Copper detoxification machinery of the brain-eating amoeba Naegleria fowleri involves copper-translocating ATPase and the antioxidant system

. 2020 Dec ; 14 () : 126-135. [epub] 20201007

Jazyk angličtina Země Nizozemsko Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid33096396
Odkazy

PubMed 33096396
PubMed Central PMC7578549
DOI 10.1016/j.ijpddr.2020.10.001
PII: S2211-3207(20)30032-4
Knihovny.cz E-zdroje

Copper is a trace metal that is necessary for all organisms but toxic when present in excess. Different mechanisms to avoid copper toxicity have been reported to date in pathogenic organisms such as Cryptococcus neoformans and Candida albicans. However, little if anything is known about pathogenic protozoans despite their importance in human and veterinary medicine. Naegleria fowleri is a free-living amoeba that occurs naturally in warm fresh water and can cause a rapid and deadly brain infection called primary amoebic meningoencephalitis (PAM). Here, we describe the mechanisms employed by N. fowleri to tolerate high copper concentrations, which include various strategies such as copper efflux mediated by a copper-translocating ATPase and upregulation of the expression of antioxidant enzymes and obscure hemerythrin-like and protoglobin-like proteins. The combination of different mechanisms efficiently protects the cell and ensures its high copper tolerance, which can be advantageous both in the natural environment and in the host. Nevertheless, we demonstrate that copper ionophores are potent antiamoebic agents; thus, copper metabolism may be considered a therapeutic target.

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Adlard P.A., Cherny R.A., Finkelstein D.I., Gautier E., Robb E., Cortes M., Volitakis I., Liu X., Smith J.P., Perez K., Laughton K., Li Q., Charman S.A., Nicolazzo J.A., Wilkins S., Deleva K., Lynch T., Kok G., Ritchie C.W., Tanzi R.E., Cappai R., Masters C.L., Barnham K.J., Bush A.I. Rapid restoration of cognition in Alzheimer's transgenic mice with 8-hydroxy quinoline analogs is associated with decreased interstitial Aß. Neuron. 2008;59:43–55. PubMed

Ahmed A.M., Lyautey E., Bonnineau C., Dabrin A., Pesce S. Environmental concentrations of copper, alone or in mixture with arsenic, can impact river sediment microbial community structure and functions. Front. Microbiol. 2018;9:1–13. PubMed PMC

Altschul S.F., Gish W., Miller W., Myers E.W., Lipman D.J. Basic local alignment search tool. J. Mol. Biol. 1990;215:403–410. PubMed

Alvarez-Carreño C., Alva V., Becerra A., Lazcano A. Structure, function and evolution of the hemerythrin-like domain superfamily. Protein Sci. 2018;27:848–860. PubMed PMC

Arbon D., Ženíšková K., Mach J., Grechnikova M., Malych R., Talacko P., Sutak R. Adaptive iron utilization compensates for the lack of an inducible uptake system in Naegleria fowleri and represents a potential target for therapeutic intervention. PLoS Negl. Trop. Dis. 2020;14:1–25. PubMed PMC

Arnér E.S.J., Holmgren A. Physiological functions of thioredoxin and thioredoxin reductase. Eur. J. Biochem. 2000;267:6102–6109. PubMed

Aurrecoechea C., Barreto A., Brestelli J., Brunk B.P., Caler E.V., Fischer S., Gajria B., Gao X., Gingle A., Grant G., Harb O.S., Heiges M., Iodice J., Kissinger J.C., Kraemer E.T., Li W., Nayak V., Pennington C., Pinney D.F., Pitts B., Roos D.S., Srinivasamoorthy G., Stoeckert C.J., Treatman C., Wang H. AmoebaDB and MicrosporidiaDB: functional genomic resources for Amoebozoa and microsporidia species. Nucleic Acids Res. 2011;39:612–619. PubMed PMC

Bailly X., Vanin S., Chabasse C., Mizuguchi K., Vinogradov S.N. A phylogenomic profile of hemerythrins, the nonheme diiron binding respiratory proteins. BMC Evol. Biol. 2008;8:1–11. PubMed PMC

Bellini N.K., Santos T.M., da Silva M.T.A., Thiemann O.H. The therapeutic strategies against Naegleria fowleri. Exp. Parasitol. 2018;187:1–11. PubMed

Bernsel A., Viklund H., Falk J., Lindahl E., Von Heijne G., Elofsson A. Prediction of membrane-protein topology from first principles. Proc. Natl. Acad. Sci. U. S. A. 2008;105:7177–7181. PubMed PMC

Biteau B., Labarre J., Toledano M.B. ATP-dependent reduction of cysteine-sulphinic acid by S. cerevisiae sulphiredoxin. Nature. 2003;425:980–984. PubMed

Brancaccio D., Gallo A., Piccioli M., Novellino E., Ciofi-Baffoni S., Banci L. [4Fe-4S] cluster assembly in mitochondria and its impairment by copper. J. Am. Chem. Soc. 2017;139:719–730. PubMed

Capdevila M., Atrian S. Metallothionein protein evolution: a miniassay. J. Biol. Inorg. Chem. 2011;16:977–989. PubMed

Cox J., Hein M.Y., Luber C.A., 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;13:2513–2526. PubMed PMC

Cunha I., Mangas-Ramirez E., Guilhermino L. Effects of copper and cadmium on cholinesterase and glutathione S-transferase activities of two marine gastropods (Monodonta lineata and Nucella lapillus) Comp. Biochem. Physiol. C Toxicol. Pharmacol. 2007;145:648–657. PubMed

Ding C., Festa R.A., Chen Y.L., Espart A., Palacios Ò., Espín J., Capdevila M., Atrian S., Heitman J., Thiele D.J. Cryptococcus neoformans copper detoxification machinery is critical for fungal virulence. Cell Host Microbe. 2013;13:265–276. PubMed PMC

Ding C., Yin J., Tovar E.M.M., Fitzpatrick D.A., Higgins D.G., Thiele D.J. The copper regulon of the human fungal pathogen Cryptococcus neoformans H99. Mol. Microbiol. 2011;81:1560–1576. PubMed PMC

Ding W.Q., Lind S.E. Metal ionophores - an emerging class of anticancer drugs. IUBMB Life. 2009;61:1013–1018. PubMed

Dobson L., Reményi I., Tusnády G.E. CCTOP: a Consensus Constrained TOPology prediction web server. Nucleic Acids Res. 2015;43:W408–W412. PubMed PMC

Eyice Ö., Myronova N., Pol A., Carrión O., Todd J.D., Smith T.J., Gurman S.J., Cuthbertson A., Mazard S., Mennink-Kersten M.A.S.H., Bugg T.D.H., Andersson K.K., Johnston A.W.B., Op Den Camp H.J.M., Schäfer H. Bacterial SBP56 identified as a Cu-dependent methanethiol oxidase widely distributed in the biosphere. ISME J. 2018;12:145–160. PubMed PMC

Fernando M.R., Nanri H., Yoshitake S., Nagata‐Kuno K., Minakami S. Thioredoxin regenerates proteins inactivated by oxidative stress in endothelial cells. Eur. J. Biochem. 1992;209:917–922. PubMed

Festa R.A., Helsel M.E., Franz K.J., Thiele D.J. Exploiting innate immune cell activation of a copper-dependent antimicrobial agent during infection. Chem. Biol. 2014;21:977–987. PubMed PMC

Findlay V.J., Townsend D.M., Morris T.E., Fraser J.P., He L., Tew K.D. A novel role for human sulfiredoxin in the reversal of glutathionylation. Canc. Res. 2006;66:6800–6806. PubMed PMC

Flemming C.A., Trevors J.T. Copper toxicity and chemistry in the environment: a review. Water. Air. Soil Pollut. 1989;44:143–158.

Fulton C. Axenic cultivation of Naegleria gruberi. Requirement for methionine. Exp. Cell Res. 1974;88:365–370. PubMed

Fung D.K.C., Lau W.Y., Chan W.T., Yan A. Copper efflux is induced during anaerobic amino acid limitation in escherichia coli to protect iron-sulfur cluster enzymes and biogenesis. J. Bacteriol. 2013;195:4556–4568. PubMed PMC

Gaetke L.M., Chow C.K. Copper toxicity, oxidative stress, and antioxidant nutrients. Toxicology. 2003;189:147–163. PubMed

Garcia-Santamarina S., Uzarska M.A., Festa R.A., Lill R., Thiele D.J. Cryptococcus neoformans iron-sulfur protein biogenesis machinery is a novel layer of protection against Cu stress. mBio. 2017;8:1–18. PubMed PMC

Gietz R.D., Schiestl R.H. High-efficiency yeast transformation using the LiAc/SS carrier DNA/PEG method. Nat. Protoc. 2007;2:38–41. PubMed

Harwood M.D., Russell M.R., Neuhoff S., Warhurst G., Rostami-Hodjegan A. Lost in centrifugation: accounting for transporter protein losses in quantitative targeted absolute proteomics. Drug Metab. Dispos. 2014;42:1766–1772. PubMed

Helsel M.E., White E.J., Razvi S.Z.A., Alies B., Franz K.J. Chemical and functional properties of metal chelators that mobilize copper to elicit fungal killing of Cryptococcus neoformans. Metallomics. 2017;9:69–81. PubMed PMC

Herman E.K., Greninger A., van der Giezen M., Ginger M.L., Ramirez-Macias I., Miller H.C., Morgan M.J., Tsaousis A.D., Velle K., Vargová R., Rodrigo Najle S., MacIntyre G., Muller N., Wittwer M., Zysset-Burri D.C., Elias M., Slamovits C., Weirauch M., Fritz-Laylin L., Marciano-Cabral F., Puzon G.J., Walsh T., Chiu C., Dacks J.B. bioRxiv; 2020. A comparative ‘omics approach to candidate pathogenicity factor discovery in the brain-eating amoeba Naegleria fowleri. 2020.01.16.908186.

Hodgkinson V., Petris M.J. Copper homeostasis at the host-pathogen interface. J. Biol. Chem. 2012;287:13549–13555. PubMed PMC

Holmgren A. Thioredoxin. Annu. Rev. Biochem. 1985;54:237–271. PubMed

Holmgren A., Lu J. Thioredoxin and thioredoxin reductase: current research with special reference to human disease. Biochem. Biophys. Res. Commun. 2010;396:120–124. PubMed

Isah M.B., Goldring J.P.D., Coetzer T.H.T. Expression and copper binding properties of the N-terminal domain of copper P-type ATPases of African trypanosomes. Mol. Biochem. Parasitol. 2020;235:111245. PubMed

Käll L., Krogh A., Sonnhammer E.L.L. A combined transmembrane topology and signal peptide prediction method. J. Mol. Biol. 2004;338:1027–1036. PubMed

Kühlbrandt W. Biology, structure and mechanism of P-type ATPases. Nat. Rev. Mol. Cell Biol. 2004;5:282–295. PubMed

Kung C.C.S., Huang W.N., Huang Y.C., Yeh K.C. Proteomic survey of copper-binding proteins in Arabidopsis roots by immobilized metal affinity chromatography and mass spectrometry. Proteomics. 2006;6:2746–2758. PubMed

Letelier M.E., Martínez M., González-Lira V., Faúndez M., Aracena-Parks P. Inhibition of cytosolic glutathione S-transferase activity from rat liver by copper. Chem. Biol. Interact. 2006;164:39–48. PubMed

Lutsenko S., LeShane E.S., Shinde U. Biochemical basis of regulation of human copper-transporting ATPases. Arch. Biochem. Biophys. 2007;463:134–148. PubMed PMC

Mach J., Bíla J., Ženíšková K., Arbon D., Malych R., Glavanakovová M., Nývltová E., Sutak R. Iron economy in Naegleria gruberi reflects its metabolic flexibility. Int. J. Parasitol. 2018;48:719–727. PubMed

Maciver S.K., Piñero J.E., Lorenzo-Morales J. Is Naegleria fowleri an emerging parasite? Trends Parasitol. 2020;36:19–28. PubMed

Mackie J., Szabo E.K., Urgast D.S., Ballou E.R., Childers D.S., MacCallum D.M., Feldmann J., Brown A.J.P. Host-imposed copper poisoning impacts fungal micronutrient acquisition during systemic Candida albicans infections. PLoS One. 2016;11:1–18. PubMed PMC

Macomber L., Imlay J.A. The iron-sulfur clusters of dehydratases are primary intracellular targets of copper toxicity. Proc. Natl. Acad. Sci. U. S. A. 2009;106:8344–8349. PubMed PMC

Meade J.C. P-type transport ATPases in Leishmania and Trypanosoma. Parasite. 2019;26:69. PubMed PMC

Moller J.A., Juul B., Maire M. le. Structural organization, ion transport, and energy transduction of P-type ATPases. Biochim. Biophys. Acta. 1996;1286:1–51. PubMed

Mull B.J., Narayanan J., Hill V.R. Improved method for the detection and quantification of Naegleria fowleri in water and sediment using immunomagnetic separation and real-time PCR. J. Parasitol. Res. 2013;2013:608367. PubMed PMC

Ogawa K., Sun J., Taketani S., Nakajima O., Nishitani C., Sassa S., Hayashi N., Yamamoto M., Shibahara S., Fujita H., Igarashi K. Heme mediates derepression of Maf recognition element through direct binding to transcription repressor Bach1. EMBO J. 2001;20:2835–2843. PubMed PMC

Pearce D.A., Sherman F. Toxicity of copper, cobalt, and nickel salts is dependent on histidine metabolism in the yeast Saccharomyces cerevisiae. J. Bacteriol. 1999;181:4774–4779. PubMed PMC

Perez-Riverol Y., Csordas A., Bai J., Bernal-Llinares M., Hewapathirana S., Kundu D.J., Inuganti A., Griss J., Mayer G., Eisenacher M., Pérez E., Uszkoreit J., Pfeuffer J., Sachsenberg T., Yilmaz Ş., Tiwary S., Cox J., Audain E., Walzer M., Jarnuczak A.F., Ternent T., Brazma A., Vizcaíno J.A. The PRIDE database and related tools and resources in 2019: improving support for quantification data. Nucleic Acids Res. 2019;47:D442–D450. PubMed PMC

Pesce A., Bolognesi M., Nardini M. vol. 63. 2013. pp. 79–96. (Protoglobin: Structure and Ligand-Binding Properties). PubMed

Rainsford K.D., Milanino R., Sorenson J.R.J., Velo G.P., editors. Copper and Zinc in Inflammatory and Degenerative Diseases. Springer Science+Business Media; Dordrecht: 1998.

Rasoloson D., Shi L., Chong C.R., Kafsack B.F., Sullivan D.J. Copper pathways in Plasmodium falciparum infected erythrocytes indicate an efflux role for the copper P-ATPase. Biochem. J. 2004;381:803–811. PubMed PMC

Reeder N.L., Xu J., Youngquist R.S., Schwartz J.R., Rust R.C., Saunders C.W. The antifungal mechanism of action of zinc pyrithione. Br. J. Dermatol. 2011;165:9–12. PubMed

Rhee J.S., Lee Y.M., Hwang D.S., Lee K.W., Kim I.C., Shin K.H., Raisuddin S., Lee J.S. Molecular cloning and characterization of omega class glutathione S-transferase (GST-O) from the polychaete Neanthes succinea: biochemical comparison with theta class glutathione S-transferase (GST-T) Comp. Biochem. Physiol. C Toxicol. Pharmacol. 2007;146:471–477. PubMed

Salazar-Medina A.J., García-Rico L., García-Orozco K.D., Valenzuela-Soto E., Contreras-Vergara C.A., Arreola R., Arvizu-Flores A., Sotelo-Mundo R.R. Inhibition by Cu2+ and Cd2+ of a Mu-class glutathione S-transferase from shrimp Litopenaeus vannamei. J. Biochem. Mol. Toxicol. 2010;24:218–222. PubMed

Sheldon J.R., Skaar E.P. Metals as phagocyte antimicrobial effectors. Curr. Opin. Immunol. 2019;60:1–9. PubMed PMC

Shimizu T. Binding of cysteine thiolate to the Fe(III) heme complex is critical for the function of heme sensor proteins. J. Inorg. Biochem. 2012;108:171–177. PubMed

Siddiqui R., Ali I.K.M., Cope J.R., Khan N.A. Biology and pathogenesis of Naegleria fowleri. Acta Trop. 2016;164:375–394. PubMed

Smith A.D., Logeman B.L., Thiele D.J. Copper acquisition and utilization in fungi. Annu. Rev. Microbiol. 2017:597–623. PubMed PMC

Söding J., Biegert A., Lupas A.N. The HHpred interactive server for protein homology detection and structure prediction. Nucleic Acids Res. 2005;33:244–248. PubMed PMC

Solioz M., Vulpe C. CPx-type ATPases: a class of P-type ATPases that pump heavy metals. Trends Biochem. Sci. 1996;21:237–241. PubMed

Song Y., Xu H., Chen W., Zhan P., Liu X. 8-Hydroxyquinoline: a privileged structure with broad-ranging pharmacological potentials. Med. Chem. Commun. 2015;6:61–74.

Sykora J.L., Keleti G., Martinez A.J. Occurrence and pathogenicity of Naegleria fowleri in artificially heated waters. Appl. Environ. Microbiol. 1983;45:974–979. PubMed PMC

Szczypka M.S., Zhu Z., Silar P., Thiele D.J. Saccharomyces cerevisiae mutants altered in vacuole function are defective in copper detoxification and iron-responsive gene transcription. Yeast. 1997;13:1423–1435. PubMed

Tyanova S., Temu T., Sinitcyn P., Carlson A., Hein M.Y., Geiger T., Mann M., Cox J. The Perseus computational platform for comprehensive analysis of (prote)omics data. Nat. Methods. 2016;13:731–740. PubMed

Vuilleumier S., Pagni M. The elusive roles of bacterial glutathione S-transferases: new lessons from genomes. Appl. Microbiol. Biotechnol. 2002;58:138–146. PubMed

Weissman Z., Berdicevsky I., Cavari B.Z., Kornitzer D. The high copper tolerance of Candida albicans is mediated by a P-type ATPase. Proc. Natl. Acad. Sci. U. S. A. 2000;97:3520–3525. PubMed PMC

White C., Lee J., Kambe T., Fritsche K., Petris M.J. A role for the ATP7A copper-transporting ATPase in macrophage bactericidal activity. J. Biol. Chem. 2009;284:33949–33956. PubMed PMC

Wiemann P., Perevitsky A., Lim F.Y., Shadkchan Y., Knox B.P., Landero Figueora J.A., Choera T., Niu M., Steinberger A.J., Wüthrich M., Idol R.A., Klein B.S., Dinauer M.C., Huttenlocher A., Osherov N., Keller N.P. Aspergillus fumigatus copper export machinery and reactive oxygen intermediate defense counter host copper-mediated oxidative antimicrobial offense. Cell Rep. 2017;19:1008–1021. PubMed PMC

Wu Z., Fernandez-Lima F.A., Russell D.H. Amino acid influence on copper binding to peptides: cysteine versus arginine. J. Am. Soc. Mass Spectrom. 2010;21:522–533. PubMed

Yang X., Cai P., Liu Q., Wu J., Yin Y., Wang X., Kong L. Novel 8-hydroxyquinoline derivatives targeting β-amyloid aggregation, metal chelation and oxidative stress against Alzheimer's disease. Bioorganic Med. Chem. 2018;26:3191–3201. PubMed

Yuan D.S., Dancis A., Klausner R.D. Restriction of copper export in Saccharomyces cerevisiae to a late Golgi or post-Golgi compartment in the secretory pathway. J. Biol. Chem. 1997;272:25787–25793. PubMed

Zhang L., Guarente L. Heme binds to a short sequence that serves a regulatory function in diverse proteins. EMBO J. 1995;14:313–340. PubMed PMC

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