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Bacteriocin-encoding genes and ExPEC virulence determinants are associated in human fecal Escherichia coli strains

BACKGROUND: A set of 1181 E. coli strains of human fecal origin isolated in the South Moravia region of the Czech Republic was collected during the years 2007–2010. Altogether, 17 virulence determinants and 31 bacteriocin-encoding genes were tested in each of them. RESULTS: The occurrence of bacteri...

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Autores principales: Micenková, Lenka, Štaudová, Barbora, Bosák, Juraj, Mikalová, Lenka, Littnerová, Simona, Vrba, Martin, Ševčíková, Alena, Woznicová, Vladana, Šmajs, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021369/
https://www.ncbi.nlm.nih.gov/pubmed/24774171
http://dx.doi.org/10.1186/1471-2180-14-109
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author Micenková, Lenka
Štaudová, Barbora
Bosák, Juraj
Mikalová, Lenka
Littnerová, Simona
Vrba, Martin
Ševčíková, Alena
Woznicová, Vladana
Šmajs, David
author_facet Micenková, Lenka
Štaudová, Barbora
Bosák, Juraj
Mikalová, Lenka
Littnerová, Simona
Vrba, Martin
Ševčíková, Alena
Woznicová, Vladana
Šmajs, David
author_sort Micenková, Lenka
collection PubMed
description BACKGROUND: A set of 1181 E. coli strains of human fecal origin isolated in the South Moravia region of the Czech Republic was collected during the years 2007–2010. Altogether, 17 virulence determinants and 31 bacteriocin-encoding genes were tested in each of them. RESULTS: The occurrence of bacteriocin-encoding genes was found to be positively correlated with the occurrence of E. coli virulence factors. Based on the presence of virulence factors and their combinations, E. coli strains were classified as non-pathogenic E. coli (n = 399), diarrhea-associated E. coli (n = 179) and ExPEC strains (n = 603). Non-pathogenic and diarrhea-associated E. coli strains had a low frequency of bacteriocinogeny (32.6% and 36.9%, respectively). ExPEC strains encoding S-fimbriae (sfa), P-fimbriae (pap) and having genes for aerobactin biosynthesis (aer, iucC), α-hemolysis (α-hly) and cytotoxic necrosis factor (cnf1) were often bacteriocinogenic (73.8%), had a high prevalence of bacteriocin multi-producers and showed a higher frequency of genes encoding microcins H47, M, V, B17 and colicins E1, Ia and S4. CONCLUSIONS: The occurrence of bacteriocin-encoding genes and ExPEC virulence determinants correlate positively in E. coli strains of human fecal origin. Bacteriocin synthesis appears to modulate the ability of E. coli strains to reside in the human intestine and/or the virulence of the corresponding strains.
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spelling pubmed-40213692014-05-16 Bacteriocin-encoding genes and ExPEC virulence determinants are associated in human fecal Escherichia coli strains Micenková, Lenka Štaudová, Barbora Bosák, Juraj Mikalová, Lenka Littnerová, Simona Vrba, Martin Ševčíková, Alena Woznicová, Vladana Šmajs, David BMC Microbiol Research Article BACKGROUND: A set of 1181 E. coli strains of human fecal origin isolated in the South Moravia region of the Czech Republic was collected during the years 2007–2010. Altogether, 17 virulence determinants and 31 bacteriocin-encoding genes were tested in each of them. RESULTS: The occurrence of bacteriocin-encoding genes was found to be positively correlated with the occurrence of E. coli virulence factors. Based on the presence of virulence factors and their combinations, E. coli strains were classified as non-pathogenic E. coli (n = 399), diarrhea-associated E. coli (n = 179) and ExPEC strains (n = 603). Non-pathogenic and diarrhea-associated E. coli strains had a low frequency of bacteriocinogeny (32.6% and 36.9%, respectively). ExPEC strains encoding S-fimbriae (sfa), P-fimbriae (pap) and having genes for aerobactin biosynthesis (aer, iucC), α-hemolysis (α-hly) and cytotoxic necrosis factor (cnf1) were often bacteriocinogenic (73.8%), had a high prevalence of bacteriocin multi-producers and showed a higher frequency of genes encoding microcins H47, M, V, B17 and colicins E1, Ia and S4. CONCLUSIONS: The occurrence of bacteriocin-encoding genes and ExPEC virulence determinants correlate positively in E. coli strains of human fecal origin. Bacteriocin synthesis appears to modulate the ability of E. coli strains to reside in the human intestine and/or the virulence of the corresponding strains. BioMed Central 2014-04-28 /pmc/articles/PMC4021369/ /pubmed/24774171 http://dx.doi.org/10.1186/1471-2180-14-109 Text en Copyright © 2014 Micenková et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Micenková, Lenka
Štaudová, Barbora
Bosák, Juraj
Mikalová, Lenka
Littnerová, Simona
Vrba, Martin
Ševčíková, Alena
Woznicová, Vladana
Šmajs, David
Bacteriocin-encoding genes and ExPEC virulence determinants are associated in human fecal Escherichia coli strains
title Bacteriocin-encoding genes and ExPEC virulence determinants are associated in human fecal Escherichia coli strains
title_full Bacteriocin-encoding genes and ExPEC virulence determinants are associated in human fecal Escherichia coli strains
title_fullStr Bacteriocin-encoding genes and ExPEC virulence determinants are associated in human fecal Escherichia coli strains
title_full_unstemmed Bacteriocin-encoding genes and ExPEC virulence determinants are associated in human fecal Escherichia coli strains
title_short Bacteriocin-encoding genes and ExPEC virulence determinants are associated in human fecal Escherichia coli strains
title_sort bacteriocin-encoding genes and expec virulence determinants are associated in human fecal escherichia coli strains
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021369/
https://www.ncbi.nlm.nih.gov/pubmed/24774171
http://dx.doi.org/10.1186/1471-2180-14-109
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