Predator-secreted sulfolipids induce defensive responses in C. elegans

Animals respond to predators by altering their behavior and physiological states, but the underlying signaling mechanisms are poorly understood. Using the interactions between Caenorhabditis elegans and its predator, Pristionchus pacificus , we show that neuronal perception by C. elegans of a predat...

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Veröffentlicht in:Nature communications 2018-03, Vol.9 (1), p.1128-13, Article 1128
Hauptverfasser: Liu, Zheng, Kariya, Maro J., Chute, Christopher D., Pribadi, Amy K., Leinwand, Sarah G., Tong, Ada, Curran, Kevin P., Bose, Neelanjan, Schroeder, Frank C., Srinivasan, Jagan, Chalasani, Sreekanth H.
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Sprache:eng
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Zusammenfassung:Animals respond to predators by altering their behavior and physiological states, but the underlying signaling mechanisms are poorly understood. Using the interactions between Caenorhabditis elegans and its predator, Pristionchus pacificus , we show that neuronal perception by C. elegans of a predator-specific molecular signature induces instantaneous escape behavior and a prolonged reduction in oviposition. Chemical analysis revealed this predator-specific signature to consist of a class of sulfolipids, produced by a biochemical pathway required for developing predacious behavior and specifically induced by starvation. These sulfolipids are detected by four pairs of C. elegans amphid sensory neurons that act redundantly and recruit cyclic nucleotide-gated (CNG) or transient receptor potential (TRP) channels to drive both escape and reduced oviposition. Functional homology of the delineated signaling pathways and abolishment of predator-evoked C. elegans responses by the anti-anxiety drug sertraline suggests a likely conserved or convergent strategy for managing predator threats. Defensive behavioral responses can be triggered by predator-released odors. Here, the authors identified the relevant Pristionchus pacificus -released sulfolipid molecules and dissected the neural circuits underlying C. elegans response to this predator.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-018-03333-6