Abstract: FR-OR128
Altered Gut Microbial Fermentation and Colonization with Methanobrevibacter smithii in Renal Transplant Recipients
Session Information
- Transplantation: Basic Research
November 08, 2019 | Location: 150, Walter E. Washington Convention Center
Abstract Time: 05:54 PM - 06:06 PM
Category: Transplantation
- 1901 Transplantation: Basic
Authors
- Knobbe, Tim J., University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- Douwes, Rianne M., University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- Kremer, Daan, University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- Swarte, J.c., University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- Eisenga, Michele F., University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- Gomes Neto, Antonio Wouter, University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- van Londen, Marco, University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- Blokzijl, H., University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- Harmsen, Hermie, University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- Nolte, Ilja M., University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
- Bakker, Stephan J.L., University Medical Center Groningen, Groningen, The Netherlands, Groningen, Netherlands
Background
The gut microbiota of kidney transplant recipients (RTR) differs from that of healthy controls (HC). This may have consequences for gut microbial fermentation. Breath hydrogen (H2) and methane (CH4) concentrations are markers of fermentation in the gut, of which CH4 is mainly produced by Methanobrevibacter smithii (M. smithii). We aimed to investigate (1) whether breath H2 and CH4 concentrations differs between RTR and HC, (2) whether the presence of M. smithii in faeces differs between RTR and HC and (3) whether presence of M. smithii is related to breath H2 and CH4.
Methods
All study subjects participated in the TransplantLines biobank cohort study. Organ donors served as HC. Breath H2 and CH4 concentrations were analysed using solid state-sensor gas-chromatography. Presence of M. smithii in faeces was determined with real-time PCR.
Results
A total of 152 RTR and 77 HC were included. Breath H2 concentrations of RTR were not significantly different from HC (median [IQR] 11.3 [4.0-30.0] ppm vs. 10.5 [4.5-28.3] ppm, p=0.92). However, RTR had significantly lower breath CH4 concentrations compared to HC (7.5 [3.9-10.6] ppm vs. 16.0 [8.0-45.5] ppm, p<0.001). In addition, M. smithii was found less frequently in RTR compared to HC (86.4% vs. 28.6%, p<0.001). In absence of M. smithii, there was a significant positive correlation between breath H2 and CH4 (r = 0.88; p<0.001). There was no correlation if M. smithii was present (r = 0.09; p=0.50).
Conclusion
Breath CH4 concentrations and the prevalence of M. smithii in faeces were significantly lower in RTR compared to HC, which indicates RTR have altered microbiota and altered gut microbial fermentation. In absence of M. smithii, CH4 is highly dependent on H2 production, while this is not the case in the presence of M. smithii. These findings provide novel insight in the alterations of gut microbiota secondary to renal transplantation and the use of immunosuppressants.
Funding
- Commercial Support –