Synergistic, collaterally sensitive β-lactam combinations suppress resistance in MRSA.
Patrick R GonzalesMitchell W PeseskyRenee A BouleyAnna BallardBrent A BiddyMark A SuckowWilliam R WolterValerie A SchroederCarey-Ann D BurnhamShahriar MobasheryMayland ChangGautam DantasPublished in: Nature chemical biology (2015)
Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most prevalent multidrug-resistant pathogens worldwide, exhibiting increasing resistance to the latest antibiotic therapies. Here we show that the triple β-lactam combination meropenem-piperacillin-tazobactam (ME/PI/TZ) acts synergistically and is bactericidal against MRSA subspecies N315 and 72 other clinical MRSA isolates in vitro and clears MRSA N315 infection in a mouse model. ME/PI/TZ suppresses evolution of resistance in MRSA via reciprocal collateral sensitivity of its constituents. We demonstrate that these activities also extend to other carbapenem-penicillin-β-lactamase inhibitor combinations. ME/PI/TZ circumvents the tight regulation of the mec and bla operons in MRSA, the basis for inducible resistance to β-lactam antibiotics. Furthermore, ME/PI/TZ subverts the function of penicillin-binding protein-2a (PBP2a) via allostery, which we propose as the mechanism for both synergy and collateral sensitivity. Showing in vivo activity similar to that of linezolid, ME/PI/TZ demonstrates that combinations of older β-lactam antibiotics could be effective against MRSA infections in humans.
Keyphrases
- methicillin resistant staphylococcus aureus
- gram negative
- multidrug resistant
- staphylococcus aureus
- klebsiella pneumoniae
- mouse model
- acinetobacter baumannii
- binding protein
- drug resistant
- escherichia coli
- signaling pathway
- physical activity
- blood brain barrier
- cystic fibrosis
- drug delivery
- antimicrobial resistance