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 language | English (US) |
---|---|
Pages (from-to) | 416-424 |
Number of pages | 9 |
Journal | Journal of Antibiotics |
Volume | 76 |
Issue number | 7 |
DOIs | |
State | Published - 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