TABLE 2.
Mutationa | No. of isolates
|
Mutationa | No. of isolates
|
|||||
---|---|---|---|---|---|---|---|---|
INHr | INHs | Total | INHr | INHs | Total | |||
katG mutations | −46 g→A | 14 | 11 | 25 | ||||
123-128-?b | 2 | 2 | −46 ΔG | 1 | 1 | |||
R128P (cgg→cCg) | 1 | 1 | −39 c→T | 4 | 4 | |||
N138H (aac→Cac) | 1 | 1 | −30 c→T | 1 | 1 | |||
N138D (aac→Gac) | 2 | 2 | −15 c→T | 1 | 1 | |||
N138S (aac→aGc) | 1 | 1 | −12 c→T | 2 | 2 | |||
A172T (gcg→Acg) | 2 | 2 | −10 c→A | 2 | 2 | |||
S315R (agc→agG) | 1 | 1 | −10 c→G | 2 | 2 | |||
S315T (agc→aCc) | 184 | 184 | −10 c→T | 7 | 7 | |||
S315N (agc→aAc) | 9 | 9 | −9 g→A | 2 | 1 | 3 | ||
S315I (agc→aTc) | 6 | 6 | −9 g→?b | 2 | 2 | |||
S315T (agc→aCA) | 21 | 21 | −8 a→?b | 1 | 1 | |||
G316D (ggc→gAc) | 1 | 1 | −6 g→A | 4 | 4 | |||
G316S (ggc→Agc) | 2 | 2 | −4::T | 3 | 3 | |||
W321G (tgg→Ggg) | 1 | 1 | ORF mutations | |||||
L336P (ctg→cGg) | 1 | 1 | T5I (acc→aTc) | 1 | 1 | |||
R515C (cgc→Tgc) | 1 | 1 | D73H (gac→Cac) | 7 | 6 | 13 | ||
L587P (ctg→cCg) | 1 | 1 | Total | 54 | 19 | 73 | ||
D735A (gac→gCc) | 1 | 1 | ||||||
Total | 235 | 3 | 238 | inhA mutations | ||||
Promoter mutationsd | ||||||||
kasA mutations | −17 g→T | 3 | 1 | 4 | ||||
D66N (gat→Aat) | 1 | 1 | 2 | −15 c→T | 31 | 31 | ||
G269S (ggt→Agt) | 36 | 87 | 123 | −8 t→A | 3 | 3 | ||
G312S (ggc→Agc) | 7 | 12 | 19 | −8 t→C | 1 | 1 | ||
Total | 44 | 100 | 144 | ORF mutations | ||||
I21V (atc→Gtc) | 1 | 1 | ||||||
ndh mutations | I21T (atc→aCc) | 2 | 2 | |||||
V18A (gtg→gCg) | 12 | 16 | 28 | I47T (att→aCt) | 1 | 1 | ||
R268H (cgc→cAc) | 2 | 2 | S94A (tcg→Gcg) | 5 | 5 | |||
Total | 14 | 16 | 30 | I194T (atc→aCc) | 2 | 1 | 3 | |
Total | 48 | 3 | 51 | |||||
oxyR-ahpC mutations | ||||||||
Promoter mutationsc | All mutations | 395 | 141 | 536 | ||||
−67 g→A | 1 | 1 |
The mutant codon is indicated, followed by the nucleotide change, shown in capital letters. When the mutation occurs in an intergenic region, the nucleotide change is indicated relative to the start site of the following ORF.
Sequences that were confirmed to be mutants by a molecular beacon assay but whose exact mutation is not known because sequencing results were inconclusive or DNA was unavailable for sequencing.
Positions in the ahpC promoter are situated relative to the transcriptional start residue.
Positions in the inhA promoter are situated relative to the start of the mabA ORF (mabA is the first gene in the mabA-inhA operon).