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Proteomic Analysis of the Effect of Salmonella Challenge on Broiler Chicken
Salmonella enteritidis is a foodborne pathogen that causes high morbidity in poultry. Proteomic analysis by liquid chromatography tandem mass spectrometry (LC-MS/MS) was used to study the effects of Salmonella infection on spleen proteome in broiler chickens. Day-old broilers were assigned to contro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9658033/ https://www.ncbi.nlm.nih.gov/pubmed/36364100 http://dx.doi.org/10.3390/molecules27217277 |
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author | Adetunji, Adedeji Casey, Theresa Franco, Jackeline Shah, Devendra Fasina, Yewande |
author_facet | Adetunji, Adedeji Casey, Theresa Franco, Jackeline Shah, Devendra Fasina, Yewande |
author_sort | Adetunji, Adedeji |
collection | PubMed |
description | Salmonella enteritidis is a foodborne pathogen that causes high morbidity in poultry. Proteomic analysis by liquid chromatography tandem mass spectrometry (LC-MS/MS) was used to study the effects of Salmonella infection on spleen proteome in broiler chickens. Day-old broilers were assigned to control (CON; n = 60) or Salmonella challenge (CON−SE; n = 60), and gavaged with Tryptic soy agar broth or SE. A subset of chicks was euthanized on D3 and D7 (n = 4/group/day) and the spleen was removed, and rapidly frozen, subsequently proteome was measured using label-free LC-MS/MS. Protein spectra were mapped to Gallus gallus Uniprot database. Differentially abundant proteins (DAP; FDR < 0.05) between days and treatments were identified using ANOVA. Cecal content of Salmonella in CON−SE was 3.37 log(10) CFU/g and CON were negative. Across the 16 samples, 2625 proteins were identified. Proteins that decreased in abundance between days mediated cell cycle progression, while those that increased in abundance function in cytoskeleton and mRNA processing. SE infection caused an increase in proteins that mediated redox homeostasis, lysosomal activities, and energy production, while proteins decreased in abundance-mediated developmental progression. Proteomic signatures of spleen suggest SE infection was metabolically costly, and energy was diverted from normal developmental processes to potentiate disease resistance mechanisms. |
format | Online Article Text |
id | pubmed-9658033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96580332022-11-15 Proteomic Analysis of the Effect of Salmonella Challenge on Broiler Chicken Adetunji, Adedeji Casey, Theresa Franco, Jackeline Shah, Devendra Fasina, Yewande Molecules Article Salmonella enteritidis is a foodborne pathogen that causes high morbidity in poultry. Proteomic analysis by liquid chromatography tandem mass spectrometry (LC-MS/MS) was used to study the effects of Salmonella infection on spleen proteome in broiler chickens. Day-old broilers were assigned to control (CON; n = 60) or Salmonella challenge (CON−SE; n = 60), and gavaged with Tryptic soy agar broth or SE. A subset of chicks was euthanized on D3 and D7 (n = 4/group/day) and the spleen was removed, and rapidly frozen, subsequently proteome was measured using label-free LC-MS/MS. Protein spectra were mapped to Gallus gallus Uniprot database. Differentially abundant proteins (DAP; FDR < 0.05) between days and treatments were identified using ANOVA. Cecal content of Salmonella in CON−SE was 3.37 log(10) CFU/g and CON were negative. Across the 16 samples, 2625 proteins were identified. Proteins that decreased in abundance between days mediated cell cycle progression, while those that increased in abundance function in cytoskeleton and mRNA processing. SE infection caused an increase in proteins that mediated redox homeostasis, lysosomal activities, and energy production, while proteins decreased in abundance-mediated developmental progression. Proteomic signatures of spleen suggest SE infection was metabolically costly, and energy was diverted from normal developmental processes to potentiate disease resistance mechanisms. MDPI 2022-10-26 /pmc/articles/PMC9658033/ /pubmed/36364100 http://dx.doi.org/10.3390/molecules27217277 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Adetunji, Adedeji Casey, Theresa Franco, Jackeline Shah, Devendra Fasina, Yewande Proteomic Analysis of the Effect of Salmonella Challenge on Broiler Chicken |
title | Proteomic Analysis of the Effect of Salmonella Challenge on Broiler Chicken |
title_full | Proteomic Analysis of the Effect of Salmonella Challenge on Broiler Chicken |
title_fullStr | Proteomic Analysis of the Effect of Salmonella Challenge on Broiler Chicken |
title_full_unstemmed | Proteomic Analysis of the Effect of Salmonella Challenge on Broiler Chicken |
title_short | Proteomic Analysis of the Effect of Salmonella Challenge on Broiler Chicken |
title_sort | proteomic analysis of the effect of salmonella challenge on broiler chicken |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9658033/ https://www.ncbi.nlm.nih.gov/pubmed/36364100 http://dx.doi.org/10.3390/molecules27217277 |
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