Evidence map›Paper›PMID 41047914›Full record

ArticleJournal of clinical laboratory analysis2025

A Comparative Evaluation of Exoenzyme Production, Biofilm Development, and Cell Surface Hydrophobicity in Dominant Genotypes of Candida albicans.

Hasti Nouraei, Neda Amirzadeh, Fatemeh Ahmadi, Keyvan Pakshir

Abstract readComparative Study
In one paragraph

Article in Journal of clinical laboratory analysis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Hasti NouraeiDepartment of Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0002-5703-5357
Neda AmirzadehDepartment of Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Fatemeh AhmadiDepartment of Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Keyvan PakshirDepartment of Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0001-7809-4690

Funding

Shiraz University of Medical Sciences 31009
6 · The paper itself

Abstract

backgroundCandida albicans exhibits significant genotypic diversity, and genotypes A and C are the most predominant clinical isolates. The aim of this study was to evaluate the virulence traits of these genotypes, focusing on exoenzyme production, biofilm formation, and cell surface hydrophobicity (CSH) property.

methodsA total of 15 genotype A and 15 genotype C clinical C. albicans isolates were evaluated for proteinase, phospholipase, and esterase activities using standard methods. Biofilm formation was quantified using a microtiter plate assay, and CSH was measured using a water-octane two-phase assay.

resultsThe study found that Genotype C had higher proteinase and phospholipase activity but no esterase production, while 40% of Genotype A isolates showed strong esterase activity. Biofilm formation and CSH did not differ significantly, though Genotype A trended toward stronger biofilm formation.

conclusionThis study highlights how genotypic variation in C. albicans influences virulence, with Genotype C exhibiting a distinct profile (high proteinase/phospholipase, no esterase) that may enhance pathogenicity, while Genotype A shows adaptability through variable enzyme production and stronger biofilm trends. These differences underscore the need for genotype-specific diagnostics and targeted therapies to improve candidiasis treatment.

Indexed as

BiofilmsCandida albicansFungal ProteinsGenotypeHumansHydrophobic and Hydrophilic InteractionsPeptide HydrolasesPhospholipasesVirulenceFungal ProteinsPeptide HydrolasesPhospholipasesbiofilmCandida albicanscell surface hydrophobicityexoenzymesgenotypes

Identifiers

PMID41047914
PMCPMC12640783

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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.