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Reproductive parasitism by worker honey bees suppressed by queens through regulation of worker mandibular secretions

Social cohesion in social insect colonies can be achieved through the use of chemical signals whose production is caste-specific and regulated by social contexts. In honey bees, queen mandibular gland pheromones (QMP) maintain reproductive dominance by inhibiting ovary activation and production of q...

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Autores principales: Mumoki, Fiona N., Pirk, Christian W. W., Yusuf, Abdullahi A., Crewe, Robin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5967312/
https://www.ncbi.nlm.nih.gov/pubmed/29799016
http://dx.doi.org/10.1038/s41598-018-26060-w
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author Mumoki, Fiona N.
Pirk, Christian W. W.
Yusuf, Abdullahi A.
Crewe, Robin M.
author_facet Mumoki, Fiona N.
Pirk, Christian W. W.
Yusuf, Abdullahi A.
Crewe, Robin M.
author_sort Mumoki, Fiona N.
collection PubMed
description Social cohesion in social insect colonies can be achieved through the use of chemical signals whose production is caste-specific and regulated by social contexts. In honey bees, queen mandibular gland pheromones (QMP) maintain reproductive dominance by inhibiting ovary activation and production of queen-like mandibular gland signals in workers. We investigated whether honey bee queens can control reproductively active workers of the intraspecific social parasite Apis mellifera capensis, parasitising A. m. scutellata host colonies. Our results show that the queen’s QMP suppresses ovarian activation and inhibits the production of QMP pheromone signals by the parasitic workers, achieved through differential expression of enzymes involved in the biosynthesis of these pheromones at two points in the biosynthetic pathway. This is the first report showing that honey bee queens can regulate reproduction in intraspecific social parasites and deepens our understanding of the molecular mechanisms involved in the regulation of worker reproduction in social insects.
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spelling pubmed-59673122018-05-30 Reproductive parasitism by worker honey bees suppressed by queens through regulation of worker mandibular secretions Mumoki, Fiona N. Pirk, Christian W. W. Yusuf, Abdullahi A. Crewe, Robin M. Sci Rep Article Social cohesion in social insect colonies can be achieved through the use of chemical signals whose production is caste-specific and regulated by social contexts. In honey bees, queen mandibular gland pheromones (QMP) maintain reproductive dominance by inhibiting ovary activation and production of queen-like mandibular gland signals in workers. We investigated whether honey bee queens can control reproductively active workers of the intraspecific social parasite Apis mellifera capensis, parasitising A. m. scutellata host colonies. Our results show that the queen’s QMP suppresses ovarian activation and inhibits the production of QMP pheromone signals by the parasitic workers, achieved through differential expression of enzymes involved in the biosynthesis of these pheromones at two points in the biosynthetic pathway. This is the first report showing that honey bee queens can regulate reproduction in intraspecific social parasites and deepens our understanding of the molecular mechanisms involved in the regulation of worker reproduction in social insects. Nature Publishing Group UK 2018-05-24 /pmc/articles/PMC5967312/ /pubmed/29799016 http://dx.doi.org/10.1038/s41598-018-26060-w Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mumoki, Fiona N.
Pirk, Christian W. W.
Yusuf, Abdullahi A.
Crewe, Robin M.
Reproductive parasitism by worker honey bees suppressed by queens through regulation of worker mandibular secretions
title Reproductive parasitism by worker honey bees suppressed by queens through regulation of worker mandibular secretions
title_full Reproductive parasitism by worker honey bees suppressed by queens through regulation of worker mandibular secretions
title_fullStr Reproductive parasitism by worker honey bees suppressed by queens through regulation of worker mandibular secretions
title_full_unstemmed Reproductive parasitism by worker honey bees suppressed by queens through regulation of worker mandibular secretions
title_short Reproductive parasitism by worker honey bees suppressed by queens through regulation of worker mandibular secretions
title_sort reproductive parasitism by worker honey bees suppressed by queens through regulation of worker mandibular secretions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5967312/
https://www.ncbi.nlm.nih.gov/pubmed/29799016
http://dx.doi.org/10.1038/s41598-018-26060-w
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