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Comparative Transcriptome Analyses of Resistant and Susceptible Near-Isogenic Wheat Lines following Inoculation with Blumeria graminis f. sp. tritici
research-article
Author(s):
Piyi Xing
1
,
2 ,
Xueying Zhang
1
,
2 ,
Yinguang Bao
2 ,
Yuhai Wang
3 ,
Honggang Wang
1
,
2 ,
Xingfeng Li
1
,
2
,
*
Publication date (Electronic):
1 May 2017
Journal:
International Journal of Genomics
Publisher:
Hindawi
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Abstract
Powdery mildew is one of the most important diseases of wheat. In this study, the leaf RNA samples of wheat NILs carrying powdery mildew resistant and susceptible Pm2 alleles (L031 and Chancellor) and its F1 hybrid at two time points (16 h and 96 h postinoculation) were used for RNA-seq analysis. We carry comparison between similar materials at different times and between different materials at same times. The overlapping DEGs between the dominant phenotypes (L031 and F1 hybrid) and the recessive phenotype (Chancellor) were 1028 and 2214 DEGs, which were clearly lower than those between the dominant and recessive parents and thus could provide relatively accurate and valuable information. GO and KEGG enrichment analysis of DEGs revealed that other than the expected defense-related genes, differential up- and downregulation of genes from many other signaling networks were also involved. Comparative transcriptome analysis also revealed that early-stage postinoculation is important and suitable time points to study expression profiles and signaling pathways of resistance-related genes following fungal inoculation. qRT-PCR analyses showed highly consistent expression patterns of genes with RNA-seq data. The results will aid in the identification of genes and signaling pathways involved in powdery mildew response in wheat.
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Most cited references30
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Gene RB cloned from Solanum bulbocastanum confers broad spectrum resistance to potato late blight.
J. Song, J. M. Bradeen, S. K. Naess … (2011)
Late blight, caused by the oomycete pathogen Phytophthora infestans, is the most devastating potato disease in the world. Control of late blight in the United States and other developed countries relies extensively on fungicide application. We previously demonstrated that the wild diploid potato species Solanum bulbocastanum is highly resistant to all known races of P. infestans. Potato germplasm derived from S. bulbocastanum has shown durable and effective resistance in the field. Here we report the cloning of the major resistance gene RB in S. bulbocastanum by using a map-based approach in combination with a long-range (LR)-PCR strategy. A cluster of four resistance genes of the CC-NBS-LRR (coiled coil-nucleotide binding site-Leu-rich repeat) class was found within the genetically mapped RB region. Transgenic plants containing a LR-PCR product of one of these four genes displayed broad spectrum late blight resistance. The cloned RB gene provides a new resource for developing late blight-resistant potato varieties. Our results also demonstrate that LR-PCR is a valuable approach to isolate genes that cannot be maintained in the bacterial artificial chromosome system.
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An important role of the pepper phenylalanine ammonia-lyase gene (PAL1) in salicylic acid-dependent signalling of the defence response to microbial pathogens
Dae-Sung Kim, Byung Kook Hwang (2014)
Introduction Plants have evolved multiple defence signalling pathways to cope with adverse environmental conditions and pathogen attack (Jones and Dangl, 2006). The levels of secondary metabolites such as phenylpropanoids are controlled in response to environmental cues (Dixon and Paiva, 1995; Payyavula et al., 2012). The evolutionary emergence of the phenylpropanoid pathway in plants is an important adaptation that enables plant defence against abiotic and biotic stresses (Ferrer et al., 2008). Phenylpropanoid compounds are precursors to a wide range of phenolic compounds, such as flavonoids, isoflavonoids, anthocyanins, plant hormones, phytoalexins, and lignins (Dixon and Paiva, 1995; La Camera, et al., 2004). Phenylpropanoids have important functions in several different pathways: in plant defence against pathogens and predators, in protection from UV irradiation, in signal transduction and communication with other organisms, and as regulatory molecules (Hahlbrock and Scheel, 1989; Dixon and Paiva, 1995; Ferrer et al., 2008; Vogt, 2010). Phenylpropanoids are derived from cinnamic acid, which is formed from phenylalanine (Vogt, 2010). Phenylalanine ammonia-lyase (PAL) catalyses the non-oxidative deamination of phenylalanine to trans-cinnamate. This is the first step in the phenylpropanoid pathway, and is an important regulation point between primary and secondary metabolism (Hahlbrock and Scheel, 1989; Dixon and Paiva, 1995; Huang et al., 2010; Vogt, 2010). PAL is an inducible enzyme that responds to biotic and abiotic stresses such as pathogens, UV irradiation, and low temperature (Dixon and Paiva, 1995; MacDonald and D’Cunha, 2007). PAL plays an important role in plant defence; it is involved in the biosynthesis of salicylic acid (SA), an essential signal involved in plant systemic resistance (Mauch-Mani and Slusarenko, 1996; Nugroho et al., 2002; Chaman et al., 2003). PAL gene expression responds to a variety of environmental stresses, including pathogen infection, wounding, nutrient depletion, UV irradiation, and extreme temperatures (Edwards et al., 1985; Liang et al., 1989a, b; Huang et al., 2010; Payyavula et al., 2012; Jin et al., 2013). Molecular genetics methods have been used to silence or disrupt PAL genes for the functional analysis of their roles in plant development and responses to external stimuli (Pallas et al., 1996; Rohde et al., 2004; Huang et al., 2010). In Arabidopsis thaliana, PAL is encoded by a small gene family with four members, denoted PAL1−PAL4 (Raes et al., 2003; Huang et al., 2010). PAL1, PAL2, and PAL4 are strongly expressed in inflorescent stems, a tissue rich in lignifying cells, whereas the PAL3 transcript is expressed at a very low level (Raes et al., 2003). Phenotypic analysis of the PAL1 and PAL2 genes was performed for both single and double mutants. The growth and development phenotypes of the pal1 and pal2 single mutants were not significantly different from the growth and development phenotypes of wild-type (WT) plants. The pal1/pal2 double mutant did show phenotypic differences from that of WT plants, such as infertility, a significant reduction in lignin accumulation, and alteration in secondary cell-wall ultrastructure (Rohde et al., 2004). Recently, morphology-based genetic analysis has been conducted on pal1/pal2 double mutants and pal1/pal2/pal3/pal4 quadruple mutants. The pal1/pal2 double mutant produced slightly yellow seeds due to the lack of condensed tannin pigments in the seed coat, it was deficient in anthocyanin pigments in various plant tissues, and it was highly sensitive to UV-B light. These results suggest that PAL1 and PAL2 have important and redundant roles in flavonoid biosynthesis (Huang et al., 2010). The pal1/pal2/pal3/pal4 quadruple mutant had a stunted phenotype, substantially reduced levels of SA accumulation, and increased susceptibility to the virulent bacterial pathogen Pseudomonas syringae (Huang et al., 2010). PAL-suppressed transgenic tobacco has undeveloped systemic acquired resistance, which correlates with the reduction of SA levels in both inoculated and uninoculated leaves (Pallas et al., 1996). The PAL inhibitor 2-aminoindan-2-phosphonic acid decreases the pathogen- or elicitor-induced SA accumulation in potato (Solanum tuberosum), cucumber (Cucumis sativus), and Arabidopsis (Meuwly et al., 1995; Mauch-Mani and Slusarenko, 1996; Coquoz et al., 1998). Mauch-Mani and Slusarenko (1996) proposed that the production of SA precursors is a major function of PAL in the resistance of Arabidopsis to Hyaloperonospora arabidopsidis (Hpa). In this study, we identified the pepper (Capsicum annuum) PAL gene, CaPAL1, using the macroarray method (Jung and Hwang, 2000). CaPAL1 was upregulated in pepper leaves by infection with avirulent Xanthomonas campestris pv. vesicatoria (Xcv) Bv5-4a. CaPAL1 loss of function and gain of function were characterized using virus-induced gene silencing (VIGS) in pepper plants (Choi et al., 2007) and ectopic overexpression in Arabidopsis plants (Kim and Hwang, 2011). CaPAL1-silenced pepper plants exhibited increased susceptibility to Xcv infection. CaPAL1 silencing promoted Xcv growth but suppressed pathogen-induced PAL activity in pepper leaves. Suppression of CaPAL1 induction in silenced leaves reduced the expression of the SA-dependent gene CaPR1, but did not reduce the expression of the jasmonic acid-dependent gene CaDEF1 (defensin). CaPAL1 silencing also compromised the SA accumulation, oxidative burst, and cell death during Xcv infection. Constitutive overexpression of CaPAL1 in Arabidopsis conferred increased PAL activity, increased reactive oxygen species (ROS) burst and cell death, induction of PR1 expression and SA accumulation, reduced susceptibility to Pseudomonas syringae pv. tomato (Pst), and increased basal resistance to infection by the obligate biotrophic oomycete Hpa. Together, these results provide convincing evidence for the involvement of pepper CaPAL1 in plant defence against pathogen attack. This suggests the potential significance of PAL genes in plant immune responses. Materials and methods Plant materials and growth conditions Pepper (C. annum L., cv. Nockwang) plants were grown in plastic pots containing a soil mix (peat moss:perlite:vermiculite, 2:1:1, v/v/v) in a growth room at 28 °C with a day length of 16h and a light intensity of 70 μmol photons m–2 s–1. All A. thaliana lines used in this study were the ecotype Columbia (Col-0). Seeds were surface sterilized and cold treated for 3 d at 4 °C before they were sown in the soil mix. Plants were grown in the soil mix in an environmental growth chamber at 24 °C under 14h light/10h dark cycles with a photosynthetic flux of 130 μmol photons m–2 s–1 and 60% relative humidity. Pathogen inoculation Xcv strains Ds1 and Bv5-4a, which are virulent and avirulent to pepper plants (cv. Nockwang), respectively, were used in this study. The bacteria were cultured in yeast nutrient (YN) broth (5g l–1 of yeast extract and 8g l–1 of nutrient broth), harvested by centrifugation at 10000g for 2min, and resuspended in sterilized tap water. To prepare the inoculum for inoculation, the bacterial suspension was diluted to an appropriate density. Leaves of pepper plants at the six-leaf stage were inoculated by infiltrating the bacterial suspension using a syringe without a needle (Choi and Hwang, 2011). Pst DC3000 and DC3000 (avrRpm1), which are virulent and avirulent to Arabidopsis Col-0, respectively, were grown in King’s B broth (10g l–1 of peptone, 1.5g l–1 of K2HPO4, 15g l–1 of glycerol, and 5g l–1 of MgSO4). Leaves of Arabidopsis plants were infiltrated with Pst in 10mM MgCl2 using a syringe without a needle. Hpa isolate Noco2, which is virulent to Arabidopsis ecotype Col-0, was used in this study. Spore suspension (5×104 conidiospores ml–1) was sprayed onto 7-d-old seedlings. Inoculated plants were domed with a plastic wrap to maintain moisture. The numbers of sporangiophores and spores on cotyledons were counted to assess disease severity at 7 d after inoculation. Isolation and sequence analysis of CaPAL1 cDNA A cDNA library was constructed from poly(A)+ mRNA of pepper leaves inoculated with the incompatible Xcv Bv5-4a strain. Pathogen-inducible cDNAs were screened using the macroarray method of Jung and Hwang (2000). Among the screened defence response genes, the PAL homologue, CaPAL1 (GenBank accession no. KF279696), was selected based on the BlastX algorithm of the NCBI website (Altschul et al., 1997). Amino acid sequence alignment of CaPAL1 and other PAL orthologues was performed using Clustal X (Thompson et al., 1997). Genomic DNA gel blot analysis For Southern blot analysis, genomic DNA was extracted from pepper leaves using Plant DNAzol® Reagent (Invitrogen, Carlsbad, CA) following the manufacturer’s instructions. Twenty micrograms of genomic DNA was digested with restriction endonucleases EcoRI and HindIII, subjected to electrophoresis through 0.7% agarose gels, and blotted onto HybondTM-N+ membranes (Amersham, Little Chalfont, UK), followed by cross-linking under UV illumination. CaPAL1 cDNA probes were [32P]dCTP labelled using Klenow enzyme (Roche, Mannheim, Germany). The membranes were hybridized to 32P-labelled probe at 65 °C overnight (Jung et al., 2003). RNA gel blot and real-time reverse transcription (RT)-PCR analyses Total RNA was extracted from pepper and Arabidopsis plants with Trizol reagent (Invitrogen) according to the manufacturer’s instructions. To generate the CaPAL1 gene-specific probe for the northern blot, the full-length CaPAL1 cDNA was [32P]dCTP-labelled using Klenow enzyme. RNA gel blot and real-time RT-PCR analyses were conducted following standard procedures, as described previously (Choi and Hwang, 2011; Choi et al., 2012). For real-time RT-PCR analysis, cDNA was synthesized from 1 μg of total RNA using avian myeloblastosis virus reverse transcriptase (Roche), synthesized oligo(dT)15 primer, and dNTPs (Takara, Shiga, Japan). The real-time PCR was performed for 45 cycles using 1 μl of cDNA as template. The PCR conditions were 94 °C for 5min; 30 cycles of 94 °C for 30 s, 55 °C for 30 s, and 72 °C for 90 s; and 72 °C for 10min for the final extension. The primers used for RT-PCR were 5′-GGTTTTGGTGCAACATCACATAGGAG-3′ (forward) and 5′-ATTGTCAAAGTTCTCTTAGCTACTTGGC-3′ (reverse) for CaPAL1, 5′-CATCAGGAAGGACTTGTACGG-3′ (forward) and 5′-GATGGACCTGACTCGTCATAC-3′ (reverse) for ACT1 in Arabidopsis, 5′-CAGGATGCAACACTCTGGTGG-3′ (forward) and 5′-ATCAAAGGCCGGTTGGTC-3′ (reverse) for CaPR1, 5′-CAAGGGAGTATGTGCTAGTGAGAC-3′ (forward) and 5′-TGCACAGCACTATCATTGCATAC-3′ (reverse) for CaDEF1, and 5′-AAACGGCTACCACATCCAAG-3′ (forward) and 5′-ACCCATCCCAAGGTTCAACT-3′ (reverse) for the 18S rRNA gene in pepper. VIGS pTRV (tobacco rattle virus)-based VIGS was conducted to generate CaPAL1 knockdown (TRV:CaPAL1) pepper plants (Liu et al., 2002; Choi et al., 2007). The N-terminal fragment of CaPAL1 cDNA (5′ 546bp) was inserted into pTRV2. pTRV1 and pTRV2:00 or pTRV2:CaPAL1 in Agrobacterium tumefaciens GV3101 were co-infiltrated into the fully expanded cotyledons of pepper plants. Gene knockdown efficacy in CaPAL1-silenced pepper plants was confirmed by RT-PCR from the leaves infected with Xcv. Plant transformation The cDNA fragment of CaPAL1 was cloned into the pBIN35S plant binary vector. The primer pairs 5′-GAGATCTAGAATGG CATCAACAATTGC-3′ (forward) and 5′-GAGAGGATCCCGCT TCCAAGATCTCAA-3′ (reverse) were used in the PCR to create XbaI- and BamHI-sited CaPAL1 cDNA. The resulting binary plasmid was transformed into A. tumefaciens strain GV3101 by electroporation. Agrobacterium-mediated transformation of Arabidopsis ecotype Col-0 was performed using the floral dipping method of Clough and Bent (1998). Transformants were selected on 0.5× Murashige and Skoog (MS) agar plates containing 50 μg ml–1 of kanamycin. Successful transformation was confirmed by RT-PCR using the CaPAL1 gene-specific primer described above. Among the selected transgenic plants, lines #2, #3, and #7 were used in this study. PAL activity assay Total proteins were extracted from pepper and Arabidopsis leaves using 100mM phosphate buffer (pH 6.0) containing 2mM EDTA, 4mM dithiothreitol, and 2% (w/w) polyvinylpyrrolidone. PAL activity in the leaf extract was determined by the method of Song and Wang (2011), with slight modifications. Briefly, the protein extract (0.2ml) was incubated at 30 °C for 60min with 2ml of 0.01M borate buffer (pH 8.7) and 1ml of 0.02M l-phenylalanine (pre-dissolved in 0.01M borate buffer pH 8.7). Absorbance was measured at 290nm before and after incubation. One unit of activity (katal) was defined as the amount of PAL that produces 1 mole of cinnamic acid in 1s and was expressed as nkatal mg–1 of protein. A reaction without the substrate was used as a blank control. Triplicate assays were performed for each extract. Measurement of H2O2 and ion conductivity H2O2 levels in pepper leaves were quantified using a xylenol orange assay (Gay et al., 1999; Choi et al., 2007). The xylenol orange assay reagent was freshly prepared. Two hundred microliters of solution [25mM FeSO4 and 25mM (NH4)2SO4 in 2.5M H2SO4] was added to 20ml of 125 μM xylenol orange in 100mM sorbitol. Eight leaf discs (0.4cm in diameter) were excised from pepper leaves and floated on 1ml of distilled water for 1h. One hundred microliters of the supernatant was immediately added to 1ml of xylenol orange assay reagent. The reaction mixture was incubated for 30min at room temperature, and H2O2 production was monitored by measuring the absorbance at 560nm using a DU 650 spectrophotometer (Beckman, Urbana, IL, USA). Ion conductivity was measured using a SensION7 conductivity meter (Hach, Loveland, CO, USA) to quantify cell death in pepper leaves. Leaf discs (1.2cm in diameter) were excised from pepper leaves inoculated with Xcv and washed for 30min in 20ml of distilled water. Ion conductivity was monitored after incubation of the leaf discs for 3h in freshly prepared distilled water (20ml). SA measurement SA and SA glycoside were extracted and measured from pepper and Arabidopsis leaves, as described previously (Aboul-Soud et al., 2004; Kim and Hwang, 2011). Leaf tissues (0.5g) were extracted in 1ml of 90% methanol following homogenization in liquid nitrogen. 3-Hydroxybenzoic acid (Sigma) was used as an internal standard. SA extracts were analysed automatically through a fluorescence detector (excitation at 305nm and emission at 405nm) in reversed-phase high-performance liquid chromatography in a Waters 515 system (Waters, Milford, MA, USA) with a C18 column. Results Isolation and sequence analyses of CaPAL1 To isolate pathogen-inducible genes from the pepper cDNA library, differential hybridization was performed based on a macroarray method (Jung and Hwang, 2000). Among the isolated clones, a full-length cDNA encoding a PAL homologue in pepper plants was selected and designated CaPAL1 based on the BlastX algorithm of the NCBI website (Altschul et al., 1997). The full-length CaPAL1 cDNA is 2318bp, and contains a 70bp 5′ untranslated region, a 2154bp coding region that encodes a protein of 717 aa, and a 94bp 3′ untranslated region (Supplementary Fig. S1A at JXB online). The deduced amino acid sequence of the CaPAL1 cDNA sequence was compared with plant PAL proteins of tomato, potato, tobacco, Ipomoea, and Arabidopsis. The sequence identities ranged from 82 to 93%. The PAL domain was placed at aa 199−215 in the CaPAL1 sequence (Supplementary Fig. S1B). The strict conservation of a PAL domain suggests that CaPAL1 may act as a PAL enzyme in nitrogen metabolism, phenylpropanoid biosynthesis, and alkaloid biosynthesis in pepper plants (Fritz et al., 2006). To determine how many PAL genes are in pepper, pepper genomic DNA was digested with restriction enzymes EcoRI and HindIII, which do not have the recognition sites within the CaPAL1 cDNA. Hybridization of the EcoRI and HindIII genome digests with the full-length CaPAL1 cDNA showed three and four bands in the range of 2.7–7.1kb, respectively (Supplementary Fig. S2 at JXB online). The full-length CaPAL1 cDNA (2154bp) was used as a positive hybridization control. These results indicated that the CaPAL gene family is composed of three to four genes in pepper plants. CaPAL1 is induced by avirulent Xcv infection Expression of the CaPAL1 gene in different pepper organs was examined by RNA gel blot analysis. CaPAL1 transcript levels were barely detectable in stem and flower tissues, but expression was constitutively much higher in roots. Healthy leaf and fruit tissues did not constitutively express CaPAL1 (Supplementary Fig. S3A at JXB online). We investigated whether CaPAL1 is induced in pepper leaves by virulent or avirulent Xcv infection (Supplementary Fig. S3B). Infection with the avirulent Xcv Bv5-4a (incompatible interaction), but not with the virulent Xcv Ds1, strongly induced CaPAL1 in pepper leaves. CaPAL1 induction remained extremely high 5–25h after avirulent Xcv Bv5-4a infection. CaPAL1 transcripts were not detected in mock-inoculated leaves. The virulent Xcv Ds1 infection did not effectively induce CaPAL1 in pepper leaves compared with the induction in response to avirulent Xcv Bv5-4a infection. CaPAL1 silencing in pepper confers increased susceptibility to Xcv infection To investigate loss of function of CaPAL1 in pepper plants, we silenced CaPAL1 in pepper plants using the tobacco rattle virus (TRV) VIGS technique (Liu et al., 2002; Chung et al., 2004; Kim and Hwang, 2011). To increase the specificity of silencing, the 5′ partial sequence (546bp) of the CaPAL1 coding region was used to construct pTRV2:CaPAL1. Silencing of CaPAL1 in pepper plants resulted in a susceptible response to Xcv infection (Fig. 1). The disease phenotypes of CaPAL1-silenced plants were compared with those of empty-vector control plants after inoculation with virulent and avirulent Xcv at 107 and 108 colony-forming units (cfu) ml–1, respectively. CaPAL1-silenced pepper leaves exhibited more severe chlorotic lesions 7 d after virulent Xcv inoculation compared with that of the empty-vector control. The susceptible regions were intensely fluorescent under UV illumination, indicating the increased accumulation of fluorescent phenolic compounds in silenced leaves (Fig. 1A). Localized hypersensitive response (HR)-like cell death was initiated in the empty-vector control leaves 2 d after inoculation with 107 cfu ml–1 of avirulent strain Bv5-4a; however, the HR-like cell death response significantly decreased in CaPAL1-silenced leaves during infection. Under UV illumination, dark yellow fluorescent lesions (characteristic of HR) were more numerous in the empty-vector control leaves than those in CaPAL1-silenced leaves (Fig. 1A). These disease phenotypes correlated with the proliferation of Xcv in silenced leaves. Xcv growth in CaPAL1-silenced leaves was significantly higher than that in empty-vector control leaves 3 d after inoculation with 5×104 cfu ml–1 virulent and avirulent Xcv strains (Fig. 1B). Fig. 1. Increased susceptibility of CaPAL1-silenced pepper plants to infection by Xcv. (A) Disease symptoms developed on empty-vector control (TRV:00) and silenced (TRV:CaPAL1) leaves 7 and 3 d after inoculation with virulent and avirulent Xcv (107 and 108 cfu ml–1), respectively. (B) Bacterial growth in empty-vector control and silenced leaves infected with Xcv (5×104 cfu ml–1). (C) PAL activity in empty-vector control and silenced leaves infected with Xcv (107 cfu ml–1). In (B) and (C), data are the means±standard deviation (SD) from three independent experiments. Asterisks indicate significant differences, as determined by Student’s t-test (*P 41. The average number of sporangiophores was significantly lower in CaPAL1-OX plants than in WT plants (Fig. 9B). Hpa produced fewer spores on the cotyledons of CaPAL1-OX seedlings than on WT cotyledons (Fig. 9C). We measured PAL activity in WT and CaPAL1-OX leaves during Hpa Noco2 infection. The induction of PAL activity in CaPAL1-OX leaves by Hpa Noco2 infection was significantly higher than that in WT leaves (Fig. 9D). Together, these results suggest that CaPAL1 overexpression confers increased basal resistance to Hpa infection in Arabidopsis plants. Fig. 9. Increased resistance of Arabidopsis CaPAL1-OX plants to Hpa infection. (A) Disease symptoms on cotyledons of WT and overexpressing transgenic plants 6 d after inoculation with Hpa isolate Noco2 (5×104 conidiospores ml–1). (B) Quantification of asexual sporangiophores on cotyledons of WT and transgenic plants 6 d after inoculation. The average numbers of sporangiophores±SD are shown below each of the lines tested. (C) Average numbers of spores on cotyledons of WT and transgenic plants. (D) PAL activity in WT and CaPAL1-OX transgenic plants infected with Hpa Noco2 (5×104 conidiospores ml–1). Data in (B) to (D) are the means±SD from three independent experiments. Statistically significant differences between the means were determined by employing the Fisher’s protected LSD test (P<0.05). (This figure is available in colour at JXB online.) Discussion PALs are encoded by a multi-gene family in plant species such as Arabidopsis (Wanner et al., 1995; Cochrane et al., 2004), Solanum lycopersicum (Guo and Wang, 2009), Bambusa oldhamii (Hsieh et al., 2010a, b), and Phyllostachys edulis (Gao et al., 2012). PALs are one of the most extensively studied plant enzymes, particularly with respect to their responses to a variety of biotic and abiotic stress (Dixon and Paiva, 1995; MacDonald and D’Cunha, 2007). The biological functions of the PAL genes have been investigated through gene silencing in tobacco and disruption of the PAL1, PAL2, PAL3, and PAL4 genes in Arabidopsis (Elkind et al., 1990; Pallas et al., 1996; Rohde et al., 2004; Huang et al., 2010). In this study, we isolated and functionally characterized the PAL gene (CaPAL1) in pepper (C. annuum) plants. Based on the observed results, CaPAL1 was proposed to function as a positive regulator of plant innate immunity. To determine the effect of the loss-of-function or gain-of-function PAL gene in pepper plants, we generated CaPAL1 knockdown pepper plants using the VIGS technique (Liu et al., 2002) and CaPAL1-OX transgenic Arabidopsis using Agrobacterium-mediated transformation (Clough and Bent, 1998). First, the strict conservation of a PAL domain in the deduced amino acid sequence of CaPAL1 suggested that CaPAL1 may function as a PAL enzyme in pepper plants. The suppression or induction of PAL activity in plants during pathogen infection was confirmed by biochemical assays (Song and Wang, 2011) on the CaPAL1-silenced pepper plants and the CaPAL1-OX transgenic Arabidopsis plants. These data suggested that CaPAL1 expression significantly increases PAL activity, which triggers the immune response in plants. PAL catalyses the first step of the phenylpropanoid pathway and the synthesis of diverse natural products based on the phenylpropane skeleton, such as hydroxycinnamic acid, stilbenes, and flavonoids, which fulfil many essential roles in higher plants (MacDonald and D’Cunha, 2007). CaPAL1 transcripts are abundant in root tissues, barely detectable in stem and flower tissues, and not constitutively expressed in leaves, green fruit, and red fruit of healthy pepper plants. Suppression of PAL in Salvia miltiorrhiza plants results in abnormal phenotypes such as delayed root formation and an underdeveloped root system (Song and Wang, 2011), indicating that PAL is required for root development in plants. Consistent with these results, the constitutive expression of CaPAL1 in pepper roots supports the hypothesis that PAL activity may be required for proper root formation and development. The upregulation of CaPAL1 in pepper leaves by avirulent Xcv infection suggests that CaPAL1 plays a crucial role in the induction of plant defence in response to microbial pathogens. Phenylpropanoid compounds have been proposed to play crucial roles in plant defence to microbial pathogens based on the correlation between rates of phenylpropanoid accumulation and expression of resistance in vivo (Dixon and Paiva, 1995; La Camera et al., 2004). CaPAL1 silencing in pepper plants confers increased susceptibility to Xcv infection. Some phenylpropanoid compounds accumulate to high levels in plants that are resistant to an invading pathogen (Dixon, 2001; La Camera et al., 2004). These pathogen-induced phenylpropanoids, such as pterocarpans, isoflavans, stilbenes, and coumarines, act as phytoalexins, which have antimicrobial activity against plant-pathogenic fungi and bacteria (Dixon and Paiva, 1995; Barber et al., 2000; La Camera et al., 2004). The induction of PAL activity by Xcv infection was significantly compromised in CaPAL1-silenced pepper plants compared with that in empty-vector control plants. The level of PAL activity in CaPAL1-silenced plants was lower than that in the empty-vector control plants. These results suggested that PAL activity in pepper plants contributes to the basal and R gene-mediated resistance to Xcv infection. SA-dependent signalling controls activation of sophisticated plant defence mechanisms to ward off attacks from microbial pathogens (Delaney et al., 1994; Lu, 2009; Vlot et al., 2009; Robert-Seilaniantz et al., 2011). CaPAL1 silencing in pepper leaves significantly compromised the induction of SA accumulation and SA-dependent CaPR1 expression during avirulent and virulent Xcv infection. CaPAL1 overexpression in Arabidopsis strongly stimulated SA induction as well as AtPR1 expression in leaves of the transgenic plants infected with both virulent Pst DC3000 and avirulent Pst DC3000 (avrRpm1). These results suggest that CaPAL1 acts as a positive regulator of SA-dependent defence signalling and downstream defence gene expression. It has been proposed that PAL activity is important for pathogen-induced SA formation in plants (Pallas et al., 1996; La Camera et al., 2004). The levels of free SA produced in pathogen-inoculated leaves of PAL-silenced Nicotiana tabacum plants were lower than those in the WT control plants (Pallas et al., 1996). The PAL inhibitor 2-aminoindan-2-phosphonic acid abolishes pathogen- or pathogen elicitor-induced SA accumulation in potato, cucumber, and Arabidopsis (Meuwly et al., 1995; Mauch-Mani and Slusarenko, 1996; Coquoz et al., 1998). Two pathways of SA biosynthesis have been proposed in plants (Chen et al., 2009). One is the phenylpropanoid pathway controlled by PAL as the first enzyme (Huang et al., 2010), and the other is the chorismate pathway controlled by isochorismate synthase (ICS) (Wildermuth et al., 2001; Catinot et al., 2008; Chen et al., 2009). Previous evidence from Arabidopsis has indicated that the chorismate pathway is the most important for SA biosynthesis after stress stimuli (Garcion et al., 2008). In fact, knockout in the two ICS genes (ics1 ics2 double mutant) in Arabidopsis completely abolishes SA accumulation after stress (Garcion et al., 2008). On the other hand, plants knocked out in the four PAL genes from Arabidopsis (pal1 pal2 pal3 pal4 quadruple mutant), which retain 10% of PAL activity, also showed a reduction in the basal levels of SA (up to 25% of WT) and in the pathogen-induced levels (50% of WT) (Huang et al., 2010). However, whether SA is produced via the chorismate pathway in pepper remains to be determined. In this study, VIGS of CaPAL1 altered pepper defence-related gene expression. Suppression of the induction of the SA-dependent marker gene CaPR1 by CaPAL1 silencing was apparent among the tested defence-related genes, suggesting that CaPAL1 is required for SA-dependent defence signalling during Xcv infection. The oxidative burst and H2O2 accumulation seem to be essential for the establishment of plant immunity (Alvarez et al., 1998; Apel and Hirt, 2004; Choi et al., 2007). Consistent with these results, VIGS of CaPAL1 compromised H2O2 accumulation and cell death during Xcv infection, suggesting that CaPAL1 expression triggers oxidative burst and cell death to promote the plant immune response. Constitutive overexpression of CaPAL1 in transgenic Arabidopsis lines was used to investigate whether CaPAL1-OX affects the defence response and PAL activity when expressed epigenetically. CaPAL1-OX plants showed increased resistance to both virulent and avirulent strains of Pseudomonas syringae pv. tomato (Pst) and to virulent Hpa Noco2. PAL activity in CaPAL1-OX Arabidopsis was significantly higher than that in non-inoculated WT plants. PAL activity was increased in both CaPAL1-OX and WT plants after Pst infection. These results suggested that constitutive expression of CaPAL1 may lead to the induction of PAL activity in response to Pst infection. Although PAL activity in CaPAL1-OX transgenic plants was significantly higher than that in WT plants, the levels of induction of PAL activity were similar in CaPAL1-OX and WT Arabidopsis infected with virulent Hpa Noco2. PAL activity in rosette leaves was generally higher than that in cotyledons, suggesting that the phenylpropanoid pathway may be more active in rosette leaves than in cotyledons. During Pst infection, the induction of ROS accumulation and ion leakage were higher in CaPAL1-OX plants. Expression of the SA-dependent AtPR1 and the ROS-producing NADPH oxidase AtRbohD in leaves of CaPAL1-OX plants was higher than that in WT plants. AtRbohD was proposed to be required for ROS accumulation in the plant defence response (Torres et al., 2002). Collectively, these results suggest that the CaPAL gene is required for the induction of SA-dependent defence signalling events in plants. Supplementary data Supplementary data are available at JXB online. Supplementary Fig. S1. (A) Nucleotide and deduced amino acid sequences of pepper CaPAL1 cDNA encoding a class family of phenylalanine ammonia-lyase. (B) Comparison of the deduced amino acid sequence of CaPAL1 with phenylalanine ammonia-lyase from other plant species. Supplementary Fig. S2. Genomic DNA gel blot analysis of CaPAL1. Genomic DNA from pepper plants was digested with restriction enzymes EcoRI and HindIII. CaPAL1 open reading frame cDNA was used as a positive control. Red arrowheads indicate the genomic DNA fragments hybridized with [32P]dCTP-labelled CaPAL1 probe. Supplementary Fig. S3. RNA gel blot analyses of CaPAL1 expression in pepper plants at the six-leaf stage. (A) Constitutive expression of CaPAL1 in various organs of pepper plants. (B) Time course of induction of CaPAL1 in leaf tissues infected with virulent strain Ds1 and avirulent strain Bv5-4a of Xanthomonas campestris pv. vesicatoria (107 cfu ml–1). The RNA gel blot was hybridized with 32P-labelled CaPAL1 probe. Supplementary Fig. S4. Real-time RT-PCR analyses of the expression of AtGST1 and AtPDF1.2 in WT and CaPAL1-OX Arabidopsis plants infected with Pseudomonas syringae pv. tomato (Pst) DC3000 and Pst DC3000 (avrRpm1). AtGST1, glutathione S-transferase; AtPDF1.2, plant defensin 1.2. Arabidopsis ACT1 was used as an internal control. The control sample was normalized to 1. Data are the means±SD from three independent experiments. Statistical significances according to Fisher’s protected LSD test (P<0.05) are indicated by different letters above the data points. Supplementary Data
Author and article information
Journal
Journal ID (nlm-ta): Int J Genomics
Journal ID (iso-abbrev): Int J Genomics
Journal ID (publisher-id): IJG
Title:
International Journal of Genomics
Publisher:
Hindawi
ISSN
(Print):
2314-436X
ISSN
(Electronic):
2314-4378
Publication date
(Print):
2017
Publication date
(Electronic):
1
May
2017
Volume: 2017
Electronic Location Identifier: 7305684
Affiliations
Author notes
Author information
Xingfeng Li
http://orcid.org/0000-0003-1943-7328
Article
DOI: 10.1155/2017/7305684
PMC ID: 5434243
SO-VID: 099d36e2-29ca-41cc-97c5-2413d36d3583
Copyright © Copyright © 2017 Piyi Xing et al.
License:
This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
History
Date
received
: 12
December
2016
Date
revision received
: 8
February
2017
Date
accepted
: 6
March
2017
Funding
Funded by: Creation and Utilization of Agriculture Biology Resource of Shandong Province
Funded by: National Key Research and Development Program of China
Award ID: 2016YFD0102000
Categories
Subject:
Research Article
Data availability: