Transcription factor Hap2p regulates antioxidant stress responses to maintain miconazole resistance in Candida albicans

Acquired resistance in Candida albicans brings about a serious challenge to the clinical application of azoles, so it is urgent to elucidate the mechanisms of azole resistance to improve the therapeutic efficiency. In the aim of searching for the potential targets mediating fluconazole resistance, w...

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Main Authors: Yulin Qin, Quanzhen Lv, Hongtao Xu, Yongbing Cao, Bing Han
Format: Article
Language:English
Published: Taylor & Francis Group 2025-01-01
Series:Mycology
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Online Access:https://www.tandfonline.com/doi/10.1080/21501203.2024.2432424
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author Yulin Qin
Quanzhen Lv
Hongtao Xu
Yongbing Cao
Bing Han
author_facet Yulin Qin
Quanzhen Lv
Hongtao Xu
Yongbing Cao
Bing Han
author_sort Yulin Qin
collection DOAJ
description Acquired resistance in Candida albicans brings about a serious challenge to the clinical application of azoles, so it is urgent to elucidate the mechanisms of azole resistance to improve the therapeutic efficiency. In the aim of searching for the potential targets mediating fluconazole resistance, we screened a mutant library of 48 transcription factor deletion Candida albicans strains. The screening results showed that hap2Δ/Δ mutants were significantly more susceptible to azoles, especially to miconazole (MCZ). Under MCZ treatment, the intracellular reactive oxygen species (ROS) were significantly higher in hap2Δ/Δ mutants compared to the control strain SN250. The addition of antioxidants reversed the MCZ-sensitive phenotype caused by the deletion of HAP2. Consistently, the expression of antioxidases responsible for scavenging ROS was shown to decrease in hap2Δ/Δ mutants, suggesting that the transcription factor Hap2p is involved in the regulation of oxidative stress responses in C. albicans. In addition, HAP2 deficiency also resulted in impaired mitochondrial function and affected cellular energy supply, which may be related to the iron deficiency regulated by HAP complex. HAP2 disruption also decreased efflux-mediated resistance of C. albicans, as demonstrated by a significant decrease in Cdr1p expression and a slight decrease in Mdr1p expression in hap2Δ/Δ strains under the action of MCZ. The above results indicate that the transcription factor Hap2p was required for the resistance of C. albicans to azoles, which could provide a new strategy to solve the clinical azoles resistance.
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institution Kabale University
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spelling doaj-art-352f0b0e6ffb4ad398a2c37aa49f28832025-01-06T11:46:13ZengTaylor & Francis GroupMycology2150-12032150-12112025-01-0111410.1080/21501203.2024.2432424Transcription factor Hap2p regulates antioxidant stress responses to maintain miconazole resistance in Candida albicansYulin Qin0Quanzhen Lv1Hongtao Xu2Yongbing Cao3Bing Han4Institute of Vascular Disease, Shanghai TCM-Integrated Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaSchool of Pharmacy, Naval Medical University, Shanghai, ChinaSchool of Pharmacy, Naval Medical University, Shanghai, ChinaInstitute of Vascular Disease, Shanghai TCM-Integrated Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaDepartment of Pharmacy, Minhang Hospital, Fudan University, Shanghai, ChinaAcquired resistance in Candida albicans brings about a serious challenge to the clinical application of azoles, so it is urgent to elucidate the mechanisms of azole resistance to improve the therapeutic efficiency. In the aim of searching for the potential targets mediating fluconazole resistance, we screened a mutant library of 48 transcription factor deletion Candida albicans strains. The screening results showed that hap2Δ/Δ mutants were significantly more susceptible to azoles, especially to miconazole (MCZ). Under MCZ treatment, the intracellular reactive oxygen species (ROS) were significantly higher in hap2Δ/Δ mutants compared to the control strain SN250. The addition of antioxidants reversed the MCZ-sensitive phenotype caused by the deletion of HAP2. Consistently, the expression of antioxidases responsible for scavenging ROS was shown to decrease in hap2Δ/Δ mutants, suggesting that the transcription factor Hap2p is involved in the regulation of oxidative stress responses in C. albicans. In addition, HAP2 deficiency also resulted in impaired mitochondrial function and affected cellular energy supply, which may be related to the iron deficiency regulated by HAP complex. HAP2 disruption also decreased efflux-mediated resistance of C. albicans, as demonstrated by a significant decrease in Cdr1p expression and a slight decrease in Mdr1p expression in hap2Δ/Δ strains under the action of MCZ. The above results indicate that the transcription factor Hap2p was required for the resistance of C. albicans to azoles, which could provide a new strategy to solve the clinical azoles resistance.https://www.tandfonline.com/doi/10.1080/21501203.2024.2432424Candida albicansazole susceptibilityHap2panti-oxidative stressmitochondrial function
spellingShingle Yulin Qin
Quanzhen Lv
Hongtao Xu
Yongbing Cao
Bing Han
Transcription factor Hap2p regulates antioxidant stress responses to maintain miconazole resistance in Candida albicans
Mycology
Candida albicans
azole susceptibility
Hap2p
anti-oxidative stress
mitochondrial function
title Transcription factor Hap2p regulates antioxidant stress responses to maintain miconazole resistance in Candida albicans
title_full Transcription factor Hap2p regulates antioxidant stress responses to maintain miconazole resistance in Candida albicans
title_fullStr Transcription factor Hap2p regulates antioxidant stress responses to maintain miconazole resistance in Candida albicans
title_full_unstemmed Transcription factor Hap2p regulates antioxidant stress responses to maintain miconazole resistance in Candida albicans
title_short Transcription factor Hap2p regulates antioxidant stress responses to maintain miconazole resistance in Candida albicans
title_sort transcription factor hap2p regulates antioxidant stress responses to maintain miconazole resistance in candida albicans
topic Candida albicans
azole susceptibility
Hap2p
anti-oxidative stress
mitochondrial function
url https://www.tandfonline.com/doi/10.1080/21501203.2024.2432424
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