Drosophila Avoids Parasitoids by Sensing Their Semiochemicals via a Dedicated Olfactory Circuit.

Drosophila Avoids Parasitoids by Sensing Their Semiochemicals via a Dedicated Olfactory Circuit.
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DOI:
10.1371/journal.pbio.1002318
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发表时间:
2015-12
期刊:
影响因子:
9.8
通讯作者:
Knaden M
Knaden M
中科院分区:
生物学1区
文献类型:
--
作者:
Ebrahim SA;Dweck HK;Stökl J;Hofferberth JE;Trona F;Weniger K;Rybak J;Seki Y;Stensmyr MC;Sachse S;Hansson BS;Knaden M

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Detecting danger is one of the foremost tasks for a neural system. Larval parasitoids constitute clear danger to Drosophila, as up to 80% of fly larvae become parasitized in nature. We show that Drosophila melanogaster larvae and adults avoid sites smelling of the main parasitoid enemies, Leptopilina wasps. This avoidance is mediated via a highly specific olfactory sensory neuron (OSN) type. While the larval OSN expresses the olfactory receptor Or49a and is tuned to the Leptopilina odor iridomyrmecin, the adult expresses both Or49a and Or85f and in addition detects the wasp odors actinidine and nepetalactol. The information is transferred via projection neurons to a specific part of the lateral horn known to be involved in mediating avoidance. Drosophila has thus developed a dedicated circuit to detect a life-threatening enemy based on the smell of its semiochemicals. Such an enemy-detecting olfactory circuit has earlier only been characterized in mice and nematodes. A dedicated olfactory circuit helps the fruit fly to implement avoidance behavior in response to semiochemicals produced by its main parasitoid enemy – wasps of the genus Leptopilina. Detecting danger is a fundamental task for an animal. Larval parasitoids constitute clear danger to the vinegar fly D. melanogaster as up to 80% of fly larvae become parasitized in nature. We show that Drosophila larvae crawl away from places that smell like the main parasitoid enemies, Leptopilina wasps. Furthermore, Drosophila adult females avoid laying eggs at those places. This avoidance is mediated via a highly specific olfactory sensory neuron type that is tuned to detect three odors of the parasitoid, including the wasps sex pheromone iridomyrmecin. We identify the neuron type, the receptors, and the odor ligands that mediate this behavior and also show that this neuronal system is both necessary and sufficient to govern the parasitoid avoidance behavior. We also find evidence that this odor-based Leptopilina wasp avoidance is conserved across several Drosophila species.