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Simultaneous spatiotemporal transcriptomics and microscopy of Bacillus subtilis swarm development reveal cooperation across generations
Development of microbial communities is a complex multiscale phenomenon with wide-ranging biomedical and ecological implications. How biological and physical processes determine emergent spatial structures in microbial communities remains poorly understood due to a lack of simultaneous measurements...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686836/ https://www.ncbi.nlm.nih.gov/pubmed/37973866 http://dx.doi.org/10.1038/s41564-023-01518-4 |
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author | Jeckel, Hannah Nosho, Kazuki Neuhaus, Konstantin Hastewell, Alasdair D. Skinner, Dominic J. Saha, Dibya Netter, Niklas Paczia, Nicole Dunkel, Jörn Drescher, Knut |
author_facet | Jeckel, Hannah Nosho, Kazuki Neuhaus, Konstantin Hastewell, Alasdair D. Skinner, Dominic J. Saha, Dibya Netter, Niklas Paczia, Nicole Dunkel, Jörn Drescher, Knut |
author_sort | Jeckel, Hannah |
collection | PubMed |
description | Development of microbial communities is a complex multiscale phenomenon with wide-ranging biomedical and ecological implications. How biological and physical processes determine emergent spatial structures in microbial communities remains poorly understood due to a lack of simultaneous measurements of gene expression and cellular behaviour in space and time. Here we combined live-cell microscopy with a robotic arm for spatiotemporal sampling, which enabled us to simultaneously acquire phenotypic imaging data and spatiotemporal transcriptomes during Bacillus subtilis swarm development. Quantitative characterization of the spatiotemporal gene expression patterns revealed correlations with cellular and collective properties, and phenotypic subpopulations. By integrating these data with spatiotemporal metabolome measurements, we discovered a spatiotemporal cross-feeding mechanism fuelling swarm development: during their migration, earlier generations deposit metabolites which are consumed by later generations that swarm across the same location. These results highlight the importance of spatiotemporal effects during the emergence of phenotypic subpopulations and their interactions in bacterial communities. |
format | Online Article Text |
id | pubmed-10686836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106868362023-12-01 Simultaneous spatiotemporal transcriptomics and microscopy of Bacillus subtilis swarm development reveal cooperation across generations Jeckel, Hannah Nosho, Kazuki Neuhaus, Konstantin Hastewell, Alasdair D. Skinner, Dominic J. Saha, Dibya Netter, Niklas Paczia, Nicole Dunkel, Jörn Drescher, Knut Nat Microbiol Article Development of microbial communities is a complex multiscale phenomenon with wide-ranging biomedical and ecological implications. How biological and physical processes determine emergent spatial structures in microbial communities remains poorly understood due to a lack of simultaneous measurements of gene expression and cellular behaviour in space and time. Here we combined live-cell microscopy with a robotic arm for spatiotemporal sampling, which enabled us to simultaneously acquire phenotypic imaging data and spatiotemporal transcriptomes during Bacillus subtilis swarm development. Quantitative characterization of the spatiotemporal gene expression patterns revealed correlations with cellular and collective properties, and phenotypic subpopulations. By integrating these data with spatiotemporal metabolome measurements, we discovered a spatiotemporal cross-feeding mechanism fuelling swarm development: during their migration, earlier generations deposit metabolites which are consumed by later generations that swarm across the same location. These results highlight the importance of spatiotemporal effects during the emergence of phenotypic subpopulations and their interactions in bacterial communities. Nature Publishing Group UK 2023-11-16 2023 /pmc/articles/PMC10686836/ /pubmed/37973866 http://dx.doi.org/10.1038/s41564-023-01518-4 Text en © The Author(s) 2023 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 Jeckel, Hannah Nosho, Kazuki Neuhaus, Konstantin Hastewell, Alasdair D. Skinner, Dominic J. Saha, Dibya Netter, Niklas Paczia, Nicole Dunkel, Jörn Drescher, Knut Simultaneous spatiotemporal transcriptomics and microscopy of Bacillus subtilis swarm development reveal cooperation across generations |
title | Simultaneous spatiotemporal transcriptomics and microscopy of Bacillus subtilis swarm development reveal cooperation across generations |
title_full | Simultaneous spatiotemporal transcriptomics and microscopy of Bacillus subtilis swarm development reveal cooperation across generations |
title_fullStr | Simultaneous spatiotemporal transcriptomics and microscopy of Bacillus subtilis swarm development reveal cooperation across generations |
title_full_unstemmed | Simultaneous spatiotemporal transcriptomics and microscopy of Bacillus subtilis swarm development reveal cooperation across generations |
title_short | Simultaneous spatiotemporal transcriptomics and microscopy of Bacillus subtilis swarm development reveal cooperation across generations |
title_sort | simultaneous spatiotemporal transcriptomics and microscopy of bacillus subtilis swarm development reveal cooperation across generations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686836/ https://www.ncbi.nlm.nih.gov/pubmed/37973866 http://dx.doi.org/10.1038/s41564-023-01518-4 |
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