Department of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 252 50, Vestec, Czech Republic.
Institute of Microbiology of the Czech Academy of Sciences, BIOCEV, 252 50, Vestec, Czech Republic.
BMC Genomics. 2017 Oct 23;18(1):814. doi: 10.1186/s12864-017-4214-4.
Yeast infections are often connected with formation of biofilms that are extremely difficult to eradicate. An excellent model system for deciphering multifactorial determinants of yeast biofilm development is the colony biofilm, composed of surface ("aerial") and invasive ("root") cells. While surface cells have been partially analyzed before, we know little about invasive root cells. In particular, information on the metabolic, chemical and morphogenetic properties of invasive versus surface cells is lacking. In this study, we used a new strategy to isolate invasive cells from agar and extracellular matrix, and employed it to perform genome wide expression profiling and biochemical analyses of surface and invasive cells.
RNA sequencing revealed expression differences in 1245 genes with high statistical significance, indicating large genetically regulated metabolic differences between surface and invasive cells. Functional annotation analyses implicated genes involved in stress defense, peroxisomal fatty acid β-oxidation, autophagy, protein degradation, storage compound metabolism and meiosis as being important in surface cells. In contrast, numerous genes with functions in nutrient transport and diverse synthetic metabolic reactions, including genes involved in ribosome biogenesis, biosynthesis and translation, were found to be important in invasive cells. Variation in gene expression correlated significantly with cell-type specific processes such as autophagy and storage compound accumulation as identified by microscopic and biochemical analyses. Expression profiling also provided indications of cell-specific regulations. Subsequent knockout strain analyses identified Gip2p, a regulatory subunit of type 1 protein phosphatase Glc7p, to be essential for glycogen accumulation in surface cells.
This is the first study reporting genome wide differences between surface and invasive cells of yeast colony biofilms. New findings show that surface and invasive cells display very different physiology, adapting to different conditions in different colony areas and contributing to development and survival of the colony biofilm as a whole. Notably, surface and invasive cells of colony biofilms differ significantly from upper and lower cells of smooth colonies adapted to plentiful laboratory conditions.
酵母菌感染通常与生物膜的形成有关,而生物膜极难根除。酵母生物膜发育的多因素决定因素的破译的一个极好的模型系统是由表面(“气生”)和侵袭(“根”)细胞组成的菌落生物膜。虽然以前已经部分分析了表面细胞,但我们对侵袭性根细胞知之甚少。特别是,关于侵袭性与表面细胞的代谢、化学和形态发生特性的信息缺乏。在这项研究中,我们使用了一种从琼脂和细胞外基质中分离侵袭性细胞的新策略,并将其用于进行表面和侵袭性细胞的全基因组表达谱分析和生化分析。
RNA 测序显示,1245 个基因的表达差异具有高度统计学意义,表明表面和侵袭性细胞之间存在大量遗传调控的代谢差异。功能注释分析表明,参与应激防御、过氧化物酶体脂肪酸 β-氧化、自噬、蛋白质降解、储存化合物代谢和减数分裂的基因在表面细胞中很重要。相比之下,许多参与营养物质运输和各种合成代谢反应的基因,包括核糖体生物发生、生物合成和翻译相关基因,在侵袭性细胞中很重要。基因表达的变化与自噬和储存化合物积累等细胞类型特异性过程显著相关,这些过程通过显微镜和生化分析得到了证实。表达谱分析还提供了细胞特异性调节的迹象。随后的敲除株分析表明,Gip2p 是 Glc7p 型 1 蛋白磷酸酶的调节亚基,对表面细胞中糖原积累是必需的。
这是第一项报道酵母菌落生物膜表面和侵袭性细胞全基因组差异的研究。新发现表明,表面和侵袭性细胞表现出非常不同的生理学,适应不同的菌落区域条件,并为整个菌落生物膜的发育和生存做出贡献。值得注意的是,与适应丰富实验室条件的光滑菌落的上、下细胞相比,菌落生物膜的表面和侵袭性细胞有显著差异。