Soil moisture severely influences crop productivity in arid and semiarid areas. Low moisture content in the soil due to low annual precipitation creates drought stress in plants. Regulating the uptake and distribution of nutrients, transport of water, and accumulation of compatible solutes and antioxidants in plant tissues can help to improve plant productivity under drought conditions (Boomsma and Vyn, 2008). Applying drought-tolerant Bacillus spp. to the soil increases the populations of these bacteria on the roots and stimulates root exudation to promote both bacterial and plant growth (Sandhya et al., 2011). Plants colonized by Bacillus spp. take up more water, which is an important mechanism for plant protection against drought-induced damage (Marulanda et al., 2009). The mitigating effects of Bacillus-induced physiological changes in plants are shown in Figure 1 and Table 2.

The uptake of N, P, and potassium (K⁺) decreases in drought-injured plants, whereas treatments with Bacillus spp. increase these macro nutrients in stressed plants (Barnawal et al., 2013). Bacterial enzymes increase the accumulation of the bioavailable forms of these macro nutrients in the soil and plants (Kang et al., 2015a; Kuan et al., 2016). In addition, these bacteria regulate high-affinity potassium transporter 1 (HKT1), which modulates Na⁺/K⁺ homeostasis, to mitigate drought stress (Gassmann et al., 1996; Vieira-Pires et al., 2013). Furthermore, K⁺ plays a key role in stomatal opening, turgor pressure maintenance, osmotic balance and controlling the transpiration rate in plants under drought stress (Loutfy et al., 2012). The scavenging activity of K⁺ helps to inhibit reactive oxygen species (ROS) formation during photosynthesis and NADPH oxidase metabolism (Cakmak, 2005). The concentrations of plant nutrients, such as Ca⁺⁺, Mg⁺⁺, Zn⁺⁺, Mn⁺⁺, and Cu⁺⁺, are increased by Bacillus megaterium, Bacillus thuringiensis and Bacillus spp. applications in drought-stressed lavandula (Lavandula angustifolia L.) and salvia (Salvia divinorum L.) plants (Armada et al., 2014). Ca⁺⁺ is involved in stabilizing membrane systems, and the accumulation of Mg⁺⁺ regulates the homeostasis of ions in the chloroplasts, vacuoles and stomata of plant tissues (Shaul-Keinan et al., 2002; Huda et al., 2013). Some Bacillus spp., enhance plant growth during drought stress by increasing Fe levels. The high level of Fe⁺⁺ in plants is probably due to siderophores derived from Bacillus spp. (Zawadzka et al., 2009). Aquaporins, particularly those encoded by the plasma membrane intrinsic protein (PIP) subfamily of aquaporin genes (Maurel et al., 2008), offer a low-resistance pathway for the movement of water across membranes to compensate for drought effects. Bacillus spp. regulate all the PIP genes to increase the hydraulic conductivity of roots in drought stressed plants, and aquaporins also transport urea, CO₂ and H₂O₂ for N metabolism, carbon fixation and stress signaling, respectively (Armada et al., 2015).

The limited uptake of water and nutrients disturbs the normal cellular physiological processes and generates ROS, which damage proteins, lipids and nucleic acids in drought-exposed plants (Zgallai et al., 2005; Miller et al., 2010). ROS accumulation affects lipid membranes and causes lipid peroxidation and enhanced electrolyte leakage. Recovery from oxidative stress-induced damage is possible via antioxidant synthesis, which inhibits ROS formation. Bacillus-based bacterial association in plants can reduce the synthesis of ROS in cells via various scavenging enzymes (Kakar et al., 2016). Bacillus spp. either increase or decrease antioxidant enzyme activities in plants to mitigate drought stress. For example, B. safensis increases catalase (CAT; EC 1.11.1.6), superoxide dismutase (SOD; EC 1.15.1.1), peroxidase (POD; EC 1.11.1.7), ascorbate peroxidase (APX; EC 1.11.1.11) and glutathione reductase (GR; EC 1.6.4.2) activities (Chakraborty et al., 2013), while B. amyloliquefaciens decreases APX, GR and dehydroascorbate reductase (DHAR; 1.8.5.1) activities in plants under drought stress (Kasim et al., 2013).

The drought-induced oversynthesis of proline is suppressed in bacteria-treated plants, reflecting bacterial-derived resistance to the detrimental effects induced by drought (Barnawal et al., 2013). The normal metabolism of carbohydrates and amino acids is disturbed in plants during drought stress, and this effect is possibly reversed by interactions with Bacillus spp. Sucrose and fructose concentrations are enhanced in plants to contribute to drought adaptation by increasing root growth (Gagne-Bourque et al., 2016). As a consequence of stress, some of the endogenous amino acid accumulation triggers the production of secondary metabolites in stress-affected plants to mitigate oxidative stress (Jia et al., 2001). The synthesis of aromatic, glutamic and aspartic amino acid families is greater in plants associated with Bacillus spp. Histidine, tyrosine, phenylalanine, valine, leucine, isoleucine, asparagine, serine and γ-aminobutyric acid levels are increased due to the effects of drought in soil (Gagne-Bourque et al., 2016).

Drought inhibits pigment synthesis and reduces photosynthesis, while Bacillus spp. stimulate the synthesis of chlorophylls a and b and carotenoid in stressed plants, which increases photosynthesis (Barnawal et al., 2013; Hashem et al., 2015). The modulation of plant hormonal signals reprograms plant growth during drought stress. The hormone- and ACC deaminase-producing Bacillus spp. regulate plant growth by enhancing levels of stress-related hormones, such as salicylic acid (SA), jasmonic acid (JA) and abscisic acid (ABA), and reducing ACC, which is responsible for generating ethylene (Barnawal et al., 2013; Castillo et al., 2013). ABA accumulation improves drought tolerance by activating antioxidant enzymes and prevents water loss by stomatal closure (Lu et al., 2009; Zhu et al., 2011). Similarly, SA induces the expression of stress-related genes to maintain membrane stability and prevent the accumulation of ROS (El-Tayeb, 2005; Jumali et al., 2011).

The normal gene expression pattern in plants is altered during drought. The expression of OsDIL (drought-induced lipid transfer protein), OsDREB1A (dehydration-responsive element-binding protein 1A), OsGAPDH (glyceraldehyde-3-phosphate dehydrogenase), OsWRKY11 (WRKY transcription factor 11), P4H (prolyl-4-hydroxylase), Cadhn (dehydrin-like protein), VA (vacuolar H⁺-ATPase), sHSP (small heat shock protein), CaPR-10 (pathogenesis-related protein 10), cAPX (cytosolic ascorbate peroxidase), rbcL (ribulose-1,5-bisphosphate carboxy/oxygenase large subunit) and rbcS (ribulose-1,5-bisphosphate carboxy/oxygenase small subunit) genes are affected during drought stress in crop plants. The lipid transfer is essential for development of lipidic orbicules and pollen exine formation, which is initiated by OsDIL genes (Zhang et al., 2010). DREB proteins involves in ABA-dependent and independent pathways to enhance the stress tolerance (Lata and Prasad, 2011). Similarly, GAPDH gene participates in cell proliferation, regulation of telomere length, apoptotic pathway and DNA repair (Kosova et al., 2017). WRKY 11 gene induces systemic resistance through JA/ethylene mediated metabolic pathway (Jiang et al., 2016). However, P4H is responsible for hydroxylating proline-rich peptides influencing carbohydrate, lipid, protein and DNA metabolisms during plant growth and development (Asif et al., 2009). DHN genes confer stress tolerance due to the structural stabilization with chaperon-like activity to protect the macromolecules in cells (Koag et al., 2003; Porat et al., 2004). The pH is a fundamental factor for biological processes. Vacuolar H⁺-ATPase regulates the pH of cells, which results to stabilize the membrane, protein degradation, transport of small molecules and several metabolisms (Forgac, 2007). During heat and osmotic stresses, sHSP genes are expressed to conserve the metabolic reactions in cells (Schoffl et al., 1998). PR-10 genes initiate and reprogramme the protein synthesis in pathogen infected or abiotic stress exposed plants (Xu P. et al., 2014). An antioxidant stimulating gene, APX plays a major role in redox condition of the electron transport machinery of chloroplast by regulating H₂O₂ levels (Davletova et al., 2005). In addition, rbcL and rbcS genes drive the synthesis of Rubisco enzymes for CO₂ fixation during photosynthesis (Andersson and Backlund, 2008).

Some studies have revealed that tolerance against drought in bacteria-treated plants is associated with higher gene expression levels of OsDIL, OsDREB1A, OsGAPDH, OsWRKY11, P4H, Cadhn, VA, sHSP, CaPR-10, cAPX, rbcL, and rbcS gene expression (Khan et al., 2011; Wang et al., 2012; Kasim et al., 2013; Lim and Kim, 2013; Timmusk et al., 2015) and lower gene expression levels of APX1 (ascorbate peroxidase 1), SAMS1 (S-adenosyl-methionine synthetase 1, which acts as methyl donor and a precursor to polyamines synthesis (Sofia et al., 2001) and HSP17.8 (heat shock protein 17.8) gene expression (Kakar et al., 2016). Plant drought tolerance may be accomplished by the interaction with Bacillus spp. resulting in enhanced water uptake, transport of nutrients, synthesis of hormones and pigments, and by the regulation of drought stress related genes and enzymes.

Climatic changes in the environment affect regular rainfall each year. Salinity in agricultural land has been spreading worldwide due to low rainfall, high water evaporation rates and improper irrigation practices (Al-Karaki, 2006). The accumulation of salt in soil reduces the soil water potential and affects water and nutrient uptake by plant roots (Porcel et al., 2012). Under conditions of salinity, crop plants face disorder in several metabolic pathways, such as those related to photosynthesis, respiration, redox system homeostasis, phytohormone regulation, and carbohydrate and amino acid synthesis, which leads to reduced seed germination, plant growth and yield (Munns and Tester, 2008; Rady, 2011; Radhakrishnan and Lee, 2013, 2014). A microbial inoculation that includes Bacillus spp. can enhance plant growth during salt stress, which is an eco-friendly approach to sustainable agriculture (Radhakrishnan et al., 2014; Hashem et al., 2015, 2016a,b). The multiple plant growth-promoting characteristics (phosphate solubilization, ammonia, IAA and siderophore production) of Bacillus licheniformis A2 mitigate the detrimental effects of salt stress and increase plant growth in stressed peanut plants (Goswami et al., 2014). The association of Bacillus spp. with plants alters the plant metabolism in stressed plants to increase plant growth (Table 2). To tolerate salt stress, plants must prevent the excess uptake of Na⁺ and Cl⁻, but they need to continue the uptake of essential nutrients, such as K⁺ and NO3- (Jeschke and Wolf, 1988). Exopolysaccharide (EPS) in the rhizosphere soil binds Na⁺ and inhibits Na⁺ transport into plant root cells (Figure 1). Inoculating wheat seedlings with EPS-producing Bacillus insolitus MAS17 and certain other Bacillus spp. covers the root zones with soil sheaths and restricts the passive flow of Na⁺ into the stele to mitigate salt stress effects (Ashraf et al., 2004). The bacteria-induced enhancement of the K⁺/Na⁺ ratio in plants grown in saline soil mitigates the effects of salinity stress (Han et al., 2014). The elevated levels of N, P, K, Ca, Mg, S, Mn, Cu, and Fe produced in salt-affected plants by the interaction with Bacillus spp. maintains plant growth during stress (Jha and Subramanian, 2012; Karlidag, 2013). The salt-tolerant bacteria increase the relative water content as well as the osmotic and turgor potential to improve the growth of salt-injured plants (Yang et al., 2016).

Bacillus spp. reduce the toxic effects of salinity in plants by inhibiting lipid peroxidation (Han et al., 2014). Hashem et al. (2015) proved that B. subtilis improved lipid synthesis, specifically that of oleic, linoleic, and linolenic acids as well as phospholipids, in plants grown under salt stress. This increase in lipid synthesis might mitigate lipid peroxidation and oxidative stress in the plants. ROS production is controlled by antioxidant enzymes. In bacteria-treated plants, APX and SOD activities are decreased, while nitrate reductase (NR; EC 1.7.1.1), CAT and POD activities are enhanced (Jha and Subramanian, 2012, 2015). Bacillus pumilus associated with the roots of salt-stressed rice plants reduces the activity of caspase (Jha and Subramanian, 2014), which is a protease that belongs to the cysteine endopeptidase family and is involved in programmed cell death in plants (Groten et al., 2006). The reduction of caspase activity decreases ROS formation and programmed cell death and reprograms the action of antioxidants to accomplish plant tolerance (Jha and Subramanian, 2014). Salt-tolerant B. subtilis RH-4 improves seed germination and plant growth by enhancing the synthesis of photosynthetic pigments, carbohydrates, proteins and osmolytes, such as proline, glycine betaine and choline, in salt-injured chickpea plants (Qurashi and Sabri, 2013). The regulation of these primary metabolic pathways in plants to protect against salinity-induced disorders promotes crop tolerance. In addition, some of the secondary metabolites, such as gallic acid, caffeic acid, syringic acid, vanillic acid, ferulic acid, cinnamic acid, and quercetin, are increased in plants associated with bacteria, which allows plants to tolerate salt stress (Tiwari et al., 2011).

The regulation of hormones under stress conditions is a complex phenomenon. Hormone levels are up- or down-regulated by environmental factors. ABA accumulation in plants grown under salt stress induces stomatal closure to reduce water loss and increases salt tolerance via stress responsive genes (Leung and Giraudat, 1998; Herrera-Medina et al., 2007), while bacterial inoculation decreases the stress-induced ABA synthesis and protects plants from the effects of stress (Kang et al., 2014b). Similarly, Bacillus spp. can produce plant hormones to enhance the concentrations of IAA and GA but reduce the synthesis of ABA in plants grown under salt stress (Mohamed and Gomaa, 2012). Several gene families are affected by salinity, and their transcriptional disorder retards plant growth. However, bacteria stimulate the expression of the NADP-Me2 (NADP malic enzyme 2), EREBP (ethylene-responsive element-binding protein), SOSI (salt overly sensitive 1), BADH (betaine aldehyde dehydrogenase) and SERK1 (somatic embryogenesis receptor-like kinase 1) genes, while the GIG (gigantea) and SAPK4 (serine threonine protein kinase) genes in plants are down-regulated due to salinity (Nautiyal et al., 2013). Overall reports suggest that plants can tolerate soil salinity by the effect of Bacillus spp. induced regulation of several genes, proteins, antioxidant enzymes, pigments, hormones, nutrient transport and prevention of excess sodium transport in plant system.

Agricultural lands contaminated with trace metals deposited from industrial effluents and agro-chemicals affect the ecological food chain, including crop cultivation, and alter microbial communities (Hu et al., 2009; Ashraf et al., 2017). Accumulated Cu, Mn, and Zn are considered major pollutants in soil and water, and these metals cannot be easily degraded into harmless substances (Ma et al., 2009; Arthur et al., 2012). Chelators are used to reduce metal toxicity but are also harmful to living organisms (Tandy et al., 2006). In contrast, microorganisms solubilize or convert toxic metals to non-toxic forms, which is applicable to the integrated management of heavy metal phytoremediation (Bosecker, 1997; Kang et al., 2015c). The inoculation of Bacillus spp. into heavy metal-contaminated soil can possibly reduce the toxic effects of these metals on plant growth. The bacteria support plant growth by increasing water uptake and reducing electrolyte leakage to mitigate Cd stress (Ahmad et al., 2014). B. licheniformis enhances Cu, Zn, Cd, Cr and Pb accumulation and distribution in plants grown in heavy metal-contaminated soil, which leads to reduced levels of toxic metals in soil (Brunetti et al., 2012). Similarly, excess amounts of Cd in soil reduce nutrient (P, Fe, Zn, and Mn) uptake in plants, but bacteria promote an increase in the levels of these nutrients in plants to protect against the effect of Cd (Malekzadeh et al., 2012 and Figure 1). The association of some Bacillus spp. increases the P and Ca contents and reduces Ni accumulation in plants grown in contaminated soil (Jamil et al., 2014). The beneficial effects of the interaction with Bacillus spp. (enhancement of water, ions, pigments and enzymes) in heavy metal-affected plants are shown in Table 2.

Heavy metal deposition in soil affects the redox state of plant metabolism by inducing signaling molecules such as ROS. Excess ROS generation damages lipid membranes and causes lipid peroxidation (Kang et al., 2015c). The contamination of soil with the most common industrial toxic metals, Pb and As, accelerates lipid peroxidation in affected plants. Bacillus spp. alleviate this stress effect by reducing lipid peroxidation and SOD activity and increasing amylase and protease to promote plant growth in heavy metal-polluted soil (Pandey et al., 2013). Similarly, bacteria support plant tolerance against Zn and Cu stress by enhancing the activities of ROS scavenging enzymes, such as POD, SOD, CAT, APX, and DHAR (Gururani et al., 2013; Wang et al., 2013). Cr stress reduces acid phosphatase activity in plants, but bacterial treatment elevates the activity of this enzyme (Riaz et al., 2010). The regulation of antioxidants in cells inhibits oxidative stress damage and triggers plant growth-promoting substances to enable plants to adapt to metal stress. Bacillus-mediated plant tolerance against Ni and Cr stresses is achieved through the enhancement of photosynthetic pigments and leghemoglobin, which leads to increased crop yield (Wani and Khan, 2010; Jamil et al., 2014). The plant growth and survival at heavy metal polluted soil can be achieved by increasing the balanced uptake of mineral nutrients and pigments synthesis, and also modulating the endogenous antioxidants due to the association of Bacillus spp. To understand the mitigation mechanisms of Bacillus spp. against heavy metal pollution, more plant physiological studies are required.

In organic farming, the use of bacterial agents is considered an environmentally friendly and safe method to increase crop productivity in the presence of pests (Dihazi et al., 2012). Plant-beneficial Bacillus spp. reduce the use of chemical fertilizers and pesticides for the sustainable production of various crops in modern agriculture (Myresiotis et al., 2015). For example, thiamethoxam is an insecticide used to control an extensive range of pests, such as aphids, beetles, lepidopteran species, thrips and whiteflies (Karmakar and Kulshrestha, 2009), but this compound causes a decline in insects beneficial to plants, such as honey bees; therefore, the use of this chemical in seed coating has been banned by the European Union (Girolami et al., 2009). Alternatively, eco-friendly microbial pesticides can fill the gap formed by the discontinuation of chemical pesticides use in the field of agriculture. A well-known bio-insecticide, B. thuringiensis, can control a broad range of diverse insects for pest management in the agricultural field (Navon, 2000). For example, the insects Helicoverpa armigera, Spodoptera littoralis, Oryzophagus oryzae, Spodoptera frugiperda, and Chilo partellus are damaging to plant growth and fruit, but B. thuringiensis inhibits the larval growth of insects and increases plant growth and yield (Brownbridge, 2001; Berlitz et al., 2012; Benfarhat-Touzri et al., 2014; Arrizubieta et al., 2016) without affecting other microbial populations within the phyllosphere (Wang et al., 2014). Some other Bacillus spp., such as B. cereus, B. subtilis, and B. amyloliquefaciens, are also involved in pest control (Gadhave and Gange, 2016).

The mechanism of Bacillus-induced pest control in plants varies with pest species as well as plant genotype (Navon, 2000; Paramasiva et al., 2014; Mnif and Ghribi, 2015; Wielkopolan and Obrepalska-Steplowska, 2016). Bacillus spp. kill pest larvae and induce systemic resistance in plants (Table 2). Pesticide-producing Bacillus spp. in soil and roots support plant growth and increase the uptake and systemic translocation of pesticide (thiamethoxam) throughout the entire plant to control pest infestations (Myresiotis et al., 2015). Bacillus spp. colonize plant parts, including the phyllosphere, and larvae and/or adult pests ingest the Bacillus-containing plant tissues during feeding. A primary site of bacterial infection begins with extensive damage to the larval midgut epithelium by bacterial crystal proteins, which interact with chitin and peritrophic membranes (Vachon et al., 2012; Feng et al., 2015; Figure 1). During later stages of infection, Bacillus spp. crystal protein endotoxin, lipopeptides and polyketides (iturin, fengycin, surfactin, bacillomycin, bacillaene, macrolactin, and difficidin) modify the vacuolization of the cytoplasm, induce vesicle formation, lyse brush border membrane, and degenerate apical membranes, leading to damage of microvilli and finally causing larval death (Ben-Khedher et al., 2015a; Boukedi et al., 2016). Surfactin attaches to the Ca²⁺ receptor site and changes the peptide composition in the cellular phospholipid bilayer (Maget-Dana and Ptak, 1995), while iturin increases cell membrane permeability via the formation of ion-conducting pores (Maget-Dana and Peypoux, 1994). Bacillus spp. elicit the JA-pathway-related genes and simultaneously increase the gene expression for other secondary metabolites (allelochemicals, which inhibit pest larval growth) in plants to defend against pests (Zebelo et al., 2016). The obtained reports suggest that Bacillus spp. control the larval population of pest and trigger the ISR mechanism and allelochemicals in plants to prevent the pest damage.

Plant disease-causing pathogenic bacteria, fungi, viruses and nematodes are major challenges in maintaining plant health and yield in agricultural lands (Hussey and McGuire, 1987; Guo et al., 2013; Narasimhan and Shivakumar, 2015). The application of plant-beneficial microorganisms is an alternative to chemical fungicides, bactericides and nematicides and an effective environmentally friendly approach to improving plant growth and controlling many plant diseases (Choudhary and Johri, 2009; Radhakrishnan et al., 2013; Adam et al., 2014; Egamberdieva et al., 2014). Bacillus spp. inhibit pathogenic microbial growth in soil and/or in plant tissues as well as the detrimental effects of the pathogens in plants. For example, pathogenic bacteria such as Ralstonia solanacearum, Pseudomonas savastanoi and Xanthomonas axonopodis infect plants and generate diseases, whereas Bacillus spp. inoculation suppresses pathogen growth and protects plants from diseases (Krid et al., 2012; Yi et al., 2013). Biofilm formation around the root surface by Bacillus spp. and their secretion of toxins (surfactin, iturin, macrolactin, bacillomycin, and fengycin) destroy the pathogenic bacterial populations and reduce disease incidence in plants (Chen et al., 2013; Huang et al., 2014; Elshakh et al., 2016; Hinarejos et al., 2016; Figure 1). The secretions of Bacillus spp. degrade the pathogenic bacterial cell walls and change the cell morphology to kill the pathogen (Elshakh et al., 2016).

In addition, pathogenic bacteria, including R. solanacearum and Xanthomonas oryzae, affect plant defense systems by decreasing phenylalanine ammonia-lyase (PAL; EC 4.3.1.24), POD, PPO, SOD, CAT, and lipoxygenase (LOX; EC 1.13.11) activities, but these defense enzyme activities are accelerated in diseased plants following the administration of Bacillus spp. (Chithrashree et al., 2011; Almoneafy et al., 2013; Kurabachew and Wydra, 2014; Table 2). PAL is involved in the biosynthesis of polyphenol compounds (lignin, flavonoids and phenylpropanoids) and triggering the plant resistance against environmental stimuli (Fritz et al., 1976; Tanaka et al., 1989). However, the systemic resistance to diseases induced in plants by Bacillus spp. is made possible by increasing SA content and the gene and protein expression of proteinase inhibitor II (Pin2) and pathogen resistant 1 (PR1) (Jiang et al., 2015; Fousia et al., 2016; Hinarejos et al., 2016).

The antagonistic activity of Bacillus spp. controls the mycelial growth of fungi, preventing plant fungal disease (Abdalla, 2015; Chowdhury et al., 2015a; Akram et al., 2016; Aydi-Ben-Abdallah et al., 2016) and increasing plant growth and yield (Narasimhan and Shivakumar, 2015). Populations of Bacillus spp. can be successfully established in the soil and root rhizospheres without any lasting effects on other bacterial populations (Chowdhury et al., 2015a). Bacillus spp. attach to the mycelial cell walls, and the chitosanase (EC 3.2.1.123), protease (EC 3.4.21.112), cellulase (EC 3.2.1.4), glucanase (EC 3.2.1.21), siderophores, and HCN of the bacteria crack and deform the hyphae, which leads to altered cell structure and functions due to vacuolation and protoplast leakage (Ben-Khedher et al., 2015b; Han et al., 2015; Narendra-Babu et al., 2015). Bacterially synthesized antifungal peptides, such as iturin, fengycin, mixirin, pumilacidin, surfactin, and a novel cyclic peptide with a molecular weight of 852.4 Da, are involved in the destruction of the pathogenic fungi in rhizospheres (Han et al., 2015; Yamamoto et al., 2015; Figure 1). Bacillus spp. mitigate pathogen-induced biotic stress via physiological changes (Table 2) in the photosynthetic and respiratory pathways and the regulation of carbohydrate, phenyl-propanoid and N metabolism and defense-related proteins in diseased plants (Jain et al., 2015). Gene expression patterns in plants are also altered during infection by pathogenic fungi, and a number of dependent genes are activated to protect the plant from biotic stresses. The expression of genes encoding β-1,3-glucanase (PR-2), chitinase (PR-3 and PR-4), peroxidase (PR-9), lipid transfer protein (PR-14), metallothionein-like protein (LfMT1), oxalate oxidase (LpOXO4), lipoxygenase (LOX), and a putative defensin (LpTHb) are upregulated, whereas the putative glycine-rich protein (LfGRP1) and PsbR protein of photosystem 2 (LfPsbR) genes are downregulated in diseased plants treated with Bacillus spp. (Liu et al., 2010; Kim et al., 2015; Rahman et al., 2015). The gene expression of major antioxidants and defense enzymes, such as POD, PAL, SOD, CAT, and PPO, is also stimulated during Bacillus spp. treatment (Narendra-Babu et al., 2015; Yang et al., 2015). The higher levels of energy, metabolism and defense-related proteins in Bacillus-treated diseased plants induce systemic resistance (Sarosh et al., 2009). The stress-induced transcriptional changes in plants trigger the production of secondary metabolites and defense enzymes to reduce oxidative damage. Antagonistic Bacillus spp. reduce lipid peroxidation and increase antioxidant enzymes, such as APX, CAT, GR, GPX, POD, PPO, other defense enzymes, such as PAL, chitinase (EC 3.2.1.14), and β-1,3-glucanase (EC 3.2.1.39), and phenolic acids to alleviate the adverse effects of pathogenic infection (Solanki et al., 2012; Chowdappa et al., 2013; Jain et al., 2013). The activity of hormones in plant immunity is well documented, and in particular, the synthesis of SA and JA plays a major role in plant defense. The cross talk among hormones is a complex process that induces disease resistance. Chowdappa et al. (2013) and Kang et al. (2015b) proved that the plant growth-promoting hormones IAA and GA are increased in Bacillus-treated plants along with SA, while JA and ABA are decreased in pathogen-infected plants. However, the studies on beneficial effect of Bacillus spp. in plants against fungal diseases conclude that the detrimental effects due to fungal infection in plants can be mitigated during the inoculation of Bacillus spp. by reprogramming the activity of plant defense enzymes and hormones. Additional physiological and molecular studies are required to elucidate the bio-control mechanisms of Bacillus spp. against pathogenic fungi-induced disease in crops.

The second largest group of plant diseases after fungi is caused by viruses. The most effective method of virus control has been accomplished by chemical treatments. The prolonged use of chemicals leads to deposits in soil and increases the drug resistance of plant pathogens (Zhao et al., 2017). Some of the Bacillus spp., produce the antiviral compounds against pathogen (Esawy et al., 2011). Very few studies have reported on the bio-control effects of bacteria in preventing or resisting viral disease. The disease rate is reduced as a consequence of induced systemic resistance (ISR) by interaction with Bacillus spp., leading to enhanced plant growth during cucumber mosaic virus infection (Zhang et al., 2004). The biofilm formation and surfactin production from B. amyloliquefaciens plantarum defense the viral disease in plants by triggering ISR machinery (Chowdhury et al., 2015b). Similarly, Bacillus spp. induce systemic resistance against viral disease caused by tobacco mosaic virus by inhibiting viral coat protein synthesis and by increasing the expression of disease-resistant signaling genes (Coil and NPR1), defense genes (PR-1a and PR-1b) and cell wall expansin (NtEXP2 and NtEXP6) genes in plants (Wang, 2009). The NPRI and Coil genes regulate the ISR- and JA-dependent pathways, respectively (Xie et al., 1998; Mou et al., 2003), which indicates that Bacillus spp. application can prevent viral damage in plants. However, crops are also damaged by nematodes, which are plant parasites and are recognized as a severe threat to plant growth. Root-knot nematodes have been recorded as the most damaging parasite relative to other types of nematodes worldwide. The host range of this nematode covers nearly 5500 plant species (Trudgill and Blok, 2001). The application of a bacterial inoculation controls the nematode populations. For example, Bacillus spp. prevent root-knot nematode infection in crops and develop resistance by reducing gall and egg masses in plants (Adam et al., 2014). Antimicrobial peptides, bacteriocins synthesized from Bacillus spp. inhibit the growth of pathogenic nematodes (Chowdhury et al., 2015b). Liu et al. (2013) identified the PZN gene cluster in B. amyloliquefaciens, and revealed that these genes are responsible for nematicidal activity against nematodes. In addition, the secretion of crystal proteins (Cry5B and Cry6A) from Bacillus spp. controls the growth of free-living (Caenorhabditis elegans) and plant-parasitic (Meloidogyne hapla) nematodes (Yu et al., 2015). Cry5B binds with glycolipids receptors, leading to intestinal damage in C. elegans. Moreover, Cry6A restricts the growth of nematodes by inhibiting egg hatch, motility and infection to host tissues (Kho et al., 2011; Yu et al., 2015). The documented results of Bacillus spp. against virus and nematode suggest that some of the metabolites synthesized from Bacillus spp. inhibit the viral and nematodes population and increase the plant resistance through the expression of defense genes.

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.