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Honeybee gut Lactobacillus modulates host learning and memory behaviors via regulating tryptophan metabolism

Honeybees are highly social insects with a rich behavioral repertoire and are a versatile model for neurobiological research. Their gut microbiota comprises a limited number of host-restricted bacterial phylotypes that are important for honeybee health. However, it remains unclear how specific gut m...

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Autores principales: Zhang, Zijing, Mu, Xiaohuan, Cao, Qina, Shi, Yao, Hu, Xiaosong, Zheng, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018956/
https://www.ncbi.nlm.nih.gov/pubmed/35440638
http://dx.doi.org/10.1038/s41467-022-29760-0
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author Zhang, Zijing
Mu, Xiaohuan
Cao, Qina
Shi, Yao
Hu, Xiaosong
Zheng, Hao
author_facet Zhang, Zijing
Mu, Xiaohuan
Cao, Qina
Shi, Yao
Hu, Xiaosong
Zheng, Hao
author_sort Zhang, Zijing
collection PubMed
description Honeybees are highly social insects with a rich behavioral repertoire and are a versatile model for neurobiological research. Their gut microbiota comprises a limited number of host-restricted bacterial phylotypes that are important for honeybee health. However, it remains unclear how specific gut members affect honeybee behaviors. Here, we find that antibiotic exposure disturbs the gut community and influences honeybee phenotypes under field conditions. Using laboratory-generated gnotobiotic bees, we show that a normal gut microbiota is required for olfactory learning and memory abilities. Brain transcriptomic profiling reveals distinct brain gene expression patterns between microbiota-free and conventional bees. Subsequent metabolomic analyses of both hemolymph and gut samples show that the microbiota mainly regulates tryptophan metabolism. Our results indicate that host-specific Lactobacillus strains promote memory behavior by transforming tryptophan to indole derivatives that activate the host aryl hydrocarbon receptor. Our findings highlight the contributions of specific gut members to honeybee neurological processes, thus providing a promising model to understand host-microbe interactions.
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spelling pubmed-90189562022-04-28 Honeybee gut Lactobacillus modulates host learning and memory behaviors via regulating tryptophan metabolism Zhang, Zijing Mu, Xiaohuan Cao, Qina Shi, Yao Hu, Xiaosong Zheng, Hao Nat Commun Article Honeybees are highly social insects with a rich behavioral repertoire and are a versatile model for neurobiological research. Their gut microbiota comprises a limited number of host-restricted bacterial phylotypes that are important for honeybee health. However, it remains unclear how specific gut members affect honeybee behaviors. Here, we find that antibiotic exposure disturbs the gut community and influences honeybee phenotypes under field conditions. Using laboratory-generated gnotobiotic bees, we show that a normal gut microbiota is required for olfactory learning and memory abilities. Brain transcriptomic profiling reveals distinct brain gene expression patterns between microbiota-free and conventional bees. Subsequent metabolomic analyses of both hemolymph and gut samples show that the microbiota mainly regulates tryptophan metabolism. Our results indicate that host-specific Lactobacillus strains promote memory behavior by transforming tryptophan to indole derivatives that activate the host aryl hydrocarbon receptor. Our findings highlight the contributions of specific gut members to honeybee neurological processes, thus providing a promising model to understand host-microbe interactions. Nature Publishing Group UK 2022-04-19 /pmc/articles/PMC9018956/ /pubmed/35440638 http://dx.doi.org/10.1038/s41467-022-29760-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhang, Zijing
Mu, Xiaohuan
Cao, Qina
Shi, Yao
Hu, Xiaosong
Zheng, Hao
Honeybee gut Lactobacillus modulates host learning and memory behaviors via regulating tryptophan metabolism
title Honeybee gut Lactobacillus modulates host learning and memory behaviors via regulating tryptophan metabolism
title_full Honeybee gut Lactobacillus modulates host learning and memory behaviors via regulating tryptophan metabolism
title_fullStr Honeybee gut Lactobacillus modulates host learning and memory behaviors via regulating tryptophan metabolism
title_full_unstemmed Honeybee gut Lactobacillus modulates host learning and memory behaviors via regulating tryptophan metabolism
title_short Honeybee gut Lactobacillus modulates host learning and memory behaviors via regulating tryptophan metabolism
title_sort honeybee gut lactobacillus modulates host learning and memory behaviors via regulating tryptophan metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018956/
https://www.ncbi.nlm.nih.gov/pubmed/35440638
http://dx.doi.org/10.1038/s41467-022-29760-0
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