4, 49 ± 2.0 and 44 ± 2.8% in the competition, exclusion Cl-amidine chemical structure and displacement assays, respectively (Figure 5). Figure 5 Inhibition of adhesion of C.albicans to vaginal epithelial cells. (a) Treatment of vaginal epithelial cells with 1×107 L. crispatus. C. albicans to Vk2/E6E7 cells was assessed by microscopy (×100) after Gram’s stain by counting the number of micro-organisms attached to 30 consecutive cells. The results of the three conditions (i.e. exclusion, competition and displacement) were expressed as the average number of C. albicans per Vk2/E6E7 cells and compared with adhesion

without lactobacilli (control value). The control values were taken as 100% of adhesion and the inhibition of C. albicans adherence was calculated by subtracting each adhesion percentage from their corresponding control

value. (b) Treatment of vaginal epithelial cells with 1.0 mg/mL EPS. C. albicans to Vk2/E6E7 cells was assessed by microscopy (×100) after Gram’s stain by counting the number of micro-organisms attached to 30 consecutive cells. The results of the three conditions (i.e. exclusion, competition and displacement) were expressed as the average number of C. albicans per Vk2/E6E7 cells and compared with adhesion without EPS (control value). The control values were taken as 100% of adhesion and the inhibition of C. albicans adherence was calculated by substracting each adhesion percentage from their corresponding control value. The data are expressed as the mean ± SD percentage of adherence in Dasatinib mw three independent experiments. The asterisks indicate a statistically significant difference between C. albicans grown in the presence of viable or heat-killed L. crispatus versus C. albicans alone. *P < 0.05, **P < 0.01. Moreover, confluent cell monolayers were treated with increasing concentrations of EPS, isolated and purified from L. crispatus L1, and successively infected with C. albicans. The AZD0156 molecular weight concentration required to interfere with yeast adhesiveness was equal to 1.0 mg∙ml−1. Figure 5b shows the effect of EPS on the adhesion of C. albicans to vaginal epithelial cells under

the conditions of exclusion, competition and displacement. The adhesion interference was of about 48% in the exclusion assay, when the monolayers were pre-treated with 1.0 mg∙ml−1 EPS for 18 h and before addition buy Rapamycin of the C. albicans suspension. In the competition and displacement tests the reduction in adherence was comparable to that obtained in the control experiment. A set of experiments was performed to determine whether HBD-2 was secreted by vaginal epithelial cells treated with increasing concentrations of EPS. HBD-2 ELISAs showed that the concentration of HBD-2 protein was significantly high in the supernatant after 18 h treatment (Figure 6). Interestingly, the plateau was reached at the same concentration (100 mg∙l−1). Figure 6 HBD-2 levels in Vk2/E6E7cells after treatment with EPS (0.01-0.1-1.0 – 5 mg/mL) secreted by L. crispatus L1.