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Involvement of a Polyketide Synthetase ClPKS18 in the Regulation of Vegetative Growth, Melanin and Toxin Synthesis, and Virulence in Curvularia lunata
The Plant Pathology Journal 2017;33:597-601
Published online December 1, 2017
© 2017 The Korean Society of Plant Pathology.

Jin-Xin Gao1,2,3, and Jie Chen1,2,3,*

1School of Agriculture and Biology, Shanghai Jiaotong University, 800 Dongchuan Road, Shanghai 200240, China, 2State Key Laboratory of Microbial Metabolism, Shanghai Jiaotong University, 800 Dongchuan Road, Shanghai 200240, China, 3Ministry of Agriculture Key Laboratory of Urban Agriculture (South), Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China
Correspondence to: Phone) +86-21-34206141, FAX) +86-21-34206141, E-mail)
Received April 11, 2017; Revised May 22, 2017; Accepted June 12, 2017.
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

The clpks18 gene was first cloned and identified in Curvularia lunata. It contains 6571 base pairs (bp) and an 6276 bp open reading frame encoding 2091 amino acids. The ClPKS18 deletion mutant displayed an albino phenotype, and almost lost the ability to product 5-(hydroxymethyl) furan-2-carboxylate (M5HF2C) toxin, implying that clpks18 gene in C. lunata is not only involved in 1,8-dihydroxynaphthalene melanin synthesis, but also relatively associated with M5HF2C toxin biosynthesis of the pathogen. The pathogenicity assays revealed that ΔClPKS18 was impaired in colonizing the maize leaves, which corresponds to the finding that ClPKS18 controls the production of melanin and M5HF2C in C. lunata. Results indicate that ClPKS18 plays a vital role in regulating pathogenicity of in C. lunata.

Keywords : melanin, PKS18, toxin

Curvularia lunata is an important fungal pathogen that causes Curvularia leaf spot (CLS), which is one of the most widely distributed maize leaf diseases worldwide (Gao et al., 2015a; Liu et al., 2016). To uncover the pathogenicity mechanisms of CLS, most researches have focused on identifying virulence factors, such as melanin (Gao et al., 2012, 2015b), and toxin (Gao et al., 2014a; Liu et al., 2009). Fungal melanins, formed by the oxidative polymerisation of phenolic compounds, are essential for enhance the mechanical strength of the infection into the host plant epidermis and contribute to virulence in numerous types of plant diseases (Gao et al., 2015e). Previous studies have also indicated that the albino C. lunata strains present in wild-type (WT) strains are weakly virulent to maize leaves, supporting the conclusion that melanin is a crucial virulence factor for C. lunata in susceptible maize leaves (Yan et al., 2005). Researchers have successfully identified a non-host-specific toxin called methyl 5-(hydroxymethyl) furan-2-carboxylate (M5HF2C). The super-virulence capability of M5HF2C was also observed on some other plant species, such as Capsicum annuum, Nicotiana tabacum, Oryzae sativa, and (Liu et al., 2009). However, few genes involved in the production of melanin (Gao et al., 2015d) and toxin (Gao et al., 2015c) have been researched.

The PKS18 protein is involved in melanin synthesis in some pathogens, such as Cochliobolus heterostrophus (Eliahu et al., 2007). However, no research has revealed the exact correlation of PKS18 with melanin production and pathogenicity in C. lunata. This study first reports the sequence and characterization of pks18 gene from C. lunata. The Bipolaris maydis PKS18 (accession number: AY495659) was used to query the C. lunata genome database (Dryad Digital Repository) for orthologs (Gao et al., 2014b). The open reading frame of clpks18 comprises 6571 bp and an 6276 bp open reading frame encoding a 209-amino-acid protein. Phylogenetic analysis indicated that the ClPKS18 protein falls in a well-supported group of dothideomycete polyketide synthetase homologs (Fig. 1A). Alignment of ClPKS18 with B. maydis BmPKS18 and Setosphaeria turcica StPKS18 showed 88% identity and 99% positives, respectively (NCBI BlastP Align). Meanwhile, alignment of them identified highly conserved Acyl transferase, Beta-ketoacyl synthase, malonyl CoA-acyl carrier protein transacylase, and dehydratase domains, characteristic of fungal polyketide synthases (Fig. 1B).

Target gene deletion strategy was employed by replacing clpks18 with a hygromycin resistance (hph) cassette to investigate the biological functions of ClPKS18 in C. lunata (Fig. 2A). The Southern hybridization pattern confirmed that homologous recombination occurs at the clpks18 locus in ΔClPKS18 (Fig. 2B). The radial growth rates of the mutant and WT on the potato dextrose agar (PDA) medium were compared. ΔClPKS18 had a significantly slower mycelial growth rate than WT on the PDA medium. However, the conidiation of ΔClPKS18 was not evidently different from those of the WT (Table 2).

In B. maydis, BmPKS18 was functionally characterized to encode a polyketide synthetase that converts malonyl-CoA to 1,3,6,8-tetradroxynaphthalene (1,3,6,8-THN) in the DHN-melanin synthesis pathway (Eliahu et al., 2007). This research showed that the ClPKS18 deletion mutant of C. lunata displayed an albino phenotype, indicating that ClPKS18 is an orthologue of PKS18 from B. maydis (Fig. 3A). We detected the expression of the polyketide synthase gene (pks18), the transcription factor gene (cmr1), and three synthase genes (brn1, brn2, and scd) related to the synthesis of DHN melanin in the mutant and WT to further confirm this observation (Gao et al., 2017). As expected, almost no expression of pks18 was detected in ΔClPKS18. Besides, the expression of scd in ΔClPKS18 has a 70.92-fold decrease, and the expression of brn1 and brn2 have above 30-fold decrease in ΔClPKS18 compared to those in WT. As for cmr1, it also showed a downward trend, which is almost 0.36-fold decrease in ΔClPKS18 compared with WT (Fig. 3B). Overall, we conclude that ClPKS18 plays a positive regulation role in the synthesis of melanin.

The mutants were cultured in Fries 3 medium for 30 days to determine whether they retained the ability to produce the virulence-related toxin M5HF2C (Liu et al., 2009). As shown in Fig. 4, the mutant lost the ability to produce M5HF2C toxin. The expression of the M5HF2C biosynthesis related gene clt-1 was analyzed by qRT-PCR to further confirm that ΔClPKS18 acts as a positive regulator of M5HF2C toxin production. Meanwhile, the expression of brn1, which is also responsible for M5HF2C biosynthesis (Liu et al., 2011), fell sharply in ΔClPKS18 (Fig. 3B). The experiment results indicate that ClPKS18 played a major role in the regulation of M5HF2C biosynthesis in C. lunata. We further assayed the infective ability of ΔClPKS18 on maize leaves because the deletion of clpks18 compromised the ability of C. lunata to produce M5HF2C. Similarly, ΔClPKS18 lost the pathogenicity, and the lesion areas also cannot be found in maize leaves which treated with ΔClPKS18 (Fig. 5), indicating that ClPKS18 was essential to the complete virulence in C. lunata. We proposed that the clpks18 gene may be one of the node genes controlling two separate metabolic pathways for melanin and toxin biosynthesis, respectively. In conclusion, this study would help us understand the synthesis mechanism of melanin and toxin in C. lunata and may provide target sites for designing a new agent to control C. lunata and a few similar fungi.


We would like to thank Zhe Li for critical reading of the manuscript. The work was supported by the National Science Foundation of China (31471734) and China Agriculture Research System (CARS-02).

Fig. 1. C. lunata PKS18 is an ortholog of Biolaris maydis PKS18. (A) Phylogenetic analysis. PKS18 protein sequences were obtained from GenBank using B. maydis BmPKS18 as a query. (B) C. lunata ClPKS18, B. maydis BmPKS18 and Setosphaeria turcica StPKS18 were aligned using ClustalW. Conserved Acyl transferase domains are highlighted in blue, Beta-ketoacyl synthase domains are highlighted in yellow, malonyl CoA-acyl carrier protein transacylase domains are highlighted in red, dehydratase domains are highlighted in green, asterisks mark identical residues, colons mark conserved residues, and periods indicate semi-conserved residues.

GenBank Accession numbers

Dothideomycetes:Alternaria alternate AaPKS18: AFN68292; Bipolaris maydis BmPKS18: AAR90272; Curvularia lunata ClPKS18: MF114294; Dothistroma septosporum DsPKS18: EME39782; Pyrenophora tritici-repentis PtPKS18: XP_001933656; Setosphaeria turcica StPKS18: AEE68981.

Sordariomycetes:Verticillium dahlia VdPKS18: AGI15329; Verticillium longisporum VlPKS18: CRK15634.

Fig. 2. Graphical representation of screening clpks18 deletion mutant. (A) clpks18 deletion strategy used by homologous recombination. clpks18 and hygromycin resistance (hph) genes are represented by green and red boxes, respectively. (B) Southern blot to confirm clpks18 was replaced using the 600 bp fragment of clpks18 as probe. All primers used for gene deletion and confirmation are showed in .
Fig. 3. ClPKS18 possively regulates the mycelial melanization of C. lunata. (A) Cultures of WT strain (CX-3), and clpks18 deletion mutant (ΔClPKS18) grown on PDA plates. Note the white mycelia of ΔClPKS18 compared to WT. (B) qRT-PCR analyses of pks18, cmr1, brn1, brn2, and scd. Error bars are the standard deviation. A single asterisk indicates the P < 0.05 while double asterisks indicate the P < 0.001 in the T-test analysis. All primers used for qRT-PCR are showed in .
Fig. 4. ClPKS18 regulates the biosynthesis of M5HF2C toxin. HPLC-MS chromatograms of the methyl 5-(hydroxymethyl)-furan-2-carboxylate standard and toxins extracted from the WT strain (CX-3) and clpks18 deletion mutant (ΔClPKS18).
Fig. 5. Virulence of the WT (CX-3), and clpks18 deletion mutant (ΔClPKS18) on maize leaves. ΔClPKS18 is impaired in the colonization of maize leaves. Detached leaves of HUANGZAO-4 were inoculated with conidial suspensions and incubated on two layers of filter papers moisturized with 10 mM 6-Benzyladenine (6-BA) in Petri dishes at 28°C for 96 h.

Primer used for this study

PrimersSequence 5′ to 3′DescriptionPCR (kb)aPurpose
pks18-FL-FATGGATGTCATCATCTTCGGclpks18 coding region, FPb6.571dclpks18 confirmation
pks18-FL-RTTATAGCTTAAGGCCTTGCCclpks18 coding region, RPc

pks18U-FACGCGTCGACACCCGCAGGATATATCAflanking region upstream of clpks18 FP0.925ΔClPKS18
pks18U-RGCTCTAGATTTAGCAAGGGTATAATTflanking region upstream of clpks18 RP

pks18D-FGGGGTACCGCATTTTGATTATTCATCflanking region downstream of clvelB FP0.943
pks18D-RCGGAATTCCCAGAGGCATGGGTCGGTflanking region downstream of clvelB RP

hyg-FCGACAGCGTCTCCGACCTGAhph coding region, FP0.811ΔClPKS18 confirmation

pks18-sb-FAGATTGTCTCTCAGGTCACCclpks18 coding region, FPb0.600
pks18-sb-RAATTGATTCTGCCAGGCGCGclpks18 coding region, RPc

gapdh_2FTCGTCGCCGTAAACGACCCCgapdh coding region, FP0.207qRT-PCR
gapdh_2RCGCCCTTGAACTGGCCGTGTgapdh coding region, RP

brn1-1FTGGCCAGCCAGTAGACATTGbrn1 coding region, FP0.075
brn1-1RACCTTTCCGTTGACCCACTCbrn1 coding region, RP

brn2-2FAACAACGGCCGTATCATCCTbrn2 coding region, FP0.078
brn2-2RAGCGTTGTAAAGAGCGTGGTbrn2 coding region, RP

cmr1-1FGTTTGGACTGACTCGCTGGTcmr1 coding region, FP0.118
cmr1-1RTAGGATGATCGGCGGGAAGAcmr1 coding region, RP

scd_1FCGGTCGTTCCTGGACAAGATGscd coding region, FP0.121

clt1-FGCACACACATACCCAAGACGclt-1 coding region, FP0.150
clt1-RAGTTGATGGGAATGTAGGCGclt-1 coding region, RP

aPCR (kb) = PCR product length in kb;

bFP = forward primer;

cRP = reverse primer;

dΔ = gene deletion. The underlined regions identify the added restriction sites.

Phenotypic analysis of ClPKS18 mutant compared with wild-type (WT) isolate CX-3a

StrainGrowth rate (mm/24 h)bConidiation (log10 CFU/ml)c
WT7.26 ± 0.19a5.90 ± 0.09a
ΔClPKS186.13 ± 0.06cb5.87 ± 0.11a

aDifferent letters in each data column indicate significant differences at P = 0.05.

bDiameter of hyphal radii.

cConidial numbers (log transformation).

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