Short-Chain Fatty Acid-Producing Gut Microbiota Is Decreased in Parkinson's Disease but Not in Rapid-Eye-Movement Sleep Behavior Disorder.

Parkinson’s disease gut microbiota meta-analysis rapid-eye-movement behavior disorder topic model

Journal

mSystems
ISSN: 2379-5077
Titre abrégé: mSystems
Pays: United States
ID NLM: 101680636

Informations de publication

Date de publication:
08 Dec 2020
Historique:
entrez: 9 12 2020
pubmed: 10 12 2020
medline: 10 12 2020
Statut: epublish

Résumé

Gut dysbiosis has been repeatedly reported in Parkinson's disease (PD) but only once in idiopathic rapid-eye-movement sleep behavior disorder (iRBD) from Germany. Abnormal aggregation of α-synuclein fibrils causing PD possibly starts from the intestine, although this is still currently under debate. iRBD patients frequently develop PD. Early-stage gut dysbiosis that is causally associated with PD is thus expected to be observed in iRBD. We analyzed gut microbiota in 26 iRBD patients and 137 controls by 16S rRNA sequencing (16S rRNA-seq). Our iRBD data set was meta-analyzed with the German iRBD data set and was compared with gut microbiota in 223 PD patients. Unsupervised clustering of gut microbiota by LIGER, a topic model-based tool for single-cell RNA sequencing (RNA-seq) analysis, revealed four enterotypes in controls, iRBD, and PD. Short-chain fatty acid (SCFA)-producing bacteria were conserved in an enterotype observed in controls and iRBD, whereas they were less conserved in enterotypes observed in PD. Genus

Identifiants

pubmed: 33293403
pii: 5/6/e00797-20
doi: 10.1128/mSystems.00797-20
pmc: PMC7771407
pii:
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

Copyright © 2020 Nishiwaki et al.

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Auteurs

Hiroshi Nishiwaki (H)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Tomonari Hamaguchi (T)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Mikako Ito (M)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Tomohiro Ishida (T)

Department of Pathophysiological Laboratory Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Tetsuya Maeda (T)

Division of Neurology and Gerontology, Department of Internal Medicine, School of Medicine, Iwate Medical University, Iwate, Japan.

Kenichi Kashihara (K)

Department of Neurology, Okayama Kyokuto Hospital, Okayama, Japan.

Yoshio Tsuboi (Y)

Department of Neurology, Fukuoka University, Fukuoka, Japan.

Jun Ueyama (J)

Department of Pathophysiological Laboratory Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Teppei Shimamura (T)

Division of Systems Biology, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Hiroshi Mori (H)

Genome Evolution Laboratory, Department of Informatics, National Institute of Genetics, Mishima, Japan.

Ken Kurokawa (K)

Genome Evolution Laboratory, Department of Informatics, National Institute of Genetics, Mishima, Japan.

Masahisa Katsuno (M)

Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Masaaki Hirayama (M)

Department of Pathophysiological Laboratory Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan hirasan@met.nagoya-u.ac.jp ohnok@med.nagoya-u.ac.jp.

Kinji Ohno (K)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan hirasan@met.nagoya-u.ac.jp ohnok@med.nagoya-u.ac.jp.

Classifications MeSH