What We Do
During brain development maturation and experience work jointly to provide the optimal neural representations of the environment to cope with future needs. By studying typically developed individuals, sensory deprivation, and sensory restoration, the SEED group explores mechanisms underlying functional and structural development, organization, and representations of the senses. Investigations on sensory neural systems that are deprived of their typical sensory input, as in the case of congenital blindness or deafness, reveal the complexity of neural systems and their adaptations: on the one hand, neural representations of specific cortical areas can be functionally preserved despite the lack of a sense, on the other hand, intra - and cross-modal plasticity, that is changes of neural responses in spared and deprived sensory modalities, disclose neural plasticity effects which can lead to compensatory abilities. The model of sensory restoration, as in the case of sight or hearing recovery, proved to be effective to test for the existence of sensitive or critical periods, during which specific experience must be available for typical development of neural circuits or, in striking contrast, to test for the existence of functions which develop independently of early input. All these approaches rely on the understanding of sensory systems development and functioning in a multisensory framework.
Research is conducted at the interface between cognitive neuroscience, psychology, and biological engineering – applying multiple methods such as computational neuroscience, electrical neuroimaging, functional and structural magnetic resonance imaging, psychophysics to elucidate complex neural dynamics.
ONGOING PROJECTS
Natural speech signals processing and development
Supramodal brain organization in sensory-deprivation
Experience dependence of audio-visual streams
Structural brain changes in large samples of congenital and late blind people
Visual dependence of auditory processing
Adaptations of visual functions following deafness
Short term plasticity of audio-visual integration
Who We Are
FEDERICI
What We Publish
Crossmodal plasticity following short-term monocular deprivation.
Federici, A., Bernardi, G., Senna, I., Fantoni, M., Ernst, M. O., Ricciardi, E., & Bottari, D. (2023).
NeuroImage.
A brief period of monocular deprivation (MD) induces short-term plasticity of the adult visual system. Whether MD elicits neural changes beyond visual processing is yet unclear. Here, we assessed the specific impact of MD on neural correlates of multisensory processes. Neural oscillations associated with visual and audio-visual processing were measured for both the deprived and the non-deprived eye. Results revealed that MD changed neural activities associated with visual and multisensory processes in an eye-specific manner. Selectively for the deprived eye, alpha synchronization was reduced within the first 150 ms of visual processing. Conversely, gamma activity was enhanced in response to audio-visual events only for the non-deprived eye within 100–300 ms after stimulus onset. The analysis of gamma responses to unisensory auditory events revealed that MD elicited a crossmodal upweight for the non-deprived eye. Distributed source modeling suggested that the right parietal cortex played a major role in neural effects induced by MD. Finally, visual and audio-visual processing alterations emerged for the induced component of the neural oscillations, indicating a prominent role of feedback connectivity. Results reveal the causal impact of MD on both unisensory (visual and auditory) and multisensory (audio-visual) processes and, their frequency-specific profiles. These findings support a model in which MD increases excitability to visual events for the deprived eye and audio-visual and auditory input for the non-deprived eye.
A modality-independent proto-organization of human multisensory areas.
Setti, F., Handjaras, G., Bottari, D., Leo, A., Diano, M., Bruno, V., Tinti, C., Cecchetti, L., Garbarini, F., Pietrini, P., Ricciardi, E. (2023).
Nature Human Behaviour.
The processing of multisensory information is based upon the capacity of brain regions, such as the superior temporal cortex, to combine information across modalities. However, it is still unclear whether the representation of coherent auditory and visual events requires any prior audiovisual experience to develop and function. Here we measured brain synchronization during the presentation of an audiovisual, audio-only or video-only version of the same narrative in distinct groups of sensory-deprived (congenitally blind and deaf) and typically developed individuals. Intersubject correlation analysis revealed that the superior temporal cortex was synchronized across auditory and visual conditions, even in sensory-deprived individuals who lack any audiovisual experience. This synchronization was primarily mediated by low-level perceptual features, and relied on a similar modality-independent topographical organization of slow temporal dynamics. The human superior temporal cortex is naturally endowed with a functional scaffolding to yield a common representation across multisensory events.
Neuroplasticity following cochlear implants.
Pavani, F., & Bottari, D. (2022).
In Handbook of Clinical Neurology (Vol. 187, pp. 89-108). Elsevier.
Delayed Auditory Brainstem Responses (ABR) in children after sight-recovery
Martinelli, A., Bianchi, B., Fratini, C., Handjaras, G., Fantoni, M., Trabalzini, F., Polizzi, S., Caputo, R., Bottari, D. (2021) Neuropsychologia. https://doi.org/10.1016/j.neuropsychologia.2021.108089Studies in non-human animal models have revealed that in early development, the onset of visual input gates the critical period closure of some auditory functions. The study of rare individuals whose sight was restored after a period of congenital blindness offers the rare opportunity to assess whether early visual input is a prerequisite for the full development of auditory functions in humans as well. Here, we investigated whether a few months of delayed visual onset would affect the development of Auditory Brainstem Responses (ABRs). ABRs are widely used in the clinical practice to assess both functionality and development of the subcortical auditory pathway and, provide reliable data at the individual level. We collected Auditory Brainstem Responses from two case studies, young children (both having less than 5 years of age) who experienced a transient visual deprivation since birth due to congenital bilateral dense cataracts (BC), and who acquired sight at about two months of age. As controls, we tested 41 children (sighted controls, SC) with typical development, as well as two children who were treated (at about two months of age) for congenital monocular cataracts (MC). The SC group data served to predict, at the individual level, wave latencies of each BC and MC participant. Statistics were performed both at the single subject as well as at the group levels on latencies of main ABR waves (I, III, V and SN10). Results revealed delayed response latencies for both BC children compared with the SC group starting from the wave III. Conversely, no difference emerged between MC children and the SC group. These findings suggest that in case the onset of patterned visual input is delayed, the functional development of the subcortical auditory pathway lags behind typical developmental trajectories. Ultimately results are in favor of the presence of a crossmodal sensitive period in the human subcortical auditory system.
Visual search performance in cerebral visual impairment is associated with altered alpha band oscillations
Bennet, C. R., Bauer, C. M., Bex, P. J., Bottari*. D., Merabet*, L. B. (2021) Neuropsychologia. https://doi.org/10.1016/j.neuropsychologia.2021.108011*sharedInteractions between auditory statistics processing and visual experience emerge only in late development
Berto, M., Ricciardi, E., Pietrini, P., Bottari. D. (2021) iScience. https://doi.org/10.1016/j.isci.2021.103383Oscillatory signatures of Repetition Suppression and Novelty Detection reveal altered induced visual responses in early deafness
Bednaya, E., Pavani, F., Ricciardi, E., Pietrini, P., Bottari. D. (2021) Cortex. https://doi.org/10.1016/j.cortex.2021.05.017The ability to differentiate between repeated and novel events represents a fundamental property of the visual system. Neural responses are typically reduced upon stimulus repetition, a phenomenon called Repetition Suppression (RS). On the contrary, following a novel visual stimulus, the neural response is generally enhanced, a phenomenon referred to as Novelty Detection (ND). Here, we aimed to investigate the impact of early deafness on the oscillatory signatures of RS and ND brain responses. To this aim, electrophysiological data were acquired in early deaf and hearing control individuals during processing of repeated and novel visual events unattended by participants. By studying evoked and induced oscillatory brain activities, as well as inter-trial phase coherence, we linked response modulations to feedback and/or feedforward processes. Results revealed selective experience-dependent changes on both RS and ND mechanisms. Compared to hearing controls, early deaf individuals displayed: (i) greater attenuation of the response following stimulus repetition, selectively in the induced theta-band (4–7 Hz); (ii) reduced desynchronization following the onset of novel visual stimuli, in the induced alpha and beta bands (8–12 and 13–25 Hz); (iii) comparable modulation of evoked responses and inter-trial phase coherence. The selectivity of the effects in the induced responses parallels findings observed in the auditory cortex of deaf animal models following intracochlear electric stimulation. The present results support the idea that early deafness alters induced oscillatory activity and the functional tuning of basic visual processing.
Social cognition in the blind brain: A coordinate‐based meta‐analysis
Arioli, M., Ricciardi, E., & Cattaneo, Z. (2021) Human Brain Mapping, 42(5), 1243–1256. https://doi.org/10.1002/hbm.25289Three factors to characterize plastic potential transitions in the visual system.
Bottari, D., & Berto, M. (2021). Neuroscience & Biobehavioral Reviews, 126, 444-446.https://doi.org/10.1016/j.neubiorev.2021.03.035EEG frequency-tagging demonstrates increased left hemispheric involvement and crossmodal plasticity for face processing in congenitally deaf signers
Bottari, D., Bednaya, E., Dormal, G., Villwock, A., Dzhelyova, M., Grin, K., ... & Röder, B. (2020). NeuroImage, 223, 117315.https://doi.org/10.1016/j.neuroimage.2020.117315The sensory-deprived brain as a unique tool to understand brain development and function
Ricciardi, E., Bottari, D., Ptito, M., Roder, B., & Pietrini, P. (2020). Neurosci. Biobehav. Rev, 108, 78-82.https://doi.org/10.1016/j.neubiorev.2019.10.017See the whole Special Issue 'Rethinking the sensory-deprived brain: hints from the Blind Brain Workshop 2018' on Neuroscience and Biobehavioral Reviews
Methods we employ
Decompositions of EEG signals in time, frequency and time-frequency
EEG encoding and decoding algorithms
fMRI encoding/
decoding algorithms
Modeling approaches
Some of our recent talks
Davide Bottari- Talk : “Experience dependence brain plasticity revealed by temporary and permanent sensory deprivation”, Milab Bicocca, March, 2023
Martina Berto, Emiliano Ricciardi, Pietro Pietrini, Davide Bottari. Interactions between auditory statistics processing and visual experience emerge only in late development IMRF 2022, Ulm
Davide Bottari- Talk : “Experience dependence brain plasticity revealed by temporary and permanent sensory deprivation”, ICON , Helsinki, May, 2021
Emiliano Ricciardi - Invited Seminar: “Rethinking the sensory deprived brain”, University of Bologna, Cesena, April 7, 2020
Our Collaborations
The Blind Brain Consortium, (a data-sharing initiative comprising many labs around the world)
Stefan Debener (University of Oldenburg, Germany)
Marc Ernst (University of Ulm, Germany)
Francesca Garbarini (Università di Torino, Italy)
Elena Nava (Università Milano Bicocca Italy)
Benedetta Bianchi (Meyer Hospital, Florence, Italy)
Eva Orzan (Burlo Hospital, Trieste Italy)
Lotfi Merabet (harvard Medical School, USA)
Milan Scheidegger (University of Zurich, Switzerland)
Brigitte Roder (University of Hamburg, Germany)
Zaira Cattaneo (University of Milan Bicocca, Italy)
Tomaso Vecchi (University of Pavia, Italy)
Francesco Pavani (University of Trento, Italy)
Silvia Chelazzi and Massimo Diodati (UIC)