Eating the brain - A multidisciplinary study provides new insights into the mechanisms underlying the cytopathogenicity of Naegleria fowleri

. 2025 Mar ; 21 (3) : e1012995. [epub] 20250317

Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid40096149
Odkazy

PubMed 40096149
PubMed Central PMC11964265
DOI 10.1371/journal.ppat.1012995
PII: PPATHOGENS-D-24-02198
Knihovny.cz E-zdroje

Naegleria fowleri, the causative agent of primary amoebic meningoencephalitis (PAM), requires increased research attention due to its high lethality and the potential for increased incidence as a result of global warming. The aim of this study was to investigate the interactions between N. fowleri and host cells in order to elucidate the mechanisms underlying the pathogenicity of this amoeba. A co-culture system comprising human fibrosarcoma cells was established to study both contact-dependent and contact-independent cytopathogenicity. Proteomic analyses of the amoebas exposed to human cell cultures or passaged through mouse brain were used to identify novel virulence factors. Our results indicate that actin dynamics, regulated by Arp2/3 and Src kinase, play a considerable role in ingestion of host cells by amoebae. We have identified three promising candidate virulence factors, namely lysozyme, cystatin and hemerythrin, which may be critical in facilitating N. fowleri evasion of host defenses, migration to the brain and induction of a lethal infection. Long-term co-culture secretome analysis revealed an increase in protease secretion, which enhances N. fowleri cytopathogenicity. Raman microspectroscopy revealed significant metabolic differences between axenic and brain-isolated amoebae, particularly in lipid storage and utilization. Taken together, our findings provide important new insights into the pathogenic mechanisms of N. fowleri and highlight potential targets for therapeutic intervention against PAM.

Zobrazit více v PubMed

Gharpure R, Gleason M, Salah Z, Blackstock AJ, Hess-Homeier D, Yoder JS, et al. Geographic range of recreational water-associated primary amebic meningoencephalitis, United States, 1978–2018. Emerg Infect Dis. 2021;27(1):271–4. doi: 10.3201/eid2701.202119 PubMed DOI PMC

Dey R, Dlusskaya E, Oloroso M, Ashbolt NJ. First evidence of free-living PubMed DOI

Martínez-Castillo M, Cárdenas-Guerra RE, Arroyo R, Debnath A, Rodríguez MA, Sabanero M, et al. Nf-GH, a glycosidase secreted by PubMed DOI PMC

Cervantes-Sandoval I, Jesús Serrano-Luna J, Pacheco-Yépez J, Silva-Olivares A, Tsutsumi V, Shibayama M. Differences between PubMed DOI

Carrasco-Yepez M, Campos-Rodriguez R, Godinez-Victoria M, Rodriguez-Monroy MA, Jarillo-Luna A, Bonilla-Lemus P, et al. PubMed DOI

Shibayama M, Martínez-Castillo M, Silva-Olivares A, Galindo-Gómez S, Navarro-García F, Escobar-Herrera J, et al. Disruption of MDCK cell tight junctions by the free-living amoeba PubMed DOI

Coronado-Velázquez D, Betanzos A, Serrano-Luna J, Shibayama M. an in vitro model of the blood-brain barrier: PubMed DOI

Jamerson M, da Rocha-Azevedo B, Cabral GA, Marciano-Cabral F. Pathogenic PubMed DOI PMC

Aldape K, Huizinga H, Bouvier J, Mckerrow J. PubMed

Vyas IK, Jamerson M, Cabral GA, Marciano-Cabral F. Identification of peptidases in highly pathogenic vs. weakly pathogenic PubMed DOI

Lam C, Jamerson M, Cabral G, Carlesso AM, Marciano-Cabral F. Expression of matrix metalloproteinases in PubMed DOI

Carrasco-Yepez MM, Contis-Montes de Oca A, Campos-Rodriguez R, Falcon-Acosta D, Pacheco-Yepez J, Rodriguez-Mera IB, et al. Mouse neutrophils release extracellular traps in response to PubMed DOI

Flores-Huerta N, Pacheco-Yépez J, Sánchez-Monroy V, Rosales-Hernández MC, Silva-Olivares A, Serrano-Luna J, et al. The MPO system participates actively in the formation of an oxidative environment produced by neutrophils and activates the antioxidant mechanism of PubMed DOI

Cleary S, Marciano-Cabral F. Activated macrophages demonstrate direct cytotoxicity, antibody-dependent cellular cytotoxicity, and enhanced binding of PubMed

Fischer-Stenger K, Cabral GA, Marciano-Cabral F. The interaction of PubMed DOI

Herbst R, Ott C, Jacobs T, Marti T, Marciano-Cabral F, Leippe M. Pore-forming polypeptides of the pathogenic protozoon PubMed DOI

Serrano-Luna J, Cervantes-Sandoval I, Tsutsumi V, Shibayama M. A biochemical comparison of proteases from pathogenic PubMed DOI

Sohn H-J, Kim J-H, Shin M-H, Song K-J, Shin H-J. The Nf-actin gene is an important factor for food-cup formation and cytotoxicity of pathogenic PubMed DOI

Russell AC, Bush P, Grigorean G, Kyle DE. Characterization of the extracellular vesicles, ultrastructural morphology, and intercellular interactions of multiple clinical isolates of the brain-eating amoeba, Naegleria fowleri. Front Microbiol. 2023;14:1264348. PubMed PMC

John DT, John RA. Enhancement of virulence of PubMed DOI

Herman EK, Greninger A, van der Giezen M, Ginger ML, Ramirez-Macias I, Miller HC, et al. Genomics and transcriptomics yields a system-level view of the biology of the pathogen PubMed DOI PMC

Joseph S, Park S, Kelley A, Roy S, Cope J, Ali I. Comparative genomic and transcriptomic analysis of PubMed DOI PMC

Arbon D, Ženíšková K, Mach J, Grechnikova M, Malych R, Talacko P, et al. 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(6):e0007759. PubMed PMC

Aucher A, Magdeleine E, Joly E, Hudrisier D. Capture of plasma membrane fragments from target cells by trogocytosis requires signaling in T cells but not in B cells. Blood. 2008;111(12):5621–8. doi: 10.1182/blood-2008-01-134155 PubMed DOI PMC

Nakada-Tsukui K, Nozaki T. AGC family kinase 1 participates in trogocytosis but not in phagocytosis in PubMed PMC

Ralston KS, Solga MD, Mackey-Lawrence NM, , Bhattacharya A, Petri WA Jr. Trogocytosis by PubMed DOI PMC

Velle KB, Fritz-Laylin LK. Conserved actin machinery drives microtubule-independent motility and phagocytosis in PubMed DOI PMC

Destaing O, Sanjay A, Itzstein C, Horne WC, Toomre D, De Camilli P, et al. The tyrosine kinase activity of c-Src regulates actin dynamics and organization of podosomes in osteoclasts. Mol Biol Cell. 2008;19(1):394–404. doi: 10.1091/mbc.e07-03-0227 PubMed DOI PMC

Olivares MJ, González-Jamett AM, Guerra MJ, Baez-Matus X, Haro-Acuña V, Martínez-Quiles N, et al. Src kinases regulate de novo actin polymerization during exocytosis in neuroendocrine chromaffin cells. PLoS One. 2014;9(6):e99001. doi: 10.1371/journal.pone.0099001 PubMed DOI PMC

Thái TL, Kang J-M, Lê HG, Lee J, Yoo WG, Shin H-J, et al. Fowlerstefin, a cysteine protease inhibitor of PubMed DOI PMC

Lê HG, Ham A-J, Kang J-M, Võ TC, Naw H, Sohn H-J, et al. A novel cysteine protease inhibitor of PubMed DOI PMC

Jung S-Y, Kim J-H, Song K-J, Lee Y-J, Kwon M-H, Kim K, et al. Gene silencing of nfa1 affects the in vitro cytotoxicity of PubMed DOI

Réveiller FL, Suh SJ, Sullivan K, Cabanes PA, Marciano-Cabral F. Isolation of a unique membrane protein from PubMed DOI

Malych R, Füssy Z, Ženíšková K, Arbon D, Hampl V, Hrdý I, et al. The response of PubMed DOI

Ma Z, Holland AA, Szlamkowicz I, Anagnostopoulos V, Caldas Nogueira ML, Caranto JD, et al. The hemerythrin-like diiron protein from PubMed DOI PMC

Albert T, Moënne-Loccoz P. Spectroscopic characterization of a diferric mycobacterial hemerythrin-like protein with unprecedented reactivity toward nitric oxide. J Am Chem Soc. 2022;144(38):17611–21. PubMed

Brunold TC, Solomon EI. Reversible dioxygen binding to hemerythrin. 1. Electronic structures of deoxy- and oxyhemerythrin. J Am Chem Soc. 1999;121(36):8277–87

Solomon EI, Park K. Structure/function correlations over binuclear non-heme iron active sites. J Biol Inorg Chem. 2016;21(5–6):575–88. doi: 10.1007/s00775-016-1372-9 PubMed DOI PMC

Enemark J, Feltham R. Principles of structure, bonding, and reactivity for metal nitrosyl complexes. Coord Chem Rev. 1974;13(4):339–406.

Martins MC, Alves CM, Teixeira M, Folgosa F. The flavodiiron protein from PubMed DOI

Abramson J, Adler J, Dunger J, Evans R, Green T, Pritzel A, et al. Accurate structure prediction of biomolecular interactions with AlphaFold 3. Nature. 2024;630(8016):493–500. doi: 10.1038/s41586-024-07487-w PubMed DOI PMC

Sheriff S, Hendrickson W, Smith J. Structure of myohemerythrin in the azidomet state at 1.71.3Å resolution. J Mol Biol. 1987;197(2):273–96. PubMed

Holmes M, Le Trong I, Turley S, Sieker L, Stenkamp R. Structures of deoxy and oxy hemerythrin at 2.0 Å resolution. J Mol Biol. 1991;218(3):583–93. PubMed

Chen K, Chuankhayan P, Wu H, Chen C, Fukuda M, Yu S. The bacteriohemerythrin from PubMed

Kopecký V Jr, Ettrich R, Pazderka T, Hofbauerová K, Řeha D, Baumruk V. Influence of ligand binding on structure and thermostability of human α1-acid glycoprotein. J Mol Recognit. 2016;29(2):70–9. doi: 10.1002/jmr.2496 PubMed DOI

Movasaghi Z, Rehman S, Rehman I. Raman spectroscopy of biological tissues. Appl Spectrosc Rev. 2007;42(5):493–541.

Rygula A, Majzner K, Marzec KM, Kaczor A, Pilarczyk M, Baranska M. Raman spectroscopy of proteins: a review. J Raman Spectrosc. 2013;44(8):1061–76. doi: 10.1002/jrs.4335 DOI

Falamas A, Kalra S, Chis V, Notingher I. Monitoring the RNA distribution in human embryonic stem cells using Raman micro-spectroscopy and fluorescence imaging. AIP Conf Proc. 2013;1565(1):43–7.

Palacký J, Vorlíčková M, Kejnovská I, Mojzeš P. Polymorphism of human telomeric quadruplex structure controlled by DNA concentration: a Raman study. Nucleic Acids Res. 2013;41(2):1005–16. doi: 10.1093/nar/gks1135 PubMed DOI PMC

Murugappan S, Tofail SAM, Thorat ND. Raman spectroscopy: a tool for molecular fingerprinting of brain cancer. ACS Omega. 2023;8(31):27845–61. doi: 10.1021/acsomega.3c01848 PubMed DOI PMC

Atkins CG, Buckley K, Blades MW, Turner RFB. Raman spectroscopy of blood and blood components. Appl Spectrosc. 2017;71(5):767–93. doi: 10.1177/0003702816686593 PubMed DOI

Czamara K, Majzner K, Pacia MZ, Kochan K, Kaczor A, Baranska M. Raman spectroscopy of lipids: a review. J Raman Spectrosc. 2014;46(1):4–20. doi: 10.1002/jrs.4607 DOI

Lendeckel U, Kähne T, Ten Have S, Bukowska A, Wolke C, Bogerts B, et al. Cathepsin K generates enkephalin from β-endorphin: a new mechanism with possible relevance for schizophrenia. Neurochem Int. 2009;54(7):410–7. PubMed

Gu Y, Kanazawa M, Hung S, Wang X, Fukuda S, Koziol J, et al. Cathepsin L acutely alters microvessel integrity within the neurovascular unit during focal cerebral ischemia. J Cereb Blood Flow Metab. 2015;35(11):1888–900. PubMed PMC

Godat E, Lecaille F, Desmazes C, Duchêne S, Weidauer E, Saftig P. Cathepsin K: a cysteine protease with unique kinin-degrading properties. Biochem J. 2004;383(3):501–6. PubMed PMC

Liu J, Hong Z, Ding J, Liu J, Zhang J, Chen S. Predominant release of lysosomal enzymes by newborn rat microglia after LPS treatment revealed by proteomic studies. J Proteome Res. 2008;7(5):2033–49. PubMed

Fischer-Stenger K, Marciano-Cabral F. The arginine-dependent cytolytic mechanism plays a role in destruction of PubMed DOI PMC

Weiss J, Elsbach P, Olsson I, Odeberg H. Purification and characterization of a potent bactericidal and membrane active protein from the granules of human polymorphonuclear leukocytes. J Biol Chem. 1978;253(8):2664–72. doi: 10.1016/s0021-9258(17)40872-6 PubMed DOI

Theprungsirikul J, Skopelja-Gardner S, Burns AS, Wierzbicki RM, Rigby WFC. Bactericidal/Permeability-increasing protein preeminently mediates clearance of PubMed DOI PMC

Bolaños J, Betanzos A, Javier-Reyna R, Rivera G, Huerta M, Pais-Morales J. EhNPC1 and EhNPC2 proteins participate in trafficking of exogenous cholesterol in PubMed DOI PMC

Rodríguez-Mera IB, Carrasco-Yépez MM, Vásquez-Moctezuma I, Correa-Basurto J, Salinas GR-, Castillo-Ramírez DA, et al. Role of cathepsin B of PubMed DOI PMC

Lê H, Kang J, Võ T, Na B. Naegleria fowleri cathepsin B induces a pro-inflammatory immune response in BV-2 microglial cells via NF-κB and AP-1 dependent-MAPK signaling pathway. Int J Mol Sci. 2022;23(15):8388. doi: 10.3390/ijms23158388 PubMed DOI PMC

Stepánek J, Kopecký V Jr, Mezzetti A, Turpin P-Y, Paulin D, Alpert B, et al. Structural and dynamic changes of the serum response element and the core domain of serum response factor induced by their association. Biochem Biophys Res Commun. 2010;391(1):203–8. doi: 10.1016/j.bbrc.2009.11.032 PubMed DOI

Pilát Z, Jonáš A, Pilátová J, Klementová T, Bernatová S, Šiler M. Analysis of bacteriophage–host interaction by Raman tweezers. Anal Chem. 2020;92(18):12304–11. PubMed

Bexkens M, Zimorski V, Sarink M, Wienk H, Brouwers J, De Jonckheere J, et al. Lipids are the preferred substrate of the protist 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. Nat Methods. 2012;9(7):676–82. doi: 10.1038/nmeth.2019 PubMed DOI PMC

Mach J, Bíla J, Ženíšková K, Arbon D, Malych R, Glavanakovová M, et al. Iron economy in PubMed

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;13(9):2513–26. doi: 10.1074/mcp.M113.031591 PubMed DOI 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. Nat Methods. 2016;13(9):731–40. doi: 10.1038/nmeth.3901 PubMed DOI

Zimmermann L, Stephens A, Nam S-Z, 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;430(15):2237–43. doi: 10.1016/j.jmb.2017.12.007 PubMed DOI

Perez-Riverol Y, Bai J, Bandla C, García-Seisdedos D, Hewapathirana S, Kamatchinathan S, et al. The PRIDE database resources in 2022: a hub for mass spectrometry-based proteomics evidences. Nucleic Acids Res. 2021;50(D1):D543–52. doi: 10.1093/nar/gkab1060 PubMed DOI PMC

Meng E, Goddard T, Pettersen E, Couch G, Pearson Z, Morris J. UCSF ChimeraX: tools for structure building and analysis. Prot Sci. 2023;32(11):e4792. doi: 10.1002/pro.4792 PubMed DOI PMC

Petasis DT, Hendrich MP. Quantitative interpretation of multifrequency multimode EPR spectra of metal containing proteins, enzymes, and biomimetic complexes. Methods Enzymol. 2015;563:171–208. doi: 10.1016/bs.mie.2015.06.025 PubMed DOI PMC

Lertjuthaporn S, Somkird J, Lekmanee K, Atipimonpat A, Sukapirom K, Sawasdipokin H, et al. Extracellular vesicles from PubMed DOI PMC

Goedhart J, Luijsterburg M. VolcaNoseR is a web app for creating, exploring, labeling and sharing volcano plots. Sci Rep. 2020;10(1):20560. PubMed PMC

Mojzeš P, Gao L, Ismagulova T, Pilátová J, Moudříková Š, Gorelova O. Guanine, a high-capacity and rapid-turnover nitrogen reserve in microalgal cells. Proc Natl Acad Sci. 2020;117(51):32722–30. PubMed PMC

Pilátová J, Tashyreva D, Týč J, Vancová M, Bokhari SNH, Skoupý R, et al. Massive accumulation of strontium and barium in diplonemid protists. mBio. 2023;14(1):e0327922. doi: 10.1128/mbio.03279-22 PubMed DOI PMC

Pilátová J, Pánek T, Oborník M, Čepička I, Mojzeš P. Revisiting biocrystallization: purine crystalline inclusions are widespread in eukaryotes. ISME J. 2022;16(9):2290–4. doi: 10.1038/s41396-022-01264-1 PubMed DOI PMC

Barcytė D, Pilátová J, Mojzeš P, Nedbalová L. The arctic cylindrocystis (Zygnematophyceae, Streptophyta) green algae are genetically and morphologically diverse and exhibit effective accumulation of polyphosphate. J Phycol. 2020;56(1):217–32. doi: 10.1111/jpy.12931 PubMed DOI

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...