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Gene expression in the chicken caecum in response to infections with non-typhoid Salmonella

Chickens can be infected with Salmonella enterica at any time during their life. However, infections within the first hours and days of their life are epidemiologically the most important, as newly hatched chickens are highly sensitive to Salmonella infection. Salmonella is initially recognized in t...

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Autores principales: Rychlik, Ivan, Elsheimer-Matulova, Marta, Kyrova, Kamila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256799/
https://www.ncbi.nlm.nih.gov/pubmed/25475706
http://dx.doi.org/10.1186/s13567-014-0119-2
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author Rychlik, Ivan
Elsheimer-Matulova, Marta
Kyrova, Kamila
author_facet Rychlik, Ivan
Elsheimer-Matulova, Marta
Kyrova, Kamila
author_sort Rychlik, Ivan
collection PubMed
description Chickens can be infected with Salmonella enterica at any time during their life. However, infections within the first hours and days of their life are epidemiologically the most important, as newly hatched chickens are highly sensitive to Salmonella infection. Salmonella is initially recognized in the chicken caecum by TLR receptors and this recognition is followed by induction of chemokines, cytokines and many effector genes. This results in infiltration of heterophils, macrophages, B- and T-lymphocytes and changes in total gene expression in the caecal lamina propria. The highest induction in expression is observed for matrix metalloproteinase 7 (MMP7). Expression of this gene is increased in the chicken caecum over 4000 fold during the first 10 days after the infection of newly hatched chickens. Additional highly inducible genes in the caecum following S. Enteritidis infection include immune responsive gene 1 (IRG1), serum amyloid A (SAA), extracellular fatty acid binding protein (ExFABP), serine protease inhibitor (SERPINB10), trappin 6-like (TRAP6), calprotectin (MRP126), mitochondrial ES1 protein homolog (ES1), interferon-induced protein with tetratricopeptide repeats 5 (IFIT5), avidin (AVD) and transglutaminase 4 (TGM4). The induction of expression of these proteins exceeds a factor of 50. Similar induction rates are also observed for chemokines and cytokines such as IL1β, IL6, IL8, IL17, IL18, IL22, IFNγ, AH221 or iNOS. Once the infection is under control, which happens approx. 2 weeks after infection, expression of IgY and IgA increases to facilitate Salmonella elimination from the gut lumen. This review outlines the function of individual proteins expressed in chickens after infection with non-typhoid Salmonella serovars.
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spelling pubmed-42567992014-12-05 Gene expression in the chicken caecum in response to infections with non-typhoid Salmonella Rychlik, Ivan Elsheimer-Matulova, Marta Kyrova, Kamila Vet Res Review Chickens can be infected with Salmonella enterica at any time during their life. However, infections within the first hours and days of their life are epidemiologically the most important, as newly hatched chickens are highly sensitive to Salmonella infection. Salmonella is initially recognized in the chicken caecum by TLR receptors and this recognition is followed by induction of chemokines, cytokines and many effector genes. This results in infiltration of heterophils, macrophages, B- and T-lymphocytes and changes in total gene expression in the caecal lamina propria. The highest induction in expression is observed for matrix metalloproteinase 7 (MMP7). Expression of this gene is increased in the chicken caecum over 4000 fold during the first 10 days after the infection of newly hatched chickens. Additional highly inducible genes in the caecum following S. Enteritidis infection include immune responsive gene 1 (IRG1), serum amyloid A (SAA), extracellular fatty acid binding protein (ExFABP), serine protease inhibitor (SERPINB10), trappin 6-like (TRAP6), calprotectin (MRP126), mitochondrial ES1 protein homolog (ES1), interferon-induced protein with tetratricopeptide repeats 5 (IFIT5), avidin (AVD) and transglutaminase 4 (TGM4). The induction of expression of these proteins exceeds a factor of 50. Similar induction rates are also observed for chemokines and cytokines such as IL1β, IL6, IL8, IL17, IL18, IL22, IFNγ, AH221 or iNOS. Once the infection is under control, which happens approx. 2 weeks after infection, expression of IgY and IgA increases to facilitate Salmonella elimination from the gut lumen. This review outlines the function of individual proteins expressed in chickens after infection with non-typhoid Salmonella serovars. BioMed Central 2014-12-05 2014 /pmc/articles/PMC4256799/ /pubmed/25475706 http://dx.doi.org/10.1186/s13567-014-0119-2 Text en © Rychlik et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), 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 Review
Rychlik, Ivan
Elsheimer-Matulova, Marta
Kyrova, Kamila
Gene expression in the chicken caecum in response to infections with non-typhoid Salmonella
title Gene expression in the chicken caecum in response to infections with non-typhoid Salmonella
title_full Gene expression in the chicken caecum in response to infections with non-typhoid Salmonella
title_fullStr Gene expression in the chicken caecum in response to infections with non-typhoid Salmonella
title_full_unstemmed Gene expression in the chicken caecum in response to infections with non-typhoid Salmonella
title_short Gene expression in the chicken caecum in response to infections with non-typhoid Salmonella
title_sort gene expression in the chicken caecum in response to infections with non-typhoid salmonella
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256799/
https://www.ncbi.nlm.nih.gov/pubmed/25475706
http://dx.doi.org/10.1186/s13567-014-0119-2
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