Experience-dependent plasticity of a highly specific olfactory circuit in Drosophila melanogaster

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Abstract

Drosophila melanogaster encounters a variety of odor cues signaling potentially harmful threats through-out its life, which are detected by highly specialized olfactory circuits enabling the animal to avoid them. We studied whether such crucial neuronal pathways are hard-wired or can be modulated by experience. Using long-term exposure to high concentrations of geosmin, an indicator of potentially lethal microorganisms, we demonstrate at the single-cell level that the underlying neuronal circuitry undergoes structural changes in the antennal lobe, while higher brain centers remain unaffected. In particular, second-order neurons show neurite extensions and synaptic remodeling after the exposure period, whereas olfactory sensory neurons and glia cells remain unaffected. Flies that were exposed to geosmin tolerate this innately aversive odorant in general choice and oviposition assays. We show that even a highly specific olfactory circuit is plastic and adaptable to environmental changes.

HIGHLIGHTS

  • The highly specific geosmin circuit is modulated by experience-dependent plasticity

  • PN dendritic extensions cause a volumetric increase of the geosmin-detecting glomerulus

  • LNs are remodeled while OSNs and glia cells remain unaffected by long-term exposure

  • Flies adapt their behavior to an odorant signaling a potential lethal threat

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  1. Excerpt

    How flies get used to the smell of death: new study shows brain changes and behavioral adaptation in Drosophila to a highly repulsive odor.