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Surface antigens on Extended-Spectrum Beta-Lactamase (ESBL)-producing Escherichia coli are structural components located on the bacterial outer membrane that serve as primary targets for the host immune system and novel therapeutic agents. These antigens include the O-antigen portion of lipopolysaccharides (LPS), capsular polysaccharides (K-antigens), flagellar proteins (H-antigens), and various outer membrane proteins (OMPs) like OmpA and fimbriae (Poolman & Wacker, 2016). In ESBL-producing strains, particularly the globally disseminated ST131 lineage, these surface structures are essential for mediating adhesion to host epithelia, biofilm formation, and resistance to serum-mediated killing (Pitout & Laupland, 2008). Because ESBL enzymes render standard beta-lactam therapies ineffective, these surface antigens are being utilized in the development of bioconjugate vaccines, such as ExPEC9V and ExPEC10V, which target the most prevalent O-serotypes associated with invasive disease (Frenck et al., 2022). Therapeutic strategies focusing on these antigens aim to induce opsonophagocytic antibodies that enhance bacterial clearance by neutrophils and macrophages, providing a narrow-spectrum approach that spares the commensal microbiome (Huttner et al., 2017).
Induction of opsonophagocytic antibodies that facilitate bacterial clearance by host immune cells and inhibition of bacterial adhesion to host tissues (Frenck et al., 2022; Huttner et al., 2017).
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