Landscape genomics of an obligate mutualism: Concordant and discordant population structures between the leafcutter ant Atta texana and its two main fungal symbiont types.

Atta texana bedassle environmental cline intergenomic epistasis mutualism population structure

Journal

Molecular ecology
ISSN: 1365-294X
Titre abrégé: Mol Ecol
Pays: England
ID NLM: 9214478

Informations de publication

Date de publication:
06 2019
Historique:
received: 09 12 2018
revised: 10 03 2019
accepted: 11 03 2019
pubmed: 30 5 2019
medline: 22 5 2020
entrez: 30 5 2019
Statut: ppublish

Résumé

To explore landscape genomics at the range limit of an obligate mutualism, we use genotyping-by-sequencing (ddRADseq) to quantify population structure and the effect of host-symbiont interactions between the northernmost fungus-farming leafcutter ant Atta texana and its two main types of cultivated fungus. Genome-wide differentiation between ants associated with either of the two fungal types is of the same order of magnitude as differentiation associated with temperature and precipitation across the ant's entire range, suggesting that specific ant-fungus genome-genome combinations may have been favoured by selection. For the ant hosts, we found a broad cline of genetic structure across the range, and a reduction of genetic diversity along the axis of range expansion towards the range margin. This population-genetic structure was concordant between the ants and one cultivar type (M-fungi, concordant clines) but discordant for the other cultivar type (T-fungi). Discordance in population-genetic structures between ant hosts and a fungal symbiont is surprising because the ant farmers codisperse with their vertically transmitted fungal symbionts. Discordance implies that (a) the fungi disperse also through between-nest horizontal transfer or other unknown mechanisms, and (b) genetic drift and gene flow can differ in magnitude between each partner and between different ant-fungus combinations. Together, these findings imply that variation in the strength of drift and gene flow experienced by each mutualistic partner affects adaptation to environmental stress at the range margin, and genome-genome interactions between host and symbiont influence adaptive genetic differentiation of the host during range evolution in this obligate mutualism.

Identifiants

pubmed: 31141257
doi: 10.1111/mec.15111
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2831-2845

Informations de copyright

© 2019 John Wiley & Sons Ltd.

Auteurs

Chad C Smith (CC)

Department of Integrative Biology, University of Texas at Austin, Austin, Texas.

Jesse N Weber (JN)

Department of Integrative Biology, University of Texas at Austin, Austin, Texas.
Department of Biological Sciences, University of Alaska, Anchorage, Alaska.

Alexander S Mikheyev (AS)

Okinawa Institute of Science & Technology, Kunigami, Japan.

Flavio Roces (F)

Department of Behavioral Physiology and Sociobiology, Biozentrum, University of Würzburg, Würzburg, Germany.

Martin Bollazzi (M)

Section of Entomology, Universidad de la República, Montevideo, Uruguay.

Katrin Kellner (K)

Department of Biology, University of Texas at Tyler, Tyler, Texas.

Jon N Seal (JN)

Department of Biology, University of Texas at Tyler, Tyler, Texas.

Ulrich G Mueller (UG)

Department of Integrative Biology, University of Texas at Austin, Austin, Texas.

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