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Escherichia coli Global Gene Expression in Urine from Women with Urinary Tract Infection

Murine models of urinary tract infection (UTI) have provided substantial data identifying uropathogenic E. coli (UPEC) virulence factors and assessing their expression in vivo. However, it is unclear how gene expression in these animal models compares to UPEC gene expression during UTI in humans. To...

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Autores principales: Hagan, Erin C., Lloyd, Amanda L., Rasko, David A., Faerber, Gary J., Mobley, Harry L. T.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978726/
https://www.ncbi.nlm.nih.gov/pubmed/21085611
http://dx.doi.org/10.1371/journal.ppat.1001187
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author Hagan, Erin C.
Lloyd, Amanda L.
Rasko, David A.
Faerber, Gary J.
Mobley, Harry L. T.
author_facet Hagan, Erin C.
Lloyd, Amanda L.
Rasko, David A.
Faerber, Gary J.
Mobley, Harry L. T.
author_sort Hagan, Erin C.
collection PubMed
description Murine models of urinary tract infection (UTI) have provided substantial data identifying uropathogenic E. coli (UPEC) virulence factors and assessing their expression in vivo. However, it is unclear how gene expression in these animal models compares to UPEC gene expression during UTI in humans. To address this, we used a UPEC strain CFT073-specific microarray to measure global gene expression in eight E. coli isolates monitored directly from the urine of eight women presenting at a clinic with bacteriuria. The resulting gene expression profiles were compared to those of the same E. coli isolates cultured statically to exponential phase in pooled, sterilized human urine ex vivo. Known fitness factors, including iron acquisition and peptide transport systems, were highly expressed during human UTI and support a model in which UPEC replicates rapidly in vivo. While these findings were often consistent with previous data obtained from the murine UTI model, host-specific differences were observed. Most strikingly, expression of type 1 fimbrial genes, which are among the most highly expressed genes during murine experimental UTI and encode an essential virulence factor for this experimental model, was undetectable in six of the eight E. coli strains from women with UTI. Despite the lack of type 1 fimbrial expression in the urine samples, these E. coli isolates were generally capable of expressing type 1 fimbriae in vitro and highly upregulated fimA upon experimental murine infection. The findings presented here provide insight into the metabolic and pathogenic profile of UPEC in urine from women with UTI and represent the first transcriptome analysis for any pathogenic E. coli during a naturally occurring infection in humans.
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spelling pubmed-29787262010-11-17 Escherichia coli Global Gene Expression in Urine from Women with Urinary Tract Infection Hagan, Erin C. Lloyd, Amanda L. Rasko, David A. Faerber, Gary J. Mobley, Harry L. T. PLoS Pathog Research Article Murine models of urinary tract infection (UTI) have provided substantial data identifying uropathogenic E. coli (UPEC) virulence factors and assessing their expression in vivo. However, it is unclear how gene expression in these animal models compares to UPEC gene expression during UTI in humans. To address this, we used a UPEC strain CFT073-specific microarray to measure global gene expression in eight E. coli isolates monitored directly from the urine of eight women presenting at a clinic with bacteriuria. The resulting gene expression profiles were compared to those of the same E. coli isolates cultured statically to exponential phase in pooled, sterilized human urine ex vivo. Known fitness factors, including iron acquisition and peptide transport systems, were highly expressed during human UTI and support a model in which UPEC replicates rapidly in vivo. While these findings were often consistent with previous data obtained from the murine UTI model, host-specific differences were observed. Most strikingly, expression of type 1 fimbrial genes, which are among the most highly expressed genes during murine experimental UTI and encode an essential virulence factor for this experimental model, was undetectable in six of the eight E. coli strains from women with UTI. Despite the lack of type 1 fimbrial expression in the urine samples, these E. coli isolates were generally capable of expressing type 1 fimbriae in vitro and highly upregulated fimA upon experimental murine infection. The findings presented here provide insight into the metabolic and pathogenic profile of UPEC in urine from women with UTI and represent the first transcriptome analysis for any pathogenic E. coli during a naturally occurring infection in humans. Public Library of Science 2010-11-11 /pmc/articles/PMC2978726/ /pubmed/21085611 http://dx.doi.org/10.1371/journal.ppat.1001187 Text en Hagan et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hagan, Erin C.
Lloyd, Amanda L.
Rasko, David A.
Faerber, Gary J.
Mobley, Harry L. T.
Escherichia coli Global Gene Expression in Urine from Women with Urinary Tract Infection
title Escherichia coli Global Gene Expression in Urine from Women with Urinary Tract Infection
title_full Escherichia coli Global Gene Expression in Urine from Women with Urinary Tract Infection
title_fullStr Escherichia coli Global Gene Expression in Urine from Women with Urinary Tract Infection
title_full_unstemmed Escherichia coli Global Gene Expression in Urine from Women with Urinary Tract Infection
title_short Escherichia coli Global Gene Expression in Urine from Women with Urinary Tract Infection
title_sort escherichia coli global gene expression in urine from women with urinary tract infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978726/
https://www.ncbi.nlm.nih.gov/pubmed/21085611
http://dx.doi.org/10.1371/journal.ppat.1001187
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