Divergent effects of itaconate isomers on Coxiella burnetii growth in macrophages and in axenic culture

• Published in: Frontiers in immunology 2024-08, Vol.15, p.1427457
• Main Authors: Siddique, Md Nur A Alam, Kellermeier, Fabian, Ölke, Martha, Zhao, Mingming, Büssow, Konrad, Oefner, Peter J, Lührmann, Anja, Dettmer, Katja, Lang, Roland
• Format: Article
• Language: English
• Subjects: ACOD1; Animals; Axenic Culture; Carboxy-Lyases - metabolism; citraconate; Coxiella burnetii - drug effects; Coxiella burnetii - growth & development; Hydro-Lyases; IRG1; itaconate; Macrophages - drug effects; Macrophages - immunology; Macrophages - metabolism; Macrophages - microbiology; mesaconate; Mice; Mice, Inbred C57BL; Mice, Knockout; Q Fever - immunology; Q Fever - microbiology; Succinates - pharmacology; uptake
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2024.1427457

Aconitate decarboxylase-1 (ACOD1) is expressed by activated macrophages and generates itaconate that exerts anti-microbial and immunoregulatory effects. ACOD1-itaconate is essential for macrophage-mediated control of the intracellular pathogen , which causes Q fever. Two isomers of itaconate, mesaconate and citraconate, have overlapping yet distinct activity on macrophage metabolism and inflammatory gene expression. Here, we found that all three isomers inhibited the growth of in axenic culture in ACCM-2 medium. However, only itaconate reduced replication efficiently in macrophages. In contrast, addition of citraconate strongly increased replication in macrophages, whereas mesaconate weakly enhanced bacterial burden in macrophages. Analysis of intracellular isomers showed that exogenous citraconate and mesaconate inhibited the generation of itaconate by infected macrophages. Uptake of added isomers into macrophages was increased after infection for itaconate and mesaconate, but not for citraconate. Mesaconate, but not citraconate, competed with itaconate for uptake into macrophages. Taken together, inhibition of itaconate generation by macrophages and interference with the uptake of extracellular itaconate could be identified as potential mechanisms behind the divergent effects of citraconate and mesaconate on replication in macrophages or in axenic culture.