Pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network.

Bacteria occupy heterogeneous environments, attaching and growing within pores in materials, living hosts, and matrices like soil. Systems that permit high-resolution visualization of dynamic bacterial processes within the physical confines of a realistic and tractable porous media environment are r...

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Main Authors: Jayde A Aufrecht, Jason D Fowlkes, Amber N Bible, Jennifer Morrell-Falvey, Mitchel J Doktycz, Scott T Retterer
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0218316
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spelling doaj-d6dd87c4eb4a41a8b1474e8f035b96e12021-03-03T20:36:17ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01146e021831610.1371/journal.pone.0218316Pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network.Jayde A AufrechtJason D FowlkesAmber N BibleJennifer Morrell-FalveyMitchel J DoktyczScott T RettererBacteria occupy heterogeneous environments, attaching and growing within pores in materials, living hosts, and matrices like soil. Systems that permit high-resolution visualization of dynamic bacterial processes within the physical confines of a realistic and tractable porous media environment are rare. Here we use microfluidics to replicate the grain shape and packing density of natural sands in a 2D platform to study the flow-induced spatial evolution of bacterial biofilms underground. We discover that initial bacterial dispersal and grain attachment is influenced by bacterial transport across pore space velocity gradients, a phenomenon otherwise known as rheotaxis. We find that gravity-driven flow conditions activate different bacterial cell-clustering phenotypes depending on the strain's ability to product extracellular polymeric substances (EPS). A wildtype, biofilm-producing bacteria formed compact, multicellular patches while an EPS-defective mutant displayed a linked-cell phenotype in the presence of flow. These phenotypes subsequently influenced the overall spatial distribution of cells across the porous media network as colonies grew and altered the fluid dynamics of their microenvironment.https://doi.org/10.1371/journal.pone.0218316
collection DOAJ
language English
format Article
sources DOAJ
author Jayde A Aufrecht
Jason D Fowlkes
Amber N Bible
Jennifer Morrell-Falvey
Mitchel J Doktycz
Scott T Retterer
spellingShingle Jayde A Aufrecht
Jason D Fowlkes
Amber N Bible
Jennifer Morrell-Falvey
Mitchel J Doktycz
Scott T Retterer
Pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network.
PLoS ONE
author_facet Jayde A Aufrecht
Jason D Fowlkes
Amber N Bible
Jennifer Morrell-Falvey
Mitchel J Doktycz
Scott T Retterer
author_sort Jayde A Aufrecht
title Pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network.
title_short Pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network.
title_full Pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network.
title_fullStr Pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network.
title_full_unstemmed Pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network.
title_sort pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Bacteria occupy heterogeneous environments, attaching and growing within pores in materials, living hosts, and matrices like soil. Systems that permit high-resolution visualization of dynamic bacterial processes within the physical confines of a realistic and tractable porous media environment are rare. Here we use microfluidics to replicate the grain shape and packing density of natural sands in a 2D platform to study the flow-induced spatial evolution of bacterial biofilms underground. We discover that initial bacterial dispersal and grain attachment is influenced by bacterial transport across pore space velocity gradients, a phenomenon otherwise known as rheotaxis. We find that gravity-driven flow conditions activate different bacterial cell-clustering phenotypes depending on the strain's ability to product extracellular polymeric substances (EPS). A wildtype, biofilm-producing bacteria formed compact, multicellular patches while an EPS-defective mutant displayed a linked-cell phenotype in the presence of flow. These phenotypes subsequently influenced the overall spatial distribution of cells across the porous media network as colonies grew and altered the fluid dynamics of their microenvironment.
url https://doi.org/10.1371/journal.pone.0218316
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