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.File | Dimensione | Formato | |
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