Role of nicotinic acetylcholine receptor subunits in the mode of action of neonicotinoid, sulfoximine and spinosyn insecticides in Drosophila melanogaster. (April 2021)
- Record Type:
- Journal Article
- Title:
- Role of nicotinic acetylcholine receptor subunits in the mode of action of neonicotinoid, sulfoximine and spinosyn insecticides in Drosophila melanogaster. (April 2021)
- Main Title:
- Role of nicotinic acetylcholine receptor subunits in the mode of action of neonicotinoid, sulfoximine and spinosyn insecticides in Drosophila melanogaster
- Authors:
- Perry, Trent
Chen, Wei
Ghazali, Razi
Yang, Ying Ting
Christesen, Danielle
Martelli, Felipe
Lumb, Chris
Bao Luong, Hang Ngoc
Mitchell, Judith
Holien, Jessica K.
Parker, Michael W.
Sparks, Thomas C.
Batterham, Philip - Abstract:
- Abstract: 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 hereAbstract: 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. Graphical abstract: Image 1 Highlights: CRISPR/Cas9 used to systematically analyse the insect nAChR gene family. Eight of the nine nAChR subunit mutants created could be maintained as homozygotes. Receptor subunit combinations targeted within and between insecticide classes vary. Insecticide targets are highly conserved across insect species. … (more)
- Is Part Of:
- Insect biochemistry and molecular biology. Volume 131(2021)
- Journal:
- Insect biochemistry and molecular biology
- Issue:
- Volume 131(2021)
- Issue Display:
- Volume 131, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 131
- Issue:
- 2021
- Issue Sort Value:
- 2021-0131-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-04
- Subjects:
- Insecticide resistance -- Nicotinic acetylcholine receptor -- Sulfoxaflor -- Spinosad -- Imidacloprid -- Nitenpyram
Imidacloprid (IMI) -- Sulfoxaflor (SFX) -- Nitenpyram (NIT) -- Spinosad (SPIN) -- Nicotinic acetylcholine receptor (nAChR) -- Insecticide Resistance Action Committee (IRAC) -- Insecticide resistance management (IRM) -- Resistance ratio RR) -- Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) -- CRISPR Associated protein 9 (Cas9)
Insect biochemistry -- Periodicals
Insects -- Physiology -- Periodicals
Insects -- Molecular aspects -- Periodicals
Biochemistry -- Periodicals
Insectes -- Biochimie -- Périodiques
Insectes -- Composition -- Périodiques
Insectes -- Physiologie -- Périodiques
Insectes -- Aspect moléculaire -- Périodiques
Biochimie -- Périodiques
Biochemistry
Insect biochemistry
Insects -- Molecular aspects
Insects -- Physiology
Periodicals
572.8157 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09651748 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.ibmb.2021.103547 ↗
- Languages:
- English
- ISSNs:
- 0965-1748
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4516.852000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 15931.xml