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Salmonella Paratyphi A lipopolysaccharide (LPS (used generically; rarely abbreviated specifically for Paratyphi A))

Target
LPS (used generically; rarely abbreviated specifically for Paratyphi A)
Molecular classification
Glycan, Surface antigen, Bacterial lipopolysaccharide, Other
01

Overview

Salmonella Paratyphi A lipopolysaccharide is a tripartite glycolipid structure embedded in the bacterial outer membrane, composed of lipid A, a nonrepeating oligosaccharide core, and a polymeric O-antigen polysaccharide (O2 antigen in Paratyphi A)[1][3][5][7]. LPS serves as a physical and immunological barrier, protecting bacteria from complement-mediated killing, opsonophagocytosis, and detergent or antibiotic assault[1][3]. The O-antigen component is both serotype-specific and highly variable in length, and is critical for immune recognition and pathogenicity[1][7]. LPS is a major target for host immune responses (notably via TLR4 signaling), diagnostic serotyping, and vaccine development for paratyphoid fever (caused by Salmonella Paratyphi A)[3][4][7]. Variations in the O-antigen structure influence serum resistance, complement evasion, and the overall virulence of Salmonella[1][3][7]. LPS is not currently directly targeted by small molecules in therapy, but is relevant in developing biologics and vaccines[3][4][7].

Other names
Paratyphi A LPSSalmonella enterica Paratyphi A LPSO-antigenO-polysaccharideOPSsurface polysaccharide
02

Mechanism of action

For antibodies or vaccines: neutralization, opsonization, and promotion of immune clearance; for innate immune sensors: induction of cytokine response via pattern recognition

03

Biological functions

Barrier to antibiotics and detergentsResistance to complement-mediated killingImmune evasionStimulation of innate immunity (via TLR4-MD2-CD14 pathway)Key virulence factor in host colonization
04

Disease associations

Infection (specifically paratyphoid fever)Inflammatory response inductionImmune evasion
05

Safety considerations

Endotoxic shock risk if LPS is released systemically (due to lipid A domain triggering strong immune response)High variability of O-antigen regions may limit broad vaccine efficacyInflammatory toxicity possible with vaccine or antibody therapy targeting LPS
06

Interacting drugs

Monoclonal antibodies

1 more in the full profile.

07

Biomarkers

Presence of anti-LPS antibodies (serodiagnosis for active or recent infection, epidemiological studies)Detection of particular O-antigen (O2) for typing

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