Phytohormones and Beneficial Microbes: Essential Components for Plants to Balance Stress and Fitness
- 1Leibniz Centre for Agricultural Landscape Research, Institute of Landscape Biogeochemistry, Müncheberg, Germany
- 2Plant Production Department, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia
- 3Botany and Microbiology Department, College of Science, King Saud University, Riyadh, Saudi Arabia
- 4Mycology and Plant Disease Survey Department, Plant Pathology Research Institute, Giza, Egypt
Plants are subjected to various abiotic stresses, such as drought, extreme temperature, salinity, and heavy metals. Abiotic stresses have negative impact on the physiology and morphology of plants through defects in the genetic regulation of cellular pathways. Plants employ several tolerance mechanisms and pathways to avert the effects of stresses that are triggered whenever alterations in metabolism are encountered. Phytohormones are among the most important growth regulators; they are known for having a prominent impact on plant metabolism, and additionally, they play a vital role in the stimulation of plant defense response mechanisms against stresses. Exogenous phytohormone supplementation has been adopted to improve growth and metabolism under stress conditions. Recent investigations have shown that phytohormones produced by root-associated microbes may prove to be important metabolic engineering targets for inducing host tolerance to abiotic stresses. Phytohormone biosynthetic pathways have been identified using several genetic and biochemical methods, and numerous reviews are currently available on this topic. Here, we review current knowledge on the function of phytohormones involved in the improvement of abiotic stress tolerance and defense response in plants exposed to different stressors. We focus on recent successes in identifying the roles of microbial phytohormones that induce stress tolerance, especially in crop plants. In doing so, this review highlights important plant morpho-physiological traits that can be exploited to identify the positive effects of phytohormones on stress tolerance. This review will therefore be helpful to plant physiologists and agricultural microbiologists in designing strategies and tools for the development of broad spectrum microbial inoculants supporting sustainable crop production under hostile environments.
The Food and Agricultural Organization has provided an estimate of the alarmingly increasing human population, expected to reach 8–9 billion by 2030 (FAO, 2010). As a result of increasing urbanization and industrialization, threats to the environment have increased, leading to the shrinkage of agricultural land on one hand and causing significant declines in crop growth on the other hand. Abiotic stresses have the potential to restrict the growth of crop plants considerably, therefore leading to significant yield losses and posing a potential threat to global food security (Mahalingam, 2015).
Environmental stresses are detrimental to the growth of plants. Drought, salinity, heavy metal contamination, flooding, temperature (cold and high), and ultraviolet radiation are the key abiotic factors that modulate the growth of plants to the extent that a reduction in yield is a certain effect. Changes in the climate patterns of different regions have resulted in shifts in vegetation, and approximately 2,000 million hectares of land worldwide has been affected by increased water scarcity and salinization (El-Beltagy and Madkour, 2012). It is believed that approximately 25% of global agricultural land is affected by drought and approximately 5–7% is affected by salt (Ruiz-Lozano et al., 2012). Abiotic stresses inhibit plant growth by reducing water uptake and altering plant physiological and biochemical processes (Ahmad et al., 2010; Hashem et al., 2016). Heavy metals, including cadmium, lead, and mercury, are toxic and are mostly present in soils at low concentrations. However, due to their high mobility in the soil–plant system, they are readily taken up by plants and delivered to the shoot (Hart et al., 1998). Increases in metal concentrations cause retardation of growth, leading to necrosis, altered nutrient uptake, reduced enzyme activity and hence phytotoxicity (Groppa et al., 2012).
A better understanding of the different tolerance strategies for maintaining crop productivity through the manipulation of environmental conditions can be helpful for maintaining the maximum genetic potential of crops as much as possible. Phytohormones are important growth regulators synthesized in defined organs of the plant that have a prominent impact on plant metabolism (Kazan, 2013) and play an important role in the mitigation of abiotic stresses (Teale et al., 2006; Hu et al., 2013). However, abiotic stresses alter the endogenous levels of phytohormones, such as auxins, gibberellins, abscisic acid (ABA), jasmonic acid and salicylic acid (SA), which causes plant growth perturbations (Debez et al., 2001; Egamberdieva, 2009; Khan et al., 2014). Drought and salt stress have also been reported to inhibit phytohormone concentrations in plant tissue.
There has been enormous progress in research regarding crop improvement in hostile environments, and the role of some tools, such as microbial technology and genetic engineering, has been acknowledged. Accordingly, several strategies for improving plant stress tolerance by root-associated microbes, such as a low-input biotechnology, have been proposed (Khan et al., 2013). Plant-associated microbes live in plant tissue endophytically or symbiotically or they colonize the root surface and cooperate with each other by producing various metabolically active substances (Egamberdieva, 2011, 2012; Berg et al., 2013; Asaf et al., 2017). The stimulation of plant growth and nutrient acquisition by beneficial rhizobacteria has been correlated to the biosynthesis of plant growth regulators, including auxins (Etesami et al., 2015; Pereira et al., 2016), gibberellins (Khan et al., 2014), cytokinins (Kudoyarova et al., 2014), and ABA (Sgroy et al., 2009). The microbial regulators modulate plant hormone levels in plant tissue, and they have been found to have effects that are similar to exogenous phytohormone application (Egamberdieva, 2009; Turan et al., 2014; Shahzad et al., 2016). Based on the currently available studies on the effect of phytohormones on plant stress tolerance, this review attempts to improve the understanding of microbial phytohormones and their interactions with plants by assessing their influence on plant physiological and morphological properties. Based on important studies on the negative effect of abiotic stresses on plant growth regulators, we have also presented some potential traits of microbial phytohormones that can be used to increase plant growth and tolerance to stress factors. In this review, we will focus on the plant growth regulators synthesized by root-associated microbes, their diversity, physiology and their involvement in stress tolerance of plants to abiotic stresses including drought, salt, and heavy metals.
Role of Phytohormones in Plant Response to Abiotic Stress
Auxins are important phytohormones, and the auxin indole-3-acetic acid (IAA) was shown to promote several growth and developmental events, such as cell division, elongation, and differentiation (Asgher et al., 2015). IAA is synthesized from and chemically similar to tryptophan. Ljung (2013) produced strong evidence favoring auxin-mediated growth and developmental control through alterations in gene expression patterns. Many reports are available depicting varied modulations in the synthesis, transport, metabolism and activity of auxins after plant exposure to stresses (Ljung, 2013); however, plenty of research reports are available advocating the role of auxins in mediating and improving plant tolerance to abiotic stresses (Kazan, 2013). Rice plants exhibited a significant decline in IAA after exposure to salinity stress. In addition, this variation in IAA can induce growth modulation through an increase in other phytohormones, such as ABA, as reported by Iqbal and Ashraf (2013). Jung and Park (2011) found a link among auxin signaling and salt stress which developed through auxin involvement in modulating the membrane bound transcription factor NTM2. These involvements were further validated by over-expression studies on the IAA30 gene of NTM2 carried out by Park et al. (2011); however, the actual mechanism of IAA-induced mitigation of salinity is unclear.
Auxins have an important role, whether directly or indirectly, in promoting heavy metal tolerance, as Hu et al. (2013) observed that heavy metals have a negative effect on the biosynthesis of auxins. The toxic effect of lead (Pb) on sunflower plant growth was alleviated by the addition of a low concentration of IAA (10-10 M), which stimulated increases in root volume, surface area and diameter (Fässler et al., 2010). IAA induced an increase in shoot biomass and increased Pb and Zn accumulation in plant tissue, indicating the potential of auxins to enhance the phytoextraction of metals. Aluminum restricts root growth in Medicago sativa by reducing the transport and synthesis of IAA from shoot to root, which was confirmed after analyzing the expression of genes; however, exogenous application of IAA was observed to mitigate aluminum stress to some extent by maintaining greater expression of the AUX1 and PIN2 genes (Wang S. et al., 2016). There was a positive effect after using auxins as priming sources. Iqbal and Ashraf (2007) have reported a significant mitigation of salt stress-induced hostile effects in wheat after seed priming with IAA, which resulted in ionic homeostasis and induction of SA biosynthesis. These studies indicate the existence of possible crosstalk between auxin and SA that mediates tolerance responses in plants. Salinity restricts the synthesis of IAA; however, the exogenous application of SA proved effective in mitigating hostile effects by causing significant alleviation of salinity-induced inhibition (Fahad and Bano, 2012).
Cytokinins (CK), an important group of plant hormones are involved in the maintaining of cellular proliferation and differentiation and the prevention of senescence, therefore leading to the inhibition of premature leaf senescence (Schmulling, 2002). However, under stress conditions, particularly water stress at the grain-filling stage, it was observed that stay-green genotypes have the potential to exhibit increased tolerance, which was ascribed to an increased concentration of cytokinin in the xylem sap (Borrell et al., 2000). Zhang et al. (2010) demonstrated that cytokinin-over-expressing transgenic cassava exhibited greater tolerance to drought in comparison to wild-type plants. The genes involved in the biosynthesis of cytokinin have been over-expressed, and their role in stress tolerance has been validated. For example, the ipt gene has been validated in field analysis (Peleg and Blumwald, 2011). Reduced cytokinin leads to ABA-induced stomatal closure, thereby reducing carbon uptake and assimilation, and under stressful conditions, the up-regulation of cytokinin oxidase may also reduce carbon metabolism; work on this topic can be fruitful in improving the plant growth and yield. Mohapatra et al. (2011) demonstrated that cytokinin improves grain filling. Currently, exogenous application of cytokinin is being employed to optimize the internal concentrations of cytokinin. It has also been documented that heavy metals, such as zinc and lead, severely hamper the seedling growth of chickpea through the inhibition of GA3 and Z concentrations in plant tissue (Atici et al., 2005). In an earlier report, the application of kinetin to chickpea stimulated plant growth and development under salt stress (Bozcuk, 1981), and in another report, kinetin alleviated cadmium stress in eggplant by enhancing its antioxidant potential (Singh and Prasad, 2014).
Like other phytohormones, ABA is known to have an important role in plants by improving stress responses and adaptation. It is a naturally occurring sesquiterpenoid, which are a group of key phytohormones involved in the regulation of growth. There have been many reports advocating the role of ABA in integrating signaling during stress exposure with subsequent control of downstream responses (Wilkinson et al., 2012). Under abiotic stress the expression of stress responsive genes regulated by ABA-induced and -mediated signaling, leading to better elicitation of tolerance responses (Sah et al., 2016). In addition, ABA has been reported to control root growth and water content under drought stress conditions (Cutler et al., 2010). However, an abrupt increase in ABA concentrations during stress exposures can lead to growth retardation and can also modulate tolerance responses against stresses (Asgher et al., 2015). Nevertheless, there are reports suggesting the positive implication of exogenous ABA in reversing the ill effects of stresses, such as salinity (Gomez et al., 2002), chilling (Nayyar et al., 2005), drought (Bano et al., 2012), and cold stress (Li et al., 2014). Bano et al. (2012) demonstrated that exogenous application of ABA protected wheat from drought-induced oxidative damage by improving the antioxidant system and relative water content. Exogenous ABA application for improving stress tolerance has been proposed as an effective tool for stress mitigation. In Solanum tuberosum, Mora-Herrera and Lopez-Delgado (2007) observed that ABA application resulted in improved stress tolerance by reducing the production of free radicals through significant increases in the activity of the antioxidant enzyme peroxidase. Zhou et al. (2014) observed a significant alteration in the proteome of tea due to exogenous application of ABA under drought stress conditions, including changes in proteins involved in transport, carbon metabolism, and stress tolerance. It has been suggested that ABA maintains the levels of other hormones, such as ethylene, leading to the maintenance of shoot and root growth in Zea mays (Spollen et al., 2000). Upon stresses, ABA synthesis and accumulation in plant tissue increases. The most important role of ABA, in addition to its role in signaling, is its ability to act as an anti-transpirant after the induction of stomatal closure and reduction of canopy expansion (Wilkinson and Davies, 2002). Exogenous ABA application to rice seedlings exposed to drought led to the protection of photosynthesis by up-regulating the expression of the OsPsbD1, OsPsbD2, OsNCED2, OsNCED3, OsNCED4 and OsNCED5 genes, leading to improved photosynthetic capacity, and stomatal regulation under normal and stressed conditions, which suggests the involvement of these genes in photosystem II induction after exogenous ABA application. In plants exposed to stress conditions, ABA is involved in developing the deeper root system and causing other necessary root modifications to mediate optimal water and nutrient acquisition (Spollen et al., 2000; Vysotskaya et al., 2009). In addition, ABA maintains the hydraulic conductivities of shoot and root to better exploit soil water content, leading to the maintenance of tissue turgor potential and improved drought tolerance through up-regulation of the antioxidant system and the accumulation of compatible osmolytes (Chaves et al., 2003), which maintains the relative water content. In Stylosanthes guianensis, Zhou et al. (2005) demonstrated that ABA-induced antioxidant defense was mediated by improved nitric oxide synthesis. Guajardo et al. (2016) also reported improved activity of antioxidant enzymes after ABA treatment, which resulted in increased desiccation tolerance by reducing oxidative stress-induced damage. Cabot et al. (2009) reported that ABA applied exogenousely inhibited accumulation of sodium and chloride in citrus plants with exogenously applied ABA. In another study, ABA treatment increased plant growth, nutrient uptake, and nitrogen fixation in the common bean under salt stress (Khadri et al., 2006).
Another important plant growth regulator is gibberellin, which has a vital role in seed dormancy formation of floral organs, and lateral shoot growth (Olszewski et al., 2002). The available literature clearly reveals the ameliorative impact of gibberellic acid against salinity. Gibberellic acid was found to stimulate plant growth and development under various abiotic stress conditions (Ahmad, 2010). Enhanced plant water uptake and reduced stomatal resistance were observed in gibberellic acid-treated tomato plants grown under saline conditions (Maggio et al., 2010). Gibberellic acid induces efficient uptake and ion partitioning within the plant system, leading to enhanced growth and maintaining the metabolism of plants under normal and stress conditions (Iqbal and Ashraf, 2013). Under salt stress conditions, improved germination and growth due to gibberellic acid has been reported by several studies (Tuna et al., 2008; Ahmad, 2010; Manjili et al., 2012). In addition, gibberellins can exhibit crosstalk with other phytohormones, which elicits important responses and mediates tolerance mechanisms for enhancing stress tolerance. The synthesis of gibberellins can also be promoted through the application of other hormones, such as auxin (Wolbang et al., 2004). Enhanced synthesis of gibberellic acid leads to enhanced ABA catabolism. Moreover, gibberellic acid directly affects growth, yield, and mineral nutrition as well as nitrogen metabolism. Khan et al. (2004) reported increases in fruit yield, leaf area, and nitrogen, phosphorous, and potassium uptake in tomato due to the exogenous application of gibberellic acid. Moreover, an increase in osmotic components was reported in plants exposed to salt stress, and their content was further increased by gibberellic acid treatment. The endogenous application of GA resulted in amendment of osmotic stress in plants and maintenance of tissue water content (Ahmad, 2010). Such effects were observed by Manjili et al. (2012) for wheat and by Tuna et al. (2008) for maize. In addition, gibberellic acid enhanced antioxidant enzyme activity by lowering the levels of reactive oxygen species (ROS) which contributed to better growth under stress (Manjili et al., 2012). In addition, exogenous application of gibberellic acid mitigates salinity-induced effects on germination and growth in Arabidopsis thaliana by mediating enhanced synthesis of SA, which causes increased activity of isochorismate synthase 1 (Alonso-Ramirez et al., 2009). The same study also demonstrated that over-expression of the gibberellin-responsive gene from Fagus sylvatica enhanced the salt tolerance of Arabidopsis.
Salicylic acid is another important phytohormone with a phenolic nature, and it has an important function in plant stress tolerance through modulation of antioxidative enzyme activities (Ahmad et al., 2011; da Silva et al., 2017). The alleviation of various abiotic stresses by application of SA was reported by Senaratna et al. (2000) for water stress, by Azooz et al. (2011) for salt stress and by Ahmad et al. (2011) for heavy metal stress. SA modulates several physiological processes involved in plant stress tolerance through stress activated signal pathways and response mechanisms (Ahmad et al., 2011; Janda et al., 2012; Khan et al., 2014). There are several reports on the alleviating effect of SA in plants, e.g., fava bean (Azooz et al., 2011), maize (Gunes et al., 2007), and wheat (Shakirova, 2007). Azooz et al. (2011) reported that the application of SA to sea water-treated Vicia faba plants not only ameliorated the negative effects on growth, biomass accumulation and antioxidant system but also caused efficient accumulation of organic osmolytes, such as proline and free amino acids. In salt-stressed Vigna radiata, L. Khan et al. (2014) reported a reduction in endogenous levels of ethylene due to SA application. The results published so far have shown that the application of SA promoted efficient sequestration and partitioning of deleterious ions, such as Na. Increased synthesis and accumulation of proline and ABA have been reported in salinity-stressed wheat seedlings, contributing to better growth and yield (Shakirova et al., 2003). In Vigna radiata, L. Khan et al. (2014) observed that treatment of seeds with SA helped to considerably mitigate salt stress-induced changes. SA-treated plants showed better growth in terms of biomass accumulation, promotion of cell division, and showed a higher photosynthetic rate and antioxidant enzyme activity (da Silva et al., 2017). In barley plants, salinity stress caused alterations in the rate of photosynthesis and membrane stability; however, these negative effects of salinity stress were ameliorated by the application of SA (Janda et al., 2012). Similar observations were reported by da Silva et al. (2017) in case of SA at 10-5 M which increased plant growth of sesame under drought stress (da Silva et al., 2017). The treatment of maize with SA reduced the accumulation of Na in plant tissue and mitigated salt-induced negative effects on plants (Gunes et al., 2007). In addition, SA inhibits lipid peroxidation, improves membrane stability (Azooz et al., 2011), sustains the transpiration rate, and decreases electrolyte leakage (Stevens et al., 2006). Tang et al. (2017) reported that SA application mitigates water stress by maintaining a lower ROS level. Several studies reported increased mitochondrial alternative oxidase (AOX) expression and activity by SA treatment; this enzyme plays an important role in tolerance to abiotic stresses (Zhang et al., 2010).
Altogether, these observations suggest that phytohormones play a vital role in plant tolerance to various abiotic stresses by modulating the physiological properties and defense system of plants. Since plants are closely associated with the microbes that live within plant tissues, microbial metabolites may have strong effect on plant physiological processes and metabolism. In earlier studies, Fulchieri et al. (1993) and Lucangeli and Bottini (1997) observed higher amounts of IAA and the gibberellin GA3 in the plant tissue of maize after the inoculation of plant growth promoting rhizobacteria (PGPR) strains. Similar observations were also reported by Fulchieri et al. (1993) in which Azospirillum increased levels of GA3 in maize seedlings. Thus, microbial phytohormones have vital importance in plant host metabolism and physiology under hostile environments.
Root-Associated Phytohormone-Producing Microbes
Soils are sources of diverse organisms, including fungi, bacteria, and plants (Mendes et al., 2013). Plant roots are heavily colonized with microorganisms (compared to soil and other habitats) because of the rich nutrient component of root exudates (Schlaeppi and Bulgarelli, 2015; Hashem et al., 2016). The rhizosphere is a relatively nutrient-rich environment containing amino acids, sugars, fatty acids and other organic compounds, which attract microbes (Vorholt, 2012) that utilize the various nutrients released by the root. In turn, the microbes synthesize biologically active compounds, including phytohormones (auxins, cytokinins, gibberellins, and ABA), antifungal compounds, enzymes, and compatible solutes. These microbial metabolites play a vital role in plant growth, nutrition and development (Ruiz-Lozano et al., 2012; Sorty et al., 2016; Egamberdieva et al., 2017a). They can stimulate plant growth development, provide resistance to various abiotic and biotic stress factors, improve nutrient acquisition and protect plants from various soil-borne pathogens (Grover et al., 2013; Cho et al., 2015). The beneficial interactions of microbes in plants, their positive effect on plant growth and their improvement of stress tolerance under extreme environmental conditions have been extensively reviewed by Nadeem et al. (2014), and the mechanisms utilized by plant growth-promoting bacteria have been reviewed by Forni et al. (2017). There are several mechanisms of plant growth stimulation, plant protection and alleviation of salt stress by PGPR, such as nitrogen fixation; synthesis of osmoprotectants, exopolysaccharides, 1-aminocyclopropane-1-carboxylate (ACC) deaminase, cell wall degrading enzymes, and phytohormones; modulation of antioxidant enzymes or nutrients; and solubilization of minerals, such as phosphorus, and potassium (Berg et al., 2013; Wang Q. et al., 2016; Mishra et al., 2017). The microbes mitigate stress responses by regulating the nutritional and hormonal balance in plants and inducing systemic tolerance to stress. One of the mechanisms of improvement of plant growth and stress tolerance by microbes is their phytohormone synthesizing ability in the rhizosphere or root tissue (Etesami et al., 2015). Microbial phytohormones affect the metabolism of endogenous growth regulators in plant tissue (Hashem et al., 2016; Sorty et al., 2016) and play a key role in changing root morphology upon exposure to drought, salinity, extreme temperature and heavy metal toxicity (Spaepen et al., 2008; Khan et al., 2011).
Root-associated microbes, including free living, symbiotic or endophytic microbes, can produce various type of phytohormones and belong to different genera and species (Sgroy et al., 2009). For example, Sorty et al. (2016) isolated diverse groups of organisms belonging to Acinetobacter, Bacillus, Enterobacter, Pantoea, Pseudomonas, Rhizobium, and Sinorhizobium from halotolerant weed (Psoralea corylifolia L.), and Egamberdieva et al. (2016) found Arthrobacter, Bacillus, Enterobacter, Pseudomonas, Rhizobium, Brevibacillus, Cellulosimicrobium, Mycobacterium, Ochrobactrum, Paenibacillus, and Pseudoxanthomonas associated with soybean root. The IAA-producing Mycobacterium species was observed in the rhizosphere of orchid (Tsavkelova et al., 2007), and Azotobacter, Azospirillum, Cellulomonas, Mycoplana, and Rahnella were found in the wheat rhizosphere (Egamberdiyeva and Hoflich, 2003; Egamberdieva et al., 2008). In other reports, Pseudomonas spp. (Lawongsa et al., 2008), Arthrobacter spp. (Piccoli et al., 2011), and Enterobacter, Pseudomonas, and Stenotrophomonas species were associated with plants that produced IAA (Khan and Doty, 2009). Piccoli et al. (2011) isolated the endophytic diazotrophic bacterium Arthrobacter koreensis which produce ABA, IAA, GA3 and jasmonic acid from the roots of the halophyte shrub Prosopis strombulifera. The endophytic strains of Klebsiella and Enterobacter isolates from sugar cane synthesize IAA (de Santi Ferrara et al., 2012). Mishra et al. (2017) isolated bacteria with IAA production ability from extreme environments, which were identified as Pseudomonas spp. and Ochrobactrum spp. In other studies Halomonas desiderata, Bacillus megaterium, Bacillus cereus, Bacillus subtilis, Escherichia coli, and Pseudomonas fluorescens G20-18 were reported to synthesize cytokinins (Salamone et al., 2001; Karadeniz et al., 2006; Großkinsky et al., 2016). Bacterial isolates from the rhizosphere of a vegetable (bitter gourd) belonging to genera Bacillus, Klebsiella, Leifsonia, and Enterobacter were able to produce IAA and improved maize growth in Cd-contaminated soil (Ahmad et al., 2016).
Naz et al. (2009) also observed cytokinin-producing species, such as Arthrobacter, Bacillus, Azospirillum, and Pseudomonas, that stimulated the root development of plants. ABA was also detected in root-associated microbes from various plants. Karadeniz et al. (2006) reported Proteus mirabilis, Phaseolus vulgaris, Klebsiella pneumoniae, B. megaterium, and B. cereus as ABA-producing bacteria. Species such as Bacillus pumilus, Bacillus licheniformis, Acetobacter sp., Bacillus sp., Azospirillium sp. were found among gibberellin-producing strains (Gutiérrez-Mañero et al., 2001; Bottini et al., 2004). Salomon et al. (2014) observed ABA-producing B. licheniformis Rt4M10 and P. fluorescens Rt6M10 in the rhizosphere of Vitis vinifera. Achromobacter xylosoxidans SF2, isolated from sunflower roots, was also able to produce ABA in minimal medium (Forchetti et al., 2007). Among IAA-producing bacteria associated with plants grown under saline soil, Rhizobia have also been shown to synthesize auxins, cytokinins and abscicic acids, increase plant growth and development and improve the yield of agricultural crops (Hayat et al., 2008). Actinobacteria have also been found to produce IAA, CK, GB-like substances (Shutsrirung et al., 2013; Vijayabharathi et al., 2016). Ruanpanun et al. (2010) found high IAA-producing nematophagous actinomycete and fungal isolates, such as Aspergillus and Streptomyces. In other studies, Streptomyces sp. Isolated from medicinal plant species Taxus chinensis and Artemisia annua showed IAA synthesis ability (Lin and Xu, 2013). Shutsrirung et al., 2013 reported IAA production in endophytic actinomycetes Streptomyces, Nocardia, Nocardiopsis, Spirillospora, Microbispora, and Micromonospora associated with mandarin.
The stress tolerance ability of bacterial strains provides important benefits to plants. The ability of root-associated microbes to synthesize phytohormones is typically not hampered by high salt concentrations (Egamberdieva and Kucharova, 2009). For example, phytohormone synthesis by endophytic actinobacteria Streptomyces coelicolor DE07 and Streptomyces geysiriensis DE27 was not inhibited under water stress (Yandigeri et al., 2012). The production of IAA by A. brasilense in osmotic stress conditions was higher than that of osmosensitive A. brasilense Sp7 (Nabti et al., 2007). In another study, Pseudomonas putida, Pseudomonas extremorientalis, Pseudomonas chlororaphis, and P. aurantiaca were able to produce IAA in a 4% NaCl conditions (Egamberdieva and Kucharova, 2009). Pseudomonas sp. and Bacillus sp. strains were able to produce IAA under high salt conditions (200–400 mM NaCl) and increased the plant biomass of Sulla carnosa under salt stress (Hidri et al., 2016).
The biosynthesis of phytohormones differs by bacterial strain. For example, Bacillus and Pseudomonas strains synthesized IAA concentrations up to 2.2 μg mL-1, GA3 production by A. xylosoxidans and B. halotolerans was between 36.5 and 75.5 μg mL-1 (Sgroy et al., 2009). In addition, ABA production was 0.3, 1.8, and 4.2 μg mL-1 in the culture medium of L. fusiformis (Ps14), B. subtilis (Ps8), and P. putida (Ps30), respectively. In another study, Bacillus amyloliquefaciens associated with rice (Oryza sativa L.) synthesized gibberellins, and the quantities of GA differed, e.g., 17.8 ng mL-1 for GA20, 5.7 ng mL-1 for GA36, 5.6 ng mL-1 for GA24, 1.02 ng mL-1 for GA4, 0.7 ng mL-1 for GA53, 0.08 ng mL-1 for GA5, and 0.01 ng mL-1 for GA8 (Shahzad et al., 2016). Endophytic fungi Aspergillus fumigatus associated with soybean roots synthesized gibberellins, such as GA4 (24.8 ng mL-1), GA9 (1.2 ng mL-1), and GA12 (9.8 ng mL-1) (Khan et al., 2011). Several studies reported SA production by root-associated bacteria, e.g., B. licheniformis MML2501 (18 μg mL-1) (Shanmugam and Narayanasamy, 2008), and Pseudomonas sp. PRGB06 (6.8 μg mL-1) (Indiragandhi et al., 2008).
Microbial Phytohormones in Plant Stress Tolerance
Microbes synthesize low amounts of phytohormones and improve stress tolerance and plant growth under various stress conditions, including salinity, heat, drought and metal toxicity, as reported in many studies (Sgroy et al., 2009; Egamberdieva et al., 2011, 2017b; Liu Y. et al., 2013). The beneficial effect of phytohormone-producing microbes on alleviating abiotic stress in plants was reported in numerous studies (Figure 1; Khan and Doty, 2009; Ngumbi and Kloepper, 2014; Hashem et al., 2016). Some examples of phytohormone-producing bacteria and their ability to mitigate abiotic stress are given in Table 1. Many studies have reported the positive effects of bacteria associated with plants and IAA production on plant growth stimulation under abiotic stress conditions. For example, bacterial strains Curtobacterium flaccumfaciens E108 and Ensifer garamanticus E110 isolated from Hordeum secalinum stimulated plant biomass and salt stress resistance in barley (Cardinale et al., 2015). The root-colonizing halotolerant bacterium B. licheniformis HSW-16 was able to mitigate salt stress-induced damage and stimulate the growth of wheat through the production of IAA under saline soil conditions (Singh and Jha, 2016). Similar observations were reported by Upadhyay et al. (2012) in which salt-tolerant bacterial strains B. subtilis and Arthrobacter sp. increased wheat biomass and total soluble sugars and reduced sodium concentration in plant tissue. Sorty et al. (2016) isolated salt-tolerant strain Enterobacter sp. NIASMVII from halotolerant weed (Psoralea corylifolia L.), which produces IAA (0.22 and 25.58 μg mL-1) and enhances seed germination of wheat (Triticum aestivum L.). In another study, Pseudomonas spp. isolated from extreme environments (close to the sites of volcanos) synthesized IAA under salt stress (500 mM NaCl) and high temperature (40°C), and they were able to stimulate increases in the root and shoot biomass of maize (Mishra et al., 2017). According to Bianco and Defez (2009), protection of plants from negative effects of abiotic stress by IAA is related to enhanced cellular defense systems. Several salt-tolerant strains synthesizing IAA in culture medium, namely, Serratia plymuthica RR-2-5-10, Stenotrophomonas rhizophila e-p10, P. fluorescens SPB2145, P. extremorientalis TSAU20, and P. fluorescens PCL1751, improved cucumber biomass and yield in greenhouse conditions (9–24%) (Egamberdieva et al., 2011). Root-associated IAA-producing bacteria were found to improve drought stress in plants. Marulanda et al. (2009) observed increased plant biomass in clover (Trifolium repens L.) after seed treatment with P. putida and B. megaterium under drought, and they found a correlation between these changes and increased IAA. IAA-producing bacteria were also found to improve plant growth and development under nutrient-poor soil conditions. Serratia sp. isolated from chickpea nodules was found to produce IAA, which led to an increased grain yield of chickpea in nutrient-deficient soil (Zaheer et al., 2016). Many fungal species were also able to produce plant growth regulators and alter plant root system and physiology. Contreras-Cornejo et al. (2009) observed increased lateral root formation, root hair growth and modified root system architecture from Trichoderma virens inoculation, which resulted in increased plant biomass of Arabidopsis thaliana.
FIGURE 1. An overview of mechanisms in microbial phytohormone-mediated plant stress tolerance. Several root associated microbes produce cytokinin (CK), gibberellin (GB), indole-3-acetic acid (IAA), salicylic acid (SA) and abscisic acid (ABA), which help plants to withstand stress by enhancing its antioxidant potential, by up-regulation of the antioxidant system and by accumulation of compatible osmolytes thus reducing oxidative stress-induced damage; improving photosynthetic capacity and membrane stability; promoting cell division and stomatal regulation; stimulating growth of root system, and acquisition of water and nutrients.
TABLE 1. Some examples of phytohormone-producing bacteria and their ability to mitigate abiotic stress.
Microbial phytohormones also play an important role in metal-plant interactions, improving phytoextraction by plants. A. xylosoxidans Ax10 improved the root system of the Brassica juncea plant through IAA production activities, which increased copper phytoextraction (Ma et al., 2008). Similar results were observed by Zaidi et al. (2006) in which B. subtilis synthesizing IAA stimulated root growth and Ni accumulation in the Indian mustard plant (B. juncea L.). B. megaterium MCR-8, which produced auxin at a concentration of 68.5 mg 25 mL-1, alleviated Ni stress in Vinca rosea and stimulated root and shoot growth. In addition, plant treatment with B. megaterium MCR-8 increased the accumulation of total phenols, flavonoids and defense-related enzymes, such superoxide dismutase (SOD), catalase (CAT), peroxidase (POD), and ascorbate peroxidase (APX), compared to uninoculated plants under Ni stress (Khan et al., 2017). In another study, Ahmad et al. (2016) observed inhibited seed germination and seedling growth of maize by Cd stress, whereas Cd-tolerant and IAA-producing bacteria Leifsonia sp. and Bacillus sp. significantly increased shoot and root growth of maize in Cd-contaminated soil compared to controls. Similar observations were reported by Dourado et al. (2013) in which Cd-tolerant multi-tolerant bacteria Burkholderia sp. SCMS54 produced IAA and improved plant growth and stress tolerance of tomato to Cd stress. Islam et al. (2016) reported that Cr toxicity significantly inhibited maize growth, negatively affecting its physiological processes, such as photosynthetic pigment and carbohydrate metabolism, and increasing its levels of proline, H2O2, and MDA. In these conditions, Cr-resistant P. mirabilis isolates T2Cr and CrP450, combined with SA, mitigated the toxic effect of Cr, improved the root and shoot growth of maize and reduced oxidative stress in maize tissue by elevating its antioxidant activities.
The tripartite interaction of root-associated microbes with symbiotic microbes and the host plant is also a mutualistic interaction that improves plant growth under stress through the induction of osmoregulation, hormonal balance, biochemical processes and changes in metabolic interfaces among partners (Nadeem et al., 2014; Park et al., 2017). IAA-producing B. subtilis NUU4 in combination with Mesorhizobium ciceri IC53 stimulated root and shoot biomass and improved nodule formation in chickpea (Cicer arietinum L.) under salt stress, as compared to uninoculated plants and plants inoculated with Mesorhizobium ciceri IC53 alone (Egamberdieva et al., 2017c) (Figure 2).
FIGURE 2. Growth of chickpea in salinated soil after inoculation with Mesorhizobium ciceri IC53 alone or with the combination of Mesorhizobium ciceri IC53 and IAA-producing Bacillus subtilis NUU4 in pots (A) and under field condition (B) (Figure as originally published in Egamberdieva et al., 2017c).
The positive effect on root development by cytokinin-producing bacterial strains was also reported in many studies. For example, inoculation of maize with cytokinin-producing bacteria Micrococcus luteus chp37 isolated from the desert of Pakistan stimulated shoot and root biomass by 54% and modulated the physiological properties of the plant, including photosynthetic pigments, under drought conditions (Raza and Faisal, 2013). The cytokinin-producing root-associated bacteria strains Arthrobacter, Bacillus, Azospirillum, and Pseudomonas increased soybean shoot and root biomass as well as proline content in plant tissue under salt stress (Naz et al., 2009). A similar observation was reported by Liu F. et al. (2013) in which cytokinin-producing B. subtilis stimulated root biomass of Platycladus orientalis (oriental thuja) by 13.9% and increased cytokinin concentration of 47.52% in leaves relative to respective controls under water stress conditions. The higher content of cytokinin in plant tissue contributed to stomatal opening and alleviated some of the detrimental effects of water stress.
Aspergillus fumigatus produced gibberellins, such as GA4 (24.8 ng mL-1), GA9 (1.2 ng mL-1), and GA12 (9.8 ng mL-1), which increased photosynthetic pigments, and shoot biomass of soybean under salt stress (Khan et al., 2011). Azospirillum lipoferum, which synthesizes GA, increased the stress tolerance of wheat to drought (Creus et al., 2004). Waqas et al. (2012) also reported improved salt and drought stress tolerance in cucumber plant by GA-producing endophytic fungi Phoma glomerata LWL2 LWL3, which produced GA1 (8.720 ng mL-1), GA3 (2.420 ng mL-1) and GA4 (0.220 ng mL-1), and Penicillium sp., which produced GA1 (5.33 ng mL-1) and GA3 (3.42 ng mL-1) in culture filtrate. The fungal inoculation resulted in increased root and shoot growth and nutrient uptake, and reduced stress by down-regulating ABA and modifying SA and jasmonic acid concentrations in plant tissue. It is known that ABA and SA act as defense signaling constituents (Shinozaki and Yamaguchi-Shinozaki, 2007).
Salomon et al. (2014) observed ABA production by B. licheniformis and P. fluorescens that stimulated plant growth of grapevine under water stress by inducing ABA synthesis. Shahzad et al. (2017) reported ABA production by Bacillus amyloliquefaciens RWL-1 (0.32 ± 0.015–0.14 ± 0.030 ng mL-1) under normal and saline conditions. Bacterial inoculation significantly increased root and shoot growth and the concentration of SA in plant tissue of rice under salt stress conditions. Park et al. (2017) isolated Bacillus aryabhattai strain SRB02 from the rhizosphere of soybean, and it significantly promoted the plant biomass and nodule number of soybean. The strains produced up to 2 ng mL-1 ABA in culture and increased the drought stress tolerance of soybean through stomatal closure under high temperatures (38°C) relative to control plants.
Similar to the effects of other phytohormones, SA-producing endophytic bacteria A. xylosoxidans and B. pumilus also enhanced the biomass of sunflower seedlings under drought conditions (Forchetti et al., 2010). Similar observations were reported by Lavania and Nautiyal (2013) in which salt-tolerant SA-producing Serratia marcescens NBRI1213 stimulated root and shoot growth as well as nutrient acquisition by maize, and furthermore increased plant stress tolerance to salinity.
Some bacteria may produce several types of phytohormones in plant tissue that interact to modulate important physiological processes in plants, including hormonal balance. Sphingomonas sp. LK11 and Serratia marcescens TP1 produced 12.31 and 10.5 μM mL-1 of IAA in the culture broths, which stimulated root and shoot growth of soybean through increases in ABA and gibberellin and a decrease in jasmonic acid content compared to levels in the control plants (Asaf et al., 2017). Trichoderma asperellum Q1, which produces IAA, GA and ABA, stimulated the biomass fresh weight of cucumber seedlings under salt stress in comparison to untreated control plants (Zhao and Zhang, 2015). In addition, the concentration of phytohormones IAA, GA and ABA in cucumber leaves were also increased after application of Trichoderma asperellum Q1 under salt stress. Similar observations were reported by Park et al. (2017) for soybean inoculated with Bacillus aryabhattai SRB02, which produces IAA, GA, and ABA. The root and shoot growth and heat stress of soybean plants increased after bacterial inoculation. In addition, higher concentrations of IAA, JA, GA12, GA4, and GA7 were observed in plant tissue of Bacillus aryabhattai SRB02-treated plants. Similar observations were reported for maize inoculated with ABA-producing Azospirillum lipoferum and A. brasilense sp. 245 in which bacterial treatment resulted in an increased concentration of ABA in plant tissue (Cohen et al., 2015). These studies demonstrate the involvement of phytohormone modulation in plant tissue by plant-associated microbes that induce the stress tolerance of plants.
Conclusion and Future Prospects
Overall, evidence was provided that the exogenous application of phytohormones of microbial origin is an important tool for increasing the abiotic and biotic stress tolerance of plants, providing potential practical applications under changing or extreme environmental conditions. The beneficial effects on plants mediated by microbes, such as the stimulation of plant growth, tolerance to abiotic stresses and resistance to pathogens, are based on the microbes’ ability to produce auxins, gibberellins, SA, ABA, and cytokinins in plant tissues. Thus, plant-associated microbes hold the potential to modulate hormone levels and metabolism in plant tissue, especially in biochemical processes that can prevent the damaging effects of external stresses, such as drought, salinity, nutrient deficiency, or heavy metal contamination. Optimizing phytohormone balance in plant tissues under stress by beneficial microbes could be a crucial challenge in the development of sustainable approaches to crop production. More experimental studies on various plant species are needed to determine whether these are plant-specific traits and to better understand the mechanisms involved in the interactions between microbial metabolites and the host that help plants optimize their responses in hostile environments. More specifically, it can be worthwhile to employ loss-of-function or gain-of-function genetic mechanisms to explore the associated mechanisms or reveal the antagonistic or synergistic interactions of phytohormones. The identification of receptors leading to the expression of specific genes after the application of a microbial phytohormone is also an important topic. Furthermore, studies on the performance of phytohormone-producing microbes in field experiments are necessary, and they should include competition for nutrients and niches between the microbial inoculant and the indigenous microflora. Moreover, investigations of host-microbe-stress interactions and their involved mechanisms using omics-based approaches, such as proteomics, genomics, metagenomics, and metabolomics, are needed.
DE, SW, and EA designed and wrote the manuscript. AH and AA edited and helped in finalizing the manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This research was supported by a Georg Forster Research Fellowship (HERMES), Alexander von Humboldt Foundation for DE. The publication of this article was funded by the Open Access Fund of the Leibniz Association. The authors would like to extend their sincere appreciation to the Deanship of Scientific Research at King Saud University for its funding this Research group NO (RG-1435-014).
Ahmad, I., Akhtar, M. J., Asghar, H. N., Ghafoor, U., and Shahid, M. (2016). Differential effects of plant growth-promoting rhizobacteria on maize growth and cadmium uptake. J. Plant Growth Regul. 35, 303–315. doi: 10.1007/s00344-015-9534-5
Ahmad, P. (2010). Growth and antioxidant responses in mustard (Brassica juncea L.) plants subjected to combined effect of gibberellic acid and salinity. Arch. Agron. Soil Sci. 56, 575–588. doi: 10.1080/03650340903164231
Ahmad, P., Jaleel, C. A., Salem, M. A., Nabi, G., and Sharma, S. (2010). Roles of enzymatic and nonenzymatic antioxidants in plants during abiotic stress. Crit. Rev. Biotechnol. 30, 161–175. doi: 10.3109/07388550903524243
Ahmad, P., Nabi, G., and Ashraf, M. (2011). Cadmium-induced oxidative damage in mustard [Brassica juncea (L.) Czern. & Coss.] plants can be alleviated by salicylic acid. South Afr. J. Bot. 77, 36–44. doi: 10.1016/j.sajb.2010.05.003
Alonso-Ramirez, A., Rodriguez, D., Reyes, D., Jimenez, J. A., Nicolas, G., Lopez-Climent, M., et al. (2009). Evidence for a role of gibberellins in salicylic acid-modulated early plant responses to abiotic stress in arabidopsis seeds. Plant Physiol. 150, 1335–1344. doi: 10.1104/pp.109.139352
Asaf, S., Khan, M. A., Khan, A. L., Waqas, M., Shahzad, R., Kim, A. Y., et al. (2017). Bacterial endophytes from arid land plants regulate endogenous hormone content and promote growth in crop plants: an example of Sphingomonas sp. and Serratia marcescens. J. Plant Interact. 12, 31–38. doi: 10.1080/17429145.2016.1274060
Azooz, M. M., Youssef, A. M., and Ahmad, P. (2011). Evaluation of salicylic acid (SA) application on growth, osmotic solutes and antioxidant enzyme activities on broad bean seedlings grown under diluted seawater. Int. J. Plant Physiol. Biochem. 3, 253–264.
Bano, A., Ullah, F., and Nosheen, A. (2012). Role of abscisic acid and drought stress on the activities of antioxidant enzymes in wheat. Plant Soil Environ. 58, 181–185. doi: 10.1371/journal.pone.0052439
Berg, G., Alavi, M., Schmidt, C. S., Zachow, C., Egamberdieva, D., Kamilova, F., et al. (2013). “Biocontrol and osmoprotection for plants under saline conditions,” in Molecular Microbial Ecology of the Rhizosphere, ed. F. J. de Bruijn (Hoboken, NJ: Wiley-Blackwell). doi: 10.1002/9781118297674.ch55
Bianco, C., and Defez, R. (2009). Medicago truncatula improves salt tolerance when nodulated by an indole-3-acetic acid-overproducing Sinorhizobium meliloti strain. J. Exp. Bot. 60, 3097–3107. doi: 10.1093/jxb/erp140
Borrell, A. K., Hammer, G. L., and Henzell, R. G. (2000). Does maintaining green leaf area in sorghum improve yield under drought? II. Dry matter production and yield. Crop Sci. 40, 1037–1048. doi: 10.2135/cropsci2000.4041037x
Bottini, R., Cassán, F., and Piccoli, P. (2004). Gibberellin production by bacteria and its involvement in plant growth promotion and yield increase. Appl. Microbiol. Biotechnol. 65, 497–503. doi: 10.1007/s00253-004-1696-1
Cabot, C., Sibole, J. V., Barcelo, J., and Poschenrieder, C. (2009). Abscisic acid decreases leaf Na+ exclusion in salt-treated Phaseolus vulgaris L. J. Plant Growth Regul. 28, 187–192. doi: 10.1007/s00344-009-9088-5
Cardinale, M., Ratering, S., Suarez, C., Montoya, A. M. Z., Geissler-Plaum, R., and Schnell, S. (2015). Paradox of plant growth promotion potential of rhizobacteria and their actual promotion effect on growth of barley (Hordeum vulgare L.) under salt stress. Microbiol. Res. 181, 22–32. doi: 10.1016/j.micres.2015.08.002
Cho, S. T., Chang, H. H., Egamberdieva, D., Kamilova, F., Lugtenberg, B., and Kuo, C. H. (2015). Genome analysis of Pseudomonas fluorescens PCL1751: a rhizobacterium that controls root diseases and alleviates salt stress for its plant host. PLOS ONE 10:e0140231. doi: 10.1371/journal.pone.0140231
Cohen, A. C., Bottini, R., Pontin, M., Berli, F. J., Moreno, D., Boccanlandro, H., et al. (2015). Azospirillum brasilense ameliorates the response of Arabidopsis thaliana to drought mainly via enhancement of ABA levels. Physiol. Plant. 153, 79–90. doi: 10.1111/ppl.12221
Contreras-Cornejo, H. A., Macías-Rodríguez, L. I., Cortés-Penagos, C., and López-Bucio, J. (2009). Trichoderma virens, a plant beneficial fungus, enhances biomass production and promotes lateral root growth through an auxin-dependent mechanism in Arabidopsis. Plant Physiol. 149, 1579–1592. doi: 10.1104/pp.108.130369
Cutler, S. R., Rodriguez, P. L., Finkelstein, R. R., and Abrams, S. R. (2010). Abscisic acid: emergence of a core signaling network. Annu. Rev. Plant Biol. 61, 651–679. doi: 10.1146/annurev-arplant-042809-112122
da Silva, A. S., Suassuna, J. F., de Melo, A. S., Costa, R. R., de Andrade, W. L., and da Silva, D. C. (2017). Salicylic acid as attenuator of drought stress on germination and initial development of sesame. Rev. Bras. Eng. Agríc. Ambient. 21, 156–162. doi: 10.1590/1807-1929/agriambi.v21n3p156-162
de Santi Ferrara, F. I., Oliveira, Z. M., Gonzales, H. H. S., Floh, E. I. S., and Barbosa, H. R. (2012). Endophytic and rhizospheric enterobacteria isolated from sugar cane have different potentials for producing plant growth-promoting substances. Plant Soil 353, 409–417. doi: 10.1007/s11104-011-1042-1
Dourado, M. N., Martins, P. F., Quecine, M. C., Piotto, F. A., Souza, L. A., Franco, M. R., et al. (2013). Burkholderia sp. SCMS54 reduces cadmium toxicity and promotes growth in tomato. Ann. Appl. Biol. 163, 494–507.
Egamberdieva, D. (2011). Survival of Pseudomonas extremorientalis TSAU20 and P. chlororaphis TSAU13 in the rhizosphere of common bean (Phaseolus vulgaris) under saline conditions. Plant Soil Environ. 57, 122–127.
Egamberdieva, D. (2012). Pseudomonas chlororaphis: a salt tolerant bacterial inoculant for plant growth stimulation under saline soil conditions. Acta Physiol. Plant. 34, 751–756. doi: 10.1007/s11738-011-0875-9
Egamberdieva, D., Kamilova, F., Validov, S., Gafurova, L., Kucharova, Z., and Lugtenberg, B. (2008). High incidence of plant growth-stimulating bacteria associated with the rhizosphere of wheat grown in salinated soil in Uzbekistan. Environ. Microbiol. 19, 1–19. doi: 10.1111/j.1462-2920.2007.01424.x
Egamberdieva, D., Kucharova, Z., Davranov, K., Berg, G., Makarova, N., Azarova, T., et al. (2011). Bacteria able to control foot and root rot and to promote growth of cucumber in salinated soils. Biol. Fertil. Soils 47, 197–205. doi: 10.1007/s00374-010-0523-3
Egamberdieva, D., Wirth, S., Behrendt, U., Abd-Allah, E. F., and Berg, G. (2016). Biochar treatment resulted in a combined effect on soybean growth promotion and a shift in plant growth promoting rhizobacteria. Front. Microbiol. 7:209. doi: 10.3389/fmicb.2016.00209
Egamberdieva, D., Wirth, S., Behrendt, U., Parvaiz, A., and Berg, G. (2017a). Antimicrobial activity of medicinal plants correlates with the proportion of antagonistic endophytes. Front. Microbiol. 8:199. doi: 10.3389/fmicb.2017.00199
Egamberdieva, D., Wirth, S., Jabborova, D., Räsänen, L. A., and Liao, H. (2017b). Coordination between Bradyrhizobium and Pseudomonas alleviates salt stress in soybean through altering root system architecture. J. Plant Interact. 12, 100–107. doi: 10.1080/17429145.2017.1294212
Egamberdieva, D., Wirth, S., Shurigin, V., Hashem, A., and Abd_Allah, E. F. (2017c). Endophytic bacteria improve plant growth, symbiotic performance of chickpea (Cicer arietinum L.) and induce suppression of root rot caused by Fusarium solani under salt stress. Front. Microbiol. 8:1887. doi: 10.3389/fmicb.2017.01887
Egamberdiyeva, D., and Hoflich, G. (2003). The effect of associative bacteria from different climates on plant growth of pea at different soils and temperatures. Arch. Agric. Soil Sci. 49, 203–213. doi: 10.1080/0365034031000101355a
Etesami, H., Alikhani, H. A., and Hosseini, H. M. (2015). Indole-3-acetic acid (IAA) production trait, a useful screening to select endophytic and rhizosphere competent bacteria for rice growth promoting agents. MethodsX 2, 72–78. doi: 10.1016/j.mex.2015.02.008
FAO (2010). FAO Land and Plant Nutrition Management Service. Available at: http://www.fao.org
Fässler, E., Evangeloua, M. W., Robinson, B. H., and Schulin, R. (2010). Effects of indole-3-acetic acid (IAA) on sunflower growth and heavy metal uptake in combination with ethylene diamine disuccinic acid (EDDS). Chemosphere 80, 901–907. doi: 10.1016/j.chemosphere.2010.04.077
Forchetti, G., Masciarelli, O., Alemano, S., Alvarez, D., and Abdala, G. (2007). Endophytic bacteria in sunflower (Helianthus annuus L.) isolation, characterization, and production of jasmonates and abscisic acid in culture medium. Appl. Microbiol. Biotechnol. 76, 1145–1152. doi: 10.1007/s00253-007-1077-7
Forchetti, G., Masciarelli, O., Izaguirre, M. J., Alemano, S., Alvarez, D., and Abdala, G. (2010). Endophytic bacteria improve seedling growth of sunflower under water stress, produce salicylic acid, and inhibit growth of pathogenic fungi. Curr. Microbiol. 61, 485–493. doi: 10.1007/s00284-010-9642-1
Gomez, C. A., Arbona, V., Jacas, J., PrimoMillo, E., and Talon, M. (2002). Abscisic acid reduces leaf abscission and increases salt tolerance in citrus plants. J. Plant Growth Regul. 21, 234–240. doi: 10.1007/s00344-002-0013-4
Groppa, M. D., Ianuzzo, M. P., Rosales, E. P., Vazquez, S. C., and Benavides, M. P. (2012). Cadmium modulates NADPH oxidase activity and expression in sunflower leaves. Biol. Plant. 56, 167–171. doi: 10.1007/s10535-012-0036-z
Grover, A., Mittal, D., Negi, M., and Lavania, D. (2013). Generating high temperature tolerant transgenic plants: achievements and challenges. Plant Sci. 20, 38–47. doi: 10.1016/j.plantsci.2013.01.005
Großkinsky, D. K., Tafner, R., Moreno, M. V., Stenglein, S. A., García de Salamone, I. E., Nelson, L. M., et al. (2016). Cytokinin production by Pseudomonas fluorescens G20-18 determines biocontrol activity against Pseudomonas syringae in Arabidopsis. Sci. Rep. 6:23310. doi: 10.1038/srep23310
Guajardo, E., Correa, J. A., and Contreras-Porcia, L. (2016). Role of abscisic acid (ABA) in activating antioxidant tolerance responses to desiccation stress in intertidal seaweed species. Planta 243, 767–781. doi: 10.1007/s00425-015-2438-6
Gunes, A., Inal, A., Alpaslam, M., Erslan, F., Bagsi, E. G., and Cicek, N. (2007). Salicylic acid induced changes on some physiological parameters symptomatic for oxidative stress and mineral nutrition in maize (Zea mays L.) grown under salinity. J. Plant Physiol. 164, 728–736. doi: 10.1016/j.jplph.2005.12.009
Gutiérrez-Mañero, F. J., Ramos, B., Probanza, A., Mehouachi, J., and Talon, M. (2001). The plant growth promoting rhizobacteria Bacillus pumilus and Bacillus licheniformis produce high amounts of physiologically active gibberellins. Physiol. Plant. 111, 206–211. doi: 10.1034/j.1399-3054.2001.1110211.x
Hart, J. J., Welch, R. M., Norvell, W. A., Sullivan, L. A., and Kochian, L. V. (1998). Characterization of cadmium binding, uptake, and translocation in intact seedlings of bread and durum wheat cultivars. Plant Physiol. 116, 1413–1420. doi: 10.1104/pp.116.4.1413
Hashem, A., Abd_Allah, E. F., Alqarawi, A., Al-Huqail, A. A., Wirth, S., and Egamberdieva, D. (2016). The interaction between arbuscular mycorrhizal fungi and endophytic bacteria enhances plant growth of Acacia gerrardii under salt stress. Front. Plant Sci. 7:1089. doi: 10.3389/fmicb.2016.01089
Hayat, S., Hasan, S. A., Fariduddin, Q., and Ahmad, A. (2008). Growth of tomato (Lycopersicon esculentum) in response to salicylic acid under water stress. J. Plant Interact. 3, 297–304. doi: 10.1080/17429140802320797
Hidri, R., Barea, J. M., Mahmoud, O. M., Abdelly, C., and Azcón, R. (2016). Impact of microbial inoculation on biomass accumulation by Sulla carnosa provenances, and in regulating nutrition, physiological and antioxidant activities of this species under non-saline and saline conditions. J. Plant Physiol. 201, 28–41. doi: 10.1016/j.jplph.2016.06.013
Hu, Y. F., Zhou, G., Na, X. F., Yang, L., Nan, W. B., Liu, X., et al. (2013). Cadmium interferes with maintenance of auxin homeostasis in Arabidopsis seedlings. J. Plant Physiol. 170, 965–975. doi: 10.1016/j.jplph.2013.02.008
Indiragandhi, P., Anandham, R., Madhaiyan, M., and Sa, T. M. (2008). Characterization of plant growth-promoting traits of bacteria isolated from larval guts of diamondback moth Plutella xylostella (Lepidoptera: Plutellidae). Curr. Microbiol. 56, 327–333. doi: 10.1007/s00284-007-9086-4
Iqbal, M., and Ashraf, M. (2007). Seed treatment with auxins modulates growth and ion partitioning in salt-stressed wheat plants. J. Integr. Plant Biol. 49, 1003–1015. doi: 10.1111/j.1672-9072.2007.00488.x
Iqbal, M., and Ashraf, M. (2013). Gibberellic acid mediated induction of salt tolerance in wheat plants: growth, ionic partitioning, photosynthesis, yield and hormonal homeostasis. Environ. Exp. Bot. 86, 76–85. doi: 10.1016/j.envexpbot.2010.06.002
Islam, F., Yasmeen, T., Arif, M. S., Riaz, M., Shahzad, S. M., Imran, Q., et al. (2016). Combined ability of chromium (Cr) tolerant plant growth promoting bacteria (PGPB) and salicylic acid (SA) in attenuation of chromium stress in maize plants. Plant Physiol. Biochem. 108, 456–467. doi: 10.1016/j.plaphy.2016.08.014
Janda, K., Éva, S. G. H., Kovács, L., and Janda, T. (2012). Salicylic acid may indirectly influence the photosynthetic electron transport. J. Plant Physiol. 169, 971–978. doi: 10.1016/j.jplph.2012.02.020
Karadeniz, A., Topcuoğlu, Ş, and İnan, S. (2006). Auxin, gibberellin, cytokinin and abscisic acid production in some bacteria. World J. Microbiol. Biotechnol. 22, 1061–1064. doi: 10.1007/s11274-005-4561-1
Khadri, M., Tejera, N. A., and Lluch, C. (2006). Alleviation of salt stress in common bean (Phaseolus vulgaris) by exogenous abscisic acid supply. J. Plant Growth Regul. 25, 110–119. doi: 10.1007/s00344-005-0004-3
Khan, A. L., Hamayun, M., Kim, Y.-H., Kang, S. M., Lee, J. H., and Lee, I. N. (2011). Gibberellins producing endophytic Aspergillus fumigatus sp. LH02 influenced endogenous phytohormonal levels, isoflavonoids production and plant growth in salinity stress. Process Biochem. 46, 440–447. doi: 10.1016/j.procbio.2010.09.013
Khan, A. L., Hussain, J., Al-Harrasi, A., Al-Rawahi, A., and Lee, I. J. (2013). Endophytic fungi: a source of gibberellins and crop resistance to abiotic stress. Crit. Rev. Biotechnol. 35, 62–74. doi: 10.3109/07388551.2013.800018
Khan, M. I. R., Asgher, M., and Khan, N. A. (2014). Alleviation of salt-induced photosynthesis and growth inhibition by salicylic acid involves glycine betaine and ethylene in mungbean (Vigna radiata L.). Plant Physiol. Biochem. 80, 67–74. doi: 10.1016/j.plaphy.2014.03.026
Khan, W. U., Ahmad, S. R., Yasin, N. A., Ali, A., Ahmad, A., and Akram, W. (2017). Application of Bacillus megaterium MCR-8 improved phytoextraction and stress alleviation of nickel in Vinca rosea. Int. J. Phytoremediation 19, 813–824. doi: 10.1080/15226514.2017.1290580
Kudoyarova, G. R., Melentiev, A. I., Martynenko, E. V., Timergalina, L. N., Arkhipova, T. N., Shendel, G. V., et al. (2014). Cytokinin producing bacteria stimulate amino acid deposition by wheat roots. Plant Physiol. Biochem. 83, 285–291. doi: 10.1016/j.plaphy.2014.08.015
Lavania, M., and Nautiyal, C. (2013). Solubilization of tricalcium phosphate by temperature and salt tolerant Serratia marcescens NBRI1213 isolated from alkaline soils. Afr. J. Microbiol. Res. 7, 4403–4413.
Lawongsa, P., Boonkerd, N., Wongkaew, S., O’Gara, F., and Teaumroong, N. (2008). Molecular and phenotypic characterization of potential plant growth-promoting Pseudomonas from rice and maize rhizospheres. World J. Microbiol. Biotechnol. 24, 1877–1884. doi: 10.1007/s11274-008-9685-7
Li, X., Cai, J., Liu, F., Dai, T., Cao, W., and Jiang, D. (2014). Exogenous abscisic acid application during grain filling in winter wheat improves cold tolerance of offspring’s seedlings. J. Agric. Crop Sci. 200, 467–478. doi: 10.1111/jac.12064
Liu, F., Xing, S., Ma, H., Du, Z., and Ma, B. (2013). Cytokinin-producing, plant growth-promoting rhizobacteria that confer resistance to drought stress in Platycladus orientalis container seedlings. Appl. Microbiol. Biotechnol. 97, 9155–9164. doi: 10.1007/s00253-013-5193-2
Liu, Y., Shi, Z., Yao, L., Yue, H., Li, H., and Li, C. (2013). Effect of IAA produced by Klebsiella oxytoca Rs-5 on cotton growth under salt stress. J. Gen. Appl. Microbiol. 59, 59–65. doi: 10.2323/jgam.59.59
Ma, Y., Rajkumar, M., and Fritas, H. (2008). Inoculation of plant growth promoting bacterium Achromobacter xylosoxidans strain Ax10 for the improvement of copper phytoextraction by Brassica juncea. J. Environ. Manag. 90, 831–837. doi: 10.1016/j.jenvman.2008.01.014
Maggio, A., Barbieri, G., Raimondi, G., and De Pascale, S. (2010). Contrasting effects of ga3 treatments on tomato plants exposed to increasing salinity. J. Plant Growth Regul. 29, 63–72. doi: 10.1007/s00344-009-9114-7
Mahalingam, R. (2015). “Consideration of combined stress: a crucial paradigm for improving multiple stress tolerance in plants,” in Combined Stresses in Plants, ed. R. Mahalingam (Berlin: Springer), 1–25. doi: 10.1007/978-3-319-07899-1
Manjili, F. A., Sedghi, M., and Pessarakli, M. (2012). Effects of phytohormones on proline content and antioxidant enzymes of various wheat cultivars under salinity stress. J. Plant Nutr. 35, 1098–1111. doi: 10.1080/01904167.2012.671411
Marulanda, A., Barea, J. M., and Azcón, R. (2009). Stimulation of plant growth and drought tolerance by native microorganisms (AM fungi and bacteria) from dry environments: mechanisms related to bacterial effectiveness. J. Plant Growth Regul. 28, 115–124. doi: 10.1007/s00344-009-9079-6
Mendes, R., Garbeva, P., and Raaijmakers, J. M. (2013). The rhizosphere microbiome: significance of plant beneficial, plant pathogenic, and human pathogenic microorganisms. FEMS Microbiol. Rev. 37, 634–663. doi: 10.1111/1574-6976.12028
Mishra, S. K., Khan, M. H., Misra, S., Dixit, K. V., Khare, P., Srivastava, S., et al. (2017). Characterisation of Pseudomonas spp. and Ochrobactrum sp. isolated from volcanic soil. Antonie Van Leeuwenhoek 110, 253–270. doi: 10.1007/s10482-016-0796-0
Mohapatra, P. K., Panigrahi, R., and Turner, N. C. (2011). Physiology of spikelet development on the rice panicle: is manipulation of apical dominance crucial for grain yield improvement? Adv. Agron. 110, 333–360. doi: 10.1016/B978-0-12-385531-2.00005-0
Mora-Herrera, M. E., and Lopez-Delgado, H. A. (2007). Freezing tolerance and antioxidant activity in potato microplants induced by abscisic acid treatment. Am. J. Potato Res. 84, 467–475. doi: 10.1007/BF02987883
Nabti, E., Sahnoune, M., Adjrad, S., Van Dommelen, A., Ghoul, M., Schmid, M., et al. (2007). A Halophilic and osmotolerant Azospirillum brasilense strain from algerian soil restores wheat growth under saline conditions. Eng. Life Sci. 7, 354–360. doi: 10.1002/elsc.200720201
Nadeem, S. M., Ahmad, M., Zahir, Z. A., Javaid, A., and Ashraf, M. (2014). The role of mycorrhizae and plant growth promoting rhizobacteria (PGPR) in improving crop productivity under stressful environments. Biotechnol. Adv. 32, 429–448. doi: 10.1016/j.biotechadv.2013.12.005
Nayyar, H., Bains, T. S., and Kumar, S. (2005). Chilling stressed chickpea seedlings: effect of cold acclimation, calcium and abscisic acid on cryoprotective solutes and oxidative damage. Environ. Exp. Bot. 54, 275–285. doi: 10.1016/j.envexpbot.2004.09.007
Naz, I., Bano, A., and Ul-Hassan, T. (2009). Isolation of phytohormones producing plant growth promoting rhizobacteria from weeds growing in Khewra salt range, Pakistan and their implication in providing salt tolerance to Glycine max L. Afr. J. Biotechnol. 8, 5762–5766. doi: 10.5897/AJB09.1176
Park, J., Kim, Y. S., Kim, S. G., Jung, J. H., Woo, J. C., and Park, C. M. (2011). Integration of auxin and salt signals by the NAC transcription factor NTM2 during seed germination in Arabidopsis. Plant Physiol. 156, 537–549. doi: 10.1104/pp.111.177071
Park, Y. G., Mun, B. G., Kang, S. M., Hussain, A., Shahzad, R., Seo, C. W., et al. (2017). Bacillus aryabhattai SRB02 tolerates oxidative and nitrosative stress and promotes the growth of soybean by modulating the production of phytohormones. PLOS ONE 12:e0173203. doi: 10.1371/journal.pone.0173203
Pereira, S. I. A., Monteiro, C., Vega, A. L., and Castro, P. M. L. (2016). Endophytic culturable bacteria colonizing Lavandula dentata L. plants: isolation, characterization and evaluation of their plant growth-promoting activities. Ecol. Eng. 87, 91–97. doi: 10.1016/j.ecoleng.2015.11.033
Piccoli, P., Travaglia, C., Cohen, A., Sosa, L., Cornejo, P., Masuelli, R., et al. (2011). An endophytic bacterium isolated from roots of the halophyte Prosopis strombulifera produces ABA, IAA, gibberellins A1 and A3 and jasmonic acid in chemically-defined culture medium. Plant Growth Regul. 64, 207–210. doi: 10.1007/s10725-010-9536-z
Ruanpanun, P., Tangchitsomkid, N., Hyde, K. D., and Lumyong, S. (2010). Actinomycetes and fungi isolated from plant-parasitic nematode infested soils: screening of the effective biocontrol potential, indole-3-acetic acid and siderophore production. World J. Microbiol. Biotechnol. 26, 1569–1578. doi: 10.1007/s11274-010-0332-8
Ruiz-Lozano, J. M., Porcel, R., Azcon, R., and Aroca, R. (2012). Regulation by arbuscular mycorrhizae of the integrated physiological response to salinity in plants. New challenges in physiological and molecular studies. J. Exp. Bot. 63, 4033–4044. doi: 10.1093/jxb/ers126
Salomon, M. V., Bottini, R., de Souza Filho, G. A., Cohen, A. C., Moreno, D., Gil, M., et al. (2014). Bacteria isolated from roots and rhizosphere of Vitis vinifera retard water losses, induce abscisic acid accumulation and synthesis of defense-related terpenes in in vitro cultured grapevine. Physiol. Plant. 51, 359–374. doi: 10.1111/ppl.12117
Senaratna, T., Touchell, D., Bunns, E., and Dixon, K. (2000). Acetyl salicylic acid (aspirin) and salicylic acid induce multiple stress tolerance in bean and tomato plants. Plant Growth Regul. 30, 157–161. doi: 10.1023/A:1006386800974
Sgroy, V., Cassán, F., Masciarelli, O., Del Papa, M. F., Lagares, A., and Luna, V. (2009). Isolation and characterization of endophytic plant growth-promoting (PGPB) or stress homeostasis-regulating (PSHB) bacteria associated to the halophyte Prosopis strombulifera. Appl. Microbiol. Biotechnol. 85, 371–381. doi: 10.1007/s00253-009-2116-3
Shahzad, R., Khan, A. L., Bilal, S., Waqas, M., Kang, S. M., and Lee, I. J. (2017). Inoculation of abscisic acid-producing endophytic bacteria enhances salinity stress tolerance in Oryza sativa. Environ. Exp. Bot. 136, 68–77. doi: 10.1016/j.envexpbot.2017.01.010
Shahzad, R., Waqas, M., Khan, A. L., Asaf, S., Khan, M. A., Kang, S. M., et al. (2016). Seed-borne endophytic Bacillus amyloliquefaciens RWL-1 produces gibberellins and regulates endogenous phytohormones of Oryza sativa. Plant Physiol. Biochem. 106, 236–243. doi: 10.1016/j.plaphy.2016.05.006
Shakirova, F. M. (2007). “Role of hormonal system in manifestation of growth promoting and antistress action of salicylic acid,” in Salicylic Acid a Plant Hormone, eds S. Hayat and A. Ahmad (Dordrecht: Springer), 69–89.
Shakirova, F. M., Sakhabutdinova, A. R., Bezrukova, M. V., Fatkhutdinova, R. A., and Fatkhutdinova, D. R. (2003). Changes in the hormonal status of wheat seedlings induced by salicylic acid and salinity. Plant Sci. 164, 317–322. doi: 10.1016/S0168-9452(02)00415-6
Shutsrirung, A., Chromkaew, Y., Pathom-Aree, W., Choonluchanon, S., and Boonkerd, N. (2013). Diversity of endophytic actinomycetes in mandarin grown in northern Thailand, their phytohormone production potential and plant growth promoting activity. Soil Sci. Plant Nutr. 59, 322–330. doi: 10.1080/00380768.2013.776935
Singh, R. P., and Jha, P. N. (2016). A halotolerant bacterium Bacillus licheniformis HSW-16 augments induced systemic tolerance to salt stress in wheat plant (Triticum aestivum). Front. Plant Sci. 7:1890. doi: 10.3389/fpls.2016.01890
Singh, S., and Prasad, S. M. (2014). Growth, photosynthesis and oxidative responses of Solanum melongena L. seedlings to cadmium stress: mechanism of toxicity amelioration by kinetin. Sci. Hortic. 176, 1–10. doi: 10.1016/j.scienta.2014.06.022
Sorty, A. M., Meena, K. K., Choudhary, K., Bitla, U. M., Minhas, P. S., and Krishnani, K. K. (2016). Effect of plant growth promoting bacteria associated with halophytic weed (Psoralea corylifolia L.) on germination and seedling growth of wheat under saline conditions. Appl. Biochem. Biotechnol. 180, 872–882. doi: 10.1007/s12010-016-2139-z
Spaepen, S., Boddelaere, S., Croonenborghs, A., and Vanderleyden, J. (2008). Effect of Azospirillum brasiliense indole-3-acetic acid production on inoculated wheat plants. Plant Soil 312, 15–23. doi: 10.1016/j.resmic.2010.01.005
Spollen, W. G., Le Noble, M. E., Samuels, T. D., Bernstein, N., and Sharp, R. E. (2000). Abscisic acid accumulation maintains maize primary root elongation at low water potentials by restricting ethylene production. Plant Physiol. 122, 967–976. doi: 10.1104/pp.122.3.967
Stevens, J., Senaratna, T., and Sivasithamparam, K. (2006). Salicylic acid induces salinity tolerance in tomato (Lycopersicon esculentum cv. Roma): associated changes in gas exchange, water relations and membrane stabilisation. Plant Growth Regul. 49, 77–83. doi: 10.1089/omi.2011.0071
Tang, Y., Sun, X., Wen, T., Liu, M., Yang, M., and Chen, X. (2017). Implications of terminal oxidase function in regulation of salicylic acid on soybean seedling photosynthetic performance under water stress. Plant Physiol. Biochem. 112, 19–28. doi: 10.1016/j.plaphy.2016.11.016
Tsavkelova, E. A., Cherdyntseva, T. A., Klimova, S. Y., Shestakov, A. I., Botina, S. G., and Netrusov, A. I. (2007). Orchid-associated bacteria produce indole-3-acetic acid, promote seed germination, and increase their microbial yield in response to exogenous auxin. Arch. Microbiol. 188, 655–664. doi: 10.1007/s00203-007-0286-x
Tuna, A. L., Kaya, C., Dikilitas, M., and Higgs, D. (2008). The combined effects of gibberellic acid and salinity on some antioxidant enzyme activities, plant growth parameters and nutritional status in maize plants. Environ. Exp. Bot. 63, 1–9. doi: 10.1016/j.envexpbot.2007.06.007
Turan, M., Ekinci, M., Yildirim, E., GneŞ, A., Karagz, K., Kotan, R., et al. (2014). Plant growth-promoting rhizobacteria improved growth, nutrient, and hormone content of cabbage (Brassica oleracea) seedlings. Turk. J. Agric. For. 38, 327–333. doi: 10.3906/tar-1308-62
Upadhyay, S. K., Singh, J. S., Saxena, A. K., and Singh, D. P. (2012). Impact of PGPR inoculation on growth and antioxidant status of wheat under saline conditions. Plant Biol. 14, 605–611. doi: 10.1111/j.1438-8677.2011.00533.x
Vijayabharathi, R., Sathya, A., and Gopalakrishnan, S. (2016). “A Renaissance in plant growth-promoting and biocontrol agents by endophytes,” in Microbial Inoculants in Sustainable Agricultural Productivity, eds D. P. Singh, H. B. Singh, and R. Prabha (New Delhi: Springer), 37–61. doi: 10.1007/978-81-322-2647-5_3
Vysotskaya, L. B., Korobova, A. V., Veselov, S. Y., Dodd, I. C., and Kudoyarova, G. R. (2009). ABA mediation of shoot cytokinin oxidase activity: assessing its impacts on cytokinin status and biomass allocation of nutrient deprived durum wheat. Funct. Plant Biol. 36, 66–72. doi: 10.1071/FP08187
Wang, Q., Dodd, I. C., Belimov, A. A., and Jiang, F. (2016). Rhizosphere bacteria containing 1-aminocyclopropane-1-carboxylate deaminase increase growth and photosynthesis of pea plants under salt stress by limiting Na+ accumulation. Funct. Plant Biol. 43, 161–172. doi: 10.1071/FP15200
Wang, S., Ren, X., Huang, B., Wang, G., Zhou, P., and An, P. (2016). Aluminium-induced reduction of plant growth in alfalfa (Medicago sativa) is mediated by interrupting auxin transport and accumulation in roots. Sci. Rep. 6:30079. doi: 10.1038/srep30079
Waqas, M., Khan, A. L., Kamran, M., Hamayun, M., Kang, S. M., Kim, Y. H., et al. (2012). Endophytic fungi produce gibberellins and indoleacetic acid and promotes host-plant growth during stress. Molecules 17, 10754–10773. doi: 10.3390/molecules170910754
Wilkinson, S., Kudoyarova, G. R., Veselov, D. S., Arkhipova, T. N., and Davies, W. J. (2012). Plant hormone interactions: innovative targets for crop breeding and management. J. Exp. Bot. 63, 3499–3509. doi: 10.1093/jxb/ers148
Wolbang, C. M., Chandler, P. M., Smith, J. J., and Ross, J. J. (2004). Auxin from the developing inflorescence is required for the biosynthesis of active gibberellins in barley stems. Plant Physiol. 134, 769–776. doi: 10.1104/pp.103.030460
Yandigeri, M. S., Meena, K. K., Singh, D., Malviya, N., Singh, D. P., Solanki, M. K. A., et al. (2012). Drought-tolerant endophytic actinobacteria promote growth of wheat (Triticum aestivum) under water stress conditions. Plant Growth Regul. 68, 411–420. doi: 10.1007/s10725-012-9730-2
Zaheer, A., Mirza, B. S., Mclean, J. E., Yasmin, S., Shah, S. M., Malik, K. A., et al. (2016). Association of plant growth-promoting Serratia spp. with the root nodules of chickpea. Res. Microbiol. 167, 510–520. doi: 10.1016/j.resmic.2016.04.001
Zaidi, S., Usmani, S., Singh, B. R., and Musarrat, J. (2006). Significance of Bacillus subtilis strain SJ-101 as a bioinoculant for concurrent plant growth promotion and nickel accumulation in Brassica juncea. Chemosphere 64, 991–997. doi: 10.1016/j.chemosphere.2005.12.057
Zhang, P., Wang, W. Q., Zhang, G. L., Kaminek, M., Dobrev, P., Xu, J., et al. (2010). Senescence-inducible expression of isopentenyl transferase extends leaf life, increases drought stress resistance and alters cytokinin metabolism in cassava. J. Integr. Plant Biol. 52, 653–669. doi: 10.1111/j.1744-7909.2010.00956.x
Zhao, L., and Zhang, Y. (2015). Effects of phosphate solubilization and phytohormone production of Trichoderma asperellum Q1 on promoting cucumber growth under salt stress. J. Integr. Agric. 14, 1588–1597. doi: 10.1016/S2095-3119(14)60966-7
Zhou, B., Guo, Z., Xing, J., and Huang, B. (2005). Nitric oxide is involved in abscisic acid-induced antioxidant activities in Stylosanthes guianensis. J. Exp. Bot. 56, 3223–3228. doi: 10.1093/jxb/eri319
Zhou, L., Xu, H., Mischke, S., Meinhardt, L. M., Zhang, D., Zhu, X., et al. (2014). Exogenous abscisic acid significantly affects proteome in tea plant (Camellia sinensis) exposed to drought stress. Hortic. Res. 1:14029. doi: 10.1038/hortres.2014.29
Keywords: abiotic stress, plant microbiome, metabolites, phytohormones
Citation: Egamberdieva D, Wirth SJ, Alqarawi AA, Abd_Allah EF and Hashem A (2017) Phytohormones and Beneficial Microbes: Essential Components for Plants to Balance Stress and Fitness. Front. Microbiol. 8:2104. doi: 10.3389/fmicb.2017.02104
Received: 19 May 2017; Accepted: 16 October 2017;
Published: 31 October 2017.
Edited by:Ying Ma, University of Coimbra, Portugal
Reviewed by:Kemal Kazan, Commonwealth Scientific and Industrial Research Organisation (CSIRO), Australia
Jose Antonio Lucas Lucas Garcia, Centro de Estudios Universitarios, Mexico
Ramon Gerardo Guevara-Gonzalez, Universidad Autónoma de Querétaro, Mexico
Copyright © 2017 Egamberdieva, Wirth, Alqarawi, Abd_Allah and Hashem. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Dilfuza Egamberdieva, firstname.lastname@example.org