Department of Molecular Microbiology, Washington University School of Medicine, Washington University, St. Louis, Missouri, USA.
Department of Molecular Microbiology, Washington University School of Medicine, Washington University, St. Louis, Missouri, USA
mBio. 2018 Nov 6;9(6):e01375-18. doi: 10.1128/mBio.01375-18.
Mitochondria are essential organelles that act in pathways including ATP production, β-oxidation, and clearance of reactive oxygen species. They occur as a complex reticular network that constantly undergoes fusion and fission, mediated by dynamin-related proteins (DRPs). DRPs include Fzo1, which mediates fusion, and Dnm1, Mdv1, and Fis1, which mediate fission. Mitochondrial morphology has been implicated in virulence in multiple fungi, as with the association between virulence and increased mitochondrial fusion in This relationship, however, has not been studied in , a related opportunistic pathogen. is an environmental yeast that can adapt to the human host environment, overcome the innate immune system, and eventually disseminate and cause lethal meningoencephalitis. We used gene deletion of key DRPs to study their role in mitochondrial morphology and pathogenesis of this yeast. Interestingly, increasing mitochondrial fusion did not increase resistance to oxidative stress, unlike in model yeast. Blocking mitochondrial fusion, however, yielded increased susceptibility to oxidative and nitrosative stresses as well as complete avirulence. This lack of virulence was not mediated by any effects of altered mitochondrial function on two major virulence factors, capsule and melanin. Instead, it was due to decreased survival within macrophages, which in turn was a consequence of increased susceptibility to oxidative and nitrosative stress. Supporting this conclusion, reactive oxygen species (ROS) scavengers rescued the ability of fusion mutants to survive intracellularly. These findings increase our understanding of cryptococcal biology and virulence and shed light on an important group of proteins and cellular processes in this pathogen. is a yeast that causes fatal brain infection in close to 200,000 people worldwide every year, mainly afflicting individuals with AIDS or others who are severely immunocompromised. One feature of this microbe that helps it cause disease is that it is able to withstand toxic molecules it encounters when host cells engulf it in their efforts to control the infection. Mitochondria are important organelles responsible for energy production and other key cellular processes. They typically exist in a complex network that changes morphology by fusing and dividing; these alterations also influence mitochondrial function. Using genetic approaches, we found that changes in mitochondrial morphology dramatically influence cryptococcal virulence. We showed that this occurs because the altered mitochondria are less able to eliminate the harmful molecules that host cells produce to kill invading microbes. These findings are important because they elucidate fundamental biology and virulence and may suggest avenues for therapy.
线粒体是一种重要的细胞器,参与包括 ATP 生成、β-氧化和活性氧物种清除在内的途径。它们呈现出一种复杂的网状结构,不断经历融合和裂变,这由与 dynamin 相关的蛋白(DRP)介导。DRP 包括介导融合的 Fzo1,以及介导裂变的 Dnm1、Mdv1 和 Fis1。线粒体形态与多种真菌的毒力有关,如在毒力增加与线粒体融合增加之间的关联, 在这种关系中,然而,在相关的机会性病原体 中尚未进行研究。 是一种环境酵母,能够适应人体宿主环境,克服先天免疫系统,最终传播并导致致命的脑膜脑炎。我们使用关键 DRP 的基因缺失来研究它们在这种酵母的线粒体形态和发病机制中的作用。有趣的是,与模型酵母不同,增加线粒体融合并没有增加对氧化应激的抵抗力。然而,阻断线粒体融合会导致对氧化和硝化应激的敏感性增加以及完全无毒力。这种无毒力不是由改变线粒体功能对两种主要毒力因子(荚膜和黑色素)的任何影响介导的。相反,这是由于在巨噬细胞内的存活率降低,而这反过来又是对氧化和硝化应激敏感性增加的结果。支持这一结论,活性氧(ROS)清除剂挽救了融合突变体在细胞内存活的能力。这些发现增加了我们对隐球菌生物学和毒力的理解,并阐明了该病原体中一组重要的蛋白质和细胞过程。 是一种导致全世界每年近 20 万人致命脑部感染的酵母,主要影响艾滋病患者或其他严重免疫功能低下的人。这种微生物有助于它引起疾病的一个特征是,它能够耐受宿主细胞吞噬它以控制感染时遇到的有毒分子。线粒体是负责能量产生和其他关键细胞过程的重要细胞器。它们通常存在于一个复杂的网络中,通过融合和分裂改变形态;这些改变也会影响线粒体的功能。通过遗传方法,我们发现线粒体形态的改变会显著影响隐球菌的毒力。我们表明,这是因为改变的线粒体更难以消除宿主细胞产生的杀死入侵微生物的有害分子。这些发现很重要,因为它们阐明了基本的生物学和毒力,并可能为治疗提供途径。