Cargando…
Social apoptosis in honey bee superorganisms
Eusocial insect colonies form superorganisms, in which nestmates cooperate and use social immunity to combat parasites. However, social immunity may fail in case of emerging diseases. This is the case for the ectoparasitic mite Varroa destructor, which switched hosts from the Eastern honeybee, Apis...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893659/ https://www.ncbi.nlm.nih.gov/pubmed/27264643 http://dx.doi.org/10.1038/srep27210 |
_version_ | 1782435597867024384 |
---|---|
author | Page, Paul Lin, Zheguang Buawangpong, Ninat Zheng, Huoqing Hu, Fuliang Neumann, Peter Chantawannakul, Panuwan Dietemann, Vincent |
author_facet | Page, Paul Lin, Zheguang Buawangpong, Ninat Zheng, Huoqing Hu, Fuliang Neumann, Peter Chantawannakul, Panuwan Dietemann, Vincent |
author_sort | Page, Paul |
collection | PubMed |
description | Eusocial insect colonies form superorganisms, in which nestmates cooperate and use social immunity to combat parasites. However, social immunity may fail in case of emerging diseases. This is the case for the ectoparasitic mite Varroa destructor, which switched hosts from the Eastern honeybee, Apis cerana, to the Western honey bee, Apis mellifera, and currently is the greatest threat to A. mellifera apiculture globally. Here, we show that immature workers of the mite’s original host, A. cerana, are more susceptible to V. destructor infestations than those of its new host, thereby enabling more efficient social immunity and contributing to colony survival. This counterintuitive result shows that susceptible individuals can foster superorganism survival, offering empirical support to theoretical arguments about the adaptive value of worker suicide in social insects. Altruistic suicide of immature bees constitutes a social analogue of apoptosis, as it prevents the spread of infections by sacrificing parts of the whole organism, and unveils a novel form of transgenerational social immunity in honey bees. Taking into account the key role of susceptible immature bees in social immunity will improve breeding efforts to mitigate the unsustainably high colony losses of Western honey bees due to V. destructor infestations worldwide. |
format | Online Article Text |
id | pubmed-4893659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48936592016-06-10 Social apoptosis in honey bee superorganisms Page, Paul Lin, Zheguang Buawangpong, Ninat Zheng, Huoqing Hu, Fuliang Neumann, Peter Chantawannakul, Panuwan Dietemann, Vincent Sci Rep Article Eusocial insect colonies form superorganisms, in which nestmates cooperate and use social immunity to combat parasites. However, social immunity may fail in case of emerging diseases. This is the case for the ectoparasitic mite Varroa destructor, which switched hosts from the Eastern honeybee, Apis cerana, to the Western honey bee, Apis mellifera, and currently is the greatest threat to A. mellifera apiculture globally. Here, we show that immature workers of the mite’s original host, A. cerana, are more susceptible to V. destructor infestations than those of its new host, thereby enabling more efficient social immunity and contributing to colony survival. This counterintuitive result shows that susceptible individuals can foster superorganism survival, offering empirical support to theoretical arguments about the adaptive value of worker suicide in social insects. Altruistic suicide of immature bees constitutes a social analogue of apoptosis, as it prevents the spread of infections by sacrificing parts of the whole organism, and unveils a novel form of transgenerational social immunity in honey bees. Taking into account the key role of susceptible immature bees in social immunity will improve breeding efforts to mitigate the unsustainably high colony losses of Western honey bees due to V. destructor infestations worldwide. Nature Publishing Group 2016-06-06 /pmc/articles/PMC4893659/ /pubmed/27264643 http://dx.doi.org/10.1038/srep27210 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 Page, Paul Lin, Zheguang Buawangpong, Ninat Zheng, Huoqing Hu, Fuliang Neumann, Peter Chantawannakul, Panuwan Dietemann, Vincent Social apoptosis in honey bee superorganisms |
title | Social apoptosis in honey bee superorganisms |
title_full | Social apoptosis in honey bee superorganisms |
title_fullStr | Social apoptosis in honey bee superorganisms |
title_full_unstemmed | Social apoptosis in honey bee superorganisms |
title_short | Social apoptosis in honey bee superorganisms |
title_sort | social apoptosis in honey bee superorganisms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893659/ https://www.ncbi.nlm.nih.gov/pubmed/27264643 http://dx.doi.org/10.1038/srep27210 |
work_keys_str_mv | AT pagepaul socialapoptosisinhoneybeesuperorganisms AT linzheguang socialapoptosisinhoneybeesuperorganisms AT buawangpongninat socialapoptosisinhoneybeesuperorganisms AT zhenghuoqing socialapoptosisinhoneybeesuperorganisms AT hufuliang socialapoptosisinhoneybeesuperorganisms AT neumannpeter socialapoptosisinhoneybeesuperorganisms AT chantawannakulpanuwan socialapoptosisinhoneybeesuperorganisms AT dietemannvincent socialapoptosisinhoneybeesuperorganisms |