Deciphering links between bacterial interactions and spatial organization in multispecies biofilms

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Standard

Deciphering links between bacterial interactions and spatial organization in multispecies biofilms. / Liu, Wenzheng; Jacquiod, Samuel; Brejnrod, Asker; Russel, Jakob; Burmølle, Mette; Sørensen, Søren J.

I: ISME Journal, Bind 13, Nr. 12, 2019, s. 3054-3066.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Liu, W, Jacquiod, S, Brejnrod, A, Russel, J, Burmølle, M & Sørensen, SJ 2019, 'Deciphering links between bacterial interactions and spatial organization in multispecies biofilms', ISME Journal, bind 13, nr. 12, s. 3054-3066. https://doi.org/10.1038/s41396-019-0494-9

APA

Liu, W., Jacquiod, S., Brejnrod, A., Russel, J., Burmølle, M., & Sørensen, S. J. (2019). Deciphering links between bacterial interactions and spatial organization in multispecies biofilms. ISME Journal, 13(12), 3054-3066. https://doi.org/10.1038/s41396-019-0494-9

Vancouver

Liu W, Jacquiod S, Brejnrod A, Russel J, Burmølle M, Sørensen SJ. Deciphering links between bacterial interactions and spatial organization in multispecies biofilms. ISME Journal. 2019;13(12):3054-3066. https://doi.org/10.1038/s41396-019-0494-9

Author

Liu, Wenzheng ; Jacquiod, Samuel ; Brejnrod, Asker ; Russel, Jakob ; Burmølle, Mette ; Sørensen, Søren J. / Deciphering links between bacterial interactions and spatial organization in multispecies biofilms. I: ISME Journal. 2019 ; Bind 13, Nr. 12. s. 3054-3066.

Bibtex

@article{a3cc056060204b938085e5798fd59642,
title = "Deciphering links between bacterial interactions and spatial organization in multispecies biofilms",
abstract = "Environmental microbes frequently live in multispecies biofilms where mutualistic relationships and co-evolution may occur, defining spatial organization for member species and overall community functions. In this context, intrinsic properties emerging from microbial interactions, such as efficient organization optimizing growth and activities in multispecies biofilms, may become the object of fitness selection. However, little is known on the nature of underlying interspecies interactions during establishment of a predictable spatial organization within multispecies biofilms. We present a comparative metatranscriptomic analysis of bacterial strains residing in triple-species and four-species biofilms, aiming at deciphering molecular mechanisms underpinning bacterial interactions responsible of the remarkably enhanced biomass production and associated typical spatial organization they display. Metatranscriptomic profiles concurred with changes in micro-site occupation in response to the addition/removal of a single species, being driven by both cooperation, competition, and facilitation processes. We conclude that the enhanced biomass production of the four-species biofilm is an intrinsic community property emerging from finely tuned space optimization achieved through concerted antagonistic and mutualistic interactions, where each species occupies a defined micro-site favoring its own growth. Our results further illustrate how molecular mechanisms can be better interpreted when supported by visual imaging of actual microscopic spatial organization, and we propose phenotypic adaptation selected by social interactions as molecular mechanisms stabilizing microbial communities.",
author = "Wenzheng Liu and Samuel Jacquiod and Asker Brejnrod and Jakob Russel and Mette Burm{\o}lle and S{\o}rensen, {S{\o}ren J.}",
year = "2019",
doi = "10.1038/s41396-019-0494-9",
language = "English",
volume = "13",
pages = "3054--3066",
journal = "I S M E Journal",
issn = "1751-7362",
publisher = "nature publishing group",
number = "12",

}

RIS

TY - JOUR

T1 - Deciphering links between bacterial interactions and spatial organization in multispecies biofilms

AU - Liu, Wenzheng

AU - Jacquiod, Samuel

AU - Brejnrod, Asker

AU - Russel, Jakob

AU - Burmølle, Mette

AU - Sørensen, Søren J.

PY - 2019

Y1 - 2019

N2 - Environmental microbes frequently live in multispecies biofilms where mutualistic relationships and co-evolution may occur, defining spatial organization for member species and overall community functions. In this context, intrinsic properties emerging from microbial interactions, such as efficient organization optimizing growth and activities in multispecies biofilms, may become the object of fitness selection. However, little is known on the nature of underlying interspecies interactions during establishment of a predictable spatial organization within multispecies biofilms. We present a comparative metatranscriptomic analysis of bacterial strains residing in triple-species and four-species biofilms, aiming at deciphering molecular mechanisms underpinning bacterial interactions responsible of the remarkably enhanced biomass production and associated typical spatial organization they display. Metatranscriptomic profiles concurred with changes in micro-site occupation in response to the addition/removal of a single species, being driven by both cooperation, competition, and facilitation processes. We conclude that the enhanced biomass production of the four-species biofilm is an intrinsic community property emerging from finely tuned space optimization achieved through concerted antagonistic and mutualistic interactions, where each species occupies a defined micro-site favoring its own growth. Our results further illustrate how molecular mechanisms can be better interpreted when supported by visual imaging of actual microscopic spatial organization, and we propose phenotypic adaptation selected by social interactions as molecular mechanisms stabilizing microbial communities.

AB - Environmental microbes frequently live in multispecies biofilms where mutualistic relationships and co-evolution may occur, defining spatial organization for member species and overall community functions. In this context, intrinsic properties emerging from microbial interactions, such as efficient organization optimizing growth and activities in multispecies biofilms, may become the object of fitness selection. However, little is known on the nature of underlying interspecies interactions during establishment of a predictable spatial organization within multispecies biofilms. We present a comparative metatranscriptomic analysis of bacterial strains residing in triple-species and four-species biofilms, aiming at deciphering molecular mechanisms underpinning bacterial interactions responsible of the remarkably enhanced biomass production and associated typical spatial organization they display. Metatranscriptomic profiles concurred with changes in micro-site occupation in response to the addition/removal of a single species, being driven by both cooperation, competition, and facilitation processes. We conclude that the enhanced biomass production of the four-species biofilm is an intrinsic community property emerging from finely tuned space optimization achieved through concerted antagonistic and mutualistic interactions, where each species occupies a defined micro-site favoring its own growth. Our results further illustrate how molecular mechanisms can be better interpreted when supported by visual imaging of actual microscopic spatial organization, and we propose phenotypic adaptation selected by social interactions as molecular mechanisms stabilizing microbial communities.

U2 - 10.1038/s41396-019-0494-9

DO - 10.1038/s41396-019-0494-9

M3 - Journal article

C2 - 31455806

AN - SCOPUS:85071623073

VL - 13

SP - 3054

EP - 3066

JO - I S M E Journal

JF - I S M E Journal

SN - 1751-7362

IS - 12

ER -

ID: 227562509