Original Research ARTICLE
Role of Trichoderma harzianum in mitigating NaCl stress in Indian mustard (Brassica juncea L) through antioxidative defense system
- 1Department of Botany, Sri Pratap College, Srinagar, India
- 2Department of Botany and Microbiology, Faculty of Science, King Saud University, Riyadh, Saudi Arabia
- 3Mycology and Plant Disease Survey Department, Plant Pathology Research Institute, Agriculture Research Center, Giza, Egypt
- 4Department of Plant Production, Faculty of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia
- 5Department of Botany, University of Kashmir, Srinagar, India
- 6Institute for Landscape Biogeochemistry, Leibniz Centre for Agricultural Landscape Research, Müncheberg, Germany
- 7Centre for Environmental Research, Near East University, Nicosia, Cyprus
Salinity stress affected crop production of more than 20% of irrigated land globally. In the present study the effect of different concentrations of NaCl (0, 100, and 200 mM) on growth, physio-biochemical attributes, antioxidant enzymes, oil content, etc. in Brassica juncea and the protective role of Trichoderma harzianum (TH) was investigated. Salinity stress deteriorates growth, physio-biochemical attributes, that ultimately leads to decreased biomass yield in mustard seedlings. Higher concentration of NaCl (200 mM) decreased the plant height by 33.7%, root length by 29.7% and plant dry weight (DW) by 34.5%. On the other hand, supplementation of TH to NaCl treated mustard seedlings showed elevation by 13.8, 11.8, and 16.7% in shoot, root length and plant DW respectively as compared to plants treated with NaCl (200 mM) alone. Oil content was drastically affected by NaCl treatment; however, TH added plants showed enhanced oil percentage from 19.4 to 23.4% in the present study. NaCl also degenerate the pigment content and the maximum drop of 52.0% was recorded in Chl. ‘a’. Enhanced pigment content was observed by the application of TH to NaCl treated plants. Proline content showed increase by NaCl stress and maximum accumulation of 59.12% was recorded at 200 mM NaCl. Further enhancement to 70.37% in proline content was recorded by supplementation of TH. NaCl stress (200 mM) affirms the increase in H2O2 by 69.5% and MDA by 36.5%, but reduction in the accumulation is recorded by addition of TH to mustard seedlings. 200 mM NaCl elevated SOD, POD, APX, GR, GST, GPX, GSH, and GSSG in the present study. Further enhancement was observed by the application of TH to the NaCl fed seedlings. NaCl stress suppresses the uptake of important elements in both roots and shoots, however, addition of TH restored the elemental uptake in the present study. Mustard seedlings treated with NaCl and TH showed restricted Na uptake as compared to seedlings treated with NaCl alone. In conclusion, TH proved to be very beneficial in imparting resistance to the mustard plants against NaCl stress through improved uptake of essential elements, modulation of osmolytes and antioxidants.
The farming land is declining gradually and the main reasons are, intensive use of agricultural practices, urbanization, biotic and abiotic stress etc. Among abiotic stresses the salinity problem is increasing at an alarming rate throughout the world. Salinity is responsible for the loss of crop production worth billions of dollars every year. It has been reported that about 7% of the total land on earth and 20% of the total arable area are affected by high salt content (Munns and Tester, 2008; Cabot et al., 2014). Salinity stress induces osmotic and ionic stress that leads to retarded growth in terms of both shoot and root length, fresh and dry weight (DW), reduced pigment content and hampers uptake of mineral elements (Ahmad et al., 2012, 2014). Sodium accumulation disturbs all physiological and biochemical processes including photosynthesis, respiration, membrane functions etc. The chlorophyll content dwindles with the increase in NaCl stress in chickpea (Rasool et al., 2013) and faba bean (Hashem et al., 2014). Accumulation of Na+ in the soil decreases the porosity, soil aeration and water conductance (Porcel et al., 2012). Mineral uptake by the plants is drastically hampered by the NaCl stress (Porcel et al., 2012), which directly affect growth biomass and yield of the plant. A prolonged salinity stress is responsible for secondary stress, i.e.; oxidative stress that generates reactive oxygen species (ROS) deleterious to biomolecules like, proteins, nucleic acids (DNA/RNA), membrane lipids etc. (Ahmad et al., 2010a,b; Ahmad, 2013). Plant cells generate ROS even under normal conditions but they are balanced by the scavenging system of the cell. When generation of ROS exceeds its quenching capacity, oxidative stress appears. Polyunsaturated fatty acids (PUFA) are more vulnerable to ROS attack and this leads to lipid peroxidation (Sánchez-Rodríguez et al., 2010). However, plants have protective mechanisms like enzymatic and non-enzymatic antioxidants against these ROSs. The enzymatic antioxidants are superoxide dismutase (SOD), ascorbate peroxidase (APX), catalase (CAT), glutathione reductase (GR) and non-enzymatic are ascorbic acid (ASA), glutathione (GSH) (Mittler, 2002; Ahmad and Sharma, 2008, 2010).
Besides the classic mycorrhizal fungi, rhizobia, and plant-growth-promoting rhizobacteria, endophytic fungi are reported to improve plant growth during stress (Egamberdieva et al., 2011, 2013; Berg et al., 2013; Hameed et al., 2014). Trichoderma sp. are endophytic plant symbionts widely used as biofertilizers for plant growth stimulation and as biocontrol agents for plant diseases (Brotman et al., 2010; Harman, 2011). Trichoderma strains are able to enhance plant tolerance to biotic and abiotic stresses such as drought and salinity (Mastouri et al., 2010; Shoresh et al., 2010), through enhanced root growth, nutritional uptake and by inducing protection against oxidative damage. Mastouri et al. (2012) reported that enhanced resistance of colonized water deficit plants by Trichoderma harzianum (TH) T22 is explained partly due to higher capacity to scavenge ROS and recycle oxidized ascorbate and glutathione, a mechanism that is expected to enhance tolerance to abiotic stresses. However, specific knowledge of mechanisms used by TH controlling multiple plant stress factors is still lacking and needs to be studied.
Brassica juncea L. (Czern and Coss) is commonly known as Indian mustard belongs to Brassicaceae family and is a multipurpose plant. The main constituent of the plant is mustard oil, which is well known in India and other countries for its edible property and medicinal importance as well. The residues of the plant can be used as biofuels, cattle feed and fertilizer for the soil (Jham et al., 2009). The mustard plant often experiences abiotic stress especially NaCl stress in arid and semi-arid regions of the world. India, inspite of being largest producer of edible oil faces shortage to meet even the daily requirements of its people. NaCl imposes hyperionic and hyperosmotic stress that interfers with the growth, biomass yield, and physio-biochemical attributes of mustard seedlings. Shrinking of cultivable land and exponential increase of human race are the two major concerns before the plant biologists. They need to look forward to make strategies to increase the crop production with the available land. One such sustainable strategy is the use of beneficial microbes in agriculture. Trichoderma species are used extensively to alleviate abiotic stress in variety of crop plants because of its high success rates. It has been observed that different hosts under stress conditions respond to beneficial micobes in a different manner. B. juncea, chosen as a model plant system for this study, is a major oil-yielding crop in India. Notably, B. juncea is susceptible to NaCl stress, which damages the crop production, hence oil yield. Use of beneficial microbes can be one of the sustainable strategies for improving B. juncea health under NaCl-salinity stress. Therefore, the present study was conducted to evaluate the effect of NaCl on growth, oil content, pigments and osmolytes and the mitigating role of TH in mustard seedlings. Production of ROS (H2O2) and during NaCl stress disrupts the membrane stability (lipid peroxidation) in mustard plants and positive role played by TH is too investigated. Protective nature of enzymatic and non-enzymatic antioxidants are also studied in mustard plants in presence and absence of NaCl and TH.
Material and Methods
Trichoderma harzianum (T22) was obtained from culture collection of already infected maize plants and used for this study. This strain showed plant growth promotion of wheat seedlings and also alleviation of the adverse effects of salinity stress in wheat (Rawat et al., 2011). For preparation of fungal inocula, 3-5 disks of fresh cultured fungus grown on Potato Dextrose Agar (PDA) plates were inoculated in 100 ml of potato dextrose broth medium (PDB, DIFCO) in flasks and kept on a shaker for 5 days at 28°C. The mycelium obtained after incubation were lyophilized under vacuum. This lyophilized powder containing mycelium was mixed with talc powder and carboxy methyl cellulose (1.0%) and the final concentration of the carrier material per gram was 2 × 109 cfu. TH was given to the pots at the rate of 10 g kg-1 soil before sowing. Pots without TH were treated as control.
Brassica juncea L. (Czern and Coss) cv. Varuna, seeds were surface sterilized with sodium hypochlorite (0.5%, v/v) for 3 min, washed thoroughly with distilled water then germinated in a sterile Petri dish with 1% water agar in the dark at 28°C for 3 days. The sterility of seeds was tested on Nutrient agar and PDA by incubating plates for 3 days at 28°C.
The soil used for the experiment has the following properties (%): sand (84.3); clay (8.2); silt (7.5); organic carbon, 0.17; total nitrogen, 0.007; (EC) = 7.12 dS/m; and pH 7.8. The soil was autoclaved for 40 min at 121°C (at 15 psi pressure), cooled down and then divided among plastic pots (300 g). After that equally germinated seeds were selected for sowing.
The seedlings were allowed to grow for an additional 3 weeks at average day/night temperatures of 28°C/15°C. After this different concentrations of NaCl (0, 100, 200 mM) were applied to the pots through Hoagland solution. TH is also applied to the soil in pots. Pots with out NaCl and TH served as control.
To maintain the moisture content of the pot, 100 ml of Hoagland nutrient solution along with dissolved NaCl was applied every alternate day to each pot except control, which received only nutrient solution. The experiment was laid out in a completely randomized design with five replicates. The plant leaves were collected for analysis after 45 days after treatment (DAT). The chemicals were procured from Sigma–Aldrich, Merck, and SRL. All chemicals were obtained in highest purity and were available commercially.
The shoot and root length was measured manually by scale (100 cm), whereas DW was determined by drying the plant samples at 65°C for 72 h and then weighed.
Estimation of Oil Content
Solvent extraction method was employed for the estimation of oil content in mustard seedlings. Seeds (3 g) were ground in Na2SO4, the powder was kept in test tubes and hexane (20 ml) was added as mobile phase. The elution, which contains oil, was kept in a vile and was placed in hot water bath to evaporate the hexane. The oil in the vile was weighed and was calculated by the following formula:
Oil percentage = oil content/seed weight × 100.
Estimation of Pigments
Chlorophyll content of the leaves was determined by the method proposed by Arnon (1949). The absorbance was read at 663, 645, and 480 nm against 80% acetone used as a blank.
Estimation of Proline Content
For the estimation of proline, the procedure of Bates et al. (1973) was followed. Optical density (OD) was measured at 520 nm by spectrophotometer (Beckman 640 D, USA). The toluene was used as a blank.
Estimation of Hydrogen Peroxide and Lipid Peroxidation
The method of Velikova et al. (2000) was applied for the estimation of hydrogen peroxide. The optical density was measured at 390 nm by spectrophotometer (Beckman 640 D, USA).
Heath and Packer (1968) method was used for the determination of lipid peroxidation (amount of malondialdehyde produced) by thiobarbituric acid reaction. The OD was recorded at 600 nm and the blank used was 1% thiobarbituric acid (TBA) in 20% trichloroacetic acid (TCA). Extinction coefficient of 155 mM cm-l was used for the calculation of malondialdehyde (MDA) concentration.
Extraction of the Enzymes
Leaf sample (10 g) were homogenized in 50 volumes of 100 mM Tris-HCl (pH 7.5) containing 5 mM DTT (Dithiothreitol), 10 mM MgCl2, 1 mM EDTA (Ethylenediaminetetraacetic acid), 5 mM magnesium acetate, 1.5% PVP-40 (Polyvinylpyrrolidone), 1 mM PMSF (phenylmethanesulfonyl fluoride) and 1 μg ml-1 aproptinin. After the filtration, the samples were centrifuged at 12,000 rpm for 10 min. The supernatant harvested was used as enzyme source. For the analysis of APX activity, tissues were separately homogenized with 2 mM AsA.
Superoxide dismutase. Estimation of SOD (EC 184.108.40.206) activity was executed following the photoreduction of nitrobluetetrazolium (NBT) (van Rossum et al., 1997). The OD was taken at 560 nm by spectrophotometer (Beckman 640 D, USA). SOD activity is inversely proportional to the NBT reduction. SOD unit is the amount of protein that restricts 50% photoreduction of NBT. SOD activity was expressed as enzyme unit (EU) mg-1 protein.
Peroxidase. Kar and Mishra (1976) method was followed for the estimation of peroxidase (POD) activity. The OD was taken at 420 nm by spectrophotometer (Beckman 640 D, USA). POD activity was expressed as change in EU mg-1 protein.
Ascorbate peroxidase. Ascorbate peroxidase activity was determined by following the method of Nakano and Asada (1981). The absorbance was read at 290 nm by spectrophotometer (Beckman 640 D, USA). EU mg-1 protein expresses the APX activity.
Monodehydroascorbate reductase (MDHAR). The method of Miyake and Asada (1992) was employed for the estimation of Monodehydroascorbate reductase (MDHAR, EC 220.127.116.11). MDAR activity was expressed as μmol NADPH oxidized/ (EU mg-1 protein).
Dehydroascorbate reductase (DHAR). Dehydroascorbate reductase (EC: 18.104.22.168) activity was determined by the procedure of Nakano and Asada (1981). The absorbance was read at 265 nm for 1 min by spectrophotometer (Beckman 640 D, USA) using extinction coefficient of 14 mM-1 cm-1.
Glutathione reductase. For the determination of GR activity (EC 22.214.171.124), the method of Carlberg and Mannervik (1985) was followed. The absorbance showed decrease and was read for 2 min at 340 nm by spectrophotometer (Beckman 640 D, USA). The GR activity was calculated using the extinction co-efficient of NADPH of 6.2 mM-1 cm-1 and expressed as EU mg-1 protein.
Glutathione S-sransferase (GST) and gaucol peroxidase (GPX) activity. Activity of GST (EC: 126.96.36.199) was estimated according to the procedure of Hasanuzzaman and Fujita (2013). The rise in absorbance was read at 340 nm for 1 min by spectrophotometer (Beckman 640 D, USA). The GST activity was considered using the extinction coefficient of 9.6 mM-1 cm-1.
The method of Elia et al. (2003) was used to determine the GPX (EC: 188.8.131.52) activity. The absorbance was measured at 340 nm for 1 min by spectrophotometer (Beckman 640 D, USA). Extinction coefficient of 6.62 mM-1 cm-1 was used for the calculation of GPX activity.
Catalase. Catalase (EC 184.108.40.206) activity was determined by following the method of Luck (1974). The activity of CAT was calculated using the extinction co-efficient of 36 × 103 mM-1 cm-1 and expressed as EU mg-1 protein.
Extraction and measurement of ascorbate and glutathione
The method of Huang et al. (2005) was employed for the determination of ascorbate content. Fresh leaves (0.8 g) were crushed in 3 ml ice-cold acidic extraction buffer (5% meta-phosphoric acid containing 1 mM EDTA). The crushed material was subjected to centrifugation at 10,000 rpm for 20 min and the supernatant harvested were analyzed for ascorbate content.
The glutathione pool was assayed by the method of Yu et al. (2003) with some modifications described by Paradiso et al. (2008). Standard curves with known concentrations of GSH and GSSG were used. The content of GSH was calculated by subtracting GSSG from total GSH.
Estimation of inorganic nutrients. Dried shoot and root materials (100 mg) were powdered and digested in H2SO4/HNO3 mixture (1/5, v/v) for 24 h, then treated with HNO3/HClO4 mixture (5/1, v/v). Atomic absorption spectrophotometer (Analyst 300, PerkinElmer, Germany) was used for the measurement of elemental concentrations in the samples.
The statistical analysis (SPSS) was performed by one-way analysis of variance (ANOVA) followed by Duncan’s Multiple Range Test (DMRT). Each value is the mean ± SE for 5 replicates in each group. P ≤ 0.05 were considered as significant.
Trichoderma Promotes Growth and Biomass Yield in NaCl Stressed Mustard Seedlings
The results related to the effect of NaCl stress in presence and absence of TH on growth and biomass yield in B. juncea is presented in Table 1. NaCl stress declined the growth in terms of length of shoot and root. The highest reduction in plant height was found to be 33.79% at 200 mM NaCl stress. Application of TH restored the plant height and increase of 14.88 and 13.81% was observed at 100 mM + TH and 200 mM + TH treatments respectively over NaCl treated plants.
TABLE 1. Effect on plant height (cm), root length (cm) and dry weight (g plant-1) under NaCl stress in presence and absence of Trichoderma harzianum (TH) in Brassica juncea seedlings.
Root length decreases by 27.56% at 100 mM and 48.74% at 200 mM NaCl treatments. However, co-application of TH mitigated the adverse effects of NaCl on root length. Length of root increases by 23.70 and 20.18% at 100 mM + TH and 200 mM+TH concentrations respectively as compared to plants treated with NaCl alone (Table 1).
Plant DW was severely affected by NaCl stress in present study. The maximum reduction of 34.50% was observed at 200 mM NaCl concentration relative to control. However, when TH was co-applied with NaCl, the DW increases by 18.18% and 16.76% at 100 mM + TH and 200 mM + TH concentrations respectively compared to plants treated with NaCl alone. The data clearly indicates that application of TH helped the mustard seedlings in restoring growth and biomass yield under NaCl stress.
Trichoderma Improved the Oil Production in Mustard Plants Under NaCl Stress
The results pertaining to the effect of NaCl and TH on oil content percentage is presented in Figure 1. NaCl treatment reduced the oil content by 25.77 and 19.35% at 100 and 200 mM NaCl treatments respectively relative to control. However, supplementation of TH improves the oil content by 30.12% at 100 mM + TH and 23.44% at 200 mM + TH treatment over the control. Increase in oil content percentage by TH proved its defensive nature to mustard seedlings against NaCl stress.
FIGURE 1. Effect on oil content (%) under NaCl stress in presence and absence of Trichoderma harzianum (TH) in Brassica juncea seedlings. Different letters indicate significant difference between means at p < 0.05 (DMRT). Values are means ± SE (n = 5).
Restoration of Pigment Content by Trichoderma in Mustard Seedlings Under NaCl Stress
The results related to the effect of NaCl and Trichoderma on pigment content is depicted in Table 2. NaCl stress decreases the pigment content and the maximum decrease of 52.00, 25.26, 42.59, and 28.57% in chl ‘a’ chl ‘b’, total chl and carotenoids respectively was observed at 200 mM NaCl concentration over the control. However application of TH to NaCl treated seedlings restored the pigment content. An increase by 15.15% in chl ‘a’, 12.34% in chl ‘b’, 13.88% in total chl and 14.63% in carotenoids was recorded at 200 mM + TH treatment as compared to 200 NaCl treatments alone. The restoration of pigments dipicts the positive role of TH in mustard seedlings under NaCl stress.
TABLE 2. Effect on chl a, b, total chlorophyll (mg g-1 FW), carotenoid (mg g-1 fw) and proline (μg g-1 fw under NaCl stress in presence and absence of TH in B. juncea seedlings.
Effect of Trichoderma on Proline Content in Mustard Seedlings Under NaCl Stress
As for proline (Table 2), it increases by 42.26% and 59.12% at 100 and 200 mM NaCl treatments respectively in comparision to control. Addition of TH further increases the proline content by 56.25% at 100 mM + TH and 70.37% at 200 mM + TH treatments over the control. Increased accumulation of proline by TH application proves its protective nature against NaCl stressed mustard seedlings.
Trichoderma Reduces Hydrogen Peroxide and Lipid Peroxidation in Mustard Seedlings Under NaCl
The results pertaining to the effect of NaCl and TH on hydrogen peroxide (H2O2) and MDA is depicted in Figures 2A,B. NaCl induces H2O2 by 59.67% at 100 mM and 69.57% at 200 mM NaCl concentration over the control. However, plants treated with TH in combination with NaCl showed less accumulation of 20.59% at 100 mM + TH and 44.50% at 200 mM + TH in H2O2 as compared with that of control.
FIGURE 2. Effect on (A) hydrogen peroxide (H2O2) and (B) malondialdehyde content (MDA) under NaCl stress in presence and absence of TH in B. juncea seedlings. Different letters indicate significant difference between means at p < 0.05. Values are means ± SE (n = 5).
Malondialdehyde, showed maximum rise of 36.56% at 200 mM and minimum of 20.12% at 100 mM NaCl concentration verses control. Decline in MDA content was observed in plants treated with TH. A decrease of 14.56 and 23.63% was observed at 100 mM + TH and 200 mM + TH respectively in MDA content as compared to 100 and 200 mM NaCl concentration (Figure 2B). From the above results it is concluded that TH plays a protective role as it mitigates the effect of H2O2 on lipid peroxidation.
Superoxide dismutase and peroxidase
Superoxide dismutase increases with the increasing concentration of NaCl and the results are depicted in Figure 3A. SOD activity increased by 20.14 and 31.17% at 100 and 200 mM NaCl concentrations respectively as compared to control. Application of TH further elevated the SOD activity by 27.82% at 100 mM + TH and 44.61% at 200 mM + TH treatments over the control.
FIGURE 3. Effect on (A) superoxide dismutase (SOD) and (B) peroxidase activity (POD) under NaCl stress in presence and absence of TH in B. juncea seedlings. Different letters indicate significant difference between means at p < 0.05. Values are means ± SE (n = 5).
Regarding POD activity, minimum hike of 23.44% and maximum of 43.15% was recorded at 100 and 200 mM NaCl concentration respectively over the control plants. However, supplementation of TH to NaCl treated plants further enhanced the POD activity by 33.56% at 100 mM + TH and 46.27% at 200 mM + TH as compared to control (Figure 3B). Increasing activity of SOD and POD by the application of TH specify the defensive nature of TH on mustard seedlings under NaCl stress.
Ascorbate peroxidase, monodehydroascorbate reductase, dehydroascorbate reductase, glutathione reductase
The results related to the effect of NaCl and TH on APX activity in mustard seedlings is presented in Figure 4A. NaCl concentration increased the APX activity by 13.00% at 100 mM and 26.25% at 200 mM NaCl concentrations relative to control. Co-inoculation of TH to NaCl treated plants showed further increase of 25.53 and 38.59% in APX activity at 100 mM + TH and 200 mM + TH treatments respectively as compared to control.
FIGURE 4. Effect on (A) ascorbate peroxidase (APX), (B) monodehydroascorbate reductase (MDHAR), (C) dehydroascorbate reductase (DHAR), and (D) glutathione reductase (GR) under NaCl stress in presence and absence of TH in B. juncea seedlings. Different letters indicate significant difference between means at p < 0.05. Values are means ± SE (n = 5).
NaCl decreases the activity of MDHAR by 27.42 and 42.60% at 100 and 200 mM NaCl concentratiosn respectively in comparison to control plants. However, addition of TH to NaCl treated plants increased the activity of MDHAR by 34.15% at 100 mM + TH as compared to 100 mM NaCl treatment. 200 mM + TH treatment also showed increase of 39.08% in MDHAR as compared to NaCl stress alone (Figure 4B).
As for DHAR (Figure 4C), NaCl stress decreased DHAR maximum by 46.51% at 200 mM NaCl concentration over the control. However, supplementation of TH to NaCl stressed plants increases the DHAR activity by 36.88% at 100 mM + TH and 58.24% at 200 mM + TH as compared to NaCl treated plants alone.
Glutathione reductase activity showed minimum rise of 15.55% and maximum of 29.78% at 100 and 200 mM NaCl respectively relative to control (Figure 4D). NaCl treated plants, inoculated with TH showed further increase in GR activity by 29.11% at 100 mM + TH and 46.94% at 200 mM + TH treatments over the control. TH maintains the activity of above antioxidant enzymes, which suggests its role in NaCl stress tolerance in mustard seedlings.
Glutathione S-transferase, guaiacol peroxidase, catalase
The results related to the effect of NaCl and TH on GST is depicted in Figure 5A. GST increases with increased concentration of NaCl and the maximum elevation by 47.07% was recorded at 200 mM NaCl treatment. Minimum hike of 20.08% in GST was observed at 100 mM NaCl treatment. However, supplementation of TH to salt stressed plants further increased the GST activity by 35.80 and 55.44% at 100 mM + TH and 200 mM + TH treatments respectively as compared with control plants.
FIGURE 5. Effect on (A) glutathione S-transferase (GST), (B) gaucol peroxidase (GPX), and (C) catalase (CAT) activity under NaCl stress in presence and absence of TH in B. juncea seedlings. Different letters indicate significant difference between means at p < 0.05 (DMRT). Values are means ± SE (n = 5).
Regarding the GPX activity (Figure 5B), NaCl stress elevated the GPX activity by 21.05 and 31.81% at 100 and 200 mM NaCl stress respectively in comparision to control. Further enhancement of 37.50% at 100 mM + TH and 50.00% at 200 mM + TH treatments was observed when salt stressed plants were supplemented with TH.
Salt stress reduced the CAT activity by 16.66% at 100 mM and 32.66% at 200 mM concentrations as compared to control (Figure 5C). Addition of TH to salt stressed plants showed increase of 10.71 and 25.18% at 100 mM + TH and 200 mM + TH respectively in CAT activity as compared to NaCl treatments alone. The above results also recommend that TH conserve the activity of above antioxidants that showed their protective responsibility against NaCl stressed mustard seedlings.
Ascorbic acid, reduced glutathione, oxidized glutathione
The results related to the effect of NaCl and TH on AsA is presented in Figure 6A. AsA declines by 33.33 and 47.91% at 100 and 200 mM treatments respectively as compared with control. However, supplementation of TH to NaCl treated plants showed accumulation of 27.27% in AsA at 100 mM + TH as compared to 100 mM NaCl treatment. 200 mM + TH treatment also showed increase of 26.47% in AsA as compared to 200 mM NaCl concentration.
FIGURE 6. Effect on (A) Ascorbic acid (nmol g-1 FW), (B) GSH (Reduced glutathione) (nmol g-1 FW), (C) GSSG (Oxidized glutathione) (nmol g-1 FW) and (D) GSH/GSSG ratio under NaCl stress in presence and absence of TH in B. juncea seedlings. Different letters indicate significant difference between means at p < 0.05 (DMRT). Values are means ± SE (n = 5).
In the present study, GSH build up with increasing concentration of NaCl. The maximum enhancement of 42.26% was observed at 200 mM NaCl concentrations with respect to control (Figure 6B). Further improvement in GSH was observed in salt stressed plants supplemented with TH. An increase of 25.00 and 22.40% in GSH at 100 mM + TH and 200 mM + TH treatments respectively was observed as compared to NaCl stress alone.
Regarding GSSG (Figure 6C), NaCl stress increased the level of GSSG by 40.32% at 100 mM and 64.50% at 200 mM NaCl treatments over the control. Further accumulation was also observed; when salt treated plants were supplemented with TH. An elevation of 51.36 and 69.67% at 100 mM + TH and 200 mM + TH respectively in GSSG were observed in the present study as compared to control.
NaCl stress decreases the GSH/GSSG ratio by 12.16 and 38.64% at 100 and 200 mM NaCl concentrations respectively in comparision to control (Figure 6D). However, TH treatment to NaCl stressed plants showed improvement in GSH/GSSG ratio by 8.19% at 100 mM + TH and 9.20% at 200 mM + TH as compared to 100 and 200 mM NaCl treatments. The above data suggests that TH application preserve the non-enzymatic antioxidants, which provides tolerance to mustard seedlings under NaCl stress.
Improved Uptake of Essential Elements by Trichoderma in NaCl Stressed Mustard Seedlings
NaCl treatments hamper the uptake of S, Mn, Mg, Ca, and K in both shoots and roots (Table 3). Maximum decrease by 25.94, 55.14, 29.86, 33.60, and 49.58% in S, Mn, Mg, Ca, and K respectively in shoots was observed at 200 mM NaCl concentration as compared to control. Roots also showed reduction by 45.56% in S, 24.42% in Mn, 21.52% in Mg, 21.89% in Ca and 28.64% in K at 200 mM NaCl treatments over the control. However, application of TH restores the uptake of above elements to appreciable level in both roots and shoots. Enhanced uptake of nutrients by TH in mustard seedlings signifies its role in tolerance against NaCl stress.
TABLE 3. Effect on uptake of minerals (μmol g-1 dry wt.) under NaCl stress in presence and absence of TH in B. juncea seedlings.
Table 4 showed elevation in Na accumulation in both shoots and roots as the NaCl concentration goes up, but supplementation of TH decreased the aggregation of Na by 45.24 and 53.67% in shoots and roots respectively at 200 mM + TH treatments in comparision to NaCl treated seedlings alone. Restricted uptake of Na by TH signifies its protective nature against NaCl stress in mustard seedlings.
TABLE 4. Effect on Na uptake under NaCl stress in presence and absence of TH in shoots and roots of B. juncea seedlings.
Trichoderma has an important role in metabolic processes of host plants that could impart tolerance against NaCl stress. Trichoderma sp have the capacity to induce systemic resistance, increase nitrogen use efficiency (Harman et al., 2004; Shoresh et al., 2010), increases water holding capacity (Berg et al., 2013; Hameed et al., 2014), induces osmolytes to protect the plants from osmotic stress, help in uptake of essential minerals, enhances photosynthetic efficiency (Hashem et al., 2014) etc.
NaCl affects the plant growth and biomass yield and is reported by different workers (Azooz et al., 2011; Rasool et al., 2013; Ahmad et al., 2014). The present study also reported reduction in shoot height, root length, plant DW and oil content under NaCl stress. Application of TH in combination with NaCl mitigated the negative effect of NaCl and the results corroborates with the findings of Mastouri et al. (2012) in tomato. Contreras-Cornejo et al. (2009) also reported enhanced biomass production on supplementation of Trichoderma to Arabidopsis. Availability of Trichoderma to the rice roots significantly enhanced root length and biomass yield and may be attributed to several growth promoting mechanisms like (i) mineral availability, (ii) availability of phytohormones, (iii) release of elicitors etc. (Doni et al., 2014). Plant growth hormones like cytokinins-like molecules, e.g. zeatin and gibberellin GA3 or GA3 related are produced in Trichoderma inoculated plants and have the ability to enhance the growth and development of the plants even under salt stress (Iqbal and Ashraf, 2013; Rawat et al., 2013; Zhang et al., 2013).
Negative effect of NaCl stress is also correlated with the decrease in oil yield in the present study and the results are in accordance with the findings of Ashraf and Akhtar (2004) in Foeniculum vulgare Mill. Increasing concentrations of NaCl resulted in decline in essential oil content in different plants (Tabatabaie and Nazari, 2007; Aziz et al., 2008). Decrease in oil content due to NaCl stress may be due to the limited supply of cytokinin from root to shoot which resulted in variations in cytokinin: abscisic acid (ABA) ratio in leaf (El-keltawi and Croteau, 1987). Application of TH resored the oil content of mustard seedlings under NaCl stress in the present study. Beneficial microbes have been reported to decrease the accumulated ABA during NaCl stress and make the transportation of cytokinins from root to shoot easy (Aroca et al., 2013; Hashem et al., 2015).
According to the published literature, NaCl stress inhibits the photosynthetic pigments in majority of plant species. Indeed the data showed in Table 2 indicated that Chl and carotenoid syntheses were negatively affected by NaCl stress. Decrease in Chl content might be due to (i) the inhibition of synthesis of important enzymes, such as δ-aminolevulinic acid dehydratase and protochlorophyllide reductase, which are involved in Chl biosynthesis and (ii) impairment in the supply of Mg2+, Fe2+, Zn2+, and Mn2+ that are required for the synthesis of Chl (Padmaja et al., 1990; Van Assche and Clijsters, 1990; Küpper et al., 1996). Carotenoids possess an antioxidant property and provides photo protection to chlorophylls by scavenging ROS (Behera et al., 2002). Thus decrease in carotenoid content by NaCl stress results in overproduction of ROS that subsequently hampers plant growth by inducing oxidative damage to DNA, RNA, and proteins (Mishra et al., 2006; Ahmad et al., 2010a,b). Application of TH has restored the chlorophyll and carotenoid content to appreciable level in the present study and the results corroborates with the findings of Rawat et al. (2011) and Zhang et al. (2013). TH increases the uptake of essential elements especially Mg2+ that was negatively affected by NaCl stress, hence the chlorophyll synthesis increases in TH inoculated plants. Another reason for increased pigment content in plants may be the production of phytohormones that contributes for the stimulation of chlorophyll content (Martínez-Medina et al., 2014; Resende et al., 2014). The increase in photosynthetic pigments by TH colonization in plants may also be due to inhibition of Na uptake (Iqbal and Ashraf, 2013).
Proline an important osmolyte maintains the cell osmoregulation under NaCl stress (Ahmad et al., 2010b; Rasool et al., 2013). Our data also reflects the increase in proline content in mustard plants under NaCl stress (Table 2). TH inoculated mustard plants showed further accumulation of proline in the present study. Evelin et al. (2009) reported that AM fungi colonized plants showed maximum accumulation of solutes that provides protection to the cell from NaCl stress. Salt treated Arabidopsis seedlings inoculated with Trichoderma sp. showed more accumulation of proline as compared to control seedlings (Contreras-Cornejo et al., 2014). Proline is reported to have antioxidant property that could scavenge the ROS and protects the cell from oxidative damage (Ahmad et al., 2010b; Jogaiah et al., 2013). Proline has also a leading role in energy storage (i.e., C and N) under NaCl stress (Aggarwal et al., 2012). Higher accumulation of proline increases the N fixation in plants (Hashem et al., 2015).
Salt stress is responsible for the generation of ROS like hydrogen peroxide in the cell (Azevedo Neto et al., 2005; Ahmad et al., 2010a,b). The increase in H2O2 in present study corroborates with the findings of Ashraf et al. (2010) in wheat. Giannakoula and Ilias (2013) also showed increased level in H2O2 in tomato on exposure to NaCl. H2O2 is the only ROS that can diffuse through aquaporins in the membranes and over larger distances within the cell (Bienert et al., 2007). However, plants treated with TH showed less accumulation of H2O2 in the present study that may be attributed to confer bioprotection against NaCl stress. Hajiboland et al. (2010) also reported that colonized tomato plants with AMF showed less accumulation of H2O2 so lower oxidative damage as compared to non-mycorrhizal plants. Citrus plants inoculated with Glomus versiforme or G. mosseae under salt stress showed lower levels of H2O2 concentration as compared to non-inoculated plants (Wu et al., 2010). Rawat et al. (2013) also observed the minimum level of H2O2 in TH treated chickpea plants, whereas significantly higher level of H2O2 was maintained in control plants under both saline and non-saline soil conditions. At cellular level these plants are better equipped with efficient free radical quenching system that offers protection against oxidative stress.
Lipid peroxidation is estimated through the accumulation of MDA and has been used as a promising criterion for determining the sensitivity of plants to saline stress (Ashraf et al., 2010; Ahmad et al., 2014). Increase in MDA content under salt stress is also reported in tomato (Li, 2009), mulberry (Ahmad et al., 2014), Okra (Saleem et al., 2011). In present study a decrease in MDA content was observed in plants treated with TH. Similar results observed for chickpea showed significantly higher accumulation of MDA in non-inoculated than inoculated Trichoderma plants (Rawat et al., 2013). Plants treated with AMF showed less accumulation of MDA content (Wu et al., 2010). AMF inoculated plants increase the antioxidant enzymes that scavenge these free radicals and minimizes the attack on lipid membranes, hence decreases lipid peroxidation. It has already been reported that Trichoderma induces phytohormones like salicylic acid (SA) and jasmonic acid (JA; Martínez-Medina et al., 2011). The intrinsic SA may reduce H2O2 content due to its role as an antioxidant in counteracting the generation of H2O2 to some extent under NaCl stress. Lipid peroxidation decreases due to accumulation of antioxidants that could scavenge the ROS and peroxidation of membranes is minimized. Trichoderma induced the expression of many antioxidant enzymes that directly or indirectly scavenges the ROS and minimizes the effect on plasma membrane. Trichoderma also induces the expression of stress related proteins like glutathione S-transferase (GST), glutathione dependent formaldehyde dehydrogenase, and POD, which could lower down the MDA content (Hashem et al., 2014).
Superoxide dismutase increases with increasing concentration of NaCl is also reported by various workers in chickpea (Rasool et al., 2013), in tomato (Abdel Latef and Chaoxing, 2011), in broad bean (Azooz et al., 2011) and in Morus alba (Ahmad et al., 2014).
NaCl induces the activity of peroxidase to protect the plants from damage. Peroxidase helps in conversion of H2O2 to water and oxygen. In present study TH treated plants showed significant increase in POD, as compared to non-inoculated plants. Gusain et al. (2014) showed that Trichoderma increased the SOD, and POD in rice cultivars provides tolerance to these plants under water stress. Inoculated plants with AMF showed higher activity of SOD than non-inoculated plants (Borde et al., 2012).
Ascorbate is vital antioxidant in ascorbate-glutathione cycle. Trichoderma treated plants have been observed to accumulate more ascorbate in its reduced form. The enzymatic unit associated with the regeneration of reduced ascorbate is MDHAR. MDHAR was shown to be crucial for the mutualistic interaction between Arabidopsis and Piriformospora indica (Vadassery et al., 2009). Interestingly, the gene responsible for expression of MDHAR is extreemly expressed in cucumber and Arabidopsis upon inoculation with Trichoderma. Pre-treatment with Trichoderma in Arabidopsis under salt stress showed induced expression of different transcripts having vital role in osmoregulation and oxidative stress management (Brotman et al., 2013). The procedure reveals that T. asperelloides can induce plant tolerance to salt stress (Brotman et al., 2013). Mastouri et al. (2012) also reported that pre- treatment of tomato seedlings with TH T22 enhances drought stress through the upregulation of antioxidant machinery. Trichoderma strains (T. asperelloides and T. harzianum) activated antioxidant machinery to recycle the oxidized ascorbate has been reported in different plants (Arabidopsis, cucumber, and tomato), so as to improve the tolerance mechanism to a wide array of abiotic stresses (Mastouri et al., 2012; Brotman et al., 2013).
Trichoderma induces changes in host plants and these changes are directly linked to stress related genes and proteins (Brotman et al., 2013). Inoculation of cucumber seedlings with Trichoderma showed induced expression of MDAR, APX1, and GST genes and impart induction of antioxidant machinery against NaCl induced oxidative stress. MDAR gene expression level was increased to 15 fold in the above study. Up-regulation of sod(Mn) and sod(cu) genes by Trichoderma have also been reported in cucumber under NaCl stress (Brotman et al., 2013).
Trichoderma harzianum increased the GR and GST activities under salt stress condition as compared to control. GR is a flavo-protein oxidoreductase, present in both prokaryotes as well as in eukaryotes (Romero-Puertas et al., 2006). It is a potential enzyme of the Ascorbate–Glutathione system. GR catalyzes the reduction of glutathione, which is associated with regulation of many plant metabolic and antioxidative processes. The main role of GR is to catalyze the NADPH dependent reaction of disulphide bond of GSSG and thus maintains the reduced pool of glutathione (Ansel et al., 2006).
Glutathione S-transferase can eliminate membrane lipid peroxides, products of oxidative DNA degredation etc. (Berhane et al., 1994). Roxas et al. (2000) demonstrated that transgenic tobacco seedlings overexpressing the GST gene showed enhanced growth under different stresses. Yu et al. (2003) also reported that overexpression of GST in transgenic rice plants showed enhanced tolerance to Cd stress.
Trichoderma harzianum treatment to NaCl stressed plants showed increase in GSH/GSSG ratio as compared to control plants. GSTs minimizes peroxides by involving GSH and provide the scavengers for cytotoxic and genotoxic compounds. GPXs use glutathione to reduce H2O2 and organic and lipid hydroperoxides, and thus helps to shield the cells from oxidative damage (Noctor et al., 2002). The decrease in the oxidative damage may be due to the high induction of stress-associated proteins like GST, glutathione dependent formaldehyde dehydrogenase (FALDH) and peroxidase. Harman et al. (2004) observed the similar results in maize by inoculating Trichoderma isolate T-22. During ROS production under environmental stress these detoxifying proteins induced by Trichoderma inoculation acts as quenching agents and protects the cell from oxidative damage (Rawat et al., 2011).
Catalase is an important antioxidant enzyme that directly dismutates hydrogen peroxide and is essential for detoxification of ROS under stress (Van Breusegem et al., 2001). In comparision to CAT and POD, APX has more affinity for H2O2, thus it may play a vital role in management or detoxification of ROS under stress.
Glutathione has been reported to react with range of ROS (Noctor et al., 2002) and is involved in reduction of H2O2 to water in ascorbate-GSH cycle (Noctor and Foyer, 1998). Herouart et al. (1993) also reported that GSH induces expression of Cu/Zn SOD in tobacco. It has been reported GSH dependent enzymes; GR and GST increases in Trichoderma treated plants (Bailey et al., 2006; Shoresh and Harman, 2008). The GR is involved in the maintainence of GSH/GSSG ratio, that is necessary for the regeneration of ascorbate and for the initiation of many important enzymes associated with CO2-fixation (Noctor and Foyer, 1998). The protective nature of glutathione transferase might be due to its role in elimination of 4-hydroxyalkenals (membrane lipid peroxide) and proponal (DNA degredation product) by conjugating them with GSH (Berhane et al., 1994). It has also been reported that glutathione transferase directly detoxify lipid peroxides (Cummins et al., 1999) because some glutathione transferase have glutathione peroxidase activity (Cummins et al., 1999).
NaCl stress has been found to hamper the uptake of mineral nutrients like, S, Mn, Mg, Ca, and K in the present study. The results corroborates with the findings of Talei et al. (2012) in Andrographis paniculatai. Patel et al. (2010) also reported reduced accumulation of K and Ca in cowpea under NaCl stress. Na ion competes with the K for binding sites thus hampers the uptake of K. Uptake of S, Mn, Mg, and Ca also got hampered due to NaCl stress and is also reported by Pandolfi et al. (2012) in pea, Kanwal et al. (2013) in wheat and Iqbal and Ashraf (2013) in wheat. TH application has restored the uptake of essential elements in mustard plants under NaCl stress. Kadian et al. (2013) reported that plants inoculated with AMF enhance K uptake under NaCl stress. Evelin et al. (2009) also reported the enhancement of K:Na ratio in roots and shoots of plants and assist the plant in maintaining the K mediated enzymatic process and protein synthesis. TH produces plant growth regulators (Zhang et al., 2013) like α-naphthaleneacetic acid (NAA), indole-3-acetic acid (IAA) and indole-3-butyric acid (IBA) that imparts significant modifications in biological reactions and may be a reason for alleviation of NaCl stress (Iqbal and Ashraf, 2013).
Accumulation of Na ions increases with rise in NaCl concentrations in the present study. Kao et al. (2006) reported that increase in Na accumulation in three genotypes of soybean under salt stress. Agglomeration of Na in salt tolernt and suceptible varieties of Azolla is reported by Masood et al. (2006). Maggio et al. (2007) also confirmed building up of Na ions with increased levels of NaCl in tomato. However, the endophytic inoculated plants showed decrease in Na accumulation in plants and the results are also confirmed by many authors (Talaat and Shawky, 2011; Evelin et al., 2012; Contreras-Cornejo et al., 2014). According to Giri et al. (2007) mycorrhizal treated plants maintains K/Na ratio. K is an important element and an osmotic regulator in the plant cell. Na competes with K in uptake because both elements have similar physico-chemical structure (Serrano and Rodriguez-Navarro, 2001). This is the main reason why NaCl increases Na accumulation and lowers K, thus disturbs K/Na ratio (Zhang et al., 2010). TH inoculated mustard seedlings clearly indicated that concentration of K increases and that of Na decreases. Improvement in growth in TH inoculated seedlings under NaCl stress has been partly correlated to decreased accumulation of Na (Giri et al., 2007; Hajiboland et al., 2010; Wu et al., 2013).
Trichoderma is responsible for release of several compounds that might help the plant to tolerate the harsh environmental conditions. The plants inoculated with Trichoderma strains showed an increased defense-and stress-related compounds like JA, SA, and ABA (Martínez-Medina et al., 2011; Rubio et al., 2014). It is reported that SA is involved in activation of antioxidants against different environmental stresses like heat, NaCl, UV, heavy metals etc. (Mishra and Choudhuri, 1999; Ahmad et al., 2011). It is also reported that Trichoderma strains apart from producing plant growth hormones, they also synthesize 1-aminocyclopropane-1-carboxylate (ACC) deaminase, which cleaves ACC, the immediate precursor of the phytohormone ethylene and confers ‘induced systemic tolerance’ (IST) against drought and salt stress in plants (Viterbo et al., 2010). Heterologous expression of ACC deaminase from T. asperellum improved the growth performance of Arabidopsis thaliana under normal and salt stress conditions (Zhang et al., 2015). The inoculation of Trichoderma sp. in plants increased deep roots, which helped in more water acquisition and uptake of nutrients and thereby increasing the plants ability to resist abiotic stresses (Azarmi et al., 2011).
NaCl stress has been found to impose deleterious effects on mustard plants. The growth, biomass yield, oil content, pigment system was negatively affected especially at higher levels of NaCl stress. However, TH was found to mitigate the detrimental effects of NaCl stress in mustard seedlings. TH inoculated plants restored the pigment content, plant growth and development. The increase in proline content was found to be very useful in providing tolerance to these plants under NaCl stress. Both enzymatic (SOD, POD, CAT, GR, APX, MDHAR, DHAR, GST, GPX), and non-enzymatic (ASA, GSH, GSSG) antioxidants got induced by NaCl and TH further enhanced the synthesis of these phytoconstituents and protects the Brassica plants from further damage. The plants inoculated with TH hold potential to induce relative salt tolerance and improve plant growth of Indian mustard under salt stress. By using this sustainable approach we can bring salt affected land under cultivation with appreciable yield.
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.
The authors would like to extend their sincere appreciation to the Deanship of Scientific Research at King Saud University for funding the Research Group Project No RGP- VPP-271.
Abdel Latef, A. A. H., and Chaoxing, H. (2011). Effect of arbuscular mycorrhizal fungi on growth, mineral nutrition, antioxidant enzymes activity and fruit yield of tomato grown under salinity stress. Sci. Hortic. 127, 228–233. doi: 10.1016/j.scienta.2010.09.020
Ahmad, P., Jaleel, C. A., and Sharma, S. (2010a). Antioxidative defense system, lipid peroxidation, proline metabolizing enzymes and biochemical activity in two genotypes of Morus alba L. subjected to NaCl stress. Russ. J. Plant Physiol. 57, 509–517. doi: 10.1134/S1021443710040084
Ahmad, P., Jaleel, C. A., Salem, M. A., Nabi, G., and Sharma, S. (2010b). Roles of enzymatic and non-enzymatic antioxidants in plants during abiotic stress. Crit. Rev. Biotechnol. 30, 161–175. doi: 10.3109/07388550903524243
Ahmad, P., Nabi, G., and Ashraf, M. (2011). Cadmium-induced oxidative damage in mustard [Brassica juncea (L.) Czern. & Coss.] plants can be alleviated by salicylic acid. S. Afr. J. Bot. 77, 36–44. doi: 10.1016/j.sajb.2010.05.003
Ahmad, P., Ozturk, M., and Gucel, S. (2012). Oxidative damage and antioxidants induced by heavy metal stress in two cultivars of mustard (Brassica juncea L.) plants. Fresenius Environ. Bull. 21, 2953–2961.
Ahmad, P., Ozturk, M., Sharma, S., and Gucel, S. (2014). Effect of sodium carbonate-induced salinity-alkalinity on some key osmoprotectants, protein profile, antioxidant enzymes, and lipid peroxidation in two mulberry (Morus alba l.) cultivars. J. Plant Interact. 9, 460–467. doi: 10.1080/17429145.2013.855271
Ansel, D. C., Franklin, M. L. T., De Carvalho, M. H. C., Lameta, A. D. A., and Fodil, Y. Z. (2006). Glutathione reductase in leaves of cowpea: cloning of two cDNAs, expression and enzymatic activity under progressive drought stress desiccation and abscissic acid treatment. Ann. Bot. 98, 1279–1287. doi: 10.1093/aob/mcl217
Aroca, R., Ruiz-Lozano, J. M., Zamarren, A. M., Paz, J. A., García-Mina, J. M., Pozo, M. J., et al. (2013). Arbuscular mycorrhizal symbiosis influences strigolactone production under salinity and alleviates salt stress in lettuce plants. J. Plant Physiol. 170, 47–55. doi: 10.1016/j.jplph.2012.08.020
Ashraf, M. A., Ashraf, M., and Ali, Q. (2010). Response of two genetically diverse wheat cultivars to salt stress at different growth stages: leaf lipid peroxidation and phenolic contents. Pak. J. Bot. 42, 559–566.
Azevedo Neto, A. D., Prisco, J. T., Eneas-Filho, J., Medeiros, J. V. R., and Gomes Filho, E. (2005). Hydrogen peroxide pre-treatment induces salt-stress acclimation in maize plants. J. Plant Physiol. 162, 1114–1122. doi: 10.1016/j.jplph.2005.01.007
Aziz, E. E., Al-Amier, H., and Craker, L. (2008). Influence of salt stress on growth and essential oil production in peppermint, pennyroyal, and apple mint. J. Herbs Spices Med. Plant 14, 77–87. doi: 10.1080/10496470802341375
Azooz, M. M., Youssef, A. M., and Ahmad, P. (2011). Evaluation of salicylic acid (SA) application on growth, osmotic solutes and antioxidant enzyme activities on broad bean seedlings grown under diluted seawater. Int. J. Plant Physiol. Biochem. 3, 253–264.
Bailey, B. A., Bae, H., Strem, M. D., Roberts, D. P., Thomas, S. E., Crozier, J., et al. (2006). Fungal and plant gene expression during the colonization of cacao seedlings by endophytic isolates of four Trichoderma species. Planta 224, 1449–1464. doi: 10.1007/s00425-006-0314-0
Behera, R. K., Mishra, P. C., and Choudhary, N. K. (2002). High irradiance and water stress induced alterations in pigment composition and chloroplast activities of primary wheat leaves. J. Plant Physiol. 159, 967–973. doi: 10.1078/0176-1617-00823
Berg, G., Alavi, M., Schmidt, C. S., Zachow, C., Egamberdieva, D., Kamilova, F., et al. (2013). “Biocontrol and osmoprotection for plants under saline conditions,” in Molecular Microbial Ecology of the Rhizosphere, ed. F. J. de Bruijn (Hoboken, NJ: John Wiley and Sons, Inc.).
Berhane, K., Widersten, M., Engstrom, A., Kozarich, J. W., and Mannervik, B. (1994). Detoxication of base propenals and other alpha, beta-unsaturated aldehyde products of radical reactions and lipid peroxidation by human glutathione transferases. Proc. Natl. Acad. Sci. U.S.A. 91, 1480–1484. doi: 10.1073/pnas.91.4.1480
Bienert, G. P., Moller, A. L., Kristiansen, K. A., Schulz, A., Moller, I. M., Schjoerring, J. K., et al. (2007). Specific aquaporins facilitate the diffusion of hydrogen peroxide across membranes. J. Biol. Chem. 282, 1183–1192. doi: 10.1074/jbc.M603761200
Borde, M., Dudhane, M., and Jite, P. (2012). Growth, water use efficiency and antioxidant defense responses of mycorrhizal and non mycorrhizal Allium sativum L. under drought stress condition. Ann. Plant Sci. 1, 6–11.
Brotman, Y., Landau, U., Cuadros-Inostroza, A., Takayuki, T., Fernie, A. R., Chet, I., et al. (2013). Trichoderma-plant root colonization: escaping early plant defense responses and activation of the antioxidant machinery for saline stress tolerance. PLoS Pathol. 9:e1003221. doi: 10.1371/journal.ppat.1003221
Contreras-Cornejo, H. A., Macías-Rodríguez, L., Alfaro-Cuevas, R., and López-Bucio, J. (2014). Trichoderma spp. Improve growth of Arabidopsis seedlings under salt stress through enhanced root development, osmolite production, and Na? elimination through root exudates. Mol. Plant Microbe Interact. 27, 503–514. doi: 10.1094/MPMI-09-13-0265-R
Contreras-Cornejo, H. A., Macías-Rodríguez, L., Cortés-Penagos, C., and López-Bucio, J. (2009). Trichoderma virens, a plant beneficial fungus, enhances biomass production andpromotes lateral root growththrough an auxin-dependent mechanism in Arabidopsis. Plant Physiol. 149, 1579–1592. doi: 10.1104/pp.108.130369
Cummins, I., Cole, D. J., and Edwards, R. (1999). A role for glutathione transferases functioning as glutathione peroxidases in resistance to multiple herbicides in black-grass. Plant J. 18, 285–292. doi: 10.1046/j.1365-313X.1999.00452.x
Doni, F., Isahak, A., Zain, C. R. C. M., Ariffin, S. M., Mohamad, W. N. W., and Yusoff, W. M. W. (2014). Formulation of Trichoderma sp. SL2 inoculants using different carriers for soil treatment in rice seedling growth. Springerplus 3, 532. doi: 10.1186/2193-1801-3-532
Egamberdieva, D., Berg, G., Lindström, K., and Räsänen, L. A. (2013). Alleviation of salt stress of symbiotic Galega officinalis L. (goat’s rue) by co-inoculation of rhizobium with root colonising Pseudomonas. Plant Soil 369, 453–465. doi: 10.1007/s11104-013-1586-3
Egamberdieva, D., Kucharova, Z., Davranov, K., Berg, G., Makarova, N., Azarova, T., et al. (2011). Bacteria able to control foot and root rot and to promote growth of cucumber in salinated soils. Biol. Fertil. Soil 47, 197–205. doi: 10.1007/s00374-010-0523-3
Elia, A. C., Galarini, R., Taticchi, M. I., Dorr, A. J. M., and Mantilacci, L. (2003). Antioxidant responses and bioaccumulation in Ictalurus melas under mercury exposure. Ecotoxicol. Environ. Saf. 55, 162–167. doi: 10.1016/S0147-6513(02)00123-9
El-keltawi, N. E., and Croteau, R. (1987). Salinity depression of growth and essential oil formation in spearmint and marjoram and its reversal by foliar applied cytokinin. Phytochemical 26, 1333–1334. doi: 10.1016/S0031-9422(00)81806-3
Evelin, H., Giri, B., and Kapoor, R. (2012). Contribution of Glomus intraradices inoculation to nutrient acquisition and mitigation of ionic imbalance in NaCl-stressed Trigonella foenum-graecum. Mycorrhiza 22, 203–217. doi: 10.1007/s00572-011-0392-0
Giannakoula, A. E., and Ilias, I. F. (2013). The effect of water stress and salinity on growth and physiology of tomato (Lycopersicon esculentum Mill.). Arch. Biol. Sci. Belgrade 65, 611–620. doi: 10.2298/ABS1302611G
Giri, B., Kapoor, R., and Mukerji, K. G. (2007). Improved tolerance of Acacia nilotica to salt stress by arbuscular mycorrhiza, Glomus fasciculatum may be partly related to elevated K/Na ratios in root and shoot tissues. Microb. Ecol. 54, 753–760. doi: 10.1007/s00248-007-9239-9
Gusain, Y. S., Singh, U. S., and Sharma, A. K. (2014). Enhance activity of stress related enzymes in rice (Oryza sativa L.) induced by plant growth promoting fungi under drought stress. Afr. J. Agric. Res. 9, 1430–1434. doi: 10.5897/AJAR2014.8575
Hajiboland, R., Aliasgharzadeh, N., Laiegh, S. F., and Poschenrieder, C. (2010). Colonization with arbuscular mycorrhizal fungi improves salinity tolerance of tomato (Solanum lycopersicum L.) plants. Plant Soil 331, 313–327. doi: 10.1007/s11104-009-0255-z
Hameed, A., Egamberdieva, D., Abd-Allah, E. F., Hashem, A., Kumar, A., and Ahmad, P. (2014). “Salinity stress and arbuscular mycorrhizal symbiosis in plants,” in Use of Microbes for the Alleviation of Soil Stresses, Vol. 1, ed. M. Miransari (New York, NY: Springer), 139–159.
Hasanuzzaman, M., and Fujita, M. (2013). Exogenous sodium nitroprusside alleviates arsenic-induced oxidative stress in wheat (Triticum aestivum L.) seedlings by enhancing antioxidant defense and glyoxalase system. Ecotoxicology 22, 584–596. doi: 10.1007/s10646-013-1050-4
Hashem, A., Abd-Allah, E. F., Alqarawi, A. A., Al Huqail, A. A., and Egamberdieva, D. (2014). Alleviation of abiotic salt stress in Ochradenus baccatus (Del.) by Trichoderma hamatum (Bonord.) Bainier. J. Plant Interact. 9, 857–868. doi: 10.1080/17429145.2014.983568
Hashem, A., Abd-Allah, E. F., Alqarawi, A. A., Alwhibi Mona, S., Alenazi, M. M., Dilfuza, E., et al. (2015). Arbuscular mycorrhizal fungi mitigates NaCl induced adverse effects on Solanum lycopersicum L. Pak. J. Bot. 47, 327–340.
Heath, R. L., and Packer, L. (1968). Photoperoxidation in isolated chloroplasts: I. kinetics and stoichiometry of fatty acid peroxidation. Arch. Biochem. Biophys. 125, 189–198. doi: 10.1016/0003-9861(68)90654-1
Herouart, D., Van Montagu, M., and Inze, D. (1993). Redox-activated expression of the cytosolic copper/zinc superoxide dismutase gene in Nicotiana. Proc. Natl. Acad. Sci. U.S.A. 90, 3108–3112. doi: 10.1073/pnas.90.7.3108
Huang, C., He, W., Guo, J., Chang, X., Su, P., and Zhang, L. (2005). Increased sensitivity to salt stress in ascorbate-deficient Arabidopsis mutant. J. Exp. Bot. 56, 3041–3049. doi: 10.1093/jxb/eri301
Iqbal, M., and Ashraf, M. (2013). Alleviation of salinity-induced perturbations in ionic and hormonal concentrations in spring wheat through seed preconditioning in synthetic auxins. Acta Physiol. Plant. 35, 1093–1112. doi: 10.1007/s11738-012-1147-z
Jham, G. N., Moser, B. R., Shah, S. N., Holser, R. A., Dhingra, O. D., Vaughn, S. F., et al. (2009). Wild Brazilian mustard (Brassica juncea L.) seed oil methyl esters as biodiesel fuel. J. Am. Oil Chem. Soc. 86, 917–926. doi: 10.1007/s11746-009-1431-2
Jogaiah, S., Govind, S. R., and Tran, L. S. (2013). Systems biology-based approaches toward understanding drought tolerance in food crops. Crit. Rev. Biotechnol. 33, 23–39. doi: 10.3109/07388551.2012.659174
Kadian, N., Yadav, K., Badda, N., and Aggarwal, A. (2013). AM fungi ameliorates growth, yield and nutrient uptake in Cicer arietinum L. under salt stress. Russ. Agri. Sci. 39, 321–329. doi: 10.3103/S1068367413040058
Kanwal, H., Ashraf, M., and Hameed, M. (2013). Water relations and ionic composition in the seedlings of some newly developed and candidate cultivars of wheat (Triticum aestivum L.) under saline conditions. Pak. J. Bot. 45, 1221–1227.
Maggio, A., Raimondi, G., Martino, A., and De Pascale, S. (2007). Salt stress response in tomato beyond the salinity tolerance threshold. Environ. Exp. Bot. 59, 276–282. doi: 10.1016/j.envexpbot.2006.02.002
Martínez-Medina, A., Alguacil, M. D. M., Pascual, J. A., and van Wees, S. C. M. (2014). Phytohormone profiles induced by Trichoderma isolates correspond with their biocontrol and plant growth-promoting activity on melon plants. J. Chem. Ecol. 40, 804–815. doi: 10.1007/s10886-014-0478-1
Martínez-Medina, A., Roldán, A., Albacete, A., and Pascual, J. A. (2011). The interaction with arbuscular mycorrhizal fungi or Trichoderma harzianum alters the shoot hormonal profile in melon plants. Phytochemistry 72, 223–229. doi: 10.1016/j.phytochem.2010.11.008
Masood, A., Shah, N. A., Zeeshan, M., and Abraham, G. (2006). Differential response of antioxidant enzymes to salinity stress in two varieties of Azolla (Azolla pinnata and Azolla filiculoides). Environ. Exp. Bot. 58, 216–222.
Mastouri, F., Bjorkman, T., and Harman, G. E. (2010). Seed treatment with Trichoderma harzianum alleviates biotic, abiotic, and physiological stresses in germinating seeds and seedlings. Phytopathology 100, 1213–1221. doi: 10.1094/PHYTO-03-10-0091
Mastouri, F., Bjorkman, T., and Harman, G. E. (2012). Trichoderma harzianum enhances antioxidant defense of tomato seedlings and resistance to water deficit. Mol. Plant Microbe Interact. 25, 1264–1271. doi: 10.1094/MPMI-09-11-0240
Mishra, A., and Choudhuri, M. A. (1999). Effects of salicylic acid on heavy metalinduced membrane deterioration mediated by lipoxygenase in rice. Biol. Plant. 42, 409–415. doi: 10.1023/A:1002469303670
Mishra, S., Srivastava, S., Tripathi, R. D., Govindarajan, R., Kuriakose, S. V., and Prasad, M. N. V. (2006). Phytochelatin synthesis and response of antioxidants during cadmium stress in Bacopa monniera. Plant Physiol. Biochem. 44, 25–37. doi: 10.1016/j.plaphy.2006.01.007
Miyake, C., and Asada, K. (1992). Thylakoid bound ascorbate peroxidase in spinach chloroplast and photoreduction of its primary oxidation product monodehydroascorbate radicals in thylakoids. Plant Cell Physiol. 33, 541–553.
Noctor, G., Gomez, L., Vanacker, H., and Foyer, C. H. (2002). Interactions between biosynthesis, compartmentation and transport in the control of glutathione homeostasis and signalling. J. Exp. Bot. 53, 1283–1304. doi: 10.1093/jexbot/53.372.1283
Paradiso, A., Berardino, R., de Pinto, M., di Toppi, L. S., Storelli, F. T., and de Gara, L. (2008). Increase in ascorbate-glutathione metabolism as local and precocious systemic responses induced by cadmium in durum wheat plants. Plant Cell Physiol. 49, 362–374. doi: 10.1093/pcp/pcn013
Patel, P. R., Kajal, S. S., Patel, V. R., Patel, V. J., and Khristi, S. M. (2010). Impact of salt stress on nutrient uptake and growth of cowpea. Braz. J. Plant Physiol. 22, 43–48. doi: 10.1590/S1677-04202010000100005
Rasool, S., Ahmad, A., Siddiqi, T. O., and Ahmad, P. (2013). Changes in growth, lipid peroxidation and some key antioxidant enzymes in chickpea genotypes under salt stress. Acta Physiol. Plant. 35, 1039–1050. doi: 10.1007/s11738-012-1142-4
Rawat, L., Singh, Y., Shukla, N., and Kumar, J. (2011). Alleviation of the adverse effects of salinity stress in wheat (Triticum aestivum L.) by seed biopriming with salinity tolerant isolates of Trichoderma harzianum. Plant Soil 347, 387–400. doi: 10.1007/s11104-011-0858-z
Rawat, L., Singh, Y., Shukla, N., and Kumar, J. (2013). Salinity tolerant Trichoderma harzianum reinforces NaCl tolerance and reduces population dynamics of Fusarium oxysporum f.sp. ciceri in chickpea (Cicer arietinum L.) under salt stress conditions. Arch. Phytopathol. Plant Prot. 146, 1442–1467. doi: 10.1080/03235408.2013.769316
Resende, M. P., Jakoby, I. C. M. C., dos Santos, L. C. R., Soares, M. A., Pereira, F. D., Souchie, E. L., et al. (2014). Phosphate solubilization and phytohormone production by endophytic and rhizosphere Trichoderma isolates of guanandi (Calophyllum Brasiliense Cambess). Afr. J. Microbiol. Res. 8, 2616–2623. doi: 10.5897/AJMR2014.6633
Romero-Puertas, M. C., Corpas, F. J., Sandalio, L. M., Leterrier, M., Rodriguez-Serrano, M., del Rio, L. A., et al. (2006). Glutathione reductase from pea leaves: response to abiotic stress and characterization of the peroxisomal isozyme. New Phytol. 170, 43–52. doi: 10.1111/j.1469-8137.2006.01643.x
Roxas, V. P., Lodhi, S. A., Garrett, D. K., Mahan, J. R., and Allen, R. D. (2000). Stress tolerance in transgenic tobacco seedlings that overexpress glutathione S-transferase/ glutathione peroxidase. Plant Cell Physiol. 41, 1229–1234. doi: 10.1093/pcp/pcd051
Rubio, M. B., Quijada, N. M., Pérez, E., Domínguez, S., Monte, E., and Hermosa, R. (2014). Identifying beneficial qualities of Trichoderma parareesei for Plants. Appl. Environ. Microbiol. 80, 1864–1873. doi: 10.1128/AEM.03375-13
Saleem, M., Ashraf, M., and Akram, N. A. (2011). Salt (NaCl)-induced modulation in some key physio-biochemical attributes in okra (Abelmoschus esculentus L.). J. Agron. Crop Sci. 197, 202–213. doi: 10.1111/j.1439-037X.2010.00453.x
Sánchez-Rodríguez, E., Rubio-Wilhelmi, M., Cervilla, L. M., Blasco, B., Rios, J., Rosales, M. A., et al. (2010). Genotypic differences in some physiological parameters symptomatic for oxidative stress under moderate drought in tomato plants. Plant Sci. 178, 30–40. doi: 10.1016/j.plantsci.2009.10.001
Shoresh, M., and Harman, G. E. (2008). The molecular basis of shoot responses of maize seedlings to Trichoderma harzianum T22 inoculation of the root: a proteomic approach. Plant Physiol. 147, 2147–2163. doi: 10.1104/pp.108.123810
Shoresh, M., Mastouri, F., and Harman, G. (2010). Induced systemic resistance and plant responses to fungal biocontrol agents. Annu. Rev. Phytopathol. 48, 21–43. doi: 10.1146/annurev-phyto-073009-114450
Tabatabaie, S. J., and Nazari, J. (2007). Influence of nutrient concentrations and NaCl salinity on the growth, photosynthesis, and essential oil content of peppermint and lemon verbena. Turk. J. Agric. For. 31, 245–253.
Talaat, N. B., and Shawky, B. T. (2011). Influence of arbuscular mycorrhizae on yield, nutrients, organic solutes, and antioxidant enzymes of two wheat cul– tivars under salt stress. J. Plant Nutr. Soil Sci. 174, 283–291. doi: 10.1002/jpln.201000051
Talei, D., Kadir, M. A., Yusop, M. K., Valdiani, A., and Abdullah, M. P. (2012). Salinity effects on macro and micronutrients uptake in medicinal plant King of Bitters (Andrographis paniculata Nees.). Plant Omic J. 5, 271–278.
Vadassery, J., Tripath, S., Prasad, R., Varma, A., and Oelmuller, R. (2009). Monodehydroascorbate reductase 2 and dehydroascorbate reductase 5 are crucial for a mutualistic interaction between Piriformospora indica and Arabidopsis. J. Plant Physiol. 166, 1263–1274. doi: 10.1016/j.jplph.2008.12.016
Velikova, V., Yordanov, I., and Edreva, A. (2000). Oxidative stress and some antioxidant systems in acid rain treated bean plants: protective role of exogenous polyamines. Plant Sci. 151, 59–66. doi: 10.1016/S0168-9452(99)00197-1
Viterbo, A., Landau, U., Kim, S., Chernin, L., and Chet, I. (2010). Characterization of ACC deaminase from the biocontrol and plant growth-promoting agent Trichoderma asperellum T203. FEMS Microbiol. Lett. 305, 42–48. doi: 10.1111/j.1574-6968.2010.01910.x
Wu, Q. S., Zou, Y. N., and He, X. H. (2010). Contribution of Arbuscular mycorrhizal fungi to growth, photosynthesis, root morphology and ionic balance of citrus seedlings under salt stress. Acta Physiol. Plant. 32, 297–304. doi: 10.1007/s11738-009-0407-z
Wu, Q. S., Zou, Y. N., and He, X. H. (2013). Mycorrhizal symbiosis enhances tolerance to NaCl stress through selective absorption but not selective transport of K+ over Na+ in trifoliate orange. Sci. Hortic. 160, 366–374. doi: 10.1016/j.scienta.2013.06.011
Yu, C. W., Murphy, T. M., and Lin, C. H. (2003). Hydrogen peroxide– induces chilling tolerance in mung beans mediated through ABA-independent glutathione accumulation. Funct. Plant Biol. 30, 955–963. doi: 10.1071/FP03091
Zhang, F., Yuan, J., Yang, X., Cui, Y., Chen, L., Ran, W., et al. (2013). Putative Trichoderma harzianum mutant promotes cucumber growth by enhanced production of indole acetic acid and plant colonization. Plant Soil 368, 433–444. doi: 10.1007/s11104-012-1519-6
Zhang, F., Zhang, J., Chen, L., Shi, X., Lui, Z., and Li, C. (2015). Heterologous expression of ACC deaminase from Trichoderma asperellum improves the growth performance of Arabidopsis thaliana under normal and salt stress conditions. Plant Physiol. Biochem. 94, 41–47. doi: 10.1016/j.plaphy.2015.05.007
Keywords: NaCl, Trichoderma harzianum (TH), mustard, growth, osmolytes, H2O2, lipid peroxidation, antioxidants
Citation: Ahmad P, Hashem A, Abd-Allah EF, Alqarawi AA, John R, Egamberdieva D and Gucel S (2015) Role of Trichoderma harzianum in mitigating NaCl stress in Indian mustard (Brassica juncea L) through antioxidative defense system. Front. Plant Sci. 6:868. doi: 10.3389/fpls.2015.00868
Received: 27 May 2015; Accepted: 01 October 2015;
Published: 14 October 2015.
Edited by:Andrea Genre, University of Turin, Italy
Reviewed by:Sheridan Lois Woo, University of Naples Federico II, Italy
Saiema Rasool, Universiti Putra Malaysia, Malaysia
Copyright © 2015 Ahmad, Hashem, Abd-Allah, Alqarawi, John, Egamberdieva and Gucel. 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.