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Extra-intestinal pathogenic Escherichia coli from human and avian origin: Detection of the most common virulence-encoding genes
Pathogenic Escherichia coli strains cause a wide range of extra intestinal infections including urinary tract infection in humans and colibacillosis in poultry. They are classified into uropathogenic E. coli (UPEC) and avian pathogenic E. coli (APEC) with genetic similarities and variations. Their p...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Urmia University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522195/ https://www.ncbi.nlm.nih.gov/pubmed/31183015 http://dx.doi.org/10.30466/vrf.2019.34307 |
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author | Najafi, Soheila Rahimi, Morad Nikousefat, Zahra |
author_facet | Najafi, Soheila Rahimi, Morad Nikousefat, Zahra |
author_sort | Najafi, Soheila |
collection | PubMed |
description | Pathogenic Escherichia coli strains cause a wide range of extra intestinal infections including urinary tract infection in humans and colibacillosis in poultry. They are classified into uropathogenic E. coli (UPEC) and avian pathogenic E. coli (APEC) with genetic similarities and variations. Their pathogenicity is related to the virulence-encoding genes like sfa, papG II, ompT, iutA, and iss with zoonotic potentials. One hundred isolated E. coli from patients with urinary tract infection and 100 E. coli from chickens with colibacillosis were evaluated for the presence of the most common virulence-encoding genes including sfa, papG II, ompT, iutA, and iss by multiplex polymerase chain reaction. While the frequency of sfa, papG II, ompT, iutA and iss encoding genes in APEC isolates were respectively 0.00%, 67.00%, 63.00%, 89.00% and 89.00%, the frequency of these encoding genes in UPEC isolates were 18.00%, 40.00%, 40.00%, 74.00% and 48.00%, respectively. Except for sfa, the frequencies of other encoding genes in APEC were more than those in UPEC isolates. The iutA as the most common UPEC encoding gene and iss as the most common APEC encoding gene were the most prevalent virulence factors in the examined E. coli isolates. Finding out the distribution of virulence-associated genes could be helpful to identify similarities and differences between APEC and UPEC isolates in order to provide more substantial evidence of their common virulence traits and potential zoonotic threats. |
format | Online Article Text |
id | pubmed-6522195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Urmia University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-65221952019-06-10 Extra-intestinal pathogenic Escherichia coli from human and avian origin: Detection of the most common virulence-encoding genes Najafi, Soheila Rahimi, Morad Nikousefat, Zahra Vet Res Forum Original Article Pathogenic Escherichia coli strains cause a wide range of extra intestinal infections including urinary tract infection in humans and colibacillosis in poultry. They are classified into uropathogenic E. coli (UPEC) and avian pathogenic E. coli (APEC) with genetic similarities and variations. Their pathogenicity is related to the virulence-encoding genes like sfa, papG II, ompT, iutA, and iss with zoonotic potentials. One hundred isolated E. coli from patients with urinary tract infection and 100 E. coli from chickens with colibacillosis were evaluated for the presence of the most common virulence-encoding genes including sfa, papG II, ompT, iutA, and iss by multiplex polymerase chain reaction. While the frequency of sfa, papG II, ompT, iutA and iss encoding genes in APEC isolates were respectively 0.00%, 67.00%, 63.00%, 89.00% and 89.00%, the frequency of these encoding genes in UPEC isolates were 18.00%, 40.00%, 40.00%, 74.00% and 48.00%, respectively. Except for sfa, the frequencies of other encoding genes in APEC were more than those in UPEC isolates. The iutA as the most common UPEC encoding gene and iss as the most common APEC encoding gene were the most prevalent virulence factors in the examined E. coli isolates. Finding out the distribution of virulence-associated genes could be helpful to identify similarities and differences between APEC and UPEC isolates in order to provide more substantial evidence of their common virulence traits and potential zoonotic threats. Urmia University Press 2019 2019-03-15 /pmc/articles/PMC6522195/ /pubmed/31183015 http://dx.doi.org/10.30466/vrf.2019.34307 Text en © 2019 Urmia University. All rights reserved. This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/)which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Original Article Najafi, Soheila Rahimi, Morad Nikousefat, Zahra Extra-intestinal pathogenic Escherichia coli from human and avian origin: Detection of the most common virulence-encoding genes |
title | Extra-intestinal pathogenic Escherichia coli from human and avian origin: Detection of the most common virulence-encoding genes |
title_full | Extra-intestinal pathogenic Escherichia coli from human and avian origin: Detection of the most common virulence-encoding genes |
title_fullStr | Extra-intestinal pathogenic Escherichia coli from human and avian origin: Detection of the most common virulence-encoding genes |
title_full_unstemmed | Extra-intestinal pathogenic Escherichia coli from human and avian origin: Detection of the most common virulence-encoding genes |
title_short | Extra-intestinal pathogenic Escherichia coli from human and avian origin: Detection of the most common virulence-encoding genes |
title_sort | extra-intestinal pathogenic escherichia coli from human and avian origin: detection of the most common virulence-encoding genes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522195/ https://www.ncbi.nlm.nih.gov/pubmed/31183015 http://dx.doi.org/10.30466/vrf.2019.34307 |
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