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. 2022 Apr 5;14(1):2052699. doi: 10.1080/19490976.2022.2052699

Table 2.

Summary of various roles of O-glycans and related structures in perpetuating microbe-dependent diseases along the GI tract

Maladaptive (O-)glycan Function General Mechanism Glycan Type Mucina Relevant Disease Model Affected Microbe(s) Reference
invasion Modulation of microbiota Blood group antigens Muc2 Intestinal infection Mouse S. Typhimurium 91
promoting growth Commensal + antibiotic-dependent Sia liberation Sialylated O-glycans Muc2b Intestinal infection Mouse C. difficile
S.Typhimurium
170
Sia metabolism by proinflammatory E. coli 2,3 linked Sialylated Milk O-ligosaccharides N/A Acute colitis Mouse E. coli 168
Pathogenic E. coli growth O-acetylated Sialic Acid N/A Intestinal infection In vitro E. coli 109
increase pathogen
adherence
Unknown Core 2-derived O-glycans MUC2 Intestinal infection In vitro/
Cell line
EPEC and EHEC:O157H7 171,172
Blood group antigen–binding adhesin (BabA) βα1,2 Fuc MUC5ACb Gastric
infection
Mouse H. pylori 84
Sialic acid binding adhesin (SabA) Sialylated O-glycans MUC5ACb 163
Promoting virulence Complex O-glycan MUC2 Intestinal infection In vitro C.jejuni 131

aNomenclature indicates original source of the mucin-type O-glycan (e.g., MUC2, human; Muc2, mouse)

bPresumed based on intestinal location where mucus was studied, but not verified in reference