Affiliation:
1. Institut für Mikrobiologie, Heinrich-Heine-Universität, D-40225 Düsseldorf, Germany
Abstract
ABSTRACT
Phenotypic switching in
Candida albicans
spontaneously generates different cellular morphologies and is manifested in strain WO-1 by the reversible switching between the white and opaque phenotypes. We present evidence that phenotypic switching is regulated by the Efg1 protein, which is known as an essential element of hyphal development (dimorphism). Firstly,
EFG1
is expressed specifically in cells of the white but not the opaque phenotype. During mass conversion from the opaque to the white phenotype, the
EFG1
transcript level correlates with competence of switching of opaque cells to the white form. Secondly, overexpression of
EFG1
by a
PCK1p-EFG1
fusion forces opaque-phase cells to switch to the white form with a high level of efficiency. Thirdly, low-level expression of
EFG1
in strain CAI-8 generates a cellular phenotype similar to that of opaque cells in that cells bud as short rods, which cannot be induced to form hyphae in standard conditions; such cells (unlike authentic opaque cells) lack typical surface “pimples.” Importantly, the opaque-specific
OP4
transcript is induced in the opaque-like cells generated by strain CAI8 as a response to low-level expression of
EFG1
. The results suggest that high
EFG1
expression levels induce and maintain the white cell form while low
EFG1
expression levels induce and maintain the opaque cell form. It is proposed that changes in
EFG1
expression determine or contribute to phenotypic switching events in
C. albicans
.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
150 articles.
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