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与急性 SARS-CoV-2 感染和炎症细胞因子反应相关的胺和犬尿氨酸代谢的系统扰动。

Systemic Perturbations in Amine and Kynurenine Metabolism Associated with Acute SARS-CoV-2 Infection and Inflammatory Cytokine Responses.

机构信息

Australian National Phenome Centre, Computational and Systems Medicine, Health Futures Institute, Murdoch University, Harry Perkins Building, Perth, WA 6150, Australia.

Bruker Pty Ltd., Preston, VIC 3072, Australia.

出版信息

J Proteome Res. 2021 May 7;20(5):2796-2811. doi: 10.1021/acs.jproteome.1c00052. Epub 2021 Mar 16.

DOI:10.1021/acs.jproteome.1c00052
PMID:33724837
Abstract

We performed quantitative metabolic phenotyping of blood plasma in parallel with cytokine/chemokine analysis from participants who were either SARS-CoV-2 (+) ( = 10) or SARS-CoV-2 (-) ( = 49). SARS-CoV-2 positivity was associated with a unique metabolic phenotype and demonstrated a complex systemic response to infection, including severe perturbations in amino acid and kynurenine metabolic pathways. Nine metabolites were elevated in plasma and strongly associated with infection (quinolinic acid, glutamic acid, nicotinic acid, aspartic acid, neopterin, kynurenine, phenylalanine, 3-hydroxykynurenine, and taurine; < 0.05), while four metabolites were lower in infection (tryptophan, histidine, indole-3-acetic acid, and citrulline; < 0.05). This signature supports a systemic metabolic phenoconversion following infection, indicating possible neurotoxicity and neurological disruption (elevations of 3-hydroxykynurenine and quinolinic acid) and liver dysfunction (reduction in Fischer's ratio and elevation of taurine). Finally, we report correlations between the key metabolite changes observed in the disease with concentrations of proinflammatory cytokines and chemokines showing strong immunometabolic disorder in response to SARS-CoV-2 infection.

摘要

我们对 SARS-CoV-2 阳性(+)(=10)和 SARS-CoV-2 阴性(-)(=49)的参与者的血浆进行了定量代谢表型分析,并同时进行了细胞因子/趋化因子分析。SARS-CoV-2 阳性与独特的代谢表型相关,并表明对感染有复杂的全身反应,包括氨基酸和犬尿氨酸代谢途径的严重紊乱。有 9 种代谢物在血浆中升高,与感染强烈相关(喹啉酸、谷氨酸、烟酸、天冬氨酸、新蝶呤、犬尿氨酸、苯丙氨酸、3-羟基犬尿氨酸和牛磺酸;<0.05),而 4 种代谢物在感染中降低(色氨酸、组氨酸、吲哚-3-乙酸和瓜氨酸;<0.05)。该特征支持感染后全身代谢表型转化,表明可能存在神经毒性和神经功能障碍(3-羟基犬尿氨酸和喹啉酸升高)和肝功能障碍(Fischer 比降低和牛磺酸升高)。最后,我们报告了疾病中观察到的关键代谢物变化与促炎细胞因子和趋化因子浓度之间的相关性,表明对 SARS-CoV-2 感染存在强烈的免疫代谢紊乱。

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