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First experimental evidence for active farming in ambrosia beetles and strong heredity of garden microbiomes
Fungal cultivation is a defining feature for advanced agriculture in fungus-farming ants and termites. In a third supposedly fungus-farming group, wood-colonizing ambrosia beetles, an experimental proof for the effectiveness of beetle activity for selective promotion of their food fungi over others...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627711/ https://www.ncbi.nlm.nih.gov/pubmed/36321493 http://dx.doi.org/10.1098/rspb.2022.1458 |
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author | Diehl, Janina M. C. Kowallik, Vienna Keller, Alexander Biedermann, Peter H. W. |
author_facet | Diehl, Janina M. C. Kowallik, Vienna Keller, Alexander Biedermann, Peter H. W. |
author_sort | Diehl, Janina M. C. |
collection | PubMed |
description | Fungal cultivation is a defining feature for advanced agriculture in fungus-farming ants and termites. In a third supposedly fungus-farming group, wood-colonizing ambrosia beetles, an experimental proof for the effectiveness of beetle activity for selective promotion of their food fungi over others is lacking and farming has only been assumed based on observations of social and hygienic behaviours. Here, we experimentally removed mothers and their offspring from young nests of the fruit-tree pinhole borer, Xyleborinus saxesenii. By amplicon sequencing of bacterial and fungal communities of nests with and without beetles we could show that beetles are indeed able to actively shift symbiont communities. Although being consumed, the Raffaelea food fungi were more abundant when beetles were present while a weed fungus (Chaetomium sp.) as well as overall bacterial diversity were reduced in comparison to nests without beetles. Core symbiont communities were generally of low diversity and there were strong signs for vertical transmission not only for the cultivars, but also for secondary symbionts. Our findings verify the existence of active farming, even though the exact mechanisms underlying the selective promotion and/or suppression of symbionts need further investigation. |
format | Online Article Text |
id | pubmed-9627711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96277112022-11-16 First experimental evidence for active farming in ambrosia beetles and strong heredity of garden microbiomes Diehl, Janina M. C. Kowallik, Vienna Keller, Alexander Biedermann, Peter H. W. Proc Biol Sci Ecology Fungal cultivation is a defining feature for advanced agriculture in fungus-farming ants and termites. In a third supposedly fungus-farming group, wood-colonizing ambrosia beetles, an experimental proof for the effectiveness of beetle activity for selective promotion of their food fungi over others is lacking and farming has only been assumed based on observations of social and hygienic behaviours. Here, we experimentally removed mothers and their offspring from young nests of the fruit-tree pinhole borer, Xyleborinus saxesenii. By amplicon sequencing of bacterial and fungal communities of nests with and without beetles we could show that beetles are indeed able to actively shift symbiont communities. Although being consumed, the Raffaelea food fungi were more abundant when beetles were present while a weed fungus (Chaetomium sp.) as well as overall bacterial diversity were reduced in comparison to nests without beetles. Core symbiont communities were generally of low diversity and there were strong signs for vertical transmission not only for the cultivars, but also for secondary symbionts. Our findings verify the existence of active farming, even though the exact mechanisms underlying the selective promotion and/or suppression of symbionts need further investigation. The Royal Society 2022-11-09 2022-11-02 /pmc/articles/PMC9627711/ /pubmed/36321493 http://dx.doi.org/10.1098/rspb.2022.1458 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Ecology Diehl, Janina M. C. Kowallik, Vienna Keller, Alexander Biedermann, Peter H. W. First experimental evidence for active farming in ambrosia beetles and strong heredity of garden microbiomes |
title | First experimental evidence for active farming in ambrosia beetles and strong heredity of garden microbiomes |
title_full | First experimental evidence for active farming in ambrosia beetles and strong heredity of garden microbiomes |
title_fullStr | First experimental evidence for active farming in ambrosia beetles and strong heredity of garden microbiomes |
title_full_unstemmed | First experimental evidence for active farming in ambrosia beetles and strong heredity of garden microbiomes |
title_short | First experimental evidence for active farming in ambrosia beetles and strong heredity of garden microbiomes |
title_sort | first experimental evidence for active farming in ambrosia beetles and strong heredity of garden microbiomes |
topic | Ecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627711/ https://www.ncbi.nlm.nih.gov/pubmed/36321493 http://dx.doi.org/10.1098/rspb.2022.1458 |
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