While no LytM-specific antibodies are documented, studies highlight antibodies targeting other staphylococcal proteins:
Targets eLtaS (elongation factor thermo unstable-associated surface antigen)
Demonstrated efficacy in murine infection models (80% survival rate vs. 20% in controls)
LytM accessibility: As an autolysin, LytM is primarily intracellular, reducing antibody exposure
Functional redundancy: S. aureus employs multiple peptidoglycan hydrolases (e.g., Atl, Sle1), diminishing therapeutic utility of targeting LytM alone
Antigenic drift: Staphylococcal surface proteins frequently evolve epitope variations, complicating antibody development
Hypothetical approaches for developing LytM antibodies could involve:
Epitope mapping of surface-exposed regions using AlphaFold-predicted structures
Conjugate vaccines combining LytM peptides with carrier proteins
Phage display libraries to identify cross-reactive antibodies against conserved zinc-binding domains
KEGG: sao:SAOUHSC_00248
STRING: 93061.SAOUHSC_00248