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Bacterial and fungal microbiota in relation to probiotic therapy (VSL#3) in pouchitis
T Kühbacher1, S J Ott, U Helwig
1Department of General Internal Medicine, Kiel, Germany.
Background:
The intestinal microbiota plays a critical role in the pathophysiology of pouchitis, a major complication after ileal pouch anal anastomosis in patients with ulcerative colitis. Recently, controlled trials have demonstrated that probiotics are effective in maintenance of remission in pouchitis patients. However, the mechanism by which therapy with probiotics works remains elusive. This study explores the role of the bacterial and fungal flora in a controlled trial for maintenance of remission in pouchitis patients with the probiotic VSL#3 compound.
Methods:
The mucosa associated pouch microbiota was investigated before and after therapy with VSL#3 by analysis of endoscopic biopsies using ribosomal DNA/RNA based community fingerprint analysis, clone libraries, real time polymerase chain reaction (PCR), and fluorescence in situ hybridisation. Patients were recruited from a placebo controlled remission maintenance trial with VSL#3.
Results:
Patients who developed pouchitis while treated with placebo had low bacterial and high fungal diversity. Bacterial diversity was increased and fungal diversity was reduced in patients in remission maintained with VSL#3 (p = 0.001). Real time PCR experiments demonstrated that VSL#3 increased the total number of bacterial cells (p = 0.002) and modified the spectrum of bacteria towards anaerobic species. Taxa specific clone libraries for Lactobacilli and Bifidobacteria showed that the richness and spectrum of these bacteria were altered under probiotic therapy.
Conclusions:
Probiotic therapy with VSL#3 increases the total number of intestinal bacterial cells as well as the richness and diversity of the bacterial microbiota, especially the anaerobic flora. The diversity of the fungal flora is repressed. Restoration of the integrity of a "protective" intestinal mucosa related microbiota could therefore be a potential mechanism of probiotic bacteria in inflammatory barrier diseases of the lower gastrointestinal tract.
Insights
Probiotic therapy with VSL#3 enhances beneficial bacteria and reduces fungi in patients with ulcerative colitis, aiding remission. This study clarifies how probiotics restore a healthy gut microbiota, crucial for inflammatory bowel diseases.
Area of Science:
- Gastroenterology and Microbiology
- Inflammatory Bowel Disease Research
- Gut Microbiome Analysis
Background:
- Pouchitis is a significant complication following ileal pouch anal anastomosis for ulcerative colitis.
- The intestinal microbiota's role in pouchitis pathophysiology is critical.
- Probiotics have shown efficacy in maintaining remission for pouchitis, but their mechanism is unclear.
Purpose of the Study:
- To investigate the impact of VSL#3 probiotic therapy on the bacterial and fungal microbiota in pouchitis patients.
- To explore the mechanisms underlying probiotic efficacy in maintaining remission for pouchitis.
Main Methods:
- Analysis of mucosa-associated microbiota from endoscopic pouch biopsies before and after VSL#3 treatment.
- Utilized ribosomal DNA/RNA-based community fingerprinting, clone libraries, real-time PCR, and fluorescence in situ hybridization.
- Patients were part of a placebo-controlled trial for VSL#3 remission maintenance.
Main Results:
- Patients with pouchitis on placebo exhibited low bacterial and high fungal diversity.
- VSL#3 treatment significantly increased bacterial diversity and decreased fungal diversity (p = 0.001).
- Real-time PCR confirmed VSL#3 increased total bacterial cells (p = 0.002) and promoted anaerobic species, altering Lactobacilli and Bifidobacteria populations.
Conclusions:
- Probiotic VSL#3 therapy enriches intestinal bacteria, particularly anaerobic species, and reduces fungal diversity.
- This restoration of a protective microbiota may be the mechanism by which probiotics benefit inflammatory diseases of the lower gastrointestinal tract.
- Findings suggest a potential therapeutic strategy for inflammatory barrier diseases via microbiota modulation.
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