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Probiotic Bacillus subtilis Protects against α-Synuclein Aggregation in C. elegans
María Eugenia Goya1, Feng Xue1, Cristina Sampedro-Torres-Quevedo1
1University of Edinburgh, Centre for Discovery Brain Sciences, Edinburgh, Scotland.
Cell Reports
|January 16, 2020
Summary
The probiotic Bacillus subtilis strain PXN21 reduces harmful alpha-synuclein clumps in a Parkinson's disease model. This gut bacteria intervention shows potential for modifying neurodegenerative disease progression.
Area of Science:
- Microbiology
- Neuroscience
- Gastroenterology
Background:
- The gut microbiome's role in Parkinson's disease (PD) is increasingly recognized, but mechanisms remain elusive.
- Alpha-synuclein aggregation is a hallmark of PD pathology.
Purpose of the Study:
- To investigate the neuroprotective effects of Bacillus subtilis (B. subtilis) in a Parkinson's disease model.
- To elucidate the mechanisms by which B. subtilis influences alpha-synuclein aggregation.
Main Methods:
- Utilized a Caenorhabditis elegans model of synucleinopathy.
- Administered B. subtilis strain PXN21 and other strains.
- Assessed alpha-synuclein aggregation, DAF-16 mediation, biofilm formation, and host metabolic pathways.
Main Results:
- B. subtilis PXN21 inhibited alpha-synuclein aggregation and cleared existing aggregates in C. elegans.
- Protection was observed in both young and aged animals, partly mediated by DAF-16.
- Biofilm formation and bacterial metabolites from multiple B. subtilis strains contributed to the protective effect, impacting host sphingolipid metabolism.
Conclusions:
- Bacillus subtilis demonstrates potential as a therapeutic agent for Parkinson's disease by mitigating alpha-synuclein pathology.
- B. subtilis's effects involve biofilm formation, metabolite release, and modulation of host sphingolipid metabolism.
- Further exploration of B. subtilis as a dietary supplement for neurodegenerative disease modification is warranted.

