Genomic insights into neonicotinoid sensitivity in the solitary bee Osmia bicornis.


Journal

PLoS genetics
ISSN: 1553-7404
Titre abrégé: PLoS Genet
Pays: United States
ID NLM: 101239074

Informations de publication

Date de publication:
02 2019
Historique:
received: 28 09 2018
accepted: 17 12 2018
revised: 14 02 2019
pubmed: 5 2 2019
medline: 12 3 2019
entrez: 5 2 2019
Statut: epublish

Résumé

The impact of pesticides on the health of bee pollinators is determined in part by the capacity of bee detoxification systems to convert these compounds to less toxic forms. For example, recent work has shown that cytochrome P450s of the CYP9Q subfamily are critically important in defining the sensitivity of honey bees and bumblebees to pesticides, including neonicotinoid insecticides. However, it is currently unclear if solitary bees have functional equivalents of these enzymes with potentially serious implications in relation to their capacity to metabolise certain insecticides. To address this question, we sequenced the genome of the red mason bee, Osmia bicornis, the most abundant and economically important solitary bee species in Central Europe. We show that O. bicornis lacks the CYP9Q subfamily of P450s but, despite this, exhibits low acute toxicity to the N-cyanoamidine neonicotinoid thiacloprid. Functional studies revealed that variation in the sensitivity of O. bicornis to N-cyanoamidine and N-nitroguanidine neonicotinoids does not reside in differences in their affinity for the nicotinic acetylcholine receptor or speed of cuticular penetration. Rather, a P450 within the CYP9BU subfamily, with recent shared ancestry to the Apidae CYP9Q subfamily, metabolises thiacloprid in vitro and confers tolerance in vivo. Our data reveal conserved detoxification pathways in model solitary and eusocial bees despite key differences in the evolution of specific pesticide-metabolising enzymes in the two species groups. The discovery that P450 enzymes of solitary bees can act as metabolic defence systems against certain pesticides can be leveraged to avoid negative pesticide impacts on these important pollinators.

Identifiants

pubmed: 30716069
doi: 10.1371/journal.pgen.1007903
pii: PGENETICS-D-18-01898
pmc: PMC6375640
doi:

Substances chimiques

Insecticides 0
Neonicotinoids 0
Thiazines 0
Cytochrome P-450 Enzyme System 9035-51-2
thiacloprid DSV3A944A4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1007903

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/OS/CP/000001
Pays : United Kingdom

Déclaration de conflit d'intérêts

This study received funding from Bayer AG, a manufacturer of neonicotinoid insecticides. Three authors of this study (M. Zaworra, M. Kohler, R. Nauen and B. Buer) are employees of Bayer AG.

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Auteurs

Katherine Beadle (K)

College of Life and Environmental Sciences, Biosciences, University of Exeter, Penryn Campus, Penryn, Cornwall, United Kingdom.

Kumar Saurabh Singh (KS)

College of Life and Environmental Sciences, Biosciences, University of Exeter, Penryn Campus, Penryn, Cornwall, United Kingdom.

Bartlomiej J Troczka (BJ)

Department of Biointeractions and Crop Protection, Rothamsted Research, Harpenden, United Kingdom.

Emma Randall (E)

College of Life and Environmental Sciences, Biosciences, University of Exeter, Penryn Campus, Penryn, Cornwall, United Kingdom.

Marion Zaworra (M)

Bayer AG, Crop Science Division, R&D, Monheim, Germany.

Christoph T Zimmer (CT)

College of Life and Environmental Sciences, Biosciences, University of Exeter, Penryn Campus, Penryn, Cornwall, United Kingdom.

Angela Hayward (A)

College of Life and Environmental Sciences, Biosciences, University of Exeter, Penryn Campus, Penryn, Cornwall, United Kingdom.

Rebecca Reid (R)

Department of Biointeractions and Crop Protection, Rothamsted Research, Harpenden, United Kingdom.

Laura Kor (L)

Department of Biointeractions and Crop Protection, Rothamsted Research, Harpenden, United Kingdom.

Maxie Kohler (M)

Bayer AG, Crop Science Division, R&D, Monheim, Germany.

Benjamin Buer (B)

Bayer AG, Crop Science Division, R&D, Monheim, Germany.

David R Nelson (DR)

Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, TN, United States of America.

Martin S Williamson (MS)

Department of Biointeractions and Crop Protection, Rothamsted Research, Harpenden, United Kingdom.

T G Emyr Davies (TGE)

Department of Biointeractions and Crop Protection, Rothamsted Research, Harpenden, United Kingdom.

Linda M Field (LM)

Department of Biointeractions and Crop Protection, Rothamsted Research, Harpenden, United Kingdom.

Ralf Nauen (R)

Bayer AG, Crop Science Division, R&D, Monheim, Germany.

Chris Bass (C)

College of Life and Environmental Sciences, Biosciences, University of Exeter, Penryn Campus, Penryn, Cornwall, United Kingdom.

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