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. 1999 Jun;43(6):1340–1346. doi: 10.1128/aac.43.6.1340

TABLE 3.

Effect of mexAB-oprM operon on LVX susceptibility of strains with multiple target mutations

gyrA or parC mutation MIC (μg/ml) for indicated strain with the following pump status:
nalBa WTb oprM::ΩHgc
None 2 (PAM1032) 0.25 (PAM1020) 0.015 (PAM1154)
gyrA (Thr83→Ile) 8 (PAM1573) 2 (PAM1548) 0.125 (PAM1665)
gyrA (Thr83→Ile) parC (Ser87→Leu) 32 (PAM1582) 4 (PAM1667) 0.5 (PAM1600)
gyrA (Thr83→Ile) parC (Ser87→Leu) gyrA (Asp87→Tyr) 128 (PAM1609) 16 (PAM1669) 2 (PAM1640)
a

The strains were obtained by stepwise selection with increasing concentrations of LVX. Strain PAM1032 was selected from wild-type strain PAM1020. The order of the strains in the column corresponds to the order in which the strains were selected, so that for example, PAM1032 is a parent of PAM1573. All mutant selections were performed with LVX at 4× the MIC for the corresponding parent. 

b

WT, wild type. PAM1548 was obtained as a spontaneous LVX-resistant mutant selected from strain PAM1020. PAM1667 and PAM1669 were constructed by transduction of the mexAB-oprM operon with the wild-type level of expression (no nalB mutation) from strain PAM1064 into PAM1582 and PAM1609, respectively, as described in Materials and Methods. 

c

Strains PAM1665, PAM1600, and PAM1640 were constructed by transduction of the Hg resistance from strain PAM1154 (PAM1020 oprM::ΩHg) into strains PAM1573, PAM1582, and PAM1609, respectively.