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. 2014 May;58(5):2825–2829. doi: 10.1128/AAC.02382-13

TABLE 3.

Fold increase in the MICs of terbinafine, itraconazole, amorolfine, and ciclopirox for drug-resistant T. rubrum mutants compared to their parental strainsa

Mutant and drug susceptibility Fold MIC increase
Terbinafine Itraconazole Amorolfine Ciclopirox
ATCC 28188
    TRB-S (n = 1) 50 ns ns ns
    ITC-S (n = 5) 4–8 4–8 4–8 ns
    AMF-S (n = 3) 4–8 ns 16–32 ns
    TRB-I (n = 3) 500–1,000 ns ns ns
    ITC-I (n = 5) 8 4–8 32 ns
    AMF-I (n = 3) 8–16 ns 64 ns
CI-1
    ITC-S (n = 5) 4–8 4–8 4–8 ns
    AMF-S (n = 1) 4 ns 16 ns
    TRB-I (n = 5) 500 ns ns ns
    ITC-I (n = 5) 8 4–8 32 ns
    AMF-I (n = 5) 8–16 ns 32–64 ns
CI-2
    TRB-S (n = 2) 500–1,000 ns ns ns
    ITC-S (n = 5) 4–8 4–8 4–8 ns
    AMF-S (n = 4) 4–8 ns 8–16 ns
a

Mutants were obtained following direct selection on plates containing inhibitory drug concentrations on the basis of selection (TBR, terbinafine; ITC, itraconazole; AMF, amorolfine) and the parental strain from which they derived. n, number of strains; ns, not significant (MIC differences of ±1 2-fold dilution were considered not significant).