Figures
Abstract
Background
The genome of P. marneffei, the most important thermal dimorphic fungus causing respiratory, skin and systemic mycosis in China and Southeast Asia, possesses 23 polyketide synthase (PKS) genes and 2 polyketide synthase nonribosomal peptide synthase hybrid (PKS-NRPS) genes, which is of high diversity compared to other thermal dimorphic pathogenic fungi. We hypothesized that the yellow pigment in the mold form of P. marneffei could also be synthesized by one or more PKS genes.
Methodology/Principal Findings
All 23 PKS and 2 PKS-NRPS genes of P. marneffei were systematically knocked down. A loss of the yellow pigment was observed in the mold form of the pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants. Sequence analysis showed that PKS11 and PKS12 are fungal non-reducing PKSs. Ultra high performance liquid chromatography-photodiode array detector/electrospray ionization-quadruple time of flight-mass spectrometry (MS) and MS/MS analysis of the culture filtrates of wild type P. marneffei and the pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants showed that the yellow pigment is composed of mitorubrinic acid and mitorubrinol. The survival of mice challenged with the pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants was significantly better than those challenged with wild type P. marneffei (P<0.05). There was also statistically significant decrease in survival of pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants compared to wild type P. marneffei in both J774 and THP1 macrophages (P<0.05).
Conclusions/Significance
The yellow pigment of the mold form of P. marneffei is composed of mitorubrinol and mitorubrinic acid. This represents the first discovery of PKS genes responsible for mitorubrinol and mitorubrinic acid biosynthesis. pks12 and pks11 are probably responsible for sequential use in the biosynthesis of mitorubrinol and mitorubrinic acid. Mitorubrinol and mitorubrinic acid are virulence factors of P. marneffei by improving its intracellular survival in macrophages.
Author Summary
Penicillium marneffei is the most important thermal dimorphic fungus causing respiratory, skin and systemic mycosis in China and Southeast Asia. Its genome possesses a large number of polyketide synthase (PKS) genes, which should be responsible for synthesis of secondary metabolites such as pigments, antibiotics and mycotoxins. Using state-of-the-art gene knockdown and ultra high performance liquid chromatography-photodiode array detector/electrospray ionization-quadruple time of flight-mass spectrometry technologies, we discovered that the yellow pigment of P. marneffei was composed of mitorubrinol and mitorubrinic acid and was synthesized by two PKS genes, named pks12 and pks11. This represents the first discovery of PKS genes responsible for mitorubrinol and mitorubrinic acid biosynthesis, in which pks12 and pks11 are probably responsible for sequential use in the biosynthesis of mitorubrinol and mitorubrinic acid. Using a mouse model and human and mouse macrophage cell line models for P. marneffei infection, we also discovered that mitorubrinol and mitorubrinic acid are virulence factors of P. marneffei by improving its intracellular survival in macrophages.
Citation: Woo PCY, Lam C-W, Tam EWT, Leung CKF, Wong SSY, Lau SKP, et al. (2012) First Discovery of Two Polyketide Synthase Genes for Mitorubrinic Acid and Mitorubrinol Yellow Pigment Biosynthesis and Implications in Virulence of Penicillium marneffei. PLoS Negl Trop Dis 6(10): e1871. https://doi.org/10.1371/journal.pntd.0001871
Editor: Pamela L. C. Small, University of Tennessee, United States of America
Received: February 17, 2012; Accepted: September 2, 2012; Published: October 18, 2012
Copyright: © Woo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was partly supported by the Research Fund for the Control of Infectious Diseases (commissioned study) of the Health, Welfare and Food Bureau of the Hong Kong SAR Government, Research Grant Council Grant, University Development Fund, Committee for Conference and Research Grant, Providence Foundation Limited in memory of the late Dr. Lui Hac Minh, HKU Award for CAE Membership, HKU Medical Faculty Award for CAE Membership, Dr. Hector T.G. Ma. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Penicillium marneffei is the most important thermal dimorphic fungus causing respiratory, skin and systemic mycosis in China and Southeast Asia [1], [2], [3], [4]. After the discovery of P. marneffei in 1956, only 18 cases of human diseases were reported until 1985 [5]. The appearance of the HIV pandemic, especially in China and Southeast Asian countries, saw the emergence of the infection as an important opportunistic mycosis in HIV positive patients. About 8% of AIDS patients in Hong Kong are infected with P. marneffei [6]. In northern Thailand, penicilliosis is the third most common indicator disease of AIDS, following tuberculosis and cryptococcosis [2]. Besides HIV positive patients, P. marneffei infections have been reported in other immunocompromised patients, such as transplant recipients, patients with systemic lupus erythematosus and those on corticosteroid therapy [7], [8], [9], [10].
Polyketides are a diverse group of secondary metabolites produced by microorganisms. Some of the best known secondary metabolites include pigments, antibiotics and mycotoxins. Polyketides are synthesized by complex enzymatic systems called polyketide synthases (PKS). In the neighborhood of the PKS genes also include additional genes that encode modifying enzymes forming biosynthetic clusters. The availability of more and more fungal genome sequences have enabled us to identify an unprecedented number of fungal PKS genes. However, relatively few fungal PKS genes have been definitely linked to the biosynthesis of specific polyketide secondary metabolites.
In 2002, the complete genome sequencing project of P. marneffei was started. At the moment, a 6× coverage of the genome has been completed [11]. Based on the genome sequence, we have assembled the complete mitochondrial genome sequence and analyzed the phylogeny, predicted the presence of a potential sexual cycle and developed a highly discriminative multilocus sequence typing scheme for P. marneffei [12], [13], [14]. Recently, we also reported a high diversity of PKS in the P. marneffei genome and characterized its melanin biosynthesis gene cluster and confirmed it as a virulence factor in P. marneffei [15]. Since the P. marneffei genome possesses 23 PKS and 2 PKS nonribosomal peptide synthase hybrid (PKS-NRPS) genes, which is of high diversity compared to other thermal dimorphic pathogenic fungi such as Histoplasma capsulatum (with only one PKS gene) and Coccidioides immitis (with 10 PKS genes), we hypothesized that the yellow pigment in the mold form of P. marneffei could also be synthesized by one or more PKS genes. To test this hypothesis, we systematically knocked down all the 23 PKS and 2 PKS-NRPS genes of P. marneffei and observed for the loss of yellow pigment in the knockdown mutants. The culture extracts of the wild type strain and the mutant strains with loss of yellow pigment were characterized using ultra high performance liquid chromatography-photodiode array detector/electrospray ionization-quadruple time of flight-mass spectrometry (UHPLC-DAD/ESI-Q-TOF-MS) to determine its chemical nature. The possible role and mechanism of the yellow pigment in virulence was also examined in a mouse model and macrophage cell line models respectively.
Methods
Ethics statement
The experimental protocols were approved by the Committee on the Use of Live Animals in Teaching and Research, The University of Hong Kong, in accordance with the Guidelines laid down by the NIH in the USA regarding the care and use of animals for experimental procedures.
Strain and culture conditions
P. marneffei strain PM1 was obtained from an already-existing collection from the clinical microbiology laboratory in Queen Mary Hospital and the strain was anonymized. The yeast form of PM1 was used for knockdown of the PKS genes. A single colony of the fungus grown on Sabouraud dextrose agar at 37°C was inoculated into yeast peptone broth and incubated in a shaker at 37°C for 10 days.
Knockdown of PKS genes
DNA extraction was performed using the DNeasy Plant Mini Kit according to manufacturer's instructions (Qiagen, Hilden, Germany). The extracted DNA was eluted in 50 µl of AE buffer and the resultant mixture was diluted 10× and 1 µl of the diluted extract was used for PCR.
Plasmid construction was performed according to our previous publication. For knockdown of pks1, plasmid pSilent-1 [16], obtained from the Fungal Genetics Stock Center, was used to construct the pPW1459 plasmid. First, the internal pks1 fragment (sense) was amplified using primers LPW11663 5′-CCGCTCGAGTTTCAACGACCTATCGCCCACTCAA-3′ and LPW11664 5′-CCCAAGCTTGGGACAACAGCACCAAGCAGTGTGGACA-3′ (Invitrogen, USA) (Table 1). The PCR mixture (25 µl) contained P. marneffei DNA, PCR buffer (10 mM Tris-HCl pH 8.3, 50 mM KCl, 2 mM MgCl2 and 0.01% gelatin), 200 µM of each deoxynucleoside triphosphates and 1.0 U Taq polymerase (Applied Biosystem, USA). The mixtures were amplified in 32 cycles of 95°C for 30 s, 56°C for 30 s and 72°C for 40 s, and a final extension at 72°C for 10 min in an automated thermal cycler (Applied Biosystem, Foster City, CA, USA). The PCR product was purified using the QIAquick Gel Extraction kit (QIAgen, Germany), digested with XhoI and HindIII, and cloned into the XhoI-HindIII site of the pSilent-1 plasmid, resulting in pPW1459-1. Second, the internal pks1 fragment (antisense) was amplified with primers LPW11665 5′-GGGGTACCTTTCAACGACCTATCGCCCACTCAA-3′ and LPW11666 5′-GAAGATCTACAACAGCACCAAGCAGTGTGGACA-3′ (Invitrogen, USA), using the PCR conditions described above. This amplified fragment was purified as described above, digested with BglII and KpnI, and cloned into the BglII-KpnI site of the pPW1459-1, resulting in pPW1459. The wild type P. marneffei strain PM1 was transformed with linearized pPW1459, using 200 µg/ml hygromycin for selection. For the other PKS genes, they were knocked down using the same protocol described above with primers listed in Table 1.
To construct the pks11pks12 double knockdown mutant, the pks11 fragment (sense) was amplified using primers LPW20378 5′-CCGCTCGAGGTATCAACACGGAAACCGACAA-3′ and LPW20379 5′-TGGCATGTGTGGTTGGTCTGCCATTCTGCGTTATCGGTAGAA-3′. The pks12 fragment (sense) was amplified using primers LPW20380 5′- CAGACCAACCACACATGCCA-3′ and LPW20381 5′- CCCAAGCTTGGGCAGGACAAGTCTCACTGCTATTGA-3′. The two PCR products were used as template for fusion PCR to construct the pks11pks12 fragment (sense) by using primers LPW20378 and LPW20381. The pks11pks12 fragment (antisense) was also amplified by the same method by replacing LPW20378 with LPW20382 5′- GGGGTACCGTATCAACACGGAAACCGACAA-3′ and LPW20381 with LPW20383 5′-GAAGATCTCAGGACAAGTCTCACTGCTATTGA-3′. The sense and antisense pks11pks12 fragments were cloned into pSilent-1 as described above.
Real-time quantitative RT-PCR
Total RNA was extracted using RiboPure-Yeast (Ambion, USA). The RNA was eluted in 70 µl of RNase-free water and was used as the template for real-time RT-PCR. Reverse transcription was performed using the SuperScript III kit (Invitrogen, USA). Real-time RT-PCR assays was performed as described previously [17], for pks1 fragment with primers LPW11663 and LPW11664 (Table 1), using actin with primers LPW8614 5′-CAYACYTTCTACAAYGARCTCC-3′ and LPW8615 5′-KGCVARRATRGAACCACC-3′ for normalization. cDNA was amplified in a LightCycler 2.0 (Roche, Switzerland) with 20 µl reaction mixtures containing FastStart DNA Master SYBR Green I Mix reagent kit (Roche, Switzerland), 2 µl cDNA, 2 mM MgCl2 and 0.5 mM primers at 95°C for 10 min followed by 50 cycles of 95°C for 10 s, 57°C (55°C for actin gene) for 5 s and 72°C for 23 s (36 s for actin gene). For the other PKS genes, real-time RT-PCR was performed using the protocol described above with primers listed in Table 1.
Sequence and phylogenetic analysis of PKS11 and PKS12
Introns were predicted by performing pairwise alignment with the annotated Talaromyces stipitatus (teleomorph of Penicillium emmonsii) complete genome sequence. Domains of PKS11 and PKS12 were predicted using the Conserved Domains Database of NCBI and PFAM (http://pfam.sanger.ac.uk/search?tab=searchSequenceBlock) and manual inspection of multiple alignments of PKS11 and PKS12 and their homologous sequences.
Extraction of yellow pigment
Conidia of seven-day-old cultures of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutant strains of P. marneffei were collected gently and immersed into 5 µl Milli-Q water. Milli-Q water without conidia was used as negative control. The mixtures were vortexed and filtered with 0.22 µm filters. Metabolic activities in the filtrates were quenched by incubating the filtrates in liquid nitrogen for 10 min. The filtrates were used for UV-Vis spectroscopic examination and UHPLC-DAD/ESI-Q-TOF-MS analysis respectively.
UV-Vis spectroscopic analysis
The maximum absorbance of the extracts was examined by a UV-Vis spectrometer (NanoDrop 1000 spectrophotometer, Thermo scientific, USA). The absorbance was measured by using the 0.2 mm path.
UHPLC-DAD/ESI-Q-TOF-MS analysis
For liquid chromatography, the separation was performed by a 1290 Agilent UHPLC with an Infinity DAD (Agilent Technologies, USA) and a C18 RRHD (Agilent Zorbax Eclipse Plus 2.1 mm×100 mm, 1.8 µm) column. The column temperature was maintained at 40°C. 15 µl of reconstituted sample was injected into the UHPLC instruments. The mobile buffer A consisted of 0.05% acetic acid and 5 mM ammonium acetate in water and mobile buffer B is methanol. Gradient started from 2% buffer B from 0 to 1 min, 2% to 40% buffer B from 1 to 10 min, 40% to 95% buffer B from 10 to 17 min, maintained at 95% buffer B from 17 to 20 min and equilibrated from 20 to 22 min. The flow rate was 0.35 ml/min. Separation was coupled to a 6540 Agilent Q-TOF mass spectrometer (Agilent Technologies, USA) with a jet stream ESI mode and infinity DAD. UV spectrum was collected from 200 to 640 nm with a 4-nm silt.
For MS, mass spectrometer acquisition was operated in the positive ESI mode with accurate mass ranged from 110 to 1700 m/z. Fragmentor was at 135 V and skimmer at 50 V. Drying gas flow rate was kept at 10 l/min at 300°C, the sheath gas flow was 10 l/min at 325°C, capillary voltage was 3500 V, and nebulizer was 45 psi. MS/MS acquisition was operated in the same parameter in MS acquisition. Collision energy was 5 eV for fragmentation of the targeted compounds. Mass spectrometry data were acquired at extended dynamic range with 4 spectra/s and 8 spectra/s in MS/MS mode. Mass accuracy was enhanced by automated calibrant system with two internal reference masses (121.0509 and 922.0098).
Animal experiments
Balb/c (H-2d) mice (6 to 8 weeks old, 18 to 22 g) were obtained from the Laboratory Animal Unit, The University of Hong Kong [18]. The experimental protocols were approved by the Committee on the Use of Live Animals in Teaching and Research, The University of Hong Kong, in accordance with the Guidelines laid down by the NIH in the USA regarding the care and use of animals for experimental procedures. The number of animals used was kept at the minimum that still ensured statistical significance of survival differences between the experimental groups. Mice were housed in cages, under standard conditions with regulated day length, temperature and humidity, and were given pelleted food and tap water ad libitum. Ten mice were challenged intravenously with 8×106 spores of wild type P. marneffei and another 10 mice each with pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants respectively. Survival of the mice was recorded daily for 60 days and analyzed by Kaplan-Meier method and Log-rank test. P<0.05 was regarded as statistically significant. The experiment was performed in duplicate.
Intracellular survival assays in J774 and THP1 macrophages
J774 macrophages (Sigma-Aldrich, USA) were grown in DMEM (Gibco, USA) supplemented with 10% fetal bovine serum and THP1 monocytes (THP1, American type culture collection, ATCC) were grown in suspension in RPMI 1640 medium (Gibco) supplemented with 10% fetal bovine serum at 37°C and 5% CO2.
J774 macrophages were seeded to 24-well tissue culture plates at 4×105 cells per well. THP1 monocytes were seeded to 24-well tissue culture plates at 1×106 cells per well and differentiated into macrophages by incubating in RPMI 1640 medium supplemented with 100 nM PMA. All cell cultures were incubated at 37°C with 5% CO2 for 24 h before adding fungal strains. Fresh culture media were replaced before addition of fungal strains. Infection was carried out by inoculating the conidia of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei at a multiplicity of infection of 1 and incubated for 2 h to allow adhesion and invasion to occur. After 2 h, the monolayers were washed with 240 U/ml of nystatin (Sigma-Aldrich) to kill the extracellular conidia. The monolayers were then washed with warm Hank's buffered salt solution (HBSS) to remove the nystatin. Macrophages were supplemented with fresh media and incubated for 24 h. After 24 h post infection, macrophages were lysed with 1% Triton X-100 (Sigma-Aldrich) for colony forming unit (CFU) count. Cell lysates were diluted and plated on Sabouraud dextrose agar and incubated at 37°C. The CFUs recovered from cell lysates after 2 h of phagocytosis were considered as the initial inocula and were used as the baseline values for intracellular survival analysis. CFUs recovered at 24 h were used to calculate the recovery rate of fungal cells in macrophages. Experiments were repeated in triplicate to calculate the mean of intracellular survival of conidia.
Intracellular survival assays in human neutrophils
Unpooled peripheral blood of three healthy blood donors was obtained from the Hong Kong Red Cross Blood Transfusion Service. Neutrophils were isolated according to published protocols with some modifications [19]. Human blood was diluted in HBSS without calcium and magnesium ions and undergone Ficoll-Paque density gradient centrifugation. The bottom layer which contained red blood cells (RBC) with granulocytes was collected and mixed with 3% dextran in 0.9% sodium chloride for 30 min sedimentation. Neutrophils rich supernatant at upper layer was collected and trace amount of RBC in the neutrophils layer was lysed by using RBC lysis buffer.
Conidia of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei were preincubated in YPD broth for 4 h at 37°C and preopsonized by incubation in autologous human serum for 30 min at 37°C [20]. Preopsonized conidia were kept at 4°C for at least 1 h before challenge. Equal number of human neutrophils and conidia were incubated in 1 ml RPMI medium containing 10% autologous serum for 2 h. After 2 h, the cultures were washed with 240 U/ml of nystatin to kill the extracellular conidia. The cultures were then washed with HBSS. Neutrophils were supplemented with fresh media and incubated for 18 h. After 18 h post-infection, Neutrophils were lysed with 1% Igepal-CA-630 for CFU count. Cell lysates were diluted and plated on Sabouraud dextrose agar. The CFUs recovered from cell lysates after 2 h of phagocytosis were considered as the initial inocula and were used as the baseline values for intracellular survival analysis. CFUs recovered at 18 h were used to calculate the recovery rate of fungal cells in neutrophils. Experiments were repeated in triplicate to calculate the mean of intracellular survival of conidia.
Susceptibility to hydrogen peroxide killing
Conidial suspensions of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei respectively were adjusted to 4×103 cells/ml in 100 mM potassium phosphate buffer (PBS) (pH 7.0) containing 25 mM hydrogen peroxide [15], [21]. At 5-min intervals, aliquots were taken, diluted in 100 mM PBS, and plated onto Sabouraud dextrose agar plates. The experiment was performed in triplicate.
Susceptibility to ultraviolet light killing
Conidial suspensions of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei respectively were adjusted to 4×103 cells/ml. Appropriate dilutions of cells were plated on Sabouraud dextrose agar plates and exposed to UV light (254 nm) generated in a Crosslinker (UVP, CA, USA) at various energy settings. Percentage survival was determined by comparing the number of colonies on irradiated plates to those on non-irradiated plates [15], [21]. The experiment was performed in triplicate.
Killing assay of antifungal peptides
Histatin 5 and PGLa were dissolved at a concentration of 1 mg/ml in 10 mM PBS, pH 7.0 respectively and stored at −20°C. Conidial suspensions of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei were adjusted to 2×106 cells/ml respectively in 100 mM PBS with a dilution series of peptides. After 1 h incubation, aliquots were taken, diluted in 100 mM PBS, and plated onto Sabouraud dextrose agar plates to determine viabilities. The experiment was performed in triplicate.
Results
pks11 and pks12 are responsible for yellow pigment production in P. marneffei
All 23 PKS and 2 PKS-NRPS genes of P. marneffei were systematically knocked down. The median transcription levels of the 25 knockdown mutants were 12.6% (range 0.1% to 40%) of that in wild type. A loss of the yellow pigment was observed exclusively in the mold form of the pks11 and pks12 knockdown mutants, which have pks11 and pks12 transcription levels 5.4% and 10.0% respectively of that in wild type (Fig. 1). A pks11pks12 double knockdown mutant was also constructed. A loss of the yellow pigment was also observed (Fig. 1). The transcription levels of pks11 and pks12 were 26.5% and 9.0% respectively of that in wild type.
(A) Wild type, (B) pks11, (C) pks12 and (D) pks11pks12 knockdown mutants of P. marneffei were grown on Sabouraud dextrose agar after 7 days incubation at 25°C.
Sequence and phylogenetic analysis of PKS11 and PKS12
The pks11 gene is 7780 bp in length. It has one intron of 52 bp (from 607 to 658 bp). The resultant putative mRNA encodes 2575 amino acid residues with a predicted molecular mass of 282.6 kDa. The pks12 gene is 5485 bp in length. It has one intron of 63 bp (from 439 to 501 bp). The resultant putative mRNA encodes 1806 amino acid residues with a predicted molecular mass of 197.9 kDa. PKS11 has one ketosynthase, one acyltransferase, one acyl carrier protein, one methyltransferase and one thioester reductase domains whereas PKS12 only has one ketosynthase, one acyltransferase and one acyl carrier protein domain (Fig. 2). The domain organization of PKS11 and PKS12 showed that both are fungal non-reducing PKSs.
Each arrow indicates the direction of transcription and relative sizes of the ORFs. Putative function is indicated for each gene. ACP, acyl carrier protein; AT, acyltransferase; KS, ketosynthase; MT, methyltransferase; R, thioester reductase.
UV-Vis spectroscopic analysis
By UV-Vis spectroscopic analysis, an absorption maximum at 360 nm was recognized in the filtrate of wild type P. marneffei. This absorption maximum was not observed in the culture filtrates of the pks11 knockdown, pks12 knockdown or pks11pks12 double knockdown mutants.
UHPLC-DAD-MS analysis
The filtrates from wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei were monitored by UV-Vis spectroscopy from 200 to 640 nm and positive ion electrospray MS. To detect the presence of yellow pigment in wild type P. marneffei but not in the pks11 knockdown, pks12 knockdown or pks11pks12 double knockdown mutants, the UHPLC profiles were monitored by DAD using UV-visible absorption at 360 nm. Peaks at 10.2 min and 11.7 min were present in wild type P. marneffei but not the pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants (Fig. 3A and Fig. 4A). The two peaks were subjected to UV absorption, MS and MS/MS analyses. For the peak at 10.2 min, UV absorption analysis showed that the isolated molecule has three absorbance maxima at 213 nm, 269 nm and 352 nm respectively (Fig. 3B). MS analysis showed that this molecule has m/z of 413.0876 [M+H]+, which matched for C21H16O9 (Fig. 3C). This chemical formula was compatible with mitorubrinic acid (Fig. 3E). The fragmentation pattern of the MS/MS analysis showed a peak at m/z 151.03895, which corresponded to C8H6O3 and another at m/z 263.05481, which corresponded to C13H10O6, further confirming the isolated molecule is mitorubrinic acid (Fig. 3D and 3E). For the peak at 11.7 min, UV absorption analysis showed that the isolated molecule has three absorbance maxima at 212 nm, 268 nm and 352 nm respectively (Fig. 4B). MS analysis showed that this molecule has m/z of 399.10834 [M+H]+ matched for C21H18O8 (Fig. 4C). This chemical formula was compatible with mitorubrinol (Fig. 4E). The fragmentation pattern of the MS/MS analysis showed a peak at m/z 151.0386, which corresponded to C8H6O3 and another at m/z 249.0755, which corresponded to C13H12O5, further confirming the isolated molecule is mitorubrinol (Fig. 4D and 4E).
(A) HPLC profiles monitored by photodiode array detector and illustrated at 360 nm, (B) UV absorption spectrum, (C) extracted ion chromatograms (m/z 413.0876), (D) MS/MS fragmentation pattern and (E) MS/MS fragmentation pathway showing the presence of mitorubrinic acid detected and identified in wild type of P. marneffei but not in pks11 or pks12 knockdown mutants.
(A) HPLC profiles monitored by photodiode array detector and illustrated at 360 nm, (B) UV absorption spectrum, (C) extracted ion chromatograms (m/z 399.10834), (D) MS/MS fragmentation pattern and (E) MS/MS fragmentation pathway showing the presence of mitorubrinol detected and identified in wild type of P. marneffei but not in pks11 or pks12 knockdown mutants.
Animal experiments
The survival of mice after intravenous challenge with wild type P. marneffei or the pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants on day 60 was summarized in Fig. 5. The survival of mice challenged with the pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants were significantly better than those challenged with wild type P. marneffei (P<0.05).
Groups of 10 BALB/c mice were challenged intravenously with 8×106 spores. Survival was recorded daily for 60 days.
Intracellular survival assays in J774 and THP1 macrophages
The survival of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei in J774 and THP1 macrophages is shown in Fig. 6. There was statistically significant decrease in survival of pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants compared to wild type P. marneffei in both J774 and THP1 macrophages (P<0.05).
Panels A and B represent the recovery rates of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei in J774 and THP1 macrophages respectively. Error bars represent as mean ± SEM. Statistical significance between groups is indicated. *: wild type versus pks11 knockdown mutant (p<0.05); **: wild type versus pks12 knockdown mutant (p<0.05), ***: wild type versus pks11pks12 double knockdown mutant (p<0.05).
Intracellular survival assays in human neutrophils
No difference was observed between the survivals of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei in human neutrophils.
Susceptibility to hydrogen peroxide killing
The relative survival of P. marneffei conidia capable of forming visible colonies was calculated and plotted as a function of time of incubation in 25 mM hydrogen peroxide. No difference was observed between the survivals of wild type, pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants of P. marneffei.
Discussion
We report the first discovery of PKS genes responsible for mitorubrinol and mitorubrinic acid biosynthesis. Mitorubrinol and mitorubrinic acid are mitorubrin derivatives, a unique subclass of azaphilones isolated from a variety of fungal species, including Penicillium species such as P. rubrum and P. funiculosum and Talaromyces (teleomorph of Penicilllium) species such as T. emodensis, T. hachijoensis, T. wortmannii var. sublevisporus, T. austrocalifornicus and T. convolutus [22], [23], [24]. Although it has been known that mitorubrinol and mitorubrinic acid are polyketides for decades, no PKS genes have been identified for their synthesis [22]. In this study, we systematically knocked down the 23 PKS and 2 PKS-NRPS genes in the P. marneffei genome and observed for loss of yellow pigment in its mold form. Two PKS genes in the same PKS gene cluster were confirmed to be responsible for biosynthesis of yellow pigment in P. marneffei. UV absorption, MS and MS/MS analyses all unambiguously confirmed that this yellow pigment consisted of mitorubrinol and mitorubrinic acid.
pks12 and pks11 are probably responsible for sequential use in the biosynthesis of mitorubrinol and mitorubrinic acid. It is well known that some polyketides, such as lovastatin and zearalenone, were synthesized by two PKSs. The first PKS serves to synthesize a starter unit for the second PKS, which possesses a starter unit ACP transacylase (SAT) domain for utilizing the advanced starter unit [25]. For zearalenone, the starter unit is a highly reduced hexaketide which encoded by a highly reducing PKS gene (PKS13) [26]. The starter unit is utilized by a second PKS gene (PKS4) which possesses SAT domain for further extension. As for mitorubrinic acid and mitorubrinol, we speculate that the first part of the biosynthesis was by PKS12, which synthesized orsellinic acid. This tetraketide is then used as a starter unit for PKS11, which possessed a putative SAT domain, in the second part of the biosynthesis. PKS11, which possessed a methyltransferase domain, also served to methylate the products, using a methyl group from S-adenosylmethionine. Interestingly, PKS12 also possessed putative SAT domain, in line with the fact that most non-reducing PKS also possess potential SAT domains irrespective of whether they require an acetate starter unit or not. Feeding experiments using isotopically or 19F labeled precursors will confirm the use of advanced starter unit for the biosynthesis of mitorubrinic acid and mitorubrinol. Notably, polyketides that are synthesized by two PKS genes commonly require a highly reducing PKS at the early stage of biosynthesis and a non-reducing PKS at the later stage, resulting in a final product consisted of a highly reducing chain and non-reducing rings. Examples include the biosynthesis of zearalenone in Gibberella zeae and asperfuranone in Aspergillus nidulans [26], [27]. However, it is rare to see a polyketide, similar to mitorubrinol and mitorubrinic acid, that is synthesized by two non-reducing PKS in a sequential manner resulting in a non-reduced polyketide product.
Mitorubrinol and mitorubrinic acid are virulence factors of P. marneffei by improving its intracellular survival in macrophages. Although P. marneffei is infecting about 8% of AIDS patients in China and Southeast Asia, the pathogenetic mechanisms of this fungus remained under studied. So far, several molecules, including superoxide dismutase and melanin, have been implicated to be associated with virulence in P. marneffei [15], [28]. Superoxide dismutase converts superoxide radicals into hydrogen peroxide and oxygen, whereas melanin contributed to virulence through decreased susceptibility to killing by hydrogen peroxide [15], [28]. In this study, these two PKS genes in the yellow pigment biosynthesis gene cluster responsible for mitorubrinol and mitorubrinic acid production were shown to be associated with virulence in a mouse model. However, unlike melanin, the mechanism of virulence is not related to increasing resistance to hydrogen peroxide killing and the decrease in virulence in the pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants were also not due to decrease in survival within neutrophils, reduced resistance to antifungal peptides, decrease in growth rates or change in electron microscopic appearances of the mutants (data not shown). On the other hand, the survival of wild type P. marneffei was significantly better than pks11 knockdown, pks12 knockdown and pks11pks12 double knockdown mutants in both murine and human macrophages. Notably, it has been shown that injection of mitorubrin to mice did not result in death of the mice, although livestock fed with feedstuff contaminated with P. rubrum could be poisoned, indicating that mitorubrin itself is not a toxic metabolite [22]. This is in line with the results of the present study, which suggested that the mechanism of virulence was mediated through enhancement of intracellular survival in macrophages. It is also noteworthy that the pks11pks12 double knockdown mutant did not survive better than the pks11 or pks12 knockdown mutants. This is because knocking down either pks11 or pks12 is sufficient to abolish the pathway for mitorubrinol and mitorubrinic acid synthesis.
Author Contributions
Conceived and designed the experiments: PCYW CWL SKPL KYY. Performed the experiments: EWTT CKFL. Analyzed the data: PCYW CWL EWTT CKFL SKPL. Contributed reagents/materials/analysis tools: PCYW CWL SSYW SKPL KYY. Wrote the paper: PCYW CWL EWTT.
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