Cited by 253Antifungal resistance and susceptibilityFungal and yeast genetics researchFungal Infections and Studies

Melanin is an essential component for the integrity of the cell wall of Aspergillus fumigatus conidia

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Pihet, Marc, Vandeputte, Patrick, Tronchin, Guy, Renier, Gilles, Saulnier, Patrick, Georgeault, Sonia, Mallet, Romain, Chabasse, Dominique +2 more·2009·BMC Microbiology

Abstract

BACKGROUND: Aspergillus fumigatus is the most common agent of invasive aspergillosis, a feared complication in severely immunocompromised patients. Despite the recent commercialisation of new antifungal drugs, the prognosis for this infection remains uncertain. Thus, there is a real need to discover new targets for therapy. Particular attention has been paid to the biochemical composition and organisation of the fungal cell wall, because it mediates the host-fungus interplay. Conidia, which are responsible for infections, have melanin as one of the cell wall components. Melanin has been established as an important virulence factor, protecting the fungus against the host's immune defences. We suggested that it might also have an indirect role in virulence, because it is required for correct assembly of the cell wall layers of the conidia. RESULTS: We used three A. fumigatus isolates which grew as white or brown powdery colonies, to demonstrate the role of melanin. Firstly, sequencing the genes responsible for biosynthesis of melanin (ALB1, AYG1, ARP1, ARP2, ABR1 and ABR2) showed point mutations (missense mutation, deletion or insertion) in the ALB1 gene for pigmentless isolates or in ARP2 for the brownish isolate. The isolates were then shown by scanning electron microscopy to produce numerous, typical conidial heads, except that the conidia were smooth-walled, as previously observed for laboratory mutants with mutations in the PKSP/ALB1 gene. Flow cytometry showed an increase in the fibronectin binding capacity of conidia from mutant isolates, together with a marked decrease in the binding of laminin to the conidial surface. A marked decrease in the electronegative charge of the conidia and cell surface hydrophobicity was also seen by microelectrophoresis and two-phase partitioning, respectively. Ultrastructural studies of mutant isolates detected considerable changes in the organisation of the conidial wall, with the loss of the outermost electron dense layer responsible for the ornamentations seen on the conidial surface in wild-type strains. Finally, analysis of the conidial surface of mutant isolates by atomic force microscopy demonstrated the absence of the outer cell wall rodlet layer which is composed of hydrophobins. CONCLUSION: These results suggest that, in addition to a protective role against the host's immune defences, melanin is also a structural component of the conidial wall that is required for correct assembly of the cell wall layers and the expression at the conidial surface of adhesins and other virulence factors.

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Crossref · 10.1186/1471-2180-9-177

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  • In Aspergillus fumigatus, melanin in conidial walls is essential for the proper expression of adhesins and other virulence factors, while inducing only minimal inflammatory cytokine responses to circumvent host antifungal defenses.

    “In A. fumigatus, melanin in conidial walls is essential for the proper expression of adhesins and other virulence factors, while inducing only minimal inflammatory cytokine responses to circumvent host antifungal defenses [40,41].”

    From Fungal Melanin in Plant Pathogens: Complex Biosynthesis Pathways and Diverse Biological Functions (2025) · cites this paper as [40]

    The Conclusion states that melanin is required for correct assembly of A. fumigatus conidial-wall layers and for surface expression of adhesins and other virulence factors. The Background and Discussion describe protection against host immune defenses, but our copy does not say melanin induces only minimal inflammatory cytokine responses; a search for cytokines found no supporting passage. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Under high-temperature conditions, melanin helps maintain cell wall integrity, preventing cell death due to wall rupture.

    “Under high-temperature conditions, the cell wall is susceptible to damage, and melanin helps maintain its integrity, thereby preventing cell death due to wall rupture [40].”

    From Fungal Melanin in Plant Pathogens: Complex Biosynthesis Pathways and Diverse Biological Functions (2025) · cites this paper as [40]

    The Conclusion says melanin is a structural component required for correct assembly of Aspergillus fumigatus conidial wall layers, and the Results report thinner walls lacking the outermost layer when melanin production is impaired. The paper does not establish that melanin prevents heat-induced wall rupture or cell death; its incubation at 37°C is not a test of high-temperature damage. No page numbers are available in our copy. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Melanin plays a vital role in fungal survival under extreme temperatures by acting as a thermal buffer through heat absorption and scattering.

    “Melanin plays a vital role in fungal survival under extreme temperatures by acting as a thermal buffer through heat absorption and scattering.”

    From Fungal Melanin in Plant Pathogens: Complex Biosynthesis Pathways and Diverse Biological Functions (2025) · cites this paper as [40]

    The Discussion and Conclusion describe melanin’s roles in protecting against host immune defenses and maintaining the conidial cell wall. A search of the indexed paper for extreme temperatures, heat absorption, scattering, and thermal buffering found no passage addressing the claimed mechanism or survival under extreme temperatures. (LLM, conf=0.75)

    Experimental — accuracy not yet measured
  • As an integral component of the fungal cell wall, melanin interacts with other wall constituents to enhance structural stability.

    “As an integral component of the fungal cell wall, melanin interacts with other wall constituents to enhance structural stability.”

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Cites

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Research works printed but not linked: 34

  1. Latgé JP Aspergillus fumigatus and aspergillosis Clin Microbiol Rev 1999 12 310 350 10194462 PMC88920
  2. Tekaia F Latgé JP Aspergillus fumigatus: saprophyte or pathogen? Curr Opin Microbiol 2005 8 385 392 10.1016/j.mib.2005.06.017 16019255 · DOI · Paper page
  3. Latgé JP The pathobiology of Aspergillus fumigatus Trends Microbiol 2001 9 382 389 10.1016/S0966-842X(01)02104-7 11514221 · DOI
  4. Tsai HF Chang YC Washburn RG Wheeler MH Kwon-Chung KJ The developmentally regulated ALB1 gene of Aspergillus fumigatus: its role in modulation of conidial morphology and virulence J Bacteriol 1998 180 3031 3038 9620950 PMC107801
  5. Jahn B Koch A Schmidt A Wanner G Gehringer H Bhakdi S Brakhage AA Isolation and characterization of a pigmentless-conidium mutant of Aspergillus fumigatus with altered conidial surface and reduced virulence Infect Immun 1997 65 5110 5117 9393803 PMC175736
  6. Jahn B Langfelder K Schneider U Schindel C Brakhage AA PKSP-dependent reduction of phagolysosome fusion and intracellular kill of Aspergillus fumigatus conidia by human monocyte-derived macrophages Cell Microbiol 2002 4 793 803 10.1046/j.1462-5822.2002.00228.x 12464010 · DOI
  7. Sugareva V Hartl A Brock M Hubner K Rohde M Heinekamp T Brakhage AA Characterisation of the laccase-encoding gene abr2 of the dihydroxynaphthalene-like melanin gene cluster of Aspergillus fumigatus Arch Microbiol 2006 186 345 355 10.1007/s00203-006-0144-2 16988817 · DOI
  8. Bouchara JP Sanchez M Esnault K Tronchin G Interactions between Aspergillus fumigatus and host matrix proteins Contrib Microbiol 1999 2 167 181 full_text 10523273
  9. Tronchin G Esnault K Sanchez M Larcher G Marot-Leblond A Bouchara JP Purification and partial characterization of a 32-kilodalton sialic acid-specific lectin from Aspergillus fumigatus Infect Immun 2002 70 6891 6895 10.1128/IAI.70.12.6891-6895.2002 12438366 PMC133100 · DOI
  10. Gil ML Peñalver MC Lopez-Ribot JL O'Connor JE Martinez JP Binding of extracellular matrix proteins to Aspergillus fumigatus conidia Infect Immun 1996 64 5239 5247 8945572 PMC174514
  11. Peñalver MC O'Connor JE Martinez JP Gil ML Binding of human fibronectin to Aspergillus fumigatus conidia Infect Immun 1996 64 1146 1153 8606071 PMC173896
  12. Langfelder K Streibel M Jahn B Haase G Brakhage AA Biosynthesis of fungal melanins and their importance for human pathogenic fungi Fungal Genet Biol 2003 38 143 158 10.1016/S1087-1845(02)00526-1 12620252 · DOI · Paper page
  13. Hamilton AJ Gomez BL Melanins in fungal pathogens J Med Microbiol 2002 51 189 191 11871612
  14. Jacobson ES Pathogenic roles for fungal melanins Clin Microbiol Rev 2000 13 708 717 10.1128/CMR.13.4.708-717.2000 11023965 PMC88958 · DOI · Paper page
  15. Kawamura C Moriwaki J Kimura N Fujita Y Fuji S Hirano T Koizumi S Tsuge T The melanin biosynthesis genes of Alternaria alternata can restore pathogenicity of the melanin-deficient mutants of Magnaporthe grisea Mol Plant Microbe Interact 1997 10 446 453 10.1094/MPMI.1997.10.4.446 9150594 · DOI
  16. Tsuji G Sugahara T Fujii I Mori Y Ebizuka Y Shiraishi T Kubo Y Evidence for involvement of two naphthol reductases in the first reduction step of melanin biosynthesis pathway of Colletotrichum lagenarium Mycol Res 2003 107 854 860 10.1017/S0953756203008001 12967213 · DOI
  17. Casadevall A Rosas AL Nosanchuk JD Melanin and virulence in Cryptococcus neoformans Curr Opin Microbiol 2000 3 354 358 10.1016/S1369-5274(00)00103-X 10972493 · DOI
  18. da Silva MB Marques AF Nosanchuk JD Casadevall A Travassos LR Taborda CP Melanin in the dimorphic fungal pathogen Paracoccidioides brasiliensis: effects on phagocytosis, intracellular resistance and drug susceptibility Microbes Infect 2006 8 197 205 10.1016/j.micinf.2005.06.018 16213179 · DOI
  19. Paolo WF Jr Dadachova E Mandal P Casadevall A Szaniszlo PJ Nosanchuk JD Effects of disrupting the polyketide synthase gene WdPKS1 in Wangiella [Exophiala] dermatitidis on melanin production and resistance to killing by antifungal compounds, enzymatic degradation, and extremes in temperature BMC Microbiol 2006 6 55 10.1186/1471-2180-6-55 16784529 PMC1569847 · DOI
  20. Romero-Martinez R Wheeler M Guerrero-Plata A Rico G Torres-Guerrero H Biosynthesis and functions of melanin in Sporothrix schenckii Infect Immun 2000 68 3696 3703 10.1128/IAI.68.6.3696-3703.2000 10816530 PMC97661 · DOI
  21. Tronchin G Esnault K Renier G Filmon R Chabasse D Bouchara JP Expression and identification of a laminin-binding protein in Aspergillus fumigatus conidia Infect Immun 1997 65 9 15 8975886 PMC174550
  22. Tronchin G Bouchara JP Larcher G Lissitzky JC Chabasse D Interaction between Aspergillus fumigatus and basement membrane laminin: binding and substrate degradation Biol Cell 1993 77 201 208 10.1016/S0248-4900(05)80189-3 8364400 · DOI
  23. Bouchara JP Tronchin G Larcher G Chabasse D The search for virulence determinants in Aspergillus fumigatus Trends Microbiol 1995 3 327 330 10.1016/S0966-842X(00)88965-9 8528619 · DOI
  24. Cunha MM Franzen AJ Alviano DS Zanardi E Alviano CS De Souza W Rozental S Inhibition of melanin synthesis pathway by tricyclazole increases susceptibility of Fonsecaea pedrosoi against mouse macrophages Microsc Res Tech 2005 68 377 384 10.1002/jemt.20260 16358282 · DOI
  25. Youngchim S Morris-Jones R Hay RJ Hamilton AJ Production of melanin by Aspergillus fumigatus J Med Microbiol 2004 53 175 181 10.1099/jmm.0.05421-0 14970241 · DOI
  26. Bernard M Latgé JP Aspergillus fumigatus cell wall: composition and biosynthesis Med Mycol 2001 39 Suppl 1 9 17 11800273
  27. Paris S Debeaupuis JP Crameri R Carey M Charles F Prevost MC Schmitt C Philippe B Latgé JP Conidial hydrophobins of Aspergillus fumigatus Appl Environ Microbiol 2003 69 1581 1588 10.1128/AEM.69.3.1581-1588.2003 12620846 PMC150101 · DOI
  28. Tronchin G Bouchara JP Ferron M Larcher G Chabasse D Cell surface properties of Aspergillus fumigatus conidia: correlation between adherence, agglutination, and rearrangements of the cell wall Can J Microbiol 1995 41 714 721 7553454
  29. Franzen AJ Cunha MM Batista EJ Seabra SH De Souza W Rozental S Effects of tricyclazole (5-methyl-1,2,4-triazol[3,4] benzothiazole), a specific DHN-melanin inhibitor, on the morphology of Fonsecaea pedrosoi conidia and sclerotic cells Microsc Res Tech 2006 69 729 737 10.1002/jemt.20344 16850396 · DOI
  30. Coulot P Bouchara JP Renier G Annaix V Planchenault C Tronchin G Chabasse D Specific interaction of Aspergillus fumigatus with fibrinogen and its role in cell adhesion Infect Immun 1994 62 2169 2177 8188338 PMC186494
  31. Clark HF Shepard CC A dialysis technique for preparing fluorescent antibody Virology 1963 20 642 644 10.1016/0042-6822(63)90292-7 14059832 · DOI
  32. Uyen HM Mei HC van der Weerkamp AH Busscher HJ Zeta potential and the adhesion of oral streptococci to polymethylmethacrylate Biomater Artif Cells Artif Organs 1989 17 385 391 2690974
  33. Kennedy MJ Rogers AL Hanselmen LR Soll DR Yancey RJ Jr Variation in adhesion and cell surface hydrophobicity in Candida albicans white and opaque phenotypes Mycopathologia 1988 102 149 156 10.1007/BF00437397 3050525 · DOI
  34. Cree RG Aleljung P Paulsson M Witte W Noble WC Ljungh A Wadström T Cell surface hydrophobicity and adherence to extra-cellular matrix proteins in two collections of methicillin-resistant Staphylococcus aureus Epidemiol Infect 1994 112 307 314 10.1017/S0950268800057721 8150005 PMC2271452 · DOI

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Authors
Pihet, M., Vandeputte, P., Tronchin, G., Renier, G., Saulnier, P., Georgeault, S., Mallet, R., Chabasse, D., Symoens, F., & Bouchara, J.-P.
Affiliations
  • Centre Hospitalier Universitaire d'Angers (FR)
  • Université d'Angers (FR)
  • Inserm (FR)
  • Institut Scientifique de Santé Publique (BE)
Corresponding author
  • Pihet, Marc
  • Bouchara, Jean-Philippe
Venue
BMC Microbiology
Published
2009
Volume
9
Issue
1
Pages
177
ISSN
1471-2180 (ISSN-L)
OpenAlex
W2094245023
Cited by
253
References
1
Citations by year
2026: 11 · 2025: 14 · 2024: 14 · 2023: 15 · 2022: 21 · 2021: 20 · 2020: 23 · 2019: 11 · 2018: 17 · 2017: 21 · 2016: 9 · 2015: 16 · 2014: 16 · 2013: 13 · 2012: 10
FWCI
6.84
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • BMC Microbiology (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, other-oa)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Topics
  • Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
  • Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
Keywords
Aspergillus fumigatus, melanin, conidia, fungal cell wall, invasive aspergillosis, virulence factors, Arp2, fibronectin binding, laminin binding, cell surface hydrophobicity, cell surface charge, hydrophobins
MeSH terms
Aspergillosis, Aspergillus fumigatus, Cell Wall, DNA, Fungal, Flow Cytometry, Fungal Proteins, Melanins, Microscopy, Electron, Scanning, Spores, Fungal, Virulence, Sequence Analysis, DNA

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