ORIGINAL RESEARCH article
Sec. Invertebrate Physiology
Volume 10 - 2019 | https://doi.org/10.3389/fphys.2019.00745
Transcriptome and Metabolome Reprogramming in Tomato Plants by Trichoderma harzianum strain T22 Primes and Enhances Defense Responses Against Aphids
- 1Department of Agricultural Sciences, Portici, Italy
- 2ENEA, Rome, Italy
- 3Task Force on Microbiome Studies, University of Naples Federico II, Naples, Italy
- 4Department of Pharmacy, University of Naples Federico II, Naples, Italy
- 5National Research Council, Institute for Sustainable Plant Protection, Portici, Italy
Beneficial fungi in the genus Trichoderma are among the most widespread biocontrol agents of plant pathogens. Their role in triggering plant defenses against pathogens has been intensely investigated, while, in contrast, very limited information is available on induced barriers active against insects. The growing experimental evidence on this latter topic looks promising, and paves the way toward the development of Trichoderma strains and/or consortia active against multiple targets. However, the predictability and reproducibility of the effects that these beneficial fungi is still somewhat limited by the lack of an in-depth understanding of the molecular mechanisms underlying the specificity of their interaction with different crop varieties, and on how the environmental factors modulate this interaction. To fill this research gap, here we studied the transcriptome changes in tomato plants (cultivar “Dwarf San Marzano”) induced by Trichoderma harzianum (strain T22) colonization and subsequent infestation by the aphid Macrosiphum euphorbiae. A wide transcriptome reprogramming, related to metabolic processes, regulation of gene expression and defense responses, was induced both by separate experimental treatments, which showed a synergistic interaction when concurrently applied. The most evident expression changes of defense genes were associated with the multitrophic interaction Trichoderma-tomato-aphid. Early and late genes involved in direct defense against insects were induced (i.e., peroxidase, GST, kinases and polyphenol oxidase, miraculin, chitinase), along with indirect defense genes, such as sesquiterpene synthase and geranylgeranyl phosphate synthase. Targeted and untargeted semi-polar metabolome analysis revealed a wide metabolome alteration showing an increased accumulation of isoprenoids in Trichoderma treated plants. The wide array of transcriptomic and metabolomics changes nicely fit with the higher mortality of aphids when feeding on Trichoderma treated plants, herein reported, and with the previously observed attractiveness of these latter toward the aphid parasitoid Aphidius ervi. Moreover, Trichoderma treated plants showed the over-expression of transcripts coding for several families of defense-related transcription factors (bZIP, MYB, NAC, AP2-ERF, WRKY), suggesting that the fungus contributes to the priming of plant responses against pest insects. Collectively, our data indicate that Trichoderma treatment of tomato plants induces transcriptomic and metabolomic changes, which underpin both direct and indirect defense responses.
Solanum lycopersicum represents one of the most widespread horticultural crops in the world, with a production of 177 million of tons in 2016 (FAOSTAT). Pests and pathogens cause remarkable crop losses only in part limited by control strategies, which are still largely based on chemical pesticides. The use of biocontrol agents and/or the implementation of bioinspired strategies of sustainable pest management (Pennacchio et al., 2012) is still limited, in spite of the health and environmental issues associated with pesticide release (Alewu and Nosiri, 2011) and the recent changes of the EU policy aiming to reduce their use (European directive 2009/128; Woo and Pepe, 2018). Among the different biocontrol options, the useof soil microorganisms to reduce crop losses and promote plant growth appears to be very promising. Indeed, many biological products (i.e., biopesticides, biostimulants, biofertilizers) already available on the market often contain beneficial fungi belonging to the genus Trichoderma (Woo et al., 2014; Woo and Pepe, 2018). Numerous strains of Trichoderma may have direct effects on plants, such as promotion of growth, nutrient uptake, efficiency of nitrogen use, seed germination rate and plant defenses against biotic and abiotic stress agents (Shoresh et al., 2010; Studholme et al., 2013; Lorito and Woo, 2015). In particular, as many other beneficial microbes (Pineda et al., 2015), some Trichoderma strains can activate Systemic Acquired Resistance (SAR) and/or Induced Systemic Resistance (ISR) (Segarra et al., 2007; Shoresh et al., 2010; Rubio et al., 2014; Martínez-Medina et al., 2017; Manganiello et al., 2018), whichconfer resistance against a wealth of phytopathogens (Van Wees et al., 2008). Indeed, Trichoderma spp. are widely used as biocontrol agents of plant pathogens (Lorito et al., 2010; Lorito and Woo, 2015; Manganiello et al., 2018), and are recognized as valuable Plant Growth Promoting Fungi (PGPFs) (Harman et al., 2004; Hermosa et al., 2012; Studholme et al., 2013; Mendoza-Mendoza et al., 2018). However, very few reports have addressed the role of these fungi in the modulation of plant defense responses against pest insects. Only in the last decade, the enhancement of indirect plant defense barriers against aphids was observed in plants colonized by Trichoderma (Guerrieri et al., 2004; Battaglia et al., 2013; Coppola et al., 2017a).
Plants have evolved both direct and indirect protection barriers to limit pest insects, such as the production of compounds able to directly interfere with physiology and reproduction of herbivores (i.e., direct defense), or to attract their natural enemies and exploit the ecological service they provide (i.e., indirect defense) (Walling, 2000; Kessler and Baldwin, 2002). The signals and the defense molecules locally produced at the damage site are often systemically circulated throughout the plant, while the released volatile blend modulates the interactions not only with higher trophic levels (i.e., herbivores and their natural enemies), but also with neighboring healthy plants, which can perceive the “alarm messages” emitted by injured conspecifics (Conrath, 2011; Coppola et al., 2017b).
The titer of different plant hormones, such as salicylic acid (SA), ethylene (ET), and jasmonic acid (JA), is modulated by damage and the induced changes activate hormone-dependent key-regulators of downstream plant defense pathways (Pieterse and van Loon, 1999, 2004; Thaler et al., 2002). Biotrophic pathogens generally trigger the SA pathway, while necrotrophic colonization activates both of ET and JA pathways (Pieterse and van Loon, 1999; Walling, 2000; Harman et al., 2004). Insect chewing on plant tissues mostly induce the JA pathway (Schilmiller et al., 2007; Pieterse et al., 2012), while sap feeders predominantly activate SA-dependent responses (Walling, 2000, 2008). However, these signaling pathways are tightly interconnected to allow a fine control of optimal resource allocation between plant growth and response to environmental stress agents; the underlying network of cross-modulating pathways is often manipulated by plant enemies to evade or actively suppress the defense barriers (Pieterse et al., 2012). The antagonism between SA, ET, and JA pathways, dictated by the need to prioritize the response against a specific type of biotic stressor, has been demonstrated in many plant species (Reymond and Farmer, 1998; Spoel and Dong, 2008; Pieterse et al., 2012). However, numerous attackers can exploit this antagonism to their own benefit by activating responses to which they are not sensitive, thus preventing/limiting energy investments in defense pathways detrimental for them (Erb et al., 2012).
This intricate network of molecular interactions among different stress agents has a further layer of complexity, which is added by the soil and plant-associated microbiota, deeply influencing the overall plant response (Berendsen et al., 2012; Bulgarelli et al., 2013; Pineda et al., 2017). Plants, along with the associated microbiota in the surrounding environment, are therefore the living milieu in which a complex network of multitrophic interactions among pests/and beneficial organisms takes place. Then, the molecular mechanisms driving plant defense responses against pests and in presence of a beneficial micro-organism can only be understood if analyzed at metaorganism level. These studies will shed light on the co-evolutionary forces shaping insect communities on plants and will offer valuable insights for developing novel strategies of pest control that can mimic and/or modulate plant defense responses.
Here we pursue this objective by investigating transcriptomic and metabolomic changes induced in Solanum lycopersicum (cv “Dwarf San Marzano”) by the beneficial fungus Trichoderma harzianum strain T22, and a pest insect, the aphid Macrosiphum euphorbiae (Thomas), when applied to the experimental plants alone or in combination.
Materials and Methods
Fungal Cultures and Insects
T. harzianum strain T22 (T22) was maintained on potato dextrose agar (PDA; Hi Media) slants at room temperature and regularly sub-cultured. Conidia were collected from the surface of sporulating fungal cultures (5–7 d) in sterile distilled water, and adjusted to a concentration of 107 spores mL−1.
The aphid M. euphorbiae was reared on tomato “Dwarf San Marzano” (hereafter indicated as SM), in a climatic chamber at 20 ± 1°C, 65 ± 10% RH, photoperiod of 16:8 hr light/dark.
Plant Material and Treatments
Seeds of Solanum lycopersicum cv “Dwarf San Marzano” (SM) were surface-sterilized in 2% (v/v) sodium hypochlorite for 20 min, then thoroughly rinsed in sterile distilled water. Seeds were treated with the fresh spore suspension of T. harzianum T22, as a seed coating (conc. 107 spores mL−1), or with water as a control treatment (CTRL); stirred frequently to cover the seed surface uniformly, left to air dry for 24 h, then stored at 4°C until use. Treated seeds were germinated on wet sterile paper disks in the dark, in an environmental chamber at 24Â°C, then transplanted to sterile potting soil upon root emergence and grown in controlled conditions at 20 ± 2°C, with a photoperiod of 16:8 h light/dark. After 3 weeks, tomato seedlings were transplanted to 14-cm diameter plastic pots containing sterilized soil and grown for 2 weeks under the same environmental conditions. Plants from the T22 coated seeds also received a supplementary watering with the T22 spore suspension (20 mL; 107sporemL−1) after the transplant and, after that, on a weekly basis. Leaf samples were collected from all tomato plants (T22 and CTRL) 2 weeks after the last T22 watering treatment.
Aphid Infestation and Bioassay
A clonal population of M. euphorbiae was reared on SM in an environmental chamber at 20 ± 2°C, 65 ± 5% RH and a 16:8 h light/dark photoperiod. For the transcriptomic analysis, the control and T. harzianum-treated plants (T22) subjected to aphid infestation after 4 weeks of growth under the same environmental conditions indicated above. Three biological replicates, both for CTRL and T22 plants, were caged and infested with synchronized 1-day-old nymphs of M. euphorbiae. Five aphids per plant were settled and allowed to feed for 48 h, then removed from the plant in order to collect aphid-free leaf samples for the subsequent RNA extraction (samples named as “Aph” or “T22Aph”).
For the aphid longevity assay, 10 plants for each CTRL or T22 treatment were infested with 5 newly born first instar nymphs of M. euphorbiae. The presence of aphids and of shed exuviae, as an indicator of molting occurrence, was daily monitored. Survival curves were compared by LogRank analysis.
Fully expanded leaves (5 leaves) of 3 tomato plants for each treatment were used for total RNA extraction: leaf samples treated with T22 (T22), infested by aphids (Aph), treated with T22 and infested by aphids (T22Aph), and untreated (CTRL). Total RNA was extracted using the Plant RNeasy mini kit (Qiagen) according to manufacturer's protocol. Samples were analyzed with the 2,100 Bioanalyzer system (Agilent Technologies) for size, quantification, and quality control of RNA. Only samples with a 260/280 nm absorbance >1.8 and a 260/230 nm absorbance >2 were sequenced. Three biological replicates were used for each experimental condition and controls. Total RNA (8 μg) of each sample was used for the library preparation and sequencing by an external sequencing service. A paired-end sequencing (2 × 30 Million of reads) on Illumina HiSeq 2,500 platform was chosen. RNA-Seq raw sequences were cleaned using Trim Galore package [http://www.bioinformatics.babraham.ac.uk/projects/trim_galore/]. Low-quality bases were trimmed from the sequences and the adapter sequences were removed by Cutadapt (Martin, 2011); default parameters for the pair-end sequences were used. Finally, if one of the pairs was filtered out due to the cleaning procedure, the other pair was also discarded from the downstream analyses.
The cleaned sequences were then mapped on the tomato genome (version 2.50) using Bowtie version 2.1.0 (Langmead and Salzberg, 2012) and Tophat version 2.0.8 (Kim et al., 2013). Quantification of the reads abundance per each gene (exon level) available from iTAG gene annotation (version 2.5) was done using AIR (https://transcriptomics.sequentiabiotech.com/).
To identify the set of Differentially Expressed Genes (DEGs) between the diverse experimental conditions, two different statistical approaches were used: the Negative Binomial test implemented in DESeq package (Anders and Huber, 2010) and the Negative Binomial test and Generalized Linear Model (GLM), as implemented in EdgeR package (Robinson et al., 2010), were used considering false discovery rate (FDR) < = 0.05. The data from the two methods were compared and where the values intersected, these results were considered and selected to compile the datasets used for the analysis of the differentially expressed genes.
RNA-Seq validation was carried out by Real Time RT-PCR, measuring the transcript levels of selected DEGs. Gene expression analysis was carried out using 2 technical replicates for each of the 3 biological replicates per sample. Relative quantification of gene expression was carried out using the 2−ΔΔCt method (Livak and Schmittgen, 2001). The housekeeping gene EF-1α was used as endogenous reference gene for the normalization of the expression level of the target genes (Marum et al., 2012; Müller et al., 2015). Ten couples of primers were used to analyze each treatment condition. Primers and their main features are reported in the Supplementary Table 1.
GO and GOslim annotations were downloaded from the Biomart section of Ensembl Plant version SL2.50 (2014-10-EnsemblPlants) (Kinsella et al., 2011). Moreover, GO was used for GO enrichment of all DEGs together and DEGs UP or DOWN regulated, independently. The analysis was carried out by the Goseq Bioconductor package (Young et al., 2010) (method “BH,” FDR ≤ 0.05).
Mapping of some enzymatic activities into specific molecular pathways was acquired from the KEGG database.
Semi-polar Metabolome Analysis
LC-ESI(+)-MS analysis of the leaf primary and secondary semi-polar metabolome was performed as previously described (Alboresi et al., 2016; Fasano et al., 2016) with slight modifications: 5 mg of freeze-dried, homogenized leaf powder were extracted with 0.75 mL cold 75% (v/v) methanol, 0.1% (v/v) formic acid, spiked with 10 μg/ml formononetin. After shaking for 40'at 20 Hz using a Mixer Mill 300 (Qiagen), samples were centrifuged for 15' at 20,000 g at 4°C; 0.6 mL of supernatant were removed and transferred to HPLC tubes. For each genotype, 4 independent biological replicates, consisting of 4 plants each, were analyzed; for each biological replicate, at least one technical replicate was carried out. LC-MS analyses were carried out using an LTQ-Orbitrap Discovery mass spectrometry system (Thermo Fisher Scientific) operating in positive electrospray ionization (ESI), coupled to an Accela U-HPLC system (Thermo Fisher Scientific, Waltham, MA). Liquid chromatography was carried out using a Phenomenex C18 Luna column (150 × 2.0 mm, 3 μm) and the mobile phase was composed by water −0.1% formic acid (A) and acetonitrile −0.1% formic acid (B). The gradient was: 95%A:5%B (1 min), a linear gradient to 25%A:75%B over 40 min, 2 min isocratic, before going back to the initial LC conditions in 18 min. Five microliter of each sample were injected and a flow of 0.2 mL was used throughout the LC runs. Detection was carried out continuously from 230 to 800 nm with an online Accela Surveyor photodiode array detector (PDA, Thermo Fisher Scientific, Waltham, MA). All solvents used were LC-MS grade quality (CHROMASOLV® from Sigma-Aldrich). Metabolites were quantified in a relative way by normalization on the internal standard (formononetin) amounts. ESI-MS ionization was performed using the following parameters: capillary voltage and temperature were set at 20V and 280°C; sheath and aux gas flow rate at, respectively, 30 and 20. Spray voltage was set to 3.5 kV and tube lens at 80 V. Targeted metabolite identification was performed by comparing chromatographic and spectral properties with authentic standards and reference spectra, in house database, literature data, and on the basis of the m/z accurate masses, as reported in the Pubchem database (http://pubchem.ncbi.nlm.nih.gov/) for monoisotopic mass identification, or on the Metabolomics Fiehn Lab Mass Spectrometry Adduct Calculator (http://fiehnlab.ucdavis.edu/staff/kind/Metabolomics/MS-Adduct-Calculator/) in the case of adduction detection.
Untargeted metabolomics was performed using the SIEVE software (Thermofisher scientific). After chromatogram alignment and retrieve of the all the detected frames (e.g., ions), an ANOVA + t-test statistical analysis was carried out to identify differentially accumulated molecules. Finally, a series of public metabolomic databases (KEGG, HMD, Golm Metabolome Database, PlantCyc) were interrogated and a list of tentative IDs was obtained. Further validation steps included isotopic pattern ratio (IPR), mass fragmentation when available and literature search.
Principal component analysis (PCA) of untargeted semipolar metabolome was performed by using the SIEVE software (Thermofisher Scientific). Venn diagram representation of differentially accumulated metabolites (DAMs) was performed using the Venny 2.1 software [Oliveros, J. C. (2007–2015)]. Metabolite heat maps and hierarchical clustering were build and colored by using the GENE-E software (http://www.broadinstitute.org/cancer/software/GENE-E/) and as previously described (Diretto et al., 2010).
Trichoderma harzianum T22 Promotes Tomato Defense Against M. euphorbiae
The treatment of tomato plants with T. harzianum T22 negatively influenced the survival rate of M. euphorbiae. T22 plants showed an increased level of resistance to aphid infestation, as indicated by the significant difference registered between the T22 survival curve and that of CTRL (LogRank analysis, χ2 = 4.72, p = 0.030, df = 1) (Figure 1).
Figure 1. Effect of T. harzianum T22 on aphid survival over time. Survival curves (percentage) of M. euphorbiae reared on the untreated water control and the T. harzianum T22 treated tomato plants are significantly different, p < 0.05 (LogRank test).
Plant Transcriptome Reprogramming Induced by Trichoderma harzianum T22 Root Colonization
In order to unravel the molecular mechanisms underlying the plant response to the combined action of Trichoderma infection and aphid infestation, transcriptomic and metabolomic analyses ofthe tomato cultivar “Dwarf San Marzano” were conducted by comparing Trichoderma treated and untreated plants, with and without aphid infestation.
Table 1 provides a general summary of differentially expressed genes for each treatment.
Table 1. General overview of the transcriptomic rearrangement of Dwarf San Marzano tomato plants imposed by experimental treatments compared to untreated SM plants.
T22 plants showed a total of 978 differentially expressed genes (DEGs) of which 515 were up-regulated and 463 were down-regulated (Supplementary Tables 2A,B). The principal defense-related categories that may be linked to the induction in T22 treated plants of a precursor state of defense against insect attack are represented by “response to stress,” “transport” and “response to stimulus” (Figure 2). The most abundant enriched Gene Ontology (GO) terms in the ontological category “Biological Process” were associated with metabolic processes, photosynthesis-related mechanisms, oxidation-reduction processes and response to stress (Supplementary Figure 1).
Figure 2. GOs distribution of differentially expressed genes in SM plants treated with T.harzianumT22. Gene Ontology (GO) terms associated with up-regulated (red bars) and down-regulated (green bars) genes based on the “Biological Process” ontological domain (sequence cut-off: 5%).
Several genes included in these categories were up-regulated. A short list of these genes is reported in Table 2. Among them, the induction of genes associated with photosynthesis, chlorophyll biosynthesis and sequestration and biosynthetic processes, may be linked with T22 beneficial effects on tomato plant physiology The up-regulation of plant genes involved in early signals of defense responses against environmental cues as, for example, Serine/threonine-protein kinase, Leucine-rich repeat protein kinase, LRKs, Glutathione S-transferase, and others (listed in Supplementary Table 2A) was also observed. Similarly, the up-regulation of genes coding for transcription factors (TF), such as Ethylene responsive transcription factors (ERF), WRKY, MYB, and bZIP TF (Supplementary Table 2A), was registered. These genes are likely involved in plant defense priming (Conrath et al., 2015).
As expected, the up-regulation of markers of SA (i.e., chitinase and1,3-B glucanase) and JA pathways (i e., metallocarboxypeptidase inhibitor and, Type I serine protease inhibitor; Supplementary Table 2A) were also observed. Overall, these data show that Trichoderma colonization of tomato plants positively affects several metabolic pathways, consistently with previous observations in tomato and other plant species (Alexandru et al., 2013; Mohapatra and Mittra, 2016; Ban et al., 2018). Since phenylpropanoids contribute to plant defenses (both direct and indirect) to insect herbivores, genes encoding for key-enzymes associated with phenylpropanoids biosynthesis were searched by using DEGs in a query to a KEGG database; in addition, a manual curation to enrich the aforementioned list was performed. Transcripts coding for 10 enzymes were retrieved among the DEGs that were up-regulated and the correspondence found between the enzymes and the gene identifiers is listed in Table 3. As shown in Figure 3, the enzymes act in different stages of phenylpropanoid biosynthesis, catalyzing key-steps as phenylalanine conversion in cinnamic acid (Phenylalanine ammonia-lyase (PAL) and Caffeoyl-CoA O-methyltransferase), or catalyzing final branches for lignin production (i.e., Peroxiredoxin) and anthocyanin synthesis and modification (Anthocyanin 5-aromatic acyl transferase and Anthocyanidin reductase). Interestingly, a transcript coding for PAL is greatly up-regulated in T22 samples. In addition, a series of genes coding for enzymes involved in early phenylpropanoid or flavonoid synthesis resulted down-regulated (Table 2). Overall, these data show that T22 colonization strongly affects and remodels phenylpropanoid pathway.
Figure 3. Schematic diagram of the phenylpropanoid biosynthesis pathway as determined by DEGs in plants treated with T22 and queried to a KEGG database. The enzymes evidenced in color are encoded by genes found in the up-regulated DEGs of the tomato. A correspondence between enzymes and DEGs is shown in Table 2.
Plant Transcriptome Reprogramming Induced by Aphids
Studies on tomato-M. euphorbiae interaction and on the relative transcriptomic changes have been already reported, although using other tomato cultivars, different time points and diverse transcriptomic approaches (Avila et al., 2012; Coppola et al., 2013). Here we carried out a transcriptomic study of the SM cultivar challenged with M. euphorbiae for 48 h, through RNA-Seq approach.
Tomato plants infested by M. euphorbiae showed 625 up-regulated and 1179 down-regulated transcripts (Supplementary Table 3). Major GO categories associated with plant defense were “response to stress,” “response to stimulus” and “oxidation-reduction process” (Figure 4). The distribution and the enrichment analysis of GO terms associated with DEGs induced by aphid infestation underlined the predominance of categories related to the regulation of gene expression as “RNA methylation,” “ncRNA processing,” “Ribosome assembly,” “rRNA metabolic process,” “translation,” “mRNA cleavage,” “defense response to bacterium” (Supplementary Figure 2). The increase of several transcripts coding for kinase/phosphatase/receptor-like kinase as well as of transcripts coding for proteins involved in oxidative burst and scavenging was observed (Supplementary Table 3A). Genes coding for several classes of pathogenesis-related proteins (PR) (PR5, PR10, Chitinase, Subtilisin), genes associated with salicylic acid and genes involved in ethylene signaling were also up-regulated upon aphid attack (Supplementary Table 3A). A large number of DEGs were down-regulated (Supplementary Table 3B and Table 4), including key genes of plant immunity, such as MAP Kinases and WRKY. Interestingly, a strong down-regulation was observed for transcripts associated with JA pathway, as those coding for lipoxygenases and protease inhibitors. Other down-regulated transcripts code for glycosyltransferases and genes associated with terpene production, such as sesquiterpene synthase 1 and geranylgeranyl reductase.
Figure 4. GOs distribution of differentially expressed genes in SM plants infested byM. euphorbiae. Gene Ontology (GO) terms associated with up-regulated (red bars) and down-regulated (green bars) genes based on the “Biological Process” ontological domain (sequence cut-off: 5%).
Overall, at primary metabolism level, aphid infestation strongly repressed transcripts of enzymes associated with sugar (i.e., Fructose-bisphosphatealdolase and Sucrose synthase) and amino acid (i.e., Threonine deaminase and Tryptophan synthase) pathways, which are involved in the plant defense responses against biotic and abiotic stresses (Conklin and Last, 1995; Brader et al., 2001; Wilkinson et al., 2001; Chen et al., 2005; Tauzin and Giardina, 2014; Lv et al., 2017). Several other down-regulated genes were involved in photosynthetic activities, chlorophyll biosynthesis, polyamine and phenylpropanoids-related metabolism (Table 4).
Plant Transcriptome Reprogramming Induced by Trichoderma harzianum T22 Root Colonization and Aphid Infestation
In order to assess the impact of T. harzianum T22 on tomato defense response against aphids, the transcriptome of tomato plants treated with Trichoderma and subsequently infested by aphids (T22Aph) was analyzed. T22Aph transcriptome reprogramming involved 1527 transcripts: 602 up- and 925 down-regulated (Supplementary Table 4). Trichoderma colonization strongly affected GO categories involved in plant metabolism and stress response during aphid infestation (Figure 5). The enrichment analysis was performed in order to underline significant over-represented GO categories relative to Biological Process ontological domain. Interestingly, some enriched GO term categories were associated with direct and indirect defenses, as they include genes involved in isoprenoid biosynthesis, induced systemic resistance and JA-mediated signaling pathway (Supplementary Figure 3; Supplementary Tables 4A,B). An example of defense-related DEGs is shown in Table 5. Among early signals, calmodulin-binding proteins and Ca2+ transporters were also over-represented as several classes of kinases and receptor-kinases (serine/threonine kinases, receptor-like kinases, LRR-RLKs, MAPKKK). Furthermore, transcripts related to ROS production and scavenging such as GST, peroxidases, oxidoreductases, catalase, superoxide dismutase, and detoxification protein were up-regulated. Other up-regulated genes coded for Lipoxygenases, involved in early stages of JA biosynthesis, Polyphenol oxidase (PPO), Leucine aminopeptidase (LapA), and proteinase inhibitor (MCPI) involved in later stages of defense besides several classes of defense genes-related TF (GRAS, WRKY, MYB, bZIP). Moreover, a transcript encoding for a cysteine protease inhibitor (Multicystatine), associated with aphid growth inhibition (Rahbé et al., 2003; Emani, 2018), was up-regulated while the number of down-regulated transcripts encoding proteinase inhibitors was reduced in comparison with what observed following aphid infestation.
Figure 5. GOs distribution of DEGs in T22-Aph plants, first treated with T. harzianum T22 and subsequently infested with aphids (SMT22 Aph). Gene Ontology (GO) terms associated with up-regulated (red bars) and down-regulated (green bars) genes based on the “Biological Process” ontological domain (sequence cut-off: 5%).
Table 5. Group of defense-related DEGs identified in San Marzano plants treated with Trichoderma T22 and infested by aphid.
A strong impact on hormone-controlled defense pathways was observed: ethylene biosynthesis and signaling as well as salicylic acid biosynthesis and signaling were up-regulated in T22Aph plants (Supplementary Table 4; Table 5). Notably, compared to T22, T22Aph were characterized by a strong down-regulation of key-steps in the phenylpropanoid pathway (Table 5).
For a selected number of genes, transcript quantification was confirmed by Real Time RT-PCR (Supplementary Figure 4).
Key Genes Regulated by the Interaction T22-Tomato-Aphid
In order to assess the contribution of T. harzianum T22 in the priming of defenses against aphids, genes specifically regulated in the tripartite interaction were analyzed. Supplementary Tables 5A,B list unique genes modulated in their expression during the T22-Tomato-Aphid interaction (T22Aph samples, Figure 6A). These genes are specifically induced by aphid challenge in presence of Trichoderma priming. Among the up-regulated ones, genes involved in ethylene biosynthesis and signaling emerge (Table 6), as well as those associated with amino acid metabolism (asparagine synthase 1, glutamate receptor 1.2, proline dehydrogenase). Unique down-regulated genes (Supplementary Table 5B; Table 6) included several members of WRKY family of transcription factors, known for their promotion of JA signaling in the negative interplay with SA pathway (Li et al., 2004; Takatsuji, 2014).
Figure 6. Venn diagram visualization of DEGs. (A) DEGs of tomato plants infested by the aphid M. euphorbiae (Aph) are crossed to DEGs of tomato plants inoculated with T. harzianum T22 and subsequently infested by aphids (T22Aph). (B) Focus on the intersection of down-regulated genes of Aph and T22Aph plants.
Figure 6A shows that aphid repression of tomato genes (1179 down-regulated genes in Aph) was reduced by T. harzianum T22 colonization in T22Aph (925 down-regulated genes in T22Aph).
The intersection between down-regulated genes of Aph and T22Aph samples is shown through a Venn diagram representation (Figure 6B). Common genes repressed in both conditions are listed in Supplementary Table 5C. A large group of genes of phenylpropanoid pathways (i.e., phenylalanine ammonia-lyase, caffeoyl-CoA O-methyltransferase, and others) resulted down-regulated in both conditions. Interestingly, a large number of glycosyltransferases resulted strongly repressed in both conditions, indicating that they could represent a peculiar aspect of tomato-aphid interaction, independently from T. harzianum T22 influence (Supplementary Table 5C). Genes specifically repressed in the bipartite interaction (Aph) are 683 (Figure 6B; Supplementary Table 5D) and include JA-related genes as those coding for Phospholipase, Lipoxygenases A, C and D, Leucine aminopeptidase A1 and several classes of proteinase inhibitors (Table 5). In order to assess if T. harzianum T22 is able to overturn the expression of aphid-repressed genes in tomato, the 683 specifically down-regulated transcripts in Aph samples were compared with genes induced by T22 (T22; Supplementary Table 2A), underlining an overturning of the expression of three genes listed in Table 7. The transcription factor bHLH may be associated with JA signaling (Zhou and Memelink, 2016) while the steroid dehydrogenase, involved in steroid and squalene biosynthesis, is a precursor of triterpenes. Finally, the GDSL esterase/lipase belong to a very large subfamily of lipolytic enzymes.
In order to analyse the downstream effects of the transcriptomic reprogramming induced by M. euphorbiae attack, in the absence or presence of the antagonist fungus T. harzianum T22, we performed a global metabolic profiling of the leaf semi-polar fraction by LC-ESI(+)-MS (for more details, see “Materials and methods). First of all, to gain a general overview of the metabolic changes occurring under the different experimental conditions, we carried an untargeted metabolomics analysis, using the SIEVE software (Thermo Fisher Scientific). Through alignment of all mass chromatograms with the subsequent retrieval of all detected ions, we built a 3D Principal Component Analysis (PCA) diagram (Supplementary Figure 5), which showed a clear separation of the leaves treated with T. harzianum and, to a lower extent, infested by aphids in the presence of the fungus. To investigate the changes of known tomato leaf metabolites, we then performed a targeted metabolomic analysis in which we quantified, in a relative way, 135 metabolites involved in primary (amino acids, amines, sugars, organic acids, lipids, vitamins, etc) and secondary (alkaloids, amides, phenylpropanoids, isoprenoids) pathways. The complete metabolite dataset is reported in Supplementary Table 7 and Supplementary Figure 6, while the lists of the differentially accumulated metabolites (DAM) in each comparison (T22/CTRL, Aph/CTRL, and T22Aph/T22) are reported in Supplementary Table 6.
Heatmap visualization was used as first attempt to understand the real impact of the aphid and fungus treatments on the leaf metabolome (Supplementary Figure 6). Globally, most of the alterations in leaves grown in the presence of M. euphorbiae or T. harzianum were of negative sign (e.g., lower levels in the treated over the control) and particularly affected secondary metabolism (alkaloids and phenylpropanoids). We used Venn diagram visualization (Figure 7; Supplementary Table 8) to highlight the number of common and specific DAMs in relation to the three interactions under study: interestingly, 29 metabolites resulted present in all the comparisons and 17 out of them displayed variations of the same sign. A group of metabolites was specifically highlighted in T22 plants, and included ADP, AMP, citric acid, dihydro-caffeic acid,2-hydroxyglutarate, phosphoenolpyruvate (PEP), coumarin, syringaldehyde and tetrahydrofolate being down-accumulated in T22 vs. CTRL and T22Aph vs. T22, and up-represented in Aph vs. CTRL; and Uroporphyrinogen III and Galactonate/Gluconate, showing an opposite trend. Interestingly, over-represented metabolites retrieved in T22 samples are precursors of salicylic acid: Salicylate β-D-glucose ester and Salicyloyl-L-aspartic acid, have a concentration three times higher than the control. Furthermore, Phenylalanine, Coumaric and chorismic acids, member of phenilpropanoids and known for their possible flow into primary steps of salicylic acid biosynthesis, in T22 samples are about 5 times higher than in control (Supplementary Table 6). Fourteen metabolites were found to be specifically associated with the presence of T. harzianum (T22 vs. CTRL and T22Aph vs. Aph comparisons), mostly with alterations of negative sign (indicated in Supplementary Table 6 with a cross). Finally, 7 DAMs each were exclusive for T22Aph vs. T22; among them, δ-tomatine (an alkaloid), N-isovalerylglycine and threonine/homoserine (amino acids) and protoporphyrinogen IX, an isoprenoid associated with tissue necrosis, were detected at lower levels over the control. At the opposite, the amino acid glutamic acid, the sugar phosphate glycerate-2-P/glycerate-3-Pand the lipid CDP-choline displayed a higher accumulation in T22Aph leaves over the CTRL. T22 and T22Aph were found to share 32 metabolites: interestingly, most of them varied differently between the two comparisons, with the exception of shikimic acid and dihydrokaempferol-7-O-glucoside, and raffinose/melezitose, respectively, down- and over-accumulated in both T22 and T22Aph. In the group of compounds showing higher accumulation in T22Aph, two relevant alkaloids were found (α-/β-tomatine), together with other compounds (indicated in Supplementary Table 6 with a hash mark). On the contrary, a group comprising the amide feruloylputrescine and other compounds (indicated in Supplementary Table 6 with an asterisk), resulted more abundant in T22 vs. CTRL than T22Aph vs. T22. Notably, no common compounds were found between T22Aph and Aph.
Figure 7. Venn diagram visualization of differentially accumulated metabolites in three comparisons between tomato plants: infested with aphids vs. water control (Aph vs. CTRL); treated with T22 vs. water control (T22 vs. CTRL); treated with T22 plus infested with aphid vs. treated with T22 (T22 Aph vs. T22).
Targeted semi-polar metabolomes were used to generate a Hierarchical Clustering (HCL), applied both on columns and rows, in order to study the global relationships within leaves treated with M. euphorbiae and/or T. harzianumT22 (Figure 8). Interestingly, two distinct groups were produced, with one-to-one interactions (aphid or fungus, Aph vs. CTRL and T22 vs. CTRL) on the left side, and the three-way interactions (T22Aph vs. T22) clustering alone. As expected, metabolites displaying similar trends of related accumulation over the controls grouped together like, for instance, a set of alkaloids in the initial part and one of phenylpropanoids in the central parts of the HCL.
Figure 8. Hierarchical Clustering (HCL) of semi-polar metabolome of tomato leaves grown in the absence and in the presence of the aphid M. euphorbiae and the fungus T. harzianum, alone or in combination. Colored squares represent the values of log2-transformed fold changes of a metabolite with respect to the corresponding control (water control CTRL for Aph and T22 samples; T22 for T22Aph), according to the color scale shown (green: down-accumulated; red: up-accumulated). Gray squares indicate no detectable accumulation of the corresponding metabolite. Hierarchical clustering was calculated both on columns and rows, applying the One Minus Pearson correlation with the average linkage algorithm.
Finally, we exploited the untargeted metabolomes to retrieve new ions not included in our targeted database and specific for the four conditions under investigation (Supplementary Table 9). Twenty-two ions were found, which were subjected to metabolomics database interrogation, and isotopic pattern ratio, literature search and standard (where available) validations. For nine of them, an identification already reported in tomato was found: this group of metabolites included three acids (5-amino-levulinic acid, hydroxypipecolic acid and glutaric acid) and one phenylpropanoid (caffeic acid hexose II), over-accumulated in T22Aph vs. T22. In addition, one ester-like (2-Amino-2-methylbutanoate), two lipids (CDP-DG(16:0/20:4(5Z,8Z,11Z,14Z)), LysoPE [22:6(4Z,7Z,10Z,13Z,16Z,19Z)/0:0)], and one alkaloid (C33H57NO8 (Jurubine-like), showing an opposite trend. Thirteen additional molecular ions were detected, which could not be identified as any of the known tomato metabolites, and were tentatively assigned according other metabolite identifications: four of them (2 acids: 3-hydroxybutyric acid-like, citric acid-like; an amine: N-methyl ethanolamine phosphate-like; a flavonoid: 6-hydroxy-4′-methoxyflavone-like; and an alkaloid: O-acetylnitraraine-like) and 3 ions (a flavonoid: 3′,4′-dihydroxychalcone-like; an alkaloid: beta-obscurine-like; and an unknown) were found at, respectively, higher and lower levels in T22Aph vs. T22. Interestingly, most of the cited molecules displayed an inverse statistically significant accumulation in the other two comparisons (Aph vs. CTRL and T22Aph vs. T22).
Plants colonized by Trichoderma have often shown multiple beneficial effects (Hermosa et al., 2012; Vitti et al., 2015). We previously demonstrated an enhancement of the indirect defense barriers in tomato plants treated with T. harzianum T22, which were more attractive toward aphid parasitoids (Coppola et al., 2017a). This plant phenotype was associated with an increased level of methyl-salicylate and β-caryophyllene, known to be among the most active compounds in promoting A. ervi flight (Sasso et al., 2009; Coppola et al., 2017a).
Here we studied the impact of T. harzianum T22 colonization of tomato plant on direct defense responses to the aphid M. euphorbiae, and used transcriptomic and metabolomic approaches to shed light on the molecular mechanisms underlying the observed phenotypic changes.
Aphid Infestation Suppresses Plant Defense Responses
Aphid feeding on the tomato cv “Dwarf San Marzano” induced dramatic changes in thetranscriptome and metabolome of the plant, despite the very limited mechanical damage caused by the insect. Transcriptomic reprogramming was characterized by the deregulation of a large number of transcripts, the majority of which are down-regulated. The total number of DEGs was much higher than previously observed (Avila et al., 2012; Coppola et al., 2013), possibly due to the higher sensitivity of the digital method (RNA-Seq with respect to the analog one (microarray and/or the different tomato cultivars used in the two studies. However, the related GO categories distribution was in general agreement with previous reports Avila et al., 2012; Coppola et al., 2013. All levels of defense responses were influenced in Aph samples: oxidative stress, signal transduction, TFs and late defenses. The down-regulation of key-genes of plant immunity such as MAP Kinases, WRKY and genes associated with direct (i.e., protease inhibitors, PIs) and indirect (i.e., sesquiterpene synthase 1) responses, is consistent with the aphid capacity to circumvent host defenses by secreting evolutionarily conserved effectors able to suppress plant immune responses (Will et al., 2007; Elzinga et al., 2014). Aphid ability to interfere with plant defense mechanisms is clearly evidenced by the down regulation of genes associated with sugar metabolism and amino acid biosynthesis. Fructose-1, 6-bisphosphate aldolase is a key-enzyme involved in glycolysis, gluconeogenesis, and the Calvin cycle. It plays significant roles in biotic and abiotic stress responses, as well as in regulating growth and development processes (Lv et al., 2017). Sucrose synthase is a glycosyltransferase enzyme that plays a key-role in sugar metabolism. Sucrose is engaged in plant defense by activating plant immune responses against pathogens (Tauzin and Giardina, 2014). Threonine deaminase is part of the phytochemical arsenal that plants use to deter herbivores. Together with PIs and other defense-related compounds, is tightly regulated by the JA signaling pathway (Chen et al., 2005). The enzyme acts in the insect gut to degrade the essential amino acids arginine and threonine, respectively. In aphids it was observed that a shortfall in threonine contribute to the poor performance of the Aphis fabae on Lamium purpureum (Wilkinson et al., 2001). Tryptophan biosynthesis and the enzymes involved are induced by a wealth of stress agents, such as for instance, ozone (Conklin and Last, 1995) and biotic stress (Brader et al., 2001). In addition, a strong down-regulation of transcripts encoding Proteinase inhibitors (PIs) and several other glycosyltransferases further demonstrated the aphid ability to repress plant defense responses. PIs are proteins involved in defense responses and are often induced upon attack by insect herbivores, as they are able to inhibit insect growth and survival by disrupting their digestive physiology (Ryan, 1990; Lawrence and Koundal, 2002; Zhu-Salzman and Zeng, 2015). In aphids, similarly to what observed in thrips, PIs may inhibit aphid salivary proteases during probing and feeding establishment (Pyati et al., 2011; van Bel and Will, 2016) reducing the insect ability to degrade sieve-tube sap that includes proteins involved in defense (Furch et al., 2015). It was proposed that plant protect sap-proteins degradation by glycosylation that appears to prevent proteolysis (Taoka et al., 2007; Russel et al., 2009). Considering that glycosyltransferases are enzymes that catalyse the transfer of a sugar residue from an activated donor to an acceptor molecule the concerted down-regulation of transcripts encoding PIs and glycosyltransferases in Aph plants could be part of the aphid strategies to reduce the effectiveness of plant defense. Interestingly, three down-regulated glycosyltransferases (Solyc10g084890.2, Solyc03g078780.2, Solyc10g085280.1) showed high homology to UGT76B, C and/or E enzymes, which in Arabidopsis are involved in flavonoid biosynthesis and/or defense responses (Yonekura-Sakakibara and Hanada, 2011). The former function is consistent with the reduction in flavonoids, particularly kaempferol and quercetin glucosides, as well in phenolic acid derivatives, observed in aphid-infested plants (Supplementary Table 6).
Other down-regulated transcripts associated with plant defense are those encoding sesquiterpene synthase 1, Z,Z-farnesyl pyrophosphate synthase and geranylgeranyl reductase (Dudareva et al., 2004; Schmidt et al., 2011). Terpenoids, including sesquiterpenes and diterpenes, constitute some of the commonly encountered chemical classes of phytoalexins, biochemicals that locally protect plant tissues (Li et al., 2015). They are pathogen- and insect-inducible, known for their role in the attraction of predators, parasitoids, and other natural antagonists (Aljbory and Chen, 2018).
Among down-regulated genes, transcripts involved in phenylalanine metabolism (PAL) were retrieved, indicating a strong perturbation in phenylpropanoid pathway. In fact, as shown by the KEGG analysis, down-regulated genes involved in phenylalanine metabolism are in the early steps of the pathway, allowing the hypothesis of a possible accumulation of phenylalanine, that has been underlined as a crucial channel of SA biosynthesis (Chen et al., 2009). This finding is consistent with the reduced accumulation of several metabolites belonging to phenylpropanoid family in Aph plants that are located downstream PAL in the pathway. The over-presence of caffeic acid glucoside and coumarin could be similarly interpreted: the effect of the partial suppression of a branch of the phenylpropanoid biosynthesis causes the accumulation of central metabolites that are not toxic per se for aphids, but are precursor of molecules toxic for other herbivores (Sun et al., 2016).
Trichoderma harzianum T22 Boosts the Plant Immune Response
The advantages conferred to the plant by Trichoderma were largely associated with biological control of phytopathogens (Woo et al., 2006; Lorito et al., 2010). However, in the past 30 years, particularly with the advancement of modern techniques to analyse plant-microbe interactions, it became increasingly evident that root colonization by Trichoderma is associated with a wealth of beneficial effects, by activating defense responses against multiple stressors (De Meyer et al., 1998; Yedidia et al., 1999; Harman et al., 2004; Lorito et al., 2010; Shoresh et al., 2010; Hermosa et al., 2012; Lorito and Woo, 2015; Manganiello et al., 2018). Regarding plant responses to phytopathogens, the production of microbe-associated molecular patterns (MAMPs) by Trichoderma enhances the sensitivity of first defense, by maintaining a level of “alert” near to the threshold of effective resistance (Lorito et al., 2010). In particular, Trichoderma is also known to be involved in priming, the activation of plant defense prior to invasion, whereby upon pathogen attack Trichoderma stimulates a faster response to the pathogen effectors or it produces compounds specifically recognized by plant receptors able to elicit defense mechanisms (Lorito et al., 2010; Mauch-Mani et al., 2017; Manganiello et al., 2018). Only very recently, this priming response was also proposed to have a role in tomato indirect defense against aphid (Balmer et al., 2015; Coppola et al., 2017a; Tan et al., 2017). Here, we observed the activation of early signals of defense responses against insects in T22 plants that indicates the ability of these plants to mount more rapid and effective direct and indirect defense responses. Similarly, the up-regulation of transcripts coding for several types of TF is a peculiar feature of adaptive plant strategies that improve their defensive potential (Khong et al., 2008; Walling, 2008). On the other hand, the concurrent down-regulation of some defense-related functions observed in T22 plants is possibly due, at least in part, to fungal effectors that allow T. harzianum T22 to colonize plant roots as an avirulent symbiont (Shoresh et al., 2005).
Trichoderma, as many beneficial plant growth promoting rhizobacteria (PGPR), tends to activate induced systemic resistance (ISR) that involve signal transduction pathways responding to JA/ET, but includes also cross-talk with SA, as well as with phytohormones associated with plant development (Harman et al., 2004; Shoresh et al., 2005; Hermosa et al., 2012). A trade-off is established between plant biosynthetic pathways involving defense or cellular/growth functions that can be regulated by Trichoderma stimuli, such as 1-aminocyclopropane-1-carboxylic acid deaminase (ACCD) activity, that modulates ET biosynthesis, or indole-3-acetic acid (IAA), that stimulates plant growth (Pieterse et al., 2009; Hermosa et al., 2012).
Our findings indicates that fungal colonization of tomato has an impact on phosphorylation dynamics of several Serine/threonine- and Leucine-rich repeat protein kinases, that were up-regulated. These kinases are involved in recruiting signals from receptors sensing environmental conditions and phytohormones and recalibrating them into appropriate outputs such as changes in metabolism, and gene expression, to activate defense/resistance against invaders (Xu and Huang, 2017). This evidence supports the hypothesis that Trichoderma T22 strain triggers a “defense mood” in the tomato cultivar “Dwarf San Marzano,” generating a pre-alerted state of “priming” to face more efficiently likely incoming attacks (Conrath, 2011; Conrath et al., 2015). However, it is of interest to note that this reinforcement of defense barriers is not univocally associated with Trichoderma infection of tomato plants. Indeed, what observed here in terms of direct defense for SM was quite different in the case of Trichoderma longibrachiatum strain MK1, which similarly increased plant attractiveness toward the aphid parasitoid A. ervi, but also promoted the development and reproduction of M. euphorbiae (Battaglia et al., 2013). This demonstrates that the plant response can be different to different fungal species, and can be specific for each tomato variety, as already suggested by Tucci et al. (2011).
The up-regulation of a Multicystatine and several other Proteinase inhibitors with the T22 treatments (observed in both T22 and T22Aph) correlated with the reduced aphid survivorship overtime. This plant defense barrier induced by T22 was reinforced by the concurrent reduction in the number of down-regulated transcripts by aphid feeding related to other protease inhibitors (4 in Aph and 2 in T22Aph), which further contributes to the disruption of the aphid-induced suppression of plant defense. Previous studies have demonstrated that Trichoderma interferes with nematode performance by inducing Protease inhibitors in tomato (Martínez-Medina et al., 2017). In addition, in wheat the fungus counteracts nematode growth, inducing chitinase, β-1, 3-glucanase and defense compounds such as total flavonoids and lignin (Zhang et al., 2017). The metabolomics analysis remarkably expands the understanding of effect induced by T. harzianum T22 on tomato defenses when coupled with insect feeding. Defense-related secondary metabolites were over-represented in T22Aph samples compared to T22 or with only aphid infestation (Aph). The defense barrier array involved alkaloids (α-/β-tomatine) that could be responsible for the reduction in aphid survival together with late defense gene products (PPO, LapA, Miraculin, and many others), phenolic acids and flavonoids.
The up-regulation of the enzymes participating at different stages in the phenylpropanoid biosynthesis, for example, involved in catalyzing key-steps such as the conversion of phenylalanine in cinnamic acid (Phenylalanine ammonia-lyase and Caffeoyl-CoA O-methyl transferase), or catalyzing final branches for lignin production (i.e., Peroxiredoxin), may be associated with the observed increased level of compounds implicated in the defense responses. In fact, phenylpropanoids or their precursors/derivates may exert direct toxicity against insect herbivores (Naoumkina et al., 2010) and, at the same time, are precursors to VOCs that contribute to plant indirect defense (Dudareva et al., 2013). Notably, PAL is the up-regulated gene with the highest fold change in T22 plants while it is down-regulated in aphid-infested plants (Aph). The observed transcriptomic reprogramming of phenylpropanoid pathway is consistent with the augmented accumulation of Phenylalanine, Coumaric and Chorismic acids, Salicylic acid precursors, as well as SA-related metabolites (Salicylate β-D-glucose ester and salicyolyl-L-aspartic acid) in T22 plants. These observations are summarized in Figure 9. Similarly, metabolites involved in PAL pathway were over-accumulated in T22 plants. This is consistent with the previously observed increased attractiveness toward A. ervi mediated by methyl-salicylate (Coppola et al., 2017a).
Figure 9. Proposed summary of transcriptomic and metabolomics changes imposed by T. harzianum T22 colonization on tomato plants responsible of the promoted direct and indirect defense responses against aphids. Starting from the left side, phenylpropanoid, and SA pathways cover a central role in T22-induced defenses at transcriptional (up) and metabolomics (down) levels. Promoted pathways are the source of MeSA, a volatile compound responsible of the increased attractiveness toward the parasitoid wasp A. ervi.
Furthermore, T22 plants showed higher accumulation of sugars quantities than CTRL plants, indicating a higher root uptake and photosynthesis efficiency, as confirmed by the over-representation of a series of transcripts of the Calvin cycle; this is in line with the reported beneficial effect of the fungus on the plant physiology (Lorito et al., 2010; Lorito and Woo, 2015) and consistent with previous observation on Trichoderma –tomato interaction (De Palma et al., 2019).
The higher content of sugar could be the result of the over-expression of a large group of genes associated with cellular and metabolic processes and many others identified by GO annotation (Figure 3; Supplementary Table 2). These processes produce substances such as nutrients, hormones, metabolites that contribute to the positive effects observed in plant growth promotion frequently induced by Trichoderma spp. (Tucci et al., 2011; Vinale et al., 2014; Lorito and Woo, 2015). It has been proposed that plant-derived sugars represent not only a carbon source for the fungus, but also a tool to modulate the extension of root colonization and the systemic induction of photosynthesis in leaves (Vargas et al., 2009). In addition, the increased expression of glycolytic enzymes can redirect the higher sugar flux to increase the carbon supply to biosynthetic pathways involved in the production of plant resistance-secondary metabolites (Fürstenberg-Hägg et al., 2013). In agreement with this hypothesis, a large group of terpenes and carotenoids/apocarotenoids genes were up-regulated in T22 leaves. In the same context, amino acid metabolism was strongly affected by Trichoderma and aphids: among the different transcript/metabolite data, a group of elements involved in glutamate metabolism was highlighted. For instance, asparagine synthetase 1 and aspartate aminotransferase, involved in glutamate production, were up-regulated in T22Aph; interestingly, a plant resistance mechanism due to increased levels of glutamate has been proved (Dixit et al., 2013). A possible explanation for this finding, besides its role in chlorophyll pathway (see below), could rely on the involvement of glutamate in tricarboxylic acidreplenishment and nitrogen remobilization upon insect attack (Ameye et al., 2018). In agreement with transcriptomic data, glutamate accumulation was observed in T22Aph vs. T22 leaves. In the same context, additional genes of glutamate synthesis/sensing/catabolism varied according the same trend: proline dehydrogenase, converting proline in Δ1-pyrroline-5-carboxylate, and which is known to contribute to the hypersensitive response and disease resistance (Cecchini et al., 2011), were up-regulated; similarly, glutamate receptor 1.2, for which a potential function as primary sensors in plant defense responses has been postulated (Forde and Roberts, 2014), displayed positive changes.On the contrary, glutamate decarboxylase, opposing glutamate accumulation by its conversion in γ-aminobutyrate, was down-expressed in T22Aph over CTRL leaves.
Key Events of the Tripartite Interaction
The hormonal balance during tomato-aphid interaction in presence of T. harzianum T22 is very delicate, variable and complex. Trichoderma spp. induction of ethylene and jasmonate (ET/JA) and salicylic acid (SA)-mediated signaling pathways has been reported in tomato cv. MicroTom (Manganiello et al., 2018). In our dataset, specific genes of the tripartite interaction are involved in ethylene biosynthesis and signaling, confirming the impact of Trichoderma on this pathway. ET production is part of the array of defense responses triggered in different plants by aphid feeding (Mantelin et al., 2009; Coppola et al., 2013). Indeed, the tomato ERF Pti5 gene confers protection against aphids, both in susceptible and resistant genotypes (War et al., 2015).
The host plant regulation by hormonal management exerted by T. harzianum T22 in the tripartite interaction is also based on the down-regulation of several members of WRKY family of transcription factors, known for their promotion of JA signaling through the negative interplay with SA pathway (Li et al., 2004; Takatsuji, 2014). WRKYs represent keystones of communication between JA and SA and are involved in multiple defense responses (Phukan et al., 2016). These TFs appear to be aphid targets in the manipulation of plant host resistance (Kloth et al., 2016). Their down-regulation in T22Aph plants promotes JA-mediated defenses, at the expenses of SA signaling which would interfere with Trichoderma colonization of plant roots. In other words, the aphid strategy based on the activation of the salycilate pathway to exert a negative regulation of JA signaling, to which they are sensitive, is outcompeted by the capacity of the Trichoderma strainT22 to counteract it, as it is is detrimental for the fungal entry and development in the plant tissues. Many TFs implicated in JA signaling have been identified and functionally characterized, including many basic helix–loop–helix (bHLH) type TFs (Zhou and Memelink, 2016). To date, four subclades of the bHLH TF family have been implicated in JA signaling in Arabidopsis, each with a different contribution to the JA response (Goossens et al., 2017). The redirection of the expression of a bHLH TF, up-regulated in T22 while down-regulated in Aph plants, represents a further contribute of Trichoderma colonization to defense priming against aphids and, possibly, other herbivores. Notably, allantoin, a purine metabolite that activates JA signaling in Arabidopsis thaliana (Takagi et al., 2016), was found to accumulate at higher levels in T22Aph vs. T22 (Supplementary Tables 6, 7). In addition, a gene encoding a steroid dehydrogenase, (upregulated in T22Aph and down regulated in Aph) is involved in plant responses to stress through lipid signaling (Fürstenberg-Hägg et al., 2013). Membrane lipids serve as substrates for the generation of numerous signaling lipids such as phosphatidic acid, phosphoinositides, sphingolipids, lysophospholipids, oxylipins, N-acylethanolamines, free fatty acids and others. These molecules are tightly regulated and can be rapidly activated upon abiotic stress signals (Hou et al., 2016) or pathogen attack (Okazaki and Saito, 2014). Interestingly, O-phosphorylethanolamine, an intermediate of ethanolamine/choline synthesis, which can take part in the stress response-signaling machinery, was over-accumulated in T22Aph leaves (Supplementary Tables 6, 7). Phloem lipids have been associated not only with intracellular signaling but also with a long-distance lipid signaling: lipid molecules could be released upon a stress perception and moving through the phloem they could bind receptors with the consequent modification of the sink tissue mediating a response (Benning et al., 2012). In this scenario, the possible alteration of lipid signaling following T. harzianum T22 colonization of tomato roots could contribute to tomato responses in the initial phase of perception and recognition of the injury.
Interestingly, among the metabolites identified by targeted/untargeted metabolomics, and previously reported in tomato, 5-amino-levulinic acid, while reduced in Aph, is highly overproduced in T22 and in T22Aph plants. This metabolite is known to be effective in counteracting the damages of different plant stressors (Yang et al., 2014). Similar accumulation pattern was registered for hydroxypipecolicacid, very recently identified as a mobile signal responsible of the induction of systemic disease resistance in Arabidopsis (Chen et al., 2018); chlorogenic and sinapic acids, which can improve host plants resistance (Nićiforović and Abramovič, 2013; Kundu and Vadassery, 2019); anthranilic acid, precursor of methyl anthranilate, which has been associated with the production of the volatile blend attracting herbivore parasitoids (Köllner et al., 2010).
Concerted regulation of genes and metabolites involved in chlorophyll metabolism is observed in the plant-fungus-insect interaction. Aphids repress, and Trichoderma induces, two early intermediates in chlorophyll biosynthesis; 5-amino-levulinic acid (ALA) and uroporphyrinogen III (UROIII); later intermediates (coproporphyrinogenIII (COPIII), protoporphyrin IX (PPIX)) show the opposite trend (Supplementary Table 10). This dual regulation is observed also for transcripts involved in chlorophyll biosynthesis: for instance, coproporphyrinogen III oxidase (CPOX) is induced by aphids, while transcripts encoding later steps (magnesium chelatase H subunit (MgCH), magnesium-protoporphyrin monomethyl ester cyclase (MPEC)) and a light harvesting chlorophyll a/b binding protein (LHC) are repressed. Trichoderma induces uroporphyrinogen decarboxylase (UROD) and protochlorophyllide reductase (POR) as well as MgCH, MPEC and two LHCs. Finally, in the triple interaction, aphid infestation seems to be epistatic over Trichoderma treatment, since it represses ALA and UROIII, strongly induces a fifth intermediate (protoporphyrinogen IX) and represses a series of transcripts involved in chlorophyll biosynthesis and sequestration (MgCH, PEC and 23 LHCs). Such a coordinated regulation of transcripts and metabolites belonging to a single pathway must have a biological meaning. Several genes in the chlorophyll pathway are known to be involved in plant defense responses: for instance, a null UROD mutation generates a disease lesion mimic phenotype in maize (Hu et al., 1998), and the accelerated cell death 2 gene of Arabidopsis, showing constitutive activation of defenses in the absence of pathogen infection, encodes a red chlorophyll catabolite reductase (Mach et al., 2001). Two hypotheses have been proposed explaining the remodeling of chorophyll metabolism in defense responses: in the first hypothesis, a reduction in chlorophyll biosynthesis and accumulation in aphid-resistant cultivars would cause a decrease in photosynthetic efficiency, thus limiting the nutrient supply to aphids (Carrillo et al., 2014). This hypothesis is consistent with the data from the tripartite (plant-fungus-aphid) interaction. A second hypothesis is based on the well-known role of some tetrapyrrole chlorophyll precursors in generating Reactive Oxygen Species in the presence of light, which in turn activate defense responses. This hypothesis is consistent with some, but not other, data presented in this paper: for instance, both UROD and CPOX silencing causes the accumulation of photosensitizing tetrapyrroles and necrotic lesions in tobacco (Mock et al., 1998). In the tomato-Trichoderma-aphid system, UROD is induced by Trichoderma (presumably a way to alleviate the production of ROS by reducing the levels of photosensitizing COPIII and PPIX) while CPOX is induced by aphid infestation (presumably a way to reduce the levels of COPIII). It is not entirely clear from our data whether the interplay of these two responses enhances or diminishes resistance to aphids in the triple interaction.
In conclusion, our study suggests a wide, articulated and sophisticated contribute of T. harzianum T22 in the promotion of tomato endogenous defenses against phloem-feeders, by the instauration of a preparation to defense. This preparation ranges from transcriptomic to metabolomics changes, from early signals to late effector of defense responses. In the specific tripartite system under investigation, the major contribute of the beneficial fungus appears to be the manipulation of phloem sap sentinel molecules, the regulation of hormonal balance and enhanced communication with natural enemies via terpenes and salycilate.
Publicly available datasets were analyzed in this study. This data can be found here: https://www.ncbi.nlm.nih.gov/Traces/study/?acc=PRJNA532377.
This article does not contain any studies with human participants or animals performed by any of the authors.
MC performed and analyzed transcriptomic data and draft the ms. GD and GG performed metabolomics, analyzed the results and contributed to manuscript writing. MD performed insect bioassays and analyzed the data. SW participated to the experimental design and contributed to manuscript writing. DM contributed to RNA isolation. ML contributed to the work plan and helped in results interpretation. FP contributed to the work plan and to data analyses and revised the manuscript. RR conceived and designed the study, supervised the experimental work and wrote the paper.
This work was supported by the European Union Horizon 2020 research and innovation programme, under grant agreement no. 773554 (EcoStack) (to FP) and by European FP7—ERANET ARIMNET2 Sustainable Tomato Production: plant defense enhancement, development of new biopesticides and optimization of environmental, water and chemical inputs—STomP (to MD). This project has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreements no. 818431 (SIMBA) and no. 677379 (G2P-SOL). JGI Community Scientific Program 2016, Proposal 1966-CSP 2016; Project ProBio - IZSM (Portici), n. D01 6309, 14/12/2016; Project LINFA - MIUR-PON, n. 03PE_00026_1, 09/04/2014; KENYA-AID, n. 10306/CEFA/KEN, 18/05/2017. This output reflects only the author's view and the Research Executive Agency (REA) cannot be held responsible for any use that may be made of the information contained therein.
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.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphys.2019.00745/full#supplementary-material
Supplementary Figure 1. GO categories distribution for plants treated with T. harzianum T22 in the “Biological Process” domain. Colors indicate the enrichment score of each GO category for (A) up-regulated and (B) down-regulated genes.
Supplementary Figure 2. GO categories distribution for SM plants infested by M. euphorbiae for 48 h in the “Biological Process” domain. Colors indicate the enrichment score of each GO category for (A) up-regulated and (B) down-regulated genes.
Supplementary Figure 3. GO categories distribution for SM plants treated with T. harzianum T22 and subsequently infested by aphids in the “Biological Process” domain. Colors indicate the enrichment score of each GO category for (A) up-regulated and (B) down-regulated genes.
Supplementary Figure 4. Expression analysis of selected defense genes from the tomato DEGs by Real Time RT-PCR in plants: treated with T. harzianum T22 (T22); infested by aphid M. euphorbiae (Aph) or treated with T22 and subsequently infested by aphid (T22Aph). Relative quantities (RQ) are calibrated to untreated plants (Ctrl), as indicated by the linear scale on the Y-axis. Asterisks indicate statistically significant differences compared to control condition (*p < 0.05; **p < 0.01; ***p < 0.001 t-test).
Supplementary Figure 5. Principal Component Analysis (PCA) of the untargeted metabolomic analysis, of the semi-polar fraction, obtained from tomato leaves grown in the absence and in the presence of the aphid M. euphorbiae, and treated with the T. harzianum T22, alone or in combination with the aphids. Dots with same colors indicate biological experimental replicates. For more details, see Materials and Methods.
Supplementary Figure 6. Heatmap (HM) of semi-polar metabolome of tomato leaves grown in the absence and in the presence of the aphid M. euphorbiae and the fungus T. harzianum T22, alone or in combination. Colored squares represent the values of log2-transformed fold changes of a metabolite in respect to the corresponding control (water control CTRL for Aph and T22 samples; T22 for T22Aph), according to the color scale shown (green: down-accumulated; red: up-accumulated). Gray squares indicate no detectable accumulation of the corresponding metabolite.
Alboresi, A., Perin, G., Vitulo, N., Diretto, G., Block, M., Jouhet, J., et al. (2016). Light remodels lipid biosynthesis in nannochloropsis gaditana by modulating carbon partitioning between organelles. Plant Physiol. 171, 2468–2482. doi: 10.1104/pp.16.00599
Alewu, B., and Nosiri, C. (2011). “Pesticides and human health,” in Pesticides in the Modern World – Effects of Pesticides Exposure, ed M. Stoytcheva (Mexicali: Autonomous University of Baja California, 231–50.
Ameye, M., Allmann, S., Verwaeren, J., Smagghe, G., Haesaert, G., Schuurink, R. C., et al. (2018). Green leaf volatile production by plants: a meta-analysis. N. Phytol. 220, 666–683. doi: 10.1111/nph.14671
Avila, C. A., Arevalo-Soliz, L. M., Jia, L. L., Navarre, D. A., Chen, Z., Howe, G. A., et al. (2012). Loss of Function of FATTY ACID DESATURASE7 in Tomato enhances basal aphid resistance in a salicylate-dependent manner. Plant Physiol. 158, 2028–2041. doi: 10.1104/pp.111.191262
Ban, Q., Han, Y., He, Y., Jin, M., Han, S., Suo, J., et al. (2018). Functional characterization of persimmon β-galactosidase gene DkGAL1 in tomato reveals cell wall modification related to fruit ripening and radicle elongation. Plant Sci. 274, 109–120. doi: 10.1016/j.plantsci.2018.05.014
Battaglia, D., Bossi, S., Cascone, P., Digilio, M. C., Prieto, J. D., Fanti, P., et al. (2013). Tomato below ground-above ground interactions: Trichoderma longibrachiatum affects the performance of Macrosiphum euphorbiae and its natural antagonists. Mol. Plant Microbe Interact 26, 1249–1256. doi: 10.1094/MPMI-02-13-0059-R
Benning, U. F., Tamot, B., Guelette, B. S., and Hoffmann-Benning, S. (2012). New aspects of phloem-mediated long-distance lipid signalling in plants. Front. Plant Sci. 3:53. doi: 10.3389/fpls.2012.00053
Brader, G., Tas, E., and Palva, E. T. (2001). Jasmonate-dependent Induction of indole glucosinolates in Arabidopsis by culture filtrates of the nonspecific pathogen Erwinia carotovora. Plant Physiol. 126, 849–860.
Bulgarelli, D., Schlaeppi, K., Spaepen, S., Ver Loren van Themaat, E., and Schulze-Lefert, P. (2013).Structure and functions of the bacterial microbiota of plants. Annu. Rev. Plant Biol. 64, 807–838. doi: 10.1146/annurev-arplant-050312-120106
Carrillo, E., Rubiales, D., and Castillejo, M. A. (2014). Proteomic analysis of pea (Pisum sativum L.) response during compatible and incompatible interactions with the pea aphid (Acyrthosiphon pisum H.). Plant Mol. Biol. Report. 32, 697–718. doi: 10.1007/s11105-013-0677-x
Cecchini, N. M., Monteoliva, M. I., and Alvarez, M. E. (2011). Proline dehydrogenase is a positive regulator of cell death in different kingdoms. Plant Signal Behav. 6, 1195–1197. doi: 10.4161/psb.6.8.15791
Chen, H., Wilkerson, C. G., Kuchar, J. A., Phinney, B. S., and Howe, G. A. (2005). Jasmonate-inducible plant enzymes degrade essential amino acids in the herbivore midgut. Proc. Natl. Acad. Sci. U.S.A. 102, 19237–19242. doi: 10.1073/pnas.0509026102
Chen, Y. C., Holmes, E. C., Rajniak, J., Kim, J. G., Tang, S., Fischer, C. R., et al. (2018). N-hydroxy-pipecolic acid is a mobile signal that induces systemic disease resistance in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 22:115. doi: 10.1101/288449
Coppola, M., Cascone, P., Chiusano, M. L., Colantuono, C., Lorito, M., Pennacchio, F., et al. (2017a). Trichoderma harzianum enhances tomato indirect defense against aphids. Insect Sci. 24, 1025–1033. doi: 10.1111/1744-7917.12475
Coppola, M., Cascone, P., Madonna, V., Di Lelio, I., Esposito, F., Avitabile, C., et al. (2017b). Plant-to-plant communication triggered by systemin primes anti-herbivore resistance in tomato. Sci. Rep. 7:15522. doi: 10.1038/s41598-017-15481-8
Coppola, V., Coppola, M., Rocco, M., Digilio, M. C., D'Ambrosio, C., Renzone, G., et al. (2013). Transcriptomic and proteomic analysis of a compatible tomato-aphid interaction reveals a predominant salicylic acid-dependent plant response. BMC Genomics 14:515. doi: 10.1186/1471-2164-14-515
De Meyer, G., Bigirimana, J., Elad, Y., and Höfte, M. (1998). Induced systemic resistance in Trichoderma harzianum T39 biocontrol of Botrytis cinerea. Eur. J. Plant Pathol. 104, 279–286. doi: 10.1023/A:1008628806616
De Palma, M., Salzano, M., Villano, C., Aversano, R., Lorito, M., Ruocco, M., et al. (2019). Transcriptome reprogramming, epigenetic modifications and alternative splicing orchestrate the tomato root response to the beneficial fungus Trichoderma harzianum. Horticul. Res. 6:5. doi: 10.1038/s41438-018-0079-1
Diretto, G., Al-Babili, S., Tavazza, R., Scossa, F., Papacchioli, V., Migliore, M., et al. (2010). Transcriptional-metabolic networks in β-carotene-enriched potato tubers: the long and winding road to the Golden phenotype. Plant Physiol. 154, 899–912. doi: 10.1104/pp.110.159368
Dixit, S., Upadhyay, S. K., Singh, H., Sidhu, O. P., Verma, P. C., and Chandrashekar, K. (2013). Enhanced methanol production in plants provides broad spectrum insect resistance. PLoS ONE 8:e79664. doi: 10.1371/journal.pone.0079664
Dudareva, N., Klempien, A., Muhlemann, J. K., and Kaplan, I. (2013). Biosynthesis, function and metabolic engineering of plant volatile organic compounds. N. Phytol. 198, 16–32. doi: 10.1111/nph.12145
Elzinga, D. A., De Vos, M., and Jander, G. (2014). Suppression of plant defenses by a Myzus persicae (green peach aphid) salivary effector protein. Mol. Plant Microbe. Interact. 27, 747–756. doi: 10.1094/MPMI-01-14-0018-R
Fasano, C., Diretto, G., Aversano, R., D'Agostino, N., Di Matteo, A., Frusciante, L., et al. (2016). Transcriptome and metabolome of synthetic Solanum autotetraploids reveal key genomic stress events following polyploidization. N. Phytol. 210, 1382–1394. doi: 10.1111/nph.13878
Guerrieri, E., Lingua, G., Digilio, M. C., Massa, N., and Berta, G. (2004). Do interactions between plant roots and the rhizosphere affect parasitoid behaviour? Ecol. Entomol. 29, 753–756. doi: 10.1111/j.0307-6946.2004.00644.x
Hu, G., Yalpani, N., Briggs, S. P., and Johal, G. S. (1998). A porphyrin pathway impairment is responsible for the phenotype of a dominant disease lesion mimic mutant of maize. Plant Cell. 10, 1095–1105. doi: 10.1105/tpc.10.7.1095
Khong, G. N., Richaud, F., Coudert, Y., Pati, P. K., Santi, C., Périn, C., et al. (2008). Modulating rice stress tolerance by transcription factors. Biotech. Genet. Eng. Rev. 25, 381–404. doi: 10.5661/bger-25-381
Kim, D., Pertea, G., Trapnell, C., Pimentel, H., Kelley, R., and Salzberg, S. (2013). TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biol. 14:36. doi: 10.1186/gb-2013-14-4-r36
Kloth, K. J., Wiegers, G. L., Busscher-Lange, J., van Haarst, J. C., Kruijer, W., Bouwmeester, H. J., et al. (2016). AtWRKY22 promotes susceptibility to aphids and modulates salicylic acid and jasmonic acid signalling. J. Exp. Bot. 67, 3383–3396. doi: 10.1093/jxb/erw159
Köllner, T. G., Lenk, C., Zhao, N., Seidl-Adams, I., Gershenzon, J., Chen, F., et al. (2010). Herbivore-induced SABATH methyltransferases of maize that methylate anthranilic acid using s-adenosyl-L-methionine. Plant Physiol. 153, 1795–1807. doi: 10.1104/pp.110.158360
Li, J., Brader, G., and Palva, E. T. (2004). The WRKY70 transcription factor: a node of convergence for jasmonate-mediated and salicylate-mediated signals in plant defense. Plant Cell. 16, 319–331. doi: 10.1105/tpc.016980
Li, R., Tee, C. S., Jiang, Y. L., Jiang, X. Y., Venkatesh, P. N., Sarojam, R., et al. (2015). A terpenoid phytoalexin plays a role in basal defense of Nicotiana benthamiana against Potato virus X. Sci. Rep. 5:9682. doi: 10.1038/srep09682
Livak, K. J., and Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2-Delta Delta CT method. Methods 25, 402–408. doi: 10.1006/meth.2001.1262
Lorito, M., and Woo, S. L. (2015). “Trichoderma: a multi-purpose tool for integrated pest management,” in Principles of Plant-Microbe Interactions, ed B. Lugtenberg (Cham: Springer International Publishing), 345–353. doi: 10.1007/978-3-319-08575-3_36
Lorito, M., Woo, S. L., Harman, G. E., and Monte, E. (2010). Translational research on Trichoderma: from'omics to the field. Annu. Rev. Phytopathol. 48, 395–417. doi: 10.1146/annurev-phyto-073009-114314
Lv, G. Y., Guo, X. G., Xie, L. P., Xie, C. G., Zhang, X. H., Yang, Y., et al. (2017). Molecular characterization, gene evolution, and expression analysis of the fructose-1, 6-bisphosphate aldolase (FBA) gene family in wheat (Triticum aestivum L.). Front. Plant Sci. 8:1030. doi: 10.3389/fpls.2017.01030
Mach, J. M., Castillo, A. R., Hoogstraten, R., and Greenberg, J. T. (2001). The Arabidopsis-accelerated cell death gene ACD2 encodes red chlorophyll catabolite reductase and suppresses the spread of disease symptoms. Proc. Natl. Acad. Sci. U.S.A. 98, 771–776. doi: 10.1073/pnas.98.2.771
Manganiello, G., Sacco, A., Ercolano, M. R., Vinale, F., Lanzuise, S., Pascale, A., et al. (2018). Modulation of tomato response to Rhizoctonia solani by Trichoderma harzianum and its secondary metabolite harzianic acid. Front. Microbiol. 9:1966. doi: 10.3389/fmicb.2018.01966
Mantelin, S., Bhattarai, K. K., and Kaloshian, I. (2009). Ethylene contributes to potato aphid susceptibility in a compatible tomato host. N. Phytol. 183, 444–456. doi: 10.1111/j.1469-8137.2009.02870.x
Martínez-Medina, A., Van Wees, S. C. M., and Pieterse, C. M. J. (2017). Airborne signals by Trichoderma fungi stimulate iron uptake responses in roots resulting in priming of jasmonic acid-dependent defences in shoots of Arabidopsis thaliana and Solanum lycopersicum. Plant Cell Environ. 40, 2691–2705. doi: 10.1111/pce.13016
Marum, L., Miguel, A., Ricardo, C. P., and Miguel, C. (2012). Reference gene selection for quantitative real-time PCR normalization in quercus suber. PLoS ONE 7:e35113. doi: 10.1371/journal.pone.0035113
Mendoza-Mendoza, A., Zaid, R., Lawry, R., Hermosa, R., Monte, E., Horwitz, B. A., et al. (2018). Molecular dialogues between Trichoderma and roots: role of the fungal secretome. Fungal Biol. Rev. 32, 62–85. doi: 10.1016/j.fbr.2017.12.001
Mock, H. P., Heller, W., Molina, A., Neubohn, B., Sandermann, H. Jr., and Grimm, B. (1998). Expression of uroporphyrinogen decarboxylase or coproporphyrinogen oxidase antisense RNA in tobacco induces pathogen defense responses conferring increased resistance to tobacco mosaic virus. J. Biol. Chem. 274, 4231–4238. doi: 10.1074/jbc.274.7.4231
Mohapatra, S., and Mittra, B. (2016). Protein glutathionylation protects wheat (Triticum aestivum Var. Sonalika) against Fusarium induced oxidative stress. Plant Physiol. Biochem. 109, 319–325. doi: 10.1016/j.plaphy.2016.10.014
Müller, O. A., Grau, J., Thieme, S., Prochaska, S., Adlung, N., Sorgatz, A., et al. (2015). Genome-wide identification and validation of reference genes in infected tomato leaves for quantitative RT-PCR analyses. PLoS ONE. 10:e0136499. doi: 10.1371/journal.pone.0136499
Naoumkina, M. A., Zhao, Q., Gallego-Giraldo, L., Dai, X., Zhao, P. X., and Dixon, R. A. (2010). Genome-wide analysis of phenylpropanoid defence pathways. Mol. Plant Pathol. 11, 829–846. doi: 10.1111/j.1364-3703.2010.00648.x
Pennacchio, F., Giordana, B., and Rao, R. (2012). “Applications of parasitoid virus and venom research in agriculture,” in Parasitoid Viruses, Symbionts and Pathogens, ed J. Drezen (Gainesville, FL: University of Florida), 269–283. doi: 10.1016/B978-0-12-384858-1.00022-9
Pieterse, C. M., Van der Does, D., Zamioudis, C., Leon-Reyes, A., and Van Wees, S. C. (2012). Hormonal modulation of plant immunity. Annu. Rev. Cell Dev. Biol. 28, 489–521. doi: 10.1146/annurev-cellbio-092910-154055
Pineda, A., Soler, R., Pozo, M. J., Rasmann, S., and Turlings, T. C. (2015). Editorial: Above-belowground interactions involving plants, microbes and insects. Front. Plant Sci. 6:318. doi: 10.3389/fpls.2015.00318
Pyati, P., Bandani, A. R., Fitches, E., and Gatehouse, J. A. (2011). Protein digestion in cereal aphids (Sitobion avenae) as a target for plant defence by endogenous proteinase inhibitors. J. Insect Physiol. 57, 881–891. doi: 10.1016/j.jinsphys.2011.03.024
Rahbé, Y., Deraison, C., Bonade-Bottino, M., Girard, C., Nardon, C., and Jouanin, L. (2003). Effects of the cysteine protease inhibitor oryzacystatin (OC-I) on different aphids and reduced performance of Myzus persicae on OC-I expressing transgenic oilseed rape. Plant Sci. 164, 441–450. doi: 10.1016/S0168-9452(02)00402-8
Robinson, M. D., McCarthy, D., and Smyth, G. K. (2010). edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics. 1, 139–40. doi: 10.1093/bioinformatics/btp616
Rubio, M. B., Quijada, N. M., Pérez, E., Domínguez, S., Monte, E., and Hermosa, R. (2014). Identifying beneficial qualities of Trichoderma parareesei for plants. Appl. Environ. Microbiol. 80, 1864–1873. doi: 10.1128/AEM.03375-13
Sasso, R., Iodice, L., Woodcock, C. M., Pickett, J. A., and Guerrieri, E. (2009). Electrophysiological and behavioural responses of Aphidius ervi (Hymenoptera: Braconidae) to tomato plant volatiles. Chemoecology 19, 195–201. doi: 10.1007/s00049-009-0023-9
Schilmiller, A. L., Koo, A. J., and Howe, G. A. (2007). Functional diversification of acyl-coenzyme A oxidases in jasmonic acid biosynthesis and action. Plant Physiol. 143, 812–824. doi: 10.1104/pp.106.092916
Schmidt, A., Nagel, R., Krekling, T., Christiansen, E., Gershenzon, J., and Krokene, P. (2011). Induction of isoprenyl diphosphate synthases, plant hormones and defense signalling genes correlates with traumatic resin duct formation in Norway spruce (Picea abies). Plant Mol. Biol. 77, 577–590. doi: 10.1007/s11103-011-9832-7
Segarra, G., Casanova, E., Bellido, D., Odena, M. A., Oliveira, E., and Trillas, I. (2007). Proteome, salicylic acid, and jasmonic acid changes in cucumber plants inoculated with Trichoderma asperellum strain T34. Proteomics 7, 3943–3952. doi: 10.1002/pmic.200700173
Shoresh, M., Harman, G. E., and Mastouri, F. (2010). Induced systemic resistance and plant responses to fungal biocontrol agents. Annu. Rev. Phytopathol. 48, 21–43. doi: 10.1146/annurev-phyto-073009-114450
Shoresh, M., Yedidia, I., and Chet, I. (2005). Involvement of jasmonic acid/ethylene signaling pathway in the systemic resistance induced in cucumber by Trichoderma asperellum T203. Phytopathology 95, 76–84. doi: 10.1094/PHYTO-95-0076
Studholme, D. J., Harris, B., Le Cocq, K., Winsbury, R., Perera, V., Ryder, L., et al. (2013). Investigating the beneficial traits of Trichoderma hamatum GD12 for sustainable agriculture— insights from genomics. Front. Plant Sci. 4:258. doi: 10.3389/fpls.2013.00258
Sun, Z., Liu, Z., Zhou, W., Jin, H., Liu, H., Zhou, A., et al. (2016). Temporal interactions of plant - insect - predator after infection of bacterial pathogen on rice plants. Sci. Rep. 6:26043. doi: 10.1038/srep26043
Takagi, H., Ishiga, Y., Watanabe, S., Konishi, T., Egusa, M., Akiyoshi, N., et al. (2016). Allantoin, a stress-related purine metabolite, can activate jasmonate signaling in a MYC2-regulated and abscisic acid-dependent manner. J. Experi. Botany 67, 2519–2532. doi: 10.1093/jxb/erw071
Tan, X. L., Chen, J. L., Benelli, G., Desneux, N., Yang, X. Q., Liu, T. X., et al. (2017). Pre-infestation of tomato plants by aphids modulates transmission-acquisition relationship among whiteflies, tomato yellow leaf curl virus (TYLCV) and plants. Front. Plant Sci. 8:1597. doi: 10.3389/fpls.2017.01597
Taoka, K., Ham, B. K., Xoconostle-Cázares, B., Rojas, M. R., and Lucas, W. J. (2007). Reciprocal phosphorylation and glycosylation recognition motifs control NCAPP1 interaction with pumpkin phloem proteins and their cell-to-cell movement. Plant Cell. 19, 1866–1884. doi: 10.1105/tpc.107.052522
Thaler, J. S., Fidantsef, A. L., and Bostock, R. M. (2002). Antagonism between jasmonate- and salicylate-mediated induced plant resistance: effects of concentration and timing of elicitation on defense-related proteins, herbivore, and pathogen performance in tomato. J. Chem. Ecol. 28, 1131–1159. doi: 10.1023/A:1016225515936
Tucci, M., Ruocco, M., De Masi, L., De Palma, M., and Lorito, M. (2011). The beneficial effect of Trichoderma spp. on tomato is modulated by the plant genotype. Mol. Plant Pathol. 12, 341–354. doi: 10.1111/j.1364-3703.2010.00674.x
Vargas, W. A., Mandawe, J. C., and Kenerley, C. M. (2009). Plant-derived sucrose is a key element in the symbiotic association between Trichoderma virens and maize plants. Plant Physiol. 151, 792–808. doi: 10.1104/pp.109.141291
Vitti, A., La Monaca, E., Sofo, A., Scopa, A., Cuypers, A., and Nuzzati, M. (2015). Beneficial effects ofTrichoderma harzianum T-22 in tomato seedlings infected by Cucumber mosaic virus (CMV). BioControl. 60, 135–147. doi: 10.1007/s10526-014-9626-3
War, A. R., Paulraj, M. G., Ignacimuthu, S., and Sharma, H. C. (2015).Induced resistance to Helicoverpa armigera through exogenous application of jasmonic acid and salicylic acid in groundnut, Arachis hypogaea. Pest Manag. Sci. 71, 72–82. doi: 10.1002/ps.3764
Will, T., Tjallingii, W. F., Thonnessen, A., and van Bel, A. J. (2007). Molecular sabotage of plant defense by aphid saliva. Proc. Natl. Acad. Scsi. U.S.A. 104, 10536–10541. doi: 10.1073/pnas.0703535104
Woo, S. L., Ruocco, M., Vinale, F., Nigro, M., Marra, R., Lombardi, N., et al. (2014). Trichoderma-based products and their widespread use in agriculture. Open Mycol. J. 8, 71–126. doi: 10.2174/1874437001408010071
Woo, S. L., Scala, F., Ruocco, M., and Lorito, M. (2006). The molecular biology of the interactions between Trichoderma spp., phytopathogenic fungi, and plants. Phytopathology 96, 181–185. doi: 10.1094/PHYTO-96-0181
Yang, Y., Sun, C., Ren, Y., Hao, S., and Jiang, D. (2014). New route toward building active ruthenium nanoparticles on ordered mesoporous carbons with extremely high stability. Sci. Rep. 4:4540. doi: 10.1038/srep04540
Yedidia, I., Benhamou, N., and Chet, I. (1999). Induction of defence responses in cucumber plants (Cucumissativus L.) by the biocontrol agent Trichoderma harzianum. Appl. Environ. Microbiol. 65:1061–1070.
Zhang, Y., Bai, Y., Wu, G., Zou, S., Chen, Y., Gao, C., et al. (2017). Simultaneous modification of three homoeologs of Ta EDR 1 by genome editing enhances powdery mildew resistance in wheat. Plant J. 91, 714–724. doi: 10.1111/tpj.13599
Keywords: San Marzano, aphid, RNA-Seq, semi-polarmetabolome, defense
Citation: Coppola M, Diretto G, Digilio MC, Woo SL, Giuliano G, Molisso D, Pennacchio F, Lorito M and Rao R (2019) Transcriptome and Metabolome Reprogramming in Tomato Plants by Trichoderma harzianum strain T22 Primes and Enhances Defense Responses Against Aphids. Front. Physiol. 10:745. doi: 10.3389/fphys.2019.00745
Received: 15 February 2019; Accepted: 31 May 2019;
Published: 21 June 2019.
Edited by:Patrizia Falabella, University of Basilicata, Italy
Reviewed by:Santiago Gutierrez, Universidad de León, Spain
Federico Martinelli, University of Florence, Italy
Copyright © 2019 Coppola, Diretto, Digilio, Woo, Giuliano, Molisso, Pennacchio, Lorito and Rao. 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) and the copyright owner(s) 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.