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Psychoactive plant- and mushroom-associated alkaloids from two behavior modifying cicada pathogens
Entomopathogenic fungi routinely kill their hosts before releasing infectious spores, but a few species keep insects alive while sporulating, which enhances dispersal. Transcriptomics- and metabolomics-based studies of entomopathogens with post-mortem dissemination from their parasitized hosts have...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876628/ https://www.ncbi.nlm.nih.gov/pubmed/31768192 http://dx.doi.org/10.1016/j.funeco.2019.06.002 |
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author | Boyce, Greg R. Gluck-Thaler, Emile Slot, Jason C. Stajich, Jason E. Davis, William J. James, Tim Y. Cooley, John R. Panaccione, Daniel G. Eilenberg, Jørgen De Fine Licht, Henrik H. Macias, Angie M. Berger, Matthew C. Wickert, Kristen L. Stauder, Cameron M. Spahr, Ellie J. Maust, Matthew D. Metheny, Amy M. Simon, Chris Kritsky, Gene Hodge, Kathie T. Humber, Richard A. Gullion, Terry Short, Dylan P.G. Kijimoto, Teiya Mozgai, Dan Arguedas, Nidia Kasson, Matt T. |
author_facet | Boyce, Greg R. Gluck-Thaler, Emile Slot, Jason C. Stajich, Jason E. Davis, William J. James, Tim Y. Cooley, John R. Panaccione, Daniel G. Eilenberg, Jørgen De Fine Licht, Henrik H. Macias, Angie M. Berger, Matthew C. Wickert, Kristen L. Stauder, Cameron M. Spahr, Ellie J. Maust, Matthew D. Metheny, Amy M. Simon, Chris Kritsky, Gene Hodge, Kathie T. Humber, Richard A. Gullion, Terry Short, Dylan P.G. Kijimoto, Teiya Mozgai, Dan Arguedas, Nidia Kasson, Matt T. |
author_sort | Boyce, Greg R. |
collection | PubMed |
description | Entomopathogenic fungi routinely kill their hosts before releasing infectious spores, but a few species keep insects alive while sporulating, which enhances dispersal. Transcriptomics- and metabolomics-based studies of entomopathogens with post-mortem dissemination from their parasitized hosts have unraveled infection processes and host responses. However, the mechanisms underlying active spore transmission by Entomophthoralean fungi in living insects remain elusive. Here we report the discovery, through metabolomics, of the plant-associated amphetamine, cathinone, in four Massospora cicadina-infected periodical cicada populations, and the mushroom-associated tryptamine, psilocybin, in annual cicadas infected with Massospora platypediae or Massospora levispora, which likely represent a single fungal species. The absence of some fungal enzymes necessary for cathinone and psilocybin biosynthesis along with the inability to detect intermediate metabolites or gene orthologs are consistent with possibly novel biosynthesis pathways in Massospora. The neurogenic activities of these compounds suggest the extended phenotype of Massospora that modifies cicada behavior to maximize dissemination is chemically-induced. |
format | Online Article Text |
id | pubmed-6876628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-68766282020-10-01 Psychoactive plant- and mushroom-associated alkaloids from two behavior modifying cicada pathogens Boyce, Greg R. Gluck-Thaler, Emile Slot, Jason C. Stajich, Jason E. Davis, William J. James, Tim Y. Cooley, John R. Panaccione, Daniel G. Eilenberg, Jørgen De Fine Licht, Henrik H. Macias, Angie M. Berger, Matthew C. Wickert, Kristen L. Stauder, Cameron M. Spahr, Ellie J. Maust, Matthew D. Metheny, Amy M. Simon, Chris Kritsky, Gene Hodge, Kathie T. Humber, Richard A. Gullion, Terry Short, Dylan P.G. Kijimoto, Teiya Mozgai, Dan Arguedas, Nidia Kasson, Matt T. Fungal Ecol Article Entomopathogenic fungi routinely kill their hosts before releasing infectious spores, but a few species keep insects alive while sporulating, which enhances dispersal. Transcriptomics- and metabolomics-based studies of entomopathogens with post-mortem dissemination from their parasitized hosts have unraveled infection processes and host responses. However, the mechanisms underlying active spore transmission by Entomophthoralean fungi in living insects remain elusive. Here we report the discovery, through metabolomics, of the plant-associated amphetamine, cathinone, in four Massospora cicadina-infected periodical cicada populations, and the mushroom-associated tryptamine, psilocybin, in annual cicadas infected with Massospora platypediae or Massospora levispora, which likely represent a single fungal species. The absence of some fungal enzymes necessary for cathinone and psilocybin biosynthesis along with the inability to detect intermediate metabolites or gene orthologs are consistent with possibly novel biosynthesis pathways in Massospora. The neurogenic activities of these compounds suggest the extended phenotype of Massospora that modifies cicada behavior to maximize dissemination is chemically-induced. 2019-06-24 2019-10 /pmc/articles/PMC6876628/ /pubmed/31768192 http://dx.doi.org/10.1016/j.funeco.2019.06.002 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Boyce, Greg R. Gluck-Thaler, Emile Slot, Jason C. Stajich, Jason E. Davis, William J. James, Tim Y. Cooley, John R. Panaccione, Daniel G. Eilenberg, Jørgen De Fine Licht, Henrik H. Macias, Angie M. Berger, Matthew C. Wickert, Kristen L. Stauder, Cameron M. Spahr, Ellie J. Maust, Matthew D. Metheny, Amy M. Simon, Chris Kritsky, Gene Hodge, Kathie T. Humber, Richard A. Gullion, Terry Short, Dylan P.G. Kijimoto, Teiya Mozgai, Dan Arguedas, Nidia Kasson, Matt T. Psychoactive plant- and mushroom-associated alkaloids from two behavior modifying cicada pathogens |
title | Psychoactive plant- and mushroom-associated alkaloids from two behavior modifying cicada pathogens |
title_full | Psychoactive plant- and mushroom-associated alkaloids from two behavior modifying cicada pathogens |
title_fullStr | Psychoactive plant- and mushroom-associated alkaloids from two behavior modifying cicada pathogens |
title_full_unstemmed | Psychoactive plant- and mushroom-associated alkaloids from two behavior modifying cicada pathogens |
title_short | Psychoactive plant- and mushroom-associated alkaloids from two behavior modifying cicada pathogens |
title_sort | psychoactive plant- and mushroom-associated alkaloids from two behavior modifying cicada pathogens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876628/ https://www.ncbi.nlm.nih.gov/pubmed/31768192 http://dx.doi.org/10.1016/j.funeco.2019.06.002 |
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