Potential strategies for the eradication of multidrug-resistant Gram-negative bacterial infections

Future Microbiol. 2016 Jul:11:955-72. doi: 10.2217/fmb-2016-0035. Epub 2016 Jun 30.

Abstract

Antimicrobial resistance is one of the leading threats to society. The increasing burden of multidrug-resistant Gram-negative infection is particularly concerning as such bacteria are demonstrating resistance to nearly all currently licensed therapies. Various strategies have been hypothesized to treat multidrug-resistant Gram-negative infections including: targeting the Gram-negative outer membrane; neutralization of lipopolysaccharide; inhibition of bacterial efflux pumps and prevention of protein folding. Silver and silver nanoparticles, fusogenic liposomes and nanotubes are potential strategies for extending the activity of licensed, Gram-positive selective, antibiotics to Gram-negatives. This may serve as a strategy to fill the current void in pharmaceutical development in the short term. This review outlines the most promising strategies that could be implemented to solve the threat of multidrug-resistant Gram-negative infections.

Keywords: Gram-negative; antibiotic resistance; antimicrobial peptides; efflux pumps; lipopolysaccharide; nanomaterial; nosocomial; outer membrane; polymyxin; porins.

Publication types

  • Review

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Antimicrobial Cationic Peptides / therapeutic use
  • Cell Wall / chemistry
  • Cell Wall / drug effects
  • Disease Eradication / methods*
  • Drug Resistance, Multiple, Bacterial*
  • Gram-Negative Bacteria / chemistry
  • Gram-Negative Bacteria / drug effects*
  • Gram-Negative Bacteria / pathogenicity
  • Gram-Negative Bacterial Infections / microbiology*
  • Gram-Negative Bacterial Infections / prevention & control
  • Humans
  • Membrane Transport Proteins
  • Metal Nanoparticles / therapeutic use
  • Polymyxins / therapeutic use

Substances

  • Anti-Bacterial Agents
  • Antimicrobial Cationic Peptides
  • Membrane Transport Proteins
  • Polymyxins