Transcriptome profiling of soybean (Glycine max) roots challenged with pathogenic and non-pathogenic isolates of Fusarium oxysporum
© Lanubile et al. 2015
Received: 30 July 2015
Accepted: 15 December 2015
Published: 21 December 2015
Fusarium oxysporum is one of the most common fungal pathogens causing soybean root rot and seedling blight in U.S.A. In a recent study, significant variation in aggressiveness was observed among isolates of F. oxysporum collected from roots in Iowa, ranging from highly pathogenic to weakly or non-pathogenic isolates.
We used RNA-seq analysis to investigate the molecular aspects of the interactions of a partially resistant soybean genotype with non-pathogenic/pathogenic isolates of F. oxysporum at 72 and 96 h post inoculation (hpi). Markedly different gene expression profiles were observed in response to the two isolates. A peak of highly differentially expressed genes (HDEGs) was triggered at 72 hpi in soybean roots and the number of HDEGs was about eight times higher in response to the pathogenic isolate compared to the non-pathogenic one (1,659 vs. 203 HDEGs, respectively). Furthermore, the magnitude of induction was much greater in response to the pathogenic isolate. This response included a stronger activation of defense-related genes, transcription factors, and genes involved in ethylene biosynthesis, secondary and sugar metabolism.
The obtained data provide an important insight into the transcriptional responses of soybean-F. oxysporum interactions and illustrate the more drastic changes in the host transcriptome in response to the pathogenic isolate. These results may be useful in the developing new methods of broadening resistance of soybean to F. oxysporum, including the over-expression of key soybean genes.
Soybean (Glycine max [L.] Merrill) is a major world crop and is the second most cultivated crop in the U.S.A. following maize. Soybean production contributes billions of dollars annually to the national economy, providing approximately 21 billion dollars in 2012 (United Nations Food and Agriculture Organization website). Limitations on maximum production are largely due to disease pressures that reduce yield. Several species of Fusarium have been associated with soybean, causing seed and seedling diseases, root rot, and vascular wilt [1–3]. F. oxysporum Schltdl. is a fungal soil-borne facultative parasite present worldwide  and is the most common species isolated from soybean roots in Iowa and other soybean-producing regions in North America [3, 5, 6]. F. oxysporum is known to consist of many “cryptic species” and, as such, it is often referred as the “F. oxysporum species complex” (FOSC). Recently, significant variation in aggressiveness was observed among isolates within the FOSC collected from soybean roots in Iowa [7, 8]. Some of these isolates caused severe root rot and dumping-off, other isolates were weakly pathogenic or non-pathogenic.
Management of soil-borne diseases like Fusarium root rot and wilt disease depends primarily on seed treatments and genetic resistance. Seed treatments are only effective during emergence and the seedling stages. Cultural practices can help in managing root rots, but these are often not adequate. Moreover, it seems clear that managing Fusarium root rot in the long-term will depend on improvements in molecular breeding for resistant genotypes .
Soybean resistance to other Fusarium species has been identified. Particularly high levels of resistance to F. graminearum have been found in the soybean cultivar Conrad, and putative QTL associated with resistance to F. graminearum have been detected [10, 11]. Previous work has identified QTL associated with resistance to sudden death syndrome (SDS), caused by F. virguliforme and other species, in Ripley  and Forrest  soybean genotypes. Progress in breeding for resistance will be improved through the analysis of new and consistent QTL for Fusarium root rot and wilt disease and by a deeper knowledge of genetic mechanisms underlying soybean-F. oxysporum interactions.
The availability of reference genome sequences and gene annotations for G. max and F. oxysporum has enabled us to study the molecular interactions between the host plant and its pathogen. Emerging massively parallel sequencing techniques allow the rapid acquisition of huge amounts of genomic or transcriptomic sequence data at relatively low costs . To date, microarray techniques have been predominantly used for gene expression analysis particularly for well-studied model organisms for which typically high-quality gene annotation data were available. Compared with microarrays, RNA-Seq is known to have a wider dynamic range, higher technical reproducibility, and provide a better estimate of absolute expression levels [15, 16]. Genome-wide expression profiling of plants infected with F. oxysporum has been reported in several crop plant species, including melon , Arabidopsis , and banana . However, little is known about transcriptional changes in soybean roots that have been infected by F. oxysporum and almost no attention has been paid to the study of differences in plant responses based on the pathogenicity of the infecting isolates. Most likely this is because of the scarce availability of isolates able to infect the same host while displaying a range of pathogenicity. This situation draws considerable interest in comparing root transcriptional responses between non-pathogenic and pathogenic F. oxysporum isolates.
To elucidate the comprehensive gene expression profiles for both G. max and F. oxysporum, we analysed the transcriptomes of plants and non-pathogenic and pathogenic fungi at 72 and 96 h post inoculation (hpi). Our aim was to characterize soybean genes that are differentially regulated by the host during infection by each pathogen, in order to identify new potential resistance mechanisms and candidate genes that have not previously been shown to play a role in defense. At the same time, we tried to strengthen our knowledge concerning novel details of infection by using two different pathogenic and non-pathogenic isolates of F. oxysporum. The results showed markedly different gene expression profiles in different host-pathogen combinations. A peak of HDEGs was observed at 72 hpi in soybean roots in response to both isolates and the number of HDEGs was about eight times higher for the pathogenic isolate compared to the non-pathogenic one. Furthermore, not only the number of genes, but also the magnitude of induction was much greater in response to the pathogenic isolate. These findings generated useful resources for the soybean research community and provided more insights into the understanding of soybean-F. oxysporum interactions.
Quantification of fungal growth and disease severity evaluation in soybean roots
To determine the appropriate time points for the investigation of soybean transcriptome profiles following the FO36 (non-pathogenic) and FO40 (pathogenic) F. oxysporum isolates inoculation, quantification of the fungal translation elongation factor 1 alpha (tef1α) gene by quantitative PCR (qPCR) was carried out in this study. Infection progression was monitored in inoculated roots of partially resistant soybean genotype Forrest over a time course of seven days. The tef1α gene was detected in samples collected 48 h post inoculation (hpi) through 168 hpi with both isolates. Two-factor analysis of variance (ANOVA) revealed significant (P ≤ 0.001) differences between the times of sampling (48, 72, 96 and 168 hpi) in the observed means for the fungal tef1α DNA quantity and between the two treatments (non-pathogenic and pathogenic inoculated samples), and their interactions (Additional file 1: Table S1).
Furthermore, disease severity index (DSI) was evaluated in seedlings at seven days after inoculation. Both isolates were able to infect and colonize soybean seedlings, although to different degrees (2.29 vs. 6.71 mean DSI for the non-pathogenic and pathogenic isolates, respectively; data not shown).
As expected, minor symptoms occurred in plants inoculated with isolate FO36, as also stated by qPCR (Fig. 1). The FO36 isolate produced fewer macroconidia in culture compared to the pathogenic one, which may have contributed to the relatively lower levels of disease and fungal DNA in seedlings over a time course of seven days.
RNA-Seq analysis of host transcriptome
Root samples were taken from plants, either noninoculated or inoculated with non-pathogenic and pathogenic isolates of F. oxysporum, at 72 and 96 hpi. To investigate the comprehensive gene expression profiles of G. max and its pathogen F. oxysporum simultaneously at the early stages of infection, we analysed transcriptomes obtained from sequencing RNA from eighteen samples, which included three biological replicates for each condition (control/inoculated) and times of inoculation (72 and 96 hpi). A total of about 126, 121 and 140 million 100 bp paired-end reads were generated from noninoculated, FO36 and FO40-inoculated samples, respectively, constituting approximately 12.6, 12.1 and 14 Gb of cDNA sequencing data (Additional file 2: Table S2). On average, 87.2 % of the total reads mapped uniquely to the soybean Williams 82 reference genome (Additional file 2: Table S2). A smaller number of uniquely aligned reads mapped to the F. oxysporum reference genome (90,770 in total), and 54,965 aligned reads were from the pathogenic isolate at 96 hpi (Additional file 2: Table S2). The fungal mapping results were consistent with the fungal DNA quantities assessed by qPCR, where fungal DNA increased throughout the course of infection, in particular for the pathogenic isolate, confirming the larger amount of reads detected for this isolate in the later inoculation stage (Fig. 1; Additional file 2: Table S2).
Unfortunately, given the very low read counts of F. oxysporum, in particular for the non-pathogenic isolate, further downstream analyses were only performed for soybean and not for F. oxysporum. The abundance of soybean transcripts are expressed in upper quartile normalized counts as calculated by HTSeq-count and QuasiSeq programs [20, 21]. One of the three biological replicates for the FO36 inoculated sample at 96 hpi was excluded for further expression level analysis due to a relatively small number of reads. We detected in total 44,026 soybean known protein coding expressed genes (Additional file 3: Table S3).
Soybean expression profiles of FO36 and FO40 F. oxysporum isolates inoculated roots were compared with their respective noninoculated controls at 72 hpi and 96 hpi. Genes were considered significantly differentially expressed (DE) if the Qvalue cut-off was below 0.05 and highly differentially expressed (HDE) if the absolute fold change (FC) was ≥ 1.9 .
Identification and functional categorization of F. oxysporum-responsive genes
A numerical overview of the differences in highly differentially expressed soybean genes at each time point and in each interaction is provided in Fig. 2. We identified 203 and 57 HDEGs in response to the non-pathogenic isolate, and 1,659 and 151 HDEGs in response to the pathogenic isolate at 72 and 96 hpi, respectively. A higher number of HDEGs was observed at 72 hpi compared to 96 hpi and this number was always higher in response to the pathogenic isolate at both times of inoculations. Some overlap in the HDEGs identified between the isolates was observed at 72 hpi, where more than 50 % of HDEGs detected in response to the non-pathogenic isolate was in common with the pathogenic one; however larger changes in expression levels were specifically identified in the interaction with the pathogenic isolate (1,441 HDEGs; Fig. 2). More limited transcriptional changes were found at 96 hpi, although the host responses against the pathogenic isolate continued to be numerically higher.
Consistent with these findings, we focused on soybean HDEGs mainly induced in response to the non-pathogenic isolate or to the pathogenic one, considering the following filters: number of normalized counts (NC) ≤0 and 0.5 in the control sample and NC ≥5 in the inoculated sample. A higher number of HDEGs was detected in response to the pathogenic isolate at both sampling times (11 vs. 48 HDEGs in total in response to the FO36 and FO40 isolates, respectively), as well as higher expression values (Additional files 6 and 7: Tables S6 and 7). These expression values ranged from 5 to 69.7 NC for the non-pathogenic isolate, and from 5 to 224.7 NC for the pathogenic one, at 72 hpi. At 96 hpi, only five genes were induced in response to FO40 isolate, with the highest expression value of 83.3 NC, while no genes were found in response to the non-pathogenic isolate. Overall, these data show that HDEGs belonging to all functional classes, in particular for the metabolic process and defense-related categories, were mainly overexpressed in the interaction with FO40 isolate, confirming a greater stimulation of soybean defense responses to the pathogenic inoculation.
Validation of representative genes by real-time RT-PCR
To validate the RNA-Seq expression profiles of soybean HDEGs, the expression levels of several known responsive genes were measured by real-time RT-PCR using gene-specific primers (Additional file 9: Table S9; Additional files 10: Figure S1). Eighteen soybean modulated genes were chosen among those expressed in planta, with a preference for defense-related genes, and some of them are marked with a star symbol in the Additional file 8: Table S8, which lists the selected set of F. oxysporum-responsive genes. The RT-PCR expression profiles of seventeen soybean genes agreed strongly with the RNA-Seq data, whereas the myb84 gene appeared to be slightly up-regulated according to RT-PCR analysis and slightly reduced from RNA-Seq results at 96 hpi in response to FO36 isolate (Additional file 10: Figure S1).
Overall, the enhancement in the expression levels and defense response revealed by RNA-Seq results in response to the pathogenic isolate were largely concordant with RT-PCR, confirming the reliability of the results.
In order to increase the understanding of transcriptomic responses produced by infection with one of the most important soybean pathogens, F. oxysporum, we performed RNA-Seq analysis to compare the global gene expression patterns in soybean roots inoculated with pathogenic and non-pathogenic isolates. The RNA-Seq method is particularly robust for gene expression studies and allows the identification of plant-targeted control strategies, as well as the detection of pathogenicity and virulence factors.
The timing of recognition for F. oxysporum infection on soybean is currently unknown, which makes it difficult to propose suitable time points for molecular analysis. We therefore began this investigation by characterizing the infection process in soybean roots inoculated with FO36 and FO40 isolates, in order to determine the optimal sampling times after inoculation. Quantification of fungal growth and disease severity evaluation reported more fungal DNA and elevated symptoms at 168 hpi, and as expected, in particular in response to the pathogenic isolate. As a consequence, this time-point was excluded from the further RNA-Seq analysis, because considered as a too late sample timing. Therefore, 72 and 96 hpi were selected to investigate early-intermediate transcriptional changes, in order to elucidate host genetic responses.
Our study provides the first large-scale investigation of gene expression changes that occur when soybean is inoculated with F. oxysporum, and is the first to compare pathogenic and non-pathogenic interactions in the same genetic background, using the partially resistant Forrest genotype. We have identified 205 soybean genes that are highly differentially expressed in pathogenic and non-pathogenic isolates versus control that encode for enzymes that are well known to be involved in defense-related networks. Of these genes, 90 were found to be significantly enriched in GO categories as determined by a Fisher’s exact or in MapMan bin categories by a Wilcox Rank Sum test (Additional files 5 and 8: Tables S5 and S8). Although the remaining 114 genes were not enriched into one of the defined categories or bins, their known relevance in the defense response literature warrants their further investigation. We placed these genes into four broad categories: signalling-related, defense response, transcriptional regulation, and modulation of secondary and sugar metabolism-related and explored their expression below.
Expression of signalling-related genes
Plants are able to recognize potential microbial pathogens through pathogen-associated molecular patterns (PAMPs) by host sensors, known as pattern-recognition receptors (PRRs) that initiate a series of defense responses called PAMP-triggered immunity (PTI). Most of these plant receptors belong to family of receptor-like kinases (RLK) [24, 25]. In our study five leucine-rich repeat (LRR) type-RLK were identified at 72 hpi in response to the FO40 isolate, four of them up-regulated. Additionally, several LRR-serine threonine protein kinase (STPK) were specifically induced after pathogenic isolate inoculation at the same time point, except one LRR-STPK (Glyma.16G169900) found down-regulated with both pathogens, and a second one (Glyma.01G004800) specifically induced in response to the non-pathogenic isolate.
Brassinosteroid insensitive 1-associated receptor kinase 1 (BAK1) is another significant PRR in plants, required for PTI triggered by bacterial flagellin and elongation factor Tu. Flagellin-sensitive 2 (FLS2) and BAK1 form a complex to initiate innate immunity in plant [26, 27]. Our results revealed the presence of two BAK1 and one FLS2 genes induced only after pathogenic isolate attack in the early stage of inoculation. As previously reported in a different pathosystem [28, 29], BAK1 played a role in the resistance response of banana roots against to F. oxysporum f. sp. cubense. Our findings are consistent with the hypothesis that BAK1 also controls plant programmed cell death and immunity to necrotrophic fungi, and bak1 mutants of Arabidopsis showed extreme susceptibility to necrotrophic fungi . These results suggest that different surveillance systems exist in response to the pathogenic and non-pathogenic isolates, and only in FO40-inoculated soybean roots the increasing BAK1 and FLS2 levels might potentiate the innate immune response.
Pathogen recognition triggers the activation of downstream signalling networks mediated by protein kinases, in particular mitogen-activated protein kinases (MAPK) [31–33]. Several MAPK and MAPK kinases (MAPKK) genes have been characterized in the response of plants to fungal infection . Consistent with this widely accepted model, we found three MAPKK kinases and two SNF1-related protein kinases specifically induced in response to the pathogenic isolate at 72 hpi.
Changes in defense response genes
One of the features of plant defense response is production of PR proteins that have been widely characterized and classified into the PR1-17 families . In our research, a high number of genes representing most of 17 different PR were clearly identified as induced after inoculation mainly in the early time point often shared by both isolates, such as three PR10, one PR4, one PR1 and four chitinases (family PR3). Other PR genes up-regulated only in response to the FO40 isolate at 72 hpi included: thaumatin-like proteins (family PR5; four genes), endoglucanases (family PR2; four genes) and lignin forming peroxidase (family PR9; one gene). Furthermore, the same three PR10 proteins and three out of four chitinases induced by both pathogens at 72 hpi, were also specifically up-regulated at 96 hpi in response to the pathogenic isolate but not by FO36. The same trend was also observed for two germin proteins (Glyma.10G168900; Glyma.20G220800), which are known to function in ROS production and biotic and abiotic stress responses . Two additional FO40-induced genes encoding bon1-associated proteins (BAP) were up-regulated at 72 hpi in FO40-inoculated roots. BAP1 and BAP2 are homologous proteins containing a calcium-dependent phospholipid-binding C2 domain and both function in the defense pathway . Furthermore, several nodulin proteins were strongly induced by FO40 at 72 hpi. Interestingly, one of them continued to be induced at 96 hpi for the pathogenic isolate (Glyma.15G049600), whereas three of them were down-regulated after non-pathogenic inoculation, suggesting a potential role in plant defense [19, 38, 39].
In our analysis another prominent class of defense-related genes was represented by protease inhibitors. In total, we identified eighteen genes up-regulated by F. oxysporum inoculation, encoding various types of protease inhibitors. Remarkably, 16 and seven out of them were strongly induced (up to 17,701 NC; Glyma.08G342000) only in response to the pathogenic isolate at 72 and 96 hpi, respectively. Indeed, fewer protease inhibitors genes, six and two, were induced by both isolates at the early and later stages of inoculation, respectively. This observation is in line with previous reports on the important role of protease inhibitors in the defense against pathogens .
Overall, the induction and greater accumulation of PR, cell wall-degrading enzymes and proteinase inhibitor genes suggested that the degradation of cell wall components of pathogens and proteolysis inhibition are important defense reactions in soybean against F. oxysporum isolates at the early infection stage (72 hpi). It could be speculated that the defense responses initiated at the early stage of fungal pathogen infection continued to play a role at the later stage following infection by isolate FO40, while these responses dropped off after 72 hpi for the non-pathogenic isolate.
Genes involved in transcriptional regulation
Transcriptome profiling analysis identified a large number of genes encoding TFs, such as ethylene-responsive transcription factors (ERF), MYB, bHLH, GATA, PLATZ and WRKY, and found that their expression was significantly changed upon FO40 inoculation. The ERF TFs play crucial roles in regulating plant responses to environmental stresses  and their overexpression in transgenic plants can confer enhanced disease resistance against different types of pathogens [42, 43]. The ERF TFs are known to be involved in ethylene signalling , and in agreement with this we also found that the pathogenic isolate infection up-regulated five genes for 1-aminocyclopropane-1-carboxylate (ACC) oxidases at 72 hpi. These enzymes participate in the last step of biosynthesis of ethylene, which has been associated with both wilting and resistance against vascular diseases [44, 45]. The induction of ACC oxidases only by the pathogenic isolate, suggests that ethylene might be involved in resistance against FO40 isolate.
Other strongly represented TF families were NAM-ATAF1/2-CUC2 (NAC) TFs. Arabidopsis NAC may play a dual role in regulating both jasmonic acid (JA)- and abscisic acid (ABA)-dependent responses and manipulate plant stress responses by activating other genes encoding MYB TFs, amylase, cold responsive protein, dehydration responsive proteins, glutathione-S-transferases, and late embryogenesis abundant (LEA) proteins [46, 47]. We observed that the percentage of up-regulated NAC and MYB TFs was between 60–70 % of total at 72 hpi for the pathogenic isolate, while no NAC and one down-regulated MYB gene were observed in response to FO36 isolate. Accordingly, two LEA genes were specifically induced by the pathogenic isolate at 72 hpi. Arabidopsis R2R3-MYB TF directly acts on the promoters of the flavonoid biosynthesis genes and in the signalling chain that causes flavonol-specific gene activation in phenylpropanoid biosynthesis . In line with this, we also observed differential expression of genes encoding enzymes related to biosynthesis of flavonol and phenylpropanoid.
Modulation of secondary and sugar metabolism-related genes
As previously stated, our results demonstrated the transcriptional induction of multiple genes involved not only in the phenylpropanoid pathway itself, but also in the downstream flavonoid and diterpenoid biosynthesis pathways. More specifically, phenylpropanoid-related genes, such as phenylalanine ammonia lyase (PAL), 4-coumarate ligase (4CL), trans-cinnamate 4-monooxygenase (C4M) and caffeoyl-o-methyltransferase (COMT) were consistently modulated upon pathogenic isolate inoculation mainly at the early time point. RNA-Seq data also revealed significant changes in genes belonging to the flavonoid pathway upon inoculation, especially with the FO40 isolate, such as chalcone isomerase (CI), flavonoid 3-hydroxylase (F3H) and flavonol synthase (FS), as well as two terpene synthases (TPs) that were identified. This finding once again indicated that lignification and cell wall strengthening are active resistance mechanisms in the soybean-pathogen interaction, as already observed in other pathosystems [49–52], as well as flavonoids and isoflavonoids, which could be crucial metabolites for the soybean infection response [53, 54].
Activation of defense responses upon pathogen infection is usually accompanied by a rapid induction of sink metabolism, possibly to satisfy the increased demand for carbohydrates as an energy source to sustain the cascade of cost-intensive direct defense responses and further mediate physiological adaptations . Additionally, pathogens try to manipulate plant carbohydrate metabolism for their own needs [56, 57]. In our study, we identified eight up-regulated genes belonging to the carbohydrate metabolic process group, seven out of them specifically induced after pathogenic inoculation at 72 hpi, and one cell wall invertase (CWI) (Glyma.15G024600) induced by the same isolate at both time points. Enhanced expression and activity of CWIs has been reported in several plant-pathogen interactions and is essential to modulate sugar partitioning necessary for the pathogen development [58, 59]. Moreover, during infection CWI activity also triggers plant defense responses, such as induction of PR genes, PAL gene expression, callose deposition and reduction of cell death, in agreement with our previous finding. One of the other possibilities for changing the sugar content is the regulation of the expression of the sugar transporters. We observed the up-regulation of five bidirectional sugar transporters only in response to the FO40 isolate at 72 hpi. In rice infected by Xanthomonas oryzae pv. Oryzae, SWEET proteins were up-regulated and sucrose accumulated in apoplast ready to be used for the pathogen growth [60, 61]. Santi and co-workers [62, 63] reported that sucrose transporter genes are first down-regulated during infection of grapevine by stolbur phytoplasma to limit the spread and then up-regulated during the recovery stage providing necessary nutrients [62, 63]. Together, these results substantiate the active mobilization of sucrose in FO40-inoculated soybean roots, providing ready-to-use sugars for pathogen growth and plant immunity.
Using RNA-Seq, we analysed the expression profiles of soybean roots inoculated with non-pathogenic/pathogenic fungal isolates at 72 and 96 hpi. We identified markedly differential responsive expression patterns in the two host-pathogen combinations and more active and drastic reactions were observed in response to the pathogenic isolate. This response included a stronger activation of many well-known defense-related genes, and several genes involved in ethylene biosynthesis and signalling, TFs, secondary and sugar metabolism. The high degree of activation of host defense signalling pathways identified in soybean was consistent with the more extensive necrosis and the highest quantity of fungal DNA observed for the pathogenic isolate. These results may be useful to understand the molecular basis of soybean-F. oxysporum interactions, and also in the development of new resistance mechanisms in soybean against F. oxysporum, including the over-expression of key soybean genes.
Plant and fungus material
Soybean [G. max (L.) Merrill] partially resistant genotype Forrest [7, 64] was evaluated after inoculation with a conidial suspension of non-pathogenic FO36 and pathogenic FO40 F. oxysporum isolates. The FO36 and FO40 isolates were collected from Lyon and Butler counties in Iowa, respectively, during a 3-year survey from 2007 to 2009 that assessed Fusarium spp. diversity and frequency from soybean roots . Aggressiveness of the two isolates was previously determined using rolled-towel assays [7, 8]. Both isolates used in this study were maintained on silica in the dark at 5 °C at Iowa State University, Seed Science Center in Ames, U.S.A.
Production of the inoculum and inoculation procedure
Inoculum for both isolates was grown for seven days on potato dextrose agar (PDA) at 25 °C with a 12-h photoperiod. Conidia were collected by rinsing plates with sterile water, scraping the agar surface with a scalpel and filtering the conidial suspension through sterile cloth. Spore suspension was adjusted to a final concentration of 1 × 106 conidia/ml based on microscopic counts using a Bürker chamber. Fifteen seeds of the partially resistant Forrest genotype were placed on a paper towel moistened with sterile distilled water and inoculated by pipette with 100 μl of 1 × 106 conidial suspension of FO36 or FO40 isolates. Another moistened paper towel was placed over the inoculated seeds, rolled up, and placed vertically in a 25-l bucket. An open plastic bag was placed over each towel to avoid cross-contamination between isolates. A black plastic bag was placed over each bucket and they were placed on a bench at room temperature (~22 °C). Noninoculated checks were included to ensure that other seed pathogens were not present. For the detection of F. oxysporum by fungal DNA assay, roots were sampled at 48, 72, 96 and 168 hpi to evaluate fungal growth and colonization. For RNA-Seq analysis, roots were collected at 72 and 96 hpi. Noninoculated control roots were sampled at the same times listed above. Three pools of five roots were prepared for each isolate and sampling time. The resulting samples were immediately frozen in liquid nitrogen and stored at −80 °C until biological analysis were carried out.
Quantitation of fungal DNA and disease severity evaluation
After inoculation, roots at 48, 72, 96 and 168 hpi were evaluated to quantify the growth of F. oxysporum by qPCR. DNA was extracted from soybean samples, as well as from FO36 and FO40 F. oxysporum isolates. To extract fungal DNA, the edge of a culture of each isolate grown for seven days on PDA plates at 25 °C with a 12-h photoperiod was scraped using a sterile loop. The mycelium and spores were transferred to a 50-ml plastic centrifuge tube (Corning Inc., Tewksbury, MA) containing 25 ml of liquid growth medium (3 g of yeast extract, 3 g of malt extract, 5 g of peptone, 20 g of dextrose, 2 g of NH4SO4 in 1 l of water). The inoculated medium was incubated at room temperature for 5 days on an Innova 2100 platform shaker (New Brunswick Scientific Co., Inc., Enfield, CT) at 100 rpm. Mycelium was harvested by filtration with sterile Miracloth (EMD Biosciences Inc., La Jolla, CA), frozen, and lyophilized. DNA from both isolates and plant tissues was extracted using a conventional CTAB chloroform: isoamyl alcohol protocol . The quality and quantity of DNA was evaluated by measuring the concentration (ng/μl) and A260/A280 and A260/A230 via a NanoDrop 2000 spectrophotometer (Thermo Scientific, Wilmington, DE). The genomic DNA was subsequently used as the template for the fungal DNA quantification using qPCR.
Quantitative PCR was carried out on the CFX-96 instrument (Bio-Rad, Hercules, CA). Each DNA sample was loaded in triplicate in a total reaction volume of 20 μl per sample with each reaction mix containing 2 × SYBR Green Mastermix (Applied Biosystems, Foster City, CA) and 0.4 μM of each primer, using primers targeting the F. oxysporum tef1α gene (JN222908.1; Additional file 9: Table S9). The following cycling conditions were used: 95 °C for a 10 min denaturation step; followed by 38 cycles of amplification at 95 °C for 15 s and 58° for 1 min; and melting curve analysis of heating to 95 °C, cooling to 60 °C for 1 min, and heating to 95 °C at a rate of 0.5 °C/5 s. DNA quantities are reported as ng of fungal DNA obtained from root tissues and determined based on the equation of the linear regression according to the instrument technical manual (Bio-Rad). Fungal DNA (20 ng) deriving from both F. oxysporum isolates was serially diluted [1:1, 1:5, 1:52, 1:53, 1:54, 1:55] in sterile water and 20 ng of each root DNA sample was compared to the dilution standard curve to determine fungal DNA quantity.
Two-factor ANOVA was performed on the observed means of the fungal tef1α DNA quantity, considering times of sampling (48, 72, 96 and 168 hpi) and treatments (non-pathogenic and pathogenic inoculated samples) as fixed factors to test the significance (P ≤ 0.05) of times of sampling, treatments and their interactions. One-factor ANOVA, followed by Tukey’s HSD test (P ≤ 0.05), was performed on the observed means of the fungal tef1α DNA quantity within each treatment to set significant differences among times of sampling. Differences between non-pathogenic and pathogenic inoculated means within the same time of sampling were performed using two-way ANOVA and considered to be significant at *P ≤ 0.05; **P ≤ 0.01; ***P ≤ 0.001.
Disease severity evaluation was performed on seedlings collected at 168 hpi. The seedlings were rated by measuring the length of hypocotyl tissue (lesion length in mm) and the total plant length (mm). DSI was calculated by dividing the total plant length and multiplying by 100 .
RNA isolation, library preparation and bioinformatic analysis
Root tissues for RNA isolation for RNA-Seq libraries were dissected from soybean samples inoculated at 72 and 96 hpi with FO36 and FO40 F. oxysporum isolates and their respective controls (18 samples overall). Frozen tissues (500 mg) were ground in liquid nitrogen with a mortar and pestle. RNA was isolated using Trizol reagent (Invitrogen, Carlsbad, CA) and then purified with the RNA Clean up protocol (Qiagen, Valencia, CA), according to the manufacturer’s instructions. RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific), as well as by agarose gel electrophoresis. Furthermore, total RNA samples were assessed for quality using an Agilent® 2100 Bioanalyzer TM (Agilent, Santa Clara, CA). RNA-Seq libraries were prepared by the Iowa State University DNA Facility and sequenced using Illumina HiSeq 2500 sequencer (Illumina Inc., San Diego, CA). 100-bp paired-end reads were generated. Mapping of the RNA-Seq data was performed at the Genome Informatics Facility, Iowa State University. Short read sequences were aligned to the soybean Williams 82 reference genome (Glyma.Wm82.a2.v1 genome assembly 2 annotation version 1; http://www.soybase.org) using GSNAP software . Only uniquely mapped reads were considered for downstream differential expression analysis. Soybean gene models were downloaded from Joint Genome Institute and read counts for each gene model were obtained using the HTSeq program developed by Anders and co-workers . Differential expression analysis was performed using the QuasiSeq package in R . For DE analysis, pathogenic isolate (FO40) was compared against non-pathogenic isolate (FO36) at each time point. Upper quartile normalization was used to normalize the read counts for library size. In QuasiSeq, the QLSpline method was used to account for over-dispersion effects. To account for multiple testing, we estimated the Qvalues for each gene model. To control false discovery rate at 5 %, gene models with Qvalues less than 0.05 were declared DE and gene models with Qvalues less than 0.05 and absolute value of FC ≥ 1.9 were declared to be HDE. For the analysis of fungal genes, the short read sequences were aligned to combined soybean and F. oxysporum f. sp. pisi HDV247 NRRL 37622 reference genome F.oxysporum HDV247 genomes (http://www.broadinstitute.org). Due to the very small number of fungal reads, the further normalized expression analysis of transcripts was not performed for F. oxysporum. Soybean GO categories were downloaded from Soybase.org. GO term enrichment (http://www.soybase.org/goslimgraphic_v2/dashboard.php; ) was determined on DEGs with a Qvalue less than 0.05. Mercator functional categories that are easily visualized as MapMan bins were annotated for all gene models. A Wilcox Rank Sum test inside MapMan was used to identify several significantly enriched bins (Additional files 4 and 5: Tables S4 and S5). Due to the high number of DEGs an additional filter of a fold change greater than 1.9 was applied for downstream analysis and visualization and we refer to these gene as HDEGs.
Sequences of HDEGs were compared with National Center for Biotechnology Information (NCBI) non redundant (NR) database with a Blast E-value of 10−3 and were functionally annotated using Blast2GO  assigning a GO term and a metabolic pathway in the Kyoto Encyclopedia of Genes and Genomes (KEGG) to the query sequences. Sequences were classified into 13 functional categories (Cell component; Cell wall; Electron/Energy; Metabolic process; Miscellanea; Photosynthesis; Proteolysis; Response to stress; Resistance; Secondary metabolism; Signal transduction; Transport; Unknown function) based on GO annotation.
The sequencing data have been submitted to Gene Expression Omnibus (GEO) database under the accession number of GSE66861.
Real-time RT-PCR validation analysis
Gene expression data from RNA-Seq analysis were validated by real-time RT-PCR. This was performed on selected soybean genes that were up- or down-regulated at 72 and 96 hpi. A 1 μg sample of total RNA after DNAse I treatment (Qiagen) was used for cDNA synthesis following the iScript cDNA synthesis kit protocol (Bio-Rad). Twenty ng of single strand cDNA determined by Nanodrop 2000 spectrophotometer (Thermo Scientific) were used for real-time RT-PCR. Relative quantitative analysis was performed under the following conditions: 95 °C for 3 min and 44 cycles at 95 °C 10 s, 60 °C 25 s. A melting curve analysis, ranging from 60 to 95 °C, was used to identify different amplicons, including non-specific products. Three technical replicates (within each biological replicate) were employed for each tested sample and template-free negative controls. Gene-specific primers were designed within consecutive exons, separated by an intron, using Primer3 software and their sequences are shown in Additional file 9: Table S9. Relative quantification was normalized to the soybean housekeeping control genes actin and FC in gene expression was calculated using the 2-ΔΔCt method .
This project was funded by the Iowa Soybean Association, U.S.A. We thank D. R. Cruz, M. L. Ellis, and D. A. Mayfield for technical assistance and cooperation in this study.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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