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Research Article

Biofilms in chronic diabetic foot ulcers—a study of 2 cases

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Pages 383-385 | Received 14 Sep 2010, Accepted 28 Feb 2011, Published online: 11 May 2011

Figures & data

Figure 1. CLSM images of biofilm on soft tissue from patient 1. Overlay projection (includes all the slices in an image stack) of the biofilm at the center of the ulcer base (A) and at the edge of the ulcer base (B). Bar represents 75 µm. CLSM examination revealed the presence of bacteria ranging from single cells to large aggregates of grape-like clusters (panel A). The bacteria in these clusters were viable, as they appeared fluorescent green after LIVE/DEAD Baclight viability stain. Calcofluor white (blue) stained the EPS excreted by the bacteria (panel B). Host nuclei and fibrous material stained red with propidium iodide (panels A and B).

Figure 1. CLSM images of biofilm on soft tissue from patient 1. Overlay projection (includes all the slices in an image stack) of the biofilm at the center of the ulcer base (A) and at the edge of the ulcer base (B). Bar represents 75 µm. CLSM examination revealed the presence of bacteria ranging from single cells to large aggregates of grape-like clusters (panel A). The bacteria in these clusters were viable, as they appeared fluorescent green after LIVE/DEAD Baclight viability stain. Calcofluor white (blue) stained the EPS excreted by the bacteria (panel B). Host nuclei and fibrous material stained red with propidium iodide (panels A and B).

Figure 2. CLSM images of biofilm on soft tissue from patient 2. Overlay projection of the biofilm (A) and a projected side-view (B), meaning the biofilm is visualized from the top and from the side (XZ-plane and YZ-plane, respectively). Bar represents 75 µm. CLSM examination showed that the biofilm distribution was patchy (panel A), with some sites containing large clusters of bacteria and other regions showing hardly any evidence of infection. The bacteria were frequently embedded within a self-produced matrix of EPS (panel B). In addition, the infected ulcer was quite superficial, as can be concluded from the biofilm thickness shown in panel B.

Figure 2. CLSM images of biofilm on soft tissue from patient 2. Overlay projection of the biofilm (A) and a projected side-view (B), meaning the biofilm is visualized from the top and from the side (XZ-plane and YZ-plane, respectively). Bar represents 75 µm. CLSM examination showed that the biofilm distribution was patchy (panel A), with some sites containing large clusters of bacteria and other regions showing hardly any evidence of infection. The bacteria were frequently embedded within a self-produced matrix of EPS (panel B). In addition, the infected ulcer was quite superficial, as can be concluded from the biofilm thickness shown in panel B.