Fluid-driven Interfacial instabilities and turbulence in bacterial biofilms
Fluid-driven Interfacial instabilities and turbulence in bacterial biofilms
Biofilms are thin layers of bacteria embedded within a slime matrix that live on surfaces. They are ubiquitous in nature and responsible for many medical and dental infections, industrial fouling and are also evident in ancient fossils. A biofilm structure is shaped by growth, detachment and response to mechanical forces acting on them. The main contribution to biofilm versatility in response to physical forces is the matrix that provides a platform for the bacteria to grow. The interaction between biofilm structure and hydrodynamics remains a fundamental question concerning biofilm dynamics. Here we document the appearance of ripples and wrinkles in biofilms grown from three species of bacteria when subjected to rapid high-velocity fluid flows. Theoretical treatment of the process as a Kelvin-Helmholtz instability indicates that the rippling process was primarily due to physics rather than chemistry or biology. The analysis also predicted a strong dependence of the instability formation on biofilm viscosity explaining the different surface corrugations observed. Turbulence through Kelvin-Helmholtz instabilities occurring at the interface demonstrated that the biofilm flows like a viscous liquid under high flow velocities applied within milliseconds. Biofilm fluid-like behavior may have important implications for our understanding of how fluid flow influences biofilm biology since turbulence will likely disrupt metabolite and signal gradients as well as community stratification.
4417-4431
Fabbri, Stefania
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Li, Jian
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Howlin, Robert P.
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Rmaile, Amir
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Gottenbos, Bart
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de Jager, Marko
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Starke, E.Michelle
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Aspiras, Marcelo
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Ward, Marilyn T.
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Cogan, Nick G.
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Stoodley, Paul
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19 November 2017
Fabbri, Stefania
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Li, Jian
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Howlin, Robert P.
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Rmaile, Amir
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Gottenbos, Bart
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de Jager, Marko
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Starke, E.Michelle
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Aspiras, Marcelo
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Ward, Marilyn T.
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Cogan, Nick G.
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Stoodley, Paul
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Fabbri, Stefania, Li, Jian, Howlin, Robert P., Rmaile, Amir, Gottenbos, Bart, de Jager, Marko, Starke, E.Michelle, Aspiras, Marcelo, Ward, Marilyn T., Cogan, Nick G. and Stoodley, Paul
(2017)
Fluid-driven Interfacial instabilities and turbulence in bacterial biofilms.
Environmental Microbiology, 19 (11), .
(doi:10.1111/1462-2920.13883).
Abstract
Biofilms are thin layers of bacteria embedded within a slime matrix that live on surfaces. They are ubiquitous in nature and responsible for many medical and dental infections, industrial fouling and are also evident in ancient fossils. A biofilm structure is shaped by growth, detachment and response to mechanical forces acting on them. The main contribution to biofilm versatility in response to physical forces is the matrix that provides a platform for the bacteria to grow. The interaction between biofilm structure and hydrodynamics remains a fundamental question concerning biofilm dynamics. Here we document the appearance of ripples and wrinkles in biofilms grown from three species of bacteria when subjected to rapid high-velocity fluid flows. Theoretical treatment of the process as a Kelvin-Helmholtz instability indicates that the rippling process was primarily due to physics rather than chemistry or biology. The analysis also predicted a strong dependence of the instability formation on biofilm viscosity explaining the different surface corrugations observed. Turbulence through Kelvin-Helmholtz instabilities occurring at the interface demonstrated that the biofilm flows like a viscous liquid under high flow velocities applied within milliseconds. Biofilm fluid-like behavior may have important implications for our understanding of how fluid flow influences biofilm biology since turbulence will likely disrupt metabolite and signal gradients as well as community stratification.
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ripples_paper_revised_SF2 PSv1
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Fabbri_et_al-2017-Environmental_Microbiology
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More information
Accepted/In Press date: 3 August 2017
e-pub ahead of print date: 14 September 2017
Published date: 19 November 2017
Identifiers
Local EPrints ID: 416468
URI: http://eprints.soton.ac.uk/id/eprint/416468
ISSN: 1462-2920
PURE UUID: d3b89d37-9d9f-4b44-9765-d4c43bf69d32
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Date deposited: 19 Dec 2017 17:31
Last modified: 16 Mar 2024 05:37
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Contributors
Author:
Stefania Fabbri
Author:
Jian Li
Author:
Robert P. Howlin
Author:
Amir Rmaile
Author:
Bart Gottenbos
Author:
Marko de Jager
Author:
E.Michelle Starke
Author:
Marcelo Aspiras
Author:
Marilyn T. Ward
Author:
Nick G. Cogan
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