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. 2014 Sep 17;9(9):e107805. doi: 10.1371/journal.pone.0107805

Figure 5. Myeloperoxidase activity of β-glucan-treated neutrophils activated by different isolates of C. albicans and C. glabrata (integrated light emission).

Figure 5

The inset represents kinetic study of MPO activity of β-glucan-treated neutrophils after 20 minutes of incubation. Neutrophils (2.0×106 cells/ml) were previously treated or not with 3 mg/ml β-glucan and incubated with the reference strain and different isolates of (A) C. albicans and (B) C. glabrata (2×107 CFU/ml) for 30 min. (a,a’) ATCC. (b,b’) ASS. (c,c’) VVC. (d,d’) RVVC. After incubation, chemiluminescence was monitored for 20 min at 37°C in a microplate luminometer using luminol as a chemical light amplifier. The data are expressed as the mean ± SD of three independent experiments. *p≤0.05, significant difference compared with the control group (neutrophils alone); # p≤0.05, significant difference compared with untreated and activated neutrophils.