African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12486

Full Length Research Paper

Comparative studies between growth regulators and nanoparticles on growth and mitotic index of pea plants under salinity

Hala G. El-Araby
  • Hala G. El-Araby
  • Biological and Environmental Science Department, Faculty of Home Economics, Al-Azhar University, Egypt.
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Sahar F.M. El-Hefnawy
  • Sahar F.M. El-Hefnawy
  • Biological and Environmental Science Department, Faculty of Home Economics, Al-Azhar University, Egypt.
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Mohammed A. Nassar
  • Mohammed A. Nassar
  • Agriculture Botany Department, Faculty of Agriculture, Al-Azhar University, Egypt.
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Nabil I. Elsheery
  • Nabil I. Elsheery
  • Agriculture Botany Department, Faculty of Agriculture, Tanta University, Egypt.
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  •  Received: 03 July 2020
  •  Accepted: 27 July 2020
  •  Published: 31 August 2020

 ABSTRACT

To our knowledge, no research study has been carried out on the effects of ascorbic acid (ASA), 5-Aminolevulinic acid (ALA) and Nano selenium (N-Se) on the cytological parameters of pea seedlings under salinity stress. Salinity treatment (60 and 120 mM NaCl) was applied. Two concentrations of ASA (50 and 100 ppm), ALA (25 and 50 ppm), and N-Se (10 and 20 ppm), respectively were used individually and in combination with NaCl (60 and 120 mM). Modifications in shoot length, number of leaves, leaf area, chromosomal aberrations and mitotic index were determined. Salinity treatment (120 mM) caused the highest reduction in shoot length, leaf area and mitotic index. A significant increase of chromosomal abnormalities percentage (%) was detected in salinity treatments compared with control.  ASA (100 ppm), ALA (50 ppm) and N-Se (10 ppm) treatments significantly reduced the damaging effect of salinity stress on growth attributes, mitotic index and chromosomal abnormalities percentage (%) and improved seedlings’ performance. These treatments can be recommended for the improvement of pea plants’ productivity under salt stress.

 

Key words: Ascorbic acid, 5-aminolevulinic acid, nano selenium, salt stress, mitosis, chromosomal aberrations, Pissum sativum L.


 INTRODUCTION

Salt stress adversely affects the morphological, physiological and biochemical responses of plant species (Nazar et al., 2011). Several researchers found that the chlorophyllian pigments were reduced with an increase in salinity level. This may be due to the disruption of the fine structure of chloroplasts and pigment-protein complex or chlorophyll   stability,   which   can   result   in  chlorophyll oxidation (Saha et al., 2010; Helaly et al., 2016; Elsheery et al., 2020c) and disturb plant growth and development (Sairam and Tyagi, 2004). Tang et al. (2017b) established that salinity inhibits plant growth, reduces yield in many crop plants and affects their commercial value (Helaly et al., 2016; Elsheery et al., 2020c). So, salinity    stress    inhibits   growth   of   basil    plants    by decreasing  a significant number  of  leaves/plant and  plant  height (Khan et al., 2009; Nassar et al., 2019). Also, the retardant effects of salinity stress on growth, physiological aspects and productivity were also recorded  on  other  different  plants  species; for instance,  Reda  (2007)  on Senna occidentalis, Dawood et al. (2014) on Faba bean, Bargaz et al. (2016) on Phaseolus vulgaris, Nassar et al. (2016) on Leucaena and Elsheery et al. (2020b) on mango. There are many ways to improve salinity tolerance in plants such as using of biofertilizer and amino acids (Helaly et al., 2016) and grafting in vegetable crops (Elsheery et al., 2020a; Helaly et al., 2016; Al-Mayahi, 2016). This study was carried out to investigate the effects of ascorbic acid (ASA) under salinity stress  on growth of pea plant. Some biochemical constituents that can promote growth and increase productivity of many species of plants grown under normal or abiotic stress conditions are highly recommended (Sharma et al., 2019). Ascorbic acid (ASA) is a small water soluble antioxidant molecule which acts as an essential substrate in the cyclic pathway of enzymatic detoxification of hydrogen peroxide. Ascorbic acid (ASA) is a naturalist product that acts as an antioxidant and enzyme and also improves cofactor. It engages in a variety of procedures. It correlates with chloroplasts in the oxidative stress of photosynthesis (Latif et al., 2016). Furthermore, ASA has a number of roles in protein modification and cell division in plant cells (Hussein et al., 2019). Nowadays, it plays an essential role in a series of physiological processes such as cofactor of key enzyme, plant defense against oxidization, growth, development, cell division, cell extension, senescence and counteracts the deleterious effects of biotic and abiotic stresses (Zhang and Sonnewald, 2017). Therefore, it is chosen to be one of the substances of the subject of our present study.

 

5-Aminolevulinic acid (ALA) is a type of non-protein amino acid that supports plant stress tolerance. However, the underlying physiological and biochemical mechanisms are not entirely understood (Anwar et al., 2020). ALA is found in all plants and animals. 5-aminolevulinic acid (ALA) is and a key precursor for the biosynthesis of porphyrins such as chlorophyll, heme and plant hormones. In addition, it has newly been reported that ALA regulates the expression level of fructose-1, 6-bisphosphatase (FBP), triose-3-phosphate isomerase (TPI), and ribulose-1, 5-bisphosphate carboxylase/ oxygenase small subunit (RBCS), which activate the Calvin cycle of photosynthesis under drought stress (Liu et al., 2016). It was found that, ALA is one of plant growth regulators (PGRs) and mitigates salinity stress effect in germinating seeds and ameliorates seedling growth. Foliar application of 5-aminolevulinic acid at low concentrations has been shown to promote salt tolerance in a lot of plants (Tang et al., 2017a). On the other hand, ALA is involved in the chlorophyll biosynthesis pathway under   salt   stress   conditions   (Wu   et  al.,  2011)  and motivates antioxidant enzyme efficiency and accumulation of endogenous hormone under many stress factors such as low-temperature in cucumber seedlings (Anwar et al., 2018). Under drought stress, spray application of ALA up-regulated the chlorophyll fluorescence indexes in oilseed rape (Brassica napus L.) (Liu et al., 2014) and gas exchange indexes, such as net photosynthetic average (Pn), stomatal behavior (gs), intercellular CO2 concentration (Ci) and the rate of transpiration (Tr), which were adversely influenced by abiotic stress (Wu et al., 2018). It is also reported that foliar application of ALA may confer plant tolerance to diverse abiotic stresses, such as chilling, high temperature, salinity, drought, weak light, and heavy metals (Wu et al., 2019a). Previous studies demonstrated that ALA encourages abiotic stress tolerance by activation of numerous types of transcription factors, signal transduction, and chlorophyll and carbohydrate biosynthesis (Nishihara et al., 2003; Anwar et al., 2020). These results submit that ALA can broadly minimize the harmful effects of environmental stress. Increasing attention has been paid to the beneficial impacts of many nanoparticles (NPs) used in low doses on diverse crops (Jampílek and Kráľová, 2017; Rastogi et al., 2019; Kumar et al., 2020; Elsheery et al., 2020c). A lot of researchers like Sonkaria et al. (2012) and Prasad et al. (2014) established that, using of NPs can promote plant growth, warrant food goodness and decrease waste. Nano-Selenium (N-Se) as Nano fertilizer has been recently used in the field (Shang et al., 2019; Elsheery et al., 2020a; Elsheery et al., 2020b). There is less documented information on the biological effects of N-Se and its application (Chau et al., 2007; Cushen et al., 2012). Bhattacharjee et al. (2014) and Kamle et al. (2020) suggest that N-Se plays a role as a reactive oxygen species (ROS) scavenger in plants under stress conditions. So, the purpose of our study was: To evaluate the (ASA, ALA and N-Se) morphological and cytological effect of application of our treatments (Soaked and foliar) on pea plants under salinity stress using hydroponic methods.


 MATERIALS AND METHODS

Plant material
 
The pea variety used in this study was obtained from El Korma Company, Egypt for seeds import. The experiment was carried out at the greenhouse of the Agriculture Botany Department, Faculty of Agriculture, Tanta University, Egypt, during winter of the two growing seasons of 2018 and 2019. In both growing seasons, the average of the daily temperature ranged between 11 and 26°C and relative humidity between 60 and 65%.
 
Hydroponic experiment for evaluating responses of tested cultivar of pea to salt stress
 
The  seeds  were  washed  and  soaked  for  6 h  before  they were planted in the treatment solutions [ASA (50, 100 ppm), ALA (25, 50 ppm) and N-se (10, 20) ppm]. Then they germinated in polyethylene bags (8 seeds per bag) filled with washed sand on a half-strength Hoagland,s nutrient solution used as macronutrient sources (Hoagland and Arnon, 1950). Then, the bags were placed in dishes containing 1 L of Hoagland,s solution (pH 5.8) in greenhouse at a temperature range of 20 to 26° during the day and 11 to 16° during the night.  Nutrient solutions were added every day and renewed every 3 days. Four replicates (each with 10 polyethylene bags containing 8 plants) were planted. After the emergence of the first real leaves (15 days after germination), the number of plants per bag was adjusted to five, by thinning out weak and less vigorous ones. Seedlings were exposed to two levels of salinized water (salt mixture of 60 and 120 mM) of a mixture salts. When the 4th true leaf emerged, foliar spraying was done twice (after 30 and 33 days from sowing) at the same concentrations [ASA (50,100 ppm), ALA (25, 50 ppm), N-Se (10, 20 ppm)[. Foliar treatments were not applied on nine pots: The first 3 pots were treated with saline; the second pot was treated with a salt mixture of 60 mM and the third was treated with a salt mixture of 120 mM.
 
The plants were collected after seven days of foliar application and their morphological parameters were recorded.
 
Growth parameters
 
The following parameters were recorded: Shoot length (cm), number of leaves and leaf area per plant (cm2) using the formula:
 
Leaf area /plant with weight method (cm2/plant) = B=L*S/ Z
 
B = Green leafy area on one plant; S = Circle space for tablets; L = Total weight of the leaves on the plant; Z = Weight of tablets.
 
For shoot length from each treatment, shoots of 10 pea plants were separated from roots; they were washed using distilled water and dried carefully with wish tissue paper. The number of leaves per plant was counted.
 
Cytological parameters
 
For mitotic screening physiologically, uniform and healthy seeds of Pisum sativum L. were used to study the effect of ASA, ALA and N-Se on the growth of pea plants under salinity stress conditions (Darlington, 1976). The dividing cells were observed and recorded. Cells were examined under a light microscope for mitotic index, numbers and types of abnormalities. At least 3000 cells were examined per treatment (1000 cell/replicate). Mitotic index (MI) and percentage of abnormal cells were calculated using the following formulas: 
 


 RESULTS AND DISCUSSION

Growth parameters
 
Plant  height  (shoot  length),  fresh  and  dry  biomass of shoot and root per pea plant, number of leaves and leaf area per plant were affected by salt stress levels. ASA, ALA, and N-Se soaking and foliar application improved the plant’s tolerance to salt stress (Table 1).
 
The data presented show that increased salt levels induced significant (mean value for two seasons) stress which resulted in a significant reduction of all growth parameters compared to control. ALA, ASA and N-Se treatments reduced the harmful effect of salinity on plants treated compared with non-treated plants.
 
Salinity is an essential environmental factor which curbs crop plants from attaining their full genetic potential; therefore, salt stress in pea plant induces a lot of growth limitation (Gama et al., 2007). Pea plant subjected to higher salt will experience delay in growth which could be attributed to the inhibition of cell elongation (Taïbi et al., 2013). These results are consistent with those obtained on rice by Yu et al. (2019), on flax by Wu et al. (2019b) or other species.
 
The inhibitory effects of salt stress on pea plant and the reduction in dry mass might be due to the toxic effect of salt stress as a result of high osmotic pressure. Salinity stress causes a significant increase of growth inhibitors and decrease of growth promoters. Disturbance of water in plants grown under salinity restricts absorption or plants are not able to uptake the water and nutrients required by them (Memon et al., 2010) (Colla et al., 2006a, b).
 
A similar tendency was observed by Shi et al. (2013). The suppression  effects of salinity lead to disturbance in ionic homeostasis, stomatal closure, reduction in photosynthesis, accumulation of toxic ions (Na+, Cl‾) which restricted the absorption of water (Shahzad et al., 2020; Kamran et al., 2020) and inhibited growth and productivity. The same trend was observed by Nassar et al. (2019) and Bargaz et al. (2016).
 
The results presented in Table 1 show that all growth characteristics of "leaf area, shoot height and number of leaves" decreased significantly with increased salt stress level.
 
Leaf area
 
Data indicate that the leaf area has been significantly affected by different salinity concentrations (Table 1). Soaking and foliar applications significantly increased the leaf area under salinized and non-salinized conditions (P < 0.05).
 
Under salinity level of 120 mM, the highest increase in leaf area was with ASA (100 ppm) (99.96 cm2) followed by ALA (50 ppm) (96.71 cm). In contrast, the lowest amounts of leaf area recorded using N-Se (20 ppm) (62.50 cm2) were 99.96, 96.71 and 62.50 cm2, respectively, compared with control plants.
 
Foliar application of ASA and ALA increased all previous parameters, improved plants’ tolerance to NaCl toxicity and  minimized  reduction  in  growth  caused  by NaCl. Meanwhile, it is evident that ASA and ALA play a vital role in the regulation of a number of metabolic processes in plants exposed to salinity. It has been concluded that, the typical effect of salt stress on plants is growth retardation due to the inhibition of cell elongation (Hanafy et al., 2013).
 
 
ALA is one of the existing PGRs used for the improvement of plants’ stress tolerance (Hotta et al., 1997; Naeem et al., 2012) and an essential precursor for the biosynthesis of tetrapyrroles such as heme and chlorophyll. It was found that ALA is formed in all animals and plants. Recently, it was found that low concentrations of ALA had a promotive effect on growth and yield of several crops and vegetables (Watanabe et al., 2000).
 
Ascorbic acid is an essential main metabolite in plants that is utilized as an enzyme cofactor, an antioxidant and a cell signaling modulator in crucial physiological processes, in biosynthesis of the cell wall, secondary metabolites and phytohormones, stress tolerance, photoprotection, cell division and growth  (Elkelish  et  al.,
2020).
 
Selenium spraying treatment had a considerable positive effect on all studied characteristics such as plant height, number of leaves, fresh weight of shoots and roots, dry weight of leaves and shoots and chlorophyll content. It could be proved that foliar application of nano selenium at 10 and 20 ppm increased vegetative growth, yield and quality as well as mineral contents in leaves of pea plants. Furthermore, the best selenium used as a foliar spray is the nano type because it is safer and more environmental friendly compared to the chemical form. These results agree with Shedeed et al. (2018).
 
Shoot length
 
Shoot length was significantly affected by different salinity concentrations. ASA (100 ppm) showed higher shoot length followed by ALA (50 ppm) (32.69 and 28.00 cm, respectively).  The  lowest shoot length was obtained with N-Se (20 ppm) treatment (22.39 cm) compared to untreated plants exclusively under high level of salt mixture (120 mM). Previous studies show that the application of some natural bio-stimulants used as a foliar spray and/or seed soaking improved growth and yield constituents of pea grown under salinity stress (Desoky et al., 2017).
 
Number of leaves
 
The data in Table 1 show that in both growing seasons, salinity caused a significant reduction in the number of leaves by different salinity concentrations. In contrast, in the treatments of ASA (100 ppm) and ALA (50 ppm), the number of leaves was higher (7 leaves and 6 leaves respectively). The lowest number of leaves was obtained with N-Se (20 ppm) treatment (5 leaves) in comparison to untreated plants, especially under high level of salinity (120 mM).
 
The decrease in growth and productivity could be attributed to the osmotic effect of salinity stress which caused increase of growth inhibitors and decrease of growth promoters, disturbance of water in plants grown under salt stress. It indicates that these inhibitory effects of salinity lead to stomatal closure, reduced photosynthesis,  unrest  in  ionic  homeostasis, accumulation of toxic Na+, Cl- and finally inhibit growth and productivity. Moreover, the decrease in the shoot length of stressed plants is actually due to senescence which is accompanied by loss and withering of plant organs as well as the transport of elaborated materials to the reproductive organs.
 
Pea seed and plant treated with ASA, ALA and N-Se used as foliar spray and seed soaking significantly promoted plant growth and productivity under the adverse effect of soil salinity. One of the compounds which has antioxidative characteristic is ASA (Zhang, 2013). This compound can reduce the harmful effects in plants under environmental stress. The ASA treatments influenced the passive effect of salinity on growth and productivity. This could be referred to as the  biochemical functions of ASA which can be divided into categories, that is, antioxidant, that changes the lipophilic antioxidants such as  tocopherol, vitamin  E, and enzyme  cofactor  for  hydroxylase  enzymes involved  in  the synthesis  of  rich-hydroxyproline glycolproteins, and  cell  wall structural  proteins (Desoky et al., 2017). It was observed that, foliar treatment with ALA stimulated growth and also partially enhanced the effects of toxic caused by high levels of salinity in root and shoot. Also, salinity damage can also be attributed to the physiological drought generated by salt stress (Hopkins, 1995; Sajid et al., 2020), due to the reduction in osmotic potential and relative water content. ALA application encouraged an increase in osmotic potential and relative water content of  the  stressed  seedlings (Naeem  et  al., 2011). Many studies have shown that ALA can stimulate crop resistance, yield and quality and can be used as a new type of plant growth regulator (Rafaqat et al., 2015; Tang et al., (2017b). A concentration of 50 mg/L of ALA could significantly mitigate seeds’ deterioration and seedlings of Perilla frutescens under NaCl stress and encourage salt resistance (Zhang et al., 2011). It was indicated that a high level of salinity damages cellular electron transport, leading to the generation of reactive oxygen species (ROS). This activates lipid peroxidation and cell membrane damage (Shalata et al., 2001).
 
Cytological parameters
 
The cytological effects on pea plants treated with ASA, ALA and N-Se under saline conditions are shown in Table 2.
 
Our results showed that, the mitotic index in root tip meristems of P. sativum treated with salt mixture (60 and120 mM) significantly decreased compared to seeds (in control treatment). Table 2 proves the effect of ASA, ALA and N-Se on mitotic index (%) in P. sativum root tips. The total number of proliferating cells and the numbers of cells at various mitotic stages of P. sativum meristemic cells were scored in root tips. Cytological analysis showed that, under harmful stress conditions (120mM NaCl), the highest value of mitotic index (%) was observed in pea treated with ascorbic acid at a concentration of 100 ppm (13.53%) followed by ALA 50 ppm (13.19%); nano selenium at a concentration of 20 ppm gave the lowest value (10.12%), compared to control (10.02%).
 
The mitotic index of root tips of seeds treated with ASA, ALA and N-Se remarkably increased in salinity samples. At the same time, ASA, ALA and N-Se + NaCl application indicated serious performance in improving the passive effects of salt stress on the mitotic activity. ÇavuÅŸoÄŸlu et al. (2007, 2013) established that, growth regulator (exogenous application) may have a positive or negative effect on seed germination and seedling growth under non-stress conditions.
 
Thus, the study aims to test the effects of ASA, ALA and N-Se application on seedling growth in non-stress and stressed conditions. Our results indicated that the shoot length, number of leaves and leaf area of treated plants were generally amplified in comparison to the control. It was stated previously that saline conditions harmfully affect growth and development actions in general, even in halophytes (ÇavuÅŸoÄŸlu et al., 2017; Ghoulam and Fares, 2001). The seedling growth and germination of P.sativum seeds, as anticipated, were prevented under saline conditions (Table 1).
 
 
 
Ali (2000) demonstrated that salinity could fulfill/replace its harmful effect in numerous ways. It may intervene with seed germination by converting the water status of the seed so that water reuptake is inhibited.  Our outcomes showed the decrease in stem length, number of leaves and leaf area under saline conditions. Other studies showed that the inhibitive effect of salt   on   root might  result  from  decreasing  cell division (McCue and Hanson, 1990), protein synthesis and nucleic acid (Prakash et al., 1988). This may be demonstrated by the failure of the roots to receive enough water due to high osmotic
pressure of the medium (Al-Karaki, 2001).
 
On the other hand, ASA, ALA and N-S treatments noticeably removed the inhibitor effect of salinity stress  on  growth  parameters,  so  our  treatments alleviate salt stress on roots due to the reduction in the salts osmotic effects. ASA might have been effective in decreasing the inhibitive impact of salinity stress on the seed germination and seedling growth by rising nucleic acid and protein synthesis, providing steadiness of cell membranes or by raising the activity of antioxidant enzyme (Al-Kaisy et al., 2018). ASA has also received special attention because it is a highly efficient antioxidant and has free radical scavenging capacity (Acosta-Motos et al., 2020).
 
There  are  no  present  studies  on  the  effects  of ALA application under salinity conditions on cytogenetical parameters as studied here.
 
In Figure 1, It was concluded that aberrations in chromosomes induced by salinity at different stages of mitosis such as prophase, metaphase, anaphase, and telophase in root meristem cells are variable. In addition, a gradual decline in mitotic index and an increase in the abnormality index were observed as the concentration of salt mixture application duration was raised. Aberrations in chromosomal behavior such as sticky and disturbed chromosomes in metaphase and anaphase, c-metaphase, bridges, laggard, and disturbed telophase were also observed. Bhattacharjee et al. (2014) confirmed that a significant reduction by N-Se in chromosomal aberration in bone marrow, and DNA damage in lymphocytes and bone marrow in mice treated with cyclophosphamide -induced hepatotoxicity and genotoxicity.
 
 
 
 
Types of chromosome aberrations in P. sativum root tips treated with ASA, ALA and N-Se under saline condition
 
In Table 3, various chromosomal aberrations like chromosomal bridges, stickiness, vagrant, broken, and lag chromosomes were recorded. In our study, the lowest value of abnormalities (%) under severe stress conditions (120 mM) was observed  when the pea was treated with ascorbic acid at a concentration of 100 ppm (13.63%) followed by ALA 50ppm (14.01%); nano selenium at a concentration of 20 ppm gave the highest value. It was 17.45% compared with control which recorded 23.42%. Cytological effects and the data obtained from the analysis of root tips treated with ALA, ASA and N-Se are summarized in Tables 1 and 2 and Figure 1.
 
 
Previously, it was reported that salt stress conditions adversely affect growth and development events. It is recognized that salinity inhibits seedling growth (Abdul Qados, 2011; Ghezal et al., 2016).
 
Salinity that inhibits shoot length and leaf number may result from decreasing cell division (McCue and Hanson, 1990). The kinds of mitotic abnormalities detected in the present study were disturbed chromosomes, sticky, vagrant, laggard, bridges and C- shaped Metaphase.
 
On the other hand, ASA, ALA and N-Se application that markedly removed the inhibitor effect of salinity on growth parameters (Tables 1 and 2) is due to the decrease in the salts osmotic effects compared to the control. In addition to all these, ASA, ALA and N-Se might have been efficacious in decreasing the inhibitive effect of salt stress on the plant growth by increasing nucleic acid and protein synthesis, stabilizing cell membranes or raising the activities of antioxidant enzyme (Liu et al., 2014;  Ekanayake et al., 2015; Germ et al., 2007).
 
According to some researchers, the harmful effects of salinity stress on mitotic activity have been known for a long time. Furthermore, the negative effects of salinity stress on chromosomal abnormalities have been planned in the last decade (Radic et al., 2009; Tabur and Demir, (2009, 2010a, b). It was demonstrated that a high concentration of salt entirely suppressed the activity of mitotic division and facilitated chromosomal abnormalities in root-tip meristem cells (Radić et al., 2009).
 
It is worth mentioning that salinity adversely affected the mitotic activity and chromosome behaviors in root meristem cells of P. sativum. Briefly, the results proved that under salinity, ASA, ALA and N-Se might act as a stimulator, triggering the protein synthesis necessary for the normal division of cells and acceleration of the mitotic cycle. Previous researches also proved that nanomaterials with low concentrations are better than high concentration alone or in a group with stress (Zedan and Omar, 2019). It was indicated that, the protective effect of selenium as nanoparticles versus numerous material induced cytotoxicity and genotoxicity effects (Bhattacharjee et al., 2014). A significant reduction by N-Se in chromosomal aberration was found in bone marrow, and DNA damage in lymphocytes and bone marrow in mice treated with cyclophosphamide -induced hepatotoxicity and genotoxicity.
 
Barakat (2003) established that, treating the roots with vitamin B6 or ascorbic acid presented a considerable increase in the mitotic index and reduced the inhibition effect of NaCl in wheat cultivars.
 
The previous results showed that ASA (100 ppm) in combination with NaCl does not only antagonize the inhibitory action of salinity but also activates the cells to inter mitosis and encourages a high mitotic activity. These results are in harmony with those obtained by Autifi et al. (2018) who proved that vitamin C reduces the influence of lead acetate on the mitotic activities. No perversion from the normal was seen in roots treated with vitamin C or vitamin B6; parallel results were observed by Bronzetti et al. (2001).
 
Harmful effects of salinity or any other stress conditions were attributed to lower endogenous levels of cytokinins and endogenous hormonal imbalance by some researchers (El-Mashed and Kamel, 2001). Plant growth inhibition refers to disturbances in natural growth regulators and mitotic chromosomal irregularities as additional factor (Hoda et al., 1991). So, the application with ascorbic acid can reform the genotoxic effect of the salinity which delays the cell in entering mitosis.
 

 


 CONCLUSIONS

Considering the data of the present study it appears that when applied at high concentrations of salinity shows cytotoxic activity. In this study some growth regulators such as ASA, ALA and N-Se were used. It was concluded that salinity treatments stimulated the genotoxic effect to throw ROS generation inside the tissues which ultimately cause oxidative disturbance. This leads to redox homeostasis imbalance and genotoxic in addition to mito-depressive effects. Using these treatments (ASA, 100 ppm; ALA, 50 ppm and N-Se, 10 ppm) causes induction of mitotic index and reduces the chromosomal aberrations.


 ACKNOWLEDGEMENTS

The authors are grateful to Prof. Amina Zedan, Biological and Environmental Sciences Department., Faculty of Home Economics, Al-Azhar University, Egypt for her support.

 



 REFERENCES

Abdul Qados MSA (2011). Effect of salt stress on plant growth and metabolism of bean plant Vicia faba (L.). Journal of the Saudi Society of Agricultural Sciences 10:7-15.
Crossref
 

Acosta-Motos JR, Penella C, Hernández JA, Díaz-Vivancos P, Sánchez-Blanco M J, Navarro JM, Gómez-Bellot MJ, Barba-Espín G (2020). Towards a Sustainable

  
 

Agriculture: Strategies Involving phytoprotectants against Salt Stress. Agronomy 10:1-32.

  
 

Ali RM (2000). Role of putrescine in salt tolerance of Atropa belladonna plant. Plant Science 152:173-179.
Crossref

  
 

Al-Kaisy W, Sahar A, Mahadi F (2018). Response of pea (Pisum sativum L.) to foliar application of ABA and vitamin C and interaction of them on some physiological characters of plant. Al-Mustansiriyah Journal of Science 29:32-37.
Crossref

  
 

Al-Karaki GN (2001). Germination, sodium and potassium concentrations of barley seeds as influenced by salinity. Journal of Plant Nutrition 24:511-522.
Crossref

  
 

Al-Mayahi AMW (2016). Influence of salicylic acid (SA) and ascorbic acid (ASA) on in vitro propagation and salt tolerance of date palm (Phoenix dactylifera L.) cv. 'Ner¬sy'. Australian Journal of Crop Science 10(7):969-976.
Crossref

  
 

Anwar A, Wang J, Yu X, He Ch, Li Y (2020). Substrate Application of 5- aminolevulinic acid enhanced low-temperature and weak-light stress tolerance in cucumber (Cucumis sativus L.). Agronomy 10:1-12.
Crossref

  
 

Anwar A, Yan Y, Liu Y, Li Y, Yu X (2018). 5-aminolevulinic acid improves nutrient uptake and endogenous hormone accumulation, enhancing low-temperature stress tolerance in cucumbers. International Journal of Molecular Science 19:33-49.
Crossref

  
 

Autifi M, Mohamed W, Abdul Haye W, Elbaz K (2018). The possible protective role of vitamin C against toxicity induced by lead acetate in liver and spleen of adult albino rats (light and electron microscopic study). The Egyptian Journal of Hospital Medicine 73:7650-7658.

  
 

Barakat H (2003). Interactive effects of salinity and certain vitamins on gene expression and cell division. International Journal of Agriculture and Biology 5:219-225.

  
 

Bargaz A, Nassar RMA, Rady MM, Gaballah MS, Thompson SM, Brestic M, Schmidhalter U, Abdelhamid MT (2016). Improved salinity tolerance by phosphorus fertilizer in two Phaseolus vulgaris recombinant inbred lines contrasting in their p-efficiency. Journal of Agronomy and Crop Science 202:497-507.
Crossref

  
 

Bhattacharjee A, Basu A, Ghosh P, Biswas J, Bhattacharya S (2014). Protective effect of Selenium nanoparticle against cyclophosphamide induced hepatotoxicity and genotoxicity in Swiss albino mice. Journal of Biomaterials Applications 29:303-317.
Crossref

  
 

Bronzetti G, Cini M, Andreoli E, Caltavuturo L, Panunzio M (2001). Protective effects of vitamins and selenium compounds in yeast. Croce CD. PubMed 496:105-115.
Crossref

  
 

ÇavuÅŸoÄŸlu K, Cadıl S, ÇavuÅŸoÄŸlu D (2017). Role of potassium nitrate (KNO3) in alleviation of detrimental effects of salt stress on some physiological and cytogenetical parameters in Allium cepa L. Cytologia 82:279-286.
Crossref

  
 

ÇavuÅŸoÄŸlu K, Kaya F, Kılıç S (2013). Effects of boric acid pretreatment on the seed germination, seedling growth and leaf anatomy of barley under saline conditions. Journal Food Agriculture and Environment 11:376-380.

  
 

ÇavuÅŸoÄŸlu K, Kılıç S, Kabar K (2007). Some morphological and anatomical observations during alleviation of salinity (NaCl) stress on seed germination and seedling growth of barley by polyamines. Acta Physiologiae Plantarum 29:551-557.
Crossref

  
 

Chau CF, Wu SH, Yen GC (2007). The development of regulations for food nanotechnology. Trends in Food Science and Technology 18:269-280.
Crossref

  
 

Colla G, RouphaelY, Cardarell M, Massa D, Salerno A, Rea, E (2006a). Yield, fruit quality and mineral composition of grafted melon plants grown under saline conditions. Horticulture Science and Biotechnology 81:146-152.
Crossref

  
 

Colla G, RouphaelY, Jawad R, Cardarell M, Rea E (2006b). Effect of salinity on yield, fruit quality, leaf gas exchange and mineral composition of grafted watermelon plants. Horticulture Science and Biotechnology 41:622-627.
Crossref

  
 

Cushen M, Kerry J, Morris M, Cruz-Romero M, Cummins E (2012). Nanotechnologies in the food industry-Recent developments, risks and regulation. Trends in Food Science and Technology 24:30-46.
Crossref

  
 

Darlington C (1976). La cour. L.R, The Handling of Chromosomes, George Alien and Unwin, London P. 182.

  
 

Dawood MG, Taie HAA, Nassar RMA, Abdel hamid MT, Schmidhalter U (2014). The changes induced in the physiological, biochemical and anatomical characteristics of Vicia faba by the exogenous application of proline under seawater stress. South African Journal of Botany 93:54-63.
Crossref

  
 

Desoky EM, Merwad AM, Elrys AS (2017). Response of pea plants to natural bio-stimulants differences and commonalities of plant responses to single and combined stresses, under soil salinity stress. American Journal and Plant Physiology 12:28-37.
Crossref

  
 

Ekanayake LJ, Thavarajah D, Vial E, Schatz B, McGee R, Thavarajah P (2015). Selenium fertilization on lentil (Lens culinaris Medikus) grain yield, seed selenium concentration and antioxidant activity. Field Crops Research 177:9-14.
Crossref

  
 

Elkelish A, Qari SH, Mazrou YSA, Abdelaal KAA, Hafez YM, Abu-Elsaoud AM, Batiha GE, El-Esawi MA, El Nahhas N (2020). Exogenous ascorbic acid induced chilling tolerance in tomato plants through modulating metabolism, osmolytes, antioxidants and transcriptional regulation of catalase and heat shock proteins. Plants 9:1-27.
Crossref

  
 

Elsheery N, Sunoj VSJ, Wen Y, Zhu JJ, Muralidharan G, Cao KF (2020a). Foliar application of nanoparticles mitigates the chilling effect on photosynthesis and photoprotection in sugarcane. Plant Physiology and Biochemistry 149:50-60.
Crossref

  
 

Elsheery N, Helaly M, El-Hoseiny H, Alam-Eldein Sh (2020b). Zinc oxide and silicone nanoparticles to improve the resistance mechanism and annual productivity of salt-stressed mango trees. Agronomy 10:953-975.
Crossref

  
 

Elsheery N, Helaly M, Omar S, John S, Zabochnicka-Swiatek M, Kalaji H, Rastogi A (2020c). Physiological and molecular mechanisms of salinity tolerance in grafted cucumber. South African Journal of Botany 130:90-102.
Crossref

  
 

Gama PBS, Inanaga S, Tanaka K, Nakazawa R (2007). Physiological response of common bean (Phaseolus vulgaris L.) seedlings to salinity stress. African Journal of Biotechnology 6:79-88.

  
 

Germ M, Kreft I, Stibilj V, Urbanc-Berčič O (2007). Combined effects of selenium and drought on photosynthesis and mitochondrial respiration in potato. Plant Physiology and Biochemistry 45:162-167.
Crossref

  
 

Ghezal N, Rinez I, Sbai H, Saad I, Farooq M, Rinez A, Zribi I, Haouala R (2016). Improvement of Pisum sativum salt stress tolerance by bio-priming their seeds using Typha angustifolia leaves aqueous extract. South African Journal of Botany 105:240-250.
Crossref

  
 

Ghoulam C, Fares K (2001). Effect of salinity on seed germination and early seedling growth of sugar beet (Beta vulgaris L.). Seed Science Technology 29:357-364.

  
 

Hanafy MS, El-Banna A, Schumacher HM, Jacobsen HJ, Hassan FS (2013). Enhanced tolerance to drought and salt stresses in transgenic faba bean (Vicia faba L.) plants by heterologous expression of the PR10a gene from potato. Plant Cell Reports 32:663-674.
Crossref

  
 

Helaly M, El-Hosieny H, Elsheery N, Kalaji H (2016). Effect of biofertilizers and putrescine amine on the physiological features and productivity of date palm (Phoenix dactylifera L.) grown on reclaimed-salinized soil. Trees 30:1149-1161.
Crossref

  
 

Hoagland DR, Arnon DI (1950). The water culture method for growing plants without soil. California Agricultural Experimental Station Circular. University of California, Berkeley 347:1-32.

  
 

Hoda Q, Bose S, Sinha S (1991). Vitamin C mediated minimization of malathion and rogor induced mito-inhibition and clastogeny. Cytologia 56:89-97.
Crossref

  
 

Hopkins WG (1995). Introduction to Plant Physiology. New York: John Wiley pp. 72-73.

  
 

Hotta Y, Tanaka T, Takaoka H, Takeuchi Y, Konnai M (1997). New physiological effects of 5-aminolevulinic acid in plants: the increase of photosynthesis, chlorophyll content, and plant growth. Bioscience, Biotechnology and Biochemistry 61:2025-2028.
Crossref

  
 

Hussein MM, Abd El-Khader A, El-Faham SY (2019). Mineral status and lupine yield responses to ascorbic acid spraying and irrigation by diluted sea water. Asian Journal of Biology 8:1-13.
Crossref

  
 

Jampílek J, Kráľová K (2017). Nanomaterials for delivery of nutrients and growth-promoting compounds to plants. Nanotechnology: An Agricultural Paradigm 9:177-226.
Crossref

  
 

Kamle M, Devi Sh, Mahato DK, Soni R, Kumar P, Tripathi V (2020). Nanotechnological interventions for plant health improvement and sustainable agriculture. Recent Patents on Food, Nutrition and Agriculture 10:168-181.
Crossref

  
 

Kamran M, Parveen A, Ahmar S, Malik Z, Hussain S, Chattha M, Saleem M, Adil M, Heidari P, Chen J (2020). An overview of hazardous impacts of soil salinity in crops, tolerance mechanisms and amelioration through selenium supplementation. International Journal of Molecular Sciences 21:1-27.
Crossref

  
 

Khan NA, Nazar R, Anjum NA (2009). Growth, photosynthesis and antioxidant metabolism in mustard (Brassica juncea L.) cultivar differing in ATP-sulfurylase activity under salinity stress. Scientia Horticulturae 122:455-460.
Crossref

  
 

Kumar KA, Sugunamma V, Sandeep N (2020). Influence of viscous dissipation on MHD flow of micropolar fluid over a slendering stretching surface with modified heat flux model. Journal of Thermal Analysis and Calorimetry 139:3661-3674.
Crossref

  
 

Latif M, Akram, NA, Ashraf M (2016). Regulation of some biochemical attributes in drought-stressed cauliflower (Brassica oleracea L.) by seed pre-treatment with ascorbic acid. Journal Horticulture Science Biotechnology 91:129-137.
Crossref

  
 

Liu D, Hu L, Ali B, Yang A, Wan G, Xu L, Zhou W (2016). Influence of 5-aminolevulinic acid on photosynthetically related parameters and gene expression in Brassica napus L. under drought stress. Soil Science and Plant Nutrient 62:254-262.
Crossref

  
 

Liu L, Nguyen NT, Ueda A, Saneoka H (2014). Effects of 5-aminolevulinic acid on swiss chard (Beta vulgaris L. subsp. cicla) seedling growth under saline conditions. Frontiers in Plant Science 74:219-228.
Crossref

  
 

McCue KF, Hanson AD (1990). Drought and salt tolerance: Towards understanding and application. Trends Biotechnology 8:358-362.
Crossref

  
 

Memon SA, Hou X, Wang LJ (2010). Morphological analysis of salt stress response of pak Choi. EJEAFCHe 9:248-254.

  
 

Naeem MS, Rasheed M, Liu D, Jin ZL, Ming DF, Yoneyama K, Takeuchi Y, Zhou WJ (2011). Role of 5-aminolevulinic acid on growth, photosynthetic parameters and antioxidant enzyme activity in NaCl-stressed Isatis indigotica. Fort. Acta Physiologiae Plantarum 518:517-528.
Crossref

  
 

Naeem MS, Warusawitharana H, Liu H, Liu D, Ahmad R, Waraich EA (2012). 5-Aminolevulinic acid alleviates the salinity-induced changes in Brassica napus as revealed by the ultrastructural study of chloroplast. Plant Physiololgy and Biochemistry 57:84-92.
Crossref

  
 

Nassar MA, Azoz DN, Wessam S, Serag El-Din M (2019). Improved growth and productivity of basil plants grown under salinity stress by foliar application with ascorbic acid. Middle East Journal of Agriculture 8:211-225.

  
 

Nassar R, Nermeen T, Reda F (2016). Active yeast extract counteracts the harmful effects of salinity stress on the growth of leucaena plant. Scienta Horticulturae 201:61-67.
Crossref

  
 

Nazar R, Iqbal N, Syeed S, Khan NA (2011). Salicylic acid alleviates decreases in photosynthesis under salt stress by enhancing nitrogen and sulfur assimilation and antioxidant metabolism differentially in two mung bean cultivars. Journal of Plant Physiology 168:807-815.
Crossref

  
 

Nishihara E, Kondo K, Masud Parvez M, Takahashi K, Watanabe K, Tanaka K (2003). Role of 5-aminolevulinic acid (ALA) on active oxygen-scavenging system in NaCl-treated spinach (Spinacia oleracea). Plant Physiology 160:1085-1091.
Crossref

  
 

Prakash L, Dutt M, Prathapasenan G (1988). NaCl alters contents of nucleic acids, proteins, polyamines and the activity of agmatine deiminase during germination and seedling growth of rice (Oryza sativa L.). Australia and Plant Physiology 15:769-776.
Crossref

  
 

Prasad R, Kumar V, Prasad KS (2014). Nanotechnology in sustainable agriculture: Present concerns and future aspect. African Journal of Biotechnology 13:705-713.
Crossref

  
 

Radić S, Pavlica M, Babić M, Pevalek-Kozlina B (2009). Cytogenetic effects of osmotic stress on the root meristem cells of Centaurea ragusina L. Environmental and Experimental Botany 54:213-218.
Crossref

  
 

Rafaqat A, Ali G, Islam F, Muhammad F, Theodore M, Zhou M (2015). Physiological and molecular analyses of black and yellow seeded Brassica napus regulated by 5-aminolivulinic acid under chromium stress. Journal of Plant Physiology and Biochemistry 94:130-143.

  
 

Rastogi D, Kumar T, Saurabh Y, Chauhan D, Živčák M, Ghorbanpour M, El-Sheery N, Brestic M (2019). Application of silicon nanoparticles in agriculture. PMC National Library of Medicine National Institutes of Health 9:90-102.
Crossref

  
 

Reda M (2007). Morphological, anatomical and physiological studies on Senna occidentalis (L.) Link plants grown under stress of different levels of salinity in irrigation water. Journal Agriculture Science, Mansoura University 32:8301-8314.

  
 

Saha P, Chatterjee P, Biswas AK (2010). NaCl pre-treatment alleviates salt stress by enhancement of antioxidant defense system and osmolyte accumulation in mungbean (Vigna radiata L. Wilczek). Indian Journal of Experimental Biology 48:593-600.

  
 

Sairam RK, Tyagi A (2004). Physiology and molecular biology of salinity stress tolerance in plants. Current Science 86:407-421.

  
 

Sajid M, Mustafa A, Niamat B, Ahmad Z, Yaseen M, Kamran M, Rafique M, Ahmar S, Chen J (2020). Alleviation of salinity-induced oxidative stress, improvement in growth, physiology and mineral nutrition of canola (Brassica napus L.) through calcium-fortified composted animal manure. Sustainability 12:1-17.
Crossref

  
 

Shahzad H, Ullah S, Iqbal M, Bilal HM, Shah GM, Ahmad S, Zakir A, Ditta A, Farooqi MA (2020). Exogenous ascorbic acid induced chilling tolerance in tomato plants through modulating metabolism, osmolytes, antioxidants, and transcriptional regulation of catalase and heat shock proteins. Plants 9:1-21.
Crossref

  
 

Shalata A, Mittova V, Volokita M, Guy M, Tal M (2001). Response of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii to salt-dependent oxidative stress: the root antioxidative system. Physiology Plant 112:487-494.
Crossref

  
 

Shang Y, Hasan K, Golam J, Li M, Yin H, Zhou J (2019). Applications of nanotechnology in plant growth and crop protection. Molecules 24:1-24.
Crossref

  
 

Sharma A, Shahzad B, Kumar V, Kohli SK, Sidhu GPS, Bali AS, Handa N, Kapoor D, Bhardwaj R, Zheng B (2019). Phytohormones regulate accumulation of osmolytes under abiotic stress. Biomolecules 9:1-36.
Crossref

  
 

Shedeed Sh, Fawzy Z, El-Bassiony A (2018). Nano and mineral selenium foliar application effect on pea plants (Pisum sativum L.). Bioscience Research 15:645-654.

  
 

Shi Y, Wang Y, Flowers T, Gong H (2013). Silicon decreases chloride transport in rice (Oryza sativa L.) in saline conditions. Journal of Plant Physiology 170:847-853.
Crossref

  
 

Sonkaria S, Ahn SH, Khare V (2012). Nanotechnology and its impact on food and nutrition. Recent Patents on Food, Nutrition and Agriculture 4:8-18.
Crossref

  
 

Tabur S, Demir K (2010a). Role of some growth regulators on cytogenetic activity of barley under salt stress. Plant Growth Regulators 60:99-104.
Crossref

  
 

Tabur S, Demir K (2010b). Protective roles of exogenous polyamines on chromosomal aberrations in Hordeum vulgare exposed to salinity. Biologia 65:947-953.
Crossref

  
 

Tabur S, Demir K (2009). Cytogenetic response of 24-epibrassinolide on the root meristem cells of barley seeds under salinity. Plant Growth Regulators 58:119-123.
Crossref

  
 

Taïbi F, Taïbi K, Belkhodja M (2013). Salinity effects on the physiological response of two bean genotypes Phaseolus vulgaris L. Arab Gulf Journal of Scientific Research 31:90-98.

  
 

Tang XQ, Wang Y, Xiao YH (2017a). role of 5-aminolevulinic acid on growth, photosynthetic parameters and antioxidant enzyme activity in NaCl-stressed Isatis indigotica Fort. Russian Journal of Plant Physiology 64:198-206.
Crossref

  
 

Tang Y, Liu K, Zhang J, Li X, Xu K, Zhang Y (2017b). JcDREB2, a physic nut AP2/ERF gene, alters plant growth and salinity stress responses in transgenic rice. Frontiers in Plant Science 8:306-324.
Crossref

  
 

Watanabe K, Tanaka T, Kuramochi H, Takeuchi Y (2000). Improving salt tolerance of cotton seedling with 5-aminolevulinic acid. Plant Growth Regulators 32:97-101.
Crossref

  
 

Wu W, Elsheery N, Wei Q, Zhang L, Huang J (2011). Defective etioplasts observed in variegation mutants may reveal the light independent regulation of white/yellow sectors of Arabidopsis leaves. Journal of Integrative Plant Biology 53:846-857.
Crossref

  
 

Wu Y, Jin X, Liao W, Hu L, Dawuda M, Zhao X, Tang Z, Gong T, Yu J (2018). 5-aminolevulinic acid (ALA) alleviated salinity stress in cucumber seedlings by enhancing chlorophyll synthesis pathway. Frontiers in Plant Science 9:635-646.
Crossref

  
 

Wu J, Zhao Q, Wu G, Yuan H, Ma Y, Lin H, Pan L, Li S, Sun D (2019a). Comprehensive analysis of differentially expressed unigenes under NaCl stress in flax (Linum usitatissimum L.) using RNA-Seq. International Journal of Molecular Science 20:2-8.

  
 

Wu Y, Liao W, Dawuda M, Hu L, Yu J (2019b). 5-Aminolevulinic acid (ALA) biosynthetic and metabolic pathways and its role in higher plants: A review. Plant Growth Regulators 87:357-374.
Crossref

  
 

Yu J, Zhao W, Tong W, He Q, Yoon M, Li F, Choi B, Heo E, Kim K, Park Y (2019). Genome-wide association study reveals candidate genes related to salt tolerance in rice (Oryza sativa) at the germination stage. International Journal of Molecular Science 19:31-45.
Crossref

  
 

Zedan A, Omar S (2019). Nano Selenium: Reduction of severe hazards of atrazine and promotion of changes in growth and gene expression patterns on Vicia faba seedlings. African Journal of Biotechnology 18:502-510.
Crossref

  
 

Zhang CP, He P, Wei PX, Du DD, Yu ZL (2011). Effect of exogenous 5- aminolevulinic acid on seed germination and antioxidase activities of Perilla frutescens seedlings under NaCl stress. Chinese Traditional and Herbal Drugs 42:1194-1200.

  
 

Zhang H, Sonnewald U (2017). Differences and commonalities of plant responses to single and combined stresses. The Plant Journal 90:839-855.
Crossref

  
 

Zhang Y (2013). Biological role of ascorbate in plants (Chapter 2). Springer Briefs in Plant Science 7-18.
Crossref

  

 




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