Voriconazole resistance genes in Aspergillus flavus clinical isolates.


Journal

Journal de mycologie medicale
ISSN: 1773-0449
Titre abrégé: J Mycol Med
Pays: France
ID NLM: 9425651

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 06 05 2019
revised: 05 01 2020
accepted: 18 03 2020
pubmed: 5 5 2020
medline: 21 10 2020
entrez: 5 5 2020
Statut: ppublish

Résumé

The present study was designed to discover novel biomarkers involved in voriconazole resistance in clinical isolates of Aspergillus flavus. Two voriconazole non-wild-type and two voriconazole-wild-type A. flavus clinical isolates were selected to evaluate possible molecular mechanism involved in A. flavus resistance to voriconazole using the mutation assessment, Quantitative real- time PCR of cyp51A and cyp51C genes and complementary DNA- amplified fragment length polymorphism technique. No mutations were seen in the cyp51A and cyp51C genes in voriconazole non-wild-type isolates compared to wild- type and reference strains. Regarding to mRNA expression results, no changes were observed in expression fold of cyp51A and cyp51C mRNA expression level in first non- wild- type isolate compared to wild-type isolate. For second isolate cyp51C mRNA expression level was down regulated (5.6 fold). The set of genes including ABC fatty acid transporter XM- 002375835 and aldehydereductase XM- 002376518 and three unknown functional genes were identified. Based on results, the over-expression of AKR1 and ABC fatty acid transporter in the voriconazole non- wild- type isolates suggests these genes could represent a novel molecular marker linked to the voriconazole resistance in A. flavus. The results obtained in this study showed a novel finding as the authors identified AKR1 and ABC fatty acid transporter genes as possible voriconazole target genes in Iranian clinical isolates of A. flavus.

Identifiants

pubmed: 32362445
pii: S1156-5233(20)30050-0
doi: 10.1016/j.mycmed.2020.100953
pii:
doi:

Substances chimiques

Antifungal Agents 0
Biomarkers 0
Fungal Proteins 0
Cytochrome P-450 Enzyme System 9035-51-2
cytochrome P-450 CYP51A, Aspergillus EC 1.14.14.-
Sterol 14-Demethylase EC 1.14.14.154
Voriconazole JFU09I87TR

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

100953

Informations de copyright

Copyright © 2020. Published by Elsevier Masson SAS.

Auteurs

F Zaini (F)

Department of Medical Parasitology and Mycology, Tehran University of Medical Sciences, Tehran, Iran.

E Lotfali (E)

Department of Medical Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

A Fattahi (A)

Center for Research and Training in Skin Diseases and Leprosy, Tehran University of Medical Sciences, Tehran, Iran. Electronic address: afattahi@sina.tums.ac.ir.

E Siddig (E)

Mycetoma Research Center, University of Khartoum, Khartoum, Sudan.

S Farahyar (S)

Microbial Biotechnology Research Center(MBIRC), School of Medicine, Iran University of Medical Sciences, Tehran, Iran; Department of Medical Mycology, Faculty of Medical Sciences, Iran University of Medical Sciences, Tehran, Iran.

E Kouhsari (E)

Clinical Microbiology Research Center, Ilam University of Medical Sciences, Ilam, Iran.

M Saffari (M)

Department of Medical Genetics, Tehran University of Medical Sciences, Tehran, Iran.

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Classifications MeSH