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Network centrality and seasonality interact to predict lice load in a social primate

Lice are socially-transmitted ectoparasites. Transmission depends upon their host’s degree of contact with conspecifics. While grooming facilitates ectoparasite transmission via body contact, it also constrains their spread through parasite removal. We investigated relations between parasite burden...

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Autores principales: Duboscq, Julie, Romano, Valeria, Sueur, Cédric, MacIntosh, Andrew J.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768153/
https://www.ncbi.nlm.nih.gov/pubmed/26915589
http://dx.doi.org/10.1038/srep22095
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author Duboscq, Julie
Romano, Valeria
Sueur, Cédric
MacIntosh, Andrew J.J.
author_facet Duboscq, Julie
Romano, Valeria
Sueur, Cédric
MacIntosh, Andrew J.J.
author_sort Duboscq, Julie
collection PubMed
description Lice are socially-transmitted ectoparasites. Transmission depends upon their host’s degree of contact with conspecifics. While grooming facilitates ectoparasite transmission via body contact, it also constrains their spread through parasite removal. We investigated relations between parasite burden and sociality in female Japanese macaques following two opposing predictions: i) central females in contact/grooming networks harbour more lice, related to their numerous contacts; ii) central females harbour fewer lice, related to receiving more grooming. We estimated lice load non-invasively using the conspicuous louse egg-picking behaviour performed by macaques during grooming. We tested for covariation in several centrality measures and lice load, controlling for season, female reproductive state and dominance rank. Results show that the interaction between degree centrality (number of partners) and seasonality predicted lice load: females interacting with more partners had fewer lice than those interacting with fewer partners in winter and summer, whereas there was no relationship between lice load and centrality in spring and fall. This is counter to the prediction that increased contact leads to greater louse burden but fits the prediction that social grooming limits louse burden. Interactions between environmental seasonality and both parasite and host biology appeared to mediate the role of social processes in louse burden.
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spelling pubmed-47681532016-03-02 Network centrality and seasonality interact to predict lice load in a social primate Duboscq, Julie Romano, Valeria Sueur, Cédric MacIntosh, Andrew J.J. Sci Rep Article Lice are socially-transmitted ectoparasites. Transmission depends upon their host’s degree of contact with conspecifics. While grooming facilitates ectoparasite transmission via body contact, it also constrains their spread through parasite removal. We investigated relations between parasite burden and sociality in female Japanese macaques following two opposing predictions: i) central females in contact/grooming networks harbour more lice, related to their numerous contacts; ii) central females harbour fewer lice, related to receiving more grooming. We estimated lice load non-invasively using the conspicuous louse egg-picking behaviour performed by macaques during grooming. We tested for covariation in several centrality measures and lice load, controlling for season, female reproductive state and dominance rank. Results show that the interaction between degree centrality (number of partners) and seasonality predicted lice load: females interacting with more partners had fewer lice than those interacting with fewer partners in winter and summer, whereas there was no relationship between lice load and centrality in spring and fall. This is counter to the prediction that increased contact leads to greater louse burden but fits the prediction that social grooming limits louse burden. Interactions between environmental seasonality and both parasite and host biology appeared to mediate the role of social processes in louse burden. Nature Publishing Group 2016-02-26 /pmc/articles/PMC4768153/ /pubmed/26915589 http://dx.doi.org/10.1038/srep22095 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Duboscq, Julie
Romano, Valeria
Sueur, Cédric
MacIntosh, Andrew J.J.
Network centrality and seasonality interact to predict lice load in a social primate
title Network centrality and seasonality interact to predict lice load in a social primate
title_full Network centrality and seasonality interact to predict lice load in a social primate
title_fullStr Network centrality and seasonality interact to predict lice load in a social primate
title_full_unstemmed Network centrality and seasonality interact to predict lice load in a social primate
title_short Network centrality and seasonality interact to predict lice load in a social primate
title_sort network centrality and seasonality interact to predict lice load in a social primate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768153/
https://www.ncbi.nlm.nih.gov/pubmed/26915589
http://dx.doi.org/10.1038/srep22095
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