Original Research ARTICLE
Role of Silicon Counteracting Cadmium Toxicity in Alfalfa (Medicago sativa L.)
- 1Plant and Crop Physiology Laboratory, Department of Botany, University of Rajshahi, Rajshahi, Bangladesh
- 2System Biology Research Center, School of Bioscience, University of Skövde, Skövde, Sweden
Cadmium (Cd) is one of the most phytotoxic elements causing an agricultural problem and human health hazards. This work investigates whether and how silicon (Si) ameliorates Cd toxicity in Alfalfa. The addition of Si in Cd-stressed plants caused significant improvement in morpho-physiological features as well as total protein and membrane stability, indicating that Si does have critical roles in Cd detoxification in Alfalfa. Furthermore, Si supplementation in Cd-stressed plants showed a significant decrease in Cd and Fe concentrations in both roots and shoots compared with Cd-stressed plants, revealing that Si-mediated tolerance to Cd stress is associated with Cd inhibition in Alfalfa. Results also showed no significant changes in the expression of two metal chelators [MsPCS1 (phytochelatin synthase) and MsMT2 (metallothionein)] and PC (phytochelatin) accumulation, indicating that there may be no metal sequestration or change in metal sequestration following Si application under Cd stress in Alfalfa. We further performed a targeted study on the effect of Si on Fe uptake mechanisms. We observed the consistent reduction in Fe reductase activity, expression of Fe-related genes [MsIRT1 (Fe transporter), MsNramp1 (metal transporter) and OsFRO1 (ferric chelate reductase] and Fe chelators (citrate and malate) by Si application to Cd stress in roots of Alfalfa. These results support that limiting Fe uptake through the down-regulation of Fe acquisition mechanisms confers Si-mediated alleviation of Cd toxicity in Alfalfa. Finally, an increase of catalase, ascorbate peroxidase, and superoxide dismutase activities along with elevated methionine and proline subjected to Si application might play roles, at least in part, to reduce H2O2 and to provide antioxidant defense against Cd stress in Alfalfa. The study shows evidence of the effect of Si on alleviating Cd toxicity in Alfalfa and can be further extended for phytoremediation of Cd toxicity in plants.
Cadmium (Cd) is a toxic heavy metal affecting plant yield and environment (Järup and Åkesson, 2009; Naeem et al., 2015). It exhibits varied degrees of phytotoxicity and may replace essential metals or cofactors at enzyme active site causing an imbalance in cellular redox status (Hattab et al., 2014). Furthermore, Cd at toxic level displaces protein structure and disrupts membrane integrity (Rascio and Navarri-Izzo, 2011). Cd is naturally high in agricultural soils due to anthropogenic release and is frequently accumulated in plants. Alfalfa (Medicago sativa L.) is an important forage crop and can accumulate heavy metals, such as Cd, Ni, Cu, Zn, Vn (Peralta-Videa et al., 2002; Yang et al., 2011; Carrasco-Gil et al., 2012). Alfalfa is a source of biological nitrogen fixation, bio-fuel and animal feed. Therefore, reducing Cd bioaccumulation in Alfalfa deserves attention.
Silicon (Si) is an abundant element in the Earth’s crust and plays a role in heavy metal alleviation in plants by different mechanisms (Ma et al., 2008; Greger et al., 2016). One mechanism of Cd detoxification is the reduction of Cd uptake into the plant (Treder and Cieslinski, 2005). Also, Si reduces the translocation of Cd from roots to shoots and thus, prevents the adverse effect of Cd on photosynthetic machinery and grains (Greger and Landberg, 2008; Zhang et al., 2008). However, Cd in high concentration is also trapped in roots through vacuolar sequestrations (Greger et al., 2016), leading to decreased Cd translocation in aerial parts of the plants (Lindberg et al., 2007; Liu et al., 2013). Phytochelatins (PCs) and metallothioneins (MTs) may bind to Cd before transporting the complexes into the vacuole or out of the cell by ATP-binding cassette transporters in few plants (Cobbett, 2000; Jasinski et al., 2003). PCs are formed from glutathione by the induction of PCS1 gene (Semane et al., 2007). Further, MTs are involved in detoxifying cytosolic environment of the cell from Cd toxicity (Cobbett and Goldsbrough, 2002; DalCorso et al., 2010).
The Cd is taken up into the cell via carriers, such as low-affinity cation transporters and Fe-regulated transporters in plants (Lindberg et al., 2004; Takahashi et al., 2011). Among the Fe transporters, IRTs and NRAMPs have been reported to take up Cd as well as Fe (Curie et al., 2000; Nakanishi et al., 2006). IRT1 is essential for root Fe uptake in response to Fe deficiency but it also accepts Cd as a substrate and is involved in the root-to-shoot transport of Cd (Rogers et al., 2000). In a transgenic study, elimination of NRAMP5 transporter reduces Cd uptake in rice (Ishikawa et al., 2012). ). Additionally, the ferric chelate reductase (FRO) gene may perform key functions in Fe acquisition in plants (Ling et al., 2002). Barcelo et al. (1993) reported the inhibition of Fe translocation when bean plants were exposed to chromium (Cr) in nutrient solutions. Also, Cr affects Fe uptake in dicots either by inhibiting the reduction of Fe(III) to Fe(II) or by competing with Fe(II) at the site of absorption (Shanker et al., 2005). In addition, IRT1 is induced in response to Fe-deficiency and is capable of transporting minerals and heavy metals (Vert et al., 2002). Further, organic acids such as citrate and malate are major chelators in both Strategy I and II plants, which bind Fe at the site of uptake and facilitate long-distance transport in plants (Abadia et al., 2002; Kabir et al., 2012). Therefore, regulation of Fe uptake has yet to be characterized in detail under Cd stress in plants.
Abiotic stresses generate excessive reactive oxygen species (ROS) which are relatively reactive compared with O2 and may lead to the unspecific oxidation of proteins and membrane lipids or may cause DNA injury (Bolwell et al., 2002; Schützendübel and Polle, 2002). In plants, the control of oxidative burst is achieved by antioxidative systems. These defense systems are composed of enzymatic scavengers, such as catalase (CAT), peroxidase (POD), superoxide dismutase (SOD), glutathione reductase (GR), ascorbate peroxidase (APX) and antioxidant metabolites. Among these enzymes, SOD is the front line of defense against ROS, dismutating reactive O2 to an oxygen molecule and H2O2 (Irfan et al., 2014). Further, an increase in the cellular ROS is subsequently converted to H2O2 (Hung et al., 2005). H2O2 can be directly decomposed through CAT or H2O2 can also be removed via recurrent oxidation–reduction reactions promoted by glutathione (Schützendübel and Polle, 2002). Further, APX enzymes use ascorbate as an electron donor to catalyze the conversion of H2O2 into H2O (Caverzan et al., 2012). In addition, some metabolites (i.e., glutathione, cysteine, glycine, methionine, proline) play critical roles to alleviate the damage induced by metal stress (Sharma and Dietz, 2006; Kumar et al., 2014; Kabir, 2016). Glutathione and proline may also function as sources of reduced-S and N under stress (Anjum et al., 2014).
Although the role of Si in Cd alleviation is reported in popular crop species, the physiological and molecular basis of Si-mediated Cd tolerance in Alfalfa is still unknown. Moreover, exact mechanisms behind the beneficial role of Si might be species dependent, which should be clearly understood for the improvement of Alfalfa. Therefore, our aim was to investigate whether, how and where Si alleviates Cd toxicity in Alfalfa by morpho-physiological investigations. Further, a combination of molecular, enzymatic and metabolomics analysis was performed in roots to elucidate the mechanisms associated with Si-mediated mitigation of Cd toxicity in Alfalfa.
Materials and Methods
We used Alfalfa var. Longdong (popularly known as drought tolerant) since this cultivar is efficient in utilizing Si. Firstly, seeds were disinfected by superficial treatment with 95% (v/v) ethanol for 10 min before germination. Only uniform seedlings were transferred to the solution culture (Hoagland and Arnon, 1950) containing the following nutrient concentrations (μM): KNO3 (16000), Ca(NO3)2.4H2O (6000), NH4H2PO4 (4000), MgSO4.7H2O (2000), KCl (50), H3BO3 (25), Fe-EDTA (25), MnSO4. 4H2O (2), ZnSO4 (2), Na2MoO4.2H2O (0.5), and CuSO4.5H2O (0.5). The nutrient medium was treated with 0 or 1 mM CdCl2 and 0 or 1 mM K2SiO3 as previously described (Greger et al., 2016). The pH of the nutrient media was adjusted to 6.0 by using NaOH or HCl. The plants were harvested for analysis after treatment for 7 days. The nutrient solutions were continuously aerated and the growth chamber was strictly maintained under 10 h light and 14 h dark (550–560 μmol s-1 per μA).
Measurement of Morphological Features and Chlorophyll Concentration
Morphological growth parameters, such as root length, root dry weight, shoot height, shoot dry weight were measured on 1-week-old plants. The roots and leaves of the plants were separated manually and then dried in an oven at 80°C for 2 days before taking the dry weight. Total chlorophyll concentration (a and b) of leaves was determined as previously described (Lichtenthaler and Wellburn, 1985). Firstly, the leaf was weighed and placed in 95% acetone in a 5 mL falcon tube. The leaf sample was then ground with mortar-pestle and centrifuged at 12000 g for 10 min. The absorbance of the separated supernatant was read at 662 nm (chlorophyll a) and 646 nm (chlorophyll b) on a spectrophotometer (UV-1650PC, Shimadzu). The amount of these pigments was calculated based on the formula given by Lichtenthaler and Wellburn (1985).
Determination of Cd and Fe by AAS (Atomic Absorption Spectroscopy)
Harvested roots and shoots were washed with CaSO4 and deionized water before drying in an oven at 80°C for 3 days. The dried samples were then digested in 3 mL HNO3 before heating at 75°C for 10 min. Further, 1 mL of H2O2 was added to each vessel through the ventilation hole and then heated at 109°C for 15 min. The samples were then analyzed for Cd and Fe concentrations by Flame atomic absorption spectroscopy (AAS) outfitted with the ASC-6100 autosampler and air-acetylene atomization gas mixture system (Model No. AA-6800, Shimadzu). Standard solutions of Cd and Fe were prepared separately from their respective concentrations of stock solutions to cover the optimum absorbance ranges for the standard calibration curve.
Determination of Total Soluble Proteins
Total soluble proteins were extracted from roots and shoots as previously described (Guy et al., 1992) with some modifications. The samples were homogenized with a chilled mortar and pestle in buffer containing ice-cold 50 mM Tris-HCl, pH 7.5; 2 mM EDTA and 0.04% (v/v) 2-mercaptoethanol. The homogenate was centrifuged at 12000 g for 30 min at room temperature and the supernatant was then transferred (100 μl) to glass cuvette containing 1 ml of Coomassie Brilliant Blue G 250 (CBB). The absorbance was recorded at 595 nm and the concentration of total soluble protein was calculated using the calibration curve of Bovine serum albumin (BSA).
Measurement of Electrolyte Leakage
Electrolyte leakage (EL) was measured in roots and shoots using an electrical conductivity meter (Lutts et al., 1996). Seedling samples were washed with deionized water to remove surface contamination, weighed and placed in individual vials containing 20 mL of deionized water. Samples were then incubated at 25°C on a shaker (100 rpm) for 2 h. The electrical conductivity of the solution was then read after incubation.
Determination of Si Concentration
Roots and leaves were washed with CaSO4 and deionized water before grinding in mortar-pestle. The samples were then centrifuged at 12000 g for 5 min and supernatant was transferred to 10% ammonium molybdate. Afterward, 10% oxalic acid was added to the sample mixture to form a silico-molybdate complex. Further, 0.5% ascorbic acid was added to the mixture and kept for 20 min at room temperature until blue color is formed. The absorbance of the reaction mixture was then measured at 660 nm in a UV spectrophotometer.
Analysis of Plant Metabolites by HPLC (High-Performance Liquid Chromatography)
Plant metabolites were analyzed in roots harvested from 1-week-old plants by HPLC (Binary Gradient HPLC System, Waters Corporation, Milford, MA, USA) with Empower2TM software as previously described with some modifications (Kabir et al., 2015). The HPLC systems comprised a Waters 515 HPLC pump and Waters In-line degasser AF. For compound separation, a C18 reverse phase-HPLC column (particle size: 5 μm, pore size: 300 A, pH Range: 1.5–10, Dimension: 250 mm × 10 mm) was attached. In mobile phase, buffer A (water and 0.1% TFA) and buffer B (80% acetonitrile and 0.1% TFA) were used at the gradient of: 1–24 min 100% A, 25–34 min 100% B and 35–40 min 100% A. Standards and sample extracts were diluted (100×) and subsequently filtered using 0.22 μm Minisart Syringe Filters (Sartorius Stedim Biotech, Germany) before injection. PC were then detected with a Waters 2489 dual absorbance detector (Waters Corporation, Milford, MA, USA) at 280 and 360 nm. For PC analysis, the peak was detected with Thlaspi arvensis in comparison with the retention times. GSH-equivalents of each PC were further used for PC quantification (Lindberg et al., 2007).
Fe Chelate Reductase Activity
Fe (III)-reductase activity was measured in roots and shoots using ferrozine [3-(2-pyridyl)-5, 6-diphenyl-1,2, 4-triazine sulfonate] as previously described (Kabir et al., 2015). Washed root tips were cut and placed in a beaker filled with ice water. About 0.1 g of tissue was soaked in 1 mM EDTA for 5 min to eliminate apoplastic Fe and washed three times with distilled water to reduce excess EDTA. The roots were then transferred to 50 mL assay solution containing 0.10 mM MES-NaOH (pH 5.5), 0.5 mM CaSO4, 100 mM Fe(III) EDTA, and 300 mM ferrozine. Samples and control tubes were incubated for 1 h in a shaking water bath at 14,000 rpm at 23°C in the dark. After incubation, a 1 mL aliquot from each tube was transferred into a cuvette and the absorbance was measured with a spectrophotometer (UV-1650PC, Shimadzu) at 562 nm wavelength. Reduced Fe [Fe(II)] was calculated with the use of an extinction coefficient of 25,200 M-1 cm-1.
RNA Isolation and Quantitative Real-Time PCR
Expression analysis of Actin, MsPCS1, MsMT2, MsIRT1, MsNRAMP1, and MsFRO1 was performed by quantitative qRT-PCR (reverse transcription PCR) in roots of 1-week-old plants. Briefly, tissues (50–100 mg) were ground with a mortar and pestle to a fine powder in liquid nitrogen. Afterward, total RNA was isolated according to the protocol supplied by SV Total RNA Isolation System (cat. no. Z3100), Promega Corporation, USA. The integrity of isolated RNA was then checked by denaturing agarose gel electrophoresis and quantified by NanoDrop 2000 UV-Vis Spectrophotometer. The first-strand cDNA was then synthesized by using GoScriptTM Reverse Transcription System (Cat no. A5001), Promega Corporation, United States. Before real-time analysis, the cDNA samples were treated with RNase to eliminate RNA contamination. Real-time PCR was performed in triplicate using the EcoTM real-time PCR system (Illumina, United States) using GoTaq® qPCR Master Mix (Promega, USA) and gene specific primers designed from the available gene sequences of Medicago sativa or Medicago truncatula (Supplementary Table S1). All primers were used to perform BLASTN searches with Arabidopsis genome database to confirm that they would specifically amplify the gene of interest. Expression data set was normalized with Actin as an internal control (Eco Software v220.127.116.11). The real-time PCR program used was as follows: 3 min at 95°C, 40 cycles of 30 s at 94°C, 15 s at 58°C and 30 s at 72°C.
Catalase, APX, POD, SOD and GR enzymes were extracted in roots of on 1-week-old plants as previously described with slight modifications (Goud and Kachole, 2012). Briefly, 100 mg of root tissue was ground in 5 mL phosphate buffer (100 mM) and centrifuged at 12000 g for 10 min to separate supernatant. For CAT analysis, the reaction mixture (2 mL) contained 100 mM potassium phosphate buffer (pH 7.0), 6% H2O2 and root extract. After adding the root extract, the decrease in absorbance was recorded at 240 nm (extinction coefficient of 0.036 mM-1 cm-1) using a UV spectrophotometer at 30 s intervals up to 1 min. APX was analyzed in a reaction mixture containing 50 mM potassium phosphate buffer (pH 7.0), 0.5 mM ascorbic acid, 0.1 mM EDTA, 0.1 mM H2O2, and 0.1 ml extract. The specific activity of the enzyme was calculated using extinction coefficient of 2.8 mM-1 cm-1 based on absorbance at 290 nm (Almeselmani et al., 2006). In case of POD, the reaction mixture (2 mL) contained 100 mM potassium phosphate buffer (pH 6.5), 0.05 M pyrogallol, 200 mM H2O2 and 100 μl root extract. Similarly, the changes in absorbance were measured at 430 nm (extinction coefficient 12 mM-1 cm-1) in a spectrophotometer from 30 s up to 1.5 min. Furthermore, SOD assay mixture contained 50 mM sodium carbonate/bicarbonate buffer (pH 9.8), 0.1 mM EDTA, 0.6 mM epinephrine and enzyme (Sun and Zigman, 1978). Once epinephrine is added, adrenochrome formation was then monitored for 4 min at 475 nm in a UV-Vis spectrophotometer. Lastly, 100 μl of root extract was added to the assay mixture containing 1 mL of 0.2 M phosphate buffer (pH 7.0) with 1 mM EDTA, 20 mM oxidized glutathione (GSSG) and 2 mM NADPH for GR analysis. Oxidation of NADPH by GR was then recorded at 340 nm (Halliwell and Foyer, 1978). The hydrogen peroxide (H2O2) content was determined in roots and shoots as previously described (Alexieva et al., 2001). Briefly, tissues were crushed in 0.1% trichloroacetic acid (TCA) and centrifuged at 10, 000 g for 15 min. The supernatant was kept in dark for 1 h before mixing with phosphate buffer (10 mM, pH 7.0) and potassium iodide ( M). The absorbance of the mixture was recorded at 390 nm.
All experiments were performed in completely randomized block design and having at least three independent replications for each sample. Statistical significance for each group of data was set at P ≤ 0.05 by ANOVA one-way followed by Duncan’s Multiple Range Test (DMRT) using SPSS Statistics 20 Software. Further, the graphical presentation was prepared using GraphPad Prism 6.
Root length, root dry weight, shoot height, shoot dry weight, and total chlorophyll concentration (a and b) significantly (P < 0.05) decreased due to Cd stress compared with non-treated controls (Table 1; Figure 1). However, these parameters significantly increased due to Si application in combination with Cd treatment compared with Cd-stressed plants. Si supplementation in non-stressed plants caused an adverse effect on root length and shoot dry weight compared to that observed for Cd-stressed plants but showed similar root dry weight and chlorophyll concentration to that of control plants (Table 1). However, results showed a non-significant change in morphological features between untreated controls and Si-treated Cd-stressed plants (Table 1).
TABLE 1. Morpho-physiological features of Alfalfa after cultivation for 7 days in nutrient medium with or without Cd and Si.
FIGURE 1. Phenotypes of 7-days-old Alfalfa plants grown under different growth conditions of Cd and Si.
Cd, Fe, and Si Contents in Roots and Shoots
Cadmium and Fe contents increased in the whole plant under Cd stress compared with non-treated controls, showing the higher amount in roots than in shoots (Figure 2A). Supplementation with Si along with Cd significantly decreased the accumulation of Cd and Fe in both roots and shoots compared with the other three (i.e., Cd-, Cd+, Cd-Si+) treatments (Figures 2A,B). Plant showed lower Si concentration in roots when plants were grown without Si treatment compared with Si-treated plants grown with or without Cd. Further, Si concentration significantly increased in roots when plants were treated with Cd along with Si compared with the plants grown with or without Cd under hydroponic conditions (Figure 2C). Plants treated by Si without Cd showed significantly decreased Si concentration in roots compared to the plants grown under dual treatment of Si and Cd. In shoots, Si concentration considerably increased when plants were grown under Si supplementation with or without Cd compared to non-treated control and Cd-stressed plants (Figure 2C).
FIGURE 2. Concentrations of Cd (A), Fe (B), and Si (C) in roots and shoots of 7-days-old Alfalfa plants grown under different growth conditions of Cd and Si. Different letters in each column indicate significant differences between mean ± SD of treatments (n = 3) at a P < 0.05 significance level.
Determination of Total Soluble Protein Content, Electrolyte Leakage, Fe Chelate Reductase Activity
Cadmium stress caused a significant decrease in total protein content in both roots and leaves compared to control plants. However, application of Si along with Cd significantly increased the protein content in both tissues compared with Cd-stressed plants. When treated solely with Si on controls, plants showed protein content similar to that of the plants grown with Si and Cd supplementation (Figure 3A). The EL significantly increased in both roots and shoots under Cd stress compared with control plants (Cd-). However, the EL significantly decreased in both tissues due to Si along with Cd treatments compared with Cd-stressed Alfalfa (Figure 3B). Si applied solely in non-treated plants showed similar EL to that of plants treated with Cd and Si along with Cd in roots and shoots, respectively (Figure 3B).
FIGURE 3. Total protein content (A) and electrolyte leakage (B) in roots and shoots of Alfalfa plants grown under different growth conditions of Cd and Si. Different letters in each column indicate significant differences between mean ± SD of treatments (n = 3) at a P < 0.05 significance level.
Cadmium toxicity caused a significant increase in Fe-chelate reductase activity in both roots and shoots in comparison with control plants (Figure 4). However, Si supplementation along with Cd showed a significant decrease in Fe-chelate reductase activity compared with Cd-stressed plants (Figure 4). Si applied solely to non-treated plants showed similar Fe-chelate reductase activity in roots to that of controls and plants treated with Si and Cd. However, Fe-chelate reductase activity significantly increased in shoots compared to controls but showed similar activity to that of plants grown under both Si and Cd supplementations (Figure 4).
FIGURE 4. Fe chelate reductase activity in roots and shoots of 7-days-old Alfalfa plants grown under different growth conditions of Cd and Si. Different letters in each column indicate significant differences between mean ± SD of treatments (n = 3) at a P < 0.05 significance level.
HPLC Analysis in Roots
In this study, phytochelatin showed no significant changes in roots among the treatments in Alfalfa plants (Table 2). Further, citrate and malate concentrations significantly decreased due to Cd stress compared with non-treated controls. However, Si application to Cd-stressed plants showed a significant increase in citrate and malate concentrations in roots compared with the plants grown under Cd stress. Si applied solely to control plants showed similar citrate and malate levels to that of control plants (Table 2).
TABLE 2. Concentrations (μg-1 FW) of total phytochelatin, citrate and malate in roots of 7-days-old Alfalfa plants grown under different growth conditions of Cd and Si.
Expression of Genes in Roots
Quantitative real-time PCR analysis showed no significant changes in the expression of two metal chelators (MsPCS1 and MsMT2) in roots of Alfalfa among the treatments (Figure 5). However, three Fe-related genes, MsIRT1, MsNramp1, and MsFRO1 significantly upregulated in roots of Alfalfa plants under Cd stress compared with control plants. Further, expression of these genes significantly decreased when plants were treated with Si along with Cd (Figure 5). Si applied to non-treated plants showed similar expression pattern for these Fe-related genes to that of control plants (Figure 5).
FIGURE 5. Quantitative expression analysis of MsPCS1, MsMT2, MsIRT1, MsNRAMP1, MsFRO1 transcripts in roots of Alfalfa plants grown under different growth conditions for 7-days. Different letters in each column indicate significant differences between mean ± SD of treatments (n = 3) at a P < 0.05 significance level.
Enzymatic Changes in Roots
Enzymatic activity of CAT, APX, and SOD significantly decreased due to Cd stress compared with controls in roots of Alfalfa. However, application of Si along with Cd showed a significant increase in CAT, APX, and SOD activities compared with Cd-stressed plants (Table 3). Si applied solely to non-treated plants showed similar activities CAT and SOD to that of control plants. Further, POD and GR activities showed no significant changes in roots of Alfalfa among the treatments. Results also demonstrated that H2O2 content significantly increased due to Cd stress compared with controls in roots. However, application of Si with or without Cd showed a significant decrease in H2O2 content compared with Cd-stressed plants (Table 3).
TABLE 3. Enzymatic activities in roots of Alfalfa after cultivation for 7 days in nutrient medium with or without Cd and Si.
Changes in Antioxidant Metabolites
We also studied the changes in some key metabolites having antioxidant properties. It was found that glutathione and cysteine showed no significant changes in roots of Alfalfa plants subjected to different treatments of Cd and Si (Table 4). However, Cd stress caused a significant decrease in methionine compared with controls but showed a significant increase when plants were treated with Cd and Si. Further, the investigation showed no significant reduction in proline concentration in response to Cd stress, application of Si along with Cd significantly increased proline concentration in roots of Alfalfa. Application of Si to control plants showed similar proline level to that of controls (Table 4).
TABLE 4. Concentrations (μg-1 FW) of antioxidant metabolites in roots of 7-days-old Alfalfa plants grown under different growth conditions of Cd and Si.
Role of Si Restoring Morphological Features
In the present study, Si supplementation under Cd showed significant improvement in root and shoot growth parameters along with total chlorophyll content in Alfalfa. Also, application of Si in Cd-treated plants restored the total protein content in both roots and shoots compared with Cd-stressed plants. The role of Si increasing total soluble protein under drought stress is associated with the reduction of free radicals and ROS regeneration (Gong et al., 2005). Furthermore, application of Si in Cd-stressed plants diminished the EL in both roots and shoots. It indicates that exogenous Si might provide membrane stability in Cd-stressed Alfalfa plants. In a similar study, lead (Pb) stress induced a significant increase in the membrane injury but Si application noticeably eliminated EL in cotton plants (Bharwana et al., 2013). Although differences were not statistically significant, Si application under Cd stress did not completely restore morphological features back to that observed for untreated controls. This could be due to the concentration of Cd and Si used and can be optimized depending on the severity of stress involved. We also observed that Si was able to withstand the adverse effect of Cd on leaf expansion and stem elongation in Alfalfa. It might coincide with the role of silicon increasing soluble protein content and maintaining chlorophyll concentrations in shoots (Zhu et al., 2004; Farooq et al., 2013). Altogether, our findings support that Si can restore the damages and significantly improved the growth parameters provoked by Cd stress in Alfalfa var. Longdong plants due to its efficiency in utilizing exogenous Si. Genotypic variation in Cd accumulation and tolerance is reported in many plant species (Metwally et al., 2004; Yan et al., 2010; Pourghasemiana et al., 2013). Therefore, Si-mediated alleviation of Cd toxicity may behave differently in other cultivars of Alfalfa.
Atomic absorption spectroscopy data further showed that dual application of Si and Cd showed a reduction of Cd concentration to its normal level in both roots and shoots. It indicates that Si inhibits Cd uptake in roots and subsequently reduces the translocation of Cd into the shoots of Alfalfa plants. Similarly, Si-mediated reduction of Cd uptake was also reported in roots of cucumber (Wu et al., 2015). In the present study, we also observed higher accumulation of Fe in roots and shoots due to Cd stress. Interestingly, Si supplementation under Cd stress showed a significant decrease in Fe concentrations in both roots and shoots, being consistent with Cd concentration. These findings support that inhibition of Cd uptake in roots of Alfalfa plants is tightly regulated with Fe transport under Si supplementation. In the light of Si concentration in roots and shoots, it is evident that Alfalfa plants require more exogenous Si under Cd stress to withstand its toxicity. In this study, it was also noticed that exogenous Si applied to non-treated plants showed a slight reduction in root parameters. It may be possible that exogenous Si when not used by plants for Cd alleviation might hamper metabolism. Taken together, our findings indicate that alleviation of Cd toxicity in Alfalfa plants is largely dependent on the regulation of Cd and Fe uptake in root systems.
Biochemical and Molecular Mechanisms Associated with Cd Detoxification
In the light of morpho-physiological observations, the mechanistic basis for Cd toxicity tolerance through Si supplementation was further investigated in roots of Alfalfa plants. We initially performed PC analysis and two candidate genes (MsPCS1, MsMT2) responsible for vacuolar sequestration in roots. HPLC analysis showed no significant changes in PC accumulation in roots under dual treatment of Si and Cd compared with control and Cd-stressed Alfalfa plants. Being consistent with PC accumulation, expression of MsPCS1 and MsMT2 showed no significant changes in roots of Alfalfa due to Si effect. Induction of PC and MT is involved in vacuolar sequestration of heavy metal is plants. However, Greger et al. (2016) suggested that the inhibition of Cd uptake in wheat closely associated with the increased Cd extrusion from the cells than PC accumulation. Our studies indicate that Cd detoxification in Alfalfa plants following Si application may not be associated with the change in metal sequestrations in roots. This observation is correlated with AAS data revealing no significant Cd accumulation in roots due to Si application. Therefore, it might be possible that effect of Si on Cd-stressed Alfalfa is dependent on the inhibition of metal transporters in root systems.
As there are no specific Cd transporters in plants, uptake of Cd is achieved by transporter genes located on plasma membranes (Morel et al., 2009). To characterize the Fe-chelating potential under Si supplementations in Alfalfa, we further studied the changes of Fe related genes (MsIRT1, OsNRAMP1, and MsFRO1) along with Fe-reductase activity in roots. Expression of these genes and Fe-reductase activity significantly decreased due to Si application under Cd stress in Alfalfa plants, indicating that regulation of Fe uptake and chelation plays a critical role in limiting Fe-mediated Cd accumulation in Alfalfa plants under Si supplementation. Fe-chelate reductase activity is known as an important biochemical mechanism regulating Fe availability in plant cells. FROs genes may be required for Fe distribution within aerial portions of the plant and/or may be involved in Fe transport mechanisms in the organelle (Jeong and Connolly, 2009). Changes of transcription factors belonging to several families demonstrate that responses of plants under Cd stress are very complex (Fusco et al., 2005; Weber et al., 2006). Transcription factors regulating genes involved in Cd detoxification following Si supplementation might provide interesting message to future researchers. Our data further showed a significant increase in two Fe chelators (citrate and malate) in roots due to Cd stress revealing that the chelation of Fe through the organic acids is associated with enhanced Fe as well as Cd uptake in Alfalfa. Interestingly, Si application to Cd-stressed plants resulted in a decrease in both citrate and malate concentrations. It indicates that Si might indirectly decrease Cd accumulation through the inhibition of Fe chelation strategies in Alfalfa plants.
Antioxidant Defense under Cd Stress
We also analyzed antioxidant enzymes involved in antioxidant defense in plants under abiotic stress. Among these enzymes, CAT and SOD activities significantly increased in roots under Si supplementation in Cd-stressed Alfalfa plants. CAT is involved in the main defense mechanism against accumulation and toxicity of ROS and may play a fundamental role in decreasing H2O2 level in plant cells (Malar et al., 2014). SOD provides a front line defense under the metal-induced oxidative damage and catalyzes the conversion of the superoxide radical to molecular oxygen and H2O2 (Romero-Puertas et al., 2007; Irfan et al., 2014). In the present work, Alfalfa plants have a tendency to increase SOD activity under Cd stress, suggesting better efficiency in converting O2 to H2O2 following Si treatment. The higher CAT and SOD activities due to Si on Cd-stressed Alfalfa plants may be partially correlated with the 0decreased H2O2 concentrations in roots. CAT mainly occurs in peroxisomes and does not require a reductant for catalyzing a dismutation reaction (Sofo et al., 2015). Wu et al. (2015) also reported that the Si-mediated increases in antioxidant enzymes might be an adaptive response to counteract Cd stress in tomato. However, the increase of APX due to Si supplementation under Cd stress indicates that inhibition of H2O2 might be associated with its increased activity. APX is largely intracellular and involved in the control of cellular H2O2 levels in chloroplasts, cytosol, mitochondria and peroxisomes, and apoplastic space (Veitch, 2004; Sofo et al., 2015). Further, APX activity increases along with other enzymes activities, such as CAT, SOD, and GSH reductase (Shigeoka et al., 2002). In another study, Cd and Cu exposures caused the increase in APX and SOD activities (Lee et al., 2007). These results emphasize that Si-mediated scavenging of Cd-induced ROS might be correlated with APX and SOD but not POD in Alfalfa plants.
Our studies also revealed the increase of methionine and proline due to Si treatment on Cd-stressed plants. Methionine can undergo ROS-mediated oxidation to methionine sulfoxide by methionine sulfoxide reductases to ameliorate oxidative damage (Dos Santos et al., 2005; Cabreiro et al., 2006). Also, methionine is a substrate for the synthesis of various polyamines (putrescine, spermidine, spermine) associated with stress tolerance (Alcázar et al., 2010) and methionine residues act as an antioxidant protein reservoir (Hoshi and Heinemann, 2001). Apart from acting as an osmolyte, proline scavenges free radicals, stabilizes sub-cellular structures and proteins under stress conditions (Sharma and Dubey, 2005). Thus, our results suggest that induction of antioxidative metabolites help Alfalfa seedlings to adapt better to the Cd stress. Metal-induced proline accumulation in plants is not directly originated from heavy metal stress, but for water balance disorder by regulating the contents of inorganic solutes (Rai, 2002; Clemens, 2006). Furthermore, proline synthesis is advantageous to NADP+ refilling and redox cycling, which is of particular importance for antioxidant defense mechanisms in plants during stress (Babiychuk et al., 1995). In this study, Si did not affect the concentration of glutathione and cysteine, which is correlated with the PC accumulation in roots as these two metabolites are involved in PC biosynthesis pathway. Therefore, it turned out that the active involvement of ROS scavenging mainly mediated by elevated SOD, methionine and proline was related, at least in part, to the Si-mediated alleviation of Cd stress in Alfalfa.
In this present study, morpho-physiological findings support that Si plays a critical role to withstand Cd toxicity and to restore the normal growth and development in Alfalfa plants. Further, simultaneous reduction of Cd and Fe in roots and shoots of Alfalfa due to Si treatment under Cd stress indicates that mechanisms counteracting Cd toxicity exist in roots. Further, no changes of metal chelator (MsPCS1 and MsMT2) genes and PC synthesis in roots suggest that changes in metal sequestration may not be involved in Si-mediated mitigation of Cd toxicity in Alfalfa. Also, reduction of Fe-reductase activity, downregulation of Fe-related genes (MsIRT1, MsNramp1, and MsFRO1) and a decrease of Fe chelators (citrate and malate) reveals that alleviation of Cd toxicity in Alfalfa plants largely depends on the inhibition of Fe uptake and Fe chelation in roots. Finally, a Si-mediated increase in antioxidant enzymes (CAT, SOD, APX) and metabolites (methionine, proline) might play an integral part against Cd-induced oxidative stress in Alfalfa plants. These findings may stimulate further researches for phytoremediation and development of Cd-tolerant crops through Si treatment.
AK conduced most of the laboratory works and prepared the draft manuscript. MH and MK performed few laboratory works. AM and SH revised the manuscript.
Conflict of Interest Statement
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.
Authors are grateful to DNA Technology, Denmark, for supplying primers on a timely basis. Tommy Landberg, Department of Ecology, Environment and Plant Sciences, Stockholm University, Sweden provided the phytochelatin standards.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fpls.2016.01117
Alcázar, R., Altabella, T., Marco, F., Bortolotti, C., Reymond, M., Koncz, C., et al. (2010). Polyamines: molecules with regulatory functions in plant abiotic stress tolerance. Planta 231, 1237–1249. doi: 10.1007/s00425-010-1130-0
Alexieva, V., Sergiev, I., Mapelli, S., and Karanov, E. (2001). The effect of drought and ultraviolet radiation on growth and stress markers in pea and wheat. Plant Cell Environ. 24, 1337–1344. doi: 10.1046/j.1365-3040.2001.00778.x
Almeselmani, M., Deshmukh, P. S., Sairam, R. K., Kushwaha, S. R., and Singh, T. P. (2006). Protective role of antioxidant enzymes under high temperature stress. Plant Sci. 171, 382–388. doi: 10.1016/j.plantsci.2006.04.009
Anjum, N. A., Aref, I. M., Duarte, A. C., Pereira, E., Ahmad, I., and Iqbal, M. (2014). Glutathione and proline can coordinately make plants withstand the joint attack of metal(loid) and salinity stresses. Front Plant Sci. 5:662. doi: 10.3389/fpls.2014.00662
Babiychuk, E., Kushnir, S., Belles-Boix, E., Van Montagu, M., and Inzé, D. (1995). Arabidopsis thaliana NADPH oxidoreductase homologs confer tolerance of yeasts toward the thiol-oxidizing drug diamide. J. Biol. Chem. 270, 26224–26231. doi: 10.1074/jbc.270.44.26224
Barcelo, J., Poschenrieder, C., Vazquez, M. D., Gunse, B., and Vernet, J. P. (1993). Beneficial and toxic effects of chromium in plants: solution culture, pot and field studies. Studies in Environmental Science No. 55. Paper Presented at the 5th International Conference on Environmental Contamination, Morges.
Bharwana, S. A., Ali, S., Farooq, M. A., Iqbal, N., Abbas, F., and Ahmad, M. S. A. (2013). alleviation of lead toxicity by silicon is related to elevated photosynthesis, antioxidant enzymes suppressed lead uptake and oxidative stress in cotton. J. Bioremed. Biodeg. 96, 242–249. doi: 10.1016/j.ecoenv.2013.07.006
Bolwell, G. P., Bindschedler, L. V., Blee, K. A., Butt, V. S., Davies, D. R., Gardner, S. L., et al. (2002). The apoplastic oxidative burst in response to biotic stress in plants: a three-component system. J. Exp. Bot. 53, 1367–1376. doi: 10.1093/jexbot/53.372.1367
Carrasco-Gil, S., Estebaranz-Yubero, M., MedelCuesta, D., Millan, R., and Hernandez, L. E. (2012). Influence of nitrate fertilization on Hg uptake and oxidative stress parameters in alfalfa plants cultivated in a Hg-polluted soil. Environ. Exp. Bot. 75, 16–24. doi: 10.1016/j.envexpbot.2011.08.013
Caverzan, A., Passaia, G., Rosa, S. B., Ribeiro, C. W., Lazzarotto, F., and Margis-Pinheiro, M. (2012). Plant responses to stresses: role of ascorbate peroxidase in the antioxidant protection. Genet. Mol. Biol. 35, 1011–1019. doi: 10.1590/S1415-47572012000600016
Cobbett, C. S., and Goldsbrough, P. (2002). Phytochelatins and metallothioneins: roles in heavy metal detoxification and homeostasis. Annu. Rev. Plant Physiol. Plant Mol. Biol. 53, 159–182. doi: 10.1146/annurev.arplant.53.100301.135154
Dos Santos, C. V., Cuiné, S., Rouhier, N., and Rey, P. (2005). The Arabidopsis plastidic methionine sulfoxide reductase B proteins. Sequence and activity characteristics, comparison of the expression with plastidic methionine sulfoxide reductase A, and induction by photooxidative stress. Plant Physiol. 138, 909–922. doi: 10.1104/pp.105.062430
Farooq, M. A., Ali, S., Hameed, A., Ishaque, W., Mahmood, K., and Iqbal, Z. (2013). Alleviation of cadmium toxicity by silicon is related to elevated photosynthesis, antioxidant enzymes; suppressed cadmium uptake and oxidative stress in cotton. Ecotoxicol. Environ. Saf. 96, 242–249. doi: 10.1016/j.ecoenv.2013.07.006
Fusco, N., Micheletto, L., Dal Corso, G., Borgato, L., and Furini, A. (2005). Identification of cadmium-regulated genes by cDNA-AFLP in the heavy metal accumulator Brassica juncea L. J. Exp. Bot. 56, 3017–3027. doi: 10.1093/jxb/eri299
Halliwell, B., and Foyer, C. H. (1978). Properties and physiological function of a glutathion reductase purified from spinach leaves by affinity chromotography. Planta 139, 9–17. doi: 10.1007/BF00390803
Hattab, S., Boussetta, H., and Banni, M. (2014). Influence of nitrate fertilization on Cd uptake and oxidative stress parameters in alfalfa plants cultivated in presence of Cd. J. Soil Sci. Plant Nutr. 14, 89–99.
Irfan, M., Ahmad, A., and Hayat, S. (2014). Effect of cadmium on the growth and antioxidant enzymes in two varieties of Brassica juncea. Saudi J. Biol. Sci. 21, 125–131. doi: 10.1016/j.sjbs.2013.08.001
Ishikawa, S., Ishimaru, Y., Igura, M., Kuramata, M., Abe, T., Senoura, T., et al. (2012). Ion-beam irradiation, gene identification, and marker-assisted breeding in the development of low-cadmium rice. Proc. Natl. Acad. Sci. U.S.A. 109, 19166–19171. doi: 10.1073/pnas.1211132109
Jasinski, M., Ducos, E., Martinoia, E., and Bountry, M. (2003). The ATP-binding cassette transporters: structure, function, and gene family comparison between rice and Arabidopsis. Plant Physiol. 131, 1169–1177. doi: 10.1104/pp.102.014720
Kabir, A. H., Paltridge, N. G., Able, A. J., Paull, J. G., and Stangoulis, J. C. R. (2012). Natural variation for Fe-efficiency is associated with upregulation of Strategy I mechanisms and enhanced citrate and ethylene synthesis in Pisum sativum L. Planta 235, 1409–1419. doi: 10.1007/s00425-011-1583-9
Kabir, A. H., Rahman, M. M., Haider, S. A., and Paul, N. K. (2015). Mechanisms associated with differential tolerance to Fe deficiency in okra (Abelmoschus esculentus Moench). Environ. Exp. Bot. 112, 16–26. doi: 10.1016/j.envexpbot.2014.11.011
Kumar, A., Dwivedi, S., Singh, R. P., Chakrabarty, D., Mallick, S., Trivedi, P. K., et al. (2014). Evaluation of amino acid profile in contrasting arsenic accumulating rice genotypes under arsenic stress. Biol. Plant. 58, 733–742. doi: 10.1016/j.jhazmat.2012.06.049
Lee, S. H., Ahsan, N., Lee, K. W., Kim, D. H., Lee, D. G., Kwak, S. S., et al. (2007). Simultaneous overexpression of both CuZn superoxide dismutase and ascorbate peroxidase in transgenic tall fescue plants confers increased tolerance to a wide range of abiotic stresses. J. Plant Physiol. 164, 1626–1638. doi: 10.1016/j.jplph.2007.01.003
Ling, H. Q., Bauer, P., Bereczky, Z., Keller, B., and Ganal, M. (2002). The tomato fer gene encoding a bHLH protein controls iron-uptake responses in roots. Proc. Nat. Aca. Sci. U.S.A. 99, 13938–13943. doi: 10.1073/pnas.212448699
Liu, J., Ma, J., He, C., Li, X., Zhang, W., Xu, F., et al. (2013). Inhibition of cadmium ion uptake in rice (Oryza sativa) cells by a wall-bound form of silicon. New Phytol. 200, 691–699. doi: 10.1111/nph.12494
Lutts, S., Kinet, J. M., and Bouharmont, J. (1996). NaCl-induced senescence in leaves of rice (Oriza sativa L.) cultivar differing in salinity resistance. Ann. Bot. 78, 389–398. doi: 10.1006/anbo.1996.0134
Ma, J. F., Yamaji, N., Mitani, N., Xu, X. X., Su, Y. H., McGrath, S. P., et al. (2008). Transporters of arsenite in rice and their role in arsenic accumulation in rice grain. Proc. Nat. Aca. Sci. U.S.A. 105, 9931–9935. doi: 10.1073/pnas.0802361105
Malar, S., Vikram, S. S., Favas, P. J. C., and Perumal, V. (2014). Lead heavy metal toxicity induced changes on growth and antioxidative enzymes level in water hyacinths [Eichhornia crassipes (Mart.)] Bot. Stud. 55:54.
Morel, M., Crouzet, J., Gravot, A., Auroy, P., Leonhardt, N., Vavasseur, A., et al. (2009). AtHMA3, a P1B-ATPase allowing Cd / Zn / Co / Pb vacuolar storage in Arabidopsis. Plant Physiol. 149, 894–904. doi: 10.1104/pp.108.130294
Naeem, A., Saifullah, Ghafoor, A., and Farooq, M. (2015). Suppression of cadmium concentration in wheat grains by silicon is related to its application rate and cadmium accumulating abilities of cultivars. J. Sci. Food Agric. 95, 2467–2472. doi: 10.1002/jsfa.6976
Nakanishi, H., Ogawa, I., Ishimaru, Y., Mori, S., and Nishizawa, N. K. (2006). Iron deficiency enhances cadmium uptake and translocation mediated by the Fe2+ transporters OsIRT1 and OsIRT2 in rice. Soil Sci. Plant Nutr. 52, 464–469. doi: 10.1111/j.1747-0765.2006.00055.x
Peralta-Videa, J. R., Gardea-Torresdey, J. L., Gomez, E., Tiemann, K. J., Parsons, J. G., and Carrillo, G. (2002). Effect of mixed cadmium, copper, nickel and zinc at different pHs upon alfalfa growth and heavy metal uptake. Environ. Pollut. 119, 291–301. doi: 10.1016/S0269-7491(02)00105-7
Pourghasemiana, N., Ehsanzadeha, P., and Greger, M. (2013). Genotypic variation in saﬄower (Carthamus spp.) cadmium accumulation and tolerance affected by temperature and cadmium levels. Environ. Exp. Bot. 87, 218–226. doi: 10.1016/j.envexpbot.2012.12.003
Rascio, N., and Navarri-Izzo, F. (2011). Heavy metal hyperaccumulating plants: how and why do they do it? And what makes them so interesting. Plant Sci. 180, 169–181. doi: 10.1016/j.plantsci.2010.08.016
Romero-Puertas, M. C., Corpas, F. J., Rodriguez-Serrano, M., Gomez, M., del Río, L. A., and Sandalio, L. M. (2007). Differential expression and regulation of antioxidative enzymes by cadmium in pea plants. J. Plant Physiol. 164, 1346–1357. doi: 10.1016/j.jplph.2006.06.018
Schützendübel, A., and Polle, A. (2002). Plant responses to abiotic stresses: heavy metal-induced oxidative stress and protection by mycorrhization. J. Exp. Bot. 53, 1351–1365. doi: 10.1093/jexbot/53.372.1351
Semane, B., Cuypers, A., Smeets, K., Van Belleghem, F., Horemans, N., Schat, H., et al. (2007). Cadmium responses in Arabidopsis thaliana: glutathione metabolism and antioxidative defence system. Physiol. Plant. 129, 519–528. doi: 10.1111/j.1399-3054.2006.00822.x
Sharma, S. S., and Dietz, K. (2006). The significance of amino acids and amino acid-derived molecules in plant responses and adaptation to heavy metal stress. J. Exp. Bot. 57, 711–726. doi: 10.1093/jxb/erj073
Sharma, P., and Dubey, R. S. (2005). Modulation of nitrate reductase activity in rice seedlings under aluminium toxicity and water stress: role of osmolytes as enzyme protectant. J. Plant Physiol. 162, 854–864. doi: 10.1016/j.jplph.2004.09.011
Shigeoka, S., Ishikawa, T., Tamoi, M., Miyagawa, Y., Takeda, T., Yabuta, Y., et al. (2002). Regulation and function of ascorbate peroxidase isoenzymes. J. Exp. Bot. 53, 1305–1319. doi: 10.1093/jexbot/53.372.1305
Sofo, A., Scopa, A., Nuzzacu, M., and Vitti, A. (2015). Ascorbate peroxidase and catalase activities and their genetic regulation in plants subjected to drought and salinity stresses. Int. J. Mol. Sci. 16, 13561–13578. doi: 10.3390/ijms160613561
Takahashi, R., Ishimaru, Y., Senoura, T., Shimo, H., Ishikawa, S., Arao, T., et al. (2011). The OsNRAMP1 iron transporter is involved in Cd accumulation in rice. J. Exp. Bot. 62, 4843–4850. doi: 10.1093/jxb/err136
Treder, W., and Cieslinski, G. (2005). Effect of silicon application on cadmium uptake and distribution in strawberry plants grown on contaminated soils. J. Plant Nutr. 28, 917–929. doi: 10.1081/PLN-200058877
Vert, G., Grotz, N., Dedaldechamp, F., Gaymard, F., Guerinot, M. L., Briat, J., et al. (2002). IRT1, an Arabidopsis transporter essential for iron uptake from the soil and for plant growth. Plant Cell 14, 1223–1233. doi: 10.1105/tpc.001388
Weber, M., Trampczynska, A., and Clemens, S. (2006). Comparative transcriptome analysis of toxic metal responses in Arabidopsis thaliana and the Cd(2+)-hypertolerant facultative metallophyte Arabidopsis halleri. Plant Cell Environ. 29, 950–963. doi: 10.1111/j.1365-3040.2005.01479.x
Wu, J., Guo, J., Hu, Y., and Gong, H. (2015). Distinct physiological responses of tomato and cucumber plants in silicon-mediated alleviation of cadmium stress. Front. Plant Sci. 6:453. doi: 10.3389/fpls.2015.00453
Zhang, C., Wang, L., Nie, Q., Zhang, W., and Zhang, F. (2008). Long-term effects of exogenous silicon on cadmium translocation and toxicity in rice (Oryza sativa L.). Environ. Exp. Bot. 62, 300–307. doi: 10.1016/j.envexpbot.2007.10.024
Keywords: Alfalfa, silicon, Fe regulation, antioxidant activities, Cd stress
Citation: Kabir AH, Hossain MM, Khatun MA, Mandal A and Haider SA (2016) Role of Silicon Counteracting Cadmium Toxicity in Alfalfa (Medicago sativa L.). Front. Plant Sci. 7:1117. doi: 10.3389/fpls.2016.01117
Received: 15 February 2016; Accepted: 13 July 2016;
Published: 27 July 2016.
Edited by:Hideyuki Inui, Kobe University, Japan
Reviewed by:Kate Warpeha, University of Illinois at Chicago, USA
Yi Ma, University of Connecticut, USA
Copyright © 2016 Kabir, Hossain, Khatun, Mandal and Haider. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ahmad H. Kabir, firstname.lastname@example.org