Functional roles of LaeA, polyketide synthase, and glucose oxidase in the regulation of ochratoxin A biosynthesis and virulence in Aspergillus carbonarius

Abstract Aspergillus carbonarius is the major producer of ochratoxin A (OTA) among Aspergillus species, but the contribution of this secondary metabolite to fungal virulence has not been assessed. We characterized the functions and addressed the roles of three factors in the regulation of OTA synthesis and pathogenicity in A. carbonarius: LaeA, a transcriptional factor regulating the production of secondary metabolites; polyketide synthase, required for OTA biosynthesis; and glucose oxidase (GOX), regulating gluconic acid (GLA) accumulation and acidification of the host tissue during fungal growth. Deletion of laeA in A. carbonarius resulted in significantly reduced OTA production in colonized nectarines and grapes. The ∆laeA mutant was unable to efficiently acidify the colonized tissue, as a direct result of diminished GLA production, leading to attenuated virulence in infected fruit compared to the wild type (WT). The designed Acpks‐knockout mutant resulted in complete inhibition of OTA production in vitro and in colonized fruit. Interestingly, physiological analysis revealed that the colonization pattern of the ∆Acpks mutant was similar to that of the WT strain, with high production of GLA in the colonized tissue, suggesting that OTA accumulation does not contribute to A. carbonarius pathogenicity. Disruption of the Acgox gene inactivated GLA production in A. carbonarius, and this mutant showed attenuated virulence in infected fruit compared to the WT strain. These data identify the global regulator LaeA and GOX as critical factors modulating A. carbonarius pathogenicity by controlling transcription of genes important for fungal secondary metabolism and infection.


| INTRODUC TI ON
Aspergillus species are widespread fungal pathogens in nature, exhibiting a saprophytic lifestyle in the soil and on a wide range of substrates, including foods and feeds. Several species are among the typical pathogens of harvested fruit and vegetables (Barkai-Golan, 2001). Most Aspergillus species occur in foods as spoilage or biodeterioration fungi (Hocking, 2007). Black Aspergillus species appear to be secondary invaders, following other fungal pathogens and insects that produce mechanical damage on fruit tissues (Varga and Kozakiewicz, 2006). Aspergillus carbonarius is frequently responsible for the postharvest decay of various fresh fruit, including grapes, peaches, pears, citrus, and nectarines, as well as grains, coffee, and nuts. Windborne spores from the soil are deposited onto the surface of those fruit (Battilani et al., 2006). The fungus frequently penetrates the commodities through harvesting wounds and bruises, or damage caused by preharvest rain, mechanical impact, and insects.
A. carbonarius is associated with maturing fruit and is responsible for a large portion of the economic losses sustained during storage and shipment. In addition to its saprophytic colonization, the pathogen is also the main producer of ochratoxin A (OTA) in grapes, dried vine fruit, and wine, especially in Mediterranean countries (Covarelli et al., 2012;Gil-Serna et al., 2018a). OTA is a potent nephrotoxin with carcinogenic, teratogenic, and immunotoxic properties in animals and possibly humans. There are several major parameters governing fungal growth and OTA production; some of them are intrinsic factors such as water availability, pH, and the composition of the substrate, and others are extrinsic factors such as temperature, moisture, and the competitive endogenous microbiota (Bellí et al., 2004;Lasram et al., 2010;Mitchell et al., 2004). Not much is known about the specific factors contributing to A. carbonarius colonization in fruit. Maor et al. (2017) demonstrated that ambient pH plays an important role in A. carbonarius pathogenicity and OTA biosynthesis. Secretion of gluconic acid (GLA) by A. carbonarius caused direct acidification of fruit tissue and induced OTA accumulation in colonized grapes (Maor et al., 2017). Previous findings have indicated that acidification of the apple fruit host environment through secretion of organic acids enhances the activation of pathogenicity factors, maceration, and colonization of the fruit by Penicillium expansum (Barad et al., 2012;Prusky et al., 2004). However, it is not clear if the similar acidification process induced during A. carbonarius infection contributes only to OTA production, the colonization process by the pathogen, or both.
Many studies have shown the involvement of global transcription factors in the regulation of secondary metabolite biosynthesis in filamentous fungi, most predominantly LaeA (Bok and Keller, 2004).
This transcription factor was first identified in Aspergillus nidulans, but is now known to be conserved in all filamentous ascomycetes (Jain and Keller, 2013). LaeA has been found to be a positive regulator of most common mycotoxins, including sterigmatocystin (Bok and Keller, 2004), aflatoxin (Kale et al., 2008), fumonisin (Butchko et al., 2012), cyclopiazonic acid (Georgianna et al., 2010), trichothecenes (Kim et al., 2013), citrinin, patulin (Kumar et al., 2018;Liu et al., 2016), and OTA (Crespo-Sempere et al., 2013). In A. carbonarius, much work has been carried out to understand the biosynthetic pathway and accumulation of OTA (Gallo et al., 2009(Gallo et al., , 2012(Gallo et al., , 2014 Disruption of AclaeA, Acpks, and Acgox genes was confirmed by several PCR analyses for introduction of the hygromycin-resistance gene-coding sequence, correct genomic placement of the 5′ and 3′ flanking sequences, and absence of the selected gene sequences (Figures S1b,S2b,and S3b). None of the ∆AclaeA, ∆Acpks, or ∆Acgox mutants showed expression of AclaeA, Acpks, or Acgox, respectively, compared to the WT strain (Figures S1c, S2c, and S3c) when grown in yeast extract sucrose (YES) medium. One of each of the validated ∆AclaeA, ∆Acpks, and ∆Acgox deletion strains were used for the following experiments. Physiological analysis of the ΔAclaeA mutant revealed that compared to the WT strain, its growth was not affected on YES synthetic medium at pH 4.0 (Figures S5 and S6a). However, loss of the laeA gene resulted in a significant reduction in conidial production as compared to the WT at all examined time points (Figures S5 and S6b). Conidial germination in the ΔAclaeA mutant strain was delayed compared to that of the WT, although 100% germination of the former conidia was observed following 8 hr of incubation ( Figure S6c).

| Loss of AcLaeA affects fruit colonization
These results indicate that AcLaeA is important for sporulation and conidial germination, and plays a significant role in A. carbonarius pathogenicity.

| AcLaeA regulates OTA biosynthesis and GLA production
Our findings indicated that inactivation of the laeA gene results in almost complete inhibition of OTA production by A. carbonarius in YES agar medium ( Figure S7). Analysis of OTA accumulation in the colonized nectarine and grape berry tissues 5 days after inoculation revealed a drastic reduction in OTA biosynthesis, from 2,041/534 ng/g by the WT strain to 3.45/17.4 ng/g by the ΔAclaeA mutant, respectively (Figures 1c and S4c). Moreover, we investigated the differential expression of all five OTA-biosynthesis cluster genes (bZIP transcription factor, pks, nonribosomal peptide synthetase [nrps], p450, and halogenase [hal]) in ΔAclaeA and WT strains during fruit infection.
The transcript levels of the five genes were down-regulated in nectarines infected with the ΔAclaeA mutant compared to the fruit colonized with the WT strain ( Figure 1d). This suggests that AcLaeA is essential for OTA production and is directly involved in regulating transcription of the genes in the OTA biosynthesis pathway.
To gain an understanding of the potential mechanism underlying the reduced pathogenicity of the ΔAclaeA strain, the mutant was assessed for some physiological characteristics that have been linked with virulence in this pathogen. We previously reported that one of the factors contributing to the pathogenicity of A. carbonarius is its ability to reduce the pH of infected fruit tissue through the production of GLA (Barda et al., 2020;Maor et al., 2017). Indeed, 5 days after inoculation, colonization of nectarine tissue by the A. carbonarius WT strain reduced the pH from 3.53 in the healthy part of the fruit to 3.16 in the decayed tissue, whereas the ΔAcleaA mutant led to a minimal pH reduction to 3.43 ( Figure 2a). Acidification of the rotten tissue by the WT strain was accompanied by the accumulation of 4.06 mg/g of GLA ( Figure 2b). In contrast, reduced GLA formation was observed in nectarines colonized by the ΔAcleaA strain (2.81 mg/g; Figure 2b). Given that GLA production requires GOX F I G U R E 1 AcLaeA is required for Aspergillus carbonarius pathogenicity and ochratoxin A (OTA) production in nectarines. (a) Disease symptoms on nectarine fruits inoculated with conidia of wild-type (WT) and ΔAclaeA strains. (b) Histogram showing the decay area of the rotten tissue on infected nectarines. (c) OTA accumulation in the nectarine tissue and (d) relative expression of OTA cluster genes in WT and ΔAclaeA strains. RNA was extracted from infected nectarines at day 5 postinoculation. Relative expression was normalized using β-tubulin as an internal control. Error bars represent standard error of three independent biological replicates. Different letters above the columns indicate statistically significant differences at p < .05 as determined using the Tukey's honestly significant difference test. Asterisks denote significant differences between strains at p < .05 enzyme activity, the observed 3-fold down-regulation of Acgox gene expression in the ΔAcleaA strain could explain the decreased GLA accumulation (Figure 2c). Similarly, during colonization of grape berries, the ΔAclaeA mutant showed poor GLA accumulation compared to the WT strain ( Figure S4d,e). These results indicate that AcLaeA may also regulate A. carbonarius pathogenicity through acidification of the ambient environment by the secretion of organic acids.

| OTA accumulation does not contribute to A. carbonarius pathogenicity
To explore the role of OTA in the pathogenicity of A. carbonarius, the Acpks gene encoding a PKS protein in the OTA cluster was disrupted using the gene-replacement strategy and Agrobacteriummediated transformation described in section 2.1 ( Figure S2). PKS is considered a key component of the OTA biosynthesis pathway (Moss, 1998). The Acpks-knockout mutant was unable to produce detectable OTA in agar medium, or in colonized fruit, as determined by HPLC analysis (Figures 3a, S8a, and S9a). The loss of Acpks re- Taken together, these results suggest that the fungus' inability to produce OTA does not affect its pathogenicity.

| AcGOX is required for A. carbonarius pathogenicity in deciduous fruit
Next, we investigated the role of Acgox in A. carbonarius pathogenesis. Deletion of Acgox completely eliminated GLA formation by A. carbonarius, both in vitro and in fruit (Figures 5a, S11a, and S12a). Quantitative reverse transcription PCR (RT-qPCR) analysis showed lack of Acgox expression in the mutant strain, confirming the loss of this gene ( Figure 5b). As shown in Figures 6a,b and S11b,c, Acgox disruption resulted in a significant reduction of decay development in nectarines and grape berries; the rotten area caused by ΔAcgox was about 10% and 18% smaller, respectively, F I G U R E 2 AcLaeA-associated regulation of gluconic acid (GLA) accumulation in colonized nectarines. (a) The pH of nectarine tissue, (b) GLA accumulation, and (c) Acgox relative expression were measured in fruits infected with the wild-type (WT) and ΔAclaeA strains at day 5 postinoculation. Error bars represent standard error of three independent biological replicates. Different letters above the columns indicate statistically significant differences at p < .05 as determined using the Tukey's honestly significant difference test. Asterisks denote significant differences between strains at p < .05 than that caused by the WT strain on day 5 postinoculation. The WT A. carbonarius showed a pH reduction from 3.83 in the healthy part of the fruit to 3.1 and 2.46 in the decayed parts of the nectarines and grape berries, respectively (Figures 5c and S11d). This additional acidification of the rotten tissues was accompanied by GLA accumulation of 2.39 and 3.34 mg/g in the nectarines and grape berries, respectively (Figures 5a and S11a). Interestingly, despite its inability to produce GLA, the ΔAcgox strain showed a reduction in pH in the inoculated fruit that was similar to that of the showing the decay area of the rotten tissue on infected nectarines. RNA was extracted from infected nectarines at day 5 postinoculation. Relative expression was normalized using β-tubulin as an internal control. Error bars represent standard error of three independent biological replicates. Different letters above the columns indicate statistically significant differences at p < .05 as determined using the Tukey's honestly significant difference test. Asterisks denote significant differences between strains at p < .05

| D ISCUSS I ON
Among the OTA-producing fungi, A. carbonarius is considered the major source of OTA contamination of a variety of fruit, especially grapes and their derived products (Battilani et al., 2006;Perrone et al., 2007). OTA has raised significant public concern worldwide and consequently has impacts on trade, as well as human and ani- The question that arose here was whether the reduced pathogenicity of the ∆AclaeA mutant is due to the decline in OTA accumulation or repressed tissue acidification.
The biological role of fungal secondary metabolites has not been elucidated, but in some studies mycotoxins have been shown to contribute to the pathogenicity of several fungi. Fusarium-produced toxins, such as deoxynivalenol and nivalenol, have been shown to be involved in the virulence of Fusarium graminearum toward wheat, F I G U R E 4 Effect of AcPKS on gluconic acid (GLA) production in colonized nectarines. (a) The pH of nectarine tissues, (b) GLA accumulation, and (c) Acgox relative expression were measured in fruits infected with the wild-type (WT) and ΔAcpks strains at day 5 postinoculation. Error bars represent standard error of three independent biological replicates. Different letters above the columns indicate statistically significant differences at p < .05 as determined using the Tukey's honestly significant difference test. Asterisks denote significant differences between strains at p < .05 maize, and barley (Boddu et al., 2007;Maier et al., 2006;Proctor et al., 2002). Several studies have demonstrated OTA phytotoxicity on the plant model organism Arabidopsis thaliana, and suggested that this toxin plays a role in the aetiology of plant diseases (Peng et al., 2010;Wang et al., 2012). Those studies indicated that OTA causes a rapid hypersensitive response and induces necrotic lesions in host leaf tissues. Exposure to OTA stimulated an oxidative burst in the plant, which resulted in a significant increase in reactive oxygen species and enhanced antioxidant enzyme defence responses, leading to plant cell death (Peng et al., 2010;Wang et al., 2012).
However, the results obtained from the current work clearly show that OTA is not associated with fungal disease development in fruit.
The deletion of Acpks in A. carbonarius, a key gene in the OTA cluster involved in OTA biosynthesis, did not affect fungal virulence on the colonized fruit (Figures 3 and S8). Similar findings have been reported in recently published studies, where deletion of patL and patK genes, encoding specific regulatory factors of the patulin-biosynthesis pathway and PKS, respectively, did not affect P. expansum virulence and demonstrated that patulin is not required by the fungus to infect apples (Ballester et al., 2015;Li et al., 2015). Interestingly, a study using a patL-knockout mutant also demonstrated that patulin is not required by P. expansum to colonize apples, but acts as a cultivar-dependent aggressiveness factor (which describes the severity of disease) (Snini et al., 2016). Given that the experiments in the current study on the involvement of OTA in the pathogenicity of A. carbonarius were conducted only on specific nectarine (Sun Snow) and grape (Zani) varieties, it is possible that OTA acts as a virulence factor in a host-dependent manner.
Our previous studies indicated that GOX, which is essential for GLA production and acidification during fruit colonization, is important for A. carbonarius pathogenicity (Barda et al., 2020;Maor et al., 2017). GOX has been reported as a virulence factor in P. expansum (Barad et al., 2012;Chen et al., 2018). Down-regulated expression of the GOX-encoding gene gox2 reduces the infection process in the fruit, resulting in a decrease in disease incidence of P. expansum. To confirm involvement of GLA in A. carbonarius virulence, the Acgox gene was disrupted. Deletion of Acgox resulted in complete inhibition of GLA formation and led to a reduction in virulence toward nectarine and grape fruit (Figures 6 and S11), further indicating that GOX is a virulence factor of A. carbonarius. It should be noted that the inoculated fruit were acidified to a similar extent by both the ΔAcgox mutant and the WT strain. The acidification by the former could be explained by its ability to pro- OTA cluster genes in WT and ΔAcgox strains. RNA was extracted from infected nectarines at day 5 postinoculation. Relative expression was normalized using β-tubulin as an internal control. Error bars represent standard error of three independent biological replicates. Different letters above the columns indicate statistically significant differences (p < .05) as determined using the Tukey's honestly significant difference test. Asterisks denote significant differences between strains at p < .05 (Student's t test) F I G U R E 7 LaeA and GOX regulate the expression of cell-wall degrading enzymes in Aspergillus carbonarius. Relative expression of cellwall degrading genes in wild-type (WT), ΔAclaeA, and ΔAcgox strains. RNA was extracted from infected nectarines 5 days postinoculation. Error bars represent standard error of three independent biological replicates. Different letters denote significant differences between the strains (p < .05) it is worth mentioning that in our study, despite the lack of GLA production, the reduction in pathogenicity of the A. carbonarius Δgox mutant was minor relative to that observed with the ΔAclaeA mutant.
Cell wall-degrading enzymes are known to contribute to the pathogenicity of fungal plant pathogens (ten Have et al., 2002).
A number of transcription factors regulating fungal virulence and secondary metabolism in filamentous fungi have been identified to control the expression of genes encoding plant cell wall-degrading enzymes. The influence of the carbon catabolite repressor protein (CreA) on the plant cell wall-degrading enzymes of several Aspergillus species has been extensively studied. In those species, CreA has been reported to act as a negative regulator of genes encoding arabinases, several endoxylanases, and pectinolytic enzymes (Bussink et al., 1991;Kester et al., 1996;Orejas et al., 1999;Ruijter et al., 1997). creA mutant strains of A. nidulans and Aspergillus niger displayed (partially) derepressed phenotypes (Ruijter et al., 1997;Shroff et al., 1997). The pH-regulatory protein PacC has also been shown to be involved in controlling genes encoding cell wall-degrading enzymes. Alkaline-and acidic-mimicking A. nidulans pacC mutants showed that the major arabinofuranosidase-encoding gene, abfB, and two genes encoding xylanases, xlnA and xlnB, are regulated by the PacC transcription factor (Gielkens et al., 1999;MacCabe et al., 1998). A recent study has suggested that PacC contributes to the pathogenesis of A. carbonarius through regulation of cell wall-degrading enzymes during fruit colonization (Barda et al., 2020). In the present study, LaeA positively regulated the expression of most of the tested genes encoding cell wall-degrading enzymes in A. carbonarius (Figure 7).
These results were in agreement with previous reports on the interaction of an endophytic fungus Epichloë festucae with perennial ryegrass, which suggested a regulatory role for LaeA in the expression of genes for plant cell wall degradation (Rahnama et al., 2019(Rahnama et al., , 2020. We assume that the deletion of AclaeA could affect A. carbonarius pathogenicity through down-regulation of the cell wall-degrading enzymes, including cellulases, hemicellulases, and pectolytic enzymes. Another key factor contributing to fungal pathogenicity in colonized fruit, GOX, has been reported to induce transcript levels of pmpg1 (encoding endopolygalacturonase) in Phomopsis mangiferae during colonization of grapes (Davidzon et al., 2010). In the current work, using the ∆Acgox mutant strain, a number of cell wall-degrading enzyme-encoding genes were shown to be regulated by GOX, although we found evidence of weaker repression of these genes in ∆Acgox compared to the ∆AcleaA-knockout strain (Figure 7).
The results of this study strongly suggest that the global regulator of secondary metabolites, LaeA, contributes to A. carbonarius pathogenicity. We showed that Acgox, which is essential for GLA production and acidification during fruit colonization, is significantly down-regulated in the ΔAclaeA mutant, suggesting that LaeA governs A. carbonarius pathogenicity through regulation of the expression of Acgox. Deletion of the Acgox gene in A. carbonarius led to a reduction in virulence toward grapes and nectarine fruit, further indicating that GOX is a virulence factor of A. carbonarius and that its expression is regulated by LaeA. It is also clear from the present data that, similar to other mycotoxins assessed to date, LaeA is a positive regulator of OTA biosynthesis both in vitro and during fruit colonization. However, our study clearly demonstrates that OTA accumulation does not contribute to the pathogenicity of A. carbonarius in grapes and nectarine fruit. The ΔAcpks mutant, which is unable to produce OTA, induced disease in fruit cultivars in a manner similar to the WT strain. Although some progress has been achieved toward understanding the mecha-

| Fungal strains and culture conditions
A. carbonarius isolate NRRL 368 was obtained from the USDA Agricultural Research Service Culture Collection. This WT strain was used to generate all derivative mutants described in the following section. Cultures were grown at 28 °C in the dark and maintained on potato dextrose agar (PDA; Becton Dickinson). Conidia were harvested using 5 ml of sterile distilled water and filtered through a 40-µm cell strainer (Biologix) to remove hyphae. Cells were visualized with a BH-2 series microscope (Olympus) and adjusted to the indicated concentrations using a haemocytometer.

| Construction of plasmids and knockout strains
The AclaeA, Acpks, and Acgox deletion vectors were generated using hygromycin B as a selectable marker. For each gene-replacement plasmid, the target gene's genomic flanking regions were PCRamplified using specific primer pairs that incorporated a single 2-deoxyuridine nucleoside near the 5′ ends. Both DNA fragments and the predigested pRFHU2 binary vector (Frandsen et al., 2008) were mixed together and treated with the USER enzyme (New England Biolabs) to obtain the deletion vector. An aliquot of the mixture was used directly for chemical transformation of high-efficiency Escherichia coli DH5α cells (New England Biolabs) without prior ligation. Kanamycin-resistant transformants were screened by PCR for validation of proper fusion events. The plasmid was then introduced into electrocompetent A. tumefaciens AGL-1 cells.

| Physiological analysis of A. carbonarius strains
Both vegetative growth and sporulation of each of the knockout and WT strains were assessed on YES agar (20 g Bacto yeast extract, 150 g sucrose, 15 g Bacto agar per litre) adjusted with HCl to pH 4, whereas germination assays were performed in YES broth (20 g Bacto yeast extract and 150 g sucrose per litre) adjusted to pH 4.
To measure the radial mycelial growth, agar plates were pointinoculated with 10 2 spores of each strain and incubated at 28 °C.
Radial growth was monitored by diameter measurements on a daily basis up to 7 days using three replicate plates per strain.
To quantify total conidia produced by the various strains, agar plates containing 10 5 spores were incubated at 28 °C in the dark.
To accurately count conidia, two 1-cm plugs from each plate were homogenized in 3 ml of 0.01% Tween 20 in water, diluted, and counted with a haemocytometer. Conidial production was quantified starting at 24 hr postinoculation using three replicate plates per strain.
Germination assays were performed in sterile 24-well culture plates (SPL Life Sciences). The spore concentration of all strains was adjusted to 10 4 spores/ml in the medium, and 0.5 ml of each spore suspension was distributed into three replicate wells. Time-course microscopy was carried out over 24 hr at 28 °C using an Eclipse Ti inverted microscope (Nikon). The germination rate was monitored regularly by capturing images of each well at 1-hr intervals. The number of spore germlings was counted for each strain and recorded.
The percentage of germinated spores was plotted against time, and the germination rates were determined.

| OTA and organic acid accumulation
A 100 µl suspension of 10 6 fungal spores/ml was inoculated onto 55-mm Petri dishes containing 10 ml of YES agar adjusted to pH 4.
The plates were incubated at 28 °C in the dark for up to 10 days as needed for sample collection.
To assess organic acid production, five 1-cm diameter discs of agar were placed in 5 ml of sterilized water and crushed to homogeneity. A 1-ml aliquot of the solution was sampled in a 1.5-ml microcentrifuge tube and centrifuged for 10 min at 20,800 × g. The supernatant was taken for GLA and citric acid analyses using test kits that apply enzymatic methods for the specific measurement of total d-gluconic acid and citric acid contents (Megazyme) according to the manufacturer's instructions. The final pH was measured directly in the agar cultures with a double-pore slim electrode connected to a Sartorius PB-11 Basic Meter.
To evaluate OTA levels, five 1-cm diameter discs of agar were added to 1.7 ml of HPLC-grade methanol (Bio-Lab) and crushed to homogeneity. OTA was extracted by shaking for 30 min at 150 rpm on an orbital shaker and centrifuged for 10 min at 20,800 × g.
The supernatant was filtered through a 0.22-µm PTFE syringe filter (Agela Technologies) and kept at −20 °C prior to HPLC analysis. OTA was quantitatively analysed by injection of 20 µl into a reversed-phase UHPLC system (Waters ACQUITY Arc, FTN-R). The mobile phase consisted of acetonitrile:water:acetic acid (99:99:2, vol/vol/vol) at 0.5 ml/min through a Kinetex 2.6 µm XB-C18 (100 × 2.1 mm) with a security guard C18 column (4 × 2 mm) (Phenomenex). The column temperature was maintained at 30 °C. The OTA peak was detected with a fluorescence detector (excitation at 330 nm and emission at 450 nm) and quantified by comparing with a calibration curve of the standard mycotoxin (Fermentek).

| Colonization and virulence assessment of A. carbonarius strains
Zani seedless grapes and Sun Snow nectarines were obtained from a local supermarket. Fruit surfaces were sterilized in 1% sodium hypochlorite solution for 1 min and immediately rinsed in sterile distilled water. A 10-µl spore suspension containing 10 6 spores/ml of either the WT or the knockout strains was injected directly into the sterilized fruit at 2 mm depth. Following inoculation, the fruit were incubated under high humidity at 28 °C for 2-7 days as needed for symptom monitoring and sample collection. The area of the necrotic lesions was recorded daily. The pH of nectarine and grape berry tissues was measured by inserting the double-pore slim electrode connected to the Sartorius PB-11 Basic Meter directly into the tested area.
To analyse the GLA content of the inoculated fruit, 1.7 g of the macerated necrotic area was homogenized in 5 ml sterilized water. A 1-ml aliquot of the solution was sampled in a 1.5-ml microcentrifuge tube and centrifuged for 10 min at 20,800 × g, and the amount of GLA produced was measured as described above (section 4.4).
For OTA analysis in colonized grapes and nectarines, 1.7 g of the macerated necrotic area was homogenized in 1.7 ml of HPLC-grade methanol. Then, OTA was quantitatively analysed as described above (section 4.4).

| RNA isolation and RT-qPCR analysis of gene expression
Mycelia grown on agar plates were harvested on day 5 postinoculation, frozen in liquid nitrogen, lyophilized for 24 hr, and kept at −80 °C until use. In colonized nectarines, mycelium-containing exocarp (peel) was removed on day 5 postinfection, frozen in liquid nitrogen, lyophilized for 24 hr, and kept at −80 °C prior to RNA extraction. Total RNA was extracted from 100 mg of lyophilized tissue of the selected samples using the Hybrid-R RNA isolation kit PCR conditions were as follows: 95 °C for 20 s, followed by 40 cycles of 95 °C for 3 s and 60 °C for 20 s. The expression of the genes analysed in this work was quantified using RT-qPCR optimization protocols (standard curve, amplification efficiency, correlation coefficient, and dissociation curve) that were previously developed by Gil-Serna et al. (2018b). The samples were normalized using β-tubulin as the endogenous control and the relative expression levels were measured using the 2 (−ΔΔCt) analysis method. Results were analysed with StepOne v. 2.3 software. The primers used for the RT-qPCR analyses are listed in Table S2.

| Statistical analysis
Student's t test was performed when data were normally distributed and the sample variances were equal. For multiple comparisons, one-way analysis of variance (ANOVA) was performed when the equal variance test was passed. If one-way ANOVA reported a p value of <.05, further analyses were performed using Tukey's singlestep honestly significant difference test to determine significant differences between the strains. All experiments described here are representative of at least three independent experiments with the same patterns of results.

ACK N OWLED G M ENTS
This study was supported by a grant (2432/18) from the Joint Israel Science Foundation (ISF) and the National Natural Science Foundation of China (NSFC) Research Program.

DATA AVA I L A B I L I T Y S TAT E M E N T
The data that support the findings of this study are available from the corresponding author upon reasonable request.