# Assessing species-specific neonicotinoid toxicity using cross-species chimeric nicotinic acetylcholine receptors in a Drosophila model

**Authors:** Anna Lassota, James J. L. Hodge, Matthias Soller

PMC · DOI: 10.1038/s41598-025-20109-3 · Scientific Reports · 2025-10-16

## TL;DR

Researchers used fruit flies to study how changes in a specific brain receptor affect sensitivity to insecticides, finding that swapping parts of the receptor reduced toxicity but impaired movement.

## Contribution

A novel cross-species chimeric nicotinic acetylcholine receptor model was created to assess neonicotinoid toxicity differences between species.

## Key findings

- Flies with the α8/β2 chimeric receptor showed impaired motor functions in climbing and flight assays.
- Flies with the chimeric receptor or β2 knock-out had increased survival after neonicotinoid exposure compared to wild-type flies.
- Combinatorial insecticide exposure did not reveal significant differences in survival.

## Abstract

Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels and the main mediators of synaptic neurotransmission in the insect brain. In insects, nAChRs are pivotal for sensory processing, cognition and motor control, and are the primary target of neonicotinoid insecticides. Neonicotinoids are potent neurotoxins, and pollinators such as honey bees are more sensitive and affected by extremely low sub-lethal doses. nAChR subtypes exist as homomers of α-subunits or heteromers composed of α and β subunits. The honey bee nAChRα8 subunit is orthologous to nAChRβ2 in Drosophila, raising the question of whether this α to β change makes flies less sensitive to neonicotinoids. To investigate species-specific aspects of neonicotinoid toxicity, we CRISPR-Cas9 engineered a cross-species chimeric nAChR subunit by swapping the ligand-binding domain in Drosophila of nAChRβ2 with honey bee nAChRα8. Phenotypic assessment revealed significantly impaired motor functions in climbing and flight assays when comparing flies carrying the α8/β2 chimeric channel to wild type or a β2 knock-out. Despite these motor deficits, both flies expressing the α8/β2 chimeric receptor and β2 knock-out flies showed significantly increased survival after exposure to neonicotinoids thiamethoxam and clothianidin, compared to wild type flies. Combinatorial exposure to different insecticides did not reveal differences. These findings highlight the critical role of nAChR subunit composition in motor control, and demonstrate how subtle structural modifications within a single nAChR subunit can profoundly impact motor function and pesticide response, offering new insights into the molecular mechanisms of neurotoxicity across species.

The online version contains supplementary material available at 10.1038/s41598-025-20109-3.

## Linked entities

- **Genes:** CHRNB2 (cholinergic receptor nicotinic beta 2 subunit) [NCBI Gene 1141], nAChRa8 (nicotinic acetylcholine receptor alpha 8 subunit) [NCBI Gene 658018]
- **Proteins:** nAChRa8 (nicotinic acetylcholine receptor alpha 8 subunit), CHRNB2 (cholinergic receptor nicotinic beta 2 subunit)
- **Chemicals:** thiamethoxam (PubChem CID 5821911), clothianidin (PubChem CID 86287519)
- **Species:** Drosophila (taxon 7215)

## Full-text entities

- **Genes:** nAChRbeta2 [NCBI Gene 726079], nAChRalpha8 [NCBI Gene 406082]
- **Diseases:** neurotoxicity (MESH:D020258), motor (MESH:D000068079), toxicity (MESH:D064420)
- **Chemicals:** neonicotinoid insecticides (-), thiamethoxam (MESH:D000077922), Neonicotinoids (MESH:D000073943), clothianidin (MESH:C480342)
- **Species:** Drosophila melanogaster (fruit fly, species) [taxon 7227], Apis mellifera (bee, species) [taxon 7460], Diptera (flies, order) [taxon 7147]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12533226