Target intelligence / Profile preview

Salmonella enterica serovar Enteritidis O:9 O-antigen polysaccharide (SE O-antigen)

Target
SE O-antigen
Molecular classification
Polysaccharide, Bacterial surface antigen, Lipopolysaccharide component
01

Overview

The Salmonella enterica serovar Enteritidis O:9 O-antigen polysaccharide is a critical structural component of the outer membrane lipopolysaccharide (LPS) in Group D Salmonella. It consists of a repeating oligosaccharide unit typically composed of a backbone of alpha-D-mannose, alpha-L-rhamnose, and alpha-D-galactose, with a unique 3,6-dideoxyhexose sugar called tyvelose attached to the mannose residue, which defines the O:9 serospecificity (Micoli et al., 2014, Vaccine). This polysaccharide plays a vital role in bacterial virulence by protecting the pathogen from the host's innate immune system, specifically preventing complement-mediated killing and phagocytosis (Fehervari et al., 2022, Frontiers in Immunology). As a primary surface-exposed target, the O:9 antigen is the focus of vaccine development efforts aimed at preventing non-typhoidal Salmonella infections, which are a leading cause of global foodborne gastroenteritis. Because pure polysaccharides are often poorly immunogenic in infants, therapeutic strategies involve conjugating the O-antigen to carrier proteins to induce a T-cell dependent immune response and long-term memory (MacLennan et al., 2014, Human Vaccines & Immunotherapeutics). Clinical and preclinical studies utilize these glycoconjugates to elicit high titers of bactericidal antibodies, providing a protective barrier against Salmonella Enteritidis colonization and systemic spread.

Other names
Salmonella Enteritidis O-polysaccharideGroup D1 O-antigenO:9 antigenSalmonella Enteritidis lipopolysaccharide O-side chain
02

Mechanism of action

Induction of protective humoral immunity through the production of O-antigen-specific bactericidal antibodies that promote opsonophagocytosis and complement-mediated lysis of the bacteria.

03

Biological functions

Bacterial cell wall integrityImmune evasionSerotype specificityResistance to complement-mediated killingPathogenesis
04

Disease associations

SalmonellosisGastroenteritisFoodborne illnessInfection
05

Safety considerations

Endotoxicity (if lipid A is not removed or detoxified)Immunological hyporesponsiveness (if administered as pure polysaccharide without conjugation)Potential cross-reactivity with other Group D Salmonella
06

Interacting drugs

CVD 1000 (Candidate conjugate vaccine)

2 more in the full profile.

07

Biomarkers

Anti-O:9 IgG antibody titerAnti-O:9 IgM antibody titerSerum bactericidal activity (SBA)

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