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Lipidomic Profiling of Influenza Infection Identifies Mediators that Induce and Resolve Inflammation
Author(s) -
Vincent C. Tam,
Oswald Quehenberger,
Christine M. Oshansky,
Rosa Suen,
Aaron M. Armando,
Piper M. Treuting,
Paul G. Thomas,
Edward A. Dennis,
Alan Aderem
Publication year - 2013
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2013.05.052
Subject(s) - biology , inflammation , immune system , influenza a virus , proinflammatory cytokine , linoleic acid , lipid signaling , pathogenicity , phenotype , virology , immunology , virus , microbiology and biotechnology , gene , genetics , fatty acid , biochemistry
Bioactive lipid mediators play a crucial role in the induction and resolution of inflammation. To elucidate their involvement during influenza infection, liquid chromatography/mass spectrometry lipidomic profiling of 141 lipid species was performed on a mouse influenza model using two viruses of significantly different pathogenicity. Infection by the low-pathogenicity strain X31/H3N2 induced a proinflammatory response followed by a distinct anti-inflammatory response; infection by the high-pathogenicity strain PR8/H1N1 resulted in overlapping pro- and anti-inflammatory states. Integration of the large-scale lipid measurements with targeted gene expression data demonstrated that 5-lipoxygenase metabolites correlated with the pathogenic phase of the infection, whereas 12/15-lipoxygenase metabolites were associated with the resolution phase. Hydroxylated linoleic acid, specifically the ratio of 13- to 9-hydroxyoctadecadienoic acid, was identified as a potential biomarker for immune status during an active infection. Importantly, some of the findings from the animal model were recapitulated in studies of human nasopharyngeal lavages obtained during the 2009-2011 influenza seasons.

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