Departamento de Ciências Farmacêuticas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil.
Departamento de Microbiologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, Brazil.
PLoS Genet. 2019 Dec 30;15(12):e1008551. doi: 10.1371/journal.pgen.1008551. eCollection 2019 Dec.
Aspergillus fumigatus causes invasive aspergillosis, the most common life-threatening fungal disease of immuno-compromised humans. The treatment of disseminated infections with antifungal drugs, including echinocandin cell wall biosynthesis inhibitors, is increasingly challenging due to the rise of drug-resistant pathogens. The fungal calcium responsive calcineurin-CrzA pathway influences cell morphology, cell wall composition, virulence, and echinocandin resistance. A screen of 395 A. fumigatus transcription factor mutants identified nine transcription factors important to calcium stress tolerance, including CrzA and ZipD. Here, comparative transcriptomics revealed CrzA and ZipD regulated the expression of shared and unique gene networks, suggesting they participate in both converged and distinct stress response mechanisms. CrzA and ZipD additively promoted calcium stress tolerance. However, ZipD also regulated cell wall organization, osmotic stress tolerance and echinocandin resistance. The absence of ZipD in A. fumigatus caused a significant virulence reduction in immunodeficient and immunocompetent mice. The ΔzipD mutant displayed altered cell wall organization and composition, while being more susceptible to macrophage killing and eliciting an increased pro-inflammatory cytokine response. A higher number of neutrophils, macrophages and activated macrophages were found in ΔzipD infected mice lungs. Collectively, this shows that ZipD-mediated regulation of the fungal cell wall contributes to the evasion of pro-inflammatory responses and tolerance of echinocandin antifungals, and in turn promoting virulence and complicating treatment options.
烟曲霉引起侵袭性曲霉病,是免疫功能低下人群最常见的危及生命的真菌病。由于耐药病原体的出现,抗真菌药物(包括棘白菌素细胞壁生物合成抑制剂)治疗播散性感染越来越具有挑战性。真菌钙反应钙调神经磷酸酶-CrzA 途径影响细胞形态、细胞壁组成、毒力和棘白菌素耐药性。对 395 种烟曲霉转录因子突变体的筛选发现了 9 种对钙胁迫耐受至关重要的转录因子,包括 CrzA 和 ZipD。在这里,比较转录组学揭示了 CrzA 和 ZipD 调节了共享和独特基因网络的表达,表明它们参与了收敛和独特的应激反应机制。CrzA 和 ZipD 可累加促进钙胁迫耐受。然而,ZipD 还调节细胞壁组织、渗透压胁迫耐受和棘白菌素耐药性。烟曲霉中 ZipD 的缺失导致免疫缺陷和免疫功能正常的小鼠的毒力显著降低。ΔzipD 突变体显示出细胞壁组织和组成的改变,同时对巨噬细胞杀伤更敏感,并引发更强的促炎细胞因子反应。在 ΔzipD 感染的小鼠肺部发现了更多的中性粒细胞、巨噬细胞和活化的巨噬细胞。总的来说,这表明 ZipD 介导的真菌细胞壁调节有助于逃避促炎反应和耐受棘白菌素抗真菌药物,进而促进毒力并使治疗选择复杂化。