Abstract
Animals that ingest toxins can themselves become toxic or unpalatable to predators and parasites. Because most animals rapidly eliminate toxins to survive toxin ingestion, it is unclear how species transition from susceptibility and toxin elimination to tolerance and accumulation as chemical defense emerges. Studies of chemical defense have generally focused on species that display active toxin sequestration and target-site insensitivity mutations that permit survival without necessitating toxin metabolism. Here we investigate whether animals that presumably rely on toxin elimination for survival can also utilize ingested toxins for defense. We use the A4 and A3 Drosophila melanogaster fly strains from the Drosophila Synthetic Population Resource (DSPR), which respectively possess elevated and reduced metabolic resistance to nicotine. We find that ingesting nicotine increased the survival of A4 but not of A3 flies against Leptopilina heterotoma wasp parasitism. Further, we find that despite possessing enhanced toxin clearance mechanisms, A4 flies accrued more nicotine than A3 individuals. Our results suggest that enhanced metabolic detoxification can allow for greater toxin intake by offsetting the cost of toxin ingestion. Passive toxin accumulation that accompanies increased toxin intake may underlie the early origins of chemical defense.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
↵+ Authors listed in alphabetical order