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. 2000 Jul;68(7):3990–3997. doi: 10.1128/iai.68.7.3990-3997.2000

TABLE 1.

Hydrogen peroxide sensitivity and production by various bacterial pathogens

Species MIC (mM)a MBC (mM)b H2O2 generated (mM)c Source or referenced
Gram-negative
H. influenzae Rd 0.4 0.5 <0.1 26
H. influenzae Eagan 0.4 0.5 <0.1 26
N. meningitidis MC58C3 0.4 5 <0.1 32
M. catarrhalis Bc1 1.1 160 <0.1 Clinical isolate
E. coli RS218 ND 15 <0.1 1
S. enterica serovar Typhimurium LT2 ND 20 <0.1 Collection of K. Sanderson
K. pneumoniae Kp1 ND 20 <0.1 Clinical isolate
P. aeruginosa PA01 ND 60 <0.1 ATCC 15692
Gram-positive
S. pyogenes P87 ND 40 <0.1 Clinical isolate
S. agalactiae P60 ND 80 <0.1 Clinical isolate
S. equisimilis P107 ND 20 <0.1 Clinical isolate
E. faecium P119 ND 80 <0.1 Clinical isolate
S. aureus A1 ND 10 <0.1 Clinical isolate
S. pneumoniae strains
 P394 (type 4) 1.6 80 TIGR genome strain
 D39 (type 2) 1.2 80 0.44 ± 0.08 4
 P383 (type 6B) ND ND 0.53 ± 0.08 22
 P384 (type 6A) ND ND 0.71 ± 0.13 22
 P878 D39 (spxB::TnphoA) 1.6 80 <0.1 38
 P62 (type 9V opaque variant) ND ND <0.1 22
 P64 (type 9V transparent variant) ND ND 0.43 ± 0.13 22
a

The MIC was determined as the minimum concentration of H2O2 necessary to prevent turbid growth of a 1-in-50 inoculum of a stationary-phase culture following overnight incubation at 37°C. ND, not determined. 

b

The MBC was determined as the minimum concentration of H2O2 necessary for >99.9% killing of washed, log-phase cells in BHI medium after 30 min at 37°C. 

c

H2O2 concentration present in culture supernatants after incubating approximately 5 × 107 washed, log-phase cells for 1 h in BHI medium at 37°C. 

d

TIGR, The Institute for Genome Research.