Introduction

Astragalus membranaceus, belonging to the Leguminosae family, is an economically important medicinal and food plant mainly distributed in North China1. A. membranaceus root is one of the most frequently used traditional medicine (Huangqi) in East Asian for the treatment of debility, chronic illness, and spleen deficiency2,3. Like most of leguminous plants, A. membranaceus root naturally contains a kind of typical phytoalexins i.e. isoflavones, among which formononetin (FO) and calycosin (CA) are two representative compounds associated with versatile health-promoting benefits as diverse as antioxidant, antiviral, anti-inflammatory, anti-fatigue, estrogenic, neuroprotective, and hematopoietic activities1,4,5. In this respect, A. membranaceus root extracts have been well recognized as functional foods/nutraceuticals according to the U.S. Dietary Supplement Health and Education Act, which can be sold as over-the-counter dietary supplements at health food markets6,7.

Considering that the slow growth rate of field cultivated A. membranaceus (3–5 years) can cause the long occupation of agriculture lands, and the fluctuation of phytochemical content due to varietal, geographical, ecological, and seasonal variations always results in the unstable function of extracts, plant cell/organ culture technology has emerged as a promising method that can supersede the field cultivation of A. membranaceus for bioactive phytochemical production in short growth cycles8. Moreover, it is worth mentioning that plant cell/organ culture technology has been endorsed by the Food and Agriculture Organization of the United Nations as a safe and feasible tool for the production of value-added foods and health compounds9,10. Previously, A. membranaceus hairy root cultures (AMHRCs) have been successfully developed, which can produce the comparable yields of FO and CA as against 3 year-old field cultivated A. membranaceus11. However, the productivity of FO and CA is still in low levels, which can be ascribed to the comfortable microenvironment of AMHRCs with the result that the two phytoalexins (FO and CA) cannot be excessively synthesized due to the lack of external stresses. To address this, elicitation, the exogenous addition of elicitors into plant cell/organ cultures that is capable of modulating defense reactions, is the most frequently adopted strategy for the enhanced production of valuable defense phytochemicals on account of the simple usage and high efficiency12,13,14. Generally, the improvement of phytochemical yield without the significant increase in cost can make plant cell/organ culture technology more attractive from the perspective of commercial application15,16. In consideration of this, an essential task is the search of cost-effective elicitors that can enhance FO and CA production in AMHRCs.

Chitosan is a naturally occurring substance that can be mainly found in the abandoned exoskeleton of abundance crustaceans, which has gained worldwide attention for diverse applications in food fields (e.g., food additive, food preservative, dietary fiber, etc.) and agriculture areas (e.g., seed coating, plant disease control, soil amendment, etc.) due to its non-toxicity (the toxicity being close to salt or sugar) as well as excellent biodegradability, biocompatibility, and bioactivity17,18,19. Notably, chitosan has been well acknowledged as a potent biotic elicitor that can induce plant stress response with the consequent enhancement in phytoalexin accumulation18,19. In consideration of the cost and safety, it is strongly recommended to use chitosan as a non-toxic elicitor for improving FO and CA productivity in AMHRCs.

Chitosan behaving as an effective “resistance elicitor” can activate plant innate immunity and defense mechanisms involving a series of biochemical and molecular reactions, in which the enhanced expression of biosynthesis genes related to the production of phytoalexins is flagged as a characteristic event17,18,19. In our recent study, it was proven that chitosan elicitation could activate the transcription of associated biosynthesis genes thus leading to the enhancement of flavonoid accumulation in Isatis tinctoria L. hairy root cultures20. However, the action mechanism of chitosan inducing phytoalexin biosynthesis is still largely unknown. The signaling cascades via chitosan elicitation that results in the phytoalexin enhancement appears to take different forms, depending upon the plan species19. Generally, mitogen-activated protein kinase (MAPK) signaling cascades play essential roles in plant immunity and stress responses21. Moreover, it is reported that chitosan can activate MAPK signaling cascades (triggering the production of reactive oxygen species, inducing the expression of MPK genes, and boosting the transcription of defense-related genes) in Cocos nucifera L. and Lycopersicon esculentum for improving their resistances to diseases22,23. However, there is no study about chitosan modifying MAPK signaling cascades on the stimulation of phytoalexin biosynthesis in plant in vitro cultures.

Based on the foregoing, the objectives of this work were to develop a feasible chitosan elicitation practice for improving the yields of two health-promoting phytoalexins (FO and CA) in AMHRCs, and to investigate whether MAPK signaling cascades can mediate the transcriptional activation of genes related to FO and CA biosynthesis. Initially, the effect of chitosan elicitation condition on FO and CA accumulation in AMHRCs was studied for achieving their optimal yields. Afterwards, the change in oxidative status, expression of genes related to MAPK signaling cascades, and transcription of pathogenesis-related genes as well as associated genes involved in FO and CA biosynthesis pathway were analyzed for understanding the mechanism of phytoalexin production induced by chitosan. To the best of our knowledge, this is the first study regarding the application of chitosan to promote isoflavone production in AMHRCs, and the exploration of chitosan inducing phytoalexin biosynthesis from the view of MAPK signaling cascades.

Results

Effect of chitosan elicitation on FO and CA accumulation in AMHRCs

Generally, the success and efficiency of a given elicitation practice for improving the yields of desired phytochemicals in plant in vitro cultures mainly depends on the elicitor dosage and exposure time14. Accordingly, it is necessary to find the appropriate chitosan concentration and elicitation time for achieving the the optimal enhancement of FO and CA in AMHRCs. As reported previously, AMHRCs harvested at day 34 can give the highest productivity of isoflavone and root biomass. Thus, chitosan elicitation experiments were carried out using 34 day-old AMHRCs in this work, with the aim of further increasing FO and CA yield without affecting the biomass amount.

As exhibited in Fig. 1, chitosan elicitation using different dosages (50, 100, and 150 mg/L) showed distinct effect on the yields of two target isoflavones in AMHRCs during the time course of 0 to 96 h. Moreover, the same chitosan dosage exerted different influences on the accumulation pattern of FO and CA during the time course of experiments. This can be ascribed to the fact that the same elicitor possesses varied abilities of inducing the biosynthesis of different phytochemicals in a given plant in vitro culture13. Additionally, it was observed from Fig. 1 that chitosan could enhance FO and CA accumulation in AMHRCs after 4 h, regardless of its concentrations. This can be attributed to the rapid defense response when plant in vitro cultures treated by elicitors, which always cause the phytochemical profile change in a very short time14. Moreover, it was noted that the enhancement of FO and CA in AMHRCs was not significant during the prolonged time course of 72 to 96 h. Taken as a whole, it was found that 100 and 150 mg/L of chitosan could induce the remarkable enhancement in the yields of FO and CA during the elicitation duration of 18 to 30 h. More exactly, 100 mg/L of chitosan showed the best elicitation effect at 24 and 30 h for FO and CA, respectively. However, it is noteworthy that CA yield at 30 h was only a little higher than that at 24 h. In view of time saving, 100 mg/L of chitosan along with 24 h of exposure time were found to be appropriate for the both compounds, where the yields of FO (764.19 ± 50.81 μg/g DW) and CA (611.53 ± 42.22 μg/g DW) were 12.45- and 6.17-fold higher than those in control (61.40 ± 2.73 and 99.07 ± 6.08 μg/g DW), respectively. Moreover, the changes in LC-MS/MS chromatograms of the two target compounds in extracts form control and chitosan-treated AMHRCs (100 mg/L and 24 h) can be obviously observed in Fig. 2.

Figure 1
figure 1

Effect of chitosan concentration (50, 100, and 150 mg/L) on the yields of FO and CA in 34 day-old AMHRCs along a 96 h time course. Results sharing different lowercase letters indicate significant differences (P < 0.05) between diverse groups of data.

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Figure 2
figure 2

Chromatograms of FO and CA in extracts form control and chitosan-treated AMHRCs (100 mg/L and 24 h) determined by LC-MS/MS using selected reaction monitoring mode.

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Assessment of oxidative burst in chitosan-treated AMHRCs

In this work, morphological comparisons of chitosan- and non-treated root cultures showed that the former one exhibited a significant indication of ROS-mediated oxidative stress (browning color) as against the later one (Fig. 3). Among all forms of ROS (O2•−, OH•, HO2•, H2O2, and RO•), H2O2 is considered as the most stable one, and can be accurately monitored22,24. Additionally, catalase (CAT) is an indispensable antioxidant enzyme that can effectively dismutate H2O2 into H2O and O224. In this regard, H2O2 content and CAT activity in chitosan- and non-treated AMHRCs harvested at different time points were determined, which aimed to verify the oxidative burst whether occur in AMHRCs following chitosan elicitation. In comparison with non-treated control, H2O2 content in chitosan-treated AMHRCs increased immediately, reached the peak value (6.19 ± 1.35 μmol/g FW) at 1 h, and decreased slowly to the control level afterwards (Fig. 3). Moreover, CAT activity was noticed to increase very rapidly, achieve the highest value (2.06 ± 0.28 U mg/g protein) at 2 h, and declined gradually to a stable level subsequently (Fig. 3). Obviously, the instantaneous increase of H2O2 lead to the fast enhancement in CAT activity during the early elicitation period, followed by the consumption of antioxidant enzyme accompanied by the decrease in H2O2 content during the late elicitation period, which indicated a positive-feedback response to fight the oxidative stress mediated by ROS.

Figure 3
figure 3

Morphological comparisons of control and chitosan-treated hairy roots (100 mg/L and 24 h); H2O2 content and CAT activity in control and chitosan-treated AMHRCs (100 mg/L) along a 96 h time course. Results sharing different lowercase letters indicate significant differences (P < 0.05) between diverse groups of data.

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MAPK gene expression in chitosan-treated AMHRCs

Factually, MAPK cascade-mediated signalling is quite essential in the regulation of many biological processes in plants, such as growth, development, and programmed cell death, and especially in immunity and stress responses21,25. Two well-characterized MAPKs, i.e. MPK3 and MPK6, are regarded as key mediators that can positively regulate various defense signaling in response to a diversity of biotic or abiotic stimuli25. More importantly, it is reported that MPK3/MPK6 cascade play an integral role in phytoalexin biosynthesis for the defense against fungal pathogen attacks26. To verify whether MPK3/MPK6 cascade can be activated by ROS in chitosan-treated AMHRCs, the corresponding gene transcripts along the time course of 0–96 h were determined by qRT-PCR. As shown in Fig. 4, the transcriptional level of MPK3 in AMHRCs was induced immediately after chitosan treatment, reached the highest level at 1 h (43.72-fold increase), and reduced rapidly to the basal level after 6 h. Meanwhile, MPK6 expression was also observed to respond rapidly following chitosan treatment, achieve the peak level (26.31-fold increase) at 2 h, and decrease significantly to the control level after 6 h (Fig. 4). As expected, the transient transcription of both genes indicated that the MPK3/MPK6 cascade was indeed activated by ROS in chitosan-treated AMHRCs.

Figure 4
figure 4

Transcriptional levels of MPK3 and MPK6 in AMHRCs treated with chitosan (100 mg/L) along a 96 h time course. Results sharing different lowercase letters indicate significant differences (P < 0.05) between diverse groups of data.

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Pathogenesis-related (PR) gene expression in chitosan-treated AMHRCs

The major actions of MAPK cascade after being activated is to relocate to the nucleus where they can induce the expression of defense-related genes through activation of specific transcription factors23,25. In this study, β-1,3-glucanase (βGlu), class 1 chitinase (Chi1), pathogen-related protein 1 (PR-1) were selected as marker defense genes to detect if they can be induced by the MPK3/MPK6 cascade in chitosan-treated AMHRCs. Also, the relative expression levels of these genes along the time course of 0–96 h were determined by qRT-PCR. It was noticed from Fig. 5 that βGlu expression was gradually induced to the highest level (13.32-fold increase) at 4 h, and decreased slowly afterwards. And, the transcriptional level of Chi1 was found to be highest (7.70-fold increase) at 6 h, after which a gradual decline tendency was observed (Fig. 5). Moreover, the significant induction of PR-1 expression (9.93 to 18.89-fold increase) was found during the time course from 2 to 12 h, whereas PR-1 transcription reduced to the value around the basal level after 18 h (Fig. 5). Obviously, chitosan treatment led to an enhanced expression of βGlu, Chi1, and PR-1 in a very short time.

Figure 5
figure 5

Expression levels of βGlu, Chi1, and PR-1 in AMHRCs treated with chitosan (100 mg/L) along a 96 h time course. Results sharing different lowercase letters indicate significant differences (P < 0.05) between diverse groups of data.

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Biosynthesis genes expression in chitosan-treated AMHRCs

Transcriptional profiles of phenylalanine ammonia lyase (PAL), cinnamate-4-hydroxylase (C4H), 4-coumarate coenzyme A ligase (4CL), chalcone synthase (CHS), chalcone reductase (CHR), chalcone isomerase (CHI), isoflavone synthase (IFS), and isoflavone 3′-hydroxylase (I3′H) that are involved in FO and CA biosynthesis pathway along the time course of experiments (6–96 h) were determined by qRT-PCR, which aimed to test whether MAPK cascade-mediated signal transduction can up-regulate the aforementioned genes in AMHRCs underlying chitosan treatment. As shown in Fig. 6, the transcriptional levels of all tested genes were significantly up-regulated in chitosan-treated AMHRCs during the period from 6 to 36 h, which indicated that MAPK-mediated signal transduction could indeed positively regulate the expression of these biosynthesis genes, thus contributing to the enhanced accumulation of FO and CA along the same time course (6 to 36 h). Taken as a whole, the transcriptional profiles of all target genes were almost consistent (Fig. 6). Their expression increased up to the highest level from 6 to 12 h, and decreased gradually to the basal level in the following experimental period (24 to 96 h). Additionally, it is noteworthy that the time point (12 h) required the highest expression levels of all biosynthesis genes was earlier than that (24 h) necessary for the maximal accumulation of FO and CA (Fig. 6), which can be attributed to a typical metabolic phenomenon that the downstream product synthesis lagged behind the upstream gene expression27. Moreover, CHI exhibited the highest expression abundances (27.72-fold) at 12 h among all tested genes (Fig. 6).

Figure 6
figure 6

Transcriptional profiles of eight biosynthesis genes involved in FO and CA pathway in AMHRCs treated with chitosan (100 mg/L) from 6 to 96 h. Results sharing different lowercase letters indicate significant differences (P < 0.05) between diverse groups of data.

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Discussion

Generally, isoflavones are considered as phytoalexins in leguminous plants that are strongly inducible and especially sensitive to pathogen and insect challenges28. It is known that chitin is a typical pathogen-associated molecule present in fungal cell walls22. Thus, chitosan (the derivative of chitin) is able to elicit plant defense response via simulating the attacks of fungal pathogen, which can eventually result in the enhancement of phytoalexin biosynthesis17. In this regard, it is not surprising that chitosan elicitation can promote FO and CA biosynthesis in AMHRCs in this work (Fig. 1).

Chitosan elicitation is reported to possess positive influence on promoting secondary metabolite accumulation in many plant in vitro cultures, such as echinacoside in Scrophularia striata Boiss. cell suspension cultures29, hydrolysable tannin in Phyllanthus debilis Klein ex Willd. cell suspension cultures30, plumbagin in Plumbago indica L. adventitious root cultures31, and withanolides in Withania somnifera (L.) Dunal adventitious root cultures32. Whereas, chitosan elicitation conditions required for the maximal enhancement of the abovementioned phytochemicals are inconsistent. Factually, plants exposed to elicitation/stress have tolerance-limit levels for activating defense secondary metabolisms and possess thresholds for biosynthesizing specific secondary metabolites, which depends upon the inherent property of plant species14. Moreover, when secondary metabolites are accumulated excessively, plants can be induced to generate special enzymes for the degradation of target metabolites via the feedback regulation15. Overall, it is inferred that 34 day-old AMHRCs treated by chitosan (100 mg/L and 24 h) (Fig. 1) might suffer from the appropriate stress for inducing FO and CA biosynthesis without degradation.

Generally, the action mechanism of elicitor inducing secondary metabolic responses in plant cells is complex owing to the existence of thousands of intertwined events13,14. The action of elicitors can alter plant cellular activities at biochemical and molecular levels, which usually triggers multiple signal transduction cascades that ultimately activate the transcription of enzymatic genes involved in the biosynthesis pathways of defense secondary metabolites12,13,14. In this regard, it is important to understand the action mechanism of chitosan inducing the biosynthesis of FO and CA.

As mentioned above, chitosan elicitation is able to simulate fungal pathogen attacks. This can be recognized by cell surface-located pathogen-recognition receptors, and cause the oxidative burst (one of the earliest cellular responses), i.e. the over-production of highly toxic reactive oxygen species (ROS)22,29. On one hand, ROS can activate antioxidant enzymes to scavenge them for detoxifying the oxidative damages to membranes, nucleic acids, lipids, and proteins in plant cells24. On the other hand, ROS can act as signal molecules, trigger many signal transduction cascades, and eventually cause the enhanced expression of specific genes related to the production of phytoalexins with antioxidant properties, which can neutralize ROS for maintaining the cellular redox status in plant cells33,34. Results in this work (Fig. 3) confirmed the actual occurrence of oxidative burst in AMHRCs undergone chitosan elicitation, which might trigger some special signaling cascades that contributed to activating the transcription of genes related to FO and CA biosynthesis.

As described previously, ROS functions as a general priming signal that can contribute to triggering multiple intracellular signalling cascades in plants, among which the activation of MAPK signaling pathways is considered as a common event33,36. Generally, external stressors/elicitors can trigger plant immunity requiring a signal transduction from receptors to downstream defense components35. Thus, the rapid and strong activation of MPK3/MPK6 cascade in chitosan-treated AMHRCs (Fig. 4) might contribute to transducing stress signals to downstream components for the enhanced expression of genes related to the production of defense-related molecules.

Generally, the activation of MAPK cascade is followed by the induction of PR genes that can encode PR proteins (e.g., β-1,3-glucanase, chitinase1, and PR-1 protein), which are major components of downstream immune signaling and consequently play a critical role in plant defense systems22,25,36. It is known that the upregulation of PR genes is correlated with the onset of plant immune response, known as systemic acquired resistance (SAR), which can make plants becomes more resistant to pathogens22,37. So, the synergistic activation of three PR genes in this work (Fig. 5) indicated that chitosan-induced stress signals can be successfully transduced via the MAPK cascade, thus leading to a typical SAR response in chitosan-treated AMHRCs for the enhanced resistance.

In addition to triggering PR gene expression, the activation of enzymatic genes related to phytoalexin biosynthesis is considered as a common event after MAPK cascade relaying the defense signals to specific transcription factors in nucleus25,26. In this work, the synergistic expression tendency of all biosynthesis genes along the time course of experiments (Fig. 6) was in accordance with the typical rule that transcription factors can activate the transcription of multiple target genes38. Also, this confirmed that MAPK cascade relayed the signals to specific transcription factors that simultaneously regulated the expression of genes involved in FO and CA biosynthesis pathway. Moreover, the highest expression abundances (27.72-fold) of CHI at 12 h among all tested genes (Fig. 6) suggested that this gene might be most susceptible to chitosan treatment for promoting FO and CA biosynthesis in AMHRCs.

Factually, CHI is capable of catalyzing the intramolecular cyclization of bicyclic chalcone to form tricyclic (2S)-flavanone, which is well recognized as the rate-limiting step controlling the downstream flavonoid metabolism39. Accordingly, CHI is a key enzyme that can effectively regulate flavonoid biosynthesis. CHI has been verified as a unique enhancer to control flavonoid biosynthesis in Arabidopsis thaliana40. And, the expression of CHI gene was found to correlate positively with flavonoid accumulation in Lycium chinense, Citrus unshiu, and Ipomoea batatas (L.) Lam41,42,43. Moreover, the overexpression of CHI gene led to a 78-fold increase in flavonol level in the transgenic tomato44. Also, the overexpression of CHI gene resulted in the transgenic Scutellaria baicalensis hairy roots containing the maximum 2.89- and 8.82-fold increase in the yields of baicalein and wogonin, respectively45. Additionally, the overexpression of CHI gene caused the enhanced accumulation of daidzein in the transgenic soybean46. In this study, the significant increase in the productivity of FO (12.45-fold increase) and CA (6.17-fold increase) in chitosan-treated AMHRCs might be partially ascribed to the remarkable up-regulation of CHI expression. However, the weakest up-regulated genes might also cause the enhanced biosynthesis of secondary metabolites in plants. Therefore, it was inferred that the synergistic effects of all up-regulated biosynthesis genes contributed to the significant improvement in FO and CA yields.

Based on the above studies, the induction of FO and CA biosynthesis in AMHRCs via chitosan-mediated MAPK signaling cascades is illustrated schematically in Fig. 7. In detail, chitosan elicitation was initially perceived by the special receptors present on plant cell membranes, which would cause the alteration of ion efflux/influx (need to be further verified), thus resulting in the massive production of ROS. Subsequently, ROS acted as a priming signal to activate the MPK3/MPK6 cascade, which relayed the stress signaling to specific transcription factors (need to be further verified) in nucleus. After that, PR genes (e.g., βGlu, Chi1, and PR-1) were activated to enhance PR protein synthesis for improving the resistance of plant cell itself. Moreover, the specific transcription factors in nucleus after being activated was to up-regulate the expression of biosynthesis genes for promoting the production of two isoflavone phytoalexins (FO and CA), both of which could scavenge the excessive ROS for restoring the intracellular redox status in equilibrium.

Figure 7
figure 7

The putative schematic diagram of chitosan-induced FO and CA biosynthesis in AMHRCs via MAPK signaling cascades. The dotted lines indicate the processes with no detailed evidence provided in this study.

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In conclusion, a simple and feasible elicitation practice using chitosan was proposed in this work for improving the yield of two health-promoting phytoalexins (FO and CA) in AMHRCs. The low cost, nontoxicity and biocompatibility of chitosan will make the proposed elicitation protocol more commercially attractive for the scale-up production of the two bioactive isoflavones. More importantly, this study preliminarily elucidated the molecular mechanisms that the enhanced biosynthesis of FO and CA in AMHRCs was achieved by chitosan-mediated MAPK signaling cascades. However, further studies need to be done to identify the specific MAPK or the upstream kinase of MPK3/MPK6 induced by chitosan in AMHRCs.

Methods

Establishment and maintenance of AMHRCs

In our previous study, A. membranaceus hairy roots were established via Agrobacterium rhizogenes LBA9402 mediated transformation of leaf explants11. A hairy root line (AMHRL II) stocked in our laboratory with the high productivity of isoflavone and biomass was adopted for the subsequent experiments. Moreover, AMHRCs used in this work were obtained by cultivating AMHRL II under the optimized conditions reported by Jiao et al.11.

Treatment of AMHRCs by chitosan

The chitosan stock solution (10 mg/mL) was prepared using acetic acid (pH = 5.5), and autoclaved prior to use. In this work, 34 day-old AMHRCs (the optimal cultures for harvesting hairy roots) would undergo chitosan elicitation with different dosage and exposure time. Before elicitation, the fresh media were used to replace the spent ones in AMHRCs, and the chitosan stock solution was added into the renewed AMHRCs to give different final concentrations (50, 100, and 150 mg/L). In addition, AMHRCs treated with the equal volume of acetic acid solution were defined as control cultures. Subsequently, all tested AMHRCs were cultured on a gyratory shaker (120 rpm) at 25 ± 1 °C without light, and sampling was performed at different time points (0, 1, 2, 4, 6, 12, 18, 24, 30, 36, 48, 72, and 96 h). After elicitation, the collected hairy roots were rinsed thoroughly with tap water and distilled water, and divided into three parts: one being directly used for the valuation of oxidative burst, one being frozen immediately using liquid nitrogen for RNA extraction, and the rest one being dried completely for isoflavone extraction.

LC-MS/MS analysis

The isoflavone extraction from dried hairy root powders and sample preparation for LC-MS/MS analysis were performed using the methods reported by Jiao et al.11. Two target isoflavones (FO and CA) in tested samples were analyzed using the established LC-MS/MS method reported by Jiao et al.11. Two ion combinations of precursor ion/product, i.e. m/z 267.0 → 252.0 and m/z 283.0 → 268.0, were used to determine FO and CA in the extracts form root samples, respectively. The content of each target compound was expressed as microgram per gram of the dry weight (DW) of root samples.

Evaluation of oxidative burst

The level of H2O2 in fresh hairy root samples was measured according to the protocols described by Dewanjee et al.47, and the amount was expressed as micromole per gram of the fresh weight (FW) of root samples. Additionally, the activity of CAT in fresh hairy root samples was determined as the descriptions of Arbona et al.48, and the value was expressed as units per microgram of protein that was detected in enzyme extracts.

qRT-PCR analyses

To study the action mechanism of chitosan inducing phytoalexin biosynthesis, the transcription levels of genes related to MAPK signaling cascades, pathogenesis-related genes, and biosynthesis genes involved in FO and CA pathway were tested by qRT-PCR, i.e. MPK3, MPK6, βGlu, Chi1, PR-1, PAL, C4H, 4CL, CHS, CHR, CHI, IFS and I3′H. Specific primers of genes (MPK3, MPK6, βGlu, Chi1, and PR-1) related to MAPK signaling cascades (Table 1) were designed based on the transcriptome sequences reported by Liu et al.49. Primers of genes (PAL, C4H, 4CL, CHS, CHR, CHI, IFS, and I3′H) associated with FO and CA biosynthesis (Table 1) were adopted as described previously50. RNA Extraction, reverse-transcription, and gene amplification were performed using the methods reported by Jiao et al.50. The relative transcription levels of all tested genes (MPK3, MPK6, βGlu, Chi1, PR-1, PAL, C4H, 4CL, CHS, CHR, CHI, IFS and I3′H) were calculated based on the internal reference 18S gene using the method reported by Livak and Schmittgen51.

Table 1 Primers of MAPK signaling cascade genes, pathogenesis-related genes, and biosynthesis genes involved in the FO and CA pathway.
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Statistical analyses

Results were obtained from the triplicate experiments, and reported as averages ± standard deviations. The SPSS statistical software (version 17.0, SPSS Inc, USA) was used to carry out all statistical analyses. One-way analysis of variance using Tukey’s test was applied to determine the significant differences (P < 0.05) between diverse groups of data.