Ecological and social cues orchestrate concerted courtship in Drosophila

Abstract Mating decisions are often attributed to the sensory signalling between prospective sexual partners. Yet these interactions are also shaped by the broader environmental context in which they unfold, to appropriately align sexual arousal with reproductive opportunities 1–6 . Here we show that in Drosophila erecta mating is strictly contingent on the ecological and social environment generated as flies densely aggregate in groups on a food patch. We find that food volatiles directly promote male sexual arousal, triggering individuals to sample and pursue potential mates, giving rise to dynamic interactions across the group. The ensuing visual motion transforms each male’s visual field, which in turn further amplifies his arousal, generating a multisensory feedback loop that coordinately promotes courtship across individuals. D. erecta ’s strict dependence on environmental cues appears latent in related species, such as Drosophila melanogaster , where food odour can promote arousal 7 but is dispensable for vigorous courtship. Comparative circuit analyses show that species-specific thresholds for sexual arousal reflect variation in how olfactory input modulates conserved nodes controlling courtship drive, rendering food volatiles a strict sensory gate only in D. erecta . Together, our findings highlight how environmental cues not directly tied to sexual signalling can profoundly influence reproductive behaviour and reorganize the social landscape to ensure mating occurs in contexts where reproductive opportunities are abundant.

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Publication Details

Journal
Nature
Published
2026-11-04
DOI
https://doi.org/10.1038/s41586-026-11209-9
Citations
3
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
Field-Weighted Citation Impact
5.88

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article

Ecological and social cues orchestrate concerted courtship in Drosophila

Philipp Brand, Lucia L. Prieto-Godino, Rory T. Coleman, Sarah Zylka et al.
3 citations
Nature
Neurobiology and Insect Physiology Research
5.88
article

Ecological and social cues orchestrate concerted courtship in Drosophila

Philipp Brand, Lucia L. Prieto-Godino, Rory T. Coleman, Sarah Zylka, Vanessa Ruta, Katherine Keller, Noelle B. Eghbali
article en
3 citations

Abstract

Abstract Mating decisions are often attributed to the sensory signalling between prospective sexual partners. Yet these interactions are also shaped by the broader environmental context in which they unfold, to appropriately align sexual arousal with reproductive opportunities 1–6 . Here we show that in Drosophila erecta mating is strictly contingent on the ecological and social environment generated as flies densely aggregate in groups on a food patch. We find that food volatiles directly promote male sexual arousal, triggering individuals to sample and pursue potential mates, giving rise to dynamic interactions across the group. The ensuing visual motion transforms each male’s visual field, which in turn further amplifies his arousal, generating a multisensory feedback loop that coordinately promotes courtship across individuals. D. erecta ’s strict dependence on environmental cues appears latent in related species, such as Drosophila melanogaster , where food odour can promote arousal 7 but is dispensable for vigorous courtship. Comparative circuit analyses show that species-specific thresholds for sexual arousal reflect variation in how olfactory input modulates conserved nodes controlling courtship drive, rendering food volatiles a strict sensory gate only in D. erecta . Together, our findings highlight how environmental cues not directly tied to sexual signalling can profoundly influence reproductive behaviour and reorganize the social landscape to ensure mating occurs in contexts where reproductive opportunities are abundant.

Nature
Boston University (US), Howard Hughes Medical Institute (US), The Francis Crick Institute (GB), Max Planck Institute for Brain Research (DE), New York University (US), Rockefeller University (US)
Howard Hughes Medical Institute, Wellcome Trust, Francis Crick Institute, Cancer Research UK, National Institutes of Health, Medical Research Council, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, H2020 European Research Council
Openalex Percentile: Top 5%
Neurobiology and Insect Physiology Research
5.88
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