Intestinal metabolites influence macrophage phagocytosis and clearance of bacterial infection
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Supplementary Information
Supplementary Information
Date
2021-07-19
Authors
O'Callaghan, Amy A.
Dempsey, Elaine
Iyer, Namrata
Stiegeler, Sarah
Mercurio, Kevin
Corr, Sinéad C.
Journal Title
Journal ISSN
Volume Title
Publisher
Frontiers Media
Published Version
Abstract
The metabolite-rich environment that is the intestinal lumen contains metabolic by-products deriving from microbial fermentation and host cell metabolism, with resident macrophages being constantly exposed to this metabolic flux. Succinate, lactate and itaconate are three metabolites secreted by primed macrophages due to a fragmented tri-carboxylic acid (TCA) cycle. Additionally, succinate and lactate are known by-products of microbial fermentation. How these metabolites impact biological functioning of resident macrophages particularly in response to bacterial infection remains poorly understood. We have investigated the potential influence of these metabolites on macrophage phagocytosis and clearance of () infection. Treatment of murine bone-marrow-derived macrophages (BMDMs) with succinate reduced numbers of intracellular early during infection, while lactate-treated BMDMs displayed no difference throughout the course of infection. Treatment of BMDMs with itaconate lead to higher levels of intracellular early in the infection with bacterial burden subsequently reduced at later time-points compared to untreated macrophages, indicative of enhanced engulfment and killing capabilities of macrophages in response to itaconate. Expression of engulfment mediators MARCKS, RhoB, and CDC42 were reduced or unchanged following succinate or lactate treatment and increased in itaconate-treated macrophages following infection. Nitric oxide (NO) levels varied while pro- and anti-inflammatory cytokines differed in secretory levels in all metabolite-treated macrophages post-infection with or in response to lipopolysaccharide (LPS) stimulation. Finally, the basal phenotypic profile of metabolite-treated macrophages was altered according to marker gene expression, describing how fluid macrophage phenotype can be in response to the microenvironment. Collectively, our data suggests that microbe- and host-derived metabolites can drive distinct macrophage functional phenotypes in response to infection, whereby succinate and itaconate regulate phagocytosis and bactericidal mechanisms, limiting the intracellular bacterial niche and impeding the pathogenesis of infection.
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Keywords
Intestinal infection , Itaconate , Lactate , Macrophage , Metabolite , Succinate
Citation
O’Callaghan, A. A., Dempsey, E., Iyer, N., Stiegeler, S., Mercurio, K. and Corr, S. C. (2021) 'Intestinal metabolites influence macrophage phagocytosis and clearance of bacterial infection', Frontiers in Cellular and Infection Microbiology, 11, 622491 (13pp). doi: 10.3389/fcimb.2021.622491