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Investigating dysregulated pathways in Staphylococcus aureus (SA) exposed macrophages based on pathway interaction network

Authors :
Wang Shuang
Li Yuehua
Wei Zhou
Zhang Zhisheng
Zhang Jingjing
Zhang Cuixia
Zhang Yan
Source :
Computational Biology and Chemistry. 66:21-25
Publication Year :
2017
Publisher :
Elsevier BV, 2017.

Abstract

Display Omitted The PIN was comprised of 8388 interactions and 1189 nodes.Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins was the seed pathway.A total of 15 dysregulated pathways were obtained for SA infected samples. ObjectiveThis work aimed to identify dysregulated pathways for Staphylococcus aureus (SA) exposed macrophages based on pathway interaction network (PIN). MethodsThe inference of dysregulated pathways was comprised of four steps: preparing gene expression data, protein-protein interaction (PPI) data and pathway data; constructing a PIN dependent on the data and Pearson correlation coefficient (PCC); selecting seed pathway from PIN by computing activity score for each pathway according to principal component analysis (PCA) method; and investigating dysregulated pathways in a minimum set of pathways (MSP) utilizing seed pathway and the area under the receiver operating characteristics curve (AUC) index implemented in support vector machines (SVM) model. ResultsA total of 20,545 genes, 449,833 interactions and 1189 pathways were obtained in the gene expression data, PPI data and pathway data, respectively. The PIN was consisted of 8388 interactions and 1189 nodes, and Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins was identified as the seed pathway. Finally, 15 dysregulated pathways in MSP (AUC=0.999) were obtained for SA infected samples, such as Respiratory electron transport and DNA Replication. ConclusionsWe have identified 15 dysregulated pathways for SA infected macrophages based on PIN. The findings might provide potential biomarkers for early detection and therapy of SA infection, and give insights to reveal the molecular mechanism underlying SA infections. However, how these dysregulated pathways worked together still needs to be studied.

Details

ISSN :
14769271
Volume :
66
Database :
OpenAIRE
Journal :
Computational Biology and Chemistry
Accession number :
edsair.doi.dedup.....1f215aca29bfa83b72dcdb16d2f996ab