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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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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. |
format | Online Article Text |
id | pubmed-10460416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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