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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eLife Sciences Publications Ltd
2021
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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) |
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phenotypic diversity bacterial chemotaxis collective behavior pattern formation langevin model agent-based simulation Medicine R Science Q Biology (General) QH301-705.5 |
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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 |
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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 |
_version_ |
1718441514850320384 |