Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1784689140012417024 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9018956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhangzijing honeybeegutlactobacillusmodulateshostlearningandmemorybehaviorsviaregulatingtryptophanmetabolism AT muxiaohuan honeybeegutlactobacillusmodulateshostlearningandmemorybehaviorsviaregulatingtryptophanmetabolism AT caoqina honeybeegutlactobacillusmodulateshostlearningandmemorybehaviorsviaregulatingtryptophanmetabolism AT shiyao honeybeegutlactobacillusmodulateshostlearningandmemorybehaviorsviaregulatingtryptophanmetabolism AT huxiaosong honeybeegutlactobacillusmodulateshostlearningandmemorybehaviorsviaregulatingtryptophanmetabolism AT zhenghao honeybeegutlactobacillusmodulateshostlearningandmemorybehaviorsviaregulatingtryptophanmetabolism |