4.7 Article

Phosphoproteomics Profile of Chicken Cecum in the Response to Salmonella enterica Serovar Enteritidis Inoculation

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ANIMALS
卷 13, 期 1, 页码 -

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MDPI
DOI: 10.3390/ani13010078

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chicken; Salmonella enterica serovar Enteritidis; cecum; phosphoproteomics

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Salmonella enterica serovar Enteritidis is a common pathogen that can cause significant public health problems and economic losses. This study investigated the genetic resistance of poultry to Salmonella infection and found that inflammatory genes were activated in chickens infected with Salmonella Enteritidis. The findings provide important insights into the molecular mechanisms and epigenetic regulation in chicken response to Salmonella infection.
Simple Summary Salmonella enterica serovar Enteritidis (S. Enteritidis) is one of the most common pathogens associated with poultry health and foodborne salmonellosis worldwide. It can cause a major public health problem and economic losses in the world. Traditional methods such as vaccines and antibiotics can make poultry and livestock resistant to drugs. Improving the genetic resistance of livestock and poultry is an effective supplement to traditional control. We found a variety of inflammatory genes were triggered at the mRNA level infected with S. Enteritidis of chickens previously. However, the phosphoproteomics profiles for chickens infected with were not clear. Phosphoproteomics was employed to dissect the molecular regulation mechanisms of F1 cross chicken cecum infected with S. Enteritidis. Functional analysis and functional classification were performed for those differentially phosphorylated proteins (DPPs). The findings in this study provide a crucial theoretical foundation to understand the molecular mechanism and epigenetic regulation in response to S. Enteritidis inoculation in chicken. Salmonella enterica serovar Enteritidis (S. Enteritidis) is a foodborne pathogen, which can cause great threats to human health through the consumption of contaminated poultry products. This research combines TMT labeling, HPLC and mass-spectrometry-based phosphoproteomics on cecum of the F1 cross of Guangxi Yao chicken and Jining Bairi chicken. The treated group was inoculated with 0.3 mL inoculum S. Enteritidis, and the control group was inoculated with 0.3 mL phosphate-buffered saline (PBS). A total of 338 differentially phosphorylated modification sites in 243 differentially phosphorylated proteins (DPPs) were chosen for downstream analyses. A total of 213 sites in 146 DPPs were up-regulated and 125 sites in 97 DPPs were down-regulated. Functional analysis was performed for DPPs based on gene ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, and the protein domain. The DPPs were mainly enriched in immune- and metabolic-related GO-BP (biological process) and KEGG pathways. We predicted and classified the subcellular structure and COG/KOG of DPPs. Furthermore, protein-protein interaction network analyses were performed by using multiple algorithms. We identified 71 motifs of the phosphorylated modification sites and selected 18 sites randomly to detect the expression level through parallel reaction monitoring (PRM). S. Enteritidis inoculation caused phosphorylation alteration in immune- and metabolic-related proteins. The invasion of S. Enteritidis may be actualized by inducing cecum cell apoptosis through the endoplasmic reticulum pathway, and chickens could resist the invasion of S. Enteritidis by affecting the function of ECM receptors. The findings herein provide a crucial theoretical foundation to understand the molecular mechanism and epigenetic regulation in response to S. Enteritidis inoculation in chickens.

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