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. 1998 Dec 8;95(25):14967–14972. doi: 10.1073/pnas.95.25.14967

Table 1.

Characteristics of SB4: Colony types W, S, and C

Characteristic Colony type
W S C
Capsule size, μm 3.9  ±  0.8 1.3  ±  0.6 1.4  ±  0.6
Cell size, μm 5.9  ±  0.8 7.0  ±  0.9 5.6  ±  0.7
Doubling times, h 1.6 1.7 2.0
AMPHOTERICIN B MIC, μg/ml 0.25 0.25 0.125
FLUCONAZOLE MIC, μg/ml 2 2 0.5
5-FC MIC, μg/ml 4 4 2
CN survival at −20°C 0.22  ±  0.10 0.07  ±  0.04 0.22  ±  0.11
CN survival at 50°C 0.19  ±  0.11 0.04  ±  0.04 0.25  ±  0.04
Mean survival of mice, days 3.2  ±  1.0 6.8  ±  1.3 11.9  ±  2.2
Inflamatory response Minimal Intermediate Intense caseous necrosis
Polysaccharide localization in vivo E ≫ 1 E > 1 1 > E
Antibody response against W extract N 76, 70 kDa 87, 76, 70, 67, 64, 61, 58, 36 kDa
Antibody response aganint S extract N 76, 70 kDa 87, 76, 70, 64, 60, 54, 50 kDa
Antibody response against C extract N 76, 70, 64 kDa 76, 70, 67, 64, 62, 61, 54 kDa

Capsule size is expressed as average capsule radius mean ± 1 SD: (n = 40–50) was determined by light microscopy (P value for S versus W is <0.001: P value for C versus S is 0.28). Cell size is average cell diameter (mean ± 1 SD; n = 40–50, not including the capsule) was determined by light microscopy (P value for S versus W is <0.001: P value for C versus W is 0.05). Susceptibility to amphotericin, fluconazole, or 5-fluorocytosine (5-FL) was determined by National Committee for Clinical Laboratory Standards macrodilution method. Survival fraction after overnight exposure to −20° relative to untreated controls represents the average of four experiments P value for S versus W is 0.025; P value for S versus C is 0.049). Survival fraction after exposure to 50°C for 5 min relative to untreated controls represents the average of three experiments (P value for S versus W is 0.09: P value for S versus C is 0.01). Mouse survival experiments were done twice with similar results (P value for C versus S is 0.002; P value for S versus W is 0.003). Inflammatory responses in rats 4 weeks after endotracheal inoculation are shown. Localization of cryptococcal polysaccharide in rat pulmonary model was determined by immunohistochemistry (E, extracellular; I, intracellular). For antibody responses, the molecular weights of major bands recognized by serum IgG in Western blot analysis are shown. Doubling times were determined by CFU experimentation. N, not detected; MIC, minimal inhibitory concentrations.