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. 2013 Feb;57(2):751–757. doi: 10.1128/AAC.01482-12

Table 3.

Effect of efflux inhibitors on the MICs of potential substrates of Mmr efflux pump

M. tuberculosis strain MIC (μg/ml)d
Ethidium bromide
Tetraphenylphosphonium
Acriflavine
Safranin O
CTAB
No inhibitor CCCP CPZ VP No inhibitor CCCP CPZ VP No inhibitor CCCP CPZ VP No inhibitor CCCP CPZ VP No inhibitor CCCP CPZ VP
H37Rv 2 2 2 0.5 12.5 3.1 12.5 12.5 3 1.5 3 3 1 0.5 1 0.5 12.5 3.1 12.5 12.5
MmrKOa 1 1 1 0.13 3.1 3.1 1.5 1.5 3 1.5 3 1.5 0.5 0.5 0.25 0.5 6.25 3.1 6.25 6.25
MmrKO::pCRS5b 2 2 2 1 12.5 3.1 12.5 12.5 3 1.5 3 3 1 0.5 1 0.5 12.5 3.1 12.5 12.5
H37Rv::pCVZ2c 4 2 4 1 12.5 6.2 12.5 12.5 6 0.18 6 6 2 0.06 2 2 12.5 0.4 12.5 12.5
a

M. tuberculosis H37Rv with mmr gene inactivated.

b

MmrKO complemented with pCRS5.

c

M. tuberculosis H37Rv containing pCVZ2.

d

CCCP, carbonyl cyanide m-chlorophenylhydrazone; CPZ, chlorpromazine; CTAB, cetyltrimethylammonium bromide; VP, verapamil. Data in bold represent at least a 4-fold reduction, considered to denote a significant MIC reduction in the presence of an efflux inhibitor.