Evidence map›Paper›PMID 26346253›Full record

ArticleBMC genomics2015

Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris.

Sharanya Chatterjee, Shuba Varshini Alampalli, Rishi Kumar Nageshan, Sivarajan T Chettiar, Sangeeta Joshi, Utpal S Tatu

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 151 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed, 1 pooled it
11.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

151 citing papers in PubMed, 1 synthesis or guideline pooled it, 243 citations in OpenAlex.

  1. Pooled it
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  7. UnderstandingJournal of medical microbiology · 2026
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  18. Inhibitory effect of copper chelators on the budding inAntimicrobial agents and chemotherapy · 2025
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91 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Sharanya ChatterjeeDepartment of Biochemistry, Indian Institute of Science, Bengaluru, Karnataka, India, 560012. sharanya@biochem.iisc.ernet.in.
Shuba Varshini AlampalliDepartment of Biochemistry, Indian Institute of Science, Bengaluru, Karnataka, India, 560012. shubavarsh@gmail.com.
Rishi Kumar NageshanDepartment of Biochemistry, Indian Institute of Science, Bengaluru, Karnataka, India, 560012. rishikumar.n@gmail.com.
Sivarajan T ChettiarDepartment of Biochemistry, Indian Institute of Science, Bengaluru, Karnataka, India, 560012. siv4who@biochem.iisc.ernet.in.
Sangeeta JoshiManipal Hospital, Bengaluru, Karnataka, India. sangeeta.joshi@manipalhospitals.com.
Utpal S TatuDepartment of Biochemistry, Indian Institute of Science, Bengaluru, Karnataka, India, 560012. tatu@biochem.iisc.ernet.in.
Manipal Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCandida auris is a multidrug resistant, emerging agent of fungemia in humans. Its actual global distribution remains obscure as the current commercial methods of clinical diagnosis misidentify it as C. haemulonii. Here we report the first draft genome of C. auris to explore the genomic basis of virulence and unique differences that could be employed for differential diagnosis.

resultsMore than 99.5 % of the C. auris genomic reads did not align to the current whole (or draft) genome sequences of Candida albicans, Candida lusitaniae, Candida glabrata and Saccharomyces cerevisiae; thereby indicating its divergence from the active Candida clade. The genome spans around 12.49 Mb with 8527 predicted genes. Functional annotation revealed that among the sequenced Candida species, it is closest to the hemiascomycete species Clavispora lusitaniae. Comparison with the well-studied species Candida albicans showed that it shares significant virulence attributes with other pathogenic Candida species such as oligopeptide transporters, mannosyl transfersases, secreted proteases and genes involved in biofilm formation. We also identified a plethora of transporters belonging to the ABC and major facilitator superfamily along with known MDR transcription factors which explained its high tolerance to antifungal drugs.

conclusionsOur study emphasizes an urgent need for accurate fungal screening methods such as PCR and electrophoretic karyotyping to ensure proper management of fungemia. Our work highlights the potential genetic mechanisms involved in virulence and pathogenicity of an important emerging human pathogen namely C. auris. Owing to its diversity at the genomic scale; we expect the genome sequence to be a useful resource to map species specific differences that will help develop accurate diagnostic markers and better drug targets.

Indexed as

Drug Resistance, FungalDrug Resistance, MultipleGenome, FungalAmino Acid SequenceAntifungal AgentsCandidaCandidiasisCodonComputational BiologyDNA, IntergenicEvolution, MolecularGenetic LociHigh-Throughput Nucleotide SequencingHumansMating FactorMicrobial Sensitivity TestsAntifungal AgentsCodonDNA, IntergenicMating FactorPeptides

Identifiers

PMID26346253
PMCPMC4562351
OpenAlexW1817471568

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.