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Adaptive evolution of Geobacter sulfurreducens in coculture with Pseudomonas aeruginosa

journal contribution
posted on 2024-12-19, 04:28 authored by Lucie Semenec, Ismael A Vergara, Andrew E Laloo, Steve PetrovskiSteve Petrovski, Philip L Bond, Ashley FranksAshley Franks

Interactions between microorganisms in mixed communities are highly complex, being either syntrophic, neutral, predatory, or competitive. Evolutionary changes can occur in the interaction dynamics between community members as they adapt to coexistence. Here, we report that the syntrophic interaction between Geobacter sulfurreducens and Pseudomonas aeruginosa coculture change in their dynamics over evolutionary time. Specifically, Geobacter sp. dominance increases with adaptation within the cocultures, as determined through quantitative PCR and fluorescence in situ hybridization. This suggests a transition from syntrophy to competition and demonstrates the rapid adaptive capacity of Geobacter spp. to dominate in cocultures with P. aeruginosa. Early in coculture establishment, two single-nucleotide variants in the G. sulfurreducens fabI and tetR genes emerged that were strongly selected for throughout coculture evolution with P. aeruginosa phenazine wild-type and phenazine-deficient mutants. Sequential window acquisition of all theoretical spectra-mass spectrometry (SWATH-MS) proteomics revealed that the tetR variant cooccurred with the upregulation of an adenylate cyclase transporter, CyaE, and a resistance-nodulationdivision (RND) efflux pump notably known for antibiotic efflux. To determine whether antibiotic production was driving the increased expression of the multidrug efflux pump, we tested Pseudomonas-derived phenazine-1-carboxylic acid (PHZ-1-CA) for its potential to inhibit Geobacter growth and drive selection of the tetR and fabI genetic variants. Despite its inhibitory properties, PHZ-1-CA did not drive variant selection, indicating that other antibiotics may drive overexpression of the efflux pump and CyaE or that a novel role exists for these proteins in the context of this interaction.

Funding

This research has been partially financially supported by the Human Protection and Performance Program of the Defense Science Institute. The Applied and Environmental Microbiology Laboratory receives support from the Defense Science and Technology Group (DSTG), Office of Naval Research Global (award N626909-13-1-N259), Asian Office of Aerospace Research and Development (AOARD; award FA2386-14-1-4032), and the Australian Research Council (ARC; award LP140100459).

History

Publication Date

2020-04-28

Journal

mBio

Volume

11

Issue

2

Article Number

e02875-19

Pagination

13p.

Publisher

American Society for Microbiology

ISSN

2150-7511

Rights Statement

© 2020 Semenec et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

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