Frontiers in Microbiology (Dec 2021)

Longitudinal Metabolomics Reveals Ornithine Cycle Dysregulation Correlates With Inflammation and Coagulation in COVID-19 Severe Patients

  • Tao Li,
  • Nianzhi Ning,
  • Bo Li,
  • Deyan Luo,
  • Enqiang Qin,
  • Wenjing Yu,
  • Jianxin Wang,
  • Guang Yang,
  • Nan Nan,
  • Zhili He,
  • Ning Yang,
  • Saisai Gong,
  • Jiajia Li,
  • Aixia Liu,
  • Yakun Sun,
  • Zhan Li,
  • Tianye Jia,
  • Jie Gao,
  • Wang Zhang,
  • Yanyu Huang,
  • Jun Hou,
  • Ying Xue,
  • Deyu Li,
  • Zhen Wei,
  • Liangyan Zhang,
  • Boan Li,
  • Hui Wang

DOI
https://doi.org/10.3389/fmicb.2021.723818
Journal volume & issue
Vol. 12

Abstract

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COVID-19 is a severe disease in humans, as highlighted by the current global pandemic. Several studies about the metabolome of COVID-19 patients have revealed metabolic disorders and some potential diagnostic markers during disease progression. However, the longitudinal changes of metabolomics in COVID-19 patients, especially their association with disease progression, are still unclear. Here, we systematically analyzed the dynamic changes of the serum metabolome of COVID-19 patients, demonstrating that most of the metabolites did not recover by 1–3 days before discharge. A prominent signature in COVID-19 patients comprised metabolites of amino acids, peptides, and analogs, involving nine essential amino acids, 10 dipeptides, and four N-acetylated amino acids. The levels of 12 metabolites in amino acid metabolism, especially three metabolites of the ornithine cycle, were significantly higher in severe patients than in mild ones, mainly on days 1–3 or 4–6 since onset. Integrating blood metabolomic, biochemical, and cytokine data, we uncovered a highly correlated network, including 6 cytokines, 13 biochemical parameters, and 49 metabolites. Significantly, five ornithine cycle-related metabolites (ornithine, N-acetylornithine, 3-amino-2-piperidone, aspartic acid, and asparagine) highly correlated with “cytokine storms” and coagulation index. We discovered that the ornithine cycle dysregulation significantly correlated with inflammation and coagulation in severe patients, which may be a potential mechanism of COVID-19 pathogenicity. Our study provided a valuable resource for detailed exploration of metabolic factors in COVID-19 patients, guiding metabolic recovery, understanding the pathogenic mechanisms, and creating drugs against SARS-CoV-2 infection.

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