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Genetic and metabolic links between the murine microbiome and memory
BACKGROUND: Recent evidence has linked the gut microbiome to host behavior via the gut–brain axis [1–3]; however, the underlying mechanisms remain unexplored. Here, we determined the links between host genetics, the gut microbiome and memory using the genetically defined Collaborative Cross (CC) mou...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164142/ https://www.ncbi.nlm.nih.gov/pubmed/32299497 http://dx.doi.org/10.1186/s40168-020-00817-w |
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author | Mao, Jian-Hua Kim, Young-Mo Zhou, Yan-Xia Hu, Dehong Zhong, Chenhan Chang, Hang Brislawn, Colin J. Fansler, Sarah Langley, Sasha Wang, Yunshan Peisl, B. Y. Loulou Celniker, Susan E. Threadgill, David W. Wilmes, Paul Orr, Galya Metz, Thomas O. Jansson, Janet K. Snijders, Antoine M. |
author_facet | Mao, Jian-Hua Kim, Young-Mo Zhou, Yan-Xia Hu, Dehong Zhong, Chenhan Chang, Hang Brislawn, Colin J. Fansler, Sarah Langley, Sasha Wang, Yunshan Peisl, B. Y. Loulou Celniker, Susan E. Threadgill, David W. Wilmes, Paul Orr, Galya Metz, Thomas O. Jansson, Janet K. Snijders, Antoine M. |
author_sort | Mao, Jian-Hua |
collection | PubMed |
description | BACKGROUND: Recent evidence has linked the gut microbiome to host behavior via the gut–brain axis [1–3]; however, the underlying mechanisms remain unexplored. Here, we determined the links between host genetics, the gut microbiome and memory using the genetically defined Collaborative Cross (CC) mouse cohort, complemented with microbiome and metabolomic analyses in conventional and germ-free (GF) mice. RESULTS: A genome-wide association analysis (GWAS) identified 715 of 76,080 single-nucleotide polymorphisms (SNPs) that were significantly associated with short-term memory using the passive avoidance model. The identified SNPs were enriched in genes known to be involved in learning and memory functions. By 16S rRNA gene sequencing of the gut microbial community in the same CC cohort, we identified specific microorganisms that were significantly correlated with longer latencies in our retention test, including a positive correlation with Lactobacillus. Inoculation of GF mice with individual species of Lactobacillus (L. reuteri F275, L. plantarum BDGP2 or L. brevis BDGP6) resulted in significantly improved memory compared to uninoculated or E. coli DH10B inoculated controls. Untargeted metabolomics analysis revealed significantly higher levels of several metabolites, including lactate, in the stools of Lactobacillus-colonized mice, when compared to GF control mice. Moreover, we demonstrate that dietary lactate treatment alone boosted memory in conventional mice. Mechanistically, we show that both inoculation with Lactobacillus or lactate treatment significantly increased the levels of the neurotransmitter, gamma-aminobutyric acid (GABA), in the hippocampus of the mice. CONCLUSION: Together, this study provides new evidence for a link between Lactobacillus and memory and our results open possible new avenues for treating memory impairment disorders using specific gut microbial inoculants and/or metabolites. |
format | Online Article Text |
id | pubmed-7164142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71641422020-04-22 Genetic and metabolic links between the murine microbiome and memory Mao, Jian-Hua Kim, Young-Mo Zhou, Yan-Xia Hu, Dehong Zhong, Chenhan Chang, Hang Brislawn, Colin J. Fansler, Sarah Langley, Sasha Wang, Yunshan Peisl, B. Y. Loulou Celniker, Susan E. Threadgill, David W. Wilmes, Paul Orr, Galya Metz, Thomas O. Jansson, Janet K. Snijders, Antoine M. Microbiome Research BACKGROUND: Recent evidence has linked the gut microbiome to host behavior via the gut–brain axis [1–3]; however, the underlying mechanisms remain unexplored. Here, we determined the links between host genetics, the gut microbiome and memory using the genetically defined Collaborative Cross (CC) mouse cohort, complemented with microbiome and metabolomic analyses in conventional and germ-free (GF) mice. RESULTS: A genome-wide association analysis (GWAS) identified 715 of 76,080 single-nucleotide polymorphisms (SNPs) that were significantly associated with short-term memory using the passive avoidance model. The identified SNPs were enriched in genes known to be involved in learning and memory functions. By 16S rRNA gene sequencing of the gut microbial community in the same CC cohort, we identified specific microorganisms that were significantly correlated with longer latencies in our retention test, including a positive correlation with Lactobacillus. Inoculation of GF mice with individual species of Lactobacillus (L. reuteri F275, L. plantarum BDGP2 or L. brevis BDGP6) resulted in significantly improved memory compared to uninoculated or E. coli DH10B inoculated controls. Untargeted metabolomics analysis revealed significantly higher levels of several metabolites, including lactate, in the stools of Lactobacillus-colonized mice, when compared to GF control mice. Moreover, we demonstrate that dietary lactate treatment alone boosted memory in conventional mice. Mechanistically, we show that both inoculation with Lactobacillus or lactate treatment significantly increased the levels of the neurotransmitter, gamma-aminobutyric acid (GABA), in the hippocampus of the mice. CONCLUSION: Together, this study provides new evidence for a link between Lactobacillus and memory and our results open possible new avenues for treating memory impairment disorders using specific gut microbial inoculants and/or metabolites. BioMed Central 2020-04-16 /pmc/articles/PMC7164142/ /pubmed/32299497 http://dx.doi.org/10.1186/s40168-020-00817-w Text en © The Author(s) 2020, corrected publication May 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Mao, Jian-Hua Kim, Young-Mo Zhou, Yan-Xia Hu, Dehong Zhong, Chenhan Chang, Hang Brislawn, Colin J. Fansler, Sarah Langley, Sasha Wang, Yunshan Peisl, B. Y. Loulou Celniker, Susan E. Threadgill, David W. Wilmes, Paul Orr, Galya Metz, Thomas O. Jansson, Janet K. Snijders, Antoine M. Genetic and metabolic links between the murine microbiome and memory |
title | Genetic and metabolic links between the murine microbiome and memory |
title_full | Genetic and metabolic links between the murine microbiome and memory |
title_fullStr | Genetic and metabolic links between the murine microbiome and memory |
title_full_unstemmed | Genetic and metabolic links between the murine microbiome and memory |
title_short | Genetic and metabolic links between the murine microbiome and memory |
title_sort | genetic and metabolic links between the murine microbiome and memory |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164142/ https://www.ncbi.nlm.nih.gov/pubmed/32299497 http://dx.doi.org/10.1186/s40168-020-00817-w |
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