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Iron metabolism and resistance to infection by invasive bacteria in the social amoeba Dictyostelium discoideum

Dictyostelium cells are forest soil amoebae, which feed on bacteria and proliferate as solitary cells until bacteria are consumed. Starvation triggers a change in life style, forcing cells to gather into aggregates to form multicellular organisms capable of cell differentiation and morphogenesis. As...

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Autores principales: Bozzaro, Salvatore, Buracco, Simona, Peracino, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777012/
https://www.ncbi.nlm.nih.gov/pubmed/24066281
http://dx.doi.org/10.3389/fcimb.2013.00050
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author Bozzaro, Salvatore
Buracco, Simona
Peracino, Barbara
author_facet Bozzaro, Salvatore
Buracco, Simona
Peracino, Barbara
author_sort Bozzaro, Salvatore
collection PubMed
description Dictyostelium cells are forest soil amoebae, which feed on bacteria and proliferate as solitary cells until bacteria are consumed. Starvation triggers a change in life style, forcing cells to gather into aggregates to form multicellular organisms capable of cell differentiation and morphogenesis. As a soil amoeba and a phagocyte that grazes on bacteria as the obligate source of food, Dictyostelium could be a natural host of pathogenic bacteria. Indeed, many pathogens that occasionally infect humans are hosted for most of their time in protozoa or free-living amoebae, where evolution of their virulence traits occurs. Due to these features and its amenability to genetic manipulation, Dictyostelium has become a valuable model organism for studying strategies of both the host to resist infection and the pathogen to escape the defense mechanisms. Similarly to higher eukaryotes, iron homeostasis is crucial for Dictyostelium resistance to invasive bacteria. Iron is essential for Dictyostelium, as both iron deficiency or overload inhibit cell growth. The Dictyostelium genome shares with mammals many genes regulating iron homeostasis. Iron transporters of the Nramp (Slc11A) family are represented with two genes, encoding Nramp1 and Nramp2. Like the mammalian ortholog, Nramp1 is recruited to phagosomes and macropinosomes, whereas Nramp2 is a membrane protein of the contractile vacuole network, which regulates osmolarity. Nramp1 and Nramp2 localization in distinct compartments suggests that both proteins synergistically regulate iron homeostasis. Rather than by absorption via membrane transporters, iron is likely gained by degradation of ingested bacteria and efflux via Nramp1 from phagosomes to the cytosol. Nramp gene disruption increases Dictyostelium sensitivity to infection, enhancing intracellular growth of Legionella or Mycobacteria. Generation of mutants in other “iron genes” will help identify genes essential for iron homeostasis and resistance to pathogens.
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spelling pubmed-37770122013-09-24 Iron metabolism and resistance to infection by invasive bacteria in the social amoeba Dictyostelium discoideum Bozzaro, Salvatore Buracco, Simona Peracino, Barbara Front Cell Infect Microbiol Microbiology Dictyostelium cells are forest soil amoebae, which feed on bacteria and proliferate as solitary cells until bacteria are consumed. Starvation triggers a change in life style, forcing cells to gather into aggregates to form multicellular organisms capable of cell differentiation and morphogenesis. As a soil amoeba and a phagocyte that grazes on bacteria as the obligate source of food, Dictyostelium could be a natural host of pathogenic bacteria. Indeed, many pathogens that occasionally infect humans are hosted for most of their time in protozoa or free-living amoebae, where evolution of their virulence traits occurs. Due to these features and its amenability to genetic manipulation, Dictyostelium has become a valuable model organism for studying strategies of both the host to resist infection and the pathogen to escape the defense mechanisms. Similarly to higher eukaryotes, iron homeostasis is crucial for Dictyostelium resistance to invasive bacteria. Iron is essential for Dictyostelium, as both iron deficiency or overload inhibit cell growth. The Dictyostelium genome shares with mammals many genes regulating iron homeostasis. Iron transporters of the Nramp (Slc11A) family are represented with two genes, encoding Nramp1 and Nramp2. Like the mammalian ortholog, Nramp1 is recruited to phagosomes and macropinosomes, whereas Nramp2 is a membrane protein of the contractile vacuole network, which regulates osmolarity. Nramp1 and Nramp2 localization in distinct compartments suggests that both proteins synergistically regulate iron homeostasis. Rather than by absorption via membrane transporters, iron is likely gained by degradation of ingested bacteria and efflux via Nramp1 from phagosomes to the cytosol. Nramp gene disruption increases Dictyostelium sensitivity to infection, enhancing intracellular growth of Legionella or Mycobacteria. Generation of mutants in other “iron genes” will help identify genes essential for iron homeostasis and resistance to pathogens. Frontiers Media S.A. 2013-09-19 /pmc/articles/PMC3777012/ /pubmed/24066281 http://dx.doi.org/10.3389/fcimb.2013.00050 Text en Copyright © 2013 Bozzaro, Buracco and Peracino. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Bozzaro, Salvatore
Buracco, Simona
Peracino, Barbara
Iron metabolism and resistance to infection by invasive bacteria in the social amoeba Dictyostelium discoideum
title Iron metabolism and resistance to infection by invasive bacteria in the social amoeba Dictyostelium discoideum
title_full Iron metabolism and resistance to infection by invasive bacteria in the social amoeba Dictyostelium discoideum
title_fullStr Iron metabolism and resistance to infection by invasive bacteria in the social amoeba Dictyostelium discoideum
title_full_unstemmed Iron metabolism and resistance to infection by invasive bacteria in the social amoeba Dictyostelium discoideum
title_short Iron metabolism and resistance to infection by invasive bacteria in the social amoeba Dictyostelium discoideum
title_sort iron metabolism and resistance to infection by invasive bacteria in the social amoeba dictyostelium discoideum
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777012/
https://www.ncbi.nlm.nih.gov/pubmed/24066281
http://dx.doi.org/10.3389/fcimb.2013.00050
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