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Spatial self-segregation of pioneer cyanobacterial species drives microbiome organization in biocrusts

Microbial communities are typically characterized by some degree of self-organization. In biological soil crust (biocrust) communities, vertical organization of resident populations at the mm scale is driven by organismal adaptations to physicochemical microniches. However, the extent of horizontal...

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Autores principales: Nelson, Corey, Giraldo-Silva, Ana, Warsop Thomas, Finlay, Garcia-Pichel, Ferran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723579/
https://www.ncbi.nlm.nih.gov/pubmed/37938289
http://dx.doi.org/10.1038/s43705-022-00199-0
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author Nelson, Corey
Giraldo-Silva, Ana
Warsop Thomas, Finlay
Garcia-Pichel, Ferran
author_facet Nelson, Corey
Giraldo-Silva, Ana
Warsop Thomas, Finlay
Garcia-Pichel, Ferran
author_sort Nelson, Corey
collection PubMed
description Microbial communities are typically characterized by some degree of self-organization. In biological soil crust (biocrust) communities, vertical organization of resident populations at the mm scale is driven by organismal adaptations to physicochemical microniches. However, the extent of horizontal organization and its driving processes are unknown. Using a combination of observational and genetic mapping, we provide evidence for a highly defined, horizontal self-organization (patchiness) at the mm to cm scale in a successionally early biocrust community dominated by the pioneer cyanobacteria, Microcoleus vaginatus (Microcoleaceae) and Parifilum sp. (Coleofasciculaceae). Experiments with representative isolates of each species demonstrate that the phenomenon is driven by active spatial segregation based on cross-species sensing through the exometabolome acted upon with motility responses. Further, we show that both species share the ability to enrich for specialized cyanospheres of heterotrophic bacteria at smaller scales, and that these cyanospheres are characterized by compositional host-specificity, thus expanding the reach of spatial patchiness beyond primary producers. Our results highlight the importance of specific microbial interactions in the emergence of microbiome compositional architecture and the enhancement of microbial diversity.
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spelling pubmed-97235792023-01-04 Spatial self-segregation of pioneer cyanobacterial species drives microbiome organization in biocrusts Nelson, Corey Giraldo-Silva, Ana Warsop Thomas, Finlay Garcia-Pichel, Ferran ISME Commun Article Microbial communities are typically characterized by some degree of self-organization. In biological soil crust (biocrust) communities, vertical organization of resident populations at the mm scale is driven by organismal adaptations to physicochemical microniches. However, the extent of horizontal organization and its driving processes are unknown. Using a combination of observational and genetic mapping, we provide evidence for a highly defined, horizontal self-organization (patchiness) at the mm to cm scale in a successionally early biocrust community dominated by the pioneer cyanobacteria, Microcoleus vaginatus (Microcoleaceae) and Parifilum sp. (Coleofasciculaceae). Experiments with representative isolates of each species demonstrate that the phenomenon is driven by active spatial segregation based on cross-species sensing through the exometabolome acted upon with motility responses. Further, we show that both species share the ability to enrich for specialized cyanospheres of heterotrophic bacteria at smaller scales, and that these cyanospheres are characterized by compositional host-specificity, thus expanding the reach of spatial patchiness beyond primary producers. Our results highlight the importance of specific microbial interactions in the emergence of microbiome compositional architecture and the enhancement of microbial diversity. Nature Publishing Group UK 2022-11-16 /pmc/articles/PMC9723579/ /pubmed/37938289 http://dx.doi.org/10.1038/s43705-022-00199-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Nelson, Corey
Giraldo-Silva, Ana
Warsop Thomas, Finlay
Garcia-Pichel, Ferran
Spatial self-segregation of pioneer cyanobacterial species drives microbiome organization in biocrusts
title Spatial self-segregation of pioneer cyanobacterial species drives microbiome organization in biocrusts
title_full Spatial self-segregation of pioneer cyanobacterial species drives microbiome organization in biocrusts
title_fullStr Spatial self-segregation of pioneer cyanobacterial species drives microbiome organization in biocrusts
title_full_unstemmed Spatial self-segregation of pioneer cyanobacterial species drives microbiome organization in biocrusts
title_short Spatial self-segregation of pioneer cyanobacterial species drives microbiome organization in biocrusts
title_sort spatial self-segregation of pioneer cyanobacterial species drives microbiome organization in biocrusts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723579/
https://www.ncbi.nlm.nih.gov/pubmed/37938289
http://dx.doi.org/10.1038/s43705-022-00199-0
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