Heavy metals are a major cause of abiotic stress in plants and their accumulation in human and animal tissues leads to serious health problems (Singh et al., in press). The oxidative stress caused by heavy metals including cadmium (Cd2+) results in membrane damage and also decreases photosynthesis (Su et al., 2017; Kaur et al., 2017). Increases in the levels of reactive oxygen species (ROS) such as hydrogen peroxide (H2O2), superoxide anion and thiobarbituric acid reactive substances (TBARS) in plant cells is the main cause of oxidative stress in plants (Tripathi et al., 2017). Cd2+ toxicity increases the accumulation of H2O2, superoxide anion and TBARS in lettuce (Wang et al., 2019) and in Arabidopsis thaliana (Song et al., 2017). The effect of Cd2+ on root morphology varies with different plant species (Li et al., 2009; Lu et al., 2013). Lambrechts et al. (2013) found that the root diameter of Lolium perenne and Trifolium repens increases in relation to a high number of short and wide adventitious roots under Cd2+ stress. Moreover, in Zea mays (Maksimovi’c et al., 2007) and in Salix alba (Lunáčková et al., 2004) plants, the root diameters increases under Cd2+ stress. The root length of lettuce (Lactuca sativa L.) plants exposed to Cd2+ decreased by 89% (Bautista, Fischer & Cárdenas, 2013). In A. thaliana, Cd2+ stress decreased root length but doubled the diameter of the lateral roots (Vitti et al., 2013). In view of the variations in the response of plants root systems to Cd2+ stress, Lu et al. (2013) indicated that the response of plants root systems to Cd2+ stress can be used in assessing their tolerance to Cd2+ stress.
Plant hormones are a group of chemical messengers that are primarily known to regulate plant growth and development (Peto’ et al., 2011) but they also play roles in plants tolerance to biotic and abiotic stresses (Krishnamurthy & Rathinasabapathi, 2013). Christmann et al. (2006) reported that increases in endogenous abscisic acid (ABA) contents in plants improve their tolerance to various stresses. The endogenous levels of ABA in rice (Kim et al., 2014) and potato tubers (Stroinski et al., 2010) as well as in the roots of two aquatic plants, Typha latifolia and Phragmites australis (Fediuc, Lips & Erdei, 2005) increased under Cd2+ stress. Veselov et al. (2003) also found that the contents of cytokinin in the shoots and roots of wheat decreased within 1–2 h of exposure to Cd2+. Auxins, including indole-3-acetic acid (IAA) also play important roles in protecting and regulating plants metabolism under stress conditions. Generally, heavy metal stress decreases the levels of endogenous auxins (Gangwar et al., 2014).
Plants tolerance to heavy metals has been associated with increase activities of antioxidant enzymes (Yang & Ye, 2015). However, Fodor (2002) reported that high Cd2+ concentrations resulted in decreased antioxidant activities in plants. The catalase (CAT) activity in several plants including, Lactuca sativa (Wang et al., 2019; Monteiro et al., 2009), Phaseolus vulgaris (Chaoui et al., 1997) and Pisum sativum (Chaoui & El Ferjani, 2005) decreased when the plants were subjected to Cd2+ stress. The CAT activity in pea seedlings was also decreased whiles the superoxide dismutase (SOD) and peroxidase (POD) activities increased under Cd2+ stress (Agrawal & Mishra, 2007). The rates of POD activity in the roots and shoots of pea seedlings were higher at lower Cd2+ (5–20 µM CdCl2) concentrations than at higher Cd2+ (50–100 µM CdCl2) concentrations (Bavi, Kholdebarin & Morashahi, 2011). Proline, which is a component of the non-specific defense systems against heavy metal toxicity acts as a chelator as well as a protein stabilizer in plants (Sharma & Dubey, 2005). The contents of proline increased in lettuce plants under Cd2+ stress (Jibril et al., 2017) and in wheat plants exposed to Pb stress (Lamhamdi et al., 2013).
Different plant species possess a wide range of protection mechanisms against Cd2+-induced stress (Mohamed et al., 2012). However, the response of plants to Cd2+ stress depend on several factors including the genotype and the Cd2+ concentration of the growing medium (Irfan, Ahmad & Hayat, 2013). The root system of plants is the foremost organ that comes into contact with Cd2+ in a growing medium. Therefore, the response of the root system to Cd2+stress could have greater impact on the tolerance of the whole plant to the stress. Richard et al. (2015) screened maize lines for Al tolerance and indicated that root tolerance should be considered in selecting cultivars for Al tolerance. In Brassica juncea seedlings exposed to Cd2+ stress, the POD and CAT activities of the root system were more efficient in scavenging ROS compared with the shoot system (Mohamed et al., 2012). Although a number of studies have reported the effect of Cd2+ on lettuce plants (Wang et al., 2019; Bautista, Fischer & Cárdenas, 2013; Monteiro et al., 2009; Monteiro et al., 2007), the root tolerance and biochemical response of the root system of different lettuce genotypes to Cd2+ stress have rarely been reported. Moreover, to the best of our knowledge, the response of the genotypes studied in the present experiment to Cd2+ stress has not been reported.
The objectives of our study were: (1) to evaluate the root tolerance of four lettuce genotypes to Cd2+ stress based on root tolerance indexes, (2) to determine the biochemical (hormones, antioxidant enzymes activities and proline) defense response of the four lettuce genotypes to Cd2+ stress.
Materials and Methods
Genotypes used for the experiment
The experiment was conducted at the College of Horticulture, Gansu Agricultural University, Lanzhou, Gansu Province, PR China (36°03′N, 103°40′E). The seeds of four improved lettuce (Lactuca sativa L.) genotypes obtained from the Gansu Academy of Agricultural Sciences, Lanzhou, China, were used in this experiment (Table 1).
Seedling growth conditions
The seeds were germinated in petri dishes within 48 h under light condition in a climate box (temperature 20 °C; light intensity 200 µmol m−2 s−1 photosynthetically active radiations, PAR; relative humidity 80%). The germinated seeds were sown in trays which were filled with vermiculite and the seedlings were raised in a greenhouse (average daily temperature 24 ± 2 °C; relative humidity 60–70%; 12 h light) for two weeks. During the first two weeks of growth, the young seedlings were irrigated with half-strength Hoagland’s nutrient solution with pH adjusted to 6.0 (Hoagland & Arnon, 1950). After the first two weeks of growth, the seedlings were grown hydroponically for another two weeks using full-strength Hoagland’s nutrient solution in a climate controlled room (25 °C/22 °C light/dark periods, 75% relative humidity and 14 h light period with 200 µmol m−2 s−1 PAR). In all, 240 seedlings were transferred to 24 opaque hydroponic containers (length 82 cm; width 30 cm; height 5 cm). Each of the containers were filled with 5 L of the full-strength Hoagland’s nutrient solution and supplied with 10 seedlings of a particular lettuce genotype. The nutrient solution was changed at 4 days interval until the seedlings were four weeks old before the 100 µM CdCl2 treatment was applied according to the experimental design.
|Genotype||Days to maturity from transplanting||Estimated yield (kg/ha)||Special attributes|
|Yidali||40||22,500||Resistant to low temperature and moisture stress, early maturing|
|Lümeng||60||22,500||Resistant to diseases and low temperature|
|Anyan||40–50||30,000–45,000||Resistant to diseases, low temperature and moderate heat stress|
Experimental design and treatments
A 4 × 2 factorial experiment in a completely randomized design with 3 replications was conducted in the climate controlled room using 28 days old seedlings. The treatments consisted of the four lettuce genotypes and two Hoagland’s nutrient solutions. Two hundred and forty seedlings (60 seedlings per genotype) were grouped into two. Half of the seedlings of each genotype were exposed to the Hoagland’s nutrient solution supplemented with 100 µM CdCl2 and the other half were maintained in the nutrient solution without 100 µM CdCl2, as control plants. We used the 100 µM CdCl2 concentration in our experiment based on previous studies that were conducted with lettuce as the test crop (Xu et al., 2014; Monteiro et al., 2009; Monteiro et al., 2007). At seven days after exposure to treatments, one plant each was taken randomly from each experimental unit and used for the analysis of root morphological indexes. At the same time, five plants were also taken randomly from each experimental unit and their root tissues were immediately stored at −80 °C for biochemical analysis.
Root morphological indexes
The roots of the sampled plants were gently separated from the shoots, rinsed in distilled water and the root systems were scanned with the aid of a root scanner (STD 4800, EPSON, Canada) to obtain the digital images. The total root length (TRL), root volume (RV), root surface area (RSA), root projected area (RPA), and numbers of root tips (NRT) and root forks (NRF) per plant were determined using the root image analysis software, Win RHIZO version 5.0 (Regent Instruments, Inc., Quebec City, Canada).
Determination of root tolerance indexes
The Cd2+ tolerance indexes (TI) of the plants root systems which indicates the resistance of the root systems to the heavy metal stress was calculated as described by Wilkins (1978) with some modifications. Since the various root morphological indexes such as total root length, root volume, number of root tips and root surface area have direct influence on Cd2+ uptake and the plants tolerance to Cd2+ stress, we calculated the Cd2+ TI for each of the root indexes at the end of the experiment. Based on the TI score, we considered the genotype which had the highest TI for most of the indexes measured as the tolerant genotype among the genotypes we evaluated. The TIs were calculated as follows:
Determination of H2O2 contents in root samples
Contents of H2O2 in the root samples were determined following the procedure described by Junglee et al. (2014) but with slight modifications. Briefly, we 0.1 g fresh root sample was ground with liquid nitrogen in mortar with pestle and the homogenate transferred into a 2 mL capacity centrifuge tube which was then kept in ice bath. We added 1.5 mL 0.1% TCA and the homogenate were centrifuged at 12,000× g for 15 min under 4 °C. Then, 0.5 ml of the supernatant was thoroughly mixed with 0.5 mL PBS (pH 7.0) and 1 mL 1 mol L−1 KI. The mixture was placed under constant temperature (28 °C) for 1 h. The absorbance was measured at 390 nm and the contents of H2O2 were calculated using the H2O2 reference standard curve (0, 1, 2, 3, 4 and 5 mmol L−1).
Determination of contents of hormones in root samples
Fresh root samples (0.5 g) of each of the four lettuce genotypes were collected from three plants in each experimental unit, quickly wrapped in alumnum foil, labeled and then put in liquid nitrogen. After this, the samples were put in labeled plastic bags and stored in a freezer at −80 °C. The contents of ABA, IAA, GA3 and Cytokinin were later determined by the Enzyme Linked Immunosorbent Assay (ELISA) technique (Shanghai Jiwei Biological Technology Co. Ltd., PR China).
Antioxidant enzymes activities and proline contents in roots
Enzymes assays were done using frozen root tissues that were stored at −80 °C. For each enzyme, about 0.5 g of the root tissue was ground in liquid nitrogen with a mortar and pestle and then homogenized in 5 ml of 0.1 M phosphate buffer (pH 7.5), containing 0.5 mM ethylene-diamine-tetra-acetic acid (EDTA). Each homogenate was centrifuged at 12,000× g for 15 min at 4 °C, and the supernatant was aliquoted for determination of enzymatic activity; superoxide dismutase (SOD, EC 184.108.40.206), catalase (CAT, EC 220.127.116.11) and peroxidase (POD, EC 18.104.22.168) activity assays. The SOD activity was measured by determining the ability of plants to inhibit the photochemical reduction of nitroblue tetrazolium (NBT). Based on the inhibition of 50% of NBT photoreduction as one unit of SOD activity, the amount of reduced NBT was monitored spectrophotometry–colorimetry at 560 nm (Giannopolitis & Ries, 1977). The POD activity was estimated at 470 nm as described by Chance & Maehly (1955). The CAT activity was measured by determining the oxidation of H2O2 and monitored as a decline spectrophotometry-colorimetry at 240 nm (Nakano & Asada, 1981). Proline contents in the root samples were determined after extraction at room temperature with 3% of 5-sulfosalicylic acid solution as previously described (Bates, Waldren & Teare, 1973).
The data were subjected to analysis of variance and the treatment means were separated by the least significance difference (LSD) test at 5% using Genstat statistical software (9th edition; Lawes Agricultural Trust, Rothamsted Experimental Station, UK). In the figures, the spread of the mean values were shown using the standard deviations. Different letters assigned to the bars indicate significant differences among the treatments by LSD (P < 0.05). Pearson’s correlation analysis was used to determine the relationship between root morphological indexes and contents of root hormones under no stress and under Cd2+ stress conditions. The correlation analyses were done using the average values for every trait × genotype × treatment. Graphs were prepared using Graphpad Prism version 8.0.
Root morphological characteristics
The results of our experiment showed that there was significant (P < 0.001) genotype × Cd2+ interaction effect on total root length (TRL), root volume (RV), root surface area (RSA), root projected area (RPA), number of root forks (NRF) and number of root tips (NRT) of the lettuce genotypes (Fig. 1). Generally, Cd2+ stress decreased all the root morphological indexes across the genotypes but Yidali was the least affected. The decrease in TRL due to Cd2+ was least (39.0%) in Lüsu and greatest (56.0%) in Yidali. The least (38.7%) decrease in RSA was observed in Yidali and the greatest (65.9%) in Lüsu. Moreover, the least (25.6%) and the greatest (59.1%) decreases in RPA were observed in Yidali and Anyan genotypes, respectively. The least (54.0%) decrease in RV also occurred in Yidali whiles the greatest (80.3%) was observed in Lümeng. Cd2+ stress also decreased NRT and NRF by 42.3%–67.9% and 36.0%–56.8%, respectively in the genotypes and in each case, Yidali was the least affected. The decreases in the root morphological indexes due to Cd2+ stress resulted in reductions in the sizes of the root systems of the four lettuce genotypes (Fig. 2).
Root tolerance to cadmium stress
Figure 3 shows the results of the root tolerance of the four genotypes to Cd2+ stress. There was significant (P < 0.001) variations in the tolerance indexes (TIs) among the four lettuce genotypes. The result showed that at seven days after plants exposure to Cd2+, Yidali, had the highest TI for most of the indexes measured including RV (46%), RSA (61%), RPA (84%), NRF (65%) and NRT (58%). Based on this result, we considered the Yidali genotype as the most tolerant genotype among the genotypes evaluated. With the exception of TI for TRL which was highest (61%) in Lüsu , the other genotypes had lower TI scores compared with Yidali and these genotypes were considered as sensitive to Cd2+ stress.
Contents of H2O2 in roots
The results showed significant (P < 0.001) genotype × Cd2+ interaction effect on contents of H2O2 in the roots of the lettuce genotypes (Fig. 4). Generally, H2O2 contents increased in all the genotypes under Cd2+ as compared to their respective control plants. In comparison with control plants, Cd2+ increased H2O2 contents in the roots of the four genotypes by 44.3–61.1%. The highest H2O2 content was found in Anyan but this was statistically similar to the H2O2 contents in the Lüsu and Lümeng genotypes. The lowest H2O2 content was found in the Yidali plants which were exposed to Cd2+ treatment.
Contents of root hormones
The results showed significant (P < 0.001) genotype × Cd2+ interaction effect on contents of abscisic acid (ABA), cytokinin, gibberellic acid (GA3) and indole-3-acitic acid (IAA) in the roots of the four lettuce genotypes (Fig. 5). The contents of ABA in Lüsu and Anyan plants under Cd2+ treatment were 19.8% and 8.9% more than their respective control plants. However, the ABA contents in Lümeng and Yidali genotypes were 17.1% and 3.9% lower compared with the control. The contents of GA3 in Anyan, Yidali and Lüsu plants under Cd2+ stress were 7.3%, 10.9% and 10.3% respectively lower than their control plants. However, the content of GA3 in Lümeng under the stress condition increased by 12.9% compared with the control plants. The contents of cytokinin in Anyan and Lüsu increased by 9.7% and 5.1% but decreased by 21.6% and 16.8% in Lümeng and Yidali under Cd2+ stress. The highest IAA content was found in the Yidali genotype under Cd2+ treatment and this was 36.2% more than the control. However, the IAA contents in Lüsu and Anyan, under Cd2+ treatment were 21.6% and 8.7%, lower than their respective control plants.
Table 2 shows the correlation analyses for root morphological indexes and root hormones of the four lettuce genotypes under Cd2+-free condition (diagonal, white background) and under Cd2+ stress (diagonal, grey background). Under no Cd2+ stress, the correlations among most of the root indexes were significantly positive. For instance, total root length (TRL) correlated positively with root surface area (RSA) (r = 0.903**), root projected area (RPA) (r = 0.756**), number of root forks (NRF) (r = 0.699*), number of root tips (NRT) (r = 0.774**) and root volume (RV) (r = 0.960**). Moreover, IAA correlated positively with RSA (r = 0.590*), NRF (r = 0.698*), NRT (r = 0.799**) and RPA (r = 0.657*). However, the correlation between cytokinin and RPA was negative (r = − 0.579*). The correlation between GA3 and IAA was positive (r = 0.765**) whiles that between ABA and cytokinin was also positive (r = 0.764**) under Cd2+-free condition. The results also showed positive and negative correlations between the hormones and root morphological indexes under Cd2+ stress condition (Table 2, above diagonal, grey background). Total root length (TRL) correlated positively with RSA (r = 0.829**), NRF (r = 0.925**) and RPA (r = 0.963**). Moreover, GA3 correlated negatively (r = − 0.768**) with NRT and IAA also correlated negatively (r = − 0.732**) with RSA. However, among the hormones, only cytokinin correlated positive with TRL (r = 0.578*), NRF (r = 0.703*) and RPA (r = 0.791**) under the Cd2+ stress condition. The correlation analysis among the hormones showed that ABA correlated positively with GA3 (r = 0.630*), cytokinin (0.786**) and IAA (r = 0.669*) under Cd2+ stress.
total root length
root surface area
number of root forks
number of root tips
root projected area
Antioxidant enzymes activities and proline contents
The results also showed significant (P < 0.001) genotype × Cd2+ interaction effect on CAT, SOD and POD activities and contents of proline in the roots of the four lettuce genotypes (Fig. 6). In comparison with their respective control plants, Cd2+ stress decreased the SOD activities in the roots of all the genotypes by 20.4–40.3%. However, the CAT and POD activities as well as the contents of proline in all the genotypes increased by 16.7–56.6%, 18.6–69.8% and 36.7–79.8%, respectively. The greatest increase in CAT activity was observed in the Yidali genotype whiles the Anyan genotype had the highest POD activity and proline content.
Cadmium (Cd2+) interferes with the uptake of water and nutrients and causes injuries to plant roots (Jibril et al., 2017). Wang et al. (2015) reported that Cd2+ stress decreases total root length (TRL), root surface area (RSA) and root volume (RV) in soybean cultivars. The decrease in root length of lettuce plants due to Cd2+ stress was as high as 89% (Bautista, Fischer & Cárdenas, 2013). The results of our experiment also showed that the addition of 100 µM CdCl2 to the nutrient solution decreased the TRL, RSA, RV and root projected area (RPA) of the lettuce genotypes. The numbers of root tips (NRT) and root forks (NRF) in the studied lettuce genotypes were also decreased. This resulted in a decrease in the size of the root systems in all four genotypes. The negative correlations observed among some of the root morphological indexes under Cd2+ stress was indicative of the adverse effect of Cd2+ on the morphological indexes of lettuce roots. The tolerance of plants to Cd2+ stress can be influenced by the characteristics of the roots. Wang et al. (2015) reported that soybean cultivars with larger root systems were tolerant to Cd2+ whiles those with smaller root systems were sensitive. However, the results of our experiment showed that Yidali, which possessed the smallest root system, had the greatest root tolerance to Cd2+ compared with the other genotypes that had larger root systems. The tolerance of Yidali to Cd2+ stress which was demonstrated by the greatest tolerance indexes for RV, RSA, RPA, NRF and NRT could largely be attributed to the diminutive nature of its root system. The smaller root system of Yidali (especially fewer root tips and smaller surface area), probably limited the amount of Cd2+ absorbed by the roots. Liu, Probst & Liao (2005) attributed the lower Cd2+ contents in the roots of S. alfedii to the smaller size of root system (smaller root length, surface area and volume). Huang et al. (2015) also indicated that pepper cultivar with shorter roots, fewer root tips and smaller surface area had lower capacity for Cd2+ uptake. Moreover, the tolerance of plants to Cd2+ stress has also been assessed based on the content of H2O2 produced when the plants were exposed to the stress. Cd2+ toxicity results in increased production of reactive oxygen species such as H2O2 and superoxide anion which causes oxidative stress (Tripathi et al., 2017). Zhang et al. (2009) indicated that Vicia sativa which had lower content of H2O2 was more tolerant to Cd2+ than Phaseolus aureus which had higher content of H2O2 when both plants were exposed to Cd2+ treatment. Increase in the accumulation of H2O2 in lettuce plants under Cd2+ stress was earlier reported (Wang et al., 2019). Our experiment also showed that Cd2+ toxicity increased the H2O2 contents in the roots of the four lettuce genotypes. However, the increase in H2O2 was least in Yidali, and this also gives an indication of the tolerance of Yidali to Cd2+ stress compared with the other genotypes. These results, therefore, suggest that lettuce genotypes with smaller root systems could be more tolerant to Cd2+ stress compared with genotypes that possess larger root systems.
Research studies have shown that almost all hormones have the capacity to act as components of Cd2+-stress signaling in plants. The content of cytokinin (Gangwar et al., 2014), abscisic acid (Kim et al., 2014), gibberellin (Zhu et al., 2012), brassinosteroid (Villiers et al., 2011) and jasmonic acid (Zaid & Mohammad, 2018; Noriega et al., 2012) in plants have all been found to change in response to various stresses. Cd2+ stress increases the levels of ABA (Kim et al., 2014; Stroinski et al., 2010; Fediuc, Lips & Erdei, 2005) and GA (Zhu et al., 2012) in plants. However, the levels of IAA (Gangwar et al., 2014) and cytokinin (Veselov et al., 2003) decreased in plants under Cd2+ stress. In our study, the effect of Cd2+ on the contents of the hormones in the roots depended on the genotype. Under Cd2+ stress, ABA increased in Anyan and Lüsu, decreased in Lümeng and remained unaffected in the Yidali genotype. Moreover, under Cd2+ stress, the contents of cytokinin increased in Anyan and Lüsu but it decreased in Yidali and Lümeng. The variations in the hormonal responses to Cd2+ among the four genotypes could be attributed to differences in their sensitivity to Cd2+ stress. Different lettuce cultivars were found to have exhibited different levels of sensitivity to heavy metals (Priac, Badot & Crini, 2017). Hsu & Kao (2003) also found that the contents of ABA increased in the roots and leaves of Cd2+-tolerant rice cultivar but not in the Cd2+-sensitive cultivar.
Under the control condition, ABA and IAA contents in roots correlated positively with most of the root indexes whiles GA3 and cytokinin correlated negatively with TRL and RPA respectively. ABA generally acts as growth inhibitor under stress free conditions (Takezawa, Komatsu & Sakata, 2011). In our study, ABA correlated positively with most of the root morphological indexes under Cd2+ stress. This suggests that ABA can play a positive role in promoting the tolerance of lettuce plants to Cd2+ stress. This observation could be attributed to the low concentrations of ABA in the roots of the genotypes tested in the current experiment. Barlow & Pilet (1984) reported that low concentrations of ABA increased root elongation, cell division and DNA synthesis whiles high concentration decreased root growth in maize. The promotion of root growth due to auxin was also demonstrated when root morphological parameters increased upon the application of 5–20 ppm IAA to grafted cucumber seedlings (Balliu & Sallaku, 2017). Although both cytokinin (Mok, 1994) and GA3 (De Souza & MacAdam, 2001) promote growth through cell division, cell expansion and cell elongation in this experiment. These hormones correlated negatively with TRL and RPA, respectively. This suggests that increasing cytokinin and GA3 contents in the roots of lettuce under Cd2+ free condition may decrease root growth. However, under Cd2+ stress, GA3 andIAA contents of roots correlated negatively with some of the root indexes but ABA correlated negatively with most of the root indexes compared with GA3 andIAA. Although under the control condition, both GA3 and IAA correlated positively with root morphological indexes, both hormones correlated negatively with the root indexes under Cd2+ stress. This suggests that the interaction effect of these hormones may not influence root growth in lettuce but could enhance the tolerance of the plants to Cd2+ stress. The positive correlation between ABA and GA3 and also between ABA and IAA under Cd2+ stress is indicative of the importance of ABA in alleviating Cd2+ stress in lettuce plants. ABA is reported to play significant role in plants response to various stresses (Kiba et al., 2011). In plants under drought stress, ABA alleviated the stress by inducing stomata closure, leaf folding and osmotic adjustment (Lipiec et al., 2013). Under stress free conditions, Cytokinin generally suppresses growth and development of roots (Werner et al., 2003) and it is usually antagonistic with IAA in roots (Nordström et al., 2004). However, in this experiment, only cytokinin correlated positively with most of the root indexes under Cd2+ stress. The positive correlation between cytokinin and most of the root morphological indexes suggests that increased level of cytokinin may be required to support the survival of lettuce plants under Cd2+ stress. Vitti et al. (2013) found that cytokinin increased root growth of A. thaliana seedlings and improved their tolerance to Cd2+ stress.
The antioxidant enzymes activities and proline response of plants to heavy metal stress depends on species, cultivar, Cd2+ concentration and duration of exposure. The enzymatic defense system in plants includes SOD, CAT, and ascorbate peroxidase (Foroozesh et al., 2012). The SOD is a major scavenger which catalyzes the conversion of superoxide to H2O2 and molecular oxygen under stress conditions (Allen, 1995). The H2O2 which is also toxic to plant cells is detoxified by CAT and/or POD, which converts it to water and oxygen (Zhu et al., 2004). Proline is also among the components of the non-specific defense systems in plants. It alleviates metal toxicity by acting as a metal chelator and also as a protein stabilizer (Sharma & Dubey, 2005). In the current experiment, antioxidant enzymes activities and proline response to Cd2+ stress in the roots of the four lettuce genotypes were similar. Although the SOD activity of the genotypes decreased at seven days after exposure to Cd2+ stress, the CAT and POD activities, as well as the contents of proline increased. The decrease in SOD activity observed in all the genotypes at seven days after the Cd2+ treatment could be due to fact that the SOD which is the first enzyme involved in the antioxidant enzyme defense system might have completed its function within few days after the Cd2+ treatment, which resulted in the increased H2O2 contents. The increase in CAT and POD activities was to enable the plants further detoxify the H2O2 which is also toxic to plant cells. Decreased SOD activity due to Cd2+ stress was reported in lettuce (Xu et al., 2014), A. thaliana (Abozeid et al., 2017) and in P. sativum L. (Rodriguez-Serrano et al., 2006). The CAT and POD activities and the contents of proline in the roots of the lettuce genotypes exposed to Cd2+ increased to counteract the Cd2+-induced oxidative stress (increased H2O2 contents) in the plants. In a previous experiment, POD, SOD and CAT activities and the content of proline in oilseed rape plants exposed to Cd2+ stress increased (Yan et al., 2015). In other experiments, the contents of proline in different lettuce varieties increased (Jibril et al., 2017) and the POD activity in pea seedlings also increased (Agrawal & Mishra, 2007) increased when these plants were exposed to Cd2+ stress.
In this study, the root tolerance and biochemical response of four lettuce genotypes to100 µM CdCl2 (Cd2+) treatment were determined. The results showed that Cd2+ stress decreased the sizes of the root systems of the four lettuce genotypes evaluated. However, the Yidali genotype, which possessed the smallest root system, exhibited the greatest tolerance to Cd2+ stress with the by exhibiting the greatest tolerance index scores for root volume, surface area, projected area and numbers of root forks and root tips. Cd2+ stress also caused increases in H2O2 contents in the roots of the genotypes but the increase was least in the Yidali genotype which showed more root tolerance to Cd2+stress. The effect of Cd2+ stress on ABA, IAA, GA3 and cytokinin was genotype dependent. Under Cd2+ stress, the correlation between ABA and IAA, GA3 and cytokinin were positive. The antioxidant enzyme activities and proline response to Cd2+ stress in the roots of the four genotypes were similar. The SOD activity decreased whiles the CAT and POD activities, as well as the contents of proline, increased under the stress condition. Greater root tolerance indexes and lower H2O2 content were found in the Yidali genotype under the stress condition, suggesting that lettuce genotypes with smaller root system could be more tolerant to Cd2+ stress. However, further research is needed to ascertain the details of the molecular and genetic mechanisms of Cd2+ tolerance in lettuce genotypes with relatively smaller root systems.