Impact Factor 4.259
2018 JCR, Web of Science Group 2019

Frontiers journals are at the top of citation and impact metrics

Original Research ARTICLE

Front. Microbiol., 28 June 2019 |

Phytophthora infestans Dihydroorotate Dehydrogenase Is a Potential Target for Chemical Control – A Comparison With the Enzyme From Solanum tuberosum

  • 1Departamento de Ciencias Biológicas, Universidad de los Andes, Bogotá, Colombia
  • 2Laboratorio de Micología y Fitopatología, Universidad de los Andes, Bogotá, Colombia
  • 3Faculty of Medicine, Department of Biology, University of Marburg, Marburg, Germany
  • 4Department of Microbiology and Plant Pathology, University of California, Riverside, Riverside, CA, United States

The oomycete Phytophthora infestans is the causal agent of tomato and potato late blight, a disease that causes tremendous economic losses in the production of solanaceous crops. The similarities between oomycetes and the apicomplexa led us to hypothesize that dihydroorotate dehydrogenase (DHODH), the enzyme catalyzing the fourth step in pyrimidine biosynthetic pathway, and a validated drug target in treatment of malaria, could be a potential target for controlling P. infestans growth. In eukaryotes, class 2 DHODHs are mitochondrially associated ubiquinone-linked enzymes that catalyze the fourth, and only redox step of de novo pyrimidine biosynthesis. We characterized the enzymes from both the pathogen and a host, Solanum tuberosum. Plant DHODHs are known to be class 2 enzymes. Sequence analysis suggested that the pathogen enzyme (PiDHODHs) also belongs to this class. We confirmed the mitochondrial localization of GFP-PiDHODH showing colocalization with mCherry-labeled ATPase in a transgenic pathogen. N-terminally truncated versions of the two DHODHs were overproduced in E. coli, purified, and kinetically characterized. StDHODH exhibited a apparent specific activity of 41 ± 1 μmol min-1 mg-1, a kcatapp of 30 ± 1 s-1, and a Kmapp of 20 ± 1 μM for L-dihydroorotate, and a Kmapp= 30 ± 3 μM for decylubiquinone (Qd). PiDHODH exhibited an apparent specific activity of 104 ± 1 μmol min-1 mg-1, a kcatapp of 75 ± 1 s-1, and a Kmapp of 57 ± 3 μM for L-dihydroorotate, and a Kmapp of 15 ± 1 μM for Qd. The two enzymes exhibited different activities with different quinones and napthoquinone derivatives, and different sensitivities to compounds known to cause inhibition of DHODHs from other organisms. The IC50 for A77 1726, a nanomolar inhibitor of human DHODH, was 2.9 ± 0.6 mM for StDHODH, and 79 ± 1 μM for PiDHODH. In vivo, 0.5 mM A77 1726 decreased mycelial growth by approximately 50%, after 92 h. Collectively, our findings suggest that the PiDHODH could be a target for selective inhibitors and we provide a biochemical background for the development of compounds that could be helpful for the control of the pathogen, opening the way to protein crystallization.


Within the Phylum Oomycota, the species of the genus Phytophthora are all considered devastating pathogens of crops and landscape plants, and are responsible annually for huge economic losses worldwide (Lamour et al., 2007; Attard et al., 2008). Phytophthora infestans causes late blight disease in potato, tomato, and other solanaceous crops. In these hosts, the entire plant is destroyed within a few days after the first lesions are observed (Fry, 2008).

Despite their economic importance, Phytophthora species remain poorly characterized at the biochemical level. The enzyme dihydroorotate dehydrogenase (DHODH, E.C., catalyzing the fourth step in de novo pyrimidine biosynthesis has been attractive for drug development for decades, with over 100 compounds that inhibit its activity in diverse organisms (Munier-Lehmann et al., 2013). In most eukaryotes, including plants (Witz et al., 2012) and some plant pathogenic fungi (Zameitat et al., 2007), class 2 DHODHs are associated with the outer surface of the inner mitochondrial membrane (Rawls et al., 2000) and transfer electrons from dihydroorotate oxidation to ubiquinone in the respiratory chain. Class 2 DHODHs are also found in gram-negative bacteria (Björnberg et al., 1999), anchored to the inner side of the periplasmic side of the inner cytoplasmic membrane, similarly transferring electrons to the respiratory chain.

Human DHODH, has been intensively studied, and is the target of A77 1726, also known as teriflunomide, the active metabolite of leflunomide, used in the treatment of rheumatoid arthritis (Fragoso and Brooks, 2015), and multiple sclerosis (Faissner and Gold, 2018). Recent work suggests that inhibitors of this enzyme show promise in the treatment of different cancers (Sykes et al., 2016). Structural differences between the human enzyme and pathogen enzymes have been exploited to develop species-specific inhibitors. For example, DSM265, a triazolopyrimidine-based compound targeting DHODH from the apicomplexan parasite Plasmodium falciparum, is currently undergoing phase 2 clinical trials (Ashley, 2017; McCarthy et al., 2017). Similarly, the antifungal properties of F901318, an inhibitor of DHODHs from pathogenic Aspergillus sp., is being tested in phase 1 trials (Oliver et al., 2016). Oomycete DHODH has been evaluated as an enzymatic target in biochemical screenings, leading to the identification of compounds that display in vitro inhibition of Pythium aphanidermatum DHODH, and in vivo whole plant control of Plasmopara viticola (Parker et al., 2002). Interestingly, gene deletion simulations in P. infestans by Rodenburg et al. (2018) identified the DHODH as one of 72 genes essential for growth, thus warranting further study.

Collectively, these observations suggest that selective inhibitors could be developed for P. infestans DHODH that would exert little or no effect on the host, or the human consumer. In the present study we produced recombinant pathogen (PiDHODH) and Solanum tuberosum (StDHODH) enzymes, measured their catalytic properties, and demonstrated differences in their activities with electron acceptors and in their sensitivities to inhibitors. We showed that PiDHODH has a micromolar IC50 for A77 1726, that is ≈37-fold lower than that of the host enzyme, and demonstrated that this compound inhibits growth of Phytophthora in vivo. Our work highlights the potential of PiDHODH as a possible target for developing novel combination strategies for pathogen control.

Materials and Methods


Reagents were purchased from Sigma–Aldrich unless otherwise specified, as follows. teriflunomide (A77 1726) Sanofi Aventis, Germany; ametoctradin (Initium) BASF, Germany; atovaquone (GlaxoSmithKline, United Kingdom); dichloroallyl lawsone (DCL/NSC-73735) NIH, United States; 2-hidroxy-1,4-naphthoquinone (lawsone) Aldrich, Germany; toltrazuril, Bayer AG, Germany. Several compounds were obtained from the Chemotherapuetic Agents Repository of the National Cancer Institute (compounds preceded by NSC). N-(3,5-difluoro-4-(trifluoromethyl)phenyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (DSM-190) was the gift of Dr. M. A. Phillips, The University of Texas at Austin, United States (Baldwin et al., 2005). N-(3-chlorobiphenyl-4-yl)-2-cyano-3-hydroxybut-2-enamide (MD-241, compound 28) (Davies et al., 2009); N-(3-chloro-2-methoxybiphenyl-4-yl)-2-cyano-3-hydroxybut-2-enamide (MD-209, compound 19) (Davies et al., 2009); 2-(4-biphenylylcarbamoyl)-1-cyclopentene-1-carboxylic acid (MD-108, compound 1) (Leban et al., 2005); 2-(4-biphenylylcarbamoyl)-2-benzoic acid (MD-129, compound 2) (Heikkilä et al., 2006); were the gift of Drs. Johnson and Fishwick, University of Leeds, United Kingdom. Restriction enzymes and other cloning enzymes were from New England Biolabs, United States. Curzate® M8 was obtained from Dupont.

Sequence Analysis

Sequences coding for the enzymes were retrieved from the genomes of P. infestans (strain T30-4), BioProject accession number PRJNA17665, and S. tuberosum, EnsemblPlants1. Additional sequences were retrieved from National Center for Biotechnology Information (NCBI). Multiple sequence alignments were performed according to sequence and 3D-structure using the STRAP program (default parameters)2. In Figure 1, the amino acid sequences of the secondary structure elements in three proteins with crystallographic structures are identified as specified in the relevant publications as follows: E. coli DHODH (Nørager et al., 2002), P. falciparum DHODH (Deng et al., 2009), human DHODH (Liu et al., 2000). Different designations for the alpha helices and beta sheets are used in these three publications; in Figure 1 we use the designations of Liu and coworkers. Mitochondrial targeting and signal peptide sequences were predicted with Mitoprot II 1.101 (default parameters) (Claros and Vincens, 1996), and TargetP 1.1 (plant network) (Nielsen et al., 1997; Emanuelsson et al., 2000), and MitoFates (plant) (Fukasawa et al., 2015). The N-terminal transmembrane domains were predicted by HMMTOP (default parameters) (Tusnady and Simon, 2001).


Figure 1. Alignment of the predicted amino acid sequences of Phytophthora infestans and Solanum tuberosum DHODHs with other class 2 DHODHs. Selected class 2 DHODHs were aligned according to sequences and 3D-structures of human, 1D3H (Liu et al., 2000), P. falciparum, 1TV5 (Hurt et al., 2006), and E. coli, 1F76 (Nørager et al., 2002) DHODHs. Secondary structures are named (blue) according to Liu and co-workers, where alpha helices are highlighted in dark gray, and beta sheets in light gray (Liu et al., 2000). The transmembrane domain is underlined in purple, and a sequence found only in plants is underlined in green. In the human DHODH sequence, residues interacting with FMN are shown in red, and residues interacting with orotate are underlined in red (Liu et al., 2000). Conserved residues are indicated with asterisks, conservative substitutions with colons, and semiconservative substitutions with periods, above the sequences. Residues in bold are conserved in more than 55% of the sequences. Four residues (P120T, I273V, I299V, and P359Q), shown in green, indicate positions where the published StDHODH sequence (PGSC0003DMG401016396) differs from the sequence of ΔN69StDHODH (P120T, I273V, I299V, and P359Q). Ecol, E. coli, 1F76 – WP_001295934; Hsap, Homo sapiens, 1D3G – NP_001352; Pfal, P. falciparum, 1TV5 – XP_966023; Pinf, P. infestans, PITG_01913; Stub, S. tuberosum, PGSC0003DMG401016396; Zmay, Zea mays, NP_001152058; Atha, A. thaliana, AAN64025.

Expression Constructs

Solanum tuberosum cDNA was prepared from commercially available potato plants (Sabanera variety). Total RNA was extracted from frozen mycelia or from 300 mg of plant leaves and cDNA was synthesized (Garcia-Bayona et al., 2014). Subsequently, a fraction of the cDNA reactions (2 μL) was used for PCR amplification. cDNA prepared from P. infestans strain 1043, a Colombian isolate from potato with A1 mating type, and also belonging to the EC-1 clonal lineage, was used for the cloning (Vargas et al., 2009). The isolates were cultured routinely on rye agar medium and incubated at 19°C for 9 days in the dark (Goodwin et al., 1998). Mycelia were collected from two plates and frozen until use.

Primers for PCR amplification were designed based on the sequences Gene ID PGSC0003DMG401016396 (StDHODH) and PITG_01913 (PiDHODH) (Supplementary Table 1). PCR products were adenylated and ligated in the pGMT-Easy vector (Promega, United States), prior to transforming in E. coli DH5-α electro-competent cells (Agilent, United States). The cloned inserts were confirmed by sequencing (Macrogen, South Korea). Recombinant plasmids containing the coding sequences, were digested with NdeI-XhoI (StDHODH) or BamHI (PiDHODH), separated by 1% agarose gel electrophoresis, purified (BIO-101, United States) and ligated into the pET-15b (StDHODH) or pET-19b (PiDHODH) expression vectors (Novagen, United States) that had been similarly treated. Linearized pET19b was treated with calf intestine alkaline phosphatase (Invitrogen, United States) prior to ligation. Constructs were transformed into E. coli BL21CodonPlus(DE3) electro-competent cells with a Micropulser Electroporator (BioRad, United States). The N-terminally truncated version of StDHODH (ΔN69StDHODH) started at residue 70 (ASTV), and the N-terminally truncated version of PiDHODH (ΔN54PiDHODH) sequence started at residue 55 (PHEW). The recombinant proteins expressed from the pET19b vector had a 26 residue N-terminal tag including 10-His, and recombinant proteins expressed from pET15b had a 19 residue N-terminal tag including 6-His. The published StDHODH sequence (PGSC0003DMG401016396) differed from the ΔN69StDHODH sequence in four positions (P120T, I273V, I299V, and P359Q).

Expression and Purification

Transformed E. coli BL21-CodonPlus(DE3)-RP electrocompetent cells were precultured overnight in Luria-Bretani broth medium (LB) with 100 μg/mL ampicillin as the selection marker at 37°C with 200 rpm agitation. The preculture was diluted to 5% in LB containing 100 μg/mL ampicillin and grown at 37°C until OD600nm = 0.5–0.6. Induction was performed with 1 mM isopropyl β-D-thiogalactopyranoside (IPTG), supplemented with 0.1 mM flavin mononucleotide (FMN) and growth was continued overnight at room temperature (Baldwin et al., 2002). Induced cultures were harvested by centrifugation at 3,500 × g for 15 min at 4°C, supernatant discarded and cell pastes were frozen at -80°C until use.

For the purification of the recombinant proteins, a pellet from 500 mL of bacterial cell culture was resuspended in Buffer A [50 mM Tris-HCl pH 8, 300 mM NaCl and 10% glycerol, 5 mM imidazole, 1 mM phenylmethanesulfonyl fluoride (PMSF) and 1 mM benzamidine] containing 2% Triton X-100. The cell suspension was incubated with lysozyme (1 mg/mL) on ice for 2 h. Cells were disrupted by sonication on ice (30 cycles of 20 s each, output control setting of 8 and 100% duty cycle) using a 250 Analog Sonifier (Branson). After sonication, insoluble and soluble fractions were separated by centrifugation (8,500 × g, 1 h, 4°C). The recombinant proteins were purified from the clarified cell lysates using Co2+ affinity columns (Thermo Scientific) equilibrated with Buffer A containing 0.5% Triton X-100 following the manufacturer’s recommendations, and eluted with buffer A containing 250 mM imidazole. The yields of purified protein were 2.0 mg/L of cell culture for StDHODH, and 1.3 mg/L of cell culture for PiDHODH. The expected sizes for the truncated recombinant proteins were: PiDHODH 43.1 kDa and StDHODH 43.7 kDa.

For enzymatic activity assays, fractions were subjected to buffer exchange performed with PD-10 columns (Sephadex G-25-M, GE Healthcare) with buffer (50 mM Tris-HCl pH 8, 150 mM NaCl, 0.1% Triton X-100 and 10% glycerol) (Ullrich et al., 2001).

SDS-PAGE and Electrotransfer

Protein samples were fractionated by SDS-PAGE on 12% running gels, with 5% stacking gels. Electrophoresis was performed in a BioRad Mini-Protean II electrophoresis cell for 1 h, at 200 volts, constant voltage. Gels were visualized by staining with Coomassie Blue G-250 dye.

Enzymatic Assays and Kinetic Analysis

In our standard activity assay we monitored the reduction of 2,6-dichlorophenol-indophenol (DCIP) at 600 nm (ε = 18,800 M-1 cm-1) at 30°C in a reaction buffer containing 50 mM Tris-HCl pH 8.0, 150 mM KCl, 0.1% Triton X-100, 10% glycerol, 1 mM L-dihydroorotate, 0.1 mM DCIP, 0.1 mM decylubiquinone (Qd) (Zameitat et al., 2007), with concentrations of 19 nM (StDHODH) or 6.6 nM (PiDHODH). The apparent kinetic constants of the substrates were determined by varying L-dihydroorotate concentration (2.5–1,250 μM) while keeping Qd constant at 100 μM, or by varying Qd (1.25–200 μM) at a fixed dihydroorotate concentration of 1 mM. The kinetic data were evaluated by fitting the data to the Michaelis–Menten equation v = Vmax[S]/ (Km + [S]) using GraphPad Prism v7 software. The apparent kcat was calculated from kcat = Vmax/[ET], where [ET] is total enzyme concentration, based on one active site monomer. Background oxidase activities due to direct reduction of DCIP by the enzyme in the absence of Qd were subtracted from the activities measured in the presence of Qd. For StDHODH the background oxidase activity was 9 ± 2 μmol min-1 mg-1, and for PiDHODH it was 6 ± 1 μmol min-1 mg-1.

To test alternative electron acceptors, stock solutions of 10–50 mM quinones, napthoquinones, and benzoquinones were prepared in absolute ethanol. Enzyme activities were measured with the standard assay described above, using 0.1 mM of the acceptor in place of Qd.

Stock solutions of all inhibitors were prepared in reaction buffer, or in dimethyl sulfoxide (DMSO). Activities were measured with the standard DCIP assay with saturating concentrations of Qd (0.1 mM) and dihydroorotate (1 mM), in the presence of 0.5 mM inhibitor. The final concentrations of 5% DMSO used in the assay solutions were found not to affect the DHODH activity of either recombinant enzyme. DHODH activities were measured by the standard assay.

Protein concentration was measured using the bicinchoninic assay (Pierce) with bovine serum albumin as the standard.

Absorbance was measured in microplates with a Thermo Scientific Multiskan GO UV/visible spectrophotometer.

P. infestans Localization Constructs, Transformation, Selection, and Imaging

To determine the subcellular localization of PiDHODH, we made a construct fused on the 3′-ends to eGFP. The desired sequences were amplified by PCR using primer pairs (Supplementary Table 1) which introduced a PacI site at the 5′ end and an NheI site at the 3′ end. The fragment was ligated to the pGEM-T Easy vector (Promega) and transformed in E. coli DH5-α chemiocompetent cells. The pGEM-T Easy plasmid was subjected to double restriction PacI-NheI, the fragment was subcloned in pGFPH (Ah-Fong and Judelson, 2011), and confirmed by sequencing. The resulting fusion construct was expressed under the control of the promoter and terminator from the Ham34 gene of Bremia lactucae. A control plasmid, pATPase-mCherryN, was used to visualize mitochondria (Ah-Fong and Judelson, 2011). Plasmid DNA for transformation was obtained using the Plasmid DNA Purification Kit NucleoBond PC 500 (Macherey-Nagel, Germany). Stable transformants were generated with isolate 1306 (A1 mating type, United States isolated from tomato) (Judelson et al., 1995), using the modifications proposed by Ah-Fong and Judelson (2011) to the original protoplast method (Judelson et al., 1991). For co-transformation, a total of 40 μg of plasmid DNA were used per experiment; 20 μg of the localization plasmid (PiDHODH-eGFP) and 20 μg of the control plasmid which expresses the b-subunit of the mitochondrial ATPase N-terminally fused to mCherry (pATPase-mCherryN). Transformed strains were grown with 30 μg mL-1 hygromycin and 10 μg mL-1 G418.

GFP- and mCherry-expressing strains were preselected by a visual inspection of the transformants by confocal laser scanning microscope using a Leica TCO-SP2. Transformants were grown in Petri dishes of rye-sucrose media for 6–8 days, mycelia from the external edge of the growth radius were mounted on drops of 10 μL of water in glass slides and sealed with transparent nail polish. GFP expression was visualized using 40X/0.8 or 63X/0.9 objectives with excitation/emission settings 488 nm/500–550 nm for GFP 543 nm/575–700 nm for mCherry. Fluorescent sporangia were obtained after 7–10 days.


The isolate Z3-2 of P. infestans, with EC-1 clonal lineage, and A1 mating type, was grown for 8 to 10 days at 18°C on rye-sucrose agar plates plus 50 μg/mL ampicillin. Plates containing sporulated mycelia were flooded with ultra pure water and rubbed with a glass rod to liberate the sporangia. The sporangia were purified from the suspension by filtration through a 50 μm nylon mesh, and counted with a hemocytometer. Then 4 × 106 sporangia/mL were incubated for 2–4 h at 10°C to induce the liberation of free-swimming zoospores. The suspension containing zoospores and sporangia (125 μL) was dispensed into five replicate wells of a 96-well flat bottom tissue culture treated plates, and combined with 75 μL of Henniger media (Henniger, 2007) and 25 μL of each compound tested. A77 1726 was resuspended in DHODH reaction buffer, and curzate was resuspended in water. Microtiter plates were covered and placed in the dark at 18°C. Growth was evaluated by measuring the OD610nm at 20–24 h intervals for 100 h with a MultiskanTM GO Microplate Spectrophotometer (Thermo Scientific). Data analysis and graphs were performed using GraphPad Prism Software v7 for Mac3.


StDHODH and PiDHODH Predicted Amino Acid Sequences Are Most Similar to Class 2 Enzymes

The gene encoding the StDHODH was identified as a single copy protein (Gene ID PGSC0003DMG401016396) in the S. tuberosum genome assembly, EnsemblPlants1. It had an open reading frame (1275 bp) comprised of 11 exons, which encoded a 48.9 kDa protein (460 residues) with an isoelectric point of 9.35 consistent with the high pI predicted for other class 2 DHODHs. The derived amino acid sequence contained typical features of the class 2 DHODHs, including an N-terminal extension, a transmembrane domain, a conserved serine (S277) that aligned with the catalytic serines of E. coli (S175), human (S215), and P. falciparum (S345) DHODHs, and conserved residues for binding the electron acceptor, FMN, and orotate (Figure 1). The identity with other plant DHODHs was high (Zea mays 73%, A. thaliana 77%), and revealed that the enzyme was more similar to the class 2 DHODHs (Homo sapiens 49%, P. falciparum 30%, P. infestans 48%, E. coli 41%) (Supplementary Table 2) than to class 1 DHODHs (T. cruzi 21%, S. cerevisiae 21%). The N-terminal extension found in plant DHODHs was longer than the extensions found in the human or the oomycete enzymes, but shorter than that found in apicomplexan enzymes. A cleavage site at residue 28 was predicted by both TargetP 1.1 (Nielsen et al., 1997; Emanuelsson et al., 2000) and MitoFates (Fukasawa et al., 2015). The StDHODH displayed a small insertion of 13 residues between positions 225 and 236 that was also present in other plant DHODHs, but not in other eukaryotic class 2 enzymes. Four positions in our cloned sequence of StDHODH (P120T, I273V, I299V, and P359Q) differed from the published sequence shown in Figure 1. Probably these differences are not significant, since all of these residues are found in other sequences shown in the alignment, for example, threonine in position 120 is observed in PiDHODH, valine in position 273 is observed in HsDHODH, valine in position 299 appears in all the eukaryotic DHODHs in Figure 1, and glutamine in position 359 is found in HsDHODH. The last of these differences is in a poorly conserved region of the sequence. Furthermore, it is relevant that cultivated S. tuberosum is a highly heterogenous autotetraploid (Manrique-Carpintero et al., 2018), and thus possesses four alleles of DHODH, which may exhibit sequence differences.

The gene encoding PiDHODH was identified as a single copy, without introns, in supercontig 2 (locus: PITG_01913) in the P. infestans genome. The open reading frame of 1275 bp encoded a 45.3 kDa protein (424 residues) with an isoelectric point of 8.74. The predicted amino acid sequence contained the class 2 DHODH N-terminal extension, transmembrane domain, conserved serine (S242), and conserved FMN and orotate binding residues. The percent identity shared with other DHODHs showed that the P. infestans enzyme was more similar to the class 2 enzymes (H. sapiens 53%, A. thaliana 46%, S. tuberosum 48%, E. coli 38%, P. falciparum 31%), than to class 1 enzymes (T. cruzi 22%, S. cerevisiae 19%) (Supplementary Table 2). As expected, alignments revealed that the DHODH from P. infestans shared the highest identity percentages with the other four Phytophthora species (P. parasitica 93%, P. capsici 90%, P. ramorum 87%, P. sojae 87%) and lower identity percentages compared to other oomycetes (Plasmopara halstedii 84%, Pythium ultimum 70%, Saprolegnia parasitica 60%, Aphanomyces invadans 57%) (Supplementary Figure 1).

PiDHODH Is Targeted to Mitochondria

The PiDHODH contains a predicted cationic mitochondrial targeting sequence (residues 1–23) at the N-terminus, followed by a predicted hydrophobic transmembrane helix sequence (residues 30–49). A proteolytic cleavage site was predicted at position 23 by MitoprotII v1.101. To confirm the mitochondrial localization we constructed an eGFP PiDHODH fusion, and co-transformed P. infestans with an mCherry tagged ATP synthase construct. PiDHOD was found to colocalize with the ATP synthase in sporangia (Figure 2).


Figure 2. The subcellular localization of P. infestans DHODH in sporangia. (A) The construct used to produce DHODH fused on the C-terminus to green fluorescent protein (GFP). (B) A sporangium doubly transformed with GFP-labeled PiDHODH (green), and with the mitochondrial marker, ATP synthase fused to mCherry (red) (Ah-Fong and Judelson, 2011) is shown. DIC, differential interference contrast. Scale bar: 10 μm.

ΔN69StDHODH and ΔN54PiDHODH Recombinant Proteins Are Produced in Soluble Form in E. coli

Class 2 DHODHs from several organisms have been produced as recombinant proteins, and in most cases these expression constructs eliminate the N-terminal sequence, which contains the hydrophobic transmembrane anchor. The elimination of these N-terminal extensions appear to exert relatively small effects on enzyme activity (Baldwin et al., 2002; Zameitat et al., 2006).

We expressed both full-length (data not shown) and N-terminally truncated recombinant proteins of StDHODH, with N-terminal polyhistidine-tags to facilitate purification. While the full-length StDHODH was found in the insoluble fraction, the truncated version, ΔN69StDHODH, was expressed in soluble form, and was purified (Supplementary Figure 2). Interestingly, both full-length and truncated versions of A. thaliana DHODH were soluble and active, although the polyhistidine-tags in these recombinant proteins were located at the C-termini (Ullrich et al., 2002). PiDHODH was expressed using a similar strategy, and only the truncated version ΔN54PiDHODH was soluble and could be purified (Supplementary Figure 2).

Apparent Kinetic Parameters of ΔN69StDHODH and ΔN54PiDHODH

Preliminary kinetic data were collected for the N-terminally truncated DHODHs (Figure 3), and the apparent kinetic parameters were compared to those of other DHODHs (Table 1) (Ullrich et al., 2001; Hortua Triana et al., 2012). ΔN69StDHODH exhibited an apparent specific activity of 41 ± 1 μmol min-1 mg-1, a kcatapp of 30 ± 1 s-1, a Kmapp of 20 ± 1 μM for L-dihydroorotate, and a Kmapp of 30 ± 3 μM for decylubiquinone (Qd). ΔN54PiDHODH exhibited an apparent specific activity of 104 ± 1 μmol min-1 mg-1, a kcatapp of 75 ± 1 s-1, a Kmapp of 57 ± 3 μM for L-dihydroorotate, and a Kmapp of 15 ± 1 μM for Qd.


Figure 3. Steady state kinetics of of purified truncated recombinant P. infestans and S. tuberosum DHODHs. ΔN54PiDHODH saturation curves for (A) L-dihydroorotate and (B) decylubiquinone are shown. ΔN69StDHODH saturation curves for (C) L-dihydroorotate and (D) decylubiquinone are shown. All curves were fit to the Michaelis–Menten equation, v = (Vmax ⋅ [S])/(Km + [S]).


Table 1. Apparent kinetic parameters of DHODHs from different organisms.

We evaluated the enzyme activities with a variety of natural and artificial electron acceptors. Activities are expressed as a percentage, taking the activity measured with Qd as 100%. ΔN69StDHODH, exhibited the highest activities for coenzyme Qs having isoprenyl side chain lengths ranging from Q1 to Q9. ΔN54PiDHODH showed a preference for a slightly shorter range of isoprenyl side chain lengths, from Q1 to Q6. The two enzymes exhibited different activities for six derivatives of napthoquinone (Table 2).


Table 2. Activities of StDHODH and PiDHODH with alternative electron acceptors.

StDHODH and PiDHODH Show Differential Sensitivities to Inhibitors

We studied the susceptibilities of the S. tuberosum and P. infestans recombinant enzymes to various compounds, which have been demonstrated to be inhibitors of DHODHs in other species (Knecht et al., 2000; Baldwin et al., 2002; Leban et al., 2005; Heikkilä et al., 2006; Davies et al., 2009; Munier-Lehmann et al., 2013). We also tested atovaquone (Munier-Lehmann et al., 2013) and amectoctradin (Dreinert et al., 2018), two inhibitors that bind to ubiquinone sites in cytochrome bc1. The first two compounds in Table 3 have similarity to the substrate (dihydroorotate), or to the product (orotate), and the remaining compounds are expected to bind in the electron acceptor (ubiquinone) site. Nine of the compounds decreased PiDHODH activity, and six decreased StDHODH activity to below 50% of the activity observed in absence of inhibitor (Table 3). Differential inhibition for StDHODH and PiDHODH was observed for compounds A77 1726, toltrazuril, MD108, MD241, and NSC61890. The greatest difference in inhibition was observed for A77 1726, where PiDHODH activity was decreased to 14%, while StDHODH activity was unaffected. This difference was confirmed by the IC50 values (Figure 4) measured for A77 1726, 2.9 ± 0.6 mM for StDHODH, and 79 ± 8 μM for PiDHODH.


Table 3. Activities of StDHODH and PiDHODH in the presence of potential inhibitors.


Figure 4. Dose-response inhibition curves of A77 1726 for truncated recombinant P. infestans and S. tuberosum DHODHs. Activities were measured with the standard DCIP assay with saturating concentrations of Qd (0.1 mM) and dihydroorotate (1 mM), in the presence of (A) 0–2,000 μM A77 1726 for ΔN54PiDHODH, and (B) 0–5.26 mM A77 1726 for ΔN69StDHODH.

A77 1726 Inhibits the Growth of P. infestans

We measured the growth of P. infestans sporangia and zoospores in liquid culture in the presence of PiDHODH inhibitor A77 1726 (Figure 5). For comparison, growth was measured in the presence of Curzate® M8, an oomyceticide containing 64% w/w mancozeb [manganese zinc ethylenebis(dithiocarbamate)] and 8% w/w cymoxanil, with the former targeted to enzymes dependent on active sulfhydryl groups (Gullino et al., 2010), and the latter implicated in amino acid synthesis (Tellier et al., 2008). Of the two treatments, Curzate® M8, is more effective, requiring only 1 to 2 μg/mL compared to 136 μg/mL (0.5 mM) required for A77 1726 to reduce the growth of the oomycete by approximately 50% at 92 h. Thus, although PiDHODH is approximately 40-fold more sensitive to A77 1726 compared to StDHODH, the compound is still a relatively poor inhibitor of the oomycete enzyme, and modifications would be needed to achieve a nanomolar IC50.


Figure 5. Effect of A77 1726 on the growth of P. infestans. Growth of zoospores and sporangia were evaluated by OD610 nm for 100 h in the presence of (A) 0, 27, 136, 277 μg/mL (0, 0.1, 0.5, and 1 mM) A77 1726, or (B) 0, 0.5, 1, and 2 μg/mL Curzate.


Oomycetes had been traditionally misclassified as fungi, since they have fungus-like growth morphology, most sharing filamentous growth habits, producing spores and occupying similar environments (Latijnhouwers et al., 2003). However, morphological features, biochemical analyses and molecular taxonomy studies indicate that oomycetes reside more closely to algae and diatoms in the Stramenopile group, and are a sister group to apicomplexa, ciliates, dinoflagellates, and amoeboids in the protists’ supergroup SAR (Adl et al., 2012). The close relation between oomycetes and apicomplexans (Haldar et al., 2006) led us to hypothesize that strategies that have demonstrated effectiveness for control of the human parasites T. gondii and P. falciparum could also be used to control the growth of P. infestans. Indeed, the reverse strategy, the use of oomyceticidal agrochemicals to control apicomplexan parasites, appears to be effective for strobilurins, such as azoxystrobin, trifloxystrobin, and dimoxystrobin, which inhibit P. falciparum with nanomolar IC50s (Witschel et al., 2012). De novo pyrimidine biosynthesis is known to be indispensable for Toxoplasma gondii (Fox and Bzik, 2002, 2010) and for more than a decade, the fourth enzyme in the pathway, DHODH, has been studied as a drug target to control malaria (Baldwin et al., 2002; Ashley, 2017). Thus, we decided to characterize these enzymes in the plant pathogen and its host.

As is the case for many organisms, P. infestans also possesses a salvage pathway for recycling nucleosides and nucleobases, that together with de novo biosynthesis, allow the pathogen to maintain the pyrimidine requirements needed for survival (Garcia-Bayona et al., 2014). Early biotrophic growth is fueled by the de novo pathway (Garcia-Bayona et al., 2014), and is also supported by the uptake of pyrimidines from the host environment, as demonstrated by apparent increases in expression of the pathogen’s nucleoside and nucleobase transporters during plant infection (Abrahamian et al., 2016). The fungal plant pathogen Magnaporthe oryzae exhibits a similar requirement for de novo synthesis for its early biotrophic growth in the case of purine nucleotides, which apparently are not sufficiently available from the plant host (Fernandez et al., 2013). In the solanaceous hosts of Phytophthora, such as potato, the de novo pathway is important in growing and developing tissues (Giermann et al., 2002). However, studies of knockdowns of pyrimidine biosynthetic enzymes in transgenic plants demonstrate that the salvage pathway can maintain the required pyrimidine pool for basic metabolism (Schroder et al., 2005) and both pathways are tuned in mutually compensatory fluxes (Zrenner et al., 2006). An additional catabolic pathway, not present in the pathogen, allows for fine-tuning of the plant pyrimidine levels (Zrenner et al., 2009).

Dihydroorotate dehydrogenase catalyze the oxidation of dihydroorotate to orotate, and are classified as follows. Class 1 enzymes are soluble, using either fumarate (class 1A) or NAD+ (class 1B) as their electron acceptors, and class 2 enzymes are membrane-associated, using ubiquinones in the electron transport chain (ETC) as electron acceptors (Reis et al., 2017). The DHODHs from both S. tuberosum and P. infestans are class 2 enzymes. The mitochondrial localization of plant DHODHs was demonstrated many years ago. In tomato, DHODH co-sediments with the mitochondrial proteins cytochrome oxidase, succinate dehydrogenase, and citrates synthase in sucrose gradients (Miersch et al., 1986). In pea, DHODH is associated with purified mitochondria, and has been shown to reduce cytochrome c in mitochondrial extracts when cytochrome oxidase is inhibited by cyanide. The N-terminus of a class 2 enzyme contains a mitochondrial targeting sequences followed by hydrophobic transmembrane domain that anchors the enzyme to the inner mitochondrial membrane (Chen and Jones, 1976; Zameitat et al., 2007) The structures available for enzymes from this class show that they are comprised of a large α/β-barrel domain containing the orotate/dihydroorotate and FMN binding sites, connected to a small domain containing two alpha helices, αA and αB, forming a hydrophobic tunnel where ubiquinone is thought to bind (Reis et al., 2017).

Differences were observed in the apparent kinetic parameters of the plant and pathogen DHODHs. The Kmapp for dihydroorotate was threefold higher for ΔN54PiDHODH compared to that of ΔN69StDHODH. In contrast, the Kmapp for the electron acceptor Qd was twofold higher for ΔN69StDHODH compared to that of ΔN54PiDHODH (Table 1). The kcatapp of the pathogen enzyme was approximately double that of the plant enzyme (Table 1). We tested the activities of the recombinant enzymes with ubiquinones having different isoprenoid tail lengths. While humans use Q10, a ubiquinone with 10 isoprenoid units, both Q9 and Q10 have been found in plants. Ubiquinone content for a few solanaceous plants are available. Tobacco contains Q10 at ≈8 mg/kg (Ohara et al., 2004). Q10 is also found in potato and tomato, but at approximately 10-fold lower concentrations, and levels of Q9 are below the detection limit (Mattila and Kumpulainen, 2001). Although the nature of the quinone in P. infestans is not known, the ubiquinone pool in Phytophthora cactorum appears to be comprised of 80% Q9, and 20% Q8 (Richards and Hemming, 1972), in agreement with a later study showing that Q9 is the major quinone in other oomycetes (Nakamura et al., 1995). Surprisingly, Q9 was not the best substrate for ΔN54PiDHODH, which exhibited approximately double the activity with ubiquinones having shorter isoprenoid tails. Similarly, ΔN69StDHODH appeared to be more active with ubiquinones having isoprenoid tails shorter than Q10 (Table 2). We also tested the activity of the recombinant enzymes with several 1,4-naphthoquinones (Table 2). These compounds, which affect diverse cellular targets because of their redox properties (Klotz et al., 2014), are alternate electron acceptors for DHODHs (Knecht et al., 2000). For ΔN69StDHODH the best acceptor was 5,8-dihydroxy-1,4-naphthoquinone, which exhibited an activity similar to Qd. In contrast, this naphthoquinone was a poor acceptor for ΔN54PiDHODH, showing sixfold less activity compared to Qd. Differences in activities for the two enzymes were also observed for lawsone, juglone, and plumbagin.

We tested compounds known to inhibit DHODHs from other organisms (Table 3). Alloxan and 5′-fluoroorotic acid, analogs of dihydroorotate and orotate, respectively, are weak inhibitors of other class 2 DHODHs (Zameitat et al., 2006; Munier-Lehmann et al., 2013), and were also poor inhibitors of ΔN69StDHODH and ΔN54PiDHODH. The remaining compounds in Table 3 have been shown to interact, or are predicted to interact, with the ubiquinone binding site, which is the target for the most effective inhibitors known to date of class 2 DHODHs (Munier-Lehmann et al., 2013). The variability in this site in class 2 DHODHs has permitted the development of species-specific inhibitors, as illustrated by DSM-265, a triazolopyrimidine inhibitor of P. falciparum DHODH (Ashley, 2017; McCarthy et al., 2017). We found that the related compound DSM190 (Gujjar et al., 2011), had similar and moderate effects on the activities of both recombinant plant and pathogen DHODHs, as did two nanomolar inhibitors of the human enzyme, redoxal (Knecht and Löffler, 2000) and dichloroallyl lawsone (Knecht et al., 2000). Brequinar, another nanomolar inhibitor of the human enzyme (Munier-Lehmann et al., 2013), caused moderate inhibition of ΔN69StDHODH, but did not decrease the activity of ΔN54PiDHODH. Greater inhibition of ΔN69StDHODH compared to ΔN54PiDHODH was also observed for toltrazuril, a weak inhibitor of Eimeria pyrimidine biosynthesis (Zameitat et al., 2006; Munier-Lehmann et al., 2013), NSC 61890, and NSC 71097. Several compounds caused greater inhibition of the Phytophthora enzyme than the plant enzyme. For example, the active metabolite of leflunomide, A77 1726, a nanomolar HsDHODH inhibitor used in the treatment rheumatoid arthritis, inhibited ΔN54PiDHODH, but was a poor inhibitor of ΔN69StDHODH. The differential effects of modifying a lead compound scaffold on the inhibition of an enzyme target is nicely illustrated by the MD compounds, a series of inhibitors that were designed in attempt to optimize the binding of A77 1726 to the active sites of PfDHODH or HsDHODH (Leban et al., 2005; Davies et al., 2009). While MD 129 did not affect either enzyme’s activity, MD 209 strongly inhibited both enzymes, and MD108 and MD241 preferentially inhibited the pathogen enzyme.

Since we had limited quantities of MD108 and MD241, we selected A77 1726 for further investigation. Measurement of IC50s revealed that the pathogen enzyme, with an IC50 of 79 μM, was 37-fold more sensitive than the plant enzyme. We found that a concentration of 0.5 mM A77 1726 reduced the growth of the oomycete by approximately 50%, at 92 h. Despite the number of DHODH inhibitor sets available (Munier-Lehmann et al., 2013), only two lipophilic inhibitors have been described and suggested as lead compounds for development of oomyceticides that target this enzyme (Parker et al., 2002). These compounds arrested Py. aphinadermatum radial growth in vitro and the addition of uridine was able to reverse this growth inhibition, suggesting that the compounds block pyrimidine metabolism. Nevertheless, these compounds were not stable enough under field conditions to be further developed as oomyceticides.

While the role played by the DHODH in de novo pyrimidine synthesis is well-defined, it is less clear what role it plays in the respiratory chain of P. infestans. In T. gondii, the mitochondrially-associated DHODH has an unknown, but essential, pyrimidine-independent function (Hortua Triana et al., 2016). In mammalian cells, physical associations between DHODH and complexes II and III have been demonstrated, and DHODH knockdown partially inhibits complex III, decreases membrane potential, and increases production of reactive oxygen species (Fang et al., 2013). Relatively little is known about the respiratory chains of plant pathogens. In P. infestans, inhibition of oxygen consumption is observed in the presence of cyanide and in the presence of antimycin A, when succinate is used as the electron donor (Scheepens and Fehrmann, 1977). Electron transport is reported to be insensitive to rotenone (Scheepens and Fehrmann, 1977). P. infestans possesses sequences with similarity to type II NADH dehydrogenases (Feng et al., 2012), plant alternate NADH dehydrogenases (Schertl and Braun, 2014), electron transfer flavoprotein ubiquinone oxidoreductase, and several so-called alternative oxidases (AOX) (Supplementary Table 3). Thus, P. infestans mitochondrial respiration appears to exhibit a complexity due to the increased number of branches, as is also observed in plants (Schertl and Braun, 2014). Oomycete respiratory chains are the target of several commercial oomyceticides, ametoctradin (Initium®), amisulbrom, and cyazofamid, bind to ubiquinone sites of respiratory complex III, and are effective against late blight disease (Mitani et al., 2001; Dreinert et al., 2018). Since complex III and DHODH both bind ubiquinone, we tested ametoctradin on the recombinant DHODs, and found it had a negligible effect on the plant enzyme, and showed a weak inhibition of the pathogen enzyme. Atovaquone, an antimicrobial ubiquinone analog that inhibits the complexes III of Plasmodium, T. gondii, and Pneumocystis carinii (Meshnick et al., 2001; Kessl et al., 2003; Mather et al., 2005) likewise showed little effect on either recombinant enzyme.

Taken together, our results highlight differences in binding of DHODH inhibitors by the plant and oomycete enzymes, and suggest that these differences could be further exploited to develop species-specific inhibitors that preferentially affect the pathogen enzyme. The inactivation of this enzyme by inhibitors would have a profound effect on pyrimidine biosynthesis, and might also have effects on the mitochondrial respiration of this pathogen. The availability of recombinant ΔN54PiDHODH should expedite the discovery of more potent agents for growth control strategies against P. infestans, and permit the screening of a large number of compounds, the examination of structure-activity relationships of inhibitors, and determination of the 3D structure of enzyme–inhibitor complexes.


To our knowledge this is first preliminary characterization of a purified recombinant oomycete DHODH and the first comparison with the corresponding plant DHODH. Whether the differences observed between the two enzymes could be further exploited to develop species-specific compounds for crop management is an intriguing question that remains to be answered. The availability and characterization of the recombinant DHODH from P. infestans in this work permitted the first preliminary screening of potential enzyme inhibitors, with the rationale of interfering with pyrimidine metabolism, and opens the way to protein crystallization, which is a prerequisite for the development of species-specific inhibitors.

Author Contributions

MG, HN-O, DP, ML, HJ, SR, and BZ conceived and designed the experiments. MG, HN-O, and DP conducted the experiments. MG, HN-O, DP, and BZ analyzed the data. ML, HJ, SR, and BZ contributed with reagents, materials, and analysis tools. MG, HN-O, and BZ contributed to the writing of the manuscript. All authors reviewed the results and approved the final version of the manuscript.


This work was supported by the Colciencias grant # 120-4521-28532 (to SR) and by a Colciencias doctoral fellowship from the Becas Doctorado Nacional (to MG). This work was also supported by funding from the Facultad de Ciencias and the Vicerrectoria de Investigaciones (Universidad de los Andes, Colombia).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The reviewer WB declared a shared affiliation, with no collaboration, with one of the authors, ML, to the handling Editor at the time of review.


We would like to thank Margaret A. Phillips (University of Texas Southwestern Medical Center); Colin W. G. Fishwick; and A. Peter Johnson (University of Leeds) for kindly providing inhibitors used in this study. We also thank Luis Eduardo Fuentes Suárez and Paola Catherine Ramírez Callejas for their excellent technical assistance.

Supplementary Material

The Supplementary Material for this article can be found online at:


  1. ^
  2. ^
  3. ^


Abrahamian, M., Ah-Fong, A. M. V., Davis, C., Andreeva, K., and Judelson, H. S. (2016). Gene expression and silencing studies in Phytophthora infestans reveal infection-specific nutrient transporters and a role for the nitrate reductase pathway in plant pathogenesis. PLoS Pathog. 12:e1006097. doi: 10.1371/journal.ppat.1006097

PubMed Abstract | CrossRef Full Text | Google Scholar

Adl, S. M., Simpson, A. G. B., Lane, C. E., Lukeš, J., Bass, D., Bowser, S. S., et al. (2012). The revised classification of eukaryotes. J. Eukaryot. Microbiol. 59, 429–514. doi: 10.1111/j.1550-7408.2012.00644.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Ah-Fong, A. M. V., and Judelson, H. S. (2011). Vectors for fluorescent protein tagging in Phytophthora: tools for functional genomics and cell biology. Fungal Biol. 115, 882–890. doi: 10.1016/j.funbio.2011.07.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Ashley, E. (2017). Investment in antimalarial drug development is bearing fruit. Lancet. Infect. Dis. 17, 568–570. doi: 10.1016/S1473-3099(17)30172-X

PubMed Abstract | CrossRef Full Text | Google Scholar

Attard, A., Gourgues, M., Galiana, E., Panabières, F., Ponchet, M., and Keller, H. (2008). Strategies of attack and defense in plant-oomycete interactions, accentuated for Phytophthora parasitica dastur (syn. P. Nicotianae Breda de Haan). J. Plant Physiol. 165, 83–94. doi: 10.1016/j.jplph.2007.06.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Baldwin, J., Farajallah, A. M., Malmquist, N. A., Rathod, P. K., and Phillips, M. A. (2002). Malarial dihydroorotate dehydrogenase. substrate and inhibitor specificity. J. Biol. Chem. 277, 41827–41834. doi: 10.1074/jbc.m206854200

PubMed Abstract | CrossRef Full Text | Google Scholar

Baldwin, J., Michnoff, C. H., Malmquist, N. A., White, J., Roth, M. G., Rathod, P. K., et al. (2005). High-throughput screening for potent and selective inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase. J. Biol. Chem. 280, 21847–21853. doi: 10.1074/jbc.M501100200

PubMed Abstract | CrossRef Full Text | Google Scholar

Björnberg, O., Grüner, A.-C., Roepstorff, P., and Jensen, K. F. (1999). The activity of Escherichia coli dihydroorotate dehydrogenase is dependent on a conserved loop identified by sequence homology. mutagenesis, and limited proteolysis. Biochemistry 38, 2899–2908. doi: 10.1021/bi982352c

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, J. J., and Jones, M. E. (1976). The cellular location of dihydroorotate dehydrogenase: relation to de novo biosynthesis of pyrimidines. Arch. Biochem. Biophys. 176, 82–90. doi: 10.1016/0003-9861(76)90143-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Claros, M. G., and Vincens, P. (1996). Computational method to predict mitochondrially imported proteins and their targeting sequences. Eur. J. Biochem. 241, 779–786. doi: 10.1111/j.1432-1033.1996.00779.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Davies, M., Heikkila, T., McConkey, G. A., Fishwick, C. W., Parsons, M. R., and Johnson, A. P. (2009). Structure-based design, synthesis, and characterization of inhibitors of human and Plasmodium falciparum dihydroorotate dehydrogenases. J. Med. Chem. 52, 2683–2693. doi: 10.1021/jm800963t

PubMed Abstract | CrossRef Full Text | Google Scholar

Deng, X., Gujjar, R., El Mazouni, F., Kaminsky, W., Malmquist, N. A., Goldsmith, E. J., et al. (2009). Structural plasticity of malaria dihydroorotate dehydrogenase allows selective binding of diverse chemical scaffolds. J. Biol. Chem. 284, 26999–27009. doi: 10.1074/jbc.M109.028589

PubMed Abstract | CrossRef Full Text | Google Scholar

Dreinert, A., Wolf, A., Mentzel, T., Meunier, B., and Fehr, M. (2018). The cytochrome bc1 complex inhibitor ametoctradin has an unusual binding mode. Biochim. Biophys. Acta Bioenerg. 1859, 567–576. doi: 10.1016/j.bbabio.2018.04.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Emanuelsson, O., Nielsen, H., Brunak, S., and von Heijne, G. (2000). Predicting subcellular localization of proteins based on their N-terminal amino acid sequence. J. Mol. Biol. 300, 1005–1016. doi: 10.1006/jmbi.2000.3903

PubMed Abstract | CrossRef Full Text | Google Scholar

Faissner, S., and Gold, R. (2018). Oral therapies for multiple sclerosis. Cold Spring Harb. Perspect. Med. 9, a032011. doi: 10.1101/cshperspect.a032011

PubMed Abstract | CrossRef Full Text | Google Scholar

Fang, J., Uchiumi, T., Yagi, M., Matsumoto, S., Amamoto, R., Takazaki, S., et al. (2013). Dihydro-orotate dehydrogenase is physically associated with the respiratory complex and its loss leads to mitochondrial dysfunction. Biosci. Rep. 33:e00021. doi: 10.1042/BSR20120097

PubMed Abstract | CrossRef Full Text | Google Scholar

Feng, Y., Li, W., Li, J., Wang, J., Ge, J., Xu, D., et al. (2012). Structural insight into the type-II mitochondrial NADH dehydrogenases. Nature 491, 478–482. doi: 10.1038/nature11541

PubMed Abstract | CrossRef Full Text | Google Scholar

Fernandez, J., Yang, K. T., Cornwell, K. M., Wright, J. D., and Wilson, R. A. (2013). Growth in rice cells requires de novo purine biosynthesis by the blast fungus Magnaporthe oryzae. Sci. Rep. 3:2398. doi: 10.1038/srep02398

PubMed Abstract | CrossRef Full Text | Google Scholar

Fox, B. A., and Bzik, D. J. (2002). De novo pyrimidine biosynthesis is required for virulence of Toxoplasma gondii. Nature 415, 926–929. doi: 10.1038/415926a

PubMed Abstract | CrossRef Full Text | Google Scholar

Fox, B. A., and Bzik, D. J. (2010). Avirulent uracil auxotrophs based on disruption of orotidine-5’-monophosphate decarboxylase elicit protective immunity to Toxoplasma gondii. Infect. Immun. 78, 3744–3752. doi: 10.1128/IAI.00287-210

CrossRef Full Text | Google Scholar

Fragoso, Y. D., and Brooks, J. B. B. (2015). Leflunomide and teriflunomide: altering the metabolism of pyrimidines for the treatment of autoimmune diseases. Expert Rev. Clin. Pharmacol. 8, 315–320. doi: 10.1586/17512433.2015.1019343

PubMed Abstract | CrossRef Full Text | Google Scholar

Fry, W. (2008). Phytophthora infestans: the plant (and R gene) destroyer. Mol. Plant Pathol. 9, 385–402. doi: 10.1111/j.1364-3703.2007.00465.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Fukasawa, Y., Tsuji, J., Fu, S.-C., Tomii, K., Horton, P., and Imai, K. (2015). MitoFates: improved prediction of mitochondrial targeting sequences and their cleavage sites. Mol. Cell. Proteomics 14, 1113–1126. doi: 10.1074/mcp.M114.043083

PubMed Abstract | CrossRef Full Text | Google Scholar

Garcia-Bayona, L., Garavito, M. F., Lozano, G. L., Vasquez, J. J., Myers, K., Fry, W. E., et al. (2014). De novo pyrimidine biosynthesis in the oomycete plant pathogen Phytophthora infestans. Gene 537, 312–321. doi: 10.1016/j.gene.2013.12.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Giermann, N., Schroder, M., Ritter, T., and Zrenner, R. (2002). Molecular analysis of de novo pyrimidine synthesis in solanaceous species. Plant Mol. Biol. 50, 393–403.

Google Scholar

Goodwin, S. B., Smart, C. D., Sandrock, R. W., Deahl, K. L., Punja, Z. K., and Fry, W. E. (1998). Genetic change within populations of Phytophthora infestans in the United States and Canada during 1994 to 1996: role of migration and recombination. Phytopathology 88, 939–949. doi: 10.1094/PHYTO.1998.88.9.939

PubMed Abstract | CrossRef Full Text | Google Scholar

Gujjar, R., El Mazouni, F., White, K. L., White, J., Creason, S., Shackleford, D. M., et al. (2011). Lead optimization of aryl and aralkyl amine-based triazolopyrimidine inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with antimalarial activity in mice. J. Med. Chem. 54, 3935–3949. doi: 10.1021/jm200265b

PubMed Abstract | CrossRef Full Text | Google Scholar

Gullino, M. L., Tinivella, F., Garibaldi, A., Kemmitt, G. M., Bacci, L., and Sheppard, B. (2010). Mancozeb, past, present, and future. Plant Dis. 94, 1076–1087. doi: 10.1094/PDIS-94-9-1076

PubMed Abstract | CrossRef Full Text | Google Scholar

Haldar, K., Kamoun, S., Hiller, N. L., Bhattacharje, S., and van Ooij, C. (2006). Common infection strategies of pathogenic eukaryotes. Nat. Rev. Microbiol. 4, 922–931. doi: 10.1038/nrmicro1549

PubMed Abstract | CrossRef Full Text | Google Scholar

Heikkilä, T., Thirumalairajan, S., Davies, M., Parsons, M. R., McConkey, A. G., Fishwick, C. W. G., et al. (2006). The first de novo designed inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase. Bioorg. Med. Chem. Lett. 16, 88–92. doi: 10.1016/j.bmcl.2005.09.045

PubMed Abstract | CrossRef Full Text | Google Scholar

Henniger, H. (2007). Zur Kultur von Phytophthora infestans auf vollsynthetischen Nährsubstraten. Z. Allg. Mikrobiol. 3, 126–135. doi: 10.1002/jobm.19630030204

CrossRef Full Text

Hortua Triana, M. A., Cajiao Herrera, D., Zimmermann, B. H., Fox, B. A., and Bzik, D. J. (2016). Pyrimidine pathway-dependent and -independent functions of the Toxoplasma gondii mitochondrial dihydroorotate dehydrogenase. Infect. Immun. 84, 2974–2981. doi: 10.1128/IAI.00187-116

PubMed Abstract | CrossRef Full Text | Google Scholar

Hortua Triana, M. A., Huynh, M.-H., Garavito, M. F., Fox, B. A., Bzik, D. J., Carruthers, V. B., et al. (2012). Biochemical and molecular characterization of the pyrimidine biosynthetic enzyme dihydroorotate dehydrogenase from Toxoplasma gondii. Mol. Biochem. Parasitol. 184, 71–81. doi: 10.1016/j.molbiopara.2012.04.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Hurt, D. E., Widom, J., and Clardy, J. (2006). Structure of Plasmodium falciparum dihydroorotate dehydrogenase with a bound inhibitor. Acta Crystallogr. Sect. D Biol. Crystallogr. 62, 312–323. doi: 10.1107/S0907444905042642

PubMed Abstract | CrossRef Full Text | Google Scholar

Judelson, H. S., Spielman, L. J., and Shattock, R. C. (1995). Genetic mapping and non-Mendelian segregation of mating type loci in the oomycete. Phytophthora infestans. Genetics 141, 503–512.

Google Scholar

Judelson, H. S., Tyler, B. M., and Michelmore, R. W. (1991). Transformation of the oomycete pathogen. Phytophthora infestans. Mol. Plant. Microbe. Interact. 4, 602–607.

Google Scholar

Kessl, J. J., Lange, B. B., Merbitz-Zahradnik, T., Zwicker, K., Hill, P., Meunier, B., et al. (2003). Molecular basis for atovaquone binding to the cytochrome bc 1 complex. J. Biol. Chem. 278, 31312–31318. doi: 10.1074/jbc.M304042200

PubMed Abstract | CrossRef Full Text | Google Scholar

Klotz, L.-O., Hou, X., and Jacob, C. (2014). 1,4-Naphthoquinones: from oxidative damage to cellular and inter-cellular signaling. Molecules 19, 14902–14918. doi: 10.3390/molecules190914902

PubMed Abstract | CrossRef Full Text | Google Scholar

Knecht, W., Henseling, J., and Löffler, M. (2000). Kinetics of inhibition of human and rat dihydroorotate dehydrogenase by atovaquone, lawsone derivatives, brequinar sodium and polyporic acid. Chem. Biol. Interact 124, 61–76. doi: 10.1016/s0009-2797(99)00144-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Knecht, W., and Löffler, M. (2000). Redoxal as a new lead structure for dihydroorotate dehydrogenase inhibitors: a kinetic study of the inhibition mechanism. FEBS Lett. 467, 27–30. doi: 10.1016/s0014-5793(00)01117-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Lamour, K. H., Win, J., and Kamoun, S. (2007). Oomycete genomics: new insights and future directions. FEMS Microbiol. Lett. 274, 1–8. doi: 10.1111/j.1574-6968.2007.00786.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Latijnhouwers, M., de Wit, P. J., and Govers, F. (2003). Oomycetes and fungi: similar weaponry to attack plants. Trends Microbiol. 11, 462–469. doi: 10.1016/j.tim.2003.08.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Leban, J., Kralik, M., Mies, J., Gassen, M., Tentschert, K., and Baumgartner, R. (2005). SAR, species specificity, and cellular activity of cyclopentene dicarboxylic acid amides as DHODH inhibitors. Bioorg. Med. Chem. Lett. 15, 4854–4857. doi: 10.1016/j.bmcl.2005.07.053

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, S., Neidhardt, E. A., Grossman, T. H., Ocain, T., and Clardy, J. (2000). Structures of human dihydroorotate dehydrogenase in complex with antiproliferative agents. Structure 8, 25–33. doi: 10.1016/s0969-2126(00)00077-0

CrossRef Full Text | Google Scholar

Manrique-Carpintero, N. C., Coombs, J. J., Pham, G. M., Laimbeer, F. P. E., Braz, G. T., Jiang, J., et al. (2018). Genome reduction in tetraploid potato reveals genetic load, haplotype variation, and loci associated with agronomic traits. Front. Plant Sci. 9:944. doi: 10.3389/fpls.2018.00944

PubMed Abstract | CrossRef Full Text | Google Scholar

Mather, M. W., Darrouzet, E., Valkova-Valchanova, M., Cooley, J. W., McIntosh, M. T., Daldal, F., et al. (2005). Uncovering the molecular mode of action of the antimalarial drug atovaquone using a bacterial system. J. Biol. Chem. 280, 27458–27465. doi: 10.1074/jbc.M502319200

PubMed Abstract | CrossRef Full Text | Google Scholar

Mattila, P., and Kumpulainen, J. (2001). Coenzymes Q9and Q10: contents in foods and dietary intake. J. Food Compos. Anal. 14, 409–417. doi: 10.1006/JFCA.2000.0983

CrossRef Full Text | Google Scholar

McCarthy, J. S., Lotharius, J., Rückle, T., Chalon, S., Phillips, M. A., Elliott, S., et al. (2017). Safety, tolerability, pharmacokinetics, and activity of the novel long-acting antimalarial DSM265: a two-part first-in-human phase 1a/1b randomised study. Lancet Infect. Dis. 17, 626–635. doi: 10.1016/S1473-3099(17)30171-30178

PubMed Abstract | CrossRef Full Text | Google Scholar

Meshnick, S. R., Berry, E. A., Nett, J., Kazanjian, P., and Trumpower, B. (2001). The interaction of atovaquone with the P. carinii cytochrome bc1 complex. J. Eukaryot. Microbiol. 48, 169S–171S. doi: 10.1111/j.1550-7408.2001.tb00505.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Miersch, J., Krauss, G.-J., and Metzger, U. (1986). Properties and subcellular localization of dihydroorotate dehydrogenase in cells of tomato suspension culture. J. Plant Physiol. 122, 55–66. doi: 10.1016/S0176-1617(86)80084-0

CrossRef Full Text | Google Scholar

Mitani, S., Araki, S., Takii, Y., Ohshima, T., Matsuo, N., and Miyoshi, H. (2001). The biochemical mode of action of the novel selective fungicide cyazofamid: specific inhibition of mitochondrial complex III in Phythium spinosum. Pestic. Biochem. Physiol. 71, 107–115. doi: 10.1006/PEST.2001.2569

CrossRef Full Text | Google Scholar

Munier-Lehmann, H., Vidalain, P.-O., Tangy, F., and Janin, Y. L. (2013). On dihydroorotate dehydrogenases and their inhibitors and uses. J. Med. Chem. 56, 3148–3167. doi: 10.1021/jm301848w

PubMed Abstract | CrossRef Full Text | Google Scholar

Nakamura, K., Yuasa, K., Sinmuk, S., Hatai, K., and Hara, N. (1995). The ubiquinone system in Oomycetes. Mycoscience 36, 121–123. doi: 10.1007/BF02268582

CrossRef Full Text | Google Scholar

Nielsen, H., Engelbrecht, J., Brunak, S., and von Heijne, G. (1997). Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites. Protein Eng. 10, 1–6. doi: 10.1093/protein/10.1.1

CrossRef Full Text | Google Scholar

Nørager, S., Jensen, K. F., Björnberg, O., and Larsen, S. (2002). E. coli dihydroorotate dehydrogenase reveals structural and functional distinctions between different classes of dihydroorotate dehydrogenases. Structure 10, 1211–1223. doi: 10.1016/s0969-2126(02)00831-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Ohara, K., Kokado, Y., Yamamoto, H., Sato, F., and Yazaki, K. (2004). Engineering of ubiquinone biosynthesis using the yeast coq2 gene confers oxidative stress tolerance in transgenic tobacco. Plant J. 40, 734–743. doi: 10.1111/j.1365-313X.2004.02246.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Oliver, J. D., Sibley, G. E. M., Beckmann, N., Dobb, K. S., Slater, M. J., McEntee, L., et al. (2016). F901318 represents a novel class of antifungal drug that inhibits dihydroorotate dehydrogenase. Proc. Natl. Acad. Sci. U.S.A. 113, 12809–12814. doi: 10.1073/pnas.1608304113

PubMed Abstract | CrossRef Full Text | Google Scholar

Parker, M. H., Durst, G. L., Hannum, A. C., Henry, M. J., Lawler, L. K., and Smith, A. J. (2002). The identification and optimization of oomycete dihydroorotate dehydrogenase inhibitors as fungicides. Synth. Chem. Agrochem. 800, 303–313. doi: 10.1021/bk-2002-0800.ch028

CrossRef Full Text | Google Scholar

Rawls, J., Knecht, W., Diekert, K., Lill, R., and Löffler, M. (2000). Requirements for the mitochondrial import and localization of dihydroorotate dehydrogenase. Eur. J. Biochem. 267, 2079–2087. doi: 10.1046/j.1432-1327.2000.01213.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Reis, R. A. G., Calil, F. A., Feliciano, P. R., Pinheiro, M. P., and Nonato, M. C. (2017). The dihydroorotate dehydrogenases: past and present. Arch. Biochem. Biophys. 632, 175–191. doi: 10.1016/

PubMed Abstract | CrossRef Full Text | Google Scholar

Richards, J. B., and Hemming, F. W. (1972). Dolichols, ubiquinones, geranylgeraniol and farnesol as the major metabolites of mevalonate in Phytophthora cactorum. Biochem. J. 128, 1345–1352. doi: 10.1042/bj1281345

PubMed Abstract | CrossRef Full Text | Google Scholar

Rodenburg, S. Y. A., Seidl, M. F., de Ridder, D., and Govers, F. (2018). Genome-wide characterization of Phytophthora infestans metabolism: a systems biology approach. Mol. Plant Pathol. 19, 1403–1413. doi: 10.1111/mpp.12623

PubMed Abstract | CrossRef Full Text | Google Scholar

Scheepens, P. C., and Fehrmann, H. (1977). Metabolic anomalies as a possible cause of biotrophy: abbreviated electron transport in Phytophthora infestans. Physiol. Plant Pathol. 11, 71–78. doi: 10.1016/0048-4059(77)90089-90083

CrossRef Full Text | Google Scholar

Schertl, P., and Braun, H.-P. (2014). Respiratory electron transfer pathways in plant mitochondria. Front. Plant Sci. 5:163. doi: 10.3389/fpls.2014.00163

PubMed Abstract | CrossRef Full Text | Google Scholar

Schroder, M., Giermann, N., and Zrenner, R. (2005). Functional analysis of the pyrimidine de novo synthesis pathway in solanaceous species. Plant Physiol. 138, 1926–1938. doi: 10.1104/pp.105.063693

PubMed Abstract | CrossRef Full Text | Google Scholar

Sykes, D. B., Kfoury, Y. S., Mercier, F. E., Wawer, M. J., Law, J. M., Haynes, M. K., et al. (2016). Inhibition of dihydroorotate dehydrogenase overcomes differentiation blockade in acute myeloid leukemia. Cell 167, 171.e–186.e. doi: 10.1016/j.cell.2016.08.057

PubMed Abstract | CrossRef Full Text | Google Scholar

Tellier, F., Fritz, R., Kerhoas, L., Ducrot, P.-H., Einhorn, J., Carlin-Sinclair, A., et al. (2008). Characterization of metabolites of fungicidal cymoxanil in a sensitive strain of Botrytis cinerea. J. Agric. Food Chem. 56, 8050–8057. doi: 10.1021/jf8010917

PubMed Abstract | CrossRef Full Text | Google Scholar

Tusnady, G. E., and Simon, I. (2001). The HMMTOP transmembrane topology prediction server. Bioinformatics 17, 849–850. doi: 10.1093/bioinformatics/17.9.849

PubMed Abstract | CrossRef Full Text | Google Scholar

Ullrich, A., Knecht, W., Fries, M., and Loffler, M. (2001). Recombinant expression of N-terminal truncated mutants of the membrane bound mouse, rat and human flavoenzyme dihydroorotate dehydrogenase. a versatile tool to rate inhibitor effects? Eur. J. Biochem. 268, 1861–1868. doi: 10.1046/j.1432-1033.2001.02061.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Ullrich, A., Knecht, W., Piskur, J., and Loffler, M. (2002). Plant dihydroorotate dehydrogenase differs significantly in substrate specificity and inhibition from the animal enzymes. FEBS Lett. 529, 346–350. doi: 10.1016/s0014-5793(02)03425-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Vargas, A. M., Quesada Ocampo, L. M., Cespedes, M. C., Carreno, N., Gonzalez, A., Rojas, A., et al. (2009). Characterization of Phytophthora infestans populations in Colombia: first report of the A2 mating type. Phytopathology 99, 82–88. doi: 10.1094/PHYTO-99-1-0082

PubMed Abstract | CrossRef Full Text | Google Scholar

Witschel, M., Rottmann, M., Kaiser, M., and Brun, R. (2012). Agrochemicals against malaria, sleeping sickness, leishmaniasis and chagas disease. PLoS Negl. Trop. Dis. 6:e1805. doi: 10.1371/journal.pntd.0001805

PubMed Abstract | CrossRef Full Text | Google Scholar

Witz, S., Jung, B., Furst, S., and Mohlmann, T. (2012). De novo pyrimidine nucleotide synthesis mainly occurs outside of plastids, but a previously undiscovered nucleobase importer provides substrates for the essential salvage pathway in Arabidopsis. Plant Cell 24, 1549–1559. doi: 10.1105/tpc.112.096743

PubMed Abstract | CrossRef Full Text | Google Scholar

Zameitat, E., Freymark, G., Dietz, C. D., Löffler, M., and Bölker, M. (2007). Functional expression of human dihydroorotate dehydrogenase (DHODH) in pyr4 mutants of ustilago maydis allows target validation of DHODH inhibitors in vivo. Appl. Env. Microbiol. 73, 3371–3379. doi: 10.1128/AEM.02569-2566

PubMed Abstract | CrossRef Full Text | Google Scholar

Zameitat, E., Gojkoviæ, Z., Knecht, W., Piškur, J., and Löffler, M. (2006). Biochemical characterization of recombinant dihydroorotate dehydrogenase from the opportunistic pathogenic yeast Candida albicans. FEBS J. 273, 3183–3191. doi: 10.1111/j.1742-4658.2006.05327.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Zrenner, R., Riegler, H., Marquard, C. R., Lange, P. R., Geserick, C., Bartosz, C. E., et al. (2009). A functional analysis of the pyrimidine catabolic pathway in Arabidopsis. New Phytol. 183, 117–132. doi: 10.1111/j.1469-8137.2009.02843.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Zrenner, R., Stitt, M., Sonnewald, U., and Boldt, R. (2006). Pyrimidine and purine biosynthesis and degradation in plants. Annu. Rev. Plant Biol. 57, 805–836. doi: 10.1146/annurev.arplant.57.032905.105421

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: dihydroorotase dehydrogenase, inhibitors, pyrimidine biosynthesis, Phytophthora infestans, Solanum tuberosum, kinetics, A77 1726

Citation: Garavito MF, Narvaez-Ortiz HY, Pulido DC, Löffler M, Judelson HS, Restrepo S and Zimmermann BH (2019) Phytophthora infestans Dihydroorotate Dehydrogenase Is a Potential Target for Chemical Control – A Comparison With the Enzyme From Solanum tuberosum. Front. Microbiol. 10:1479. doi: 10.3389/fmicb.2019.01479

Received: 05 February 2019; Accepted: 13 June 2019;
Published: 28 June 2019.

Edited by:

Felipe Cava, Umeå University, Sweden

Reviewed by:

Maria Cristina Nonato, University of São Paulo, Brazil
Wolfgang Buckel, University of Marburg, Germany

Copyright © 2019 Garavito, Narvaez-Ortiz, Pulido, Löffler, Judelson, Restrepo and Zimmermann. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Barbara H. Zimmermann,

Shared first authorship

Present address: Manuel F. Garavito, Wisconsin Institute for Discovery and Department of Plant Pathology, University of Wisconsin, Madison, WI, United States Heidy Y. Narvaez-Ortiz, Institute of Molecular Biology, University of Oregon, Eugene, OR, United States Dania Camila Pulido, Boyce Thompson Institute and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY, United States