Evidence map›Paper›PMID 42246768›Full record

ArticleBioMed research international2026

Molecular Identification and Antifungal Susceptibility Patterns of Candida Species in Pediatric Patients at Tabriz Children's Hospital.

Kamran Hosseini, Behrooz Naghili Hokmabadi, Narges Aslani, Taraneh Mirzai, Mahdieh Manafi Shabestari, Mohammad Ahangarzadeh Rezaee, Mohammad Bagher Hosseini, Azita Dilmaghani

Abstract read
In one paragraph

Article in BioMed research international, 2026. 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

8 authors.

Kamran HosseiniShiraz Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran, sums.ac.ir.ORCID https://orcid.org/0000-0003-1189-7143
Behrooz Naghili HokmabadiInfectious and Tropical Diseases Research Center, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0009-0003-1939-2016
Narges AslaniDepartment of Parasitology and Mycology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran, umsu.ac.ir.ORCID https://orcid.org/0000-0003-4142-2173
Taraneh MirzaiDepartment of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0009-0007-5316-8279
Mahdieh Manafi ShabestariDepartment of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.
Mohammad Ahangarzadeh RezaeePediatric Health Research Center, Tabriz University of Medical Science, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0000-0003-2172-0587
Mohammad Bagher HosseiniDepartment of Microbiology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0000-0001-9067-9392
Azita DilmaghaniDepartment of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0000-0001-6556-8332

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Candida species are significant opportunistic pathogens, particularly in immunocompromised pediatric populations. With the increasing incidence of invasive candidiasis in neonatal and pediatric intensive care units, accurate species identification and antifungal susceptibility profiling have become critical for effective treatment. This dual-phase study is aimed at: (1) identifying Candida species from clinical samples using conventional and molecular methods (rDNA-ITS sequencing), and (2) evaluating antifungal susceptibility patterns against fluconazole, itraconazole, amphotericin B, and caspofungin. A total of 97 clinical isolates were obtained from pediatric patients for molecular identification, with 67 isolates successfully subcultured and evaluated for antifungal susceptibility testing. Species identification involved culture on selective media, microscopic examination, DNA extraction, and ITS region sequencing. Antifungal susceptibility testing was performed using the broth microdilution method (CLSI M27 standard) with RPMI-1640 medium, incubating at 35°C for 48 h. Minimum inhibitory concentration (MIC) endpoints were determined visually. Molecular identification revealed the following distribution: C. glabrata (50 isolates, 51.5%), C. albicans/dubliniensis complex (34, 35.1%), C. kefyr (5, 5.2%), C. krusei (6, 6.2%), and C. tropicalis (2, 2.1%). Susceptibility testing showed widespread resistance to fluconazole (particularly in C. glabrata, C. albicans, and C. krusei) and amphotericin B; variable resistance to itraconazole (with 100% susceptibility in C. kefyr); and universal susceptibility to caspofungin (97.4%-100% across species). Our findings highlight a concerning epidemiological shift toward nonalbicans species, predominantly C. glabrata, with distinct resistance profiles. While caspofungin remains highly effective, the observed resistance patterns underscore the necessity of routine antifungal susceptibility testing to guide therapy and prevent treatment failure in pediatric candidiasis.

Indexed as

Antifungal AgentsCandidaCandidiasisAmphotericin BCaspofunginChildChild, PreschoolDrug Resistance, FungalFemaleFluconazoleHospitals, PediatricHumansInfantItraconazoleLipopeptidesMaleAmphotericin BAntifungal AgentsCaspofunginFluconazoleItraconazoleLipopeptidesantifungal susceptibilitybroth microdilutionC. albicansCandida speciesdrug resistanceITS sequencingpediatric candidiasis

Identifiers

PMID42246768
PMCPMC13238512

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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.