Leishmania donovani Induces Multiple Dynamic Responses in the Metabolome Associated with Amastigote Differentiation and Maturation Inside the Human Macrophage

代谢组 杜氏利什曼原虫 生物 无鞭毛体 代谢组学 巨噬细胞 鞘脂 甘油磷脂 代谢物 细胞生物学 磷酸戊糖途径 生物化学 利什曼原虫 糖酵解 新陈代谢 免疫学 内脏利什曼病 寄生虫寄主 体外 利什曼病 生物信息学 万维网 计算机科学 磷脂
作者
Miguel Fernández-García,Inês Mesquita,Carolina Ferreira,Marta Araújo,Bhaskar Saha,Fernanda Rey-Stolle,Antonia Garcı́a,Ricardo Silvestre,Coral Barbas
出处
期刊:Journal of Proteome Research [American Chemical Society]
卷期号:22 (7): 2256-2270 被引量:1
标识
DOI:10.1021/acs.jproteome.2c00845
摘要

Leishmania donovani infection of macrophages drives profound changes in the metabolism of both the host macrophage and the parasite, which undergoes different phases of development culminating in replication and propagation. However, the dynamics of this parasite–macrophage cometabolome are poorly understood. In this study, a multiplatform metabolomics pipeline combining untargeted, high-resolution CE-TOF/MS and LC-QTOF/MS with targeted LC-QqQ/MS was followed to characterize the metabolome alterations induced in L. donovani-infected human monocyte-derived macrophages from different donors at 12, 36, and 72 h post-infection. The set of alterations known to occur during Leishmania infection of macrophages, substantially expanded in this investigation, characterized the dynamics of the glycerophospholipid, sphingolipid, purine, pentose phosphate, glycolytic, TCA, and amino acid metabolism. Our results showed that only citrulline, arginine, and glutamine exhibited constant trends across all studied infection time points, while most metabolite alterations underwent a partial recovery during amastigote maturation. We determined a major metabolite response pointing to an early induction of sphingomyelinase and phospholipase activities and correlated with amino acid depletion. These data represent a comprehensive overview of the metabolome alterations occurring during promastigote-to-amastigote differentiation and maturation of L. donovani inside macrophages that contributes to our understanding of the relationship between L. donovani pathogenesis and metabolic dysregulation.
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