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Cardiolipin Biosynthesis Genes Are Not Required for Salmonella enterica Serovar Typhimurium Pathogenesis in C57BL/6J Mice

Salmonella enterica serovar Typhimurium is an intracellular pathogen that parasitizes macrophages from within a vacuole. The vacuolar environment prompts the bacterium to regulate the lipid composition of the outer membrane (OM), and this influences host inflammation. . Typhimurium regulates the lev...

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Bibliographic Details
Published in:Microbiology spectrum 2022-06, Vol.10 (3), p.e0261721-e0261721
Main Authors: Cian, Melina B, Mettlach, Joshua A, Zahn, Aaron E, Giordano, Nicole P, Minor, Keaton E, McClelland, Michael, Dalebroux, Zachary D
Format: Article
Language:English
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Summary:Salmonella enterica serovar Typhimurium is an intracellular pathogen that parasitizes macrophages from within a vacuole. The vacuolar environment prompts the bacterium to regulate the lipid composition of the outer membrane (OM), and this influences host inflammation. . Typhimurium regulates the levels of acidic glycerophospholipids known as cardiolipins (CL) within the OM, and mitochondrial CL molecules can prime and activate host inflammasomes. However, the contribution of . Typhimurium's CL biosynthesis genes to intracellular survival, inflammasome activation, and pathogenesis had not been examined. . Typhimurium genes encode three CL synthases. Single, double, and triple mutants were constructed. Similar to other , ClsA is the primary CL synthase for . Typhimurium during logarithmic growth, while ClsB and ClsC contribute CL production in stationary phase. It was necessary to delete all three genes to diminish the CL content of the envelope. Despite being devoid of CL molecules, Δ mutants were highly virulent during oral and systemic infection for C57BL/6J mice. In macrophages, Δ , Δ , Δ , and Δ mutants behaved like the wild type, whereas Δ , Δ , and Δ mutants were attenuated and elicited reduced amounts of secreted interleukin-1 beta (IL-1β), IL-18, and lactate dehydrogenase. Hence, when and are deleted, is necessary and sufficient to promote intracellular survival and inflammasome activation. Similarly, when is deleted, and are necessary and sufficient. Therefore, the three CL synthase genes cooperatively and redundantly influence . Typhimurium inflammasome activation and intracellular survival in C57BL/6J mouse macrophages but are dispensable for virulence in mice. Salmonella enterica serovar Typhimurium is a pathogenic Gram-negative bacterium that regulates the cardiolipin (CL) and lipopolysaccharide (LPS) composition of the outer membrane (OM) during infection. Mitochondrial CL molecules activate the inflammasome and its effector caspase-1, which initiates an inflammatory process called pyroptosis. Purified bacterial CL molecules also influence LPS activation of Toll-like receptor 4 (Tlr4). . Typhimurium resides within macrophage vacuoles and activates Tlr4 and the inflammasome during infection. However, the contribution of the three bacterial CL synthase genes ( ) to microbial pathogenesis and inflammation had not been tested. This study supports that the genes encoding the CL synthases work coordinately to promote intracellular survival in macrop
ISSN:2165-0497
2165-0497
DOI:10.1128/spectrum.02617-21