Candida albicans is an opportunistic pathogen causing morbidity and mortality in patients with immuno-dysfunction. Multidrug resistant Candida has emerged as significant health problem. The White laboratory is at the forefront in studying the cellular and molecular mechanisms of multidrug resistance in Candida. We propose to further define the transcriptional controls involved in the drug resistant phenotype of a well-defined series of isolates from a single AIDS patient.
The specific aims of this proposal are: 1) to identify the transcriptional controls of the MDR1 promoter from the azole-sensitive and azole-resistant isolates, 2) to determine the domains interacting with transcription factors involved in azole-resistance, drug induction and specified environmental states, and 3) to determine if the CAP1p or other transcription factors interact with MDR1 promoter. Promoter deletion analysis will be used to identify the basal level transcription, silencers and enhancers utilized by these promoters. Gel mobility shift assays, competition experiments and DNase I footprint analysis will further define protein:DNA interactions. Finally, characterized transcription factors such as CAP1 will be used in gel mobility shift assays, competition experiments and antibody supershifts to determine the interactions between these factors and the drug resistant MDR1 promoter. This project is designed to generate valuable information that could lead to development of drugs or methods to control multidrug resistance in Candida. In addition, it will further Candida research by being a comprehensive study on the transcriptional controls important in a multidrug resistance phenotype.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
3F32AI010497-01S1
Application #
6420821
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Program Officer
Baron, Patricia A
Project Start
2000-04-01
Project End
Budget Start
2001-04-01
Budget End
2002-03-31
Support Year
1
Fiscal Year
2001
Total Cost
$45,560
Indirect Cost
Name
Seattle Biomedical Research Institute
Department
Type
DUNS #
City
Seattle
State
WA
Country
United States
Zip Code
98109
Johnson, Britney; VanBlargan, Laura A; Xu, Wei et al. (2018) Human IFIT3 Modulates IFIT1 RNA Binding Specificity and Protein Stability. Immunity 48:487-499.e5
Harry, Jo Beth; Oliver, Brian G; Song, Jia L et al. (2005) Drug-induced regulation of the MDR1 promoter in Candida albicans. Antimicrob Agents Chemother 49:2785-92
Song, Jia L; Harry, Jo Beth; Eastman, Richard T et al. (2004) The Candida albicans lanosterol 14-alpha-demethylase (ERG11) gene promoter is maximally induced after prolonged growth with antifungal drugs. Antimicrob Agents Chemother 48:1136-44
Harry, J B; Song, J L; Lyons, C N et al. (2002) Transcription initiation of genes associated with azole resistance in Candida albicans. Med Mycol 40:73-81