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Whole Genome Sequencing of Candida glabrata for Detection of Markers of Antifungal Drug Resistance
Published on: December 28, 2017
Sequence and analysis of the genome of the pathogenic yeast Candida orthopsilosis
Alessandro Riccombeni1, Genevieve Vidanes, Estelle Proux-Wéra
1School of Biomolecular and Biomedical Science, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
Abstract:
Candida orthopsilosis is closely related to the fungal pathogen Candida parapsilosis. However, whereas C. parapsilosis is a major cause of disease in immunosuppressed individuals and in premature neonates, C. orthopsilosis is more rarely associated with infection. We sequenced the C. orthopsilosis genome to facilitate the identification of genes associated with virulence. Here, we report the de novo assembly and annotation of the genome of a Type 2 isolate of C. orthopsilosis. The sequence was obtained by combining data from next generation sequencing (454 Life Sciences and Illumina) with paired-end Sanger reads from a fosmid library. The final assembly contains 12.6 Mb on 8 chromosomes. The genome was annotated using an automated pipeline based on comparative analysis of genomes of Candida species, together with manual identification of introns. We identified 5700 protein-coding genes in C. orthopsilosis, of which 5570 have an ortholog in C. parapsilosis. The time of divergence between C. orthopsilosis and C. parapsilosis is estimated to be twice as great as that between Candida albicans and Candida dubliniensis. There has been an expansion of the Hyr/Iff family of cell wall genes and the JEN family of monocarboxylic transporters in C. parapsilosis relative to C. orthopsilosis. We identified one gene from a Maltose/Galactoside O-acetyltransferase family that originated by horizontal gene transfer from a bacterium to the common ancestor of C. orthopsilosis and C. parapsilosis. We report that TFB3, a component of the general transcription factor TFIIH, undergoes alternative splicing by intron retention in multiple Candida species. We also show that an intein in the vacuolar ATPase gene VMA1 is present in C. orthopsilosis but not C. parapsilosis, and has a patchy distribution in Candida species. Our results suggest that the difference in virulence between C. parapsilosis and C. orthopsilosis may be associated with expansion of gene families.
Insights
The genome of Candida orthopsilosis was sequenced, revealing gene expansions in Candida parapsilosis that may explain differences in virulence between these closely related fungi.
Area of Science:
- Mycology
- Genomics
- Comparative genomics
Background:
- Candida orthopsilosis is closely related to the pathogenic fungus Candida parapsilosis.
- Unlike C. parapsilosis, C. orthopsilosis is rarely associated with human infections.
Purpose of the Study:
- To sequence and annotate the genome of Candida orthopsilosis.
- To identify genes potentially associated with virulence and understand evolutionary divergence.
Main Methods:
- De novo genome assembly using next-generation sequencing (Illumina, 454) and Sanger sequencing.
- Automated genome annotation pipeline with comparative analysis and manual curation.
- Phylogenetic analysis to estimate divergence times.
Main Results:
- A 12.6 Mb genome assembly on 8 chromosomes with 5700 protein-coding genes.
- High ortholog similarity (5570 genes) with C. parapsilosis, but a greater divergence time.
- Identified gene family expansions (Hyr/Iff, JEN) in C. parapsilosis and horizontal gene transfer of a Maltose/Galactoside O-acetyltransferase gene.
- Observed alternative splicing of TFB3 and presence of a VMA1 intein in C. orthopsilosis.
Conclusions:
- Genome sequencing provides a foundation for studying C. orthopsilosis virulence.
- Gene family expansions in C. parapsilosis relative to C. orthopsilosis may contribute to differential virulence.
- Comparative genomics reveals insights into fungal evolution and gene gain/loss events.
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