Diversification, selective sweep, and body size in the invasive Palearctic alfalfa weevil infected with Wolbachia.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
06 05 2021
Historique:
received: 30 08 2020
accepted: 15 04 2021
entrez: 7 5 2021
pubmed: 8 5 2021
medline: 21 10 2021
Statut: epublish

Résumé

The alfalfa weevil Hypera postica, native to the Western Palearctic, is an invasive legume pest with two divergent mitochondrial clades in its invading regions, the Western clade and the Eastern/Egyptian clade. However, knowledge regarding the native populations is limited. The Western clade is infected with the endosymbiotic bacteria Wolbachia that cause cytoplasmic incompatibility in host weevils. Our aim was to elucidate the spatial genetic structure of this insect and the effect of Wolbachia on its population diversity. We analyzed two mitochondrial and two nuclear genes of the weevil from its native ranges. The Western clade was distributed in western/central Europe, whereas the Eastern/Egyptian clade was distributed from the Mediterranean basin to central Asia. Intermediate mitotypes were found from the Balkans to central Asia. Most Western clade individuals in western Europe were infected with an identical Wolbachia strain. Mitochondrial genetic diversity of the infected individuals was minimal. The infected clades demonstrated a higher nonsynonymous/synonymous substitution rate ratio than the uninfected clades, suggesting a higher fixation of nonsynonymous mutations due to a selective sweep by Wolbachia. Trans-Mediterranean and within-European dispersal routes were supported. We suggest that the ancestral populations diversified by geographic isolation due to glaciations and that the diversity was reduced in the west by a recent Wolbachia-driven sweep(s). The intermediate clade exhibited a body size and host plant that differed from the other clades. Pros and cons of the possible use of infected-clade males to control uninfected populations are discussed.

Identifiants

pubmed: 33958611
doi: 10.1038/s41598-021-88770-y
pii: 10.1038/s41598-021-88770-y
pmc: PMC8102540
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

9664

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Auteurs

Midori Tuda (M)

Institute of Biological Control, Faculty of Agriculture, Kyushu University, Fukuoka, 819-0395, Japan. tuda@grt.kyushu-u.ac.jp.
Laboratory of Insect Natural Enemies, Department of Bioresource Sciences, Faculty of Agriculture, Kyushu University, Fukuoka, Japan. tuda@grt.kyushu-u.ac.jp.

Shun-Ichiro Iwase (SI)

Institute of Biological Control, Faculty of Agriculture, Kyushu University, Fukuoka, 819-0395, Japan.
Research Institute of Environment, Agriculture and Fisheries, Osaka Prefecture, Japan.

Khadim Kébé (K)

GRBA-BE, LE3PI Laboratory, Department of Chemical Engineering and Applied Biology, Polytechnic Higher School of Dakar, Dakar, Senegal.

Julien Haran (J)

CBGP, Cirad, Montpellier SupAgro, INRA, IRD, Univ. Montpellier, Montpellier, France.

Jiri Skuhrovec (J)

Group Function of Invertebrate and Plant Biodiversity in Agro-Ecosystems, Crop Research Institute, Drnovska, Praha, Czech Republic.

Ehsan Sanaei (E)

School of Biological Sciences, University of Queensland, Brisbane, Australia.

Naomichi Tsuji (N)

Entomological Laboratory, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Fukuoka, Japan.

Attila Podlussány (A)

Hungarian Natural History Museum, Budapest, Hungary.

Ottó Merkl (O)

Hungarian Natural History Museum, Budapest, Hungary.

Ahmed H El-Heneidy (AH)

Department of Biological Control, Plant Protection Research Institute, Agricultural Research Center, Giza, Egypt.

Katsura Morimoto (K)

Nata-Danchi, Fukuoka, Japan.

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