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Termites shape their collective behavioural response based on stage of infection

Social insects employ a range of behaviours to protect their colonies against disease, but little is known about how such collective behaviours are orchestrated. This is especially true for the social Blattodea (termites). We developed an experimental approach that allowed us to explore how the soci...

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Autores principales: Davis, Hannah E., Meconcelli, Stefania, Radek, Renate, McMahon, Dino P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158180/
https://www.ncbi.nlm.nih.gov/pubmed/30258216
http://dx.doi.org/10.1038/s41598-018-32721-7
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author Davis, Hannah E.
Meconcelli, Stefania
Radek, Renate
McMahon, Dino P.
author_facet Davis, Hannah E.
Meconcelli, Stefania
Radek, Renate
McMahon, Dino P.
author_sort Davis, Hannah E.
collection PubMed
description Social insects employ a range of behaviours to protect their colonies against disease, but little is known about how such collective behaviours are orchestrated. This is especially true for the social Blattodea (termites). We developed an experimental approach that allowed us to explore how the social response to disease is co-ordinated by multistep host-pathogen interactions. We infected the eastern subterranean termite Reticulitermes flavipes with the entomopathogenic fungus Metarhizium anisopliae, and then, at different stages of infection, reintroduced them to healthy nestmates and recorded behavioural responses. As expected, termites groomed pathogen-exposed individuals significantly more than controls; however, grooming was significantly elevated after fungal germination than before, demonstrating the importance of fungal status to hygienic behaviour. Significantly, we found that cannibalism became prevalent only after exposed termites became visibly ill, highlighting the importance of host condition as a cue for social hygienic behaviour. Our study reveals the presence of a coordinated social response to disease that depends on stage of infection. Specifically, we show how the host may play a key role in triggering its own sacrifice. Sacrificial self-flagging has been observed in other social insects: our results demonstrate that termites have independently evolved to both recognize and destructively respond to sickness.
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spelling pubmed-61581802018-09-28 Termites shape their collective behavioural response based on stage of infection Davis, Hannah E. Meconcelli, Stefania Radek, Renate McMahon, Dino P. Sci Rep Article Social insects employ a range of behaviours to protect their colonies against disease, but little is known about how such collective behaviours are orchestrated. This is especially true for the social Blattodea (termites). We developed an experimental approach that allowed us to explore how the social response to disease is co-ordinated by multistep host-pathogen interactions. We infected the eastern subterranean termite Reticulitermes flavipes with the entomopathogenic fungus Metarhizium anisopliae, and then, at different stages of infection, reintroduced them to healthy nestmates and recorded behavioural responses. As expected, termites groomed pathogen-exposed individuals significantly more than controls; however, grooming was significantly elevated after fungal germination than before, demonstrating the importance of fungal status to hygienic behaviour. Significantly, we found that cannibalism became prevalent only after exposed termites became visibly ill, highlighting the importance of host condition as a cue for social hygienic behaviour. Our study reveals the presence of a coordinated social response to disease that depends on stage of infection. Specifically, we show how the host may play a key role in triggering its own sacrifice. Sacrificial self-flagging has been observed in other social insects: our results demonstrate that termites have independently evolved to both recognize and destructively respond to sickness. Nature Publishing Group UK 2018-09-26 /pmc/articles/PMC6158180/ /pubmed/30258216 http://dx.doi.org/10.1038/s41598-018-32721-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Davis, Hannah E.
Meconcelli, Stefania
Radek, Renate
McMahon, Dino P.
Termites shape their collective behavioural response based on stage of infection
title Termites shape their collective behavioural response based on stage of infection
title_full Termites shape their collective behavioural response based on stage of infection
title_fullStr Termites shape their collective behavioural response based on stage of infection
title_full_unstemmed Termites shape their collective behavioural response based on stage of infection
title_short Termites shape their collective behavioural response based on stage of infection
title_sort termites shape their collective behavioural response based on stage of infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158180/
https://www.ncbi.nlm.nih.gov/pubmed/30258216
http://dx.doi.org/10.1038/s41598-018-32721-7
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