Description of biofilm formation by determination of developmental axis

2000 ◽  
Vol 41 (4-5) ◽  
pp. 121-127 ◽  
Author(s):  
J.B. Xavier ◽  
R. Mahló ◽  
A.M. Reis ◽  
J.S. Almeida

The formation of a multispecies denitrifying biofilm was monitored by confocal scanning laser microscopy (CSLM). The time series of tri-dimensional reconstitutions was used to develop a methodology for biofilm structural characterization based on the identification of axis of development. The algorithm is an adaptation of the standard medial axis transform technique (MAT) and was applied to both 2D sections and to the 3D stack. The use of development axis as the primary structural feature is a well-established practice to the study of morphogenesis of superior organisms. The extension of the concept to microbial aggregates is justified by the experimental realization of its highly structured nature. The determination of development axis (DA) is scalable and can be applied to structures with time resolution (effectively corresponding to four dimension structures) in order to define unifying measures of biofilm morphogenesis. Practical applications of DA characterization include the determination of how density of specific biofilms will be reflected in pore turtuosity, which in turn will condition the internal mass transfer limitations.

2001 ◽  
Vol 183 (18) ◽  
pp. 5385-5394 ◽  
Author(s):  
Jyotsna Chandra ◽  
Duncan M. Kuhn ◽  
Pranab K. Mukherjee ◽  
Lois L. Hoyer ◽  
Thomas McCormick ◽  
...  

ABSTRACT Biofilms are a protected niche for microorganisms, where they are safe from antibiotic treatment and can create a source of persistent infection. Using two clinically relevant Candida albicans biofilm models formed on bioprosthetic materials, we demonstrated that biofilm formation proceeds through three distinct developmental phases. These growth phases transform adherent blastospores to well-defined cellular communities encased in a polysaccharide matrix. Fluorescence and confocal scanning laser microscopy revealed that C. albicans biofilms have a highly heterogeneous architecture composed of cellular and noncellular elements. In both models, antifungal resistance of biofilm-grown cells increased in conjunction with biofilm formation. The expression of agglutinin-like (ALS) genes, which encode a family of proteins implicated in adhesion to host surfaces, was differentially regulated between planktonic and biofilm-grown cells. The ability ofC. albicans to form biofilms contrasts sharply with that of Saccharomyces cerevisiae, which adhered to bioprosthetic surfaces but failed to form a mature biofilm. The studies described here form the basis for investigations into the molecular mechanisms of Candida biofilm biology and antifungal resistance and provide the means to design novel therapies for biofilm-based infections.


2015 ◽  
Vol 26 (1) ◽  
pp. 54-56

Candida albicans may colonize natural or artificial surfaces, leading to formation of the biofilm. Infections associated with the biofilm formation are important therapeutic problem. In this paper, we present data concerning the biofilm formation under static conditions by oropharyngeal isolates of C. albicans on a glass surface using confocal scanning laser microscopy (CSLM). The areal parameters describing the architecture of biofilm and its development, i.e. the areal porosity, the length of edge line, the length of skeleton line, were calculated. The changes in values of these parameters during the biofilm formation by C. albicans were similar for biofilm consisting of only blastospores as well as the biofilm consisting of blastospores and filamentous elements (hyphae or/and pseudohyphae). However, the thickness of C. albicans biofilm consisting of blastospores and filamentous elements was much higher than that consisting of only blastospores. The heterogeneity may be regarded as an important feature of the yeast biofilm including C. albicans.


Author(s):  
M Wessendorf ◽  
A Beuning ◽  
D Cameron ◽  
J Williams ◽  
C Knox

Multi-color confocal scanning-laser microscopy (CSLM) allows examination of the relationships between neuronal somata and the nerve fibers surrounding them at sub-micron resolution in x,y, and z. Given these properties, it should be possible to use multi-color CSLM to identify relationships that might be synapses and eliminate those that are clearly too distant to be synapses. In previous studies of this type, pairs of images (e.g., red and green images for tissue stained with rhodamine and fluorescein) have been merged and examined for nerve terminals that appose a stained cell (see, for instance, Mason et al.). The above method suffers from two disadvantages, though. First, although it is possible to recognize appositions in which the varicosity abuts the cell in the x or y axes, it is more difficult to recognize them if the apposition is oriented at all in the z-axis—e.g., if the varicosity lies above or below the neuron rather than next to it. Second, using this method to identify potential appositions over an entire cell is time-consuming and tedious.


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