An Update on Staphylococcus aureus NorA Efflux Pump Inhibitors

Curr Top Med Chem. 2020;20(24):2168-2185. doi: 10.2174/1568026620666200704135837.

Abstract

Background: Methicillin-resistant and vancomycin-resistant Staphylococcus aureus are pathogens causing severe infectious diseases that pose real public health threats problems worldwide. In S. aureus, the most efficient multidrug-resistant system is the NorA efflux pump. For this reason, it is critical to identify efflux pump inhibitors.

Objective: In this paper, we present an update of the new natural and synthetic compounds that act as modulators of antibiotic resistance through the inhibition of the S. aureus NorA efflux pump.

Results: Several classes of compounds capable of restoring the antibiotic activity have been identified against resistant-S. aureus strains, acting as NorA efflux pump inhibitors. The most promising classes of compounds were quinolines, indoles, pyridines, phenols, and sulfur-containing heterocycles. However, the substantial degree structural diversity of these compounds makes it difficult to establish good structure- activity correlations that allow the design of compounds with more promising activities and properties.

Conclusion: Despite substantial efforts put forth in the search for new antibiotic adjuvants that act as efflux pump inhibitors, and despite several promising results, there are currently no efflux pump inhibitors authorized for human or veterinary use, or in clinical trials. Unfortunately, it appears that infection control strategies have remained the same since the discovery of penicillin, and that most efforts remain focused on discovering new classes of antibiotics, rather than trying to prolong the life of available antibiotics, and simultaneously fighting mechanisms of bacterial resistance.

Keywords: Antibacterial agents; Drug design; Efflux pump inhibitors; Methicilin-resistant Staphylococcus aureus; Multidrug resistance; NorA efflux pump.

Publication types

  • Review

MeSH terms

  • Anti-Bacterial Agents / chemistry*
  • Anti-Bacterial Agents / pharmacology
  • Bacterial Proteins / antagonists & inhibitors*
  • Drug Discovery
  • Drug Resistance, Bacterial
  • Humans
  • Indoles / chemistry
  • Methicillin-Resistant Staphylococcus aureus / drug effects
  • Microbial Sensitivity Tests
  • Multidrug Resistance-Associated Proteins / antagonists & inhibitors*
  • Phenols / chemistry
  • Protein Conformation
  • Pyridines / chemistry
  • Quinolines / chemistry
  • Staphylococcal Infections / drug therapy*
  • Structure-Activity Relationship
  • Vancomycin-Resistant Staphylococcus aureus / drug effects

Substances

  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Indoles
  • Multidrug Resistance-Associated Proteins
  • Phenols
  • Pyridines
  • Quinolines
  • NorA protein, Staphylococcus