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Encrustations on ureteral stents from patients without urinary tract infection reveal distinct urotypes and a low bacterial load

BACKGROUND: Current knowledge of the urinary tract microbiome is limited to urine analysis and analysis of biofilms formed on Foley catheters. Bacterial biofilms on ureteral stents have rarely been investigated, and no cultivation-independent data are available on the microbiome of the encrustations...

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Autores principales: Buhmann, Matthias T., Abt, Dominik, Nolte, Oliver, Neu, Thomas R., Strempel, Sebastian, Albrich, Werner C., Betschart, Patrick, Zumstein, Valentin, Neels, Antonia, Maniura-Weber, Katharina, Ren, Qun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462311/
https://www.ncbi.nlm.nih.gov/pubmed/30981280
http://dx.doi.org/10.1186/s40168-019-0674-x
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author Buhmann, Matthias T.
Abt, Dominik
Nolte, Oliver
Neu, Thomas R.
Strempel, Sebastian
Albrich, Werner C.
Betschart, Patrick
Zumstein, Valentin
Neels, Antonia
Maniura-Weber, Katharina
Ren, Qun
author_facet Buhmann, Matthias T.
Abt, Dominik
Nolte, Oliver
Neu, Thomas R.
Strempel, Sebastian
Albrich, Werner C.
Betschart, Patrick
Zumstein, Valentin
Neels, Antonia
Maniura-Weber, Katharina
Ren, Qun
author_sort Buhmann, Matthias T.
collection PubMed
description BACKGROUND: Current knowledge of the urinary tract microbiome is limited to urine analysis and analysis of biofilms formed on Foley catheters. Bacterial biofilms on ureteral stents have rarely been investigated, and no cultivation-independent data are available on the microbiome of the encrustations on the stents. RESULTS: The typical encrustations of organic and inorganic urine-derived material, including microbial biofilms formed during 3–6 weeks on ureteral stents in patients treated for kidney and ureteral stones, and without reported urinary tract infection at the time of stent insertion, were analysed. Next-generation sequencing of the 16S rRNA gene V3–V4 region revealed presence of different urotypes, distinct bacterial communities. Analysis of bacterial load was performed by combining quantification of 16S rRNA gene copy numbers by qPCR with microscopy and cultivation-dependent analysis methods, which revealed that ureteral stent biofilms mostly contain low numbers of bacteria. Fluorescence microscopy indicates the presence of extracellular DNA. Bacteria identified in biofilms by microscopy had mostly morphogenic similarities to gram-positive bacteria, in few cases to Lactobacillus and Corynebacterium, while sequencing showed many additional bacterial genera. Weddellite crystals were absent in biofilms of patients with Enterobacterales and Corynebacterium-dominated microbiomes. CONCLUSIONS: This study provides novel insights into the bacterial burden in ureteral stent encrustations and the urinary tract microbiome. Short-term (3–6 weeks) ureteral stenting is associated with a low load of viable and visible bacteria in ureteral stent encrustations, which may be different from long-term stenting. Patients could be classified according to different urotypes, some of which were dominated by potentially pathogenic species. Facultative pathogens however appear to be a common feature in patients without clinically manifested urinary tract infection. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02845726. Registered on 30 June 2016—retrospectively registered. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0674-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-64623112019-04-22 Encrustations on ureteral stents from patients without urinary tract infection reveal distinct urotypes and a low bacterial load Buhmann, Matthias T. Abt, Dominik Nolte, Oliver Neu, Thomas R. Strempel, Sebastian Albrich, Werner C. Betschart, Patrick Zumstein, Valentin Neels, Antonia Maniura-Weber, Katharina Ren, Qun Microbiome Research BACKGROUND: Current knowledge of the urinary tract microbiome is limited to urine analysis and analysis of biofilms formed on Foley catheters. Bacterial biofilms on ureteral stents have rarely been investigated, and no cultivation-independent data are available on the microbiome of the encrustations on the stents. RESULTS: The typical encrustations of organic and inorganic urine-derived material, including microbial biofilms formed during 3–6 weeks on ureteral stents in patients treated for kidney and ureteral stones, and without reported urinary tract infection at the time of stent insertion, were analysed. Next-generation sequencing of the 16S rRNA gene V3–V4 region revealed presence of different urotypes, distinct bacterial communities. Analysis of bacterial load was performed by combining quantification of 16S rRNA gene copy numbers by qPCR with microscopy and cultivation-dependent analysis methods, which revealed that ureteral stent biofilms mostly contain low numbers of bacteria. Fluorescence microscopy indicates the presence of extracellular DNA. Bacteria identified in biofilms by microscopy had mostly morphogenic similarities to gram-positive bacteria, in few cases to Lactobacillus and Corynebacterium, while sequencing showed many additional bacterial genera. Weddellite crystals were absent in biofilms of patients with Enterobacterales and Corynebacterium-dominated microbiomes. CONCLUSIONS: This study provides novel insights into the bacterial burden in ureteral stent encrustations and the urinary tract microbiome. Short-term (3–6 weeks) ureteral stenting is associated with a low load of viable and visible bacteria in ureteral stent encrustations, which may be different from long-term stenting. Patients could be classified according to different urotypes, some of which were dominated by potentially pathogenic species. Facultative pathogens however appear to be a common feature in patients without clinically manifested urinary tract infection. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02845726. Registered on 30 June 2016—retrospectively registered. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0674-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-13 /pmc/articles/PMC6462311/ /pubmed/30981280 http://dx.doi.org/10.1186/s40168-019-0674-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Buhmann, Matthias T.
Abt, Dominik
Nolte, Oliver
Neu, Thomas R.
Strempel, Sebastian
Albrich, Werner C.
Betschart, Patrick
Zumstein, Valentin
Neels, Antonia
Maniura-Weber, Katharina
Ren, Qun
Encrustations on ureteral stents from patients without urinary tract infection reveal distinct urotypes and a low bacterial load
title Encrustations on ureteral stents from patients without urinary tract infection reveal distinct urotypes and a low bacterial load
title_full Encrustations on ureteral stents from patients without urinary tract infection reveal distinct urotypes and a low bacterial load
title_fullStr Encrustations on ureteral stents from patients without urinary tract infection reveal distinct urotypes and a low bacterial load
title_full_unstemmed Encrustations on ureteral stents from patients without urinary tract infection reveal distinct urotypes and a low bacterial load
title_short Encrustations on ureteral stents from patients without urinary tract infection reveal distinct urotypes and a low bacterial load
title_sort encrustations on ureteral stents from patients without urinary tract infection reveal distinct urotypes and a low bacterial load
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462311/
https://www.ncbi.nlm.nih.gov/pubmed/30981280
http://dx.doi.org/10.1186/s40168-019-0674-x
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