Target intelligence / Profile preview

O-specific polysaccharide of Vibrio cholerae O1 (O-SP)

Target
O-SP
Molecular classification
Other (bacterial polysaccharide, lipopolysaccharide [LPS] O-antigen component), Not a protein/enzyme/receptor, but a polysaccharide epitope on bacterial surface
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Overview

The O-specific polysaccharide (O-SP) of Vibrio cholerae O1 is the distal carbohydrate polymer of the O-antigen domain of V. cholerae lipopolysaccharide (LPS), covalently linked to the core oligosaccharide and lipid A in the bacterial outer membrane. In O1 strains, O-SP consists of a homopolymer of α-(1→2)-linked 4-amino-4,6-dideoxy-D-mannopyranose (perosamine) residues, in which the amino group is acylated with 3-deoxy-L-glycero-tetronic acid. The O-SP's terminal perosamine may be methylated (Ogawa serotype) or unmethylated (Inaba serotype), producing specific B-cell epitopes. O-SP is key for defining serogroup O1 and for classification into Ogawa and Inaba serotypes. This polysaccharide is the dominant target for vibriocidal antibodies and is the principal antigen in cholera immunity acquired after infection or vaccination. O-SP, while not a classical therapeutic target like an enzyme or receptor, is a critical vaccine antigen, and manipulation of its structure (e.g., via vaccine design) is a leading strategy for cholera prevention.

Other names
O-antigen of Vibrio cholerae O1O1 O-antigen polysaccharideO-specific antigen of Vibrio cholerae O1O-SP of V. cholerae O1O1 O-SP
02

Mechanism of action

Induction of protective humoral immune response, especially vibriocidal antibodies targeting O-SP on bacterial surface, leading to bacterial clearance by the immune system

03

Biological functions

Immune recognition (major B-cell antigen)Structural component of the bacterial outer membraneSerotype determinant (basis for O1 Inaba/Ogawa classification)Host-pathogen interaction (important for virulence and immune evasion)Elicits protective antibody response after infection or vaccination
04

Disease associations

Infection (major virulence/antigenic determinant in Vibrio cholerae O1, the principal cause of pandemic cholera)Other (determines serogroup classification for epidemiology and diagnosis)
05

Safety considerations

Minimal for O-SP as an antigen; vaccines based on O-SP are generally safe (main issues are general to polysaccharide vaccines: limited immunogenicity in young children unless conjugated)Polysaccharide from bacterial LPS is not associated with major autoimmunity or toxicity; main risk is insufficient immune activation, not overactivation.
06

Interacting drugs

No small-molecule drugs interact specifically, but:

1 more in the full profile.

07

Biomarkers

Anti-O-SP (anti-LPS/O-antigen) IgA, IgM, IgG levels as correlates of immune protection and vaccine response

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