No Arabic abstract
We propose a modeling approach to study how mature biofilms spread and colonize new surfaces by predicting the formation and growth of satellite colonies generated by dispersing biofilms. This model provides the basis for better understanding the fate and behavior of dispersal cells, phenomenon that cannot, as yet, be predicted from knowledge of the genome. The model results were promising as supported by the experimental results. The proposed approach allows for further improvements through more detailed sub-models for front propagation, seeding, availability and depletion of resources. The present study was a successful proof-of-concept in answering the following questions: Can we predict the colonization of new sites following biofilm dispersal? Can we generate patterns in space and time to shed light on seeding dispersal? That are fundamental issues for developing novel approaches to manipulate biofilm formation in industrial, environmental and medical applications.
Biofilms are communities of bacteria adhered to surfaces. Recently, biofilms of rod-shaped bacteria were observed at single-cell resolution and shown to develop from a disordered, two-dimensional layer of founder cells into a three-dimensional structure with a vertically-aligned core. Here, we elucidate the physical mechanism underpinning this transition using a combination of agent-based and continuum modeling. We find that verticalization proceeds through a series of localized mechanical instabilities on the cellular scale. For short cells, these instabilities are primarily triggered by cell division, whereas long cells are more likely to be peeled off the surface by nearby vertical cells, creating an inverse domino effect. The interplay between cell growth and cell verticalization gives rise to an exotic mechanical state in which the effective surface pressure becomes constant throughout the growing core of the biofilm surface layer. This dynamical isobaricity determines the expansion speed of a biofilm cluster and thereby governs how cells access the third dimension. In particular, theory predicts that a longer average cell length yields more rapidly expanding, flatter biofilms. We experimentally show that such changes in biofilm development occur by exploiting chemicals that modulate cell length.
We present models of dormancy in a planktonic culture and in biofilm, and examine the relative advantage of short dormancy versus long dormancy times in each case. Simulations and analyses indicate that in planktonic batch cultures and in chemostats, live biomass is maximized by the fastest possible exit from dormancy. The lower limit of time to reawakening is thus perhaps governed by physiological, biochemical or other constraints within the cells. In biofilm we see that the slower waker has a defensive advantage over the fast waker due to a larger amount of dormant biomass, without an appreciable difference in total live biomass. Thus it would seem that typical laboratory culture conditions can be unrepresentative of the natural state. We discuss the computational methods developed for this work.
Despite their importance in many biological, ecological and physical processes, microorganismal fluid flows under tight confinement have not been investigated experimentally. Strong screening of Stokelets in this geometry suggests that the flow fields of different microorganisms should be universally dominated by the 2D source dipole from the swimmers finite-size body. Confinement therefore is poised to collapse differences across microorganisms, that are instead well-established in bulk. Here we combine experiments and theoretical modelling to show that, in general, this is not correct. Our results demonstrate that potentially minute details like microswimmers spinning and the physical arrangement of the propulsion appendages have in fact a leading role in setting qualitative topological properties of the hydrodynamic flow fields of micro-swimmers under confinement. This is well captured by an effective 2D model, even under relatively weak confinement. These results imply that active confined hydrodynamics is much richer than in bulk, and depends in a subtle manner on size, shape and propulsion mechanisms of the active components.
Excitable membranes are an important type of nonlinear dynamical system and their study can be used to provide a connection between physical and biological circuits. We discuss two models of excitable membranes important in cardiac and neural tissues. One model is based on the Fitzhugh-Nagumo equations and the other is based on a three-transistor excitable circuit. We construct a circuit that simulates reentrant tachycardia and its treatment by surgical ablation. This project is appropriate for advanced undergraduates as a laboratory capstone project, or as a senior thesis or honors project, and can also be a collaborative project, with one student responsible for the computational predictions and another for the circuit construction and measurements.
Marine microorganisms often reach high swimming speeds, either to take advantage of evanescent nutrient patches or to beat Brownian forces. Since this implies that a sizable part of their energetic budget must be allocated to motion, it is reasonable to assume that some fast-swimming microorganisms may increase their nutrient intake by increasing their speed v. We formulate a model to investigate this hypothesis and its consequences, finding the steady state solutions and analyzing their stability. Surprisingly, we find that even modest increases in nutrient absorption may lead to a significant increase of the microbial speed. In fact, evaluations obtained using realistic parameter values for bacteria indicate that the speed increase due to the enhanced nutrient absorption may be quite large.