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Repository series · ncbi-prjeb32538

Persistence and spread of Candida auris in various hospitals across Kuwait and their susceptibility to antifungal drugs

KuwaitPathogen genomics and infectious diseaseRepository record

Background: Candida auris has recently attracted worldwide attention because of its intrinsic resistance to multiple antifungal agents and proclivity of nosocomial transmission despite normal decontamination procedures. Here, we describe isolation frequency and spread of C. auris among patients in various hospitals in Kuwait during 2014-2018. Susceptibility to antifungal drugs and molecular basis of resistance to fluconazole, voriconazole and micafungin was also studied.Methods: A total of 314 C. auris isolates obtained from 126 patients in eight hospitals were studied. All isolates were identified by PCR amplification and/or PCR-sequencing of rDNA. Antifungal susceptibility was determined by Etest. Fluconazole resistance was studied by PCR-sequencing of ERG11 gene fragment while resistance to micafungin was studied by PCR-sequencing of hotspot 1 region of FKS1 gene.Results: Of 314 C. auris isolates, 58 (18.4%) came from blood specimens of 43 patients including 42 strains isolated from 30 patients in 2018. Most non-blood isolates (n=256) were cultured from urine (n=124) and respiratory specimens (n=98). The isolation frequency of bloodstream C. auris strains was statistically higher (42 of 307, 13.7%) in 2018 as compared to 2014-2017 (16 of 964, 1.7%) (P=0.000). Similarly, isolation frequency of C. auris was statistically higher (P=0.000) from non-blood specimens in 2018 (97 of 722, 13.4%) as compared to 2014-2017 (159 of 2847, 6.4%). Of total C. auris isolates during the two period, more bloodstream isolates (42 of 139) were cultured in 2018 than during 2014-2017 (16 of 175) (P=0.000). Resistance to amphotericin B, fluconazole, voriconazole and micafungin was detected in 27.1%, 100%, 41.1% and 1.7% isolates, respectively. No isolate was resistant to flucytosine. Fluconazole-resistant isolates contained either Y132F or K143R mutation in ERG11. Isolates with K143R mutation were additionally resistant to voriconazole. Micafungin-resistant isolates contained S639F mutation in hotspot 1 region of FKS1. Conclusions: Our study highlights continued spread of C. auris in major hospitals across Kuwait and its increasing role as a bloodstream pathogen in 2018 warranting continuous surveillance. Cross-resistance to voriconazole was seen only in isolates with K143R mutation in ERG11 while micafungin-resistant isolates harbored S639F mutation in hotspot 1 of FKS1.

Repository interpretation

The accession and its GCC connection are verified. Registration alone does not establish that the broader research programme remains active.

01 / Project overview

What the record establishes.

Geographic scope
Kuwait connection indexed in BioProject metadata
Project type
Repository project
Research domain
Pathogen genomics and infectious disease
Years
2019–
Lifecycle status
repository_recorded
Status basis
Registered in NCBI BioProject on 2019/05/15; operational lifecycle is not asserted.
Status evidence date
2019-05-15
Scale
1 BioProject accession grouped by matching submitter, date, data type and narrative.

02 / Organizations and population

Who and what the project connects.

Lead organizations
Kuwait University
Partner organizations
Not stated
Organism / population
Not stated

03 / Data and access

What exists and how it can be reached.

Data types

  • Transcriptome or Gene expression
  • Sequencing
  • Genome

Data access

Public repository metadata with linked data where supplied by the submitter

Identifiers

  • BioProjectPRJEB32538

04 / Evidence and provenance

Why the record is included.

Inclusion basis

Exact country-name match in authoritative NCBI BioProject metadata; repeated submissions are grouped into one Atlas series.

Editorial note

Repository verification confirms the accession and regional connection, not whether the broader research programme remains active.

Sources

  1. primary record source Verified 2026-08-15

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