Evaluation of mRNA Expression Levels of <i>cyp51A</i> and <i>mdr1</i>, Candidate Genes for Voriconazole Resistance in <i>Aspergillus flavus</i>

AuthorAzam Fattahien
AuthorFarideh Zainien
AuthorParivash Kordbachehen
AuthorSasan Rezaieen
AuthorMahin Safaraen
AuthorRoohollah Fatehen
AuthorShirin Farahyaren
AuthorAli Kananien
AuthorMansour Heidarien
Issued Date2015-12-31en
AbstractBackground:: 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.en
DOIhttps://doi.org/10.5812/jjm.26990en
KeywordDrug Resistanceen
KeywordMinimum Inhibitory Concentrationen
Keyword<i>cyp51A</i>en
Keyword<i>mdr1</i>en
PublisherBrieflandsen
TitleEvaluation of mRNA Expression Levels of <i>cyp51A</i> and <i>mdr1</i>, Candidate Genes for Voriconazole Resistance in <i>Aspergillus flavus</i>en
TypeResearch Articleen

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
jjm-08-12-26990.pdf
Size:
396.44 KB
Format:
Adobe Portable Document Format
Description:
Article/s PDF