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  Symbiosis and horizontal gene transfer promote herbivory in the megadiverse leaf beetles

Kirsch, R., Okamura, Y., García-Lozano, M., Weiss, B., Keller, J., Vogel, H., et al. (2025). Symbiosis and horizontal gene transfer promote herbivory in the megadiverse leaf beetles. Current Biology, 35(3), 640-654. doi:10.1016/j.cub.2024.12.028.

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Kirsch, R, Author
Okamura, Y, Author
García-Lozano, M1, Author                 
Weiss, B, Author
Keller, J, Author
Vogel, H, Author
Fukumori, K, Author
Fukatsu, T, Author
Konstantinov, AS, Author
Montagna, M, Author
Moseyko, AG, Author
Riley, EG, Author
Slipinski, A, Author
Vencl, FV, Author
Windsor, DM, Author
Salem, H1, Author                 
Kaltenpoth, M, Author
Pauchet, Y, Author
Affiliations:
1Research Group on Mutualisms, Max Planck Institute for Biology Tübingen, Max Planck Society, ou_3375056              

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 Abstract: Beetles that feed on the nutritionally depauperate and recalcitrant tissues provided by the leaves, stems, and roots of living plants comprise one-quarter of herbivorous insect species. Among the key adaptations for herbivory are plant cell wall-degrading enzymes (PCWDEs) that break down the fastidious polymers in the cell wall and grant access to the nutritious cell content. While largely absent from the non-herbivorous ancestors of beetles, such PCWDEs were occasionally acquired via horizontal gene transfer (HGT) or by the uptake of digestive symbionts. However, the macroevolutionary dynamics of PCWDEs and their impact on evolutionary transitions in herbivorous insects remained poorly understood. Through genomic and transcriptomic analyses of 74 leaf beetle species and 50 symbionts, we show that multiple independent events of microbe-to-beetle HGT and specialized symbioses drove convergent evolutionary innovations in approximately 21,000 and 13,500 leaf beetle species, respectively. Enzymatic assays indicate that these events significantly expanded the beetles’ digestive repertoires and thereby contributed to their adaptation and diversification. Our results exemplify how recurring HGT and symbiont acquisition catalyzed digestive and nutritional adaptations to herbivory and thereby contributed to the evolutionary success of a megadiverse insect taxon.

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 Dates: 2025-012025-02
 Publication Status: Issued
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 Identifiers: DOI: 10.1016/j.cub.2024.12.028
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Title: Current Biology
  Abbreviation : Curr. Biol.
Source Genre: Journal
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Publ. Info: London, UK : Cell Press
Pages: - Volume / Issue: 35 (3) Sequence Number: - Start / End Page: 640 - 654 Identifier: ISSN: 0960-9822
CoNE: https://pure.mpg.de/cone/journals/resource/954925579107