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Microbiome diversity in carriers of fluoroquinolone resistant Escherichia coli

PURPOSE: Fluoroquinolone-resistant (FQR) Escherichia coli causes transrectal prostate biopsy infections. In order to reduce colonization of these bacteria in carriers, we would like to understand the surrounding microbiome to determine targets for decolonization. MATERIALS AND METHODS: We perform an...

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Autores principales: Liss, Michael A., Leach, Robin J., Rourke, Elizabeth, Sherrill, Allison, Johnson-Pais, Teresa, Lai, Zhao, Basler, Joseph, White, James R., Patterson, Jan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Urological Association 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397931/
https://www.ncbi.nlm.nih.gov/pubmed/30838339
http://dx.doi.org/10.4111/icu.2019.60.2.75
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author Liss, Michael A.
Leach, Robin J.
Rourke, Elizabeth
Sherrill, Allison
Johnson-Pais, Teresa
Lai, Zhao
Basler, Joseph
White, James R.
Patterson, Jan E.
author_facet Liss, Michael A.
Leach, Robin J.
Rourke, Elizabeth
Sherrill, Allison
Johnson-Pais, Teresa
Lai, Zhao
Basler, Joseph
White, James R.
Patterson, Jan E.
author_sort Liss, Michael A.
collection PubMed
description PURPOSE: Fluoroquinolone-resistant (FQR) Escherichia coli causes transrectal prostate biopsy infections. In order to reduce colonization of these bacteria in carriers, we would like to understand the surrounding microbiome to determine targets for decolonization. MATERIALS AND METHODS: We perform an observational study to investigate the microbiome differences in men with and without FQR organisms found on rectal culture. A rectal swab with two culturettes was performed on men before an upcoming prostate biopsy procedure as standard of care to perform “targeted prophylaxis.” Detection of FQR was performed by the standard microbiology lab inoculates the swab onto MacConkey agar containing ciprofloxacin. The extra swab was sent for 16S rRNA amplicon sequencing (MiSeq paired-end) using the V1V2 primer. Alpha and beta-diversity analysis were performed using QIIME. We used PERMANOVA to evaluate the statistical significance of beta-diversity distances within and between groups of interest. RESULTS: We collected 116 rectal swab samples before biopsy for 16S rRNA amplicon sequencing. We identified 18 isolates (15.5%, 18/116) that were positive and had relative reduced diversity profiles (p<0.05). Enterobacteriaceae were significantly over-represented in the FQR subjects (adjusted p=0.03). CONCLUSIONS: Microbiome analysis determined that men colonized with FQR bacteria have less diverse bacterial communities (dysbiosis), higher levels of Enterobacteriaceae and reduced levels of Prevotella disiens. These results may have implications in pre/probiotic intervention studies.
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spelling pubmed-63979312019-03-05 Microbiome diversity in carriers of fluoroquinolone resistant Escherichia coli Liss, Michael A. Leach, Robin J. Rourke, Elizabeth Sherrill, Allison Johnson-Pais, Teresa Lai, Zhao Basler, Joseph White, James R. Patterson, Jan E. Investig Clin Urol Original Article PURPOSE: Fluoroquinolone-resistant (FQR) Escherichia coli causes transrectal prostate biopsy infections. In order to reduce colonization of these bacteria in carriers, we would like to understand the surrounding microbiome to determine targets for decolonization. MATERIALS AND METHODS: We perform an observational study to investigate the microbiome differences in men with and without FQR organisms found on rectal culture. A rectal swab with two culturettes was performed on men before an upcoming prostate biopsy procedure as standard of care to perform “targeted prophylaxis.” Detection of FQR was performed by the standard microbiology lab inoculates the swab onto MacConkey agar containing ciprofloxacin. The extra swab was sent for 16S rRNA amplicon sequencing (MiSeq paired-end) using the V1V2 primer. Alpha and beta-diversity analysis were performed using QIIME. We used PERMANOVA to evaluate the statistical significance of beta-diversity distances within and between groups of interest. RESULTS: We collected 116 rectal swab samples before biopsy for 16S rRNA amplicon sequencing. We identified 18 isolates (15.5%, 18/116) that were positive and had relative reduced diversity profiles (p<0.05). Enterobacteriaceae were significantly over-represented in the FQR subjects (adjusted p=0.03). CONCLUSIONS: Microbiome analysis determined that men colonized with FQR bacteria have less diverse bacterial communities (dysbiosis), higher levels of Enterobacteriaceae and reduced levels of Prevotella disiens. These results may have implications in pre/probiotic intervention studies. The Korean Urological Association 2019-03 2019-02-27 /pmc/articles/PMC6397931/ /pubmed/30838339 http://dx.doi.org/10.4111/icu.2019.60.2.75 Text en © The Korean Urological Association, 2019 http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Liss, Michael A.
Leach, Robin J.
Rourke, Elizabeth
Sherrill, Allison
Johnson-Pais, Teresa
Lai, Zhao
Basler, Joseph
White, James R.
Patterson, Jan E.
Microbiome diversity in carriers of fluoroquinolone resistant Escherichia coli
title Microbiome diversity in carriers of fluoroquinolone resistant Escherichia coli
title_full Microbiome diversity in carriers of fluoroquinolone resistant Escherichia coli
title_fullStr Microbiome diversity in carriers of fluoroquinolone resistant Escherichia coli
title_full_unstemmed Microbiome diversity in carriers of fluoroquinolone resistant Escherichia coli
title_short Microbiome diversity in carriers of fluoroquinolone resistant Escherichia coli
title_sort microbiome diversity in carriers of fluoroquinolone resistant escherichia coli
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397931/
https://www.ncbi.nlm.nih.gov/pubmed/30838339
http://dx.doi.org/10.4111/icu.2019.60.2.75
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