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Asexual and sexual reproduction are two separate developmental pathways in a Termitomyces species

Although mutualistic symbioses per definition are beneficial for interacting species, conflict may arise if partners reproduce independently. We address how this reproductive conflict is regulated in the obligate mutualistic symbiosis between fungus-growing termites and Termitomyces fungi. Even thou...

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Autores principales: Vreeburg, Sabine M. E., de Ruijter, Norbert C. A., Zwaan, Bas J., da Costa, Rafael R., Poulsen, Michael, Aanen, Duur K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480157/
https://www.ncbi.nlm.nih.gov/pubmed/32781906
http://dx.doi.org/10.1098/rsbl.2020.0394
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author Vreeburg, Sabine M. E.
de Ruijter, Norbert C. A.
Zwaan, Bas J.
da Costa, Rafael R.
Poulsen, Michael
Aanen, Duur K.
author_facet Vreeburg, Sabine M. E.
de Ruijter, Norbert C. A.
Zwaan, Bas J.
da Costa, Rafael R.
Poulsen, Michael
Aanen, Duur K.
author_sort Vreeburg, Sabine M. E.
collection PubMed
description Although mutualistic symbioses per definition are beneficial for interacting species, conflict may arise if partners reproduce independently. We address how this reproductive conflict is regulated in the obligate mutualistic symbiosis between fungus-growing termites and Termitomyces fungi. Even though the termites and their fungal symbiont disperse independently to establish new colonies, dispersal is correlated in time. The fungal symbiont typically forms mushrooms a few weeks after the colony has produced dispersing alates. It is thought that this timing is due to a trade-off between alate and worker production; alate production reduces resources available for worker production. As workers consume the fungus, reduced numbers of workers will allow mushrooms to ‘escape’ from the host colony. Here, we test a specific version of this hypothesis: the typical asexual structures found in all species of Termitomyces—nodules—are immature stages of mushrooms that are normally harvested by the termites at a primordial stage. We refute this hypothesis by showing that nodules and mushroom primordia are macro- and microscopically different structures and by showing that in the absence of workers, primordia do, and nodules do not grow out into mushrooms. It remains to be tested whether termite control of primordia formation or of primordia outgrowth mitigates the reproductive conflict.
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spelling pubmed-74801572020-09-14 Asexual and sexual reproduction are two separate developmental pathways in a Termitomyces species Vreeburg, Sabine M. E. de Ruijter, Norbert C. A. Zwaan, Bas J. da Costa, Rafael R. Poulsen, Michael Aanen, Duur K. Biol Lett Evolutionary Biology Although mutualistic symbioses per definition are beneficial for interacting species, conflict may arise if partners reproduce independently. We address how this reproductive conflict is regulated in the obligate mutualistic symbiosis between fungus-growing termites and Termitomyces fungi. Even though the termites and their fungal symbiont disperse independently to establish new colonies, dispersal is correlated in time. The fungal symbiont typically forms mushrooms a few weeks after the colony has produced dispersing alates. It is thought that this timing is due to a trade-off between alate and worker production; alate production reduces resources available for worker production. As workers consume the fungus, reduced numbers of workers will allow mushrooms to ‘escape’ from the host colony. Here, we test a specific version of this hypothesis: the typical asexual structures found in all species of Termitomyces—nodules—are immature stages of mushrooms that are normally harvested by the termites at a primordial stage. We refute this hypothesis by showing that nodules and mushroom primordia are macro- and microscopically different structures and by showing that in the absence of workers, primordia do, and nodules do not grow out into mushrooms. It remains to be tested whether termite control of primordia formation or of primordia outgrowth mitigates the reproductive conflict. The Royal Society 2020-08 2020-08-12 /pmc/articles/PMC7480157/ /pubmed/32781906 http://dx.doi.org/10.1098/rsbl.2020.0394 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://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/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolutionary Biology
Vreeburg, Sabine M. E.
de Ruijter, Norbert C. A.
Zwaan, Bas J.
da Costa, Rafael R.
Poulsen, Michael
Aanen, Duur K.
Asexual and sexual reproduction are two separate developmental pathways in a Termitomyces species
title Asexual and sexual reproduction are two separate developmental pathways in a Termitomyces species
title_full Asexual and sexual reproduction are two separate developmental pathways in a Termitomyces species
title_fullStr Asexual and sexual reproduction are two separate developmental pathways in a Termitomyces species
title_full_unstemmed Asexual and sexual reproduction are two separate developmental pathways in a Termitomyces species
title_short Asexual and sexual reproduction are two separate developmental pathways in a Termitomyces species
title_sort asexual and sexual reproduction are two separate developmental pathways in a termitomyces species
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480157/
https://www.ncbi.nlm.nih.gov/pubmed/32781906
http://dx.doi.org/10.1098/rsbl.2020.0394
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