RESUMO
Quorum sensing is almost always regarded as a population density effect in three-dimensional bulk samples of bacteria. Here we create two-dimensional samples of Vibrio fischeri cells adhered onto glass surfaces to examine the effect of local population densities on quorum sensing. This is done by measuring the luminescent response. The 2-D bacterial populations enable us to simultaneously account for time and distance effects on quorum sensing, which were previously very challenging to access in typical three-dimensional bulk samples. Thus, we are able to consider quorum sensing in terms of signal diffusion. A diffusion model of quorum sensing signals guides the experiments and shows that for a given cell spacing (density) and diffusion time there exists a "true quorum"- a number of cells necessary for quorum sensing. We find that quorum sensing can occur locally in 2-D surface samples and is a function of cell population density as well as signal diffusion time.
Assuntos
Aliivibrio fischeri/fisiologia , Percepção de Quorum/fisiologia , Algoritmos , Aderência Bacteriana , Meios de Cultura , Difusão , Luminescência , Modelos Estatísticos , Propriedades de SuperfícieRESUMO
Chemotaxis is the movement of organisms toward or away from a chemical attractant or toxin by a biased random walk process. Here we describe the first experimental example of chemotaxis outside biological systems. Platinum-gold rods 2.0 microm long exhibit directed movement toward higher hydrogen peroxide concentrations through "active diffusion." Brownian dynamics simulations reveal that no "temporal sensing" algorithm, commonly attributed to bacteria, is necessary; rather, the observed chemotaxis can be explained by random walk physics in a gradient of the active diffusion coefficient.