QTLs and eQTLs mapping related to citrandarins’ resistance to citrus gummosis disease

Background Phytophthora nicotianae Breda de Haan (Phytophthora parasitica Dastur) causes severe damage to citrus crops worldwide. A population of citrandarins was created from the cross between the susceptible parent Citrus sunki Hort. Ex Tan. and the resistant parent Poncirus trifoliata (L.) Raf. cv. Rubidoux, both parents and two reference rootstocks (Rangpur lime and Swingle citrumelo) were grafted in a greenhouse on Rangpur lime. Inoculations were performed at 10 cm and 15 cm above the grafting region and the resulting lesions were evaluated by measuring the lesion length 60 days after inoculation. As control, non-inoculated plants of each genotype were used. In addition, we evaluated the expression of 19 candidate genes involved in citrus defense response 48 h after pathogen infection by quantitative Real-Time PCR (qPCR). We mapped genomic regions of Quantitative Trait Loci (QTLs) and Expression Quantitative Trait Loci (eQTLs) associated with resistance to P. parasitica in the linkage groups (LGs) of the previously constructed maps of C. sunki and P. trifoliata. Results We found disease severity differences among the generated hybrids, with lesion lengths varying from 1.15 to 11.13 mm. The heritability of the character was 65%. These results indicate that there is a great possibility of success in the selection of resistant hybrids within this experiment. The analysis of gene expression profile demonstrated a great variation of responses regarding the activation of plant defense pathways, indicating that citrandarins have several defense strategies to control oomycete infection. The information of the phenotypic and gene expression data made possible to detect genomic regions associated with resistance. Three QTLs and 84 eQTLs were detected in the linkage map of P. trifoliata, while one QTL and 110 eQTLs were detected in C. sunki. Conclusions This is the first study to use eQTLs mapping in the Phytophthora-citrus interaction. Our results from the QTLs and eQTLs mapping allow us to conclude that the resistance of some citrandarins to the infection by P. parasitica is due to a favorable combination of QTLs and eQTLs transmitted by both parents. Electronic supplementary material The online version of this article (10.1186/s12864-018-4888-2) contains supplementary material, which is available to authorized users.


Background
Hybrids of microtangerines, such as the ones obtained from the cross of Sunki mandarin (Citrus sunki Hort. Ex Tan.) with trifoliate [Poncirus trifoliata (L.) Raf.], are called citrandarins. They are part of a new generation of rootstocks for citrus and combine the advantageous characteristics of mandarins, such as tolerance to Citrus blight and Citrus sudden death, with the qualities of trifoliates, which correspond to high resistance to Phytophthora, immunity to Citrus tristeza virus and resistance to citrus nematode, besides the great ability to form compact, productive plants with good fruit quality [1]. In a study on the Phytophthora-Citrus pathosystem, a F1 population from the crossing between C. sunki (susceptible parent) and P. trifoliata cv. Rubidoux (resistant parent) was obtained and evaluated for Phytophthora gummosis. Differences in the level of symptoms in both parents and progeny were observed [2]. Root rot, caused by Phytophthora, and gummosis and its various synonyms (foot rot, neck rot and trunk gum disease) are among the diseases that damage citrus crops. Citrus nurseries and orchards worldwide have been severely damaged by Phytophthora nicotianae Breda de Haan (Phytophthora parasitica Dastur) and Phytophthora citrophthora (Smith & Smith). In Brazil, P. parasitica is the most predominant species associated with the disease [3]. These pathogens can infect the main branches of the plants, inducing the formation of cankers with gum exudation of the lesions [3,4]. Infected plants usually lose their vigor and may die prematurely [5].
P. parasitica is an oomycete, which belongs to the kingdom Stramenopila, comprising a diversified group of organisms [6]. During infection, oomycetes establish intimate relationships with their hosts through the formation of haustoria, structures used to obtain nutrients from plants, reprogramming the host defense metabolism. Species from the genus Phytophthora are hemibiotrophic pathogens, which means they initiate the infection as biotrophic agents in the first 36-48 h and colonize the host as necrotrophic pathogens, alternating the way of obtaining nutrients in order to guarantee its dissemination from necrotic plant tissues [7]. Gummosis is considered the most serious disease caused by Phytophthora spp. The lesions caused by the Phytophthora grow around the tree trunk damaging the cambium and inner bark killing it [8].
It is known that more than one mechanism of resistance and/or tolerance are involved in the citrus defense response to Phytophthora due to the large differences in types of affected tissues, and consequently to different citrus species' responses to the infection. In general, responses that are common to all plant species affected by phytopathogens can be activated, such as hypersensitivity reaction (HR), the development of structural barriers and the production of antimicrobial compounds called phytoalexins. In addition, induction of specific responses to a given population of Phytophthora may occur, which are controlled by host resistance genes [9].
The great volume of information generated by genome sequencing projects has allowed a large-scale approach to differential gene expression analysis using techniques such as microarray, RNA Sequencing and qPCR (Real Time Quantitative PCR). Some information has already been produced to elucidate the molecular basis of the host response to Phytophthora gummosis disease [10,11]. These studies have reported on changes in global gene expression profile and have shown differentially expressed genes involved in processes such as cellular defense and metabolism of carbohydrates, lipids and proteins. Defense genes are activated in response to pathogen infection by signal transduction mechanisms, which are regulated by phytohormones pathways, with salicylic acid (SA), jasmonic acid (JA), ethylene (ET) and abscisic acid (ABA) being the most common ones [12].
According to Pieterse et al. [13], the crosstalk that occurs between the SA, JA and ET pathways confers a directed defense response against different plant pathogens. There is a synergy between the JA and ET pathways, while there is a mutual repression between these two pathways with the SA pathway. In addition, it has been shown that ABA, which is known as the abiotic stress hormone in plants and is considered a negative regulator of resistance to phytopathogens, may be involved in increasing plant resistance to disease through its positive effect on callose deposition. ABA may also contribute to plant defense by the convergence of signaling with the JA pathway, which synergistically triggers the expression of defense genes responsive to both hormones [13,14].
Genomics emerges as a technique that encompasses quantitative loci mapping and gene expression analysis to identify the association between the allelic status of a genome region and the quantification of gene transcripts [15]. These genomic regions are referred to as Expression Quantitative Trait Loci (eQTLs). The study of QTLs and eQTLs is of great importance for understanding pathogen-host interaction and to understand mechanisms of resistance and response to diseases.
In this study, we mapped the genomic regions associated with resistance to P. parasitica by means of phenotypic (QTLs) and expression (eQTLs) analyses in the linkage groups (LGs) of previously constructed maps of C. sunki and P. trifoliata. We evaluated the resistance of C. sunki x P. trifoliata hybrids to P. parasitica, as well as the expression of candidate genes related to resistance to P. parasitica by qPCR in the parents and hybrids used in the experiment.

Plant material and inoculation of P. parasitica
A population of 110 hybrids of C. sunki (susceptible to Phytophthora) x P. trifoliata (resistant) and parents was established in a greenhouse. Rangpur lime (Citrus limonia Osbeck) and Swingle citrumelo [Citrus paradisi Macfad. cv. Duncan x Poncirus trifoliata (L.) Raf.], two reference rootstocks in citrus cultivation, were also evaluated. Plants were multiplied by bud grafting using Rangpur lime as rootstock, and were kept in a greenhouse until the stem reached a diameter of approximately 0.8 to 1.0 cm.
The isolate IAC-01/95 from the isolates' collection of the Plant Pathology Clinic of Sylvio Moreira Citrus Center, which was obtained from infected soil, was used in this assay. Mycelial disks of the pathogen growing in carrot-agar culture medium [16], containing 1 ml of Rifampicin, 1 ml of Ampicillin and 2 ml of Benomyl per 1000 ml of the medium, were removed from the colonies and transferred to Petri dishes containing 15 ml of this medium.
To activate the pathogenicity of the isolate, a re-isolation was performed from the lesion sections of tissue infected with the pathogen's mycelium (pre-inoculation). Small portions of the lesions were taken and inoculated in Sicilian lemon fruits. These fruits were incubated at 25°C with a photoperiod of 16 h for nine days. Then, they were carefully opened under brief asepsis inside a flow cabinet. With the disease affecting a large area of the fruit, the contaminated seeds were removed and transferred to Petri dishes containing the selective culture medium with carrot-agar. They were subsequently kept at 25°C in the dark for six days, until the formation of the pathogenic mycelium.
The experimental design was a completely randomized assay with two replicates of each genotype and one plant per plot. Each hybrid was conducted with a single stem and inoculation was performed at 10 cm and 15 cm above the grafting region, totalizing two inoculations per genotype, as described by Siviero et al. [2]. This method consists of: disinfestation with alcohol of the surface of the trunk region to be inoculated; incision in the bark using a cork borer and removing a 5 mm diameter disc, thus exposing the cambium zone; introduction of a disk of equal diameter of virulent P. parasitica mycelium maintained in culture medium; placing back the same disc of the bark and protection of the wound site caused by inoculation with cotton and tape. As a control, and to remove the effect of the stress caused by the wound, only the incision itself was made in the bark of plants with a cork borer, without inoculation of the pathogen, in each genotype of the experimental population.

Evaluation of lesions and statistical analysis of phenotypic data
To evaluate the lesions, plants were maintained in an artificial lighting environment with a photoperiod of 16 h, a temperature of 25°C and a relative humidity of 85%, with daily irrigations. The resulting lesions were evaluated 60 days after inoculation by measuring the length of the injured area after bark removal of the trunk with the aid of a digital caliper, totally exposing the developed lesion.
For the normality's hypothesis of the data and for the statistical analysis, were used the average lengths of the lesions from inoculated individuals (LLI -Lesion length by inoculation) minus the average lengths obtained from control individuals (LLC -Lesion length in control), which were around 5 mm, due to the cork borer's diameter used to cause injury to the plant, resulting in the variable RLL (Real lesion length) [LLI -LLC = RLL]. A QQ-plot for the distribution of lesion means was obtained using the Minitab 18 software (http://www.minitab.com/), based on the Kolmogorov-Smirnov normality test, with log (base 10)-transformed phenotypic data.
Statistical analyses were performed using the SASM-AGRI software [17], applying the F-test for analysis of variance and using the appropriate statistical model in a completely randomized design. In addition, the Scott-Knott test for comparison of treatments means was also used.
The averages of the phenotypic data from the RLL evaluation of the progeny of the crossing between P. trifoliata and C. sunki were used to calculate the genetic parameters (heritability, variance, and coefficient of variation) for the variable measured using the model 83 of the SELEGEN-REML/BLUP software [18].

Leaf collection, RNA extraction and cDNA synthesis
Leaf collection was performed 48 h after inoculation of the pathogen in the plants. Leaves were placed in liquid nitrogen and stored in a − 80°C freezer until the extraction of RNA. The choice of collection time was based on previous time course studies that evaluated the systemic response of plants using the expression of genes involved in the Phytophthora-citrus interaction [11,19] and associated with the signaling pathways of phytohormones that activate several defense mechanisms in the plant.
Total RNA extraction from plant material was performed according to the lithium chloride (LiCl) method described by Chang et al. [20]. To avoid contamination with genomic DNA, samples were treated with DNase I, RNase-Free kit (Fermentas Life Sciences), following the manufacturer's recommendations. 300 mg of leaves from the same genotype were ground with liquid nitrogen and three tubes of the resulting macerate (100 mg each) were collected, totaling three biological replicates per genotype. Total RNA was then quantified in NanoDrop ND-8000 spectrophotometer (Thermo Scientific), and its integrity was evaluated with 1.2% denaturing agarose gel electrophoresis.
The cDNA was synthesized according to instructions from the Revertaid H Minus First Strand cDNA Synthesis Kit (Fermentas), using oligo (dT) primers, and then treated with RNAse H (1 U) to remove any RNA contamination. Subsequently, the obtained cDNA was diluted in RNAse-free water at the ratio of 1:50, with the three biological replicates of cDNA (50 μL each) being mixed. This formed a pool of samples represented in a single tube containing 150 μL of diluted cDNA from each genotype to be analyzed in gene expression and eQTL mapping assays.

qPCR for validation of gene expression
The expression of 19 candidate genes by qPCR (Additional file 1: Table S1), selected in previous studies with microarray and gene expression [10,11], was evaluated in 51 hybrids, the two parents (C. sunki and P. trifoliata), Rangpur lime and Swingle citrumelo. The selection of hybrids for the qPCR assays was performed based in the application of the Scott-Knott test on the phenotypic data, which were separated into three groups (susceptible [S]; moderately susceptible [MS]; and tolerant and/or resistant [T/R]). Six hybrids were selected and formed the S group together with the two susceptible rootstocks (C. sunki and Rangpur lime). Three hybrids formed the MS group, and 42 hybrids together with the two resistant rootstocks (P. trifoliata and Swingle citrumelo) formed the T/R group. In general, we screened for genes related to cellular defense processes, which involve the main pathways of phytohormones such as SA, JA, ET and ABA. Moreover, some genes, such as LEA5 and RPS4, found differentially expressed by microarray among P. trifoliata, C. sunki and in some hybrids, in order to be a strong candidate in Phytophthora resistance [10], and other genes, such as PR2, PR3 and PAL, which were induced within 48 h after infestation in previous time course studies evaluating target genes related to the pathosystem formed by Phytophthora with two citrus species phenotypically opposed to the invader, corresponding to P. trifoliata (resistant) and C. sunki (susceptible) [11], were also evaluated. As endogenous controls, the FBOX (F-box family protein), SAND (SAND protein family) and GAPC2 (Glyceraldehyde-3-phosphate dehydrigenase C2) genes were analyzed.
The oligonucleotides primers flanking the gene regions were synthesized using the Primer Express 2.0 software (Applied Biosystems), and checked for specificity by Primer-BLAST tool in the NCBI (National Center for Biotechnology Information) database. Their sequences were found in the literature, in studies evaluating qPCR experiments with Arabidopsis, tobacco, rice and in the CitEST database for citrus plants.
The amplifications by qPCR for the gene expression assays were performed using 7.5 μL of GoTaq qPCR Master Mix (Promega), 3 μL of cDNA (1:50 dilution), which was taken from the pool formed by the three replicates (150 μL each), 200 nM of each primer and water to complete a final volume of 15 μL, and carried out in a 7500 Fast Real Time PCR System (Applied Biosystems) with cycles of: 50°C for 2 min; 95°C for 10 min; 40 cycles of 95°C for 15 s and 60°C for 1 min. For each reaction, a dissociation curve was performed to verify possible non-specific contaminations and reactions. In addition, the reactions for each pair of primers were made in duplicates, always using control without cDNA to detect possible contaminations.

Normalization of qPCR data and gene expression analyses
Expression stability for each housekeeping gene was evaluated using the GenEx v. 6 (http://www.multid.se/) software, which provides the GeNorm algorithm to make paired comparisons between the endogenous genes, determining the best combination (two or more genes) to be used and calculating the average value of the Expression stability, called the M value (m-value) for each gene. The data that served as input for the calculation of the M value by the GeNorm algorithm were the relative quantities of each sample together with the efficiency of the primer, according to Mafra et al. [21].
For the detection of relative quantities, expression levels, fold change values and stability of endogenous genes, two treatments were considered in the study of the Phytophthora-citrus complex: plants inoculated with P. parasitica (infected group) and non-inoculated plants (control group). Calculations were made based on the number of amplification cycles required to reach a fixed threshold (cut-off cycle -Ct) in the exponential phase of PCR. The amplification efficiency and Ct data were calculated for each qPCR reaction by the Real-time PCR Miner software [22], which implements a normalizing algorithm to the raw fluorescence data according to the function of the PCR cycles. For each gene, an average efficiency of all PCRs was calculated. The mean of the Ct values of the two technical replicates of each genotype analyzed was also estimated (Additional file 2: Table S2). With these data, the relative quantification was calculated. It was determined by the 2 -ΔΔCT method between the conditions of qPCR [23], which serves as parameter for the calculation of the expression levels of each sample. Hence, a methodology derived from this procedure was established, which does not consider the efficiency value (E) of the gene equal to 100%. Instead, the actual value of E was used in the calculations of the relative quantities (Q) of each sample by the formula Q = E ΔC T .
Expression levels of each genotype were calculated by a normalization factor, given by the geometric mean of the estimated relative quantities for the two reference genes that had a smaller M value in the two treatments evaluated by the GeNorm algorithm. The calculation of expression levels in each sample was done by the ratio between the value of the relative quantity found in the target gene and the normalization factor of that genotype under analysis.
At last, the Fold change values of each inoculated individual were calculated in relation to the non-inoculated ones, by the ratio of the expression levels of the infected group on the control group. For statistical analysis, Fold change data were transformed into logarithmic scale (base 2), to meet the data normality using the Minitab 18 software (http:// www.minitab.com/). An F-test (ANOVA: a criterion) was made to compare log 2 Fold change results for each gene between the three groups (S, MS and T/ R). If the obtained p-value was significant, a post-hoc paired Student's t-test was applied to compare the differences between the sample means of the three groups.

Gene expression profile
To obtain the gene expression profile of the experiment, by comparing the 19 candidate genes among the 51 hybrids, the two parents, Rangpur lime and Swingle citrumelo, Log 2 Fold change values served as input to the MeV (MultiExperiment Viewer) program v. 4.9 (http:// sourceforge.net/projects/mev-tm4/). It was possible to group both the genes and the samples by the Hierarchical clustering (HCL), using the Pearson correlation as metric distance, which resulted in the gathering of genes with closer expressions and the separation of the genotypes in clusters. These parameters were visualized in a graphical representation called heatmap.
In addition, to better understand the relationship between the candidate genes, a dissimilarity matrix was obtained from the Euclidean Distance, so that this comparative analysis could also be demonstrated with a heatmap.

QTLs and eQTLs mapping
In the present study, we used pre-built linkage maps of C. sunki and P. trifoliata [24], that were constructed using DArT-seq™ molecular markers and the OneMap software [25]. The analyses were performed using the FullsibQTL package of the programming language R [26]. For the QTLs mapping, the means of the RLL phenotypic data in logarithmic transformation (base 10) in the segregating population of 110 hybrids were considered. For the eQTLs mapping, the Log 2 Fold change values calculated by the relative expression in the segregating population composed of 51 selected hybrids were used to map the eQTLs on the two parental linkage maps, as well as the phenotypic trait, thus detecting polymorphisms associated with gene expression. The strategy of composite interval mapping (CIM) [27] was used. A maximum of 20 cofactors were stipulated to locate QTLs and eQTLs outside the mapping range. The calculation of the critical LOD score to determine the presence of true QTL and eQTL was done by the random permutation test (α = 0.05; n = 1000 replicates) [28], available in FullsibQTL. The percentages of phenotypic variation (R 2 ) explained by QTLs and eQTLs were also estimated.

Evaluation of lesions caused by P. parasitica and phenotypic analyses
The means of lesions by inoculation of the 110 hybrids, C. sunki, P. trifoliata, Rangpur lime and Swingle citrumelo with P. parasitica are shown in Fig. 1.
The RLL from the population composed by P. trifoliata, C. sunki, the 110 hybrids, Rangpur lime and Swingle citrumelo met the expectation of normal distribution data by the Kolmogorov-Smirnov (KS) normality test.
There were significant differences between the RLL means of the 114 genotypes (Additional file 3: Broad-sense heritability coefficient was considered high (65%) for the RLL character (Table 1).

Gene expression and genotypic analyses
Three endogenous normalizing genes were analyzed and all of them presented high expression stability (Table 2), with M values varying from 0.16 for the best candidates to Normalizers (FBOX and SAND) at 0.21 (GAPC2), which had the highest m-value recorded. Therefore, the FBOX and SAND genes were selected as normalizing genes for the analyses of candidate genes, related to resistance to P. parasitica.
The results of the relative gene expression in the population composed of P. trifoliata, C. sunki, 51 hybrids, Rangpur lime and the Swingle citrumelo satisfied the expectation of normal distribution. The p-value obtained by the KS test was bigger than 0.150 for 17 analyzed genes, which made the log 2 Fold change values highly significant (p ≥ 0.01 and p ≥ 0.05) and allowed the development of the following comparative analyses. Only the PR2 and PR4 genes had a smaller p-value (0.038 and 0.077, respectively).
The F-test (ANOVA: a criterion) results for variance analysis using log 2 Fold change values from 19 target genes evaluated in the P. trifoliata, C. sunki, 51 hybrids, Rangpur lime and Swingle citrumelo revealed that only five genes (EDS1, WRKY46, WRKY62, Chitinase and LEA5) had significant different expression among the three groups (S, MS and T/R). The EDS1, WRKY46 and LEA5 genes had a smaller p-value (0.0079, 0.0073 and 0.0022, respectively), and were highly significant at 1% (p-value ≤0.01) compared to WRKY62 and Chitinase (0.0254 and 0.0495, respectively), with significant difference at 5% (p-value ≤0.05).
After the F-test, a paired Student's t-test was applied to the five genes with statistically significant difference, comparing the sample means of the three groups in pairs (Fig. 2).
The heatmap (Fig. 3), based on the comparative analysis performed by the Hierarchical clustering (HCL) of 19 target genes and the 55 selected genotypes (51 hybrids, their two parents, Rangpur lime and Swingle citrumelo), allowed the grouping of genes and related genotypes, using the Pearson correlation as metric distance to obtain the best intra and intervariable grouping possible. The genotypes were separated into five secondary clusters distributed in two main clusters, while the genes in three secondary clusters arranged in two main clusters. The color scale representing the log 2 Fold change values showed that the gene expression data ranged from − 8.29 to 5.53.
Another heatmap (Fig. 4) was constructed for a more accurate analysis of the relationship among the candidate genes, from a dissimilarity matrix, which uses as a metric distance the measure called Euclidean Distance, allowing to observe the difference degree among genes in a range of 0 to 1.

QTLs analysis and mapping
Using the two genetic maps previously constructed for each parent of the hybrids progeny [22] and according to RLL phenotypic data, it was possible to detect QTLs associated with the lesion length character caused by Phytophthora in citrus.
Based on the methodology of composite interval mapping (CIM), four QTLs were detected with LOD score higher than or equal to 3.0, three for the P. trifoliata (resistant parent) map and one for the C. sunki (susceptible parent) map (Figs. 5 and 6). In this model, only the additive effect was estimated, and the signal indicates the linkage phase between the marker and the QTL.
QTLs were found in LGs 3, 5 and 7 of the P. trifoliata map with 1:1 segregation due to the significant additive effect for this parent (Fig. 5). Regarding the QTLs analysis in the C. sunki linkage map, there was only one QTL located in LG 2 that showed 1:1 segregation ratio, also with significant additive effect for this parent (Fig. 6). Table 3 shows the results of the QTLs mapping. "LOD scores" of the detected QTLs ranged from 4.06 to 7.67 while R 2 values presented small to moderate effects, ranging from 1.77 to 16.8%.

eQTLs analysis and mapping
Using the two genetic maps previously constructed for the progeny of the citrandarins [22] and according to gene expression profile from relative expression values (log 2 Fold change) of 19 target genes evaluated with the 51 selected hybrids, it was possible to detect eQTLs in response to infection caused by P. parasitica. Only those Overall mean 4.0065 a genotipic variance (V g ); residual variance (V r ); phenotypic variance (V p ); broadsense heritability coefficient (H 2 ); coefficient of variation for genotypic variance (CV g %); coefficient of variation for residual variance (CV r %) and overall character mean with LOD score higher than or equal to 3.0, calculated by the random permutation test for each analyzed gene, with a confidence interval of 95%, were considered as consistent eQTLs. In this model, there is only one effect's type (additive effect) and the signal indicates the linkage phase between the marker and the eQTL. According to the methodology of composite interval mapping (CIM), 164 eQTLs with LOD ≥ 3.0 were detected for 19 evaluated genes: 84 of them for the P. trifoliata map, with mean of approximately four eQTLs per gene and 1:1 segregation due to the significant additive effect for this parent; and 110 for the C. sunki map, with mean of approximately six eQTLs per gene that showed 1:1 segregation, with significant additive effect for this parent. All target genes possessed at least one eQTL associated with their expression on both the Rubidoux trifoliate map and the Sunki mandarin map (Figs. 7, 8 and 9).
In general, the calculated LOD scores were close to 3.0 for all evaluated genes in the two maps. The LOD scores of the eQTLs were consistent and ranged from 3.58 to 19.02 for the P. trifoliata map (Additional file 4: Table S4), while ranging from 3.39 to 33.13 for the C. sunki map (Additional file 5: Table S5).
Twenty three hotspots were identified on the Rubidoux trifoliate map, with mean of approximately two hotspots per LG, as well as 31 hotspots on the Sunki mandarin map, with approximately three hotspots per LG. Genes that had overlapping eQTLs localized in hotspots ranged from two to eight on genetic maps (Table 4). In addition, the interposition between an eQTL from the WRKY46 gene and a QTL in the same genomic position was found exactly on the marker 100,087,520|F|0 in the LG7 of the P. trifoliata map at 190.66 cM, indicating a complex network that regulates both gene expression and phenotype.

Discussion
The RLL means of the hybrids ranged from 1.15 to 11.13 mm, which is in accordance with previous study carried out by Siviero et al. [2], that worked with the same population, using as inoculum a 3 mm disc (cork borer) of oomycete mycelium. The parents represented the extreme points in lesion lengths, with about 15.10 mm for C. sunki, and 2.30 mm for P. trifoliata. The lesion length values for the F1 individuals ranged from 5.8 to 12.2 mm (discounting 3 mm from the mean values obtained) [2]. In our study, the parents had very contrasting results for the lesion developed by the infection with P. parasitica, with P. trifoliata (Rubidoux trifoliate) reaching 2.71 mm and C. sunki (Sunki mandarin), 8.36 mm (Fig. 1). According to the literature, Sunki mandarin is susceptible to Phytophthora, while trifoliate behaves as resistant rootstock [29,30]. The lesion in the Rangpur lime reached 10.52 mm, surpassing the Sunki mandarin, in order to be classified as susceptible; and in the Swingle citrumelo, the RLL mean was 1.72 mm, reaching values smaller than P. trifoliata. Swingle citrumelo rootstock is known as being tolerant for trunk and root infections [31]. The results also indicated that hybrids from the crosses between Sunki mandarin and Rubidoux trifoliate present great genetic variability, being few (17%) susceptible or moderately susceptible to Phytophthora (Additional file 3: Table S3).
The value of broad-sense heritability coefficient in Table 1 indicates that 65% of the phenotypic variation is due to the action of genes, demonstrating good genetic control and great chance of success in the selection of individuals within the experiment. This result disagrees with Siviero [32], which found a low value of heritability (18.7%) when evaluating the lesion caused by inoculation of P. parasitica.
Considering gene expression results, the M values of endogenous normalizing genes are in accordance with the literature [33] and with the GeNorm manual, because they are below the limit of 1.5 (Table 2). Thus, FBOX and SAND genes were classified as the most uniform by both the SD and the GeNorm algorithm, surpassing the GAPC2 housekeeping gene, which is commonly used for the normalization of gene expression assays by qPCR in plants [34,35].
Three expression patterns were found after the F-test and paired Student's t-test (Fig. 2). In the first one, there was a significant difference within the MS and T/R groups for the Chitinase gene (Fig. 2a). The expression    of Chitinase was down-regulated in these two groups, but there was a higher repression in the MS group. According to Punja & Zhang [36], there are different classes of plant chitinases from molecular, biochemical and physicochemical criteria, that are constitutively expressed at high levels in the plant in response to several abiotic and biotic factors. In addition, the same author stated that the level of protection is variable in transgenic plants that express cloned genes of chitinases in response to a fungal pathogen.
In the second pattern, significant differences for the WRKY62 gene were found when comparing log 2 Fold change means between S and MS, as well as MS and T/ R (Fig. 2b). In relation to the combination S and MS, this gene was found induced in most genotypes belonging to the MS group, predominantly evidencing the existence of S hybrids that repressed the WRKY62 gene. This may show a small participation of this gene in the defense response to P. parasitica, considering that genotypes with intermediate lesion lengths express it more than others with larger lesion length. On the other hand, the results with the combination MS and T/R indicate that tolerant and/or resistant hybrids of C. sunki x P. trifoliata don't response to P. parasitica infection with WRKY62 gene, since the mean is down-regulated for this group and consequently smaller than the mean of the MS group, which was up-regulated. Previous studies state that the transcription factor WRKY62 has a different performance in comparison to other members of the WRKY family, negatively regulating the SA-mediated response and positively regulating a typical PTI (PAMP-triggered immunity) response, by interacting with an also negative regulator of the SA downstream pathway called HDA19 (histone deacetylase 19) [37,38].
In addition to the second pattern of expression, a third one was detected, in which there were significant differences for three genes (EDS1, WRKY46 and LEA5) when comparing the log 2 Fold change means between S and MS, as well as T/R and S (Figs. 2c, d and e). The genes were induced in most genotypes belonging to the S group, evidencing the predominant existence of MS and T/R hybrids that repressed the EDS1, WRKY46 and LEA5 genes.
Perhaps resistant citrandarins activate other defense mechanisms, such as the production of ROS (Reactive Oxygen Species) and phytoalexins that are enough to contain the advance of P. parasitica. In the literature, it is described that resistance to pathogenic fungi belonging to the genus Verticillium, which attack the tomato crop, involves a more basal and nonspecific response, with resistant plants producing depositions (callose, among others) on cell walls and synthesizing antimicrobial agents, including phytoalexins [39]. In addition, previous studies using the microarray technique and qPCR to evaluate differential gene expression in susceptible and resistant tomato varieties to the isolates of Table 3 Map, linkage group (LG), flanking markers, position of the QTL in centiMorgans (cM position), LOD score, proportion of phenotypic variation (R 2 ) explained by QTL in % and additive effect by the QTLs mapping Map LG Verticillium dahliae, identified genes induced to this pathosystem, such as those coding for PR proteins; and found a larger induction, as well as a larger number of genes differentially expressed in susceptible plants to the pathogen. Thus, these results indicate that the increase of systemic gene expression in susceptible plants does not protect them, and that this exaggerated and inductive reaction may trigger the symptoms of the disease [40][41][42]. In fact, according to Dalio et al. [43], in the susceptible plant (C. sunki), P. parasitica deploys effectors, such as elicitins, NPP1 (Necrosis-inducing Phytophthora protein 1), CBEL (Cellulose-binding elicitor and lectin activity), RxLR and CRN (Crinkler), whereas the host responds by activating the main defense signaling pathways, resulting in hypersensitive response and necrosis. Despite its strength, this defense response fails to withstand P. parasitica invasion, confirming its hemibiotrophic life style. In P. trifoliata, the effectors were strongly expressed, nevertheless failing to induce any immunity manipulation and disease development, suggesting a non-host resistance type, in which the plant relies on preformed biochemical and anatomical barriers. The LEA5 gene, in addition to play an important role in resistance to abiotic stresses, may also be related in defense responses to pathogen infection, being responsive to increased levels of JA and ABA [44]. The transcription factor WRKY46, as well as WRKY70, acts as a positive regulator of the SA signaling pathway [45]. At last, the EDS1 gene acts on the SA upstream pathway, and consequently in its biosynthesis from an ETI (effector-triggered immunity) [46,47].
In the cluster analysis of the first heatmap (Fig. 3), there was a higher variation in log 2 Fold change values within the sampled individuals than in the genes. The BSMT1 and SGT1b genes were predominantly up regulated. These genes are part of the SA metabolism [47] and may therefore have a greater participation in the resistance of this population to P. parasitica. On the other hand, most hybrids and four analyzed rootstocks were down-regulated for the EIN3 gene (Fig. 3), an important regulator of the ET downstream pathway [48], indicating that it may not interfere in the defense response of the different phenotypes to P. parasitica.
In relation to the genotypes, it was found that the Sunki mandarin and Rangpur lime rootstocks, described The comparison of the congruence pattern of the gene expression is presented in Fig. 4. The Euclidean Distance is widely used as a parameter to investigate how much an object differs from the other, being efficient to evaluate the intravariable divergence [49]. The darker the color, the more intense the interaction between two genes, demonstrating a larger congruence between expressions. Therefore, smaller distance was observed between the PR2 and EDS1 genes, which are part of SA signaling pathway. EDS1 acts on the biosynthesis of this phytohormone and PR2 consists of a responsive defense gene to SA accumulation. PR2 encodes the β-1,3-glucanase protein with anti-oomycetes properties, because it constitutes an enzyme that degrades the cell wall of these organisms that is composed of β-glucans [37]. However, the less intense the color, the more distant the genes will be, which denotes a smaller congruence of the expressions between genes. It was found that three genes (BSMT1, PR4 and ABF) in comparison with WRKY46 obtained the largest distances. It is known that WRKY46 is a transcription factor belonging to the large WRKY family, and acts as a positive regulator of the SA downstream pathway. The BSMT1 gene is known to be part of SA metabolism, converting this phytohormone into MeSA (Methyl Salicylate), and has functions as a defense signal for the expression of JA-dependent defense genes. The PR4 gene encodes a chitinase (PR protein) that is activated by the JA pathway in the ERF branch, contributing to the synergy between the JA/ET pathways. The ABF gene is essential in downstream regulation of the ABA pathway, inducing the expression of many responsive defense genes to this gaseous hormone [45,50,51]. Hence, there is a smaller relationship between their expressions when evaluating the specific resistance response to Phytophthora.
Regarding the QTL mapping in both linkage maps (Figs. 5 and 6), Siviero et al. [2] in their study of QTLs mapping for evaluation of resistance to Phytophthora in hybrids of C. sunki x P. trifoliata, using maps previously constructed by Cristofani-Yaly et al. [52], also found three QTLs for the Rubidoux trifoliate parent. In addition, Siviero et al. [2] also detected only one QTL for Sunki mandarin.
According to Anderson et al. [53], many studies with mapping reveal QTLs in a few loci with moderate R 2 values (10 to 20%), while there are several other loci with small effects (R 2 smaller than 10%), which is similar to those found in the present study. QTLs identified in LGs 3, 5 and 7 on the P. trifoliata map explain 1.77; 6.3 and 7.41% of the phenotypic variation, respectively. The QTL for C. sunki parent, located in LG 2, was responsible for most of the phenotypic variation of the RLL values, explaining 16.8% of it (Table 3). Thus, this suggests that Sunki mandarin has greater contribution in transmitting alleles for gummosis response to the progeny. Some studies with QTLs mapping in other plants reported about resistance alleles located in the susceptible parent, as well as susceptibility alleles in the resistant one [54,55]. In addition, Siviero et al. [2] also detected a QTL with moderate effect, which explained 18% of the phenotypic variation.
The high value found for heritability (65%) shows that the genetic nature presents a predominant role in the phenotype manifestation, a fact that was not shown in previous studies, in which heritability values found for the character were low, reaching less than 20%, as in the study of Siviero et al. [2].
The detection of several QTLs associated with resistance to Phytophthora and the variation of RLL phenotypic data of the hybrids in response to inoculation with P. parasitica are indicative that the lesion length character is complex, being controlled by polygenes, as mentioned in the literature [30,31]. This study of Phytophthora-citrus pathosystem demonstrates a great possibility of success in the selection of resistant hybrids within the experiment, an important scenario in a breeding program. The QTLs location and the understanding of their genetic effects contribute to the detection and selection of possible candidate genes responsible for the variation of the studied phenotype [56].
According to Shi et al. [57], a high detection power of eQTLs can be found even in small populations (population size below or close to 50). In addition, as the methodology established by the software for QTLs mapping is similar to eQTLs mapping, a population size larger than 50 is sufficient to provide high resolution to the activity of mapping and detecting QTLs/eQTLs of small effect. The larger the population size, the saturation of the genetic map and the heritability of the phenotypic character, the larger the genomic information related to the mapping [58][59][60]. As a high heritability (65%) for the RLL character was found in the present study, a high saturation of the two maps of each parent and the population of selected hybrids for the eQTLs mapping being equal to 51, a large volume of eQTLs from the differential gene expression profiles for each candidate gene analyzed via RT-qPCR was found.
PR4, PR3, ACO and PAL2 genes presented the highest number of eQTLs on the P. trifoliata map, each one with six of them, while on the C. sunki map there was a larger number for the MKP1 gene, totalizing nine eQTLs (Fig. 7). The PR4, Chitinase and PR3 genes, which are responsive to the JA/ET pathways, encode a class of enzymes called chitinases, which degrade cell wall [61]. They detained a larger number of chromosomal regions that affect their transcription levels in response to infection caused by P. parasitica on both the Rubidoux trifoliate map and the Sunki mandarin map. On the other hand, a smaller number (only one eQTL) for the EDS1 gene was found, which is below the mean of eQTLs per gene in both maps. One of the main regulators of the SA upstream pathway, EDS1 acts to promote SA biosynthesis due to effector-triggered immunity (ETI) [47]. This gene may not have much participation in the defense response of the interaction Phytophthora-citrus, a fact explained by its expression pattern and by smaller quantity of genomic regions in the two contrasting parents, responsible for the variation of its gene expression in the segregating progeny.
Regarding the phenotypic variation (R 2 ) values explained by the eQTLs, both on the maps of the Rubidoux trifoliate and the Sunki mandarin (Additional file 4: Table S4 and Additional file 5: Table S5), R 2 values reached up to 11.54% for the P. trifoliata map; and up to 24.97% for the C. sunki map. Equivalent to the phenotypic variation values explained by QTLs in mapping studies [53], many eQTLs in the present study are composed of loci with small effects (R 2 less than 10%), while few are formed by chromosome regions with moderate effects (10 to 20%).
Studies with eQTLs allow the identification of chromosomal regions that affect the expression of multiple genes (hotspots). Such phenomenon can be seen by a series of overlapping eQTLs on the LGs of genetic maps, and its consequence can be attributed to genome regions rich in closely linked genes, by identifying nearby eQTLs; or to a single genomic region regulating the transcription levels of many genes, from the detection of distant eQTLs. Nonetheless, it is reported in the literature that many hotspots control the expression of enzyme-coding genes involved in various metabolic pathways, and some hotspots may even regulate the pathway as a whole [62][63][64][65].
It could be verified that there was an intense overlap of eQTLs from the quantification of the 19 gene transcripts (Table 4), independent of the signaling pathway involved, as observed in Figs. 8 and 9. Thus, the interposition between eQTLs does not seem to follow the relationship between the genes, including eQTLs from the transcripts associated with different signaling pathways of phytohormone, which were overlapping exactly at the same position or in the proximal regions of hotspots, both on the P. trifoliata map and on the C. sunk map.
Co-regulated genes in plants have been extensively identified in genetic analyses by eQTLs mapping, with the concept that different transcription levels from distinct genes may be under control of the same loci regulators. In addition, this type of methodology allows the detection of other regulatory networks, from the co-location between QTLs and eQTLs, identifying associations between the allelic state of a genomic region with the quantification of gene transcripts within QTLs involved in the variation of complex agronomic traits. The overlap of QTLs and eQTLs may corroborate to a strong association between gene transcript levels and phenotypic data [66][67][68]. The WRKY46 gene is a transcription factor of the WRKY family and its activation is involved in plant responses against phytopathogen infection [37,45]. It has a gene expression pattern and co-location of QTL and eQTL in P. trifoliata map that suggest a larger participation in the interaction of P. parasitica with hybrids of C. sunki x P. trifoliata.
Kirst et al. [69], using the pseudo-testcross strategy to map eQTLs on two parental genetic maps in hybrids of eucalyptus, suggested that different genotypes of the progeny have distinct regulatory loci in the parents, which may explain the genetic differences in the gene expression. In the present study, the susceptible parent Sunki mandarin seemed to have a greater contribution in the transmission of alleles to the progeny, since it was detected in comparison with the map of the trifoliate Rubidoux: a single QTL of moderate effect; higher number of eQTLs; and greater number of hotspots and consequently greater overlap. However, it is worth mentioning that there was an expressive identification of QTLs, eQTLs and hotspots in the Rubidoux trifoliate map, suggesting that there is an interaction between the two parents to confer a favorable combination of QTLs/eQTLs to be transmitted to citrandarins in response to infection of the causal agent of citrus gummosis disease.
According to Dalio et al. [43], that studied the contrasting interactions of Sunki mandarin (susceptible) and trifoliata Rubidoux (resistant) in Phytophthora, they noticed that SA, JA and ET pathways seem to be activated in susceptible rootstock upon infection. The plant responds by strongly activating several genes related to all three main defense signaling pathways (SA, JA and ET). This major transcriptional shift results in HR. Nonetheless, this is not efficient to kill or stop pathogen colonization. Since P. parasitica has a hemibiotrophic life style, it might benefit from cell death and release of nutrients. On the other hand, trifoliata Rubidoux, even in contact with several P. parasitica effectors, does not activate SA, JA or ET pathways.
In our work, in relation to inoculation, the bark was removed as according to Boava et al. [11]. These authors reported the induction of defense-related genes in P. trifoliata plants and smaller lesion induced by the pathogen, when compared to C. sunki. We also observe this fact, but we observed in general that the eQTLs for C. sunki had higher values of phenotypic variations (R 2 ) than those observed for P. trifoliata.
As argued by Dalio et al. [43], inoculation method by wounding used in our work might favor a first establishment of the pathogen and a concomitant defense response of the plant in P. trifoliata, which impairs further development of the pathogen. But we also observed defense response in Sunki and it was not enough to contain the infection. So it seems to us that the genes studied here are not the main ones involved in resistance. It appears that P. trifoliata and citrandarins presents other defense mechanisms that may be related to structural and chemical barriers as well as hypothesized by Dalio et al. [43].

Conclusions
We have identified citrandarins that are promising genotypes for future research related to gummosis disease. The heritability for the lesion length character caused by P. parasitica is considered high, demonstrating that genetics exerts larger influence than the environment. From our genetic maps constructed for both parents of the segregating progeny, QTLs that act in the process of expression of the lesion length character related to the inheritance of the citrus gummosis have been identified. The performance of both parents is of extreme importance for the transmission of a favorable combination of QTLs to their hybrids.