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Individual colonization varies.
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Here, acetyl-CoA generated from citrate is used for epigenetic modifications via acetylation of histones, citrate itself can be used to generate ROS, NOS, and prostaglandins, and cis-aconitate can be metabolized into itaconate, which besides being an anti-microbial substance has immune-modulatory effects by inhibiting the succinate dehydrogenase (resulting in succinate accumulation, see below), modifying either glycolysis enzymes or the inflammasome nucleotide-binding leucine-rich repeat receptor (NLR) family pyrin domain containing 3 protein (NLRP3), thereby reducing IL-1β, IL-18, and gasdermin D (GSDMD) maturation, and activating the transcription factor nuclear factor erythroid 2-related factor 2 (Nrf2) with its widespread down-stream signaling events [reviewed in ( Figure 1B )
