Both O157 strains grown in DMEM and pre-incubated with pooled, polyclonal antisera generated against the LEE (Tir, EspA, EspB, and Intimin) and flagellar H7 proteins, or the anti-Intimin antisera alone, at 1:5 and 1:10 dilution, continued to adhere to the RSE cells, irrespective of the presence/absence of D + Mannose. Data is shown for one of the O157 strains in the Ganetespib clinical trial presence of D + Mannose (Additional file Selleck SHP099 1, Figure 1, panel A, Figure 2). These results were consistent between all trials, irrespective of toluidine blue or immunofluorescent staining, and did not show any differences in the adherence patterns compared to the controls. The same O157-RSE cell-adherence

pattern was observed in the controls with normal rabbit sera added at 1:5 dilution (data not shown), and in the absence of any sera (Additional file 1, Figure 1, panel B; Figure 2) [5], irrespective of the presence/absence of selleck kinase inhibitor D + Mannose. The continued adherence of O157 to the RSE cells in the presence of antibodies to the LEE proteins may have been due to the masking of these antigens and the unmasking of other O157 adhesins targeting the receptors on the RSE cells. To that effect an increase in the total number of RSE cells with adherent bacteria and decrease in the total number of RSE cells with no adherent bacteria

was observed, in the presence of pooled and anti-Intimin antisera (Figure 2). We intentionally included antisera targeting the flagellar antigen H7 as flagella have been demonstrated to play a role in initial adherence to plant cells and the FAE [28, 29]. These results suggest that additional mechanisms of adherence, distinct from those attributable to LEE, Intimin and flagellar H7 proteins, are involved in O157 attachment to the RAJ squamous epithelial

cells. Figure 1 Adherence patterns of O157 strain EDL 933 on RSE cells, in the presence of D + Mannose and +/− antisera. Panel A, in the presence of “pooled antisera” against LEE, Intimin and flagellar H7 proteins, and the anti-Intimin antisera alone, at 1:5 dilutions. Panel B, in the absence of any sera (No sera). The immunofluorescence (IF) stained slides are shown at 40x magnification. O157 have green fluorescence, cytokeratins’ of RSE cells have orange-red fluorescence, and their nuclei have blue fluorescence. The arrows in the Phospholipase D1 adjacent toluidine blue (TB) stained slides, at 40x magnification, point to RSE-adherent O157. Figure 2 Quantitative representation of the adherence patterns of O157 strains EDL 933, and 86–24 along with its mutant derivatives, on RSE and HEp-2 cells. Percent mean ± standard error of mean of cells with adherent bacteria or no bacteria, in the ranges shown in the legend, are depicted in each graph. On the other hand, the LEE-encoded proteins were critical to O157 adherence to HEp-2 cells as demonstrated previously [22], with or without D + Mannose.