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Lipopolysaccharide from *Shigella flexneri* is a complex glycolipid located in the outer membrane of this Gram-negative bacterium. LPS consists of three main domains: lipid A (the toxic component), a core oligosaccharide, and a highly variable O-antigen polysaccharide responsible for serotype specificity. The O-antigen undergoes various modifications—such as glucosylation, O-acetylation, and phosphoethanolamine addition—which create different serotypes and enable immune evasion. LPS protects *S. flexneri* from acid stress, bile salts, and antibiotics, and plays a key role in pathogenesis and the host immune response. Although LPS is central to infection and immunity, it is not a classical therapeutic target (e.g. receptor or enzyme); instead, it represents a molecular signature used for bacterial serotyping and epidemiological tracking, and is considered in vaccine development as an immunodominant antigen.
Disruption of bacterial outer membrane integrity (e.g., polymyxin mechanism) Neutralization of endotoxin effect (e.g., LPS-binding peptides for sepsis; not serotype-specific)
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