Geometry and Mechanics of Microdomains in Growing Bacterial Colonies

Bacterial colonies are abundant on living and nonliving surfaces and are known to mediate a broad range of processes in ecology, medicine, and industry. Although extensively researched, from single cells to demographic scales, a comprehensive biomechanical picture, highlighting the cell-to-colony dy...

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Main Authors: Zhihong You, Daniel J. G. Pearce, Anupam Sengupta, Luca Giomi
Format: Article
Language:English
Published: American Physical Society 2018-09-01
Series:Physical Review X
Online Access:http://doi.org/10.1103/PhysRevX.8.031065
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spelling doaj-4bab96191d5940edbb17fefb60514d1d2020-11-25T00:53:15ZengAmerican Physical SocietyPhysical Review X2160-33082018-09-018303106510.1103/PhysRevX.8.031065Geometry and Mechanics of Microdomains in Growing Bacterial ColoniesZhihong YouDaniel J. G. PearceAnupam SenguptaLuca GiomiBacterial colonies are abundant on living and nonliving surfaces and are known to mediate a broad range of processes in ecology, medicine, and industry. Although extensively researched, from single cells to demographic scales, a comprehensive biomechanical picture, highlighting the cell-to-colony dynamics, is still lacking. Here, using molecular dynamics simulations and continuous modeling, we investigate the geometrical and mechanical properties of a bacterial colony growing on a substrate with a free boundary and demonstrate that such an expanding colony self-organizes into a “mosaic” of microdomains consisting of highly aligned cells. The emergence of microdomains is mediated by two competing forces: the steric forces between neighboring cells, which favor cell alignment, and the extensile stresses due to cell growth that tend to reduce the local orientational order and thereby distort the system. This interplay results in an exponential distribution of the domain areas and sets a characteristic length scale proportional to the square root of the ratio between the system orientational stiffness and the magnitude of the extensile active stress. Our theoretical predictions are finally compared with experiments with freely growing E. coli microcolonies, finding quantitative agreement.http://doi.org/10.1103/PhysRevX.8.031065
collection DOAJ
language English
format Article
sources DOAJ
author Zhihong You
Daniel J. G. Pearce
Anupam Sengupta
Luca Giomi
spellingShingle Zhihong You
Daniel J. G. Pearce
Anupam Sengupta
Luca Giomi
Geometry and Mechanics of Microdomains in Growing Bacterial Colonies
Physical Review X
author_facet Zhihong You
Daniel J. G. Pearce
Anupam Sengupta
Luca Giomi
author_sort Zhihong You
title Geometry and Mechanics of Microdomains in Growing Bacterial Colonies
title_short Geometry and Mechanics of Microdomains in Growing Bacterial Colonies
title_full Geometry and Mechanics of Microdomains in Growing Bacterial Colonies
title_fullStr Geometry and Mechanics of Microdomains in Growing Bacterial Colonies
title_full_unstemmed Geometry and Mechanics of Microdomains in Growing Bacterial Colonies
title_sort geometry and mechanics of microdomains in growing bacterial colonies
publisher American Physical Society
series Physical Review X
issn 2160-3308
publishDate 2018-09-01
description Bacterial colonies are abundant on living and nonliving surfaces and are known to mediate a broad range of processes in ecology, medicine, and industry. Although extensively researched, from single cells to demographic scales, a comprehensive biomechanical picture, highlighting the cell-to-colony dynamics, is still lacking. Here, using molecular dynamics simulations and continuous modeling, we investigate the geometrical and mechanical properties of a bacterial colony growing on a substrate with a free boundary and demonstrate that such an expanding colony self-organizes into a “mosaic” of microdomains consisting of highly aligned cells. The emergence of microdomains is mediated by two competing forces: the steric forces between neighboring cells, which favor cell alignment, and the extensile stresses due to cell growth that tend to reduce the local orientational order and thereby distort the system. This interplay results in an exponential distribution of the domain areas and sets a characteristic length scale proportional to the square root of the ratio between the system orientational stiffness and the magnitude of the extensile active stress. Our theoretical predictions are finally compared with experiments with freely growing E. coli microcolonies, finding quantitative agreement.
url http://doi.org/10.1103/PhysRevX.8.031065
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