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Feces production as a form of social immunity in an insect with facultative maternal care

BACKGROUND: Social animals have the unique capability of mounting social defenses against pathogens. Over the last decades, social immunity has been extensively studied in species with obligatory and permanent forms of social life. However, its occurrence in less derived social systems and thus its...

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Autores principales: Diehl, Janina MC, Körner, Maximilian, Pietsch, Michael, Meunier, Joël
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4408575/
https://www.ncbi.nlm.nih.gov/pubmed/25888183
http://dx.doi.org/10.1186/s12862-015-0330-4
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author Diehl, Janina MC
Körner, Maximilian
Pietsch, Michael
Meunier, Joël
author_facet Diehl, Janina MC
Körner, Maximilian
Pietsch, Michael
Meunier, Joël
author_sort Diehl, Janina MC
collection PubMed
description BACKGROUND: Social animals have the unique capability of mounting social defenses against pathogens. Over the last decades, social immunity has been extensively studied in species with obligatory and permanent forms of social life. However, its occurrence in less derived social systems and thus its role in the early evolution of group-living remains unclear. Here, we investigated whether lining nests with feces is a form of social immunity against microbial growth in the European earwig Forficula auricularia, an insect with temporary family life and facultative maternal care. RESULTS: Using a total of 415 inhibition zone assays, we showed that earwig feces inhibit the growth of two GRAM+ bacteria, two fungi, but not of a GRAM- bacteria. These inhibitions did not result from the consumed food or the nesting environment. We then demonstrated that the antimicrobial activity against fungus was higher in offspring than maternal feces, but that this difference was absent against bacteria. Finally, we showed that family interactions inhibited the antibacterial activity of maternal feces against one of the two GRAM+ bacteria, whereas it had no effect on the one of nymphal feces. By contrast, antifungal activities of the feces were independent of mother-offspring interactions. CONCLUSION: These results demonstrate that social immunity occurs in a species with simple and facultative social life, and thus shed light on the general importance of this process in the evolution of group-living. These results also emphasize that defecation can be under selection for other life-history traits than simple waste disposal.
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spelling pubmed-44085752015-04-25 Feces production as a form of social immunity in an insect with facultative maternal care Diehl, Janina MC Körner, Maximilian Pietsch, Michael Meunier, Joël BMC Evol Biol Research Article BACKGROUND: Social animals have the unique capability of mounting social defenses against pathogens. Over the last decades, social immunity has been extensively studied in species with obligatory and permanent forms of social life. However, its occurrence in less derived social systems and thus its role in the early evolution of group-living remains unclear. Here, we investigated whether lining nests with feces is a form of social immunity against microbial growth in the European earwig Forficula auricularia, an insect with temporary family life and facultative maternal care. RESULTS: Using a total of 415 inhibition zone assays, we showed that earwig feces inhibit the growth of two GRAM+ bacteria, two fungi, but not of a GRAM- bacteria. These inhibitions did not result from the consumed food or the nesting environment. We then demonstrated that the antimicrobial activity against fungus was higher in offspring than maternal feces, but that this difference was absent against bacteria. Finally, we showed that family interactions inhibited the antibacterial activity of maternal feces against one of the two GRAM+ bacteria, whereas it had no effect on the one of nymphal feces. By contrast, antifungal activities of the feces were independent of mother-offspring interactions. CONCLUSION: These results demonstrate that social immunity occurs in a species with simple and facultative social life, and thus shed light on the general importance of this process in the evolution of group-living. These results also emphasize that defecation can be under selection for other life-history traits than simple waste disposal. BioMed Central 2015-03-12 /pmc/articles/PMC4408575/ /pubmed/25888183 http://dx.doi.org/10.1186/s12862-015-0330-4 Text en © Diehl et al.; licensee BioMed Central. 2015 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
Diehl, Janina MC
Körner, Maximilian
Pietsch, Michael
Meunier, Joël
Feces production as a form of social immunity in an insect with facultative maternal care
title Feces production as a form of social immunity in an insect with facultative maternal care
title_full Feces production as a form of social immunity in an insect with facultative maternal care
title_fullStr Feces production as a form of social immunity in an insect with facultative maternal care
title_full_unstemmed Feces production as a form of social immunity in an insect with facultative maternal care
title_short Feces production as a form of social immunity in an insect with facultative maternal care
title_sort feces production as a form of social immunity in an insect with facultative maternal care
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4408575/
https://www.ncbi.nlm.nih.gov/pubmed/25888183
http://dx.doi.org/10.1186/s12862-015-0330-4
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