Cargando…

Parasites modulate within-colony activity and accelerate the temporal polyethism schedule of a social insect, the honey bee

Task allocation in social insect colonies is generally organised into an age-related division of labour, termed the temporal polyethism schedule, which may in part have evolved to reduce infection of the colony’s brood by pests and pathogens. The temporal polyethism schedule is sensitive to colony p...

Descripción completa

Detalles Bibliográficos
Autores principales: Natsopoulou, Myrsini E., McMahon, Dino P., Paxton, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917585/
https://www.ncbi.nlm.nih.gov/pubmed/27397965
http://dx.doi.org/10.1007/s00265-015-2019-5
_version_ 1782438964546764800
author Natsopoulou, Myrsini E.
McMahon, Dino P.
Paxton, Robert J.
author_facet Natsopoulou, Myrsini E.
McMahon, Dino P.
Paxton, Robert J.
author_sort Natsopoulou, Myrsini E.
collection PubMed
description Task allocation in social insect colonies is generally organised into an age-related division of labour, termed the temporal polyethism schedule, which may in part have evolved to reduce infection of the colony’s brood by pests and pathogens. The temporal polyethism schedule is sensitive to colony perturbations that may lead to adaptive changes in task allocation, maintaining colony homeostasis. Though social insects can be infected by a range of parasites, little is known of how these parasites impact within-colony behaviour and the temporal polyethism schedule. We use honey bees (Apis mellifera) experimentally infected by two of their emerging pathogens, Deformed wing virus (DWV), which is relatively understudied concerning its behavioural impact on its host, and the exotic microsporidian Nosema ceranae. We examined parasite effects on host temporal polyethism and patterns of activity within the colony. We found that pathogens accelerated the temporal polyethism schedule, but without reducing host behavioural repertoire. Infected hosts exhibited increased hyperactivity, allocating more time to self-grooming and foraging-related tasks. The strength of behavioural alterations we observed was found to be pathogen specific; behavioural modifications were more pronounced in virus-treated hosts versus N. ceranae-treated hosts, with potential benefits for the colony in terms of reducing within-colony transmission. Investigating the effects of multiple pathogens on behavioural patterns of social insects could play a crucial role in understanding pathogen spread within a colony and their effects on colony social organisation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00265-015-2019-5) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4917585
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-49175852016-07-07 Parasites modulate within-colony activity and accelerate the temporal polyethism schedule of a social insect, the honey bee Natsopoulou, Myrsini E. McMahon, Dino P. Paxton, Robert J. Behav Ecol Sociobiol Original Article Task allocation in social insect colonies is generally organised into an age-related division of labour, termed the temporal polyethism schedule, which may in part have evolved to reduce infection of the colony’s brood by pests and pathogens. The temporal polyethism schedule is sensitive to colony perturbations that may lead to adaptive changes in task allocation, maintaining colony homeostasis. Though social insects can be infected by a range of parasites, little is known of how these parasites impact within-colony behaviour and the temporal polyethism schedule. We use honey bees (Apis mellifera) experimentally infected by two of their emerging pathogens, Deformed wing virus (DWV), which is relatively understudied concerning its behavioural impact on its host, and the exotic microsporidian Nosema ceranae. We examined parasite effects on host temporal polyethism and patterns of activity within the colony. We found that pathogens accelerated the temporal polyethism schedule, but without reducing host behavioural repertoire. Infected hosts exhibited increased hyperactivity, allocating more time to self-grooming and foraging-related tasks. The strength of behavioural alterations we observed was found to be pathogen specific; behavioural modifications were more pronounced in virus-treated hosts versus N. ceranae-treated hosts, with potential benefits for the colony in terms of reducing within-colony transmission. Investigating the effects of multiple pathogens on behavioural patterns of social insects could play a crucial role in understanding pathogen spread within a colony and their effects on colony social organisation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00265-015-2019-5) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-10-07 2016 /pmc/articles/PMC4917585/ /pubmed/27397965 http://dx.doi.org/10.1007/s00265-015-2019-5 Text en © Springer-Verlag Berlin Heidelberg 2015
spellingShingle Original Article
Natsopoulou, Myrsini E.
McMahon, Dino P.
Paxton, Robert J.
Parasites modulate within-colony activity and accelerate the temporal polyethism schedule of a social insect, the honey bee
title Parasites modulate within-colony activity and accelerate the temporal polyethism schedule of a social insect, the honey bee
title_full Parasites modulate within-colony activity and accelerate the temporal polyethism schedule of a social insect, the honey bee
title_fullStr Parasites modulate within-colony activity and accelerate the temporal polyethism schedule of a social insect, the honey bee
title_full_unstemmed Parasites modulate within-colony activity and accelerate the temporal polyethism schedule of a social insect, the honey bee
title_short Parasites modulate within-colony activity and accelerate the temporal polyethism schedule of a social insect, the honey bee
title_sort parasites modulate within-colony activity and accelerate the temporal polyethism schedule of a social insect, the honey bee
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917585/
https://www.ncbi.nlm.nih.gov/pubmed/27397965
http://dx.doi.org/10.1007/s00265-015-2019-5
work_keys_str_mv AT natsopouloumyrsinie parasitesmodulatewithincolonyactivityandacceleratethetemporalpolyethismscheduleofasocialinsectthehoneybee
AT mcmahondinop parasitesmodulatewithincolonyactivityandacceleratethetemporalpolyethismscheduleofasocialinsectthehoneybee
AT paxtonrobertj parasitesmodulatewithincolonyactivityandacceleratethetemporalpolyethismscheduleofasocialinsectthehoneybee