ORIGINAL RESEARCH article
A Jasmonate-Inducible Defense Trait Transferred from Wild into Cultivated Tomato Establishes Increased Whitefly Resistance and Reduced Viral Disease Incidence
- 1Instituto de Hortofruticultura Subtropical y Mediterránea “La Mayora”, Universidad de Málaga – Consejo Superior de Investigaciones Científicas, Algarrobo-Costa, Spain
- 2Department of Population Biology, Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, Netherlands
- 3Instituto de Biología Molecular y Celular de Plantas, Consejo Superior de Investigaciones Científicas – Universidad Politécnica de Valencia, Valencia, Spain
Whiteflies damage tomatoes mostly via the viruses they transmit. Cultivated tomatoes lack many of the resistances of their wild relatives. In order to increase protection to its major pest, the whitefly Bemisia tabaci and its transmitted Tomato Yellow Leaf Curl Virus (TYLCV), we introgressed a trichome-based resistance trait from the wild tomato Solanum pimpinellifolium into cultivated tomato, Solanum lycopersicum. The tomato backcross line BC5S2 contains acylsucrose-producing type-IV trichomes, unlike cultivated tomatoes, and exhibits increased, yet limited protection to whiteflies at early development stages. Treatment of young plants with methyl jasmonate (MeJA) resulted in a 60% increase in type-IV trichome density, acylsucrose production, and enhanced resistance to whiteflies, leading to 50% decrease in the virus disease incidence compared to cultivated tomato. Using transcriptomics, metabolite analysis, and insect bioassays we established the basis of this inducible resistance. We found that MeJA activated the expression of the genes involved in the biosynthesis of the defensive acylsugars in young BC5S2 plants leading to enhanced chemical defenses in their acquired type-IV trichomes. Our results show that not only constitutive but also these inducible defenses can be transferred from wild into cultivated crops to aid sustainable protection, suggesting that conventional breeding strategies provide a feasible alternative to increase pest resistance in tomato.
Tomato (Solanum lycopersicum L.) is one of the most important and consumed vegetables worldwide. Production, however, is severely threatened since tomatoes are susceptible to diseases caused by all type of pathogens (i.e., viruses, bacteria, and fungi), and animal pests such as nematodes, insects, and mites. The low level of genetic variation within the cultivated species makes difficult to find natural sources of resistance for breeding programs. This is due to the consecutive strong genetic bottlenecks performed during domestication, where marketable genotypes were selected by using low numbers of plants from the existing germplasms (Bai and Lindhout, 2007). Consequently, current cultivated tomato varieties present a large diversity in growth habit, leaf morphology and fruits-related traits, but they lack resistances to pests and diseases (Schauer et al., 2005; Foolad, 2007). One of the major arthropod pests of cultivated tomato is the whitefly (Hemiptera: Aleyrodidae) Bemisia tabaci [Gennadius]. Whitefly feeding affects plant development (Inbar and Gerling, 2008) but, most importantly, results in acquisition and transmission of several viral plant diseases (Navas-Castillo et al., 2011). Whitefly-transmitted virus diseases have become an emerging problem in vegetable production for which no efficient solutions have been developed (Moriones and Navas-Castillo, 2000; Navas-Castillo et al., 2011). One of the most destructive of these viral diseases in tomato is Tomato yellow curl disease (TYLCD) caused by Tomato yellow leaf curl virus (TYLCV) (Moriones and Navas-Castillo, 2009). Host–plant resistance may be decisive to conduct successful integrated pest management (IPM) of whiteflies in order to prevent plant viral diseases (Nombela and Muñiz, 2009). This notion is reinforced by the observation that insect-transmitted virus diseases are more restricted when the performance of their vectors is lower (Mutschler and Wintermantel, 2006; Broekgaarden et al., 2011). In this sense, plant breeding for insect resistance has received an increased interest since resistances from wild tomato species can be introgressed into susceptible cultivars (Foolad, 2007).
Resistance to herbivores largely depends on physical and chemical plant defenses that deter or inhibit feeding, oviposition and development of larvae or adults. Among these resistance traits, presence of glandular trichomes and their production of allelochemicals – e.g., acylsugars, sesquiterpenes, and methyl ketones – found in wild tomato species have been shown to confer a high level of resistance against whiteflies (Mutschler et al., 1996; Freitas et al., 2002; Muigai et al., 2002; Bleeker et al., 2009; Firdaus et al., 2012). Cultivated tomato lacks many of these secondary metabolites and its glandular trichomes produce insufficient levels of anti-herbivore substances making them relatively susceptible to a wide range of pests (Besser et al., 2009; McDowell et al., 2011). Only a few breeding programs for plant resistance to whiteflies were successful in transferring constitutive trichome-based resistances from wild into susceptible cultivated tomatoes (Goffreda et al., 1989; Maluf et al., 2010; Leckie et al., 2012), but to our knowledge no such commercial cultivar has been released commercially yet.
Previously we reported that the wild tomato species Solanum pimpinellifolium accession TO-937 was resistant to the two-spotted spider mite Tetranychus urticae and the whitefly B. tabaci (Fernández-Muñoz et al., 2000; Alba, 2006; Rodríguez-López et al., 2011). Genetic and biochemical studies revealed that resistance in TO-937 was associated with acylsucroses-producing type-IV glandular leaf trichomes (Fernández-Muñoz et al., 2003; Alba et al., 2009). The close phylogenetic relationship of this wild species with the cultivated tomato made TO-937 suitable as a resistance donor. Accordingly, acylsucrose-producing advanced backcross (BC) lines were generated (at BC3 and BC5 levels of introgression) using the tomato (S. lycopersicum) cultivar ‘Moneymaker’ as a recipient for the trait. The line in BC3 (ABL 14-8) was tested for resistance to whitefly and TYLCV transmission (Rodríguez-López et al., 2011). Results showed that this acylsucrose-producer line was repellent to whiteflies and this reduced the incidence of TYLCD. However, in ABL 14-8, as well as in more advanced backcross lines, the density of acylsucroses-producing type-IV trichomes varied across different plant ages. Therefore, low levels of acylsucrose production were detected in young plants. This resulted in a limited protection against whiteflies and lower effectiveness in reducing TYLCD transmission in 4–5 leaf stage ABL 14-8 plants (Rodríguez-López et al., 2011). Because, TYLCD infections during early growth stages may have a devastating effect on tomato yield (Moriones and Navas-Castillo, 2000; Srinivasan et al., 2012), it was necessary to obtain plants displaying an earlier expression of these resistance traits. We reasoned that an alternative approach, i.e., by artificially inducing such trichomes in early growth stages of BC lines, might enhance plant protection. Artificial induction of plant defenses against herbivores can be accomplished by the application of elicitors, such as plant hormones (Thaler et al., 1999; Andreu et al., 2006). For example, expression of anti-herbivore direct and indirect defenses such as the biosynthesis of defensive secondary metabolites and enzymes (Takabayashi et al., 2000; Kant et al., 2004; Chen et al., 2006), and trichome production (Boughton et al., 2005; Campos et al., 2009; Maes and Goossens, 2010) can be induced by the plant hormone jasmonic acid (JA) or its derivative volatile form methyl jasmonate (MeJA).
In the present study, we investigated whether MeJA application might promote an early expression of the TO-937 derived trichome-based resistance traits against whiteflies present in an acylsucrose-producing BC5 line, BC5S2. Using the two near-isogenic lines, i.e., BC5S2 and its recurrent parent ‘Moneymaker,’ we assessed to which extent MeJA induces the trichome-based defense traits of TO-937 and if such induction suffices for enhancing protection against whiteflies and the viral disease they transmit, TYLCD. For this we tested the inducibility of type-IV trichome densities and exudates, and the effect on tomato resistance against whiteflies. Moreover, we assessed the transcriptomic profiles of BC5S2 and ‘Moneymaker’ in order to provide a mechanistic explanation for the differences observed between the two plant lines. Here, we show that the constitutive defenses based on acylsucrose-producing type-IV trichomes can be modulated by MeJA in the tomato breeding line BC5S2, but not in ‘Moneymaker.’ We argue that we have transferred an MeJA-inducible defense from a wild tomato into a cultivated breeding line.
Materials and Methods
Plant Material and Hormone Treatments
The tomato cultivar ‘Moneymaker’ (MM) and its near-isogenic line BC5S2 were used for the experiments. BC5S2 was generated from the initial cross S. lycopersicum cv. Moneymaker ×S. pimpinellifolium acc. TO-937 followed by five cycles of combined recurrent crosses toward ‘Moneymaker’ and subsequent selfing steps with selection for high type-IV trichome density and acylsugar production, plus two additional final selfing steps (Supplementary Figure S1). Seedlings were sown in plastic pots of 12 cm containing 15% plant-nutrient loaded zeolite and 85% coconut fiber substrate. Plants were grown within a glasshouse under natural lighting with loose temperature control (22–27°C day, 17–20°C night) and watered when needed. Two leaf growth-stage plantlets were sprayed with 7.5 mM methyl jasmonate (MeJA) (Sigma-Aldrich) in 0.8% ethanol aqueous solution until the point of run-off. Mock treatment with 0.8% ethanol aqueous solution was used as control. Multiple MeJA inductions were performed by three applications on days 0, 7, and 14.
Whitefly Colony and Virus Inoculation
Non-viruliferous B. tabaci whiteflies [Mediterranean (MED) species, formerly Q biotype] originating from field individuals collected in Málaga (Spain) were reared on melon plants (Cucumis melo L. ‘ANC42,’ IHSM La Mayora-CSIC germplasm collection; or cultivar Primal F1, S&G Vegetables) within wooden cages covered with insect-proof nets, in a glasshouse with loose temperature control (22–27°C day, 17–20°C night) and supplemental light when needed. Viruliferous whiteflies were obtained by allowing B. tabaci adults a 48-h acquisition access period (AAP) on TYLCV-infected MM plants. The infectious clone of the worldwide distributed IL strain of TYLCV begomovirus associated to TYLCD (TYLCV-IL) (Morilla et al., 2005) was used to infect tomato plants by using the Agrobacterium tumefaciens-mediated inoculation (further on referred to as “agroinoculation”) method described in Monci et al. (2005). Detection of TYLCV-IL was performed by squash-blot hybridization following the indications described by Navas-Castillo et al. (2000).
MeJA Effect on Glandular Trichome Induction and Targeted Trichome-Associated Secretions
Trichome density and targeted associated secretions in leaf exudates were measured on leaflets of the third youngest leaf at 21 days after the initial hormone treatment (dai). Two independent replicated experiments were carried out. Type-IV trichome density was measured following the indications by Alba et al. (2009). Previous analysis of TO-937 and the derived S. lycopersicum introgression lines indicated that these produced sucrosyl esters. Epicuticular leaf acylsucroses were extracted and de-esterified using the method described by Goffreda et al. (1990), and the resulting free-sugar moiety was quantified spectrophotometrically using a hexokinase-based glucose assay. In short, aliquots of acylsucroses were concentrated by evaporation, re-dissolved in methanol and saponified adding 0.04 N NaOH. Free sucrose was hydrolyzed to glucose and fructose by adding invertase (Sigma-Aldrich), and then phosphorylated by adenosine triphosphate (Sigma-Aldrich) in the reaction catalyzed by hexokinase (Sigma-Aldrich). The resulting glucose-6-phosphate was oxidized to 6-phosphogluconate in the presence of nicotinamide adenine dinucleotide in a reaction catalyzed by glucose-6-phosphate dehydrogenase (Sigma-Aldrich). The increase in absorbance at 340 nm was recorded, and initial sucrose quantities were determined by using a sucrose standard curve in the range of 0.15–5.8 mM, and expressed as nmol of sucrose esters per cm2 of leaf area. Phenolic compounds from leaf exudates were extracted by using a method described by Antonious et al. (2003) and quantified using the Folin-Ciocalteu colorimetric method (Hagerman et al., 1997) (for more details see Supplementary Method 1). The concentration of phenolics was determined using chlorogenic acid as a standard, and expressed as chlorogenic acid equivalents in micrograms per cm2 of leaf area. In addition, phenolics were visualized locally in planta by diphenylboric acid-2-aminoethyl ester (DPBA) staining following the indications described by Buer et al. (2007).
Whitefly Preference Bioassays
Whitefly settling behavior was assessed under no-choice conditions following the experimental design described by Rodríguez-López et al. (2012). Six detached leaflets of control and MeJA-treated MM or BC5S2 plants were collected at 21 dai and placed inside a plastic tray (25 cm × 25 cm) forming a circle. The petiolules of the leaflets were inserted in perforated small petri dishes filled with nutrient solution (0.25 g/l of Nutrichem 60, Miller Chemical, Hanover, PA, USA). Thirty adult B. tabaci whiteflies were then released in the center of the circle after a short cold treatment. Plastic trays were closed with a lid where a perforated hole covered with muslin allowed ventilation. The trays were placed in a growth chamber (25°C and 16:8°h photoperiod). Number of whiteflies settled on each leaflet side was recorded at 0.5, 1, 2, 4, 8, 24, and 48 h after release. Six replicates (i.e., six trays per genotype and treatment) of this experiment were performed.
TYLCV Primary Transmission Experiments
An experiment to assess TYLCD primary transmission was conducted following the no-choice design described by Rodríguez-López et al. (2011). For this, 21 days after the initial mock and MeJA treatments, MM and BC5S2 plants were placed within separated walk-in insect-proof net structures (5 m length × 5 m width × 2 m height). Then, twenty TYLCV-IL-viruliferous B. tabaci individuals per plant were released at the center of a circle (2 m of diameter) of 22 control or MeJA-treated MM or BC5S2 plants. After 48 h, insects were eliminated by insecticide treatment, and plants were moved to a glasshouse until analysis. Detection of TYLCV-IL infection was performed in the youngest newly emerged leaf at 7, 14, 21, and 28 days post-inoculation (dpi).
RNA was isolated from young leaves of multiple MeJA-treated and mock-treated MM and BC5S2 plants at 21 dai (hormone treatments applied at days 0, 7, and 14) by using RNeasy Mini kit (Qiagen) followed by DNase treatment (Ambion) and checked for integrity and quality. Three biological replicates of each treatment were fragmented, labeled and hybridized to the EUTOM3 tomato exon array according to the manufacturer’s instructions (Affymetrix®, Santa Clara, CA, USA) at Unitat Central d’Investigació (Universitat de Valencia, Spain), as described in Powell et al. (2012). Microarray design and experimental data are available in the ArrayExpress database1 under the accession numbers of A-MEXP-2227 and E-MTAB-2898, respectively.
Up-regulated or down-regulated genes at least 1.5-fold greater in MeJA-treated BC5S2 than in mock-treated BC5S2 plants and in MeJA-treated MM than mock-treated MM plants were first selected (FDR-corrected P-value ≤ 0.05 for both the ANOVA and the post hoc test). Then, a second statistics filter was used to select genes up-regulated or down-regulated more in MeJA-treated BC5S2 than in MeJA-treated MM plants. For a more detailed description of the design and analysis see Supplementary Method 2. The identified differentially expressed genes classified into clusters were used to calculate MapMan term enrichment scores against molecular function categories by applying Fisher Exact tests using a local, customized version of the ‘catscore.pl’ Perl script described in Cheung et al. (2003). MapMan terms with a P < 0.05, and more than three regulated genes for the Mapman-term were defined as over-represented (Supplementary Data sheet 1).
Gene Expression Analysis by RT-qPCR
To test the early MeJA-mediated induction of acylsugar metabolism-related genes in the BC5S2 genotype, semi-quantitative RT-PCR analyses were first conducted (data not shown) at 1 day after initial MeJA application. Genes up-regulated according to the microarray analysis, together with other acylsugar biosynthesis-related genes reported as highly expressed in type-IV glandular trichomes of the acylsugar-producing wild tomato species Solanum pennellii (Slocombe et al., 2008) were analyzed. Those genes showing higher up-regulation were then analyzed by RT-qPCR in a time-course experiment. For this, BC5S2 and MM plants were multiple treated with MeJA or mock solution at days 0, 7, and 14. Samples for gene expression analysis were taken at 1, 3, 7, 8, 14, and 15 days after initial induction (dai). Three leaflets per plant were detached and homogenized in liquid nitrogen and total RNA was isolated using a phenol LiCl-based method (Verdonk et al., 2003) and treated with DNase (Ambion). First strand cDNA was synthesized from 4 μg of total RNA using M-MuLV Reverse Transcriptase (Fermentas), as described by the manufacturer, in a 20 μl reaction. PCR was performed in ABI7500 Real-Time PCR system (Applied Biosystems) using Platinum SYBR Green qPCR SuperMix-UDG (Invitrogen). PCR reactions of 20 μl contained 0.25 μM of each primer, 0.1 μl ROX reference dye and 1 μl of cDNA. The cycling program was set to 5 min at 50°C, 2 min at 95°C, 40 cycles of 15 s at 95°C and 1 min at 60°C, followed by a melting curve analysis. Five biological replicates (i.e., each obtained from an individual plant) were analyzed per treatment and time point with two technical qRT-PCR replicates per individual sample. Expression levels for all the genes were normalized to the expression of the endogenous control gene Actin. The normalized expression (NE) data were calculated by the ΔCt method NE = -(PEtargetˆCttarget)/(PEreferenceˆCtreference) (PE = primer efficiency; Ct = cycle threshold). The PEs were determined by fitting a linear regression on the Ct-values of a standard cDNA dilution series. To plot the relative expression, NE values were scaled the lowest average NE within the plot, being the lowest average in each plot set to 1. The gene-specific primers used for the PCRs are listed in Supplementary Table S1.
Effect of Whitefly Infestation on JA-Associated Defenses and Acylsucrose Secretions in MeJA-Induced BC5S2 Plants
To test the effect of whitefly infestation on JA-induced acylsucrose secretions in BC5S2, we measured the acylsucrose secretions in leaf exudates and assessed the expression of the JA-marker gene WIPI-II (wound inducible proteinase inhibitor-II) (called PI-IIf in Alba et al., 2015) and the acylsugar biosynthesis-related gene BCKD-E2 in control and MeJA-treated plants after infestation with non-viruliferous B. tabaci. To obtain this material, young BC5S2 plants were treated three times with MeJA or mock solution at 0, 7, and 14 days. At 21 days after the initial hormone or mock treatment, 22 plants per treatment were placed in a circle in separated walk-in insect-proof net structures. Two blocks per treatment were set, each block corresponding to one walk-in insect-proof net structure. B. tabaci whiteflies (60 individuals per plant) were then released in the center of the circle of mock-treated or MeJA-treated BC5S2 plants and allowed to develop a new population until the end of the experiment. Plants were sampled for acylsucrose production and gene expression analysis at 7 and 14 days after whitefly release.
All data were first analyzed using Levene and Kolmogorov–Smirnov tests to determine the heteroscedasticity of variance and normality, respectively. Differences in type-IV trichome density and acylsugar content in leaf exudates of mock-treated and MeJA-treated BC5S2 plants were tested by t-test. To normalize the data and stabilize the variance, acylsucrose measurements were Log (x+1) transformed prior to analysis. Differences in phenolic content among groups, i.e., mock-treated and MeJA-treated MM and BC5S2 plants, were tested by generalized linear models (GLMs), using Linear distribution and identity link function, followed by Fisher’s least significant difference (LSD) post hoc test. Whitefly preference data were analyzed by GLM using Log (x+1) as the link function and Poisson as the probability distribution. Results of three replicated experiments assessing TYLCD primary transmission were homogeneous, as determined by contingency tables and associated chi-squared test (P ≤ 0.05), and pooled data were statistically analyzed. For this, differences between number of infected vs. non-infected BC5S2 and MM plants were analyzed by GLM using Logit as the link function and Binomial as the probability distribution. Pair-wise comparisons among groups at each time point were performed by LSD post hoc test. For the TYLCV agroinoculation experiments, differences between infected vs. non-infected BC5S2 or MM plants were analyzed by t-test at each time point. Data of gene expression analysis by RT-qPCR of acylsugar biosynthesis-related genes for mock-treated and MeJA-treated plants were analyzed by one-way nested ANOVA. For this, univariate analysis was used with hormone treatment and technical replicate nested within hormone treatment as fixed factors. Pooled data of acylsucrose production between non-infested and whitefly infested mock-treated or MeJA-treated BC5S2 plants were analyzed by Student’s t-test. Prior analysis, heterogeneity of pooled data was statistically tested using contingency tables and associated chi-squared test (P ≤ 0.05). Differences in WIPI-II and BCKD-E2 expression levels between non-infested and whitefly-infested plants were analyzed by one-way nested ANOVA. For this, normalized expression data were Log transformed when needed prior analysis. Univariate analysis was used with whitefly infestation and technical replicate nested within whitefly infestation as fixed factors.
MeJA Promotes Type-IV Glandular Trichome Density and Secretion of Acylsugars and Phenolics in BC5S2
Moneymaker and its near-isogenic line BC5S2 differ in their leaf trichome composition. In MM, type-I and -VI glandular, but especially type-V non-glandular trichomes, constitute the majority of trichomes on abaxial and adaxial leaf surfaces. Conversely, in BC5S2 the acylsucrose-producing type-IV glandular trichomes, which are absent in MM, densely cover the abaxial leaf surface; non-glandular type-V, and glandular type-I and type-VI trichomes are also present in BC5S2 plants albeit at low densities (Supplementary Figure S2). After multiple MeJA applications, type-IV glandular trichome density and acylsucrose production significantly increased in BC5S2 plants, but MM remained lacking these traits (Figures 1A,B). Phenolic compounds were present in the leaf exudates of both genotypes and significantly induced by MeJA (Figure 1C). Though, the presence of phenolics was previously associated with type-VI trichomes (Kennedy, 2003), these compounds were also detected in the glands of type-IV trichomes of DPBA-stained BC5S2 leaves (Figures 1D,F,G). No DBPA-fluorescence was detected in abaxial leaf surface of MeJA-treated MM plants (Figure 1E).
FIGURE 1. Effect of multiple methyl jasmonate (MeJA) applications on type-IV glandular trichome density and targeted secretions at 21 days after the initial hormone induction in BC5S2 and ‘Moneymaker’ (MM). Two independent experiments were performed. Representative data from one experiment are shown. (A) Mean values + SEM (n = 12–15) of type-IV glandular trichome densities measured in mock- and MeJA-treated plants. (B) Mean values + SEM (n = 15) of acylsucrose secretions in mock-treated and MeJA-treated MM and BC5S2 plants. Significant differences between treatments in BC5S2 plants were tested by t-test. Asterisks denote significant differences at P ≤ 0.001. (C) Mean values + SEM (n = 15) of phenolic content in leaf exudates of mock-treated and MeJA-treated MM and BC5S2 plants. Bars with different letters indicate significant differences among groups compared by Fisher’s least significant differences (LSD) test at P ≤ 0.05. Representative micrographs of phenolics accumulation in diphenylboric acid-2-aminoethyl ester (DPBA)-flavonoid stained abaxial leaf surfaces of mock-treated (D,F) and MeJA-treated (G) BC5S2 plants. Black arrows point golden fluorescence associated to the presence of phenolic compounds in the glands of type-IV trichomes of BC5S2 plants. (E) Absence of type-IV trichomes and gold fluorescence was observed in DPBA-treated abaxial leaf surfaces of MeJA-treated MM plants.
Whitefly Preference and TYLCV-IL Primary Transmission Are Reduced in MeJA-Treated BC5S2 Plants
Lower numbers of whiteflies settled on the leaflets of the acylsugar-producing genotype BC5S2 when compared to MM (Figures 2A,B). When treated with MeJA, however, both MM and BC5S2 plants were less preferred by whiteflies. In MeJA-treated MM plants, the number of whiteflies settled in abaxial leaf surfaces at 4, 6, and 24 h was significantly lower than in mock-treated controls, though no differences were observed in the adaxial sides (Figures 2A,C). Reduced whitefly preference was observed in the abaxial leaf sides of MeJA-treated BC5S2 plants at 4 and 24 h (Figure 2B) and at 4 and 6 h on adaxial leaf sides (Figure 2D) when compared to their controls.
FIGURE 2. Evaluation of Bemisia tabaci biotype Q preference and Tomato yellow leaf curl disease (TYLCD) primary transmission in mock-treated and multiple methyl jasmonate (MeJA)-treated ‘Moneymaker’ (MM) and BC5S2 plants under no-choice experimental conditions. Plants received three MeJA applications at 0, 7, and 14 days. At 21 days after initial hormone treatments whitefly preference and virus primary transmission experiments were performed. Mean number + SEM of whiteflies (wf) per six leaflets settled on adaxial (A,B), and abaxial (C,D) leaflet surfaces of mock-treated and MeJA-treated MM and BC5S2 plants at different time points after release of 30 unsexed adult whiteflies. Asterisks indicate significant differences (P ≤ 0.05) between treatments at each time point. (E) Estimation of primary TYLCD transmission in mock-treated and MeJA-treated BC5S2 and MM plants. Percentage (mean + SEM) of TYLCV-infected plants at different time points after viruliferous whiteflies were given a 48-h inoculation access period (IAP) are shown. Pooled data of three replicated experiments were homogeneous and are shown in the figure. Pair-wise comparisons among groups at each time point were performed by Fisher’s LSD post hoc test. Different letters indicate significant differences among groups at P ≤ 0.05.
To further investigate the impact of the MeJA treatments on the incidence of the whitefly-transmitted TYLCV-IL, primary transmission of the virus was estimated in mock-treated and MeJA-treated MM and BC5S2 plants at 21 dai (Figure 2E). A significant reduction in TYLCV-IL transmission was observed in mock-treated BC5S2 plants when compared to MM (Figure 2E). Conversely, virus transmission was diminished in MeJA-treated BC5S2 plants when compared to mock-treated BC5S2 plants at 21 and 28 dpi. In contrast, no such differences were observed between mock-treated and MeJA-treated MM plants at either time point. To determine whether MeJA treatment may affect infectivity by TYLCV-IL, TYLCV-IL agroinoculation of mock-treated and MeJA-treated BC5S2 and MM plants was conducted at 21 dai (Figure 3). No significant reduction in susceptibility to TYLCV-IL was observed in MeJA-treated BC5S2 plants in the two replicated experiments (Figures 3A,B), reinforcing the notion that the reduction of virus transmission observed in MeJA-treated BC5S2 plants correlates strongly with the enhancement of acylsucrose production and the effect on whiteflies. Higher susceptibility to TYLCV, however, was observed for hormone-treated MM plants in one of the replicated experiments (Figure 3D). Activation of JA defenses can disrupt geminivirus infection (Lozano-Durán et al., 2011). As Agrobacterium tumefaciens and TYLCV can induce salicylic acid (SA) signaling pathway in plants (Sheikh et al., 2014; Sade et al., 2015; Villarroel et al., 2016), a stronger and negative SA-JA crosstalk might have diminished induced JA defenses and explain the higher susceptibility to TYLCV in the MeJA-induced tomato plants.
FIGURE 3. Effect of Methyl jasmonate (MeJA) applications (on days 0, 7, and 14) on TYLCD incidence in MM and BC5S2 plants. TYLCV-IL agroinoculation was performed at 21 days after initial MeJA treatment. Percentage (mean + SEM) (n = 12) of infection at several time points after TYLCV-IL agroinoculation of mock-treated and multiple MeJA-treated BC5S2 (A,B) and MM (C,D) plants is shown. The experiment was repeated twice, in February (A–C) and May (B,D). Number of infected vs. non-infected plants were analyzed by Generalized Linear Models using Logit as the link function and Binomial as the probability distribution. Asterisks indicate significant differences between treatments (P < 0.05) for each time point.
MM and BC5S2 Show Differences in their Gene Expression Profiles after MeJA Treatments
To get a better understanding of the mechanistic basis of the MeJA-mediated induced resistance to whiteflies, changes in transcriptome profiles of BC5S2 and its recurrent parent MM was analyzed by means of microarray.
A total of 2,309 genes (∼26% of EUTOM3 probes) were up- or down-regulated in BC5S2 and/or MM by MeJA at 21 dai (mean fold change ≥ 1.5 relative to their controls, P-value and FDR ≤ 0.05 in both ANOVA test factor and post hoc test). Then these genes were filtered and classified according to their ratio between BC5S2 and MM MeJA- treated plants. Out of them, 1,089 genes were up- or down- regulated by MeJA and showed differences between BC5S2 and MM MeJA-treated plants higher than 1.5 folds (Figure 4). Of these genes, 95 were up-regulated and 33 were down-regulated in both MM and BC5S2 plants. Functional categories of genes up- or down-regulated by MeJA in both plant genotypes matched to those of JA-, SA-, ethylene- and biotic stress-related genes. In agreement with the observation that MeJA increased the production of surface phenolics in MM and BC5S2 (Figure 1C), aromatic amino acid and phenylpropanoid biosynthesis-related genes were up-regulated in both genotypes. Moreover, our analysis showed the MeJA-induced expression of the AGAMOUS gene TAG1 in MM and BC5S2, which has been described to increase glandular trichome density (Pnueli et al., 1994). However, among the genes up-regulated by MeJA in both plant genotypes, 91 showed higher levels of up-regulation in BC5S2 than in MM plants. This set predominantly (P < 0.05 and genes > 3) consisted of genes annotated to be involved in amino acid and lipid metabolism (mainly degradation), secondary metabolism and stress (Supplementary Data sheet 1). This cluster contained several genes related to JA biosynthesis, as well as WRKY transcription factors of which several are involved in the regulation of pathogen/plant immunity, senescence and trichome development (Eulgem et al., 2000; Pandey et al., 2011). In MM and BC5S2 plants, MeJA treatment down-regulated genes related to protein post-translational modification, including phosphatases and kinases and, among them, genes similar to SOS3- interacting proteins, HAB, ABI1 and PP2C, most of which are negative regulators of ABA signaling in Arabidopsis (Santiago et al., 2009). These genes (30 of a total of 33) showed stronger level of down-regulation in BC5S2 than in MeJA-treated MM plants.
FIGURE 4. Venn diagram of genes significantly induced (A) and repressed (B) by multiple methyl jasmonate (MeJA) applications in ‘Moneymaker’ (MM) and BC5S2 plants at 21 days after the initial hormone treatment. Numbers in red denote genes showing higher expression levels in MeJA-treated BC5S2 plants when compared to MeJA-treated MM plants. In black, number of genes showing lower expression levels in MeJA-treated BC5S2 plants when compared to MeJA-treated MM plants.
We also found sets of genes differentially expressed in the advanced backcross line BC5S2 or its recurrent parent MM. Genes that responded to the MeJA-treatment only in BC5S2 were considered to be the most important candidates directly or indirectly related to the introgressions from TO-937 and, consequently, related to the increase in acylsugar-producing type-IV trichomes observed in response to the hormone treatment (Table 1). Indeed, the acylsugar metabolism-related genes Dihydrolipoyl dehydrogenase, Dihydrolipoyllysine-residue acetyltransferase, 2-isopropylmalate synthase 1 and the Fatty acid elongase 3-ketoacyl-CoA synthase, and Threonine deaminase were only up-regulated in MeJA-treated BC5S2 plants. In addition, several tomato trichome-specific acyltransferases, responsible for the acylation of the sucrose backbones of acylsucroses, were up-regulated by MeJA only in BC5S2. The analysis showed a twofold increase in the expression of the S. lycopersicum acylsucrose acyltransferase 2 gene (Sl-ASAT2) in BC5S2 after MeJA treatments, and when compared to the expression levels in MeJA-treated MM plants this gene was fourfold more expressed. The product of the Sl-ASAT2 gene has very recently been described to catalyze, together with another S. lycopersicum BAHD [BEAT, AHT, HCBT, DAT (D’Auria, 2006)] acyltransferase, Sl-ASAT1, consecutive reactions to produce di-acylsucrose intermediates (Fan et al., 2016). Interestingly, the BAHD-type acylsucrose acyltransferase gene Acylsugar acyltransferase3 (ASAT3), which was described to catalyze acylation on the five-member furanose ring of diacylsucroses in the tip cells of acylsugar producing type-I trichomes (Schilmiller et al., 2010, 2015) was also induced in MeJA-treated BC5S2 plants. This gene was twofold induced in BC5S2 after the hormone treatments, and it was nine times more expressed than in MeJA-treated MM plants. The analysis also showed that BC5S2 up-regulated more defense -related genes than MM after MeJA treatments, since a higher number of genes involved in biotic and abiotic stress-related responses, signal transduction, and secondary metabolites production were differentially induced only in the former genotype after the hormone treatments. Notably, the effect of MeJA on down-regulation of genes related to the photosynthetic apparatus was also stronger in BC5S2 when compared to MM.
TABLE 1. Ratio of expression levels (log2 transformed; mock-treated versus MeJA-treated) of tomato genes involved in acylsugar biosynthesis that are differentially up-regulated by MeJA treatments in the acylsucrose producing breeding line BC5S2 when compared to the parental line Moneymaker (MM).
Expression analysis on MeJA-treated MM plants revealed fewer induced or repressed genes in this genotype when compared to those regulated in BC5S2 after the hormone treatments. A total of 88 genes were up-regulated specifically in MM after MeJA treatment. Out of them, seven genes showed higher expression levels in MeJA-treated BC5S2 line than in MeJA-treated MM plants, though they were not induced by MeJA in this genotype. Those genes were related to lipid, hormone metabolism, and stress.
To validate the microarray data, four genes whose expression was significantly different between MeJA-treated and control MM and BC5S2 plants were selected to be re-analyzed via RT-qPCR. The expression levels and differences observed on the microarray matched those observed via RT-qPCR (Supplementary Figure S3; Supplementary Table S2).
MeJA Induces Expression of Acylsugar Biosynthesis-Related Genes in BC5S2
The preliminary semiquantitative PCR analysis revealed that Dihydrolipoyllysine-residue acetyltransferase, also called Branched chain keto-acid dehydrogenase subunit 2 (BCKD-E2) gene (Slocombe et al., 2008), a component of the branched-chain keto-acid dehydrogenase complex (BCKD) responsible for the production of acyl-CoAs, was up-regulated 24 h after the first MeJA application. This gene was then selected for analysis of its expression over time by means of RT-qPCR expression analysis. Expression of BCKD-E2 was induced by MeJA in BC5S2 plants (Figure 5A). A slight induction was detected 1 day after application, which significantly increased at day 3 but ceased again at day 7. After the second MeJA application (day 8), a stronger induction of BCKD-E2 was observed. This induced expression was not maintained over time, with no significant differences observed between mock-treated and MeJA-treated BC5S2 plants at 14 dai. After the third MeJA application (day 15), the induction of BCKD-E2 was considerably stronger than in previous applications (Figure 5A). In MM plants treated with MeJA the BCKD-E2 gene was slightly up-regulated at 1, 3 and 8 dai, albeit at much lower levels than in BC5S2, and at 15 dai no induction was observed.
FIGURE 5. Relative transcript levels of acylsugar biosynthesis-related genes after multiple methyl jasmonate (MeJA) applications. Exogenous MeJA was applied at day 0, 7, and 14. (A) Time-course expression analysis of the Dihydrolipoyllysine-residue acetyltransferase or also called Branched-chain keto-acid dehydrogenase-E2 subunit (BCKD-E2) in mock-treated and MeJA-treated BC5S2 and MM plants at 1, 3, 7, 8, 14, and 15 days after the first MeJA application. Black arrows indicate time-points at which MeJA applications were done. (B) Expression analysis performed in BC5S2 plants at 1 day after the second and third MeJA application (8 and 15 days, respectively) of acylsugar biosynthesis-related genes involved in the following processes: conversion of keto-acids to acyl-CoAs, Dihydrolipoyllysine-residue acetyltransferase or also called Branched chain keto-acid dehydrogenase subunit 3 (BCKD-E3); fatty acid elongation, 3-ketoacyl-CoA synthase (FAE-3); leucine biosynthesis, 2-isopropylmalate synthase 1 (IPMS-1); branched-chain keto-acid precursors biosynthesis, Threonine deaminase (TD), respectively. The mean + SEM fold induction calculated respect to mock treatment values is shown. Data from five biological replicates and two technical replicates were analyzed and normalized to Actin gene. Normalized expression data were Log transformed prior analysis when needed. Differences between mock-treated and MeJA-treated BC5S2 plants were analyzed separately for each gene and time point by one way nested ANOVA. Asterisks denote significant differences between treatments at P ≤ 0.05.
We selected the samples from 8 and 15 dai, when expression of BCKD-E2 was higher, to assess the expression levels of four other acylsugar biosynthesis-related genes involved in different steps of this pathway and that according to the microarray analysis were upregulated by MeJA (Figure 5B). These four genes were Dihydrolipoyllysine-residue acetyltransferase or also called Branched chain keto-acid dehydrogenase subunit 3 (BCKD-E3), 3-ketoacyl-CoA synthase (FAE-3), 2-isopropylmalate synthase 1 (IPMS-1) and Threonine deaminase (TD). Our results showed that the BCKD-E3 gene was also significantly up-regulated in MeJA-treated BC5S2 plants at 8 dai (Figure 5B). However, this induction was not as high as for BCKD-E2, and no significant differences in the expression levels were observed at 15 dai. Similarly, expression of FAE-3 was significantly up-regulated in MeJA-treated BC5S2 plants at 8 days, but not at 15 dai. Finally, IPMS-1 was significantly down-regulated in MeJA-treated BC5S2 plants at 8 and 15 dai, and TD was down-regulated at 8 dai.
MeJA-Mediated Induction of Defenses in BC5S2 is Enhanced by Whitefly Infestation
Our results showed that infestation with B. tabaci whiteflies induced higher accumulation of acylsucroses in leaf exudates of infested MeJA-treated BC5S2 plants than in non-infested MeJA-treated plants (Figure 6A). Acylsucrose levels, however, did not differ between infested and non-infested mock-treated BC5S2 plants. To determine whether the enhanced acylsucrose secretion in infested MeJA-treated BC5S2 plants is accompanied by the induction of JA-mediated responses, expression levels of the JA-marker gene WIPI-II and the acylsugar-related gene BCKD-E2 were assessed at 7 and 14 days after whitefly release. At 7 days, WIPI-II was significantly up-regulated in infested MeJA-treated BC5S2 plants when compared to non-infested MeJA-treated plants (Figure 6B). No significant differences were observed at 14 days. However, WIPI-II was slightly induced in whitefly-infested mock treated plants at 14 days. Up-regulation of BCKD-E2 gene coincided with up-regulation of WIPI-II. Hence, BCKD-E2 gene was up-regulated in whitefly infested MeJA-treated BC5S2 plants at 7 days and up-regulated in whitefly-infested mock treated plants at 14 days (Figure 6C). At 7 days, however, BCKD-E2 was down-regulated in infested mock-treated BC5S2 plants which coincided with lower, though not significant, levels of WIPI-II.
FIGURE 6. Effect of B. tabaci whitefly infestation on acylsucrose metabolism and JA-mediated signaling defense in mock- and MeJA-treated BC5S2 plants. (A) Acylsucrose secretions (mean + SEM, n = 21–22) measured in mock-treated and MeJA-treated BC5S2 plants uninfested (- whiteflies) or infested with B. tabaci whiteflies (+ whiteflies) at 7 and 14 days after whitefly release. Pooled data of the two blocks per treament are shown. Asterisks denote significant differences between treatments by t-test (P ≤ 0.05). (B) Gene expression levels of the JA-responsive gene Wound inducible proteinase inhibitor-II (WIPI-II) and (C) the acylsugar metabolism bio-marker gene Branched-chain keto-acid dehydrogenase-E2 subunit, (BCKD-E2) were analyzed by real time RT-PCR at 7 and 14 days after whitefly release. Bars indicate mean + SEM fold induction of each treatment group (n = 4–5 biological replicates, two technical replicates). Normalized expression data were Log transformed when needed and differences between non-infested and whitefly infested plants were analyzed by one-way nested ANOVA. Univariate analysis was used with whitefly infestation and technical replicate nested within whitefly infestation as fixed factors. Asterisks denote significant differences at P ≤ 0.05.
Here, we have shown that an inducible defense can be transferred from a wild tomato into a commercial variety such that it increases protection against a virus-transmitting whitefly in young plants of the generated BC5S2 breeding line. In particular, we transferred MeJA-inducible type-IV trichomes and acylsugar production associated to these trichomes into the cultivar ‘Moneymaker’ thus rendering the plants less attractive to whiteflies and deceasing TYLCV disease incidence.
First, our results show that repeated MeJA applications on MM and BC5S2 plants enhanced their repellence properties against whiteflies. The use of jasmonates and other elicitors for plant defense induction has been described extensively in the literature (Dicke and Hilker, 2003). Application of the elicitor MeJA can establish direct and indirect plant resistance resulting in the reduction of herbivore development and survival (Thaler et al., 2002a; Rohwer and Erwin, 2008). When compared to BC5S2, however, MM leaves showed higher attractiveness to whiteflies even after MeJA treatments. This might be explained by the absence of effective constitutive and inducible resistance traits against whiteflies in MM, such as type-IV glandular trichomes and acylsucrose production, only present in BC5S2. In both genotypes, however, MeJA increased the phenolic content in leaf exudates. We hypothesized that this might be due to the increase in type-VI leaf glandular trichome densities in both MM and BC5S2 plants, since type-VI trichomes on adaxial leaf sides can be induced by MeJA (Boughton et al., 2005; Maes and Goossens, 2010) and produce and store different allelochemicals, i.e., terpenes, defensive proteins, and phenolic compounds (Wagner, 1991; Besser et al., 2009; McDowell et al., 2011). Interestingly, production of phenolics was higher in leaf exudates of BC5S2 plants. This might be in part associated with the induction of type-IV trichome densities and metabolism, as phenolic compounds were detected therein (Figure 1D). In tomato, leaf glandular trichomes and production of their associated allelochemicals play an important role in plant defenses (Kang et al., 2010a,b; McDowell et al., 2011; Glas et al., 2012) and, therefore, their induction might confer additional protection against herbivory. Deterrent properties of phenolics, however, have been reported for some herbivore species but not for whiteflies (Duffey and Isman, 1981; Mitchell et al., 1993; Kang et al., 2010a,b). Moreover, adult B. tabaci whiteflies locate preferentially on abaxial leaf surfaces (Freeman et al., 2001; Rodríguez-López et al., 2012). This indicates that higher production of phenolics by type-VI trichomes in adaxial leaf sides of MM plants might be ineffective to deter whitefly feeding. Nevertheless, JA-mediated induction of other defense and trichome-related compounds in MM, i.e., terpenes, might account for the enhanced repellence to whiteflies (Bleeker et al., 2009). For BC5S2, the role of type-IV trichomes-mediated production of phenolics in plant resistance against whiteflies is an aspect that would need further investigation.
Here, we also show that repeated MeJA applications resulted in reduced TYLCV-IL transmission by whiteflies in BC5S2 plants, but not in MM. Our previous studies reported on the generation of acylsucrose-producing backcross lines displaying high resistance to whiteflies and reduction of TYLCD incidence (Rodríguez-López et al., 2011). Acylsugar-producing type-IV glandular trichomes are known as effective barriers against aphids (Goffreda et al., 1989), spider mites (Fernández-Muñoz et al., 2000, 2003), leafminers (Hawthorne et al., 1992; Oliveira et al., 2012), and whiteflies (Firdaus et al., 2012; Leckie et al., 2012). Still, this trichome-based resistance is compromised in young developmental stages of our BC lines due to lower type-IV trichome densities and acylsucroses production (Rodríguez-López et al., 2011). Reinforcement of these constitutive defenses by treating young BC5S2 plants with MeJA might explain the observed differences in TYLCV transmission by whiteflies described here, in agreement with previous reports (Sippell et al., 1987; Walker, 1988; Snyder et al., 1998; Muigai et al., 2002; Sadasivan and Thayumanavan, 2003; Oriani and Vendramim, 2010). This increase in acylsucrose secretions is probably associated with the induction of type-IV glandular trichome density that is only present in BC5S2. Hence, though Maes and Goossens (2010) demonstrated that MeJA can induce higher densities of type-I trichomes in tomato, and this trichome-type is also reported to produce acylsugars (Schilmiller et al., 2010), leaf type-I trichomes were only and scarcely present in the main nerves of BC5S2 leaves (Supplementary Figure S2). Furthermore, acylsucroses were not detected in MM in our analysis. This confirms the idea that acylsugar levels produced in pest-susceptible tomato cultivars by type-I trichomes are insignificant when compared to those found in pest-resistant wild species (Alba et al., 2009; McDowell et al., 2011), and that, even after trichome induction, they are not really effective for pest control purposes.
Overall, our results strongly support that induced type-IV trichomes, as well as their secondary defense metabolism after MeJA treatments, accounted for the increased JA-induced resistance to whiteflies and reduced TYLCD transmission in BC5S2 plants. BC5S2 and MM are near-isogenic lines. Generation of BC5S2 was performed by recurrent backcrosses to MM and subsequent phenotypic selection of resistant plants based on type-IV glandular trichomes density and secretion of acylsucroses. This breeding process could result in the selection of genomic regions coding for trichome-associated traits from the wild donor while enriching the genetic background in genes from the susceptible parent MM. Differences in JA-induced defenses between BC5S2 and MM would be expected, therefore, to be largely centered around the activation of genes related to type-IV trichomes production and acylsucrose content in leaf exudates in the breeding line, absent in MM. Moreover, while type-IV trichome densities were approximately 1.9-fold induced after MeJA application in BC5S2 plants, acylsucrose content in the leaf exudates was increased 10 times (Figures 1A,B), suggesting a higher production of these compounds per trichome. To test this hypothesis we analyzed the transcriptomic responses of MM and BC5S2 plants to multiple MeJA applications at 21 dai. Comparative transcriptome analysis of these two near-isogenic lines revealed that overall the trichome-associated defenses were activated more strongly in the acylsugar producing line BC5S2 than in MM. This is not surprising since production and secretion of acylsugars is a complex phenotypic trait controlled by multiple genetic factors (Lawson et al., 1997). Several metabolic pathways are involved in their biosynthesis and, in agreement with this, numerous quantitative trait loci (QTL) located on different chromosomes have been associated with changes in acylsugar production and type-IV trichome density. Thus, distinct genetic configurations of these QTLs have been associated to changes in the sugar moiety, fatty acid esters composition, and total acylsugar production in wild tomato species (Mutschler et al., 1996; Blauth et al., 1998; Leckie et al., 2012, 2013).
Acylsugar biosynthesis results from a combined synthesis of branched chain amino acids (Leu, Val, and Ile), precursors for keto-acids biosynthesis, followed by their conversion into branched-chain acyl-CoAs by BCKD complex. These acyl-CoAs can act as substrates for the fatty acid synthase complex (FAS), reported as the major pathway responsible for providing medium-branched acylCoAs to acylsugar production and wax alkane biosynthesis (Slocombe et al., 2008). In addition, components of α-keto elongation (αKAE), associated with leucine precursor biosynthesis play an important role, as they provide precursors for keto-acids biosynthesis (Kroumova and Wagner, 2003; Ning et al., 2015). In line with this, genes involved in lipid and amino acid metabolism were among the enriched categories up-regulated in MeJA-treated BC5S2. Next, transfer of acyl chains to sucrose has been proposed to occur mainly via an Acetyl-coA dependent pathway (Schilmiller et al., 2012, Schilmiller et al., 2015). Accordingly, in the microarray analysis, two type-IV/I trichome-specific BAHD acyltransferases (Sl-ASAT2 and Sl-ASAT3) (Schilmiller et al., 2015; Fan et al., 2016) were induced in MeJA-treated BC5S2 plants and showed higher expression levels when compared to MeJA-treated MM plants. Our time-course experiments confirmed the induction of some of the above-mentioned acylsugar-related biosynthetic genes after sequential MeJA applications. We showed that the component of the BCKD complex, BCKD-E2 gene, was highly up-regulated after each hormone treatment when compared to MM (Figure 5A). Similarly, other key components of this metabolic pathway, BCKD-E3 and FAE-3, were induced, emphasizing the successful transfer of constitutive, but also inducible, S. pimpinellifolium resistant-associated genes into the susceptible S. lycopersicum cultivar. By contrast, FAE-3, involved in fatty acid elongation, and TD and IPSM-1 genes, responsible for the biosynthesis of keto-acid precursors, did not show higher expression levels at 15 dai. Moreover, in the case of TD and IPSM-1 genes, they were down-regulated after hormone applications at 7 and 15 dai, respectively. Differences in expression of FAE-3, TD and IPSM-1 genes between the microarray and RT-qPCR analyses might be explained by the different time point at which plants were sampled, 21 and 15 dai, respectively. Overall, these results also suggest that in BC5S2, MeJA positively induced the acylsugar biosynthesis pathway mainly by prioritizing the production of AcylCoAs through the activation of BCKD complex. Interestingly, BCKD-E2 showed higher and faster inductions after pre-treatment of BC5S2 plants with MeJA. An increased density of type-IV trichomes might account for this stronger expression of BCKD-E2. Nevertheless, significant higher trichome densities were only detected at 21 dai in preliminary experiments, suggesting that the positive regulation of the acylsugar biosynthesis machinery might occur within pre-existing type-IV trichomes at 15 dai. We hypothesize that higher expression levels of BCKD-E2 after previous MeJA treatments might be explained by a priming effect. Baldwin and Schmelz (1996) reported that previous treatment of Nicotiana sylvestris plants with MeJA gave rise to more rapid nicotine accumulation after induction compared (Schilmiller et al., 2015) to untreated plants. This form of sensitization is referred to as ‘priming’ and can be established by a treatment with defense elicitors, e.g., chemicals, but also previous contact with necrotizing pathogens, mycorrizhal fungi and herbivores, that enables plants to display a more robust and accelerated induced defense responses upon subsequent herbivore or pathogen attack (Engelberth et al., 2004; Conrath et al., 2006; Frost et al., 2008). Whether enhanced acylsucrose secretions in BC5S2 are influenced by JA-mediated priming will need further analysis. The relevant role of acylsucroses in plant defense, and the fact that a strong response in their biosynthesis machinery upon previous JA-mediated activation might occur, provides new opportunities for utilizing this trait in plant protection. Additionally, among the differences between MM and BC5S2 we observed that the photosynthetic apparatus gene set was down-regulated stronger in BC5S2. In tomato, MeJA has been reported to reduce the photosynthetic capacity of treated leaves and increase N:C ratio, a signal that can stimulate production of defensive compounds involved in direct and indirect plant defenses (Gómez et al., 2010). This response might be related to the stronger induction of defense secondary metabolites, such as acylsucroses, in MeJA-treated BC5S2 plants.
Finally, our study also showed that MeJA-induced BC5S2 plants activated JA-mediated responses and induced even higher production of acylsucroses at 14 days after whitefly infestation (Figure 6A), providing therefore a durable protection. It is known that the whitefly B. tabaci can alter plant hormone-mediated responses in infested tomato plants by promoting induction of SA-mediated defenses while suppressing JA defense responses (Zarate et al., 2007; Estrada-Hernández et al., 2009; Puthoff et al., 2010). Whiteflies are phloem feeding insects alleged to be experts in avoiding and manipulating JA-mediated plant defense responses. Adult whiteflies avoid induction causing little damage in plant tissues, and nymphs manipulate induction by activating (harmless) SA-responses, which antagonize the (harmful) JA-responses (Zarate et al., 2007; Walling, 2008; Zhang et al., 2009). Then, it would be possible that previous JA-induction in BC5S2 plants might have altered the effectiveness of adult whiteflies to dodge and avoid their detection. Prior to feeding, whiteflies use their stylets to make shallow probes on the leaf surface of plant hosts, and if they detect physical and/or chemical defense barriers, not appropriate for colonization, they leave and search for another host (Walling, 2008; Bleeker et al., 2012). Whiteflies might have induced JA-mediated plant responses during these shallow probes in MeJA-treated BC5S2 plants. Yet, it is also unknown whether a more hairy leaf surface will sense a herbivore more easily via trichomes being ruptured (Peiffer et al., 2009). In addition, the effectiveness of the JA-mediated induction of acylsucrose-producing trichomes against other pests/pathogens that do not avoid activation of the JA signaling pathway (Thaler et al., 2002b; Zhao et al., 2003), but whose colonization might be affected by the trichome defenses, not present in cultivated tomatoes, would need further research.
RE-B, RF-M, EM, JA, and MK designed the research. RE-B performed the hormone, insect and virus experiments, chemical analyses and RT-qPCRs. Data analysis and interpretation was performed by RE-B, RF-M, EM, JA, MK, CP, and AG. Microarray experiment was performed by CP and its analysis and interpretation was made by CP, RE-B, AG, and MK. RE-B drafted the manuscript with critical review by all the authors.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This work was funded by grants AGL2013-48913-C2-01-R/AGR (Spanish MICINN, co-financed by EU FEDER) and P10-AGR-6516 (Consejería de Economía, Innovación y Ciencia, Junta de Andalucía, Spain). RE-B was recipient of a FPI grant by MICINN. JA was supported by the Netherlands Organization for Scientific Research NWO (Earth and Life Sciences ALW/TOP 854.11.005). MK was supported by Netherlands Organization for Scientific Research NWO (Technology Foundation STW/VIDI 13492). EM and RF-M are members of AGR-214 and AGR-129 research groups, respectively, partially funded by the Consejería de Economía, Innovación y Ciencia, Junta de Andalucía, Spain (co-financed by EU FEDER-FSE). AG was funded by TRADITOM (634561) under the H2020 SFS-07a-2014 EU Program, the Spanish Ministry BIO2013-42193-R, and the EU COST-FA1106.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fpls.2016.01732/full#supplementary-material
Alba, J. M., Montserrat, M., and Fernández-Muãoz, R. (2009). Resistance to the two-spotted spider mite (Tetranychus urticae) by acylsucroses of wild tomato (Solanum pimpinellifolium) trichomes studied in a recombinant inbred line population. Exp. Appl. Acarol. 47, 35–47. doi: 10.1007/s10493-008-9192-4
Alba, J. M., Schimmel, B. C., Glas, J. J., Ataíde, L. M., Pappas, M. L., Villarroel, C. A., et al. (2015). Spider mites suppress tomato defenses downstream of jasmonate and salicylate independently of hormonal crosstalk. New Phythol. 205, 828–840. doi: 10.1111/nph.13075
Andreu, A. B., Guevara, M. G., Wolski, E. A., Daleo, G. R., and Caldiz, D. O. (2006). Enhancement of natural disease resistance in potatoes by chemicals. Pest Manag. Sci. 62, 162–170. doi: 10.1002/ps.1142
Besser, K., Harper, A., Welsby, N., Schauvinhold, I., Slocombe, S., Li, Y., et al. (2009). Divergent regulation of terpenoid metabolism in the trichomes of wild and cultivated tomato species. Plant Physiol. 149, 499–514. doi: 10.1104/pp.108.126276
Blauth, S., Churchill, G., and Mutschler, M. (1998). Identification of quantitative trait loci associated with acylsugar accumulation using intraspecific populations of the wild tomato, Lycopersicon pennellii. Theor. Appl. Genet. 96, 458–467. doi: 10.1007/s001220050762
Bleeker, P. M., Diergaarde, P. J., Ament, K., Guerra, J., Weidner, M., Schütz, S., et al. (2009). The role of specific tomato volatiles in tomato-whitefly interaction. Plant Physiol. 151, 925–935. doi: 10.1104/pp.109.142661
Bleeker, P. M., Mirabella, R., Diergaarde, P. J., Vandoorn, A., Tissier, A., Kant, M. R., et al. (2012). Improved herbivore resistance in cultivated tomato with the sesquiterpene biosynthetic pathway from a wild relative. Proc. Natl. Acad. Sci. U.S.A. 109, 20124–20129. doi: 10.1073/pnas.1208756109
Boughton, A. J., Hoover, K., and Felton, G. W. (2005). Methyl jasmonate application induces increased densities of glandular trichomes on tomato, Lycopersicon esculentum. J. Chem. Ecol. 31, 2211–2216. doi: 10.1007/s10886-005-6228-7
Broekgaarden, C., Snoeren, T. A., Dicke, M., and Vosman, B. (2011). Exploiting natural variation to identify insect-resistance genes. Plant Biotechnol. J. 9, 819–825. doi: 10.1111/j.1467-7652.2011.00635.x
Campos, M. L., De Almeida, M., Rossi, M. L., Martinelli, A. P., Junior, C. G. L., Figueira, A., et al. (2009). Brassinosteroids interact negatively with jasmonates in the formation of anti-herbivory traits in tomato. J. Exp. Bot. 60, 4347–4361. doi: 10.1093/jxb/erp270
Chen, H., Jones, A. D., and Howe, G. A. (2006). Constitutive activation of the jasmonate signaling pathway enhances the production of secondary metabolites in tomato. FEBS Lett. 580, 2540–2546. doi: 10.1016/j.febslet.2006.03.070
Cheung, K. J., Badarinarayana, V., Selinger, D. W., Janse, D., and Church, G. M. (2003). A microarray-based antibiotic screen identifies a regulatory role for supercoiling in the osmotic stress response of Escherichia coli. Genome Res. 13, 206–215. doi: 10.1101/gr.401003
Conrath, U., Beckers, G. J., Flors, V., García-Agustín, P., Jakab, G., Mauch, F., et al. (2006). Priming: getting ready for battle. Mol. Plant Microbe Interact. 19, 1062–1071. doi: 10.1094/MPMI-19-1062
Engelberth, J., Alborn, H. T., Schmelz, E. A., and Tumlinson, J. H. (2004). Airborne signals prime plants against insect herbivore attack. Proc. Natl. Acad. Sci. U.S.A. 101, 1781–1785. doi: 10.1073/pnas.0308037100
Estrada-Hernández, M. G., Valenzuela-Soto, J. H., Ibarra-Laclette, E., and Délano-Frier, J. P. (2009). Differential gene expression in whitefly Bemisia tabaci-infested tomato (Solanum lycopersicum) plants at progressing developmental stages of the insect’s life cycle. Physiol. Plant 137, 44–60. doi: 10.1111/j.1399-3054.2009.01260.x
Fan, P., Miller, A. M., Schilmiller, A. L., Liu, X., Ofner, I., Jones, A. D., et al. (2016). In vitro reconstruction and analysis of evolutionary variation of the tomato acylsucrose metabolic network. Proc. Natl. Acad. Sci. U.S.A. 113, E239–E248. doi: 10.1073/pnas.1517930113
Fernández-Muñoz, R., Domínguez, E., and Cuartero, J. (2000). A novel source of resistance to the two-spotted spider mite in Lycopersicon pimpinellifolium (Jusl.) Mill.: its genetics as affected by interplot interference. Euphytica 111, 169–173. doi: 10.1023/A:1003893432676
Fernández-Muñoz, R., Salinas, M., Álvarez, M., and Cuartero, J. (2003). Inheritance of resistance to two-spotted spider mite and glandular leaf trichomes in wild tomato Lycopersicon pimpinellifolium (Jusl.) Mill. J. Am. Soc. Hortic. Sci. 128, 188–195.
Firdaus, S., Van Heusden, A. W., Hidayati, N., Supena, E. D. J., Visser, R. G., and Vosman, B. (2012). Resistance to Bemisia tabaci in tomato wild relatives. Euphytica 187, 31–45. doi: 10.1007/s10681-012-0704-2
Freeman, T. P., Buckner, J. S., Nelson, D. R., Chu, C.-C., and Henneberry, T. J. (2001). Stylet penetration by Bemisia argentifolii (Homoptera: Aleyrodidae) into host leaf tissue. Ann. Entomol. Soc. Am. 94, 761–768. doi: 10.1603/0013-8746(2001)094[0761:SPBBAH]2.0.CO;2
Freitas, J. A., Maluf, W. R., Cardoso, M., Gomes, L. A., and Bearzotti, E. (2002). Inheritance of foliar zingiberene contents and their relationship to trichome densities and whitefly resistance in tomatoes. Euphytica 127, 275–287. doi: 10.1023/A:1020239512598
Frost, C. J., Mescher, M. C., Carlson, J. E., and De Moraes, C. M. (2008). Plant defense priming against herbivores: getting ready for a different battle. Plant Physiol. 146, 818–824. doi: 10.1104/pp.107.113027
Glas, J. J., Schimmel, B. C., Alba, J. M., Escobar-Bravo, R., Schuurink, R. C., and Kant, M. R. (2012). Plant glandular trichomes as targets for breeding or engineering of resistance to herbivores. Int. J. Mol. Sci. 13, 17077–17103. doi: 10.3390/ijms131217077
Goffreda, J. C., Mutschler, M. A., Avé, D. A., Tingey, W. M., and Steffens, J. C. (1989). Aphid deterrence by glucose esters in glandular trichome exudate of the wild tomato, Lycopersicon pennellii. J. Chem. Ecol. 15, 2135–2147. doi: 10.1007/BF01207444
Gómez, S., Ferrieri, R. A., Schueller, M., and Orians, C. M. (2010). Methyl jasmonate elicits rapid changes in carbon and nitrogen dynamics in tomato. New Phytol. 188, 835–844. doi: 10.1111/j.1469-8137.2010.03414.x
Hagerman, A. E., Zhao, Y., and Johnson, S. (1997). “Methods for determination of condensed and hydrolyzable tannins,” in Proceedings of the 210th National Meeting of the American Chemical Society, Chicago, IL.
Hawthorne, D., Shapiro, J., Tingey, W., and Mutschler, M. (1992). Trichome-borne and artificially applied acylsugars of wild tomato deter feeding and oviposition of the leafminer Liriomyza trifolii. Entomol. Exp. Appl. 65, 65–73. doi: 10.1111/j.1570-7458.1992.tb01628.x
Kang, J.-H., Liu, G., Shi, F., Jones, A. D., Beaudry, R. M., and Howe, G. A. (2010a). The tomato odorless-2 mutant is defective in trichome-based production of diverse specialized metabolites and broad-spectrum resistance to insect herbivores. Plant Physiol. 154, 262–272. doi: 10.1104/pp.110.160192
Kang, J.-H., Shi, F., Jones, A. D., Marks, M. D., and Howe, G. A. (2010b). Distortion of trichome morphology by the hairless mutation of tomato affects leaf surface chemistry. J. Exp. Bot. 61, 1053–1064. doi: 10.1093/jxb/erp370
Kant, M. R., Ament, K., Sabelis, M. W., Haring, M. A., and Schuurink, R. C. (2004). Differential timing of spider mite-induced direct and indirect defenses in tomato plants. Plant Physiol. 135, 483–495. doi: 10.1104/pp.103.038315
Lawson, D. M., Lunde, C. F., and Mutschler, M. A. (1997). Marker-assisted transfer of acylsugar-mediated pest resistance from the wild tomato, Lycopersicon pennellii, to the cultivated tomato, Lycopersicon esculentum. Mol. Breed. 3, 307–317. doi: 10.1023/A:1009677412902
Leckie, B. M., De Jong, D. M., and Mutschler, M. A. (2012). Quantitative trait loci increasing acylsugars in tomato breeding lines and their impacts on silver leaf whiteflies. Mol. Breed. 30, 1621–1634. doi: 10.1007/s11032-012-9746-3
Lozano-Durán, R., Rosas-Díaz, T., Gusmaroli, G., Luna, A. P., Taconnat, L., Deng, X. W., et al. (2011). Geminiviruses subvert ubiquitination by altering CSN-mediated derubylation of SCF E3 ligase complexes and inhibit jasmonate signaling in Arabidopsis thaliana. Plant Cell 23, 1014–1032. doi: 10.1105/tpc.110.080267
Maes, L., and Goossens, A. (2010). Hormone-mediated promotion of trichome initiation in plants is conserved but utilizes species and trichome-specific regulatory mechanisms. Plant Signal. Behav. 5, 205–207. doi: 10.4161/psb.5.2.11214
Maluf, W. R., Maciel, G. M., Gomes, L. A. A., Cardoso, M. D. G., Gonçalves, L. D., Da Silva, E. C., et al. (2010). Broad-spectrum arthropod resistance in hybrids between high-and low-acylsugar tomato lines. Crop Sci. 50, 439–450. doi: 10.2135/cropsci2009.01.0045
McDowell, E. T., Kapteyn, J., Schmidt, A., Li, C., Kang, J.-H., Descour, A., et al. (2011). Comparative functional genomic analysis of Solanum glandular trichome types. Plant Physiol. 155, 524–539. doi: 10.1104/pp.110.167114
Mitchell, M. J., Keogh, D. P., Crooks, J. R., and Smith, S. L. (1993). Effects of plant flavonoids and other allelochemicals on insect cytochrome P-450 dependent steroid hydroxylase activity. Insect Biochem. Mol. Biol. 23, 65–71. doi: 10.1016/0965-1748(93)90083-5
Monci, F., García-Andrés, S., Maldonado, J. A., and Moriones, E. (2005). Resistance to monopartite begomoviruses associated with the bean leaf crumple disease in Phaseolus vulgaris controlled by a single dominant gene. Phytopathology 95, 819–826. doi: 10.1094/PHYTO-95-0819
Morilla, G., Janssen, D., García-Andrés, S., Moriones, E., Cuadrado, I., and Bejarano, E. (2005). Pepper (Capsicum annuum) is a dead-end host for Tomato yellow leaf curl virus. Phytopathology 95, 1089–1097. doi: 10.1094/PHYTO-95-1089
Moriones, E., and Navas-Castillo, J. (2009). “Tomato yellow leaf curl disease epidemics,” in Bemisia: Bionomics and Management of a Global Pest, eds P. Stansly and S. E. Naranjo (Dordrecht: Springer), 259–282.
Muigai, S. G., Schuster, D. J., Snyder, J. C., Scott, J. W., Bassett, M. J., and Mcauslane, H. J. (2002). Mechanisms of resistance in Lycopersicon germplasm to the whitefly Bemisia argentifolii. Phytoparasitica 30, 347–360. doi: 10.1007/BF02979682
Mutschler, M., Doerge, R., Liu, S., Kuai, J., Liedl, B., and Shapiro, J. (1996). QTL analysis of pest resistance in the wild tomato Lycopersicon pennellii: QTLs controlling acylsugar level and composition. Theor. Appl. Genet. 92, 709–718. doi: 10.1007/BF00226093
Mutschler, M. A., and Wintermantel, W. M. (2006). “Reducing virus associated crop loss through resistance to insect vectors”, in Natural Resistance Mechanisms of Plants to Viruses, eds G. Loebenstein and J. P. Carr (New York: Springer), 241–260.
Navas-Castillo, J., Sánchez-Campos, S., Noris, E., Louro, D., Accotto, G. P., and Moriones, E. (2000). Natural recombination between Tomato yellow leaf curl virus-Is and Tomato leaf curl virus. J. Gen. Virol. 81, 2797–2801. doi: 10.1099/0022-1317-81-11-2797
Ning, J., Moghe, G. D., Leong, B., Kim, J., Ofner, I., Wang, Z., et al. (2015). A feedback-insensitive isopropylmalate synthase affects acylsugar composition in cultivated and wild tomato. Plant Physiol. 169, 1821–1835.
Nombela, G., and Muñiz, M. (2009). “Host plant resistance for the management of Bemisia tabaci: a multi-crop survey with emphasis on tomato,” in Bemisia: Bionomics and Management of a Global Pest, eds P. A. Stansly and S. E. Naranjo (Dordrecht: Springer), 357–383.
Oliveira, C. M. D., Andrade Júnior, V. C. D., Maluf, W. R., Neiva, I. P., and Maciel, G. M. (2012). Resistance of tomato strains to the moth Tuta absoluta imparted by allelochemicals and trichome density. Ciênc. Agrotecnol. 36, 45–52.
Oriani, M. A. G., and Vendramim, J. D. (2010). Influence of trichomes on attractiveness and ovipositional preference of Bemisia tabaci (Genn.) B biotype (Hemiptera: Aleyrodidae) on tomato genotypes. Neotrop. Entomol. 39, 1002–1007. doi: 10.1590/S1519-566X2010000600024
Pandey, A. K., Yang, C., Zhang, C., Graham, M. A., Horstman, H. D., Lee, Y., et al. (2011). Functional analysis of the Asian soybean rust resistance pathway mediated by Rpp2. Mol. Plant Microbe Interact. 24, 194–206. doi: 10.1094/MPMI-08-10-0187
Peiffer, M., Tooker, J. F., Luthe, D. S., and Felton, G. W. (2009). Plants on early alert: glandular trichomes as sensors for insect herbivores. New Phytol. 184, 644–656. doi: 10.1111/j.1469-8137.2009.03002.x
Pnueli, L., Hareven, D., Rounsley, S. D., Yanofsky, M. F., and Lifschitz, E. (1994). Isolation of the tomato AGAMOUS gene TAG1 and analysis of its homeotic role in transgenic plants. Plant Cell 6, 163–173. doi: 10.2307/3869636
Powell, A. L., Nguyen, C. V., Hill, T., Cheng, K. L., Figueroa-Balderas, R., Aktas, H., et al. (2012). Uniform ripening encodes a Golden 2-like transcription factor regulating tomato fruit chloroplast development. Science 336, 1711–1715. doi: 10.1126/science.1222218
Puthoff, D. P., Holzer, F. M., Perring, T. M., and Walling, L. L. (2010). Tomato pathogenesis-related protein genes are expressed in response to Trialeurodes vaporariorum and Bemisia tabaci biotype B feeding. J. Chem. Ecol. 36, 1271–1285. doi: 10.1007/s10886-010-9868-1
Rodríguez-López, M., Garzo, E., Bonani, J., Fereres, A., Fernández-Muñoz, R., and Moriones, E. (2011). Whitefly resistance traits derived from the wild tomato Solanum pimpinellifolium affect the preference and feeding behavior of Bemisia tabaci and reduce the spread of Tomato yellow leaf curl virus. Phytopathology 101, 1191–1201. doi: 10.1094/PHYTO-01-11-0028
Rodríguez-López, M. J., Garzo, E., Bonani, J. P., Fernández-Muñoz, R., Moriones, E., and Fereres, A. (2012). Acylsucrose-producing tomato plants forces Bemisia tabaci to shift its preferred settling and feeding site. PLoS ONE 7:e33064. doi: 10.1371/journal.pone.0033064
Sade, D., Shriki, O., Cuadros-Inostroza, A., Tohge, T., Semel, Y., Haviv, Y., et al. (2015). Comparative metabolomics and transcriptomics of plant response to Tomato yellow leaf curl virus infection in resistant and susceptible tomato cultivars. Metabolomics 11, 81–97. doi: 10.1007/s11306-014-0670-x
Schauer, N., Zamir, D., and Fernie, A. R. (2005). Metabolic profiling of leaves and fruit of wild species tomato: a survey of the Solanum lycopersicum complex. J. Exp. Bot. 56, 297–307. doi: 10.1093/jxb/eri057
Schilmiller, A., Shi, F., Kim, J., Charbonneau, A. L., Holmes, D., Daniel Jones, A., et al. (2010). Mass spectrometry screening reveals widespread diversity in trichome specialized metabolites of tomato chromosomal substitution lines. Plant J. 62, 391–403. doi: 10.1111/j.1365-313X.2010.04154.x
Schilmiller, A. L., Charbonneau, A. L., and Last, R. L. (2012). Identification of a BAHD acetyltransferase that produces protective acyl sugars in tomato trichomes. Proc. Natl. Acad. Sci. U.S.A. 109, 16377–16382. doi: 10.1073/pnas.1207906109
Schilmiller, A. L., Moghe, G. D., Fan, P., Ghosh, B., Ning, J., Jones, A. D., et al. (2015). Functionally divergent alleles and duplicated loci encoding an acyltransferase contribute to acylsugar metabolite diversity in Solanum trichomes. Plant Cell 27, 1002–1017. doi: 10.1105/tpc.15.00087
Sheikh, A. H., Raghuram, B., Eschen-Lippold, L., Scheel, D., Lee, J., and Sinha, A. K. (2014). Agroinfiltration by cytokinin-producing Agrobacterium sp. strain GV3101 primes defense responses in Nicotiana tabacum. Mol. Plant Microbe Interact. 27, 1175–1185. doi: 10.1094/MPMI-04-14-0114-R
Slocombe, S. P., Schauvinhold, I., Mcquinn, R. P., Besser, K., Welsby, N. A., Harper, A., et al. (2008). Transcriptomic and reverse genetic analysesof branched-chain fatty acid and acyl sugar production in Solanum pennellii and Nicotiana benthamiana. Plant Physiol. 148, 1830–1846. doi: 10.1104/pp.108.129510
Snyder, J., Simmons, A., and Thacker, R. (1998). Attractancy and ovipositional response of adult Bemisia argentifolii (Homoptera: Aleyrodidae) to type IV trichome density on leaves of Lycopersicon hirsutum grown in three day-length regimes. J. Entomol. Sci. 33, 270–281.
Srinivasan, R., Riley, D., Diffie, S., Sparks, A., and Adkins, S. (2012). Whitefly population dynamics and evaluation of whitefly-transmitted tomato yellow leaf curl virus (TYLCV)-resistant tomato genotypes as whitefly and TYLCV reservoirs. J. Econ. Entomol. 105, 1447–1456. doi: 10.1603/EC11402
Takabayashi, J., Shimoda, T., Dicke, M., Ashihara, W., and Takafuji, A. (2000). Induced response of tomato plants to injury by green and red strains of Tetranychus urticae. Exp. Appl. Acarol. 24, 377–383. doi: 10.1023/A:1006497024175
Thaler, J. S., Farag, M. A., Paré, P. W., and Dicke, M. (2002a). Jasmonate-deficient plants have reduced direct and indirect defences against herbivores. Ecol. Lett. 5, 764–774. doi: 10.1046/j.1461-0248.2002.00388.x
Thaler, J. S., Karban, R., Ullman, D. E., Boege, K., and Bostock, R. M. (2002b). Cross-talk between jasmonate and salicylate plant defense pathways: effects on several plant parasites. Oecologia 131, 227–235. doi: 10.1007/s00442-002-0885-9
Thaler, J. S., Fidantsef, A. L., Duffey, S. S., and Bostock, R. M. (1999). Trade-offs in plant defense against pathogens and herbivores: a field demonstration of chemical elicitors of induced resistance. J. Chem. Ecol. 25, 1597–1609. doi: 10.1023/A:1020840900595
Verdonk, J. C., De Vos, C. R., Verhoeven, H. A., Haring, M. A., Van Tunen, A. J., and Schuurink, R. C. (2003). Regulation of floral scent production in petunia revealed by targeted metabolomics. Phytochemistry 62, 997–1008. doi: 10.1016/S0031-9422(02)00707-0
Villarroel, C. A., Jonckheere, W., Alba, J. M., Glas, J. J., Dermauw, W., Haring, M. A., et al. (2016). Salivary proteins of spider mites suppress defenses in Nicotiana benthamiana and promote mite reproduction. Plant J. 86, 119–131. doi: 10.1111/tpj.13152
Zarate, S. I., Kempema, L. A., and Walling, L. L. (2007). Silverleaf whitefly induces salicylic acid defenses and suppresses effectual jasmonic acid defenses. Plant Physiol. 143, 866–875. doi: 10.1104/pp.106.090035
Zhang, P. J., Zheng, S. J., van Loon, J. J., Boland, W., David, A., Mumm, R., et al. (2009). Whiteflies interfere with indirect plant defense against spider mites in Lima bean. Proc. Natl. Acad. Sci. U.S.A. 106, 21202–21207. doi: 10.1073/pnas.0907890106
Zhao, Y., Thilmony, R., Bender, C. L., Schaller, A., He, S. Y., and Howe, G. A. (2003). Virulence systems of Pseudomonas syringae pv. tomato promote bacterial speck disease in tomato by targeting the jasmonate signaling pathway. Plant J. 36, 485–499. doi: 10.1046/j.1365-313X.2003.01895.x
Keywords: acylsugars, Bemisia tabaci, plant breeding, methyl jasmonate, tomato, Tomato yellow leaf curl virus, trichomes, whitefly
Citation: Escobar-Bravo R, Alba JM, Pons C, Granell A, Kant MR, Moriones E and Fernández-Muñoz R (2016) A Jasmonate-Inducible Defense Trait Transferred from Wild into Cultivated Tomato Establishes Increased Whitefly Resistance and Reduced Viral Disease Incidence. Front. Plant Sci. 7:1732. doi: 10.3389/fpls.2016.01732
Received: 21 September 2016; Accepted: 03 November 2016;
Published: 22 November 2016.
Edited by:Mario Tavazza, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, Italy
Reviewed by:Donato Gallitelli, University of Bari, Italy
Joe Hull, Agricultural Research Service (USDA), USA
Copyright © 2016 Escobar-Bravo, Alba, Pons, Granell, Kant, Moriones and Fernández-Muñoz. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Rafael Fernández-Muñoz, email@example.com
†Present address: Rocío Escobar-Bravo, Department of Plant Ecology and Phytochemistry, Institute of Biology, Leiden University, Leiden, Netherlands