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Urobiome composition after renal transplantation: an exploratory study
David Harriman1, Alex Ng2, Monica Bronowski2
1Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada. David.Harriman@ubc.ca.
Renal transplantation significantly alters the urobiome, with specific microbial changes linked to acute rejection and declining kidney function. Further research is needed to explore the urobiome
Area of Science:
- Microbiology
- Transplant Immunology
- Urology
Background:
- The urinary microbiome (urobiome) in renal transplant recipients remains largely undefined.
- Understanding urobiome dynamics is crucial for post-transplant allograft health.
- Investigating urobiome changes in relation to rejection and graft function is critical.
Purpose of the Study:
- To characterize urobiome alterations in renal transplant recipients.
- To compare pre- to post-transplant urobiome states.
- To assess urobiome differences between acute T-cell mediated rejection (TCMR) and non-rejector cohorts, and across varying allograft function levels.
Main Methods:
- Urine samples from 41 renal transplant recipients (10 rejectors, 16 women, 15 men) were analyzed.
- Samples were collected pre-transplant, at TCMR diagnosis, and at 1 and 3 months post-transplant.
- 16S rRNA sequencing was performed, followed by diversity and differential abundance analyses.
Main Results:
- The urobiome composition significantly changed post-transplant, differing from pre-transplant states by ~75%.
- Rejectors showed an increase in Corynebacterium and Pseudomonas, while non-rejectors gained Lactobacillus.
- Urobiome composition varied by sex, and a loss of Lactobacillus correlated with decreased eGFR (estimated glomerular filtration rate) at 3 months post-transplant.
Conclusions:
- Renal transplantation profoundly impacts individual urobiome composition, but not necessarily diversity.
- Microbial imbalances in the urobiome may be associated with acute rejection and impaired post-transplant renal function.
- The urobiome holds potential as a biomarker for, or contributor to, post-transplant allograft health, warranting further investigation.
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