- Research article
- Open Access
RNA-Seq analysis of Citrus reticulata in the early stages of Xylella fastidiosa infection reveals auxin-related genes as a defense response
© Rodrigues et al.; licensee BioMed Central Ltd. 2013
- Received: 1 March 2013
- Accepted: 25 September 2013
- Published: 3 October 2013
Citrus variegated chlorosis (CVC), caused by Xylella fastidiosa, is one the most important citrus diseases, and affects all varieties of sweet orange (Citrus sinensis L. Osb). On the other hand, among the Citrus genus there are different sources of resistance against X. fastidiosa. For these species identifying these defense genes could be an important step towards obtaining sweet orange resistant varieties through breeding or genetic engineering. To assess these genes we made use of mandarin (C. reticulata Blanco) that is known to be resistant to CVC and shares agronomical characteristics with sweet orange. Thus, we investigated the gene expression in Ponkan mandarin at one day after infection with X. fastidiosa, using RNA-seq. A set of genes considered key elements in the resistance was used to confirm its regulation in mandarin compared with the susceptible sweet orange.
Gene expression analysis of mock inoculated and infected tissues of Ponkan mandarin identified 667 transcripts repressed and 724 significantly induced in the later. Among the induced transcripts, we identified genes encoding proteins similar to Pattern Recognition Receptors. Furthermore, many genes involved in secondary metabolism, biosynthesis and cell wall modification were upregulated as well as in synthesis of abscisic acid, jasmonic acid and auxin.
This work demonstrated that the defense response to the perception of bacteria involves cell wall modification and activation of hormone pathways, which probably lead to the induction of other defense-related genes. We also hypothesized the induction of auxin-related genes indicates that resistant plants initially recognize X. fastidiosa as a necrotrophic pathogen.
- Gene expression
- Plant-pathogen interaction
- Ponkan mandarin
- Pera sweet orange
The Brazilian citrus industry accounts for 30% of sweet orange production and 85% of exports of frozen-concentrated orange juice in the world, despite the large number of pests and diseases that affect the Brazilian orchards. Among these diseases, Citrus Variegated Chlorosis (CVC), caused by the bacterium Xylella fastidiosa, costs around 120 million US dollars a year to chemically control the bacterial vectors and for replanting new orchards .
Citrus species show varying responses to CVC. While the sweet orange (Citrus sinensis L. Osb) is very susceptible, the Ponkan mandarin (Citrus reticulata Blanco) is considered resistant because it shows no symptoms, yet the bacteria can be isolated from the plants at 30 days after inoculation. However, after 60 days of inoculation the bacteria cannot be isolated from the plant. The resistance of mandarin is not related to the number and/or diameter of xylem vessels, suggesting that resistance is caused by active defense responses . Based on this, the pattern of gene expression in Ponkan mandarin was assessed by sequencing expressed sequence tags in mandarins inoculated with X. fastidiosa at 30 and 60 days after infection. The results revealed differential expression patterns for several defense-related genes of the salicylic acid (SA), jasmonate (JA), and ethylene (ET) signaling pathways [6, 7]. These results indicate a crosstalk between regulatory pathways that control different cellular processes in the mandarin-X. fastidiosa interaction. However, it is unclear whether these pathways are activated during the initial response of Ponkan mandarin to this phytopathogen. Thus, the present study aimed to evaluate which genes are activated in the preliminary stages of infection, as this phase may involve an important strategy for avoiding pathogen establishment and colonization, and consequently the progress of the disease. Identifying these defense genes could be an important step towards obtaining sweet orange resistant varieties through breeding or genetic engineering.
Overview of RNA-seq analysis
In recent years the number of works using global expression analysis to study plant-pathogen interactions has grown considerably. By comparing specific mRNAs present in different tissues, such as infected or not infected, differentially expressed genes can be identified and their functions inferred.
In the present study, we used RNA-seq to analyze the differential expression of Ponkan mandarin mRNAs one day after X. fastidiosa infection (compared with mock inoculated plants). The presence or absence of bacteria in the plants used in this analysis was confirmed by real-time quantitative PCR (RT-qPCR) (Additional file 1). Three biological replicates for each condition were selected for performing transcriptome analyses.
RNA-seq generated 35,344,265 and 37,326,339 single end reads of 101 bp for the non-infected and infected libraries, respectively. Tophat was used to align the reads to the Citrus clementina reference genome, with approximately 74% of success. The expression level of 27,889 coding sequences was quantified using the software Cufflink. A total of 1,391 transcripts showed significant variation in expression by Cuffdiff analysis: 724 were induced and 667 were repressed (P ≤ 0.001) in the infected Ponkan mandarin (Additional file 2).
Induction of a PAMP - Triggered Immunity (PTI) – like response in Ponkan mandarin
Differentially expressed genes in Ponkan mandarin in response to infection by X. fastidiosa
gene id_Citrus clementina*
P ≤ 0.001
leucine-rich repeat family protein
leucine-rich repeat protein kinase family protein
receptor like protein 12
nb-arc domain-containing disease resistance protein
as1 (asymmetric leaves 1); transcription factor
myb domain protein 66); transcription factor
glucan synthase-like 7
cellulose synthase like A9
pectate lyase family protein
BURP domain-containing protei
pectate lyase family protein
nine-cis-epoxycarotenoid dioxygenase 6
carotenoid clevage dioxygenase 7
ap2 domain-containing transcription factor, putative
zinc finger (c3hc4-type ring finger) family protein
indole-3-acetic acid inducible 9
ubiquitin protein ligase 5
ARF-GAP DOMAIN 8
arf gtpase activator
auxin transport protein (big)
xyloglucan endotransglycosylase, putative
engoxyloglucan transferase A4
A gene encoding a coiled-coil motif nucleotide-binding site–leucine-rich repeat (CC-NBS-LRR) protein was upregulated in Ponkan mandarin challenged with X. fastidiosa (Table 1). CC-NBS-LRR is a cytoplasmic receptor normally involved in responses triggered after recognition of Avr proteins secreted by the pathogen. However, this bacterium does not have the type III secretion apparatus or Avr proteins . This leads us to believe that this receptor may be involved in perception of damage-associated molecular patterns (DAMPs), because the recognition of cytoplasmic danger signals depends on cytoplasmic sensors like NB-LRR resistance proteins [16–18]. This hypothesis is consistent with X. fastidiosa’s ability to produce danger molecules by degrading plant cell walls . However, this hypothesis needs to be further investigated.
A main feature of the PTI response is strengthening of the cell wall . Many genes related with cell wall modification were upregulated in Ponkan mandarin infected with X. fastidiosa, which reinforced our hypothesis that PTI is involved in this early response.
Genes related to secondary metabolism and the cell wall
In response to X. fastidiosa infection, Ponkan mandarin appears to activate genes for the formation and alteration of secondary xylem cells as a defense mechanism. Induction of the transcription factor AS1, which has a MYB domain (Ciclev10012089m) was also observed. It is suggested that the abundance of MYB proteins in the xylem could be involved in transcriptional regulation of the formation of the secondary xylem  (Table 1). Furthermore, a myo gene (Ciclev10010780m), which encodes actin, was strongly induced (Table 1). Many studies suggest that actin displays a similar expression pattern to microtubules, which are suggested to determine the location for deposition of the secondary cell wall, cellulose, lignin, hemicellulose, and proteins . Another transcription factor induced in this study was MYB66 (Ciclev10017556m), which is probably involved in the regulation of flavonoids biosynthesis and lignification [22–24] (Table 1). To corroborate these observations, we verified the activation of genes related to phenylpropanoid and flavonoids biosynthesis, which act as anti-pathogenic molecules . Some of them such as phenylalanine ammonium lyase are involved in lignin biosynthesis (Table 1; Figure 2 and Additional file 3). In addition to lignification, callose deposition is also an important defense mechanism in plants and one callose synthase (Ciclev10030560m) was induced in Ponkan mandarin infected with X. fastidiosa (Table 1; Figure 2 and Additional file 3). Additionally, genes encoding cellulose synthases (Ciclev10031284m, Ciclev10014155m and Ciclev10018639m) were significantly induced, such as CESA8 and CESA4, which are key enzymes in the biosynthesis of the xylem cell wall . Among the repressed genes it is remarkable the presence of those encoding proteins related to cell wall degradation (Table 1; Figure 2 and Additional file 3). These results indicate that the molecular defense response of Ponkan mandarin against X. fastidiosa involves the participation of genes related to cell wall biosynthesis. This could represent an important strategy of the plant for restrict the movement of X. fastidiosa through the xylem cells.
Hormone related-genes in the Ponkan mandarin defense response
Defense-genes upregulated in Ponkan mandarin in response to X. fastidiosa infection
Gene id_Citrus clementina*
P ≤ 0.001
calcium-binding EF hand family protein
calmodulin-dependent protein kinase
calcium-binding EF hand family protein
GTP binding / GTPase
guanyl-nucleotide exchange factor/ protein binding
WD-40 repeat family protein
MAP kinase kinase 9
shikimate dehydrogenase, putative
heat shock protein 70
17.6 kda class II heat shock protein
heat shock protein 90.1
dnaJ heat shock N-terminal domain-containing protein
homogentisate phytyltransferase 1
cytochrome P450, family 706, subfamily A, polypeptide 6
glutathione S-transferase TAU 8
udp-glucosyl transferase 72E1
trypsin and protease inhibitor family protein
With regard to ABA-related genes, AP2 (Ciclev10010403m), nced 6 (Ciclev10006710m), and ccd 7 (Ciclev10027500m) were induced in response to X. fastidiosa infection (Table 1; Figure 3 and Additional file 4). AP2 is involved in the activation of genes related to ABA biosynthesis , while nced 6 and ccd 7 are associated with biosynthesis and transport of this hormone, respectively. Additionally the aip 2 gene (Ciclev10008969m) was repressed (Table 1; Figure 3 and Additional file 4) and this gene encodes an E3 ligase that negatively regulates ABA signaling by targeting ABI3, a central regulator of this pathway, for degradation .
So the repression of this gene strengthens the idea that ABA biosynthesis is activated in Ponkan mandarin in response to X. fastidiosa infection.
Many studies have reported that auxin promotes susceptibility to bacterial diseases [42, 43]. However, this affirmation is only true for biotrophic organisms: auxin signaling is an important component involved in plant resistance to necrotrophic pathogens [30, 44]. Auxin signaling is upregulated in Ponkan mandarin in response to X. fastidiosa and this plant is resistant to this pathogen; therefore, we speculated that in the early stage of infection Ponkan mandarin recognizes X. fastidiosa as a necrotrophic organism, even though this bacterium does not cause massive destruction of host tissue. This is consistent with the direct injection of the bacteria by the insect vector into the xylem vessels, which is composed mainly of dead cells, and the fact that X. fastidiosa is able to degrade plant cell wall, which is an important factor for its colonization in susceptible plants . Therefore, substantial tissue destruction is not necessary to trigger necrotroph-related responses mediated by X. fastidiosa in the resistant plant host.
The evidence in this paper indicates that activation of the auxin signaling pathway does not promoting susceptibility of Ponkan mandarin after infection with the bacterium. The involvement of this hormone in pathogen susceptibility disease development appears to include rapid elongation of plant tissues by increasing the extensibility of the cell wall . Proteins that participate in acid-induced cell wall extension are endo-β-1,4-glucanases (EGases), xyloglucan endotransglycosylases (XETs), and expansins . We did not observed induction of a major set of these proteins. In fact some of them such as XETs (Ciclev10005561m and Ciclev10028851m) and expansin (Ciclev10012518m) were repressed in Ponkan mandarin in response to X. fastidiosa, suggesting that auxin signaling related genes found in this work are not primarily promoting cell expansion (Table 1). On the other hand, auxin synergistically with jasmonic acid/ethylene-signaling is required for necrotrophic resistance. In addition some members of ARF positively regulate camalexin biosynthesis resulting in resistance to necrotrophic pathogens . This defense system, involving the interaction between auxin and JA signaling pathways, which probably occurs in Ponkan mandarin, given the significant induction of genes associated with both signaling pathways. Camalexin is produced through the tryptophan pathway and in our analysis two genes involved in the biosynthesis of tryptophan, dehydroquinate-shikimate dehydrogenase (Ciclev10000874m) and MAPK 9 (Ciclev10021170m), were induced in Ponkan mandarin, suggesting that camalexin biosynthesis may be induced in response to X. fastidiosa infection. Taken together all these evidences suggest us that the resistant Ponkan mandarin recognizes X. fastidiosa in early stage of infection as a necrotrophic pathogen.
To confirm the participation of different genes related to pathogen recognition, cell wall synthesis, and hormone signaling pathways in the mandarin resistance response, we also tested their expression in Pera sweet orange. The analysis confirmed that genes encoding LRR-RLK and CC-NBS-LRR (pathogen recognition), AP2 (ABA signaling), MYO and CESA4 (cell wall synthesis) were not only specifically induced in mandarin but also repressed in sweet orange (Additional file 6).
Validation of RNA-seq data by RT-qPCR
This work demonstrated that the defense response of Ponkan mandarin to X. fastidiosa involves induction of genes related to PAMP receptors, cell wall synthesis, and ABA, JA and auxin signaling pathways, which will probably culminate in the induction of other defense-related genes. We also hypothesize that Ponkan mandarin initially recognizes X. fastidiosa as a necrotrophic pathogen, inducing genes related to the auxin signaling pathway and later it changes the response to a biotrophic pathogen.
The genes found in this work are important tools to be used in breeding programs to accelerate the selection of hybrid from C. reticulata and C. sinensis carrying defense responses from mandarin. Moreover these genes can be also used for genetic engineering aiming the development of resistant sweet orange varieties.
Plant materials and bacterial detection
The experiments were conducted with physiologically mature plants, of uniform size and production of young leaves. When the shoots reached a length of approximately 10 cm, they were artificially inoculated by needle prick with 10 μL suspension (108 cells mL-1) of X. fastidiosa strain 9a5c in PBS buffer at five different points on the same stem. Negative controls comprising Ponkan mandarin (C. reticulata Blanco) and Pera sweet orange (Citrus sinensis L. Osb) were mock inoculated with PBS buffer.
Total genomic DNA (plant + bacteria) was extracted from inoculated cambial tissue enriched with xylem after 1 day using a CTAB method adapted from . These samples were used for detection of bacteria using real-time PCR reactions. The analyses were carried out with an ABI PRISM 7500 Sequence Detector System (Applied Biosystems, Foster City, CA, USA). The reaction was performed in a total volume of 25 μL, containing 12.5 μL of TaqMan PCR Master Mix fast (Applied Biosystems), 200 ng of DNA template and 525 nM of primers CVC-1 and CCSM-1 . Each sample was tested in triplicate and with five biological replicates. Negative (no template DNA) and positive (DNA from X. fastidiosa) controls were included in all experiments to exclude or detect any possible contamination. The samples were considered positive for the presence of X. fastidiosa when they presented Ct (Cycle Threshold) below or equal to 37; negative samples did not present amplification up to this Ct value (unpublished data). From these results, we selected the three biological replicates for different conditions and performed transcriptome analyses.
RNA isolation and expression analysis in RNA-seq
For transcriptome analysis we used cambial tissue enriched with xylem from Ponkan mandarin. Total RNA was extracted with Trizol (Invitrogen Life Technologies Foster City, CA, USA) and treated with DNase RNase-Free Set (Qiagen, Valencia, CA, USA), according to the manufacturer’s instructions. We extracted RNA samples from a pool of three independent biological replicates infected after one day and their respective controls (not infected). The concentration of RNA was measured in a NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE). RNA quality was evaluated using an Agilent Bioanalyzer Model 2100 (Agilent Technologies, Palo Alto, CA).
A total of 10 μg of RNA from Ponkan mandarin (control and infected with X. fastidiosa) were sent to Macrogen Inc. (South Korea) for sequencing using the Genome Analyzer IIx platform (Illumina Inc.). All procedures were performed according to Illumina’s protocols. Purified cDNA libraries were dispersed onto an Illumina single-end flow cell composed of eight lanes using the Illumina Cluster Station (Illumina Inc.). One lane was used per sample of the treated and control plants. The 101 bp reads were collected using the Illumina GA II and sequencing-by-synthesis technology. The sequences of Ponkan mandarin were mapped against the Citrus clementina reference genome (http://www.phytozome.net/clementine.php) using TopHat . After alignment, the relative abundance of the transcripts was measured with the Cufflink software, which measures the transcripts abundance as RPKM (Reads Per Kilobase of exon model per Million mapped reads). The differential expression between Ponkan mandarins inoculated or not with bacteria, and its significance, was calculated in Cuffdiff . The differentially expressed transcripts were annotated and automatically categorized using GO (Gene Ontology - http://www.blast2go.com/b2ghome). These sequences were also used to search for similar protein sequences available in GenBank using the BLASTX tool.
In addition, the differentially expressed genes were also functionally analyzed using the MapMan software, which is a user-driven tool that displays large genomics datasets onto diagrams of metabolic pathways or other processes .
Expression analysis by RT-qPCR
Twelve genes that were identified by RNA-seq to be induced or repressed in Ponkan mandarin in response to X. fastidiosa, were selected for validation by RT-qPCR: ATEXPA 4; CLV 1; CC-NBS-LRR; RLK; P 12; LOX; AIP; MYO; AP 2; HSP 90; CCR 4 and IAA 9 (Additional file 7).
Furthermore, we used RT-qPCR to compare the level of expression of some genes involved in the auxin pathway, pathogen recognition, ABA signal transduction, and cell wall synthesis in Ponkan mandarin and in Pera sweet orange, a susceptible variety, one day after infection with the bacteria. We evaluated the IAA9 (Aux/IAA), ARF 19, TIR 1, BIG and E 3 genes (auxin pathway); LRR-RLK and CC-NBS-LRR (pathogen recognition); AP2 (ABA); MYO and CESA4 (cell wall synthesis).
Additionally, we checked the relative quantification of genes encoding IAA9 and PR1 in Citrus plants, by RT-qPCR, using RNA extracted from a mixture of leaves and petioles of Ponkan mandarin and Pera sweet orange at 1, 7, 14, and 21 days after inoculation of X. fastidiosa or mock inoculated (control).
The primers for these genes were designed using PrimerExpress software (Applied Biosystems, Foster City, CA, USA) (Additional file 9).
The specificity of the primers was checked in silico against the NCBI database (http://www.ncbi.nlm.nih.gov/) using the Primer-BLAST tool. All the primer sequences showed specificity with the sequences of target genes. Additionally, we checked the pattern of dissociation obtained after RT-qPCR, using a meting curve for each primer. This showed a single peak for all the evaluated genes, confirming the existence of only one amplicon (Additional file 10).
The efficiency of the primers was estimated in each experiment using the software Miner (http://www.miner.ewindup.info/). This software quantifies the results of RT-qPCR based on the kinetics of the PCR amplification individually for each sample, without the need for a standard curve. This allows a direct calculation of the efficiency and values of cycle quantification (cq) . All primers showed amplification efficiencies between 90 - 100% (Additional file 10).
To find a reference gene to normalize the RT-qPCR results, the stability of five endogenous control genes in Citrus was analyzed to confirm their stability using geNorm software  and to ensure the existence of gene expression variation due to the experimental conditions. The primers for these genes were obtained from a previous work . In this evaluation we used samples of Pera sweet orange and Ponkan mandarin (control and infected with X. fastidiosa). Ubiquitin (UBQ) and cyclophilin (CYC) were the most stable and were selected for further analysis. However, the other three genes, eukaryotic translation elongation factor 2, NADP-isocitrate dehydrogenase and tubulin also showed satisfactory mean values (M-value) (Additional file 11). These M-values are within acceptable values at a cutoff value of 0.15 .
For the analyses of gene expression by RT-qPCR, we used RNA isolated as described above, with three independent biological replicates, infected or not with X. fastidiosa. These RNAs were used for the cDNA synthesis according to the instructions of the Thermo Scientific for the RevertAid H Minus First Strand cDNA Synthesis Kit. After synthesis, the cDNAs were diluted at 1:25 and used in RT-qPCR. The evaluations were performed on an ABI Prism 7500 Sequence Detector System (Applied Biosystems, Foster City, CA, USA) using absolute quantification analysis. The detection of PCR products was measured by monitoring the increase in fluorescence emitted by SYBR green marker. For all amplifications performed in RT-qPCR, we produced dissociation curves to check for nonspecific amplification resulting from possible contamination.
The analysis and normalization of gene expression were performed in the Genex software (version 188.8.131.52; http://www.multid.se), using the efficiencies and Cqs generated in the Miner software, and transformed into non-standardized data (Q). Uninfected samples were used as calibrators for each genotype evaluated. We used two endogenous genes for the normalization of the data.
The present study was conducted with the financial support of Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP) (Process n. 2007/07944-3), which provided a scholarship to CMR and Instituto Nacional de Ciência e Tecnologia (INCT) de Genômica para Melhoramento de Citros (Process n. 573848/2008-4), with the financial support of FAPESP and Conselho Nacional de Pesquisa de Desenvolvimento (CNPq). MAM, AAS, and MAT are CNPq fellows.
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