RRC ID 46766
Author Takahata S, Kubota N, Takei-Masuda N, Yamada T, Maeda M, Alshahni MM, Abe S, Tabata Y, Maebashi K.
Title Mechanism of Action of ME1111, a Novel Antifungal Agent for Topical Treatment of Onychomycosis.
Journal Antimicrob. Agents Chemother.
Abstract Despite the existing treatment options for onychomycosis, there remains a strong demand for potent topical medications. ME1111 is a novel antifungal agent that is active against dermatophytes, has an excellent ability to penetrate human nails, and is being developed as a topical agent for onychomycosis. In the present study, we investigated its mechanism of action. Trichophyton mentagrophytes mutants with reduced susceptibility to ME1111 were selected in our laboratory, and genome sequences were determined for 3 resistant mutants. The inhibitory effect on a candidate target was evaluated by a spectrophotometric enzyme assay using mitochondrial fractions. Point mutations were introduced into candidate genes by a reverse genetics approach. Whole-genome analysis of the 3 selected mutants revealed point mutations in the structural regions of genes encoding subunits of succinate dehydrogenase (complex II). All of the laboratory-generated resistant mutants tested harbored a mutation in one of the subunits of succinate dehydrogenase (SdhB, SdhC, or SdhD). Most of the mutants showed cross-resistance to carboxin and boscalid, which are succinate dehydrogenase inhibitors. ME1111 strongly inhibited the succinate-2,6-dichlorophenolindophenol reductase reaction in Trichophyton rubrum and T. mentagrophytes (50% inhibitory concentrations [IC50s] of 0.029 and 0.025 μg/ml, respectively) but demonstrated only moderate inhibition of the same reaction in human cell lines. Furthermore, the target protein of ME1111 was confirmed by the introduction of point mutations causing the amino acid substitutions in SdhB, SdhC, and SdhD found in the laboratory-generated resistant mutants, which resulted in reduced susceptibility to ME1111. Thus, ME1111 is a novel inhibitor of the succinate dehydrogenase of Trichophyton species, and its mechanism of action indicates its selective profile.
Volume 60(2)
Pages 873-80
Published 2016-2
DOI 10.1128/AAC.01790-15
PII AAC.01790-15
PMID 26596944
PMC PMC4750688
MeSH Administration, Topical Amino Acid Substitution / genetics Antifungal Agents / pharmacology* Arthrodermataceae / drug effects Base Sequence Cell Line DNA, Fungal / genetics Drug Resistance, Fungal / genetics* Humans Molecular Sequence Data Onychomycosis / drug therapy* Onychomycosis / microbiology Phenols / pharmacology* Pyrazoles / pharmacology* Sequence Analysis, DNA Succinate Dehydrogenase / genetics* Trichophyton / drug effects* Trichophyton / genetics*
IF 4.256
Times Cited 5
WOS Category PHARMACOLOGY & PHARMACY MICROBIOLOGY
Resource
Pathogenic microorganisms ?