TABLE 2.
K. pneumoniae strain no. | MIC (μg/ml)a |
FICb |
|||||||
---|---|---|---|---|---|---|---|---|---|
AMK | COL | DOR | TGC | TMP-SMX | AMK-COL | AMK-DOR | AMK-TGC | AMK–TMP-SMX | |
615 | 4 | >64 | 128 | 1 | >128 | 1 | 0.75 | 2 | 0.25 |
383 | 16 | 0.125 | 8 | 2 | >128 | 0.75 | 0.5 | 0.75 | 0.375 |
871 | 16 | 0.125 | 16 | 2 | >128 | 1 | 0.625 | 0.75 | 0.375 |
930 | 16 | 0.25 | 32 | 1 | 0.125 | 1 | 0.375 | 0.75 | 2 |
1 | 16 | >64 | 64 | 0.25 | >128 | 0.265 | 0.5156 | 0.75 | 0.25 |
136 | 16 | >64 | 64 | 2 | 16 | 0.375 | 0.5 | 0.75 | 0.5 |
294 | 16 | 0.5 | 4 | 0.25 | >128 | 0.75 | 0.5 | 0.75 | 0.25 |
584 | 16 | 64 | >128 | 2 | 128 | 0.375 | 0.5156 | 2 | 0.5 |
928 | 16 | 32 | 4 | 1 | >128 | 0.375 | 0.25 | 1 | 0.3125 |
184 | 32 | 16 | 64 | 0.25 | >128 | 0.75 | 1 | 2 | 0.375 |
216 | 32 | 16 | 4 | 0.25 | >128 | 0.5 | 0.75 | 0.5625 | 0.25 |
484 | 32 | 0.5 | >128 | 2 | >128 | 0.75 | 0.5 | 0.5625 | 0.5 |
539 | 32 | 0.25 | 64 | 0.5 | >128 | 1.5 | 1 | 2 | 0.3125 |
587 | 32 | 0.25 | 64 | 0.5 | >128 | 0.75 | 1 | 2 | 0.375 |
669 | 32 | 0.25 | 128 | 2 | 1 | 1 | 0.5 | 0.75 | 0.56 |
705 | 32 | 0.125 | 128 | 0.5 | >128 | 0.675 | 0.75 | 1 | 0.375 |
709 | 32 | 0.125 | 16 | 2 | >128 | 1 | 0.5625 | 0.75 | 0.375 |
94 | 32 | 64 | 128 | 2 | >128 | 0.5 | 1 | 0.5625 | 0.3125 |
649 | 32 | 64 | >128 | 1 | >128 | 0.625 | 0.75 | 0.625 | 0.375 |
692 | 32 | 0.25 | 8 | 2 | >128 | 2 | 0.75 | 0.75 | 0.3125 |
AMK, amikacin; COL, colistin; DOR, doripenem; TGC, tigecycline; TMP-SMX, trimethoprim-sulfamethoxazole.
The following concentrations were tested for each agent: AMK, 2 to 128 μg/ml; COL, 0.06 to 64 μg/ml; DOR, 0.125 to 128 μg/ml; TGC, 0.06 to 64 μg/ml; TMP-SMX, 0.125 to 128 μg/ml. TMP and SMX were tested at a fixed ratio of 1:19 in accordance with CLSI susceptibility testing guidelines (10). The percentages of synergy (FIC of ≤0.5) were as follows: AMK-COL, 30%; AMK-DOR, 35%; AMK-TGC, 0%; and AMK–TMP-SMX, 90%.