Pharmacology · Antimicrobials (Cell Wall Inhibitors, Protein Synthesis Inhibitors, Fluoroquinolones)

Ceftaroline is a fifth-generation cephalosporin with activity against MRSA. Its mechanism compared to earlier cephalosporins is BEST explained by:

  • A Beta-lactamase inhibition combined with beta-lactam antibacterial activity
  • B High binding affinity for the modified PBP2a (PBP2') expressed by MRSA
  • C Disruption of bacterial cell membrane integrity via lipophilic interactions
  • D Inhibition of D-Ala-D-Ala ligase preventing peptidoglycan precursor synthesis
Correct answer: B. High binding affinity for the modified PBP2a (PBP2') expressed by MRSA

Explanation

MRSA resistance to beta-lactams is due to expression of PBP2a (encoded by mecA), which has very low affinity for conventional beta-lactams. Ceftaroline has a unique side chain that allows it to bind PBP2a with high affinity, inhibiting its transpeptidase activity. It is not a beta-lactamase inhibitor, does not act on cell membranes, and does not target D-Ala-D-Ala ligase (which is vancomycin's mechanism).

Reference: KD Tripathi, Essentials of Medical Pharmacology, 8th ed.

High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP

Written and medically reviewed by the StethoPrep medical team.

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