Viana Romeu, Carreiro Tiago, Couceiro Diogo, Dias Oscar, Rocha Isabel, Teixeira Miguel Cacho
Department of Bioengineering, Instituto Superior Técnico, University of Lisbon, 1049-001 Lisboa, Portugal.
iBB - Institute for Bioengineering and Biosciences, Associate Laboratory Institute for Health and Bioeconomy - i4HB, 1049-001 Lisboa, Portugal.
FEMS Yeast Res. 2023 Jan 4;23. doi: 10.1093/femsyr/foad045.
Candida auris is an emerging human pathogen, associated with antifungal drug resistance and hospital candidiasis outbreaks. In this work, we present iRV973, the first reconstructed Genome-scale metabolic model (GSMM) for C. auris. The model was manually curated and experimentally validated, being able to accurately predict the specific growth rate of C. auris and the utilization of several sole carbon and nitrogen sources. The model was compared to GSMMs available for other pathogenic Candida species and exploited as a platform for cross-species comparison, aiming the analysis of their metabolic features and the identification of potential new antifungal targets common to the most prevalent pathogenic Candida species. From a metabolic point of view, we were able to identify unique enzymes in C. auris in comparison with other Candida species, which may represent unique metabolic features. Additionally, 50 enzymes were identified as potential drug targets, given their essentiality in conditions mimicking human serum, common to all four different Candida models analysed. These enzymes represent interesting drug targets for antifungal therapy, including some known targets of antifungal agents used in clinical practice, but also new potential drug targets without any human homolog or drug association in Candida species.
耳念珠菌是一种新出现的人类病原体,与抗真菌药物耐药性及医院念珠菌病暴发有关。在这项研究中,我们展示了iRV973,这是首个针对耳念珠菌构建的基因组规模代谢模型(GSMM)。该模型经过人工精心策划和实验验证,能够准确预测耳念珠菌的比生长速率以及几种单一碳源和氮源的利用情况。该模型与其他致病性念珠菌物种的可用GSMM进行了比较,并被用作跨物种比较的平台,旨在分析它们的代谢特征并识别最常见致病性念珠菌物种共有的潜在新抗真菌靶点。从代谢角度来看,与其他念珠菌物种相比,我们能够在耳念珠菌中鉴定出独特的酶,这可能代表了独特的代谢特征。此外,鉴于在模拟人血清的条件下(这是所分析的所有四种不同念珠菌模型共有的)这些酶的必要性,有50种酶被鉴定为潜在的药物靶点。这些酶是抗真菌治疗中有趣的药物靶点,包括临床实践中使用的一些抗真菌药物的已知靶点,但也包括念珠菌物种中没有任何人类同源物或药物关联的新潜在药物靶点。