Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Evaluation of Mrna Expression Levels of Cyp51a and Mdr1, Candidate Genes for Voriconazole Resistance in Aspergillus Flavus Publisher



Fattahi A1 ; Zaini F1 ; Kordbacheh P1 ; Rezaie S1 ; Safara M1 ; Fateh R2 ; Farahyar S3 ; Kanani A1 ; Heidari M4, 5
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Medical Mycology and Parasitology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Medical Mycology and Parasitology, Iran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Microbiology and Immunology, Qom University of Medical Sciences, Qom, Iran
  4. 4. Department of Medical Genetics, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Experimental Research Center, Tehran University of Medical Sciences, Tehran, Iran

Source: Jundishapur Journal of Microbiology Published:2015


Abstract

Background: Voriconazole Resistance (VRC-R) in Aspergillus flavus isolates impacts the management of aspergillosis, since azoles are the first choice for prophylaxis and therapy. However, to the best of our knowledge, the mechanisms underlying voriconazole resistance are poorly understood. Objectives: The present study was designed to evaluate mRNA expression levels of cyp51A and mdr1 genes in voriconazole resistant A. flavus by a Real-Time Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) technique. Materials and Methods: Five A. flavus isolates with resistance to VRC were examined by a RT-PCR approach. Results: Four out of five isolates revealed cyp51A and mdr1 mRNA overexpression. Interestingly, the isolate, which was negative for cyp51A and mdr1 mRNA expression showed a high voriconazole Minimum Inhibitory Concentration (MIC). Furthermore, a computational-based analysis predicted that voriconazole resistance could be mediated through cooperation with a network protein interaction. Conclusions: Our experimental and in silico findings may provide new insight in the complex molecular pathways of drug resistance and also could assist design an efficient therapeutic strategy for aspergillosis treatment. © 2015 Ahvaz Jundishapur University of Medical Sciences.
Experts (# of related papers)