Figures
Abstract
Salt stress limits plant growth and crop productivity and is an increasing threat to agriculture worldwide. In this study, proteomic and physiological responses of Brassica napus leaves under salt stress were investigated. Seedlings under salt treatment showed growth inhibition and photosynthesis reduction. A comparative proteomic analysis of seedling leaves exposed to 200 mM NaCl for 24 h, 48 h and 72 h was conducted. Forty-four protein spots were differentially accumulated upon NaCl treatment and 42 of them were identified, including several novel salt-responsive proteins. To determine the functional roles of these proteins in salt adaptation, their dynamic changes in abundance were analyzed. The results suggested that the up-accumulated proteins, which were associated with protein metabolism, damage repair and defense response, might contribute to the alleviation of the deleterious effect of salt stress on chlorophyll biosynthesis, photosynthesis, energy synthesis and respiration in Brassica napus leaves. This study will lead to a better understanding of the molecular basis of salt stress adaptation in Brassica napus and provides a basis for genetic engineering of plants with improved salt tolerance in the future.
Citation: Jia H, Shao M, He Y, Guan R, Chu P, Jiang H (2015) Proteome Dynamics and Physiological Responses to Short-Term Salt Stress in Brassica napus Leaves. PLoS ONE 10(12): e0144808. https://doi.org/10.1371/journal.pone.0144808
Editor: Shao Jun Dai, Northeast Forestry University, CHINA
Received: July 3, 2015; Accepted: November 24, 2015; Published: December 21, 2015
Copyright: © 2015 Jia et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by the National Natural Science Foundation of China (No. 31270386 and 31301352), the Fundamental Research Funds for the Central Universities of China (KYZ201202-7 and KJQN201423), the National Basic Research Program of China (973 Program) (No. 2011CB109300), and the Jiangsu Agricultural Science and Technology Innovation Fund (JASTIF) (CX (14)2003). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Salt stress is one of the most severe environmental challenges and limits crop production throughout the world [1]. Research to determine the mechanism of salinity adaptation and improving salt tolerance of plants has attracted increasing attention. NaCl is the main component of salinity [2] and exposure to high concentrations of NaCl can trigger various adverse effects, including water deficit, ionic toxicity, nutritional disorders, plant growth stunt, photosynthesis and protein synthesis depression, excess reactive oxygen species (ROS) generation and oxidative stress [3–6]. To cope with the deleterious effects of salt stress, plants have evolved a series of regulatory mechanisms. Ion homeostasis maintenance, compatible solute accumulation, antioxidant systems, hormonal control, Ca2+ signaling and SOS signaling pathways are important in salt-stress tolerance [6,7].
Salt stress can induce extensive proteome alteration in plants and proteomic analysis has proved to be an effective approach to study plant salt-stress tolerance [1,8]. Recently, a database containing 2171 salt-responsive proteins was constructed based on proteomics studies from 34 plant species, which has helped our understanding of the mechanisms underlying plant salt response and tolerance [9]. Two-dimensional polyacrylamide gel electrophoresis (2-DE) remains the primary approach in proteomic research [8] and has been applied commonly in studies on salt stress in plants [10–12].
Brassica napus is the third most important source of edible oil in the world and has considerable economic and nutritional values as an oilseed crop [13]. However, Brassica napus seedlings are sensitive to salt stress and their growth is markedly inhibited by salinity [14]. Few proteomic studies on the salt-stress response have been reported for Brassica napus. A previous study on canola under salt stress detected 44 and 31 differentially accumulated proteins in leaf proteome of the salt-tolerant genotype Hyola 308 and salt-susceptible genotype Sarigol, respectively; 46 proteins were identified using mass spectrometry (MS) analysis [15]. Recently, a proteomic analysis of seedling roots from Hyola 308 and Sarigol detected 20 and 21 proteins that responded to salt-stress treatments, respectively; However, only 19 proteins were identified [16]. The proteome dynamics during salt treatment and the roles of the salt-responsive proteins in salt stress adaptation remain unclear and require further exploration.
To better understand the mechanism of salt-stress adaptation in Brassica napus, proteomic and physiological responses to salt stress were analyzed in seedling leaves. Salt-responsive proteins were separated by 2-DE and identified by MS analysis. The functions of these proteins and the dynamic changes in their abundance are investigated and discussed.
Materials and Methods
Plant growth and salt treatments
Seeds of Brassica napus (var. Nannongyou No.3, salt tolerant) were collected from the Nanjing Agriculture University Agronomy farm in Nanjing city, Jiangsu Province, China. Plants were grown in greenhouse pots filled with a mixture of sand and vermiculite (1:1 v/v) under a light intensity of 120 μmol m-2 s-1 with a 16 h/8 h photoperiod and temperatures of 23 ± 2°C. The plants were irrigated daily with half-strength Murashige and Skoog solution. Six-week-old seedlings were treated with half-strength Murashige and Skoog solution containing either 200 mM NaCl (salt-stressed treatment group) or no NaCl (unstressed control group) for 24 h, 48 h and 72 h. The third leaves were harvested from control and salt-treated plants, immediately frozen in liquid nitrogen and kept at −80°C until use. At least three independent biological replicates were prepared for physiological and proteomic analyses.
Biomass and water content
The fresh weight (FW) of Brassica napus seedlings and leaves was measured immediately after harvesting. To determine the determination of water content (WC), the plant samples were maintained at 105°C for 5 min and then at 80°C for 72 h in an oven; the dry weight (DW) of the samples was then measured. The WC of the sample was calculated using the following formula: WC = (FW − DW)/FW×100%.
Pigment determination
Chlorophyll (Chl) was extracted from 0.5 g samples of fresh leaves using 80% acetone. The extract was centrifuged at 12 000 rpm at 4°C for 5 min and the supernatant was collected. Absorbance of the extract was measured at 663 nm and 646 nm spectrophotometrically and the contents of total Chl (Chl a + Chl b), Chl a, and Chl b of leaves were determined as previously described [17]. Three biological replicates were prepared for analysis.
Leaf gas-exchange measurement
The third leaves of control and salt stressed plants were used for gas-exchange analysis. Net photosynthesis and stomatal conductance were determined by a Li-Cor 6400 portable photosynthesis system (Li-Cor Inc. Lincoln, NE, USA) using the built-in light source set at 1,000 μmol photons m-2 s-1 [18]. During the measurements, the leaf temperature was adjusted to 25°C.
Protein extraction and quantification
Protein extraction was performed using the trichloroacetic acid/acetone method, as described previously [19] with some modifications. Leaf samples (1 g) were ground in liquid nitrogen with a mortar and pestle. The tissue powder was transferred to 50 mL centrifuge tubes and suspended in 10% trichloroacetic acid (TCA) and 65 mM DTT in ice-cold acetone and incubated at −20°C overnight. Proteins were pelleted by centrifugation at 40,000 × g for 25 min at 4°C, and then resuspended in cold acetone containing 65mM DTT. The mixture was kept at −20°C for 1 h before centrifugation at 40,000 × g for 15 min at 4°C. Protein pellets were washed twice with cold acetone and lyophilized in a vacuum. The resulting pellet was solubilized in lysis buffer (7 M urea, 2 M thiourea, 4% CHAPS, 65 mM DTT, and 0.2% w/v Bio-Lyte) for 2 h at room temperature and then centrifuged at 16,000 × g for 30 min. The supernatant was collected and stored at −80°C until use. The protein concentration of each sample was measured using the Bradford method [20].
2-DE and image analysis
For isoelectric focusing (IEF) in the first dimension, traces of bromophenol blue were added to the protein samples. A total of 450 μg of protein samples was loaded into the immobilized pH gradient (IPG) strips (pH 4–7, 17 cm, Bio-Rad, Hercules, CA, USA). The strips were then covered with mineral oil and rehydrated at 50 V for 14 h at 20°C. Electrophoresis was carried out at 250 V for 1 h, followed by 500 V for 1 h, 1000V for 1h, 2000V for 1h, 10,000 for 4h with a linear ramp and 10,000 V for 80,000 Vh with a rapid ramp. Focused IPG strips were equilibrated as previously described [21] and after equilibration, the strip was placed on the top of 11.5% SDS-PAGE and sealed with 0.5% agarose. Electrophoresis was carried out at 10 mA/gel for 30 min followed by 20 mA/gel until the bromophenol blue dye reached the bottom of the gel. The gels were stained with silver nitrate [22] and analyzed using PDQuest software (version 8.0.1, Bio-Rad, Hercules, CA, USA) for spot detection and protein quantification according to the user manual. Three gel replicates were used for the 2-DE gels quantification. The proteins with at least a two-fold change between the control and treatment samples were considered differentially accumulated proteins (p < 0.05 by Student’s t-test). Spots with significant changes were selected and manually excised from the gel for further protein identification.
In-gel digestion and protein identification
The selected spots were in-gel digested with trypsin as previously described [23,24] with minor modification. Briefly, protein spots were washed twice with ultrapure water, destained twice with 25mM NH4HCO3 in 50% acetonitrile (ACN), dehydrated with 50% ACN and 100% ACN, and then lyophilized in an ALPHA 2–4 LSC Freeze Dryer (Martin Christ, GmbH, Osterode, Germany). The gels pieces were reduced with 10 mM DTT in 25 mM NH4HCO3 at 56°C for 1 h, alkylated with 50 mM iodoacetamide in 25 mM NH4HCO3 at 37°C for 30 min, dried with 50% ACN and 100% ACN and digested with trypsin (Promega, Madison, WI, USA) in 25 mM NH4HCO3 overnight at 37°C. The peptides were extracted twice with 5% trifluoroacetic acid (TFA) in 67% ACN after digestion. All extracts were pooled and lyophilized in the concentrator. The tryptic peptides were prepared by dissolving the extracts with 0.1% TFA and stored at −80°C until MS analysis.
MS analysis was conducted using a matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF/TOF) mass spectrometer 4800 Proteomics Analyzer (AB SCIEX, Framingham, MA, USA). Data were analyzed using GPS 3.6 Explorer software (AB SCIEX, Framingham, MA, USA) and searched using MASCOT 2.1 software (Matrix Science Ltd., London, UK) against the NCBInr database, which contained accessible Arabidopsis and Brassica protein sequences. The peptide MS and MS/MS tolerances were set as 15 ppm and 0.25 Da, respectively. The search parameters were as follows: specificity of protease digestion was set to trypsin, and a maximum of one missed cleavage was allowed per protein. Carbamidomethyl on Cys was set as a fixed modification and oxidation of Met was set as a variable modification. The probability-based Mowse score was used to determine the confidence of protein identification and only significant hits with a confidence interval (CI) greater than 95% (p < 0.05) were accepted as correctly identified.
Hierarchical cluster analysis
Hierarchical clustering of the relative abundance profiles of differentially accumulated protein was performed on the log2-transformed fold change values of protein spots, using Cluster 3.0 [25]. The complete linkage algorithm was used for data aggregation [21] and TreeView version 1.6 was used to generate a heatmap [18].
Enzymatic assays
Superoxide dismutase (SOD) activity assay.
To assess SOD activity, 0.5 g of leaf sample was ground in an ice-chilled mortar with 0.1 M potassium phosphate buffer (pH 7.8) and was centrifuged at 12,000 × g for 20 min at 4°C. The supernatant was used for the enzymatic assay, according to a previously described method [26]. Briefly, 50 μl of the supernatant was added to the 100 mM phosphate buffer (pH 7.8) containing 1.3 μM riboflavin, 13 mM methionine and 65 μM nitro blue tetrazolium (NBT). After the reaction mixture was illuminated for 15 min with luminescent lamps, absorbance was measured at 560 nm. One unit of SOD was defined as the amount of enzyme that induced 50% inhibition of the NBT reduction, and SOD activity was expressed as unit g fresh weight-1.
Chitinase activity assay.
Chitinase activity in leaf samples was measured as previously described [27]. The crude protein extracts were prepared using sodium acetate buffer (pH4.5). After centrifugation at 10,000 × g for 15 min at 4°C, the supernatants were used for the colorimetric determination of N-acetylglucosamine (GlcNAc) with 1% colloidal chitin (w/v) as the substrate. Chitinase activity was calculated from a GlcNAc (Funakoshi, Tokyo, Japan) standard curve. One unit of chitinase activity was defined as the release of 1 μmol of GlcNAc per hour at 37°C.
ATPase activity assay.
ATPase activity in leaf samples was measured as previously described with modifications [28]. Briefly, 1 g leaf sample was ground in an ice-chilled mortar with 0.05 M potassium phosphate buffer (pH 7.8) containing 0.4 M sucrose and 0.01M NaCl. The supernatants were collected by centrifugation at 1500 × g for 5 min and the pellets were resuspended in 0.05 M potassium phosphate buffer (pH 7.8), 0.4 M sucrose and 0.01 M NaCl at a Chl concentration of 0.5 mg ml−1. ATPase activity was determined in a reaction mixture that contained 50 mM Tris-HCl (pH 8.0), 5 mM ATP, and 5 mM CaCl2. After incubation at 37°C for 10 min, 20% trichloroacetic acid was added into the mixture to stop the reaction and the concentration of inorganic phosphate (Pi) was determined as described previously [29].
Results
Effect of salt stress on plant growth
Salt stress with 200 mM NaCl significantly (p < 0.01) decreased the FW, DW and WC of the Brassica napus ‘Nannongyou No.3’ seedlings (Fig 1). We further analyzed the effect of salinity on Brassica napus leaves, and the results showed that compared with the control plants, the FW and WC of the third leaves was reduced by 43% and 3%, respectively, after salt treatment for 3 d. However, the effect of salinity on the DW of the third leaves was not statistically significant (Fig 1).
Values shown are means ± SD from three biological replicates. ** indicates a significant difference (compared with the control) at p < 0.01.
Effect of salt stress on pigments and photosynthesis
No significant decrease in chlorophyll a (Chl a), chlorophyll a (Chl b), total chlorophyll and carotenoid concentrations was observed in the leaves of salt-stressed ‘Nannongyou No.3’ seedlings after salt treatment for 3 d, compared with untreated controls (Fig 2). No significant changes were detected in the Chla to Chlb ratio, and the chlorophyll to carotenoid ratio after salt-stress treatment (Fig 2).
Values shown are means ± SD from three biological replicates.
Leaf gas-exchange measurements revealed that net photosynthesis (Pn) was dramatically reduced by salinity (Table 1). Salt-stress treatment significantly decreased the stomatal conductance (Gs), intercellular CO2 concentration (Ci) and transpiration rate (Tr) by 84%, 27% and 80%, respectively.
Leaf proteome dynamics in response to salt stress
The effects of salt stress on the leaf protein profiles of ‘Nannongyou No.3’ were analyzed using 2-DE. To analyze proteome dynamics in response to salt stress, we measured several time points, from 24 to 72 h, after 200 mM NaCl treatment (S1 Fig). Approximately 800 protein spots were detected on silver-stained 2-DE gels in the pH range of 4–7 by the PDQuest software (Fig 3). Differential protein abundance between the control and salt stressed plants under different NaCl treatment time points was assessed. Forty-four protein spots were observed to be reproducibly and significantly (p < 0.05) altered in abundance by more than two-fold in at least one time point after salt treatment. Among these 44 spots, 42 were identified by MS/MS analysis (Table 1, S1 Table and S1 Dataset). ATP synthase (chloroplast) was identified in seven spots (spot 13, 18, 28, 31, 32, 36 and 37), and 60-kDa chaperonin was identified in three spots (spot 4, 16, and 19), whereas chloroplast ribulose-1, 5-bisphosphate carboxylase/oxygenase activase (spot 7 and 30), heat shock protein 70 (spot 20 and 25), and chitinase (spot 26 and 29) were identified in two spots. These phenomena are commonly observed in 2-DE gel analysis and may result from the presence of different isoforms, differential post-translational modification or degradation in the protein extracts; they can also be related to allelic polymorphism [30–33].
The 42 salt-stress-responsive protein spots identified by tandem mass spectrometry (MS/MS), which are numbered and indicated by arrows, correspond to the spot numbers in Table 2.
The identified salt-stress-responsive proteins were further divided into seven categories on the basis of their functions (Fig 4), including Chl biosynthesis (2.38%), photosynthesis (28.57%), energy synthesis (19.05%), respiration (4.76%), protein metabolism (23.81%), and damage repair and defense response (21.43%). At the 24-h time point, 12 protein spots exhibited increased abundance and 16 spots exhibited decreased abundance. The number of down-accumulated proteins upon salt stress decreased and was much lower than the number of salt-induced proteins. Only five spots were down-accumulated, while 15 protein spots were up-accumulated, at the 48-h time point. The changes persisted and at the 72-h time point, the abundance of 18 protein spots was increased and only four spots showed decreases in abundance.
The salinity-responsive proteins displayed different dynamic patterns during the time course experiments. For example, no significant change in protein abundance was detected for chitinase (spot 29) at 24 h; however, it was up-accumulated at 48 h (Fig 5A). The abundance of the ATP synthase beta subunit (spot 37) was significantly decreased at 24 h, and then increased at 48 h (Fig 5B). However, for FtSH2 (spot 35) and transketolase 1(spot 39), no significant alteration was detected at 48 h, compared with the increased abundance of these two spots at 24 h and 72 h (Fig 5C and 5D). To further reveal the leaf proteome dynamics in response to salt stress, hierarchical cluster analysis was performed (Fig 6). The results indicated that leaves at 24 h and 48 h were grouped into a single group, and leaves at 72 h were in another cluster. The 42 differentially accumulated protein spots in response to salt stress were grouped in two main clusters. The first cluster (Cluster I) included 14 protein spots whose abundance mainly decreased upon high salinity. Most of these proteins are involved in Chl biosynthesis, photosynthesis, respiration and energy synthesis. This cluster could be separated into two subgroups according to the changing patterns of the spots. In subgroup A, the abundance of most down-accumulated proteins at time point 24 h was increased at time point 48 h and 72 h, while the highest depression effect of salinity on the accumulation of proteins in subgroup B was observed at time point 72 h. The second cluster (Cluster II) included 28 protein spots whose abundance was increased by salt treatment. Most of them belong to protein families for protein metabolism, damage repair and defense response. This cluster could be further divided into three subgroups. The first subgroup (subgroup C) included 10 protein spots showing the highest up-regulation upon salt stress treatment at time point 72 h. The accumulation levels of 11 spots in the second subgroup (subgroup D) and seven spots in the third subgroup (subgroup E) was strongly induced by salinity at time point 24 h and 48 h, respectively.
Fold changes of protein abundance were log 2 transformed. Columns 1, 2, and 3 represent 200 mM NaCl treatment for 24 h, 48 h, and 72 h, respectively. The rows represent individual proteins. Protein names and spot numbers are labeled to the right of the corresponding heat maps. The proteins that increased and decreased in abundance are indicated in red and green, respectively. Proteins showing no significant changes are indicated in black. The intensity of the colors increases with increasing accumulation differences, as shown to the left of the bar. I and II indicated Cluster I and II, while A-E indicated subgroup A-E.
Changes in enzyme activities in response to salt stress
The changes in protein abundance identified by 2-DE analysis were further validated by enzyme activity assay. Salt stressed leaves at different time points (24 h, 48 h and 72 h after 200mM NaCl treatment) were tested. In agreement with the data from the proteomics analysis, the activities of SOD and chitinase were significantly increased at 72 h and 48 h of salt stress treatment, respectively, while the ATPase activity was significantly reduced at all three time points (Fig 7).
Values shown are means ± SD from three biological replicates. ** indicates a significant difference (compared with the control) at p < 0.01.
Discussion
In this study, the proteomic and physiological responses to salt stress in Brassica napus seedling leaves were analyzed. Seedling biomass was reduced after NaCl treatment (Fig 1), implying that plant growth was repressed by salinity. NaCl treatment resulted in a reduction of the Gs and Tr (Table 1), which might be associated with the water deficiency in salt-stressed leaves. Forty-four salt-stress-responsive proteins were detected, of which 42 were identified (Table 2). The identified proteins were classified into different functional categories. Most of the up-accumulated proteins during NaCl treatment were associated with protein metabolism, damage repair and defense response, which might account for the alleviation of the adverse effect of salt stress on Chl biosynthesis, photosynthesis, energy synthesis and respiration in Brassica napus leaves.
Chl biosynthesis and photosynthesis under salt stress
Salt stress can impair photosynthesis indirectly by reducing Chl content [6]. However, the impact of salinity on Chl biosynthesis remains unclear. A recent study on rice seedlings suggested that downregulation of Chl biosynthesis by salt stress could be attributed to decreased activities of Chl biosynthetic pathway enzymes [34]. Glutamate 1-semialdehyde aminotransferase (GSA-AT) is a key enzyme in plant Chl synthesis [35], and GSA-AT antisense transformants showed varying degrees of Chl deficiency [36,37]. In this study, the abundance of GSA-AT (spot 1) decreased after 24 h of salt-stress treatment. However, the GSA-AT protein level recovered to control levels at 48 h and 72 h of NaCl treatment (Fig 6), which might be attributed to salt tolerance mechanisms in Brassica napus seedlings. Consistent with this finding, the reduction in Chl content in salt-stressed seedlings was not significant after 72 h of treatment (Fig 2).
Photosynthesis is one of the primary processes affected by salinity [38,39]. The decrease in photosynthesis capacity in salt-stressed plants might result from damage to the photosynthetic apparatus and decreased CO2 availability caused by stomatal limitations [40,41], other than by reduction of the Chl content. In this study, leaf gas-exchange measurements revealed that net photosynthesis was significantly reduced in salt-stressed seedlings (Table 1). Proteomic analysis showed that 12 proteins related to photosynthesis were salinity responsive, including six photosynthetic proteins and six enzymes crucial for CO2 fixation (Table 2). Interestingly, most of the proteins involved in the light reaction, including photosystem I subunit VII (spot 3), Lhcb6 protein (spot 12), 33 kDa oxygen-evolving protein (spot 14), Chl a/b binding protein (spot 17), and 23kD protein of oxygen evolving system of photosystem II (spot 23), were up-accumulated in response to salt stress. However, the protein abundance of enzymes in CO2 assimilation, including Ribulose bisphosphate carboxylase (RuBisCO) large chain (spot 38), sedoheptulose-1, 7-bisphosphatase (spot 5) and phosphoribulokinase (spot 10), was significantly decreased after salt-stress treatment, especially at the 24-h time point. In support of this finding, the reduction in stomatal conductance and transpiration rate was far larger than the reduction in intercellular CO2 concentration after salt stress treatment (Table 1). These observations suggested that the salt-induced reduction in photosynthesis capacity could be mainly attributed to impaired CO2 fixation in Brassica napus seedlings. Photosynthesis limited by a reduction in the rate of CO2 assimilation by salinity has been reported in wheat [11], rice [42] and Arabidopsis [43].
Two spots (spot 7, 30) corresponding to RuBisCO activase (RCA) were significantly up-accumulated in Brassica napus seedlings after salt stress treatment, especially at the 48 h time point. RCA is a key regulatory enzyme that catalyzes the activation of RuBisCO [41]. RCA has been implicated in the maintenance of CO2 assimilation at low CO2 levels because of the reduction in stomatal conductance caused by salinity [44,45]. The induction of RCA by salinity has been reported previously [15,46] and might explain the recovery of the abundance of RuBisCO at the 48-h and 72-h time point of salt-stress treatment. Therefore, the up-accumulation of RCA might contribute to salt tolerance in Brassica napus seedlings.
Energy synthesis and respiration under salt stress
ATP synthase is a salt-responsive enzyme and plays crucial roles in plant salt tolerance [22,47]. In this study, proteomic analysis identified eight spots (spots 13, 18, 27, 28, 31, 32, 36, 37) as ATP synthase subunits, whose abundances changed under salt-stress conditions. Most of these proteins were down-accumulated, especially at the 24 h time point, and the enzyme activity analysis result was consistent with this finding (Fig 7). These results suggested that energy synthesis might be repressed in salt-stressed Brassica napus seedlings. In agreement with this observation, the downregulation of ATP synthase by salt stress has been reported in soybean leaves [48]. However, the response of ATP synthase to salinity depends on the plant species and genotype. For example, the studies in rice [49] and black locust [50] showed that ATP synthase was induced upon salinity. ATP synthase was significantly down-regulated in a salt tolerant cowpea cultivar, but up-regulated in a salt-sensitive cowpea cultivar after salt treatment [44].
Plant respiration response to salt stress has been studied [51]. However, the regulation of respiration by salinity stress appears to be complex, depending on species, tissue or cell type, and stress levels [4,32]. In this study, the abundance of the respiration enzyme pyruvate dehydrogenase (spot 6) was 2.2-fold higher after 72 h of salt stress treatment, while malate dehydrogenase (spot 34) was decreased by 0.66-fold at the 24 h time point. The pyruvate dehydrogenase in mung bean seedlings was reduced in 50 mM NaCl but increased in 100 mM and 150 mM NaCl, while the activity of malate dehydrogenase was decreased in salt-stressed seedlings [52]. The up-regulation of pyruvate dehydrogenase and malate dehydrogenase was reported in tomato leaves under salt stress treatment, especially in a salt-tolerant genotype [53].
Protein metabolism under salt stress
Salt stress can severely affect protein synthesis [54] and disrupt protein folding in the endoplasmic reticulum (ER), leading to the accumulation of unfolded proteins and ER stress in plants [55]. Proteomic analysis in the present study indicated that elongation factor Tu (spot 33), which is involved in protein biosynthesis and chaperones (cyclophilin, 60 kDa chaperonin/HSP60 and HSP70) related to protein folding, was significantly induced in salt-stressed leaves. By contrast, a protein associated with protein degradation (20S proteasome) was decreased by salinity stress treatment.
The up-accumulation of elongation factor Tu might enhance protein biosynthesis and thus repair the damage of salt stress on photosynthetic proteins in chloroplasts. Similar observations have been reported in cucumber [21] and soybean seedlings [12]. Chaperonins assist protein folding and assembly [56], and may function to protect and repair vulnerable protein targets under stress conditions [33,57,58]. In contrast to our findings, a previous proteomic analysis of Brassica napus seedling roots identified chaperonin hsp60 as a down-regulated protein in response to salinity [16]. This differential response could reflect the varying plant genotypes or different tissues used. Cyclophilins are implicated in protection against multiple abiotic stresses, and have been identified as salt-stress-responsive proteins in rapeseed [15], barley [19] and creeping bentgrass [59], consistent with our results. The results suggested that these proteins related to protein metabolism might participate in salt-stress tolerance in Brassica napus seedlings.
Damage repair and defense response under salt stress
Oxidative stress caused by the generation of excess ROS is a well-documented indirect form of damage caused by salt stress [60]. The up-accumulation of antioxidant enzymes, such as FeSOD 1 (spot 8), glutathione transferase (spot 9), and dehydroascorbate reductase (spot 22), might promote ROS scavenging and mitigate the oxidative damage under salt stress in Brassica napus leaves. The thiazole biosynthetic enzyme (THI) protein (spot 11) plays a role in thiamine biosynthesis, and its involvement in DNA damage repair and stress-tolerance mechanisms has been observed in bacteria, yeast and Arabidopsis thaliana [61–63]. The up-accumulation of THI might help to restore DNA stability and alleviate oxidative stress caused by NaCl treatment in Brassica napus leaves. Cell division protein FtSH was suggested to play a role in attenuating the detrimental effects of salinity on the photosynthetic machinery [4], and the enhanced abundance of FtSH2 in salt-stressed Brassica napus leaves might have contributed to the restoring of the photosynthetic proteins at 48 h and 72 h after salt-stress treatment (Fig 5).
Three up-accumulated proteins related to the defense response were identified in Brassica napus leaves, including cinnamyl alcohol dehydrogenase (spot 24), chitinase (spot 26 and 29) and N-glyceraldehyde-2-phosphotransferase-like protein (spot 40). Cinnamyl alcohol dehydrogenase (CAD) is a key enzyme in lignin biosynthesis and enhanced CAD might increase the extent of lignification, which might represent a salt-adaptation response in plant roots [64–66]. Functional analysis in tea plants suggested that CAD in leaves might play a role in defense against biotic stresses and adaptation to abiotic stresses [67]. However, the function of CAD in salt tolerance in plant leaves is still poorly understood. Chitinase belongs to the pathogenesis-related (PR) protein family, which plays important roles in biotic and abiotic stress resistance [57]. The up-regulation of chitinase by salt stress has been reported in Brassica rapa [68], Nicotiana tabacum [10] and Halogeton glomeratus [69].The increased abundance of chitinase in salt-stressed leaves was further validated and supported by the enzyme assay in the present study (Fig 7). These results suggested that chitinase might help to enhance resistance against salt stress in Brassica napus. A study in Brassica carinata showed that N-glyceraldehyde-2-phosphotransferase was up-regulated in the resistant genotype upon pathogen attack [70]. The involvement of N-glyceraldehyde-2-phosphotransferase in salt stress resistance/tolerance is unclear, and to the best of our knowledge, it represents a novel salt-stress-responsive protein in Brassica napus leaves.
Conclusions
The present study identified 42 proteins affected by salt stress in Brassica napus, including several novel salt stress responsive proteins in plant leaves, such as cinnamyl alcohol dehydrogenase and N-glyceraldehyde-2-phosphotransferase. Proteome dynamics under different time points after NaCl treatment were analyzed. The results suggested that Chl biosynthesis, photosynthesis, respiration and energy synthesis were negatively affected by salt stress at the 24 h time point, and then recovered at the 48 h and 72 h time point. By contrast, protein biosynthesis, damage repair and defense response were significantly induced by NaCl during the stress treatment, implying that proteins in these categories might alleviate the damage caused by NaCl and promote salt adaptation in Brassica napus. In this study, analysis of the physiological responses to salt stress supported the proteomic data. This study expanded our knowledge of the mechanisms underlying salt-stress adaptation and will promote molecular breeding of salt-tolerant plants in the future.
Supporting Information
S1 Dataset. The MS/MS spectra for the proteins identified by single peptide.
https://doi.org/10.1371/journal.pone.0144808.s001
(RAR)
S1 Fig. Two-dimensional electrophoresis (2-DE) gel images of proteins extracted from leaf 3 of B. napus ‘Nannongyou No. 3’.
https://doi.org/10.1371/journal.pone.0144808.s002
(TIF)
S1 Table. Quantification summary of differentially accumulated proteins under salt stress in leaves of B. napus.
Fold change is expressed as the intensity ratio of treatment/control protein spot. Values are presented as means ± SD of the replicates.
https://doi.org/10.1371/journal.pone.0144808.s003
(XLSX)
Author Contributions
Conceived and designed the experiments: PC RG. Performed the experiments: H. Jia MS YH. Analyzed the data: PC RG. Contributed reagents/materials/analysis tools: RG PC H. Jiang. Wrote the paper: PC H. Jiang.
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