Crabbé Aurélie, Nielsen-Preiss Sheila M, Woolley Christine M, Barrila Jennifer, Buchanan Kent, McCracken James, Inglis Diane O, Searles Stephen C, Nelman-Gonzalez Mayra A, Ott C Mark, Wilson James W, Pierson Duane L, Stefanyshyn-Piper Heidemarie M, Hyman Linda E, Nickerson Cheryl A
Center for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, Arizona, United States of America.
PLoS One. 2013 Dec 4;8(12):e80677. doi: 10.1371/journal.pone.0080677. eCollection 2013.
This study presents the first global transcriptional profiling and phenotypic characterization of the major human opportunistic fungal pathogen, Candida albicans, grown in spaceflight conditions. Microarray analysis revealed that C. albicans subjected to short-term spaceflight culture differentially regulated 452 genes compared to synchronous ground controls, which represented 8.3% of the analyzed ORFs. Spaceflight-cultured C. albicans-induced genes involved in cell aggregation (similar to flocculation), which was validated by microscopic and flow cytometry analysis. We also observed enhanced random budding of spaceflight-cultured cells as opposed to bipolar budding patterns for ground samples, in accordance with the gene expression data. Furthermore, genes involved in antifungal agent and stress resistance were differentially regulated in spaceflight, including induction of ABC transporters and members of the major facilitator family, downregulation of ergosterol-encoding genes, and upregulation of genes involved in oxidative stress resistance. Finally, downregulation of genes involved in actin cytoskeleton was observed. Interestingly, the transcriptional regulator Cap1 and over 30% of the Cap1 regulon was differentially expressed in spaceflight-cultured C. albicans. A potential role for Cap1 in the spaceflight response of C. albicans is suggested, as this regulator is involved in random budding, cell aggregation, and oxidative stress resistance; all related to observed spaceflight-associated changes of C. albicans. While culture of C. albicans in microgravity potentiates a global change in gene expression that could induce a virulence-related phenotype, no increased virulence in a murine intraperitoneal (i.p.) infection model was observed under the conditions of this study. Collectively, our data represent an important basis for the assessment of the risk that commensal flora could play during human spaceflight missions. Furthermore, since the low fluid-shear environment of microgravity is relevant to physical forces encountered by pathogens during the infection process, insights gained from this study could identify novel infectious disease mechanisms, with downstream benefits for the general public.
本研究展示了在航天飞行条件下生长的主要人类机会性真菌病原体白色念珠菌的首次全球转录谱分析和表型特征。微阵列分析显示,与同步地面对照相比,经历短期航天飞行培养的白色念珠菌差异调节了452个基因,占分析的开放阅读框的8.3%。航天飞行培养的白色念珠菌诱导的基因参与细胞聚集(类似于絮凝),这通过显微镜和流式细胞术分析得到了验证。根据基因表达数据,我们还观察到航天飞行培养的细胞随机出芽增强,而地面样本为双极出芽模式。此外,参与抗真菌剂和应激抗性的基因在航天飞行中差异调节,包括ABC转运蛋白和主要易化子家族成员的诱导、麦角固醇编码基因的下调以及参与氧化应激抗性的基因的上调。最后,观察到参与肌动蛋白细胞骨架的基因下调。有趣的是,转录调节因子Cap1以及超过30%的Cap1调控子在航天飞行培养的白色念珠菌中差异表达。由于该调节因子参与随机出芽、细胞聚集和氧化应激抗性,而这些都与观察到的白色念珠菌与航天飞行相关的变化有关,因此提示Cap1在白色念珠菌的航天飞行反应中具有潜在作用。虽然白色念珠菌在微重力条件下培养会增强基因表达的全局变化,这可能诱导与毒力相关的表型,但在本研究条件下,在小鼠腹腔内感染模型中未观察到毒力增加。总体而言,我们的数据为评估共生菌群在人类航天飞行任务中可能发挥的风险提供了重要依据。此外,由于微重力的低流体剪切环境与病原体在感染过程中遇到的物理力相关,本研究获得的见解可以识别新的传染病机制,从而为普通大众带来下游益处。