Bursts boost nonlinear encoding in electroreceptor afferents

Nonlinear mechanisms are at the heart of neuronal information processing, for example to fire an action potential, the membrane voltage must exceed a threshold nonlinearity. Even though, linear encoding schemes are commonly used and often successfully describe large parts of sensory encoding nonlinear mechanisms such as thresholds and saturations are well known to be crucial to encode behaviorally relevant features in the stimulus space not captured by linear methods. Here we analyze the role of bursts in p-type electroreceptor afferents (P-units) in the weakly electric fish Apteronotus leptorhynchus . It is long known that subpopulations of these cells fire bursts of action potentials while others do not. Previous research suggests, that the non-bursting cells are better at encoding the stimulus time-course while bursting neurons are better suited to encode special features in the stimulus. We here show, based on the analysis of experimental data and modeling, that bursts affect the linear as well as the nonlinear encoding. Theoretical work predicts that in simple leaky-integrate-and-fire model neurons, two periodic stimuli interact nonlinearly when the sum of the two frequencies matches the neuron’s baseline firing rate as quantified by the second-order susceptibility. Indeed, such nonlinear responses have been found in non-bursting P-units when stimulated by two beats simultaneously but only in those cells, that exhibit very low levels of intrinsic noise. In this study, we found that bursts strongly enhance these nonlinear responses which may play a critical role in the detection of weak intruder signals in the presence of a strong female signal, i.e. an electrosensory cocktail party.