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Updated: May 10, 2025

Topical Application Bioassay to Quantify Insecticide Toxicity for Mosquitoes and Fruit Flies
Published on: January 19, 2022
Impacts of short-term ivermectin exposures on fruit flies
M Yusuf Ali1, Carl K Namini2, John M Clark3
1Department of Biological Sciences, Southern Illinois University, Edwardsville, IL 62026, USA.
Abstract:
A short-term ivermectin (IVM) exposure method was newly established to demonstrate effects of sublethal concentrations of IVM on the wild-type fruit fly, Drosophila melanogaster. Using a conventional glass-vial contact approach, exposures to IVM (0.01 to 1000 ppm) for 12 h durations or less were selected to assess the downstream impacts of short-term IVM exposures (STIEs) on fruit flies. Under these conditions, all female flies produced significantly higher levels of reactive oxygen species and malondialdehydes in their ovaries. Additionally, females treated with IVM for 12 h under the STIE conditions exhibited significantly increased levels of DNA damages in their ovaries. Despite the negative impacts described above, the mean percent hatchability values obtained from the eggs oviposited by the IVM-exposed females were not statistically different when compared to the hatchability of the unexposed females. Two concentrations (1 and 10 ppm) of IVM were selected to determine transgenerational effects following short-term IVM exposures. F1, F2 and F8 flies exposed to IVM showed significantly delayed developments (2.5-3.2, 2.5-3.0, and 0.9-1.3 days delayed, respectively). F5, F11 and F17 females showed significantly delayed IVM-induced sluggish behaviors in the presence of lethal IVM (1 %, w/v). F18 females transgenerationally exposed to 1 ppm IVM exhibited significantly increased levels of Mrp1 (8.7-fold) and Cyp6g2 (5.9-fold) transcripts compared to unexposed flies. Comparatively, F18 females transgenerationally exposed to 10 ppm IVM showed significantly increased levels of Cyp9f2 (2.6-fold) transcripts. Current study clearly demonstrated the effects of sublethal IVM on parent and filial generations of fruit flies, providing an important step toward understanding development of IVM resistance under the STIE conditions.
Insights
Short-term ivermectin exposure in fruit flies caused ovarian damage but did not affect egg hatchability. Subsequent generations showed developmental delays and altered gene expression, indicating potential ivermectin resistance development.
Area of Science:
- Toxicology
- Genetics
- Entomology
Background:
- Ivermectin (IVM) is a widely used antiparasitic drug.
- Understanding the effects of sublethal IVM concentrations is crucial for assessing environmental and health risks.
- The fruit fly, Drosophila melanogaster, serves as a model organism for studying toxicological impacts.
Purpose of the Study:
- To establish a short-term ivermectin exposure (STIE) method for Drosophila melanogaster.
- To investigate the downstream impacts of STIEs on parent and filial generations of fruit flies.
- To explore the potential development of IVM resistance.
Main Methods:
- Fruit flies were exposed to varying concentrations of IVM (0.01–1000 ppm) for durations of 12 hours or less.
- Ovarian damage was assessed by measuring reactive oxygen species and malondialdehydes.
- DNA damage, egg hatchability, developmental delays, behavioral changes, and gene expression (Mrp1, Cyp6g2, Cyp9f2) were analyzed across generations.
Main Results:
- Short-term ivermectin exposure led to increased reactive oxygen species, malondialdehydes, and DNA damage in female fruit fly ovaries.
- Despite ovarian damage, egg hatchability remained unaffected.
- Transgenerational effects included significantly delayed development in F1, F2, and F8 generations, and altered expression of detoxification genes (Mrp1, Cyp6g2, Cyp9f2) in F18 females.
Conclusions:
- Sublethal ivermectin exposure has detrimental effects on the parent generation of fruit flies.
- Short-term ivermectin exposures can induce transgenerational effects, including developmental delays and altered gene expression.
- The findings provide insights into the mechanisms underlying ivermectin resistance development.

