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Author: Harrison, JJ
Author: Turner, RJ
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Methods Article

The use of microscopy and three-dimensional visualization to evaluate the structure of microbial biofilms cultivated in the Calgary Biofilm Device

Joe J. Harrison2, Howard Ceri2, Jerome Yerly3, Carol A. Stremick2, Yaoping Hu3, Robert Martinuzzi4 and Raymond J. Turner1*

1 Department of Biological Sciences, University of Calgary. T2N 1N4. Canada.
2 Department of Biological Sciences and Biofilm Research Group, University of Calgary. T2N 1N4. Canada.
3 Electrical and Computer Engineering, Schulich School of Engineering, University of Calgary. T2N 1N4. Canada.
4 Mechanical and Manufacturing Engineering, Schulich School of Engineering, University of Calgary. 2500 University Drive N.W., Calgary, AB T2N 1N4. Canada.

* To whom correspondence should be addressed: Raymond J. Turner, Department of Biological Sciences, University of Calgary. T2N 1N4. Canada. Phone: 403-220-4308. Email: turnerr@ucalgary.ca

Biol. Proced. Online 2006;8:194-215. doi:10.1251/bpo127
Submitted: September 06, 2006; Accepted: October 28, 2006; Published: December 19, 2006.

Indexing terms: Biofilms; Imaging, Three-Dimensional.


Figure 5 Enlarged

Fig. 5:

TRITC-conjugated lectin staining of C. tropicalis and B. cenocepacia biofilms. A. An overlay image of a C. tropicalis biofilm that was stained with AO (green emission) and TRITC-ConA (red emission). B. AO staining of the section illustrated in panel A. C. TRITC-ConA staining of the section illustrated in panel A. D. An overlay image of a B. cenocepacia biofilm that was stained with Syto-9 and TRITC-PNA. E. Syto-9 staining of the section illustrated in panel D. F. TRITC-PNA staining of the section illustrated in panel D. Each panel represents a square surface area of approximately 238 × 238 μm.

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