This study used 16S rRNA sequencing to compare gut microbiota among healthy controls, untreated PD patients, and piribedil-treated PD patients, and identified differences in microbial composition associated with piribedil treatment.
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Research Article
This study used 16S rRNA sequencing to compare gut microbiota among healthy controls, untreated PD patients, and piribedil-treated PD patients, and identified differences in microbial composition associated with piribedil treatment.
This study aimed to determine whether piribedil therapy alters the gut microbiota of patients with Parkinson’s disease (PD), providing a theoretical reference for understanding gut microbiota alterations induced by piribedil and their potential clinical implications. Fecal samples were analyzed using 16S ribosomal RNA (16S rRNA) gene sequencing. Comparisons were made between patients with PD who took piribedil (piribedil group), patients with PD who did not take piribedil (PD group), and healthy controls (blank group). Compared with the blank group, the relative abundance of Staphylococcus, Rhodococcus, and other genera was higher in the PD group, whereas the relative abundance of Achromobacter and Delftia was lower. Furthermore, the relative abundance of Achromobacter, Delftia, and Stenotrophomonas was higher in the piribedil group compared to the PD group, whereas the relative abundance of Staphylococcus, Rhodococcus, and other species was lower. Compared to healthy individuals, the gut microbiota of patients with PD exhibited significant changes. The gut microbiota of patients taking piribedil significantly differs from that of untreated patients. These results suggest an association between piribedil and altered gut microbiota in patients with PD.
The incidence of Parkinson’s disease (PD) is gradually increasing; however, its etiology and pathogenesis have not yet been fully clarified. More studies have indicated that the gut microbiota is closely related to the onset and development of PD. He et al.1documented that the gut microbiota composition in patients with PD varies from that of healthy people, and that an increase in intestinal pathogens may be associated with the onset of PD. Scheperans et al.2confirmed that the relative abundance of Prevotella and Bacteroides in the gut of patients with PD is reduced, and that these bacterial gene....
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This study was reviewed by the Ethics Committee of the First Affiliated Hospital of Anhui University of Chinese Medicine (Ethics review number: 2025AH-101, Ethical approval date: 2025-07-02).
Research subjects
Patients with PD and healthy controls at the First Affiliated Hospital of Anhui University of Chinese Medicine were enrolled. Fresh fecal samples were collected for follow-up analysis. Fresh fecal samples were collected, aliquoted into sterile EP tubes, immediately snap-frozen in liquid nitrogen, and then stored at −80 °C for long-term preservation. The inclusion criteria of pati....
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Microbial diversity differences associated with piribedil treatment
DNA extraction quality control results (concentration range, purity) are provided in Supplementary Table 1. PCR amplification quality control (band size, recovery concentrations) is shown in Supplementary Table 2. Sequencing quality control metrics (read counts, depth, coverage) are detailed in Supplementary Table 3. The ACE, Chao1, InvSimpson, Shannon, and Simpson indices wer.......
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Parkinson’s disease ranks as the second most common neurodegenerative disorder globally, only preceded by Alzheimer’s disease23. Since 1970, piribedil, as a dopamine receptor agonist, has been widely used in the treatment of PD24. However, in clinical practice, piribedil may cause some adverse reactions, such as nausea, vomiting, and gastrointestinal discomfort. Growing research demonstrates that the development of Parkinson’s disease, as well as therapeut.......
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The authors state that there are no competing interests.
This research was supported by the Anhui Province Academic Leader Reserve Candidate Funding Project (No. 2022H287), the Anhui Province Hygiene and Health Outstanding Talents Project (No. ahsjhmypygc20230074), the Anhui Provincial Scientific Research Project on Inheritance and Innovation of Traditional Chinese Medicine (2025CCCX017), and the Special Project for Basic-Clinical Integration of Anhui University of Chinese Medicine (JCLCA2025009).
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| Name | Company | Catalog Number | Comments |
|---|---|---|---|
| 2× reaction buffer (Taq MasterMix) | Kangweii | CW0690 | |
| Agarose | (general) | not applicable | molecular biology grade |
| AxyPrep DNA Gel Extraction Kit | Axygen Biosciences | (not provided) | |
| Benchtop high-speed freezing centrifuge | Hunan Kosei | GTR116C | |
| DNA extraction reagents (SDS, phenol, chloroform, ethanol) | (general) | not applicable | |
| DNBSEQ-G99 PE300 sequencing platform | MGI Tech Co., Ltd | DNBSEQ-G99 | |
| Gel electrophoresis apparatus | Beijing Liuyi | DYY-8C | |
| Gel imaging system | Shanghai Jiapeng | JP-2880 | |
| LEfSe software | (open source) | online version | |
| NanoDrop spectrophotometer | Hangzhou Haipe | Aurora-900 | |
| PCR machine | Hangzhou Langji | A200 | |
| Piribedil | Servier | 6094078 | |
| Primers: 341F and 806R (synthesized) | (custom synthesis) | not applicable | |
| QIIME software | (open source) | http://qiime.org | version 1.8.0 |
| Quantus Fluorometer | Promega | E6150 | |
| Qubit 4.0 Fluorometer | Invitrogen | Q33226 | |
| SDS (sodium dodecyl sulfate) | (general) | not applicable | |
| UPARSE software | (open source) | http://drive5.com/uparse | version 7.0.1090 |
| VAHTS Universal Plus DNA Library Prep Kit for MGI V2 | Vazyme | NDM627-01 |