Caryologia. International Journal of Cytology, Cytosystematics and Cytogenetics 74(1): 33-41, 2021 Firenze University Press www.fupress.com/caryologia ISSN 0008-7114 (print) | ISSN 2165-5391 (online) | DOI: 10.36253/caryologia-783 Caryologia International Journal of Cytology, Cytosystematics and Cytogenetics Citation: S. Farahnaz Talebi, M. Jamal Saharkhiz, M. Jafarkhani Kermani, Y. Sharafi (2021) Polyploidy increases tol- erance to salt stress in Anise hys- sop (Agastache foeniculum [Pursh.] Kuntze). Caryologia 74(1): 33-41. doi: 10.36253/caryologia-783 Received: December 18, 2019 Accepted: April 26, 2021 Published: July 20, 2021 Copyright: © 2021 S. Farahnaz Talebi, M. Jamal Saharkhiz, M. Jafarkhani Kerm- ani, Y. Sharafi. This is an open access, peer-reviewed article published by Firenze University Press (http://www. fupress.com/caryologia) and distributed under the terms of the Creative Com- mons Attribution License, which per- mits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Data Availability Statement: All rel- evant data are within the paper and its Supporting Information files. Competing Interests: The Author(s) declare(s) no conflict of interest. Polyploidy increases tolerance to salt stress in Anise hyssop (Agastache foeniculum [Pursh.] Kuntze) Seyyedeh Farahnaz Talebi1, Mohammad Jamal Saharkhiz2, Maryam Jafarkhani Kermani3, Yavar Sharafi4,* 1 Department of Horticultural Sciences, Faculty of Agriculture, Shiraz University, Shiraz, Iran 2 Medicinal Plants Processing Research Center, Shiraz University of Medical Sciences, Shi- raz, Iran 3 Department of Tissue and Cell Culture, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran, P.O. Box: 31535-1897 4 Department of Horticultural Sciences, Shahed University, Tehran, Iran *Corresponding author. E-mail, y.sharafi@shahed.ac.ir Abstract. Salinization is one of the most serious environmental problems in agricul- ture. Polyploid induction could increase abiotic stress tolerance in plants. In this study, the effect of different NaCl concentrations (0, 50, 100 and 150 mM) was studied on dip- loid (2x) and tetraploid (4x) plants of anise hyssop (Agastache foeniculum) in vitro. The results indicated that salt stress reduced survival percentage, stem length, and leaf and shoot number in both tetraploid and diploid plants. However, tetraploid plants had better survival and growth rates compared with diploids. The highest antioxidant enzyme activ- ity was observed in the plants treated with 100 mM NaCl, while increasing the salinity to 150 mM NaCl lowered the activity of antioxidant enzymes significantly. Essential oil con- tent in diploid and tetraploid plants decreased as the concentration of NaCl was elevated. Also, salinity stress affected the chemical composition of essential oil in both diploid and tetraploid plants. In conclusion, the results indicated that tetraploids showed greater tol- erance to salt stress compared with diploids, and polyploidy might be a useful breeding method in anise hyssop to amplify its tolerance to salt stress under soil salinity. Keywords: anise hyssop, essential oil, polyploidy, salt tolerance. Abbreviations: EO - essential oil; ROS - reactive oxygen species; O2– - super- oxide radicals; H2O2 - hydrogen peroxide; OH• - hydroxyl radicals; SOD - superoxide dismutases; CAT - catalases; APX - ascorbate peroxidases; GST - glutathione S-transferases; GPX - glutathione peroxidases. INTRODUCTION Anise hyssop (Agastache foeniculum) from the family Lamiaceae is as an important medicinal plant. The essential oil (EO) of anise hyssop is mainly 34 Seyyedeh Farahnaz Talebi, Mohammad Jamal Saharkhiz, Maryam Jafarkhani Kermani , Yavar Sharafi biosynthesized in its leaves and flowers which contain significant amounts of methyl chavicol. In medicinal plants, secondary metabolites are fundamentally pro- duced by genetic pathways, although environmental fac- tors also strongly influence their biosynthesis (Zhang, 2015). Biotic and abiotic environmental factors, spe- cifically salinity and drought conditions, affect growth parameters, medicinal plants’ survival, and their essen- tial oil yield (Heidari et al. 2008, Heydari et al. 2020, sharafi et al. 2017). Podda et al. (2013) stated that salin- ity is one of the most important abiotic stresses in agri- culture affecting the plant growth and agricultural pro- ductivity. High levels of soil salinity have toxic effects on the absorption of nutrients from the root system in the plant through osmotic processes which, in turn, reduc- es essential oil production and modifies their composi- tion in medicinal and aromatic species (Sarmoum et al. 2019). It is essential to determine the environmental factors under which medicinal and aromatic plants offer higher yields and improve quality. High salinity can dis- turb essential physiological processes due to factors such as water deficits, nutritional imbalance, hyper-osmotic stress, ion imbalance, metabolic disorders, and appear- ance or disappearance of some proteins which may eventually lead to death (Meng et al. 2016). These culmi- nate in reduction of growth, yield, and quality of plants. Therefore, the over expression of genes encoding the bio- synthetic enzymes may increase proline concentration in plant cells (Apse and Blumwald, 2002; Rabiei et al. 2011). On the other hand, oxidation reactions from cho- line to glycine betaine enhance plant resistance to salin- ity (Apse and Blumwald, 2002). Saline stress increases production of reactive oxygen species (ROS) including superoxide radicals (O2 –), hydrogen peroxide (H2O2), and hydroxyl radicals (OH•) which cause oxidative dam- age to different cellular components including mem- brane lipids, proteins, and nucleic acids (Hasanuzzaman et al., 2020). Plants use low molecular mass antioxidants such as ascorbic acid, superoxide dismutase (SOD), cata- lases (CAT), ascorbate peroxidases (APX), glutathione S-transferases (GST) and glutathione peroxidases (GPX) to scavenge ROS (Apse and Blumwald, 2002). Several mechanisms have been developed in plants under salt stress, one of which is the control of ion movement across tonoplasts to maintain a low Na+  concentration in the cytoplasm (Brini and Masmoudi, 2012). Apse and Blumwald (2002) showed that plants could use several strategies to keep a high K+/Na+ ratio in the cytosol to control the entry of Na+ ions into and out of cells. Polyploidy has been used in horticulture as a breed- ing tool to improve morphological, physiological, and physio-biochemical characteristics (Kermani et al. 2003, Talebi et al. 2017). Some polyploids are tolerant to envi- ronmental stresses such as drought (Li et al. 2009), heat (Zhang et al. 2010), nutrient-poor soils (Kolar et al. 2014), and salinity (Mouhaya et al. 2010, Podda et al. 2013). This increased tolerance may be related to dupli- cate gene expression or simply associated with evolution- ary processes. Meanwhile, few studies have specifically reported the relationship between ploidy level and abi- otic tolerance in plants (Podda et al. 2013). Polyploidy plants had enabled better adaptation to some detrimen- tal environmental conditions (Parisod et  al., 2010) and enhanced tolerance to a range of abiotic stresses and biotic, souch as soil salinity (Chao et al., 2013). Poly- ploidy improved resistance to salt stress in rice (Tu et al., 2014), and citrus tetraploid genotypes (Mouhaya et al., 2010). Salt resistance in polyploidy plants was related to reduced sensitivity of plasma membrane K+- permeable channels in the meristem root zone and increased sensi- tivity of Ca2+-permeable channels in the elongation and mature root zones to H2O2 (Liu et al., 2019). Omami et al. (2006) reported that CAT is one of the major antioxidant enzymes which breaks down H2O2 to oxygen and water. Chao et al. (2013) reported that autopolyploidy induces resistance to salinity and may represent an adaptive outcome of the enhanced K+ accumulation of plants with higher ploidy. Bagheri and Mansouri (2014) found that polyploidy raised protein and sugar content under saline conditions. In another study, Munns (2002) suggested that the soil salt reduced water absorption and growth rate which could be due to loss of cellular turgor pressure and hormonal signals produced by the roots. When the amounts of salt rise to toxic levels in the plant cell, it is transported to leaves, which results in reduction of the photosynthetic leaf area and premature leaf senescence (Munns, 2002). In salt- tolerant plants, there is a low rate of Na+ and Cl- trans- port to leaves where these ions are sorted in vacuoles in a way to prevent their build-up in cytoplasm, cell walls, and avoid salt toxicity (Greenway and Munns, 1980). Aromatic plants that are salt stress tolerant should also maintain their growth and secondary metabolite production (Aziz et al. 2008; Ahmadi et al. 2013). Taba- tabaie et al. (2007) showed that abiotic stress changed the quantity and quality of essential oil and thus reduced the market value of the Mentha piperita plants. Aziz et al. (2008) reported that essential oil yields of Peppermint (Mentha piperita L.), Pennyroyal (Mentha pulegium L.), and Apple mint (Mentha suaveolens Ehrh.) diminished under salt stress, compared with controls. Currently, there is no information available regard- ing the effects of salt stress on induced polyploid anise hyssop plants compared with diploid parents. Accord- 35Polyploidy increases tolerance to salt stress in Anise hyssop (Agastache foeniculum [Pursh.] Kuntze) ingly, the purpose of this study was to compare the effect of salt stress on tetraploid and diploid plants by measuring growth rate, antioxidant enzyme activity, and essential oil content of this plant. MATERIALS AND METHODS The tetraploid (2n=4x=36) and diploid (2n=2x=18) explants of anise hyssop (Agastache foeniculum [Pursh.] Kuntze) that were used in this study were obtained from our previous study (Talebi et al. 2017). These plants were grown under greenhouse conditions (16/8 h light/dark cycle, 21°C and 15°C day/night temperature and 60 % humidity). The tetraploid and diploid explants were cul- tured on an Murashige and Skoog medium medium contain- ing 0.6 mg/l 6-benzylaminopurine (BAP) and 0.2 mg/l 1-naphthaleneacetic acid (NAA) and sub-cultured every four weeks (Fig. 1). The cultures were incubated under controlled conditions of temperature (25±2°C), light (2000- 2500 lux for 16 h/d provided by fluorescent tubes), and 60-70% humidity. Adaptation of micropropagated plantlets was car- ried out in pots filled with sand and vermiculite (1:1, v:v) in a greenhouse. Initially, all plants were irrigated with a nutrient solution with half strength Hoagland’s for 4 weeks and then irrigated every 3 days with full-strength Hoagland’s solution containing salt (NaCl) at 0, 50, 100, and 150 mM (Hoagland and Arnon 1950). The cultures were then incubated under a photoperiod of 16 hr light and 8 hr dark, light intensity of 2000- 2500 lux, and at a temperature of 21°C day and 15°C night and 60% humidity. Morphological traits such as survival per- centage and plant growth (leaf and shoot number, stem length) were measured. Essential oil content was measured after three months. This content was determined using hydro-dis- tillation by placing the aerial parts of dried plants (10 g) in a modified Clevenger apparatus for 3 hours (Ozturk et al. 2004) whereafter the essential oil content (w/w %) was calculated. The composition of essential oil was ana- lyzed by GC-MS (Agilent Technologies 5977A GC/MSD System, USA) analysis, using a fused silica capillary HP-5 column (30 m × 0.32 mm i.d.; film thickness 0.25 µm with an Agilent gas chromatograph series 7890A equipped with a flame ionization detector (FID). The injector and detector temperatures were kept at 250°C and 280°C, respectively. Nitrogen was used as carrier gas at a flow rate of 1 ml/min; oven temperature program was 60210°C at the rate of 4°C.min, which was then pro- grammed to 240°C at the rate of 20°C.min, and finally, held isothermally for 8.5 min. The split ratio was 1:50 and the GC-MS analysis was carried out by Agilent gas chromatograph equipped with fused silica capillary HP- 5MS column (30 m × 0.25 mm i.d.; film thickness 0.25 µm) coupled with 5975C mass spectrometer. Helium was used as carrier gas with an ionization voltage of 70 eV. Ion source and interface temperatures were 230°C and 280°C, respectively. Finally, the mass ranged from 45 to 550 amu (atomic mass unit). The activity of antioxidant enzymes such as CAT and POD was measured accord- ing to the method of Chance and Maehly (1955). Experi- ments were analyzed in a factorial design based on a completely randomized design. Analysis of variance was performed and comparisons of means were conducted using Duncan’s multiple range test (DMRT) at the 0.01 or 0.05 levels of probability. All analyses were performed using SAS and MSTATC software. RESULTS It was observed that the survival percentage of dip- loid and tetraploid plants decreased with elevation of NaCl concentrations. The diploids survived at 100mM NaCl, while tetraploids were able to survive at a higher salt concentration of 150 mM (Fig. 2, 3). Diploid plants did not tolerate 150 mM NaCl and died under these con- ditions, while 21% tetraploid plants survived at 150 mM NaCl. The results revealed that stem length, leaf and shoot number significantly declined in tetraploid and diploid plantlets of anise hyssop under salt stress. In diploids and tetraploids, the highest stem length and number Figure 1. Micropropagation of tetraploid and diploid plants of anise hyssop. 36 Seyyedeh Farahnaz Talebi, Mohammad Jamal Saharkhiz, Maryam Jafarkhani Kermani , Yavar Sharafi of leaves and shoots was observed in the control, while the lowest stem length and leaf and shoot number was detected at 150 mM NaCl (Figs. 4, 5, 6). Th e results indicated that CAT activity was enhanced at 50 and 100 mM NaCl treatments in diploids and tetraploids of Anise hyssop. Although the CAT activity decreased at 150 mM NaCl in both diploids and tetra- ploids, it remained higher in 150 mM NaCl treatment compared with the control (Table 1). Fig 8? illustrates that the plants treated with 100 mM NaCl had the high- est POD activity. However, the activity of antioxidant enzymes was higher in the tetraploid plants (Table 1). Th e essential oil content extracted from the diploid and tetraploid plants is displayed in Fig. 7. Th e results indicated that salinity reduced the essential oil con- tent in diploid and tetraploid plants as compared with essential oil produced in control plants. Th e maximum essential oil percentages in diploid (1.37%) and tetraploid (2.82%) plants were obtained from control plants. Th e minimum essential oil content was observed in 150 mM NaCl in diploid (0.71%) and tetraploid (1.97%) plants. Th e reductions in essential oil content were greater in diploids than in tetraploids under salt conditions. Th e results of components identifi ed through gas chromatography (GC/MS) in diploid and tetraploid plants are reported in Table 2. In tetraploid plants, with an increase in salt stress, the percentage of methyl chavi- col, anisaldehyde, and β-caryophyllene rose, while the percentage of α-Th ujene, Terpinene, and Germacrene D did not change. However, several other constituents decreased at the maximum salt concentration tested. Figure 2. Eff ect of salt stress on survival percent in diploid and tetraploid plants. Figure 3. Eff ect of salt stress on survival of diploid and tetraploid plants. Figure 4. Eff ect of salt stress on leaf number in diploid and tetra- ploid plants. Figure 5. Eff ect of salt stress on shoot number in diploid and tetra- ploid plants. Figure 6. Eff ect of salt stress on stem length in diploid and tetra- ploid plants. 37Polyploidy increases tolerance to salt stress in Anise hyssop (Agastache foeniculum [Pursh.] Kuntze) Data revealed that the percentage of all chemical constit- uents of essential oil in the diploid plants decreased with elevated NaCl concentration. In contrast, the changes in the essential oil constituent levels in the tetraploid plants were relatively lower than in diploid plants under the salt stress conditions. DISCUSSION According to the results of this study, salt stress reduced survival percentage and plant growth in tetra- ploid and diploid plants. Th e main reason for this reduc- tion may be attributed to suppression of growth due to changes in developmental pathways under saline condi- tions. Salt stress reduced leaf growth and leaves exhib- ited wilting and chlorosis in diploid plants (Meng et al. 2011, Wang et al. 2013). Studies of Munns (2002) showed that plants treated under saline conditions had decreased water availability as well as sodium chlo- ride toxicity. Munns (2002) reported that salt-induced drought stress decreased the ability of the plant to absorb water and nutrients from the soil. Th e ability of plant cells to prevent Na+ transport into the growing tis- sues is critically important for maintaining metabolic processes during cell growth against the toxic eff ects of Na+ (Khorasaninejad et al. 2010). Khorasaninejad et al. (2010) reported that reduction in dry weight under salinity stress may be related to inhibition of hydrolysis of reserved foods and their translocation to the growing shoots. Similar decreases in growth parameters under salt stress were found in Salvia offi cinalis (Ben Taarit et al., 2009), thyme (Ezz El-Din et al. 2009), and basil (Said-Al Ahl and Mahmoud, 2010). In this study, the highest activity of antioxidant enzymes was observed in the plants treated with 100 mM NaCl. Increasing salinity beyond 100 mM NaCl sig- nifi cantly decreased the activity of antioxidant enzymes. Under salt stress conditions, reactive oxygen species (ROS) increase in chloroplasts (Meng et al. 2016). Gen- erally, salt stress results in an increased accumulation of ROS, such as H2O2, which may act as a signal molecule during stress conditions, which in turn induces gene expression encoding antioxidant enzymes (Breusegem et al. 2001). Tseng (2007) showed that salt stress tolerance in cabbage was enhanced with the production of cuprozinc- superoxide dismutase (Cu/Zn SOD) and catalase (CAT) in chloroplasts. Th e levels of plant hormones such as absci- sic acid (ABA) increase with high salt concentrations. ABA plays an important role in the mechanism of salt tolerance (Omami et al. 2006). Chao et al. (2013) found that autopolyploid plants have greater tolerance to salin- ity compared with diploids, which could be related to the enhanced K+ in the tetraploid plants. Meng et al. (2016) reported that salt stress facilitated increased H2O2 pro- duction, antioxidative enzymes, non-enzymatic antioxi- dants, and protein activity in tetraploid plants compared with diploid plants. On the other hand, gene expression and synthesis of plant hormones such as ABA grow under salt conditions (Riddle et al. 2010). Tu et al. (2014) found that tetraploid rice showed less root growth inhibition, accumulated a higher proline content and lower malondi- aldehyde (MDA) content, and exhibited a higher frequen- cy of normal epidermal cells than diploid rice did under salt conditions. Th e response of salt-tolerant organisms to salinity stress involves synthesis and accumulation of osmo-protective compounds, which are small, non-toxic compounds and can stabilize proteins, cellular structures and increase the osmotic pressure of the cell (Yancey et al. 1982). Th e high levels of proline and glycine betaine were correlated with improved tolerance to salinity (Apse and Blumwald, 2002). Similar results were observed in Melissa offi cinalis (Ozturk et al. 2004), Majorana hortensis (Shalan et al. 2006), Th ymus vulgaris (Najafi an et al. 2009), and Mentha pulegium (Queslati et al. 2010). Figure 7. Eff ect of salt stress on essential oil content in diploid and tetraploid plants. Table 1. Infl uence of diff erent concentrations of NaCl on selected antioxidant enzyme activity. Means with the same letters in each column are not signifi cantly diff erent at p < 0.01%. POD activity (µmol min-1 mg-1 protein) CAT activity (µmol min-1 mg-1 protein) Tetraploid (%) Diploid (%) Tetraploid (%) Diploid (%) Treatment 1.17 d 0.67d 2.31 d 1.07 d Control 1.33 b 0.84 b 2.43 b 1.24 b 50mM 1.62 a 1.16 a 2.50 a 1.34 a 100mM 1.21 c 0.71 c 2.37 c 1.14 c 150mM 38 Seyyedeh Farahnaz Talebi, Mohammad Jamal Saharkhiz, Maryam Jafarkhani Kermani , Yavar Sharafi Table 2. The effect of salt stress on essential oil composition in diploid and tetraploid plants. ** Means followed by the same letter in each row are not significantly different by LSD test (P< 0.05). Compounds Diploid NaCl (mM) Tetraploid NaCl (mM) control 50mM 100mM 150mM control 50mM 100mM 150mM α-Thujene 0.52a 0.51b 0.46c 0.44d 0.64a 0.61c 0.63b 0.64a α-Pinene 0.61a 0.59b 0.54c 0.52d 0.42a 0.41b 0.34c 0.27d Camphene 0.52a 0.50b 0.42c 0.39d 0.41a 0.41a 0.32b 0.22c 1 -Octen-3-ol 0.28a 0.17b 0.11c 0.09d 0.35a 0.31b 0.23c 0.22d 3-Octanone 0.37a 0.31b 0.22c 0.16d 0.14a 0.09b 0.00c 0.00c Sabinene 0.18a 0.14b 0.7c 0.00d 0.30a 0.23b 0.11c 0.02d β-Pinene 0.52a 0.44b 0.39c 0.21d 0.34a 0.26b 0.16c 0.06d 3-Octanol 0.04a 0.00b 0.00b 0.00b 0.10a 0.05b 0.00c 0.00c myrcene 0.04a 0.00b 0.00b 0.00b 0.06a 0.00b 0.00c 0.00c p-Cymene 0.63a 0.54b 0.49c 0.36d 0.84a 0.84a 0.75b 0.73c 1 ,8Cineole 3.24a 3.23b 3.18c 3.13d 3.05a 2.98b 2.87c 2.86d Limonene 2.69a 2.61b 2.56c 2.53d 3.02a 2.92b 2.94c 2.93d γ-Terpinene 0.37a 0.29b 0.15c 0.07d 0.32a 0.30b 0.29c 0.32d Trans-sabinene hydrate 0.04a 0.00b 0.00b 0.00b 0.04a 0.00b 0.00b 0.00b Cis-linalool oxide 0.08a 0.03b 0.00c 0.00c 0.05a 0.00b 0.00b 0.00b Trans-linalool oxide 0.05a 0.00b 0.00b 0.00b 0.06a 0.00b 0.00b 0.00b Linalool 0.55a 0.46b 0.43c 0.39d 0.61a 0.53b 0.47c 0.42d 1 -Octen-3-yl acetate 0.28a 0.19b 0.12c 0.09d 0.37a 0.31b 0.27c 0.26d α-Campholenal 0.02a 0.00b 0.00b 0.00b 0.02a 0.00b 0.00b 0.00b Camphor 0.04a 0.00b 0.00b 0.00b 0.07a 0.03b 0.00c 0.00c Trans-pinocarveol 0.27a 0.16b 0.08c 0.00d 0.30a 0.26b 0.18c 0.09d Trans-verbenol 0.04a 0.00b 0.00b 0.00b 0.02a 0.00b 0.00b 0.00b Pinocawone 0.03a 0.00b 0.00b 0.00b 0.03a 0.00b 0.00b 0.00b Borneol 0.52a 0.47b 0.42c 0.39d 0.28a 0.22b 0.19c 0.11d Terpinen-4-ol 0.02a 0.00b 0.00b 0.00b 0.05a 0.00b 0.00b 0.00b Methyl chavicol 78.77a 78.73b 78.68c 78.61d 81.11d 81.13a 81.13b 81.15a Piperitone 0.35a 0.26b 0.18c 0.03d 0.20a 0.14b 0.09c 0.00d Anisaldehyde 0.68a 0.54b 0.43c 0.34d 0.81b 0.80c 0.82ba 0.82a Bornylacetate 0.54a 0.47b 0.31c 0.28d 0.42a 0.37b 0.33c 0.26d β-Bourbonene 0.58a 0.56b 0.51c 0.45d 0.44a 0.40b 0.39c 0.37d β-Caryophyllene 0.72a 0.65b 0.41c 0.35d 0.61c 0.56d 0.63b 0.65a (E)-α-Bergamotene 0.05a 0.00b 0.00b 0.00b 0.03a 0.00b 0.00b 0.00b α-Humulene 0.04a 0.00b 0.00b 0.00b 0.02a 0.00b 0.00b 0.00b Germacrene D 0.24a 0.17b 0.00c 0.00c 0.30a 0.30a 0.29b 0.30a β-Selinene 0.02a 0.00b 0.00b 0.00b 0.03a 0.00b 0.00b 0.00b Valencene 0.02a 0.00b 0.00b 0.00b 0.03a 0.00b 0.00b 0.00b Bicyclogermacrene 0.20a 0.13b 0.00c 0.00c 0.21a 0.17b 0.08c 0.00d β-Bisabolene 0.02a 0.00b 0.00b 0.00b 0.01a 0.00b 0.00b 0.00b γ-Cadinene 0.04a 0.00b 0.00b 0.00b 0.02a 0.00b 0.00b 0.00b δ-Cadinene 0.04a 0.00b 0.00b 0.00b 0.06a 0.00b 0.00b 0.00b Spathulenol 0.33a 0.26b 0.23c 0.10d 0.45a 0.39b 0.36c 0.27d Caryophyllene oxide 0.30a 0.33b 0.25c 0.07d 0.48a 0.42b 0.31c 0.27d Globulol 1.45a 1.29b 1.13c 0.57d 1.72a 1.72a 1.67b 1.67b 39Polyploidy increases tolerance to salt stress in Anise hyssop (Agastache foeniculum [Pursh.] Kuntze) In our study, salinity reduced the essential oil con- tent in diploid and tetraploid plants compared with control plants. Data showed that treatment of tetraploid plants with different concentrations of NaCl had a dif- ferent response in terms of essential oil composition and production. In the diploid plants, the percentage of all chemical constituents of essential oil decreased with elevation of NaCl concentration. Aziz et al. (2008) found that essential oil synthesis in peppermint was very sen- sitive to stress. Further, Olfa et al. (2009) reported that essential oil content in marjoram (Origanum majorana) was reduced consistently with rising salt concentration. Salinity stress requires additional energy for plant cells; therefore, the amount of carbon for growth and flower initiation and essential oil synthesis is reduced during stress (Cheesman 1988). Reductions in essential oil con- tent could be due to decreases and changes in photosyn- thesis systems, essential oil biosynthesis and metabolic pathways (Aziz et al. 2008). However, Belaqziz et al. (2009) reported that oil content of Thymus maroccanus did not change with elevation of salt concentration. The results of the present investigation demonstrat- ed that anise hyssop is sensitive to salt stress. However, tetraploid plants were more resistant to salt stress than diploids. This was most probably due to the bigger cell size and fewer cells in the unit area in tetraploids com- pared with diploids (Comai, 2005). Thus, the responses of polyploid plants may differ in terms of morpho- logical, physiological, cellular and biochemical aspects (Shafieizargar et al. 2013). Riddle et al. (2010) reported that polyploidy induction increased chromosome num- ber, DNA content, gene expression, and enzyme activ- ity per cell. In addition, according to our previous study, the polyploid plants of anise hyssop had a larger sto- mata size and density, chloroplast number, morphologi- cal features (leaf length and width, distance between the nodes, leaf area, plant height, fresh and dry weight, and spikes length), and physio-biochemical characteristics (net photosynthesis, protein content, catalase and perox- idase activity) (Talebi et al. 2017). Thus, tetraploid plants could naturally tolerate salt stress better than diploid plants. According to Zhang et al. (2015), the response of the autotetraploid apple seedlings to salt stress was bet- ter than that of the diploid. Other reports have also sug- gested that polyploidy induction is an efficient way to increase abiotic stress tolerance in Spathiphyllum wallisii (Van Laere et al. 2010), Dendranthema nankingense (Liu et al. 2011), Brassica rapa L. (Meng et al. 2011), and Nico- tiana benthamiana (Deng et al. 2012). CONCLUSION According to the results obtained in the present study, salt stress reduced survival percentage, stem length, leaf and shoot number in tetraploid and dip- loid plants. The minimum growth rates were detected at 150 mM NaCl in both diploids and tetraploids. How- ever, since tetraploid plants had higher rates of growth compared with diploids, they showed a higher percent- age survival and growth compared with diploids under salt stress conditions. The highest activity of antioxidant enzymes for the two ploidy levels was observed in the plants treated with 100 mM NaCl. Tetraploid plants were more resistant to salt stress than diploids. Increasing salt concentration caused a significant reduction in the essential oil content in both tetraploid and diploid plants. Nonetheless, tetraploid plants showed different responses under different salinity stress conditions when the per- centage of essential oil composition was measured. 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