Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Toyama, Shinjuku-ku, Tokyo, Japan.
Department of Biological Science and Technology, Faculty of Industrial Science and Technology, Tokyo University of Science, Niijuku, Katsushika-ku, Tokyo, Japan.
PLoS One. 2019 Aug 9;14(8):e0220989. doi: 10.1371/journal.pone.0220989. eCollection 2019.
Cryptococcus gattii is a capsular fungal pathogen, which causes life-threatening cryptococcosis in immunocompetent individuals. This emerging pathogen is less likely to be recognized by innate immunity compared to traditional Cryptococcus neoformans strains. Previous studies indicate that C-type lectin receptors (CLRs), including dectin-1 and dectin-2, play a role in recognizing cryptococcal cells; however, it remains to be elucidated whether the receptors physically associate with C. gattii yeast cell surfaces. Based on the previous findings, we hypothesized that culture conditions influence the expression or exposure of CLR ligands on C. gattii. Therefore, in the present study, we first investigated the culture conditions that induce exposure of CLR ligands on C. gattii yeast cells via the binding assay using recombinant fusion proteins of mouse CLR and IgG Fc, Fc dectin-1 and Fc dectin-2. Common fungal culture media, such as yeast extract-peptone-dextrose (YPD) broth, Sabouraud broth, and potato dextrose agar, did not induce the exposure of dectin-1 ligands, including β-1,3-glucan, on both capsular and acapsular C. gattii strains, in contrast to Fc dectin-1 and Fc dectin-2 bound to C. gattii cells growing in the conventional synthetic dextrose (SD) medium [may also be referred to as a yeast nitrogen base with glucose medium]. The medium also induced the exposure of dectin-1 ligands on C. neoformans, whereas all tested media induced dectin-1 and dectin-2 ligands in a control fungus Candida albicans. Notably, C. gattii did not expose dectin-1 ligands in SD medium supplemented with yeast extract or neutral buffer. In addition, compared to YPD medium-induced C. gattii, SD medium-induced C. gattii more efficiently induced the phosphorylation of Syk, Akt, and Erk1/2 in murine dendritic cells (DCs). Afterwards, the cells were considerably engulfed by DCs and remarkably induced DCs to secrete the inflammatory cytokines. Overall, the findings suggest that C. gattii alters its immunostimulatory potential in response to the environment.
格特隐球菌是一种荚膜真菌病原体,可导致免疫功能正常的个体发生致命性 cryptococcosis。与传统的新型隐球菌株相比,这种新出现的病原体不太可能被先天免疫识别。先前的研究表明,C 型凝集素受体(CLR),包括 dectin-1 和 dectin-2,在识别 cryptococcal 细胞中发挥作用;然而,受体是否与 C. gattii 酵母细胞表面物理结合仍有待阐明。基于先前的发现,我们假设培养条件会影响 C. gattii 上 CLR 配体的表达或暴露。因此,在本研究中,我们首先通过使用小鼠 CLR 和 IgG Fc、Fc dectin-1 和 Fc dectin-2 的重组融合蛋白进行结合测定,研究了诱导 C. gattii 酵母细胞 CLR 配体暴露的培养条件。与 Fc dectin-1 和 Fc dectin-2 结合的 C. gattii 细胞不同,常见的真菌培养基,如酵母提取物-蛋白胨-葡萄糖(YPD)肉汤、沙氏葡萄糖琼脂和土豆葡萄糖琼脂,均未诱导荚膜和无荚膜 C. gattii 菌株上 dectin-1 配体(包括β-1,3-葡聚糖)的暴露,而在传统合成葡萄糖(SD)培养基[也可能称为含葡萄糖的酵母氮基础培养基]中生长的 C. gattii 细胞则诱导了 dectin-1 配体的暴露。所有测试的培养基均在对照真菌白色念珠菌中诱导了 dectin-1 和 dectin-2 配体。值得注意的是,C. gattii 在补充了酵母提取物或中性缓冲液的 SD 培养基中不暴露 dectin-1 配体。此外,与 YPD 培养基诱导的 C. gattii 相比,SD 培养基诱导的 C. gattii 更有效地诱导了小鼠树突状细胞(DC)中 Syk、Akt 和 Erk1/2 的磷酸化。之后,细胞被 DC 大量吞噬,并显著诱导 DC 分泌炎症细胞因子。总的来说,这些发现表明 C. gattii 会根据环境改变其免疫刺激潜力。