J Biol Chem, Vol. 275, Issue 19, 14242-14247, May 12, 2000

Ornithine Decarboxylase of Stagonospora (Septoria) nodorum Is Required for Virulence toward Wheat^*

Andy Bailey, Elisabeth Mueller^§, and Paul Bowyer^¶

From the Institute of Arable Crop Research-Long Ashton Research Station, Department of Agricultural Sciences, University of Bristol, Long Ashton, Bristol, BS41 9AF, United Kingdom

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

A knockout strain of Stagonospora (Septoria) nodorum lacking the single ornithine decarboxylase (ODC) allele has been created by targeted gene replacement. A central region of the S. nodorum ODC gene was isolated by polymerase chain reaction using degenerate oligonucleotides and used to probe a  genomic library. The gene was sequenced and the encoded ODC protein sequence was shown to be similar to those from other fungi. The functionality of the S. nodorum ODC was confirmed by complementation of an Aspergillus nidulans mutant (puA) strain devoid of ODC activity, restoring growth in the absence of exogenous polyamines. Sporulation of the transformants was reduced suggesting abberant regulation of the S. nodorum gene in A. nidulans. Transformation-mediated gene replacement was used to create strains which were auxotrophic for putrescine and lack ODC coding sequences. Pathogenicity studies on these mutants showed that they are greatly reduced in virulence compared with non-disrupted transformants. This confirms that the strains carrying an ODC disruption cannot obtain sufficient polyamines from the host plant for normal growth and, thus, that fungal ODC may be a suitable target for chemical intervention.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Polyamines are a class of positively charged molecules found in all organisms (1-3). They are required for cell growth and are reported to have various functions in stabilizing DNA or membrane structure, and in resistance to oxidative stress. Ornithine decarboxylase (ODC)¹ catalyzes the conversion of ornithine to putrescine and is the first and rate-limiting step in polyamine biosynthesis in most organisms (4). ODC is an effective therapeutic target in the treatment of human protozoal pathogens (5-9) and has been proposed as a target in treatment of certain cancers and in the eradication of economically damaging plant pathogenic fungi (10). Inhibition of the polyamine biosynthetic enzyme ODC using the specific and highly potent inhibitor, di-fluoromethylornithine (DFMO) (11), is an effective therapy in treatment of Trypanosomiasis and other diseases caused by Plasmodia, Giardia, and Leishmania (5-9).

Control of fungal disease in humans and plants has relied on compounds that specifically interdict fungal metabolic pathways, in particular, ergosterol biosynthesis. Resistance to such fungicides generally arises within a few years either as a result of mutation in the native population or because of the introduction of resistant strains from other areas. Many effective fungicides are being withdrawn from use due to public concern about their toxicity. The search for new classes of fungicide is becoming increasingly urgent due to the limited number of targets for fungicide action so far identified. Most fungi (including the economically important plant pathogens, Rhizoctonia solani, Botrytis cinerea, Fusarium oxysporum f.sp. lycopersici, Verticillium dahliae, Cochliobolus carbonum, and Phytophthora infestans) are prevented from growing by low concentrations of DFMO (10, 12, 13). The same concentration of DFMO does not inhibit plant growth, because plants can synthesize polyamines from arginine (14). For example, DFMO applied to R. solani-infected tomato plants markedly reduced disease severity without adversely affecting plant growth. Polyamine biosynthesis (and in particular ODCase) has therefore been proposed as a good candidate target for developing a new type of fungicidal chemical.

Although DFMO is not toxic to plants per se, its toxicity to animals and high cost make it unsuitable for development as a fungicide. Moreover, certain important fungal plant pathogens, such as Septoria tritici, Stagonospora nodorum, Pyrenophora avenae, and Ophiostoma ulmi, are reportedly insensitive to DFMO (10, 15), suggesting the presence of divergent ODCase enzymes or an alternative route to polyamine biosynthesis in these organisms. Beneficial soil fungi, such as mycorrhiza, are reportedly insensitive to DFMO due to the presence of the agmatine route to polyamine biosynthesis (10) but other ODCase inhibitors have not been tested.

In theory, plants contain sufficient polyamines to support fungal growth. It is possible that, even after inhibition of ODC, pathogenic fungi may be able to obtain enough polyamines from the plant to support invasion of plant tissues. The ability to disrupt chromosomal gene loci in haploid fungi is well established and allows a direct test of gene function in growth and pathogenicity. ODC genes have been isolated and disrupted in yeast (16), Neurospora crassa (17), and Ustilago maydis (18). Yeast and N. crassa are non-pathogens and disruption in U. maydis prevents formation of the diploid state, which is a pre-requisite for pathogenicity. A recent paper describes an ODC gene knockout in Leishmania (19) but does not describe effects of the lesion on pathogenicity, hence it is not yet known whether ODC is required for virulence of any pathogen. We have now isolated ODC gene sequences from the ascomycete fungus, S. nodorum, which is one of the major causes of cereal crop loss throughout the world. To define the role of ODC in polyamine biosynthesis and pathogenicity in this pathogen, gene function was tested genetically by gene disruption. Disruptants demonstrated the essential function of ODC in polyamine metabolism, growth, and pathogenesis. This provides the first demonstration for the requirement for ODC in disease development.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Strains and Media-- The following fungal isolates were used in this work: S. nodorum BS171, and Aspergillus nidulans G0171. Septoria nodorum was maintained at 25 °C on Czapek minimal agar with the addition of V8 juice at 5% (v/v) (Cz-V8). A. nidulans was maintained at 37 °C on Aspergillus minimal medium agar (26) with appropriate supplements. For DNA isolation, the fungi were grown in liquid culture with shaking. Where appropriate, wheat varieties Avalon and Cadenza were used for pathogenicity studies. Fungi were transformed using standard methods (20-22). Cultures were routinely maintained as plug inocula from master plates or frozen conidial suspensions in water or 15% glycerol. ODC mutants were grown on Czapek agar medium supplemented with trace elements (46 mg MnSO₄·7H₂O, 65.9 mg of ZnSO₄·7H₂O, 59 mg of CuSO₄·5H₂O, 75 mg of FeSO₄·7H₂O, 37.8 mg of Na₂MoO₄·2H₂O added to 1000 ml of H₂O), and 60 µM putrescine. For mycelial suspensions, plugs were inoculated into Czapek Dox (Oxoid)/V8 (Cz-V8) media and grown in a shaking incubator for 2 days at 18 °C and 250 rpm. A. nidulans strain G0171 (puA2;biA1) was grown on complete media (20.0 g of Difco malt extract. 1.0 g of Bacto-Peptone, 20.0 g of glucose, 20.0 g of Bacto-agar, and appropriate supplements in 1000 ml of H₂O).

Inoculation of Plants and Pathogenicity Assays-- Leaf 3 of 14-day-old wheat seedlings was attached to horizontal plastic sheet using double-sided sticky tape. Inoculum consisting of 10⁵ fresh fungal spores was applied to leaves in 20-µl water drops at 5 drops per leaf. Inoculated plants were sealed in large plastic bags to maintain humidity and incubated at 20 °C with a 16-h photoperiod. Disease severity was scored after 7 days as described previously (23).

PCR of Ornithine Decarboxylase from S. nodorum-- For PCR, 100 ng of genomic DNA of S. nodorum was used in a "hot-start" PCR reaction. The amplification conditions were as follows: 94 °C for 5 min, 75 °C for 5 min, then 35 cycles of 94 °C for 1 min, 52 °C for 2 min, and 72 °C for 3 min. The degenerate primers were used at a final concentration of 2.5 µM. One-hundredth of the first-round product was used in the second-round PCR with the inner pair of nested primers, under identical amplification conditions. The outer pair of primers were the 5'-primer (5'-CCNT(T/C)TA(T/C)GCNGTNAA(A/G)TG(T/C)AA-3'), representing the amino acid sequence PFYAVKCN, and the 3'-primer (5'-CC(A/G)TC(A/G)CANGTNGGNCCCCA-3'), representing the sequence (W)GPTCDG. The second-round internal pair of primers were the 5'-primer (5'-TNATNT(T/A)(T/C)GCNAA(T/C)CCNTG-3'), representing the amino acid sequence I(F/Y)ANPC, and the 3'-primer (5'-TNCC(A/G)TANACNCCA(A/G)TC(A/G)TT-3'), representing the sequence NDGVYG(S/N). The products of several PCRs were pooled and size-fractionated on a 1.5% (w/v) agarose gel. After the second round of PCR, only one distinct band of the right size was visible after ethidium bromide staining and DNA from that band was isolated and cloned as a blunt-ended fragment into the EcoRV site of the vector pBluescript II SK⁺ (Stratagene). The identity of the cloned fragment was determined by sequencing the PCR product.

Genomic Library Screening-- 50,000 clones from a S. nodorum  GEM11 genomic library were screened with the ODC PCR product radioactively labeled using the High Prime Kit (Roche Molecular Biochemicals). The labeled DNA was separated from unincorporated nucleotides by running the reaction mixture over a small gel filtration column (Nick Column; Amersham Pharmacia Biotech).

Sequencing-- All sequencing reactions were performed on double-stranded plasmid DNA using a Perkin-Elmer ABI PRISM Dye Terminatior Cycle Sequencing Ready Reaction Kit. The sequence of both strands of the genomic ODC clone was determined by a combination of oligonucleotide primer walking and subcloning into pUC18. Sequence determination was carried out with an ABI377 automated sequencer and analyzed using the GCG package (24).

Plasmid Construction-- The plasmids used in the transformation of S. nodorum were as follows: pST28 was constructed by ligating a 1.4-kb HpaI fragment from pCB1004 (25), containing the hygromycin resistance gene from Escherichia coli under control of the TrpC promoter from A. nidulans, into pLitmus28 (New England Biolabs). Plasmid pAN7-1 contains the hygromycin resistance gene from E. coli flanked by the highly expressed A. nidulans gpd promoter and the terminator region of the A. nidulans trpC gene (26). A 4.8-kb XmnI fragment of genomic DNA containing the complete open reading frame of ODC was cloned into pUC18 to form pXmnI. Construction of plasmids for disruption of the S. nodorum ODC gene is illustrated in Fig. 2A. To construct vectors for replacement of ODC a 1011-bp SalI-HindIII fragment containing ODC promoter sequences was cut from pXmnI and cloned into pBluescript SK⁺ to form plasmid pFRONT2. A 1062-bp fragment containing 3'-non-coding sequences was amplified by PCR from pXmnI using primers odcA 5'-GCGGATCCGTACCACATTGGCGTC and a standard pBluescript SK⁺ flanking primer. The resulting PCR product was cloned as a SacI-BamHI fragment into pBluescript SK⁺ to form plasmid pBACK2. The SalI-HindIII fragment from pFRONT2 was then cloned into SalI-HindIII cut pBACK2 to form plasmid pDIS3. The hygromycin resistance cassette from pAN7-1 was excised with BglII and HindIII and cloned into BamHI-HindIII digested pDIS3 to form plasmid pSNODCDIS. This plasmid was linearized with KpnI prior to transformation into S. nodorum. Plasmid DNA was isolated by a modification of the alkaline lysis method (27).

DNA Isolation and Southern Blotting-- Genomic DNA was purified by a modification of the method by Specht et al. (28). Liquid cultures were collected on Miracloth in a funnel and washed with TSE (150 mM NaCl, 100 mM EDTA, 50 mM Tris-HCl, pH 8). The washed mycelia were subsequently freeze-dried. Mycelium (1 g dry weight) was ground to a fine powder and transferred to a 250-ml conical flask; 25 ml of extraction buffer (TSE + 2% SDS) and 0.2 volumes of toluene was added. The flask was shaken very slowly on a rotary shaker for 3 days. The DNA was separated from the toluene by spinning at 15,000 × g for 15 min in a SS34 rotor. The DNA is concentrated in the interphase between the water and the toluene phase. The DNA was removed and spun again to remove the toluene. 0.25 volumes of 7.5 M NH₄Ac was added and the polysaccharides were precipitated overnight at 4 °C. Polysaccharides were pelleted at 39,000 × g for 30 min in a SS34 rotor. The DNA was precipitated with 0.7 volumes of isopropyl alcohol. The precipitate was removed with a sealed-off Pasteur pipette and resuspended in 750 µl of TE (10 mM Tris-HCl, pH 7.5, 1 mM EDTA) and 50 µg/ml RNase. The RNase digestion was performed at 37 °C for 30 min. Proteinase K was added to 100 µg/ml and left to incubate for another 2 h at 37 °C. The DNA solution was extracted with phenol/CHCl₃. The DNA was once more precipitated and resuspended in TE. For Southern analysis, 5 µg of genomic fungal DNA was digested with appropriate restriction enzymes overnight at the appropriate temperature. The DNA was separated on a 0.8% agarose gel and standard techniques (29) were employed for treating and blotting the DNA onto a Nylon membrane (Amersham Pharmacia Biotech). Pre-hybridization and hybridization solutions were 5 × Denhardts (2% gelatin, 2% Ficoll 400, 2% polyvinylpyrolidone 360, 10% SDS), 100 µg/ml denatured calf thymus DNA, 0.2% SDS, and 1 × HSB (3 M NaCl, 0.1 M PIPES, 20 mM EDTA, pH 6.8). Hybridization was performed overnight at 65 °C. All washes were performed at high stringency: 0.1 × SSC and 0.5% SDS at 65 °C (twice for 30 min).

Transformation of S. nodorum-- S. nodorum was transformed essentially as described by Cooley et al. (25). After transformation, the plates were incubated overnight at 18 °C and the next day overlaid with Cz-V8 agar containing 1 mM putrescine and 100 µg/ml hygromycin B or 500 µg/ml zeacin (Invitrogen), as appropriate. The plates were incubated at 18 °C under near UV light until the first emerging colonies were visible; these were transferred weekly to new selective media.

Transformation of A. nidulans-- The method was essentially as reported by De Graaff (30). Plates of transformed protoplasts were incubated at 37 °C in the dark until the first emerging colonies were visible. Spores from these were removed and streaked out to single colonies on MM plates (MM, 1.2% agar and appropriate supplements). Spores from a single colony were transferred into 100 µl of water and subsequently propagated and tested for complementation of putrescine auxotrophy.

ODC Enzyme Assay-- Fungal ODC activity was measured by following the release of ¹⁴CO₂ from [1-¹⁴C]ornithine in a protocol adapted from Stevens et al. (31). Spores were harvested from confluently sporulating Cz-V8 plates and washed extensively with sterile distilled water. They were suspended in Cz-Dox liquid media (100 ml) at 1 × 10⁷/ml and incubated at 25 °C with shaking. Material was harvested by filtration through Miracloth (Calbiochem). Samples were ground to a fine powder in liquid nitrogen with glass beads, then resuspended in 2-3 ml of extraction buffer (10 mM potassium phosphate, 2 mM dithiothreitol, 1 mM MgCl₂, 0.1 mM EDTA, 0.1 mM pyridoxal phosphate, pH 7.6) and briefly vortexed. The resulting extract was centrifuged at 25,000 × g to remove cell debris then desalted to remove other decarboxylase substrates by buffer exchange in a Nap 10 column (Amersham Pharmacia Biotech) according to the manufacturers instructions. Reactions (0.4 ml) containing 50 mM Tris, 0.05 mM ornithine, 0.32 mM pyridoxal phosphate, 4.625 MBq (0.125 mCi) of [¹⁴C]ornithine, pH 8.0, and 0.2 ml of extract were carried out in 14-ml snap-top Falcon tubes. CO₂ was captured in suspended 0.5 ml of Eppendorf tubes containing 50 µl of 2-methoxyethanol/ethanolamine (2:1, v/v). Reactions were incubated at 25 °C for 30 min and stopped by addition of 0.1 ml of 50% trichloroacetic acid then left for an additional 1 h to trap released CO₂. Trapped CO₂ was measured in a scintillation counter. Protein was measured in 0.2-ml samples using the Bio-Rad Protein Assay kit according to the manufacturer's instructions.

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

ODC Gene Isolation-- Degenerate oligonucleotides designed against conserved amino acids within the ODC proteins of human (32), yeast (16), N. crassa (17), and Datura otramanium (33) were used as PCR primers to amplify an internal fragment of the S. nodorum ODC gene. A product of 609 bp was obtained using S. nodorum DNA as a template and this was cloned into pBluescript SK (Stratagene) and sequenced to confirm its identity. The fragment was purified, labeled with [³²P]dCTP and then used as a hybridization probe to screen a genomic DNA library of S. nodorum in the vector GEM11. 20 Positive plaques were identified, purified by a further two rounds of screening and DNA purified. Digested DNA was electrophoresed, blotted onto nylon membranes, and probed to identify those fragments corresponding to the ODC gene. These were subcloned into pUC18 and sequenced. A 4.8-kb region was fully sequenced (GenBank accession number AJ249387). This contained an open reading frame that encoded a protein of 462 amino acids and was interrupted by a single intron of 51 bp. The intron is bounded by sequences typical of fungal introns (34). The predicted amino acid sequence of this protein is shown in Fig. 1. The protein encoded by this gene is typical of ornithine decarboxylase proteins and contains all of the motifs conserved in those of other species. However, analysis of the sequence failed to reveal the PEST sequences which are believed to be important for the rapid protein degradation (35) observed in ODCs from some other species. The mRNA of ODC from N. crassa has a long 450-bp 5'-leader sequence and it has been suggested that this may allow for post-transcriptional control of ODC by enabling regulation of mRNA stability (36). Although we have not precisely determined the transcription start site for S. nodorum ODC, reverse transcriptase-PCR using primer pairs from the ODC promoter region has shown that this occurs within a region 470-600-bp upstream of the predicted methionine initiation codon, so it is possible that the S. nodorum ODC is also regulated in the same manner (data not shown).

View larger version (24K): [in this window] [in a new window]   Fig. 1.   Predicted S. nodorum ODC amino acid sequence.

Expression of S. nodorum ODC in A. nidulans-- The identity of the cloned gene was confirmed by co-transforming the 4.8-kb genomic fragment containing the proposed S. nodorum ODC gene, pXmnI, with pGM32 a plasmid containing pyr-4 into an ODC minus pyrG mutant (puA, pyrG) of A. nidulans that is auxotrophic for putrescine and uridine (37). Transformants were recovered on the basis of their ability to grow in the absence of uridine. A number of these transformants were able to grow in the absence of exogenous polyamine demonstrating that the S. nodorum ODC gene was capable of complementing the puA mutation.

Although the transformed colonies had the same radial growth rate as wild-type A. nidulans, they exhibited delayed and reduced conidiation. It is known that high levels of polyamines are needed for conidiation in A. parasiticus and that conidiation can be prevented by the addition of diamino butanone (a polyamine biosynthesis inhibitor) at concentrations that do not inhibit mycelial growth (38). This suggested that although sufficient putrescine was being produced for mycelial growth, there was not enough polyamine synthesized to fully support sporulation and so presumably this heterologous gene was not properly regulated or fully functional.

ODC Gene Disruption-- In order to examine the effect of ODC mutation in S. nodorum, a two-step gene disruption strategy was devised. Having cloned the gene, it was necessary to make a construct suitable for gene disruption. A 1-kb region from upstream of the N-terminal methionine and 1 kb from downstream of the stop codon were isolated, and ligated into pUC19 along with the hygromycin resistance cassette so that they flanked the hygromycin gene (Fig. 2A). This construct was transformed into S. nodorum using standard protocols (21) and transformants recovered on media containing both 100 µg/ml hygromycin and 100 µM putrescine. The transformants were purified and tested for putrescine-dependant growth. Of 150 transformants tested, numbers 26, 128, 132, and 143 were unable to grow in the absence of exogenous putrescine and so were presumably devoid of ODC activity. DNA was isolated from these transformants and analyzed to confirm that the ODC gene had indeed been deleted from these isolates. Fig. 2B shows a Southern blot of DNA from wild-type and candidate disruptant colonies probed with the ODC encoding region. The ODC coding region has been deleted from three of the candidate disruptants, 26, 128, and 135; these strains have been renamed mutants 26, 128, and 135, respectively. Transformant 143 has a complex rearrangement at this locus. This confirms that the colonies that were unable to grow without putrescine have indeed lost the ODC coding sequence, and that a functional ODC gene is required for growth when no exogenous polyamines are available. Since deletion of a single copy of the ODC gene from this haploid organism removes all hybridizing bands on this Southern blot, this result also confirms the presence of a single copy of the ODC gene in the S. nodorum genome.

View larger version (55K): [in this window] [in a new window]   Fig. 2.   Plasmid constructs and Southern blot analysis for ODC gene replacement. A, restriction map of ODC genomic DNA and the disruption construct pSNODCDIS, showing the region used to probe Southern blots. B, 5 µg of genomic DNA from wild-type BS171 (lane 1), wild-type LAW95 (lane 2), transformant 26 (lane 3), transformant 128 (lane 4), transformant 132 (lane 5), and transformant 143 (lane 6) was digested with HindIII electrophoresed on an 0.8% agarose gel and transferred to a Nylon membrane. The membrane was then hybridized to a probe derived from the coding region of ODC.

ODC Enzyme Activity in Wild-type and Mutant Fungus-- ODC enzyme activity was determined in wild-type and ODC S. nodorum. As ODC activity was difficult to detect in mycelia we determined activity in germinating spores where activity was expected to be high. The highest level of ODC activity is observed at the same time as germination occurs (Fig. 3). No ODC activity could be detected in any ODC mutant strain. This observation agrees well with a role for polyamines in the differentiation of fungi.

View larger version (24K): [in this window] [in a new window]   Fig. 3.   ODC activity in wild-type and disruptant fungi. ODC activity was measured in triplicate in extracts from germinating spores of wild-type () or mutant 26 () fungi at various times. The percentage of spores that had germinated at each time point () is also shown. Percentage germination is representative of three experiments, each of which yielded similar results.

Nutritional Requirements of ODC Pathogens-- To test the ability of different polyamines to restore growth of the ODC mutant, strains were grown on minimal agar medium containing 60 µM putrescine, spermine, and spermidine, with or without the addition of DFMO. We note that DFMO has been reported to be a poor inhibitor of growth for a number of fungal species, among them S. nodorum. These inhibition experiments relied on measurements of growth rate on rich media, such as potato dextrose agar (PDA) or Czapek Malt agar (CMA). Therefore, growth rates for wild-type and ODC S. nodorum were determined using PDA, CMA, and a defined minimal medium (MM) in combination with added polyamines and DFMO to determine the effects of ODC inhibition. DFMO is a potent inhibitor of wild-type S. nodorum growth on defined minimal medium but not on rich medium such as PDA or CMA (Fig. 4A). However, the ODC mutant is restored to wild-type growth rate on MM with the addition of 60 µM putrescine, spermine, or spermidine (Fig. 4B). The antagonistic effects of DFMO on growth on defined minimal medium can be completely reversed by addition of 60 µM putrescine, spermine, or spermidine, which suggests that the PDA and CMA media contain sufficient amounts of polyamines to counteract the effects of DFMO. This may explain the poor inhibition of fungal growth previously reported on these media. It would be interesting to re-examine the inhibitory effects of DFMO on "insensitive" fungi using defined minimal media. Furthermore, interesting questions are raised concerning polyamine uptake and ODC turnover in those fungi which were DFMO-sensitive on rich media.

View larger version (25K): [in this window] [in a new window]   Fig. 4.   Growth of wild-type and ODC fungi in the presence or absence of polyamines and DFMO. A, the inhibitory effect of DFMO was tested on defined minimal medium (), defined minimal medium + 60 µM putrescine (), Czapek-malt medium (), and potato dextrose agar (). B, radial growth rates of wild-type and mutant fungi were measured in the presence or absence of 2 mM DFMO during growth on PDA, CMA, un-supplemented defined MM, defined minimal media supplemented with 60 µM putrescine (MM + Pu), spermidine (MM + Spd), and spermine (MM + Spm). Growth rates were measured for 10 separate experiments then subjected to statistical analysis.

Virulence of ODC Mutants-- Spores isolated from wild-type and mutant strains of S. nodorum were used to inoculate wheat plants in our standard bioassay procedure and the strains were assessed for virulence (23). Disease scores after 7 days are shown in Fig. 5; ODC disruptants are severely reduced in their ability to cause disease. After 10 days, it was clear that the ODC mutants were still able to infect and could occasionally produce lesions which were much smaller than those formed by the wild-type strain. This demonstrated that the ODC-disrupted strains have reduced virulence and thus, presumably cannot obtain sufficient polyamines from the plant during infection to support normal growth and disease development.

View larger version (13K): [in this window] [in a new window]   Fig. 5.   Pathogenicity of wild-type and ODC S. nodorum to wheat. Disease was scored 7 days post-inoculation as described previously (41). Average scores from 20 inoculations are presented.

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

We have cloned and sequenced the ODC gene from S. nodorum and shown that it is functional in A. nidulans by restoring putrescine prototrophy to a putrescine auxotroph. Sporulation of the A. nidulans transformants was reduced compared with the wild-type; this may indicate that the S. nodorum gene cannot provide sufficient putrescine to support the normal levels of conidiation of A. nidulans. It may be because the heterologous enzyme is expressed at a reduced rate, is not assembled correctly, cannot be fully induced in the heterologous host, or that some control regions were not present in the construct used for complementation. It does, however, confirm that a supply of polyamines is essential for the sporulation process and that even if normal vegetative growth can proceed, sporulation and, hence, disease dissemination may be impaired by inhibition of the polyamine pathway in a fungus. Targeted gene replacement of ODC in S. nodorum demonstrates the essential housekeeping function of this enzyme in this species. These mutants are strict auxotrophs, showing germination but almost no growth on minimal medium in the absence of exogenous polyamines. These ODC disruptants grow at a rate similar to the wild-type when supplemented with sufficient exogenous putrescine. Putrescine, spermine, and spermidine were equally able to complement the polyamine auxotrophy in the ODC null mutant cells, suggesting that there is no strict requirement for putrescine in growth. ODC-deficient mutants of N. crassa, A. nidulans, and mammals also require polyamines for growth suggesting a similarly vital role for ODC in these organisms. This result also confirms that ODC is the sole route to polyamine biosynthesis in S. nodorum. Together with the observation that previous reports of ODC inhibitor insensitivity may well have arisen from unintentional contamination of media with polyamines, this suggests that inhibition of polyamine biosynthesis may be a useful therapeutic target for this class of pathogens. It is not known whether the fungus has a strict requirement for spermidine in growth and disease development. A S. nodorum spermidine synthase genomic clone has been isolated and work is underway to create spermidine synthase knockout mutants to test the validity of this enzyme as a therapeutic target.

Deletion of the ODC genes from Leishmania donovani (19) results in a requirement for either putrescine or spermidine but not for spermine, hence, this protozoan seems to lack a catabolic pathway for spermine. Spermine is the major polyamine in mammals and, thus, ODC null mutants of this parasite are unlikely to be able to scavenge usable polyamines from their host. Plants contain significant amounts of spermidine and putrescine. ODC-deficient S. nodorum and other fungi can utilize all three polyamines to maintain growth suggesting that ODC mutants could scavenge sufficient polyamine from the plant host to maintain growth during disease development. Pathogenicity assays of the mutant strains using spore inoculum resulted in greatly reduced lesions compared with the wild-type. This shows that although the strains are still pathogenic, their virulence is greatly reduced. We believe this to be the first demonstration of a role for ODC in pathogenesis of any organism. The limited growth of the ODC disruptants in planta is presumably sustained by utilizing plant-derived polyamines. The possibility that spores used in the assay have reserves of polyamines that allow limited growth within the plant cannot be disregarded. Attempts to produce polyamine-starved spores were unsuccessful, because continued growth of ODC mutants in the absence of polyamines did not occur. Progressive reduction of polyamine levels in the medium also resulted in greatly reduced sporulation, preventing reliable pathogenicity tests. If it were possible to find a compound that completely inhibited fungal ODC activity during plant infection, mimicking the effects of the mutation, then presumably the same degree of reduction in lesion development would be observed. It would be interesting to investigate whether ODC strains are more sensitive to toxic polyamine analogues (39-41) than the wild-type, since they must be utilizing a polyamine uptake system to supply their requirement, raising the possibility of a dual control approach. It is also noteworthy that a number of plant defense compounds are polyamine conjugates. Due to the need for uptake of exogenous polyamines, it is possible that the mutants would be more sensitive to such compounds. Our work has demonstrated that ornithine decarboxylase is essential for virulence of a fungal pathogen and that inhibition of ODC may be a valid approach to the design of new fungicides. This disease is a prime target for chemical or biological control in winter cereals and the demonstration of a requirement for ODC in virulence and growth has important implications in the consideration of polyamine biosynthesis as a fungicide target.

	FOOTNOTES

^* This work was supported by the Institute of Arable Crop Research-Long Ashton Research Station, supported by the Biotechnology and Biological Sciences Research Council (BBSRC).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Recipient of a BBSRC Biological Chemistry Initiative grant. Current address: Dept. of Biological Sciences, University of Bristol, Bristol, UK.

^§ Supported by a BBSRC Cooperative Awards in Science and Engineering studentship award co-funded by Zeneca Agrochemicals.

^¶ To whom all correspondence should be addressed. Tel.: 1275-549297; Fax: 1275-394281; E-mail: bowyerp@bbsrc.ac.uk.

	ABBREVIATIONS

The abbreviations used are: ODC, ornithine decarboxylase; DFMO, difluoromethylornithine; PCR, polymerase chain reaction; kb, kilobase(s); bp, base pair(s); PIPES, 1,4-piperazinediethanesulfonic acid; PDA, potato dextrose agar; CMA, Czapek Malt agar; MM, minimal medium.

	REFERENCES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES