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. 2018 Jan 25;62(2):e02222-17. doi: 10.1128/AAC.02222-17

TABLE 2.

Activity of IQG-607, INH, ETH, and MFX against several laboratory strains of M. tuberculosis

Strain katG genotype inhA promoter genotype inhA genotype MIC (mg/liter) fora
INH ETH MFX IQG-607
H37Rv WT WT WT 0.39 3.13 0.08 1.56
IQG1b 120del1 WT WT >100 3.13 0.16 >100
IQG2 120del1 WT WT >100 1.56 0.08 >100
IQG3 T(271)C WT WT >100 3.13 0.16 >100
IQG4 1298del1 WT WT >100 1.56 0.08 >100
IQG5 120del1 WT WT >100 1.56 0.02 >100
IQG6 C(1249)G WT WT >100 3.13 0.08 >100
pNIP::furA+katG(WT) WT WT WT <0.2 3.13 <0.2 0.78
pNIP::furA+katG(S315T) G(944)Cc WT WT >100 0.78 <0.2 >100
pNIP::Ø WT WT WT 0.39 6.25 <0.2 1.56
pNIP::InhA(WT) WT WT WT 0.39 6.25 <0.2 3.13
pNIP::InhA(S94A) WT WT T(280)Gd 25 >100 <0.2 >100
a

MIC values reported here were observed in two independent experiments or were the highest value found among three independent tests. ETH, ethionamide.

b

IQG1-6 refers to the IQG-607 spontaneous mutant strains.

c

This mutation changes the serine-315 residue by a threonine (S315T).

d

This strain still expresses the underlying level of the wild-type inhA gene but carries the mutant inhA gene [T(280)G], cloned into the integrative plasmid pNIP40/b. This mutation changes the serine-94 residue by an alanine (S94A).