Abstract
Soft rot of konjac (Amorphophallus spp.) is a devastating disease caused by the bacterium Pectobacterium carotovorum subsp. carotovorum (Pcc) with serious adverse effects on plantation development, corm quality and crop yield due to the current lack of effective control measures. The main objective of the present study was to elucidate the mechanisms underlying plant resistance to soft rot disease. A combination of transcriptomic and metabolomic analyses demonstrated significant enrichment of differentially expressed genes (DEG) and differentially accumulated metabolites (DAM) associated with plant hormones, phenylpropanoid biosynthesis and, in particular, alkaloid metabolism, in Amorphophallus muelleri following Pcc infection compared with A. konjac, these data implicate alkaloid metabolism as the dominant mechanism underlying disease resistance of A. muelleri. Quantitative real-time polymerase chain reaction analysis further revealed involvement of PAL, CYP73A16, CCOAOMT1, RBOHD and CDPK20 genes in the response of konjac to Pcc. Analysis of the bacteriostatic activities of total alkaloid from A. muelleri validated the assumption that alkaloid metabolism positively regulates disease resistance of konjac. Our collective results provide a foundation for further research on the resistance mechanisms of konjac against soft rot disease.
1 Introduction
Konjac (Amorphophallus spp.), an economically important tuber taro species belonging to the family Araceae, is widely distributed among Asian countries including China, Japan and Burma. The corm of konjac is used as a thickening and gelation agent within the food processing, biotechnology, and pharmaceutical industries due to its high glucomannan content (; ). Moreover, health protection effects of konjac through reduction of blood glucose and lipids levels and metabolic regulation have been reported (). Due to its application prospects and economic value, planting of konjac has become the main pillar industry for farmers to lift themselves out of poverty in the Yunnan province of China. However, owing to expansion of the planting area, continuous cropping, and unreasonable preventive measures, outbreaks of konjac soft rot disease involving various symptoms, such as plants turning yellow and wilting, tissue decay, and emission of a foul odor, are a common occurrence (). Soft rot disease can severely affect growth of Amorphophallus spp., resulting in a significant decrease in quality and yield (). The pathogens of soft rot disease of Amorphophallus spp. have been identified as Pectobacterium spp. (), Dicyeya spp (), and Erwinia spp (), of which Pectobacterium carotovorum subsp. Carotovorum (Pcc) is the prevalent disease-causing agent in the major planting areas of Kunming, Qujing, Chuxiong, and Yunnan provinces. Current strategies to control soft rot include application of pesticides and biocontrol (). However, long-term use of chemical pesticides could not only increase the resistance of pathogenic bacteria but also cause serious damage to the ecological environment. Biocontrol is greatly influenced by both biotic and abiotic factors in the environment, resulting in unstable effects. One long-term and effective method of controlling plant diseases is to improve the plant’s own resistance. However, to our knowledge, few studies to date have focused on the mechanisms contributing to molecular resistance of Amorphophallus spp. against soft rot disease.
Under stress conditions, plants often enhance their resistance to disease-causing organisms by regulating the expression of specific genes and accumulation of metabolites. Metabolomics techniques can be effectively applied to assess changes in the metabolite profiles of plants during pathogen infection and identify a series of resistance-related metabolites. The data obtained not only inform further research into the defense mechanisms of plants but also facilitate the identification of functional genes involved in plant metabolism through comprehensive transcriptome analysis (). Integration of transcriptomic and metabolomic analyses to predict the regulatory networks of biological traits and gene functions provides a valuable tool to evaluate the resistance response of plants to pathogenic infection. For example, salicylic acid metabolism was shown to be enriched in cabbage (Brassica oleracea) following infection with Xanthomonas campestris pv. campestris (Xcc) and the flavonoid pathway metabolites chlorogenic acid and caffeic acid effectively inhibited growth of Xcc (). Flavonoid and steroidal saponin contents were increased while that of asparagusic acid glucose ester was decreased in resistant wild-type Asparagus kiusianus following infection with Phomopsis asparagi (). Moreover, phenylpropanoids, flavonoids, alkaloids and terpenoid biosynthesis pathway resistance genes were shown to be strongly induced in association with resistance of potato (Solanum tuberosum) to late blight caused by Phytophthora infestans (). Therefore, comprehensive analysis of changes in gene expression patterns in the transcriptome and metabolite accumulation in the metabolome should facilitate elucidation of the regulatory mechanisms of plant responses to pathogen infection, which will be useful for breeding and quality improvement of disease-resistant crops.
Identification and utilization of the factors involved in resistance of Amorphophallus spp. may provide a basis for a viable control strategy for soft rot disease. During the cultivation process, we observed that compared to Amorphophallus konjac, A. muelleri showed stronger resistance to soft rot disease. Recently, our group conducted a preliminary study on the resistance of konjac to soft rot disease using non-parametric transcriptome analysis (). However, since our team has successfully completed the whole genome sequencing of A. konjac, we re-applied the reference transcriptome to further explore the mechanisms underlying disease resistance of Amorphophallus spp. To this end, transcriptomics and metabolomics methodologies were employed to determine changes in gene expression profiles and metabolite accumulation between resistant and susceptible species. Moreover, correlations between transcriptomic and metabolomic data were examined with the expectation of developing a better understanding of the resistance mechanisms. Finally, real-time fluorescence quantitative polymerase chain reaction (qRT-PCR) and bacteriostasis test were conducted to validate the transcriptomic and metabolomic findings. This study provides valuable molecular information on the responses of Amorphophallus spp. to Pcc infection and the most significant biological pathways implicated in resistance against soft rot disease. Our collective findings should aid in greatly enhancing resistance breeding and biocontrol of plant growth and development and improving post-harvest storage of crops with higher resistance to Amorphophallus spp. soft rot disease.
2 Materials and methods
2.1 Plant growth and cultivation conditions
Three-month-old seedlings of A. muelleri and A. konjac were kindly provided by a Konjac germplasm resource nursery (Research Center for Engineering and Technology Urban Agricultural of Yunnan Province, Kunming, Yunnan Province, China; 24°97’E, 102°79’N). Each seedling was planted in a plastic pot (upper diameter of 20 cm, lower diameter of 12 cm, and depth of 14 cm) containing sterile nutrient soil and cultivated in an environmentally controlled greenhouse at Kunming University (Kunming, China) under a temperature of 27 ± 2°C, relative humidity of 80%, and a light/dark photoperiod of 16 h/8 h with a light intensity of 2000 Lux.
2.2 Pathogen inoculation and symptom analysis of soft rot disease
Bacteria (Pcc) causing soft rot disease of A. muelleri and A. konjac were stored at the Plant Pathology Laboratory of the Agriculture and Life Sciences College (Kunming University). Three-month-old seedlings of A. muelleri and A. konjac cultivated in greenhouses of Kunming University were used for inoculation. The surface of the inoculation site on a disease-free petiole of A. muelleri and A. konjac was cleaned with wet sterile cotton, and injected with Pcc bacterial suspension (50 µL; 108 cfu/mL) using a disposable syringe. Inoculation sites injected with sterile Luria-Bertani (LB) medium served as the control group. One inoculation site was used for each plant (). Sixty seedlings of each species of konjac were used for experiments, of which 15 uninfected seedlings were used as the control group. All inoculated seedlings were cultured in a greenhouse at Kunming University under the above cultivation conditions. Evaluation of soft rot disease in A. muelleri and A. konjac was conducted at 24 h and 48 h post-inoculation (hpi).
2.3 RNA-seq and data analysis
RNA-seq analyses of resistant A. muelleri (M) and susceptible A. konjac (K) species following Pcc infection at 0, 24 and 48 hpi were conducted, including control groups (inoculated with LB), which were designated MJ24, MJ48, KJ24, KJ48, MJ0 and KJ0 according to the time-point of study. Petiole samples were obtained at a 2.0 cm distance from the lesion spot (KJ24, KJ48, MJ24 and MJ48) or the inoculation site (KJ0 and MJ0). Three biological replicates were collected for each treatment. Each replicate contained mixed petiole samples of different seedlings from at least six sample sites. All samples were immediately frozen in liquid nitrogen and stored at −80°C until experimental use.
Total RNA was extracted using a TRIzol reagent kit (TransGen, Beijing, China) according to the manufacturer’s instructions, followed by evaluation with an Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA). Agarose gel electrophoresis was employed to determine the quality of total RNA. Fragmentation of total RNA was followed by reverse transcription into cDNA using the NEBNext Ultra RNA Library Prep Kit for Illumina (NEB#7530; New England Biolabs, Ipswich, MA, USA). The purified product was subsequently ligated to Illumina sequencing adapters following the addition of A base. After purification of the ligation reaction, appropriately sized fragments were selected and sequenced using Illumina Novaseq6000 by Gene Denovo Biotechnology Co. (Guangzhou, China) to obtain a cDNA library. Firstly, fastp (version 0.18.0) () was utilized to remove data containing adapters, >10% unknown nucleotides (N) and >50% low quality (Q-value ≤ 20) bases from the raw data, resulting in clean data, followed by ribosome and reference genome alignment. Mapped reads of each test sample were reconstructed using StringTie v1.3.1 (, ) and fragment per kilobase of transcript per million mapped reads (FPKM) calculated using RSEM software (). Principal component analysis (PCA) and Pearson correlation coefficient were applied to evaluate repeatability between samples. Differentially expressed genes (DEG) between the groups were analyzed with DESeq2 software (). Genes with false discovery rates (FDR) below 0.05 (FDR P-value < 0.05) and absolute fold change |log2FC| ≥ 2 were considered DEGs. To determine the potential functions of these genes and the metabolic pathways involved, Gene Ontology (GO) () and Kyoto Encyclopedia of Genes and Genomes (KEGG) (; ; ) were employed for enrichment analysis.
2.4 Metabolite extraction and data analysis
Metabolome analysis was conducted by Guangzhou Genedenovo Biotechnology Co., Ltd. (Guangzhou, China). The petiole was ground into powder in liquid nitrogen, and 80 mg of petiole powder extracted with 1 mL of methanol/acetonitrile/H2O (2:2:1, v/v/v) under low-temperature ultrasound for 60 mins, followed by incubation at −20°C for 10 min. Following centrifugation of the mixture for 20 mins (14000 g, 4°C), the supernatant obtained was vacuum-dried, dissolved in water and after filtration with a 0.22 μm microporous membrane prior to analysis on an Ultra High-Performance Liquid Chromatography System (UPLC, Vanquish UHPLC, ThermoFisher Technologies) using a 2.1 mm × 100 mm ACQUITY UPLC BEH 1.9 µm column (ThermoFisher Technologies). The mobile phase contained solvent A (25 mM ammonium acetate and 25 mM ammonium hydroxide in water) and solvent B (acetonitrile). The following gradient was used: 90% B for 1 min, linearly reduced to 65% in 11 min, further reduced to 40% in 0.1 min and maintained for 4 min, then increased to 85% in 0.1 min, with a 5 min re-equilibration period. The quality control (QC) sample was composed of equal volumes of all 18 test samples. QC samples were inserted into the sample queue for monitoring and evaluating the stability of the system and the reliability of experimental data. Primary and secondary spectra were collected with the AB Triple TOF 6600 mass spectrometry system (AB Sciex, USA). Qualitative analysis of metabolomic data was performed by searching the internal database using a self-compiled index (Guangzhou Genedenovo Biotechnology Co., Ltd, Guangzhou, China). Principal component analysis (PCA), partial least squares-discriminant analysis (PLS-DA), and orthogonal projection to latent structures-discriminant analysis (OPLS-DA) were performed on metabolomic data obtained using the corresponding R language package (). Differentially accumulated metabolites (DAM) were screened based on t-test p values of < 0.05 and a variable importance in projection (VIP) ≥ 1. Finally, the functions of DAMs were annotated using the KEGG database (; ; ) to establish the pathways highly correlated with resistance of Amorphophallus spp. to Pcc infection.
2.5 Validation of gene expression
The sampled petioles of A. muelleri and A. konjac were the same as those used for RNA-seq analysis, specifically, MJ0, MJ24, MJ48, KJ0, KJ24 and KJ48 (Supplementary Table S1). Total RNA was extracted with a TRIzol reagent kit (TransGen, Beijing, China) and cDNA synthesized using TransScript® One-Step RT-PCR SuperMix (TransGen). qRT-PCR was conducted using TransStart® Top Green qPCR SuperMix (+Dye I) (TransGen). All protocols were performed according to the manufacturers’ instructions. The qRT-PCR assay was conducted in a total reaction volume of 20 μL under the following conditions: one cycle at 95°C for 30 s, 45 cycles at 95°C for 5 s, 60°C for 30 s and 72°C for 10 s. Three technical replicates were analyzed for each reaction. The actin gene of A. konjac was used as an internal reference and relative expression levels of the target genes were quantified using the 2−(ΔΔCt) method ().
2.6 Bacteriostatic activities of alkaloids from A. muelleri on Pcc
The effects of alkaloids on propagates of Pcc were additionally examined. The Pcc propagation experiment was performed according to the methods of reported by Khan et al (). and Ramkissoon et al (), with minor modifications. Fresh konjac corms were dried at 50 °C to a constant weight, ground into powder, sieved through a 40 mesh sieve, and 1 kg of konjac powder was weighed and extracted in 95% alcohol for 24 hours (konjac powder: 95% alcohol = 1:20). Therefore, the alcohol extract is vacuum filtered using a vacuum rotary evaporator until it becomes viscous (temperature = 55°C). The concentrated viscous liquid was adjusted to pH 9.0 with 1mol/L NaOH, extracted five times with ethyl acetate, and concentrated again after merging the organic layers. The viscous liquid obtained from the final separation was total alkaloids. With spectrophotometer method, a total alkaloid content determination kit (Grace Biotechnology Co., Ltd., Suzhou, China) was used to determine the total alkaloid content of the obtained extract.
A stock solution of alkaloids (100 mg/mL) was prepared using methanol as the solvent and sterilized through a 0.22 μM microfilter. The final concentrations of alkaloids in LB were 0.1, 0.2, 0.4, 1 and 2 mg/mL. A control experiment was conducted by adding the corresponding volume of methanol into LB and the culture medium was used as the blank control. Bacterial suspensions (10 μL) at OD600 of 0.02 were added to 1 mL LB containing alkaloids and cultured at 27 ± 2°C and 150 g until the logarithmic growth phase of the blank control was reached. The absorbance value of bacterial suspensions was measured at a wavelength of 600 nm.
Under sterile conditions, the Pcc strain at the logarithmic stage was inoculated into LB liquid medium alone and that containing total alkaloid (1 mg/mL). Supernatant fractions were obtained via centrifugation (3400 g, 4°C, 10 min) after overnight incubation and absorbance values at 260 nm determined (.). Five replicates were analyzed for each treatment concentration of alkaloids and all experiments were repeated twice.
3 Results
3.1 Differences in soft rot disease between A. muelleri and A. konjac
Symptoms of soft rot disease in A. muelleri and A. konjac were used as indicators of plant resistance (Figure 1). After inoculation with Pcc for 0 h, the petioles of A. konjac and A. muelleri showed no symptoms (Figures 1A, E). With the development of disease after 24 hpi, A. konjac displayed water soaking with gummosis while no obvious symptoms were observed in A. muelleri (Figures 1B, F). Upon extension of the inoculation time, the diseased area of A. konjac expanded rapidly and A. muelleri presented slight soft rot symptoms (Figures 1C, G). After inoculation with Pcc for 96 h, the petioles of A. konjac showed considerable decay with progressive damage and death of the entire plant. At this time-point (Figure 1D), while the petioles of A. muelleri became hollow, growth was maintained (Figure 1H). The significant differences in disease symptoms between the species clearly indicate that A. konjac is more susceptible while A. muelleri is more resistant to Pcc infection.
Figure 1
3.2 Transcriptome analysis of A. muelleri and A. konjac petioles responsive to Pcc infection
Three independent replicates of A. muelleri and A. konjac species responsive to Pcc infection at 24 hpi and 48 hpi were subjected to RNA-seq analyses, with a view to clarifying the potential mechanisms contributing to disease resistance. A total of 18 libraries (KJ0, KJ24, KJ48, MJ0, MJ24, and MJ48; three biological replicates per treatment) were combined into one pool, resulting in ~58.8 Gb clean data, a Q20 value above 97.58% and GC content between 50.95% and 52.52% (Supplementary Table S2). The data obtained could be successfully used for subsequent analyses. Principal component analysis (PCA) showed that the differences between control and infected plants were attributable to PC1 (56.4%) and those between A. muelleri and A. konjac to PC2 (17.1%) (Figure 2A). The correlation between the three biological replicates for each treatment was >0.75, indicating significant similarities in gene expression patterns (Supplementary Figure S1). Seven comparative DEG analyses (KJ0 vs KJ24, KJ0 vs KJ48, MJ0 vs MJ24, MJ0 vs MJ48, KJ0 vs MJ0, KJ24 vs MJ24 and KJ48 vs MJ48) revealed 4816, 7616, 3163, 1140, 7282, 8676 and 10001 DEGs, respectively. Among these, 2590, 3545, 1596, 565, 2281, 2553 and 3720 genes were up-regulated while 2226, 4071, 1567, 575, 5001, 6123 and 6281 genes were down-regulated in response to infection, respectively, clearly demonstrating that infection with Pcc induces significant changes in plant gene expression patterns (Figure 2B).
Figure 2
Venn diagram analysis showed that 920 common genes were up-regulated in KJ0 vs KJ24 and MJ0 vs MJ24, whereas 597 common genes were down-regulated (Figure 2C); 643 common genes were up-regulated in KJ0 vs KJ48 and MJ0 vs MJ48, whereas 472 common genes were down-regulated (Figure 2D). Additionally, 717 and 253 up-regulated DEGs were found in MJ24 and MJ48, respectively, whereas 2539 and 3346 up-regulated DEGs were found in KJ24 and KJ48, respectively (Figures 2C, D). These up-regulated DEGs, unique to MJ24 and MJ48, may be involved in resistance against bacterial infection.
To explore the key pathways activated by Pcc infection, KEGG annotations of up-regulated and down-regulated DEGs of A. konjac and A. muelleri infected with Pcc. The results showed that in both A. konjac and A. muelleri, the down-regulated genes were mainly enriched in pathways of “photosynthesis,” “photosynthesis-antenna protein” and “porphyrin metabolism” (Figures 2E, F) while up-regulated genes were the most highly represented in “biosynthesis of secondary metabolites,” “alpha-linolenic acid metabolism,” “MAPK signaling pathway-plant,” and “phenylpropanoid biosynthesis” pathways (Figures 2G, H). These findings support the conclusion that Pcc infection activates A. konjac and A. muelleri resistance responses and induces the expression of genes associated with metabolic pathways implicated in disease resistance.
To clarify the functions of DEGs at different time points of Pcc infection in A. muelleri and A. konjac, KEGG annotations of these genes were analyzed between groups (KJ0 vs MJ0, KJ24 vs MJ24, and KJ48 vs MJ48). DEGs between KJ0 and MJ0 were mainly enriched in “metabolic pathways,” “biosynthesis of secondary metabolites,” “flavone and flavonol biosynthesis,” “tropane, piperidine and pyridine alkaloid biosynthesis” and “glutathione metabolism” (Figure 3A). DEGs between KJ24 and MJ24 were mainly enriched in “ubiquinone and other terpenoid-quinone biosynthesis,” “glutathione metabolism,” “biosynthesis of secondary metabolites” and “ubiquinone and other terpenoid-quinone biosynthesis” (Figure 3B). DEGs between KJ48 and MJ48 were mainly enriched in “metabolic pathways,” “ubiquinone and other terpenoid-quinone biosynthesis,” “isoquinoline alkaloid biosynthesis,” “MAPK signaling pathway-plant,” “phenylpropanoid biosynthesis” and “amino sugar and nucleotide sugar metabolism” (Figure 3C). The results support the potential involvement of “MAPK signaling pathway-plant,” “phenylpropanoid biosynthesis,” “glutathione metabolism” and alkaloid metabolic pathways in the response of konjac to Pcc.
Figure 3
Heatmaps of DEGs subclusters were developed to better understand the key DEGs associated with the resistance of konjac to Pcc (Supplementary Table S3). The resulting heatmaps showed DEGs involved in plant-pathogen interactions. Based on their functional annotation, these genes included 27 phenylpropanoid biosynthesis pathway genes (Figure 4A), 13 isoquinoline alkaloid biosynthesis pathway genes (Figure 4B), four calcium-binding protein genes, six calcium-dependent protein kinase genes (Figure 4C), and six respiratory burst oxidase genes (Figure 4D).
Figure 4
3.3 Metabolome analysis of A. muelleri and A. konjac petioles responsive to Pcc infection
A non-targeted metabolome analysis was performed on Pcc-infected A. muelleri and A. konjac petiole samples at 0, 24 and 48 hpi, designated M0, MJ24, MJ48 and KJ0, KJ24 and KJ48, respectively. A total of 1658 metabolites (1047 in the positive ion mode (POS) and 611 in the negative ion mode (NEG) were identified from all samples. The orthogonal Projections to Latent Structures Discriminant Analysis (OPLS-DA) method was employed for subsequent model tests and DAM screening (Supplementary Figure S2). Based on VIP ≥1 and t-test P <0.05, DAMs were identified (Figure 5A). After Pcc infection, the number of DAMs in susceptible A. konjac was higher than that in resistant A. muelleri. Further comparative analysis of each group revealed a total of 152 DAMs between KJ0 and MJ0, among which 28 metabolites were up-regulated and 124 were down-regulated in MJ0 relative to KJ0. Comparison of KJ24 and MJ24 revealed a total of 133 DAMs, among which 93 metabolites were up-regulated and 40 were down-regulated in MJ24. Comparison of KJ48 and MJ48 led to the identification of 82 DAMs, among which 19 metabolites were up-regulated and 63 were down-regulated in MJ48 (Figure 5B). The collective data clearly indicate significant differences between the metabolomes of A. muelleri and A. konjac petioles following Pcc infection.
Figure 5
Overall, 141 DAMs were detected between KJ0 and KJ24, with 15 up-regulated and 126 down-regulated metabolites at 24 hpi. Comparison of KJ0 and KJ48 revealed a total of 156 DAMs, among which 33 metabolites were up-regulated and 123 were down-regulated at 48 hpi (Figure 5C). We detected 76 DAMs between MJ0 and MJ24, among which 63 metabolites were up-regulated and 13 were down-regulated at 24 hpi. A total of 28 DAMs were identified in comparative analysis of MJ0 and MJ48, with 15 up-regulated and 13 down-regulated metabolites at 48 hpi (Figure 5D). The DAMs in A. muelleri and A. konjac petioles responsive to Pcc infection were mainly classified into 10 categories, specifically, organic acids and derivatives, alkaloids and derivatives, phenylpropanoids and polyketides, organoheterocyclic compounds, lipids and lipid-like molecules, organic oxygen compounds, benzenoids, nucleotides and analogs, lignans, neolignans and related compounds, and others (Supplementary Table S4).
Venn diagram analysis showed that 8 common DAMs in KJ0 vs KJ24 and MJ0 vs MJ24 and 4 common DAMs in KJ0 vs KJ48 and MJ0 vs MJ48. Additionally, 68 and 24 DAMs were uniquely found in MJ24 and MJ48, respectively; and 133 and 152 DAMs were uniquely found in KJ24 and KJ48, respectively (Figure 6A). These DAMs may be involved in resistance against bacterial infection.
Figure 6
To understand the main pathways activated by Pcc infection, KEGG annotations of these unique DAMs of A. muelleri and A. konjac were analyzed. In A. konjac, The DAMs were mainly involved in “Flavone and flavonol biosynthesis,” “biosynthesis of phenylpropanoids” and “biosynthesis of secondary metabolites,” (Figure 6B); In A. muelleri, three cluster modes were significantly enriched and their DAM contents markedly increased compared with MJ0. These DAMs were mainly involved in “isoquinoline alkaloid biosynthesis,” “biosynthesis of plant secondary metabolites,” “Biosynthesis of alkaloids derived from shikimate pathway,” “Biosynthesis of plant hormones,” and “phenylpropanoid biosynthesis” pathways (Figure 6C). Interestingly, DAMs of the “biosynthesis of plant secondary metabolites” pathway were mainly involved in synthesis of alkaloids and plant hormones. Our results suggest that “phenylpropanoid biosynthesis,” “biosynthesis of plant hormones” and “biosynthesis of plant secondary metabolites” pathways are potentially involved in the defense mechanisms of A. muelleri and A. konjac.
DAMs between KJ0 and MJ0 were mainly enriched in “tropane, piperidine and pyridine alkaloid biosynthesis,” “nicotinate and nicotinamide metabolism” and “indole alkaloid biosynthesis” pathways (Supplementary Figure S3). DAMs between KJ24 and MJ24 were mainly enriched in “glycerophospholipid metabolism,” “monoterpenoid biosynthesis” and “indole alkaloid biosynthesis” and DAMs between KJ48 and MJ48 were mainly enriched in “tryptophan metabolism,” “diterpenoid biosynthesis,” “biosynthesis of alkaloids derived from shikimate pathway” and “biosynthesis of plant secondary metabolites” (Supplementary Figure S3). The collective results indicate that alkaloid metabolites may participate in A. muelleri resistance to Pcc infection.
3.4 Involvement of the phenylpropanoid biosynthesis pathway in resistance of A. muelleri and A. konjac against soft rot disease
Phenylpropanoid metabolism is one of the most important mechanisms in plants, with multiple branching pathways producing flavonoids, coumarins, lignans, lignin, and other metabolites that participate in growth and development and response to various biotic and abiotic stresses stimuli (). In this study, a total of nine phenylpropanoid metabolites were identified, including cinnamic acids and derivatives (4), cinnamyl alcohols (1), phenols (1) and other phenylpropane metabolites (3). Compared with MJ0, the contents of ferulic acid, 4-hydroxycinnamic acid and eleutheroside b were significantly increased and p-coumaryl alcohol, sinapic acid and sinapyl alcohol levels relatively increased in MJ24 and MJ48. No marked differences in the other metabolites were observed among the groups. However, these metabolites exhibited different patterns in A. konjac. Compared with KJ0, the contents of ferulic acid, trans-3,5-dimethoxy-4-hydroxycinnamaldehyde and eleutheroside b in KJ24 and KJ48 were significantly increased while those of other metabolites were significantly decreased (Figure 7). The comprehensive results of these analyses indicate that Pcc infection triggers the phenylpropanoid metabolism process of A. muelleri and A. konjac, leading to changes in the contents of secondary metabolites of this pathway.
Figure 7
3.5 qRT-PCR-based validation of candidate DEGs
The phenylpropanoid metabolism pathway produces secondary metabolites, such as lignans, lignin, and flavonoids, through a series of enzymatic reactions that participate in plant growth, development, and stress response. Phenylalanine amine lyase, trans-cinnamate 4-monooxygenase, and caffeoyl-CoA O-methyltransferase are key enzymes in the phenylpropanoid metabolic pathway in plants and are involved in the biosynthesis of secondary metabolites, such as lignin and flavonoids. CYP73A16s and CCOAOMT1s are involved in the synthesis of phenylalanine ammonia-lyase, trans-cinnamate 4-monooxygenase, and caffeoyl-CoA O-methyltransferase. Therefore, to determine whether candidate DEGs were involved in the responses of A. muelleri and A. Konjac to Pcc, the expression of three phenylpropane biosynthesis pathway genes (PAL, CYP73A16 and CCOAOMT1) was screened via qRT-PCR (Figure 8). Furthermore, an oxidative stress-related gene (RBOHD) and a calcium ion channel-related gene (CDPK20) were screened by qRT-PCR (Figure 8). All five genes were significantly induced in A. muelleri and A. Konjac in response to infection with Pcc, supporting their utility as candidates for further evaluation of the disease resistance mechanism of konjac.
Figure 8
3.6 Involvement of total alkaloid of A. muelleri on Pcc growth
Alkaloids are important bioactive substances in plants that participate in defense against a variety of biotic and abiotic stress conditions. Transcriptome and metabolome analyses suggest that alkaloids of A. muelleri play an important role in inhibiting growth of Pcc. To establish the effect of total alkaloid from A. muelleri on Pcc growth, total alkaloid was isolated from healthy petioles for antibacterial experiments, with an extract yield of ~2.76 mg/g. Compared with the control group, alkaloids from A. muelleri inhibited the growth of Pcc in a dose-dependent manner. At alkaloid concentrations of >1 mg/mL, the cell density of Pcc was only one-third that of the control Pcc group (Figure 9A). The cell membrane maintains cellular integrity and is the basis of energy metabolism. Following damage, the cell membrane releases nucleic acids, which absorb light at a wavelength of 260 nm. Growth of Pcc was markedly inhibited and the OD260 value was significantly higher than that of the control group after incubation for 24 h with 1 mg/mL total alkaloid (Figure 9B), indicating that total alkaloids of A. muelleri cause damage to the cell membrane of Pcc, resulting in nucleic acid leakage. Our findings strongly support the theory that alkaloids in A. muelleri serve as a contributory factor to its resistance to soft rot disease.
Figure 9
3.7 Co-joint analysis
A co-joint KEGG enrichment analysis showed 42, 23, 48, and 63 co-mapping pathways across the pairwise comparisons of KJ0 vs KJ24, KJ0 vs KJ48, MJ0 vs MJ24, and MJ0 vs MJ48, respectively (Supplementary Table S5). Pearson correlation coefficients were used to explore the correlations between DEGs and DAMs. The correlations between the top 250 DEGs and their related DAMs were selected and represented as a heat map (Supplementary Table S6; Supplementary Figure S4).
4 Discussion
Long-term and effective strategies to control plant diseases can be achieved by improving the resistance of plants themselves. Soft rot disease is widely prevalent throughout the whole planting area of Amorphophallus spp. Our conclusions are consistent with earlier reports that A. muelleri is resistant while A. konjac is susceptible to soft rot disease (). Screening and identification of species resistant to Amorphophallus spp. through artificial inoculation should provide a foundation for further research on the defense mechanisms of plants against soft rot disease.
During plant-bacteria interactions, complex systems in plants are activated to participate in the defense response to pathogens. The plant mitogen-activated protein kinase (MAPK) cascade reaction (), hormones (), and secondary metabolites, such as alkaloids, flavonoids, phenolic acids (), are collectively involved in mediating plant defense against pathogen infection. The MAPK cascade activates downstream transcription factors through a series of protein phosphorylation reactions, triggering various defense reactions in plants (; , ; ). In addition, the MAPK cascade reaction interacts with a host of signaling pathways, such as plant hormones (), reactive oxygen species (), calmodulins, and calcium-dependent protein kinases (), to regulate the same defense process, forming a complex defense network. Plant hormones have been shown to induce defense genes, regulate the synthesis of secondary metabolites, and participate in the resistance response to pathogens (; ). In this study, DEGs were enriched in the pathways of “alpha-linolenic acid metabolism,” “glutathione metabolism,” “phenylpropanoid biosynthesis,” and “MAPK signaling pathway - plant” in A. muelleri and A. konjac. In response to Pcc infection, downstream defense genes of pathogen pattern-triggered immunity (PTI) were induced, including MAPK, respiratory burst oxidase (RBOH), calmodulin (CML), calcium-dependent protein kinase (CDPK), WRKY transcription factors, abscisic acid receptor (PYL, PP2C) and ethylene receptor (ETR, EIN). Recently, our group showed that methyl jasmonate administered as a spray could enhance the resistance of A. konjac to Pcc (). Here, “alpha-linolenic acid metabolism” pathway genes were extensively activated that participated in the synthesis of jasmonic acid (JA). Glutathione relies on both its antioxidant capacity and modulation of plant hormones to regulate plant defense against pathogens (). Our results showed induction of “glutathione metabolism” pathway genes in response to oxidative stress induced by Pcc. The “phenylpropanoid biosynthesis” pathway is closely related to plant resistance to disease and its phenylalanine ammonia-lyase (PAL) activity serves as a critical physiological indicator for assessing resistance. Following Pcc infection, PAL and lignin synthesis-related (4-coumarate-CoA ligase (4CL), 5-O-(4-coumaroyl)-D-quinate 3’-monooxygenase (CYP98A)) and defense (peroxidase (POD), beta-glucosidase (BGLU)) genes of A. muelleri and A. konjac were induced (Figure 10; Supplementary Table S7). Taken together, the results suggest that konjac forms a complex defense network system through activating plant hormones, regulating signal transduction processes, and inducing disease resistance and antioxidant genes that collectively participate in resistance to Pcc infection.
Figure 10
Following pathogenic infection, plants ultimately synthesize antitoxins that function in resistance through changes in their metabolites (). Previous study showed that alkaloids are important antibacterial components of plants (; ). And the intermediate metabolites of phenylpropanoid biosynthesis pathways are related to plant defense against pathogens (; ; ).Under Pcc stress, up-regulated DAMs were mainly enriched in disease-resistant metabolic pathways, including “biosynthesis of plant hormones,” “biosynthesis of plant secondary metabolites” and “biosynthesis of phenylpropanoids,” in both A. muelleri and A. konjac. Interestingly, we observed an increase in the alkaloid metabolite content in A. muelleri. Our results are in keeping with earlier findings implicating phenylpropanoid and indole alkaloids in the resistance response of rice (Oryza sativa) to Xanthomonas oryzae pv. oryzicola (), Pueraria lobata to Synchytrium puerariae Miy (), and Musa acuminata to Fusarium wilt (Fusarium oxysporum f. sp. cubense) ().
In response to Pcc infection, the contents of intermediate metabolites in biosynthesis of phenylpropanoids of A. muelleri and A. konjac exhibited different trends. We propose that these differences in alkaloid and phenylpropanoid metabolites potentially contribute to the stronger resistance of A. muelleri to Pcc relative to A. konjac.
Alkaloids are natural products widely present in animals and plants that have a range of physiological properties, such as insecticidal, antifungal, anti-tumor, and cytotoxic activities (; ). Earlier, isolated a jerveratrum-type steroidal alkaloid from Veratrum californicum with inhibitory effects on Botrytis cinerea and Puccinia recondita. Similarly, the group of reported antibacterial activities of seven main alkaloids in an extract of Chelidonium majus (). In the present study, compared with A. konjac, DAMs in Pcc-infected A. muelleri were mainly enriched in two alkaloid metabolism pathways, specifically, “biosynthesis of alkaloids derived from shikimate pathway” and “isoquinoline alkaloid biosynthesis.” Harmine and mescaline levels were significantly increased in both A. muelleri and A. konjac, with relatively higher contents in A. muelleri. Moreover, Pcc infection promoted the expression of genes in the alkaloid metabolism pathway in both A. muelleri and A. konjac, including polyphenol oxidase (PPO), (S)-stylopine/(S)-canadine/(S)-nandinine synthase (CYP719A13), and aspartate-prephenate aminotransferase (AAT) genes. In vitro analysis of the antibacterial activity of total alkaloids from A. muelleri against Pcc showed that LB containing 0.4 mg/mL total alkaloids could effectively inhibit bacterial growth. Our results are consistent with previous reports showing that alkaloids function in plant resistance to pathogens.
5 Conclusion
RNA-seq and metabolomic analyses were effectively employed to elucidate the defense mechanisms of Amorphophallus spp. against Pcc infection. Under Pcc-induced stress, the following disease resistance-related pathways were activated: “alpha-linolenic acid metabolism,” “isoquinoline alkaloid biosynthesis,” “MAPK signaling pathway-plant” and “phenylpropanoid biosynthesis.” Moreover, PAL, CYP73A16, CCOAOMT1, RBOHD and CDPK20 genes were implicated in the response of Amorphophallus spp. to Pcc. Consistently, metabolomic results revealed the involvement of both phenylpropanoid biosynthesis and alkaloid metabolism pathways in response to infection. Interestingly, following infection with Pcc, the numbers of DEGs and DAMs in resistant A. muelleri were lower than those in A. konjac. These differential alterations in the phenylpropanoid and alkaloid metabolite contents between A. muelleri and A. konjac after Pcc infection could explain the stronger resistance of A. muelleri. Total alkaloid of A. muelleri was identified as a component that could effectively inhibit Pcc growth.
Statements
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: BioProject, PRJNA1017648.
Author contributions
PG: Writing – original draft, Writing – review & editing. YQ: Funding acquisition, Software, Writing – review & editing. LL: Investigation, Software, Writing – review & editing. SY: Methodology, Writing – review & editing. JG: Methodology, Writing – review & editing. JL: Resources, Writing – review & editing. FH: Conceptualization, Formal analysis, Writing – original draft, Writing – review & editing. LY: Funding acquisition, Resources, Supervision, Writing – original draft, Writing – review & editing. HW: Methodology, Writing – review & editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was funded by Yunnan Province Youth Talent Support Program (Grant No. YNWR-QNBJ-2018-324), Yunnan Provincial Science and Technology Department (grant no. 202101BA070001-163, 202101BA070001-174, 202201AU070043), Yunnan Education Department Research Project (grant no. 2022J0644, 2023J0827), Applied Basic Research Foundation of Yunnan Province (grant no. 202301AU070136, 202301AT070055), Kunming University Talent Program (grant no. YJL23010, YJL23005, YJL23007).
Acknowledgments
We are thankful to Min Yang from Kunming University for her assistance with the experiment.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2024.1334996/full#supplementary-material
Supplementary Figure 1Correlation heat map of expression of genes in KJ0, KJ24, KJ48, MJ0, MJ24 and MJ48.
Supplementary Figure 2OPLS-DA analysis of DAMs for KJ0, KJ24, KJ48, MJ0, MJ24 and MJ48.
Supplementary Figure 3KEGG enrichment bubble diagrams of DAMs between KJ0 and MJ0 (A), KJ24 and MJ24 (B), and KJ48 and MJ48 (C). We obtained the appropriate copyright permission to modify the KEGG image.
Supplementary Figure 4Heatmap of the top 250 DEGs and relevant metabolites.
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Summary
Keywords
konjac, phenylpropane biosynthesis, alkaloid metabolism, Pectobacterium carotovorum subsp. carotovorum, RNA-SeqTab
Citation
Gao P, Qi Y, Li L, Yang S, Guo J, Liu J, Wei H, Huang F and Yu L (2024) Phenylpropane biosynthesis and alkaloid metabolism pathways involved in resistance of Amorphophallus spp. against soft rot disease. Front. Plant Sci. 15:1334996. doi: 10.3389/fpls.2024.1334996
Received
08 November 2023
Accepted
05 February 2024
Published
20 February 2024
Volume
15 - 2024
Edited by
Zhaohui Chu, Wuhan University, China
Reviewed by
Li Lu, Wuhan University, China
Gothandapani Sellamuthu, Czech University of Life Sciences Prague, Czechia
Updates
Copyright
© 2024 Gao, Qi, Li, Yang, Guo, Liu, Wei, Huang and Yu.
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*Correspondence: Feiyan Huang, 125593879@qq.com; Lei Yu, yulei0425@163.com
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.