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. Author manuscript; available in PMC: 2021 Jan 1.
Published in final edited form as: Autism Res. 2018 Aug 14;11(9):1286–1299. doi: 10.1002/aur.1972

Table 5.

Metabolic Pathways Differentially Regulated in the Oral Microbiome of ASD, TD, and DD Children

KEGG pathway χ2 FDR Mann–Whitney KO Phyla R FDR

Energy metabolism 24.8 0.00047 ASD > TD ASD > DD K04043 Spirochaetes 0.44 9.7E-16
K00415 Ascomycota 0.45 1.6E-16
K00415 Cyanobacteria 0.46 2.8E-17
Translation ribosomal structure and biogenesis 18.2 0.0062 ASD > TD ASD > DD K01979 Cyanobacteria 0.47 2.1E-18
Pyrimidine metabolism 15.8 0.013 ASD < TD ASD < DD
Lysine degradation 15.3 0.013 ASD > TD K04069 Spirochaetes 0.42 2.2E-14
Nucleotide metabolism 14.5 0.016 ASD < TD ASD < DD
Carbon metabolism 12.6 0.030 ASD > TD ASD > DD
Nucleotide transport and metabolism 12.6 0.030 ASD < TD ASD < DD K14226 Ascomycota 0.58 1.5E-30
K14221 Ascomycota 0.53 4.5E-24

Note. Nonparametric Kruskal–Wallis testing was used to interrogate 113 KEGG pathways for differences in representation among the oral microbiome in children with ASD, TD, or nonautistic DD. KEGG pathways with FDR < 0.05 are shown. A Mann–Whitney test was used as a post hoc contrast between the groups. Individual KO pathways significantly (R > 0.40) associated with individual phylogenies across samples are displayed. Abbreviations: ASD, autism spectrum disorder; DD, developmental delay; FDR, false detection rate; KEGG, Kyoto Encyclopedia of Genes and Genomes; KO, KEGG Orthology; TD, typical development.