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Species-specific ant brain manipulation by a specialized fungal parasite
BACKGROUND: A compelling demonstration of adaptation by natural selection is the ability of parasites to manipulate host behavior. One dramatic example involves fungal species from the genus Ophiocordyceps that control their ant hosts by inducing a biting behavior. Intensive sampling across the glob...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174324/ https://www.ncbi.nlm.nih.gov/pubmed/25085339 http://dx.doi.org/10.1186/s12862-014-0166-3 |
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author | de Bekker, Charissa Quevillon, Lauren E Smith, Philip B Fleming, Kimberly R Ghosh, Debashis Patterson, Andrew D Hughes, David P |
author_facet | de Bekker, Charissa Quevillon, Lauren E Smith, Philip B Fleming, Kimberly R Ghosh, Debashis Patterson, Andrew D Hughes, David P |
author_sort | de Bekker, Charissa |
collection | PubMed |
description | BACKGROUND: A compelling demonstration of adaptation by natural selection is the ability of parasites to manipulate host behavior. One dramatic example involves fungal species from the genus Ophiocordyceps that control their ant hosts by inducing a biting behavior. Intensive sampling across the globe of ants that died after being manipulated by Ophiocordyceps suggests that this phenomenon is highly species-specific. We advance our understanding of this system by reconstructing host manipulation by Ophiocordyceps parasites under controlled laboratory conditions and combining this with field observations of infection rates and a metabolomics survey. RESULTS: We report on a newly discovered species of Ophiocordyceps unilateralis sensu lato from North America that we use to address the species-specificity of Ophiocordyceps-induced manipulation of ant behavior. We show that the fungus can kill all ant species tested, but only manipulates the behavior of those it infects in nature. To investigate if this could be explained at the molecular level, we used ex vivo culturing assays to measure the metabolites that are secreted by the fungus to mediate fungus-ant tissue interactions. We show the fungus reacts heterogeneously to brains of different ant species by secreting a different array of metabolites. By determining which ion peaks are significantly enriched when the fungus is grown alongside brains of its naturally occurring host, we discovered candidate compounds that could be involved in behavioral manipulation by O. unilateralis s.l.. Two of these candidates are known to be involved in neurological diseases and cancer. CONCLUSIONS: The integrative work presented here shows that ant brain manipulation by O. unilateralis s.l. is species-specific seemingly because the fungus produces a specific array of compounds as a reaction to the presence of the host brain it has evolved to manipulate. These studies have resulted in the discovery of candidate compounds involved in establishing behavioral manipulation by this specialized fungus and therefore represent a major advancement towards an understanding of the molecular mechanisms underlying this phenomenon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-014-0166-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4174324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41743242014-09-26 Species-specific ant brain manipulation by a specialized fungal parasite de Bekker, Charissa Quevillon, Lauren E Smith, Philip B Fleming, Kimberly R Ghosh, Debashis Patterson, Andrew D Hughes, David P BMC Evol Biol Research Article BACKGROUND: A compelling demonstration of adaptation by natural selection is the ability of parasites to manipulate host behavior. One dramatic example involves fungal species from the genus Ophiocordyceps that control their ant hosts by inducing a biting behavior. Intensive sampling across the globe of ants that died after being manipulated by Ophiocordyceps suggests that this phenomenon is highly species-specific. We advance our understanding of this system by reconstructing host manipulation by Ophiocordyceps parasites under controlled laboratory conditions and combining this with field observations of infection rates and a metabolomics survey. RESULTS: We report on a newly discovered species of Ophiocordyceps unilateralis sensu lato from North America that we use to address the species-specificity of Ophiocordyceps-induced manipulation of ant behavior. We show that the fungus can kill all ant species tested, but only manipulates the behavior of those it infects in nature. To investigate if this could be explained at the molecular level, we used ex vivo culturing assays to measure the metabolites that are secreted by the fungus to mediate fungus-ant tissue interactions. We show the fungus reacts heterogeneously to brains of different ant species by secreting a different array of metabolites. By determining which ion peaks are significantly enriched when the fungus is grown alongside brains of its naturally occurring host, we discovered candidate compounds that could be involved in behavioral manipulation by O. unilateralis s.l.. Two of these candidates are known to be involved in neurological diseases and cancer. CONCLUSIONS: The integrative work presented here shows that ant brain manipulation by O. unilateralis s.l. is species-specific seemingly because the fungus produces a specific array of compounds as a reaction to the presence of the host brain it has evolved to manipulate. These studies have resulted in the discovery of candidate compounds involved in establishing behavioral manipulation by this specialized fungus and therefore represent a major advancement towards an understanding of the molecular mechanisms underlying this phenomenon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-014-0166-3) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-29 /pmc/articles/PMC4174324/ /pubmed/25085339 http://dx.doi.org/10.1186/s12862-014-0166-3 Text en © de Bekker et al.; licensee BioMed Central Ltd 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article de Bekker, Charissa Quevillon, Lauren E Smith, Philip B Fleming, Kimberly R Ghosh, Debashis Patterson, Andrew D Hughes, David P Species-specific ant brain manipulation by a specialized fungal parasite |
title | Species-specific ant brain manipulation
by a specialized fungal parasite |
title_full | Species-specific ant brain manipulation
by a specialized fungal parasite |
title_fullStr | Species-specific ant brain manipulation
by a specialized fungal parasite |
title_full_unstemmed | Species-specific ant brain manipulation
by a specialized fungal parasite |
title_short | Species-specific ant brain manipulation
by a specialized fungal parasite |
title_sort | species-specific ant brain manipulation
by a specialized fungal parasite |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174324/ https://www.ncbi.nlm.nih.gov/pubmed/25085339 http://dx.doi.org/10.1186/s12862-014-0166-3 |
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