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Updated: Feb 26, 2026

Whole Genome Sequencing of Candida glabrata for Detection of Markers of Antifungal Drug Resistance
Published on: December 28, 2017
Whole Genome Sequence of the Heterozygous Clinical Isolate Candida krusei 81-B-5
Christina A Cuomo1, Terrance Shea2, Bo Yang3
1Infectious Disease and Microbiome Program, and cuomo@broadinstitute.org aforche@bowdoin.edu.
Abstract:
Candida krusei is a diploid, heterozygous yeast that is an opportunistic fungal pathogen in immunocompromised patients. This species also is utilized for fermenting cocoa beans during chocolate production. One major concern in the clinical setting is the innate resistance of this species to the most commonly used antifungal drug fluconazole. Here, we report a high-quality genome sequence and assembly for the first clinical isolate of C. krusei, strain 81-B-5, into 11 scaffolds generated with PacBio sequencing technology. Gene annotation and comparative analysis revealed a unique profile of transporters that could play a role in drug resistance or adaptation to different environments. In addition, we show that, while 82% of the genome is highly heterozygous, a 2.0 Mb region of the largest scaffold has undergone loss of heterozygosity. This genome will serve as a reference for further genetic studies of this pathogen.
Insights
We sequenced the Candida krusei genome, revealing unique transporters linked to fluconazole resistance in this opportunistic pathogen. This reference genome aids future studies on antifungal drug resistance and adaptation.
Area of Science:
- Medical Mycology
- Genomics
- Antimicrobial Resistance
Background:
- Candida krusei is an opportunistic fungal pathogen causing infections in immunocompromised individuals.
- This yeast exhibits inherent resistance to fluconazole, a primary antifungal medication.
- C. krusei is also used in cocoa fermentation for chocolate production.
Purpose of the Study:
- To generate a high-quality genome sequence and assembly for a clinical isolate of Candida krusei.
- To identify genetic elements potentially contributing to drug resistance and environmental adaptation.
Main Methods:
- PacBio sequencing technology was employed for genome sequencing and assembly.
- Gene annotation and comparative genomic analysis were performed.
- Analysis of heterozygosity and loss of heterozygosity regions was conducted.
Main Results:
- A high-quality genome sequence and assembly for the clinical isolate C. krusei 81-B-5 were generated into 11 scaffolds.
- A unique profile of transporters potentially involved in drug resistance was identified.
- While 82% of the genome is heterozygous, a 2.0 Mb region showed loss of heterozygosity.
Conclusions:
- The generated genome serves as a valuable reference for Candida krusei.
- Understanding genetic factors, such as transporters and heterozygosity, is crucial for addressing fluconazole resistance.
- This genomic resource will facilitate future research into C. krusei pathogenesis and adaptation.
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