Role of nicotinic acetylcholine receptor subunits in the mode of action of neonicotinoid, sulfoximine and spinosyn insecticides in Drosophila melanogaster.
Animals
Drosophila Proteins
/ metabolism
Drosophila melanogaster
/ genetics
Drug Combinations
Insecticide Resistance
/ genetics
Insecticides
/ pharmacology
Macrolides
/ pharmacology
Mutation
Neonicotinoids
/ pharmacology
Pyridines
/ pharmacology
Receptors, Nicotinic
/ drug effects
Sulfur Compounds
/ pharmacology
Imidacloprid
Insecticide resistance
Nicotinic acetylcholine receptor
Nitenpyram
Spinosad
Sulfoxaflor
Journal
Insect biochemistry and molecular biology
ISSN: 1879-0240
Titre abrégé: Insect Biochem Mol Biol
Pays: England
ID NLM: 9207282
Informations de publication
Date de publication:
04 2021
04 2021
Historique:
received:
07
09
2020
revised:
28
01
2021
accepted:
29
01
2021
pubmed:
7
2
2021
medline:
30
7
2021
entrez:
6
2
2021
Statut:
ppublish
Résumé
Insecticides remain valuable tools for the control of insect pests that significantly impact human health and agriculture. A deeper understanding of insecticide targets is important in maintaining this control over pests. Our study systematically investigates the nicotinic acetylcholine receptor (nAChR) gene family, in order to identify the receptor subunits critical to the insect response to insecticides from three distinct chemical classes (neonicotinoids, spinosyns and sulfoximines). Applying the CRISPR/Cas9 gene editing technology in D. melanogaster, we were able to generate and maintain homozygous mutants for eight nAChR subunit genes. A ninth gene (Dβ1) was investigated using somatic CRISPR in neural cells to overcome the low viability of the homozygous germline knockout mutant. These findings highlight the specificity of the spinosyn class insecticide, spinosad, to receptors containing the Dα6 subunit. By way of contrast, neonicotinoids are likely to target multiple receptor subtypes, beyond those receptor subunit combinations previously identified. Significant differences in the impacts of specific nAChR subunit deletions on the resistance level of flies to neonicotinoids imidacloprid and nitenpyram indicate that the receptor subtypes they target do not completely overlap. While an R81T mutation in β1 subunits has revealed residues co-ordinating binding of sulfoximines and neonicotinoids differ, the resistance profiles of a deletion of Dβ1 examined here provide new insights into the mode of action of sulfoxaflor (sulfoximine) and identify Dβ1 as a key component of nAChRs targeted by both these insecticide classes. A comparison of resistance phenotypes found in this study to resistance reported in insect pests reveals a strong conservation of subunit targets across many different insect species and that mutations have been identified in most of the receptor subunits that our findings would predict to have the potential to confer resistance.
Identifiants
pubmed: 33548485
pii: S0965-1748(21)00030-8
doi: 10.1016/j.ibmb.2021.103547
pii:
doi:
Substances chimiques
Drosophila Proteins
0
Drug Combinations
0
Insecticides
0
Macrolides
0
Neonicotinoids
0
Pyridines
0
Receptors, Nicotinic
0
Sulfur Compounds
0
sulfoxaflor
671W88OY8K
spinosad
XPA88EAP6V
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
103547Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.