Related Experiment Video
Updated: May 6, 2026

The Nematode Caenorhabditis Elegans - A Versatile In Vivo Model to Study Host-microbe Interactions
Published on: October 18, 2017
Ctr9 promotes virulence of Candida albicans by regulating methionine metabolism
Jiyeon Park1, Shinae Park1, Jueun Kim1
1Department of Molecular Bioscience, College of Biomedical Science, Kangwon National University, Chuncheon, Republic of Korea.
Abstract:
Candida albicans, a part of normal flora, is an opportunistic fungal pathogen and causes severe health issues in immunocompromised patients. Its pathogenicity is intricately linked to the transcriptional regulation of its metabolic pathways. Paf1 complex (Paf1C) is a crucial transcriptional regulator that is highly conserved in eukaryotes. The objective of this study was to explore the role of Paf1C in the metabolic pathways and how it influences the pathogenicity of C. albicans. Paf1C knockout mutant strains of C. albicans (ctr9Δ/Δ, leo1Δ/Δ, and cdc73Δ/Δ) were generated using the CRISPR-Cas9 system. To investigate the effect of Paf1C on pathogenicity, macrophage interaction assays and mouse survival tests were conducted. The growth patterns of the Paf1C knockout mutants were analyzed through spotting assays and growth curve measurements. Transcriptome analysis was conducted under yeast conditions (30°C without serum) and hyphal conditions (37°C with 10% FBS), to further elucidate the role of Paf1C in the pathogenicity of C. albicans. CTR9 deletion resulted in the attenuation of C. albicans virulence, in macrophage and mouse models. Furthermore, we confirmed that the reduced virulence of the ctr9Δ/Δ mutant can be attributed to a decrease in C. albicans cell abundance. Moreover, transcriptome analysis revealed that metabolic processes required for cell proliferation are impaired in ctr9Δ/Δ mutant. Notably, CTR9 deletion led to the downregulation of methionine biosynthetic genes and the cAMP-PKA signaling pathway-related hypha essential genes, which are pivotal for virulence. Our results suggest that Ctr9-regulated methionine metabolism is a crucial factor for determining C. albicans pathogenicity.
Insights
The Paf1 complex (Paf1C) regulates metabolic pathways in Candida albicans. Deleting CTR9, a Paf1C component, reduces fungal virulence by impairing methionine metabolism and cell proliferation.
Area of Science:
- Mycology
- Molecular Biology
- Pathogenesis
Background:
- Candida albicans is an opportunistic fungal pathogen.
- Its pathogenicity is linked to metabolic pathway regulation.
- The Paf1 complex (Paf1C) is a conserved transcriptional regulator.
Purpose of the Study:
- To investigate the role of Paf1C in C. albicans metabolic pathways.
- To determine how Paf1C influences C. albicans pathogenicity.
Main Methods:
- Generated Paf1C knockout mutant strains using CRISPR-Cas9.
- Assessed pathogenicity via macrophage interaction and mouse survival assays.
- Analyzed growth patterns and performed transcriptome analysis under various conditions.
Main Results:
- CTR9 deletion attenuated C. albicans virulence in vitro and in vivo.
- Reduced virulence correlated with decreased cell abundance and impaired metabolic processes.
- CTR9 deletion downregulated methionine biosynthesis and essential hyphal genes.
Conclusions:
- Ctr9 plays a vital role in C. albicans pathogenicity.
- Methionine metabolism regulated by Ctr9 is crucial for virulence.
- Paf1C is a key regulator of C. albicans virulence and metabolic processes.
Related Concept Videos
Amino Acid Catabolism
Gene Regulation in Microbial Communities: Quorum Sensing
Transduction
Fungal Phylum Microsporidia
Regulation of Bacterial Virulence

