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Longitudinal multi-omics analyses link gut microbiome dysbiosis with recurrent urinary tract infections in women.
Worby, Colin J; Schreiber, Henry L; Straub, Timothy J; van Dijk, Lucas R; Bronson, Ryan A; Olson, Benjamin S; Pinkner, Jerome S; Obernuefemann, Chloe L P; Muñoz, Vanessa L; Paharik, Alexandra E; Azimzadeh, Philippe N; Walker, Bruce J; Desjardins, Christopher A; Chou, Wen-Chi; Bergeron, Karla; Chapman, Sinéad B; Klim, Aleksandra; Manson, Abigail L; Hannan, Thomas J; Hooton, Thomas M; Kau, Andrew L; Lai, H Henry; Dodson, Karen W; Hultgren, Scott J; Earl, Ashlee M.
Afiliación
  • Worby CJ; Infectious Disease and Microbiome Program, Broad Institute, Cambridge, MA, USA.
  • Schreiber HL; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO, USA.
  • Straub TJ; Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, MO, USA.
  • van Dijk LR; Division of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
  • Bronson RA; Infectious Disease and Microbiome Program, Broad Institute, Cambridge, MA, USA.
  • Olson BS; Infectious Disease and Microbiome Program, Broad Institute, Cambridge, MA, USA.
  • Pinkner JS; Delft Bioinformatics Lab, Delft University of Technology, Delft, the Netherlands.
  • Obernuefemann CLP; Infectious Disease and Microbiome Program, Broad Institute, Cambridge, MA, USA.
  • Muñoz VL; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO, USA.
  • Paharik AE; Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, MO, USA.
  • Azimzadeh PN; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO, USA.
  • Walker BJ; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO, USA.
  • Desjardins CA; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO, USA.
  • Chou WC; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO, USA.
  • Bergeron K; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO, USA.
  • Chapman SB; Applied Invention, Cambridge, MA, USA.
  • Klim A; Infectious Disease and Microbiome Program, Broad Institute, Cambridge, MA, USA.
  • Manson AL; Infectious Disease and Microbiome Program, Broad Institute, Cambridge, MA, USA.
  • Hannan TJ; Department of Surgery, Division of Urologic Surgery, Washington University School of Medicine, St. Louis, MO, USA.
  • Hooton TM; Infectious Disease and Microbiome Program, Broad Institute, Cambridge, MA, USA.
  • Kau AL; Department of Surgery, Division of Urologic Surgery, Washington University School of Medicine, St. Louis, MO, USA.
  • Lai HH; Infectious Disease and Microbiome Program, Broad Institute, Cambridge, MA, USA.
  • Dodson KW; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.
  • Hultgren SJ; Department of Medicine, University of Miami, Miami, FL, USA.
  • Earl AM; Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, MO, USA.
Nat Microbiol ; 7(5): 630-639, 2022 05.
Article en En | MEDLINE | ID: mdl-35505248
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones Urinarias / Infecciones por Escherichia coli / Microbioma Gastrointestinal Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Nat Microbiol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones Urinarias / Infecciones por Escherichia coli / Microbioma Gastrointestinal Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Nat Microbiol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido