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Register a new userCollective motion and nonequilibrium cluster formation in colonies of gliding bacteria
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We characterize cell motion in experiments and show that the transition to collective motion in colonies of gliding bacterial cells confined to a monolayer appears through the organization of cells into larger moving clusters. Collective motion by non-equilibrium cluster formation is detected for a critical cell packing fraction around 17%. This transition is characterized by a scale-free power-law cluster size distribution, with an exponent $0.88pm0.07$, and the appearance of giant number fluctuations. Our findings are in quantitative agreement with simulations of self-propelled rods. This suggests that the interplay of self-propulsion of bacteria and the rod-shape of bacteria is sufficient to induce collective motion.
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The near-surface swimming patterns of bacteria are strongly determined by the hydrodynamic interactions between bacteria and the surface, which trap bacteria in smooth circular trajectories that lead to inefficient surface exploration. Here, we show by combining experiments and a data-driven mathematical model that surface exploration of enterohemorrhagic Escherichia coli (EHEC) -- a pathogenic strain of E. coli causing serious illnesses such as bloody diarrhea -- results from a complex interplay between motility and transient surface adhesion events. These events allow EHEC to break the smooth circular trajectories and regulate their transport properties by the use stop-adhesion events that lead to a characteristic intermittent motion on surfaces. We find that the experimentally measured frequency of stop-adhesion events in EHEC is located at the value predicted by the developed mathematical model that maximizes bacterial surface diffusivity. We indicate that these results and the developed model apply to other bacterial strains on different surfaces, which suggests that swimming bacteria use transient adhesion to regulate surface motion.
Collective motion is found in various animal systems, active suspensions and robotic or virtual agents. This is often understood using high level models that directly encode selected empirical features, such as co-alignment and cohesion. Can these features be shown to emerge from an underlying, low-level principle? We find that they emerge naturally under Future State Maximisation (FSM). Here agents perceive a visual representation of the world around them, such as might be recorded on a simple retina, and then move to maximise the number of different visual environments that they expect to be able to access in the future. Such a control principle may confer evolutionary fitness in an uncertain world by enabling agents to deal with a wide variety of future scenarios. The collective dynamics that spontaneously emerge under FSM resemble animal systems in several qualitative aspects, including cohesion, co-alignment and collision suppression, none of which are explicitly encoded in the model. A multi-layered neural network trained on simulated trajectories is shown to represent a heuristic mimicking FSM. Similar levels of reasoning would seem to be accessible under animal cognition, demonstrating a possible route to the emergence of collective motion in social animals directly from the control principle underlying FSM. Such models may also be good candidates for encoding into possible future realisations of artificial intelligent matter, able to sense light, process information and move.
The prospect of new biological and industrial applications that require communication in micro-scale, encourages research on the design of bio-compatible communication networks using networking primitives already available in nature. One of the most promising candidates for constructing such networks is to adapt and engineer specific types of bacteria that are capable of sensing, actuation, and above all, communication with each other. In this paper, we describe a new architecture for networks of bacteria to form a data collecting network, as in traditional sensor networks. The key to this architecture is the fact that the node in the network itself is a bacterial colony; as an individual bacterium (biological agent) is a tiny unreliable element with limited capabilities. We describe such a network under two different scenarios. We study the data gathering (sensing and multihop communication) scenario as in sensor networks followed by the consensus problem in a multi-node network. We will explain as to how the bacteria in the colony collectively orchestrate their actions as a node to perform sensing and relaying tasks that would not be possible (at least reliably) by an individual bacterium. Each single bacterium in the colony forms a belief by sensing external parameter (e.g., a molecular signal from another node) from the medium and shares its belief with other bacteria in the colony. Then, after some interactions, all the bacteria in the colony form a common belief and act as a single node. We will model the reception process of each individual bacteria and will study its impact on the overall functionality of a node. We will present results on the reliability of the multihop communication for data gathering scenario as well as the speed of convergence in the consensus scenario.
In the growth of bacterial colonies, a great variety of complex patterns are observed in experiments, depending on external conditions and the bacterial species. Typically, existing models employ systems of reaction-diffusion equations or consist of growth processes based on rules, and are limited to a discrete lattice. In contrast, the two-dimensional model proposed here is an off-lattice simulation, where bacteria are modelled as rigid circles and nutrients are point-like, Brownian particles. Varying the nutrient diffusion and concentration, we simulate a wide range of morphologies compatible with experimental observations, from round and compact to extremely branched patterns. A scaling relationship is found between the number of cells in the interface and the total number of cells, with two characteristic regimes. These regimes correspond to the compact and branched patterns, which are exhibited for sufficiently small and large colonies, respectively. In addition, we characterise the screening effect observed in the structures by analysing the multifractal properties of the growth probability.
Locomotion and transport of microorganisms in fluids is an essential aspect of life. Search for food, orientation toward light, spreading of off-spring, and the formation of colonies are only possible due to locomotion. Swimming at the microscale occurs at low Reynolds numbers, where fluid friction and viscosity dominates over inertia. Here, evolution achieved propulsion mechanisms, which overcome and even exploit drag. Prominent propulsion mechanisms are rotating helical flagella, exploited by many bacteria, and snake-like or whip-like motion of eukaryotic flagella, utilized by sperm and algae. For artificial microswimmers, alternative concepts to convert chemical energy or heat into directed motion can be employed, which are potentially more efficient. The dynamics of microswimmers comprises many facets, which are all required to achieve locomotion. In this article, we review the physics of locomotion of biological and synthetic microswimmers, and the collective behavior of their assemblies. Starting from individual microswimmers, we describe the various propulsion mechanism of biological and synthetic systems and address the hydrodynamic aspects of swimming. This comprises synchronization and the concerted beating of flagella and cilia. In addition, the swimming behavior next to surfaces is examined. Finally, collective and cooperate phenomena of various types of isotropic and anisotropic swimmers with and without hydrodynamic interactions are discussed.
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