Next Article in Journal
Nasal Polyposis: Insights in Epithelial-Mesenchymal Transition and Differentiation of Polyp Mesenchymal Stem Cells
Previous Article in Journal
Role of Microglia in Modulating Adult Neurogenesis in Health and Neurodegeneration
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 21
Issue 18
10.3390/ijms21186876
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Biocontrol Root-Oomycete, Pythium Oligandrum, Triggers Grapevine Resistance and Shifts in the Transcriptome of the Trunk Pathogenic Fungus, Phaeomoniella Chlamydospora

by
Amira Yacoub
1,†,
Noel Magnin
1,†,
Jonathan Gerbore
2,†,
Rana Haidar
1,
Emilie Bruez
1,
Stéphane Compant
3,
Rémy Guyoneaud
4 and
Patrice Rey
1,*
1
INRAE, UMR 1065 Santé et Agroécologie du Vignoble (SAVE), Institut des Sciences de la vigne et du Vin (ISVV), 33883 Villenave d’Ornon, France
2
BIOVITIS, 15400 Saint-Étienne-de-Chomeil, France
3
Bioresources Unit, Center for Health & Bioresources, AIT Austrian Institute of Technology GmbH, Konrad Lorenz Strasse 24, 3430 Tulln, Austria
4
Institut des Sciences Analytiques et de Physicochimie pour l‘Environnement et les Matériaux—UMR 5254, Microbial Ecology, Université de Pau et des Pays de l’Adour/E2S UPPA/CNRS, IBEAS Avenue de l’Université, 64013 Pau, France
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Int. J. Mol. Sci. 2020, 21(18), 6876; https://doi.org/10.3390/ijms21186876
Submission received: 8 September 2020 / Accepted: 15 September 2020 / Published: 19 September 2020
(This article belongs to the Section Molecular Plant Sciences)
Browse Figures
Versions Notes

Abstract

:
The worldwide increase in grapevine trunk diseases, mainly esca, represents a major threat for vineyard sustainability. Biocontrol of a pioneer fungus of esca, Phaeomoniella chlamydospora, was investigated here by deciphering the tripartite interaction between this trunk-esca pathogen, grapevine and the biocontrol-oomycete, Pythium oligandrum. When P. oligandrum colonizes grapevine roots, it was observed that the wood necroses caused by P. chlamydospora were significantly reduced. Transcriptomic analyses of plant and fungus responses were performed to determine the molecular events occurring, with the aim to relate P. chlamydospora degradation of wood to gene expression modulation. Following P. oligandrum-root colonization, major transcriptomic changes occurred both, in the grapevine-defense system and in the P. chlamydospore-virulence factors. Grapevine-defense was enhanced in response to P. chlamydospora attacks, with P. oligandrum acting as a plant-systemic resistance inducer, promoting jasmonic/ethylene signaling pathways and grapevine priming. P. chlamydospora pathogenicity genes, such as those related to secondary metabolite biosynthesis, carbohydrate-active enzymes and transcription regulators, were also affected in their expression. Shifts in grapevine responses and key-fungal functions were associated with the reduction of P. chlamydospora wood necroses. This study provides evidence of wood fungal pathogen transcriptional changes induced by a root biocontrol agent, P. oligandrum, in which there is no contact between the two microorganisms.

1. Introduction

Applying biocontrol agents (BCAs) to plants can be useful to control diseases, particularly when chemical pesticides have been banned or do not exist [1,2]. This is the case for grapevine trunk diseases (GTDs), which have increased worldwide over the last two decades following the ban, in Europe in the early 2000s, of sodium arsenite, due to its toxic effect on the environment and humans [1,3]. GTDs, especially esca, cause considerable economic losses to the viticulture sector [4], with decreases in plant productivity and longevity, and wine quality alteration [5,6]. The worldwide annual incidence and cost for the replacement of dead plants due to GTDs is very high. In Italy, for instance, depending on the cultivars, the incidence of GTDs ranged from 8% to 19% and around 10% in Spain; in France, approximately 12% of French vineyards are unproductive during the period of 2012-2017 [7], with losses, in 2014, estimated at around € 1 billion.
In order to control esca, various beneficial microorganisms, used as BCAs, have been tested to control the fungal pathogens associated with this disease [1,3,8]. Two biocontrol products called Esquive WP® and Vintec® based on two different strains of Trichoderma atroviride, I-1237 and SC1, respectively, have been registered to control esca on the adult grapevine [9,10]. However, their protection levels usually vary from year to year. Consequently, the few BCAs available against GTDs, particularly esca, need their levels of protection to be optimized. Improving our understanding of the molecular mechanisms involved in a defined grapevine, esca-pathogen and biocontrol agent interaction would facilitate the development of this control method.
Among the potential microbial BCAs, we have selected here the oomycete, Pythium oligandrum, because it is naturally present in the rhizosphere of many plants, including vineyards [11], and has shown potential in controlling many plant pathogens [12,13]. As regards the plant protection provided by P. oligandrum, it results from: (1) the direct effect of the oomycete on the pathogens by destroying them via mycoparasitism, antibiosis and/or competition for nutrient elements and (2) the indirect effect P. oligandrum has on plants by inducing host resistance. Scientists generally considered plant-induced resistance as the main mode of action of P. oligandrum [13]. Three elicitin-like proteins produced by P. oligandrum, such as oligandrin, POD1 and POD2, are also able to trigger this host-resistance when they are applied on plants.
Regarding grapevines, previous studies showed that treating Vitis vinifera L. roots with P. oligandrum was associated with a reduction in Botrytis cinerea infection at the leaf level [14]. It also reduced the wood attacks of two fungal pathogens involved in GTDs [15], Phaeomoniella chlamydospora and Neofusicoccum parvum [16,17]. Hence, the use of a BCA to control esca could well prove an interesting approach for growers in developing sustainable viticulture.
Various molecular aspects of a grapevine, esca-pathogen and biocontrol agent interaction will be investigated here, since little is known about the molecular events associated with GTD pathogens. The complete genome sequencing of several GTD pathogens [18,19,20] has also paved the way for obtaining molecular insights about the genes involved in the pathological process. Moreover, this enables improved understanding of the plant resistance induced by the BCA.
In the present study, our objective is to extensively decipher the tripartite interaction between the grapevine and a trunk fungal pathogen involved in esca, P. chlamydospora and P. oligandrum, as a biocontrol agent colonizing the root system, using transcriptomic analyses. First, grapevine microarrays have been used to study the grapevine transcriptomic responses associated with the trunk-infection by the pathogen, P. chlamydospora, and root-inoculation with P. oligandrum, the main aim being to identify grapevine defense genes specific to this tripartite interaction. Then, the indirect effect of P. oligandrum-root colonization on the transcriptome of the wood pathogen, P. chlamydospora was studied by RNAseq. This complementary approach using two methodologies provides useful information both on the transcriptomic changes induced in the grapevine and pathogen. To the best of our knowledge, this is the first experiment that studies trunk pathogen transcriptome shifts indirectly induced by a BCA, inoculated at the root level.

2. Results

2.1. Evaluation of Grapevine Transcriptomic Responses

Differentially expressed (DE) genes in the plant wood tissues were investigated using a time- frame approach with V. vinifera microarrays (0- vs. 14-dpi corresponding to 2 h and 14 days after pathogen infection).

2.1.1. Grapevine Trunk Transcriptional Response to P. oligandrum Root Colonization

Transcriptomic analysis of P. oligandrum-treated plants at 0- vs. 14-dpi revealed that a total of 189 genes were differentially expressed. Seventy percent of these genes (green genes) were overexpressed at 0-dpi. A few functional categories showed statistical significance (Figure 1). Stress-associated genes showed overexpression at 0-dpi (PR-proteins and heat shock protein). On the contrary, polyamine metabolism (two S-adenosylmethionine decarboxylase genes, SAM) and three GCN5-related-N-acetyltransferase associated genes showed overexpression at 14-dpi. As regards the hormone metabolism category, whereas DE genes related to ethylene (ET), gibberellin and salicylic acid were induced at 0-dpi, those concerning cytokinin were overexpressed at 14-dpi.
Other important functional categories, albeit of lesser statistical significance, concerned transcriptional regulation factors: apetala2 ethylene-responsive element binding protein transcription factor family (AP2-EREBP), which was overexpressed, at 0-dpi (3 genes), and basic helix-loop-helix type transcription factor (bHLH), overexpressed at 14-dpi (1 gene).

2.1.2. Transcriptomic Changes in Grapevine Wood Tissues Following P. chlamydospora or P. oligandrum + P. chlamydospora inoculations

In order to evaluate grapevine transcriptomic changes, plant responses to the different treatments (mock inoculation, P. chlamydospora and P. oligandrum + P. chlamydospora) were compared. DE genes between 0- and 14-dpi were obtained using Limma analysis (p < 0.01), which gave the following results: mock treatment (1371 genes), pathogen treatment (2235 genes) and pathogen treatment in the presence of the root BCA (1858 genes). The number of specific and common DE genes detected is shown in the Venn diagram (Figure 2). Specific genes for each treatment were thus obtained, and their biological significance compared (Mapman functional category enrichment).
The combined effect of all treatments revealed numerous DE genes (898), and analysis by functional categories using Mapman software indicated that the amplitude of expression appeared to play a major role. Although many interesting features can be obtained from these microarray result analyses, it is important to focus on the optimal points in high-throughput data regarding the biological system under investigation. In our case, these concerned (1) V. vinifera defense induction by P. chlamydospora and (2) V. vinifera induced resistance by P. oligandrum. The expected differences among treatments at the induction level for the most important DE genes, and statistically significant functional categories related to induced systemic resistance, ISR, (hormones, secondary metabolites, transcription factors and stress related genes), were effectively found. These results were observed when the genes were considered as common to all treatments, rather than when they were considered as specific to each treatment. Our analysis compared the expression of genes at 0-dpi against those at 14-dpi. Overexpression, for the most important functional categories involved in the establishment of ISR, took place at 0-dpi.
In all conditions where wounding occurred (mock inoculation and P. chlamydospora infection), the functional category presenting the strongest statistical significance was “secondary metabolism”. More detailed analyses revealed that several genes involved in phenylpropanoid biosynthesis (Figure 3) presented overexpression at 0-dpi (green genes) in the different treatments. These genes included four phenyl-alanine-ammonia lyase genes (PAL), one gene for 4-coumarate-CoA ligase (4CL) and three cinnamyl alcohol dehydrogenase (CAD) genes. One of the CAD genes was highly overexpressed at 0-dpi in plants treated with both microorganisms.
The “hormone” functional category was statistically significant for all treatments considered, with the jasmonate functional category having the largest number of DE genes (51) in the case of plants inoculated by both P. oligandrum and P. chlamydospora. Selected genes common to all treatments are presented in Figure 4. Two genes were particularly overexpressed at 0-dpi, but only in the joint presence of P. oligandrum and P. chlamydospora. One of the genes was involved in ET hormone regulation (log2 (FC) = −5.23), and the other one, annotated as allene oxide cyclase (log2(FC) = −6.12), was involved in the jasmonic acid (JA) biosynthesis pathway. Seven other genes of that pathway were induced at 0-dpi at various levels. One was lipoxygenase, two allene oxide synthase, and four related to 12 oxo-phytodienoic acid reductase, thereby confirming the strong involvement of the jasmonate pathway in the P. oligandrum induction of plant defenses.
Two other functional categories, stress-related genes and transcription factors, presented the induction of numerous genes in all treatments at 0-dpi. In the case of stress-related genes induction of abiotic- (heat shock proteins, wounding) and biotic-related genes (pathogenesis-related proteins and receptors), slight differences were detected according to the treatment. However, for transcription factors (Figure 5), P. oligandrum + P. chlamydospora treated plants showed globally a higher gene induction at 0-dpi than those inoculated with P. chlamydospora. Numerous functional categories were presented such as the Apetala2-Ethylene responsive element-binding protein (AP2-EREBP), Basic Helix-Loop-Helix (bHLH), MYB domain and WRKY domain. Moreover, AP2-EREBP was the most represented family, with several genes showing a stronger induction in the presence of P. oligandrum and P. chlamydospora.

2.2. Evaluation of P. chlamydospora Transcriptomic Responses

RNAseq experiments were designed to compare samples treated with the P. chlamydospora pathogen in the presence or not of the BCA, P. oligandrum, 14 days after pathogen infection.
The P. chlamydospora genome used in our analysis is a draft comprising of 7,279 genes annotated on a BlastP analysis [18]. A relatively high number of transcripts (2347—32% of the total predicted genes) were detected in our RNAseq data: 1,130 different transcripts in both treatments, 754 transcripts specific to the pathogen + BCA treatment and 463 transcripts to the pathogen treatment only (Figure 6). Of the sequences detected in both treatments, 573 were overexpressed and 557 underexpressed in the P. chlamydospora + P. oligandrum treatment. A more detailed annotation was undertaken in order to obtain further information about the biological signification of our RNAseq data.
The peptide fasta file [18] was used to obtain precise annotations concerning the presence of carbohydrate-active enzymes (CAZymes), and also of peptides involved in secondary metabolite production. The genes potentially involved in secondary metabolite production and detected in our experiment are given in Figure 7. The “Antismash” analysis found gene clusters involved in terpene synthesis: five genes concerned non-ribosomal peptide synthesis (Nrps), and seven others were attributed to type I polyketide synthases (T1pks). In our RNAseq data, five sequences belonging to T1pks clusters were expressed in both treatments (pathogen/BCA and pathogen). Four of these were expressed at a higher level in the pathogen + BCA treatment. Genes expressed only in the pathogen + BCA treatment belonged to the Nrps, T1pks, terpene and Nrps-t1pks hybrid clusters, whereas genes expressed only in the pathogen treatment were restricted to the Nrps and T1pks.
Genes annotated as CAZymes, genes implicated in the degradation of plant polysaccharides and divided into six groups [21], were detected in our samples (Table 1). Most sequences predicted in the P. chlamydospora genome belonged to the glycoside hydrolase (GH) families (345), 107 sequences to the carbohydrate esterase (CE) families, 4 sequences to the polysaccharide lyases (PL) families, 268 to the glycosyl transferase (GT) families and 141 to the carbohydrate-binding module (CBM) families. Out of these 921 sequences identified as CAZymes, 142 enzymes could be potentially secreted (SignalP positive), mainly those of the GH families.
In our experiment, several CAZymes were found in the two conditions, P. chlamydospora and P. oligandrum + P. chlamydospora (Table 1). Overall, the highest number of expressed genes occurred in the pathogen + BCA treatment, with 279 vs. 230 genes for the pathogen treatment. Out of the detected CAZymes, 27 and 29 enzymes could be potentially secreted, respectively, in the P. chlamydospora and P. chlamydospora + P. oligandrum treatment. Interestingly, the number of expressed genes was different according to the condition. In P. chlamydospora + P. oligandrum samples, the number of GH expressed genes was higher than in the P. chlamydospora treatment (70 vs. 60, respectively). Inversely, for the same family, the number of expressed genes related to CAZymes was higher in the P. chlamydospora than in P. chlamydospora + P. oligandrum treatment. Regarding the GT family, the number of expressed genes was higher in the P. chlamydospora + P. oligandrum than in P. chlamydospora treatment. The CAZyme gene expression was clearly modified in the presence of the BCA at the root level.
The genes potentially involved in the regulation of metabolic processes in P. chlamydospora were sought within BlastP annotations (against NCBI database). Their potential identifications were further tentatively confirmed by BlastP analysis against the Uniprot fungi database. In all, 34 genes were expressed in our RNAseq dataset. Out of these, 19 were present in both treatments, and 22 were expressed at a higher rate in the pathogen/BCA treatment. Most of these genes were involved in protein kinase (PK) pathways, such as cell wall remodeling, antifungal-resistance and invasive-growth (Figure 8). Most of genes involved in the “cell wall strengthening” and “Antifungal resistance” functional categories showed a higher expression in P. chlamydospora + P. oligandrum than in P. chlamydospora treatment (Wsc2, Wsc3, Mkk1 and Swi6). However, all genes (6) involved in the “invasive growth”, “Osmoregulation” and “Differentiation Infection-related morphogenesis” functional categories were expressed at a higher level in the P. chlamydospora treatment (Figure 8).
Six other genes were involved in a secondary metabolism regulation, such as those involved in the redox status, pH regulation and the carbon source (Figure 9). Four of those genes were implicated in redox status regulation. Interestingly, two of them (HapE and Fkh1/2) showed expression levels at 0 FPKM, when only the pathogen was present. However, in the presence of the BCA at the root level, the expression levels of these genes were strongly upregulated (Figure 9). The expression levels of the two other genes involved in the redox status (Yap1 and HapC) were higher in the pathogen treatment than in the BCA + pathogen treatment. The PacC and CreC genes, involved in pH regulation and the carbon source were, respectively, more expressed in P. chlamydospora/P. oligandrum than in the P. chlamydospora treatment.

3. Discussion

P. oligandrum establishes a somewhat relatively complex relationship with the roots of many plants [12,13] as shown in a recent report describing the transcriptomic changes in the roots of V. vinifera when colonized by the oomycete [24]. The expression of several transcripts suggests that the plant sets up defense systems against the oomycete, while certain similarities with symbiotic microorganisms have also been observed [24].
In addition to its complex relationship with roots, P. oligandrum’s role in protecting grapevine from the attacks of many pathogens has been frequently reported [12,13]. These include a pathogenic fungus, P. chlamydospora, involved in esca [16,17]. It was shown that necrosis of grapevine cuttings caused by P. chlamydospora was significantly reduced when P. oligandrum colonized the plant root systems [17]. Thus, we decided to further analyze this BCA–pathogen–host interactome to throw light on how the presence of the BCA, at the root level, had led to the grapevine-trunk pathogen being less invasive. The present study showed that, by using high-throughput of transcriptome analyses, following P. oligandrum grapevine-root colonization, transcriptional changes occurred in the wood tissues of a perennial species such as the grapevine. Equally, transcriptional changes in a pathogenic fungus colonizing the trunk wood were, to the best of our knowledge, shown for the first time in this kind of biocontrol experiment.

3.1. P. oligandrum Induced Genes Involved in the Jasmonic/Ethylene Signaling Pathways

Grapevine global molecular responses were studied between 0- and 14-dpi at the trunk level. The wood samples of P. oligandrum-treated plants showed 189 DE genes comparing to control plants. The same result has already been observed, at the root level, in an earlier study [24]. This suggests that this type of plant response occurs throughout the whole plant, including the upper part of the grapevine.
In order to understand the specific effect of P. oligandrum on P. chlamydospora-infected grapevine responses, the expression levels of ISR-related genes in (i) mock inoculated plants, (ii) plants infected with the pathogen and (iii) plants pretreated with the BCA and infected with the pathogen, were compared. In order to understand the specific effect of P. oligandrum on P. chlamydospora-infected grapevine responses, the expression levels of ISR-related genes in (i) mock inoculated plants, (ii) plants infected with the pathogen and (iii) plants pretreated with the BCA and infected with the pathogen were compared. In all treatments, expression levels of ISR-related genes, i.e., phenylpropanoid biosynthesis, signaling hormone pathways and transcription factors, were more expressed at 0-dpi than those observed at 14-dpi. These results are in accordance with previous studies showing that grapevine defense genes are, generally, induced a few hours following biotic stress applications [25,26,27,28,29] as it is the case in our experiment where 0-dpi corresponded to 2 h after plant inoculation with the pathogen, P. chlamydospora.
A more detailed analysis of expression profiles revealed that certain genes involved in JA/ET pathways were more expressed in the grapevine treated with both the BCA, P. oligandrum, and the pathogen, than in those only infected with P. chlamydospora alone. Hence, it can be assumed that P. oligandrum promotes priming, in which the plant mobilizes its defense reactions more intensely when pathogen infection occurred. Previous studies have also demonstrated the implication of JA/ET signaling pathways in P. oligandrum tomato-induced resistance against other pathogens [30,31,32,33]. Genes involved in ET and JA pathways, and specifically activated in P. oligandrum-treated grapevine in response to P. chlamydospora attacks, encoded for ACC synthase, allene oxide cyclase, bHLH and AP2-ERBP transcription factors, which are involved in the regulation of disease resistance as reviewed by [34].
Moreover, Pré et al. (2008) [35] have demonstrated that the overexpression of an ORA59 gene from the AP2/ERBF family induced resistance against B. cinerea, and that the ORA59 mutant plants were more susceptible than control plants to infection. All these grapevine genes represent a valuable tool in characterizing the tri-partite interaction between P. oligandrum, V. vinifera and P. chlamydospora.

3.2. P. oligandrum Indirectly Modulates the Expression Level of P. chlamydospora Pathogencity Related-Genes

Characterization of P. chlamydospora pathogenicity related-genes, especially those involved in the colonization of the plant and effectors, is of importance. Our results showed that 463 P. chlamydospora recovered transcripts were identified in grapevines treated with the pathogen, whereas a higher number of transcripts, 754, were exclusively detected in grapevines treated with the BCA, P. oligandrum, and the pathogen, P. chlamydospora. Thus, the presence of P. oligandrum, at the grapevine root level, indirectly affected the transcriptomic responses of P. chlamydospora, when inoculated at the trunk level. To the best of our knowledge, this study provides the first dataset on wood fungal pathogen transcriptional changes induced by a root BCA, in which there is no contact between the two microorganisms.
Numerous studies have shown that P. chlamydopora produces several secondary metabolites with phytotoxic activity (i.e., toxins) [36,37,38,39]. When P. oligandrum colonized grapevine roots, three P. chlamydospora sequences encoding NRPS were not expressed, these peptides being reported as potentially responsible for the synthesis of toxic polypeptides [40]. Additionally, most t1pks genes were also more overexpressed when P. oligandrum was present at the root level, these genes participating in the production of the naphtelenone pentaketide toxins were found in the P. chlamydospora liquid culture [36,40,41]. These results evidenced the indirect effect induced by the P. oligandrum strain on secondary metabolite gene expression by the pathogen. It can be hypothesized that the potential regulation of specific transcripts encoding for these toxins corresponds to a stress state of the pathogen induced by the presence of the BCA, P. oligandrum, at the root level.
CAZymes transcripts are also affected. CAZymes are proteins that catalyze the breakdown, biosynthesis or modification of carbohydrates and glycoconjugates [42,43,44,45]. Differences in the expression levels of P. chlamydospora CAZyme-related transcripts detected in our dataset were observed, between treatments. Results obtained in our study also revealed that the secretion of the expression level of P. chlamydospora genes encoding for GHs, involved in the degradation of cellulose and hemicelluloses, was greatly reduced in the presence of P. oligandrum at the root level. On the contrary, the GTs responsible for the biosynthesis glycosidic bonds from phospho-activated sugar donors [45] were more secreted. Accordingly, it could be supposed that, as the trunk pathogen is stressed in grapevines treated with P. oligandrum, it is unable to progress in planta and it needs to secrete enzymes to obtain a source of energy. Overall, these results confirmed the indirect effect of P. oligandrum root inoculation on the P. chlamydospora transcriptome at the trunk level.
The P. chlamydospora transcripts of genes related to several proteins important for the pathogen–host relationship, namely transcription factors and protein kinases [22,23], were identified. Several of the above-mentioned protein genes, especially those involved in the cell wall strengthening pathway (Wsc family, Swi6 gene) and regulation of the redox status (HapE and Fkh1 genes), presented a high level of expression in P. chlamydospora + P. oligandrum, than in the P. chlamydospora one. One explanation could be that effectors, produced by P. oligandrum at the root level, were transported via the grapevine vascular system and induce stresses on P. chlamydospora, when they reach the trunk level.
Other P. chlamydospora genes possibly involved in invasive growth, Ste7, Ste20 and Sho1, showed the highest expression levels in the pathogen condition. In the presence of P. oligandrum, expression levels of these three genes were strongly reduced and when combined with other factors, it may be involved in reducing the wood necroses caused by P. chlamydospora.
To conclude, our data showed that during the tripartite interaction grapevine + P. chlamydosporum and P. oligandrum, the JA/ET signaling pathways are promoted with certain genes being more induced when plants were pretreated with the BCA, P. oligandrum, thus highlighting a priming effect. The indirect effect of P. oligandrum on the P. chlamydospora transcriptome was also demonstrated, which contributes to a better understanding of the protection mechanisms induced by the potential oomycete-BCA.

4. Methods

4.1. Plant and Microorganism Materials

In order to choose the best samples to characterize the tripartite interaction between P. oligandrum, the grapevine and P. chlamydospora, using high throughput transcriptomic techniques such as a microarray and RNAseq, a preliminary study has been already carried out [17]. In that previous study, three inocula of P. oligandrum were assessed to protect the grapevine against P. chlamydospora. Plant responses were evaluated using a set of 22 genes globally involved in grapevine defenses against different biotic stresses. For the present study, depending on our previous results [17], we selected the samples showing the P. oligandrum mean root colonization level of 39% (P. oligandrum, inoculum Po2), and the highest plant protection level (50%) against the pathogen (P. chlamydospora, strain SO37). The different control treatments were integrated in the analysis.
The assay was conducted in a greenhouse and at 7–8 leaf stage, grapevine plants (V. vinifera L. cv. Cabernet Sauvignon) were infected with P. chlamydospora (strain SO37, INRA-UMR SAVE collection, Bordeaux, France) at the stem level. P. oligandrum root inoculation (at 2 × 104 oospores per mL suspension) was performed twice at intervals of 4 days, with the first inoculation being carried out 7 days before pathogen infection, and the second one 3 days before. The P. oligandrum inocula were composed of an oospore-mycelium homogenate of a mixture of two strains (Sto-1 and Oth-4), they were prepared by Biovitis (Saint-Étienne-de-Chomeil, France) as described previously [46].
The experimental design consisted of five conditions composed of grapevines (i) inoculated on roots with P. oligandrum; (ii) infected in the wood trunk by the pathogenic agent P. chlamydospora; (iii) pretreated on roots with P. oligandrum and then infected with P. chlamydospora; (iv) mock inoculated (cuttings with a hole) and (v) control (cuttings without any treatment).
For the transcriptome analyses, the stems of nine grapevines per treatment were collected, at each sampling time point, and pooled on three replicates (three plants per replicate) in order to reduce biological variation-related noise. For each plant, collected wood samples were measured at about 4 cm (2 cm above and 2 cm below the inoculation point). Collected materials at 0-dpi (2 h post pathogen inoculation) and 14-dpi (14 days post pathogen inoculation) were immediately frozen in liquid nitrogen and stored at −80 °C until use.

4.2. RNA Extraction

Grapevine wood samples were ground in liquid nitrogen, and 200 mg aliquots were used for RNA extraction. A commercial RNA extraction kit (RNeasy Plant Mini Kit, Qiagen, Hilden, Germany) was employed, with modifications as previously described [17]. Total RNA samples were subjected to standard quality controls: Nanodrop (ND-1000, ThermoScientific, Waltham, MA, USA) for all samples and the BioAnalyzer (Agilent, Carpinteria, CA, USA) for the microarray and RNAseq samples. All samples were stored at −80 °C before use in RT-qPCR experiments, or else stored at −80 °C before being shipped in dry ice, either to the GeT (Genome & Transcriptome) platform (Toulouse, France) for subsequent microarray analyses, or to the IGBMC (Institut de génétique et de biologie moléculaire et cellulaire) sequencing platform (Strasbourg, France) for RNAseq analyses.

4.3. Microarray Analyses, Data Processing and Deposition

The microarrays used were the grapevine whole-genome microarrays by Nimblegen, Roche, Basel, Switzerland (Design name 090918 Vitus exp HX12). Microarray hybridizations were performed by the Get Platform (Toulouse, France) in accordance with the manufacturer’s instructions. The microarray data were analyzed using the statistical package R, version 2.14.0 with various Bioconductor packages [47] (http://www.bioconductor.org). Microarray quality controls were performed using the ArrayQualityMetrics package [48]. Expression intensities were background corrected, quantile-normalized and summarized using the RMA function of the oligo package [49]. The raw and normalized microarray data are available in the ArrayExpress database under accession number E-MTAB-12345.
Differentially expressed (DE) genes were identified using the Limma package [50] at a p value < 0.01 using the MultiExperiment Viewer software MeV [51]. The log2 of the fold change (FC) was used to obtain contrastingly regulated genes between 0 and 14 dpi, for each treatment.

4.4. RNAseq Analyses

RNAseq library preparation was performed using an rRNA-depletion kit (RiboZero, Qiagen, Hilden, Germany), as recommended by the manufacturer. Sequencing was performed by the IGBMC Microarray and Sequencing platform, a member of the “France Génomique” consortium (ANR-10-INBS-0009). The libraries were sequenced on an Illumina Hiseq 2500 as paired-end 100 base reads, in accordance with Illumina’s instructions. Image analysis and base calling were performed using RTA 1.17.21.3 and CASAVA 1.8.2. Files containing raw data (fastq files) obtained from the IGBMC Sequencing platform were transferred to the bioinformatics servers of the GenoToul bioinformatics facility and analyzed remotely by connecting to the linux cluster. The procedure that we followed for RNAseq analyses has already been described [52]. RNAseq data are available in the ArrayExpress database under accession number E-MTAB-3966. The widely used computational tool Antismash [53] to identify different gene clusters involved in pathogen secondary metabolite biosynthesis.

4.5. Reverse Transcriptase Quantitative PCR Experiments

RNA retro-transcription was performed with the Superscript III kit from Invitrogen (using oligo(dT) primers, 1.5 µg of RNA and in accordance with to the manufacturer’s instructions). Gene expression was analyzed on a Stratagene MX3005P PCR machine (Agilent Technologies), with a kit MESA BLUE qPCR for SYBR Assay (Eurogentec, Liége, Belgium). Each reaction was performed in duplicate, using 1 µL of each primer (forward and reverse) at 1 µM, 7 µL of the fluorescein mix and 5 µL of cDNAs [54]. All qRT-PCR reactions were performed as follows: 95 °C for 10 min, followed by 40 cycles of 95 °C for 3 s and 60 °C for 30 s. Determination of the relative quantity of the target gene transcript was performed using the 2−ΔΔCT method [55].
The raw data were exported using the software from the PCR equipment, and then analyzed using the LinRegPCR software [56]. Primers were designed on the NCBI (National Center for Biotechnology Information) website using the Primer-Blast utility [57]. The sequences used for RT-qPCR and corresponding primers are given in Table S1, and those used as references are given in Table S2. The comparison between the microarray and qPCR levels of expression was carried out using regression analysis (Figure S1).

Supplementary Materials

Supplementary materials can be found at https://www.mdpi.com/1422-0067/21/18/6876/s1. Figure S1. Comparison of microarray and qPCR expression levels Log2 (FC) by regression analysis. Table S1. Genes used for microarray validation by RT-qPCR. Table S2. Genes used as reference in RT-qPCR analyses.

Author Contributions

A.Y. and J.G. performed the experiments. N.M. analyzed the data. A.Y., J.G., N.M., R.H., E.B., S.C., R.G. and P.R. wrote and corrected the manuscript. P.R. directed the research. All authors have read and agreed to the published version of the manuscript.

Funding

This work is supported by the Industrial Chair GTDfree funded by ANR (French National Research Agency) and the Hennessy Company. We would also like to thank the French Ministry of Agriculture (V1302 Casdar research project on Grapevine Trunk Diseases), the Tunisian Ministry of Scientific Research and Biovitis for their financial supports.

Acknowledgments

We appreciate the technical support provided by: the Toulouse Get Biopuce Platform for microarray experiments (LeBerre, V., Trouilh, L., Jouanillou, A. and Lamarre, S.); the Strasbourg IGBMC platform (Jost, B., Keime, C. and Velt, A.) concerning RNAseq experiments; the Toulouse GenoToul Bioinformatics facility (Trotard, M.S.) for advice about bioinformatic analyses on the server and the Bordeaux Functional Genomics Platform (Petit, J.) for the RNA quality controls.

Conflicts of Interest

The authors declare no conflict interests. The funders had no role in the design of the study; in the collection, analyses or interpretation of data; in the writing of the manuscript or in the decision to publish the results.

References

  1. Gramaje, D.; Úrbez-Torres, J.R.; Sosnowski, M.R. Managing grapevine trunk diseases with respect to etiology and epidemiology: Current strategies and future prospects. Plant Dis. 2018, 102, 12–39. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Mondello, V.; Songy, A.; Battiston, E.; Pinto, C.; Coppin, C.; Trotel-Aziz, P.; Clément, C.; Mugnai, L.; Fontaine, F. Grapevine trunk diseases: A review of fifteen years of trials for their control with chemicals and biocontrol agents. Plant Dis. 2018, 102, 1189–1217. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Bertsch, C.; Ramírez-Suero, M.; Magnin-Robert, M.; Larignon, P.; Chong, J.; Abou-Mansour, E.; Spagnolo, A.; Clément, C.; Fontaine, F. Grapevine trunk diseases: Complex and still poorly understood. Plant Pathol. 2013, 62, 243–265. [Google Scholar] [CrossRef] [Green Version]
  4. Kaplan, J.; Travadon, R.; Cooper, M.; Hillis, V.; Lubell, M.; Baumgartner, K. Identifying economic hurdles to early adoption of preventative practices: The case of trunk diseases in California winegrape vineyards. Wine Econ. Policy 2016, 5, 127–141. [Google Scholar] [CrossRef]
  5. Calzarano, F.; Marco, S.D.; Cesari, A. Benefit of fungicide treatment after trunk renewal of vines with different types of esca necrosis. Phytopathol. Mediterr. 2004, 43, 10. [Google Scholar]
  6. Lorrain, B.; Ky, I.; Pasquier, G.; Jourdes, M.; Dubrana, L.G.; Gény, L.; Rey, P.; Donèche, B.; Teissedre, P.-L. Effect of Esca disease on the phenolic and sensory attributes of Cabernet Sauvignon grapes, musts and wines: Esca effect on grapes and wines composition. Aust. J. Grape Wine Res. 2012, 18, 64–72. [Google Scholar] [CrossRef]
  7. Les Maladies du Bois de la Vigne—Réunion du Groupe de Travail Maladies du Bois. Available online: https://www.maladie-du-bois-vigne.fr/Zoom-sur/Reunion-du-Groupe-de-travail-Maladies-du-bois (accessed on 30 June 2020).
  8. Compant, S.; Brader, G.; Muzammil, S.; Sessitsch, A.; Lebrihi, A.; Mathieu, F. Use of beneficial bacteria and their secondary metabolites to control grapevine pathogen diseases. BioControl 2013, 58, 435–455. [Google Scholar] [CrossRef] [Green Version]
  9. Mounier, E.; Boulisset, F.; Elbaz, N.; Dubournet, P.; Pajot, E. Esquive® WP limits development of grapevine wood diseases and reductions in the productive potential of land. In Proceedings of the 5th Conférence Internationale sur les Méthodes Alternatives de Protection des Plantes, Nouceau Sièle, Lille, France, 11–13 March 2015; Association Française de Protection des Plantes (AFPP): Alfortville, France, 2015; pp. 251–261. [Google Scholar]
  10. Blundell, R.; Lynch, M.; Haden, T.; Arreguin, M.; Gallagher, T.; Eskalen, A. Final Report: Evaluation of Vintec (Trichoderma atroviride_SC1) as Pruning Wound Protectants Against Selected Fungi Associated with Grapevine Trunk Diseases; Department of Plant Pathology, University of California: Davis, CA, USA, 2020. [Google Scholar]
  11. Gerbore, J.; Vallance, J.; Yacoub, A.; Delmotte, F.; Grizard, D.; Regnault-Roger, C.; Rey, P. Characterization of Pythium oligandrum populations that colonize the rhizosphere of vines from the Bordeaux region. FEMS Microbiol. Ecol. 2014, 90, 153–167. [Google Scholar] [CrossRef] [Green Version]
  12. Benhamou, N.; le Floch, G.; Vallance, J.; Gerbore, J.; Grizard, D.; Rey, P. Pythium oligandrum: An example of opportunistic success. Microbiology 2012, 158, 2679–2694. [Google Scholar] [CrossRef]
  13. Gerbore, J.; Benhamou, N.; Vallance, J.; Le Floch, G.; Grizard, D.; Regnault-Roger, C.; Rey, P. Biological control of plant pathogens: Advantages and limitations seen through the case study of Pythium oligandrum. Environ. Sci. Pollut. Res. 2014, 21, 4847–4860. [Google Scholar] [CrossRef] [Green Version]
  14. Mohamed, N.; Lherminier, J.; Farmer, M.-J.; Fromentin, J.; Béno, N.; Houot, V.; Milat, M.-L.; Blein, J.-P. Defense responses in grapevine leaves against Botrytis cinerea induced by application of a Pythium oligandrum strain or its elicitin, oligandrin, to roots. Phytopathology 2007, 97, 611–620. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Laveau, C.; Letouze, A.; Louvet, G.; Bastien, S.; Guérin-Dubrana, L. Differential aggressiveness of fungi implicated in esca and associated diseases of grapevine in France. Phytopathol. Mediterr. 2009, 48, 15. [Google Scholar]
  16. Daraignes, L.; Gerbore, J.; Yacoub, A.; Dubois, L.; Romand, C.; Zekri, O.; Roudet, J.; Chambon, P.; Fermaud, M. Efficacy of P. oligandrum affected by its association with bacterial BCAs and rootstock effect in controlling grapevine trunk diseases. Biol. Control 2018, 119, 59–67. [Google Scholar] [CrossRef]
  17. Yacoub, A.; Gerbore, J.; Magnin, N.; Chambon, P.; Dufour, M.-C.; Corio-Costet, M.-F.; Guyoneaud, R.; Rey, P. Ability of Pythium oligandrum strains to protect Vitis vinifera L., by inducing plant resistance against Phaeomoniella chlamydospora, a pathogen involved in Esca, a grapevine trunk disease. Biol. Control 2016, 92, 7–16. [Google Scholar] [CrossRef]
  18. Antonielli, L.; Compant, S.; Strauss, J.; Sessitsch, A.; Berger, H. Draft genome sequence of Phaeomoniella chlamydospora strain RR-HG1, a grapevine trunk disease (esca)-related member of the ascomycota. Genome Announc. 2014, 2, e00098-14. [Google Scholar] [CrossRef] [Green Version]
  19. Blanco-Ulate, B.; Rolshausen, P.; Cantu, D. Draft genome sequence of the Ascomycete Phaeoacremonium aleophilum strain UCR-PA7, a causal agent of the esca disease complex in grapevines. Genome Announc. 2013, 1, e00390-13. [Google Scholar] [CrossRef] [Green Version]
  20. Robert-Siegwald, G.; Vallet, J.; Abou-Mansour, E.; Xu, J.; Rey, P.; Bertsch, C.; Rego, C.; Larignon, P.; Fontaine, F.; Lebrun, M.-H. Draft genome sequence of Diplodia seriata F98.1, a fungal species involved in grapevine trunk diseases. Genome Announc. 2017, 5, e00061-17. [Google Scholar] [CrossRef] [Green Version]
  21. Lombard, V.; Golaconda Ramulu, H.; Drula, E.; Coutinho, P.M.; Henrissat, B. The carbohydrate-active enzymes database (CAZy) in 2013. Nucleic Acids Res. 2014, 42, D490–D495. [Google Scholar] [CrossRef] [Green Version]
  22. Turrà, D.; Segorbe, D.; Di Pietro, A. Protein kinases in plant-pathogenic fungi: Conserved regulators of infection. Annu. Rev. Phytopathol. 2014, 52, 267–288. [Google Scholar] [CrossRef]
  23. Brakhage, A.A. Regulation of fungal secondary metabolism. Nat. Rev. Microbiol. 2013, 11, 21–32. [Google Scholar] [CrossRef]
  24. Yacoub, A.; Gerbore, J.; Magnin, N.; Haidar, R.; Compant, S.; Rey, P. Transcriptional analysis of the interaction between the oomycete biocontrol agent, Pythium oligandrum, and the roots of Vitis vinifera L. Biol. Control 2018, 120, 26–35. [Google Scholar] [CrossRef]
  25. Armijo, G.; Schlechter, R.; Agurto, M.; Muñoz, D.; Nuñez, C.; Arce-Johnson, P. Grapevine pathogenic microorganisms: Understanding infection strategies and host response scenarios. Front. Plant Sci. 2016, 7. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. De Bona, G.S.; Adrian, M.; Negrel, J.; Chiltz, A.; Klinguer, A.; Poinssot, B.; Héloir, M.-C.; Angelini, E.; Vincenzi, S.; Bertazzon, N. Dual mode of action of grape cane extracts against Botrytis cinerea. J. Agric. Food Chem. 2019, 67, 5512–5520. [Google Scholar] [CrossRef] [PubMed]
  27. Esmaeel, Q.; Jacquard, C.; Clément, C.; Sanchez, L.; Ait Barka, E. Genome sequencing and traits analysis of Burkholderia strains reveal a promising biocontrol effect against grey mould disease in grapevine (Vitis vinifera L.). World J. Microbiol. Biotechnol. 2019, 35, 40. [Google Scholar] [CrossRef] [PubMed]
  28. Haidar, R.; Roudet, J.; Bonnard, O.; Dufour, M.C.; Corio-Costet, M.F.; Fert, M.; Gautier, T.; Deschamps, A.; Fermaud, M. Screening and modes of action of antagonistic bacteria to control the fungal pathogen Phaeomoniella chlamydospora involved in grapevine trunk diseases. Microbiol. Res. 2016, 192, 172–184. [Google Scholar] [CrossRef]
  29. Zhang, W.; Yan, J.; Li, X.; Xing, Q.; Chethana, K.W.T.; Zhao, W. Transcriptional response of grapevine to infection with the fungal pathogen Lasiodiplodia theobromae. Sci. Rep. 2019, 9. [Google Scholar] [CrossRef]
  30. Hase, S.; Shimizu, A.; Nakaho, K.; Takenaka, S.; Takahashi, H. Induction of transient ethylene and reduction in severity of tomato bacterial wilt by Pythium oligandrum. Plant Pathol. 2006, 55, 537–543. [Google Scholar] [CrossRef]
  31. Hase, S.; Takahashi, S.; Takenaka, S.; Nakaho, K.; Arie, T.; Seo, S.; Ohashi, Y.; Takahashi, H. Involvement of jasmonic acid signalling in bacterial wilt disease resistance induced by biocontrol agent Pythium oligandrum in tomato. Plant Pathol. 2008, 57, 870–876. [Google Scholar] [CrossRef]
  32. Ouyang, Z.; Li, X.; Huang, L.; Hong, Y.; Zhang, Y.; Zhang, H.; Li, D.; Song, F. Elicitin-like proteins Oli-D1 and Oli-D2 from Pythium oligandrum trigger hypersensitive response in Nicotiana benthamiana and induce resistance against Botrytis cinerea in tomato: Oligandrins induce resistance in tomato. Mol. Plant Pathol. 2015, 16, 238–250. [Google Scholar] [CrossRef]
  33. Wang, A.; Lou, B.; Xu, T.; Lin, C. Defense responses in tomato fruit induced by oligandrin against Botrytis cinerea. Afr. J. Biotechnol. 2011, 10, 4596–4601. [Google Scholar]
  34. Gutterson, N.; Reuber, T.L. Regulation of disease resistance pathways by AP2/ERF transcription factors. Curr. Opin. Plant Biol. 2004, 7, 465–471. [Google Scholar] [CrossRef] [PubMed]
  35. Pré, M.; Atallah, M.; Champion, A.; De Vos, M.; Pieterse, C.M.J.; Memelink, J. The AP2/ERF domain transcription factor ORA59 integrates jasmonic acid and ethylene signals in plant defense. Plant Physiol. 2008, 147, 1347–1357. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Andolfi, A.; Mugnai, L.; Luque, J.; Surico, G.; Cimmino, A.; Evidente, A. Phytotoxins produced by fungi associated with grapevine trunk diseases. Toxins 2011, 3, 1569–1605. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Bruno, G.; Sparapano, L. Effects of three esca-associated fungi on Vitis vinifera L.: I. Characterization of secondary metabolites in culture media and host responses to the pathogens in calli. Physiol. Mol. Plant Pathol. 2006, 69, 209–223. [Google Scholar] [CrossRef]
  38. Bruno, G.; Sparapano, L. Effects of three esca-associated fungi on Vitis vinifera L.: II. Characterization of biomolecules in xylem sap and leaves of healthy and diseased vines. Physiol. Mol. Plant Pathol. 2006, 69, 195–208. [Google Scholar] [CrossRef]
  39. Bruno, G.; Sparapano, L. Effects of three esca-associated fungi on Vitis vinifera L.: III. Enzymes produced by the pathogens and their role in fungus-to-plant or in fungus-to-fungus interactions. Physiol. Mol. Plant Pathol. 2006, 69, 182–194. [Google Scholar] [CrossRef]
  40. Morales-Cruz, A.; Amrine, K.C.H.; Blanco-Ulate, B.; Lawrence, D.P.; Travadon, R.; Rolshausen, P.E.; Baumgartner, K.; Cantu, D. Distinctive expansion of gene families associated with plant cell wall degradation, secondary metabolism, and nutrient uptake in the genomes of grapevine trunk pathogens. BMC Genom. 2015, 16. [Google Scholar] [CrossRef] [Green Version]
  41. Luini, E.; Fleurat-Lessard, P.; Rousseau, L.; Roblin, G.; Berjeaud, J.-M. Inhibitory effects of polypeptides secreted by the grapevine pathogens Phaeomoniella chlamydospora and Phaeoacremonium aleophilum on plant cell activities. Physiol. Mol. Plant Pathol. 2010, 74, 403–411. [Google Scholar] [CrossRef]
  42. Cantarel, B.L.; Coutinho, P.M.; Rancurel, C.; Bernard, T.; Lombard, V.; Henrissat, B. The Carbohydrate-Active EnZymes database (CAZy): An expert resource for Glycogenomics. Nucleic Acids Res. 2009, 37, D233–D238. [Google Scholar] [CrossRef]
  43. Zhao, Z.; Liu, H.; Wang, C.; Xu, J.-R. Comparative analysis of fungal genomes reveals different plant cell wall degrading capacity in fungi. BMC Genom. 2013, 14, 274. [Google Scholar] [CrossRef] [Green Version]
  44. Sista Kameshwar, A.K.; Qin, W. Comparative study of genome-wide plant biomass-degrading CAZymes in white rot, brown rot and soft rot fungi. Mycology 2018, 9, 93–105. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Yip, V.L.; Withers, S.G. Breakdown of oligosaccharides by the process of elimination. Curr. Opin. Chem. Biol. 2006, 10, 147–155. [Google Scholar] [CrossRef] [PubMed]
  46. Le Floch, G.; Rey, P.; Déniel, F.; Benhamou, N.; Picard, K.; Tirilly, Y. Enhancement of development and induction of resistance in tomato plants by the antagonist, Pythium oligandrum. Agronomie 2003, 23, 455–460. [Google Scholar] [CrossRef] [Green Version]
  47. Gentleman, R.C.; Carey, V.J.; Bates, D.M.; Bolstad, B.; Dettling, M.; Dudoit, S.; Ellis, B.; Gautier, L.; Ge, Y.; Gentry, J.; et al. Bioconductor: Open software development for computational biology and bioinformatics. Genome Biol. 2004, 10, R80. [Google Scholar] [CrossRef] [Green Version]
  48. Kauffmann, A.; Gentleman, R.; Huber, W. arrayQualityMetrics—A bioconductor package for quality assessment of microarray data. Bioinformatics 2009, 25, 415–416. [Google Scholar] [CrossRef] [Green Version]
  49. Carvalho, B.S.; Irizarry, R.A. A framework for oligonucleotide microarray preprocessing. Bioinformatics 2010, 26, 2363–2367. [Google Scholar] [CrossRef]
  50. Bioinformatics and Computational Biology Solutions Using R and Bioconductor; Gentleman, R. (Ed.) Statistics for Biology and Health; Springer Science + Business Media: New York, NY, USA, 2005; ISBN 978-0-387-25146-2. [Google Scholar]
  51. Saeed, A.I.; Sharov, V.; White, J.; Li, J.; Liang, W.; Bhagabati, N.; Braisted, J.; Klapa, M.; Currier, T.; Thiagarajan, M.; et al. TM4: A Free, Open-Source System for Microarray Data Management and Analysis. BioTechniques 2003, 34, 374–378. [Google Scholar] [CrossRef] [Green Version]
  52. Trapnell, C.; Roberts, A.; Goff, L.; Pertea, G.; Kim, D.; Kelley, D.R.; Pimentel, H.; Salzberg, S.L.; Rinn, J.L.; Pachter, L. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. Nat. Protoc. 2012, 7, 562–578. [Google Scholar] [CrossRef] [Green Version]
  53. Medema, M.H.; Blin, K.; Cimermancic, P.; de Jager, V.; Zakrzewski, P.; Fischbach, M.A.; Weber, T.; Takano, E.; Breitling, R. antiSMASH: Rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences. Nucleic Acids Res. 2011, 39, W339–W346. [Google Scholar] [CrossRef]
  54. Dufour, M.C.; Lambert, C.; Bouscaut, J.; Mérillon, J.M.; Corio-Costet, M.F. Benzothiadiazole-primed defence responses and enhanced differential expression of defence genes in Vitis vinifera infected with biotrophic pathogens Erysiphe necator and Plasmopara viticola: Elicitation and grapevine responses to mildews. Plant Pathol. 2013, 62, 370–382. [Google Scholar] [CrossRef]
  55. Livak, K.J.; Schmittgen, T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods 2001, 25, 402–408. [Google Scholar] [CrossRef] [PubMed]
  56. Ruijter, J.M.; Ramakers, C.; Hoogaars, W.M.H.; Karlen, Y.; Bakker, O.; van den Hoff, M.J.B.; Moorman, A.F.M. Amplification efficiency: Linking baseline and bias in the analysis of quantitative PCR data. Nucleic Acids Res. 2009, 37, e45. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Ye, J.; Coulouris, G.; Zaretskaya, I.; Cutcutache, I.; Rozen, S.; Madden, T.L. Primer-BLAST: A tool to design target-specific primers for polymerase chain reaction. BMC Bioinform. 2012, 13, 134. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Ijms 21 06876 g001 550
Figure 1. Global aspects of the grapevine transcriptome evolution from 0- to 14-dpi according to the treatments. Major functional categories obtained after Limma analysis and Mapman classification for root-inoculated grapevine with Pythium oligandrum, in the absence of pathogen infection. The red color means overexpression at 14-dpi and the green color means overexpression at 0-dpi.
Figure 1. Global aspects of the grapevine transcriptome evolution from 0- to 14-dpi according to the treatments. Major functional categories obtained after Limma analysis and Mapman classification for root-inoculated grapevine with Pythium oligandrum, in the absence of pathogen infection. The red color means overexpression at 14-dpi and the green color means overexpression at 0-dpi.
Ijms 21 06876 g001
Ijms 21 06876 g002 550
Figure 2. Venn diagram showing gene numbers in grapevine wood tissues common or specific to the three conditions considered ((i) mock inoculation, (ii) Phaeomoniella chlamydospora-wood infection, (iii) Phaeomoniella chlamydospora-wood infection and Pythium oligandrum Po2-root inoculation). Mock: mock inoculation; Po: P. oligandrum; Pch: P. chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
Figure 2. Venn diagram showing gene numbers in grapevine wood tissues common or specific to the three conditions considered ((i) mock inoculation, (ii) Phaeomoniella chlamydospora-wood infection, (iii) Phaeomoniella chlamydospora-wood infection and Pythium oligandrum Po2-root inoculation). Mock: mock inoculation; Po: P. oligandrum; Pch: P. chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
Ijms 21 06876 g002
Ijms 21 06876 g003 550
Figure 3. Characteristics of the grapevine transcriptome evolution for genes involved in the phenylpropanoid biosynthesis pathway between 0- and 14-dpi. Expression level values of phenylpropanoid genes (PAL: phenyl-alanine-ammonia lyase, 4CL: 4-coumarate-CoA ligase and CAD: cinnamyl alcohol dehydrogenase) are given as the fold change on a log2 basis. The red color means overexpression at 14-dpi and the green color means overexpression at 0-dpi. Mock: mock inoculation; Po: Pythium oligandrum; Pch: Phaeomoniella chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
Figure 3. Characteristics of the grapevine transcriptome evolution for genes involved in the phenylpropanoid biosynthesis pathway between 0- and 14-dpi. Expression level values of phenylpropanoid genes (PAL: phenyl-alanine-ammonia lyase, 4CL: 4-coumarate-CoA ligase and CAD: cinnamyl alcohol dehydrogenase) are given as the fold change on a log2 basis. The red color means overexpression at 14-dpi and the green color means overexpression at 0-dpi. Mock: mock inoculation; Po: Pythium oligandrum; Pch: Phaeomoniella chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
Ijms 21 06876 g003
Ijms 21 06876 g004 550
Figure 4. Characteristics of the grapevine transcriptome evolution for genes involved in hormone biosynthesis pathways between 0- and 14-dpi. Expression level values of genes encoding proteins involved in the synthesis or regulation of hormones (ABA: abscisic acid, ACC: 1-aminocyclopropane 1-carboxylate and GA: gibberellin) are given as the fold change on a log2 basis. The red color means overexpression at 14-dpi and the green color means overexpression at 0-dpi. Mock: mock inoculation; Po: Pythium oligandrum; Pch: Phaeomoniella chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
Figure 4. Characteristics of the grapevine transcriptome evolution for genes involved in hormone biosynthesis pathways between 0- and 14-dpi. Expression level values of genes encoding proteins involved in the synthesis or regulation of hormones (ABA: abscisic acid, ACC: 1-aminocyclopropane 1-carboxylate and GA: gibberellin) are given as the fold change on a log2 basis. The red color means overexpression at 14-dpi and the green color means overexpression at 0-dpi. Mock: mock inoculation; Po: Pythium oligandrum; Pch: Phaeomoniella chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
Ijms 21 06876 g004
Ijms 21 06876 g005 550
Figure 5. Global aspects of the grapevine transcriptome evolution for the transcription factor functional category between 0- and 14-dpi. Expression level values are given as a fold change on a log2 basis. The red color means overexpression at 14-dpi and the green color means overexpression at 0-dpi. Mock: mock inoculation; Po: Pythium oligandrum; Pch: Phaeomoniella chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
Figure 5. Global aspects of the grapevine transcriptome evolution for the transcription factor functional category between 0- and 14-dpi. Expression level values are given as a fold change on a log2 basis. The red color means overexpression at 14-dpi and the green color means overexpression at 0-dpi. Mock: mock inoculation; Po: Pythium oligandrum; Pch: Phaeomoniella chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
Ijms 21 06876 g005
Ijms 21 06876 g006 550
Figure 6. Phaeomoniella chlamydospora transcripts detected by RNAseq analysis in grapevine wood tissues according to the treatment (Pch: P. chlamydospora; PoPch: Pythium oligandrum and P. chlamydospora).
Figure 6. Phaeomoniella chlamydospora transcripts detected by RNAseq analysis in grapevine wood tissues according to the treatment (Pch: P. chlamydospora; PoPch: Pythium oligandrum and P. chlamydospora).
Ijms 21 06876 g006
Ijms 21 06876 g007 550
Figure 7. Expression level of Phaeomoniella chlamydospora genes predicted as secondary metabolites producers obtained in the RNAseq experiment. Expression level values are given as FPKM (fragments per kilobase per million mapped fragments). nrps = non-ribosomal peptide synthetase; t1pks = type 1 polyketide synthase. Pch: P. chlamydospora; PoPch: Pythium oligandrum and P. chlamydospora. Light blue means that the number of transcripts is lower than in the other treatment. Dark blue means the number of transcripts is higher than in the other treatment. Blank means no transcripts detected in the samples.
Figure 7. Expression level of Phaeomoniella chlamydospora genes predicted as secondary metabolites producers obtained in the RNAseq experiment. Expression level values are given as FPKM (fragments per kilobase per million mapped fragments). nrps = non-ribosomal peptide synthetase; t1pks = type 1 polyketide synthase. Pch: P. chlamydospora; PoPch: Pythium oligandrum and P. chlamydospora. Light blue means that the number of transcripts is lower than in the other treatment. Dark blue means the number of transcripts is higher than in the other treatment. Blank means no transcripts detected in the samples.
Ijms 21 06876 g007
Ijms 21 06876 g008 550
Figure 8. Protein kinase (PK) pathways in plant pathogenic fungi [22]. PKs are shown in colors. PKs involved in the same pathway have the same color. PKs involved in two different pathways are presented in two colors. Red circles containing the letter P indicate phosphorylated amino acid residues. Pie charts correspond to the expression level of Phaeomoniella chlamydospora genes encoding PKs in P. chlamydospora treatment (Black), and Pythium oligandrum + P. chlamydospora (yellow) treatments. Only PK genes detected in our data are shown. Expression level values are given as FPKM (fragments per kilobase per million mapped fragments). Abbreviations: AC, adenylate cyclase; PKAc, protein kinase A catalytic subunit; TORC1, target of rapamycin complex 1.
Figure 8. Protein kinase (PK) pathways in plant pathogenic fungi [22]. PKs are shown in colors. PKs involved in the same pathway have the same color. PKs involved in two different pathways are presented in two colors. Red circles containing the letter P indicate phosphorylated amino acid residues. Pie charts correspond to the expression level of Phaeomoniella chlamydospora genes encoding PKs in P. chlamydospora treatment (Black), and Pythium oligandrum + P. chlamydospora (yellow) treatments. Only PK genes detected in our data are shown. Expression level values are given as FPKM (fragments per kilobase per million mapped fragments). Abbreviations: AC, adenylate cyclase; PKAc, protein kinase A catalytic subunit; TORC1, target of rapamycin complex 1.
Ijms 21 06876 g008
Ijms 21 06876 g009 550
Figure 9. Regulatory proteins (RP) involved in the regulation of secondary metabolism gene clusters in fungi [23]. Regulatory proteins are shown in colors. Arrows and bars refer to direct interactions. Pie charts correspond to the expression level of Phaeomoniella chlamydospora genes encoding these RP in P. chlamydospora treatment (black), and Pythium oligandrum + P. chlamydospora (yellow) treatments. Only regulatory RP genes detected in our data are shown. Expression level values are given as FPKM (fragments per kilobase per million mapped fragments). Abbreviations: CBC: CCAAT-binding complex; CpcR1: cephalosporin C regulator 1; LaeA: loss of aflR expression A; RsmA: restorer of secondary metabolism A; SAGA-ADA: Spt-Ada-Gcn55-acetyltransferase-ADA. Reprinted by permission from Nature Publishers [24].
Figure 9. Regulatory proteins (RP) involved in the regulation of secondary metabolism gene clusters in fungi [23]. Regulatory proteins are shown in colors. Arrows and bars refer to direct interactions. Pie charts correspond to the expression level of Phaeomoniella chlamydospora genes encoding these RP in P. chlamydospora treatment (black), and Pythium oligandrum + P. chlamydospora (yellow) treatments. Only regulatory RP genes detected in our data are shown. Expression level values are given as FPKM (fragments per kilobase per million mapped fragments). Abbreviations: CBC: CCAAT-binding complex; CpcR1: cephalosporin C regulator 1; LaeA: loss of aflR expression A; RsmA: restorer of secondary metabolism A; SAGA-ADA: Spt-Ada-Gcn55-acetyltransferase-ADA. Reprinted by permission from Nature Publishers [24].
Ijms 21 06876 g009
Table
Table 1. CAZymes genes predicted in the Phaeomoniella chlamydospora genome and transcripts detected in the RNAseq samples. Within parentheses: the number of genes related to CAZymes that could be potentially secreted (SignalP positive). Pch: P. chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
Table 1. CAZymes genes predicted in the Phaeomoniella chlamydospora genome and transcripts detected in the RNAseq samples. Within parentheses: the number of genes related to CAZymes that could be potentially secreted (SignalP positive). Pch: P. chlamydospora; PoPch: P. oligandrum and P. chlamydospora.
FamiliesNumber of Genes Predicted in the GenomeNumber of Genes Detected in Samples
PchPoPch
Glycoside hydrolases (GH)345 (72)60 (17)70 (9)
Glycosyl transferases (GT)268 (17)34 (3)69 (7)
Carbohydrate-binding module (CBM)141 (26)27 (6)37 (4)
Carbohydrate esterases (CE)107 (12)13 (1)10 (3)
Auxiliary Activities (AA)56 (14)9 (0)7 (2)
Polysaccharide Lyases (PL)4 (1)2 (0)1 (1)

Share and Cite

MDPI and ACS Style

Yacoub, A.; Magnin, N.; Gerbore, J.; Haidar, R.; Bruez, E.; Compant, S.; Guyoneaud, R.; Rey, P. The Biocontrol Root-Oomycete, Pythium Oligandrum, Triggers Grapevine Resistance and Shifts in the Transcriptome of the Trunk Pathogenic Fungus, Phaeomoniella Chlamydospora. Int. J. Mol. Sci. 2020, 21, 6876. https://doi.org/10.3390/ijms21186876

AMA Style

Yacoub A, Magnin N, Gerbore J, Haidar R, Bruez E, Compant S, Guyoneaud R, Rey P. The Biocontrol Root-Oomycete, Pythium Oligandrum, Triggers Grapevine Resistance and Shifts in the Transcriptome of the Trunk Pathogenic Fungus, Phaeomoniella Chlamydospora. International Journal of Molecular Sciences. 2020; 21(18):6876. https://doi.org/10.3390/ijms21186876

Chicago/Turabian Style

Yacoub, Amira, Noel Magnin, Jonathan Gerbore, Rana Haidar, Emilie Bruez, Stéphane Compant, Rémy Guyoneaud, and Patrice Rey. 2020. "The Biocontrol Root-Oomycete, Pythium Oligandrum, Triggers Grapevine Resistance and Shifts in the Transcriptome of the Trunk Pathogenic Fungus, Phaeomoniella Chlamydospora" International Journal of Molecular Sciences 21, no. 18: 6876. https://doi.org/10.3390/ijms21186876

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop