Target intelligence / Profile preview

O-antigen polysaccharide from Shigella sonnei (OAg (O-antigen))

Target
OAg (O-antigen)
Molecular classification
Other (Bacterial surface polysaccharide), Bacterial antigen, Lipopolysaccharide component (O-specific chain)
01

Overview

O-antigen polysaccharide from Shigella sonnei is a high-molecular-weight carbohydrate chain comprising repeating units unique to S. sonnei, including 2-acetamido-2-deoxy-L-altruronic acid and 2-acetamido-2-deoxy-L-fucose[1][5][9]. It forms the O-specific region of the bacterial lipopolysaccharide (LPS) and, in S. sonnei, also exists as a capsule (group 4 capsule) attached to an alternative lipid anchor[4][5]. This antigen is the primary target for protective immune responses, particularly vaccine-induced anti-OAg antibodies, and is critical for evasion of host immunity, resistance to complement-mediated killing, and modulation of bacterial virulence[1][3][4][5][9]. The biosynthetic genes for the O-antigen are carried on the S. sonnei virulence plasmid (pSS), rather than the chromosome, and are highly similar to those in Plesiomonas shigelloides, reflecting recent horizontal gene transfer[2][5]. S. sonnei O-antigen is essential for pathogenesis and is a validated vaccine target, with several human monoclonal antibodies and OMV (outer membrane vesicle/GMMA) vaccines in clinical development[3][9].

Other names
S. sonnei O-antigenShigella sonnei OAgO-antigen capsule (sometimes referred to for the high-molecular-weight form)S. sonnei O-antigen polysaccharide
02

Mechanism of action

Antibody-mediated complement-dependent bactericidal activity[3][9]; Vaccine-induced immunity (production of anti-OAg IgG that can kill bacteria or prevent invasion/extracellular survival)[3][9]

03

Biological functions

Immune evasionInduction of protective immunity in hostModulation of bacterial virulenceResistance to complement-mediated killing
04

Disease associations

Infection (key antigen and virulence factor in Shigella sonnei pathogenesis)Protective antigen (vaccine target in shigellosis)
05

Safety considerations

Potential risk for endotoxicity, as part of lipopolysaccharide (LPS)Variability in O-antigen expression may affect vaccine efficacy and required coverage[3][1]No major target-specific therapeutic safety concerns known; standard LPS-related concerns apply
06

Interacting drugs

Human monoclonal antibody C-0302B17[9]

2 more in the full profile.

07

Biomarkers

Anti-O-antigen antibody titers (biomarker for vaccine efficacy and protective immunity in both clinical trial and experimental models)[3][9]

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