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. 2010 Jul 16;192(18):4680–4693. doi: 10.1128/JB.00543-10

TABLE 5.

Determination of the MICs and survival rates

Type of compound Compounds MIC,a,b survival ratec for:
Wild type ΔliaF mutant ΔliaIH mutant
Cell wall antibiotics Bacitracin 300 300 300
Cefotaxime 0.1, 100 0.1, 100 0.05, 10−2
Cephalexin 0.25, 100 0.25, 102 0.125, 101
Daptomycin 1.25, 100 1.25, 100 0.6, 10−1 to 10−2
Enduracidin 25, 100 12.5, 100 12.5, 10−3
Nisin 10 2.5 10
Fosfomycin 100, 100 200, 100 50, 10−3
Vancomycin 0.5 0.5 0.5
Oxidative stress reagents Cumene hydroperoxide 0.006, 100 0.006, 100 0.006, 10−2
Hydrogen peroxide 1.5 0.5 1.0
Menadione 5, 100 1.25, 100 2.5, 10−1
Plumbagin 5, 100 2.5, 100 1.25, 10−1
Sodium selenite 500, 100 500, 100 125, 10−2
t-Butyl hydroperoxide 1, 100 1, 100 0.5, 10−1
Others Cetylpyridinium chloride 0.5 0.5 0.5
Domiphen bromide 0.125 0.03 0.125
Phenylarsine oxide 0.1 0.1 0.05
a

MICs are in μg/ml with the exception of cumene hydroperoxide (%), t-butylhydroperoxide (mM) and hydrogen peroxide (%).

b

Values indicating explicit sensitivity or resistance of the ΔliaF and ΔliaIH mutant strains versus that of the wild-type are highlighted in bold.

c

Survival rates were determined by serial dilution spot tests on Mueller-Hinton agar plates at the following “critical” compound concentrations: fosfomycin, 250 μg ml−1; cefotaxime, 0.1 μg ml−1; enduracidin, 0.01 μg ml−1; daptomycin, 0.15 μg ml−1; cephalexin, 0.2 μg ml−1; plumbagin, 2.5 μg ml−1; menadione, 1.25 μg ml−1; t-butyl hydroperoxide, 0.3 mM; cumene hydroperoxide, 0.003%; sodium selenite, 125 μg ml−1. All values are given relative to the result for the wild type as a reference, which was therefore set to 100. See Fig. S3 in the supplemental material for the original data and experimental details.