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. 2018 Jan 19;8:1278. doi: 10.1038/s41598-018-19754-8

Table 3.

Top significant pathways (p < 0.05) predicted by IPA for NDV vs. Control by line and day post infection (2 dpi or 6 dpi).

Group Pathways DEGs in the Pathway P-value Ratios
Leghorn 2 dpi Retinoic acid mediated apoptosis signaling* APAF1, PARP9, PARP12, PARP13 2.8E-05 4/61
Death receptor signaling* APAF1, PARP9, PARP12, PARP13 1.4E-04 4/92
Role of PKR in interferon induction and antiviral response APAF1, EIF2AK2, STAT1 2.1E-04 3/40
Interferon signaling STAT1, TAP1 4.8E-03 2/36
Complement system C1S, SERPING1 5.1E-03 2/37
Fayoumi 2 dpi Role of lipids/lipid rafts in the pathogenesis of influenza RSAD2 0.014 1/22
Complement system C1S 0.024 1/37
Role of PKR in interferon induction and antiviral response EIF2AK2 0.026 1/40
Role of RIG1-like receptors in antiviral innate immunity TRIM25 0.028 1/43
Retinoic acid mediated apoptosis signaling PARP9 0.040 1/61
Leghorn 6 dpi Granzyme A signaling GZMA 0.011 1/20
Role of lipids/lipid rafts in the pathogenesis of influenza RSAD2 0.012 1/22

Note: Pathways labeled with * were predicted to be significantly upregulated (z-score >2). All differentially expressed genes (DEGs) were significantly upregulated (False discovery rate <0.05). No pathway was predicted for Fayoumi at 6 dpi. Ratios = (Number of DEGs in a pathways)/(Total number of genes in the pathway).