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Repository series · ncbi-prjeb26553

ERG6 and ERG2 are major targets conferring reduced susceptibility to amphotericin B in clinical Candida glabrata isolates in Kuwait

KuwaitPathogen genomics and infectious diseaseRepository record

Objectives: Candida glabrata is intrinsically less susceptible to azoles and resistance to echinocandins and amphotericin B has also been detected. Molecular mechanisms of reduced susceptibility (RS) to amphotericin B (AMB) were investigated in C. glabrata strains in Kuwait by sequence analyses of genes involved in ergosterol biosynthesis. Methods: Eight RS-AMB and 5 AMB-susceptible C. glabrata isolates were used. Antifungal susceptibility testing was done by Etest and by reference broth microdilution. PCR-sequencing of three (ERG2, ERG6 and ERG11) genes was performed by using gene-specific primers. Total cell sterol content was analyzed by gas chromatography-mass spectrometry. Phylogenetic relationship among the isolates was investigated by multilocus sequence typing. Results: AMB-susceptible isolates contained only synonymous mutations in ERG2, ERG6 or ERG11 and total sterol content of 1 isolate was similar to reference strain. A nonsynonymous (AGA48AAA, R48K) ERG6 mutation was found in both RS-AMB and AMB-susceptible isolates. Four RS-AMB isolates contained novel nonsense mutations at Trp286/Tyr192/Leu341 and two isolates contained nonsynonymous (V126F or C198F) mutation in ERG6 and their sterol content were consistent with ERG6 deficiency. Two other RS-AMB isolates contained novel nonsynonymous (G119S or G122S) ERG2 mutation and their sterol content were consistent with ERG2 deficiency. Isolate Kw861/13 also contained Y141H + L381M mutations while 7 RS-AMB isolates contained only synonymous mutations in ERG11. All isolates with ERG6/ERG2/ERG11 mutations were genotypically distinct strains. Conclusions: Our data show that ERG6 and ERG2 are major targets conferring RS-AMB in clinical C. glabrata isolates in Kuwait.

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
2018–
Lifecycle status
repository_recorded
Status basis
Registered in NCBI BioProject on 2018/05/03; operational lifecycle is not asserted.
Status evidence date
2018-05-03
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

  • Other
  • Sequencing
  • Genome

Data access

Public repository metadata with linked data where supplied by the submitter

Identifiers

  • BioProjectPRJEB26553

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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