首页> 外文期刊>Molecular & cellular proteomics: MCP >Comparative Ploidy Proteomics of Candida albicans Biofilms Unraveled the Role of the AHP1 Gene in the Biofilm Persistence Against Amphotericin B
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Comparative Ploidy Proteomics of Candida albicans Biofilms Unraveled the Role of the AHP1 Gene in the Biofilm Persistence Against Amphotericin B

机译:Candida albicils Biofilms的比较倍性蛋白质组学解开了AHP1基因在Biofilm持久性上对两性霉素B的作用

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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.
机译:念珠菌白醛是一种主要的真菌病原体,导致免疫疗效患者的致死感染。 C. albicans形成抗真菌耐受性生物膜,其促进治疗失败。最近建立的单倍体C. albicans生物膜模型提供了一种新的工具箱,用于揭示揭示生物膜抗真菌耐受性的机制。在这里,我们全面地检查了标准二倍体(SC5314和BWP17)和稳定的单倍体(GZY792和GZY803)C. albicans Biofilms的蛋白质组学和抗真菌敏感性。随后的下游分析鉴定烷基氢过氧化物还原酶1(AHP1)作为C. albicans生物膜的临界决定因子。在32μg/ ml两性霉素B中,GZY803单倍体Biofilms显示出0.1%的抗泄漏群,而1%二倍体生物膜。在GZY803生物膜中发现AHP1表达降低,GZY803中的AHP1过表达恢复了抗泄固群体的百分比。一致地,删除二倍体菌株BWP17中的AHP1导致两性霉素B易感性增加。 AHP1表达与抗氧化潜力也呈正相关。此外,C. albicans IRA2 Delta / Delta Biofilms易于两性霉素B,并且具有减少的抗氧化能力。有趣的是,IRA2 Delta / delta菌株中的AHP1过表达恢复了抗氧化剂潜力,并增强了对两性霉素B的抗血液群体,并在IRA2 Delta / Delta Biofilms中关闭AHP1表达逆转效果。总之,我们提供了通过维持持久性抗氧化能力来确定AHP1基因的证据表明AHP1基因批判性地确定C. albicans Biofilms的两性霉素B容差。这一发现将开辟新的途径,用于制定针对抗病患者的抗体群体的疗法。质谱蛋白质组学数据通过蛋白质Xchange获得标识符PXD004274。

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  • 来源
    《Molecular & cellular proteomics: MCP》 |2016年第11期|共13页
  • 作者单位

    Natl Univ Singapore Fac Dent Oral Sci 11 Lower Kent Ridge Rd Singapore 119083 Singapore;

    Agcy Sci Technol &

    Res Inst Mol &

    Cell Biol Biopolis Dr Singapore 138673 Singapore;

    Natl Univ Singapore Fac Sci Dept Biol Sci Singapore 117543 Singapore;

    Natl Univ Singapore Fac Sci Dept Biol Sci Singapore 117543 Singapore;

    Natl Univ Singapore Fac Dent Oral Sci 11 Lower Kent Ridge Rd Singapore 119083 Singapore;

    Agcy Sci Technol &

    Res Inst Mol &

    Cell Biol Biopolis Dr Singapore 138673 Singapore;

    Agcy Sci Technol &

    Res Inst Mol &

    Cell Biol Biopolis Dr Singapore 138673 Singapore;

    Natl Univ Singapore Fac Dent Oral Sci 11 Lower Kent Ridge Rd Singapore 119083 Singapore;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

  • 入库时间 2022-08-20 04:07:04

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