Run-and-tumble dynamics of E. coli is governed by its mechanical properties

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This paper studied how mechanical properties of the bacterium Escherichia coli—including cell/body geometry, flagellar bending rigidity and hook rigidity, polymorphic transformations that change flagellar helicity, and the number and arrangement of helical flagella—govern its run-and-tumble motility. Using a detailed coupled model with fluid flow described by dissipative particle dynamics, the authors performed mesoscale simulations and compared the results with direct experiments. They found that swimming velocity is nearly independent of the number of flagella, while hook rigidity, flagellar helicity polymorphic transformation, and flagellar arrangement strongly influence run-and-tumble behavior, with simulation results agreeing well with experiments. The limitation is that the model is focused on E. coli peritrichous motility and is designed for use in exploring more complex environments, rather than directly addressing host-tissue or disease contexts. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

The huge variety of microorganisms motivates fundamental studies of their behavior with a possibility to construct artificial mimics. A prominent example is the E. coli bacterium which employs several helical flagella to exhibit a motility pattern that alternates between run (directional swimming) and tumble (change in swimming direction) phases. We establish a detailed E. coli model, coupled to fluid flow described by the dissipative particle dynamics method, and investigate its run-and-tumble behavior. Different E. coli characteristics, including body geometry, flagella bending rigidity, the number of flagella and their arrangement at the body are considered. Experiments are also performed to directly compare with the model. Interestingly, in both simulations and experiments, the swimming velocity is nearly independent of the number of flagella. The rigidity of a hook (the short part of a flagellum which connects it directly to the motor), polymorphic transformation (spontaneous change in flagella helicity) of flagella, and their arrangement at the body surface strongly influence the run-and-tumble behavior. Mesoscale hydrodynamics simulations with the developed model help us better understand physical mechanisms which govern E. coli dynamics, yielding the run-and-tumble behavior that compares well with experimental observations. This model can further be used to explore the behavior of E. coli and other peritrichous bacteria in more complex realistic environments.
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Abstract The huge variety of microorganisms motivates fundamental studies of their behavior with a possibility to construct artificial mimics. A prominent example is the E. coli bacterium which employs several helical flagella to exhibit a motility pattern that alternates between run (directional swimming) and tumble (change in swimming direction) phases. We establish a detailed E. coli model, coupled to fluid flow described by the dissipative particle dynamics method, and investigate its run-and-tumble behavior. Different E. coli characteristics, including body geometry, flagella bending rigidity, the number of flagella and their arrangement at the body are considered. Experiments are also performed to directly compare with the model. Interestingly, in both simulations and experiments, the swimming velocity is nearly independent of the number of flagella. The rigidity of a hook (the short part of a flagellum which connects it directly to the motor), polymorphic transformation (spontaneous change in flagella helicity) of flagella, and their arrangement at the body surface strongly influence the run-and-tumble behavior. Mesoscale hydrodynamics simulations with the developed model help us better understand physical mechanisms which govern E. coli dynamics, yielding the run-and-tumble behavior that compares well with experimental observations. This model can further be used to explore the behavior of E. coli and other peritrichous bacteria in more complex realistic environments. Competing Interest Statement The authors have declared no competing interest.

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last seen: 2026-05-20T01:45:00.602351+00:00