Phenotypic characterization of a Candida albicans strain deficient in its major exoglucanase
Abstract
Summary: Both alleles of the XOG1 gene of Candida albicans, which encodes a protein with exoglucanase activity, were sequentially disrupted. Enzymic analysis of either cell extracts or culture supernatants of disrupted strains revealed that this gene is responsible for the major exoglucanase activity in C. albicans, although residual exoglucanase activity could still be detected.xog1 null mutants showed similar growth rates in both rich and minimal liquid medium as compared to the wild-type strain, indicating that the enzyme is not essential for C. albicans growth. In addition, no differences were observed between wild-type and xog1 null mutants with respect to their ability to undergo dimorphic transition. However, small but repeatable differences were found between the wild-type and the null mutant with respect to susceptibility to chitin and glucan synthesis inhibitors. Using a murine model of experimental infection, no significant differences in virulence were observed. The xog 1null strain is thus a suitable recipient for studying Candida gene expression using the exoglucanase as a reporter gene.
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Among the regulated cell wall genes were homologues of C. albicans glucanase genes (XOG1 and ENG1) as well as genes encoding putative adhesins (ALS4, IFF4, and PGA6).
“Among the regulated cell wall genes were homologues of C. albicans glucanase genes (XOG1 and ENG1) (46, 47) as well as genes encoding putative adhesins (ALS4, IFF4, and PGA6) (48–50).”
From Transcriptomics and Phenotyping Define Genetic Signatures Associated with Echinocandin Resistance in Candida auris (2022) · cites this paper as [46]
PGA6 (B9J08_001366) was among the upregulated cell wall-related genes in ECN-R isolates, in addition to Putative GPI-anchored protein (PGA31) and the exoglucanase gene XOG1.
“PGA6 (B9J08_001366), a homologue of a putative C. albicans glycosylphosphatidylinositol (GPI)-anchored adhesion molecule (49), was among the upregulated cell wall-related genes in ECN-R isolates, in addition to Putative GPI-anchored protein (PGA31) and the exoglucanase gene XOG1 (46) (Fig. 3A).”
From Transcriptomics and Phenotyping Define Genetic Signatures Associated with Echinocandin Resistance in Candida auris (2022) · cites this paper as [46]
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References 55 · Cited by 47
- Authors
- del Mar González, M., Díez-Orejas, R., Molero, G., álvarez, A. M., Pla, J., Pla, J., Nombela, C., & Sánchez-PéArez, M.
- Affiliations
- Department of Microbiology II, Faculty of Pharmacy, University Complutense of Madrid, 28040 Madrid, Spain
- Universidad Complutense de Madrid (ES)
- Flow and Confocal Cytometry Unit (CCF), Faculty of Pharmacy, University Complutense of Madrid, 28040 Madrid, Spain
- ORCID
- Molero, Gloria
- Venue
- Microbiology
- Publisher
- Microbiology Society
- Published
- 1997-09-01
- Volume
- 143
- Issue
- 9
- Pages
- 3023-3032
- ISSN
- 1350-0872 (ISSN-L)
- 1465-2080
- OpenAlex
- W2141096783
- Cited by
- 47
- References
- 55
- Citations by year
- 2025: 2 · 2024: 2 · 2022: 3 · 2021: 2 · 2020: 1 · 2019: 3 · 2018: 2 · 2017: 1 · 2016: 2 · 2014: 3 · 2012: 3
- FWCI
- 0.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
- Keywords
- Candida albicans, cellobiohydrolase, gene disruption, knockout mutants, chitin synthesis inhibitors, dimorphic transition, virulence, reporter genes, fungal cell wall
- MeSH terms
- Animals, Base Sequence, beta-Glucosidase, Candida albicans, Cell Wall, Genes, Fungal, Mutation, Phenotype, Virulence, Gene Expression, Polymerase Chain Reaction, Genes, Reporter, DNA Primers, Glucan 1,3-beta-Glucosidase, Mice
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