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Rapid parallel evolution overcomes global honey bee parasite
In eusocial insect colonies nestmates cooperate to combat parasites, a trait called social immunity. However, social immunity failed for Western honey bees (Apis mellifera) when the ectoparasitic mite Varroa destructor switched hosts from Eastern honey bees (Apis cerana). This mite has since become...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955925/ https://www.ncbi.nlm.nih.gov/pubmed/29769608 http://dx.doi.org/10.1038/s41598-018-26001-7 |
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author | Oddie, Melissa Büchler, Ralph Dahle, Bjørn Kovacic, Marin Le Conte, Yves Locke, Barbara de Miranda, Joachim R. Mondet, Fanny Neumann, Peter |
author_facet | Oddie, Melissa Büchler, Ralph Dahle, Bjørn Kovacic, Marin Le Conte, Yves Locke, Barbara de Miranda, Joachim R. Mondet, Fanny Neumann, Peter |
author_sort | Oddie, Melissa |
collection | PubMed |
description | In eusocial insect colonies nestmates cooperate to combat parasites, a trait called social immunity. However, social immunity failed for Western honey bees (Apis mellifera) when the ectoparasitic mite Varroa destructor switched hosts from Eastern honey bees (Apis cerana). This mite has since become the most severe threat to A. mellifera world-wide. Despite this, some isolated A. mellifera populations are known to survive infestations by means of natural selection, largely by supressing mite reproduction, but the underlying mechanisms of this are poorly understood. Here, we show that a cost-effective social immunity mechanism has evolved rapidly and independently in four naturally V. destructor-surviving A. mellifera populations. Worker bees of all four ‘surviving’ populations uncapped/recapped worker brood cells more frequently and targeted mite-infested cells more effectively than workers in local susceptible colonies. Direct experiments confirmed the ability of uncapping/recapping to reduce mite reproductive success without sacrificing nestmates. Our results provide striking evidence that honey bees can overcome exotic parasites with simple qualitative and quantitative adaptive shifts in behaviour. Due to rapid, parallel evolution in four host populations this appears to be a key mechanism explaining survival of mite infested colonies. |
format | Online Article Text |
id | pubmed-5955925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59559252018-05-21 Rapid parallel evolution overcomes global honey bee parasite Oddie, Melissa Büchler, Ralph Dahle, Bjørn Kovacic, Marin Le Conte, Yves Locke, Barbara de Miranda, Joachim R. Mondet, Fanny Neumann, Peter Sci Rep Article In eusocial insect colonies nestmates cooperate to combat parasites, a trait called social immunity. However, social immunity failed for Western honey bees (Apis mellifera) when the ectoparasitic mite Varroa destructor switched hosts from Eastern honey bees (Apis cerana). This mite has since become the most severe threat to A. mellifera world-wide. Despite this, some isolated A. mellifera populations are known to survive infestations by means of natural selection, largely by supressing mite reproduction, but the underlying mechanisms of this are poorly understood. Here, we show that a cost-effective social immunity mechanism has evolved rapidly and independently in four naturally V. destructor-surviving A. mellifera populations. Worker bees of all four ‘surviving’ populations uncapped/recapped worker brood cells more frequently and targeted mite-infested cells more effectively than workers in local susceptible colonies. Direct experiments confirmed the ability of uncapping/recapping to reduce mite reproductive success without sacrificing nestmates. Our results provide striking evidence that honey bees can overcome exotic parasites with simple qualitative and quantitative adaptive shifts in behaviour. Due to rapid, parallel evolution in four host populations this appears to be a key mechanism explaining survival of mite infested colonies. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955925/ /pubmed/29769608 http://dx.doi.org/10.1038/s41598-018-26001-7 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 Oddie, Melissa Büchler, Ralph Dahle, Bjørn Kovacic, Marin Le Conte, Yves Locke, Barbara de Miranda, Joachim R. Mondet, Fanny Neumann, Peter Rapid parallel evolution overcomes global honey bee parasite |
title | Rapid parallel evolution overcomes global honey bee parasite |
title_full | Rapid parallel evolution overcomes global honey bee parasite |
title_fullStr | Rapid parallel evolution overcomes global honey bee parasite |
title_full_unstemmed | Rapid parallel evolution overcomes global honey bee parasite |
title_short | Rapid parallel evolution overcomes global honey bee parasite |
title_sort | rapid parallel evolution overcomes global honey bee parasite |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955925/ https://www.ncbi.nlm.nih.gov/pubmed/29769608 http://dx.doi.org/10.1038/s41598-018-26001-7 |
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