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      Rapid, High-Throughput Tracking of Bacterial Motility in 3D via Phase-Contrast Holographic Video Microscopy

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          Abstract

          Tracking fast-swimming bacteria in three dimensions can be extremely challenging with current optical techniques and a microscopic approach that can rapidly acquire volumetric information is required. Here, we introduce phase-contrast holographic video microscopy as a solution for the simultaneous tracking of multiple fast moving cells in three dimensions. This technique uses interference patterns formed between the scattered and the incident field to infer the three-dimensional (3D) position and size of bacteria. Using this optical approach, motility dynamics of multiple bacteria in three dimensions, such as speed and turn angles, can be obtained within minutes. We demonstrated the feasibility of this method by effectively tracking multiple bacteria species, including Escherichia coli, Agrobacterium tumefaciens, and Pseudomonas aeruginosa. In addition, we combined our fast 3D imaging technique with a microfluidic device to present an example of a drug/chemical assay to study effects on bacterial motility.

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          Most cited references40

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          Monolithic microfabricated valves and pumps by multilayer soft lithography.

          Soft lithography is an alternative to silicon-based micromachining that uses replica molding of nontraditional elastomeric materials to fabricate stamps and microfluidic channels. We describe here an extension to the soft lithography paradigm, multilayer soft lithography, with which devices consisting of multiple layers may be fabricated from soft materials. We used this technique to build active microfluidic systems containing on-off valves, switching valves, and pumps entirely out of elastomer. The softness of these materials allows the device areas to be reduced by more than two orders of magnitude compared with silicon-based devices. The other advantages of soft lithography, such as rapid prototyping, ease of fabrication, and biocompatibility, are retained.
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            Chemotaxis in Escherichia coli analysed by three-dimensional tracking.

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              Escherichia coli swim on the right-hand side.

              The motion of peritrichously flagellated bacteria close to surfaces is relevant to understanding the early stages of biofilm formation and of pathogenic infection. This motion differs from the random-walk trajectories of cells in free solution. Individual Escherichia coli cells swim in clockwise, circular trajectories near planar glass surfaces. On a semi-solid agar substrate, cells differentiate into an elongated, hyperflagellated phenotype and migrate cooperatively over the surface, a phenomenon called swarming. We have developed a technique for observing isolated E. coli swarmer cells moving on an agar substrate and confined in shallow, oxidized poly(dimethylsiloxane) (PDMS) microchannels. Here we show that cells in these microchannels preferentially 'drive on the right', swimming preferentially along the right wall of the microchannel (viewed from behind the moving cell, with the agar on the bottom). We propose that when cells are confined between two interfaces--one an agar gel and the second PDMS--they swim closer to the agar surface than to the PDMS surface (and for much longer periods of time), leading to the preferential movement on the right of the microchannel. Thus, the choice of materials guides the motion of cells in microchannels.
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                Author and article information

                Contributors
                Journal
                Biophys J
                Biophys. J
                Biophysical Journal
                The Biophysical Society
                0006-3495
                1542-0086
                10 March 2015
                10 March 2015
                : 108
                : 5
                : 1248-1256
                Affiliations
                [1 ]Mechanobiology Institute, National University of Singapore, Singapore
                [2 ]School of Mechanical Engineering & Department of Global Biomedical Engineering, Sungkyunkwan University, Suwon, Korea
                [3 ]Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois
                [4 ]Department of Microbiology & Immunology, University of Illinois-Chicago, Chicago, Illinois
                [5 ]Department of Biomedical Engineering, National University of Singapore, Singapore
                [6 ]Department of Mechanical Engineering, National University of Singapore, Singapore
                Author notes
                []Corresponding author ctlim@ 123456nus.edu.sg
                Article
                S0006-3495(15)00081-8
                10.1016/j.bpj.2015.01.018
                4375448
                25762336
                68beb07f-fac4-4ee5-bb89-360dee0aa7ea
                © 2015 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).

                History
                : 6 February 2014
                : 8 January 2015
                Categories
                Systems Biophysics

                Biophysics
                Biophysics

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