Parallel mutations result in a wide range of cooperation and community consequences in a two-species bacterial consortium

Sarah M. Douglas, Lon M. Chubiz, William R. Harcombe, F. Marty Ytreberg, Christopher J. Marx

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Multi-species microbial communities play a critical role in human health, industry, and waste remediation. Recently, the evolution of synthetic consortia in the laboratory has enabled adaptation to be addressed in the context of interacting species. Using an engineered bacterial consortium, we repeatedly evolved cooperative genotypes and examined both the predictability of evolution and the phenotypes that determine community dynamics. Eight Salmonella enterica serovar Typhimurium strains evolved methionine excretion sufficient to support growth of an Escherichia coli methionine auxotroph, from whom they required excreted growth substrates. Non-synonymous mutations in metA, encoding homoserine trans-succinylase (HTS), were detected in each evolved S. enterica methionine cooperator and were shown to be necessary for cooperative consortia growth. Molecular modeling was used to predict that most of the non-synonymous mutations slightly increase the binding affinity for HTS homodimer formation. Despite this genetic parallelism and trend of increasing protein binding stability, these metA alleles gave rise to a wide range of phenotypic diversity in terms of individual versus group benefit. The cooperators with the highest methionine excretion permitted nearly two-fold faster consortia growth and supported the highest fraction of E. coli, yet also had the slowest individual growth rates compared to less cooperative strains. Thus, although the genetic basis of adaptation was quite similar across independent origins of cooperative phenotypes, quantitative measurements of metabolite production were required to predict either the individual-level growth consequences or how these propagate to community-level behavior.

Original languageEnglish (US)
Article numbere0161837
JournalPloS one
Volume11
Issue number9
DOIs
StatePublished - Sep 2016

Bibliographical note

Funding Information:
This work was funded with an NIH (www. nih.gov) NRSA Award to WRH and a DOE (www. energy.gov) award to CJM (DE-SC0006731). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We wouldliketothankLionelloBossiforpSUB11andthemembersoftheMarxlab, Stephen Lory, Andrew Murray, Karine Gibbs, and two anonymous reviewers for their manuscript suggestions and feedback.

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