Fusarium graminearum ATP-Binding Cassette Transporter Gene FgABCC9 Is Required for Its Transportation of Salicylic Acid, Fungicide Resistance, Mycelial Growth and Pathogenicity towards Wheat

ATP-binding cassette (ABC) transporters hydrolyze ATP to transport a wide range of substrates. Fusarium graminearum is a major causal agent of Fusarium head blight, which is a severe disease in wheat worldwide. FgABCC9 (FG05_07325) encodes an ABC-C (ABC transporter family C) transporter in F. graminearum, which was highly expressed during the infection in wheat and was up-regulated by the plant defense hormone salicylic acid (SA) and the fungicide tebuconazole. The predicted tertiary structure of the FgABCC9 protein was consistent with the schematic of the ABC exporter. Deletion of FgABCC9 resulted in decreased mycelial growth, increased sensitivity to SA and tebuconazole, reduced accumulation of deoxynivalenol (DON), and less pathogenicity towards wheat. Re-introduction of a functional FgABCC9 gene into ΔFgABCC9 recovered the phenotypes of the wild type strain. Transgenic expression of FgABCC9 in Arabidopsis thaliana increased the accumulation of SA in its leaves without activating SA signaling, which suggests that FgABCC9 functions as an SA exporter. Taken together, FgABCC9 encodes an ABC exporter, which is critical for fungal exportation of SA, response to tebuconazole, mycelial growth, and pathogenicity towards wheat.


Introduction
Fusarium head blight (FHB) is a severe disease of wheat in the world, which is mainly caused by the ascomycete fungus Fusarium graminearum [1][2][3]. FHB causes yield loss and contamination of seeds by the accumulation of trichothecene mycotoxins (mainly deoxynivalenol [DON]), which threatens food and feed security [4,5]. FHB has not been well-controlled due to the complexity of wheat resistance to F. graminearum. Therefore, it is necessary to understand the molecular mechanism of interaction between F. graminearum and wheat, which would be valuable for designing a proper strategy for FHB disease management. 2 of 15 ATP-binding cassette (ABC) transporters hydrolyze ATP to transport a wide range of substrates and can be broadly categorized as importers or exporters in the cell membrane depending on the direction of transportation relative to the cytoplasm [6,7]. Members of this superfamily have conserved domain architecture and have been divided into seven families (A-G) in fungi, plants, and animals [8][9][10]. Recent studies demonstrated that the ABC transporter family C (ABC-C) as a cell membrane protein is important for fungal pathogens in response to fungicide [11][12][13].
In the genome of F. graminearum, there are 16 genes belonging to ABC-C [9]. Many of them are expressed at much higher or lower levels during the infection process when compared with their expression in an axenic culture [14][15][16]. FgABCC15 (FG05_10995) played important and diverse roles in both fungicide resistance and pathogenesis of F. graminearum [9,15]. Considering the importance of ABC-C transporters and the hazards of FHB, it is still necessary to characterize other ABC-C transporters in F. graminearum.
Salicylic acid (SA) is a critical plant defense hormone, which contributes to plant defense against a wide range of pathogens with biotrophic and hemibiotrophic lifestyles [17][18][19]. SA triggers systemic acquired resistance (SAR) in plants and upregulates the expression of a set of genes encoding pathogenesis-related (PR) proteins in tobacco and Arabidopsis thaliana [20,21].
The contribution of SA to the wheat/F. graminearum interaction remains unclear. Infection of wheat spikes with F. graminearum resulted in a significant increase in the accumulation of SA [22], which suggests that SA is important in wheat defense against F. graminearum. Over-expression of Nonexpresser of PR Genes 1 (NPR1) of A. thaliana enhanced the FHB resistance level in transgenic wheat [23]. SA has a significant and direct impact on F. graminearum by reducing the efficiency of germination and growth [24]. Nevertheless, exogenous application of SA in wheat spikes cannot increase its resistance against FHB as expected, which possibly resulted from the capacity of F. graminearum to metabolize and export SA [24]. However, the molecular mechanism on the exportation of SA in F. graminearum is still not well understood.
In this paper, we characterized an ABC-C transporter gene (FG05_07325) in F. graminearum. It was named FgABCC9 following Kovalchuk and Driessen [9]. FgABCC9 was highly expressed during the infection of wheat and was upregulated by SA and by the fungicide tebuconazole [12,22,25]. The objective of this research was to understand the mechanism for the exportation of SA in F. graminearum by analyzing the function of FgABCC9 and elevating its effect on fungal mycelial growth and pathogenicity towards wheat. This research would be helpful for understanding the contribution of SA to the wheat/F. graminearum interaction.

Sequence Analysis
FgABCC9 gene is 4533 bp in length with 3 exons and 2 introns and its open reading frame is 4359 bp. Its deduced amino acid sequence (Appendix A Figure A1a) includes the ABC transporter transmembrane region 1 (ATTR1, pfam00116, 190-503 aa), the ABC transporter C family MRP domain 1 (AMD1, cd03250, 546-783 aa), the ABC transporter transmembrane region 2 (ATTR2, pfam00664, 873-1138 aa), and the ABC transporter C family MRP domain 2 (AMD2, cd03250, 1180-1411 aa). The predicted tertiary structure of FgABCC9 was shown in Appendix A Figure A1b, which is consistent with the model structure (Appendix A Figure A1c) for ABC exporters [26] indicating that FgABCC9 encodes an ABC exporter.

Deletion and Complementation of FgABCC9 in F. graminearum
To disrupt the function of FgABCC9 in F. graminearum, the two flanking regions of FgABCC9 were amplified from the genomic DNA of F. graminearum by using P1-F + P2-R and P3-F + P4-R, respectively (Figure 1a), which were then inserted into the pRF-HU2 vector (Figure 1a). Deletion mutants (∆FgABCC9) were created by replacing the entire FgABCC9 gene with HPH, which is known as a fungal selectable marker gene, using a targeted gene replacement strategy through homologous recombination.
To ensure that the construct was integrated at the intended homologous site (Figure 1b), the primer pairs ∆J-U-F + ∆J-U-R and ∆J-D-F + ∆J-D-F were used to test ∆FgABCC9, which is shown in Figure 1a. The two primer pairs provided expected PCR bands in ∆FgABCC9 (Figure 1b), which were confirmed by sequencing. These results show that FgABCC9 was successfully removed from the genome of ∆FgABCC9.
To create complementation mutants (C-FgABCC9), a fragment containing the promoter and open reading frame of FgABCC9 was introduced into ∆FgABCC9 (Figure 1c). Reverse transcription PCR (RT-PCR) showed that the FgABCC9 gene was normally expressed in C-FgABCC9 as in WT and no expression was observed in ∆FgABCC9 (Figure 1d). respectively (Figure 1a), which were then inserted into the pRF-HU2 vector (Figure 1a). Deletion mutants (ΔFgABCC9) were created by replacing the entire FgABCC9 gene with HPH, which is known as a fungal selectable marker gene, using a targeted gene replacement strategy through homologous recombination.
To ensure that the construct was integrated at the intended homologous site (Figure 1b), the primer pairs ΔJ-U-F + ΔJ-U-R and ΔJ-D-F + ΔJ-D-F were used to test ΔFgABCC9, which is shown in Figure 1a. The two primer pairs provided expected PCR bands in ΔFgABCC9 (Figure 1b), which were confirmed by sequencing. These results show that FgABCC9 was successfully removed from the genome of ΔFgABCC9.
To create complementation mutants (C-FgABCC9), a fragment containing the promoter and open reading frame of FgABCC9 was introduced into ΔFgABCC9 (Figure 1c). Reverse transcription PCR (RT-PCR) showed that the FgABCC9 gene was normally expressed in C-FgABCC9 as in WT and no expression was observed in ΔFgABCC9 (Figure 1d).  Table 1. LB-F + LB-R, RB-F + RB-R, C-FgABCC9-F + C-FgABCC9-R were located in the genomic sequence of FgABCC9 of the WT strain. P1-F + P2-R and P3-F + P4-R were mapped in the T-DNA fragment of the pRF-HU2 vector. ΔJ-U-F, ΔJ-U-R, ΔJ-D-F, and ΔJ-D-R were, respectively, positioned into the upstream and downstream of inserted T-DNA sequence of ΔFgABCC9. All the PCR products were verified by sequencing in the commercial company (Qingke, Chengdu, China).

Importance of FgABCC9 for Mycelial Growth and Fungal Response to Stress Conditions
Mycelial growth of WT (wild type), ΔFgABCC9, and C-FgABCC9 strains was compared on mSNA (modified Synthetischer Nährstoffarmer Agar) plates ( Figure 2a). ΔFgABCC9 grew much slower than WT and C-FgABCC9. The expression of FgABCC9 could be induced by the plant defense hormone SA and the fungicide tebuconazole (Figure 2d), which was previously reported [12,24]. To clarify whether FgABCC9 was involved in mechanisms alleviating SA and tebuconazole, mycelial growth of WT, ΔFgABCC9 and C-FgABCC9 were elevated on mSNA plates supplemented with 0.9  Table 1. LB-F + LB-R, RB-F + RB-R, C-FgABCC9-F + C-FgABCC9-R were located in the genomic sequence of FgABCC9 of the WT strain. P1-F + P2-R and P3-F + P4-R were mapped in the T-DNA fragment of the pRF-HU2 vector. ∆J-U-F, ∆J-U-R, ∆J-D-F, and ∆J-D-R were, respectively, positioned into the upstream and downstream of inserted T-DNA sequence of ∆FgABCC9. All the PCR products were verified by sequencing in the commercial company (Qingke, Chengdu, China).

Importance of FgABCC9 for Mycelial Growth and Fungal Response to Stress Conditions
Mycelial growth of WT (wild type), ∆FgABCC9, and C-FgABCC9 strains was compared on mSNA (modified Synthetischer Nährstoffarmer Agar) plates ( Figure 2a). ∆FgABCC9 grew much slower than WT and C-FgABCC9. The expression of FgABCC9 could be induced by the plant defense hormone SA and the fungicide tebuconazole (Figure 2d), which was previously reported [12,24]. To clarify whether FgABCC9 was involved in mechanisms alleviating SA and tebuconazole, mycelial growth of WT, ∆FgABCC9 and C-FgABCC9 were elevated on mSNA plates supplemented with 0.9 mM SA and 0.5 mM tebuconazole, respectively ( Figure 2a). When compared to WT, ∆FgABCC9 was more sensitive to SA and tebuconazole, which reveals the important role of FgABCC9 in a fungal response to SA and tebuconazole (Figure 2b,c).
The FgABCC9 protein was usually distributed in the septa zone and the cell membrane ( Figure 2e). Consistent with its expression at the RNA level, the accumulation of the FgABCC9 protein in the fungal cell membrane was enhanced when treated with SA and tebuconazole (Figure 2e), which further demonstrates the key role of FgABCC9 in the transportation of SA and tebuconazole in F. graminearum.

FgABCC9 Affects Pathogenicity and DON Production
To clarify whether FgABCC9 affected pathogenicity of the F. graminearum, two fully developed florets of a central spikelet were point-inoculated with conidial suspensions of WT, ∆FgABCC9, and C-FgABCC9, respectively. In agreement with its slower mycelial growth on plates and increased sensitivity to SA (Figure 2a), spikes inoculated with ∆FgABCC9 show much less visual disease symptom and a lower fungal biomass when compared with those inoculated with WT and C-FgABCC9 (Figure 3a-c). The concentrations of DON in the liquid culture and in wheat spikes were compared as well. ∆FgABCC9 had a much lower DON production than WT and C-FgABCC9 (Figure 3d,e).
Considering that FgABCC9 encodes an SA exporter, we compared the contents of SA in spikes inoculated with WT and ∆FgABCC9. Spikes infected with ∆FgABCC9 accumulated a higher concentration of SA (Figure 3f), which suggests that the export of SA by FgABCC9 is critical for the balance between the degradation of wheat endogenous SA by F. graminearum and the toxicity of SA to F. graminearum (reduction in mycelial growth and conidial germination [24]) during the infection in wheat.

FgABCC9 Affects Pathogenicity and DON Production
To clarify whether FgABCC9 affected pathogenicity of the F. graminearum, two fully developed florets of a central spikelet were point-inoculated with conidial suspensions of WT, ΔFgABCC9, and C-FgABCC9, respectively. In agreement with its slower mycelial growth on plates and increased sensitivity to SA (Figure 2a), spikes inoculated with ΔFgABCC9 show much less visual disease symptom and a lower fungal biomass when compared with those inoculated with WT and C-FgABCC9 (Figure 3a-c). The concentrations of DON in the liquid culture and in wheat spikes were compared as well. ΔFgABCC9 had a much lower DON production than WT and C-FgABCC9 ( Figure  3d,e).
Considering that FgABCC9 encodes an SA exporter, we compared the contents of SA in spikes inoculated with WT and ΔFgABCC9. Spikes infected with ΔFgABCC9 accumulated a higher concentration of SA (Figure 3f), which suggests that the export of SA by FgABCC9 is critical for the balance between the degradation of wheat endogenous SA by F. graminearum and the toxicity of SA to F. graminearum (reduction in mycelial growth and conidial germination [24]) during the infection in wheat.

Evaluation of the Function of FgABCC9 in A. thaliana
To confirm its function, FgABCC9 was expressed in A. thaliana. The leaves of AtFgABCC9 accumulated more SA than those of Col-0 (Figure 4e) even though there was no visual difference between Col-0 and AtFgABCC9 plants (Figure 4a,b). To make sure the increased accumulation of SA affected expression of SA-related genes, we compared the expression of NPR1, EDS1, PAD4, and PR1 in the leaves of transgenic and WT plants (Figure 4f). NPR1 is a master regulator of SA-mediated transcriptional reprogramming and immunity and it functions as a transcriptional coactivator [27]. EDS1 and PAD4 as part of a central regulator complex contribute to the positive feedback loop of SA accumulation [28]. PR1 is one of the genes that is induced by SA and often used as the marker for SA signaling [29]. Unexpectedly, only the expression of NPR1 was affected, which indicated that transgenic expression of FgABCC9 did not activate SA signaling.

Discussion
The superfamily of the ABC transporter is one of the largest gene families in fungi. It is involved in the transport of a broad range of substrates across biological membranes. ABC transporters, particularly those with a multidrug resistance (MDR) domain or a pleiotropic drug resistance (PDR) domain, are important in the resistance of fungal pathogens to xenobiotics [11]. F. graminearum, which is an ascomycete fungus, is a major causal pathogen for FHB disease in wheat. F. graminearum has 62 To clarify whether FgABCC9 affected A. thaliana resistance against F. graminearum, the leaves of AtFgABCC9 and Col-0 were point-inoculated with conidial suspension of the WT strain. Consistent with the qPCR data in Figure 4f, there was no significant difference between the resistance levels of AtFgABCC9 and Col-0 (Figure 4c,d).

Discussion
The superfamily of the ABC transporter is one of the largest gene families in fungi. It is involved in the transport of a broad range of substrates across biological membranes. ABC transporters, particularly those with a multidrug resistance (MDR) domain or a pleiotropic drug resistance (PDR) domain, are important in the resistance of fungal pathogens to xenobiotics [11]. F. graminearum, which is an ascomycete fungus, is a major causal pathogen for FHB disease in wheat. F. graminearum has 62 ABC transporter genes, which were divided into seven families (A-G) according to domain architecture and phylogenetic data [9]. FgABCG6 (FG05_04580) with a PDR domain plays a role in protecting the fungus from antifungal compounds and helps combat unidentified wheat defense compounds during disease development [30]. FgABCC15 (FG05_10995) with an MRP domain plays important and diverse roles in both fungicide resistance and pathogenesis of F. graminearum [15]. In this study, we characterized a new ABC-C transporter gene with an MRP domain (FgABCC9; FG05_07325). Our data demonstrated that FgABCC9 was an ABC exporter, which was important for the export of SA by F. graminearum under SA stress and for fungal response to tebuconazole and pathogenesis in wheat. Our results together with the previous reports suggested that manipulation of the expression level or activity of ABC transporters would be a hopeful way to manage FHB disease.
SA is one of the key plant defense hormones, which is associated with resistance against F. graminearum in wheat [22][23][24]. Nevertheless, the contribution of SA to wheat/F. graminearum interaction remains unclear. SA has a significant and direct impact on F. graminearum since it reduces the efficiency of germination and mycelial growth at higher concentrations [24] by down regulating the chitin synthase gene FgCHS8 and the cis-12 linoleic acid isomerase gene FgLAI12 [31,32]. Wheat spikes accumulate more SA when infected with F. graminearum [22], which suggests an important role of SA in wheat FHB resistance. Unexpectedly, exogenous application of SA cannot improve the wheat resistance level against FHB possibly due to the fact that F. graminearum can reduce the toxicity of SA by its capacity to metabolize and export SA [24]. This research showed the importance of FgABCC9 as an SA exporter for F. graminearum under SA stress and during infection in wheat. Deletion of the FgABCC9 gene resulted in enhanced fungal sensitivity to SA (Figure 2a), increased accumulation of SA (Figure 3f), lower fungal biomass (Figure 3c), and less disease symptom (Figure 3a,b) in wheat spikes after inoculation. The presence of FgABCC9 was critical for fungal degradation of SA under SA stress (Figure 2a). Therefore, we speculated that ∆FgABCC9 could not efficiently degrade SA in wheat spikes as the WT strain, which results in enhanced accumulation of SA in spikes inoculated with ∆FgABCC9 (Figure 3f). It also suggested that F. graminearum reduced the accumulation of SA in spikes when FgABCC9 functioned normally and made sure that the concentration of endogenous SA was below the toxicity threshold. ∆FgABCC9 might not completely lose the ability to export SA from the cytoplasm to the extracellular space since it is hard to identify all the SA exporters in one experiment. However, even the partial reduction of this ability led to lower fungal biomass and less disease symptom, which indicated the contribution of the SA exporter to deal with SA during the infection of F. graminearum. These results demonstrated that SA did contribute to wheat resistance against F. graminearum.
Transgenic expression of the FgABCC9 gene did not activate the expression of the PR1 that is the marker gene for SA signaling (Figure 4f), even though it increased the concentration of SA in the leaves of A. thaliana (Figure 4e). Considering that FgABCC9 functions as an SA exporter, we speculated that the content of SA within cytoplasm would not increase.
Tebuconazole is a sterol demethylation inhibitor and is effective in controlling FHB in agricultural production [33,34]. Recent studies show that the 14-α-demethylase encoded by the Cyp51 gene as a target enzyme affected fungal cell wall sensitivity to tebuconazole. ABC transporters used as efflux pumps were involved in the transportation of tebuconazole in fungi [35,36]. In this study, the expression of the FgABCC9 gene was upregulated by tebuconazole (Figure 2d,e) and deletion of the FgABCC9 gene led to increased sensitivity to tebuconazole on mSNA plates (Figure 2a,c). These results suggest that the FgABCC9 gene is involved in mechanisms alleviating to tebuconazole and that FgABCC9 is an exporter for the fungicide tebuconazole in F. graminearum as well.
FHB threatens food and feed security by contaminating seeds with trichothecene mycotoxins. We previously showed that SA significantly inhibited DON production [24] and SA also significantly upregulated the expression level of FgABCC9 (Figure 2d). In the present study, disruption of the FgABCC9 gene in F. graminearum resulted in reduced accumulation of DON production in wheat spikes and in liquid media (Figure 3d,e). However, the reduced DON contents in spikes inoculated with ∆FgABCC9 was possibly due to the less fungal biomass (Figure 3c). In the liquid media, the same amount of mycelia (0.2 mg) was used, which demonstrates that the expression of the FgABCC9 gene was positively associated with DON production in F. graminearum. It seems likely that the FgABCC9 may not be a regulatory target for SA to downregulate DON production in F. graminearum.
Members in the ABC-C subfamily have been recognized as export pumps for amphiphilic anions especially for conjugates of lipophilic compounds with glutathione or several other non-toxic anionic residues in Saccharomyces cerevisiae [10,[37][38][39]. ∆FgABCC9 showed slower mycelial growth on mSNA plates than WT and C-FgABCC9 (Figure 2a), which suggested that FgABCC9 is also an exporter for other materials that are essential for normal growth of F. graminearum.

Materials
A virulent isolate of F. graminearum (DAOM180378) was used for the fungal experiment throughout the paper. Triticum aestivum cv. "Roblin" was used for wheat inoculation, which is susceptible to FHB disease. Wheat plants were grown in green houses under 16/8 h day/night cycles at 23/18 • C. Plants were watered as needed and fertilized before sowing with 15-15-15 (N-P-K). Unless specifically noted, all chemicals were purchased from Sigma-Aldrich (St. Louis, MO, USA).
A. thaliana ecotype Col-0 was used. Seeds were sown on Murashige and Skoog (MS) medium with 0.7% (weight/volume) agar and were kept at 4 • C for 3 d before being moved to a growth chamber. The WT and transgenic plants were grown side-by-side in the same tray to minimize possible variation of growth conditions. Plants were first grown at 22 • C under a short day (SD) condition for 30 d with a 10 h light/14 h dark photoperiod for an extended vegetative growth phase and were then moved to a long day (LD) (16 h light/8 h dark) condition for reproductive growth. The pCAMBIA1302 vector carrying FgABCC9 was frozen and then thawed into the Agrobacterium tumefaciens strain AGL-1 (Tiangen, Beijing, China). It was transformed into the Col-0 through the floral dip method [40]. Six resistant T 1 transgenic lines were selected in 50 µg·mL −1 hygromycin (HPH) and verified by using PCR. Phenotypic analyses were performed in the T 2 generation and confirmed in the T 3 generation. Homozygous plants were used in all experiments.

Sequence Analysis
Nucleotide sequence of FgABCC9 (FG05_07325) was downloaded from the Ensembl fungi database (Available at: http://fungi.ensembl.org/index.html). Primer Premier 5.0 (Premier Biosoft, Palo Alto, CA, USA) software was used to design PCR primers ( Table 1). The analysis of sequence similarity and identification of conserved domains were performed using BLASTp on NCBI (Available at: http://blast.ncbi.nlm.nih.gov/Blast.cgi) (Figure 1a). The 3D-protein structure was predicted by Phyre2 [41] and made by PyMol 1.8 (Figure 1b). The underlined are cutting sites for restriction enzymes.

Construction of Deletion and Complementation Mutants
Fresh mycelia cultured on mSNA (1 g KH 2 PO 4 , 1 g KNO 3 , 0.5 g MgSO 4 , 0.5 g KCl, 1 g glucose, 1 g sucrose and 20 g agar per liter) plates [24] were used to extract the genomic DNA of F. graminearum by using a CTAB method [45]. Disruption of the FgABCC9 gene in F. graminearum was performed, which is shown in Figure 1a. The pRF-HU2 vector [46] was used to create ∆FgABCC9 mutants through homologous recombination. Transformation of F. graminearum was carried out similarly to our previous study [31].
To restore its function, the genomic sequence of FgABCC9 was amplified by primer pair C-FgABCC9-F + C-FgABCC9-R, ligated into pCAMBIA1302 vector, and transformed into ∆FgABCC9 to create C-FgABCC9 mutants. All the C-FgABCC9 mutants were verified by RT (reverse transcription)-PCR by using the primer pair RJ-FgABCC9-F + RJ-FgABCC9-CJ-R (Table 1).

Conidial and Mycelial Growth Conditions
Conidia were produced in CMC (carboxymethyl cellulose) medium at 28 • C by shaking (180 rpm) for 5 d [47]. The concentration of conidia was determined with a hemocytometer by microscopy.
The effects of SA and tebuconazole on mycelial growth were tested on mSNA plates. SA (0.9 mM SA) and tebuconazole (0.5 mM) were supplemented after autoclaving. A total of 1000 conidia were inoculated on each mSNA plate and the plates were maintained at 28 • C in darkness. Ten replicates were done for each treatment. The growing mycelia on mSNA plates were scanned by using the EPSON Perfection V700 Photo (Seiko Epson, Bekasi, Indonesia) on day 5 after inoculation. Thereafter, the area of mycelia was measured by Computer Aided Design (CAD) software (version 2007). The B-spline curve for mycelia growth was calculated as Fang et al. [48].

Virulence Assay
To determine the effect of FgABCC9 on the pathogenicity of F. graminearum in wheat heads, two flowering florets of a central spikelet of one head were each inoculated with 1 × 10 3 conidia. The inoculated heads were sprayed with water and enclosed with a plastic wrap for 48 h at 25 • C. Wheat plants were placed in a controlled-environment room at 25 • C. FHB symptoms were assessed 4 to 12 d after inoculation. Ten plants were used per treatment.
To examine whether FgABCC9 affected pathogenicity of F. graminearum in leaves of A. thaliana, 1 × 10 3 conidia was point inoculated in the middle of leaves wounded by brush. The inoculated leaves were maintained on MS medium at 25 • C for 48 h. Subsequently, the inoculated leaves were scanned by using the EPSON Perfection V700 Photo and ground to powder in liquid nitrogen.
To test whether FgABCC9 was related to the production of mycotoxin DON in liquid media, a two-stage protocol from References [24,49] was used. The concentration of DON was measured by using the DON ELISA kit (Beacon, Saco, ME, USA) and the Multiskan Spectrum (Thermo Scientific, Vantaa, Finland).
To test whether FgABCC9 affected the production of DON in wheat spikes, two florets of fully developed spikelets at mid-anthesis were each inoculated with 1 × 10 3 conidia. After inoculation, the wheat plants were placed in a room as described above. The inoculated spikelets were harvested at the 48 th hour (for the following gene expression analysis) and on day 8 after inoculation (for DON analysis). The spikelets were ground into a fine powder in liquid nitrogen. DON was extracted from 100 mg spikelet powder with one mL sterile water at 4 • C for 12 h. Three biological replicates were conducted with at least ten heads per treatment.

Gene Expression Analysis
Total RNA was extracted from fresh powders of mycelia, wheat spikelets, and A. thaliana leaves by using the E.Z.N.A. ® Total RNA Kit I (Omega Bio-Tek, Norcross, GA, USA) in accordance with the manufacturer's instructions. RNA was reverse transcribed using the PrimeScript™ RT Reagent Kit with genomic DNA Eraser (Takara, Dalian, China) following the manufacturer's protocol.
The primer pair Rj-FgABCC9-F + Rj-FgABCC9-R was used to measure the expression level of FgABCC9 in F. graminearum and A. thaliana. Gene expression of PR1, EDS1, PAD4, and NPR1 was detected in the leaves of A. thaliana by using PR1-F + PR1-R, EDS1-F + EDS1-R, PAD4-F + PAD4-R, and NPR1-F + NPR1-R, respectively ( Table 1). The FgGAPDH (FG05_06257), β-tubulin (FG05_09530) and elongation factor 1 (FG05_08811) genes were used as reference genes when performing qPCR for the samples of F. graminearum [24]. The relative amount of F. graminearum was estimated by measuring the expression level of FgGAPDH in wheat spike tissue by using qPCR with normalization to three wheat reference genes (w-GAPDH (glyceraldehyde-3-phosphate dehydrogenase gene in wheat), NCBI UniGene Ta.66461; Aox (aldehyde oxidase gene), Ta.6172; hn-RNP-Q (heterogeneous nuclear ribonucleoprotein Q gene), Ta.10105) [24]. The ACT2, UBQ10, and EF-1α genes [42] were used as reference genes when doing qPCR in the samples of A. thaliana. qPCR was performed by a MyiQ Real-Time PCR Detection System (Bio-Rad, Hercules, CA, USA). All of the primers mentioned above were listed in Table 1.

Quantification of SA
The wheat spikelet and A. thaliana leaf samples for qPCR analysis were utilized for the quantification of SA as well. To prepare samples of A. thaliana, leaves of WT and transgenic plants grown under the SD condition without inoculation were harvested and ground to a fine powder in liquid nitrogen, respectively. Three biological replicates were conducted with at least six plants per treatment. Quantification of SA was performed as described previously [50].

Microscopic Assay
The C-FgABCC9 strains harboring a green fluorescent protein gene (GFP) tag were used to examine the subcellular localization of the FgABCC9 protein. Hyphae were used to detect GFP fluorescence. The optical microscopic and fluorescence microscopic assays were carried out as shown in Reference [31] by using a Nikon-80i fluorescence microscope (Nikon, Tokyo, Japan).