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. 1999 Oct;43(10):2520–2523. doi: 10.1128/aac.43.10.2520

TABLE 1.

Susceptibilities of strains to selected Fqs and mutations in the parC, parE, gyrA, and gyrB genesa

Strain MIC (μg/ml)
Amino acid change (codon change)b
Cp
SPA
CLX, agar dilution
E test Agar dilution E test Agar dilution ParCc ParE GyrAd GyrB
S. pneumoniae R6 0.5 0.5 0.25 0.25 0.125
S. oralis NCTC11427 4 2 0.5 0.5 0.125 ND
S. oralis ATCC10557 2 2 0.5 0.5 0.125 ND
S. mitis NCTC12261 1 1 0.25 0.25 0.06 ND
S. mitis V1e 16 4 1 0.25 0.125 ND ND
S. mitis V2 16 4 1 0.5 0.125 ND ND
S. mitis V3 16 4 1 0.25 0.125 ND ND
S. mitis V4 16 4 1 0.5 0.125 ND ND
S. sanguis V5 16 4 1 0.5 0.125 ND 425A→G (GCT→GGT)
S. mitis V6 16 4 2 0.5 0.125 425A→G (GCT→GGT)
S. mitis V10 16 4 1 0.5 0.125 79S→F (TCT→TTT) ND
S. mitis V8 >32 16 2 1 0.25 79S→F (TCT→TTT)
S. oralis V9 >32 32 2 1 0.5 79S→Y (TCT→TAT)
a

SPA, sparfloxacin; CLX, clinafloxacin; ND, not determined. 

b

Positions of substitutions are according to the coordinates for S. pneumoniae R6. —, no change. 

c

The sequenced strains had an additional 91N→D (AAC→GAC) change compared to the sequence of S. pneumoniae R6. 

d

The sequenced strains had an additional 114S→G (AGT→GGT) change compared to the sequence of S. pneumoniae R6. 

e

Classification of the VGS clinical isolates to the species level was done with the API 20-Strep and ID 32-Strep systems.