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. 2010 Mar 8;54(5):2125–2134. doi: 10.1128/AAC.01420-09

TABLE 2.

MICs and levels of MarA-mediated MDR in the wild-type and parental strains

Strain Description or genotype MIC (μg/ml)a,b
FOX NOR CHL MIN
BW25113 Wild type 4.0 0.09 10.7 3.3
CR2000 BW25113 ΔmarRA (MarA-free parental strain) 3.2 0.07 8.1 2.4
CR1000 BW25113 ΔmarR (MarA-overproducing parental strain) 10.6 0.21 23.9 4.9
a

The results are presented as the average MICs (the standard errors of the means were 0 to 15% [n = 3 to 9]) for cefoxitin (FOX), norfloxacin (NOR), chloramphenicol (CHL), and minocycline (MIN). MarA mediated low-level resistance to all four antibiotics, as shown by the significant increase in MICs in the ΔmarR parental strain compared to the levels for the ΔmarRA parental and wild-type strains. MarA also mediated resistance to other antibiotics tested (ampicillin, cephalothin, nalidixic acid, rifampin, erythromycin, tetracycline, and doxycycline) but had no effect on susceptibility to aminoglycosides, trimethoprim-sulfamethoxazole, imipenem, or fosfomycin (data not shown).

b

The CR1000 MIC/CR2000 MIC ratios were as follows: for FOX, 3.3; for NOR, 3.1; for CHL, 3.0; and for MIN, 2.0. These ratios represent 100% MarA-mediated resistance to each antibiotic (see Table 3), that is, the increase in the MIC resulting from physiological overexpression of marA in the ΔmarR parental strain (CR1000) compared to the MIC for the ΔmarRA parental strain (CR2000).