Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Oddie, Melissa, Büchler, Ralph, Dahle, Bjørn, Kovacic, Marin, Le Conte, Yves, Locke, Barbara, de Miranda, Joachim R., Mondet, Fanny, Neumann, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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
_version_ 1783323790213644288
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
work_keys_str_mv AT oddiemelissa rapidparallelevolutionovercomesglobalhoneybeeparasite
AT buchlerralph rapidparallelevolutionovercomesglobalhoneybeeparasite
AT dahlebjørn rapidparallelevolutionovercomesglobalhoneybeeparasite
AT kovacicmarin rapidparallelevolutionovercomesglobalhoneybeeparasite
AT leconteyves rapidparallelevolutionovercomesglobalhoneybeeparasite
AT lockebarbara rapidparallelevolutionovercomesglobalhoneybeeparasite
AT demirandajoachimr rapidparallelevolutionovercomesglobalhoneybeeparasite
AT mondetfanny rapidparallelevolutionovercomesglobalhoneybeeparasite
AT neumannpeter rapidparallelevolutionovercomesglobalhoneybeeparasite