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Genetic relatedness of the Escherichia coli fecal population and strains causing urinary tract infection in the same host

It is common knowledge that fecal microbiota is a primary source of Escherichia coli causing urinary tract infections (UTIs) via the fecal‐perineal‐urethral route. But, it is still unknown whether E. coli UTI is mainly caused by dominant fecal E. coli isolates (prevalence hypothesis) or the isolates...

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Autores principales: Bahadori, Maryam, Motamedifar, Mohammad, Derakhshandeh, Abdollah, Firouzi, Roya, Motamedi Boroojeni, Azar, Alinejad, Mohsen, Naziri, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562127/
https://www.ncbi.nlm.nih.gov/pubmed/30358940
http://dx.doi.org/10.1002/mbo3.759
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author Bahadori, Maryam
Motamedifar, Mohammad
Derakhshandeh, Abdollah
Firouzi, Roya
Motamedi Boroojeni, Azar
Alinejad, Mohsen
Naziri, Zahra
author_facet Bahadori, Maryam
Motamedifar, Mohammad
Derakhshandeh, Abdollah
Firouzi, Roya
Motamedi Boroojeni, Azar
Alinejad, Mohsen
Naziri, Zahra
author_sort Bahadori, Maryam
collection PubMed
description It is common knowledge that fecal microbiota is a primary source of Escherichia coli causing urinary tract infections (UTIs) via the fecal‐perineal‐urethral route. But, it is still unknown whether E. coli UTI is mainly caused by dominant fecal E. coli isolates (prevalence hypothesis) or the isolates that possess more virulence factors (special pathogenicity hypothesis). In the present study, the urine E. coli isolates of 30 women with UTI were compared with the fecal E. coli isolates of the same patients and healthy control individuals according to the phylogenetic group, virulence genotype, and antibiotic susceptibility pattern. The genetic relatedness of the isolates was specified and compared by pulsed‐field gel electrophoresis (PFGE). PFGE analysis showed that most patients (73.3%) had distinct urine isolates which were not similar to any of their fecal isolates. Based on the phylogenetic analysis, most of the urine and fecal isolates of healthy women were assigned to phylogenetic group B2, followed by D. The distribution of phylogenetic groups was significantly different between the urine and the fecal isolates of patients (p < 0.05). The prevalence of fimH and ompT among urine isolates was significantly more than that among fecal isolates. The level of multidrug resistance was higher among urine isolates. Although more in‐depth researches are required, the present study could be supported by pathogenicity hypothesis. Furthermore, concerning the antibiotic resistance pattern among uropathogenic E. coli should be highly considered.
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spelling pubmed-65621272019-06-17 Genetic relatedness of the Escherichia coli fecal population and strains causing urinary tract infection in the same host Bahadori, Maryam Motamedifar, Mohammad Derakhshandeh, Abdollah Firouzi, Roya Motamedi Boroojeni, Azar Alinejad, Mohsen Naziri, Zahra Microbiologyopen Original Articles It is common knowledge that fecal microbiota is a primary source of Escherichia coli causing urinary tract infections (UTIs) via the fecal‐perineal‐urethral route. But, it is still unknown whether E. coli UTI is mainly caused by dominant fecal E. coli isolates (prevalence hypothesis) or the isolates that possess more virulence factors (special pathogenicity hypothesis). In the present study, the urine E. coli isolates of 30 women with UTI were compared with the fecal E. coli isolates of the same patients and healthy control individuals according to the phylogenetic group, virulence genotype, and antibiotic susceptibility pattern. The genetic relatedness of the isolates was specified and compared by pulsed‐field gel electrophoresis (PFGE). PFGE analysis showed that most patients (73.3%) had distinct urine isolates which were not similar to any of their fecal isolates. Based on the phylogenetic analysis, most of the urine and fecal isolates of healthy women were assigned to phylogenetic group B2, followed by D. The distribution of phylogenetic groups was significantly different between the urine and the fecal isolates of patients (p < 0.05). The prevalence of fimH and ompT among urine isolates was significantly more than that among fecal isolates. The level of multidrug resistance was higher among urine isolates. Although more in‐depth researches are required, the present study could be supported by pathogenicity hypothesis. Furthermore, concerning the antibiotic resistance pattern among uropathogenic E. coli should be highly considered. John Wiley and Sons Inc. 2018-10-25 /pmc/articles/PMC6562127/ /pubmed/30358940 http://dx.doi.org/10.1002/mbo3.759 Text en © 2018 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Bahadori, Maryam
Motamedifar, Mohammad
Derakhshandeh, Abdollah
Firouzi, Roya
Motamedi Boroojeni, Azar
Alinejad, Mohsen
Naziri, Zahra
Genetic relatedness of the Escherichia coli fecal population and strains causing urinary tract infection in the same host
title Genetic relatedness of the Escherichia coli fecal population and strains causing urinary tract infection in the same host
title_full Genetic relatedness of the Escherichia coli fecal population and strains causing urinary tract infection in the same host
title_fullStr Genetic relatedness of the Escherichia coli fecal population and strains causing urinary tract infection in the same host
title_full_unstemmed Genetic relatedness of the Escherichia coli fecal population and strains causing urinary tract infection in the same host
title_short Genetic relatedness of the Escherichia coli fecal population and strains causing urinary tract infection in the same host
title_sort genetic relatedness of the escherichia coli fecal population and strains causing urinary tract infection in the same host
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562127/
https://www.ncbi.nlm.nih.gov/pubmed/30358940
http://dx.doi.org/10.1002/mbo3.759
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