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Protein nutrition governs within-host race of honey bee pathogens
Multiple infections are common in honey bees, Apis mellifera, but the possible role of nutrition in this regard is poorly understood. Microsporidian infections, which are promoted by protein-fed, can negatively correlate with virus infections, but the role of protein nutrition for the microsporidian...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678143/ https://www.ncbi.nlm.nih.gov/pubmed/29118416 http://dx.doi.org/10.1038/s41598-017-15358-w |
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author | Tritschler, Manuel Vollmann, Jutta J. Yañez, Orlando Chejanovsky, Nor Crailsheim, Karl Neumann, Peter |
author_facet | Tritschler, Manuel Vollmann, Jutta J. Yañez, Orlando Chejanovsky, Nor Crailsheim, Karl Neumann, Peter |
author_sort | Tritschler, Manuel |
collection | PubMed |
description | Multiple infections are common in honey bees, Apis mellifera, but the possible role of nutrition in this regard is poorly understood. Microsporidian infections, which are promoted by protein-fed, can negatively correlate with virus infections, but the role of protein nutrition for the microsporidian-virus interface is unknown. Here, we challenged naturally deformed wing virus - B (DWV-B) infected adult honey bee workers fed with or without pollen ( = protein) in hoarding cages, with the microsporidian Nosema ceranae. Bee mortality was recorded for 14 days and N. ceranae spore loads and DWV-B titers were quantified. Amongst the groups inoculated with N. ceranae, more spores were counted in protein-fed bees. However, N. ceranae infected bees without protein-diet had reduced longevity compared to all other groups. N. ceranae infection had no effect on protein-fed bee’s longevity, whereas bees supplied only with sugar-water showed reduced survival. Our data also support that protein-feeding can have a significant negative impact on virus infections in insects. The negative correlation between N. ceranae spore loads and DWV-B titers was stronger expressed in protein-fed hosts. Proteins not only enhance survival of infected hosts, but also significantly shape the microsporidian-virus interface, probably due to increased spore production and enhanced host immunity. |
format | Online Article Text |
id | pubmed-5678143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56781432017-11-17 Protein nutrition governs within-host race of honey bee pathogens Tritschler, Manuel Vollmann, Jutta J. Yañez, Orlando Chejanovsky, Nor Crailsheim, Karl Neumann, Peter Sci Rep Article Multiple infections are common in honey bees, Apis mellifera, but the possible role of nutrition in this regard is poorly understood. Microsporidian infections, which are promoted by protein-fed, can negatively correlate with virus infections, but the role of protein nutrition for the microsporidian-virus interface is unknown. Here, we challenged naturally deformed wing virus - B (DWV-B) infected adult honey bee workers fed with or without pollen ( = protein) in hoarding cages, with the microsporidian Nosema ceranae. Bee mortality was recorded for 14 days and N. ceranae spore loads and DWV-B titers were quantified. Amongst the groups inoculated with N. ceranae, more spores were counted in protein-fed bees. However, N. ceranae infected bees without protein-diet had reduced longevity compared to all other groups. N. ceranae infection had no effect on protein-fed bee’s longevity, whereas bees supplied only with sugar-water showed reduced survival. Our data also support that protein-feeding can have a significant negative impact on virus infections in insects. The negative correlation between N. ceranae spore loads and DWV-B titers was stronger expressed in protein-fed hosts. Proteins not only enhance survival of infected hosts, but also significantly shape the microsporidian-virus interface, probably due to increased spore production and enhanced host immunity. Nature Publishing Group UK 2017-11-08 /pmc/articles/PMC5678143/ /pubmed/29118416 http://dx.doi.org/10.1038/s41598-017-15358-w Text en © The Author(s) 2017 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 Tritschler, Manuel Vollmann, Jutta J. Yañez, Orlando Chejanovsky, Nor Crailsheim, Karl Neumann, Peter Protein nutrition governs within-host race of honey bee pathogens |
title | Protein nutrition governs within-host race of honey bee pathogens |
title_full | Protein nutrition governs within-host race of honey bee pathogens |
title_fullStr | Protein nutrition governs within-host race of honey bee pathogens |
title_full_unstemmed | Protein nutrition governs within-host race of honey bee pathogens |
title_short | Protein nutrition governs within-host race of honey bee pathogens |
title_sort | protein nutrition governs within-host race of honey bee pathogens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678143/ https://www.ncbi.nlm.nih.gov/pubmed/29118416 http://dx.doi.org/10.1038/s41598-017-15358-w |
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