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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9723579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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