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Systems view of Bacillus subtilis pellicle development

In this study, we link pellicle development at the water–air interface with the vertical distribution and viability of the individual B. subtilis PS-216 cells throughout the water column. Real-time interfacial rheology and time-lapse confocal laser scanning microscopy were combined to correlate mech...

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Autores principales: Krajnc, Mojca, Stefanic, Polonca, Kostanjšek, Rok, Mandic-Mulec, Ines, Dogsa, Iztok, Stopar, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9005697/
https://www.ncbi.nlm.nih.gov/pubmed/35414070
http://dx.doi.org/10.1038/s41522-022-00293-0
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author Krajnc, Mojca
Stefanic, Polonca
Kostanjšek, Rok
Mandic-Mulec, Ines
Dogsa, Iztok
Stopar, David
author_facet Krajnc, Mojca
Stefanic, Polonca
Kostanjšek, Rok
Mandic-Mulec, Ines
Dogsa, Iztok
Stopar, David
author_sort Krajnc, Mojca
collection PubMed
description In this study, we link pellicle development at the water–air interface with the vertical distribution and viability of the individual B. subtilis PS-216 cells throughout the water column. Real-time interfacial rheology and time-lapse confocal laser scanning microscopy were combined to correlate mechanical properties with morphological changes (aggregation status, filament formation, pellicle thickness, spore formation) of the growing pellicle. Six key events were identified in B. subtilis pellicle formation that are accompanied by a major change in viscoelastic and morphology behaviour of the pellicle. The results imply that pellicle development is a multifaceted response to a changing environment induced by bacterial growth that causes population redistribution within the model system, reduction of the viable habitat to the water–air interface, cell development, and morphogenesis. The outcome is a build-up of mechanical stress supporting structure that eventually, due to nutrient deprivation, reaches the finite thickness. After prolonged incubation, the formed pellicle collapses, which correlates with the spore releasing process. The pellicle loses the ability to support mechanical stress, which marks the end of the pellicle life cycle and entry of the system into the dormant state.
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spelling pubmed-90056972022-04-27 Systems view of Bacillus subtilis pellicle development Krajnc, Mojca Stefanic, Polonca Kostanjšek, Rok Mandic-Mulec, Ines Dogsa, Iztok Stopar, David NPJ Biofilms Microbiomes Article In this study, we link pellicle development at the water–air interface with the vertical distribution and viability of the individual B. subtilis PS-216 cells throughout the water column. Real-time interfacial rheology and time-lapse confocal laser scanning microscopy were combined to correlate mechanical properties with morphological changes (aggregation status, filament formation, pellicle thickness, spore formation) of the growing pellicle. Six key events were identified in B. subtilis pellicle formation that are accompanied by a major change in viscoelastic and morphology behaviour of the pellicle. The results imply that pellicle development is a multifaceted response to a changing environment induced by bacterial growth that causes population redistribution within the model system, reduction of the viable habitat to the water–air interface, cell development, and morphogenesis. The outcome is a build-up of mechanical stress supporting structure that eventually, due to nutrient deprivation, reaches the finite thickness. After prolonged incubation, the formed pellicle collapses, which correlates with the spore releasing process. The pellicle loses the ability to support mechanical stress, which marks the end of the pellicle life cycle and entry of the system into the dormant state. Nature Publishing Group UK 2022-04-12 /pmc/articles/PMC9005697/ /pubmed/35414070 http://dx.doi.org/10.1038/s41522-022-00293-0 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
Krajnc, Mojca
Stefanic, Polonca
Kostanjšek, Rok
Mandic-Mulec, Ines
Dogsa, Iztok
Stopar, David
Systems view of Bacillus subtilis pellicle development
title Systems view of Bacillus subtilis pellicle development
title_full Systems view of Bacillus subtilis pellicle development
title_fullStr Systems view of Bacillus subtilis pellicle development
title_full_unstemmed Systems view of Bacillus subtilis pellicle development
title_short Systems view of Bacillus subtilis pellicle development
title_sort systems view of bacillus subtilis pellicle development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9005697/
https://www.ncbi.nlm.nih.gov/pubmed/35414070
http://dx.doi.org/10.1038/s41522-022-00293-0
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