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Carrara, S.

Publications and source records attributed to Carrara, S..

2 recordsLinked to original sources

Orsay virus infection is associated with reduced locomotion and alters cue-dependent food choice in Caenorhabditis elegans

Behavioral responses are an important component of host defense; however, most evidence in Caenorhabditis elegans comes from bacterial pathogens. Here, we tested whether infection with Orsay virus (OrV) alters host dispersal and food choice and whether these responses involve the RNA-processing factor EOL-1. When measuring distance travelled over a certain period of time in control and infected wild-type animals, we observed that OrV infection was associated with lower locomotion. Moreover, when presenting infected and control animals with food choices, we observed that infected animals preferred OrV infected food sources only when the alternative was a pure food source, preferring a non-inoculated food source when both control and viral food sources contained a C. elegans filtrate. Moreover, loss of EOL-1 altered baseline locomotion and attenuated the infection-associated reduction detected in the earlier motility assay, while also modifying the food choice response, suggesting that eol-1 contributes to the motility and behavioral changes induced by OrV infection. Collectively, these results support an overall association between OrV infection and reduced host dispersal, whereas its effect on food choice depends on the sensory context. These findings extend infection-associated behavioral responses to a natural viral pathogen and identify eol-1 as a modulator of their expression.

microbiology↗

Flow-Triggered Regeneration of Electrochemical Aptasensor for Continuous Monitoring of 17β-Estradiol

Continuous biomarker monitoring with affinity biosensors remains limited by probe saturation, slow dissociation, signal carryover, and regeneration methods that require chemical washing, harsh buffers, or external reset modules. Here, we report a flow-programmed, self-regenerative electrochemical aptamer-based biosensor for continuous 17{beta}-estradiol monitoring. The platform restores the sensing interface by tuning buffer flow through the device, enabling repeated sensing-regeneration cycles without chemical stripping or active-reset hardware. The biosensor achieves a 1.46 pM limit of detection, and a log-linear dynamic range from 100 pM to 1 M in real human sweat, covering physiologically relevant estradiol concentrations. It exhibits high selectivity, with responses to potential molecularly similar interferents remaining below 10% of the 17{beta}-estradiol signal. Under dynamic flow operation, the device shows reversible signal recovery and stable electrochemical performance, with higher buffer-wash flow reducing baseline carryover between measurements. A coupled binding-transport simulation captures the flow-dependent regeneration trends and maps how wash-flow rate, wash duration, and apparent aptamer affinity affect regeneration efficiency. Ex vivo testing in real human sweat, including samples from pregnant women, supports translational relevance. This work establishes buffer-flow programming as a reagent-free route to regenerable electrochemical aptamer sensing for automated, wearable-compatible estradiol monitoring.

bioengineering↗