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首页> 外文期刊>Frontiers in Microbiology >Serum Metabolic Profiling of Oocyst-Induced Toxoplasma gondii Acute and Chronic Infections in Mice Using Mass-Spectrometry
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Serum Metabolic Profiling of Oocyst-Induced Toxoplasma gondii Acute and Chronic Infections in Mice Using Mass-Spectrometry

机译:质谱法测定小鼠卵囊诱发的刚地弓形虫急性和慢性感染的血清代谢谱

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Toxoplasma gondii is an obligate intracellular parasite causing severe diseases in immunocompromised individuals and congenitally infected neonates, such as encephalitis and chorioretinitis. This study aimed to determine whether serum metabolic profiling can (i) identify metabolites associated with oocyst-induced T. gondii infection and (ii) detect systemic metabolic differences between T. gondii -infected mice and controls. We performed the first global metabolomics analysis of mice serum challenged with 100 sporulated T. gondii Pru oocysts (Genotype II). Sera from acutely infected mice (11 days post-infection, dpi), chronically infected mice (33 dpi) and control mice were collected and analyzed using LC-MS/MS platform. Following False Discovery Rate filtering, we identified 3871 and 2825 ions in ESI+ or ESI? mode, respectively. Principal Component Analysis (PCA) and Partial Least Squares Discriminant Analysis (PLS-DA) identified metabolomic profiles that clearly differentiated T. gondii -infected and -uninfected serum samples. Acute infection significantly influenced the serum metabolome. Our results identified common and uniquely perturbed metabolites and pathways. Acutely infected mice showed perturbations in metabolites associated with glycerophospholipid metabolism, biosynthesis of amino acid, and tyrosine metabolism. These findings demonstrated that acute T. gondii infection induces a global perturbation of mice serum metabolome, providing new insights into the mechanisms underlying systemic metabolic changes during early stage of T. gondii infection.
机译:弓形虫是专性的细胞内寄生虫,在免疫功能低下的个体和先天感染的新生儿中引起严重的疾病,例如脑炎和脉络膜视网膜炎。这项研究旨在确定血清代谢谱分析能否(i)鉴定与卵囊诱导的弓形虫感染相关的代谢物,以及(ii)检测弓形虫感染的小鼠和对照组之间的全身代谢差异。我们对小鼠血清进行了首次全球代谢组学分析,该小鼠血清受到100个带孢子的弓形虫Pru卵囊(基因型II)攻击。收集急性感染小鼠(感染后11天,dpi),慢性感染小鼠(33 dpi)和对照小鼠的血清,并使用LC-MS / MS平台进行分析。经过错误发现率过滤后,我们在ESI +或ESI?中识别了3871和2825个离子。模式。主成分分析(PCA)和偏最小二乘判别分析(PLS-DA)确定了代谢组学谱,可以清楚地区分弓形虫感染和未感染的血清样品。急性感染显着影响血清代谢组。我们的结果确定了常见且独特的代谢物和途径。急性感染的小鼠表现出与甘油磷脂代谢,氨基酸的生物合成和酪氨酸代谢有关的代谢产物扰动。这些发现表明,急性刚地弓形虫感染可引起小鼠血清代谢组的整体扰动,从而为刚地弓形虫感染早期系统性代谢变化的潜在机制提供新见解。

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