Antibacterial effect of rose bengal against colistin-resistant gram-negative bacteria

Michio Kurosu, Katsuhiko Mitachi, Edward V. Pershing, Bruce D. Horowitz, Eric A. Wachter, John W. Lacey, Yinduo Ji, Dominic J. Rodrigues

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Increasing drug resistance in Gram-negative bacteria presents significant health problems worldwide. Despite notable advances in the development of a new generation of β-lactams, aminoglycosides, and fluoroquinolones, it remains challenging to treat multi-drug resistant Gram-negative bacterial infections. Colistin (polymyxin E) is one of the most efficacious antibiotics for the treatment of multiple drug-resistant Gram-negative bacteria and has been used clinically as a last-resort option. However, the rapid spread of the transferable gene, mcr-1 which confers colistin resistance by encoding a phosphoethanolamine transferase that modifies lipid A of the bacterial membrane, threatens the efficacy of colistin for the treatment of drug-resistant bacterial infections. Colistin-resistant strains of Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae often reduce their susceptibility to other anti-Gram-negative bacterial agents. Thus, drugs effective against colistin-resistant strains or methods to prevent the acquisition of colistin-resistance during treatment are urgently needed. To perform cell-based screenings of the collected small molecules, we have generated colistin-resistant strains of E. coli, A. baumannii, K. pneumoniae, P. aeruginosa, and S. enterica Typhimurium. In-house MIC assay screenings, we have identified that rose bengal (4,5,6,7-tetrachloro-2’,4’,5’,7’-tetraiodofluorescein) is the only molecule that displays unique bactericidal activity against these strains at low concentrations under illumination conditions. This article reports the antibacterial activity of a pharmaceutical-grade rose bengal against colistin-resistant Gram-negative bacteria.

Original languageEnglish (US)
Pages (from-to)416-424
Number of pages9
JournalJournal of Antibiotics
Volume76
Issue number7
DOIs
StatePublished - Jul 2023

Bibliographical note

Funding Information:
We MK and KM are grateful to Provectus Biopharmaceuticals for financial support. M. K. thanks UTRF (University of Tennessee Health Science Center) for generous financial support (Innovation award R079700292). The wild-type bacterial strains used here were obtained through BEI Resources, NIAID, NIH.

Funding Information:
We MK and KM are grateful to Provectus Biopharmaceuticals for financial support. M. K. thanks UTRF (University of Tennessee Health Science Center) for generous financial support (Innovation award R079700292). The wild-type bacterial strains used here were obtained through BEI Resources, NIAID, NIH.

Publisher Copyright:
© 2023, The Author(s), under exclusive licence to the Japan Antibiotics Research Association.

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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