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. 2017 Jul 13;170(2):249–259.e25. doi: 10.1016/j.cell.2017.06.025

Table 2.

TAM16 MIC Values for Mtb Strains with Different Drug-Susceptibility Profiles, Related to Tables S4 and S5

Strain and resistance statusa Number of strains MIC90b range for multiple strains (μM) Median MIC90 (μM)
H37Rv, fully susceptible lab strain 1 - 0.125-0.25
H37RvMa, fully susceptible lab strain 1 - 0.125
Mtb, fully susceptible clinical isolates 12 0.060-0.250 0.100
Mtb, poly-resistant clinical isolate 1 - 0.420
Mtb, MDR clinical isolates 7 0.060-0.210 0.210
Mtb, pre-XDR clinical isolates 5 0.125-0.420 0.420
Mtb, XDR clinical isolates 5 0.125-0.250 0.125
Mtb, INH mono-resistant, clinical 6 0.050-0.125 0.100
Mtb, RIF mono-resistant, clinical 1 - 0.125
Mtb, SM mono-resistant, clinical 1 - 0.420

Poly-resistant, Mtb-strain resistant to isoniazid (INH), ethionamide, and streptomycin (SM); MDR, resistant to both INH and rifampicin (RIF), with or without resistance to other anti-TB drugs; pre-XDR, MDR strains with additional resistance to either a fluoroquinolone or an injectable but not both; XDR, MDR strains that are also resistant to any fluoroquinolone and to any of the three second-line injectables (amikacin, capreomycin, and kanamycin).

a

Detailed description of the strains with their drug-resistance phenotypes is given in Tables S4 and S5.

b

The lowest concentration of drug that inhibited growth of more than 90% of the bacterial population was considered to be the MIC90. The MIC90 values were determined using MGIT 960 system.