Spatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration

Coordination of diverse individuals often requires sophisticated communications and high-order computational abilities. Microbial populations can exhibit diverse individualistic behaviors, and yet can engage in collective migratory patterns with a spatially sorted arrangement of phenotypes. However,...

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Autores principales: Yang Bai, Caiyun He, Pan Chu, Junjiajia Long, Xuefei Li, Xiongfei Fu
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Publicado: eLife Sciences Publications Ltd 2021
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Acceso en línea:https://doaj.org/article/c455e94f3b914dbcb0de31da36890ffb
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spelling oai:doaj.org-article:c455e94f3b914dbcb0de31da36890ffb2021-11-08T17:16:00ZSpatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration10.7554/eLife.673162050-084Xe67316https://doaj.org/article/c455e94f3b914dbcb0de31da36890ffb2021-11-01T00:00:00Zhttps://elifesciences.org/articles/67316https://doaj.org/toc/2050-084XCoordination of diverse individuals often requires sophisticated communications and high-order computational abilities. Microbial populations can exhibit diverse individualistic behaviors, and yet can engage in collective migratory patterns with a spatially sorted arrangement of phenotypes. However, it is unclear how such spatially sorted patterns emerge from diverse individuals without complex computational abilities. Here, by investigating the single-cell trajectories during group migration, we discovered that, despite the constant migrating speed of a group, the drift velocities of individual bacteria decrease from the back to the front. With a Langevin-type modeling framework, we showed that this decreasing profile of drift velocities implies the spatial modulation of individual run-and-tumble random motions, and enables the bacterial population to migrate as a pushed wave front. Theoretical analysis and stochastic simulations further predicted that the pushed wave front can help a diverse population to stay in a tight group, while diverse individuals perform the same type of mean reverting processes around centers orderly aligned by their chemotactic abilities. This mechanism about the emergence of orderly collective migration from diverse individuals is experimentally demonstrated by titration of bacterial chemoreceptor abundance. These results reveal a simple computational principle for emergent ordered behaviors from heterogeneous individuals.Yang BaiCaiyun HePan ChuJunjiajia LongXuefei LiXiongfei FueLife Sciences Publications Ltdarticlephenotypic diversitybacterial chemotaxiscollective behaviorpattern formationlangevin modelagent-based simulationMedicineRScienceQBiology (General)QH301-705.5ENeLife, Vol 10 (2021)
institution DOAJ
collection DOAJ
language EN
topic phenotypic diversity
bacterial chemotaxis
collective behavior
pattern formation
langevin model
agent-based simulation
Medicine
R
Science
Q
Biology (General)
QH301-705.5
spellingShingle phenotypic diversity
bacterial chemotaxis
collective behavior
pattern formation
langevin model
agent-based simulation
Medicine
R
Science
Q
Biology (General)
QH301-705.5
Yang Bai
Caiyun He
Pan Chu
Junjiajia Long
Xuefei Li
Xiongfei Fu
Spatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration
description Coordination of diverse individuals often requires sophisticated communications and high-order computational abilities. Microbial populations can exhibit diverse individualistic behaviors, and yet can engage in collective migratory patterns with a spatially sorted arrangement of phenotypes. However, it is unclear how such spatially sorted patterns emerge from diverse individuals without complex computational abilities. Here, by investigating the single-cell trajectories during group migration, we discovered that, despite the constant migrating speed of a group, the drift velocities of individual bacteria decrease from the back to the front. With a Langevin-type modeling framework, we showed that this decreasing profile of drift velocities implies the spatial modulation of individual run-and-tumble random motions, and enables the bacterial population to migrate as a pushed wave front. Theoretical analysis and stochastic simulations further predicted that the pushed wave front can help a diverse population to stay in a tight group, while diverse individuals perform the same type of mean reverting processes around centers orderly aligned by their chemotactic abilities. This mechanism about the emergence of orderly collective migration from diverse individuals is experimentally demonstrated by titration of bacterial chemoreceptor abundance. These results reveal a simple computational principle for emergent ordered behaviors from heterogeneous individuals.
format article
author Yang Bai
Caiyun He
Pan Chu
Junjiajia Long
Xuefei Li
Xiongfei Fu
author_facet Yang Bai
Caiyun He
Pan Chu
Junjiajia Long
Xuefei Li
Xiongfei Fu
author_sort Yang Bai
title Spatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration
title_short Spatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration
title_full Spatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration
title_fullStr Spatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration
title_full_unstemmed Spatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration
title_sort spatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration
publisher eLife Sciences Publications Ltd
publishDate 2021
url https://doaj.org/article/c455e94f3b914dbcb0de31da36890ffb
work_keys_str_mv AT yangbai spatialmodulationofindividualbehaviorsenablesanorderedstructureofdiversephenotypesduringbacterialgroupmigration
AT caiyunhe spatialmodulationofindividualbehaviorsenablesanorderedstructureofdiversephenotypesduringbacterialgroupmigration
AT panchu spatialmodulationofindividualbehaviorsenablesanorderedstructureofdiversephenotypesduringbacterialgroupmigration
AT junjiajialong spatialmodulationofindividualbehaviorsenablesanorderedstructureofdiversephenotypesduringbacterialgroupmigration
AT xuefeili spatialmodulationofindividualbehaviorsenablesanorderedstructureofdiversephenotypesduringbacterialgroupmigration
AT xiongfeifu spatialmodulationofindividualbehaviorsenablesanorderedstructureofdiversephenotypesduringbacterialgroupmigration
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