1. Academic Validation
  2. Avibactam Sensitizes Carbapenem-Resistant NDM-1-Producing Klebsiella pneumoniae to Innate Immune Clearance

Avibactam Sensitizes Carbapenem-Resistant NDM-1-Producing Klebsiella pneumoniae to Innate Immune Clearance

  • J Infect Dis. 2019 Jul 2;220(3):484-493. doi: 10.1093/infdis/jiz128.
Erlinda R Ulloa 1 2 Nicholas Dillon 1 Hannah Tsunemoto 3 Joe Pogliano 3 George Sakoulas 1 4 Victor Nizet 1 5
Affiliations

Affiliations

  • 1 Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, La Jolla.
  • 2 Division of Infectious Disease, Department of Pediatrics, Children's Hospital of Philadelphia, Pennsylvania.
  • 3 Division of Biological Sciences, University of California-San Diego, La Jolla.
  • 4 Sharp Healthcare System, San Diego, California.
  • 5 Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California-San Diego, La Jolla.
Abstract

Infections caused by New Delhi Metallo-β-lactamase (NDM)-producing strains of multidrug-resistant Klebsiella pneumoniae are a global public health threat lacking reliable therapies. NDM is impervious to all existing β-lactamase inhibitor (BLI) drugs, including the non-β-lactam BLI avibactam (AVI). Though lacking direct activity against NDMs, AVI can interact with penicillin-binding protein 2 in a manner that may influence cell wall dynamics. We found that exposure of NDM-1-producing K. pneumoniae to AVI led to striking bactericidal interactions with human cathelicidin antimicrobial peptide LL-37, a frontline component of host innate immunity. Moreover, AVI markedly sensitized NDM-1-producing K. pneumoniae to killing by freshly isolated human neutrophils, platelets, and serum when complement was active. Finally, AVI monotherapy reduced lung counts of NDM-1-producing K. pneumoniae in a murine pulmonary challenge model. AVI sensitizes NDM-1-producing K. pneumoniae to innate immune clearance in ways that are not appreciated by standard Antibiotic testing and that merit further study.

Keywords

Klebsiella pneumoniae; New Delhi metallo-β-lactamase (NDM); avibactam; human serum; innate immunity; neutrophil; non–β-lactam β-lactamase inhibitors; platelet.

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