The pbrB Gene Encodes a Laccase Required for DHN-Melanin Synthesis in Conidia of Talaromyces (Penicillium) marneffei

Talaromyces marneffei (Basionym: Penicillium marneffei) is a significant opportunistic fungal pathogen in patients infected with human immunodeficiency virus in Southeast Asia. T. marneffei cells have been shown to become melanized in vivo. Melanins are pigment biopolymers which act as a non-specific protectant against various stressors and which play an important role during virulence in fungi. The synthesis of the two most commonly found melanins in fungi, the eumelanin DOPA-melanin and the allomelanin DHN-melanin, requires the action of laccase enzymes. The T. marneffei genome encodes a number of laccases and this study describes the characterization of one of these, pbrB, during growth and development. A strain carrying a PbrB-GFP fusion shows that pbrB is expressed at high levels during asexual development (conidiation) but not in cells growing vegetatively. The pbrB gene is required for the synthesis of DHN-melanin in conidia and when deleted results in brown pigmented conidia, in contrast to the green conidia of the wild type.


Introduction
Talaromyces marneffei (Basionym: Penicillium marneffei) is an opportunistic human fungal pathogen endemic to Southeast Asia and Southern China [1][2][3]. Most cases of T. marneffei infection occur in immune-deficient hosts, especially those infected with human immunodeficiency virus (HIV), however, infections have also been reported in non-HIV children with the underlying immune defects (e.g. severe combined immunodeficiency (SCID), congenital lymphopenia, hyper-IgM syndrome, and hyper-IgE syndrome). Failure to treat infections is fatal, especially in children with primary immunodeficiency [2,3]. T. marneffei is a dimorphic fungus with a thermally regulated dimorphic switch. As such, T. marneffei is capable of undergoing a transition from the saprophytic filamentous multicellular hyphae found in the environment (or in vitro at 25°C) to a unicellular yeast growth form in vitro at 37°C and during infection. During growth at 25°C, hyphae can also undergo asexual development (conidiation) to produce conidia, the infectious propagules. Hyphae differentiate by sequential production of an aerial stalk followed by the budding of the metula and phialide cell types from the stalk tip PLOS ONE | DOI: 10 All transformants were produced from a uracil auxotrophic strain (G526, ΔpkuA pyrG -) derived from Talaromyces marneffei FRR2161 (CBS 334.59, ATCC18224) [26,27]. Strain G526 lacks the pkuA gene encoding the ku70 protein which functions in non-homologous DNA end joining repair [28]. Therefore, genetic transformation is mediated via homologous recombination only. G526 harbors a spontaneous, loss-of-function mutation in pyrG (orotidine-5'-phosphate decarboxylase encoding gene) selected by growth in the presence of 5-fluoroorotic acid [27]. All pyrG + transformants and the T. marneffei G681 (ΔpkuA::pyrG + ) strain used as a control, were maintained on ANM medium containing 1% (w/v) glucose, 10 mM ammonium sulfate [26]. The T. marneffei F4 strain isolated from an AIDS patient (CBS 119456) [29] was maintained on malt extract (ME) agar. Conidial suspensions of transformants and the G526 strain were harvested from conidiating colonies growing on ANM solid medium at 28°C for 1 week. Colonies on petri dishes were flooded with sterilized phosphate buffer saline, gently scraped, filtered through Miracloth (Calbiochem), and recovered by centrifugation.

Inhibition of reductase enzyme function assay
Conidia were harvested from T. marneffei F4 colonies cultured on ME agar at 28°C for 1 week. A suspension of 10 6 conidia was spread on ME agar with and without 30 μg/ml tricyclazole in 6-well plate. The plate was incubated at 28°C for 1 week.

RT-PCR
The expression of pbrB was investigated by RT-PCR. RNA samples were extracted from T. marneffei F4 cultured in brain heart infusion (BHI) broth at 28°C and 37°C for 3 days. RNA was extracted and used as a template to produce cDNA using Omniscript reverse transcription kit (Qiagen). The pbrB cDNA was then amplified using specific primers PmLac25-F and L25Re. The 18s rRNA was amplified as a control using Pm1 and Pm2 primers [30]. Primers used in this study are listed in Table 1. Talaromyces (Penicillium) marneffei pbrB Gene

Construction of transformation vectors
To construct the ΔpbrB plasmid, PmLac25U and PmLac25L primers were used to amplify the pbrB gene containing approximately 1.4 kb of upstream and downstream untranslated regions (UTRs) from T. marneffei strain G681. Purified PCR product (4,747 bp) was ligated into pGEM-T Easy (Promega) to produce the pbrB plasmid (plac25). This plasmid was digested with BglII and StuI to remove the pbrB coding region (138 bp before ATG to 155 bp before stop codon). The BglII/StuI pbrB plasmid was ligated to a BamHI/EcoRV fragment containing the pyrG blaster selectable marker cassette (pAB4342 [27]) to generate pplilac25. The linearized insert from pplilac25 was excised by NotI and purified before transformation. For the complementation construct, p25N9, the NotI fragment from plac25 was ligated into a NotI-digested/ dephosphorylated pAB4342 vector. In order to generate the pbrB(p)::pbrB::GFP strain, plac25 was amplified by inverse PCR using iLL25EC1/iUL25EC1 primers. The PCR product was digested with EcoRV and AclI and then ligated with EcoRV/ClaI fragment containing egfp to produce plac25GFP. The egfp coding region was inserted at the 5' end of pbrB, 87 bases after the start codon. The egfp coding region was amplified from the pEGFP-C1 vector (kindly provided by Dr. Amornrat O'Brien [31]) using fpEGFPC1/rpEGFPC1 primers. The whole pbrB(p)::pbrB::GFPfragment was excised from plac25GFP by NotI digestion and cloned into NotI-digested/dephosphorelated pAB4342 to generate pGFPLac4N.

Generation of transformants
T. marneffei strain G526 was used to generate the ΔpbrB::pyrG + mutant and pbrB(p)::pbrB:: GFP strain. DNA-mediated transformation was performed using PEG-mediated transformation protocol described previously [27]. The PyrG + transformants were selected on medium without uracil. To generate a ΔpbrB pyrGstrain, the ΔpbrB::pyrG + strain was inoculated onto ANM agar containing 1 mg/ml 5-fluoroorotic acid to select for loss of the pyrG cassette via homologous recombination between the inverted CAT repeats that flank pyrG in the construct [32]. To generate the ΔpbrB pbrB + complementation strain, the ΔpbrB pyrGstrain was transformed with p25N9 and PyrG + transformants were selected.
Genetically modified T. marneffei transformants were examined by PCR and/or Southern blot analysis [26]. The pbrB amplification was performed using PmLac25F/L25Re primers, while fpEGFPC1/L25Re primers were for egfp-pbrB amplification. The T. marneffei fetC gene (PMAA_057450) was amplified as an internal control of PCR using PmLac4F/PmLac4R primers. The hybridization probe for Southern blot analysis was the pbrB gene amplified by PCR using PmLac25U/PmLac25L primers.

Germination and growth rate assays
For germination assays, conidia (10 6 ) of each strain were inoculated in a six well microtitre plate containing BHI broth and the plate was incubated at 28°C or 37°C for 24 hours. Aliquots of the broth culture were placed on slides to count germinating conidia. Three replicates were performed counting at least 100 cells each time. For growth rate assays, approximately 10 conidia were spread onto 3 plates of ANM agar and incubated at 28°C for 3 days. The diameter of 5 individual colonies was measured daily over a period of 7 days. Mean and standard error of the mean (SEM) values were calculated and analyzed for statistical significance using Graph-Pad software (http://www.graphpad.com/).

Fluorescence microscopy
Conidia (10 6 ) of the pbrB(p)::pbrB::GFP strain were inoculated into two flasks containing 50 ml of BHI broth. Each flask was incubated in a shaking incubator at 28°C or 37°C for 3 days. Mycelia from the 28°C culture were poured onto Miracloth and rinsed with cold PBS before microscopic examination. Fungal cells from the 37°C culture were harvested by centrifugation, washed with cold PBS, placed on a microscope slide and examined using an Olympus Provis AX70 fluorescence microscope.
To examine conidiating fungal cells, a piece of ANM agar block (about 10 x 10 x 5 mm) was placed on a sterile glass slide. Conidia from the pbrB(p)::pbrB::GFP strain were inoculated on each side of agar block. A cover glass was placed on the top of the agar block. The slide culture was incubated in a humidified chamber at 28°C for 10 days. The agar block was removed and fungal cells that remained attached to the slide were fixed with absolute ethanol before air drying in a biosafety cabinet. Fungal cells on the slide were incubated with 5 mg/ml Trichoderma harzianum cell wall lysing enzyme (Sigma-Aldrich, UK) dissolved in osmotic buffer [27] at 37°C for 30 minutes and then the solution was poured off. Fungal cells were permeabilized by the addition of 0.2% Triton X-100 in PBS for 5 minutes. Slides were washed with cold PBS solution. Immunofluorescence staining was performed as previously described [20]. Briefly, slide cultures were blocked with Superblock Blocking Buffer (Pierce, USA) at 37°C for 2 hours. The slides were incubated with 10 μg/ml of anti-melanin IgM antibody, kindly provided by Dr. Sirida Youngchim [20], at 37°C for 1.5 hours. Slides were washed with PBS and then incubated with a dilution 1:100 of rhodamine-labeled goat anti-mouse IgM antibody (Jackson Immunoresearch Laboratories, USA) at 37°C for 1.5 hours. After washing, cells were observed under a fluorescence microscope. The negative control samples were produced by omitting the antimelanin IgM binding step in order to assess the background caused by non-specific binding of secondary antibody. The Superblock Blocking buffer used to dilute anti-melanin IgM was added, instead of using anti-melanin IgM, before incubating with secondary antibody.
To examine chitin deposition, calcofluor white staining was performed as previously described [33]. Three-day-old fungal cells were harvested from BHI broth culture as described above and the cells were washed with PBS before staining.

Results
The green pigment synthesized during conidiation in T. marneffei is dihydroxynaphthalene melanin To examine if the green coloration of conidia was attributed to DHN-melanin, T. marneffei conidia were inoculated onto medium with or without the inhibitor tricyclazole. Tricyclazole inhibits the two hydroxynaphthalene reductases functioning in DHN-melanin synthetic pathway ( Fig 1A) [23][24][25]. In the absence of tricyclazole, T. marneffei conidia appeared green ( Fig 1B). In contrast, in a presence of tricyclazole, the T. marneffei conidia appeared yellow (Fig 1B). This suggests that the synthesis of DHN-melanin contributes to the green coloration of conidia during asexual development.
The T. marneffei genome encodes ten multicopper oxidases Laccases are members of the multicopper oxidase (MCO) family, which also includes ferroxidases and ascorbate oxidases. To identify laccase encoding genes in T. marneffei the C. neoformans Lac1 and A. fumigatus Abr2 (Fig 2A) encoding genes were used as a query sequence in blast searches of the T. marneffei ATCC 18224 genome sequence (GenBank, NCBI). This identified two highly homologous genes (PMAA_072680 and PMAA_085520) (Cnlac1 homology of 88% and 78%, respectively) that were then also used for additional blast searches to retrieve related sequences in the T. marneffei genome. These homology searches identified 10 genes encoding putative multicopper oxidases (PMAA_008350, PMAA_050860, PMAA_055370, PMAA_057450, PMAA_062880, PMAA_072680, PMAA_082010, PMAA_082060, PMAA_085520, and PMAA_100410). Generally, laccases contain four copper atoms including type1 Cu, type 2 Cu, and a pair of type 3 Cu. The patterns of conserved amino acids coordinated with each type of copper are HXHG, HXH, HCHXXXHXXXM/F/L, and HXXHXH, which occupy the L1-L4 signature sequences starting from the N-terminus [34][35][36]. We found that 9 of the T. marneffei MCOs (excluding PMAA_062880) have these conserved patterns (see S1 Fig). Previous phylogenetic studies reveal that MCO sequences are often clustered with other genes according to function, fungal division, and source organism [10,11,13]. To predict which T. marneffei MCO participates in conidial DHN-melanin synthesis, we combined 55 fungal MCO sequences and performed alignments using CLUSTALW (http://www.genome.jp/ tools/clustalw/). Tree construction was conducted in MEGA version 6 [37] using the Neighbor--Joining method. The 55 fungal MCO sequences were separated into 5 clades with wellsupported branches (>90% bootstrap support) (Fig 2A). Each clade was highlighted and named according to sequences with known functions and fungal divisions. The ascomycete laccase lineage can be divided into 2 clades supported with very high bootstrap values (99% and 100%). Focusing on the second clade containing T. marneffei PbrB, this clade comprises of characterized laccases functioning in conidial DHN-melanin synthesis. T. marneffei PbrB is more closely related to A. fumigatus Abr2 than A. nidulans YA [16][17][18].
pbrB is expressed during asexual development and localizes to all cell types of the conidiophore The expression of pbrB was investigated by RT-PCR. RNA samples were extracted from T. marneffei F4 grown in BHI broth at 28°C and 37°C for 3 days. A transcript was not detected under these conditions suggesting there is little or no pbrB expression in vegetative hyphal or yeast cells (data not shown). To analyze pbrB expression further, a strain was generated that expresses a fusion construct in which pbrB, expressed from the native promoter, is fused to GFP (pbrB(p)::pbrB::GFP). Conidia of the pbrB(p)::pbrB::GFP strain were inoculated into BHI broth and cultured at 28°C and 37°C for 3 days. In support of the RT PCR analysis, GFP fluorescence was not detected in vegetative hyphal cells at 28°C or vegetative yeast cells at 37°C  nlm.nih.gov/protein/) and used to build sequence alignments in CLUSTALW. The alignment was then used to construct a relatedness tree using MEGA 6 software. Phylogenetic relationships of the 55 MCOs were inferred using the Neighbor-Joining method and bootstrap tested (1000 replicates). Branch lengths of the tree under standard conditions (Fig 3A and 3B). In addition, vegetative cells were grown at 28°C and 37°C in a variety of other types of medium (ANM, Synthetic Dextrose and Malt Extract) and in the presence of copper with low glucose (0.2%) or under acidic condition pH 5.0, which are known laccase inducing conditions [38]. No signal from PbrB::GFP could be detected under any of these conditions after 3, 5 and 7 days of incubation (data not shown).
A slide culture of the pbrB(p)::pbrB::GFP strain was prepared to observe expression of pbrB during conidiation. Compared to the negative control (Fig 3C), strong GFP fluorescence was observed in conidiophores of the pbrB(p)::pbrB::GFP strain, suggesting that PbrB is expressed during asexual development (Fig 3D). The PbrB::GFP protein was localized as distinct spots in metulae and phialides (Fig 3D).
To investigate if PbrB co-localizes with melanin, melanin was detected in the pbrB(p)::pbrB:: GFP strained by immunolabeling with an anti-melanin antibody. Immunostaining detected strong fluorescence in phialide cells with some weaker staining in the stalk, metulae and conidial cell types. There was also some punctate melanin staining in the various cell types. This staining are drawn to scale and bootstrap support indicating at the branch sites. Fungal MCOs that share a common ancestry with more than 60% bootstrap value are shaded in gray. Functions are defined at each clade based on characterized function of MCO members. (B) A partial alignment representing the conserved motifs of copper binding sites and L1-L4 signature sequences found in T. marneffei PbrB (PMAA_082060) and its orthologs A. fumigatus Abr2 (AFUA_2G17530) and A. nidulans YA (AN6635). The numbers in front of each sequence indicate the amino acid position of a particular protein. Cu binding motifs are identified above the sequences, numbers including 1, 2, and 3 are type 1 Cu, type 2 Cu, and type 3 Cu. The asterisk indicates the potential proton donor for the reaction intermediates.  was highly co-localised with the fluorescence form the PbrB::GFP fusion protein (Fig 4). This supports the hypothesis that PbrB is likely to be involved in melanin biosynthesis during conidiation.

T. marneffei pbrB is required for the melanization of conidia
To characterize the role of pbrB in T. marneffei, ΔpbrB mutants were generated. Two independent mutants were characterized with respect to conidiation, germination and growth. In order to examine morphogenesis during conidiation, ΔpbrB conidia were grown on ANM plates. In contrast to the wild type control, which exhibits green colored conidiation at 28°C after 14 days, conidiation of the ΔpbrB mutants appeared a light brown color (Fig 5). Reintroduction of a wild type copy of pbrB at the native locus (Materials and Methods) in the ΔpbrB mutant complemented the conidiation phenotype (Fig 5). Slide cultures of the ΔpbrB and ΔpbrB pbrB + complemented strains growing on ANM agar at 28°C for 7 days were prepared to examine the morphology of conidiophores. Deletion of pbrB did not result in any morphological defects in any of the conidiophore cell types (Fig 6C and 6D). The change in phenotype indicates that PbrB has a unique function that cannot be compensated by other T. marneffei laccases.
To assess if deletion of pbrB and the consequent change in pigmentation of the conidia affected germination, 10 6 conidia of the ΔpbrB and ΔpbrB pbrB + strains were inoculated in BHI broth and incubated at 28°C or 37°C for 24 hours then the number of germinated conidia were counted. There was no difference in the germination of the ΔpbrB and ΔpbrB pbrB + strains at 28°C (Fig 6A and 6B) or 37°C (data not shown). Hyphal cells from the ΔpbrB and ΔpbrB pbrB + strains were grown at 28°C for 3 days and examined microscopically. Staining of hyphae with 1 μg/μl calcofluor white showed no defects in chitin deposition nor was any morphological difference detected (data not shown).
Growth rates of the ΔpbrB and ΔpbrB pbrB + strains were determined by measuring colony diameters daily over the course of 7 days on ANM medium at 28°C. Mean and standard error of the mean (SEM) were calculated and statistical differences were assessed using the t-test. The differences in growth rates between ΔpbrB and ΔpbrB pbrB + strains at 6 and 7 days were found to be statistical significant (p = 0.002 and 0.015, respectively) (Fig 7).

Loss of T. marneffei pbrB does not affect sensitivity to stressors
Deletion of pbrB results in brown conidiation color, in contrast to the green coloration of wild type. This suggests that like A. fumigatus and A. nidulans, pbrB in T. marneffei is required for the synthesis of DHN-melanin. As melanins protect fungal cells against environmental assaults, the susceptibility of the ΔpbrB mutant to a variety of stresses was determined. Ten-fold dilutions of ΔpbrB and ΔpbrB pbrB + conidial suspensions were dropped on ANM and BHI agar containing 2% H 2 O 2 (oxidative stress), 20 μg/ml SDS (cell wall stress), 3 μM Congo Red (cell wall stress), 1 M sorbitol (osmotic stress), 0.6 M NaCl (salt stress), 5 mM NaNO 2 (nitrosative stress) or antifungals (0.15 μg/ml amphotericin B, 0.1 μg/ml clotrimazole, 40 μg/ml fluconazole, and 0.04 μg/ml itraconazole) and incubated at either 28°C and 37°C for 7 days. In addition, susceptibility to antifungal activity of macrophage (J774) was examined. However, no differences in stress susceptibility were observed (data not shown).   Talaromyces (Penicillium) marneffei pbrB Gene Cytoplasmic protein extracts from the wild type and ΔpbrB mutant cultured in brain heart infusion broth at 37°C for 3 days were capable of catalyzing L-DOPA (data not shown). In addition, ΔpbrB cells growing in BHI medium at 37°C for 5 days showed equivalent staining as the wild type using the anti-melanin antibody. These results suggest that melanization of vegetative cell types is not dependent on pbrB and this is consistent with the results from the susceptibility tests using the various stress agents.

Discussion
The multicopper oxidase (MCO) family comprises enzymes that typically contain four copper atoms classified into three types (type 1 Cu, type 2 Cu and type 3 Cu). Members of MCO family include laccases, ferroxidases, ascorbate oxidases, bilirubin oxidases, CueO, and ceruloplasmin [10,11,34,35]. Among MCO members, laccases can be found in various organisms (e.g. plants, fungi, bacteria and insects), but not in humans. A large number of laccases are produced in many basidiomycete and ascomycete fungal species and a variety of physiological roles have been reported including morphogenesis, stress defense, fungal pathogen/host interaction and delignification [7,12,36]. In pathogenic fungi, laccases have attracted attention due to their involvement in melanization and the correlation with host invasion and protection against host immunity. Laccases contribute to the melanization pathways producing the most commonly isolated fungal melanins; DOPA-and DHN-melanin [7,9]. Generally, melanins are deposited in the cell wall of conidia and fungal cells [6,15]. This study has determined the role of a developmentally regulated laccase, encoded by pbrB, during DHN-melanin synthesis in conidia. Neither the pbrB transcript nor the GFP-tagged protein in a pbrB(p)::pbrB::GFP strain could be detected during vegetative hyphal or yeast growth. However, GFP fluorescence was observed in conidiophores of the pbrB(p)::pbrB::GFP strain, suggesting that pbrB is only expressed during asexual development in T. marneffei. Likewise in A. fumigatus and A. nidulans, expression of the orthologous abr2 and yA genes characteristically occurs during conidiophore development but not during vegetative growth [16,18]. Phylogenetic examination showed that T. marneffei PbrB is more closed to A. fumigatus Abr2 than A. nidulans YA (Fig 2A). Moreover, T. marneffei ΔpbrB colonies displayed brown-pigmented conidia that resemble those of the Δabr2 strain [17,18]. Our data suggests that T. marneffei PbrB is polymerizing polymers of 1,8-DHN to form DHN-melanin, as has been shown in A. fumigatus [39]. T. marneffei pbrB is located within a genomic cluster of genes with homology to those required for conidial pigment biosynthesis in other systems and includes PMAA_082010 (conidial biosynthesis oxidase AbrA), PMAA_082020 (conidial biosynthesis protein AygA), PMAA_082030 (1,3,6,8-tetrahydroxynaphthalene reductase ArpA), PMAA_082040 (conidial pigment biosynthesis scytalone dehydrogenase ArpA) and PMAA_082120 (conidial pigment polyketide synthase AlbA) (see S2A  Fig). This cluster is conserved in A. fumigatus (S2B Fig). The biochemical pathway for DHN-melanin production was first described by Wheeler and Bell (1988) and has been well characterized both biochemically and genetically in many ascomycetes. The genus Aspergillus comprises many species and pigmented conidia appear in various colors among species. Effects of inhibitors on DHN-melanin synthesis (using tricyclazole and phthalide) and DOPA-melanin synthesis (using kojic acid and tropolone) in a range of Aspergillus species demonstrate that differences in the amounts and types of pigments and melanins synthesized by related species are likely to be a common theme [40,41]. Among Aspergillus and Penicillium species, most exhibit green to bluish green conidial pigments and the use of inhibitors of melanization pathways has revealed that most of these pigments are made from pentaketide metabolites [41]. The starting carbon units are acetate [25,42], malonyl CoA and/or acetyl CoA [6,15,43] and are catalyzed by a polyketide synthase (PKS) in the first step before subsequent processing through enzymatic steps to produce DHN-melanin [6,9,12,23]. Mutation of the gene encoding the PKS in A. nidulans (wA), A. fumigatus (pksP) and T. marneffei (wA) similarly results in white, non-melanized conidia [44,45,22]. While this early part of the pathway seems to be conserved amongst these fungi, differing results have been shown when tests are conducted with the DHN-melanin synthesis inhibitor tricyclazole. Tricyclazole specifically affects the reductases that reduce 1,3,6,8-tetrahydroxynaphthalene to scytalone and 1,3,8-trihydroxynaphthalene to vermelone [23][24][25]46]. Tricyclazole alters the conidial color phenotype of A. fumigatus but it does not affect conidial coloration of A. nidulans, A. flavus, and A. parasiticus [41,47]. Further studies showed that the conidial pigment biosynthesis in A. fumigatus and A. nidulans possess some steps that are distinct from the general model of DHN-melanin biosynthetic pathway (Fig 8) [6,15]. Instead of producing tetrahydroxynaphthalene (THN) from the starter units, A. nidulans and A. fumigatus utilize malonyl CoA and Acetyl CoA to produce heptaketide naphthopyrone YWA1 by heptaketide synthase (HKS) [44,48]. Although YWA1 is a precursor for green conidial pigmentation in both A. nidulans and A. fumigatus, the downstream metabolic steps are different in the two organisms. In A. nidulans, YA laccase catalyzes YWA1 to produce the green pigment of conidia. In contrast, A. fumigatus YWA1 is catalyzed through a hydrolytic polyketide-based shortening step to produce 1,3,6,8-THN by Ayg1 [49]. A homolog of A. fumigatus ayg1 is also presents in T. marneffei genome (see S2 Fig). As the addition of tricyclazole affected conidial color of T. marneffei, it suggests that hydroxynaphthalene reductases function in DHNmelanin synthetic pathway (Fig 8). Similar to A. fumigatus, YWA1 should be converted to 1,3,6,8-THN in T. marneffei. Then 1,3,6,8-THN is processed through additional steps to produce 1,8-DHN. Finally, 1,8-DHN is polymerized by PbrB laccase to form DHN-melanin, which appears as the green color of T. marneffei conidia (Fig 8).