Gut microbiota and urobiota in liver cirrhosis with urinary tract infections
https://doi.org/10.30629/0023-2149-2026-104-3-204-212
Abstract
The purpose of the study was to examine the differences and commonality of the gut microbiota and urobiota in patients with liver cirrhosis (LC), depending on the presence of urinary tract infections (UTI).
Material and methods. A prospective cohort study was conducted on 125 patients with LC, including 41 — without UTI, 22 — with asymptomatic bacteriuria (ABU), and 62 — with UTI.
The results and their discussion. The beta diversity of the gut microbiota and urobiota differs in LC without UTI, with ABU, and with UTI (p = 0.002 and p = 0.001). In the gut microbiota in LC without UTI — with ABU — with UTI, there is an increase in the abundance of Pseudomonadota taxa (1.25 [0.49; 3.15]% — 5.76 [1.34; 10.29]% — 6.40 [1.78; 31.23]%, p = 0.0003), Gammaproteobacteria (0.57 [0.05; 2.59]% — 4.06 [0.63; 7.16]% — 4.47 [0.9; 29.82]%, p = 0.0004), Bacilli (2.52 [1.28; 7.96]% — 6.75 [2.51; 15.91]% — 13.86 [3.5; 26.52]%, p = 0.006) and decreased Bacteroidota density (42.94 [31.77; 67.78]% without UTI, 25.38 [0.95; 44.58]% with UTI, p = 0.003). Urobiota in LC without UTI — with ABU — with UTI are characterized by an increase in Pseudomonadota taxa (68.48 [38.7; 90.69]% — 71,57 [20,3; 88,4]% — 80.51 [8.85; 93.07]%, p = 0.029), Gammaproteobacteria (33.59 [26.5; 48.95]% — 38.95 [14.08; 78.94]% — 52.8 [5.25; 86.88]%, p = 0.004) and a decrease in Actinomycetota (2.89 [1.24; 5.59]% — 1.63 [0.22; 4.08]% — 0.5 [0.08; 3.8]%, р = 0.03), Clostridia (0.94 [0.07; 2.36]% — 0.4 [0.06; 5.98]% — 0.24 [0.03; 0.93]%, p = 0.011). The commonality between the urobiota and the gut microbiota in patients with LC with UTI ranges from 96% at the department level to 61.5% at the species level.
Conclusion. In patients with LC with UTI, there is a change in the beta diversity of the gut microbiota and urobiota, an increase in the abundance of pathogenic taxa (Pseudomonadota, Gammaproteobacteria, Bacilli), and a decrease in the abundance of commensal taxa (Bacteroidota, Actinomycetota, Clostridia) compared to the group without UTI.
About the Authors
E. G. MalaevaBelarus
Ekaterina G. Malaeva — Candidate of Medical Sciences, Associate Professor, Head of the Department of Internal Diseases No. 1 with the courses of Endocrinology and Hematology
Gomel
I. O. Stoma
Belarus
Igor O. Stoma — Doctor of Medical Sciences, Рrofessor, Rector
Gomel
E. V. Voropaev
Belarus
Evgeny V. Voropaev — Candidate of Medical Sciences, Associate Professor, Vice-rector for Scientific Work
Gomel
O. V. Osipkina
Belarus
Olga V. Osipkina — Head of the Scientific Research Laboratory
Gomel
A. A. Kovalev
Belarus
Alexey A. Kovalev — Senior Lecturer, Department of Medical and Biological Physics
Gomel
References
1. Choi J., Thanert R., Reske K.A., Nickel K.B., Olsen M.A., Hink T. et al. Gut microbiome correlates of recurrent urinary tract infection: A longitudinal, multi-center study. EClinicalMedicine. 2024; 71:102490. DOI: 10.1016/j.eclinm.2024.102490
2. Sturov N.V., Popov S.V., Zhukov V.A. Pathogenetic Role and Possibilities for Correction of Gut Microbiota Disorders in Urinary Tract Infections. Antibiotiki i Khimioterapiya = Antibiotics and Chemotherapy. 2021;66(7–8):100–108. (In Russ.). DOI: 10.24411/0235-2990-2021-66-7-8-100-108.
3. Malaeva E.G. Urinary tract infections and microbiota. Problemy zdorov’ya i ekologii = Health and Ecology Issues. 2021;18(3):5–14. (In Russ.). DOI: 10.51523/2708-6011.2021-18-3-1
4. Gromova G.G., Verizhnikova L.N., Karpin V.A. Role of intestinal dysbiosis in occur rence of urinary tract infection. Vestnik SurGU. Meditsina. 2019;2 (40):86–89. (In Russ.). URL: https://cyberleninka.ru/article/n/rol-disbakterioza-kishechnika-v-vozniknovenii-infektsii-mochevyhputey (date of request: 15.09.2025).
5. Iqbal Z.S., Halkjær S.I., Ghathian K.S.A., Heintz J.E., Petersen A.M. The role of the gut microbiome in urinary tract infec tions: a narrative review. Nutrients. 2024;16(21):3615. DOI: 10.3390/nu16213615
6. Malaeva E.G., Stoma I.O., Voropaev E.V., Osipkina O.V., Kovalev A.A. Urobiota and urinary tract infections in liver cirrhosis. Sibirskij nauchnyj medicinskij zhurnal = Siberian Scientifi c Medical Journal. 2025;45(1):148– 157. (In Russ.). DOI: 10.18699/SSMJ20250116
7. Bajaj J.S., Reddy K.R., Tandon P., Garcia-Tsao G., Kamath P.S., O’Leary J.G. et al. Association of serum metabolites and gut microbiota at hospital admission with nosocomial infection development in patients with cirrhosis. Liver Transpl. 2022;28(12):1831–1840. DOI: 10.1002/lt.26552
8. Saenz C.N., Neugent M.L., De Nisco N.J. The Human Urinary Microbiome and Its Potential Role in Urinary Tract Infections. Eur. Urol. Focus. 2024;10(6):889–892. DOI: 10.1016/j.euf.2024.12.005
9. Worby C.J., Schreiber H.L.t., Straub T.J., van Dijk L.R., Bronson R.A., Olson B.S. et al. Longitudinal multi-omics analyses link gut microbiome dysbiosis with recurrent urinary tract infections in women. Nat. Microbiol. 2022;7:630–639. DOI: 10.1038/s41564-022-01107-x
10. Magruder M., Sholi A.N., Gong C., Zhang L., Edusei E., Huang J. et al. Gut uropathogen abundance is a risk factor for development of bacteriuria and urinary tract infection. Nat. Commun. 2019;10(1):5521. DOI: 10.1038/s41467-019-13467-w
11. Paalanne N., Husso A., Salo J., Pieviläinen O., Tejesvi M.V., Koivusaari P. et al. Intestinal microbiome as a risk factor for urinary tract infections in children. Eur. J. Clin. Microbiol. Infect. Dis. 2018;37:1881–1891. DOI: 10.1007/s10096-018-3322-7
12. Thänert R., Reske K.A., Hink T., Wallace M.A., Wang B., Schwartz D.J. et al. Comparative genomics of antibiotic-resistant uropathogens implicates three routes for recurrence of urinary tract infections. mBio. 2019;10(4):e01977-19. DOI: 10.1128/mBio.01977-19
13. Lingiah V.A., Pyrsopoulos N.T. Bacterial infections in cirrhotic patients in a tertiary care hospital. J. Clin. Transl. Hepatol. 2021;9(1):32–39. DOI: 10.14218/JCTH.2020.00076
14. Reuken P.A., Stallmach A., Bruns T. Mortality after urinary tract infections in patients with advanced cirrhosis – relevance of acute kidney injury and comorbidities. Liver Int. 2013;33(2):220–230. DOI: 10.1111/liv.12029
15. Nielsen K.L., Stegger M., Kiil K., Godfrey P.A., Feldgarden M., Lilje B., Andersen P.S., Frimodt-Møller N. Whole-genome Comparison of Urinary Pathogenic Escherichia coli and Faecal Isolates of UTI Patients and Healthy Controls. Int. J. Med. Microbiol. 2017;307(8):497–507. DOI: 10.1016/j.ijmm.2017.09.007
16. Dubourg G., Morand A., Mekhalif F., Godefroy R., Corthier A., Yacouba A. et al. Deciphering the urinary microbiota repertoire by culturomics reveals mostly anaerobic bacteria from the gut. Front. Microbiol. 2020;11:513305. DOI: 10.3389/fmicb.2020.513305
17. Tariq R., Pardi D.S., Tosh P.K., Walker R.C., Razonable R.R., Khanna S. Fecal microbiota transplantation for recurrent Clostridium diffi cile infection reduces recurrent urinary tract infection frequency. Clin. Infect. Dis. 2017;65(10):1745–1747. DOI: 10.1093/cid/cix618
18. Urakami C., Yamanouchi S., Kimata T., Tsuji S., Akagawa S., Kino J. et al. Abnormal Development of microbiota may be a risk factor for febrile urinary tract infection in infancy. Microorganisms. 2023;11(10):2574. DOI: 10.3390/microorganisms11102574
19. Maslennikov R., Ivashkin V., Efremova I., Alieva A., Kashuh E., Tsvetaeva E., Poluektova E., Shirokova E., Ivashkin K. Gut dysbiosis is associated with poorer long-term prognosis in cirrhosis. World J. Hepatol. 2021;13(5):557–570. DOI: 10.4254/wjh.v13.i5.557
20. Giannelli V., Di Gregorio V., Iebba V., Giusto M., Schippa S., Merli M., Thalheimer U. Microbiota and the gut-liver axis: bacterial trans location, infl ammation and infection in cirrhosis. World J. Gas troenterol. 2014;20:16795–16810. DOI: 10.3748/wjg.v20.i45.16795
21. Microbiota of the lungs, skin, and urogenital tract. N.A. Belyakov, I.O. Stoma, E.G. Malaeva, T.N. Trofi mova. Human Biocenosis and Hospital Environment. Saint Petersburg: Baltic Medical Educational Center, 2023:36–64. (In Russ.).
22. Ryan R.P., Monchy S., Cardinale M., Taghavi S., Crossman L., Avison M.B., Berg G., van der Lelie D., Dow J.M. The versatility and adaptation of bacteria from the genus Stenotrophomonas. Na.t Rev. Microbiol. 2009;7(7):514–25. DOI: 10.1038/nrmicro2163
23. Almas S., Carpenter R.E., Rowan C., Tamrakar V.K., Bishop J., Sharma R. Advantage of precision metagenomics for urinary tract infection diagnostics. Front. Cell. Infect. Microbiol. 2023;13:1221289. DOI: 10.3389/fcimb.2023.1221289
24. Dalvi H., De Nisco N.J. The evolving world of the urinary microbiome. Curr. Opin. Urol. 2024;34(6):422–427. DOI: 10.1097/MOU.0000000000001222
25. Sturov N.V., Popov S.V., Zhukov V.A., Lyapunova T.V. Correction of gut microbiota in urinary tract infection (a review). Farmakologiya & farmakoterapiya = Pharmacology & Pharmacotherapy. 2022;(3):24–27. (In Russ.). DOI: 10.46393/27132129_2022_3_24
26. Magruder M., Edusei E., Zhang L., Albakry S., Satlin M.J., Westblade L.F. et al. Gut commensal microbiota and decreased risk for Enterobacteriaceae bacteriuria and urinary tract infection. Gut Microbes. 2020;12(1):1805281. DOI: 10.1080/19490976.2020.1805281
27. Moreland R.B., Brubaker L., Wolfe A.J. Polymicrobial urine cultures: reconciling contamination with the urobiome while recognizing the pathogens. Front. Cell. Infect. Microbiol. 2025;15:1562687. DOI: 10.3389/fcimb.2025.1562687
Review
For citations:
Malaeva E.G., Stoma I.O., Voropaev E.V., Osipkina O.V., Kovalev A.A. Gut microbiota and urobiota in liver cirrhosis with urinary tract infections. Clinical Medicine (Russian Journal). 2026;104(3):204-212. (In Russ.) https://doi.org/10.30629/0023-2149-2026-104-3-204-212
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