TY - JOUR
T1 - Gut Microbiota Regulate Motor Deficits and Neuroinflammation in a Model of Parkinson's Disease
AU - Sampson, Timothy R.
AU - Debelius, Justine W.
AU - Thron, Taren
AU - Janssen, Stefan
AU - Shastri, Gauri G.
AU - Ilhan, Zehra Esra
AU - Challis, Collin
AU - Schretter, Catherine E.
AU - Rocha, Sandra
AU - Gradinaru, Viviana
AU - Chesselet, Marie Francoise
AU - Keshavarzian, Ali
AU - Shannon, Kathleen M.
AU - Krajmalnik-Brown, Rosa
AU - Wittung-Stafshede, Pernilla
AU - Knight, Rob
AU - Mazmanian, Sarkis K.
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - The intestinal microbiota influence neurodevelopment, modulate behavior, and contribute to neurological disorders. However, a functional link between gut bacteria and neurodegenerative diseases remains unexplored. Synucleinopathies are characterized by aggregation of the protein α-synuclein (αSyn), often resulting in motor dysfunction as exemplified by Parkinson's disease (PD). Using mice that overexpress αSyn, we report herein that gut microbiota are required for motor deficits, microglia activation, and αSyn pathology. Antibiotic treatment ameliorates, while microbial re-colonization promotes, pathophysiology in adult animals, suggesting that postnatal signaling between the gut and the brain modulates disease. Indeed, oral administration of specific microbial metabolites to germ-free mice promotes neuroinflammation and motor symptoms. Remarkably, colonization of αSyn-overexpressing mice with microbiota from PD-affected patients enhances physical impairments compared to microbiota transplants from healthy human donors. These findings reveal that gut bacteria regulate movement disorders in mice and suggest that alterations in the human microbiome represent a risk factor for PD.
AB - The intestinal microbiota influence neurodevelopment, modulate behavior, and contribute to neurological disorders. However, a functional link between gut bacteria and neurodegenerative diseases remains unexplored. Synucleinopathies are characterized by aggregation of the protein α-synuclein (αSyn), often resulting in motor dysfunction as exemplified by Parkinson's disease (PD). Using mice that overexpress αSyn, we report herein that gut microbiota are required for motor deficits, microglia activation, and αSyn pathology. Antibiotic treatment ameliorates, while microbial re-colonization promotes, pathophysiology in adult animals, suggesting that postnatal signaling between the gut and the brain modulates disease. Indeed, oral administration of specific microbial metabolites to germ-free mice promotes neuroinflammation and motor symptoms. Remarkably, colonization of αSyn-overexpressing mice with microbiota from PD-affected patients enhances physical impairments compared to microbiota transplants from healthy human donors. These findings reveal that gut bacteria regulate movement disorders in mice and suggest that alterations in the human microbiome represent a risk factor for PD.
KW - Parkinson's disease
KW - gut-brain axis
KW - microbiome
KW - microglia
KW - mouse model
KW - short chain fatty acids
KW - synuclein
UR - http://www.scopus.com/inward/record.url?scp=85001930733&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85001930733&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2016.11.018
DO - 10.1016/j.cell.2016.11.018
M3 - Article
C2 - 27912057
AN - SCOPUS:85001930733
SN - 0092-8674
VL - 167
SP - 1469-1480.e12
JO - Cell
JF - Cell
IS - 6
ER -