Evidence map›Paper›PMID 42348119›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2026

Unraveling clade-specific differences in Candida auris: evolution, adaptation, and pathogenicity.

Preeti Sharma, Vinay Kumar Bari, Ritu Pasrija

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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Preeti SharmaDepartment of Biochemistry, Maharshi Dayanand University, Rohtak, Haryana, 124001, India.
Vinay Kumar BariDepartment of Biochemistry, School of Basic Sciences, Central University of Punjab, Bathinda, India.
Ritu PasrijaDepartment of Biochemistry, Maharshi Dayanand University, Rohtak, Haryana, 124001, India. ritupasrija@yahoo.com.ORCID https://orcid.org/0000-0003-2851-5391

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since its 2009 emergence, Candida auris (now also known as Candidozyma auris) has evolved from a rare isolate into a global "critical priority" pathogen. This rapid expansion is defined by its unique population structure consisting of six distinct genomic clades with starkly different evolutionary trajectories, phenotypic traits, and clinical risks. We conducted a systematic synthesis of literature from PubMed, Scopus, and Google Scholar (2009-2026), focusing on comparative genomics, clade-specific virulence, and diagnostic accuracy. A total of 64 studies were analyzed to identify patterns in clade divergence and antifungal resistance. Our analysis reveals that C. auris is not a monolithic threat but a complex of diverse lineages with specialized adaptations. Clade I (South Asian) and Clade IV (South American) represent the highest clinical risk due to hyper-virulence and high rates of multi-drug resistant (MDR) strains. In contrast, Clade II (East Asian) was initially associated with localized ear infections; recent genomic data show an expanding pathogenic profile with emerging bloodstream infections. Our review also identifies Clade V (Iranian) as a genetically distinct group and highlights the recent identification of Clade VI (Indomalayan) as a distinct lineage, suggesting a long-standing environmental reservoir. Furthermore, we identify critical "blind spots" in automated diagnostic platforms (VITEK

Indexed as

BiofilmC. aurisCladesMelaninMulti-drug resistanceVirulence

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