Vancomycin
The iconic glycopeptide antibiotic — the gold-standard MRSA treatment for over 60 years, acting by binding D-Ala-D-Ala to block cell wall synthesis.
A branched tricyclic glycopeptide antibiotic that binds the D-Ala-D-Ala terminus of peptidoglycan precursors, sterically blocking transglycosylation and transpeptidation of the gram-positive bacterial cell wall.
Mechanism of action
Binds with high affinity to the D-Ala-D-Ala dipeptide terminus of lipid II (the peptidoglycan precursor), forming a non-covalent complex that sterically prevents both transglycosylation and transpeptidation. This blocks cell wall synthesis. VRE resistance arises from D-Ala-D-Lac substitution, which reduces binding affinity 1000-fold.
Primary uses
- MRSA infections (IV)
- Clostridioides difficile colitis (oral)
- Prosthetic device infections
- Surgical prophylaxis (beta-lactam allergy)
Typical dosing
IV for systemic infections. Oral vancomycin is not absorbed and acts locally in the gut for C. difficile.
Regulatory status
FDA-approved in 1958. Indicated for serious gram-positive infections including MRSA, C. difficile colitis (oral), and surgical prophylaxis in beta-lactam-allergic patients. Multiple generic formulations available.
References
- [review] Rybak MJ, et al. "Therapeutic monitoring of vancomycin for serious methicillin-resistant Staphylococcus aureus infections." Clin Infect Dis, 2020;71:1361-1364.
Related peptides
This entry is for educational purposes only and does not constitute medical advice. Dosing information reflects published regulatory or research data and is not a recommendation. Many compounds described here are not approved for human use in the United States. Consult a licensed medical professional before considering any peptide therapy.