Vancomycin Analogue Restores Meropenem Activity against NDM-1 Gram-Negative Pathogens

ACS Infect Dis. 2018 Jul 13;4(7):1093-1101. doi: 10.1021/acsinfecdis.8b00011. Epub 2018 May 14.

Abstract

New Delhi metallo-β-lactamase-1 (NDM-1) is the major contributor to the emergence of carbapenem resistance in Gram-negative pathogens (GNPs) and has caused many clinically available β-lactam antibiotics to become obsolete. A clinically approved inhibitor of metallo-β-lactamase (MBL) that could restore the activity of carbapenems against resistant GNPs has not yet been found, making NDM-1 a serious threat to human health. Here, we have rationally developed an inhibitor for the NDM-1 enzyme, which has the ability to penetrate the outer membrane of GNPs and inactivate the enzyme by depleting the metal ion (Zn2+) from the active site. The inhibitor reinstated the activity of meropenem against NDM-1 producing clinical isolates of GNPs like Klebsiella pneumoniae and Escherichia coli. Further, the inhibitor efficiently restored meropenem activity against NDM-1 producing K. pneumoniae in a murine sepsis infection model. These findings demonstrate that a combination of the present inhibitor and meropenem has high potential to be translated clinically to combat carbapenem-resistant GNPs.

Keywords: NDM-1 Gram-negative bacteria; antibacterial activity; antibiotic resistance; glycopeptide antibiotics; meropenem; vancomycin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology*
  • Cell Membrane Permeability
  • Drug Synergism
  • Enzyme Activation / drug effects
  • Female
  • Gene Expression Regulation, Bacterial / drug effects
  • Gram-Negative Bacteria / drug effects*
  • Gram-Negative Bacteria / genetics
  • Gram-Negative Bacteria / metabolism*
  • Klebsiella Infections / drug therapy
  • Klebsiella Infections / microbiology
  • Klebsiella pneumoniae / drug effects
  • Klebsiella pneumoniae / genetics
  • Klebsiella pneumoniae / metabolism
  • Meropenem / pharmacology*
  • Mice
  • Molecular Structure
  • Vancomycin / analogs & derivatives
  • Vancomycin / chemical synthesis
  • Vancomycin / pharmacology*
  • beta-Lactam Resistance
  • beta-Lactamases / genetics
  • beta-Lactamases / metabolism*

Substances

  • Anti-Bacterial Agents
  • Vancomycin
  • beta-Lactamases
  • beta-lactamase NDM-1
  • Meropenem