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Kinetics of Uropathogenic Escherichia coli Metapopulation Movement during Urinary Tract Infection

The urinary tract is one of the most frequent sites of bacterial infection in humans. Uropathogenic Escherichia coli (UPEC) strains are the leading cause of urinary tract infections (UTIs) and are responsible for greater than 80% of uncomplicated cases in adults. Infection of the urinary tract occur...

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Autores principales: Walters, Matthew S., Lane, M. Chelsea, Vigil, Patrick D., Smith, Sara N., Walk, Seth T., Mobley, Harry L. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3273315/
https://www.ncbi.nlm.nih.gov/pubmed/22318320
http://dx.doi.org/10.1128/mBio.00303-11
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author Walters, Matthew S.
Lane, M. Chelsea
Vigil, Patrick D.
Smith, Sara N.
Walk, Seth T.
Mobley, Harry L. T.
author_facet Walters, Matthew S.
Lane, M. Chelsea
Vigil, Patrick D.
Smith, Sara N.
Walk, Seth T.
Mobley, Harry L. T.
author_sort Walters, Matthew S.
collection PubMed
description The urinary tract is one of the most frequent sites of bacterial infection in humans. Uropathogenic Escherichia coli (UPEC) strains are the leading cause of urinary tract infections (UTIs) and are responsible for greater than 80% of uncomplicated cases in adults. Infection of the urinary tract occurs in an ascending manner, with colonization of the bladder leading to possible kidney infection and bacteremia. The goal of this study was to examine the population dynamics of UPEC in vivo using a murine model of ascending UTI. To track individual UPEC lineages within a host, we constructed 10 isogenic clones of UPEC strain CFT073 by inserting unique signature tag sequences between the pstS and glmS genes at the attTn7 chromosomal site. Mice were transurethrally inoculated with a mixture containing equal numbers of unique clones. After 4 and 48 h, the tags present in the bladders, kidneys, and spleens of infected mice were enumerated using tag-specific primers and quantitative real-time PCR. The results indicated that kidney infection and bacteremia associated with UTI are most likely the result of multiple rounds of ascension and dissemination from motile UPEC subpopulations, with a distinct bottleneck existing between the kidney and bloodstream. The abundance of tagged lineages became more variable as infection progressed, especially after bacterial ascension to the upper urinary tract. Analysis of the population kinetics of UPEC during UTI revealed metapopulation dynamics, with lineages that constantly increased and decreased in abundance as they migrated from one organ to another.
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spelling pubmed-32733152012-02-23 Kinetics of Uropathogenic Escherichia coli Metapopulation Movement during Urinary Tract Infection Walters, Matthew S. Lane, M. Chelsea Vigil, Patrick D. Smith, Sara N. Walk, Seth T. Mobley, Harry L. T. mBio Research Article The urinary tract is one of the most frequent sites of bacterial infection in humans. Uropathogenic Escherichia coli (UPEC) strains are the leading cause of urinary tract infections (UTIs) and are responsible for greater than 80% of uncomplicated cases in adults. Infection of the urinary tract occurs in an ascending manner, with colonization of the bladder leading to possible kidney infection and bacteremia. The goal of this study was to examine the population dynamics of UPEC in vivo using a murine model of ascending UTI. To track individual UPEC lineages within a host, we constructed 10 isogenic clones of UPEC strain CFT073 by inserting unique signature tag sequences between the pstS and glmS genes at the attTn7 chromosomal site. Mice were transurethrally inoculated with a mixture containing equal numbers of unique clones. After 4 and 48 h, the tags present in the bladders, kidneys, and spleens of infected mice were enumerated using tag-specific primers and quantitative real-time PCR. The results indicated that kidney infection and bacteremia associated with UTI are most likely the result of multiple rounds of ascension and dissemination from motile UPEC subpopulations, with a distinct bottleneck existing between the kidney and bloodstream. The abundance of tagged lineages became more variable as infection progressed, especially after bacterial ascension to the upper urinary tract. Analysis of the population kinetics of UPEC during UTI revealed metapopulation dynamics, with lineages that constantly increased and decreased in abundance as they migrated from one organ to another. American Society of Microbiology 2012-02-07 /pmc/articles/PMC3273315/ /pubmed/22318320 http://dx.doi.org/10.1128/mBio.00303-11 Text en Copyright © 2012 Walters et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Walters, Matthew S.
Lane, M. Chelsea
Vigil, Patrick D.
Smith, Sara N.
Walk, Seth T.
Mobley, Harry L. T.
Kinetics of Uropathogenic Escherichia coli Metapopulation Movement during Urinary Tract Infection
title Kinetics of Uropathogenic Escherichia coli Metapopulation Movement during Urinary Tract Infection
title_full Kinetics of Uropathogenic Escherichia coli Metapopulation Movement during Urinary Tract Infection
title_fullStr Kinetics of Uropathogenic Escherichia coli Metapopulation Movement during Urinary Tract Infection
title_full_unstemmed Kinetics of Uropathogenic Escherichia coli Metapopulation Movement during Urinary Tract Infection
title_short Kinetics of Uropathogenic Escherichia coli Metapopulation Movement during Urinary Tract Infection
title_sort kinetics of uropathogenic escherichia coli metapopulation movement during urinary tract infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3273315/
https://www.ncbi.nlm.nih.gov/pubmed/22318320
http://dx.doi.org/10.1128/mBio.00303-11
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