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The human urinary microbiome; bacterial DNA in voided urine of asymptomatic adults

The urinary microbiome of healthy individuals and the way it alters with ageing have not been characterized and may influence disease processes. Conventional microbiological methods have limited scope to capture the full spectrum of urinary bacterial species. We studied the urinary microbiota from a...

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Autores principales: Lewis, Debbie A., Brown, Richard, Williams, Jon, White, Paul, Jacobson, S. Kim, Marchesi, Julian R., Drake, Marcus J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3744036/
https://www.ncbi.nlm.nih.gov/pubmed/23967406
http://dx.doi.org/10.3389/fcimb.2013.00041
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author Lewis, Debbie A.
Brown, Richard
Williams, Jon
White, Paul
Jacobson, S. Kim
Marchesi, Julian R.
Drake, Marcus J.
author_facet Lewis, Debbie A.
Brown, Richard
Williams, Jon
White, Paul
Jacobson, S. Kim
Marchesi, Julian R.
Drake, Marcus J.
author_sort Lewis, Debbie A.
collection PubMed
description The urinary microbiome of healthy individuals and the way it alters with ageing have not been characterized and may influence disease processes. Conventional microbiological methods have limited scope to capture the full spectrum of urinary bacterial species. We studied the urinary microbiota from a population of healthy individuals, ranging from 26 to 90 years of age, by amplification of the 16S rRNA gene, with resulting amplicons analyzed by 454 pyrosequencing. Mid-stream urine (MSU) was collected by the “clean-catch” method. Quantitative PCR of 16S rRNA genes in urine samples, allowed relative enumeration of the bacterial loads. Analysis of the samples indicates that females had a more heterogeneous mix of bacterial genera compared to the male samples and generally had representative members of the phyla Actinobacteria and Bacteroidetes. Analysis of the data leads us to conclude that a “core” urinary microbiome could potentially exist, when samples are grouped by age with fluctuation in abundance between age groups. The study also revealed age-specific genera Jonquetella, Parvimonas, Proteiniphilum, and Saccharofermentans. In conclusion, conventional microbiological methods are inadequate to fully identify around two-thirds of the bacteria identified in this study. Whilst this proof-of-principle study has limitations due to the sample size, the discoveries evident in this sample data are strongly suggestive that a larger study on the urinary microbiome should be encouraged and that the identification of specific genera at particular ages may be relevant to pathogenesis of clinical conditions.
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spelling pubmed-37440362013-08-21 The human urinary microbiome; bacterial DNA in voided urine of asymptomatic adults Lewis, Debbie A. Brown, Richard Williams, Jon White, Paul Jacobson, S. Kim Marchesi, Julian R. Drake, Marcus J. Front Cell Infect Microbiol Microbiology The urinary microbiome of healthy individuals and the way it alters with ageing have not been characterized and may influence disease processes. Conventional microbiological methods have limited scope to capture the full spectrum of urinary bacterial species. We studied the urinary microbiota from a population of healthy individuals, ranging from 26 to 90 years of age, by amplification of the 16S rRNA gene, with resulting amplicons analyzed by 454 pyrosequencing. Mid-stream urine (MSU) was collected by the “clean-catch” method. Quantitative PCR of 16S rRNA genes in urine samples, allowed relative enumeration of the bacterial loads. Analysis of the samples indicates that females had a more heterogeneous mix of bacterial genera compared to the male samples and generally had representative members of the phyla Actinobacteria and Bacteroidetes. Analysis of the data leads us to conclude that a “core” urinary microbiome could potentially exist, when samples are grouped by age with fluctuation in abundance between age groups. The study also revealed age-specific genera Jonquetella, Parvimonas, Proteiniphilum, and Saccharofermentans. In conclusion, conventional microbiological methods are inadequate to fully identify around two-thirds of the bacteria identified in this study. Whilst this proof-of-principle study has limitations due to the sample size, the discoveries evident in this sample data are strongly suggestive that a larger study on the urinary microbiome should be encouraged and that the identification of specific genera at particular ages may be relevant to pathogenesis of clinical conditions. Frontiers Media S.A. 2013-08-15 /pmc/articles/PMC3744036/ /pubmed/23967406 http://dx.doi.org/10.3389/fcimb.2013.00041 Text en Copyright © 2013 Lewis, Brown, Williams, White, Jacobson, Marchesi and Drake. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Lewis, Debbie A.
Brown, Richard
Williams, Jon
White, Paul
Jacobson, S. Kim
Marchesi, Julian R.
Drake, Marcus J.
The human urinary microbiome; bacterial DNA in voided urine of asymptomatic adults
title The human urinary microbiome; bacterial DNA in voided urine of asymptomatic adults
title_full The human urinary microbiome; bacterial DNA in voided urine of asymptomatic adults
title_fullStr The human urinary microbiome; bacterial DNA in voided urine of asymptomatic adults
title_full_unstemmed The human urinary microbiome; bacterial DNA in voided urine of asymptomatic adults
title_short The human urinary microbiome; bacterial DNA in voided urine of asymptomatic adults
title_sort human urinary microbiome; bacterial dna in voided urine of asymptomatic adults
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3744036/
https://www.ncbi.nlm.nih.gov/pubmed/23967406
http://dx.doi.org/10.3389/fcimb.2013.00041
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