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Biology subjects

Cavaliere, C.

Publications and source records attributed to Cavaliere, C..

4 recordsLinked to original sources

Sustained dynamics of saccadic inhibition and adaptive oculomotor responses during continuous exploration

In natural environments, stimuli often recur across time and space, requiring the visual system to remain sensitive to novelty while managing predictability. A central question in systems neuroscience is how motor systems adapt to repeated sensory events without compromising responsiveness. We investigated this adaptive capacity using saccadic inhibition (SI)--a reflexive suppression of eye movements triggered by sudden visual transients--as a probe of oculomotor dynamics during naturalistic viewing. Human participants (N = 21) freely explored visual arrays while brief gaze-contingent flashes appeared five times at random intervals, either foveally or parafoveally. SI reliably occurred [~]120 ms post-flash across repetitions and locations, indicating robust sensory-driven inhibition. However, the rebound phase--reflecting saccade reprogramming--showed a progressive decline. In a second experiment (N = 19), only the first or the fifth flash was visible on each trial. In this case, neither inhibition nor rebound was altered, suggesting that the rebound decline is driven by repeated sensory stimulation rather than exploration time. This dissociation reveals selective habituation of motor re-engagement mechanisms, while reflexive inhibitory gating remains stable. We propose that inhibition is mediated by circuitry that transiently suppresses saccade initiation and resists habituation. By contrast, the weakening rebound reflects a separate, habituation-prone route that reduces saccade generation to irrelevant events. Functionally, this imbalance implies a recalibration within the saccade generator, preserving inhibitory capacity while constraining motor output. Our findings uncover a distinct form of oculomotor habituation and demonstrate how SI reveals dynamic decoupling of sensory input and motor output under repeated stimulation. Significance StatementThe ability to interrupt and resume eye movements in response to environmental changes is fundamental to visual exploration. We investigated how this process unfolds across repeated visual transients in naturalistic conditions. Our findings show that saccadic inhibition remains stable across time, whereas the subsequent rebound phase habituates. This dissociation suggests that distinct processes mediate reflexive interruption and motor recovery habituation. Our data indicate that dynamic modulation of motor gating circuits is a mechanism for optimizing oculomotor behavior. These results deepen our understanding of visual-motor coordination, provide insight about the constraints governing the underlying system circuitry, and may inform clinical tools for assessing sensorimotor adaptability in health and disease.

neuroscience↗

Clinical connectome fingerprints of cognitive decline

Brain connectome fingerprinting is rapidly rising as a novel influential field in brain network analysis. Yet, it is still unclear whether connectivity fingerprints could be effectively used for mapping and predicting disease progression from human brain data. We hypothesize that dysregulation of brain activity in disease would reflect in worse subject identification. Hence, we propose a novel framework, Clinical Connectome Fingerprinting, to detect individual connectome features from clinical populations. We show that "clinical fingerprints" can map individual variations between elderly healthy subjects and patients undergoing cognitive decline in functional connectomes extracted from magnetoencephalography data. We find that identifiability is reduced in patients as compared to controls, and show that these connectivity features are predictive of the individual Mini-Mental State Examination (MMSE) score in patients. We hope that the proposed methodology can help in bridging the gap between connectivity features and biomarkers of brain dysfunction in large-scale brain networks.

neuroscience↗

Single species RNA purification with DNA nanoswitches

We report a novel method to purify individual RNA species using programmable DNA nanoswitches to facilitate RNA capture, release, and isolation. We validate sequence-based purification of microRNA, rRNA, and an mRNA fragment from total RNA, demonstrate multiplexing with two different RNA species, and show an application with downstream LC/MS analysis to identify RNA modifications. The simplicity, low cost, and low sample requirements of our method make it suitable for easy adoption.Competing Interest StatementLZ, ARC, and KH have intellectual property related to DNA nanoswitches. All other authors declare no competing interests.View Full Text

molecular biology↗

Programmable low-cost DNA-based platform for viral RNA detection

Viral detection is critical for controlling disease spread and progression. Recent emerging viral threats including Zika, Ebola, and the current COVID-19 outbreak highlight the cost and difficulty in responding rapidly. To address these challenges, we develop a platform for low-cost and rapid detection of viral RNA with DNA nanoswitches designed to mechanically reconfigure in response to specific viruses. Using Zika virus as a model system, we show non-enzymatic detection of viral RNA to the attomole level, with selective and multiplexed detection between related viruses and viral strains. For clinical-level sensitivity in biological fluids, we paired the assay with a sample preparation step using either RNA extraction or isothermal pre-amplification. Our assay can be performed with minimal or no lab infrastructure, and is readily adaptable to detect other viruses. We demonstrate the adaptability of our method by quickly developing and testing DNA nanoswitches for detecting a fragment of SARS-CoV-2 RNA in human saliva. Given this versatility, we expect that further development and field implementation will improve our ability to detect emergent viral threats and ultimately limit their impact.

bioengineering↗