Enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus

Roots of most terrestrial plants form symbiotic associations (mycorrhiza) with soil- borne arbuscular mycorrhizal fungi (AMF). Many studies show that mycorrhizal colonization enhances plant resistance against pathogenic fungi. However, the mechanism of mycorrhiza-induced disease resistance remains equivocal. In this study, we found that mycorrhizal inoculation with AMF Funneliformis mosseae significantly alleviated tomato (Solanum lycopersicum Mill.) early blight disease caused by Alternaria solani Sorauer. AMF pre-inoculation led to significant increases in activities of β-1,3-glucanase, chitinase, phenylalanine ammonia-lyase (PAL) and lipoxygenase (LOX) in tomato leaves upon pathogen inoculation. Mycorrhizal inoculation alone did not influence the transcripts of most genes tested. However, pathogen attack on AMF-inoculated plants provoked strong defense responses of three genes encoding pathogenesis-related proteins, PR1, PR2, and PR3, as well as defense-related genes LOX, AOC, and PAL, in tomato leaves. The induction of defense responses in AMF pre-inoculated plants was much higher and more rapid than that in un-inoculated plants in present of pathogen infection. Three tomato genotypes: a Castlemart wild-type (WT) plant, a jasmonate (JA) biosynthesis mutant (spr2), and a prosystemin-overexpressing 35S::PS plant were used to examine the role of the JA signaling pathway in AMF-primed disease defense. Pathogen infection on mycorrhizal 35S::PS plants led to higher induction of defense-related genes and enzymes relative to WT plants. However, pathogen infection did not induce these genes and enzymes in mycorrhizal spr2 mutant plants. Bioassays showed that 35S::PS plants were more resistant and spr2 plants were more susceptible to early blight compared with WT plants. Our finding indicates that mycorrhizal colonization enhances tomato resistance to early blight by priming systemic defense response, and the JA signaling pathway is essential for mycorrhiza-primed disease resistance.


Introduction
In response to various abiotic stresses and biotic attack by herbivorous insects or pathogens, plants have evolved an array of sophisticated strategies to protect themselves against these agents. One strategy is the ability of plant root systems to form mycorrhizal associations, which are mutualistic and reciprocally beneficial symbiotic relationships between plant roots and some specific soil-borne fungi. Mycorrhizal fungi are the most important symbionts for the majority of plant species in terrestrial ecosystems (Smith and Read, 2008). It has been estimated that over 90% of land plants form arbuscular mycorrhizas (AM) with fungi belonging to the phylum Glomeromycota (Brundrett, 2002). The presence of widespread extra radical mycelium networks of mycorrhizal fungi in soils helps plants to acquire nutrients and water in soils which plant roots can not reach. Mycorrhizal associations facilitated the plant colonization on land (Redecker et al., 2000). Mycorrhizas also influence plant physiology (Smith et al., 2010) and soil structure (Rillig and Mummey, 2006;Fellbaum et al., 2012), as well as a series of important ecosystem processes, including plant diversity, nutrient cycling, and ecosystem productivity (van der Heijden et al., 1998;Vogelsang et al., 2006;Cheng et al., 2012).
Colonization or infection by certain beneficial microbes or necrotizing pathogens provokes a specific physiological state in plants called "priming" (Hao et al., 2012;Aimé et al., 2013). The primed state in plants can also be induced by various natural and artificial compounds, such as β-aminobutyric acid (BABA), jasmonic acid (JA), and salicylic acid (SA) (Jakab et al., 2001;Worrall et al., 2012). The primed plants show quicker and/or stronger induction of various cellular defense responses following exposure to either pathogens herbivore insects, or abiotic stress (Kuc, 1987;Ton et al., 2006;Jung et al., 2009;Slaughter et al., 2012;Ye et al., 2013). Recent studies demonstrate that the defense priming in Arabidopsis thaliana plants can be transferred to their progeny, conferring better protection from pathogen attack (Slaughter et al., 2012). Tomato plants grown from seeds treated with JA and BABA displayed enhanced resistance against insect herbivory and powdery mildew disease (Worrall et al., 2012).
The objectives of this study are to investigate the effects of pre-inoculation of tomato plants with Funneliformis mosseae on resistance to early blight disease caused by Alternaria solani, as well as on defense responses in pre-inoculated and un-inoculated tomato plants. We hypothesized that AMF pre-colonization primes tomato plants and initiates host defense response upon subsequent pathogen attack. In general, SA signaling triggers resistance against biotrophic and hemibiotrophic pathogens, whereas the JA pathway activates resistance against necrotrophic pathogens (Glazebrook, 2005;Robert-Seilaniantz et al., 2011). Since the pathogen A. solani exhibits a necrotrophic lifestyle, we examined the role of the JA pathway in AMF-induced priming in tomato by using transgenic tomato plants that overexpress the prosystemin gene (35S::PS) and plants with a mutation in the JA biosynthetic pathway (spr2). In tomato plants, systemic induction of JA-dependent defense responses is mediated by an 18-amino-acid peptide signal called systemin (Howe and Ryan, 1999). Tomato transgenic line 35S::prosystemin (35S::PS) that overexpress prosystemin, the systemin precursor, exhibit constitutive expression of several JA-regulated defensive proteins including proteinase inhibitors and polyphenol oxidase (Chen et al., 2006).

Plant and Fungal Materials
Tomato seeds were sterilized with H 2 O 2 (10%) for 10 min and rinsed five times with sterile distilled water. The seeds were then sowed in autoclaved sand-soil mixture (1:1).
The inocula of F. mosseae were propagated by using corn plants (Zea mays L.) cultured in autoclaved sand (Chellappan et al., 2002). A mixture of corn roots and rhizospheric sand from trap cultures containing approximate 35 AMF propagules per gram was used for AM inoculation.
The pathogen was cultured for 6 day on potato dextrose broth with 100 mg/l streptomycin sulfate, at 28 • C in darkness and on a shaker at 150 rpm. Then the fungal culture was centrifuged at 1000 g, re-suspended in sterilized distilled water, and recentrifuged. The concentration of AMF spores was measured and adjusted to 10 6 conidia per milliliter using a hemacytometer.
To reveal the role of the jasmonate (JA) signaling pathway in mycorrhiza-induced systemic priming of disease resistance against A. solani, both overexpressing 35S::prosystemin and defective spr2 mutant lines, as well as their corresponsive wildtype (WT) tomato plants, were used to compare their differential responses to A. solani infection after mycorrhizal colonization by AMF F. mosseae. Tomato cv Castlemart was used as the WT parent, the mutant line suppressor of prosystemin-mediated responses2 (spr2) was derived from cv Castlemart (Li et al., 2003). The 35S::PS transgenic plants were developed from the seeds collected from a 35S::prosys/35S::prosys homozygous line (Chen et al., 2006) that was backcrossed five times using the recurrent parent cv Castlemart.

Bioassay
To determine mycorrhizal colonization on tomato disease resistance, a bioassay was carried out to compare the disease incidence and disease severity index (see definitions below) between non-mycorrhizal and mycorrhizal tomato plants. The brown loam soil collected from the campus of South China Agricultural University in Guangzhou (China) contained 1.52% organic matter, 0.789 g/kg total N, 0.42 g/kg total P, 1.76 g/kg total K, 35.93 mg/kg available N, 1.30 mg/kg available P, and 37.14 mg/kg available K with a pH of 4.68. The soil autoclaved at 121 • C for 2 h was mixed with sterilized sand at a ratio of 2:1. The mixture was used as culture medium of tomato plants. The inocula (225 g) of AMF F. mosseae were incorporated into the obtained mixture (1.5 kg) for mycorrhizal inoculation. The same amount of mixture (1.5 kg) and sterilized sand (225 g) was applied to each non-mycorrhizal control pot. The control pots were watered with a soil filtrate obtained by shaking nonpasteurized rhizospheric sand with sterilized water then filtering it through a Watman No 1 filter, to exclude possible effect of other soil microorganisms. The filtrate contained the natural soil microbial population without AMF inocula.
Two pre-germinated tomato seeds were transplanted into each plastic pot with the growth substrate. Ten days later, the seedlings were thinned to one plant per pot. The plants were grown in a growth chamber at 25 ± 1 • C with a 16 h photoperiod, 150 Md/m 2 /s PAR and 60% relative humidity. The seedlings were watered daily and fertilized every 5 days with 50 mL of Hoagland nutrient solution (5 ml 1 M KNO 3 , 5 ml 1 M Ca(NO 3 ) 2 , 1 ml 1 M MgSO 4 , 2 ml 1 M KH 2 PO 4 , 1 ml 46 mM H 3 BO 3 , 1 ml 11 mM MnCl 2 , 1 ml 1 mM ZnSO 4 , 1 ml 3.5 mM CuSO 4 and 1 ml 17.7 mM FeEDTA in one liter water). Thirty-five days after transplanting, tomato leaves in each pot were carefully sprayed with 30 ml of a conidia suspension (10 6 conidia/ml) of A. solani. All plants were covered with an air-tight plastic bag during pathogen infection to maintain the high relative humidity facilitating spore germination.
The incidence and severity of tomato early blight were measured 10 d post pathogen inoculation. Disease incidence was indicated by percentage of diseased tomato leaves. Disease severity was estimated using a Disease Index (DI) calculated from disease grades 0-5 (Sriram et al., 1997), using the following formula: (1) Individual leaf ratings in the formula refer to disease grade of each leaf of tomato. The maximum disease score refers to the maximum disease grade observed during the entire period of the experiment. Fifty root samples (1 cm in length) were collected from each plant, cleaned and stained to examine AM colonization by the ink-vinegar staining method (Vierheilig et al., 1998;Mukerji et al., 2002).

Enzyme Assays
The experiment setups for enzyme assays and real-time RT-PCR analysis were the same as those for disease bioassays. PAL activity was determined as the rate of the conversion of L-phenylalanine to trans-cinnamic acid at 290 nm. Leaf samples (0.2 g) were harvested from the different treatment conditions (CK, Fm, As, and Fm+As) and ground using liquid nitrogen and homogenized in 1 ml ice cold 0.05 M sulfate buffer, pH 8.8 containing 7 mM 2-mercaptoethanol and 0.1 g insoluble polyvinylpyrrolidone.
The homogenate was centrifuged at 12000 g for 20 min. The supernatant was used for enzyme analysis. PAL activity was determined spectrophotometrically (Edwards and Kessmann, 1992). Lipoxygenase (LOX) activity was measured as conjugated diene formation (Macri et al., 1994). Leaf samples (0.2 g) were ground using liquid nitrogen and extracted with 1 ml ice-cold 0.5 M TRIS-HCl buffer (pH 7.6) and centrifuged at 12 000 g for 15 min at 4 • C. The supernatant was kept at 4 • C until used. The substrate contained 1.6 mM linoleic acid and 0.5% (v/v) Tween 20 in 0.1 M phosphate buffer (pH 7.6). The reaction was initiated by the addition of 0.2 ml crude extract in 4.8 ml of the substrate. Diene formation was followed as increase of absorbance at 234 nm.
Leaf samples (0.1 g) were ground in liquid nitrogen and extracted with 2 ml 0.05 M sodium acetate buffer (pH 5.0) and centrifuged at 12 000 g for 15 min at 4 • C. The supernatant was used for the enzyme assay of β-1,3-glucanase and chitinase. β-1,3-Glucanase activity was assayed by the laminarindinitrosalicylic acid method (Pan et al., 1991). The chitinase activity was analyzed as described (Boller and Mauch, 1988).

Real-time RT-PCR Analysis
Differential expression of selected genes was verified by real time -polymerase chain reaction (RT-PCR) using the RNA samples isolated from tomato leaves obtained from the four treatments. The total RNA was extracted and isolated as described by Kiefer et al. (2000), with slight modification. Fresh leaves (0.2 g) were ground with a mortar and pestle in liquid nitrogen, and the powdered tissue transferred to a 2 ml Eppendorf tube, then 1000 μl TRIzol reagent (Invitrogen) was added and mixed. After incubation for 8-10 min on ice, 200 μl chloroform was added and mixed. Following 5 min incubation at room temperature, the mixture was centrifuged at 12,000 g for 15 min at 4 • C. The supernatant was transferred to a 1.5 ml Eppendorf tube and 500 μl isoamylalcohol was added, followed by vortexing at room temperature for 10 min and centrifugation at 13,000 g for another 10 min at 4 • C. The supernatant was discarded and the pellet was washed with 1 ml 75% ethanol (v/v), dissolved in 30 μl RNAse free water and kept at −80 • C until used. RNA integrity was checked on a denaturing agarose gel electrophoresis; the concentration was determined spectrophotometrically before further use.
The expression patterns of defense-related genes (PAL, LOX, AOC, PR1, PR2, and PR3) in different treated tomato leaves were analyzed by using Real Time-PCR. The primers for target genes PAL, LOX, AOC, PR1, PR2, and PR3 were designed by Primer 3.0 software (Applied Biosystems, http://fokker.wi. mit.edu/primer3/input.htm) based on tomato mRNA sequences deposited in GenBank. The gene-specific primer sequences used are listed in Table 1. Ubi3 (Accession No. X58253) was used as a reference. Proteinase inhibitor II (Pin2) gene was chosen because it is typical jasmonic acid responsive gene systemically induced upon wounding (Farmer and Ryan, 1992). Real-time PCR reactions were carried out with 0.2 μl (0.15 μM) of each specific primers, 1 μl (50 ng) cDNA, and 12.5 μl of the SYBR green master mix (Quanti Tech SYBR Green kit, Qiagen, Gmbh Hilden, Germany), and the final volume was made up to 25 μl with RNase-free water. In the negative control, cDNA was replaced by RNase free water. The reactions were performed on a DNA Engine Opticon 2 Continuous Fluorescence Detection System (MJ Research Inc., Waltham, MA, US). The program used for real-time PCR was 3 min initial denaturation at 95 • C, followed by 35 cycles of denaturation for 20 s at 95 • C, annealing for 20 s (PAL: 57 • C; LOX: 56.9 • C; AOC: 56.5 • C; PR1: 55.4 • C; PR2: 56 • C; PR3: 58 • C; Pin2: 60.0 • C; Ubi3: 58 • C) and extension for 20 s at 72 • C. The fluorescence signal was measured immediately after incubation for 2 s at 75 • C following the extension step, which eliminates possible primer dimer detection. At the end of the cycles, melting temperatures of the PCR products was determined between 65 and 95 • C. The specificity of amplicons was verified by melting curve analysis and agarose gel electrophoresis. Three independent biological replicates for each treatment were used for qRT-PCR analyses.

Statistical Analysis
For each treatment, three replicates were maintained in a completely randomized design. SAS 8.0 (SAS Institute, Cary, North Carolina) package for windows was used for statistical analysis. The data were analyzed with a oneway analysis of variance with the significant differences among means identified by Tukey's multiple range test (P < 0.05).

Induction of Disease resistance by Mycorrhizal Colonization
Inoculation of tomato plants with the AMF, F. mosseae, led to a significant decrease in disease incidence and disease severity of early blight compared to the control plants without mycorrhizal inoculation ( Table 2). Disease incidences and indices were reduced in mycorrhizal plants by 54.3% and 72.8%, respectively, 10 d after pathogen inoculation. Mycorrhizal plants had significantly fewer disease symptoms than non-mycorrhizal plants (Figure 1). Furthermore, disease development in AMF-inoculated plants  was significantly slower. Microscopic observation showed that the mycorrhizal infection rate was 55.1% in the inoculated plants ( Table 2).

Induction of Defense-related Enzymes by Mycorrhizal Colonization
To examine effects of mycorrhizal colonization on defense responses in host plants in presence of pathogen infection tomato plants were subjected to four treatments: (1) CK: control without fungal inoculation; (2) As: inoculation with A. solani; (3) Fm: inoculation with F. mosseae; (4) Fm+As: inoculation with both F. mosseae and A. solani. Four defense-related enzymes, including PAL, LOX, chitinase, and β-1,3-glucanase were analyzed in the leaves of tomato plants. Mycorrhizal preinoculation significantly enhanced activities of the four enzymes in the leaves upon pathogen infection (Figures 2A-D). The activities of all tested enzymes were significantly higher in treatment Fm+As after the pathogen inoculation and reached a maximum at 65 h. The activity of β-1,3-glucanase was increased by 34.7, 33.3, and 28.8%, respectively, relative to those in treatments CK, As, and Fm 65 h post the pathogen inoculation (Figure 2A). However, the activity of β-1,3-glucanase did not differ significantly between the other treatments (CK, As, and Fm) (Figure 2A). The enzymatic activity of LOX in treatment Fm+As was significantly higher after pathogen inoculation ( Figure 2B). LOX activity in treatment Fm+As increased by 48.1, 32.2, and 99.5% at 18 h after pathogen inoculation compared to treatments CK, As, and Fm, respectively, and increased by 38.1, 37.8, and 68.1% at 65 h after pathogen inoculation, respectively.
Although mycorrhization led to some increase in PAL activity in treatment Fm, the PAL induction was more pronounced in treatment Fm+As. The PAL activity in treatment Fm+As was, on average, higher by 104.3, 74.9, and 79.5% than that of treatment CK, As, and Fm, respectively, at 65 h after pathogen inoculation ( Figure 2C). In contrast, the difference in PAL activity among treatments CK, As, and Fm were less variable. In particular, the PAL activity was not significantly different among treatment CK, As, and Fm at 18 and 65 h following pathogen inoculation.
Chitinase activity in mycorrhizal pre-inoculated plants (Fm+As) was significantly higher at 18, 65, and 100 h after the pathogen inoculation ( Figure 2D). It displayed increases of 44.1, 62.1, and 55.1% in treatment Fm+As compared to treatments CK, As, and Fm, respectively, at 65 h after pathogen inoculation.

Transcript Induction of Defense-related Genes by Mycorrhizal Colonization
To determine whether mycorrhizal colonization enhances the disease resistance and defense response by inducing transcription of defense-related genes , the expression patterns of the six genes (PAL, LOX, AOC (encoding allene oxide cyclase for JA biosynthesis), PR1, PR2, and PR3) were analyzed by using real-time RT-PCR from tomato leaves 18, 65, 100, and 140 h post pathogen inoculation. Mycorrhizal pre-inoculation of tomato plants with F. mosseae and later pathogen inoculation with A. solani (treatment Fm+As) induced accumulation of PAL, LOX, AOC, PR1, PR2, and PR3 transcripts over basal levels present in the leaves of un-inoculated control (CK), sole A. solani inoculation (As), and F. mosseae colonization (Fm) treatments 18, 65, 100, and 140 h after pathogen inoculation (Figure 3). The expression levels of PAL, LOX, and AOC were induced approximately 3.0, 7.1, and 18.8-fold at 100 h, and by 4.1, 5.3, and 5.8-fold at 140 h post pathogen inoculation, respectively, in response to dual inoculation with the AMF and the pathogen (Fm+As) relative to the non-mycorrhizal control (CK) (Figures 3A-C). Mycorrhizal pre-colonization induced transcripts of PR1, PR2, and PR3 by 20.4, 35.5, and 47.7fold at 65 h, by 8.0, 37.7, and 22.9-fold at 100 h, respectively (CK) (Figures 3D-F). Pathogen infection alone (treatment As) induced transcripts of the six genes in the leaves of nonpreinoculated tomato plants, but the induction was much less and slower compared with that in mycorrhizal and pathogeninfected plants (treatment Fm+As). Mycorrhizal colonization (treatment Fm) alone did not induce gene expression of PAL and PR3 (Figures 3A,F). Although sole mycorrhization upregulated transcripts of PR1, PR2, and AOC at 100 and 140 h, the induction was even weaker than that by pathogen infection.

Role of Jasmonate Signaling Pathway in AMF-induced Disease Resistance
Three tomato genotypes: a WT plant, a JA biosynthesis mutant (spr2), and a prosystemin-overexpressing 35S::PS plant, were used to identify the role of the JA signaling pathway in mycorrhiza-induced disease resistance against A. solani. The plants of the three genotypes were subjected to the same four treatments as above. There was no significant difference in activities of the four defense-related enzymes in control plants of the three genotypes (Figures 4A-D). However, the three genotypes showed large differences in activities of the four defense-related enzymes in response to pathogen infection (As) and dual inoculation with the pathogen and mycorrhizal fungus (Fm+As). The 35S::PS plants showed higher induction of enzymatic activities in A. solani-inoculated plants compared to the other two genotypes. Most importantly, mycorrhizal pre-inoculated 35S::PS plants showed the highest induction of enzymatic activities (Figures 4A-D). β-1,3-Glucanase activity in treatment Fm+As was increased by 1083.7, 291.3, and 495.5% at 100 h post pathogen inoculation compared with that in treatments CK, As, and Fm, respectively (Figure 4Ac). Similarly, chitinase activity in treatment Fm+As was increased by 795.2, 161.5, and 498.8% at 65 h compared with the other three treatments (Figure 4Db). Similar trends were observed for LOX and PAL activities (Figures 4B,C). The LOX and PAL activities were increased in mycorrhizal preinoculated 35S::PS and WT plants after pathogen inoculation, but 35S::PS plants exhibited significantly higher LOX and PAL activities as compared to WT plants (Figures 4B,C). The 35S::PS plants showed 48.5, 125.0, 56.0, and 111.4% higher PAL activity in treatment Fm+As than that of WT plants 18, 65, 100, and 140 h after pathogen inoculation, respectively (Figure 4Ca-d).
In contrast, the four tested enzymes were not induced in the spr2 plants in response to pathogen inoculation (As) and dual inoculation (Fm+As) (Figures 4A-D).
Mycorrhizal pre-inoculation on 35S::PS and WT tomato plants resulted in strong induction of transcripts of defenserelated genes (PAL, LOX, Pin2, PR1, PR2, and PR3) upon pathogen attack (treatment Fm+As) (Figures 5A-F). The highest induction of the six defense-related genes was found in the mycorrhizal 35S::PS plants. While no induction of PAL expression was found with pathogen inoculation alone (As) or AMF inoculation alone (Fm), dual inoculation with the AMF, and pathogen induced PAL 24.0-and 10.2fold in 35S::PS and WT plants, respectively, 65 h after pathogen inoculation (Figure 5Ab). Similarly, AMF preinoculation and later pathogen infection induced PR1 18.3-, 6.5-, and 17.5-fold in 35S::PS plants as compared to that in treatments CK, As, and Fm, respectively, 100 h after pathogen inoculation (Figure 5Dc). Although pathogen infection alone induced PR1 transcripts in 35S::PS and WT plants, the induction was significantly lower relative to treatment Fm+As ( Figure 5D). No induction was found in the spr2 plants in response to pathogen inoculation (As) or dual inoculation (Fm+As) (Figures 5A-F). Similar inductions of PR3 and Values are means ± SE from three sets of independent experiments with three pots per treatment for each set of experiments. Significant differences (P < 0.05 using Tukey post hoc test) among treatments in a group are indicated by different letters above bars.
Pin2 transcripts were observed in 35S::PS and WT plants, but there was no induction in the JA-deficient spr2 mutant (Figures 5C,F).
Bioassays showed that mycorrhizal pre-inoculation on 35S::PS and WT tomato plants significantly reduced disease incidence and disease severity of early blight relative to AMF un-inoculated control plants (Table 3). Mycorrhizal colonization led to 17.6 and 15.6% reductions in the disease incidence and disease severity, respectively, in WT plants, and 19.7 and 20.4% reductions, respectively, in 35S::PS plants. In contrast, mycorrhizal inoculation did not affect the disease incidence and severity of the spr2 mutant plants. On the other hand, the spr2 plants had the lowest mycorrhizal colonization rate and the highest disease incidence and severity among the three tomato genotypes ( Table 3).

Discussion
In last two decades, early blight has become a major disease of tomato in many parts of China (Dong et al., 2015). This study shows that tomato early blight can be alleviated through mycorrhizal inoculation, which is consistent with previous finding by Fritz et al. (2006). The enhanced disease resistance was not due to improved phosphorus nutrient, though the underlying mechanism was not clear (Fritz et al., 2006). Mycorrhizal fungi are ideal biocontrol agents because they are natural soil-borne biota and can establish stable and long lasting mutualistic symbiosis with the roots of most vascular plant species, including most crops (Smith and Read, 2008). Mycorrhizal associations benefit not only plant nutrient absorption (Smith and Read, 2008), but also plant resistance to diverse abiotic stresses (Ruiz-Lozano et al., 1996) and soil-borne fungal pathogens (Harrier and  , 2004;Bi et al., 2007). More interestingly, AM symbiosis also enhances plant resistance against foliar pathogens such as fungal pathogens [e.g., Botrytis cinerea (Pozo et al., 2010;Fiorilli et al., 2011) and A. solani (Fritz et al., 2006)], bacteria [e.g., Xamantomonas campestris (Liu et al., 2007) and viruses (e.g., Tomato yellow leaf curl Sardinia virus (Maffei et al., 2014)].

Watson
Induction of pathogenesis-related (PR) proteins is believed an indicator of plant induced defense responses. Accumulation of chitinase and β-1,3-glucanase has been associated previously with induced systemic resistance in tomato to A. solani (Lawrence et al., 1996) and Fusarium oxysporum (Pozo et al., 2002). Basic isozymes of chitinase and β-1,3-glucanase inhibit A. solani in vitro (Lawrence et al., 1996). Early blight-resistant tomato lines possess higher levels of chitinase and β-1,3-glucanase than susceptible genotypes (Lawrence et al., 2000). PR genes have been frequently used as marker genes for systemic acquired resistance in many plant species (Mitsuhara et al., 2008). Our study showed that mycorrhizal pre-inoculation in tomato roots systemically induced both enzyme activities of chitinase and β-1,3-glucanase, and transcripts of the genes PR1, PR2, and PR3 encoding PR proteins in the leaves of tomato. Pozo et al. (2002) found that F. mosseae colonization in tomato plants reduced both local and systemic disease symptoms caused by Phytophthora parasitica infection, as well as provoked local and systemic induction of chitinase, β-1,3-glucanase and superoxide dismutase.
Our study showed that mycorrhizal inoculation itself did not affect most enzyme activities and only slightly induced transcripts of AOC, PR1, and PR2. However, upon pathogen attack AMF pre-inoculation strongly induced defense responses of all six tested genes and four defense-related enzymes in tomato plants. Based on the results that plants inoculated  with both F. mosseae and A. solani had less disease damage, higher levels of defense-related enzymatic activities and gene expression than the controls, or pathogen or mycorrhizal inoculations alone, we suggest that mycorrhizal colonization on tomato can prime plant defense responses against early blight disease.
Most studies on defense priming focus on priming signals triggered by herbivore-induced volatile compounds Heil and Silva Bueno, 2007;Ramadan et al., 2011). Some studies show that priming of plant defense can also be triggered by certain beneficial micro-organisms van Hulten et al., 2006;van Wees et al., 2008), including AMF (Pozo and Azcón-Aguilar, 2007;Pozo et al., 2009;Jung et al., 2012). Mycorrhizal pre-inoculation results in significantly higher production of PR-1a and basic β-1,3-glucanases in tomato plants upon Phytophthora infection (Cordier et al., 1998;Pozo et al., 1999;Maldonado-Bonilla et al., 2008). RNAseq-based transcriptome analysis showed that mycorrhization led to the transcriptional changes in categories of signaling, hormone metabolism, biotic, and abiotic stresses, and several differentially expressed genes were related to systemic defense priming (Cervantes-Gámez et al., 2015). Our study confirms that priming is an important mechanism operating in mycorrhizainduced disease resistance.
Plant disease resistance is tightly manipulated through an interconnected network of signaling pathways of JA and SA. PAL is the key enzyme involved in the biosynthesis of the signal molecule, SA (Mauch-mani and Slusarenko, 1996). SA accumulates in cells undergoing hypersensitive response and it is essential for local and systemic resistance response (Gaffney et al., 1993;Makandar et al., 2012). Induction of PAL activity is a reliable indicator of plant resistance expression (Mauch-mani and Slusarenko, 1996). An increase in of PAL activity indicates that, upon pathogen attack, mycorrhizal colonization initiates SA signaling pathways and increase accumulation of phenolic compounds.
The JA signaling pathway has been demonstrated to play a vital role in mediating plant defense responses to chewing herbivore insects (Howe and Jander, 2008;Bosch et al., 2014) and necrotrophic pathogens (Glazebrook, 2005;Robert-Seilaniantz et al., 2011). External application of methyl JA primes Arabidopsis defense against caterpillar herbivory (Rasmann et al., 2012).
Since A. solani is a necrotrophic pathogen, we examined the roles of the JA pathway in AMF-induced priming in tomato. LOX, AOC, and AOS (allene oxide synthase) are three important enzymes in JA biosynthesis (Hause et al., 2002;Schaller et al., 2005). Stronger and quicker induction of LOX and AOC in mycorrhizal plants suggest that mycorrhizal colonization can also provoke the JA pathway, which thereby increases broad-spectrum disease resistance (De Vos et al., 2005).
Use of JA biosynthesis (spr2) mutant and prosysteminoverexpressing 35S::PS plants revealed that the JA signaling pathway mediated AMF-primed defense in tomato plants. Mycorrhizal 35S::PS plants had significantly higher levels of defense-related enzyme activity and gene expression than mycorrhizal WT plants and non-mycorrhizal 35S::PS plants in response to A. solani infection (Figures 4 and 5). Although pathogenic infection alone induced enzymatic activities and gene transcripts in WT plants, the induction was lower than that of pathogen-infected mycorrhizal plants. However, AMF preinoculation and pathogenic infection did not lead to induction of defense-related enzymes and genes in spr2 plants. The mycorrhizal 35S::PS plants were the most resistant to early blight and mycorrhizal spr2 plants were the most susceptible (Table 3). Non-mycorrhizal 35S::PS plants showed similar level of disease resistance to mycorrhizal WT plants. These results suggest that the JA pathway is required for AMF-induced systemic priming of defense against A. solani. Rasmann et al. (2012) showed that herbivory in the previous generation primed Arabidopsis and tomato for enhanced insect resistance, and Arabidopsis mutants that were deficient in JA perception did not exhibit inherited resistance, demonstrating that the JA pathway is required in mother plants for priming resistance in the next generation. Low mycorrhizal colonization rate ( Table 3) may suggest that JA signalings are necessary for establishment of mycorrhizal association.

Conclusion
Pre-inoculation of tomato plants with F. mosseae enhanced tomato resistance to early blight. Root colonization by AMF systematically induced the defense-related enzymes and genes in the leaves of tomato upon pathogen challenge. Our results suggest that mycorrhizal-induced disease resistance in tomato is associated with priming for an efficient activation of defense responses upon pathogen attack. The AMF-induced primed responses were systemic and the JA pathway is required for such responses. Since most land plants have symbiotic association with mycorrhizal fungi (Brundrett, 2002), use of mycorrhizal fungi as defense priming elicitors may be an important evolutionary strategy for plant defense against pathogens and it may serve as an important alternative for management of crop disease in sustainable agriculture.