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Symbionts shape host innate immunity in honeybees
The gut microbiome plays a critical role in the health of many animals. Honeybees are no exception, as they host a core microbiome that affects their nutrition and immune function. However, the relationship between the honeybee immune system and its gut symbionts is poorly understood. Here, we explo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482289/ https://www.ncbi.nlm.nih.gov/pubmed/32842927 http://dx.doi.org/10.1098/rspb.2020.1184 |
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author | Horak, Richard D. Leonard, Sean P. Moran, Nancy A. |
author_facet | Horak, Richard D. Leonard, Sean P. Moran, Nancy A. |
author_sort | Horak, Richard D. |
collection | PubMed |
description | The gut microbiome plays a critical role in the health of many animals. Honeybees are no exception, as they host a core microbiome that affects their nutrition and immune function. However, the relationship between the honeybee immune system and its gut symbionts is poorly understood. Here, we explore how the beneficial symbiont Snodgrassella alvi affects honeybee immune gene expression. We show that both live and heat-killed S. alvi protect honeybees from the opportunistic pathogen Serratia marcescens and lead to the expression of host antimicrobial peptides. Honeybee immune genes respond differently to live S. alvi compared to heat-killed S. alvi, the latter causing a more extensive immune expression response. We show a preference for Toll pathway upregulation over the Imd pathway in the presence of both live and heat-killed S. alvi. Finally, we find that live S. alvi aids in clearance of S. marcescens from the honeybee gut, supporting a potential role for the symbiont in colonization resistance. Our results show that colonization by the beneficial symbiont S. alvi triggers a replicable honeybee immune response. These responses may benefit the host and the symbiont, by helping to regulate gut microbial members and preventing overgrowth or invasion by opportunists. |
format | Online Article Text |
id | pubmed-7482289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74822892020-09-21 Symbionts shape host innate immunity in honeybees Horak, Richard D. Leonard, Sean P. Moran, Nancy A. Proc Biol Sci Development and Physiology The gut microbiome plays a critical role in the health of many animals. Honeybees are no exception, as they host a core microbiome that affects their nutrition and immune function. However, the relationship between the honeybee immune system and its gut symbionts is poorly understood. Here, we explore how the beneficial symbiont Snodgrassella alvi affects honeybee immune gene expression. We show that both live and heat-killed S. alvi protect honeybees from the opportunistic pathogen Serratia marcescens and lead to the expression of host antimicrobial peptides. Honeybee immune genes respond differently to live S. alvi compared to heat-killed S. alvi, the latter causing a more extensive immune expression response. We show a preference for Toll pathway upregulation over the Imd pathway in the presence of both live and heat-killed S. alvi. Finally, we find that live S. alvi aids in clearance of S. marcescens from the honeybee gut, supporting a potential role for the symbiont in colonization resistance. Our results show that colonization by the beneficial symbiont S. alvi triggers a replicable honeybee immune response. These responses may benefit the host and the symbiont, by helping to regulate gut microbial members and preventing overgrowth or invasion by opportunists. The Royal Society 2020-08-26 2020-08-26 /pmc/articles/PMC7482289/ /pubmed/32842927 http://dx.doi.org/10.1098/rspb.2020.1184 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Development and Physiology Horak, Richard D. Leonard, Sean P. Moran, Nancy A. Symbionts shape host innate immunity in honeybees |
title | Symbionts shape host innate immunity in honeybees |
title_full | Symbionts shape host innate immunity in honeybees |
title_fullStr | Symbionts shape host innate immunity in honeybees |
title_full_unstemmed | Symbionts shape host innate immunity in honeybees |
title_short | Symbionts shape host innate immunity in honeybees |
title_sort | symbionts shape host innate immunity in honeybees |
topic | Development and Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482289/ https://www.ncbi.nlm.nih.gov/pubmed/32842927 http://dx.doi.org/10.1098/rspb.2020.1184 |
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