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.

G3 (Bethesda, Md.)
|July 12, 2017
PubMed

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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