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. 2020 Oct 6;12(1):1801964. doi: 10.1080/19490976.2020.1801964

Figure 4.

Figure 4.

Expression of functional gene profile for carbohydrates metabolism in AE group. Arrows indicate significant differential expression of functional gene in AE compared to control group (p < .05). (a-Red Box) Perturbation of carbohydrate metabolism attributed by the depletion of butyrate- and propionate-producing bacteria. Several key carbohydrate metabolism genes were significantly reduced in AE (adj p < .05) from the glycolysis pathway (K15633 2,3-bisphosphoglycerate-independent phosphoglycerate mutase, K01571 oxaloacetate decarboxylase and K01960 pyruvate carboxylase subunit B); butyrate biosynthesis pathway (K00634 phosphate butyryltransferase, K00929 butyrate kinase); acetate biosynthesis pathway (K04020 phosphotransacetylase, K00625 phosphate acetyltransferase) and propionate biosynthesis pathway (K01734 methylglyoxal synthase, K00005 glycerol dehydrogenase, K01699 propanediol dehydratase, K13922 propionaldehyde dehydrogenase, K11381 2-oxoisovalerate dehydrogenase, K00625 phosphate acetyltransferase). (b-Green Box) Pathway attributed by the enrichment of potentially pathogenic bacteria. In contrast, several key genes were found to be enriched in AE compared to controls (adj p < .05) in the trehalose metabolism pathway (K05343 maltose alpha-D-glucosyltransferase/alpha-amylase, K05342 alpha,alpha-trehalose phosphorylase and K01194 alpha,alpha-trehalase); lipopolysaccharide (LPS) biosynthesis (K02847 O-antigen ligase, K00979 3-deoxy-manno-octulosonate cytidylyltransferase, K12975 KDO II ethanol-amine-phosphotransferase and K00912 tetra-acyl-disaccharide 4ʹ-kinase) and virulence components biosynthesis pathways (K13735 adhesin/invasin, K02406 flagellin). List of metatranscriptomics functional annotation that are significantly different between AE and controls is shown in Supplementary Table 5.