Longitudinal multi-omics analyses link gut microbiome dysbiosis with recurrent urinary tract infections in women

CJ Worby, HL Schreiber IV, TJ Straub, LR van Dijk… - Nature …, 2022 - nature.com
CJ Worby, HL Schreiber IV, TJ Straub, LR van Dijk, RA Bronson, BS Olson, JS Pinkner…
Nature microbiology, 2022nature.com
Recurrent urinary tract infections (rUTIs) are a major health burden worldwide, with history of
infection being a significant risk factor. While the gut is a known reservoir for uropathogenic
bacteria, the role of the microbiota in rUTI remains unclear. We conducted a year-long study
of women with (n= 15) and without (n= 16) history of rUTI, from whom we collected urine,
blood and monthly faecal samples for metagenomic and transcriptomic interrogation. During
the study 24 UTIs were reported, with additional samples collected during and after infection …
Abstract
Recurrent urinary tract infections (rUTIs) are a major health burden worldwide, with history of infection being a significant risk factor. While the gut is a known reservoir for uropathogenic bacteria, the role of the microbiota in rUTI remains unclear. We conducted a year-long study of women with (n = 15) and without (n = 16) history of rUTI, from whom we collected urine, blood and monthly faecal samples for metagenomic and transcriptomic interrogation. During the study 24 UTIs were reported, with additional samples collected during and after infection. The gut microbiome of individuals with a history of rUTI was significantly depleted in microbial richness and butyrate-producing bacteria compared with controls, reminiscent of other inflammatory conditions. However, Escherichia coli gut and bladder populations were comparable between cohorts in both relative abundance and phylogroup. Transcriptional analysis of peripheral blood mononuclear cells revealed expression profiles indicative of differential systemic immunity between cohorts. Altogether, these results suggest that rUTI susceptibility is in part mediated through the gut–bladder axis, comprising gut dysbiosis and differential immune response to bacterial bladder colonization, manifesting in symptoms.
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