Background

Rosellinia necatrix is a soilborne ascomycete, belonging to the order Xylariales, which causes white root rot (WRR) disease in a wide range of commercially important crops and ornamental plants. It has been reported that R. necatrix can infect over 170 plant species from 63 genera and 30 families [1], listed in 344 R. necatrix-host combinations by the United States Department of Agriculture [2]. This pathogen has a worldwide distribution being able to survive in temperate, tropical and subtropical climates [3,4,5,6].

In the Mediterranean region of Spain, WRR is especially damaging due to the co-occurrence of favorable environmental conditions for the development of the fungus and susceptible hosts such as avocado (Persea americana Mill.) and mango (Mangifera indica L.) [7, 8]. Nowadays it is considered as one of the most important threats affecting avocado productivity [7].

Affected avocado trees show rotten roots and are characterized by a yellowing of the leaves that eventually wilt and ultimately, results in death of the tree. R. necatrix root invasion usually occurs by the formation of mycelial aggregates over the root surface which penetrate the root tissues among epidermal and cortical cells and finally, collapse the vascular system of the plant [9]. Neither chemical nor physical methods have proven to be fully effective to control this disease due to the capacity of the fungus to survive in acidic soils as well as to colonize numerous hosts; in addition, the pathogen is quite resistant to drought [4, 7]. Nowadays, the obtainment of tolerant rootstocks appears as the most promising approach to control this disease and efforts are underway to reach this goal [10].To add future developments in disease resistance, systematic analysis of pathogenic fungi’s genomes and transcriptomes has become a top priority. Thus, in recent years, many researchers have addressed transcriptomics studies of plant pathogenic fungi/host interactions [11,12,13]. The analyses of gene expression profiles associated with the fungal infection provides key sources for understanding fungal biology, leading to the identification of potential pathogenicity determinants [11, 14,15,16,17]. Recently, Shimizu et al. [13] provided a 44-Mb draft genome sequence of R. necatrix virulent strain W97, in which 12,444 protein encoding genes were predicted. The transcriptome analysis of the hypovirulent strain W97, infected with the megabirnavirus 1 (RNmbv1), revealed that primary and secondary metabolism, as well as genes encoding transcriptional regulators, plant cell wall-degradating enzymes (CWDE), and toxin production such as cytochalasin E, were greatly disturbed in the hypovirulent strain. In another study, the transcriptome analysis of the virulent R. necatrix strain (KACC40445) identified 10,616 full-length transcripts among which, pathogen related effectors and CWDE encoding genes were predicted [12]. Data presented in both transcriptomics studies are a valuable resource of genetic information; however, to get a deep insight into pathogenesis of R. necatrix a comprehensive transcriptomic analysis of a virulent R. necatrix strain interacting with its host is necessary. With this aim, this research addresses the comparison of the transcriptomic profiles of R. necatrix during infection of susceptible avocado `Dusa´ roots (RGA) and in vitro growth on PDA (Potato Dextrose Agar) media (RGPDA) using RNA-Seq technology. Functional classification based on assignments to publicly available datasets was conducted, and potential pathogenicity genes related to R. necatrix virulence were identified providing a better understanding of the WRR disease.

Results

Comparative transcriptome analysis of R. necatrix growing on avocado roots vs PDA medium

A transcriptome analysis was carried out to capture genes expressed during R. necatrix growth on susceptible `Dusa´ avocado roots and on PDA medium, in order to compare their expression profiles (Fig. 1). The RNA-Seq data including the raw reads from three biological replicates of R. necatrix CH53 virulent strain colonizing avocado roots (RGA1; RGA2 and RGA3) and growing on culture medium (RGPDA1; RGPDA2 and RGPDA3) were processed. A total of 12,104 transcripts were obtained, among which 11,807 were present in both conditions, while 137 and 160 transcripts were exclusively expressed in either RGA or RGPDA, respectively (Fig. 2). Total transcripts were subjected to statistical analysis to evaluate differential gene expression between RGA vs RGPDA test situations. Analyses resulted in 1937 differentially expressed genes (DEG), 61.9% induced and 38.1% repressed (− 2 > fold change (FC) > 2; P-value < 0.05) (Fig. 3). A heat map of DEGs showed consistence in expression patterns among RGA1, RGA2 and RGA3 and among RGPDA1, RGPDA2 and RGPDA3, supporting the reliability of the RNA-Seq data (Fig. 4).

Fig. 1
figure 1

RNA-Seq Experimental Design. Schematic representation of the transcriptome analysis carried out in R. necatrix growing on avocado roots in comparison with its growth on Potato Dextrose Agar (PDA) media

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Fig. 2
figure 2

Venn diagram of transcripts expressed during R. necatrix growth on avocado roots vs rich medium. Numbers of common and specific transcripts obtained in the transcriptome analysis of R. necatrix growing on avocado roots (RGA) in comparison with its growth on Potato Dextrose Agar media (RGPDA). Unique transcripts are shown in only one of the two circles while shared transcripts are illustrated where the circles meet

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Fig. 3
figure 3

Volcano Plot analysis of differentially expressed genes. Volcano plot summarizing the RNA-Seq DEGs. Significantly up-regulated (right side) or down-regulated (left side) DEGs in R. necatrix that also passed the 2 fold-change threshold is shown in green, or in red if the threshold criteria were not met. Non-significantly expressed genes are shown in orange if above or below the fold-change threshold, or black if no criteria were passed

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Fig. 4
figure 4

Hierarchical clustering of differentially expressed genes (DEGs). Hierarchical clustering during R. necatrix infection on avocado roots (RGA1, RGA2 and RGA3) in comparison with its in vitro growth on Potato Dextrose Agar media (RGPDA1, RGPDA2, RGPDA3). Red and green indicate up- and down regulation, respectively

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Validation of the RNA-Seq analysis

Differences found in gene expression profiles between RGA vs RGPDA were further verified through a quantitative real time PCR (qRT-PCR) assay on total cDNA samples from mycelia of three biological replicates. For this, five randomly selected genes over-expressed in RGA vs RGPDA and with different FC, were analyzed. Actin gene was used as reference gene for data normalization. The expression levels of these genes amplified by qRT-PCR are shown in Table 1. Although higher expression values were obtained by qRT-PCR than those observed on the RNA-Seq, results corroborated the overall differences found between the two samples (RGA and RGPDA) in the RNA-Seq analysis.

Table 1 qRT-PCR and RNA-Seq expression data of selected contigs over-expressed during R. necatrix growth on avocado roots
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Functional annotation and pathways analysis of differentially expressed genes (DEGs)

To better understand the infection process of R. necatrix colonizing susceptible avocado roots, all differentially expressed genes were functionally enriched and categorized based on blast sequence homologies and gene ontology (GO) annotations using Blast2GO software [18] (P < 0.05), selecting the NCBI blast Fungi as taxonomy filter and default parameters. DEGs were significantly grouped into the regulation of eight molecular function (MF), such as heme binding (GO:0020037), iron ion binding (GO:0005506), oxidoreductase activity acting on CH-OH group of donors (GO:0016614), flavin adenine dinucleotide binding (GO:0050660), cellulose binding (GO:0030248), NADP binding (GO:0050661), peroxidase activity (GO:0004601) and N,N-dimethylaniline monooxygenase activity (GO:0004499), and three biological process (BP), such as carbohydrate transport (GO:0008643), cellular oxidant detoxification (GO:0098869) and mycotoxin biosynthesis (GO:0043386) (Fig. 5a). To identify processes and functions over-represented in R. necatrix during infection, GO term enrichment analysis was also applied to the Top 100 over-expressed genes (Fig. 5b). The functions of these DEGs were significantly enriched in the regulation of five BP, such as oxido-reduction process (GO:0055114), cellulose catabolic process (GO:0030245), mycotoxin biosynthesis (GO:0043386), glucose import (GO:0046323) and response to hydrogen peroxide (GO:0042542), and 13 MF (Fig. 5b) among which activities related to plant cell wall degradation, including glucosidase activity (GO:0015926); endo-1,4-β-xylanase activity (G0:0031176); cellulose 1,4-beta-cellobiosidase activity (GO:0016162); xyloglucan-specific exo-β-1,4-glucanase activity (GO:0033950) and arabinogalactan endo-1,4-β-galactosidase activity (GO:0031218) were found.To investigate the metabolic pathways affected in R. necatrix during avocado root infection, a KEGG pathway analysis was performed with Blast2go [18]. For the total of 1937 DEGs, 100 metabolic pathways that involved 208 genes were identified (P-value < 0.05). The metabolic pathways were reorganized into eleven categories (Table 2) being the nucleotides metabolism the one with the highest number of genes (n = 64). Interestingly, metabolic pathways involved in antibiotic and drug metabolism were also affected, in accordance with GO enrichment analysis results, where mycotoxin biosynthetic process was one of the molecular functions over-represented.

Fig. 5
figure 5

Gene Ontology (GO) enrichment analysis of differentially expressed genes (DEGs). a. GO enrichment analysis of DEGs obtained in the transcriptome analysis of R. necatrix growing on avocado roots (RGA) in comparison with its growth on Potato Dextrose Agar media (RGPDA). b. GO enrichment analysis of the TOP100 DEGs obtained in the transcriptome analysis of RGA vs RGPDA. Enrichment GO terms were obtained by Blast2GO using a cut-off of P < 0.05. (BP) biological process; (MF) molecular function

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Table 2 The KEGG pathway analysis using differentially expressed genes (DEGs)
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Candidate genes involved in the pathogenesis of R. necatrix

At least 69 transcripts showing homology to genes previously reported to be involved in fungal infection were identified among the 1937 DEGs. These include homologs to genes involved in the production of CWDE (Table 3), proteases, fungal toxins, detoxification and transport of toxic compounds, gibberellin biosynthesis and gene silencing (Table 4) as well as gene effectors (Table 5). Out of the 69 selected genes, 30 were associated with cell wall hydrolysis, among which 16 showed fold change (FC) values above 50, with three of them (SAMD00023353_0503130, SAMD00023353_6500680 and SAMD00023353_4001240) allocated in the top20 over-expressed genes in R. necatrix during avocado root-colonization (Table 3 and Additional file 1). Five genes were identified as proteases, two aspartic proteases and three serine proteases, with the contig SAMD00023353_1500930 expressed over 411 times in RGA vs RGPDA (Table 4). Five contigs showed homology to genes encoding fungal toxins, among which the contig SAMD00023353_5500610 encoding the putative aflatoxin B1 aldehyde reductase member 2 showed the higher transcript abundance with a FC value of 18.65 (Table 4).

Table 3 R. necatrix genes encoding cell wall degrading enzymes
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Table 4 Genes of R. necatrix potentially involved in pathogenesis
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Table 5 List of candidate effectors genes in R. necatrix
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Nineteen genes were related to degradation of toxic compounds such as reactive oxygen species (SAMD00023353_5200870), aflatoxins (SAMD00023353_0902760, SAMD00023353_12800020, SAMD00023353_3200110), and antibiotics (SAMD00023353_3600430, SAMD00023353_6600160, SAMD00023353_0702510, SAMD00023353_0100280, SAMD00023353_2201610), among other drugs. R. necatrix also over-expressed genes related to transport of toxic compounds, in particular, four (SAMD00023353_2601150, SAMD00023353_2501030, SAMD00023353_3000620 and SAMD00023353_6200040) and two contigs (SAMD00023353_10000080 and SAMD00023353_2200710) showed homology with genes encoding ATP-binding cassette (ABC) transporters and major facilitator superfamily (MFS) transporters, respectively. Expression values of genes homologous to ABC transporters were higher (FC values ranging from 5 to 7) than those observed for MFS transporters (ranging from 2 to 3) (Table 4).

Two genes were selected for being associated with hormone biosynthesis (GA4 desaturase family protein SAMD00023353_10100030 and gibberellin 20-oxidase SAMD00023353_1901120) showing FC values of 38.2 and 2.39 respectively and one gene, the argonaute siRNA chaperone complex subunit Arb1 (SAMD00023353_0801000), postulated to play a role in RNA induced transcriptional silencing (Table 4).

The RNAseq analysis also revealed 137 genes only expressed in R. necatrix during its growth on avocado roots. From those contigs, 24 were predicted as candidate effector proteins (CEP) by the CSIRO tool EffectorP2 (a machine learning method for fungal effector prediction in secretomes) [19] with a probability above 60% (Table 5). All CEPs, except for SAMD00023353_2100110, SAMD00023353_2801560, SAMD00023353_3900800, SAMD00023353_11900020 and SAMD00023353_1700590, showed no similarity with proteins in the public database. Out of the 24 CEP, 13 were predicted to be secreted by SignalP3 server and ten were determined to have an apoplastic localization by the CSIRO tool ApoplastP (a machine learning method for predicting localization of proteins) [20] (Table 5).

To test any existing relationship within the candidate effectors proteins identified in this study with previously described effectors proteins, the PHI (Pathogen Host Interaction) database was used; i.e., PHI-base is a database of virulence and effector genes that have been experimentally proven via pathogen-host interaction [21]. Blastp was used to match PHI-base with an e-value cutoff of 1E-03 and 30% identity. As result, 3 R. necatrix candidate effectors were annotated, SAMD00023353_11900020 encoding a putative glycoside hydrolase, showed the higher percentage of identity with the effector Lysm from Penicillium expansum (Identity 44.58%, E-value 9.94 E-53). SAMD00023353_2100110 and SAMD00023353_1700590 showed identity with effectors BEC1040 and Mocapn7 from Blumeria graminis (Identity 32.76%, E-value 1.32 E-05) and Magnaporthe oryzae (Identity 35.82%, E-value 1.32 E-03), respectively.

Discussion

Transcriptome analysis of R. necatrix strains growing on rich medium, has recently been addressed as an alternative to provide insights into plant pathogenicity mechanisms used by this ascomycete [12, 13]. However, neither of the two studies was carried out using R. necatrix directly interacting with a host. This current study fills this gap, obtaining and analyzing the transcriptomes of the virulent CH53 strain during infection of avocado roots and comparing it with that obtained from the fungus cultured in rich medium.

The number of predicted genes (12,104) obtained in this study is congruent with data from previous transcriptomes from R. necatrix (10,616 [12];), as well as other plant pathogenic Ascomycota, such as Fusarium graminearum (13,332 genes [22];), Valsa mali (13,046 genes [11];), or Magnaporte oryzae (11,101 genes [23];). When comparing gene expression profiles between R. necatrix infecting avocado roots or growing on PDA medium, a number of transcripts were related with major fungal traits involved in the interaction with the host, among others, CWDE [24], production of toxic compounds and detoxification of those produced by the host, or potential effectors.

Phytopathogenic fungi usually produce numerous extracellular enzymes in order to penetrate the host tissue, being cell wall hydrolases and pectinases the most important ones [25]. The high number of CWDE over-expressed during the infection process correlates with previous visualization studies of R. necatrix hyphae that directly penetrate through the avocado root cells [9]. In addition, five putative proteases were also identified. Interestingly, gene expression studies carried out on avocado revealed that three protease inhibitors were highly over-expressed in tolerant rootstocks to R. necatrix following inoculation with the pathogen but not in susceptible genotypes [10]. This finding suggests that these proteases, up-regulated in R. necatrix during the infection process, could play an important role in degrading basal defense proteins on susceptible avocado roots, however, future experiments need to be carried out to confirm this hypothesis.

Several studies support the idea that R. necatrix produce toxins that are likely responsible for the symptoms observed in the aerial parts of the plant [26, 27]. Cytochalasin E and rosnecatrone toxins produced by R. necatrix [28, 29] are believed to be involved in the onset of disease symptoms in young apple shoots and detached apple leaves [27]. Shimizu et al., [13], identified the cytochalasin biosynthetic gene cluster, containing fourteen genes, within a 36 kb region of the R. necatrix strain W97 genome. In the present study, only one gene (putative aflatoxin B1 aldehyde reductase protein) of the putative cytochalasin cluster was highly up-regulated, while it was down-regulated in transcriptomic analyses carried out in the hypovirulent R. necatrix strain [13] (Additional file 2). Taking this into consideration, this gene could play an important role in the pathogenicity of R. necatrix CH53 on avocado roots, however the role of the cytochalasin E in virulence remains unclear as suggested by other authors [30]. Four more genes related with the production of fungal toxins were up-regulated during the infection process, two of them (putative sterigmatocystin 8-O-methyltransferase and the averantin oxidoreductase) had been previously described to be involved in aflatoxin biosynthesis [31]. Aflatoxins are considered as the most toxic and carcinogenic compounds among the known mycotoxins and 25 clustered genes have been reported to be involved in its biosynthesis [31, 32]. Although the expression of other genes potentially involved in aflatoxin biosynthesis was not observed and no aflatoxin production, even at minimum concentration (< 1 μg/Kg), was detected in wheat grains infected with R necatrix (data not shown), future studies should address the detection of this compound on infected roots due to its high toxigenic nature.

As other necrotrophic pathogens, R. necatrix seems to have adapted mechanisms to detoxify host metabolites that can interfere with its virulence [33]. Nineteen genes potentially involved in detoxification of antimicrobial compounds were significantly over-expressed. Interestingly, SAMD00023353_12800020 and SAMD00023353_3200110, both repressed in the hypovirulent R. necatrix strain [13], showed homology to genes previously described to be involved in detoxification of phytoalexins. The importance of phytoalexin degradation ability in pathogenesis has been proved through transformation experiments [34]. To date, no phytoalexin production has been reported in ‘Dusa’ avocado rootstocks however, mutation experiments of these two genes would be of great interest to reveal their role in degradation of possible fungal toxic compounds produced by avocado roots.

Other contigs were related to transport mechanisms by which endogenous and exogenous toxicants can be secreted. Two major classes of transporter proteins were represented in R. necatrix DEGs such as ABC and MFS transporters. Members of both classes can have broad and overlapping substrate specificities for toxic compounds and have been considered as a “first-line fungus defense barrier” [35].

Some necrotrophs are also able to influence host phytohormone levels or employ their own hormone biosynthesis machinery thereby disrupting defense signaling [24, 36,37,38,39,40,41]. Two genes involved in gibberellin biosynthesis, GA4 desaturase family protein and Gibberellin 20-oxidase, were up-regulated during the infection process. Role of GAs in plant-pathogen interactions is not well known [42]; i.e., Studt et al. [43] showed the positive relation between GA production and bakanae disease in rice while Manka [44] found no correlation between GA production and pathogenesis of Fusarium.

Throughout the infection process, fungi can actively manipulate host cellular machinery in order to suppress defenses and/or aid disease progression throughout the release of the so-called ‘effector’ proteins [45]. These effectors are usually secreted proteins that act at the host cell surface [46] or are taken up by the plant cell and act internally [47]. In this investigation, a total of 23 genes were predicted to be effectors (with probability above 60%), among which 19 encoded for hypothetical proteins and 10 were predicted as apoplastic effectors, being their place of action the interphase between the hyphae and the host cell. One of the predicted effectors, showed homology to the Lysm1 effector of Penycilium expansum. Lysm-containing proteins have been proposed to be involved in binding and sequestering chitin oligosaccharides in order to prevent elicitation of host immune responses [48] and/or to protect fungal hyphae against chitinases secreted by competitors [49]. In this sense, the expression of this effector during R. necatrix infection correlates with previous studies in which the overexpression of chitinases on susceptible avocado rootstocks/R. necatrix interaction, was reported [10]. Finally, other contig showed homology with the previously described Blumeria graminis effector gene BEC1040, which reduces haustoria formation in barley powdery mildew when silenced [50]. These results confirm previous observations by [12], in which BEC1040 homologous effectors in the virulent R. necatrix strain KACC40445 were found.

Conclusion

This study revealed, for the first time, several genes potentially associated with R. necatrix pathogenesis on avocado roots. The analysis of the full-length transcriptome of R. necatrix during the infection process suggests that the success of this fungus to infect diverse crops might be attributed to a number of produced compounds such as CWDE, toxins, antimicrobial detoxification compounds, transporters, effectors which, singly or in combination, likely interfere with defense or signaling mechanisms found on different plant families [24]. These results are revealing the complexity underlying R. necatrix pathogenesis being consistent with the difficulty of WRR management.

Functional characterization of these genes could help to understand how the fungus interferes with the host machinery and the development of white root rot disease. Along this line, a genetic manipulation protocol for transformation of R. necatrix has been established, although its efficiency needs to be improved [9]. Nevertheless, the transcriptome analysis of R. necatrix during the infection process provides useful information and facilitates further research to a more in -depth understanding of the biology and virulence of this pathogen. In turn, this will make possible to evolve novel strategies for white root rot management in avocado.

Methods

Plant material, fungal isolate and inoculation

Clonal 1 year old ‘Dusa™’ plants, described as susceptible to R. necatrix [51] and provided by Brokaw nursery (Brokaw España S.L), were potted in 1.5 L plastic pots, previously disinfected with hypochlorite solution (2%) with an sterilized substrate consisting in peat, coconut fibre and perlite mixture (10:10:1) supplemented with 12 g osmocote® and placed into a semi-controlled greenhouse conditions (~ 20 °C temperature and ~ 60% relative humidity). The virulent CH53 fungal strain, isolated at Almuñecar (Granada, Spain) [52], was used in this study and cultured on potato dextrose agar (PDA; Difco Laboratories, Detroit, USA) at 25 °C.

For transcriptome analysis of R. necatrix growing on rich medium, the isolate was cultured on PDA covered with a perforated layer of cellophane and incubated 5 days at 25 °C.

For RNA-Seq analysis of R. necatrix during infection, plants were removed from the pot and roots were washed with distilled water to remove soil debris. Roots were cut and placed into 15 cm diameter Petri dishes covered with three layers of filter paper soaked with sterilized distilled water. Three perforated cellophane discs, 6 cm diameter, were placed along the roots (Fig. 1). The inoculation was carried out by placing two wheat grains infected with R. necatrix onto each cellophane disc. Petri dishes were closed, sealed with parafilm and incubated in dark for 5 days.

RNA isolation and sequencing

For RNA extractions, cellophane discs covered with grown mycelium, were collected and macerated with liquid nitrogen using a mortar and pestle. One g of frozen powder was collected in a 2 ml Eppendorf and resuspended in 1 ml of denaturation solution (guanidine thiocyanate, 4 M, Na-citrate 25 mM sarcosyl, 0.5%) (Fluka; Switzerland) and saturated phenol pH 4.3 (1:1) plus 7 μl of β-Mercaptoethanol. One hundred μl chloroform were added to the mixture; samples were vortexed and incubated 3 min at room temperature and centrifuged at 12,000 g for 10 min at 4 °C. Afterwards, RNA was extracted using NucleoSpin RNA plant kit (Macherey-Nagel, Germany) following manufacturer’s instructions.

DNAase I (DNase I, Thermo, USA) treatment was carried out twice, during and after the extraction process. RNA quantity and quality were determined based on absorbance ratios at 260 nm/280 nm and 260 nm/230 nm using a NanoDrop® ND-1000 (Nanodrop Technologies, Inc., Montchanin, USA) spectrophotometer. RNA integrity was confirmed by the appearance of ribosomal RNA bands and lack of degradation products after separation on a 2% agarose gel and Red Safe staining.

The integrity of the RNA samples was further verified using the 2100 Bioanalyzer (Agilent Technologies, Inc., Santa Clara, USA) and submitted to the Centre Nacional d’Anàlisi Genòmica (CNAG, Barcelona, Spain) for sequencing. Two μg RNA from each sample were used for RNA library preparation using the TruSeq RNA Sample Preparation Kit (Illumina Inc) according to the protocols recommended by the manufacturer. Each library was paired-end sequenced (2 × 76 bp) by using the TruSeq SBS Kit v3-HS, in a HiSeq2000 platform. More than 40 million reads were generated for each sample. The RNA-Seq reads from six libraries (three biological replicates per condition) were processed to remove adaptor sequences, empty reads, low-quality sequences with a Phred score lower than 20 and short reads (< 25 bp). Resulting reads were stored in FASTQ format. High quality reads were aligned to the R. necatrix reference genome [13] for generation of read counts and differential expression analysis. CH53 RNA-seq reads were mapped to the W97 genome and consensus sequences were made of the mapped reads. The overall rate of base changes in the mapped regions between the CH53 and W97 strains was 0.75%. Raw reads from three biological replicates of R. necatrix growing on avocado roots and PDA media, are available from the NCBI Gene Expression Omnibus under accession number GSE134243.

A statistical analysis of the expression data of R. necatrix growing on avocado roots (RGA) vs Potato Dextrose Agar (RGPDA) media was performed by the Empirical analysis of DGE (EDGE) in CLC Genomics Workbench 10.0.0 (CLC Bio, Aarhus, Denmark). The DEGs were identified using the following conditions: − 2 > fold change > 2 and FDR (P < 0.05). A visual representation of DEGs log10 FDR P-value vs log2 Fold change was plotted in R (version 3.6) with a simple scatterplot color coding the different conditions.

Gene predictions and annotations

R. necatrix predicted genes were searched against NCBI Fungi databases to assign associated Gen Ontology (GO) annotations using Blast2Go [18]. GO enrichment analysis (Fisher’s Exact test, [53]) and KEGG pathway analyses were carried out by Blast2go 5.2.4. Default parameters were used with a cut-off FDR of 0.05. GO enrichment analysis (Fisher’s Exact test, [53]) describing the enriched biological processes (BP), molecular functions (MF) and cellular components (CC) of DEGs was performed with B2G according to the following parameters: filter mode as P-Value and 0.05 as filter value. Kyoto Encyclopedia of Genes and Genomes (KEGG) annotations [54] of DEGs was performed with B2G.

Genes were clustered using TIGR Multi Experiment Viewer 4.6.1 [55] with Euclidean distances and Average linkage.

SignalP 3.0 server [56] was used to predict the presence and location of signal peptide cleavage sites in amino acid sequences. Localization of proteins to the plant apoplast was predicted by the CSIRO tool ApoplastP [20]. Relationships within the candidate effectors proteins identified in this study with previously described effectors proteins was tested using the PHI (Pathogen Host Interaction) database [21].

Quantitative real-time PCR

Validation of gene expression levels obtained from the transcriptome analysis was performed using qRT-PCR.

One μg of total RNA was treated with DNase RNase-free (Promega, Madison, USA) following the manufacturer’s instructions. Single-stranded cDNA was synthesized using the iScript cDNA synthesis kit (BIO-RAD, California, USA) following the manufacturer’s instructions. The expression of five R. necatrix genes was studied. One endogenous control gene, actin, was used for normalization. Primer sequences for endogenous control gene and the five R. necatrix genes are presented in Additional file 3. Primer pairs were chosen to generate fragments between 50 and 150 bp with melting temperature of 60 °C and designed using Primer 3 software [57, 58].

Primer specificity was tested by first performing a conventional PCR and confirmed by the presence of a single melting curve during qRT-PCR. Serial dilutions (1∶10, 1∶20, 1∶50, 1∶200) were made from a pool of cDNA and calibration curves were performed for each gene. The qRT-PCR reaction mixture consisted of cDNA first-strand template, primers (500 nmol final concentration) and SYBR Green Master Mix (SsoAdvanced Universal SYBR Green Supermix, Bio-Rad) in a total volume of 20 μl. The PCR conditions were as follows: 30 s at 95 °C, followed by 40 cycles of 10 s at 95 °C and 15 s at 60 °C. The reactions were performed using an iQ5 real-time PCR detection system (Bio-Rad). Relative quantification of the expression levels for the target was performed using the comparative Ct method [59]. Three biological replicates of RGA or RGPDA vs control samples were performed in triplicate. Statistical significance of the data was determined by a Student’s t-test carried out with Sigma Stat version 4.0 software (Systat Software GmbH).