Prediction of key regulators and downstream targets of E. coli induced mastitis.
Somayeh SharifiAbbas PakdelEsmaeil EbrahimieYalda AryanMostafa Ghaderi ZefreheeJames M ReecyPublished in: Journal of applied genetics (2019)
Mastitis, an inflammatory response of mammary glands to invading bacteria, is one of the most economically costly diseases affecting dairy animals. Escherichia coli can be introduced as a major etiological agent of bovine mastitis in well-managed dairy farms. It is of great significance to understand the regulatory mechanisms by which the disease can be controlled. High-throughput technologies combined with novel computational systems biology tools have provided new opportunities for a better understanding of the molecular mechanisms that underlie disease. In the current study, the results of microarray meta-analysis research were used to perform a network analysis to potentially identify molecular mechanisms that regulate gene expression profile in response to E. coli mastitis. In our result, transcription factors, TP53, SP1, ligands, INS, IFNG, EGF, and protein kinases, MAPK1, MAPK14, AKT1, were identified as the key upstream regulators whereas protein kinases, MAPK3, MAPK8, MAPK14, ligands, VEGFA, IL10, an extracellular protein, MMP2, and a mitochondrial membrane protein, BCL2, were identified as the key downstream targets of differentially expressed genes. The results of this research revealed important genes that have the key functions in immune response, inflammation, or mastitis which can provide the basis for strategies to improve the diagnosis and treatment of mastitis in dairy cows.
Keyphrases
- signaling pathway
- oxidative stress
- escherichia coli
- transcription factor
- pi k akt
- inflammatory response
- systematic review
- genome wide identification
- network analysis
- immune response
- genome wide
- high throughput
- diabetic rats
- dairy cows
- protein protein
- binding protein
- amino acid
- small molecule
- single cell
- randomized controlled trial
- dna methylation
- meta analyses
- growth factor
- dendritic cells
- pseudomonas aeruginosa
- case control