Role of nicotinic acetylcholine receptor subunits in the mode of action of neonicotinoid, sulfoximine and spinosyn insecticides in Drosophila melanogaster.


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
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

103547

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Trent Perry (T)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia. Electronic address: trentp@unimelb.edu.au.

Wei Chen (W)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia.

Razi Ghazali (R)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia.

Ying Ting Yang (YT)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia.

Danielle Christesen (D)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia.

Felipe Martelli (F)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia.

Chris Lumb (C)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia; Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Parkville, Victoria, 3052, Australia.

Hang Ngoc Bao Luong (HN)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia.

Judith Mitchell (J)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia.

Jessica K Holien (JK)

St. Vincent's Institute of Medical Research, 9 Princes St, Fitzroy, Victoria, 3065, Australia.

Michael W Parker (MW)

St. Vincent's Institute of Medical Research, 9 Princes St, Fitzroy, Victoria, 3065, Australia; Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia.

Thomas C Sparks (TC)

Corteva Agriscience, 9330 Zionville Road, Indianapolis, IN, 46268, USA.

Philip Batterham (P)

School of BioSciences, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, Victoria, 3010, Australia.

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Classifications MeSH