Rescued chlorhexidine activity by resveratrol against carbapenem-resistant Acinetobacter baumannii via down-regulation of AdeB efflux pump

PLoS One. 2020 Dec 2;15(12):e0243082. doi: 10.1371/journal.pone.0243082. eCollection 2020.

Abstract

The aim of this study was to determine the activity and synergistic mechanisms of resveratrol in combination with chlorhexidine against carbapenem-resistant Acinetobacter baumannii clinical isolates. The activity of resveratrol plus antimicrobial agents was determined by checkerboard and time-kill assay against carbapenem-resistant A. baumannii isolated from patients at the King Chulalongkorn Memorial Hospital, Bangkok, Thailand. Overexpression of efflux pumps that mediates chlorhexidine susceptibility was characterized by the ethidium bromide accumulation assay. The effect of resveratrol on the expression of efflux pump genes (adeB, adeJ, adeG abeS, and aceI) and the two-component regulators, adeR and adeS was determined by RT-qPCR. The combination of resveratrol and chlorhexidine resulted in strong synergistic and bactericidal activity against carbapenem-resistant A. baumannii. Up-regulation of adeB and aceI was induced by chlorhexidine. However, the addition of resveratrol increased chlorhexidine susceptibility with increased intracellular accumulation of ethidium bromide in A. baumannii indicating that resveratrol acts as an efflux pump inhibitor. Expression of adeB was significantly reduced in the combination of resveratrol with chlorhexidine indicating that resveratrol inhibits the AdeB efflux pump and restores chlorhexidine effect on A. baumannii. In conclusion, reduced adeB expression in A. baumannii was mediated by resveratrol suggesting that AdeB efflux pump inhibition contributes to the synergistic mechanism of resveratrol with chlorhexidine. Our finding highlights the potential importance of resveratrol in clinical applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acinetobacter baumannii / drug effects*
  • Acinetobacter baumannii / genetics
  • Bacterial Proteins / genetics*
  • Carbapenems / pharmacology*
  • Chlorhexidine / pharmacology*
  • Down-Regulation / drug effects*
  • Drug Resistance, Bacterial / drug effects*
  • Drug Synergism
  • Gene Expression Regulation, Bacterial / drug effects
  • Membrane Transport Proteins / genetics*
  • Resveratrol / pharmacology*

Substances

  • AdeB protein, Acinetobacter baumannii
  • Bacterial Proteins
  • Carbapenems
  • Membrane Transport Proteins
  • Resveratrol
  • Chlorhexidine

Grants and funding

This work was funded by Ratchadapisek Somphot Fund for Postdoctoral Fellowship, Chulalongkorn University, the 90th Anniversary of Chulalongkorn University Fund (Ratchadaphiseksompot Endowment Fund) from Graduate School, Chulalongkorn University, and the Ratchadapiseksompotch Fund, Faculty of Medicine, Chulalongkorn University to Uthaibhorn Singkham-in. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.