Metabolomic Profiling of Lungs from Mice Reveals the Variability of Metabolites in Infection and the Metabolic Abnormalities in BAFF-R-Deficient Mice.

Purpose: The incidence of pneumonia (PCP) in patients without human immunodeficiency virus (HIV) has been increasing. In this study, we aimed to investigate the metabolic changes in infection and the metabolic abnormalities in B-cell-activating factor receptor (BAFF-R)-deficient mice with infection.

Methods: The important function of B cells during infection is increasingly recognized. In this study, a -infected mouse model was constructed in BAFF-R mice and wild-type (WT) mice. Lungs of uninfected WT C57BL/6, WT -infected, and BAFF-R -infected mice were used for metabolomic analyses to compare the metabolomic profiles among the groups, with the aim of exploring the metabolic influence of infection and the influence of mature B-cell deficiency during infection.

Results: The results indicated that many metabolites, mainly lipids and lipid-like molecules, were dysregulated in infected WT mice compared with uninfected WT C57BL/6 mice. The data also demonstrated significant changes in tryptophan metabolism, and the expression levels of key enzymes of tryptophan metabolism, such as indoleamine 2,3-dioxygenase 1 (IDO1), were significantly upregulated. In addition, B-cell development and function might be associated with lipid metabolism. We found a lower level of alitretinoin and the abnormalities of fatty acid metabolism in BAFF-R -infected mice. The mRNA levels of enzymes associated with fatty acid metabolism in the lung were upregulated in BAFF-R -infected mice and positively correlated with the level of IL17A, thus suggesting that the abnormalities of fatty acid metabolism may be associated with greater inflammatory cell infiltration in the lung tissue of BAFF-R -infected mice compared with the WT -infected mice.

Conclusion: Our data revealed the variability of metabolites in -infected mice, suggesting that the metabolism plays a vital role in the immune response to infection.