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Confinement-induced self-organization in growing bacterial colonies

We investigate the emergence of global alignment in colonies of dividing rod-shaped cells under confinement. Using molecular dynamics simulations and continuous modeling, we demonstrate that geometrical anisotropies in the confining environment give rise to an imbalance in the normal stresses, which...

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Detalles Bibliográficos
Autores principales: You, Zhihong, Pearce, Daniel J. G., Giomi, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10670964/
https://www.ncbi.nlm.nih.gov/pubmed/33523940
http://dx.doi.org/10.1126/sciadv.abc8685
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author You, Zhihong
Pearce, Daniel J. G.
Giomi, Luca
author_facet You, Zhihong
Pearce, Daniel J. G.
Giomi, Luca
author_sort You, Zhihong
collection PubMed
description We investigate the emergence of global alignment in colonies of dividing rod-shaped cells under confinement. Using molecular dynamics simulations and continuous modeling, we demonstrate that geometrical anisotropies in the confining environment give rise to an imbalance in the normal stresses, which, in turn, drives a collective rearrangement of the cells. This behavior crucially relies on the colony’s solid-like mechanical response at short time scales and can be recovered within the framework of active hydrodynamics upon modeling bacterial colonies as growing viscoelastic gels characterized by Maxwell-like stress relaxation.
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spelling pubmed-106709642021-01-22 Confinement-induced self-organization in growing bacterial colonies You, Zhihong Pearce, Daniel J. G. Giomi, Luca Sci Adv Research Articles We investigate the emergence of global alignment in colonies of dividing rod-shaped cells under confinement. Using molecular dynamics simulations and continuous modeling, we demonstrate that geometrical anisotropies in the confining environment give rise to an imbalance in the normal stresses, which, in turn, drives a collective rearrangement of the cells. This behavior crucially relies on the colony’s solid-like mechanical response at short time scales and can be recovered within the framework of active hydrodynamics upon modeling bacterial colonies as growing viscoelastic gels characterized by Maxwell-like stress relaxation. American Association for the Advancement of Science 2021-01-22 /pmc/articles/PMC10670964/ /pubmed/33523940 http://dx.doi.org/10.1126/sciadv.abc8685 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
You, Zhihong
Pearce, Daniel J. G.
Giomi, Luca
Confinement-induced self-organization in growing bacterial colonies
title Confinement-induced self-organization in growing bacterial colonies
title_full Confinement-induced self-organization in growing bacterial colonies
title_fullStr Confinement-induced self-organization in growing bacterial colonies
title_full_unstemmed Confinement-induced self-organization in growing bacterial colonies
title_short Confinement-induced self-organization in growing bacterial colonies
title_sort confinement-induced self-organization in growing bacterial colonies
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10670964/
https://www.ncbi.nlm.nih.gov/pubmed/33523940
http://dx.doi.org/10.1126/sciadv.abc8685
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