Comparative Ploidy Proteomics of Candida albicans Biofilms Unraveled the Role of the AHP1 Gene in the Biofilm Persistence Against Amphotericin B

被引:35
|
作者
Thuyen Truong [1 ]
Zeng, Guisheng [2 ]
Lin Qingsong [3 ]
Kwang, Lim Teck [3 ]
Tong, Cao [1 ]
Chan, Fong Yee [2 ]
Wang, Yue [2 ]
Seneviratne, Chaminda Jayampath [1 ]
机构
[1] Natl Univ Singapore, Fac Dent, Oral Sci, 11 Lower Kent Ridge Rd, Singapore 119083, Singapore
[2] Agcy Sci Technol & Res, Inst Mol & Cell Biol, Biopolis Dr, Singapore 138673, Singapore
[3] Natl Univ Singapore, Fac Sci, Dept Biol Sci, Singapore 117543, Singapore
关键词
SACCHAROMYCES-CEREVISIAE; ASPERGILLUS-FUMIGATUS; FUNGAL-INFECTIONS; STRESS-RESPONSE; CELL-WALL; PROTEIN; RESISTANCE; REGULATOR; YEAST; EXPRESSION;
D O I
10.1074/mcp.M116.061523
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Candida albicans is a major fungal pathogen causing lethal infections in immunocompromised patients. C. albicans forms antifungal tolerant biofilms contributing significantly to therapeutic failure. The recently established haploid C. albicans biofilm model provides a new toolbox to uncover the mechanism governing the higher antifungal tolerance of biofilms. Here, we comprehensively examined the proteomics and antifungal susceptibility of standard diploid (SC5314 and BWP17) and stable haploid (GZY792 and GZY803) strains of C. albicans biofilms. Subsequent downstream analyses identified alkyl hydroperoxide reductase 1 (AHP1) as a critical determinant of C. albicans biofilm's tolerance of amphotericin B. At 32 mu g/ml of amphotericin B, GZY803 haploid biofilms showed 0.1% of persister population as compared with 1% of the diploid biofilms. AHP1 expression was found to be lower in GZY803 biofilms, and AHP1 overexpression in GZY803 restored the percentage of persister population. Consistently, deleting AHP1 in the diploid strain BWP17 caused a similar increase in amphotericin B susceptibility. AHP1 expression was also positively correlated with the antioxidant potential. Furthermore, C. albicans ira2 Delta/Delta biofilms were susceptible to amphotericin B and had a diminished antioxidant capacity. Interestingly, AHP1 overexpression in the ira2 Delta/Delta strain restored the antioxidant potential and enhanced the persister population against amphotericin B, and shutting down the AHP1 expression in ira2 Delta/Delta biofilms reversed the effect. In conclusion, we provide evidence that the AHP1 gene critically determines the amphotericin B tolerance of C. albicans biofilms possibly by maintaining the persisters' antioxidant capacity. This finding will open up new avenues for developing therapies targeting the persister population of C. albicans biofilms. The mass spectrometry proteomics data are available via ProteomeXchange with identifier PXD004274.
引用
收藏
页码:3488 / 3500
页数:13
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