Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses

Joe Dan Dunn(University of Geneva), Cristina Bosmani(University of Geneva), Caroline Barisch(University of Geneva), Lyudmil Raykov(University of Geneva), Louise Lefrançois(University of Geneva), Elena Cardenal‐Muñoz(University of Geneva), Ana T. López-Jiménez(University of Geneva), Thierry Soldati(University of Geneva)
Frontiers in Immunology
January 4, 2018
Cited by 200Open Access
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Abstract

The soil-dwelling social amoeba Dictyostelium discoideum feeds on bacteria. Each meal is a potential infection because some bacteria have evolved mechanisms to resist predation. To survive such a hostile environment, D. discoideum has in turn evolved efficient antimicrobial responses that are intertwined with phagocytosis and autophagy, its nutrient acquisition pathways. The core machinery and antimicrobial functions of these pathways are conserved in the mononuclear phagocytes of mammals, which mediate the initial, innate-immune response to infection. In this review, we discuss the advantages and relevance of D. discoideum as a model phagocyte to study cellautonomous defenses. We cover the antimicrobial functions of phagocytosis and autophagy and describe the processes that create a microbicidal phagosome: acidification and delivery of lytic enzymes, generation of reactive oxygen species, and the regulation of Zn 2+ , Cu 2+ , and Fe 2+ availability. High concentrations of metals poison microbes while metal sequestration inhibits their metabolic activity. We also describe microbial interference with these defenses and highlight observations made first in D. discoideum. Finally, we discuss galectins, TNF receptor-associated factors, tripartite motif-containing proteins, and signal transducers and activators of transcription, microbial restriction factors initially characterized in mammalian phagocytes that have either homologs or functional analogs in D. discoideum.


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