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  4. Reduction of Abeta amyloid pathology in APPPS1 transgenic mice in the absence of gut microbiota
 
research article

Reduction of Abeta amyloid pathology in APPPS1 transgenic mice in the absence of gut microbiota

Harach, Taoufiq  
•
Marungruang, Nittaya
•
Duthilleul, Nicolas
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2017
Scientific Reports

Alzheimer’s disease is the most common form of dementia in the western world, however there is no cure available for this devastating neurodegenerative disorder. Despite clinical and experimental evidence implicating the intestinal microbiota in a number of brain disorders, its impact on Alzheimer’s disease is not known. To this end we sequenced bacterial 16S rRNA from fecal samples of Aβ precursor protein (APP) transgenic mouse model and found a remarkable shift in the gut microbiota as compared to non-transgenic wild-type mice. Subsequently we generated germ-free APP transgenic mice and found a drastic reduction of cerebral Aβ amyloid pathology when compared to control mice with intestinal microbiota. Importantly, colonization of germ-free APP transgenic mice with microbiota from conventionally-raised APP transgenic mice increased cerebral Aβ pathology, while colonization with microbiota from wild-type mice was less effective in increasing cerebral Aβ levels. Our results indicate a microbial involvement in the development of Abeta amyloid pathology, and suggest that microbiota may contribute to the development of neurodegenerative diseases.

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Type
research article
DOI
10.1038/srep41802
Web of Science ID

WOS:000393636100001

Author(s)
Harach, Taoufiq  
Marungruang, Nittaya
Duthilleul, Nicolas
Cheatham, Victoria
Mc Coy, Kathleen
Frisoni, Giovanni
Neher, J. J.
Fak, Frida
Jucker, Matthias
Lasser, Theo  
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Date Issued

2017

Publisher

Nature Research

Published in
Scientific Reports
Volume

7

Article Number

41802

Subjects

Alzheimer

•

gastro-intestinal tract

•

microbiota germ free

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LOB  
Available on Infoscience
February 7, 2017
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/134213
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