Abstract
Bacterial keratitis causes significant blindness, yet antimicrobial resistance has rendered current treatments ineffective. Polymyxin B-trimethoprim (PT) plus rifampin has potent in vitro activity against Staphylococcus aureus and Pseudomonas aeruginosa, two important causes of keratitis. Here we further characterize this combination against P. aeruginosa in a murine keratitis model. PT plus rifampin performed comparably to or better than moxifloxacin, the gold standard, suggesting that the combination may be a promising therapy for bacterial keratitis.
Keywords:
antimicrobial combinations; drug discovery; eye; keratitis.
Copyright © 2019 American Society for Microbiology.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Anti-Bacterial Agents / pharmacology*
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Cornea / drug effects
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Cornea / microbiology
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Drug Resistance, Multiple, Bacterial / drug effects
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Drug Therapy, Combination / methods
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Eye Infections, Bacterial / drug therapy*
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Eye Infections, Bacterial / microbiology
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Female
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Keratitis / drug therapy
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Keratitis / microbiology
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Mice
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Mice, Inbred C57BL
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Microbial Sensitivity Tests / methods
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Polymyxin B / pharmacology
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Pseudomonas Infections / drug therapy*
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Pseudomonas aeruginosa / drug effects*
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Rifampin / pharmacology
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Staphylococcal Infections / drug therapy
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Staphylococcal Infections / microbiology
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Staphylococcus aureus / drug effects
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Trimethoprim / pharmacology
Substances
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Anti-Bacterial Agents
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Trimethoprim
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Polymyxin B
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Rifampin