The role of phenotypic switching in the basic biology and pathogenesis of Candida albicans

71Citations
Citations of this article
165Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The "white-opaque" transition in Candida albicans was discovered in 1987. For the next fifteen years, a significant body of knowledge accumulated that included differences between the cell types in gene expression, cellular architecture and virulence in cutaneous and systemic mouse models. However, it was not until 2002 that we began to understand the role of switching in the life history of this pathogen, the role of the mating type locus and the molecular pathways that regulated it. Then in 2006, both the master switch locus WORI and the pheromone-induced white cell biofilm were discovered. Since that year, a number of new observations on the regulation and biology of switching have been made that have significantly increased the perceived complexity of this fascinating phenotypic transition. © 2014 David R. Soll.

Figures

  • Fig. 1. Scanning electron micrographs of white opaque switching, which involves a dramatic change in cellular phenotype and differences in the capacity to colonize skin. A. The transition is between the white (a/a or a/a) budding yeast cell and a unique oblong, pimpled opaque (a/a, a/a) cell. The frequencies given vary according to the method used to measure them, the strains used, environmental conditions, etc. B. Transmission electron micrograph of an opaque cell reveals wall pimples and a giant vacuole. Arrow heads indicate pimples; V indicates a large vacuole. C. The transition from the white budding cell to oblong opaque cell involves an elongate intermediate phenotype. D. Opaque cells, but not white cells, readily colonize the skin of a newborn mouse, in many cases sinking into an induced cavity. E. Removal of opaque cells from skin reveals cavities (C) formed under them in the skin cells.
  • Fig. 2. While formation of a ‘pathogenic’ MTL-heterozygous (a/a) biofilm is regulated by the Ras1/cAMP pathway, formation of a sexual MTL-homozygous biofilm is regulated by the MAP kinase pathway (72). Regulation in this case was analyzed in a/a, and alternatively in a/a or a/a biofilms, formed on silicone elastomer for 48 hours at 258C in air, in RPMI 1640 medium. Note that even though the final biofilms are architecturally similar, the characteristics resulting from different matrices differ.
  • Fig. 3. The evolving complexity of the regulation of the white opaque transition. The arrows denote upregulation ( ) or down regulation (¡).
  • Fig. 4. Landmark discoveries directly related to the white opaque transition in C. albicans. This represents an incomplete list based on this author’s view of the field.

References Powered by Scopus

This article is free to access.

This article is free to access.

Cited by Powered by Scopus

141Citations
338Readers
Get full text
135Citations
495Readers

This article is free to access.

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Soll, D. R. (2014). The role of phenotypic switching in the basic biology and pathogenesis of Candida albicans. Journal of Oral Microbiology. Co-Action Publishing. https://doi.org/10.3402/jom.v6.22993

Readers over time

‘14‘15‘16‘17‘18‘19‘20‘21‘22‘23‘24‘2507142128

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 62

70%

Researcher 19

21%

Professor / Associate Prof. 4

4%

Lecturer / Post doc 4

4%

Readers' Discipline

Tooltip

Agricultural and Biological Sciences 44

42%

Biochemistry, Genetics and Molecular Bi... 29

28%

Medicine and Dentistry 18

17%

Immunology and Microbiology 14

13%

Article Metrics

Tooltip
Mentions
References: 3
Social Media
Shares, Likes & Comments: 12

Save time finding and organizing research with Mendeley

Sign up for free
0