TABLE 2.
Isolate | Genotype | Susceptibility status | Drug resistance profile | MIC (μg/ml) of VXc-486 |
---|---|---|---|---|
TT135 | Atypical Beijing | XDR | H, R, E, Z, ET, S, A, C, O, M, PAS | 0.08 |
R179 | Atypical Beijing | MDR | H, R, E, ET, S | 0.08 |
R884 | Low copy number | Pre-XDR | H, R, E, Z, ET, S, O | 0.08 |
X_3 | Beijing | XDR | H, R, E, K, S, C, O | 0.68 |
X_27 | Beijing | XDR | H, R, ET, O, A | 0.68 |
X_60 | Beijing | XDR | H, R, E, A, ET, O, S, C, K | 0.68 |
X_61 | Beijing | XDR | H, R, ET, A, O, K, S | 0.68 |
X_131 | F11 | Pre-XDR | H, R, K, S, O | 0.17 |
TT149 | Atypical Beijing | XDR | H, R, ET, S, A, C, O, M | 5.48 |
Mycobacterial growth was measured by using mycobacterial growth indicator tubes (MGIT), and the MIC (μg/ml) of VXc-486 was determined. The growth units were recorded once the 1:100 controls reached a GU (gas unit) of 400, and the MIC is regarded as a concentration that gives a GU of 0. The isolates grew well in the presence of isoniazid, confirming resistance to this drug. Abbreviations: H, isoniazid; R, rifampin; E, ethionamide; ET, ethambutol; S, streptomycin; A, amikacin; C, capreomycin; O, ofloxacin; M, moxifloxacin; PAS, para-aminosalicylic acid; Z, pyrazinamide.