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Spatial scales of competition and a growth–motility trade-off interact to determine bacterial coexistence

The coexistence of competing species is a long-lasting puzzle in evolutionary ecology research. Despite abundant experimental evidence showing that the opportunity for coexistence decreases as niche overlap increases between species, bacterial species and strains competing for the same resources are...

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Autores principales: Kuhn, Thierry, Mamin, Marine, Bindschedler, Saskia, Bshary, Redouan, Estoppey, Aislinn, Gonzalez, Diego, Palmieri, Fabio, Junier, Pilar, Richter, Xiang-Yi Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727664/
https://www.ncbi.nlm.nih.gov/pubmed/36483758
http://dx.doi.org/10.1098/rsos.211592
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author Kuhn, Thierry
Mamin, Marine
Bindschedler, Saskia
Bshary, Redouan
Estoppey, Aislinn
Gonzalez, Diego
Palmieri, Fabio
Junier, Pilar
Richter, Xiang-Yi Li
author_facet Kuhn, Thierry
Mamin, Marine
Bindschedler, Saskia
Bshary, Redouan
Estoppey, Aislinn
Gonzalez, Diego
Palmieri, Fabio
Junier, Pilar
Richter, Xiang-Yi Li
author_sort Kuhn, Thierry
collection PubMed
description The coexistence of competing species is a long-lasting puzzle in evolutionary ecology research. Despite abundant experimental evidence showing that the opportunity for coexistence decreases as niche overlap increases between species, bacterial species and strains competing for the same resources are commonly found across diverse spatially heterogeneous habitats. We thus hypothesized that the spatial scale of competition may play a key role in determining bacterial coexistence, and interact with other mechanisms that promote coexistence, including a growth–motility trade-off. To test this hypothesis, we let two Pseudomonas putida strains compete at local and regional scales by inoculating them either in a mixed droplet or in separate droplets in the same Petri dish, respectively. We also created conditions that allow the bacterial strains to disperse across abiotic or fungal hyphae networks. We found that competition at the local scale led to competitive exclusion while regional competition promoted coexistence. When competing in the presence of dispersal networks, the growth–motility trade-off promoted coexistence only when the strains were inoculated in separate droplets. Our results provide a mechanism by which existing laboratory data suggesting competitive exclusion at a local scale is reconciled with the widespread coexistence of competing bacterial strains in complex natural environments with dispersal.
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spelling pubmed-97276642022-12-07 Spatial scales of competition and a growth–motility trade-off interact to determine bacterial coexistence Kuhn, Thierry Mamin, Marine Bindschedler, Saskia Bshary, Redouan Estoppey, Aislinn Gonzalez, Diego Palmieri, Fabio Junier, Pilar Richter, Xiang-Yi Li R Soc Open Sci Ecology, Conservation and Global Change Biology The coexistence of competing species is a long-lasting puzzle in evolutionary ecology research. Despite abundant experimental evidence showing that the opportunity for coexistence decreases as niche overlap increases between species, bacterial species and strains competing for the same resources are commonly found across diverse spatially heterogeneous habitats. We thus hypothesized that the spatial scale of competition may play a key role in determining bacterial coexistence, and interact with other mechanisms that promote coexistence, including a growth–motility trade-off. To test this hypothesis, we let two Pseudomonas putida strains compete at local and regional scales by inoculating them either in a mixed droplet or in separate droplets in the same Petri dish, respectively. We also created conditions that allow the bacterial strains to disperse across abiotic or fungal hyphae networks. We found that competition at the local scale led to competitive exclusion while regional competition promoted coexistence. When competing in the presence of dispersal networks, the growth–motility trade-off promoted coexistence only when the strains were inoculated in separate droplets. Our results provide a mechanism by which existing laboratory data suggesting competitive exclusion at a local scale is reconciled with the widespread coexistence of competing bacterial strains in complex natural environments with dispersal. The Royal Society 2022-12-07 /pmc/articles/PMC9727664/ /pubmed/36483758 http://dx.doi.org/10.1098/rsos.211592 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Ecology, Conservation and Global Change Biology
Kuhn, Thierry
Mamin, Marine
Bindschedler, Saskia
Bshary, Redouan
Estoppey, Aislinn
Gonzalez, Diego
Palmieri, Fabio
Junier, Pilar
Richter, Xiang-Yi Li
Spatial scales of competition and a growth–motility trade-off interact to determine bacterial coexistence
title Spatial scales of competition and a growth–motility trade-off interact to determine bacterial coexistence
title_full Spatial scales of competition and a growth–motility trade-off interact to determine bacterial coexistence
title_fullStr Spatial scales of competition and a growth–motility trade-off interact to determine bacterial coexistence
title_full_unstemmed Spatial scales of competition and a growth–motility trade-off interact to determine bacterial coexistence
title_short Spatial scales of competition and a growth–motility trade-off interact to determine bacterial coexistence
title_sort spatial scales of competition and a growth–motility trade-off interact to determine bacterial coexistence
topic Ecology, Conservation and Global Change Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727664/
https://www.ncbi.nlm.nih.gov/pubmed/36483758
http://dx.doi.org/10.1098/rsos.211592
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