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. 2016 Jan 28;54(2):449–452. doi: 10.1128/JCM.02730-15

TABLE 2.

Rate of identification of B. melitensis 16M, cultivated under different conditions and inactivated with the solvent mixture before MALDI-TOF MS

Strain Mediuma Incubation conditions No. identified/
no. analyzed (%)b
16M COS-B 24 h 2/2 (100)
16M COS-B 48 h 10/11 (91)
16M COS-B 48 h, +5% CO2 2/2 (100)
16M COS-B 72 h 2/2 (100)
16M COS-B 96 h 2/2 (100)
16M COS-B 96 h, +5% CO2 2/2 (100)
16M COS-O 48 h 2/2 (100)
16M MHB 48 h 3/4 (75)
16M MHF 48 h 3/4 (75)
16M BAS 48 h 6/6 (100)
16M BBA 48 h 4/4 (100)
16M CHOC 48 h 4/4 (100)
16M TS 48 h 2/2 (100)
16M TSA-S 48 h 3/4 (75)
bIN1983c COS-B 48 h 7/7 (100)
a

COS-B, Columbia agar with 5% sheep blood (bioMérieux); COS-O, Columbia agar with 5% sheep blood (Oxoid); MHB, Mueller-Hinton agar with 5% sheep blood (Bio-Rad); MHF, Mueller-Hinton agar with 5% horse blood and β-NAD (Bio-Rad); BAS, Brucella agar with 5% sheep blood, hemin, and vitamin K1 (Becton, Dickinson); BBA, Brucella blood agar (bioMérieux); CHOC, chocolate agar with vitox (Oxoid); TS, homemade trypticase soy agar; TSA-S, trypticase soy agar with 5% sheep blood (Becton, Dickinson).

b

Shown are the numbers of successful identifications/number of spectra analyzed, as well as the rate of success.

c

bIN1983, strain 16M plus pMR10-GFP.