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Plasmalogen Loss in Sepsis and SARS-CoV-2 Infection.
Pike, Daniel P; McGuffee, Reagan M; Geerling, Elizabeth; Albert, Carolyn J; Hoft, Daniel F; Shashaty, Michael G S; Meyer, Nuala J; Pinto, Amelia K; Ford, David A.
  • Pike DP; Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • McGuffee RM; Center for Cardiovascular Research, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • Geerling E; Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • Albert CJ; Center for Cardiovascular Research, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • Hoft DF; Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • Shashaty MGS; Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • Meyer NJ; Center for Cardiovascular Research, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • Pinto AK; Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • Ford DA; Department of Internal Medicine, Division of Infectious Diseases, Allergy and Immunology, Saint Louis University School of Medicine, St. Louis, MO, United States.
Front Cell Dev Biol ; 10: 912880, 2022.
Article in English | MEDLINE | ID: covidwho-2276495
ABSTRACT
Plasmalogens are plasma-borne antioxidant phospholipid species that provide protection as cellular lipid components during cellular oxidative stress. In this study we investigated plasma plasmalogen levels in human sepsis as well as in rodent models of infection. In humans, levels of multiple plasmenylethanolamine molecular species were decreased in septic patient plasma compared to control subject plasma as well as an age-aligned control subject cohort. Additionally, lysoplasmenylcholine levels were significantly decreased in septic patients compared to the control cohorts. In contrast, plasma diacyl phosphatidylethanolamine and phosphatidylcholine levels were elevated in septic patients. Lipid changes were also determined in rats subjected to cecal slurry sepsis. Plasma plasmenylcholine, plasmenylethanolamine, and lysoplasmenylcholine levels were decreased while diacyl phosphatidylethanolamine levels were increased in septic rats compared to control treated rats. Kidney levels of lysoplasmenylcholine as well as plasmenylethanolamine molecular species were decreased in septic rats. Interestingly, liver plasmenylcholine and plasmenylethanolamine levels were increased in septic rats. Since COVID-19 is associated with sepsis-like acute respiratory distress syndrome and oxidative stress, plasmalogen levels were also determined in a mouse model of COVID-19 (intranasal inoculation of K18 mice with SARS-CoV-2). 3 days following infection, lung infection was confirmed as well as cytokine expression in the lung. Multiple molecular species of lung plasmenylcholine and plasmenylethanolamine were decreased in infected mice. In contrast, the predominant lung phospholipid, dipalmitoyl phosphatidylcholine, was not decreased following SARS-CoV-2 infection. Additionally total plasmenylcholine levels were decreased in the plasma of SARS-CoV-2 infected mice. Collectively, these data demonstrate the loss of plasmalogens during both sepsis and SARS-CoV-2 infection. This study also indicates plasma plasmalogens should be considered in future studies as biomarkers of infection and as prognostic indicators for sepsis and COVID-19 outcomes.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Language: English Journal: Front Cell Dev Biol Year: 2022 Document Type: Article Affiliation country: Fcell.2022.912880

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Language: English Journal: Front Cell Dev Biol Year: 2022 Document Type: Article Affiliation country: Fcell.2022.912880