Microbial cross-feeding stabilized by segregation of a dependent mutant from its independent ancestor
Microbial gene loss is hypothesized to be beneficial when gene function is costly, and the gene product can be replaced via cross-feeding from a neighbor. However, cross-fed metabolites are often only available at low concentrations, limiting the growth rates of gene-loss mutants that are dependent on those metabolites. Here we define conditions that support a loss of function mutant in a three-member bacterial community of (i) N2-utilizing Rhodopseudomonas palustris as an NH4+-excreting producer, (ii) N2-utilizing Vibrio natriegens as the ancestor, and (iii) a V. natriegens N2-utilizaton mutant that is dependent on the producer for NH4+. Using experimental and simulated cocultures, we found that the ancestor outcompeted the mutant due to low NH4+ availability under uniform conditions where both V. natriegens strains had equal access to nutrients. However, spatial structuring that increasingly segregated the mutant from the ancestor, while maintaining access to NH4+ from the producer, allowed the mutant to avoid extinction. Counter to predictions, mutant enrichment under spatially structured conditions did not require a growth rate advantage from gene loss and the mutant coexisted with its ancestor. Thus, cross-feeding can originate from loss-of-function mutations that are otherwise detrimental, provided that the mutant can segregate from a competitive ancestor.
Authors
- Sima Setayeshgar (ORCID: https://orcid.org/0000-0002-7273-0809)
- James B. McKinlay (ORCID: https://orcid.org/0000-0003-2401-6229)
- Anthony J. Zmuda
- Ryan K. Fritts (ORCID: https://orcid.org/0000-0002-5528-4982)
- Olivia F Schakel (ORCID: https://orcid.org/0009-0009-9585-1556)
Institutions
- University of Minnesota (US)
- Cooperative Institute for Research in Environmental Sciences (US)
- Twin Cities Public Television (US)
- Indiana University Bloomington (US)
Publication Details
- Journal
- The ISME Journal
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1093/ismejo/wraf131
- Citations
- 1
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- National Science Foundation
- Eli Lilly and Company
- Lilly Endowment
- Division of Biological Infrastructure
- Army Research Office