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系统代谢分析鉴定出鞘脂合成与假菌丝相关,对白色念珠菌菌丝形成是必需的。

Systematic Metabolic Profiling Identifies Sphingolipid Synthesis as Hypha Associated and Essential for Candida albicans Filamentation.

机构信息

Septomics Research Center, Friedrich Schiller University and Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute, Jena, Germany.

BioControl Jena, Jena, Germany.

出版信息

mSystems. 2022 Dec 20;7(6):e0053922. doi: 10.1128/msystems.00539-22. Epub 2022 Oct 20.

Abstract

The yeast-to-hypha transition is a key virulence attribute of the opportunistic human fungal pathogen Candida albicans, since it is closely tied to infection-associated processes such as tissue invasion and escape from phagocytes. While the nature of hypha-associated gene expression required for fungal virulence has been thoroughly investigated, potential morphotype-dependent activity of metabolic pathways remained unclear. Here, we combined global transcriptome and metabolome analyses for the wild-type SC5314 and the hypha-defective Δ and ΔΔ strains under three hypha-inducing (human serum, -acetylglucosamine, and alkaline pH) and two yeast-promoting conditions to identify metabolic adaptions that accompany the filamentation process. We identified morphotype-related activities of distinct pathways and a metabolic core signature of 26 metabolites with consistent depletion or enrichment during the yeast-to-hypha transition. Most strikingly, we found a hypha-associated activation of sphingolipid biosynthesis, indicating a connection of this pathway and filamentous growth. Consequently, pharmacological inhibition of this partially fungus-specific pathway resulted in strongly impaired filamentation, verifying the necessity of sphingolipid biosynthesis for proper hypha formation. The reversible switch of Candida albicans between unicellular yeast and multicellular hyphal growth is accompanied by a well-studied hypha-associated gene expression, encoding virulence factors like adhesins, toxins, or nutrient scavengers. The investigation of this gene expression consequently led to fundamental insights into the pathogenesis of this fungus. In this study, we applied this concept to hypha-associated metabolic adaptations and identified morphotype-dependent activities of distinct pathways and a stimulus-independent metabolic signature of hyphae. Most strikingly, we found the induction of sphingolipid biosynthesis as hypha associated and essential for the filamentation of C. albicans. These findings verified the presence of morphotype-specific metabolic traits in the fungus, which appear connected to the fungal virulence. Furthermore, the here-provided comprehensive description of the fungal metabolome will help to foster future research and lead to a better understanding of fungal physiology.

摘要

酵母到菌丝的转变是机会性人类真菌病原体白色念珠菌的一个关键毒力属性,因为它与感染相关的过程密切相关,如组织侵袭和逃避吞噬细胞。虽然与真菌毒力相关的菌丝相关基因表达的性质已经得到了彻底的研究,但潜在的形态依赖代谢途径的活性仍然不清楚。在这里,我们结合了全球转录组和代谢组分析,用于野生型 SC5314 以及菌丝缺陷型 Δ 和 ΔΔ 菌株在三种诱导菌丝形成的条件(人血清、N-乙酰葡萄糖胺和碱性 pH)和两种促进酵母生长的条件下,以确定伴随丝状形成过程的代谢适应。我们确定了不同途径的形态相关活性和代谢核心特征的 26 种代谢物,这些代谢物在酵母到菌丝的转变过程中持续消耗或富集。最引人注目的是,我们发现了一种与菌丝相关的鞘脂生物合成的激活,表明该途径与丝状生长有关。因此,该部分真菌特异性途径的药理学抑制导致丝状形成严重受损,验证了鞘脂生物合成对正确菌丝形成的必要性。白色念珠菌从单细胞酵母到多细胞菌丝生长的可逆转换伴随着菌丝相关基因表达的深入研究,这些基因编码了黏附素、毒素或营养物质 scavengers 等毒力因子。对这种基因表达的研究导致了对这种真菌发病机制的基本了解。在这项研究中,我们将这一概念应用于菌丝相关的代谢适应,并确定了不同途径的形态相关活性和一种不依赖刺激的菌丝代谢特征。最引人注目的是,我们发现了鞘脂生物合成的诱导与菌丝相关,是白色念珠菌丝状形成所必需的。这些发现验证了真菌中存在形态特有的代谢特征,这些特征似乎与真菌毒力有关。此外,这里提供的真菌代谢组的全面描述将有助于促进未来的研究,并导致对真菌生理学的更好理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef48/9765226/d119b535e6b0/msystems.00539-22-f001.jpg

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