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PMID: 21085611 Published · epublish English Journal Article Research Support, N.I.H., Extramural

Escherichia coli global gene expression in urine from women with urinary tract infection.

PLoS pathogens ·Vol. 6 ·No. 11 ·2010-11-11 ·Pages e1001187

Hagan EC, Lloyd AL, Rasko DA, Faerber GJ, Mobley HL

Abstract

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.

MeSH Terms
Adult Aged Aged, 80 and over Animals Biomarkers/urine Blotting, Western Escherichia coli/genetics,metabolism,pathogenicity Escherichia coli Infections/genetics,microbiology,urine Escherichia coli Proteins/genetics,urine Female Gene Expression Profiling Hemagglutination Humans Mice Mice, Inbred CBA Middle Aged Oligonucleotide Array Sequence Analysis RNA, Bacterial/genetics RNA, Messenger/genetics Reverse Transcriptase Polymerase Chain Reaction Urinary Tract Infections/genetics,microbiology,urine Virulence Factors/genetics,urine Young Adult
Chemicals
Biomarkers Escherichia coli Proteins RNA, Bacterial RNA, Messenger Virulence Factors
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hagan Erin C
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
Lloyd Amanda L
Rasko David A
Faerber Gary J
Mobley Harry L T
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Article Info
Journal
PLoS pathogens
Abbr.
PLoS Pathog
ISSN
1553-7374
Published
2010-11-11
Epub
2010-00-11
Pages
e1001187
Language
English
Region
United States
NLM ID
101238921
PMCID
PMC2978726
Subset
IM
Grants
NIAID NIH HHS · R01 AI043363 · United States
NIAID NIH HHS · R56 AI043363 · United States
NIAID NIH HHS · AI43363 · United States
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