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. 2014 Aug;52(8):2876–2880. doi: 10.1128/JCM.00398-14

TABLE 2.

MTBDRsl patterns versus gyrA mutations detected by DNA sequencing among 25 of the 32 DNA extracts, by WHO patient category

Type of patienta gyrA MTBDRsl patternb gyrA sequencing data, codons, and amino acid (nucleotide) substitutions No. (%) detected
Cat. 4 ΔWT3 plus MUT3C 94Gly (GGC) 2 (8)
ΔWT2 plus ΔWT3 plus MUT3C 80Ala (GCC), 90Gly (GGG), 94Gly (GGC) 1 (4)
MUT3A plus MUT3C 94Ala (GCC) 1 (4)
Cat. 2 MUT3A 94Tyr (TAC), 94Ala (GCC) 1 (4)
MUT3A 80Ala (GCC), 90Gly (GGG), 94Ala (GCC) 1 (4)
ΔWT2 80Ala (GCC), 90Gly (GGG) 9 (36)
ΔWT2 WTc 1 (4)
Cat. 1 ΔWT2 plus MUT1 90Val (GTG) 1 (4)
ΔWT2 plus MUT1 80Ala (GCC), 90Val (GTG) 1 (4)
ΔWT2 plus MUT2 91Pro (CCG) 1 (4)
ΔWT2 80Ala (GCC), 90Gly (GGG) 4 (16)
ΔWT2 80Ala (GCC), 90Arg (AGG) 1 (4)
ΔWT2 WT 1 (4)
a

Cat. 1, 2, and 4, WHO patient categories of recurrences after first-line primary treatment, first-line re-treatment, and second-line treatment, respectively.

b

ΔWT, omission of the respective wild-type band.

c

WT, only wild-type DNA detected.