Assessment of the potential for inducing resistance in multidrug-resistant organisms from exposure to minocycline, rifampin, and chlorhexidine used to treat intravascular devices

Joel Rosenblatt, Nylev Vargas-Cruz, Ruth A. Reitzel, Issam I. Raad

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

To assess the potential for the induction of antimicrobial resistance following repeated subinhibitory exposures to the combination minocycline (MIN), rifampin (RIF), and chlorhexidine (CHX), a total of 29 clinical microbial pathogenic isolates were repeatedly exposed to subinhibitory concentrations of MIN, RIF, and CHX for 20 passages. MICs of the MIN, RIF, and CHX combination were assessed at each passage to evaluate the potential for resistance to have been induced. The combination of MIN, RIF, and CHX showed significant antimicrobial efficacy and synergy against organisms resistant to all 3 individual components (MIC of 16 g/ml for MIN or MIC of 4 g/ml for RIF or CHX). Among the organisms originally resistant to 2 or more individual components and the organisms originally susceptible to 2 or more individual components, there was no evidence that organisms became resistant following 20 repeated subinhibitory exposure cycles to the triple combination. The risk of resistance developing to the triple combination is extremely low because microbes are inhibited or killed before resistance can simultaneously emerge to all three agents. Surveillance studies monitoring the development of resistance should be conducted in a clinical setting.

Original languageEnglish (US)
Article numbere00040-19
JournalAntimicrobial agents and chemotherapy
Volume63
Issue number5
DOIs
StatePublished - May 2019

Keywords

  • Chlorhexidine
  • Intravascular devices
  • Intravascular infections
  • Minocycline
  • Multidrug-resistant organisms
  • Rifampin

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)
  • Infectious Diseases

MD Anderson CCSG core facilities

  • Clinical Trials Office

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