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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...

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Autores principales: Jeckel, Hannah, Nosho, Kazuki, Neuhaus, Konstantin, Hastewell, Alasdair D., Skinner, Dominic J., Saha, Dibya, Netter, Niklas, Paczia, Nicole, Dunkel, Jörn, Drescher, Knut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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.
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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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