Faecal microbiota transplant from aged donor mice affects spatial learning and memory via modulating hippocampal synaptic plasticity- and neurotransmission-related proteins in young recipients.


Journal

Microbiome
ISSN: 2049-2618
Titre abrégé: Microbiome
Pays: England
ID NLM: 101615147

Informations de publication

Date de publication:
01 10 2020
Historique:
received: 30 03 2020
accepted: 31 08 2020
entrez: 2 10 2020
pubmed: 3 10 2020
medline: 31 3 2021
Statut: epublish

Résumé

The gut-brain axis and the intestinal microbiota are emerging as key players in health and disease. Shifts in intestinal microbiota composition affect a variety of systems; however, evidence of their direct impact on cognitive functions is still lacking. We tested whether faecal microbiota transplant (FMT) from aged donor mice into young adult recipients altered the hippocampus, an area of the central nervous system (CNS) known to be affected by the ageing process and related functions. Young adult mice were transplanted with the microbiota from either aged or age-matched donor mice. Following transplantation, characterization of the microbiotas and metabolomics profiles along with a battery of cognitive and behavioural tests were performed. Label-free quantitative proteomics was employed to monitor protein expression in the hippocampus of the recipients. We report that FMT from aged donors led to impaired spatial learning and memory in young adult recipients, whereas anxiety, explorative behaviour and locomotor activity remained unaffected. This was paralleled by altered expression of proteins involved in synaptic plasticity and neurotransmission in the hippocampus. Also, a strong reduction of bacteria associated with short-chain fatty acids (SCFAs) production (Lachnospiraceae, Faecalibaculum, and Ruminococcaceae) and disorders of the CNS (Prevotellaceae and Ruminococcaceae) was observed. Finally, the detrimental effect of FMT from aged donors on the CNS was confirmed by the observation that microglia cells of the hippocampus fimbria, acquired an ageing-like phenotype; on the contrary, gut permeability and levels of systemic and local (hippocampus) cytokines were not affected. These results demonstrate that age-associated shifts of the microbiota have an impact on protein expression and key functions of the CNS. Furthermore, these results highlight the paramount importance of the gut-brain axis in ageing and provide a strong rationale to devise therapies aiming to restore a young-like microbiota to improve cognitive functions and the declining quality of life in the elderly. Video Abstract.

Sections du résumé

BACKGROUND
The gut-brain axis and the intestinal microbiota are emerging as key players in health and disease. Shifts in intestinal microbiota composition affect a variety of systems; however, evidence of their direct impact on cognitive functions is still lacking. We tested whether faecal microbiota transplant (FMT) from aged donor mice into young adult recipients altered the hippocampus, an area of the central nervous system (CNS) known to be affected by the ageing process and related functions.
RESULTS
Young adult mice were transplanted with the microbiota from either aged or age-matched donor mice. Following transplantation, characterization of the microbiotas and metabolomics profiles along with a battery of cognitive and behavioural tests were performed. Label-free quantitative proteomics was employed to monitor protein expression in the hippocampus of the recipients. We report that FMT from aged donors led to impaired spatial learning and memory in young adult recipients, whereas anxiety, explorative behaviour and locomotor activity remained unaffected. This was paralleled by altered expression of proteins involved in synaptic plasticity and neurotransmission in the hippocampus. Also, a strong reduction of bacteria associated with short-chain fatty acids (SCFAs) production (Lachnospiraceae, Faecalibaculum, and Ruminococcaceae) and disorders of the CNS (Prevotellaceae and Ruminococcaceae) was observed. Finally, the detrimental effect of FMT from aged donors on the CNS was confirmed by the observation that microglia cells of the hippocampus fimbria, acquired an ageing-like phenotype; on the contrary, gut permeability and levels of systemic and local (hippocampus) cytokines were not affected.
CONCLUSION
These results demonstrate that age-associated shifts of the microbiota have an impact on protein expression and key functions of the CNS. Furthermore, these results highlight the paramount importance of the gut-brain axis in ageing and provide a strong rationale to devise therapies aiming to restore a young-like microbiota to improve cognitive functions and the declining quality of life in the elderly. Video Abstract.

Identifiants

pubmed: 33004079
doi: 10.1186/s40168-020-00914-w
pii: 10.1186/s40168-020-00914-w
pmc: PMC7532115
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

140

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/F/00044453
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/J004529/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L01632X/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/F/000PR10353
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/F/000PR10356
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/F/000PR10355
Pays : United Kingdom

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Auteurs

Alfonsina D'Amato (A)

Dept. of Pharmaceutical Sciences, University of Milan, Milan, Italy.

Lorenzo Di Cesare Mannelli (L)

NEUROFARBA Department., University of Florence, Florence, Italy.

Elena Lucarini (E)

NEUROFARBA Department., University of Florence, Florence, Italy.

Angela L Man (AL)

Earlham Institute, Norwich, UK.

Gwenaelle Le Gall (G)

Norwich Medical School, Biomedical Research Centre, University of East Anglia, Norwich, NR4 7TJ, UK.

Jacopo J V Branca (JJV)

Dept. of Experimental and Clinical Medicine, University of Florence, 50134, Florence, Italy.

Carla Ghelardini (C)

NEUROFARBA Department., University of Florence, Florence, Italy.

Amedeo Amedei (A)

Dept. of Experimental and Clinical Medicine, University of Florence, 50134, Florence, Italy.

Eugenio Bertelli (E)

Dept. of Developmental and Molecular Medicine, University of Siena, Siena, Italy.

Mari Regoli (M)

Dept. of Developmental and Molecular Medicine, University of Siena, Siena, Italy.

Alessandra Pacini (A)

Dept. of Experimental and Clinical Medicine, University of Florence, 50134, Florence, Italy.

Giulia Luciani (G)

Dept. of Experimental and Clinical Medicine, University of Florence, 50134, Florence, Italy.

Pasquale Gallina (P)

NEUROFARBA Department., University of Florence, Florence, Italy.
Neurosurgery Unit, Careggi University Hospital, Florence, Italy.

Annalisa Altera (A)

Dept. of Developmental and Molecular Medicine, University of Siena, Siena, Italy.

Arjan Narbad (A)

The Quadram Institute Bioscience, Norwich, UK.

Massimo Gulisano (M)

Dept. of Experimental and Clinical Medicine, University of Florence, 50134, Florence, Italy.

Lesley Hoyles (L)

Dept. of Biosciences, School of Science and Technology, Nottingham Trent University, Nottingham, UK.

David Vauzour (D)

Norwich Medical School, Biomedical Research Centre, University of East Anglia, Norwich, NR4 7TJ, UK. D.Vauzour@uea.ac.uk.

Claudio Nicoletti (C)

Dept. of Experimental and Clinical Medicine, University of Florence, 50134, Florence, Italy. claudio.nicoletti@unifi.it.

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Classifications MeSH