There is a need for imaging and sensing instrumentation that can monitor transitions in a biofilm structure in order to better understand biofilm development and emergent properties such as anti-microbial resistance. Herein, we describe the design, manufacture, and use of a microfluidic flow cell to visualize the surface structure of bacterial biofilms with white-light interferometry (WLI). The novel imaging chip enabled the use of this non-disruptive imaging method for the capture of high resolution three-dimensional profile images of biofilm growth over time. The fine axial resolution (3 nm) and the wide field of view (>1 mm by 1 mm) enabled the detection of biofilm formation as early as 3 h after inoculation of the flow cell with a live bacterial culture (Pseudomonas fluorescens). WLI imaging facilitated the monitoring of the early stages of biofilm development and subtle variations in the structure of mature biofilms. Minimally-invasive imaging enabled the monitoring of biofilm structure with surface metrology metrics (e.g., surface roughness). The system was used to observe a transition in the biofilm structure that occurred in response to exposure to a common antiseptic. In the future, WLI and the biofilm imaging cell described herein may be used to test the effectiveness of biofilm-specific therapies to combat common diseases associated with biofilm formation such as cystic fibrosis and periodontitis.
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July 2017
Research Article|
August 18 2017
Monitoring bacterial biofilms with a microfluidic flow chip designed for imaging with white-light interferometry
Michelle Brann;
Michelle Brann
a)
1
Pacific Northwest National Laboratory
, Richland, Washington, 99325, USA
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Jonathan D. Suter;
Jonathan D. Suter
2
Signatures Science and Technology Division, Pacific Northwest National Laboratory. Battelle for the USDOE
, P.O. Box 999, MSIN P7-50, Richland, Washington 99354, USA
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R. Shane Addleman;
R. Shane Addleman
2
Signatures Science and Technology Division, Pacific Northwest National Laboratory. Battelle for the USDOE
, P.O. Box 999, MSIN P7-50, Richland, Washington 99354, USA
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Curtis Larimer
Curtis Larimer
b)
2
Signatures Science and Technology Division, Pacific Northwest National Laboratory. Battelle for the USDOE
, P.O. Box 999, MSIN P7-50, Richland, Washington 99354, USA
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Michelle Brann
1,a)
Jonathan D. Suter
2
R. Shane Addleman
2
Curtis Larimer
2,b)
1
Pacific Northwest National Laboratory
, Richland, Washington, 99325, USA
2
Signatures Science and Technology Division, Pacific Northwest National Laboratory. Battelle for the USDOE
, P.O. Box 999, MSIN P7-50, Richland, Washington 99354, USA
a)
Present address: Department of Chemistry, The University of Chicago, Chicago, Illinois 60637, USA.
b)
Author to whom correspondence should be addressed: [email protected].
Biomicrofluidics 11, 044113 (2017)
Article history
Received:
June 01 2017
Accepted:
August 07 2017
Citation
Michelle Brann, Jonathan D. Suter, R. Shane Addleman, Curtis Larimer; Monitoring bacterial biofilms with a microfluidic flow chip designed for imaging with white-light interferometry. Biomicrofluidics 1 July 2017; 11 (4): 044113. https://doi.org/10.1063/1.4985773
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