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Live Imaging and Quantification of Viral Infection in K18 hACE2 Transgenic Mice Using Reporter-Expressing Recombinant SARS-CoV-2
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SARS-CoV2 variants differentially impact on the plasma metabolome
Tina Kramaric1, Onn Shaun Thein2,3, Dhruv Parekh2,3
1Department of Life Sciences, Aberystwyth University, Penglais Campus, Aberystwyth, SY23 3DA, UK.
Summary
COVID19 patient plasma metabolomes differ based on SARS-CoV-2 variant, reflecting disease severity. Key changes in phospholipids and other metabolites correlate with clinical markers.
Area of Science:
- Biochemistry
- Immunology
- Infectious Diseases
Background:
- Severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) caused a global pandemic, with evolving variants altering disease presentation.
- Current SARS-CoV-2 infections are generally less severe than those observed in the initial pandemic wave.
Purpose of the Study:
- To investigate variations in plasma metabolomes among COVID-19 patients infected with different SARS-CoV-2 variants.
- To determine if plasma metabolomic profiles can indicate disease severity and specific variant infections.
Main Methods:
- Plasma samples were collected from COVID-19 patients infected with Alpha, Delta, and Omicron variants and compared to healthy controls.
- Metabolomic analysis was performed using flow injection electrospray mass spectrometry (FIE-MS).
- Data analysis utilized the R-based MetaboAnalyst platform for statistical assessment.
Main Results:
- Distinct plasma metabolomic profiles were observed between COVID-19 patients and control groups.
- Metabolite variations correlated with specific SARS-CoV-2 variants, including differences in phospholipids, ganglioside GD1a, and dihydroxyvitamin D3 derivatives.
- Negative correlations were found between certain phospholipids and clinical markers of inflammation and severity (C-reactive protein, creatinine, neutrophil count, D-dimer).
Conclusions:
- Plasma metabolomic alterations in COVID-19 patients are associated with SARS-CoV-2 variant type.
- These metabolic changes, particularly in phospholipids, may serve as indicators of disease severity and variant-specific infection patterns.
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