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Biology subjects

Halder, N.

Publications and source records attributed to Halder, N..

2 recordsLinked to original sources

Nutritional Regulation of DN1a-Dh44 Signaling Modulates Sleep Across the Lifespan

Across species, sleep amount and timing are tightly linked to the nutritional environment. While early life sleep and sleep in mature organisms are both dramatically influenced by reductions in the dietary environment, the mechanisms linking nutritional cues to conserved sleep-regulatory circuitry are not well understood. Using both early 3rd instar (L3) Drosophila larvae and adults, we examined the plasticity of sleep responses under shifting nutrient environments across the lifespan. We find that L3 larvae and adults exhibit changes in sleep duration in low sugar environments with L3 showing a loss of sleep-wake rhythms that can be rescued with additional nutrients. We show that larval and adult sleep plasticity is regulated by CCHamide-1 signaling between DN1a and Dh44 neurons and glucose metabolic genes in Dh44 neurons. Additionally, our data indicate that sleep plasticity is not dependent on anatomical and functional connectivity between clock-arousal circuitry, suggesting that peptidergic signaling alone is sufficient for diet-dependent sleep regulation. Finally, we demonstrate that Dh44 neurons in both L3 larvae and adults adjust mRNA levels of CCHamide-1 receptor (CCHa1-R) in response to changes in dietary sugar. Together, our findings suggest that organisms utilize conserved molecular signaling pathways across the lifespan to dynamically regulate their sleep in a changing environment.

neuroscience↗

Development and Analytical Evaluation of a Point-of-Care Electrochemical Biosensor for Rapid and Accurate SARS-CoV-2 Detection

The COVID-19 pandemic has underscored the critical need for rapid and accurate screening and diagnostic methods for potential respiratory viruses. Existing COVID-19 diagnostic approaches face limitations either in terms of turnaround time or accuracy. In this study, we present an electrochemical biosensor that offers nearly instantaneous and precise SARS-CoV-2 detection, suitable for point-of-care and environmental monitoring applications. The biosensor employs a stapled hACE-2 N-terminal alpha helix peptide to functionalize an in-situ grown polypyrrole conductive polymer on a nitrocellulose membrane backbone through a chemical process. We assessed the biosensors analytical performance using heat-inactivated omicron and delta variants of the SARS-CoV-2 virus in artificial saliva (AS) and nasal swabs (NS) samples diluted in a strong ionic solution. Virus identification was achieved through electrochemical impedance spectroscopy (EIS) and frequency analyses. The assay demonstrated a limit of detection of 40 TCID50/mL, with 95% sensitivity and 100% specificity. Notably, the biosensor exhibited no cross-reactivity when tested against the influenza virus. The entire testing process using the biosensor takes less than a minute. In summary, our biosensor exhibits promising potential in the battle against pandemic respiratory viruses, offering a platform for the creation of rapid, compact, portable, and point-of-care devices capable of multiplexing various viruses. This groundbreaking development has the capacity to significantly bolster our readiness and response to future viral outbreaks.

bioengineering↗