Mem Inst Oswaldo Cruz, Rio de Janeiro, 113(8) August 2018
Original Article

Melanin particles isolated from the fungus Fonsecaea pedrosoi activates the human complement system

Lysianne Pinto1, Luiz Fernando Zmetek Granja1, Mariana Amorim de Almeida2, Daniela Sales Alviano1, Maria Helena da Silva1, Regina Ejzemberg1/†, Sonia Rozental3, Celuta Sales Alviano1/+

1Universidade Federal do Rio de Janeiro, Instituto de Microbiologia Professor Paulo de Góes, Rio de Janeiro, RJ, Brasil
2Universidade Federal do Rio de Janeiro, Instituto de Macromoléculas Professora Eloisa Mano, Rio de Janeiro, RJ, Brasil
3Universidade Federal do Rio de Janeiro, Instituto de Biofísica Carlos Chagas Filho, Rio de Janeiro, RJ, Brasil

DOI: 10.1590/0074-02760180120
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BACKGROUND Melanin production has been associated with virulence in various pathogenic fungi, including Fonsecaea pedrosoi, the major etiological agent for chromoblastomycosis, a subcutaneous fungal disease that occurs in South America.

OBJECTIVE The aim of this study was to evaluate the effects of acid-basic extracted F. pedrosoi melanin particles and fungal cell ghosts obtained by Novozym 234 treatment on their ability to activate the human complement system.

METHODS The ability of melanin particles and fungal cell ghosts to activate the human complement system was evaluated by complement consumption, immunofluorescence, and enzyme-linked immunosorbent assay (ELISA).

FINDINGS Unsensitised melanin particles and melanin ghosts presented complement consumption of 82.67 ± 2.08% and 96.04 ± 1.13%, respectively. Immunofluorescence assays revealed intense deposition of the C3 and C4 fragments on the surface of melanin particles and ghosts extracted from F. pedrosoi. Deposition of the C3, C4, and C5 fragments onto melanin samples and zymosan was confirmed by ELISA. Deposition of small amounts of C1q and C9 onto melanin samples and zymosan was detected by ELISA.

CONCLUSION Fonsecaea pedrosoi melanin particles and fungal cell ghosts activated the complement system mainly through an alternative pathway.

Chromoblastomycosis is a chronic progressive fungal infection of the mammalian skin and subcutaneous tissue caused by transcutaneous inoculation of a group of melanised fungi that belong to the Dematiaceae family (Torres-Guerrero et al. 2012 29 ). These fungi are saprophytes normally found in the mycelial form in tropical and sub-tropical soil and vegetation. Rounded fungal forms with transverse and longitudinal division are observed in the lesions and referred to as “sclerotic cells”. The etiological agent most commonly found in Brazil is Fonsecaea pedrosoi, which appears as thick-walled, brownish coloured cells because of the melanotic pigmentation in their cell walls (Correia et al. 2010 4 ).

F. pedrosoi constitutively produces melanin, a pigment and important virulence factor because of its anti-oxidative, thermostable, anti-radioactive, paramagnetic, and metal-binding properties (Cunha et al. 2010 6 ). Melanin production has been associated with virulence in various microorganisms and has been widely studied in several fungi such as Aspergillus spp, Sporothrix schenckii, and Cryptococcus neoformans (Romero-Martinez et al. 2000 19 , Rosas et al. 2000 21 , Gómez and Nosanchuck 2003 8 ). Fungi can produce melanin through several metabolic pathways. The most prevalent is the constitutive dihydroxynaphthalene pathway, found in F. pedrosoi, Wangiella dermatitidis, and S. schenckii. Another frequently described pathway is the dihydroxyphenylalanine (DOPA) pathway, based on melanin synthesis from the L-DOPA amino acid, and is present in C. neoformans (Nosanchuk et al. 2000 16 , Cunha et al. 2005 5 ).

The complement system is an important part of innate immunity and plays an essential role in host defence against infectious agents and in inflammatory processes. It contains more than 30 proteins with enzymatic or binding properties and comprises multiple cell-surface receptors specific for fragments generated from the activation. These receptors are differentially expressed on the eosinophils, neutrophils, macrophages, monocytes, and B and T lymphocytes (Ricklin et al. 2010 18 ).

The complement system can be activated through classical pathways, typically involving an antigen-antibody complex, or by an alternative pathway, where the initial activation step occurs by spontaneous hydrolysis of the C3 molecule. C3 plays a central role in activation of the complement system, which is required for both classical and alternative complement activation pathways. C3 deficiencies increase the susceptibility to microorganism infections. Additionally, the complement can be activated by the lectin pathway, which involves activation through an interaction of mannose binding lectin or ficolins with carbohydrates expressed on microbial surfaces (Runza et al. 2008 23 ).

Numerous fungi such as Aspergillus fumigatus, Candida albicans, C. neoformans, and Mucor spp activate the complement system, mainly by the alternative pathway (Speth et al. 2008 27 , Granja et al. 2010 9 ). Wünthrich et al. (2015) demonstrated that dectin-2 (and to a lesser extent dectin-1)-mediated recognition of F. pedrosoi is largely responsible for the development of Ag-specific Th17 cells, while Mincle appears to inhibit the development of this T-helper subset.

In the present study, we evaluated the role of melanin particles and fungal cell ghosts extracted from F. pedrosoi in activating the human complement system by complement consumption, immunofluorescence, and enzyme-linked immunosorbent assay (ELISA).




Reagents and buffers - The following buffers were used: PBS (10 mM phosphate, 15 mM saline, pH 7.2), PBS-Tween (PBS containing 0.05% of Tween 20), VBS (5 mM Veronal-buffered saline, pH 7.35-5 mM Veronal, 142 mM), GVB (VBS containing 0,1% gelatine), GVB2+ (GVB containing 0.15 mM CaCl2 and 1 mM MgCl2), GVB-EGTA-Mg2+ (GVB containing 10 mM EGTA (ethylene glycol-bis(b-aminoethyl ether)-N,N,N´,N´-tetraacetic acid) and 10 mM MgCl2), and GVB-EDTA (GVB containing 10 mM EDTA), 10 mM sodium citrate-phosphate, pH 5.1. The following antibodies were used: rabbit serum anti-human C3c conjugated with fluorescein isothiocyanate and rabbit serum anti-human C4 purchased from Dako (Carpinteria, CA, USA) and goat serum anti-human C1q, goat serum anti-human C3c, rabbit serum anti-human C4, rabbit serum anti-human C5, rabbit serum anti-human C9, goat serum anti-rabbit IgG and rabbit serum anti-goat IgG conjugated with peroxidase and rabbit serum anti-sheep erythrocytes (haemolysin), and rabbit anti-guinea pig immunoglobulins (g-1 and/or g-2) purchased from Sigma Chemical Co. (St. Louis, MO, USA). All antibody dilutions were carried out according to the manufacturer’s instructions.


F. pedrosoi and zymosan - A pathogenic strain F. pedrosoi (ATCC 46428, formerly 5VLP) isolated from a human case of chromoblastomycosis was used. Stock cultures were maintained on Sabouraud-dextrose-agar under mineral oil and kept at 4ºC. For the experiments, a sample of F. pedrosoi was grown in Czapeck-Dox medium for 14 days at room temperature.

Zymosan A particles (Sigma Chemical Co.) were used as a positive control for complement activation. To loosen the mannan structures, zymosan particles were boiled for 30 min, washed with PBS, and resuspended in the same buffer (10 mg mL-1).


Melanin particle extraction - F. pedrosoi melanin particles were extracted from the mycelia using a Waring Blender with 0.5 M NaOH solution for 10 min. The mixture was kept under constant agitation for 24 h to completely extract the melanin. The sample was centrifuged at 5000 × g for 30 min and the supernatant was collected and treated with 6 M HCl until the pH reached 1.5. The resulting pigmented sample was washed several times with distilled water and lyophilised (Alviano et al. 1991 1 ).


Melanin ghosts - Melanin ghost isolation involved incubating the fungus with 1 M sorbitol in 0.1 M sodium citrate, pH 5.0. After washing in the same solution, the mycelia were treated with 10 mg Novozym 234 (Sigma Chemical Co.) in the same solution for 1 h at 37ºC. The cells were separated by centrifugation at 1500 × g and resuspended in a 4 M guanidine isothiocyanate solution for 30 min at room temperature. The mixture was centrifuged and the pigmented material was transfer to 6 M HCl solution and heated to 100ºC for 60 min. This material was extensively washed in distilled water, lyophilised, and analysed by light microscopy and infrared spectroscopy.


Melanin sample spectrometry analyses - In this study, a Frontier FT-IR spectrometer from PerkinElmer (Waltham, MA, USA) was used to compare the spectra of a commercial melanin sample obtained from Sepia officinalis (Sigma Chemical Co., M2649), melanin obtained from fungal supernatant, melanin in the ghost particle sample, and melanin treated with sodium hydroxide (NaOH). The spectra were obtained in transmission mode by the potassium bromide (KBr) pellet method. The previously dried samples were macerated together with KBr and then the mixture was pressed until pellets were formed. The KBr pellets were analysed from 4000 to 400 cm-1 with 4 cm-1 of resolution and 20 scans.


Guinea pig immunisation - Melanin particles were suspended (1 mg mL-1) in a sterile and apyrogenic saline solution. The suspension was mixed 1:1 (v v-1) with Freund’s complete adjuvant (Sigma Chemical Co.). Intramuscular inoculation of two guinea pigs (Cavia cobaya) weighing approximately 1.2 and 1.3 kg each was carried out with 0.5 mL of the emulsified material. After 50 days, blood was collected and the obtained sera were aliquoted and stored at -80ºC. One week later, both animals were administered another melanin intramuscular inoculation, but with Freund’s incomplete adjuvant (Sigma Chemical Co.). After 21 days, blood was once more collected and the obtained sera were aliquoted and stored at -80ºC. The antibody response was evaluated by agglutination with the melanin particles and melanin ghosts and observed under light microscopy. Pre-immune sera, collected before the immunisation process, were also maintained at -80ºC. All animal experiments followed the guidelines of the local ethics committee.


Human serum - Peripheral blood was collected from healthy adult volunteers after obtaining informed consent. The sera were pooled and absorbed three times, 30 min each, with sheep red blood cells (1 × 109 cells mL-1), all absorptions were carried out at 4ºC. The sera were then absorbed three times with melanin particles (20 mg mL-1). This pool was used as the source of the human complement system. Serum was heated at 56ºC for 30 min for studies requiring heat-inactivated serum. All serum samples were aliquoted and stored at -80ºC.


Opsonisation of sheep erythrocytes - A sheep erythrocyte suspension (1 × 109 cells mL-1) was opsonised by incubation with an equal volume of previously titrated haemolysin (erythrocyte-antibody, EA) at 37ºC with agitation for 20 min, washed three times, and resuspended in GVB2+ to obtain a sample of 5 × 108 cells mL-1.


Complement activation - Activation of the complement system by melanin (5 mg), melanin ghost (5 mg), and zymosan (5 mg) was carried out as follows. The samples were incubated with absorbed serum in either GVB++, GVB-Mg-EGTA, or GVB-EDTA. After 60 min at 37ºC, the samples were centrifuged at 1500 × g under refrigeration and the supernatants were collected and residual complement was measured in a spectrophotometer (Beckman Coulter, Brea, CA, USA) at 540 nm using the haemolytic system (Granja et al. 2010 9 ). Melanin and melanin ghost samples sensitised with guinea pig anti-melanin antibodies (1/200 dilution, previously titrated) were subjected to the same activation process but without the addition of chelators. Zymosan was used as a positive control and serum alone, without cells, was used as a negative control. Haemolysis percentage was calculated by considering the positive and negative controls. The pellets were collected and washed three times with PBS-Tween for use in immunofluorescence assays and ELISA.


Direct immunofluorescence assay - After incubation and washing with PBS Tween, all samples and zymosan particles were washed with PBS. The particles were diluted 1/10 in PBS and incubated with fluorescein-conjugated rabbit anti-human C3c (dilution 1/25) for 30 min. The cells were washed and resuspended with PBS. One drop of each cell suspension was placed on a microscope slide, covered with a cover-slip, and examined under an epifluorescence microscope (Zeiss, Oberkochen, Germany).


Indirect immunofluorescence assay - After incubation and washing with PBS Tween, all samples and zymosan particles were washed with PBS. The particles were diluted 1/10 in PBS and incubated with rabbit anti-human C4 (dilution 1/25) for 30 min. Goat anti-rabbit secondary antibodies conjugated with fluorescein (1/50) were then added to react for 60 min at 37ºC. The particles were washed and resuspended with PBS. One drop of each cell suspension was placed on a microscope slide, covered with a cover-slip, and examined under an epifluorescence microscope (Zeiss).


ELISA - To detect the deposition of the complement fragments (C1q, C3c, C4b, C5, and C9) on the surface of all samples, 96-well polystyrene plates (Corning, Inc., Corning, NY, USA) were coated with the particles obtained from complement activation (100 mL well-1). The plates were incubated for 1 h at 37ºC, and then overnight at 4ºC. The samples were washed with PBS-Tween 20 and blocking buffer (2% BSA in PBS) was added and incubated for 2 h at 37ºC. The previously described primary antibodies were added to detect the fragments. The plates were incubated for 1 h at 37ºC, and then washed three times with PBS-Tween 20. Secondary antibodies conjugated with peroxidase were added for 60 min at 37ºC. The terminal complexes were detected after incubation for 30 min with substrate solution pH 5.0 (4 mL H2O2 and 4 mg OPD in 10 mL of 100 mM citric acid, 100 mM NaH2PO4). The absorbance was measured at 492 nm (SLT-Spectra, Tecan, Männedorf, Switzerland) after the reaction had been stopped with 2N H2SO4.


Statistical analysis - Complement activation, ELISA, and immunofluorescence assays were repeated at least three times. Complement consumption mean values were used for evaluation. Analysis of variance and two-tailed two-sample t-test were applied to compare results from each activation. Results were considered significant at P values of < 0.05 for a two-sided test.




Results of FT-IR spectroscopy - The infrared spectra of the melanin samples are presented in Fig. 1 A-D. All samples of melanin showed a strong band at 3401 cm-1 corresponding to the primary amine (-NH2) or associated -OH; the other two bands at 2923 and 2852 cm-1 corresponded to -CH3 and -CH2 of the aliphatic structure. These bands agree with those found in the literature for other melanin samples (Alviano et al. 1991 1 , Selvakumar et al. 2008 26 , Kumar et al. 2011 14 ). The band at 1711 cm-1 observed in ghost melanin (Fig. 1C) corresponded to the aliphatic ketone (-C = O). The bands at 1654 cm-1 (ghost melanin and melanin treated with NaOH) (Fig. 1C-D); 1632 cm-1 (melanin supernatant) (Fig. 1B), and 1620 cm-1 (commercial melanin) (Fig. 1A) corresponded to C = C. Finally, the bands at 1089 and 1037 cm-1 present in the ghost melanin and melanin supernatant, respectively, corresponded to C-O.


Guinea pig antibodies to F. pedrosoi melanin - An agglutination test was conducted using pre-immunised guinea pig serum to show that non-specific antibodies did not detect agglutinate melanin or melanin ghost particles (Fig. 2C, C’), also that hydrophobicity was not sufficient to aggregate both melanin samples suspended in PBS under optical microscopy in the absence of serum. However, when melanin and melanin ghost particles were incubated with immunised serum, they clearly aggregated, indicating an antigen-antibody reaction even at high serum dilutions (Fig. 2).


Complement activation - The complement consumption percentage of melanin extracted from F. pedrosoi after incubation with serum chelated or not with magnesium EGTA was evaluated. Zymosan was used as a positive control of human complement activation in vitro, as this particle activates the complement system mainly through the alternative pathway and shows consumption of 100% of complement activity (Table). Normal serum was used as a negative control and presented consumption of only 1.2% of complement (Table).

Our results showed that unsensitised melanin particles and melanin ghosts presented a complement consumption of 82.67 ± 2.08% and 96.04 ± 1.13%, respectively, when incubated in normal serum. When incubated with serum pre-treated with EGTA-Mg2+, which prevents activation of the classical pathway by chelating Ca2+, consumption of complement activity of approximately 61.07 ± 2.82% and 80.33 ± 1.92%, respectively, was observed. Sensitised melanin particles and melanin ghost showed improved complement consumption after activation, and both samples showed 100% complement consumption when sensitised (Table). Such sensitised particles did not show improved complement consumption in serum treated with EGTA-Mg2+. Reduced complement activity by melanin particles, melanin ghost, or positive control in the serum treated with EDTA was not observed (data not shown).


Direct immunofluorescence assay - Deposition of serum C3 fragments on the sample surfaces was examined by immunofluorescence microscopy. As shown in Fig. 3, a similar pattern and intensity for C3 fragments was observed on the surface of both melanin ghosts (Fig. 3A-C) and melanin particles (Fig. 3D-F) when the samples were incubated in serum containing EGTA-Mg2+ (Fig. 3A, D) or not (Fig. 3B, E). Intense deposition of C3 was also observed on both sensitised melanin particles and melanin ghosts (Fig. 3C, F). No immunofluorescence was observed on melanin or melanin ghost particles when the complement activation used serum treated with EDTA (data not shown).


Indirect immunofluorescence assay - Deposition of C4b onto the sample surfaces was examined by immunofluorescence microscopy. Fig. 4 shows that the component tested was found on the surface of both melanin ghosts (Fig. 4A-C) and melanin particles (Fig. 4D-F) when incubated with (Fig. 4A, D) or without EGTA-Mg2+ (Fig. 4B, D). C4b deposits were also observed on both sensitised melanin particles and melanin ghosts (Fig. 2C, F) and appeared to show stronger fluorescence in all cases compared to unsensitised samples. No immunofluorescence was observed on melanin or melanin ghost particles when the complement activation used serum treated with EDTA (data not shown).


ELISA - Complement component deposition onto the samples, after incubation in human serum, was further assayed by ELISA (Fig. 5). C3 fragments bound to both melanin particles and ghosts in the experiments using human serum treated or not with EGTA-Mg2+, confirming the pattern previously observed by microscopy (Fig. 5). As described above, melanin sensitisation with antibodies increased the number of bound C3 fragments (Fig. 5). Assays to detect C4 fragments on the surface of melanin samples showed that a small amount bound to their surface in the presence of EGTA-Mg2+, which supports the absence of the classical pathway. When samples were incubated with serum without chelators, the amount of C4 fragments bound doubled (Fig. 5). Sensitised melanin samples also showed a significant increase in bound C4 fragments (Fig. 5). C5b was detected on all melanin samples, sensitised or not, either in the presence or absence of EGTA-Mg2+ (Fig. 6). For C9 detection, a small amount bound to the unsensitised samples. However, sensitised melanin showed a noticeable improvement in the amount of this component (Fig. 6). A very small amount of bound C1q was detected on both melanin particles and ghost, while a considerable increase was observed in sensitised melanin samples (Fig. 6).




Melanin pigment has been implicated in the pathogenesis of several microbial infections and is important for virulence. Previous studies demonstrated that melanin has antigenic and anti-inflammatory properties (Rosas et al. 2002 20 ). These findings led us to explore the interaction of F. pedrosoi melanin and the immune system. In a previous study, we demonstrated that the black fungus F. pedrosoi activated the complement system in human serum in vitro (mainly via the alternative pathway).Comparison of highly pigmented and hypopigmented fungal cells revealed that complement consumption was higher when pigmented mycelia were used (Pinto et al. 2011 17 ).

To confirm that the previous effect was related to melanin and not to others components exposed on the fungal cell surface, we extracted melanin particles and melanin ghosts from F. pedrosoi pigmented cells and evaluated their effects on complement activation. Data extracted from complement consumption by melanin particle or ghost (Table) illustrated that melanin elicited the complement mainly via an alternative pathway.

When samples were incubated in the serum not treated with chelators, increased complement consumption was observed (Table). Nevertheless, the results suggest mainly alternative pathway activation. Our data also show that, in all cases, the amount of C4 (Fig. 5) fragment deposited was considerably smaller on samples incubated with serum chelated with EGTA-Mg2+ than without chelators, supporting that the alternative pathway is mainly responsible for activation under these conditions. Because consumption was higher without the addition of EGTA, the difference observed may be related to classical pathway activation. As serum was previously absorbed with melanin and sheep erythrocytes, it did not contain specific antibodies that could activate the classical pathway by an antigen/antibody complex. However, the participation of the classical pathway by the action of acute phase proteins cannot be excluded (Gupta and Surolia 2004 11 ). Another possible explanation for this increased consumption is the presence of mannose binding lectin (MBL) and MBL-associated serine proteases (MASPs) in human serum (Selander et al. 2006 25 ). Together, MBL can recognise mannose patterns on the microorganism surface and MASPs can activate the system via the lectin pathway. The presence of rhamnose, mannose, galactose, and glucose residues in the melanin moiety may trigger the lectin pathway (Alviano et al. 1991 1 ).

Immunofluorescence analyses demonstrated the deposition of C3 and C4 fragments on the different melanin samples used in this study (Figs 3-4). Because Evan’s blue dye causes non-fluorescent structures to emit red fluorescence, the samples can show three possible outcomes: red colour for non-reactant structures, yellow colour for few reactant structures, and greener as the number of reactions increases. The tested melanin samples showed that deposition occurred on most of the pigment surface.

Non-specific deposition was not examined because of the lack of C3 and C4 fragment detection onto melanin and melanin ghost after complement activation with serum treated with EDTA (data not shown). EDTA inhibits all complement activation pathways but does not inhibit non-specific deposition of serum proteins such as complement components under the conditions in this study. Additionally, all samples including zymosan were washed three times with PBS-Tween before the immunofluorescence or ELISA assays, and thus complement components were present because of covalent binding, reflecting actual complement activation.

The results of Torinuki et al. (1984) 28 using sclerotic cells of F. pedrosoi also suggested that the activation and conversion of C3, analysed by immunoelectrophoresis, occurs entirely via the alternative pathway, as complement activation was not affected when the classical pathway was blocked by EGTA-Mg2+. Rosas et al. (2002) obtained similar results using melanin ghosts from C. neoformans and Aspergillus niger.

The ELISA results demonstrate that C3b, C4b, and C5b was present on the fungus, while C9 was very limited (Fig. 3). These results indicate that in the presence of human serum, the fungus activates and develops the cascade of complement activation but not to completion. Nonetheless, melanin’s ability to bind C3b and C5b after complement activation may be important in spreading F. pedrosoi in the host. This indicates the formation of C3a and C5a, which can in turn function as chemoattractants for neutrophils and dendritic cells (Gutzmer et al. 2006 12 ). C5a is also involved in the activation of phagocytic cells, release of granule-based enzymes, and generation of oxidants (Guo and Ward 2005 10 ). Neutrophils, for example, recognise cells coated with C3 fragments (C3b and iC3b) through their complement receptors (CR3 and CR4 which bind iC3b or CR1 which binds to C3b) (Ricklin et al. 2010 18 ) as well as to the C5a anaphylatoxin (Guo and Ward 2005 10 ). The ability of melanin to quench free radicals is thought  to reduce the susceptibility of fungal cells to oxidative damage (Nosanchuk and Casadevall 2006 15 , Cunha et al. 2010 6 ), a fungal mechanism enabling escape from host immune defence processes (Chai et al. 2009 3 ).

Notably, F. pedrosoi secretes melanin during neutrophil infection (Rozental et al. 1996 22 ). Melanin fungal ghosts are also observed during the infection because even when the host cell successfully kills the fungus, melanin ghosts are not digested and can persist for a long time during infection (Nosanchuk et al. 2000 16 ). Sera from patients with chromoblastomycosis reacted with melanin secreted into the culture medium during fungal growth, suggesting that melanin synthesis also occurs in vivo during infection (Alviano et al. 2004 2 ).

We showed that melanin sensitisation with anti-melanin antibodies elicited full complement consumption (Table), indicating that through specific antibodies, the classical pathway is activated, greatly enhancing the complement response to this pigment. All results from sensitised samples showed improvement compared to unsensitised tests (Figs 3-6). C1q (Fig. 6) also strongly indicates classical pathway activation in these situations, as agglutination was observed when higher concentrations of antibodies were added (data not shown). However, C3 deposition is typically much faster by the classical pathway compared to the alternative pathway (Kozel 1998 13 ), indicating that its usage is much more valuable than the alternative. In contrast, to use the classical pathway, IgG or IgM is often necessary (Gadjeva et al. 2008 7 ). Adaptive immunity inclusion is typically necessary to obtain these antibodies. Thus, responses towards the antigen may be delayed for some time. For this reason, alternative pathway activation is crucial, as it contributes to antigen presentation to phagocytes, and therefore induces an adaptive immunity response, particularly Th17 lymphocytes (Wüthrich et al. 2015 30 ).

We found that melanin particles and ghosts extracted from F. pedrosoi activate the complement system, mainly via the alternative pathway. Additionally, melanin present on the cell surface of this fungus directly influences the activation, acting as an acceptor for complement proteins. C5b ensures anaphylatoxin formation and thus results in chemotaxis and activation of polymorphonuclear neutrophils. Indirectly, melanin may promote pathogen internalisation by phagocytic cells via complement receptors (CR1, CR3, CR4) as a strategy to allow their persistence on the host, as melanin inhibits nitric oxide production (Cunha et al. 2010 6 ). Furthermore, the presence of C1q and C9 indicate that the activation process reaches its full potential from the initial steps to membrane attack complex formation when the classical pathway is involved. However, deposited C9 cannot form intermembrane canals on F. pedrosoi because of the cell wall thickness (Santos et al. 2007 24 ).

The complement system is an important branch of innate immunity, and its activation by F. pedrosoi melanin may be important in the balance of the host cell response and progress of infection and fungal elimination.




The authors thank Fundação Oswaldo Cruz (FIOCRUZ) for providing sheep’s blood, Fátima Regina de V Goulart and Ana Regina M de Sousa for technical support.




LP and LFZG performed the experiments, analysed and discussed the results; MAA performed the spectrometer experiments and analysed the results; DSA cultured fungal cells, obtained melanin, and discussed the results; MHS and SR analysed the experiments, wrote and revised the manuscript; CSA designed the experiments, discussed the results, and revised the manuscript. All authors analysed results and approved this manuscript.

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Financial support: CAPES, FAPERJ, CNPq.† In memoriam
+ Corresponding author:
Received 4 March 2018
Accepted 23 May 2018

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