Cargando…

Meta-analysis of honey bee neurogenomic response links Deformed wing virus type A to precocious behavioral maturation

Crop pollination by the western honey bee Apis mellifera is vital to agriculture but threatened by alarmingly high levels of colony mortality, especially in Europe and North America. Colony loss is due, in part, to the high viral loads of Deformed wing virus (DWV), transmitted by the ectoparasitic m...

Descripción completa

Detalles Bibliográficos
Autores principales: Traniello, Ian M., Bukhari, Syed Abbas, Kevill, Jessica, Ahmed, Amy Cash, Hamilton, Adam R., Naeger, Nicholas L., Schroeder, Declan C., Robinson, Gene E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033282/
https://www.ncbi.nlm.nih.gov/pubmed/32080242
http://dx.doi.org/10.1038/s41598-020-59808-4
_version_ 1783499632278503424
author Traniello, Ian M.
Bukhari, Syed Abbas
Kevill, Jessica
Ahmed, Amy Cash
Hamilton, Adam R.
Naeger, Nicholas L.
Schroeder, Declan C.
Robinson, Gene E.
author_facet Traniello, Ian M.
Bukhari, Syed Abbas
Kevill, Jessica
Ahmed, Amy Cash
Hamilton, Adam R.
Naeger, Nicholas L.
Schroeder, Declan C.
Robinson, Gene E.
author_sort Traniello, Ian M.
collection PubMed
description Crop pollination by the western honey bee Apis mellifera is vital to agriculture but threatened by alarmingly high levels of colony mortality, especially in Europe and North America. Colony loss is due, in part, to the high viral loads of Deformed wing virus (DWV), transmitted by the ectoparasitic mite Varroa destructor, especially throughout the overwintering period of a honey bee colony. Covert DWV infection is commonplace and has been causally linked to precocious foraging, which itself has been linked to colony loss. Taking advantage of four brain transcriptome studies that unexpectedly revealed evidence of covert DWV-A infection, we set out to explore whether this effect is due to DWV-A mimicking naturally occurring changes in brain gene expression that are associated with behavioral maturation. Consistent with this hypothesis, we found that brain gene expression profiles of DWV-A infected bees resembled those of foragers, even in individuals that were much younger than typical foragers. In addition, brain transcriptional regulatory network analysis revealed a positive association between DWV-A infection and transcription factors previously associated with honey bee foraging behavior. Surprisingly, single-cell RNA-Sequencing implicated glia, not neurons, in this effect; there are relatively few glial cells in the insect brain and they are rarely associated with behavioral plasticity. Covert DWV-A infection also has been linked to impaired learning, which together with precocious foraging can lead to increased occurrence of infected bees from one colony mistakenly entering another colony, especially under crowded modern apiary conditions. These findings provide new insights into the mechanisms by which DWV-A affects honey bee health and colony survival.
format Online
Article
Text
id pubmed-7033282
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-70332822020-02-28 Meta-analysis of honey bee neurogenomic response links Deformed wing virus type A to precocious behavioral maturation Traniello, Ian M. Bukhari, Syed Abbas Kevill, Jessica Ahmed, Amy Cash Hamilton, Adam R. Naeger, Nicholas L. Schroeder, Declan C. Robinson, Gene E. Sci Rep Article Crop pollination by the western honey bee Apis mellifera is vital to agriculture but threatened by alarmingly high levels of colony mortality, especially in Europe and North America. Colony loss is due, in part, to the high viral loads of Deformed wing virus (DWV), transmitted by the ectoparasitic mite Varroa destructor, especially throughout the overwintering period of a honey bee colony. Covert DWV infection is commonplace and has been causally linked to precocious foraging, which itself has been linked to colony loss. Taking advantage of four brain transcriptome studies that unexpectedly revealed evidence of covert DWV-A infection, we set out to explore whether this effect is due to DWV-A mimicking naturally occurring changes in brain gene expression that are associated with behavioral maturation. Consistent with this hypothesis, we found that brain gene expression profiles of DWV-A infected bees resembled those of foragers, even in individuals that were much younger than typical foragers. In addition, brain transcriptional regulatory network analysis revealed a positive association between DWV-A infection and transcription factors previously associated with honey bee foraging behavior. Surprisingly, single-cell RNA-Sequencing implicated glia, not neurons, in this effect; there are relatively few glial cells in the insect brain and they are rarely associated with behavioral plasticity. Covert DWV-A infection also has been linked to impaired learning, which together with precocious foraging can lead to increased occurrence of infected bees from one colony mistakenly entering another colony, especially under crowded modern apiary conditions. These findings provide new insights into the mechanisms by which DWV-A affects honey bee health and colony survival. Nature Publishing Group UK 2020-02-20 /pmc/articles/PMC7033282/ /pubmed/32080242 http://dx.doi.org/10.1038/s41598-020-59808-4 Text en © The Author(s) 2020 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
Traniello, Ian M.
Bukhari, Syed Abbas
Kevill, Jessica
Ahmed, Amy Cash
Hamilton, Adam R.
Naeger, Nicholas L.
Schroeder, Declan C.
Robinson, Gene E.
Meta-analysis of honey bee neurogenomic response links Deformed wing virus type A to precocious behavioral maturation
title Meta-analysis of honey bee neurogenomic response links Deformed wing virus type A to precocious behavioral maturation
title_full Meta-analysis of honey bee neurogenomic response links Deformed wing virus type A to precocious behavioral maturation
title_fullStr Meta-analysis of honey bee neurogenomic response links Deformed wing virus type A to precocious behavioral maturation
title_full_unstemmed Meta-analysis of honey bee neurogenomic response links Deformed wing virus type A to precocious behavioral maturation
title_short Meta-analysis of honey bee neurogenomic response links Deformed wing virus type A to precocious behavioral maturation
title_sort meta-analysis of honey bee neurogenomic response links deformed wing virus type a to precocious behavioral maturation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033282/
https://www.ncbi.nlm.nih.gov/pubmed/32080242
http://dx.doi.org/10.1038/s41598-020-59808-4
work_keys_str_mv AT tranielloianm metaanalysisofhoneybeeneurogenomicresponselinksdeformedwingvirustypeatoprecociousbehavioralmaturation
AT bukharisyedabbas metaanalysisofhoneybeeneurogenomicresponselinksdeformedwingvirustypeatoprecociousbehavioralmaturation
AT kevilljessica metaanalysisofhoneybeeneurogenomicresponselinksdeformedwingvirustypeatoprecociousbehavioralmaturation
AT ahmedamycash metaanalysisofhoneybeeneurogenomicresponselinksdeformedwingvirustypeatoprecociousbehavioralmaturation
AT hamiltonadamr metaanalysisofhoneybeeneurogenomicresponselinksdeformedwingvirustypeatoprecociousbehavioralmaturation
AT naegernicholasl metaanalysisofhoneybeeneurogenomicresponselinksdeformedwingvirustypeatoprecociousbehavioralmaturation
AT schroederdeclanc metaanalysisofhoneybeeneurogenomicresponselinksdeformedwingvirustypeatoprecociousbehavioralmaturation
AT robinsongenee metaanalysisofhoneybeeneurogenomicresponselinksdeformedwingvirustypeatoprecociousbehavioralmaturation