SsMet1 is a critical gene in methionine biosynthesis in Sclerotinia sclerotiorum
Nickisha Pierre-Pierre, Wei Wei, Richard Manasseh, Michelle Mendoza, George J. Vandemark, Weidong Chen
TL;DR
This study shows that the SsMet1 gene is essential for methionine production and survival in the fungus Sclerotinia sclerotiorum.
Contribution
The study identifies SsMet1 as a critical gene in methionine biosynthesis in Sclerotinia sclerotiorum.
Findings
SsMet1-deletion mutants cannot grow on minimal medium and fail to produce sclerotia.
Methionine and homocysteine rescue mycelial growth but not sclerotial development in mutants.
SsMet1-deletion mutants are avirulent but regain virulence with methionine supplementation.
Abstract
Methionine, a key sulfur-containing amino acid, is involved in various important functions in cellular metabolism. Genes that encode enzymes to catalyze steps of the methionine biosynthesis pathway are essential for survival of fungi. The SsMet1 (SS1G_11000) gene in Sclerotinia sclerotiorum is an orthologue of BcStr2, a gene characterized in Botrytis cinerea that plays a key role in methionine biosynthesis. In this study, we characterized SsMet1 in S. sclerotiorum by creating SsMet1-deletion mutants, Met1–2 and Met1-4, using a split marker technique. The SsMet1-deletion mutants were unable to grow on minimal medium and did not produce sclerotia. Supplementation with methionine and homocysteine rescued the defects in mycelial growth, but not sclerotial development of the SsMet1-deletion mutants. These results indicate that SsMet1-deletion mutants are auxotrophic for methionine. In…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Click any figure to enlarge with its caption.
Figure 1
Figure 2
Figure 3
Figure 4
Figure 5
Figure 6
Figure 7| PCR primers | Sequence (5’ to 3’) | Purpose |
|---|---|---|
| 11Hind-L | AAGCTTTCCTGGACGCCGATAGCGGATA | Knockout of |
| 11Sal-R | GTCGACCTGAGGGCTTTTTGGGTTT | Knockout of |
| 11Xba-L | TCTAGACGAATGGAGGTTATGGTGGA | Knockout of |
| 11Knp-R | GGTACCAAGGCTTCCAGGTTGTTAGTTC | Knockout of |
| 11-L | GAGCTCATGTCCGTCATCGAACTTGGAGAGT | Complementation of |
| 11-R | CCCGGGAGACGTTGAATCTGCCGCAGCTTTC | Complementation of |
| 11delF6 | GAGAATGCAACGTCATGGGC | Confirmation of |
| 11delR6 | ACCAAGGGATGGGATCGAAG | Confirmation of |
| Species | Amino Acid Identity % |
|---|---|
|
| 100 |
|
| 91.89 |
|
| 91.72 |
|
| 80.53 |
|
| 75.00 |
|
| 72.94 |
|
| 72.64 |
|
| 72.44 |
|
| 64.93 |
|
| 60.07 |
|
| 57.62 |
|
| 57.17 |
|
| 57.10 |
|
| 56.42 |
|
| 54.62 |
|
| 47.70 |
|
| 37.25 |
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsPlant pathogens and resistance mechanisms · Yeasts and Rust Fungi Studies · Turfgrass Adaptation and Management
Introduction
Sclerotinia sclerotiorum is one of the most destructive plant pathogens. There are more than 60 names that have been used to describe the diseases it causes (Purdy, 1979), including white mold, watery soft rot and stem rot (Bolton et al., 2006). S. sclerotiorum is known to infect dicotyledonous crops such as sunflower, soybean, dry bean, dry pea and chickpea, but has also some monocotyledonous species such as onion and Chinese chive (Boland and Hall, 1994; Choi et al., 2017). S. sclerotiorum’s mechanism to attack host plants includes cell wall and middle lamella degrading enzymes, toxins, defense substances and rapidity of infection (Lumsden, 1979). Annual losses from S. sclerotiorum in the United States have exceeded $200 million due to a lack of high levels of host resistance (Bolton et al., 2006).
S. sclerotiorum is a robust pathogen that thrives under diverse environmental conditions and survives as sclerotia for four to five years and up to eight years in soil (Adams and Ayers, 1979; Bolton et al., 2006). Management of S. sclerotiorum is difficult due to the fungus targeting different stages of crop development; infection can cause damping-off of seedlings, stem rot, and soft rot of fruits and flowers (Bolton et al., 2006). Successful disease control usually requires implementation and integration of multiple management practices. In the past, cultural practices such as field burning to reduce the number of sclerotia in the soil (Hind-Lanoiselet et al., 2005; Brooks et al., 2018) were used. Currently, the disease is managed in fields of many crop species using applications of fungicides, which can have negative environmental implications (Leroux et al., 2002; Mir et al., 2023). However, in many cases, especially for high value crops or on highly specialized farms, these methods are insufficient for white mold control.
Because of the central role of methionine in metabolism (Jastrzębowska and Gabriel, 2015) and growth control in fungi, methionine biosynthesis inhibition by fungicides has been explored in several filamentous fungi (Masner et al., 1994; Fritz et al., 1997; Scott et al., 2020). Methionine (Met), a key sulfur-containing amino acid, is not only a key amino acid of proteins, but is also involved in many essential functions in cellular metabolism through its main derivative S-adenosylmethionine (SAM). The pathways of methionine biosynthesis have been characterized extensively in some plants, bacteria, and fungi (Jastrzębowska and Gabriel, 2015) but have not been reported in Sclerotinia.
Recently, targeted disruption of genes involved in the metabolism of cysteine and methionine in Alternaria alternata, AaMetB, AaMetC and AaMetX, have been investigated as these genes are required for vegetative growth, conidiation, and pathogenicity of A. alternata (Gai et al., 2021). Fungal mutants that lack AaMetB, AaMetC, or AaMetX exhibited developmental deficiencies such as decreased aerial hyphae and conidia production, and inability to grow on minimal media. However, the defects in cell growth and development of these mutants were restored by exogenous applications of methionine or homocysteine, but not cysteine. This restoration indicated that AaMetB, AaMetC, and AaMetX mutants are typical methionine auxotrophs rather than cysteine auxotrophs (Gai et al., 2021).
In the study on B. cinerea, Shao et al. (2016) observed that the deletion mutant ΔBcStr2, an orthologue of Str2 encoding a cystathionine γ-synthase (CGS) in yeast Saccharomyces cerevisiae, exhibited a decrease in virulence on different plant tissues. They also found that ΔBcStr2 produced significantly fewer conidia compared to the wildtype and complemented strains. The mutant strain also showed increased sensitivity to agents that damage the cell wall and increased sensitivity to osmotic stress, which led to reduced mycelial growth of the mutant strain in host tissue.
In Magnaporthe oryzae, the methionine synthase, MET6, catalyzes the last step of methionine biosynthesis. MET6-deletion mutants were obtained by targeted gene replacement (Saint-Macary et al., 2015). The Δmet6 mutants were unable to grow on minimal media unless supplemented with methionine*. M. oryzae Δmet6* mutants were non-pathogenic on intact and wounded barley and rice leaves. These results indicated that the Met biosynthesis pathway may be essential for fungal development, survival, and pathogenicity (Saint-Macary et al., 2015).
In this study, we investigated the role of SsMet1, a gene hypothesized to be involved in methionine biosynthesis, in S. sclerotiorum. Thus, we generated gene deletion mutants of SsMet1, characterized the function of SsMet1 in mutant strains to evaluate the role of SsMet1 in the regulation of various cellular processes in S. sclerotiorum. The deletion of the methionine biosynthesis gene demonstrated its role in growth, virulence, sclerotial development, and response to environmental stresses.
Experimental methods
SsMet1 sequence acquisition and phylogenetic analysis
First, the sequence of SsMet1 was identified as an orthologue sequence to BcStr2 of B. cinerea on EnsemblFungi (Yates et al., 2022; Martin et al., 2023). These two sequences as well as 15 additional sequences highlighted as orthologues of SS1G_11000 were obtained by EnsemblFungi (Yates et al., 2022; Martin et al., 2023) and on the Basic Local Alignment Search Tool (BLAST) (https://blast.ncbi.nlm.nih.gov/Blast.cgi; Sayers et al., 2022). We searched against the NCBI genome database with a cut-off E-value of 1e^–10^. The translated protein sequences were aligned using the National Center for Biotechnology Information multiple alignment tool (COBALT: Multiple Alignment Tool; Papadopoulos and Agarwala, 2007). For phylogenetic analysis, maximum-likelihood phylogenetic dendrograms were constructed using MEGA11 with 1000 bootstraps (Tamura et al., 2021).
Knockout of SsMet1 in S. sclerotiorum
Gene replacement mutants for SsMet1 were created with a split-marker technique (Goswami, 2012). For the target gene, both the 5’ (840 bp) and the 3’ (507 bp) flanking sequences of the ORF were amplified from genomic DNA of the wildtype strain WMA1 (ATCC MYA-4521), with PCR primers 11HindL/11SalR and 11XbaL/11KpnR (Table 1) and cloned into the pJET1.2 cloning vector (Promega, Madison, Wisconsin) (Figure 1). The amplified 5’ and 3’ flanking sequences of SsMet1 were then subcloned into pUCH18 (Lu et al., 1994) to generate pCU18-ORF-5’and pCU18-ORF-3’, which harbor a hygromycin-resistance gene (HYG) and the 5’ or 3’ flanking sequences at the 5’ and 3’ ends of the HYG gene (Figure 1). The 5’ and 3’ flanking sequences with their corresponding truncated HYG were amplified (Figure 1). Purified 5’-HY and YG-3’ fragments were then used to co-transform S. sclerotiorum protoplasts (Rollins, 2003). Transformants were selected and purified through repeated hyphal tipping on potato dextrose agar (PDA) containing hygromycin (100 ug/L). In the hygromycin-resistant transformants, the target gene was replaced by reconstituted HYG via homologous recombination mediated by the flanking sequences (Figure 1).
Knockout of the SsMet1 gene in S. sclerotiorum. The schematic diagram illustrates the knockout strategy of SsMet1 gene with the hygromycin-resistance gene (HYG) as the replacement (not drawn to scale).
The deletion of SsMet1 and gene replacement in Met1–2 and Met1–4 mutants were confirmed by rt-PCR assays with the 11delF6/11delR6 primers (Table 1). For rt-PCR, mycelia were harvested, freeze dried and total RNA was isolated using the RNeasy Plant Mini Kit (Qiagen, Germantown, MD), according to the manufacturer’s instructions. All RNA samples were diluted to 400 ng/µl and cDNA was synthesized using the 5X all-in-one RT Mastermix (Applied Biological Materials Inc., Richmond, Canada), according to the manufacturer’s instructions.
Complementation of SsMet1
The SsMet1-deletion mutant was complemented with the full-length wildtype allele of SsMet1 gene. The full-length SsMet1 gene was amplified from the cDNA of the wildtype WMA1 strain with 11-L/11-R primers (Table 1). The PCR product was cloned into a pJET1.2 blunt cloning vector (Promega, Madison, Wisconsin) and digested with SacI and SmaI. The resulting SacI-SmaI fragment was cloned into a complementation vector (pCETNS) in the Sac1/Sma1 sites and used for Agrobacterium-mediated transformation. Transformants were selected on PDA plates containing 150 μg/ml geneticin (G418; Ameresco, Ohio) for two rounds of hyphal tip transfers under geneticin selection, and the presence and expression of the wildtype SsMet1 allele were confirmed by rt-PCR assay using primers 11delF6/11delR6 (Table 1).
Characterization of SsMet1-deletion mutants
The SsMet1-deletion mutants were compared with the wildtype strain for growth rate and sensitivity to various stress agents. To compare their growth rates, colonized agar plugs (4 mm in diameter) of wildtype WMA1 and mutant strains Met1–2 and Met1–4 were taken from the edge of a 2-day-old culture, placed on the center of a fresh PDA plate, and incubated at 22°C. Cultures were monitored for three days for evaluation of colony morphology and diameter, and up to 30 days for sclerotial formation. Mycelial growth tests under various conditions were performed on minimal medium (MM) (10 mM K_2_HPO_4_, 10 mM KH_2_PO_4_, 4 mM (NH_4_)2_SO_4, 2.5 mM NaCl, 2 mM MgSO_4_, 0.45 mM CaCl_2_, 9 mM FeSO_4_. 7H_2_O, 10 mM glucose and 1 L water, pH 6.9) and MM amended with four different supplements: methionine (1 mM), cysteine (1 mM), homocysteine (0.5 mg/mL), or glutathione (0.5 mg/mL). Each plate was inoculated with a 4-mm-diameter mycelial-colonized agar plug taken from the edge of a 2-day-old colony on PDA. The diameter of the mycelium was measured with a digital caliper three days post inoculation. Each treatment was replicated three times for each strain and the experiment was repeated three times.
To test the sensitivity of each strain to various environmental stressors, colonized agar plugs (4 mm in diameter) taken from the margin of a 2-day-old colony on PDA were placed onto PDA plates amended with one the following six stressors: a cell wall stress agent, congo red (CR, 0.5 mg/mL); two osmotic stress generators, sodium chloride (NaCl, 1 M) and potassium chloride (KCl, 1 M); and three oxidative stress generators, sorbitol (1 M), hydrogen peroxide (H_2_O_2_, 10 mM) and calcofluor white (CFW, 0.5 g/liter). After incubation at 22°C for three days, the mycelial diameter in each plate was measured. Each experiment was repeated three times with three replications for each strain. The overall average of mycelia growth was obtained. Thermal stress sensitivity was tested by incubating 2-day-old colonies grown on PDA and then placed on fresh PDA plates under four temperature conditions (15, 20, 25, and 28°C) and measuring mycelial diameter after three days.
Pathogenicity assays
Detached leaf disease assays on bean were conducted using mycelium of the wildtype and mutant strains grown on PDA. After a two-day growth on PDA, mycelium colonized agar plugs (4 mm in diameter) were placed on the leaves for observance of disease development. Lesion sizes were measured 48 hours post inoculation. This experiment was repeated three times with three replications for each strain. Supplementation of MM with methionine was also used to investigate pathogenicity restoration of the deletion mutants on detached been leaves. We inoculated the wildtype strain and deletion mutants on to MM amended with methionine and after two days of growth we used the fungal plugs to evaluate virulence on detached bean leaves.
Statistical analysis
A linear model in conjunction with an analysis of variances (ANOVA) (R Core Team, 2020) were used to compare the mean growth rates of the wildtype, complement and mutant strains (Met1–2 and Met1-4) inoculated on PDA and MM with amendments, which are the environmental stressors for PDA and the additions of methionine, homocysteine, cysteine and glutathione for MM. For the linear model and ANOVA, the fungus type and the media type were used as factors. The same approach was used to compare the growth responses to the different thermal stressors on PDA. For this analysis, the fungus type and temperature were used as factors. A linear model in conjunction with an ANOVA were also used to analyze the lesion sizes induced by the wildtype, complement and mutant strains on bean. For this analysis, the fungus type was used as a factor. The linear model provided the standard error. After each ANOVA, pairwise comparisons with Tukey’s HSD test were used to find means that were significantly different from each other. The alpha value of 0.05 was used for the ANOVA computation.
Results
Identification of SsMet1 in S. sclerotiorum
SsMet1 of S. sclerotiorum is an orthologue of BcStr2 of B. cinerea. The homologous sequence for BcStr2 gene from B. cinerea was found in S. sclerotiorum following a BLAST search against the NCBI genome database. The SsMet1 protein shares 91.72% identity with that of BcStr2. Because of the high similarity of their amino acid sequences, SsMet1 was identified as an orthologue of BcStr2 in the B. cinerea genome database. We named this gene SsMet1 due to BcStr2 (an orthologue of Saccharomyces cerevisiae, Str2) being involved in methionine biosynthesis. The SsMet1 gene is 1815 bp in length and encodes 604 amino acids. The structure of the nucleotide sequence was predicted to contain two introns of 96 and 71 bp located at positions 625 and 816 of the sequence, respectively. Analysis of the characteristic domains of the SsMet1 protein with EnsemblFungi indicated that SsMet1 contains a pyridoxal phosphate-dependent transferase domain (Yates et al., 2022; Martin et al., 2023).
Sequence acquisition and phylogenetic analysis of SsMet1 orthologues
BLAST search of the NCBI genome database and EnsemblFungi using the SS1G_11000 protein sequence as the query identified homologous sequences in 16 other fungi (including BcStr2). We found this protein sequence to be highly conserved among the 17 fungi compared, with amino acid identity varying from 37.25% to 91.89% (Table 2). S. cerevisiae was used as an outgroup and has the least identity at 37.25%. To further elaborate the phylogenetic relationships for this gene among the 17 fungal species, Maximum-likelihood phylogenetic dendrograms were constructed with MEGA11 (Tamura et al., 2021) (Figure 2). Regarding the protein sequence, the phylogenetic tree shows that S. sclerotiorum and B. cinerea are sister taxa. In addition, S. sclerotiorum, B. cinerea, S. borealis and Rutstroemia sp. NJR-2017a WRK4 form one monophyletic group. The taxa including Cadophora sp. DSE1049*, R. secalis*, M. brunnea and D. rosae form another monophyletic group and these two groups as a whole share a common ancestor. A third monophyletic group includes F. solani, U. virens, N. crassa, and M. oryzae. The tree also displays an ancestor further back in time that connects this monophyetic group to the previous two discussed that includes S. sclerotiorum. Lastly, the furthest ancestor highlighted in this tree shows that S. sclerotiorum and S. cervisiae share a distant common ancestor.
Evolutionary analysis by Maximum Likelihood method. The evolutionary history was inferred based on amino acid sequences using the Maximum Likelihood method and JTT matrix-based model. The tree with the highest log likelihood (–9941.71) is shown. The percentage of trees in which the associated taxa clustered together is shown next to the branches. Initial tree(s) for the heuristic search were obtained by applying the Neighbor-Joining method to a matrix of pairwise distances estimated using the JTT model. All positions containing gaps and missing data were excluded (complete deletion option). Evolutionary analyses were conducted in MEGA11.
Knockout and complementation of SsMet1 in S. sclerotiorum
To confirm SsMet1 gene knockout and complementation in S. sclerotiorum, rt-PCR was conducted with 11delF6/11delR6 primers (Table 1). The rt-PCR confirmed that the wildtype and complement strains of S. sclerotiorum have a band corresponding to the expected size of 217 bps, which was absent in the mutants (Figure 3), confirming that the SsMet1 was deleted.
Verification of SsMet1 knockout in S. sclerotiorum by PCR. (A) Confirmation of gene deletion of Met1–2 and Met1–4 using RT-PCR with SsMet1 specific primers 11delF/11delR (217 bps). (B) PCR with SsGAR1 primers (NADPH-utilizing reductase) to check the RNA quality.
Role of SsMet1 in S. sclerotiorum pathogenicity
To analyze the role of SsMet1 in pathogenicity, SsMet1 infection capability was evaluated on detached bean leaves. As shown in Figure 4, the wildtype and complement strains, WMA1 (average size of 26.3 mm) and Met1C (average size of 26.3 mm) respectively, caused disease lesions on detached leaves of bean 48 hours after inoculation. In contrast, the mycelia of Met1–2 and Met1–4 mutants were unable to infect bean leaves (Figure 4A). When the wildtype and deletion mutants were grown on MM amended with methionine and then used to inoculate detached bean leaves to observe virulence, the deletion mutants, Met1–2 and Met1–4 were able to cause disease on detached bean leaves (Figure 4B). The average disease lesion size for Met1–2 and Met1–4 were 21.1 mm and 20.8 mm respectively (Figure 4D).
Pathogenicity assay of mutants in comparison to wildtype and complement strains. Pathogenicity assay on common bean leaves with (A) Wildtype, WMA1, complement, Met1C and SsMet1-deletion mutants, Met1–2 and Met1–4 grown on PDA. (B) WMA1 and mutants Met1–2 and Met1–4 after being inoculated on MM amended with methionine. Disease lesions were measured, and photos were taken 48h after inoculation. (C, D) Average lesion diameter. A one-way ANOVA in R and the Tukey HSD test were used to determine the significant differences of means from the wildtype, WMA1. The means of three replicates are presented and the error bars are standard errors. A significance threshold of 0.05 was used. Signif. codes: *** P < 0.001, ** P < 0.01.
SsMet1 is required for differentiation and sclerotial development
To study the growth of SsMet1-deletion mutants, Met1–2 and Met1-4, wildtype WMA1 and the complement Met1C, were grown on PDA for three days at 22°C. The average colony diameter of WMA1 and Met1C strains were 82.2 mm and 82.4 mm, respectively. The SsMet1-deletion mutants Met1–2 and Met1–4 diameters were 72.2 mm and 72.6 mm respectively. The results show that the deletion mutants, Met1–2 and Met1-4, grew slower on PDA than the wildtype and complemented strains, WMA1 and Met1C, respectively (Figures 5A, C).
Sensitivity of the wildtype WMA1, complement Met1C and mutant strains Met1–2 and Met1–4 to cell wall-damaging, osmotic, and oxidative stress. (A) Comparisons of colony morphology on PDA plates amended with cell wall-damaging agent (0.5 mg/mL Congo Red), oxidative stress generators (1 M Sorbitol, 0.5 g/liter CFW and 10 mM H2O2) or osmotic stress agents (1 M NaCl and 1 M KCl). Photos were taken three days after incubation. (B) Sclerotial formation of the wildtype WMA1, SsMet1-deletion mutants Met1–2 and Met1-4, and complement Met1C strains on PDA, and PDA amended with the above environmental stressors at 7 days and up to 30 days post inoculation. (C) Colony diameter. A one-way ANOVA in R and the Tukey HSD test were used to determine the significant differences of means from the wildtype, WMA1. The means of three replicates are presented and the error bars are standard errors. A significance threshold of 0.05 was used. Signif. codes: *** P < 0.001, * P < 0.05.
Naturally, we wanted to observe how sclerotial formation of the deletion mutants compared to the wildtype and complemented strains due to sclerotia being an important form of survival for S. sclerotiorum. Twelve days post inoculation on PDA, Met1–2 and Met1–4 mutants did not produce prominent sclerotia whereas the wildtype WMA1, and the complemented strain, Met1C, both produced normal sized sclerotia after seven days (Figure 5B). These results indicate that SsMet1 is required for sclerotial development in S. sclerotiorum. In addition, the mutants were unable to grow on MM (Figure 6A), suggesting that SsMet1 plays a role in mycelial growth and differentiation.
Chemical complementation assays of SsMet1-deletion mutants. (A) Mycelial growth of WMA1, mutant strains Met1–2 and Met1–4 and complement, Met1C on MM and MM amended with Methionine (1 mM), Homocysteine (0.5 mg/mL), Cysteine (1 mM) and Glutathione (0.5 mg/mL). (B) Colony diameter. A one-way ANOVA in R and the Tukey HSD test were used to determine the significant differences of means from wildtype, WMA1. The means of three replicates are presented and the error bars are standard errors. A significance threshold of 0.05 was used. Signif. codes: *** P < 0.001.
SsMet1 is crucial for stress response in S. sclerotiorum
To investigate the functions of SsMet1 in S. sclerotiorum tolerance to environmental stresses, we observed the growth of wildtype WMA1, complement Met1C, and mutants Met1–2 and Met1–4 strains under conditions of osmotic and oxidative stresses, cell wall-damaging agents and thermal stress. To analyze the growth response associated with exposure to these environmental stressors the four strains were grown on PDA for two days at 22°C and then agar plugs from these 2-day-old cultures were inoculated onto PDA amended with the above listed stress agents stated in the methods section. Colony diameters were measured after three days of inoculation. Compared with the wildtype and complemented strains, Met1–2 and Met1–4 showed increased sensitivity to osmotic stress (reduced radial growth) generated by NaCl (1 M) (P < 0.001) and KCl (1 M) (P < 0.001), and the cell wall stress agent, congo red (0.5 mg/mL) (P < 0.001) (Figures 5A, C). Met1–2 and Met1–4 both exhibited increased sensitivity as shown by reduced growth to oxidative stress generated by H_2_O_2_ (10 mM) (P < 0.001), CFW (0.5 g/liter) (P < 0.001) and sorbitol (1 M) (P < 0.05) (Figures 5A, C). After fifteen days, the mutants were able to grow their mycelial to the edge of the PDA plate amended with H_2_O_2_. The initial growth size (measured after three days) for the SsMet1-deletion mutants was 1 mm and after 15 days the growth size increased to 82 mm. This increase in growth may be due to the instability of H_2_O_2_ and the loss of inhibitory effect over time. On exposure to thermal stress, the mutants showed sensitivity to temperatures both lower and higher than the optimal growth temperature of 20 °C (Figure 7A). At 15 °C and 28 °C, both Met1–2 and Met1–4 showed a significant decrease in growth compared to the wildtype after three days (Figure 7B).
Sensitivity of WMA1, mutants Met1–2 and Met1–4 and complement strain Met1C to thermal stress. (A) Comparisons on PDA after incubation at 15, 20, 25 and 28°C for 3 days. (B) Colony diameter of wildtype, WMA1, complement, Met1C and SsMet1-deletion mutant strains Met1–2 and Met1-4. A one-way ANOVA in R and the Tukey HSD test were used to determine the significant differences of means from the wildtype, WMA1. The means of three replicates are presented and the error bars are standard errors. A significance threshold of 0.05 was used. Signif. codes: *** P < 0.001.
Mycelial growth restoration of SsMet1 phenotype
Mycelium viability is very important for S. sclerotiorum growth. Minimal medium (MM) provides the minimal nutrients required for the fungus to grow. The mutants were not able to grow on MM because it lacks methionine. Our results show that in comparison with the wildtype (79.9 mm) and complemented (79.3 mm) strains, the SsMet1-deletion mutants, Met1–2 and Met1–4 were unable to grow on MM (0.0 mm) (Figures 6A, B). Supplementation with methionine (1 mM) and homocysteine (0.5 mg/mL) restored the growth defect of *SsMet1-*deletion mutants, Met1–2 and Met1-4, on MM, although not to wildtype levels. The average mycelial growth for the wildtype, complement and mutants, Met1–2 and Met1–4 on MM amended with methionine were 71 mm, 70.8 mm, 46 mm, 45.6 mm respectively. The average mycelial growth for the wildtype, complement and mutants, Met1–2 and Met1–4 on MM amended with homocysteine were 76.6 mm, 76.5 mm, 46.4 mm, 47.5 mm respectively. Supplementation with cysteine (1 mM) and glutathione (0.5 mg/mL) also partially restored the growth defect of the SsMet1-deletion mutants, (Figures 6A, B). The average mycelial growth for the wildtype, complement and mutants, Met1–2 and Met1–4 on MM amended with cysteine were 75.8 mm, 74.8 mm, 22 mm, 23.9 mm respectively. The average mycelial growth for the wildtype, complement and mutants, Met1–2 and Met1–4 on MM amended with glutathione were 79.3 mm, 78.8 mm, 25 mm, 24.2 mm respectively. These results indicate that SsMet1 is an auxotroph of methionine and methionine is required for processes like the initiation of translation, DNA synthesis, and the utilization of nutrients for optimal growth (Jastrzębowska and Gabriel, 2015).
Discussion
The biosynthesis of methionine
The methionine biosynthesis pathway has been studied in fungi (Saint-Macary et al., 2015; Shao et al., 2016; Gai et al., 2021). The main fungal route of methionine biosynthesis starts from homoserine, a branch point in the aspartate pathway leading to methionine or isoleucine through threonine production (Ejim et al., 2004). L-Homoserine first undergoes O-acetylation catalyzed by L-homoserine transacetylase Met2p. The sulfur atom is then introduced into the rising amino acid chain, either from inorganic sulfide via direct sulfhydrylation or from L-cysteine through the transsulfurylation pathway (Hébert et al., 2011; Kulikova et al., 2019). The sulfhydrylation reaction catalyzed by O-acetylhomoserine(thiol)-lyase Met15p leads to the conversion of O-acetylhomoserine to L-homoserine. Introduction of a sulfur atom through the transsulfurylation pathway requires the participation of two enzymes: cystathionine-γ-synthase (CGS) (Str2p) and cystathionine-β-lyase (Str3p). Str2p utilizes O-acetyl-homoserine and L-cysteine to produce L-cystathionine which, upon the action of cystathionine β-lyase Str3p, is converted to L-homocysteine. Finally, in all fungi, L-homocysteine is S-methylated by methionine synthase Met6p to generate methionine using 5-methyltetrahydrofolate as the methyl donor (Jastrzębowska and Gabriel, 2015; Shao et al., 2016).
SsMet1-deletion mutants are methionine auxotrophic
In this study, we characterized SsMet1, a gene we believe that is implicated in methionine metabolism in S. sclerotiorum. We created SsMet1-deletion mutants, Met1–2 and Met1-4. Methionine is a sulfur containing amino acid and plays a key role in cell proliferation, metabolism, protein synthesis and DNA methylation (Gai et al., 2019). The mutants grew slowly on PDA and were unable to grow on MM and did not produce sclerotia on MM. The sclerotia produced on PDA were abnormally small (Figure 5B). Supplementation with methionine and homocysteine to MM partially rescued the defects in mycelial growth, but not sclerotial development of the *SsMet1-*deletion mutants. These results indicate that the SsMet1-deletion mutants Met1–2 and Met1–4 are methionine auxotrophic, thus SsMet1 is required for the regulation of cellular processes in S. sclerotiorum which includes amino acid biosynthesis and formation, and transferase activity. Thus, SsMet1 is important for growth, pathogenicity, stress response and long-term survival. SsMet1 is an orthologue of BcStr2 found in B. cinerea. The Str2 gene encodes a cystathionine γ‐synthase (CGS) that is a key enzyme in methionine biosynthesis in Saccharomyces cerevisiae. Therefore, CGS has been regarded as an attractive target for fungicide discovery (Leroux et al., 2002).
SsMet1 is necessary for virulence of Sclerotinia sclerotiorum
The Met1–2 and Met1–4 mutants were avirulent on detached bean leaves. This behavior is like that reported for the ΔBcStr2 mutant in B. cinerea, which exhibited decreased virulence on host plants (Shao et al., 2016). Gai et al. (2021) showed that AaMetB, AaMetC, and AaMetX are required for full virulence in A. alternata. The defects in virulence of the Met1–2 and Met1–4 mutants on detached bean leaves were also restored by exogenous supply of methionine as reported by Gai et al. (2021). This suggests that SsMet1 is essential for virulence of S. sclerotiorum.
SsMet1 is required for sclerotial formation of S. sclerotiorum
The Met1–2 and Met1–4 mutants were also unable to produce prominent sclerotial development. These results are consistent with ΔBcStr2, which exhibited decreased conidiation and impaired sclerotial development (Shao et al., 2016), whereas in A. alternata, mutants AaMetB/MetC/MetX showed defects in conidiation. We were able to restore the virulence of Met1–2 and Met1–4 by adding exogenous methionine to MM, but sclerotial development was not restored using the same method. This suggests that virulence and sclerotial development can be controlled by separate downstream factors.
SsMet1-deletion mutants are more sensitive to stresses
The Met1–2 and Met1–4 mutants in the present study showed increased sensitivity to all environmental stresses. Both mutants grew slowly on sorbitol medium than the wildtype and complement strains but produced large sclerotia on PDA plates amended with 1 M sorbitol (Figure 5B), suggesting that exposure to sorbitol does not induce oxidative stress in these mutants to the point of not being able to produce resting structures. The mutants were not able to produce prominent sclerotia on PDA alone so the addition of sorbitol to PDA somehow reversed those effects. Growth was significantly reduced on PDA amended with H_2_O_2_ in the first 7 days, but both mutants were able to recover from the exposure to this H_2_O_2_ exposure and grow fully (15 days post inoculation), likely because H_2_O_2_ became ineffective with increased incubation time due to its short half-life. In addition, the deletion mutants, Met1–2 and Met1–4 were not able to produce sclerotia in the H_2_O_2_-amended medium. AaMetR was primarily sensitive to H_2_O_2_ and many reactive oxygen species (ROS)-generating compounds (Gai et al., 2021). The inactivation of MetR in A. alternata resulted in severe inhibition of methionine synthesis and increased sensitivity to H_2_O_2_ (Gai et al., 2021). In addition, ΔBcStr2, showed increased sensitivity to osmotic and oxidative stresses, cell-wall damaging agents and thermal stress (Shao et al., 2016). These results indicate that the SsMet1-deletion mutants were extremely affected by the environmental stressors and perhaps SsMet1 is essential for ROS tolerance. The knockout and replacement of SsMet1 has resulted in methionine metabolism being blocked. This can possibly affect the biosynthesis and expression of other metabolism related genes (Gai et al., 2021). In addition, SsMet1 may interact with the genes that play a key role in cell wall synthesis and integrity, osmotic stress, and oxidative stress.
Methionine and homocysteine amendments were able to restore growth of the mutants on MM, but not to wildtype levels. Methionine supplementation to MM was able to restore virulence to the Met1–2 and Met1–4 mutants on detached bean leaves. In the research conducted by Das et al. (2024) exogenous methionine restored disease infection on rice and facilitated growth of Rs_MET13‐silenced Rhizoctonia solani gene in the presence of MM amended with 10 mM of H_2_O_2._ Homocysteine can be converted back to methionine through a process requiring folate, vitamin B12 and methionine synthase (McCaddon and Miller, 2023) and thus homocysteine was able to restore growth of the mutants to the same level as methionine on MM. We infer that homocysteine can also restore virulence to the SsMet1-deletion mutants. Glutathione and cysteine restored mycelial growth of the SsMet1-deletion mutants partially and in comparison to methionine and homocysteine, it was nearly 50% less after three days. Cysteine and glutathione cannot be converted back to methionine, resulting in poor growth restoration of the SsMet1-deletion mutants on MM. This slow rate of growth does indicate to us that virulence would be affected negatively and not be restored. This growth and virulence restoration indicates Met1–2 and Met1–4 are methionine auxotrophic mutants. In A. alternata, exogenous cysteine restored the growth and virulence defects of AaMetR suggesting that AaMetR is essential for cysteine biosynthesis (Gai et al., 2021). SsMet1 is required for methionine synthesis and its deletion may prevent the initiation of other metabolic pathways such as cysteine biosynthesis due to it being described as a pyridoxal phosphate-dependent enzyme involved in Cys/Met metabolism (Martin et al., 2023). For SsMet1 to be involved in Cys/Met metabolism (Martin et al., 2023), this allosteric dependence needs further investigation. In the transsulfuration pathway, homocysteine is converted to cysteine. Cysteine is then used to build glutathione. It is also important to note that fungi also have an alternative pathway (DUG pathway) to generate cysteine by degrading glutathione. In S. sclerotiorum, there are two genes, SS1G_04565 and SS1G_02111, related to the DUG pathway, DUG1 and DUG2 respectively. There is a possibility that the function of these genes can be dependent on SsMet1 and in the absence of SsMet1, growth is not fully restored in the presence of exogenous cysteine and glutathione.
Conclusion
Overall, we infer that methionine synthesis interacts with various biochemical pathways in S. sclerotiorum. The deletion of SsMet1 demonstrated its role in growth, virulence, sclerotial development, and is important for the response to environmental stresses. SsMet1 is a potential antifungal drug target in S. sclerotiorum. The Str2 gene encodes a cystathionine γ‐synthase (CGS) that is a key enzyme in methionine biosynthesis in Saccharomyces cerevisiae. Therefore, CGS has been regarded as an attractive target for fungicide discovery. Further analysis can be done on the mutants for their sensitivity to fungicides. CGS is a proposed target of anilinopyrimidine (AP) fungicides (Leroux et al., 2002).
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Adams P. B.Ayers W. A. (1979). Ecology of Sclerotinia species. Phytopathology 69, 896–898. doi: 10.1094/Phyto-69-896 · doi ↗
- 2Boland G. J.Hall R. (1994). Index of plant hosts of Sclerotinia sclerotiorum . Can. J. Plant Pathol. 16, 93–108. doi: 10.1080/07060669409500766 · doi ↗
- 3Bolton M. D.Thomma B. P. H. J.Nelson B. D. (2006). Sclerotinia sclerotiorum (Lib.) de Bary: Biology and Molecular Traits of a Cosmopolitan Pathogen. Mol. Plant Pathol. 7, 1–16. doi: 10.1111/j.1364-3703.2005.00316.x 20507424 · doi ↗ · pubmed ↗
- 4Brooks K. D.Bennett S. J.Hodgson L. M.Ashworth M. B. (2018). Narrow Windrow Burning Canola (Brassica napus L.) Residue for Sclerotinia sclerotiorum (Lib.) de Bary Sclerotia Destruction. Pest Manage. Sci. 74, 2594–2600. doi: 10.1002/PS.5049 29687565 · doi ↗ · pubmed ↗
- 5Choi I. Y.Kim J.Lee W. H.Cho S. E.Shin H. D. (2017). First report of Sclerotinia stem rot caused by Sclerotinia sclerotiorum on Chinese chives in Korea. Plant Dis. 101, 1953. doi: 10.1094/PDIS-04-17-0587-PDN · doi ↗
- 6Das J.Ghosh S.Tyagi K.Sahoo D.Jha G. (2024). Methionine biosynthetic genes and methionine sulfoxide reductase A are required for Rhizoctonia solani AG 1-IA to cause sheath blight disease in rice. Microbial Biotechnol. 17(4), 1–12. doi: 10.1111/1751-7915.14441 PMC 1099004638568774 · doi ↗ · pubmed ↗
- 7Ejim L.Mirza I. A.Capone C.Nazi I.Jenkins S.Chee G. L.. (2004). New phenolic inhibitors of yeast homoserine dehydrogenase. Bioorganic Medicinal Chem. 12, 3825–3830. doi: 10.1016/j.bmc.2004.05.009 15210149 · doi ↗ · pubmed ↗
- 8Fritz R.Lanen C.Colas V.Leroux P. (1997). Inhibition of methionine biosynthesis in Botrytis cinerea by the anilinopyrimidine fungicide pyrimethanil. Pesticide Sci. 49, 40–46. doi: 10.1002/(SICI)1096-9063(199701)49:1<40::AID-PS 470>3.0.CO;2-Y · doi ↗