Cooperative microbial interactions drive spatial segregation in porous environments

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Cooperative microbial interactions drive spatial segregation in porous environments. / Wu, Yichao; Fu, Chengxia; Peacock, Caroline L.; Sørensen, Søren J.; Redmile-Gordon, Marc A.; Xiao, Ke Qing; Gao, Chunhui; Liu, Jun; Huang, Qiaoyun; Li, Zixue; Song, Peiyi; Zhu, Yongguan; Zhou, Jizhong; Cai, Peng.

In: Nature Communications, Vol. 14, No. 1, 4226, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Wu, Y, Fu, C, Peacock, CL, Sørensen, SJ, Redmile-Gordon, MA, Xiao, KQ, Gao, C, Liu, J, Huang, Q, Li, Z, Song, P, Zhu, Y, Zhou, J & Cai, P 2023, 'Cooperative microbial interactions drive spatial segregation in porous environments', Nature Communications, vol. 14, no. 1, 4226. https://doi.org/10.1038/s41467-023-39991-4

APA

Wu, Y., Fu, C., Peacock, C. L., Sørensen, S. J., Redmile-Gordon, M. A., Xiao, K. Q., Gao, C., Liu, J., Huang, Q., Li, Z., Song, P., Zhu, Y., Zhou, J., & Cai, P. (2023). Cooperative microbial interactions drive spatial segregation in porous environments. Nature Communications, 14(1), [4226]. https://doi.org/10.1038/s41467-023-39991-4

Vancouver

Wu Y, Fu C, Peacock CL, Sørensen SJ, Redmile-Gordon MA, Xiao KQ et al. Cooperative microbial interactions drive spatial segregation in porous environments. Nature Communications. 2023;14(1). 4226. https://doi.org/10.1038/s41467-023-39991-4

Author

Wu, Yichao ; Fu, Chengxia ; Peacock, Caroline L. ; Sørensen, Søren J. ; Redmile-Gordon, Marc A. ; Xiao, Ke Qing ; Gao, Chunhui ; Liu, Jun ; Huang, Qiaoyun ; Li, Zixue ; Song, Peiyi ; Zhu, Yongguan ; Zhou, Jizhong ; Cai, Peng. / Cooperative microbial interactions drive spatial segregation in porous environments. In: Nature Communications. 2023 ; Vol. 14, No. 1.

Bibtex

@article{a43019b438174c7ab200bb540d434cf0,
title = "Cooperative microbial interactions drive spatial segregation in porous environments",
abstract = "The role of microbial interactions and the underlying mechanisms that shape complex biofilm communities are poorly understood. Here we employ a microfluidic chip to represent porous subsurface environments and show that cooperative microbial interactions between free-living and biofilm-forming bacteria trigger active spatial segregation to promote their respective dominance in segregated microhabitats. During initial colonization, free-living and biofilm-forming microbes are segregated from the mixed planktonic inoculum to occupy the ambient fluid and grain surface. Contrary to spatial exclusion through competition, the active spatial segregation is induced by cooperative interactions which improves the fitness of both biofilm and planktonic populations. We further show that free-living Arthrobacter induces the surface colonization by scavenging the biofilm inhibitor, D-amino acids and receives benefits from the public goods secreted by the biofilm-forming strains. Collectively, our results reveal how cooperative microbial interactions may contribute to microbial coexistence in segregated microhabitats and drive subsurface biofilm community succession.",
author = "Yichao Wu and Chengxia Fu and Peacock, {Caroline L.} and S{\o}rensen, {S{\o}ren J.} and Redmile-Gordon, {Marc A.} and Xiao, {Ke Qing} and Chunhui Gao and Jun Liu and Qiaoyun Huang and Zixue Li and Peiyi Song and Yongguan Zhu and Jizhong Zhou and Peng Cai",
note = "Publisher Copyright: {\textcopyright} 2023. The Author(s).",
year = "2023",
doi = "10.1038/s41467-023-39991-4",
language = "English",
volume = "14",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "nature publishing group",
number = "1",

}

RIS

TY - JOUR

T1 - Cooperative microbial interactions drive spatial segregation in porous environments

AU - Wu, Yichao

AU - Fu, Chengxia

AU - Peacock, Caroline L.

AU - Sørensen, Søren J.

AU - Redmile-Gordon, Marc A.

AU - Xiao, Ke Qing

AU - Gao, Chunhui

AU - Liu, Jun

AU - Huang, Qiaoyun

AU - Li, Zixue

AU - Song, Peiyi

AU - Zhu, Yongguan

AU - Zhou, Jizhong

AU - Cai, Peng

N1 - Publisher Copyright: © 2023. The Author(s).

PY - 2023

Y1 - 2023

N2 - The role of microbial interactions and the underlying mechanisms that shape complex biofilm communities are poorly understood. Here we employ a microfluidic chip to represent porous subsurface environments and show that cooperative microbial interactions between free-living and biofilm-forming bacteria trigger active spatial segregation to promote their respective dominance in segregated microhabitats. During initial colonization, free-living and biofilm-forming microbes are segregated from the mixed planktonic inoculum to occupy the ambient fluid and grain surface. Contrary to spatial exclusion through competition, the active spatial segregation is induced by cooperative interactions which improves the fitness of both biofilm and planktonic populations. We further show that free-living Arthrobacter induces the surface colonization by scavenging the biofilm inhibitor, D-amino acids and receives benefits from the public goods secreted by the biofilm-forming strains. Collectively, our results reveal how cooperative microbial interactions may contribute to microbial coexistence in segregated microhabitats and drive subsurface biofilm community succession.

AB - The role of microbial interactions and the underlying mechanisms that shape complex biofilm communities are poorly understood. Here we employ a microfluidic chip to represent porous subsurface environments and show that cooperative microbial interactions between free-living and biofilm-forming bacteria trigger active spatial segregation to promote their respective dominance in segregated microhabitats. During initial colonization, free-living and biofilm-forming microbes are segregated from the mixed planktonic inoculum to occupy the ambient fluid and grain surface. Contrary to spatial exclusion through competition, the active spatial segregation is induced by cooperative interactions which improves the fitness of both biofilm and planktonic populations. We further show that free-living Arthrobacter induces the surface colonization by scavenging the biofilm inhibitor, D-amino acids and receives benefits from the public goods secreted by the biofilm-forming strains. Collectively, our results reveal how cooperative microbial interactions may contribute to microbial coexistence in segregated microhabitats and drive subsurface biofilm community succession.

U2 - 10.1038/s41467-023-39991-4

DO - 10.1038/s41467-023-39991-4

M3 - Journal article

C2 - 37454222

AN - SCOPUS:85164754809

VL - 14

JO - Nature Communications

JF - Nature Communications

SN - 2041-1723

IS - 1

M1 - 4226

ER -

ID: 360248712