Adaptive iron utilization compensates for the lack of an inducible uptake system in Naegleria fowleri and represents a potential target for therapeutic intervention
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
32555641
PubMed Central
PMC7326272
DOI
10.1371/journal.pntd.0007759
PII: PNTD-D-19-01499
Knihovny.cz E-zdroje
- MeSH
- buněčné dýchání MeSH
- fyziologická adaptace * MeSH
- mitochondrie metabolismus MeSH
- Naegleria fowleri genetika metabolismus MeSH
- regulace genové exprese * MeSH
- stopové prvky metabolismus MeSH
- železo metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- stopové prvky MeSH
- železo MeSH
Naegleria fowleri is a single-cell organism living in warm freshwater that can become a deadly human pathogen known as a brain-eating amoeba. The condition caused by N. fowleri, primary amoebic meningoencephalitis, is usually a fatal infection of the brain with rapid and severe onset. Iron is a common element on earth and a crucial cofactor for all living organisms. However, its bioavailable form can be scarce in certain niches, where it becomes a factor that limits growth. To obtain iron, many pathogens use different machineries to exploit an iron-withholding strategy that has evolved in mammals and is important to host-parasite interactions. The present study demonstrates the importance of iron in the biology of N. fowleri and explores the plausibility of exploiting iron as a potential target for therapeutic intervention. We used different biochemical and analytical methods to explore the effect of decreased iron availability on the cellular processes of the amoeba. We show that, under iron starvation, nonessential, iron-dependent, mostly cytosolic pathways in N. fowleri are downregulated, while the metal is utilized in the mitochondria to maintain vital respiratory processes. Surprisingly, N. fowleri fails to respond to acute shortages of iron by inducing the reductive iron uptake system that seems to be the main iron-obtaining strategy of the parasite. Our findings suggest that iron restriction may be used to slow the progression of infection, which may make the difference between life and death for patients.
BIOCEV proteomics core facility Faculty of Science BIOCEV Charles University Vestec Czech Republic
Department of Parasitology Faculty of Science BIOCEV Charles University Vestec Czech Republic
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De Jonckheere JF. What do we know by now about the genus PubMed
Kelly RB, Francine M-C, Charles PG. Occurrence of
Visvesvara GS, Moura H, Schuster FL. Pathogenic and opportunistic free-living amoebae: PubMed DOI
Grace E, Asbill S, Virga K. PubMed DOI PMC
Ma P, Visvesvara GS, Martinez AJ, Theodore FH, Daggett PM, Sawyer TK. PubMed
Centers for Disease Control and Prevention,
Linam WM, Ahmed M, Cope JR, Chu C, Visvesvara GS, Da Silva AJ, et al. Successful treatment of an adolescent with PubMed DOI PMC
Pana A, Vijayan V, Anilkumar AC. Amebic meningoencephalitis [Internet]. StatPearls. 2019. PubMed
Cabello‐Vílchez AM, Chura‐Araujo MA, Anicama Lima WE, Vela C, Asencio AY, García H, et al. Fatal granulomatous amoebic encephalitis due to free‐living amoebae in two boys in two different hospitals in Lima, Perú. Neuropathology. 2019. November 22;neup.12617. PubMed
Crichton R. Iron metabolism: From molecular mechanisms to clinical consequences: Fourth edition. Chichester, UK: John Wiley & Sons, Ltd; 2016. 1–556 p.
Lill R, Broderick JB, Dean DR. Special issue on iron-sulfur proteins: Structure, function, biogenesis and diseases. Biochim Biophys Acta—Mol Cell Res. 2015. June 1;1853(6):1251–2. PubMed PMC
Boyd PW, Jickells T, Law CS, Blain S, Boyle EA, Buesseler KO, et al. Mesoscale iron enrichment experiments 1993–2005: Synthesis and future directions. Science (80-). 2007. February 2;315(5812):612–7. PubMed
Koka S, Föller M, Lamprecht G, Boini KM, Lang C, Huber SM, et al. Iron deficiency influences the course of malaria in PubMed DOI
Kabyemela ER, Fried M, Kurtis JD, Mutabingwa TK, Duffy PE. Decreased susceptibility to PubMed DOI
Ganz T. Iron in innate immunity: Starve the invaders. Curr Opin Immunol. 2009;21(1):63–7. 10.1016/j.coi.2009.01.011 PubMed DOI PMC
Sutak R, Lesuisse E, Tachezy J, Richardson DR. Crusade for iron: Iron uptake in unicellular eukaryotes and its significance for virulence. Trends Microbiol. 2008. June 1;16(6):261–8. 10.1016/j.tim.2008.03.005 PubMed DOI
Singh N, Haldar S, Tripathi AK, Horback K, Wong J, Sharma D, et al. Brain iron homeostasis: From molecular mechanisms to clinical significance and therapeutic opportunities. Antioxidants Redox Signal. 2014. March 10;20(8):1324–63. PubMed PMC
Leitner DF, Connor JR. Functional roles of transferrin in the brain. Vol. 1820, Biochimica et Biophysica Acta—General Subjects. 2012. p. 393–402. PubMed
Mobarra N, Shanaki M, Ehteram H, Nasiri H, Sahmani M, Saeidi M, et al. A review on iron chelators in treatment of iron overload syndromes. Vol. 10, International Journal of Hematology-Oncology and Stem Cell Research Tehran University of Medical Sciences (TUMS); 2016. p. 239–47. PubMed PMC
Cruz-Castañeda A, López-Casamichana M, Olivares-Trejo JJ. PubMed DOI
Basu S, Horáková E, Lukeš J. Iron-associated biology of PubMed
Tsaousis AD, Nývltová E, Šuták R, Hrdý I, Tachezy J. A Nonmitochondrial hydrogen production in PubMed DOI PMC
Marciano-Cabral FM, Patterson M, John DT, Bradley SG. Cytopathogenicity of PubMed
Martínez-Castillo M, Ramírez-Rico G, Serrano-Luna J, Shibayama M. Iron-binding protein degradation by cysteine proteases of PubMed PMC
Dancis A, Roman DG, Anderson GJ, Hinnebusch AG, Klausner RD. Ferric reductase of PubMed DOI PMC
Sutak R, Chamot C, Tachezy J, Camadro JM, Lesuisse E. Siderophore and haem iron use by PubMed
Alonso P, Zubiaur E. Phagocytic activity of three PubMed DOI
Scaglia M, Gatti S, Brustia R, Chichino G, Rondanelli EG. Phagocytosis of human erythrocytes by PubMed
Létoffé S, Heuck G, Delepelaire P, Lange N, Wandersman C. Bacteria capture iron from heme by keeping tetrapyrrol skeleton intact. Proc Natl Acad Sci U S A. 2009. July 14;106(28):11719–24. 10.1073/pnas.0903842106 PubMed DOI PMC
Bradley SG, Toney DM, Zhang Y, Marciano-Cabral F. Dependence of growth, metabolic expression, and pathogenicity of PubMed
Jung SY, Kim JH, Song KJ, Lee YJ, Kwon MH, Kim K, et al. Gene silencing of nfa1 affects the PubMed DOI
Shakoury-Elizeh M, Protchenko O, Berger A, Cox J, Gable K, Dunn TM, et al. Metabolic response to iron deficiency in PubMed DOI PMC
Bexkens ML, Zimorski V, Sarink MJ, Wienk H, Brouwers JF, De Jonckheere JF, et al. Lipids Are the Preferred Substrate of the Protist PubMed DOI PMC
Mach J, Bíla J, Ženíšková K, Arbon D, Malych R, Glavanakovová M, et al. Iron economy in PubMed DOI
Kulda J, Tachezy J, Čerkasovová A. PubMed DOI
Li X, Li J, Hu X, Huang L, Xiao J, Chan J, et al. Differential roles of the hemerythrin-like proteins of PubMed DOI PMC
Ma Z, Strickland KT, Cherne MD, Sehanobish E, Rohde KH, Self WT, et al. The Rv2633c protein of PubMed DOI PMC
Selote D, Samira R, Matthiadis A, Gillikin JW, Long TA. Iron-binding e3 ligase mediates iron response in plants by targeting basic helix-loop-helix transcription factors1[open]. Plant Physiol. 2015. January;167(1):273–86. 10.1104/pp.114.250837 PubMed DOI PMC
Zeng WB, Chen WB, Yan QP, Lin GF, Qin YX. Hemerythrin is required for PubMed
Newsome AL, Wilhelm WE. Inhibition of PubMed PMC
Romeo AM, Christen L, Niles EG, Kosman DJ. Intracellular chelation of iron by bipyridyl inhibits DNA virus replication: Ribonucleotide reductase maturation as a probe of intracellular iron pools. J Biol Chem. 2001. June 29;276(26):24301–8. 10.1074/jbc.M010806200 PubMed DOI
Megger N, Welte L, Zamora F, Müller J. Metal-mediated aggregation of DNA comprising 2,2′-bipyridine nucleoside, an asymmetrically substituted chiral bidentate ligand. Dalt Trans. 2011. February 8;40(8):1802–7. PubMed
Nyayapati S, Afshan G, Lornitzo F, Byrnes RW, Petering DH. Depletion of cellular iron by BPS and ascorbate: Effect on toxicity of adriamycin. Free Radic Biol Med. 1996. January 1;20(3):319–29. 10.1016/0891-5849(96)02054-0 PubMed DOI
Ihnat PM, Vennerstrom JL, Robinson DH. Synthesis and solution properties of deferoxamine amides. J Pharm Sci. 2000. December;89(12):1525–36. 10.1002/1520-6017(200012)89:12<1525::aid-jps3>3.0.co;2-t PubMed DOI
Kontoghiorghe CN, Kontoghiorghes GJ. Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes. Drug Des Devel Ther. 2016;10:465–81. 10.2147/DDDT.S79458 PubMed DOI PMC
Porter JB. Deferoxamine pharmacokinetics. Semin Hematol. 2001. January;38(1 Suppl 1):63–8. 10.1016/s0037-1963(01)90061-7 PubMed DOI
Crichton RR, Ward RJ, Hider RC. The efficacy of iron chelators for removing iron from specific brain regions and the pituitary—Ironing out the brain. Vol. 12, Pharmaceuticals. MDPI AG; 2019. PubMed PMC
Tyanova S, Temu T, Sinitcyn P, Carlson A, Hein MY, Geiger T, et al. The Perseus computational platform for comprehensive analysis of (prote)omics data. Nature Methods. Nature Publishing Group; 2016;13 p. 731–40. 10.1038/nmeth.3901 PubMed DOI
Tyanova S, Temu T, Cox J. The MaxQuant computational platform for mass spectrometry-based shotgun proteomics. Nat Protoc. 2016. December 1;11(12):2301–19. 10.1038/nprot.2016.136 PubMed DOI
Cox J, Hein MY, Luber CA, Paron I, Nagaraj N, Mann M. Accurate proteome-wide label-free quantification by delayed normalization and maximal peptide ratio extraction, termed MaxLFQ. Mol Cell Proteomics. 2014. September 1;13(9):2513–26. 10.1074/mcp.M113.031591 PubMed DOI PMC
Schindelin J, Arganda-Carreras I, Frise E, Kaynig V, Longair M, Pietzsch T, et al. Fiji: An open-source platform for biological-image analysis. Vol. 9, Nature Methods. 2012. p. 676–82. 10.1038/nmeth.2019 PubMed DOI PMC
Stookey LL. Ferrozine-a new spectrophotometric reagent for iron. Anal Chem. 1970. June;42(7):779–81.
Aurrecoechea C, Barreto A, Brestelli J, Brunk BP, Caler E V., Fischer S, et al. AmoebaDB and MicrosporidiaDB: Functional genomic resources for PubMed PMC
Scheiber IF, Pilátová J, Malych R, Kotabova E, Krijt M, Vyoral D, et al. Copper and iron metabolism in: PubMed DOI
Zimmermann L, Stephens A, Nam SZ, Rau D, Kübler J, Lozajic M, et al. A Completely Reimplemented MPI Bioinformatics Toolkit with a New HHpred Server at its Core. J Mol Biol. 2018. July 20;430(15):2237–43. 10.1016/j.jmb.2017.12.007 PubMed DOI
Indiveri C, Iacobazzi V, Tonazzi A, Giangregorio N, Infantino V, Convertini P, et al. The mitochondrial carnitine/acylcarnitine carrier: Function, structure and physiopathology. Mol Aspects Med. 2011. August 1;32(4–6):223–33. 10.1016/j.mam.2011.10.008 PubMed DOI
Hamel P, Saint-Georges Y, De Pinto B, Lachacinski N, Altamura N, Dujardin G. Redundancy in the function of mitochondrial phosphate transport in PubMed DOI
Šmíd O, Horáková E, Vilimova V, Hrdý I, Cammack R, Horvath A, et al. Knock-downs of iron-sulfur cluster assembly proteins IscS and IscU down-regulate the active mitochondrion of procyclic PubMed DOI
Hoff KG, Cupp-Vickery JR, Vickery LE. Contributions of the LPPVK motif of the iron-sulfur template protein IscU to interactions with the Hsc66-Hsc20 chaperone system. J Biol Chem. 2003. September 26;278(39):37582–9. 10.1074/jbc.M305292200 PubMed DOI
Mittra B, Laranjeira-Silva MF, Perrone Bezerra de Menezes J, Jensen J, Michailowsky V, Andrews NW. A trypanosomatid iron transporter that regulates mitochondrial function is required for PubMed DOI PMC
Brazzolotto X, Pierrel F, Pelosi L. Three conserved histidine residues contribute to mitochondrial iron transport through mitoferrins. Biochem J. 2014. May 15;460(1):79–89. 10.1042/BJ20140107 PubMed DOI
Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970. August;227(5259):680–5. 10.1038/227680a0 PubMed DOI
Anders S, Huber W. Differential expression analysis for sequence count data. Genome Biol. 2010. October 27;11(10):R106 10.1186/gb-2010-11-10-r106 PubMed DOI PMC
MacLean B, Tomazela DM, Shulman N, Chambers M, Finney GL, Frewen B, et al. Skyline: An open source document editor for creating and analyzing targeted proteomics experiments. Bioinformatics. 2010. April 1;26(7):966–8. 10.1093/bioinformatics/btq054 PubMed DOI PMC
Rasoloson D, Vaňáčová Š, Tomková E, Rázga J, Hrdý I, Tachezy J, et al. Mechanisms of in vitro development of resistance to metronidazole in PubMed
Verner Z, Čermáková P, Škodová I, Kriegová E, Horváth A, Lukeš J. Complex I (NADH:ubiquinone oxidoreductase) is active in but non-essential for procyclic PubMed DOI
IC50 Calculator, available at: https://www.aatbio.com/tools/ic50-calculator, accessed 07/03/2019 [Internet].
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