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Joseph W. Larkin

Publications and source records attributed to Joseph W. Larkin.

4 recordsLinked to original sources

Distinguishable spreading dynamics in microbial communities

A packed community of exponentially proliferating microbes will spread in size exponentially. However, due to nutrient depletion, mechanical constraints, or other limitations, exponential proliferation is not indefinite, and the spreading slows. Here, we theoretically explore a fundamental question: is it possible to infer the dominant limitation type from the spreading dynamics? Using a continuum active fluid model, we consider three limitations to cell proliferation: intrinsic growth arrest (e.g., due to sporulation), pressure from other cells, and nutrient access. We find that memoryless growth arrest still results in superlinear (accelerating) spreading, but at a reduced rate. In contrast, pressure-limited growth results in linear (constant-speed) spreading in the long-time limit. We characterize how the expansion speed depends on the maximum growth rate, the limiting pressure value, and the effective fluid friction. Interestingly, nutrient-limited growth results in a phase transition: depending on the nutrient supply and how efficiently nutrient is converted to biomass, the spreading can be either superlinear or sublinear (decelerating). We predict the phase boundary in terms of these parameters and confirm with simulations. Thus, our results suggest that when an expansion slowdown is observed, its dominant cause is likely nutrient depletion. More generally, our work suggests that cell-level growth limitations can be inferred from population-level dynamics, and it offers a methodology for connecting these two scales.

physics.bio-ph

Microscale 3-D Capacitance Tomography with a CMOS Sensor Array

Electrical capacitance tomography (ECT) is a nonoptical imaging technique in which a map of the interior permittivity of a volume is estimated by making capacitance measurements at its boundary and solving an inverse problem. While previous ECT demonstrations have often been at centimeter scales, ECT is not limited to macroscopic systems. In this paper, we demonstrate ECT imaging of polymer microspheres and bacterial biofilms using a CMOS microelectrode array, achieving spatial resolution of 10 microns. Additionally, we propose a deep learning architecture and an improved multi-objective training scheme for reconstructing out-of-plane permittivity maps from the sensor measurements. Experimental results show that the proposed approach is able to resolve microscopic 3-D structures, achieving 91.5% prediction accuracy on the microsphere dataset and 82.7% on the biofilm dataset, including an average of 4.6% improvement over baseline computational methods.

cs.CV

Spiral wave propagation in communities with spatially correlated heterogeneity

Many multicellular communities propagate signals in a directed manner via excitable waves. Cell-to-cell heterogeneity is a ubiquitous feature of multicellular communities, but the effects of heterogeneity on wave propagation are still unclear. Here we use a minimal FitHugh-Nagumo-type model to investigate excitable wave propagation in a two-dimensional heterogeneous community. The model shows three dynamic regimes in which waves either propagate directionally, die out, or spiral indefinitely, and we characterize how these regimes depend on the heterogeneity parameters. We find that in some parameter regimes, spatial correlations in the heterogeneity enhance directional propagation and suppress spiraling. However, in other regimes, spatial correlations promote spiraling, a surprising feature that we explain by demonstrating that these spirals form by a second, distinct mechanism. Finally, we characterize the dependence of the spiral period on the degree of heterogeneity in the system by using techniques from percolation theory. Our results reveal that the spatial structure of cell-to-cell heterogeneity can have important consequences for signal propagation in cellular communities.

physics.bio-ph

Statistics of correlated percolation in a bacterial community

Signal propagation over long distances is a ubiquitous feature of multicellular communities. In biofilms of the bacterium Bacillus subtilis, we recently discovered that some, but not all, cells participate in the propagation of an electrical signal, and the ones that do are organized in a way that is statistically consistent with percolation theory. However, two key assumptions of percolation theory are violated in this system. First, we find here that the probability for a cell to signal is not independent from other cells but instead is correlated with its nearby neighbors. We develop a mechanistic model, in which correlated signaling emerges from cell division, phenotypic inheritance, and cell displacement, that reproduces the experimental results. Second, we observed previously that the fraction of signaling cells is not constant but instead varies from biofilm to biofilm. We use our model to understand why percolation theory remains a valid description of the system despite these two violations of its assumptions. We find that the first violation does not significantly affect the spatial statistics, which we rationalize using a renormalization argument. We find that the second violation widens the range of signaling fractions around the percolation threshold at which one observes the characteristic power-law statistics of cluster sizes, consistent with our previous experimental results. We validate our model using a mutant biofilm whose signaling probability decays along the propagation direction. Our results identify key statistical features of a correlated percolating system and demonstrate their functional utility for a multicellular community.

physics.bio-ph