Oxylipins are important signalling compounds that are significantly involved in the regulation of the immune system and the resolution of inflammation. Lipid metabolism is strongly activated upon SARS-CoV-2 infection, however the modulating effects of oxylipins induced by different variants remain unexplored.Here, we compare the plasma profiles of thirty-seven oxylipins and four PUFAs in subjects infected with Wild type, Alpha (B.1.1.7), Delta (B.1.617.2), and Omicron (B.1.1.529) variants.The results suggest that oxidative stress and inflammation resulting from COVID-19 were highly dependent on the SARS-CoV-2 variant, and that the Wild-type elicited the strongest inflammatory storm. The Alpha and Delta variants induced a comparable lipid profile alteration upon infection, which differed significantly from Omicron. The latter variant increased the levels of pro-inflammatory mediators and decreased the levels of omega-3 PUFA in infected patients.We speculate that changes in therapeutics, vaccination, and prior infections may have a role in the alteration of the oxylipin profile besides viral mutations. The results shed new light on the evolution of the inflammatory response in COVID-19.

The effect of SARS-CoV-2 variants on the plasma oxylipins and PUFAs of COVID-19 patients

Biagini, Denise
Primo
;
Lomonaco, Tommaso;Ghimenti, Silvia;Lenzi, Alessio;Vivaldi, Federico;Di Francesco, Fabio
Ultimo
2023-01-01

Abstract

Oxylipins are important signalling compounds that are significantly involved in the regulation of the immune system and the resolution of inflammation. Lipid metabolism is strongly activated upon SARS-CoV-2 infection, however the modulating effects of oxylipins induced by different variants remain unexplored.Here, we compare the plasma profiles of thirty-seven oxylipins and four PUFAs in subjects infected with Wild type, Alpha (B.1.1.7), Delta (B.1.617.2), and Omicron (B.1.1.529) variants.The results suggest that oxidative stress and inflammation resulting from COVID-19 were highly dependent on the SARS-CoV-2 variant, and that the Wild-type elicited the strongest inflammatory storm. The Alpha and Delta variants induced a comparable lipid profile alteration upon infection, which differed significantly from Omicron. The latter variant increased the levels of pro-inflammatory mediators and decreased the levels of omega-3 PUFA in infected patients.We speculate that changes in therapeutics, vaccination, and prior infections may have a role in the alteration of the oxylipin profile besides viral mutations. The results shed new light on the evolution of the inflammatory response in COVID-19.
2023
Biagini, Denise; Oliveri, Paolo; Baj, Andreina; Gasperina, Daniela Dalla; Ferrante, Francesca Drago; Lomonaco, Tommaso; Ghimenti, Silvia; Lenzi, Alessio; Bonini, Andrea; Vivaldi, Federico; Oger, Camille; Galano, Jean-Marie; Balas, Laurence; Durand, Thierry; Maggi, Fabrizio; Di Francesco, Fabio
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1207651
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