Evidence map›Paper›PMID 40240922›Full record

Observational studyBMC microbiology2025

Short- and mid-term temporal variability of the human urinary microbiota: a prospective observational cohort study.

Vojtěch Tláskal, Jan Hrbáček, Vítězslav Hanáček, Petra Baránková, Pavel Čermák, Roman Zachoval, Priscila Thiago Dobbler

Abstract readObservational Study
In one paragraph

Observational study in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Vojtěch TláskalDepartment of Urology, Thomayer University Hospital, Prague, Czech Republic. vojtech.tlaskal@bc.cas.cz.ORCID http://orcid.org/0000-0002-2924-9470
Jan HrbáčekDepartment of Urology, Thomayer University Hospital, Prague, Czech Republic. jan.hrbacek@bulovka.cz.ORCID http://orcid.org/0000-0002-4243-8698
Vítězslav HanáčekDepartment of Urology, Thomayer University Hospital, Prague, Czech Republic.
Petra BaránkováDepartment of Urology, Thomayer University Hospital, Prague, Czech Republic.
Pavel ČermákDepartment of Clinical Microbiology, Thomayer University Hospital, Prague, Czech Republic.
Roman ZachovalDepartment of Urology, Thomayer University Hospital, Prague, Czech Republic.
Priscila Thiago DobblerInstitute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic.ORCID http://orcid.org/0000-0002-7681-5463

Funding

Fakultní Thomayerova nemocnice 00064190Grantová Agentura České Republiky 23-07434O
6 · The paper itself

Abstract

backgroundUnderstanding the temporal variability of the microbiome is critical for translating associations of the microbiome with health and disease into clinical practice. The aim of this study is to assess the extent of temporal variability of the human urinary microbiota. A pair of urine samples were collected from study participants at 3-40-month interval. DNA was extracted and the bacterial V4 hypervariable region of the 16S rRNA gene was sequenced on the Illumina MiSeq platform. The alpha diversity of paired samples was analyzed using Chao1 and Shannon indices and PERMANOVA was used to test the factors influencing beta diversity.

resultsA total of 63 participants (43 men and 20 women with a mean age of 63.0 and 57.1 years, respectively) were included in the final analysis. An average of 152 ± 128 bacterial operational taxonomic units (OTUs) were identified in each urine sample from the entire cohort. There was an average of 41 ± 32 overlapping OTUs in each sample pair, accounting for 66.3 ± 29.4% of the relative abundance. There was a clear correlation between the number of overlapping OTUs and the relative abundance covered. The difference in Chao1 index between paired samples was statistically significant; the difference in Shannon index was not. Beta diversity did not differ significantly within the paired samples. Neither age nor sex of the participants influenced the variation in community composition. With a longer interval between the collections, the relative abundance covered by the overlapping OTUs changed significantly but not the number of OTUs.

conclusionOur findings demonstrated that, while the relative abundance of dominant bacteria varied, repeated collections generally shared more than 60% of the bacterial community. Furthermore, we observed little variation in the alpha and beta diversity of the microbial community in human urine. These results help to understand the dynamics of human urinary microbiota and enable interpretation of future studies.

Indexed as

BacteriaMicrobiotaUrineBiodiversityDNA, BacterialFemaleHumansMaleMiddle AgedProspective StudiesRNA, Ribosomal, 16SSequence Analysis, DNATime FactorsDNA, BacterialRNA, Ribosomal, 16S16S rRNA geneBacterial communityNext-generation sequencingStabilityUrinary microbiotaVariability

Identifiers

PMID40240922
PMCPMC12001408

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.