Department of Microbial Pathogenicity Mechanisms, Leibniz Institute for Natural Product Research and Infection Biology, Hans-Knoell-Institute, Jena, Germany.
PLoS One. 2012;7(12):e52850. doi: 10.1371/journal.pone.0052850. Epub 2012 Dec 21.
Neutrophils are key players during Candida albicans infection. However, the relative contributions of neutrophil activities to fungal clearance and the relative importance of the fungal responses that counteract these activities remain unclear. We studied the contributions of the intra- and extracellular antifungal activities of human neutrophils using diagnostic Green Fluorescent Protein (GFP)-marked C. albicans strains. We found that a carbohydrate starvation response, as indicated by up-regulation of glyoxylate cycle genes, was only induced upon phagocytosis of the fungus. Similarly, the nitrosative stress response was only observed in internalised fungal cells. In contrast, the response to oxidative stress was observed in both phagocytosed and non-phagocytosed fungal cells, indicating that oxidative stress is imposed both intra- and extracellularly. We assessed the contributions of carbohydrate starvation, oxidative and nitrosative stress as antifungal activities by analysing the resistance to neutrophil killing of C. albicans mutants lacking key glyoxylate cycle, oxidative and nitrosative stress genes. We found that the glyoxylate cycle plays a crucial role in fungal resistance against neutrophils. The inability to respond to oxidative stress (in cells lacking superoxide dismutase 5 or glutathione reductase 2) renders C. albicans susceptible to neutrophil killing, due to the accumulation of reactive oxygen species (ROS). We also show that neutrophil-derived nitric oxide is crucial for the killing of C. albicans: a yhb1Δ/Δ mutant, unable to detoxify NO•, was more susceptible to neutrophils, and this phenotype was rescued by the nitric oxide scavenger carboxy-PTIO. The stress responses of C. albicans to neutrophils are partially regulated via the stress regulator Hog1 since a hog1Δ/Δ mutant was clearly less resistant to neutrophils and unable to respond properly to neutrophil-derived attack. Our data indicate that an appropriate fungal response to all three antifungal activities, carbohydrate starvation, nitrosative stress and oxidative stress, is essential for full wild type resistance to neutrophils.
中性粒细胞是白色念珠菌感染过程中的关键角色。然而,中性粒细胞活性对真菌清除的相对贡献,以及对抗这些活性的真菌反应的相对重要性仍不清楚。我们使用诊断性绿色荧光蛋白(GFP)标记的白色念珠菌菌株研究了人中性粒细胞的细胞内和细胞外抗真菌活性的贡献。我们发现,碳水化合物饥饿反应(糖异生途径基因上调)仅在吞噬真菌时被诱导。同样,硝化应激反应仅在被内化的真菌细胞中观察到。相比之下,氧化应激反应在被吞噬和未被吞噬的真菌细胞中均被观察到,这表明氧化应激既在细胞内也在细胞外发生。我们通过分析缺乏关键糖异生、氧化和硝化应激基因的白色念珠菌突变体对中性粒细胞杀伤的抗性,评估了碳水化合物饥饿、氧化和硝化应激作为抗真菌活性的贡献。我们发现,糖异生途径在真菌抵抗中性粒细胞方面起着至关重要的作用。由于活性氧(ROS)的积累,无法对氧化应激(在缺乏超氧化物歧化酶 5 或谷胱甘肽还原酶 2 的细胞中)做出反应,使白色念珠菌易受中性粒细胞杀伤。我们还表明,中性粒细胞衍生的一氧化氮对于白色念珠菌的杀伤至关重要:一个无法解毒 NO•的 yhb1Δ/Δ 突变体对中性粒细胞更敏感,而这种表型可以通过一氧化氮清除剂 carboxy-PTIO 挽救。白色念珠菌对中性粒细胞的应激反应部分通过应激调节因子 Hog1 调节,因为 hog1Δ/Δ 突变体对中性粒细胞的抵抗力明显降低,并且无法对中性粒细胞衍生的攻击做出适当反应。我们的数据表明,适当的真菌反应对所有三种抗真菌活性(碳水化合物饥饿、硝化应激和氧化应激)对于完全抵抗野生型中性粒细胞至关重要。