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Untargeted Lipidomics Reveals Lipid Alterations in Colonic Contents of C57BL/6J Mice with Acute Toxoplasma gondii
Wen-Jie Cheng1,2, Bo-Fang Duan3,4, Cai-Qin Deng3,5
1Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China.
Background:
Although Toxoplasma gondii has been recognized as an obligate intracellular parasite, the lipid metabolic alterations it induces in colonic contents during acute infection remain poorly characterized.
Methods:
An acute infection model was established using C57BL/6J mice by oral inoculation with the T. gondii ME49 strain. Untargeted lipidomics analysis was performed on the colonic contents collected at day 10 post-infection.
Results:
Acute infection significantly elevated glycerophospholipids (GPs) and reduced glycerolipids (GLs), and prenol lipids (PRs), leading to 136 differentially abundant lipids. Pathway enrichment analysis identified the two most significantly affected pathways: choline metabolism in cancer and glycerophospholipid metabolism, with lysophosphatidic acid (LPA(16:0)) and lysophosphatidylcholine (LPC(18:1)) functioning as core hub nodes. Receiver operating characteristic (ROC) analysis identified phosphatidylethanolamine (PE(20:1e_22:4)), PE(16:0_22:6), hexosylceramide (Hex1Cer(m18:0_20:4)), and Hex1Cer(t17:0_22:6) as exploratory candidate biomarkers with high discriminatory performance (AUC > 0.94).
Conclusions:
Acute T. gondii infection induces lipid metabolic reprogramming in colonic contents of C57BL/6J mice. The findings provide a novel metabolic perspective on the intestinal pathogenesis of toxoplasmosis and offer exploratory candidate lipid markers for diagnosing acute infection.
