Cargando…

Fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of Parkinson’s disease

Parkinson’s disease (PD) is a neurological disorder characterized by motor dysfunction, dopaminergic neuron loss, and alpha-synuclein (αSyn) inclusions. Many PD risk factors are known, but those affecting disease progression are not. Lifestyle and microbial dysbiosis are candidates in this context....

Descripción completa

Detalles Bibliográficos
Autores principales: Schmit, Kristopher J., Garcia, Pierre, Sciortino, Alessia, Aho, Velma T.E., Pardo Rodriguez, Beatriz, Thomas, Mélanie H., Gérardy, Jean-Jacques, Bastero Acha, Irati, Halder, Rashi, Cialini, Camille, Heurtaux, Tony, Ostahi, Irina, Busi, Susheel B., Grandmougin, Léa, Lowndes, Tuesday, Singh, Yogesh, Martens, Eric C., Mittelbronn, Michel, Buttini, Manuel, Wilmes, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548091/
https://www.ncbi.nlm.nih.gov/pubmed/37676767
http://dx.doi.org/10.1016/j.celrep.2023.113071
_version_ 1785115201625915392
author Schmit, Kristopher J.
Garcia, Pierre
Sciortino, Alessia
Aho, Velma T.E.
Pardo Rodriguez, Beatriz
Thomas, Mélanie H.
Gérardy, Jean-Jacques
Bastero Acha, Irati
Halder, Rashi
Cialini, Camille
Heurtaux, Tony
Ostahi, Irina
Busi, Susheel B.
Grandmougin, Léa
Lowndes, Tuesday
Singh, Yogesh
Martens, Eric C.
Mittelbronn, Michel
Buttini, Manuel
Wilmes, Paul
author_facet Schmit, Kristopher J.
Garcia, Pierre
Sciortino, Alessia
Aho, Velma T.E.
Pardo Rodriguez, Beatriz
Thomas, Mélanie H.
Gérardy, Jean-Jacques
Bastero Acha, Irati
Halder, Rashi
Cialini, Camille
Heurtaux, Tony
Ostahi, Irina
Busi, Susheel B.
Grandmougin, Léa
Lowndes, Tuesday
Singh, Yogesh
Martens, Eric C.
Mittelbronn, Michel
Buttini, Manuel
Wilmes, Paul
author_sort Schmit, Kristopher J.
collection PubMed
description Parkinson’s disease (PD) is a neurological disorder characterized by motor dysfunction, dopaminergic neuron loss, and alpha-synuclein (αSyn) inclusions. Many PD risk factors are known, but those affecting disease progression are not. Lifestyle and microbial dysbiosis are candidates in this context. Diet-driven gut dysbiosis and reduced barrier function may increase exposure of enteric neurons to toxins. Here, we study whether fiber deprivation and exposure to bacterial curli, a protein cross-seeding with αSyn, individually or together, exacerbate disease in the enteric and central nervous systems of a transgenic PD mouse model. We analyze the gut microbiome, motor behavior, and gastrointestinal and brain pathologies. We find that diet and bacterial curli alter the microbiome and exacerbate motor performance, as well as intestinal and brain pathologies, but to different extents. Our results shed important insights on how diet and microbiome-borne insults modulate PD progression via the gut-brain axis and have implications for lifestyle management of PD.
format Online
Article
Text
id pubmed-10548091
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cell Press
record_format MEDLINE/PubMed
spelling pubmed-105480912023-10-05 Fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of Parkinson’s disease Schmit, Kristopher J. Garcia, Pierre Sciortino, Alessia Aho, Velma T.E. Pardo Rodriguez, Beatriz Thomas, Mélanie H. Gérardy, Jean-Jacques Bastero Acha, Irati Halder, Rashi Cialini, Camille Heurtaux, Tony Ostahi, Irina Busi, Susheel B. Grandmougin, Léa Lowndes, Tuesday Singh, Yogesh Martens, Eric C. Mittelbronn, Michel Buttini, Manuel Wilmes, Paul Cell Rep Article Parkinson’s disease (PD) is a neurological disorder characterized by motor dysfunction, dopaminergic neuron loss, and alpha-synuclein (αSyn) inclusions. Many PD risk factors are known, but those affecting disease progression are not. Lifestyle and microbial dysbiosis are candidates in this context. Diet-driven gut dysbiosis and reduced barrier function may increase exposure of enteric neurons to toxins. Here, we study whether fiber deprivation and exposure to bacterial curli, a protein cross-seeding with αSyn, individually or together, exacerbate disease in the enteric and central nervous systems of a transgenic PD mouse model. We analyze the gut microbiome, motor behavior, and gastrointestinal and brain pathologies. We find that diet and bacterial curli alter the microbiome and exacerbate motor performance, as well as intestinal and brain pathologies, but to different extents. Our results shed important insights on how diet and microbiome-borne insults modulate PD progression via the gut-brain axis and have implications for lifestyle management of PD. Cell Press 2023-09-08 /pmc/articles/PMC10548091/ /pubmed/37676767 http://dx.doi.org/10.1016/j.celrep.2023.113071 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Schmit, Kristopher J.
Garcia, Pierre
Sciortino, Alessia
Aho, Velma T.E.
Pardo Rodriguez, Beatriz
Thomas, Mélanie H.
Gérardy, Jean-Jacques
Bastero Acha, Irati
Halder, Rashi
Cialini, Camille
Heurtaux, Tony
Ostahi, Irina
Busi, Susheel B.
Grandmougin, Léa
Lowndes, Tuesday
Singh, Yogesh
Martens, Eric C.
Mittelbronn, Michel
Buttini, Manuel
Wilmes, Paul
Fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of Parkinson’s disease
title Fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of Parkinson’s disease
title_full Fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of Parkinson’s disease
title_fullStr Fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of Parkinson’s disease
title_full_unstemmed Fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of Parkinson’s disease
title_short Fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of Parkinson’s disease
title_sort fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548091/
https://www.ncbi.nlm.nih.gov/pubmed/37676767
http://dx.doi.org/10.1016/j.celrep.2023.113071
work_keys_str_mv AT schmitkristopherj fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT garciapierre fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT sciortinoalessia fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT ahovelmate fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT pardorodriguezbeatriz fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT thomasmelanieh fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT gerardyjeanjacques fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT basteroachairati fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT halderrashi fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT cialinicamille fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT heurtauxtony fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT ostahiirina fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT busisusheelb fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT grandmouginlea fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT lowndestuesday fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT singhyogesh fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT martensericc fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT mittelbronnmichel fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT buttinimanuel fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease
AT wilmespaul fiberdeprivationandmicrobiomebornecurlishiftgutbacterialpopulationsandacceleratediseaseinamousemodelofparkinsonsdisease