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Caspase-1-induced pyroptosis is an innate immune effector mechanism against intracellular bacteria (111.33)
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2011
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Microbial PathogensApoptosisImmunologyImmune RegulationCell DeathInnate Immune SystemInnate ImmunityImmune SystemBacterial PathogensCaspase-1-dependent ProcessingInflammationHost ResponseCaspase-1-induced PyroptosisCell SignalingHost-pathogen InteractionsPyroptosisAbstract MacrophagesVirulence FactorImmune FunctionHost-microbe InteractionIntracellular BacteriaCell BiologyPhagocyteCytokineImmune Effector FunctionsPathogenesisMicrobiologyMedicine
Abstract Macrophages mediate crucial innate immune responses via caspase-1-dependent processing and secretion of IL-1β and IL-18. While wild type Salmonella typhimurium infection is lethal to mice, a strain that persistently expresses flagellin was cleared by the cytosolic flagellin detection pathway via NLRC4 activation of caspase-1; however, this clearance was independent of IL-1β and IL-18. Instead, caspase-1 induced pyroptotic cell death released bacteria from macrophages, exposing them to uptake and killing by reactive oxygen species in neutrophils. Similarly, caspase-1 cleared Legionella and Burkholderia by cytokine independent mechanisms. Our results show, for the first time, that caspase-1 can clear intracellular bacteria in vivo independent of IL-1β and IL-18, and establish pyroptosis as an efficient mechanism of bacterial clearance by the innate immune system.