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. 2009 Oct 7;47(12):4161–4163. doi: 10.1128/JCM.01374-09

TABLE 1.

Color detection for beta-hemolytic GBS strains by the use of three pigment-detecting broth mediaa

Medium and test dateb No. (%) of strains with pigment at indicated concn (CFU/ml)
No. of isolates negative for pigment production and positive on BAP subculture at indicated concn (CFU/ml)/total no. of subcultured isolates
After incubation at 24 h
Only after incubation at 48 h
102 101 102 101 102 101
Carrot (SBCB)
    TD-1 45 (97.8) 45 (97.8) 1 (2.1) 1 (2.1)
    TD-2 46 (100) 46 (100)
    TD-3 46 (100) 45 (97.8) 0 0/1
Granada (IGLB)
    TD-1 46 (100) 46 (100)
    TD-2 46 (100) 45 (97.8) 0 0/1
    TD-3 46 (100) 44 (95.7) 1 (2.1) 0/1c
    TD-4 46 (100) 43 (93.5) 0 0/3
NEL-GBS
    TD-1 37 (80.4) 38 (82.6) 2 (4.3) 4 (8.6) 6/7c 4/4
    TD-2 43 (93.4) 43 (93.4) 2 (4.3) 2 (4.3) 1/1 1/1
    TD-3 37 (80.4) 37 (80.4) 3 (6.5) 4 (8.6) 6/6 3/5
    TD-4 40 (86.9) 39 (84.7) 4 (8.6) 3 (6.5) 2/2 2/4
a

Forty-six strains were used.

b

TD-1, test date 1; TD-2, test date 2; TD-3, test date 3; TD-4, test date 4.

c

Subculture to BAP for one isolate that was negative after 24 h in broth was not determined.