Impact of the structure-activity relationship of AHL analogues on quorum sensing in Gram-negative bacteria

Bioorg Med Chem. 2020 Feb 1;28(3):115282. doi: 10.1016/j.bmc.2019.115282. Epub 2019 Dec 28.

Abstract

With the emergence of microbial resistance pathogens, recent research aims at studying new mechanisms of action of antibiotics. This review discusses the mechanisms and types of quorum sensing (QS) inhibitors in Gram negative bacteria. It illustrates all published data available in literature pertaining to novel compounds that showed activity against different targets in the quorum sensing pathways in Gram negative bacteria. A systemic overview has been conducted by searching PubMed, Medline, and the Cochrane Library and data extraction of all quorum sensing inhibitors with their mechanisms of action have been collected. This review will focus on signaling autoinducer AI-1 in Gram negative bacteria. The biological activity of the antagonists is mainly reported as IC50 (the concentration of an inhibitor where the response is reduced by half).

Keywords: Acyl homoserine lactone (AHL); Gram negative bacteria; Quorum sensing; Structure activity relationship.

Publication types

  • Review

MeSH terms

  • Acyl-Butyrolactones / chemistry
  • Acyl-Butyrolactones / pharmacology*
  • Animals
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Gram-Negative Bacteria / drug effects*
  • Humans
  • Microbial Sensitivity Tests
  • Molecular Conformation
  • Quorum Sensing / drug effects
  • Structure-Activity Relationship

Substances

  • Acyl-Butyrolactones
  • Anti-Bacterial Agents