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Behavioural individuality determines infection risk in clonal ant colonies

In social groups, infection risk is not distributed evenly across individuals. Individual behaviour is a key source of variation in infection risk, yet its effects are difficult to separate from other factors (e.g., age). Here, we combine epidemiological experiments with chemical, transcriptomic, an...

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Autores principales: Li, Zimai, Bhat, Bhoomika, Frank, Erik T., Oliveira-Honorato, Thalita, Azuma, Fumika, Bachmann, Valérie, Parker, Darren J., Schmitt, Thomas, Economo, Evan P., Ulrich, Yuko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460416/
https://www.ncbi.nlm.nih.gov/pubmed/37634010
http://dx.doi.org/10.1038/s41467-023-40983-7
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author Li, Zimai
Bhat, Bhoomika
Frank, Erik T.
Oliveira-Honorato, Thalita
Azuma, Fumika
Bachmann, Valérie
Parker, Darren J.
Schmitt, Thomas
Economo, Evan P.
Ulrich, Yuko
author_facet Li, Zimai
Bhat, Bhoomika
Frank, Erik T.
Oliveira-Honorato, Thalita
Azuma, Fumika
Bachmann, Valérie
Parker, Darren J.
Schmitt, Thomas
Economo, Evan P.
Ulrich, Yuko
author_sort Li, Zimai
collection PubMed
description In social groups, infection risk is not distributed evenly across individuals. Individual behaviour is a key source of variation in infection risk, yet its effects are difficult to separate from other factors (e.g., age). Here, we combine epidemiological experiments with chemical, transcriptomic, and automated behavioural analyses in clonal ant colonies, where behavioural individuality emerges among identical workers. We find that: (1) Caenorhabditis-related nematodes parasitise ant heads and affect their survival and physiology, (2) differences in infection emerge from behavioural variation alone, and reflect spatially-organised division of labour, (3) infections affect colony social organisation by causing infected workers to stay in the nest. By disproportionately infecting some workers and shifting their spatial distribution, infections reduce division of labour and increase spatial overlap between hosts, which should facilitate parasite transmission. Thus, division of labour, a defining feature of societies, not only shapes infection risk and distribution but is also modulated by parasites.
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spelling pubmed-104604162023-08-28 Behavioural individuality determines infection risk in clonal ant colonies Li, Zimai Bhat, Bhoomika Frank, Erik T. Oliveira-Honorato, Thalita Azuma, Fumika Bachmann, Valérie Parker, Darren J. Schmitt, Thomas Economo, Evan P. Ulrich, Yuko Nat Commun Article In social groups, infection risk is not distributed evenly across individuals. Individual behaviour is a key source of variation in infection risk, yet its effects are difficult to separate from other factors (e.g., age). Here, we combine epidemiological experiments with chemical, transcriptomic, and automated behavioural analyses in clonal ant colonies, where behavioural individuality emerges among identical workers. We find that: (1) Caenorhabditis-related nematodes parasitise ant heads and affect their survival and physiology, (2) differences in infection emerge from behavioural variation alone, and reflect spatially-organised division of labour, (3) infections affect colony social organisation by causing infected workers to stay in the nest. By disproportionately infecting some workers and shifting their spatial distribution, infections reduce division of labour and increase spatial overlap between hosts, which should facilitate parasite transmission. Thus, division of labour, a defining feature of societies, not only shapes infection risk and distribution but is also modulated by parasites. Nature Publishing Group UK 2023-08-26 /pmc/articles/PMC10460416/ /pubmed/37634010 http://dx.doi.org/10.1038/s41467-023-40983-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Zimai
Bhat, Bhoomika
Frank, Erik T.
Oliveira-Honorato, Thalita
Azuma, Fumika
Bachmann, Valérie
Parker, Darren J.
Schmitt, Thomas
Economo, Evan P.
Ulrich, Yuko
Behavioural individuality determines infection risk in clonal ant colonies
title Behavioural individuality determines infection risk in clonal ant colonies
title_full Behavioural individuality determines infection risk in clonal ant colonies
title_fullStr Behavioural individuality determines infection risk in clonal ant colonies
title_full_unstemmed Behavioural individuality determines infection risk in clonal ant colonies
title_short Behavioural individuality determines infection risk in clonal ant colonies
title_sort behavioural individuality determines infection risk in clonal ant colonies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460416/
https://www.ncbi.nlm.nih.gov/pubmed/37634010
http://dx.doi.org/10.1038/s41467-023-40983-7
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