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Molecular identification, genotyping of virulence-associated genes, and pathogenicity of cellulitis-derived Escherichia coli

BACKGROUND AND AIM: Avian colibacillosis, which is caused by avian pathogenic Escherichia coli (APEC), is a major bacterial disease that affects birds of all ages worldwide, causing significant economic losses. APEC manifests in several clinical forms, including cellulitis, and its high pathogenicit...

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Autores principales: Amer, Mohamed M., Mekky, Hoda M., Fedawy, Hanaa S., EL-Shemy, A., Bosila, M. A., Elbayoumi, Kh. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Veterinary World 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811558/
https://www.ncbi.nlm.nih.gov/pubmed/33487989
http://dx.doi.org/10.14202/vetworld.2020.2703-2712
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author Amer, Mohamed M.
Mekky, Hoda M.
Fedawy, Hanaa S.
EL-Shemy, A.
Bosila, M. A.
Elbayoumi, Kh. M.
author_facet Amer, Mohamed M.
Mekky, Hoda M.
Fedawy, Hanaa S.
EL-Shemy, A.
Bosila, M. A.
Elbayoumi, Kh. M.
author_sort Amer, Mohamed M.
collection PubMed
description BACKGROUND AND AIM: Avian colibacillosis, which is caused by avian pathogenic Escherichia coli (APEC), is a major bacterial disease that affects birds of all ages worldwide, causing significant economic losses. APEC manifests in several clinical forms, including cellulitis, and its high pathogenicity is attributed to harboring numerous virulence-associated genes (VGs). This study evaluated the pathogenicity of the cellulitis-derived E. coli (O78) strain through molecular identification of genes coding for seven virulence factors and by conducting an in vivo assessment of capability for cellulitis induction in broiler chickens. MATERIALS AND METHODS: This study was performed using a previously isolated and identified cellulitis-derived E. coli (O78), which was screened for seven VGs using molecular detection and identification through polymerase chain reaction followed by nucleotide sequencing and phylogenetic analysis. Experimental infection by subcutaneous (SC) inoculation in broilers and its pathogenicity was confirmed in vivo by cellulitis induction. The impact of cellulitis on broiler performance was assessed. RESULTS: Molecular genotyping proved that the isolate harbored five virulence genes (iroN, iutA, tsh, iss, and papC) and was negative for stx1 and hly genes. The amplified products for iroN, iss, and iutA were subjected to sequencing and phylogenetic analysis, and the results indicate the highest similarity and matching with E. coli submitted to the National Center for Biotechnology Information GenBank. SC inoculation of bacteria in broiler chickens resulted in cellulitis, as indicated by thick red edematous skin with yellowish-white material in the SC tissue at the inoculation site, and the abdominal muscle showed redness and increased vacuolization. Histopathological examination revealed moderate-to-severe caseous inflammatory reaction with a marked accumulation of heterophils and mononuclear cells in the SC fatty tissue. The average feed intake, body weight gain (BWG), and feed conversion ratio (FCR) were lower in infected chickens in comparison with those of the control non-infected chickens. CONCLUSION: This study proves that molecular techniques are accurate for pathogenicity determination in virulent bacteria, with the advantages of being rapid, time-saving, and economical. Cellulitis is associated with economic losses that are represented by a lower BWG and FCR.
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spelling pubmed-78115582021-01-22 Molecular identification, genotyping of virulence-associated genes, and pathogenicity of cellulitis-derived Escherichia coli Amer, Mohamed M. Mekky, Hoda M. Fedawy, Hanaa S. EL-Shemy, A. Bosila, M. A. Elbayoumi, Kh. M. Vet World Research Article BACKGROUND AND AIM: Avian colibacillosis, which is caused by avian pathogenic Escherichia coli (APEC), is a major bacterial disease that affects birds of all ages worldwide, causing significant economic losses. APEC manifests in several clinical forms, including cellulitis, and its high pathogenicity is attributed to harboring numerous virulence-associated genes (VGs). This study evaluated the pathogenicity of the cellulitis-derived E. coli (O78) strain through molecular identification of genes coding for seven virulence factors and by conducting an in vivo assessment of capability for cellulitis induction in broiler chickens. MATERIALS AND METHODS: This study was performed using a previously isolated and identified cellulitis-derived E. coli (O78), which was screened for seven VGs using molecular detection and identification through polymerase chain reaction followed by nucleotide sequencing and phylogenetic analysis. Experimental infection by subcutaneous (SC) inoculation in broilers and its pathogenicity was confirmed in vivo by cellulitis induction. The impact of cellulitis on broiler performance was assessed. RESULTS: Molecular genotyping proved that the isolate harbored five virulence genes (iroN, iutA, tsh, iss, and papC) and was negative for stx1 and hly genes. The amplified products for iroN, iss, and iutA were subjected to sequencing and phylogenetic analysis, and the results indicate the highest similarity and matching with E. coli submitted to the National Center for Biotechnology Information GenBank. SC inoculation of bacteria in broiler chickens resulted in cellulitis, as indicated by thick red edematous skin with yellowish-white material in the SC tissue at the inoculation site, and the abdominal muscle showed redness and increased vacuolization. Histopathological examination revealed moderate-to-severe caseous inflammatory reaction with a marked accumulation of heterophils and mononuclear cells in the SC fatty tissue. The average feed intake, body weight gain (BWG), and feed conversion ratio (FCR) were lower in infected chickens in comparison with those of the control non-infected chickens. CONCLUSION: This study proves that molecular techniques are accurate for pathogenicity determination in virulent bacteria, with the advantages of being rapid, time-saving, and economical. Cellulitis is associated with economic losses that are represented by a lower BWG and FCR. Veterinary World 2020-12 2020-12-19 /pmc/articles/PMC7811558/ /pubmed/33487989 http://dx.doi.org/10.14202/vetworld.2020.2703-2712 Text en Copyright: © Amer, et al. http://creativecommons.org/licenses/by/4.0 Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Amer, Mohamed M.
Mekky, Hoda M.
Fedawy, Hanaa S.
EL-Shemy, A.
Bosila, M. A.
Elbayoumi, Kh. M.
Molecular identification, genotyping of virulence-associated genes, and pathogenicity of cellulitis-derived Escherichia coli
title Molecular identification, genotyping of virulence-associated genes, and pathogenicity of cellulitis-derived Escherichia coli
title_full Molecular identification, genotyping of virulence-associated genes, and pathogenicity of cellulitis-derived Escherichia coli
title_fullStr Molecular identification, genotyping of virulence-associated genes, and pathogenicity of cellulitis-derived Escherichia coli
title_full_unstemmed Molecular identification, genotyping of virulence-associated genes, and pathogenicity of cellulitis-derived Escherichia coli
title_short Molecular identification, genotyping of virulence-associated genes, and pathogenicity of cellulitis-derived Escherichia coli
title_sort molecular identification, genotyping of virulence-associated genes, and pathogenicity of cellulitis-derived escherichia coli
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811558/
https://www.ncbi.nlm.nih.gov/pubmed/33487989
http://dx.doi.org/10.14202/vetworld.2020.2703-2712
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