Omics for understanding synergistic action of validamycin A and Trichoderma asperellum GDFS1009 against maize sheath blight pathogen

Sheath blight, causes by Rhizoctonia spp., threaten maize yield every year throughout the world. Trichoderma could degrade Rhizoctonia solani on maize mainly via competition and hyperparasitism, whereas validamycin A could efficiently inhibit the growth of R. solani via disturbing the energy system. By contrast, validamycin A is efficient but it takes effect in a short period, while Trichoderma takes effect in a long period though time-consuming. To overcome the disadvantages, Trichoderma asperellum GDFS1009 was used together with validamycin A. In vitro tests proved that the combined pathogen-inhibiting efficiency was significantly improved. Furthermore, results based on transcriptome and metabolome showed that validamycin A had no significant effects on growth, basic metabolism and main bio-control mechanisms of T. asperellum GDFS1009. Such few impacts may be attributed to detoxification and tolerance mechanism of T. asperellum GDFS1009. In addition, T. asperellum GDFS1009 has an ability to relieve the stress caused by validaymicn A. Meanwhile, liquid chromatography-mass spectrometry (LC-MS) results showed that only minor degradation (20%) of validamycin A was caused by T. asperellum GDFS1009 during cofermentation. All results together provide solid bases for validamycin A synergy with T. asperellum GDFS1009 in their combined biocontrol application.


Results
The synergistic antibiotic effect of validamycin A and T. asperellum GDFS1009 on sheath blight. After incubation for 1 d, validamycin A could be efficiently absorbed by R. solani (R. zeae) and its bacteriostasis was highly significant. At this stage, the colony area of R. solani (R. zeae) was barely 222.34 ± 5.29 mm 2 (357.14 ± 7.25 mm 2 ) in the validamycin A experimental group, while it reached 2544.94 ± 92.13 mm 2 (1893.21 ± 9.55 mm 2 ) in the blank control group. Though T. asperellum GDFS1009 which grew rapidly had a relatively obvious bacteriostatic efficacy, its impact on bacteriostasis was weaker than that of validamycin A. After T. asperellum GDFS1009 experimental treatment, the colony area of R. solani (R. zeae) was 1699.33 ± 14.39 mm 2 (2153.05 ± 62.11 mm 2 ). Furthermore, the synergistic effect of validamycin A combined with T. asperellum GDFS1009 was not present at this stage. The colony area of R. solani (R. zeae) was barely 221.17 ± 11.06 mm 2 (335.92 ± 35.63 mm 2 ) in the experiment with validamycin A combined with T. asperellum GDFS1009, which demonstrated no significant difference compared with validamycin A experimental treatment alone.
However, with increased experimental time, the bacteriostasis of validamycin A began to attenuate and gradually removed. After incubation for 4 d, the colony area of R. solani (R. zeae) increased to 3956.08 ± 70.52 mm 2 (1912.26 ± 102.48 mm 2 ) in the validamycin A experimental group, while it was 6351.89 ± 40.97 mm 2 (6352.66 ± 40.95 mm 2 ) in the blank control group. Nevertheless the advantage of biological containment of T. asperellum GDFS1009 was represented at this stage, and the colony area of highly inhibited R. solani (R. zeae) decreased to merely 1565.78 ± 46.53 mm 2 (2310.5 2 ± 107.04 mm 2 ). Furthermore, the synergistic effect of validamycin A combined with T. asperellum GDFS1009 was reflected. Under successive impacts of antibiosis, competition, and hyperparasitism, the colony diameter of R. solani (R. zeae) was 1058.46 ± 68.08 mm 2 (724.16 ± 17.28 mm 2 ), significantly less than any single factor treatment ( Fig. 1 and Supplementary Figure S1). From 24 h and 48 h cultures of T. asperellum GDFS1009, 11,845 genes and 11,801 genes were obtained, respectively. After treatment with validamycin A for 24 h and 48 h, the differentially expressed genes in T. asperellum GDFS1009 were 8.93% and 6.78%, respectively, when compared with the control sample (Supplementary Figure S2a and Figure S2c). Comprehensive analysis showed that, compared with the control sample, the sample after validamycin A treated had only five compounds with significant changed, which were: fatty acids, carbohydrates, amino acids, and amines. Their proportion was very small, only 4.81%.

Global impact of validamycin A on T. asperellum GDFS1009 based on RNA-seq and GC-MS data.
Effect of validamycin A on growth and competition of T. asperellum GDFS1009. In 4 d of culture, compared with the control, the colony size, mycelium morphology and mycelium ultrastructure were not changed in T. asperellum GDFS1009 treated with validamycin A (Fig. 2a,b,c).
After treated with validamycin A for 4 d, T. asperellum GDFS1009 displayed the same level of competition on Fusarium graminearum (Fig. 2d).
As the tricarboxylic acid cycle (TCA) cycle is the basis for biological metabolism and is the hub of carbohydrate, fatty acid, and amino acid metabolism pathways 17,18 , which is related to growth and competition of T. asperellum GDFS1009, corresponding RNA-seq data of 24 h and 48 h cultures was analyzed and the results showed that, compared to the control T. asperellum GDFS1009, T. asperellum GDFS1009 treated with validamycin A had only increased aconitase, but not the rate-limiting enzymes. GC-MS metabolomics 24 h data analysis showed that, in T. asperellum GDFS1009 treated with validamycin A and control, the yield of citric acid, succinate, and malic acid was not significantly different. Comprehensive analysis of RNA-seq and GC-MS results showed that, validamycin A had no significant effect on the TCA cycle in T. asperellum GDFS1009 (Fig. 3 and  Supplementary Tables S2-S4). RNA-seq results showed that, in T. asperellum GDFS1009 treated with validamycin A for 24 h, in 13 amino acid metabolic pathways, a total of 72 genes were up-regulated and 11 were down-regulated. After treatment for 48 h, in 12 amino acid metabolic pathways, a total of 28 genes were up-regulated, and 2 genes were decreased (Supplementary Table S3). GC-MS metabolomics data of 24 h showed that, there is no significant difference in the yield of these amino acids between the control and validamycin A treated T. asperellum GDFS1009 (Supplementary Table S5). Comprehensive analysis of the results of gene expression profiles and GC-MS metabolomics showed that, validamycin A had no significant effect on the synthesis and degradation pathways of amino acids in T. asperellum GDFS1009. In addition, RNA-seq results showed that, few genes were changed in fatty acid metabolic pathways (Supplementary Table S3). GC-MS results showed that, there is no significant difference in yields of these fatty acids between control T. asperellum GDFS1009 and T. asperellum GDFS1009 treated with validamycin A (Supplementary Table S6). There is also no significant difference in yields of glucose between control T. asperellum GDFS1009 and T. asperellum GDFS1009 treated with validamycin A (Supplementary Table S7). Comprehensive analysis of the above RNA-seq and GC-MS results showed that, validamycin A had no significant effect on the TCA cycle and related carbohydrates, lipids, and amino acid metabolism in T. asperellum GDFS1009, namely validamycin A does not affect the basal metabolic pathways of T. asperellum GDFS1009.
Effect of validamycin A on the hyperparasitism of T. asperellum GDFS1009. Results of optical and scanning electron microscopy showed that after treatment with validamycin A, T. asperellum GDFS1009 displayed the same level of hyperparasitism on F. graminearum (Fig. 4a). During fermentation for 3-4 d, the chitinase production of T. asperellum GDFS1009 reached a plateau. The enzyme activity in the T. asperellum GDFS1009 treated with validamycin A at 4 d fermentation is 121.48 ± 9.11 U/mL, compared with 119.84 ± 6.23 U/mL in control, showing that validamycin A had no effect on the production of T. asperellum GDFS1009 chitinase (Supplementary Figure S3a). Meanwhile, validamycin A had no influence on cellulase production in T. asperellum GDFS1009. After fermentation of 3 d, the enzyme activity reached the maximum, the enzyme activity after validamycin A treatment was: 1.717 ± 0.212 U/mL, compared with 1.72 ± 0.11 U/mL in control (Supplementary Figure S3b).
In Trichoderma, G protein-MAPK (Mitogen-activated protein kinases)-cAMP (protein kinase A system) signaling pathway is associated with hyperparasitism 19,20 . After treatment with validamycin A at 24 h, RNA-seq data showed that only G-protein gene was significantly up-regulated, while, AC, PKA, TMK1, ECH42 genes and so on in G protein-MAPK-cAMP signaling pathway were not significantly changed. Then, at 48 h, all the genes were not significantly changed ( Fig. 4b and Supplementary Table S8). Furthermore, qRT-PCR validation showed conformably results (Supplementary Figure S3c and d). Therefore, we may infer that validamycin A does not affect the hyperparasitism of T. asperellum GDFS1009.

The degradation and absorption rate of validamycin A by T. asperellum GDFS1009. LC-MS
results showed that, co-fermentation of T. asperellum GDFS1009 and validamycin A in PD broth for 7 d, resulted in a limited 20% degradation of validamycin A, indicating that T. asperellum GDFS1009 has no significant effect on validamycin A ( Fig. 5a and b). Additionally, gas chromatography/time-of-flight mass spectrometry (GC-TOF-MS) results showed that no validamycin A was detected in the mycelium of T. asperellum GDFS1009 (Fig. 5c) exposed to validamycin A.

Transient impacts of validamycin A on T. asperellum GDFS1009 detoxification genes.
Peroxidase, monooxygenase, glutathione transferase, catalase, and ABC translocatorare related to biological detoxification and stress 21,22 . After 24 h treatment with validamycin A, 8 peroxidase genes, 6 monooxygenase genes, 1 superoxide dismutase gene and 2 catalase genes in T. asperellum GDFS1009 were significantly up-regulated, but none of which were still significantly up-regulated at 48 h. Additionally, 3 glutathione S-transferase genes, 1 thioredoxin gene and 6 ABC translocator genes in T. asperellum GDFS1009 were significantly up-regulated at 24 h, while at 48 h only 1 glutathione S-transferase gene, 1 thioredoxin genes and 4 ABC translocator genes were still significantly up-regulated. It is notable that there were 3 ABC translocator genes significantly down-regulated (Table 1).

Discussion
T. asperellum GDFS1009 could inhibit R. solani on maize mainly via competition and hyperparasitism, and further degrade it, whereas validamycin A, as a widely used antibiotic, could be absorbed by R. solani, efficiently disturbs its highly depended energy system, trehalose pathway, and inhibits the growth of R. solani, but could not degrade it [3][4][5][6][7]13 . By contrast, validamycin A is efficient but it takes effect in a short period, while T. asperellum GDFS1009 takes effect in a long period though time-consuming. It was proven that, as compared to a single agent, when validamycin A and T. asperellum GDFS1009 are used together and complementary advantages, the control effect on sheath blight was significantly enhanced (Fig. 1). Similarly, it is showed that T. harzianum and T. asperelloides can develop tolerance to fungicides without compromising their biological activity (growth and parasitism against Fusarium) 23 .
However, this is the first detailed report on the possible effects of validamycin A on Trichoderma. The results showed that, validamycin A had no obvious effect on growth, mycelium morphology, mycelium ultrastructure and the effect of competition of T. asperellum GDFS1009 (Fig. 2). In consideration of primary metabolism which is the energy basis for Trichoderma growth and competition, we used two approaches of metabolomics and transcriptomics to globally explore the sensitive metabolism pathway upon validamycin A interaction. Comprehensive analysis suggested that there were no obvious effect on its TCA cycle, glycolytic pathway, lipid and amino acid metabolism ( Fig. 3 and Supplementary Tables S2-S7). To sum up, validamycin A does not affect the function of competition of T. asperellum GDFS1009.
In Trichoderma, G protein-MAPK-cAMP signaling pathway is associated with hyperparasitism 19,20 . MAPK gene tmk1 in T. atroviride is an important signal gene in hyperparasitism. After knockout of tmk1, the hyperparasitic capacity of T. atroviride was decreased, while the expressions of chitinase gene nag1 and ech42 were significantly induced. In this study, as the hyperparasitism related genes were analyzed via RNA-seq and qRT-PCR, together with dual culture tests, we could infer that validamycin A had no significant effect on hyperparasitism of T. asperellum GDFS1009 (Figs 2d and 4 and Supplementary Tables S8). Meanwhile, LC-MS analysis showed that the absorption and degradation of validamycin A by T. asperellum GDFS1009 was limited (Fig. 5). These researches provided a strong theoretical basis for synergistic effect of validamycin A and T. asperellum GDFS1009, and also provide a theoretical basis for combined use via more modes (for example, validamycin A with biocontrol factors or spores granules of T. asperellum GDFS1009).
In order to uncover the co-exist mechanism of validamycin A and T. asperellum GDFS1009, detoxification and tolerance related genes should be analyzed. It is reported that peroxidase, monooxygenase, glutathione transferase, and catalase are related to biological detoxification and stress. Invasion of external toxic substances could stimulate fungal overexpression of a large number of enzymes, including monooxygenase and peroxidase, which could produce a lot of reactive oxygen species (ROS). Then, toxic substances could be oxidized, form toxic substances-glutathione (GSH) complex via glutathione transferase, and be eliminated from the fungi by catalase etc 21 . After 24 h treatment with validamycin A, lots of related genes in T. asperellum GDFS1009 were significantly up regulated, almost all of which were down to normal levels at 48 h (Table 1). It is explained that the ability of Trichoderma to withstand relatively high concentrations of a variety of synthetic and natural toxic compounds, including its own antibiotics, depends on efficient cell detoxification mechanisms supported by a complex system of membrane pumps 24 . It is well known that the genome of Trichoderma includes ABC transporters (ATP binding cassette (ABC) transporters), which are members of a protein superfamily that efflux drugs from cells of target organisms. Thus transporters may provide a mechanism of protection against cytotoxic drugs and xenobiotic agents. The natural function of ABC transporters in plant pathogenic fungi may relate to transport of plant-defense compounds or fungal pathogenicity factors. The ABC transporters may explain the natural tolerance of Trichoderma to fungicides, and their ability to successfully survive in extreme environments 22 . After 24 h treatment with validamycin A, 6 ABC transporter genes were significantly up-regulated, while after 48 h treatment, 4 ABC transporter genes remains significantly up-regulated expression, but there are 3 ABC transporter genes appearing significantly down regulation (Table 1). According to all the results, we speculated that validamycin A may have a slight stimulation on T. asperellum GDFS1009 but without toxicity. Within 24 h, T. asperellum GDFS1009 spores began germination, and the mycelium is immature. It is more sensitive to external stimuli, so the expression of some genes related to detoxification and stress tolerance were significantly increased; at 48 h, the mycelium is matured and prosperous, and gradually adapts to external stimuli, so the expression of these detoxification genes were decreased.
It is already known that the trehalose pathway in sheath blight pathogen (Rhizoctonia spp.) is a target of validamycin A attacks 13 . Validamycin A could be absorbed in abundance by R. solani, efficiently disturbs its highly depended energy system, trehalose pathway, impacts the glucose production and inhibits the growth of R. solani. But in our study, the glucose production was not impacted in T. asperellum GDFS1009 (Supplementary Table S7), and the growth of T. asperellum GDFS1009 was not impacted by validamycin A (Fig. 2a,b and c), indicating that the trehalose pathway in T. asperellum GDFS1009 is not the target of validamycin A, which is distinguished to R. solani. This may also be the reason why validamycin A and T. asperellum GDFS1009 could co-exist together. It is notable that this study was simply performed at the primary metabolism level to understand the impact of validamycin A on T. asperellum GDFS1009, so the influence at the secondary metabolism level cannot be explained. Whereas, based on our findings from culture tests, we assumed a certain impact of validamycin A over T. asperellum GDFS1009 secondary metabolism, if it did happen, the slight changes of secondary metabolites may not associate with pathogen antagonistic activity since not all secondary metabolites are inhibitory to sheath blight pathogen.
At present we cannot confirm the impact of validamycin A on T. asperellum GDFS1009 in vivo since most of the experiments were completed in vitro which cannot reflect the whole situation of validamycin A-Trichoderma in its natural condition. Therefore, our next study will evaluate what happens to the interaction of T. asperellum-validamycin A in the presence of pathogen and maize plants.

Fungal strains. The biocontrol fungus T. asperellum GDFS1009 was preserved in China General
Microbiological Culture Collection Center (CGMCC NO. 9512), Beijing, China. R. solani, R. zeae and F. graminearum on maize were used as target pathogens for examination of biocontrol effects.

Analysis of the effect of synergetic inhibition of T. asperellum GDFS1009 and validamycin A on maize sheath blight.
T. asperellum GDFS1009, R. solani, and R. zeae were cultured in a PDA dish for 3 d. Holes were then punched into the dish using 7 mm punchers and turned upside down on the following PDA plates: (1) R. solani or R. zeae dish on PDA plate containing 500 μ g/mL validamycin A; (2) R. solani or R. zeae dish on PDA plate without validamycin A and separated by 4 cm from T. asperellum GDFS1009 dish; (3) R. solani or R. zeae dish on PDA plate with 500 μ g/mL validamycin A and also separated 4 cm from T. asperellum GDFS1009 dish; (4) R. solani or R. zeae dish on PDA plate without validamycin A 25 . The plates were incubated at 28 °C and the inhibition effects were photographed after 1 d and 4 d and quantified with Image J software 26 .

Detection of growth and competition of T. asperellum GDFS1009 treated with validamycin A.
T. asperellum GDFS1009 was cultured in PDA dishes for 3 d, after which holes were punched in the dish containing T. asperellum GDFS1009 culture with 7 mm punchers. The dish was then turned upside down on fresh PDA plate containing 500 μ g/mL of validamycin A (or on a control PDA plate without validamycin A). The plates were incubated at 28 °C for 4 d. On day 2, the edge of the colony was cut to observe the mycelium morphology under an optical microscope and also the cellular structure under a transmission electron microscope 27,28 . On day 3, the overall status of growth and sporulation of T. asperellum GDFS1009 was observed and photographed.
T. asperellum GDFS1009 and F. graminearum were cultured in a PDA dish for 3 d. Holes were then punched in the dish with 7 mm punchers, after which it was turned upside down on a PDA plate containing 500 μ g/mL of validamycin A (or on a control plate without validamycin A). In both cases, the two dishes were 4 cm apart 25 . After incubation at 28 °C for 5 d, competition of T. asperellum GDFS1009 with F. graminearum was observed and photographed.

Detection of hyperparasitism of T. asperellum GDFS1009 upon treatment with validamycin A.
T. asperellum GDFS1009 and F. graminearum were co-cultured on PDA plates containing 500 μ g/mL of validamycin A (or on a control plate without validamycin A, as mentioned above) 25 . After sufficient length of incubation at 28 °C to allow the colonies to contact each other, the part in contact was cut to observe hyperparasitism of T. asperellum GDFS1009 under an optical microscope.
In addition, the activities of enzymes chitinase and cellulase, associated with hyperparasitism, were induced in enzyme-inducing medium containing 500 μ g/mL validamycin A (control without validamycin) and measured by the 3, 5-dinitrosalicylic acid (DNS) method [29][30][31] . A GlcNAc standard curve was prepared according to Reissig et al. 32 . One unit (U) of the chitinase activity was defined as the amount of enzyme required to release 1 μ g of GlcNAc per hour at 37 °C temperature and pH 5.2. A glucose standard curve was established as per the People's Republic of China Light Industry standard (QB 2583(QB -2003. A unit of enzyme activity was defined as the amount of enzyme needed for production of 1 mg of glucose per milliliter of broth at 50 °C temperature and pH 4.8.

JGI gene accession number
Gene function Detection of global impact of validamycin A on T. asperellum GDFS1009 transcription by RNA-sequencing. The spore suspension of T. asperellum GDFS1009 was transferred to PD medium containing 500 μ g/mL analytical standard validamycin A (HPLC degrade, Kexing, China; control without validamycin A) to a final spore concentration of 10 6 cfu/mL. After culturing at 28 °C, 180 rpm, for 24 h, the mycelia were collected by vacuum filtration. RNA was extracted and cDNA library was built. Solexa sequencing of single-ends (1 × 50) was then performed that produced 20 million reads per sample. To generate additional data, 48 h samples were also sequenced using Solexa (Single-ends: 1 × 50; 10 million reads). Conventional analysis was performed on the sequencing data obtained from the transcriptome samples, including data preprocessing, genomic mapping, gene expression analysis, transcript expression analysis, alternative splicing analysis, analysis of differential genes, and GO/KEGG enrichment analysis between differentially expressed genes and nondifferentially expressed genes 33,34 . The reference genome for transcriptome analysis was derived from http://genome.jgi.doe.gov/Trias1/Trias1.download.html. Fold change < 0.05 represents significantly down-regulated, and fold change > 2 represents significantly up-regulated.
Specific analysis about TCA cycle, G protein-MAPK-cAMP signaling pathway was via JGI (Joint Genome Institute) online blast with related reference genes, and the highest homology genes were selected for the expression analysis based RNA-seq data and drawing diagrams [17][18][19][20]35 .
Representative genes were validated by qRT-PCR in an ABI 7900 HT Sequence Detection System. The primers used are listed in Supplementary Table S1 17,36 . The qRT-PCR reaction system (10 μ L) was set up as follows: 5 μ L of 2× SYBR Green PCR buffer, 1 μ L of 10 μ M forward primer, 1 μ L of 10 μ M reverse primer, 5 ng of cDNA, ddH 2 O up to 10 μ L. qRT-PCR amplification conditions were as follows: 50 °C for 2 min; 95 °C for 10 min; 95 °C for 15 s, and 60 °C for 1 min, for a total of 40 cycles. Data analysis was carried out as the method outlined in the Bio-Rad quantitative PCR Application Guide 2 −ΔΔCT (Livak).

Detection of global impact of validamycin A on T. asperellum GDFS1009 metabolome by GC-MS analysis.
The spore suspension of T. asperellum GDFS1009 was transferred to PD medium containing 500 μ g/mL validamycin A (or in control medium without validamycin A), to a final spore concentration of 10 6 cfu/mL. After culturing at 28 °C, 180 rpm, for 24 h, 4 volumes of pre-cooled 60% methanol at − 50 °C was added to quench for 20 min, and the mixture was centrifuged at 4 °C at 6,000 rpm for 5 min. The precipitate containing mycelia was collected, washed twice with sterile water at 4 °C and freeze-dried under vacuum till all water was removed. After extraction and derivation, intracellular substances were analyzed by gas chromatography-mass spectrometry (GC-MS) (Agilent 7890 A/5975 C GC-MS). The chromatography conditions were as follows: HP-5MS capillary column (5% phenyl methyl silox: 30 m × 250 μ m id, 0.25-μ m; Agilent J & W scientific, Folsom, CA); split injection, injection volume of 1 μ L, split ratio of 20:1. Inlet temperature was 280 °C; ion source temperature was 250 °C; interface temperature was 150 °C. The temperature program was started at 40 °C for 5 min, raised to 300 °C at 10 °C/min stepwise intervals, and held for 5 min. The carrier gas was helium, with a carrier gas flow rate of 1 mL/min. MS conditions were set as follows: Electrospray ionization (ESI) source, full scan mode, electron energy of 70 eV, quadrupole scan range of m/z 35-780.
Data obtained by comparison and analysis of the information derived from the samples was further analyzed by bioinformatics, which included preprocessing of data, identification of compounds and differential screening of compounds 37,38 . Metabolites were annotated based on metabolome databases from the NIST commercial database (NIST 2008) and Wiley 9 39,40 . P < 0.05 and VIP > 1 represent significantly changed.

Detection of degradation and absorption of validamycin A by T. asperellum GDFS1009 by LC-MS and GC-TOF-MS.
T. asperellum GDFS1009 spore suspension was transferred to PD medium containing 500 μ g/mL validamycin A to a final spore concentration of 10 6 cfu/mL. After culturing at 28 °C, 180 rpm, for 7 d, the culture was filtered through a 0.22 μ m membrane filter. The filtrate was subjected to LC-MS for detection of validamycin A (PD medium containing 500 μ g/mL of validamycin A was used as control) by Waters Quattro Premier XE triple quadrupole mass spectrometer equipped with Ultra Performance Liquid Chromatography (UPLC). Chromatography conditions were: C18 column (1.7 μ m, 2.1 × 100 mm), 2 μ L injection volume, column temperature 40 °C, automatic feed injector temperature maintained at 4 °C, mobile phase A was ultrapure water, mobile phase B was HPLC grade acetonitrile, mobile phase with 0.1% formic acid (v/v), flow rate was 0.3 mL/min; elution was with linear gradient of mobile phase B: 10% initial for 1 min, 10-90% for 1-6 min, 90% equilibrium for 3 min, 90-10% for 0.5 min after the next sample collection. MS conditions: ESI source, positive and negative ionization mode. Source temperature was 150 °C, desolvation temperature was 350 °C, desolvation gas flow was 500 L/h, cone gas flow was 50 L/h. Positive and negative ion mode ionization capillary voltage was 3.0 kV, sampling cone was 20 eV, extraction cone was 2 eV, quadrupole scan ranged between m/z 100-1500 41 .
The spore suspension of T. asperellum GDFS1009 was transferred to PD medium with 500 μ g/mL validamycin A at a final spore concentration of 10 8 cfu/mL. After culturing at 28 °C, 180 rpm, for 4 d, the mycelia of T. asperellum GDFS1009 were collected by vacuum filtration and washed twice with 4 °C sterile deionized water. Intracellular substances were extracted (Validamycin A standard was used as positive control), derived and detected using Agilent 7890 GC-TOF-MS equipped with Rxi-5Sil MS capillary column (30 m × 250 μ m × 0.25 μ m, Restek, USA). Detection conditions were as follows injection volume was 1 μ L with non-shunt mode; carrier gas was helium; forward flow velocity was 3 mL/ min; column temperature was 40 °C for 1 h, increased to 330 °C at 10 °C per minute rate, and held for 10 min; forward sampling temperature was 280 °C; transmission line temperature was 280 °C; ion source temperature was 220 °C; ionization voltage was − 70 eV; scanning mode was 85-600 m/z; scanning rate was 20 spectra/sec; solvent delay was 366 s 42 .