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Biology subjects

Probst, R.

Publications and source records attributed to Probst, R..

2 recordsLinked to original sources

Social context modulates cannibalistic attraction in Drosophila larvae

Animals often face conflicting decisions to ensure survival. Under food limitation, cannibalism can provide a nutritional advantage despite substantial costs. In Drosophila melanogaster larvae, feeding is essential for successful metamorphosis, making food source decisions critical. We find that dead conspecifics act as attractive cues, but this attraction is weak for live larval groups. It is enhanced when dead larvae are injured or homogenized, or after repeated exposure. Larvae are also more attracted to dead individuals from other Drosophila or insect species. Testing live larvae individually revealed the strongest attraction, indicating that social context suppresses feeding-related attraction. Attraction to dead conspecifics depends on multiple chemosensory and mechanosensory modalities, highlighting the complex integration of social and nutritional cues in larval decision-making. Our results indicate that fly larvae flexibly balance attraction and avoidance based on social context to optimize resource use under ecological constraints. Short summaryDrosophila melanogaster larvae flexibly balance attraction and social avoidance when encountering dead conspecifics. Attraction depends on carcass condition, prior experience, and social context, and is mediated by chemosensory, gustatory, and mechanosensory pathways. These findings reveal how larvae integrate multimodal social and nutritional cues to guide context-dependent feeding decisions.

neuroscience↗

A polymer gel index-matched to water enables diverse applications in fluorescence microscopy

We demonstrate diffraction-limited and super-resolution imaging through thick layers (tens-hundreds of microns) of BIO-133, a biocompatible, UV-curable, commercially available polymer with a refractive index (RI) matched to water. We show that cells can be directly grown on BIO-133 substrates without the need for surface passivation and use this capability to perform extended time-lapse volumetric imaging of cellular dynamics 1) at isotropic resolution using dual-view light-sheet microscopy, and 2) at super-resolution using instant structured illumination microscopy. BIO-133 also enables immobilization of 1) Drosophila tissue, allowing us to track membrane puncta in pioneer neurons, and 2) Caenorhabditis elegans, which allows us to image and inspect fine neural structure and to track pan-neuronal calcium activity over hundreds of volumes. Finally, BIO-133 is compatible with other microfluidic materials, enabling optical and chemical perturbation of immobilized samples, as we demonstrate by performing drug and optogenetic stimulation on cells and C. elegans.

bioengineering↗