Mutations in transcription factor Mrr2p contribute to fluconazole resistance in clinical isolates of Candida albicans

Wang, Y; Liu, JY; Shi, C; Li, WJ; Zhao, Y; Yan, L; Xiang, MJ

HERO ID

3044641

Reference Type

Journal Article

Year

2015

Language

English

PMID

26404130

HERO ID 3044641
In Press No
Year 2015
Title Mutations in transcription factor Mrr2p contribute to fluconazole resistance in clinical isolates of Candida albicans
Authors Wang, Y; Liu, JY; Shi, C; Li, WJ; Zhao, Y; Yan, L; Xiang, MJ
Journal International Journal of Antimicrobial Agents
Volume 46
Issue 5
Page Numbers 552-559
Abstract The Candida albicans zinc cluster proteins are a family of transcription factors (TFs) that play essential roles in the development of antifungal drug resistance. Gain-of-function mutations in several TFs, such as Tac1p, Mrr1p and Upc2p, have been previously well documented in azole-resistant clinical C. albicans isolates. Mrr2p (multidrug resistance regulator 2) is a novel TF controlling expression of the ABC transporter gene CDR1 and mediating fluconazole resistance. In this study, the relationship between naturally occurring mutations in MRR2 and fluconazole resistance in clinical C. albicans isolates was investigated. Among a group of 20 fluconazole-resistant clinical C. albicans and 10 fluconazole-susceptible C. albicans, 12 fluconazole-resistant isolates overexpressed CDR1 by at least two-fold compared with the fluconazole-susceptible isolates. Of these 12 resistant isolates, three (C7, C9, C15) contained 11 identical missense mutations, 6 of which occurred only in the azole-resistant isolates. The contribution of these mutations to CDR1 overexpression and therefore to fluconazole resistance was further verified by generating recombinant strains containing the mutated MRR2 gene. The mutated MRR2 alleles from isolate C9 contributed to an almost six-fold increase in CDR1 expression and an eight-fold increase in fluconazole resistance; the missense mutations S466L and T470N resulted in an increase in CDR1 expression of more than two-fold and a four-fold increase in fluconazole resistance. In contrast, the other four missense mutations conferred only two- to four-fold increases in fluconazole resistance, with no significant increase in CDR1 expression. These findings provide some insight into the mechanism by which MRR2 regulates C. albicans multidrug resistance.
Doi 10.1016/j.ijantimicag.2015.08.001
Pmid 26404130
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English