作者
Nathan G Lawler, Nicola Gray, Torben Kimhofer, Berin Boughton, Melvin Gay, Rongchang Yang, Aude-Claire Morillon, Sung-Tong Chin, Monique Ryan, Sofina Begum, Sze How Bong, Jerome D Coudert, Dale Edgar, Edward Raby, Sven Pettersson, Toby Richards, Elaine Holmes, Luke Whiley, Jeremy K Nicholson
发表日期
2021/3/16
期刊
Journal of Proteome Research
卷号
20
期号
5
页码范围
2796-2811
出版商
American Chemical Society
简介
We performed quantitative metabolic phenotyping of blood plasma in parallel with cytokine/chemokine analysis from participants who were either SARS-CoV-2 (+) (n = 10) or SARS-CoV-2 (-) (n = 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; p < 0.05), while four metabolites were lower in infection (tryptophan, histidine, indole-3-acetic acid, and citrulline; p < 0.05). This signature supports a systemic metabolic phenoconversion following infection, indicating possible neurotoxicity and neurological disruption (elevations of 3 …
引用总数