Implications of 3-step swimming patterns in bacterial chemotaxis

We recently found that marine bacteria Vibrio alginolyticus execute a cyclic 3-step (run- reverse-flick) motility pattern that is distinctively different from the 2-step (run-tumble) pattern of Escherichia coli. How this novel swimming pattern is regulated by cells of V. alginolyticus is not currently known, but its significance for bacterial chemotaxis is self- evident and will be delineated herein. Using an approach introduced by de Gennes, we calculated the migration speed of a cell executing the 3-step pattern in a linear chemical gradient, and found that a biphasic chemotactic response arises naturally. The implication of such a response for the cells to adapt to ocean environments and its possible connection to E. coli 's response are also discussed.Comment: 18 pages, 4 figures, submitted to biophysical journa

Bacterial Motility Patterns Reveal Importance of Exploitation over Exploration in Marine Microhabitats. Part I: Theory

AbstractBacteria use different motility patterns to navigate and explore natural habitats. However, how these motility patterns are selected, and what their benefits may be, are not understood. In this article, we analyze the effect of motility patterns on a cell’s ability to migrate in a chemical gradient and to localize at the top of the gradient, the two most important characteristics of bacterial chemotaxis. We will focus on two motility patterns, run-tumble and run-reverse-flick, that are observed and characterized in enteric bacterium Escherichia coli and marine bacterium Vibrio alginolyticus, respectively. To make an objective comparison, master equations are developed on the basis of microscopic motions of the bacteria. An unexpected yet significant result is that by adopting the run-reverse-flick motility pattern, a bacterium can reduce its diffusivity without compromising its drift in the chemical gradient. This finding is biologically important as it suggests that the motility pattern can improve a microorganism’s ability to sequester nutrients in a competitive environment

Dynamic bandwidth allocation using infinitesimal perturbation analysis

Advances in network management and switching technologies make dynamic bandwidth allocation of logical networks built on top of a physical network possible. Previous proposed dynamic bandwidth allocation algorithms are based on simplified network model. The analytical model is valid only under restrictive assumptions. Infinitesimal Perturbation Analysis, a technique which estimates the gradients of the functions in discrete event dynamic systems by passively observing the system, is used to estimate delay sensitivities under general traffic patterns. A new dynamic bandwidth allocation algorithm using on-line sensitivity estimation is proposed. Simulation results show that the approach further improves network performance. Implementation of the proposed algorithm in operational networks is also discussed.published_or_final_versio

An Element of Determinism in a Stochastic Flagellar Motor Switch

Marine bacterium Vibrio alginolyticus uses a single polar flagellum to navigate in an aqueous environment. Similar to Escherichia coli cells, the polar flagellar motor has two states; when the motor is counter-clockwise, the cell swims forward and when the motor is clockwise, the cell swims backward. V. alginolyticus also incorporates a direction randomization step at the start of the forward swimming interval by flicking its flagellum. To gain an understanding on how the polar flagellar motor switch is regulated, distributions of the forward Δf and backward Δb intervals are investigated herein. We found that the steady-state probability density functions, P(Δf) and P(Δb), of freely swimming bacteria are strongly peaked at a finite time, suggesting that the motor switch is not Poissonian. The short-time inhibition is sufficiently strong and long lasting, i.e., several hundred milliseconds for both intervals, which is readily observed and characterized. Treating motor reversal dynamics as a first-passage problem, which results from conformation fluctuations of the motor switch, we calculated P(Δf) and P(Δb) and found good agreement with the measurements