Ecological succession and the competition-colonization trade-off in microbial communities

Abstract Background During range expansion in spatially distributed habitats, organisms differ from one another in terms of their patterns of localization versus propagation. To exploit locations or explore the landscape? This is the competition-colonization trade-off, a dichotomy at the core of eco...

Full description

Bibliographic Details
Main Authors: Miles T. Wetherington, Krisztina Nagy, László Dér, Ágnes Ábrahám, Janneke Noorlag, Peter Galajda, Juan E. Keymer
Format: Article
Language:English
Published: BMC 2022-11-01
Series:BMC Biology
Subjects:
Online Access:https://doi.org/10.1186/s12915-022-01462-5
_version_ 1811310768654647296
author Miles T. Wetherington
Krisztina Nagy
László Dér
Ágnes Ábrahám
Janneke Noorlag
Peter Galajda
Juan E. Keymer
author_facet Miles T. Wetherington
Krisztina Nagy
László Dér
Ágnes Ábrahám
Janneke Noorlag
Peter Galajda
Juan E. Keymer
author_sort Miles T. Wetherington
collection DOAJ
description Abstract Background During range expansion in spatially distributed habitats, organisms differ from one another in terms of their patterns of localization versus propagation. To exploit locations or explore the landscape? This is the competition-colonization trade-off, a dichotomy at the core of ecological succession. In bacterial communities, this trade-off is a fundamental mechanism towards understanding spatio-temporal fluxes in microbiome composition. Results Using microfluidics devices as structured bacterial habitats, we show that, in a synthetic two-species community of motile strains, Escherichia coli is a fugitive species, whereas Pseudomonas aeruginosa is a slower colonizer but superior competitor. We provide evidence highlighting the role of succession and the relevance of this trade-off in the community assembly of bacteria in spatially distributed patchy landscapes. Furthermore, aggregation-dependent priority effects enhance coexistence which is not possible in well-mixed environments. Conclusions Our findings underscore the interplay between micron-scale landscape structure and dispersal in shaping biodiversity patterns in microbial ecosystems. Understanding this interplay is key to unleash the technological revolution of microbiome applications.
first_indexed 2024-04-13T10:06:00Z
format Article
id doaj.art-27be3bcf02274885b840410d35bea152
institution Directory Open Access Journal
issn 1741-7007
language English
last_indexed 2024-04-13T10:06:00Z
publishDate 2022-11-01
publisher BMC
record_format Article
series BMC Biology
spelling doaj.art-27be3bcf02274885b840410d35bea1522022-12-22T02:51:05ZengBMCBMC Biology1741-70072022-11-0120111410.1186/s12915-022-01462-5Ecological succession and the competition-colonization trade-off in microbial communitiesMiles T. Wetherington0Krisztina Nagy1László Dér2Ágnes Ábrahám3Janneke Noorlag4Peter Galajda5Juan E. Keymer6Department of Ecology, School of Biological Sciences, P. Catholic University of ChileBiological Research Centre, Institute of BiophysicsBiological Research Centre, Institute of BiophysicsBiological Research Centre, Institute of BiophysicsDepartment of Ecology, School of Biological Sciences, P. Catholic University of ChileBiological Research Centre, Institute of BiophysicsDepartment of Ecology, School of Biological Sciences, P. Catholic University of ChileAbstract Background During range expansion in spatially distributed habitats, organisms differ from one another in terms of their patterns of localization versus propagation. To exploit locations or explore the landscape? This is the competition-colonization trade-off, a dichotomy at the core of ecological succession. In bacterial communities, this trade-off is a fundamental mechanism towards understanding spatio-temporal fluxes in microbiome composition. Results Using microfluidics devices as structured bacterial habitats, we show that, in a synthetic two-species community of motile strains, Escherichia coli is a fugitive species, whereas Pseudomonas aeruginosa is a slower colonizer but superior competitor. We provide evidence highlighting the role of succession and the relevance of this trade-off in the community assembly of bacteria in spatially distributed patchy landscapes. Furthermore, aggregation-dependent priority effects enhance coexistence which is not possible in well-mixed environments. Conclusions Our findings underscore the interplay between micron-scale landscape structure and dispersal in shaping biodiversity patterns in microbial ecosystems. Understanding this interplay is key to unleash the technological revolution of microbiome applications.https://doi.org/10.1186/s12915-022-01462-5Ecological successionCompetition-colonization trade-offMicrobial landscape ecologyMetacommunitiesMicrofluidics
spellingShingle Miles T. Wetherington
Krisztina Nagy
László Dér
Ágnes Ábrahám
Janneke Noorlag
Peter Galajda
Juan E. Keymer
Ecological succession and the competition-colonization trade-off in microbial communities
BMC Biology
Ecological succession
Competition-colonization trade-off
Microbial landscape ecology
Metacommunities
Microfluidics
title Ecological succession and the competition-colonization trade-off in microbial communities
title_full Ecological succession and the competition-colonization trade-off in microbial communities
title_fullStr Ecological succession and the competition-colonization trade-off in microbial communities
title_full_unstemmed Ecological succession and the competition-colonization trade-off in microbial communities
title_short Ecological succession and the competition-colonization trade-off in microbial communities
title_sort ecological succession and the competition colonization trade off in microbial communities
topic Ecological succession
Competition-colonization trade-off
Microbial landscape ecology
Metacommunities
Microfluidics
url https://doi.org/10.1186/s12915-022-01462-5
work_keys_str_mv AT milestwetherington ecologicalsuccessionandthecompetitioncolonizationtradeoffinmicrobialcommunities
AT krisztinanagy ecologicalsuccessionandthecompetitioncolonizationtradeoffinmicrobialcommunities
AT laszloder ecologicalsuccessionandthecompetitioncolonizationtradeoffinmicrobialcommunities
AT agnesabraham ecologicalsuccessionandthecompetitioncolonizationtradeoffinmicrobialcommunities
AT jannekenoorlag ecologicalsuccessionandthecompetitioncolonizationtradeoffinmicrobialcommunities
AT petergalajda ecologicalsuccessionandthecompetitioncolonizationtradeoffinmicrobialcommunities
AT juanekeymer ecologicalsuccessionandthecompetitioncolonizationtradeoffinmicrobialcommunities