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Immune challenges increase network centrality in a queenless ant

Social animals display a wide range of behavioural defences against infectious diseases, some of which increase social contacts with infectious individuals (e.g. mutual grooming), while others decrease them (e.g. social exclusion). These defences often rely on the detection of infectious individuals...

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Autores principales: Alciatore, Giacomo, Ugelvig, Line V., Frank, Erik, Bidaux, Jérémie, Gal, Asaf, Schmitt, Thomas, Kronauer, Daniel J. C., Ulrich, Yuko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424377/
https://www.ncbi.nlm.nih.gov/pubmed/34493081
http://dx.doi.org/10.1098/rspb.2021.1456
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author Alciatore, Giacomo
Ugelvig, Line V.
Frank, Erik
Bidaux, Jérémie
Gal, Asaf
Schmitt, Thomas
Kronauer, Daniel J. C.
Ulrich, Yuko
author_facet Alciatore, Giacomo
Ugelvig, Line V.
Frank, Erik
Bidaux, Jérémie
Gal, Asaf
Schmitt, Thomas
Kronauer, Daniel J. C.
Ulrich, Yuko
author_sort Alciatore, Giacomo
collection PubMed
description Social animals display a wide range of behavioural defences against infectious diseases, some of which increase social contacts with infectious individuals (e.g. mutual grooming), while others decrease them (e.g. social exclusion). These defences often rely on the detection of infectious individuals, but this can be achieved in several ways that are difficult to differentiate. Here, we combine non-pathogenic immune challenges with automated tracking in colonies of the clonal raider ant to ask whether ants can detect the immune status of their social partners and to quantify their behavioural responses to this perceived infection risk. We first show that a key behavioural response elicited by live pathogens (allogrooming) can be qualitatively recapitulated by immune challenges alone. Automated scoring of interactions between all colony members reveals that this behavioural response increases the network centrality of immune-challenged individuals through a general increase in physical contacts. These results show that ants can detect the immune status of their nest-mates and respond with a general ‘caring’ strategy, rather than avoidance, towards social partners that are perceived to be infectious. Finally, we find no evidence that changes in cuticular hydrocarbon profiles drive these behavioural effects.
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spelling pubmed-84243772021-09-09 Immune challenges increase network centrality in a queenless ant Alciatore, Giacomo Ugelvig, Line V. Frank, Erik Bidaux, Jérémie Gal, Asaf Schmitt, Thomas Kronauer, Daniel J. C. Ulrich, Yuko Proc Biol Sci Behaviour Social animals display a wide range of behavioural defences against infectious diseases, some of which increase social contacts with infectious individuals (e.g. mutual grooming), while others decrease them (e.g. social exclusion). These defences often rely on the detection of infectious individuals, but this can be achieved in several ways that are difficult to differentiate. Here, we combine non-pathogenic immune challenges with automated tracking in colonies of the clonal raider ant to ask whether ants can detect the immune status of their social partners and to quantify their behavioural responses to this perceived infection risk. We first show that a key behavioural response elicited by live pathogens (allogrooming) can be qualitatively recapitulated by immune challenges alone. Automated scoring of interactions between all colony members reveals that this behavioural response increases the network centrality of immune-challenged individuals through a general increase in physical contacts. These results show that ants can detect the immune status of their nest-mates and respond with a general ‘caring’ strategy, rather than avoidance, towards social partners that are perceived to be infectious. Finally, we find no evidence that changes in cuticular hydrocarbon profiles drive these behavioural effects. The Royal Society 2021-09-08 2021-09-08 /pmc/articles/PMC8424377/ /pubmed/34493081 http://dx.doi.org/10.1098/rspb.2021.1456 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Behaviour
Alciatore, Giacomo
Ugelvig, Line V.
Frank, Erik
Bidaux, Jérémie
Gal, Asaf
Schmitt, Thomas
Kronauer, Daniel J. C.
Ulrich, Yuko
Immune challenges increase network centrality in a queenless ant
title Immune challenges increase network centrality in a queenless ant
title_full Immune challenges increase network centrality in a queenless ant
title_fullStr Immune challenges increase network centrality in a queenless ant
title_full_unstemmed Immune challenges increase network centrality in a queenless ant
title_short Immune challenges increase network centrality in a queenless ant
title_sort immune challenges increase network centrality in a queenless ant
topic Behaviour
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424377/
https://www.ncbi.nlm.nih.gov/pubmed/34493081
http://dx.doi.org/10.1098/rspb.2021.1456
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