Comparison of gene expression profiles of Candida albicans azole-resistant clinical isolates and laboratory strains exposed to drugs inducing multidrug transporters

Détails

ID Serval
serval:BIB_076596EEE6FB
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Comparison of gene expression profiles of Candida albicans azole-resistant clinical isolates and laboratory strains exposed to drugs inducing multidrug transporters
Périodique
Antimicrobial Agents and Chemotherapy
Auteur(s)
Karababa  M., Coste  A. T., Rognon  B., Bille  J., Sanglard  D.
ISSN
0066-4804 (Print)
Statut éditorial
Publié
Date de publication
08/2004
Volume
48
Numéro
8
Pages
3064-79
Notes
Comparative Study
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Aug
Résumé
Azole resistance in Candida albicans can be due to upregulation of multidrug transporters belonging to ABC (ATP-binding cassette) transporters (CDR1 and CDR2) or major facilitators (CaMDR1). Upregulation of these genes can also be achieved by exposure to fluphenazine, resulting in specific upregulation of CDR1 and CDR2 and by exposure to benomyl, resulting in specific CaMDR1 upregulation. In this study, these two different states of gene upregulation were used to determine coregulated genes that often share similar functions or similar regulatory regions. The transcript profiles of a laboratory strain exposed to these drugs were therefore determined and compared with those of two matched pairs of azole-susceptible and -resistant strains expressing CDR1 and CDR2 (CDR strains) or CaMDR1 (MDR isolates). The results obtained revealed that, among 42 commonly regulated genes (8.6% of all regulated genes) between fluphenazine-exposed cells and CDR isolates, the most upregulated were CDR1 and CDR2 as expected, but also IFU5, RTA3 (which encodes putative membrane proteins), HSP12 (which encodes heat shock protein), and IPF4065 (which is potentially involved in stress response). Interestingly, all but HSP12 and IPF4065 contain a putative cis-acting drug responsive element in their promoters. Among the 57 genes (11.5% of all regulated genes) commonly regulated between benomyl-exposed cells and MDR isolates, the most upregulated were CaMDR1 as expected but also genes with oxido-reductive functions such as IFD genes, IPF5987, GRP2 (all belonging to the aldo-keto reductase family), IPF7817 [NAD(P)H oxido-reductase], and IPF17186. Taken together, these results show that in vitro drug-induced gene expression only partially mimics expression profiles observed in azole-resistant clinical strains. Upregulated genes in both drug-exposed conditions and clinical strains are drug resistance genes but also genes that could be activated under cell damage conditions.
Mots-clé
Antifungal Agents/*pharmacology Azoles/*pharmacology Benomyl/pharmacology Blotting, Northern Candida albicans/drug effects/*genetics Candidiasis/*microbiology Cluster Analysis Fluphenazine/pharmacology Fungal Proteins/biosynthesis/genetics Fungicides, Industrial/pharmacology Gene Expression Regulation, Fungal/*genetics Membrane Transport Proteins/biosynthesis/genetics Oligonucleotide Array Sequence Analysis P-Glycoprotein/biosynthesis/genetics P-Glycoproteins/*biosynthesis/*genetics RNA, Fungal/biosynthesis/genetics Regulatory Sequences, Nucleic Acid/genetics Reproducibility of Results Reverse Transcriptase Polymerase Chain Reaction Transcription, Genetic/genetics Up-Regulation/genetics
Pubmed
Web of science
Création de la notice
25/01/2008 15:40
Dernière modification de la notice
03/03/2018 13:28
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