학술논문

Dysbiosis of the beneficial gut bacteria in patients with Parkinson's disease from India.
Document Type
Article
Source
Annals of Indian Academy of Neurology. Nov/Dec2023, Vol. 26 Issue 6, p908-916. 9p.
Subject
*RNA analysis
*DNA analysis
*FECAL analysis
*KRUSKAL-Wallis Test
*PATHOGENESIS
*SEQUENCE analysis
*CLOSTRIDIA
*ANALYSIS of variance
*GUT microbiome
*CONSTIPATION
*MULTIVARIATE analysis
*EFFECT sizes (Statistics)
*CASE-control method
*RANDOM forest algorithms
*DISCRIMINANT analysis
*MANN Whitney U Test
*BIOINFORMATICS
*PARKINSON'S disease
*QUESTIONNAIRES
*DESCRIPTIVE statistics
*POLYMERASE chain reaction
*BODY mass index
*BACTERIA
*SHORT-chain fatty acids
Language
ISSN
0972-2327
Abstract
Objectives: Recent advancement in understanding neurological disorders has revealed the involvement of dysbiosis of the gut microbiota in the pathophysiology of Parkinson's disease (PD). We sequenced microbial DNA using fecal samples collected from PD cases and healthy controls (HCs) to evaluate the role of gut microbiota. Methods: Full-length bacterial 16S rRNA gene sequencing of fecal samples was performed using amplified polymerase chain reaction (PCR) products on the GridION Nanopore sequencer. Sequenced data were analyzed using web-based tools BugSeq and MicrobiomeAnalyst. Results: We found that certain bacterial families like Clostridia UCG 014, Cristensenellaceae, and Oscillospiraceae are higher in abundance, and Lachinospiracea, Coriobacteriaceae and genera associated with short-chain fatty acid production, Faecalibacterium, Fusicatenibacter, Roseburia and Blautia, are lower in abundance among PD cases when compared with the HC. Genus Akkermansia, Dialister, Bacteroides, and Lachnospiraceae NK4A136 group positively correlated with constipation in PD. Conclusion: Observations from this study support the other global research on the PD gut microbiome background and provide fresh insight into the gut microbial composition of PD patients from a south Indian population. We report a higher abundance of Clostridia UCG 014 group, previously not linked to PD. [ABSTRACT FROM AUTHOR]