TABLE 4.
β-Lactam challenge-induced β-lactamase expression in B. ubonensisa
| Gene | Treatment |
|||||||
|---|---|---|---|---|---|---|---|---|
| Untreated |
MEM |
IMP |
CAZ |
|||||
| Normalized fold mRNA expression ± SD |
P
value |
Normalized fold mRNA expression ± SD |
P
value |
Normalized fold mRNA expression ± SD |
P
value |
Normalized fold mRNA expression ± SD |
P
value |
|
| penA* | 1.00 ± 0.05 | NA | 0.79 ± 0.10 | 0.98 | 0.47 ± 0.03 | 0.94 | 0.75 ± 0.05 | 0.35 |
| penB | 1.00 ± 0.13 | NA | 336.94 ± 35.58 | <0.001 | 371.00 ± 45.40 | <0.001 | 17.65 ± 1.41 | <0.001 |
| ampC | 1.00 ± 0.12 | NA | 64.43 ± 9.03 | <0.001 | 99.31 ± 6.81 | <0.001 | 9.09 ± 0.77 | <0.001 |
| oxa | 1.00 ± 0.07 | NA | 0.80 ± 0.17 | 0.98 | 0.86 ± 0.05 | 0.99 | 0.70 ± 0.07 | 0.28 |
Cells of Bu278 (wild type) were grown to log phase in LB medium. Equal portions of the cell cultures remained untreated or were treated with subinhibitory concentrations of meropenem (MEM; 8 μg/ml), imipenem (IMP; 8 μg/ml), or ceftazidime (CAZ; 3 μg/ml). Total RNA was isolated after an additional 1 h of incubation at 37°C. The penA*, penB, ampC, and oxa mRNA levels were determined by RT-qPCR. The penA*, penB, ampC, and oxa mRNA levels were determined by RT-qPCR. Standard deviations (SD) between three biological replicates are indicated. Two-way ANOVA and Sidak’s multiple-comparison test were used to determine the significance of the change in fold mRNA expression levels between treated (with MEM, IPM, or CAZ) and untreated strains. P values of <0.05 were considered significant. NA, not applicable.