Everything about Candida Albicans totally explained
Candida albicans is a
diploid fungus (a form of
yeast), which is capable of mating but not of meiosis, and a causal agent of
opportunistic and
genital infections in humans. Systemic fungal infections (
fungemias) have emerged as important causes of
morbidity and
mortality in
immunocompromised patients (for example,
AIDS, cancer
chemotherapy, organ or
bone marrow transplantation). In addition, hospital-related infections in patients not previously considered at risk (for example patients in an intensive care unit) have become a cause of major health concern.
C. albicans is among the
gut flora, the many organisms which live in the human mouth and
gastrointestinal tract. Under normal circumstances,
C. albicans lives in 80% of the human population with no harmful effects, although overgrowth results in
candidiasis. Candidiasis is often observed in
immunocompromised individuals such as
HIV-positive patients. Candidiasis also may occur in the
blood and in the
genital tract. Candidiasis, also known as "thrush", is a common condition which is usually easily cured in people who are not immunocompromised. To infect host tissue, the usual
unicellular yeast-like form of
Candida albicans reacts to environmental cues and switches into an invasive, multicellular filamentous forms. The genome of the WO1 strain was sequenced by the
Broad Institute of MIT and Harvard.
The sequencing of the
C. albicans genome and subsequently of the genomes of several other medically relevant
Candida species has profoundly and irreversibly changed the way
Candida species are now investigated and understood. The
C. albicans genome sequencing effort was launched in October 1996. Successive releases of the sequencing data and genome assemblies have marked the last 10 years, culminating with the release of the diploid assembly 19 which provided a haploid version of the genome along with data on allelic regions in the genome. A refined assembly 20 with the eight assembled
C. albicans chromosomes was released in the summer of 2006. Importantly, the availability of sequencing data prior to the completion of the genome sequence has made it possible to start
C. albicans post-genomics early on. In this regard, genome databases have been made available to the research community providing different forms of genome annotation. These have been merged in a community-based annotation hosted by the
Candida Genome Database. The availability of the genome sequence has paved the way for the implementation of post-genomic approaches to the study of
C. albicans: macroarrays and then microarrays have been developed and used to study the
C. albicans transcriptome; proteomics has also been developed and complements transcriptional analyses; furthermore, systematic approaches are becoming available to study the contribution of each
C. albicans gene in different contexts. Other
Candida genome sequences have been, or are being, determined:
C. glabrata,
C. dubliniensis,
C. parapsilosis,
C. guilliermondii,
C. lusitaniae, and
C. tropicalis. These species will soon enter the post-genomic era as well and provide interesting comparative data. The genome sequences obtained for the different
Candida species along with those of non-pathogenic hemiascomycetes provide a wealth of knowledge on the evolutionary processes which have shaped the hemiascomycete group as well as those which may have contributed to the success of different
Candida species as pathogens.
The genome of
C. albicans is highly dynamic and this variability has been used advantageously for molecular epidemiological studies of
C. albicans and population studies in this species. A remarkable discovery which has arisen from the genome sequence is the presence of a parasexual cycle in
C. albicans. This parasexual cycle is under the control of mating-type loci and switching between white and opaque phenotypes. Investigating the role which the mating process plays in the dynamics of the
C. albicans population or in other aspects of
C. albicans biology and pathogenicity will undoubtedly represent an important focus for future research.
Dimorphism
In a process which superficially resembles
dimorphism,
C. albicans undergoes a process called
phenotypic switching, in which different cellular morphologies are generated spontaneously. One of the classically studied strains which undergoes phenotypic switching is WO-1, which consists of two phases - one which grows as smooth white colonies and one which is rod-like and grows as flat gray colonies. The other strain known to undergo switching is 3153A; this strain produces at least seven different colony morphologies. In both the WO-1 and 3153A strains, the different phases convert spontaneously to the other(s) at a low frequency. The switching is reversible, and colony type can be inherited from one generation to another. While several
genes which are
expressed differently in different colony morphologies have been identified, some recent efforts have focused on what might be controlling these changes. Further, whether there's a potential molecular link between dimorphism and phenotypic switching is a tantalizing question.
In the 3153A strain, a gene called SIR2 (for silent information regulator) has been found which seems to be important for phenotypic switching. SIR2 was originally found in
Saccharomyces cerevisiae (brewer's yeast), where it's involved in
chromosomal silencing — a form of
transcriptional regulation in which regions of the
genome are reversibly inactivated by changes in
chromatin structure (chromatin is the complex of
DNA and proteins which make
chromosomes). In yeast, genes involved in the control of mating type are found in these silent regions, and SIR2 represses their expression by maintaining a silent-competent chromatin structure in this region. The discovery of a
C. albicans SIR2 which is implicated in phenotypic switching suggests that it too has silent regions controlled by SIR2, in which the phenotype-specific genes may perhaps reside.
Another potential regulatory molecule is Efg1p, a
transcription factor found in the WO-1 strain which regulates dimorphism, and more recently has been suggested to help regulate phenotypic switching. Efg1p is expressed only in the white and not in the gray cell-type, and overexpression of Efg1p in the gray form causes a rapid conversion to the white form.
So far there are few data which say that dimorphism and phenotypic switching use common molecular components. However, it isn't inconceivable that phenotypic switching may occur in response to some change in the environment as well as being a spontaneous event. How SIR2 itself is regulated in
Saccharomyces cerevisiae may yet provide clues as to the switching mechanisms of
C. albicans.
Heterozygosity
The
heterozygosity of the
Candida genome exceeds that found in other genomes and is widespread among clinical isolates. Non-synonymous
single base polymorphisms result in two proteins that differ in one or several amino acids that may confer functional differences for each protein. This situation considerably increases the number of different proteins encoded by the genome.
Further Information
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