Abstract
Background: Halophytes possess efficient salt-tolerance mechanisms and can complete their life cycles in naturally saline soils with NaCl contents exceeding 200 mM. While a significant progress have been made in recent decades elucidating underlying salt-tolerance mechanisms, these studies have been mostly confined to the vegetative growth stage. At the same time, the capacity to generate high-quality seeds and to survive early developmental stages under saline conditions, are both critically important for plants. Halophytes perform well in both regards, whereas non-halophytes cannot normally complete their life cycles under saline conditions.
Scope: Research into the effects of salinity on plant reproductive biology has gained momentum in recent years. However, it remains unclear whether the reproductive biology of halophytes differs from that of non-halophytes, and whether their reproductive processes benefit, like their vegetative growth, from the presence of salt in the rhizosphere. Here, we summarize current knowledge of the mechanisms underlying the superior reproductive biology of halophytes, focusing on critical aspects including control of flowering time, changes in plant hormonal status and their impact on anther and pollen development and viability, plant carbohydrate status and seed formation, mechanisms behind the early germination of halophyte seeds, and the role of seed polymorphism.
Conclusion: Salt has beneficial effects on halophyte reproductive growth that include late flowering, increased flower numbers and pollen vitality, and high seed yield. This improved performance is due to optimal nutrition during vegetative growth, alterations in plant hormonal status, and regulation of flowering genes. In addition, the seeds of halophytes harvested under saline conditions show higher salt tolerance than those obtained under non-saline condition, largely due to increased osmolyte accumulation, more optimal hormonal composition (e.g., high gibberellic acid and low abcisic acid content) and, in some species, seed dimorphism. In the near future, identifying key genes involved in halophyte reproductive physiology and using them to transform crops could be a promising approach to developing saline agriculture.
Introduction
Coastal salt marshes and inland lakes contain significant amounts of salt, and inappropriate agricultural irrigation has also created large areas of saline environment (Galvan-Ampudia and Christa, 2011; Yuan et al., 2016a), contaminating both freshwater reservoirs and soil, particularly in arid and semiarid climatic zones (Rozema and Flowers, 2008). While soil salinization threatens the life cycle of most plants, approximately 1% of known terrestrial plant species flourish in saline conditions and are referred to as halophytes (Rozema and Flowers, 2008). The definition of a halophyte is somewhat subjective and varies in the literature. The most salt-tolerant halophytes can complete their life cycles in soils containing concentrations of NaCl, equal to, or even exceeding, that of seawater, e.g., 500 mM (Shabala, 2013; Song and Wang, 2015). However, the conventional definition used in the literature is that plants possess halophytism if they are able to survive and reproduce at NaCl concentrations exceeding 200 mM NaCl (Flowers and Colmer, 2008; Flowers et al., 2015; Santos et al., 2015; Yuan et al., 2016a). Based on mechanisms employed to deal with salinity load, halophytes can be divided into three categories: euhalophytes [which can actively compartmentalize toxic ions into their vacuoles, such as Suaeda salsa (Song et al., 2011; Li X. et al., 2012)], recretohalophytes [which directly secret salt outside by salt-secretory structures, e.g., Chenopodium quinoa (Shabala et al., 2014) and Limonium bicolor (Yuan et al., 2016a, 2018)], and pseudo-halophytes [which can exclude rather than absorb salt in their roots, such as Avicennia officinalis (Krishnamurthy et al., 2014)].
Heredity determines the geographical distribution of halophytes and non-halophytes and their responses to salinity (Ding et al., 2010a,b; Zhao K.F. et al., 2010; Guo et al., 2012a,b). The two groups show distinct differences in their maximum salt tolerance, and tend to form natural halophytic and non-halophytic populations in saline soil and non-saline alkali soil, respectively (Chen et al., 2010; Sui et al., 2010; Zhao S.Z. et al., 2010; Sun et al., 2013). Across the globe, halophytes are found in two typical kinds of saline environments: intertidal zones (Figures 1A,B) and inland saline soils (Figures 1C,D). They can grow to maturity and complete their life cycles in seawater or in highly saline soil (Chen et al., 2016); examples include mangrove (Tan et al., 2013), S. salsa (Song et al., 2008), and L. bicolor (Feng et al., 2014, 2015; Yuan et al., 2016b). In contrast, non-halophytes (such as most crop plants) are found only in non-saline soils. Though non-halophytes have also evolved various strategies to respond to salt stress, their growth declines sharply with increased NaCl concentration, whereas halophytes can benefit from higher salt concentrations, within reason, and show an optimal growth in the presence of significant amounts of NaCl: e.g., 200 mM for S. salsa (Yang et al., 2010) and Suaeda fruticosa (Khan et al., 2000), 150 mM for Chenopodium quinoa (Shabala et al., 2012), and 100 mM for Cakile maritima (Debez et al., 2004).
FIGURE 1
Typical saline habitats and halophytes across the globe. (A)Suaeda salsa grows well and forms a community in the intertidal zone, which is flooded regularly by seawater. The photograph was taken in the Yellow River Delta (N 37°25′; E 118°54′). (B) Mangroves grow in a sea water. The photograph was taken in the Dongzhai Harbor National Nature Reserve in Haikou (N 19°51′–20°1′; E 110°32′–110°37′). (C) Halophyte communities (Nitraria tangutorum and Alhagi sparsifolia) live in inland saline soil. The photograph was taken near Ebinur Lake (N 44°50′; E 82°45′) in North Xinjiang. (D) Photograph of Tamarix gallica in Luntai County (N 41°47′; E 84°14′) in South Xinjiang.
Numerous papers have been published dealing with various aspects of halophyte physiology (Shabala, 2013; Shabala et al., 2014; Song and Wang, 2015; Yuan et al., 2016b; Dassanayake and Larkin, 2017; Leng et al., 2018; Liu Q. et al., 2018), biochemistry and molecular biology (Kirch et al., 2000; Oh et al., 2015; Himabindu et al., 2016; Ozfidankonakci et al., 2016), ecology (Flowers and Colmer, 2008; Rozema and Flowers, 2008), and evolution (Flowers et al., 2010). Moreover, the practical use of halophytes in saline agriculture has been actively advocated (Ruan et al., 2010). All these papers have provided insightful suggestions about the mechanisms underlying the superior vegetative growth of halophytes under saline conditions.
While vegetative growth is important throughout the life of a plant, the capacity to set seeds in a hostile environment, such as saline soil, is equally critical for completing the life cycle. During the reproductive phase of plant growth, the meristem growth is almost always determinate, although the extent of determinacy depends on the inflorescence architecture (Kwiatkowska, 2008). Salinity stress strongly affects reproductive growth. Non-halophytes cannot naturally form seeds under saline conditions, and therefore fail to complete their life cycles. The reproductive growth is an essential stage of the plant life cycle, and early germination is equally important to establishing a population in a saline soil. While research into the effects of salinity on plant reproductive biology has been gaining momentum in recent years, it remains unclear whether the reproductive biology of halophytes differ from that of non-halophytes, and whether aspects of halophyte biology relevant to reproduction traits benefit from the presence of salt, like those related to vegetative growth. In the current review, we focus on the reproductive biology of halophytes and non-halophytes grown in saline environment.
Halophyte Reproductive Growth Under Saline Conditions
Being grown under high-salinity conditions, halophytes often show increased flower number, decreased sterility, and high seed quality (Guo et al., 2018). At the same time, salinity markedly reduces the flower and seed numbers of non-halophytes grown under same conditions (Sohrabi et al., 2008; Khan et al., 2015). This difference may be attributed to the limited resource allocation to flowers and developing seeds in non-halophytes, which results in a lower fertilization efficiency and less seed formation (Ledesma and Sugiyama, 2005; Guo et al., 2015).
Halophyte Flowering Time Benefits From Salinity
Halophytes typically show delayed flowering time under appropriate salinity. For example, treating plants of the euhalophyte S. salsa with 400 mM NaCl significantly delays the time of the first flowering as compared to that in S. salsa not subjected to saline treatment (Guo et al., 2018). In contrast, in non-halophytes, salt stress can often cause an early flowering (Lee et al., 1994) and abortion of flower buds (Sulpice et al., 2003). Halophytes can also undergo longer flowering periods (florescence) under saline as compared to non-saline conditions (Guo et al., 2018).
The underlying mechanisms controlling flowering time may be explained by genes, domestication, and sustainable productivity (Cockram et al., 2007), but whether these factors are affected by salt has been largely not investigated in halophytes. Some clues may be found in studies from Arabidopsis thaliana (Arabidopsis). It was shown that in this species, a good flower onset may benefit from the synthesis of the osmoregulator glycine betaine (Sulpice et al., 2003). Recent studies have investigated several genes related to the flowering time and their protein products. BFT (BROTHER OF FT AND TFL1), a floral repressor, participates in the inhibition of flowering under high salinity by competing with FT (FLOWERING LOCUS T) for binding to the FD transcription factor (Ryu et al., 2014). CDKG2 (CYCLIN-DEPENDENT KINASE G2) also plays a role in the control of flowering time under saline conditions (Ma et al., 2015). In addition, DDF1 (DWARF AND DELAYED-FLOWERING 1) is also involved in controlling late flowering, and its expression has been found to always accompany gibberellic acid (GA) synthesis (Magome et al., 2008).
Halophyte Anther and Pollen Maintain High Vitality in Saline Conditions Due to Altered Hormonal Status
Male reproductive development is extremely sensitive to salt stress as a result of a variety of factors associated with cytoskeletal alterations, tapetal irregularities, altered sugar utilization, and meiotic defects or abortion (Nico and Danny, 2014). Pollen development involves a series of stages, including specification of stamen identity, archesporial cell initiation, anther cell establishment, and meiosis (Zhao D. et al., 2003). In most species, the more mature pollen is, the more susceptible to abiotic stress it is. The anther and pollen vitality is an indispensable factor inducing sterility of non-halophytes under salinity stress. However, in S. salsa, the pollen number and pollen activity under saline conditions are higher than, or equal to those, under non-saline conditions, implying that high NaCl concentration markedly improves the reproductive capacity (Guo et al., 2018).
The mechanisms behind the decreased pollen vitality in non-halophytes under salinity stress remain to be identified. In rice and Arabidopsis, the plant hormone gibberellin (GA) participates in stamen development and tapetum function (Plackett et al., 2011), and is tightly intertwined with the secretion of callose and the synthesis and secretion of proteins and lipids for the pollen coat into the anther locule (Parish and Li, 2010). In addition to GA’s direct roles in the pollen mother cells, a loss of GA signal in the tapetum could indirectly block further development of the gametophytes. In a late stamen development, GA signal transduction acts partially through a jasmonic acid (JA) signal via regulation of JA biosynthesis (Plackett et al., 2011). However, the question of whether GA maintains a stable level in halophytes requires further investigation.
Salinity can also promote senescence and induce the production of two other stress-related hormones, ethylene and abcisic acid (ABA) (Nandwal et al., 2007), which can increase the number of aborted flowers. Reproductive growth is coordinated with vegetative growth based on the balance or homeostasis between ethylene and its receptors. When non-halophytes suffer from salinity stress, enhanced ethylene production leads to small rosettes and relatively early flowering, limiting energy and resource utilization for production of seeds (Cao et al., 2008). In halophytes, NaCl participates in the conversion of the precursor l-aminocyclopropane-l-carboxylic acid (ACC) to ethylene (Chrominski et al., 1986, 1988), and this process is enhanced under salinity stress in Allenrolfea occidentalis (Chrominski et al., 1989).
Halophyte Seed Formation and Yield Benefit From the Presence of Salt
A high positive correlation between leaf area and yield in the presence of salt exists in many crop species (Richards, 1992). NaCl treatment did not specifically decrease the development of reproductive organs in these species, and the production losses caused by high salinity may result from a reduction in flower production and/or a decrease in the flower fertility (Khatun and Flowers, 1995). Interestingly, our recent study found that the halophyte S. salsa produces a greater weight of seeds under high salinity than without saline treatment (Figure 2B; Guo et al., 2018); the same phenomenon has been observed in Suaeda corniculata (Yang et al., 2017). Similarly, in the halophyte C. maritima, seed production is stimulated by 50 to 100 mM NaCl as compared to a no-salt control treatment (Debez et al., 2004). Another halophyte, Salicornia bigelovii, displayed high seed yield and biomass production when irrigated with seawater (Glenn et al., 1998). Its increased seed yield was mainly due to increased flower number (Figure 2A) and reduced abortion ratio, which may be related to an increase in pollen vitality or stigma receptivity (Guo et al., 2015).
FIGURE 2
Flower number (A) and seed weights (B) of Suaeda salsa grown with NaCl were markedly enhanced compared with those of S. salsa grown without NaCl. Data shown in panel A are from our laboratory, bar = 1 mm. Seed photos in (B) originated (Guo et al., 2018), bar = 250 μm. Treatments were applied to the sand in which the seeds were sown and then continued until seed maturity. The seeds were watered twice a day with either a no-NaCl solution (Hoagland nutrient solution, as control) or 200 mM of NaCl dissolved in Hoagland nutrient solution.
Higher Carbohydrate Supply Improves Halophyte Reproductive Growth
In rice, agronomic characteristics related to grain yield show significant decreases at 50 mM NaCl, mainly due to limitation in the soluble carbohydrate translocation in spikelets and a significant inhibition of starch synthase activity (Abdullah et al., 2010). The situation is rather different in halophytes. The higher net photosynthetic rates and adequate carbon supply under saline conditions promote the reproductive growth of S. salsa and improve the flower fertility and seed size, compared to non-saline conditions (Guo et al., 2018). Thus, the superior reproductive growth of halophytes may be fundamentally attributable to their better resource allocation to flower and developing seeds, as compared with non-halophytes (Monteiro et al., 2003; Wang et al., 2017). In non-halophytes, maternal plants grown under saline conditions are unable to provide sufficient nutrients to the floral organ, leading to poor reproductive growth or reproductive failure.
Possible Genes Involved in Salt Response During Reproductive Growth
Plant reproductive development is controlled by multiple key regulators of floral identity. APETALA1 (AP1)/CAULIFLOWER (CAL) and LEAFY (LFY) are redundantly activated by FT [reviewed by Ruiz-García et al. (1997); Komeda (2004); Blázquez et al. (2006)]. FLC (FLOWERING LOCUS C, a negative regulatory gene) and FT (a positive regulatory gene) are two important flowering-related and determined genes that regulate the induction of flowering (Lee, 2011; Xu et al., 2012). Signaling by EXCESS MICROSPOROCYTES1/TAPETUM DETERMINANT1 (EMS1/TPD1) determines cell fate during plant sexual reproduction (Jia et al., 2008). Kim and Park (2007) have found that the transcription factor NTL8 (NTM1-Like’s 8) regulates flowering time under salt stress by downregulating FT. EARLY FLOWERING3 (ELF3) may also be involved in salt tolerance (Sakuraba et al., 2017). CYCLIN-DEPENDENT KINASE G2 (CDKG2) negatively regulates flowering time in response to salinity stress (Ma et al., 2015). However, it should be kept in mind that all this knowledge comes from studies on non-halophytes and thus, cannot be directly extrapolated to halophytes without additional studies.
Early Germination of Halophytes Under Saline Conditions
Seed formation is the end of a plant life cycle for annual plants, but also a new start for the next generation. From the perspective of generational reproduction and population formation, whether a new plant can survive, or a population can develop under saline conditions, is also determined by the germination process. In the next section, we therefore review current knowledge about the early survival of halophytes under saline conditions. Halophytes have evolved several strategies to cope with salinity during germination, including seed dormancy and heteromorphism, which are well described in previous reviews (Gul et al., 2013). Here we focus on the in-depth mechanisms that may explain the higher germination frequencies of halophytes as compared to non-halophytes under saline conditions.
Halophytes Show Higher Seed Germination Than Non-halophytes at High Salinity
Halophytes can germinate at salinities that kill 99% of non-halophytes (Manousaki and Kalogerakis, 2011), indicating that they are more salt tolerant at the germination stage (Ungar, 1978). Though the seeds of both halophytes and non-halophytes are able to imbibe water from a saline substrate in a similar manner, their behavior is otherwise strikingly different (Malcolm et al., 2003). To date, the seeds of at least ten species of halophytes have been shown to have higher germination percentages at slightly elevated salinity (0.5%, around 50–90 mM) than in distilled water (Qu et al., 2007; Zhang et al., 2012). In the halophyte C. maritima, NaCl inhibits germination only at concentrations higher than 200 mM, mainly through an osmotic effect (which is fully reversible if the seeds are transferred to water) (Debez et al., 2004). This is consistent with the reported beneficial effects of salt on halophyte vegetative growth (Flowers and Colmer, 2008).
The above notion is further illustrated by Figure 3, which shows the germination percentages of typical halophytes and non-halophytes under an NaCl concentration gradient and over time. Though beneficial effects of salt on germination have been reported for some halophytes (Debez et al., 2004), the majority of halophytes still show a decreased germination even under low concentration of salinity. Interestingly, the same salinity levels that can promoting vegetative growth [e.g., 200 mM in S. salsa in their natural habitats (Song et al., 2008) and 100 mM in Plantago crassifolia (Vicente et al., 2004)] suppress the seed germination of the same species. Spergularia marina even fails to germinate in the 2% NaCl treatment (Keiffer and Ungar, 1997). Thus, seed germination trait appears to be more sensitive to salt stress compared to vegetative growth. Nevertheless, halophytes still perform much better than non-halophytes at the germination stage. The germination percentages for non-halophytes decrease sharply at even low concentrations of NaCl, and some species fail to germinate above 100 mM NaCl. In contrast, halophytes maintain relatively high germination percentages under saline conditions, which decline slowly with increasing concentrations of NaCl. There is also a large genetic variability in germination ability/rate amongst halophytes grown under saline conditions. S. salsa maintains more than 90% of its germination percentage being exposed to 700 mM NaCl as compared to non-saline conditions (Figure 3A). S. salsa and Kalidium capsicum can rapidly reach more than 50% germination percentages in the first day, while other halophytes (Suaeda physophora and Haloxylon persicum) keep slowly increasing germination with time (Figure 3B). Comparative analysis of the time course of germination in 100–200 mM NaCl between halophytes and non-halophytes reveals that maximum germination of halophytes is achieved in the first 3 days.
FIGURE 3
Effect of increasing salinity on the germination percentage (A) and the time course of germination percentage under 100–200 mM NaCl (B) in halophytes and non-halophytes. Halophytes (solid lines): Suaeda japonica (Yokoishi and Tanimoto, 1994), Chloris virgata (Zhang et al., 2012), Kalidium capsicum (Tobe et al., 2000), Suaeda physophora (Song et al., 2005), Haloxylon persicum, Haloxylon ammodendron, Suaeda physophora (Song et al., 2005), and Suaeda salsa (Song et al., 2008). Non-halophytes (dotted lines): Cyperus conglomeratus (Keblawy et al., 2011), Oryza sativa (Jiang et al., 2013), Glycine max (Neves et al., 2005), Nigella sativa (Papastylianou et al., 2017), Cucumis melo (Sohrabikertabad et al., 2013), Impatiens balsamina (Jiang et al., 2014), and Arabidopsis thaliana (Wilson et al., 2014).
Another advantage of halophytes compared with non-halophytes is that the former can easily get recovery when transferred to water or solutions of lower salinity. Similar to germination, the recovery phenomenon also varies between different halophytes. Some species show high recovery rate of full germination (reach the control), such as Suaeda fruticosa (Khan and Ungar, 1997), P. crassifolia (Vicente et al., 2004) and Haloxylon recurvum (Khan and Ungar, 1996). Other halophytes exhibit low or little recovery, e.g., Zygophyllum simplex (Khan and Ungar, 1997).
Inhibition of halophyte germination under high salt concentration can be alleviated by mild saline pretreatment. For example, seeds of the halophyte Crithmum maritimum that are pretreated with 50 mM NaCl show a higher germination percentage and faster germination at 500 mM NaCl than untreated seeds (Meot-Duros and Magné, 2008), and the same phenomenon has been observed for Arthrocnemum macrostachyum and Sarcocornia fruticosa, in which osmotic pretreatments (with salts such as NaCl and MgCl2) promote germination, doubling the germination percentage under saline conditions compared to that of plants pretreated with distilled water (Pujol et al., 2000). The germination of halophyte P. crassifolia can reach the control after salt priming (Vicente et al., 2004). Further details and mechanisms behind this osmopriming effect in halophytes have been reviewed by Gul et al. (2013).
Halophytes Accumulate High Levels of Osmolytes During Seed Formation
Seeds of S. salsa harvested under saline conditions for three successive generations showed higher germination percentage than those harvested under non-saline conditions (Li W. et al., 2011; Guo et al., 2015), mainly as a result of the increased accumulation of osmoregulating substances (such as Na+, soluble sugars, and seed starch) in saline-grown seeds. These substances can reduce the water potential of seeds, thus contributing to quick imbibition under saline conditions.
The seed coat plays a significant role in maintaining seed viability under hypersaline conditions (Song et al., 2017). Lipid mobilization (as evidenced by a high transition ratio of phosphatidylglycerol to sulfoquinovosyldiacylglycerol) (Li X. et al., 2011), chlorophyll accumulation (Li X. et al., 2012; Zhou J.C. et al., 2016), soluble sugar accumulation, and sufficient storage of energy from photosynthesis in seeds (Rolletschek et al., 2003; Weber et al., 2005) all facilitate rapid germination under saline conditions (Song and Wang, 2015). Interestingly, in some halophytes, such as Haloxylon ammodendron and Suaeda physophora, chlorophyll is found in both dry and imbibed seeds (Zhang et al., 2010), regardless of whether they were treated with NaCl. In non-halophyte species, chlorophyll is found in some immature (Tasaki, 2008) but not in mature seeds. Increased chlorophyll concentration and oxygen production observed in the embryos of maturing S. salsa seeds may enhance the salt tolerance of the seeds and seedlings by changing the lipid composition of membranes (Zhou J.C. et al., 2016). It has also been suggested that nitrates provided to seeds by maternal plants may act as signaling molecules to enhance germination, enabling plant adaptation to saline environments (Song et al., 2016). It remains to be determined whether this observation can be extrapolated to all halophytes.
Phytohormones Participate in Halophyte Early Germination
Plant hormones play a pivotal role in seed germination and seed formation under saline conditions (Wang et al., 2015). Studies of non-halophytes have indicated that the reduced seed germination of Arabidopsis under saline conditions is caused by alterations in plant hormonal status (Jung and Park, 2011). Several genes are strongly induced by NaCl and appear to be involved in the regulation of seed germination through ABA–GA crosstalk during salt stress (Yuan et al., 2011). In particular, the ABA level increases several fold under saline conditions due to the dramatic increase in expression of the genes ABA-INSENSITIVE 3 (ABI3) and ABA-INSENSITIVE 5 (ABI5), which in turn activates the ABA signaling pathway, resulting in inhibition of seed germination (Piskurewicz et al., 2008). Meanwhile, REPRESSOR OF GA-LIKE2 (RLG2) transcription is also activated by salt or by the ABI3/ABI5 pathway, leading to inactivation of the GA signaling pathway, which further inhibits germination by blocking or limiting GA signaling (Yuan et al., 2011). In addition, NaCl has been observed to induce a negative regulation of GA and a positive biogenesis of ABA, which delays soybean seed germination (Shu et al., 2017). Mechanisms underlying osmopriming are also directly related to the ABA-GA network (Nakaune et al., 2012).
In addition, ethylene has been reported to promote seed germination of non-halophytes such as Arabidopsis and lettuce under salinity stress by upregulating the gene ETHYLENE-INSENSITIVE 3 (EIN3) (Verma et al., 1973; Lin et al., 2013). It has been verified in 22 species of halophytes that the application of exogenous ethylene significantly promotes seed germination (Khan et al., 2009), especially during later stages of seed germination (such as radicle breaching of the seed coat) (Li and Tran, 2017). Thus, it appears that the genes related to ABA, GA, and ethylene may coordinate and participate in the response of halophytes to salt that allows them to maintain high germination rates. In non-halophytes, salt induces an increase in ABA and a decrease in GA in the embryo, thus preventing germination. It may be envisaged that in halophyte seeds, comparatively less ABA is released, more GA accumulates, and more ethylene synthesis occurs during germination, explaining their stronger performance under saline conditions. However, as only few studies have been performed in halophytes to explain the molecular mechanisms underlying their good germination under saline conditions, this hypothesis requires further confirmation.
Ca2+ Is Involved in the Alleviation of Salt Toxicity
Salinity stress symptoms in plants can be ameliorated by exogenous Ca2+ application (Rengel, 1992b). Ca2+ participated in salt alleviation to some degree NaCl stress/toxicity for certain types of soils (Rengel, 1992a; Zhu, 2016), involved in enhancing seed germination of halophyte Kalidium caspicum (Tobe et al., 2002, 2004), facilitating radicle survival (Tobe et al., 2000) of K. caspicum and promoting polar vegetative growth (Mori and Schroeder, 2004) in non-halophyte species. The beneficial effects of Ca2+ treatment are mainly attributed to both reducing the rate of Na+ uptake by roots resulting from blockage of non-selective cation channels (NSCC) by millimolar Ca2+ concentrations (Demidchik and Tester, 2002), as well as to its ability to prevent NaCl-induced K+ leak via outward-rectifying channels (Shabala et al., 2007). Calcium also operates as a second messenger in both SOS (Mario and Zhu, 2009) and ABA signal pathway (Macrobbie, 2000; Sokolovski et al., 2008). Salt-tolerant genotypes appear to have a larger population of Ca2+-sensitive NSCC channels, compared with salt-sensitive counterparts such as barley (Chen et al., 2007). It remains to be answered if increased sensitivity to Ca2+ and/or its cross-talk with other signaling hormones may explain better performance of halophyte seeds under saline conditions.
Physiology and Metabolic Profiles of Halophyte Dimorphic Seeds
Another possible explanation for the better seed germination and population establishment of halophytes under saline conditions is the presence of seed dimorphism (Liu R. et al., 2018), a feature of some annual halophyte species that can help plants adapt to a changing environment (Song and Wang, 2015). For example, soft brown seeds (with a higher germination percentage) and hard black seeds (dormant) are found in S. salsa (Li W. et al., 2008; Song et al., 2008) and Suaeda acuminate (Wang et al., 2012). Green seeds (long-winged type) and yellow seeds (short-winged type) are found in Salsola komarovii (Takeno and Yamaguchi, 1991), and the former show higher germination than latter. The same seed dimorphism is observed in Salicornia europaea with large seeds (formed from large flowers) and small seeds (small flowers) (Ungar, 1979; Gasparri et al., 2016). In general, the larger seeds are the main type showing rapid germination in most halophytes with dimorphic seeds, such as Atriplex prostrata (Wertis and Ungar, 1986), Suaeda aralocaspica (Wang et al., 2008), S. salsa (Song and Wang, 2015), and S. europaea (Orlovsky et al., 2016).
In addition to differences in germination percentages and appearance, dimorphic seeds also show differences in physiology and metabolic profiles related to the underlying mechanisms of their different behaviors. For example, the seed coats of brown S. salsa seeds contain more phenolics than black seeds (Xu et al., 2016), while the latter contain abundant waxes that can form a protective layer to shield the embryo from ion toxicity under saline conditions (Song et al., 2016). The black seeds of S. corniculata have an annual dormancy/non-dormancy cycle, while the brown seeds remain non-dormant. Salinity stress induces dormancy in black seeds, but decreases the viability of brown seeds (Cao et al., 2012). Thus, black seeds can better maintain their viability under long-time salinity than brown seeds (Song et al., 2017). In ecological terms, the black seeds can serve as a seed bank for long-term preservation in saline environments. Another difference between the two types of dimorphic seeds lies in their levels of endogenous hormones, including indole-3-acetic acid (IAA), free zeatin riboside (ZR), and ABA, which in S. salsa are much greater in brown seeds than in black seeds (Wang et al., 2015). These characteristics may help the species to ensure seedling establishment and population succession in variable saline environments. Finally, though the seeds of S. corniculata are collected from two distant population (F0), the descendants (F1 and F2) still kept phenotypic differences regardless of whether grown in low or high salinity, indicating that the traits of dimorphic seeds are genetically determined and that soil salinity only plays an ecological role in influencing heteromorphic seed production (high salinity results in fewer seeds and more non-dormant brown seeds) (Yang et al., 2017). Recently, Xu et al. (2017) used dimorphic seeds of S. salsa to perform differential expression analysis by transcriptome and identified a series of genes related to embryo development, fatty acid metabolism, osmoregulatory substances, and plant hormones that may regulate seed dormancy or germination. In this context, experiments with dimorphic seeds are a highly promising tool to reveal the mechanism of seed germination competence in halophytes.
Perspectives
The reproductive growth and early germination are two critical processes that all plants must carry out, in order to survive under saline conditions, since only plants that can reproduce and germinate have a chance to complete their life cycle and establish descendant populations. Halophytes perform well in both respects under saline conditions. The current review mainly pay attention to the majority of halophytes that show promoted reproductive growth; however, it is worth noting that not all halophytes show the stimulation of growth or germination at low or moderate salinities, and some especial exceptions exist in different germplasms of the same species. For example, one accession (from Tabarka, Tunisian) of halophyte Cakile maritime behaves limited growth under 100 mM NaCl (Ben Amor et al., 2010), while other accessions of this species have enhanced biomass (Ksouri et al., 2007).
In the future, analyzing the in-depth mechanisms of salt tolerance in halophytes, isolating the unique genes involved, and creating new salt-tolerant plants by genetic engineering represents a promising approach toward developing saline agriculture. However, few reports have uncovered the key genes involved in the reproductive growth and early germination of halophytes. To date, certain salt-tolerance genes involved in vegetative growth have been cloned, and many key genes have been transformed into non-halophytes to verify their functions (Table 1). The maximum salt concentration tolerated by such transgenic plants was 400 mM (Li W. et al., 2011; Jha et al., 2012). Heterologous expression of halophytic salt-tolerance genes indeed improves the salt resistance of non-halophytes to a certain degree; however, no reports have demonstrated the stable expression of such genes in the next generation. The reason for this lies in a fact that the targeted traits were related to vegetative growth but not to seed formation or early germination. As a result, transgenic plants grew reasonably well in controlled condition but could not complete their life cycle in saline land.
Table 1
| Halophyte species | Gene | Probable function of gene product in salt tolerance | Effect when transformed into non-halophyte | Reference |
|---|---|---|---|---|
| Aeluropus littoralis | AlNHX | Vacuolar-type Na+/H+ antiporter | Transgenic tobacco overexpression lines had high salt tolerance (400 mM NaCl) and compartmentalized more Na+ in the roots to maintain a relatively high K+/Na+ ratio in the leaves. | Zhang et al., 2008 |
| Kalidium foliatum | KfVP1 | H+-pyrophosphatase | Transgenic Arabidopsis showed more vigorous growth than the wild type and accumulated more Na+ in the leaves in 120 mM NaCl | Yao et al., 2012 |
| Salicornia brachiata | SbASR-1 | Abscisic acid stress ripening-1 | Transgenic T0 tobacco seeds showed better germination and seedling growth than the wild type in 400 mM NaCl | Jha et al., 2012 |
| SbSOS1 | Plasma membrane Na+/H+ antiporter | Transgenic tobacco showed high seed germination and a high degree of salt tolerance in 200 mM NaCl | Yadav et al., 2012 | |
| SbpAPX | Peroxisomal ascorbate peroxidase | Transgenic tobacco showed enhanced salt and drought tolerance, with enhanced vegetative growth and higher germination rates than the wild type in 300 mM NaCl | Singh et al., 2014 | |
| Salsola soda | SsNHX1 | Putative vacuolar Na+/H+ antiporter | Transgenic Medicago sativa grew in high concentrations of NaCl (up to 400 mM) as a result of improved Na+ sequestration in vacuoles | Li W. et al., 2011 |
| Sesuvium portulacastrum | SpAQP1 | Aquaporin-related protein whose expression is induced by salt | Transgenic tobacco had increased activity of antioxidative enzymes, and enhanced seed germination and root growth in 200 mM NaCl | Chang et al., 2016 |
| Spartina alterniflora | SaVHAc1 | A vacuolar ATPase subunit c1 | Transgenic rice showed early stomata closure and increased K+/Na+ ratio | Niranjan et al., 2012 |
| Suaeda salsa | SsVP | Vacuolar H+-pyrophosphatase | Higher salt tolerance in transgenic Arabidopsis was related to higher activities of V-ATPase and V-PPase | Guo et al., 2006 |
| SsHKT1;1 | High-affinity K+ transporter | Transgenic Arabidopsis showed enhanced salt tolerance and increased shoot K+ concentration | Shao et al., 2014 | |
| Ss.sAPX | Stroma ascorbate peroxidase | Transgenic Arabidopsis overexpression lines had increased germination rates, cotyledon growth, and survival under saline conditions | Li K. et al., 2012 | |
| Suaeda asparagoides | SaDhn and SaRBP1 | Dehydrin and RNA-binding protein | Transgenic yeast overexpression lines showed enhanced tolerance to osmotic, freezing, and heat-shock stresses | Ayarpadikannan et al., 2012 |
| Zoysia matrella | ZmVP1 | A type I VP homolog gene induced by salt | Transgenic Arabidopsis grew more vigorously than the wild type in 300 mM NaCl because of higher activities of V-ATPase and V-PPase | Chen et al., 2015 |
Cloned halophyte genes related to salt tolerance and their effects after transformation into non-halophytes.
Therefore, to improve salinity tolerance in non-halophytes, key genes related to seed germination and formation should be also targeted and pyramided in the transformed plants. The utility of this approach was confirmed in a preliminary fashion by an assessment of Arabidopsis transformed with the gene coda involved in reproductive growth, which showed improved reproductive growth due to the resulting accumulation of the osmoregulator glycine betaine, especially in flowers and siliques (Sulpice et al., 2003).
Until now, with a single exception of KcNHX in Karelinia caspica (Liu L. et al., 2012), all salt-tolerance genes cloned in halophytes have been heterologously expressed in non-halophytes to illustrate their function. The usefulness of this approach is jeopardized by the fact that salinity tolerance is a complex trait that cannot be controlled by a single or a few genes, prompting a need for a pyramiding approach and targeting gene networks. This results in a need to obtain genetic evidence for the functional role of specific gene(s) in the “native” (i.e., halophyte) systems. The recent development of transformation systems for certain halophytes (Ishimaru, 1999; Sun and Hong, 2012; Yuan et al., 2014) opens prospects for validating the functions of the key halophyte genes by knockout, CRISPR-cas9, or overexpression studies in halophytes themselves. Moreover, many halophytes such as S. europaea is a promising crop (crop adapted halophyte), and present on food market as a tea, juice, powder, etc. (Gunning, 2016). Thus, the domestication of existing halophytic plants is another approach that should be considered for developing crops that can grow under saline conditions.
Given the paucity of the existing data, many aspects of the reproductive biology of halophytes remain to be elucidated. An important step in this process is the recent genome sequencing of Z. marina (Olsen et al., 2016) and Chenopodium quinoa (Jarvis et al., 2017; Zou et al., 2017). In the near future, it will be necessary to obtain more genome sequences so as to study salt-tolerance mechanisms in a broader range of halophytes – such as L. bicolor, which has salt glands; and S. salsa, which shows leaf and stem succulence – to detect the key genes and networks underlying these traits.
Halophytes provide good material for studying salt-tolerance mechanisms, especially those involved in seed formation and germination under saline conditions. Subsequent salt-tolerance studies may thus be focused on halophytes instead of non-halophytes. Moreover, mutant libraries for halophytes should be constructed to verify the functions of salt-tolerance genes. The use of ethyl methanesulfonate (EMS) or gamma ray mutagenesis and/or CRISPR-cas9 in halophytes may represent feasible approaches to obtaining mutants with differences in salt tolerance (Yuan et al., 2013, 2015). We hope to obtain salt-sensitive halophyte strains by applying the above mutagenesis techniques followed by transcriptome or expression profiling. Such work would allow us to accurately identify a series of salt-related genes by comparing the mutants’ profiles with those of the wild type. Therefore, more efficient transformation systems for different types of halophytes urgently need to be established. The detailed mechanisms underlying the good reproductive growth and early germination of halophytes can then be further investigated at the molecular level.
Statements
Author contributions
BW designed the manuscript. FY and JG wrote the manuscript. BW and SS revised the manuscript.
Funding
This work was supported by the National Natural Science Foundation of China (NSFC, Project Nos. 31570251, 31600200, and 31770288), the Shandong Province Key Research and Development Plan (2015ZDJS03002 and 2017CXGC0313), the Natural Science Foundation of Shandong Province (ZR2014CZ002 and ZR2017MC003), the Higher Educational Science and Technology Program of Shandong Province (J15LE08 and J17KA136), and Foshan University.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
abscisic acid, dimorphism, osmolyte, reproductive biology, salt tolerance, salinity, survival
Citation
Yuan F, Guo J, Shabala S and Wang B (2019) Reproductive Physiology of Halophytes: Current Standing. Front. Plant Sci. 9:1954. doi: 10.3389/fpls.2018.01954
Received
22 October 2018
Accepted
17 December 2018
Published
09 January 2019
Volume
9 - 2018
Edited by
Oscar Vicente, Universitat Politècnica de València, Spain
Reviewed by
Viktor Zarsky, Charles University, Czechia; Agnieszka Piernik, Nicolaus Copernicus University in Toruñ, Poland
Updates
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© 2019 Yuan, Guo, Shabala and Wang.
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*Correspondence: Sergey Shabala, Sergey.Shabala@utas.edu.au Baoshan Wang, bswang@sdnu.edu.cn
This article was submitted to Plant Abiotic Stress, a section of the journal Frontiers in Plant Science
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