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Jörn Dunkel. Mok, Rachel V.(Rachel Verla) Massachusetts Institute of Technology. Department of Mechanical Engineering. Massachusetts Institute of Technology. Department of Mechanical Engineering 2019-09-16T21:16:05Z 2019-09-16T21:16:05Z 2019 2019 https://hdl.handle.net/1721.1/122136 1117713879 Thesis: Ph. D., Massachusetts Institute of Technology, Department of Mechanical Engineering, 2019 Cataloged from PDF version of thesis. Includes bibliographical references (pages 121-133). With recent technological advancements, observations and measurements of complex bacterial communities at single-cell resolution are now possible. Guided by these rich experimental data sets, we develop minimal individual-based models to uncover the governing forces driving the dynamics in microbial systems. Our model incorporates the biophysical processes of cell growth and division, viscous drag, bacteria self-propulsion, and mechanical cell-surface and cell-cell interactions through interaction potentials. In particular, our cell-cell interaction potential accounts for hard steric and osmotic repulsion as well as attraction mediated through secreted components which bind cells together. Implementing this model on graphics processing units (GPUs) such that the computational time scales linearly with the system size, we achieve a 10x speedup over a comparable code written on central processing units (CPUs). With this simulation framework, we investigate the collective dynamics of Bacillus subtilis swarm expansion and Vibrio cholerae biofilm formation. Our experimental and numerical results imply that mechanical cell-cell interactions dominate the swarming motility phases and can account for the emergence of order and structure seen in growing biofilms. Furthermore, this model is used to explore the effectiveness of surface topography on deterring biofilm formation by investigating how locally varying boundary curvature impact the scattering and accumulation dynamics of swimming bacteria. This work shows great promise at increasing our understanding of the physics governing microbial communities, which knowledge is essential to control and inhibit bacterial populations. Supported by a James S. McDonnell Foundation Complex Systems Scholar Award, an Edmund F. Kelly Research Award, a MITGermany MISTI seed grant, a MIT ODGE Childbirth Accommodation Fund, a MIT OGE Chyn Duog Shiah Memorial Fellowship, and the MIT Mechanical Engineering Department by Rachel Verla Mok. Ph.D. Ph.D. Massachusetts Institute of Technology, Department of Mechanical Engineering 133 pages eng Massachusetts Institute of Technology MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission. http://dspace.mit.edu/handle/1721.1/7582 Mechanical Engineering. An individual-based GPU simulation framework for collective bacterial dynamics in swarms and biofilms Thesis application/pdf 2019-09-16T21:16:01Z Publication Doctoral MechE unknown unknown <Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="873fa2fb-745e-49f7-a422-8e1ce1bb05a7"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>An individual-based GPU simulation framework for collective bacterial dynamics in swarms and biofilms</Title> <PublishedIn> <Publication> </Publication> </PublishedIn> <PublicationDate>2019</PublicationDate> <Authors> <Author> <DisplayName>Mok, Rachel V.(Rachel Verla)</DisplayName> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Massachusetts Institute of Technology</DisplayName> <OrgUnit /> </Publisher> </Publishers> <License>http://dspace.mit.edu/handle/1721.1/7582</License> <Keyword>Mechanical Engineering.</Keyword> <Abstract>With recent technological advancements, observations and measurements of complex bacterial communities at single-cell resolution are now possible. Guided by these rich experimental data sets, we develop minimal individual-based models to uncover the governing forces driving the dynamics in microbial systems. Our model incorporates the biophysical processes of cell growth and division, viscous drag, bacteria self-propulsion, and mechanical cell-surface and cell-cell interactions through interaction potentials. In particular, our cell-cell interaction potential accounts for hard steric and osmotic repulsion as well as attraction mediated through secreted components which bind cells together. Implementing this model on graphics processing units (GPUs) such that the computational time scales linearly with the system size, we achieve a 10x speedup over a comparable code written on central processing units (CPUs). With this simulation framework, we investigate the collective dynamics of Bacillus subtilis swarm expansion and Vibrio cholerae biofilm formation. Our experimental and numerical results imply that mechanical cell-cell interactions dominate the swarming motility phases and can account for the emergence of order and structure seen in growing biofilms. Furthermore, this model is used to explore the effectiveness of surface topography on deterring biofilm formation by investigating how locally varying boundary curvature impact the scattering and accumulation dynamics of swimming bacteria. This work shows great promise at increasing our understanding of the physics governing microbial communities, which knowledge is essential to control and inhibit bacterial populations.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication>