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Gene expression during zombie ant biting behavior reflects the complexity underlying fungal parasitic behavioral manipulation

BACKGROUND: Adaptive manipulation of animal behavior by parasites functions to increase parasite transmission through changes in host behavior. These changes can range from slight alterations in existing behaviors of the host to the establishment of wholly novel behaviors. The biting behavior observ...

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Autores principales: de Bekker, Charissa, Ohm, Robin A., Loreto, Raquel G., Sebastian, Aswathy, Albert, Istvan, Merrow, Martha, Brachmann, Andreas, Hughes, David P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545319/
https://www.ncbi.nlm.nih.gov/pubmed/26285697
http://dx.doi.org/10.1186/s12864-015-1812-x
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author de Bekker, Charissa
Ohm, Robin A.
Loreto, Raquel G.
Sebastian, Aswathy
Albert, Istvan
Merrow, Martha
Brachmann, Andreas
Hughes, David P.
author_facet de Bekker, Charissa
Ohm, Robin A.
Loreto, Raquel G.
Sebastian, Aswathy
Albert, Istvan
Merrow, Martha
Brachmann, Andreas
Hughes, David P.
author_sort de Bekker, Charissa
collection PubMed
description BACKGROUND: Adaptive manipulation of animal behavior by parasites functions to increase parasite transmission through changes in host behavior. These changes can range from slight alterations in existing behaviors of the host to the establishment of wholly novel behaviors. The biting behavior observed in Carpenter ants infected by the specialized fungus Ophiocordyceps unilateralis s.l. is an example of the latter. Though parasitic manipulation of host behavior is generally assumed to be due to the parasite’s gene expression, few studies have set out to test this. RESULTS: We experimentally infected Carpenter ants to collect tissue from both parasite and host during the time period when manipulated biting behavior is experienced. Upon observation of synchronized biting, samples were collected and subjected to mixed RNA-Seq analysis. We also sequenced and annotated the O. unilateralis s.l. genome as a reference for the fungal sequencing reads. CONCLUSIONS: Our mixed transcriptomics approach, together with a comparative genomics study, shows that the majority of the fungal genes that are up-regulated during manipulated biting behavior are unique to the O. unilateralis s.l. genome. This study furthermore reveals that the fungal parasite might be regulating immune- and neuronal stress responses in the host during manipulated biting, as well as impairing its chemosensory communication and causing apoptosis. Moreover, we found genes up-regulated during manipulation that putatively encode for proteins with reported effects on behavioral outputs, proteins involved in various neuropathologies and proteins involved in the biosynthesis of secondary metabolites such as alkaloids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1812-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-45453192015-08-23 Gene expression during zombie ant biting behavior reflects the complexity underlying fungal parasitic behavioral manipulation de Bekker, Charissa Ohm, Robin A. Loreto, Raquel G. Sebastian, Aswathy Albert, Istvan Merrow, Martha Brachmann, Andreas Hughes, David P. BMC Genomics Research Article BACKGROUND: Adaptive manipulation of animal behavior by parasites functions to increase parasite transmission through changes in host behavior. These changes can range from slight alterations in existing behaviors of the host to the establishment of wholly novel behaviors. The biting behavior observed in Carpenter ants infected by the specialized fungus Ophiocordyceps unilateralis s.l. is an example of the latter. Though parasitic manipulation of host behavior is generally assumed to be due to the parasite’s gene expression, few studies have set out to test this. RESULTS: We experimentally infected Carpenter ants to collect tissue from both parasite and host during the time period when manipulated biting behavior is experienced. Upon observation of synchronized biting, samples were collected and subjected to mixed RNA-Seq analysis. We also sequenced and annotated the O. unilateralis s.l. genome as a reference for the fungal sequencing reads. CONCLUSIONS: Our mixed transcriptomics approach, together with a comparative genomics study, shows that the majority of the fungal genes that are up-regulated during manipulated biting behavior are unique to the O. unilateralis s.l. genome. This study furthermore reveals that the fungal parasite might be regulating immune- and neuronal stress responses in the host during manipulated biting, as well as impairing its chemosensory communication and causing apoptosis. Moreover, we found genes up-regulated during manipulation that putatively encode for proteins with reported effects on behavioral outputs, proteins involved in various neuropathologies and proteins involved in the biosynthesis of secondary metabolites such as alkaloids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1812-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-19 /pmc/articles/PMC4545319/ /pubmed/26285697 http://dx.doi.org/10.1186/s12864-015-1812-x Text en © de Bekker et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Ohm, Robin A.
Loreto, Raquel G.
Sebastian, Aswathy
Albert, Istvan
Merrow, Martha
Brachmann, Andreas
Hughes, David P.
Gene expression during zombie ant biting behavior reflects the complexity underlying fungal parasitic behavioral manipulation
title Gene expression during zombie ant biting behavior reflects the complexity underlying fungal parasitic behavioral manipulation
title_full Gene expression during zombie ant biting behavior reflects the complexity underlying fungal parasitic behavioral manipulation
title_fullStr Gene expression during zombie ant biting behavior reflects the complexity underlying fungal parasitic behavioral manipulation
title_full_unstemmed Gene expression during zombie ant biting behavior reflects the complexity underlying fungal parasitic behavioral manipulation
title_short Gene expression during zombie ant biting behavior reflects the complexity underlying fungal parasitic behavioral manipulation
title_sort gene expression during zombie ant biting behavior reflects the complexity underlying fungal parasitic behavioral manipulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545319/
https://www.ncbi.nlm.nih.gov/pubmed/26285697
http://dx.doi.org/10.1186/s12864-015-1812-x
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