus assignment of coding sequences, we have also been able to determine that the three biphenyl to benzoate pathways are carried out by Rhodococcus strains. In turn, strains belonging to Pseudomonas and Bordetella are the main responsible of three of the benzoate to TCA pathways while the benzoate conversion into TCA cycle intermediates via benzoyl-CoA and the catechol meta-cleavage pathways are carried out by beta proteobacteria belonging to genera such as Achromobacter and Variovorax. We have isolated a Rhodococcus strain WAY2 from the consortium which contains the genes encoding the three biphenyl to benzoate pathways indicating that this strain is responsible for all the biphenyl to benzoate transformations. The presented results show that metagenomic analysis of consortia allows the identification of bacteria active in biodegradation processes and the assignment of specific reactions and pathways to specific bacterial groups.

Highlights

  • Biphenyl has been widely used as a mineralizable polychlorinated biphenyls (PCBs) analog in biodegradation studies (Leigh et al, 2006; Uhlik et al, 2009; Leewis et al, 2016; Vergani et al, 2017a)

  • We show that reducing the community complexity to a lower number of bacterial populations by means of enrichment cultures, the metagenomic analysis allows to identify the populations playing a role in biphenyl and benzoate degradation and to assign specific reactions and pathways to specific populations and elucidating the trophic relationships occurring within the consortium to a higher detail

  • Some genera, such as Bordetella and Achromobacter, have a lower relative coding DNA sequences (CDSs) representation than in the 16S rRNA. This could be explained by an incomplete metagenome, given that around 120 Mpb metagenome size was expected to achieve a full genomic representation of the 24 operational taxonomic units (OTUs) identified in the biphenyl-degrading consortium

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Summary

Introduction

Biphenyl has been widely used as a mineralizable polychlorinated biphenyls (PCBs) analog in biodegradation studies (Leigh et al, 2006; Uhlik et al, 2009; Leewis et al, 2016; Vergani et al, 2017a). The three bph gene clusters identified in the whole metagenome of the biphenyl-degrading consortium were screened by PCR on the genome of the isolated Rhodococcus sp.

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