- 1Department of Plant Pathology and Microbiology, Iowa State University, Ames, IA, United States
- 2School of Life Sciences, Peking University, Beijing, China
- 3Peking University – Tsinghua University Joint Center for Life Sciences, Beijing, China
Different from the conventional biocidal agrochemicals, synthetic chemical inducers of plant immunity activate, bolster, or prime plant defense machineries rather than directly acting on the pathogens. Advances in combinatorial synthesis and high-throughput screening methods have led to the discovery of various synthetic plant immune activators as well as priming agents. The availability of their structures and recent progress in the mechanistic understanding of plant immune responses have opened up the possibility of identifying new or more potent chemical inducers through rational design. In this review, we first summarize the chemical inducers identified through large-scale screening and then discuss the emerging trends in the identification and development of novel plant immune inducers including natural elicitor based chemical derivation, bifunctional combination, and computer-aided design.
Introduction
While plants are important nutritional source of humans, they are also consumed by various heterotrophic microorganisms, which cause diverse plant diseases and considerable economic loss to agriculture. To reduce the yield loss, conventional chemical pesticides have been developed. They exert their functions through direct biocidal effects on the pathogens. However, besides the toxicity on the pathogens, conventional pesticides may also have negative impacts on the crops, beneficial microorganisms and the health of farmers and consumers. Furthermore, continuous application of conventional pesticides can result in the selection of pesticide-resistant pathogen strains and eventually voids the use of the specific pesticide (Burketova et al., 2015). Synthetic chemical inducers of plant immunity are attractive and promising alternatives. They stimulate or prime the endogenous immunity of plants to combat pathogenic invasions rather than kill the pathogens directly.
Unlike animals that have evolved specific immune cells, nearly each cell in plants is able to act as an “immune cell” to fight against pathogen attacks. Plants can perceive the presence of pathogens through recognition of microbe-associated molecular patterns (MAMPs) or damage-associated molecular patterns (DAMPs) by pattern recognition receptors (PRRs). MAMPs are highly conserved molecular signature within different classes of microbes, for instance, flagellin and elongation factor Tu (EF-Tu) from bacteria, chitin and xylanase from fungi and heptaglucan from oomycetes. DAMPs are plant endogenous immune elicitors released by the pathogen-triggered mechanical stress or enzymatic activities controlled by pathogens, e.g., oligogalacturonides (Schwessinger and Ronald, 2012). The downstream defense activation events following PRR activation include changes of ion fluxes across the plasma membrane, the oxidative burst, activation of mitogen activated protein kinase (MAPK) cascades, gene activation and callose deposition. This MAMPs/DAMPs-triggered immunity (MTI) is the first layer of plant immune system (Jones and Dangl, 2006; Zipfel, 2009). Some pathogens have evolved effectors to interfere with MTI (Dangl et al., 2013). Through co-evolution, plants have developed intracellular immune receptors, Resistance (R) proteins, to recognize the presence of effectors and activate effector-triggered immunity (ETI), which is the second layer of plant immune system (Spoel and Dong, 2012). These two layers of immunity are usually referred to as plant innate immunity (Schwessinger and Ronald, 2012).
The activation of plant innate immunity in local tissue (the infected part) leads to transportation of the mobile defense signals to systemic (uninfected) tissue, resulting in a long-lasting resistance to a broad spectrum of pathogens. This acquired immunity is known as systemic acquired resistance (SAR). The induction of SAR usually confers by ETI, however, it has been reported that MTI can also trigger SAR under some circumstances (Mishina and Zeier, 2007). In addition to pathogens, SAR can be induced by exogenous application of chemical inducers, including salicylic acid (SA), its analogs 2, 6-dichloroisonicotinic acid (INA) and benzothiadiazole S-methyl ester (BTH), its derivatives acetylsalicylic acid (aspirin) and methyl SA (MeSA) (White, 1979; Uknes et al., 1992; Cao et al., 1994; Lawton et al., 1996; Durrant and Dong, 2004; Park et al., 2007), nitric oxide (NO), reactive oxygen species (ROS) (Wang et al., 2014), dicarboxylic acid azelaic acid (AzA) (Jung et al., 2009), the phosphorylated sugar glycerol-3-phosphate (G3P) (Chanda et al., 2011), the abietane diterpenoid dehydroabietinal (DA) (Chaturvedi et al., 2012), the amino-acid derivative pipeolic acid (Pip) (Navarova et al., 2012), and N-hydroxypipecolic acid (NHP) (Chen et al., 2018; Hartmann et al., 2018).
To communicate with the systemic tissue, mobile signals are generated in local tissue and then transported to systemic tissue through phloem. Although, it is well-known that SAR is associated with the accumulation of SA in both local and systemic tissues, grafting studies demonstrated that SA is not the mobile SAR signal (Vernooij et al., 1994). Several chemical candidates for this long-distance signal have been proposed, including MeSA (Park et al., 2007), AzA (Jung et al., 2009), glycerol-3-phosphate (G3P) (Chanda et al., 2011), DA (Chaturvedi et al., 2012), Pip (Navarova et al., 2012), and more recently, its derivative, NHP (Hartmann et al., 2018). Key protein players involved have also been identified including Defective in Induced Resistance 1 (DIR1) (Maldonado et al., 2002; Carella et al., 2017), AzA Insensitive 1 (AZI1) (Jung et al., 2009), and Lipid Transfer Protein 2 (LTP2). Plasmodesmata (PD) is considered to be the transportation route of these signals (Lim et al., 2016). These putative SAR signals might function coordinately to achieve long-distance signal transduction (Dempsey and Klessig, 2012; Shah et al., 2014; Wang et al., 2014).
Once SAR signals are perceived, systemic tissues generate SA to activate a key immune regulator, NON-EXPRESSER OF PR1 (NPR1) to trigger massive transcriptional reprogramming, including the induction of Pathogenesis-related (PR) genes and endoplasmic reticulum (ER)-resident genes, which aid secretion of PR proteins (Wang et al., 2005, 2006; Spoel and Dong, 2012; Fu and Dong, 2013). Continuous efforts have been made to study the mechanism of how NPR1 responds to SA and regulates downstream defense genes. SA or pathogen infection could cause changes in cellular redox status (Mou et al., 2003). As a result of the cellular redox changes, the cysteine residues of NPR1 (C82 and C216) are reduced by thioredoxins, leading to an oligomer-to-monomer switch in NPR1 conformation and nuclear translocation of the monomer NPR1 (Tada et al., 2008). Nuclear NPR1 monomer then undergoes phosphorylation to promote its transcriptional activity in SAR and its turnover (Spoel et al., 2009). As a transcription co-factor, nuclear NPR1 interacts with TGAs and NIMI-interacting (NIMIN) TFs to regulate the expression of downstream defense genes (Despres, 2003; Kesarwani et al., 2007). TGAs mainly activate NPR1-mediated genes; while NIMIN represses the expression of defense genes (Zhou et al., 2000; Johnson et al., 2003). After fulfillment of its function, ubiquitination of “exhausted” NPR1 leads to its degradation by the proteasomes, allowing “fresh” NPR1 to reinitiate the transcription cycle (Spoel et al., 2009). Recently NPR1 and its paralogs, NPR3 and NPR4, have been found to directly bind SA and serve as its receptors to mediate transcriptional reprogramming (Fu et al., 2012; Wu et al., 2012; Ding et al., 2018). Besides SA, indolic compounds, jasmonic acid (JA), monoterpenes, NO, ROS and intact cuticle also contribute to the establishment of SAR (Truman et al., 2007, 2010; Xia et al., 2009; Navarova et al., 2012; Wendehenne et al., 2014; Riedlmeier et al., 2017).
Induced systemic resistance (ISR) is another form of systemic immunity, which is triggered by non-pathogenic beneficial microbes (Pieterse et al., 2014). Although ISR and SAR are both systemic defense mechanism, they differ in several ways. First, the triggers of ISR and SAR are fundamentally different. SAR is triggered by either compatible or incompatible pathogenic interactions while ISR is initiated by non-pathogenic microbes. Second, although ISR and SAR are both broad-spectrum, their effective spectrum only partially overlaps (Ton et al., 2002). Third, SA is critical to SAR but ISR is less dependent on SA and mainly regulated by JA and ethylene (ET) (Pieterse et al., 1998; Pieterse et al., 2014). Fourth, SAR is accompanied with induction of PR genes and proteins while SA-independent ISR is not (Hoffland et al., 1995). Instead of direct induction of defense machineries, ISR-conditioned plants can elicit faster and/or stronger defenses upon subsequent pathogenic interactions. This sensitization mechanism is called priming (Conrath et al., 2006). It has been shown that priming can reduce the fitness cost associated with constitutive activation of defenses (van Hulten et al., 2006; Walters et al., 2008; Vos et al., 2013). Despite these distinctions between ISR and SAR, SA-independent ISR also depends on NPR1, the key component of SA signaling pathway (Pieterse et al., 1998; Iavicoli et al., 2003; Ryu et al., 2003; Ahn et al., 2007; Hossain et al., 2008; Stein et al., 2008; Segarra et al., 2009; Weller et al., 2012). Cumulating studies suggest that ISR may mainly rely on the cytosolic function of NPR1 while SAR more depends on the nuclear role of NPR1 (Pieterse et al., 2014).
Synthetic Chemical Inducers of Plant Immunity
Synthetic chemical inducers of plant immunity are structurally different from the natural plant defense elicitors. They may activate or prime plant immunity by simply mimicking the structures of natural immune inducers. Alternatively, they can also be structurally unrelated to natural elicitors and target a subset of defense signaling components. In general, they do not have in vitro antimicrobial activity. In this section, we mainly focus on the legacy inducers related to the recently discovered ones, which will be discussed in the “Emerging trends” section.
SA Derivatives
As a major plant immune hormone, SA plays a pivotal role in the establishment of plant immunity. SA is among the first plant endogenous chemicals reported to induce SAR, which is accompanied by accumulation of PR proteins and resistance to TMV in tomato (White, 1979). In the same study, the famous synthetic SA derivative, Aspirin, was also shown to induce SAR (White, 1979). Later mono- and di-chloro substituted SA derivatives including 4-chloro-SA, 5-chloro-SA and 3, 5-chloro-SA were found to induce PR proteins accumulation and resistance against TMV infection in tobacco (Conrath et al., 1995). More comprehensive investigations of mono- and multiple-substituted SA suggest that 3- and 5-position substitutions are more active than 4- and 6-position substitution. Electron-withdrawing substituents are important to the enhanced activity. Except for 6-fluoro-SA, all fluoro- and chloro-SA tested induced more resistance against TMV than SA (Silverman et al., 2005). Aside from the simple substituted SA, a new class of salicyl glycoconjugates containing hydrazide and hydrazone moieties were synthesized and studied on their in vitro and in vivo antifungal activity using cucumber (Cui et al., 2014). While the SA hydrazine derivative showed little in vitro antifungal activity, significant in vivo antifungal activity against Colletotrichum orbiculare, Fusarium oxysporum, Rhizoctonia solani, and Phytophthora capsici was demonstrated. Intriguingly, while the SA hydrazine derivative is structurally derived from SA, it did not induce the expression of SA marker genes but rather induce JA marker genes. This suggests that the SA hydrazine derivative may not be an SA agonist and function through targeting of other immune signaling components.
Isonicotinic Acid Derivatives
INA was first identified by Ciba-Geigy, the predecessor of Syngenta, through large-scale screening to identify chemicals that can induce resistance in cucumber against the fungal pathogen Colletotrichum lagenarium (Metraux et al., 1991). INA has been shown to induce pathogen resistance in various plants including Arabidopsis, tobacco, pear, pepper, rice, cucumber, and beans (Kuc, 1982; Metraux et al., 1991; Ward et al., 1991; Uknes et al., 1992). INA can trigger similar immune responses as SA but independent of SA accumulation as it can still induces SAR in transgenic plants expressing SA hydrolase (NahG) in which SA accumulation is compromised (Delaney et al., 1994; Vernooij, 1995). Therefore it functions downstream of the SA accumulation. Recent identifications of SA receptors, NPR3 and NPR4 suggest that INA is likely to be a genuine SA agonist. Similar to SA, INA can also promote the interactions between NPR1 and NPR3. Furthermore, in a competition binding assay, INA was shown to compete with SA to bind its receptors, NPR3 and NPR4 (Fu et al., 2012). Besides the interaction with NPR3 and NPR4, interactions between INA and other SA-binding proteins may also contribute to its role in elicitation of immunity (Durner and Klessig, 1995). However, due to its phytotoxicity effects, INA or its derivatives have not been commercialized for agricultural use.
N-cyanomethyl-2-chloro isonicotinic acid (NCI) is another potent plant immune inducer, which belongs to the isonicotinic acid derivative family. It was identified in a screen of 2-chloroisonicotinamide derivatives for control of rice blast (Yoshida et al., 1990a,b). NCI did not show biocidal effects on rice blast in vitro even when a high dose was used. However, its in vivo antifungal activity against rice blast can last 30 days after a single application. In tobacco, NCI induces expression of PR genes even in nahG plants (Nakashita, 2002). This suggests that the immune inducing effect of NCI does not rely on SA accumulation. In Arabidopsis, NCI-induced immunity is independent of SA accumulation but depends on NPR1 (Yasuda et al., 2003; Yasuda, 2007). Therefore NCI appears to interact with the signaling steps between SA and NPR1.
Thiadiazole and Isothiazole Derivatives
BTH is another potent synthetic SAR inducer identified by Ciba-Geigy through a large-scale screening of thiadiazole derivatives (Schurter et al., 1993; Kunz et al., 1997; Oostendorp et al., 2001). BTH does not exhibit antimicrobial activity in vitro. However, it can trigger disease resistance against a diverse spectrum of pathogens in various plant species. BTH has been tested in more than 120 pathosystems including resistance in apple and pear against fire blight, tomato against bacterial canker, grapefruit against canker, canola against blackleg disease, cowpea against anthracnose, etc. (Latunde-Dada and Lucas, 2001; Brisset et al., 2002; Soylu et al., 2003; Potlakayala et al., 2007; Graham and Myers, 2011). BTH induces the expression of PR genes and BTH-triggered SAR in Arabidopsis is dependent on NPR1 (Lawton et al., 1996). In rice, however, BTH-induced defense responses against rice blast does not require rice ortholog of Arabidopsis NPR1 but rather involves WRKY family transcription factor, OsWRKY45 (Shimono et al., 2007). Similar to INA, BTH is also able to induce SAR and expression of PR genes in nahG plants (Molina et al., 1998). BTH can be converted by methyl SA esterase to acibenzolar. This conversion is required for BTH-induced PR protein expression as BTH failed to induce PR1 in the methyl SA esterase silenced tobacco seedlings (Tripathi et al., 2010). Besides direct induction of plant defense responses, low doses of BTH can prime plant immunity. In Arabidopsis, this priming effect is dependent on NPR1 (Kohler et al., 2002; Goellner and Conrath, 2008). Induction of MAPKs and histone modifications have also been found to associate with and may explain this priming effect (Beckers et al., 2009; Jaskiewicz et al., 2011). Different from INA, BTH has been commercialized as an effective agrochemical.
The isothiazole-based synthetic plant immune inducer, Isotianil, was identified by Bayer AG and Sumitomo Chemical Co., Ltd., through comprehensive search for this type of compounds as protectant against both rice blast and rice blight. Besides rice, Isotianil has also been shown to protect wheat against powdery mildew, cucumber against anthracnose and bacterial leaf spot, Chinese cabbage against Alternaria leaf spot, pumpkin against powdery mildew, strawberry against anthracnose and peach against bacterial shot hole (Ogawa et al., 2011; Krämer et al., 2012). Isotianil does not have antimicrobial activity in vitro but relies on its strong immune inducing power to protect rice against rice blast. An exceptionally low dosage is enough to assure its in vivo antimicrobial effect (Ogawa et al., 2011). Its effective dose is lower than any other existing plant defense activators (Ogawa et al., 2011). Transcriptome profiling revealed that Isotianil induces the expression of defense-related genes in rice including NPR1, NPR3, and WRKY family transcription factors as well as gene involved in SA catabolism (Krämer et al., 2012). Up till now, more in-depth molecular basis of how Isotianil achieves its immune eliciting activity has not been reported (Maienfisch and Edmunds, 2017).
JA Analog
While SA regulates defense against biotrophic pathogens, JA and methyl-JA (MeJA) mainly control the immunity against necrotrophic pathogens and herbivores (Santino et al., 2013). JA can be metabolized to MeJA and JA-isoleucine (JA-Ile) which is a biologically active form (Svoboda and Boland, 2010; Pieterse et al., 2012). JA signal is transduced to transcription through JA-Ile triggered degradation of Jasmonate ZIM-domain (JAZ)-type transcriptional repressors by the JA receptor, Coronatine Insensitive 1 (COI1) (Yan et al., 2013, 2018). With the removal of these repressors, JA-responsive genes are de-repressed and JA-dependent defense responses are activated (Browse, 2009; Pieterse et al., 2012; Monte et al., 2014). The phytotoxin, coronatine, is a natural structural and functional mimic of JA-Ile (Weiler et al., 1994; Fonseca et al., 2009). Coronatine can elicit similar responses as JA. In an effort to identify more potent mimics of coronatine, the synthetic JA mimic coronalon was synthesized (Schuler et al., 2001). Coronalon was later shown to mediate stress responses in various plants species (Schuler et al., 2004). It can induce known MeJA-activated defense products as well as MeJA-responsive genes (Pluskota et al., 2007). Besides coronalon, several synthetic JA mimics have been studied and shown to induce JA signaling and defense responses in lima bean, soybean and coyote tobacco (Krumm et al., 1995; Fliegmann et al., 2003; Pluskota et al., 2007). However, whether these JA mimics bind COI1 has not been investigated. Based on the co-receptor structure, a coronatine derivative, coronatine-O-methyloxime (COR-MO), was synthesized through direct chemical derivation and identified as a potent competitive antagonist of jasmonate perception (Monte et al., 2014).
β-Aminobutyric Acid (BABA)
BABA is a non-protein amino acid that has been known to induce plant resistance since 1963 (Papavizas and Davey, 1963). It has been shown to protect about 40 different plant species against a diverse range of pathogen and pests including virus, bacteria, oomycetes, fungi, nematode, and arthropods (Cohen et al., 2016). BABA primes multiple defense mechanisms regulated by SA-dependent and SA-independent pathways (Zimmerli et al., 2000; Ton et al., 2005). The priming effects elicited by BABA can be maintained to the next generation, making BABA the first plant immune inducer with transgenerational efficacy (Slaughter et al., 2012). BABA is sensed by an aspartyl-tRNA synthetase, IBI1 (Luna et al., 2014). Binding of BABA to IBI1 primes it for alternative defense activity. However, the inhibition of BABA on the aspartyl-tRNA synthetase activity leads to toxicity in plants, which makes BABA unsuitable for agricultural use. While BABA has long been considered as a synthetic plant immune priming agent, a recent study has unequivocally identified BABA as an endogenously metabolite synthesized by various plant species including Arabidopsis, Chinese cabbage, maize, teosinte, and wheat (Thevenet et al., 2017).
Emerging Trends
Large-scale screens performed by the private sector identified the first-generation synthetic elicitors including INA and BTH. Over the last 15 years, advances in combinatorial chemistry and development of high-throughput screening systems have equipped the scientists outside the private sector with the ability to carry out comprehensive screens for synthetic plant immune inducers. This has led to the discovery of a rich arsenal of the second-generation synthetic elicitors (Bektas and Eulgem, 2015). While systematic screens will continue to help us unveil new and better synthetic elicitors, approaches based on the knowledge of known synthetic and/or natural elicitors are emerging.
Chemical Derivation
Simple chemical derivation of known immune inducers has been and continues to be a shortcut to the identification of more potent immune elicitors. Recently, a new class of SA derivative, benzoylsalicylic acid (BzSA) was identified from seed coats of Givotia rottleriformis, a soft-wood tree species (Kamatham et al., 2016). BzSA induces SAR-related gene expression more effectively than SA. It also induced more local and systemic resistance against TMV in tobacco than SA. Through relatively simple chemical derivation, Kamatham et al. (2017) synthesized 14 BzSA derivatives and tested their bioefficacy using the tobacco-TMV pathosystem. When low dosage was tested, all 14 derivatives caused more reduction of the lesion size than both SA and BzSA. The immune-inducing effects of BzSA derivatives are not dependent on SA accumulation as they can still induce resistance in nahG plants.
With the availability of a diverse collection of known synthetic and nature plant immune inducers, comparison between known elicitors may help identify specific moiety critical to the immune inducing ability. The 3-methylfuran-containing natural products like menthofuran, furanoeremophilane, caclol, and tanshinone are plant secondary metabolites involved in plant defense (Hägele and Rowell-Rahier, 2000; Maffei et al., 2012; Liu et al., 2013). Based on the prediction that 3-methylfuran moiety may be important to the antimicrobial activity of these secondary metabolites, He et al. (2017) used diversity-oriented synthesis to generate a small natural-products-like library containing the 3-methylfuran scaffold. Five 3-methylfuran derivatives were found to significantly induce the resistance in rice against brown planthopper, supporting the initial speculation on the critical role of 3-methylfuran (He et al., 2017).
Besides specific functional moiety, the pattern of known immune elicitors can also be useful information for the design of new ones. Rhamnolipids and lipopeptides have been found as a new class of MAMPs (Jourdan et al., 2009; Sanchez et al., 2012; Farace et al., 2015). Both rhamnolipids and lipopeptides are amphiphilic compounds. Due to the biocompatibility and biodegradability, rhamnoside-based bolaamphiphiles surfactants have been increasingly recognized and investigated (Gatard et al., 2013; Akong and Sandrine, 2015). The bolaamphiphiles surfactants contains a long hydrophobic spacer connecting two hydrophilic moieties. Luzuriaga-Loaiza et al. (2018) synthesized rhamnolipid bolaforms (SRBs) and tested their immune induction activity. Depending on the acyl chain length, SRBs differentially induce defense responses and confer local resistance in Arabidopsis against the hemibiotrophic bacteria Pseudomonas syringae but not the necrotrophic fungal pathogen Botrytis cinerea.
Chemical derivation based on known natural immune inducers has great expedited the invention of better synthetic immune inducers. However, the lack of the mechanistic understanding of the interactions between the new synthetic immune inducers and their cognate targets in plants has limited our ability to improve the efficacy or lower the phytotoxicity in a more rational manner. More comprehensive biochemical studies using the new synthetic immune inducers will provide a promising guide.
Bifunctional Combination
Bifunctional combination approaches combine a known synthetic plant immune inducer with another compound, which brings other functions to the final product. Strobilurins are a class of broad spectrum fungicides. Widespread use of strobilurins have caused pathogen resistance (Gisi et al., 2002; Leiminger et al., 2014). 3,4-dichloroisothiazole derivatives have diverse biological activities including immune-inducing activity. For example, as mentioned in Section 2.3, Isotianil, a 3,4-dichloroisothiazole derivative, is a very potent immune elicitor. In an effort to identify new strobilurins for future market, Chen et al. (2017) combined 3,4-dichloroisothiazoles with strobilurins. Through the incorporation of 3,4-dichloroisothiazole, new strobilurins with good in vivo and in vitro fungicide activities were identified.
JA-Ile is a natural conjugation of JA and isoleucine and was previously identified as the sole endogenous bioactive JA molecule. In an effort to identify additional endogenous bioactive jasmonates, Yan et al. (2016) coupled 20 natural amino acids with coronafacic acid (CFA) which is a part of the phytotoxic natural JA-Ile mimic, coronatine, and identified 5 non-polar amino acid conjugates of CFA including CFA-Ile, CFA-Leu, CFA-Val, CFA-Met, and CFA-Ala as new synthetic JA signaling pathway elicitors. Following these findings, JA-Leu, JA-Val, JA-Met, and JA-Ala were further discovered as new endogenous bioactive JA molecules. Through integration of the structural information of all these bioactive JA molecules, general rules of bioactive JA conjugates were proposed. Based on these rules, two additional JA signaling pathway elicitors, CFA-N-Leu and CFA-Ch-Gly were identified (Yan et al., 2016).
Besides covalent combination, ionic pairing is another attractive method, since one can choose ions independently. The same plant immune inducer can be paired with surfactant-type cation for better wetting or tetrabutylammonium cation for faster dissolution. Using this strategy, 15 immunity inducers including SA, BTH, INA, BABA, etc., were paired with the cholinium cation to form ionic liquids (Kukawka et al., 2018). Their abilities to induce SAR were tested using the tobacco-TMV pathosystem. Cholinium is an essential nutrient. Pairing with cholinium reduced phytotoxicity of these immune inducers while only mild perturbation to the immune-inducing ability was recorded.
While bifunctional combination approaches have shown the potential to either improve the efficacy or reduce phytotoxicity, the introduction of the second chemical moiety has also brought more complications. For example, Pip, a SAR mobile signal candidate, showed significantly reduced SAR-inducing activity when paired with cholinium (Kukawka et al., 2018). On the other hand, while isonicotinate did not induce SAR, its cholinium ionic liquid was shown to induce SAR (Kukawka et al., 2018). Therefore bifunctional combination is not merely the addition of the biological activities of the two chemical moieties but rather results in potentially complicated interactions between the signaling pathways induced by the two moieties. Careful characterization is thus essential to understand the full spectrum of the biological activities of the new synthetic immune inducers identified through bifunctional combination approaches.
Computer-Aided Design
Manual inspection can only process a handful of immune elicitors for recognition of potentially critical bioactive substructures and patterns of known immune inducers (He et al., 2017; Luzuriaga-Loaiza et al., 2018). Advances in high-performance computing have made it possible to screen tens of thousands of lead-like molecules computationally. This computer-aided design (CAD) drug design strategy has been increasingly recognized and utilized in pesticide discovery and property analysis (Xia et al., 2014; Veselinovi et al., 2015; Burden et al., 2016). Using SA, MeSA, BTH, and Tiadinil, the four known immune inducers as query templates, Chang et al. (2017) performed virtual screening against the 5,3000 hit-like and lead-like compounds in the Maybridge database and identified three benzotriazole scaffolds as promising leading compounds. One of them, L1 shows high 3D structure similarity to BTH despite their differences in 2D topology. Furthermore, L1 also shares similar pharmacophore features to BTH. In vivo screening of L1 derivatives identified new immune inducers with comparable or improved efficacy against Mycosphaerella melonis, Corynespora cassiicola, P. syringae, B. cinerea, and F. oxysporum in cucumber, Phytophthora infestans in tomato and R. solani in rice.
Besides the knowledge of the small lead-like compounds, structural understanding of plant receptors can also lend power to the virtual screening of new leading compounds. Using the high quality structural model of JA receptor, COI1, 767 JA analogs were analyzed in terms of their ability to bind COI1 (Pathak et al., 2017). Two such analogs ZINC27640214 and ZINC43772052 showed higher binding affinity compared to JA. ZINC27640214 appears to have efficient, stable and good cell permeability properties, making it a good candidate for experimental validation. Buswell et al. (2018) combined the knowledge of the structural information on the BABA receptor, IBI1 and small-scale screening of β-amino acids using the ibi1 mutant to search for BABA analogs, which induce plant immunity without severe growth inhibition. Out of the seven resistance-inducing compounds, five of them showed no inhibition on growth. Among these five, (R)-β-homoserine (RBH) showed the strongest resistance-inducing activity without affecting vegetative growth or global plant metabolism. Interestingly, RBH appears to elicit partially different signaling pathways from those affected by BABA, making it a promising new crop protectant. Through in silico docking and subsequent molecular dynamics simulation, the keto group of a stereoisomer of coronatine showed the potential to control the binding selectivity between its derivatives and different subtypes of JAZ (Takaoka et al., 2018). An oxime derivative of this coronatine stereoisomer was then developed as a synthetic JAZ subtype-selective agonist, specifically targeting JAZ9 and JAZ10. This selectivity in JAZ enabled induction of pathogen resistance without a cost on growth. It is noteworthy that small-scale targeted characterization of synthetic agonist candidates rather than large-scale screening was realized in this study owing to the integration of the structural information on both the ligands and the receptor.
As an emerging trend, application of CAD in the discoveries of new synthetic immune inducers awaits further exploitation. While lead-like compound databases have provided a critical foundation for virtual chemical screening, they also restrain the chemical diversity and may potentially hinder the discovery of completely novel scaffolds. On the other side, CAD based on the structural information of plant defense signaling components does not set a limit on the chemical diversity. However, synthetic immune activators identified through this route may be only effective in the specific plant species studied due to the sequence variation among different plant species. Integration of evolutional conservation information may help alleviate this issue.
Conclusion and Perspectives
In this review, we provided a focused overview on the discovery and functional properties of synthetic plant immune inducers and emerging trends in the search for new and improved synthetic inducers. A rich knowledge of the structural, chemical and pharmacological properties of the known inducers has opened up some shortcuts to expedite the discovery procedure. Instead of in vivo screening tens of thousands small molecules, small-scale screening involves only a few dozens or even a handful of compounds is able to identify new inducer derivatives or even completely new scaffolds through integration of prior knowledge. While the availability of the structures of small compounds is the major drive for this advancement, we anticipate that integration of more prior information will greatly facilitate the discovery of novel and better plant immune elicitors. This includes the structural information, biological function and evolutional conservation of key plant immune-related signaling components, physical and biochemical features of the small compounds as well as the structural basis and evolutional conservation of the molecular interactions between small compounds and their cognate plant immune signaling components.
The great expansion of synthetic immune inducers has also provided opportunities to dissect the signaling networks of plant immune system that is not accessible to genetic screens due to the lethality and gene redundancy. With the discovery of the hidden drug-able targets in plant immune system, new synthetic immune inducers may be developed to target these hidden points. Then in turn, these new inducers can again enhance our ability to dissect plant immune system and keep this discovery cycle going on.
Author Contributions
All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.
Funding
This work was supported by the funds from School of Life Sciences, Peking University – Tsinghua University Joint Center for Life to WW.
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.
References
Ahn, I. P., Lee, S. W., and Suh, S. C. (2007). Rhizobacteria-induced priming in Arabidopsis is dependent on ethylene, jasmonic acid, and NPR1. Mol. Plant Microbe Interact. 20, 759–768. doi: 10.1094/MPMI-20-7-0759
Akong, F. O., and Sandrine, B. (2015). Efficient syntheses of bolaform surfactants from L-rhamnose and/or 3-(4-hydroxyphenyl)propionic acid. Green Chem. 17, 3290–3300. doi: 10.1039/C5GC00448A
Beckers, G. J. M., Jaskiewicz, M., Liu, Y., Underwood, W. R., He, S. Y., Zhang, S., et al. (2009). Mitogen-activated protein kinases 3 and 6 are required for full priming of stress responses in Arabidopsis thaliana. Plant Cell 21, 944–953. doi: 10.1105/tpc.108.062158
Bektas, Y., and Eulgem, T. (2015). Synthetic plant defense elicitors. Front. Plant Sci. 5:804. doi: 10.3389/fpls.2014.00804
Brisset, M. N., Faize, M., Heintz, C., Cesbron, S., Chartier, R., Tharaud, M., et al. (2002). Induced resistance to Erwinia amylovora in apple and pear. Acta Hortic. 590, 335–338. doi: 10.17660/ActaHortic.2002.590.49
Browse, J. (2009). Jasmonate passes muster: a receptor and targets for the defense hormone. Annu. Rev. Plant Biol. 60, 183–205. doi: 10.1146/annurev.arplant.043008.092007
Burden, N., Maynard, S. K., Weltje, L., and Wheeler, J. R. (2016). The utility of QSARs in predicting acute fish toxicity of pesticide metabolites: a retrospective validation approach. Regul. Toxicol. Pharmacol. 80, 241–246. doi: 10.1016/j.yrtph.2016.05.032
Burketova, L., Trda, L., Ott, P. G., and Valentova, O. (2015). Bio-based resistance inducers for sustainable plant protection against pathogens. Biotechnol. Adv. 33, 994–1004. doi: 10.1016/j.biotechadv.2015.01.004
Buswell, W., Schwarzenbacher, R. E., Luna, E., Sellwood, M., Chen, B. N., Flors, V., et al. (2018). Chemical priming of immunity without costs to plant growth. New Phytol. 218, 1205–1216. doi: 10.1111/nph.15062
Cao, H., Bowling, S. A., Gordon, A. S., and Dong, X. N. (1994). Characterization of an Arabidopsis mutant that is nonresponsive to inducers of systemic acquired-resistance. Plant Cell 6, 1583–1592. doi: 10.1105/tpc.6.11.1583
Carella, P., Kempthorne, C. J., Wilson, D. C., Isaacs, M., and Cameron, R. K. (2017). Exploring the role of DIR1, DIR1-like and other lipid transfer proteins during systemic immunity in Arabidopsis. Physiol. Mol. Plant Pathol. 97, 49–57. doi: 10.1016/j.pmpp.2016.12.005
Chanda, B., Xia, Y., Mandal, M. K., Yu, K., Sekine, K. T., Gao, Q. M., et al. (2011). Glycerol-3-phosphate is a critical mobile inducer of systemic immunity in plants. Nat. Genet. 43, 421–427. doi: 10.1038/ng.798
Chang, K., Chen, J. Q., Shi, Y. X., Sun, M. J., Li, P. F., Zhao, Z. J., et al. (2017). The discovery of new scaffold of plant activators: from salicylic acid to benzotriazole. Chin. Chem. Lett. 28, 919–926. doi: 10.1016/j.cclet.2017.02.004
Chaturvedi, R., Venables, B., Petros, R. A., Nalam, V., Li, M. Y., Wang, X. M., et al. (2012). An abietane diterpenoid is a potent activator of systemic acquired resistance. Plant J. 71, 161–172. doi: 10.1111/j.1365-313X.2012.04981.x
Chen, L., Guo, X. F., Fan, Z. J., Zhang, N. L., Zhu, Y. J., Zhang, Z. M., et al. (2017). Synthesis and fungicidal activity of 3,4-dichloroisothiazole based strobilurins as potent fungicide candidates. RSC Adv. 7, 3145–3151. doi: 10.1021/acs.jafc.6b05128
Chen, Y. C., Holmes, E. C., Rajniak, J., Kim, J. G., Tang, S., Fischer, C. R., et al. (2018). N-hydroxy-pipecolic acid is a mobile metabolite that induces systemic disease resistance in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 115, E4920–E4929. doi: 10.1073/pnas.1805291115
Cohen, Y., Vaknin, M., and Mauch-Mani, B. (2016). BABA-induced resistance: milestones along a 55-year journey. Phytoparasitica 44, 513–538. doi: 10.1007/s12600-016-0546-x
Conrath, U., Beckers, G. J. M., Flors, V., Garcia-Agustin, P., Jakab, G., Mauch, F., et al. (2006). Priming: getting ready for battle. Mol. Plant Microbe Interact. 19, 1062–1071. doi: 10.1094/MPMI-19-1062
Conrath, U., Chen, Z., Ricigliano, J. R., and Klessig, D. F. (1995). Two inducers of plant defense responses, 2,6-dichloroisonicotinec acid and salicylic acid, inhibit catalase activity in tobacco. Proc. Natl. Acad. Sci. U.S.A. 92, 7143–7147. doi: 10.1073/pnas.92.16.7143
Cui, Z. N., Ito, J., Dohi, H., Amemiya, Y., and Nishida, Y. (2014). Molecular design and synthesis of novel salicyl glycoconjugates as elicitors against plant diseases. PLoS One 9:e108338. doi: 10.1371/journal.pone.0108338
Dangl, J. L., Horvath, D. M., and Staskawicz, B. J. (2013). Pivoting the plant immune system from dissection to deployment. Science 341, 746–751. doi: 10.1126/science.1236011
Delaney, T. P., Uknes, S., Vernooij, B., Friedrich, L., Weymann, K., Negrotto, D., et al. (1994). A central role of salicylic acid in plant disease resistance. Science 266, 1247–1250. doi: 10.1126/science.266.5188.1247
Dempsey, D. A., and Klessig, D. F. (2012). SOS - too many signals for systemic acquired resistance? Trends Plant Sci. 17, 538–545. doi: 10.1016/j.tplants.2012.05.011
Despres, C. (2003). The Arabidopsis NPR1 disease resistance protein is a novel cofactor that confers redox regulation of DNA binding activity to the basic domain/leucine zipper transcription factor TGA1. Plant Cell 15, 2181–2191. doi: 10.1105/tpc.012849
Ding, Y., Sun, T., Ao, K., Peng, Y., Zhang, Y., Li, X., et al. (2018). Opposite roles of salicylic acid receptors NPR1 and NPR3/NPR4 in transcriptional regulation of plant immunity. Cell 173, 1454.e–1467.e. doi: 10.1016/j.cell.2018.03.044
Durner, J., and Klessig, D. F. (1995). Inhibition of ascorbate peroxidase by salicylic acid and 2,6-dichloroisonicotinic acid, two inducers of plant defense responses. Proc. Natl. Acad. Sci. U.S.A. 92, 11312–11316. doi: 10.1073/pnas.92.24.11312
Durrant, W. E., and Dong, X. (2004). Systemic acquired resistance. Annu. Rev. Phytopathol. 42, 185–209. doi: 10.1146/annurev.phyto.42.040803.140421
Farace, G., Fernandez, O., Jacquens, L., Coutte, F., Krier, F., Jacques, P., et al. (2015). Cyclic lipopeptides from Bacillus subtilis activate distinct patterns of defence responses in grapevine. Mol. Plant Pathol. 16, 177–187. doi: 10.1111/mpp.12170
Fliegmann, J., Schuler, G., Boland, W., Ebel, J., and Mithofer, A. (2003). The role of octadecanoids and functional mimics in soybean defense responses. Biol. Chem. 384, 437–446. doi: 10.1515/BC.2003.049
Fonseca, S., Chini, A., Hamberg, M., Adie, B., Porzel, A., Kramell, R., et al. (2009). (+)-7-iso-Jasmonoyl-L-isoleucine is the endogenous bioactive jasmonate. Nat. Chem. Biol. 5, 344–350. doi: 10.1038/nchembio.161
Fu, Z. Q., and Dong, X. (2013). Systemic acquired resistance: turning local infection into global defense. Annu. Rev. Plant Biol. 64, 839–863. doi: 10.1146/annurev-arplant-042811-105606
Fu, Z. Q., Yan, S., Saleh, A., Wang, W., Ruble, J., Oka, N., et al. (2012). NPR3 and NPR4 are receptors for the immune signal salicylic acid in plants. Nature 486, 228–232. doi: 10.1038/nature11162
Gatard, S., Nasir, M. N., Deleu, M., Klai, N., Legrand, V., and Bouquillon, S. (2013). Bolaamphiphiles derived from alkenyl L-rhamnosides and alkenyl D-Xylosides: importance of the hydrophilic head. Molecules 18, 6101–6112. doi: 10.3390/molecules18056101
Gisi, U., Sierotzki, H., Cook, A., and Mccaffery, A. (2002). Mechanisms influencing the evolution of resistance to Qo inhibitor fungicides. Pestic. Manag. Sci. 58, 859–867. doi: 10.1002/ps.565
Goellner, K., and Conrath, U. (2008). Priming: it’s all the world to induced disease resistance. Eur. J. Plant Pathol. 121, 233–242. doi: 10.1007/s10658-007-9251-4
Graham, J. H., and Myers, M. E. (2011). Soil application of sar inducers imidacloprid, thiamethoxam, and acibenzolar-S-Methyl for citrus canker control in young grapefruit trees. Plant Dis. 95, 725–728. doi: 10.1094/PDIS-09-10-0653
Hägele and Rowell-Rahier (2000). Choice, performance and heritability of performance of specialist and generalist insect herbivores towards cacalol and seneciphylline, two allelochemicals of Adenostyles alpina (Asteraceae). J. Evol. Biol. 13, 131–142. doi: 10.1046/j.1420-9101.2000.00145.x
Hartmann, M., Zeier, T., Bernsdorff, F., Reichel-Deland, V., Kim, D., Hohmann, M., et al. (2018). Flavin monooxygenase-generated N-hydroxypipecolic acid is a critical element of plant systemic immunity. Cell 173, 456.e16–469.e16. doi: 10.1016/j.cell.2018.02.049
He, X. R., Chen, X., Lin, S. B., Mo, X. C., Zhou, P. Y., Zhang, Z. H., et al. (2017). Diversity-oriented synthesis of natural-product-like libraries containing a 3-methylbenzofuran moiety for the discovery of new chemical elicitors. Chemistryopen 6, 102–111. doi: 10.1002/open.201600118
Hoffland, E., Pieterse, C., Bik, L., and Van Den Pelt, J. (1995). Induced systemic resistance in radish is not associated with accumulation of pathogenesis-related proteins. Physiol. Mol. Plant Pathol. 46, 309–320. doi: 10.1006/pmpp.1995.1024
Hossain, M. M., Sultana, F., Kubota, M., and Hyakumachi, M. (2008). Differential inducible defense mechanisms against bacterial speck pathogen in Arabidopsis thaliana by plant-growth-promoting-fungus Penicillium sp GP16-2 and its cell free filtrate. Plant Soil 304, 227–239. doi: 10.1007/s11104-008-9542-3
Iavicoli, A., Boutet, E., Buchala, A., and Metraux, J. P. (2003). Induced systemic resistance in Arabidopsis thaliana in response to root inoculation with Pseudomonas fluorescens CHA0. Mol. Plant Microbe Interact. 16, 851–858. doi: 10.1094/MPMI.2003.16.10.851
Jaskiewicz, M., Conrath, U., and Peterhansel, C. (2011). Chromatin modification acts as a memory for systemic acquired resistance in the plant stress response. EMBO Rep. 12, 50–55. doi: 10.1038/embor.2010.186
Johnson, C., Boden, E., and Arias, J. (2003). Salicylic acid and NPR1 induce the recruitment of trans-activating TGA factors to a defense gene promoter in Arabidopsis. Plant Cell 15, 1846–1858. doi: 10.1105/tpc.012211
Jones, J. D., and Dangl, J. L. (2006). The plant immune system. Nature 444, 323–329. doi: 10.1038/nature05286
Jourdan, E., Henry, G., Duby, F., Dommes, J., Barthelemy, J. P., Thonart, P., et al. (2009). Insights into the defense-related events occurring in plant cells following perception of surfactin-type lipopeptide from Bacillus subtilis. Mol. Plant Microbe Interact. 22, 456–468. doi: 10.1094/MPMI-22-4-0456
Jung, H. W., Tschaplinski, T. J., Wang, L., Glazebrook, J., and Greenberg, J. T. (2009). Priming in systemic plant immunity. Science 324, 89–91. doi: 10.1126/science.1170025
Kamatham, S., Neela, K. B., Pasupulati, A. K., Pallu, R., Singh, S. S., and Gudipalli, P. (2016). Benzoylsalicylic acid isolated from seed coats of Givotia rottleriformis induces systemic acquired resistance in tobacco and Arabidopsis. Phytochemistry 126, 11–22. doi: 10.1016/j.phytochem.2016.03.002
Kamatham, S., Pallu, R., Pasupulati, A. K., Singh, S. S., and Gudipalli, P. (2017). Benzoylsalicylic acid derivatives as defense activators in tobacco and Arabidopsis. Phytochemistry 143, 160–169. doi: 10.1016/j.phytochem.2017.07.014
Kesarwani, M., Yoo, J., and Dong, X. (2007). Genetic interactions of TGA transcription factors in the regulation of pathogenesis-related genes and disease resistance in Arabidopsis. Plant Physiol. 144, 336–346. doi: 10.1104/pp.106.095299
Kohler, A., Schwindling, S., and Conrath, U. (2002). Benzothiadiazole-induced priming for potentiated responses to pathogen infection, wounding, and infiltration of water into leaves requires the NPR1/NIM1 gene in Arabidopsis. Plant Physiol. 128, 1046–1056. doi: 10.1104/pp.010744
Krämer, W., Schirmer, U., Jeschke, P., and Witschel, M. (2012). Modern Crop Protection Compounds, 2nd Edn. Hoboken, NJ: Wiley.
Krumm, T., Bandemer, K., and Boland, W. (1995). Induction of volatile biosynthesis in the Lima bean (Phaseolus lunatus) by leucine- and isoleucine conjugates of 1-oxo- and 1-hydroxyindan-4-carboxylic acid: evidence for amino acid conjugates of jasmonic acid as intermediates in the octadecanoid signalling pathway. FEBS Lett. 377, 523–529. doi: 10.1016/0014-5793(95)01398-9
Kukawka, R., Czerwoniec, P., Lewandowski, P., Pospieszny, H., and Smiglak, M. (2018). New ionic liquids based on systemic acquired resistance inducers combined with the phytotoxicity reducing cholinium cation. N. J. Chem. 42, 11984–11990. doi: 10.1039/C8NJ00778K
Kunz, W., Schurter, R., and Maetzke, T. (1997). The chemistry of benzothiadiazole plant activators. Pestic. Sci. 50, 275–282. doi: 10.1002/(SICI)1096-9063(199708)50:4<275::AID-PS593>3.0.CO;2-7
Latunde-Dada, A. O., and Lucas, J. A. (2001). The plant defence activator acibenzolar-S-methyl primes cowpea [Vigna unguiculata(L.) Walp.] seedlings for rapid induction of resistance. Physiol. Mol. Plant Pathol. 58, 199–208. doi: 10.1006/pmpp.2001.0327
Lawton, K. A., Friedrich, L., Hunt, M., Weymann, K., Delaney, T., Kessmann, H., et al. (1996). Benzothiadiazole induces disease resistance in Arabidopsis by activation of the systemic acquired resistance signal transduction pathway. Plant J. 10, 71–82. doi: 10.1046/j.1365-313X.1996.10010071.x
Leiminger, J. H., Adolf, B., and Hausladen, H. (2014). Occurrence of the F129L mutation in Alternaria solani populations in Germany in response to QoI application, and its effect on sensitivity. Plant Pathol. 63, 640–650. doi: 10.1111/ppa.12120
Lim, G. H., Shine, M. B., De Lorenzo, L., Yu, K., Cui, W., Navarre, D., et al. (2016). Plasmodesmata localizing proteins regulate transport and signaling during systemic acquired immunity in plants. Cell Host Microbe 19, 541–549. doi: 10.1016/j.chom.2016.03.006
Liu, Y.-P., Lai, R., Yao, Y.-G., Zhang, Z.-K., Pu, E.-T., Cai, X.-H., et al. (2013). Induced furoeudesmanes: a defense mechanism against stress in Laggera pterodonta, a Chinese herbal plant. Org. Lett. 15, 4940–4943. doi: 10.1021/ol4024826
Luna, E., Van Hulten, M., Zhang, Y., Berkowitz, O., López, A., Pétriacq, P., et al. (2014). Plant perception of β-aminobutyric acid is mediated by an aspartyl-tRNA synthetase. Nat. Chem. Biol. 10, 450–456. doi: 10.1038/nchembio.1520
Luzuriaga-Loaiza, W. P., Schellenberger, R., De Gaetano, Y., Akong, F. O., Villaume, S., Crouzet, J., et al. (2018). Synthetic Rhamnolipid Bolaforms trigger an innate immune response in Arabidopsis thaliana. Sci. Rep. 8:8534. doi: 10.1038/s41598-018-26838-y
Maffei, M. E., Arimura, G.-I., and Mithöfer, A. (2012). Natural elicitors, effectors and modulators of plant responses. Nat. Prod. Rep. 29, 1288–1303. doi: 10.1039/c2np20053h
Maienfisch, P., and Edmunds, A. J. F. (2017). “Thiazole and isothiazole ring-containing compounds in crop protection,” in Heterocyclic Chemistry in the 21st Century: A Tribute to Alan Katritzky, eds E. F. V. Scriven and C. A. Ramsden (San Diego: Elsevier Academic Press Inc), 35–88.
Maldonado, A. M., Doerner, P., Dixon, R. A., Lamb, C. J., and Cameron, R. K. (2002). A putative lipid transfer protein involved in systemic resistance signalling in Arabidopsis. Nature 419, 399–403. doi: 10.1038/nature00962
Metraux, J. P., Ahlgoy, P., Staub, T., Speich, J., Steinemann, A., Ryals, J., et al. (1991). Induced Systemic Resistance in Cucumber in Response to 2,6-Dichloro-Isonicotinic Acid and Pathogens. Dordrecht: Springer Netherlands. doi: 10.1007/978-94-015-7934-6_66
Mishina, T. E., and Zeier, J. (2007). Pathogen-associated molecular pattern recognition rather than development of tissue necrosis contributes to bacterial induction of systemic acquired resistance in Arabidopsis. Plant J. 50, 500–513. doi: 10.1111/j.1365-313X.2007.03067.x
Molina, A., Hunt, M. D., and Ryals, J. A. (1998). Impaired fungicide activity in plants blocked in disease resistance signal transduction. Plant Cell 10, 1903–1914. doi: 10.1105/tpc.10.11.1903
Monte, I., Hamberg, M., Chini, A., Gimenez-Ibanez, S., Garcia-Casado, G., Porzel, A., et al. (2014). Rational design of a ligand-based antagonist of jasmonate perception. Nat. Chem. Biol. 10, 671–676. doi: 10.1038/nchembio.1575
Mou, Z., Fan, W. H., and Dong, X. N. (2003). Inducers of plant systemic acquired resistance regulate NPR1 function through redox changes. Cell 113, 935–944. doi: 10.1016/S0092-8674(03)00429-X
Nakashita, H. (2002). Chloroisonicotinamide derivative induces a broad range of disease resistance in rice [Oryza sativa] and tobacco [Nicotiana tabacum]. Plant Cell Physiol. 43, 823–831. doi: 10.1093/pcp/pcf097
Navarova, H., Bernsdorff, F., Doring, A. C., and Zeier, J. (2012). Pipecolic acid, an endogenous mediator of defense amplification and priming, is a critical regulator of inducible plant immunity. Plant Cell 24, 5123–5141. doi: 10.1105/tpc.112.103564
Ogawa, M., Kadowaki, A., and Yamada, T. (2011). Applied development of a novel fungicide isotianil (STOUT). Sumitomo Kagaku 2011, 1–15.
Oostendorp, M., Kunz, W., Dietrich, B., and Staub, T. (2001). Induced disease resistance in plants by chemicals. Eur. J. Plant Pathol. 107, 19–28. doi: 10.1023/A:1008760518772
Papavizas, G. C., and Davey, C. B. (1963). Effect of amino compounds and related substances lacking sulfur on aphanomyces root rot of peas. Phytopathology 53, 116–122.
Park, S. W., Kaimoyo, E., Kumar, D., Mosher, S., and Klessig, D. F. (2007). Methyl salicylate is a critical mobile signal for plant systemic acquired resistance. Science 318, 113–116. doi: 10.1126/science.1147113
Pathak, R. K., Baunthiyal, M., Shukla, R., Pandey, D., Taj, G., and Kumar, A. (2017). In silico identification of mimicking molecules as defense inducers triggering jasmonic acid mediated immunity against alternaria blight disease in Brassica species. Front. Plant Sci. 8:609. doi: 10.3389/fpls.2017.00609
Pieterse, C. M., Van Der Does, D., Zamioudis, C., Leon-Reyes, A., and Van Wees, S. C. (2012). Hormonal modulation of plant immunity. Annu. Rev. Cell Dev. Biol. 28, 489–521. doi: 10.1146/annurev-cellbio-092910-154055
Pieterse, C. M. J., Van Wees, S. C. M., Van Pelt, J. A., Knoester, M., Laan, R., Gerrits, N., et al. (1998). A novel signaling pathway controlling induced systemic resistance in Arabidopsis. Plant Cell 10, 1571–1580. doi: 10.1105/tpc.10.9.1571
Pieterse, C. M. J., Zamioudis, C., Berendsen, R. L., Weller, D. M., Van Wees, S. C. M., and Bakker, P. A. H. M. (2014). Induced systemic resistance by beneficial microbes. Annu. Rev. Phytopathol. 52, 347–375. doi: 10.1146/annurev-phyto-082712-102340
Pluskota, W. E., Qu, N., Maitrejean, M., Boland, W., and Baldwin, I. T. (2007). Jasmonates and its mimics differentially elicit systemic defence responses in Nicotiana attenuata. J. Exp. Bot. 58, 4071–4082. doi: 10.1093/jxb/erm263
Potlakayala, S. D., Reed, D. W., Covello, P. S., and Fobert, P. R. (2007). Systemic acquired resistance in canola is linked with pathogenesis-related gene expression and requires salicylic Acid. Phytopathology 97, 794–802. doi: 10.1094/PHYTO-97-7-0794
Riedlmeier, M., Ghirardo, A., Wenig, M., Knappe, C., Koch, K., Georgii, E., et al. (2017). Monoterpenes support systemic acquired resistance within and between plants. Plant Cell 29, 1440–1459. doi: 10.1105/tpc.16.00898
Ryu, C. M., Hu, C. H., Reddy, M. S., and Kloepper, J. W. (2003). Different signaling pathways of induced resistance by rhizobacteria in Arabidopsis thaliana against two pathovars of Pseudomonas syringae. New Phytol. 160, 413–420. doi: 10.1046/j.1469-8137.2003.00883.x
Sanchez, L., Courteaux, B., Hubert, J., Kauffmann, S., Renault, J. H., Clement, C., et al. (2012). Rhamnolipids elicit defense responses and induce disease resistance against biotrophic, hemibiotrophic, and necrotrophic pathogens that require different signaling pathways in Arabidopsis and highlight a central role for salicylic acid. Plant Physiol. 160, 1630–1641. doi: 10.1104/pp.112.201913
Santino, A., Taurino, M., De Domenico, S., Bonsegna, S., Poltronieri, P., Pastor, V., et al. (2013). Jasmonate signaling in plant development and defense response to multiple (a)biotic stresses. Plant Cell Rep. 32, 1085–1098. doi: 10.1007/s00299-013-1441-2
Schuler, G., Gorls, H., and Boland, W. (2001). 6-Substituted indanoyl isoleucine conjugates mimic the biological activity of coronatine. Eur. J. Organ. Chem. 2001, 1663–1668. doi: 10.1002/1099-0690(200105)2001:9<1663::AID-EJOC1663>3.0.CO;2-I
Schuler, G., Mithofer, A., Baldwin, I. T., Berger, S., Ebel, J., Santos, J. G., et al. (2004). Coronalon: a powerful tool in plant stress physiology. FEBS Lett. 563, 17–22. doi: 10.1016/S0014-5793(04)00239-X
Schurter, R., Kunz, W., and Nyfeler, R. (1993). Process and a composition for immunizing plants against diseases. US4931581A. Toms River: Ciba-Geigy Corp.
Schwessinger, B., and Ronald, P. C. (2012). Plant innate immunity: perception of conserved microbial signatures. Annu. Rev. Plant Biol. 63, 451–482. doi: 10.1146/annurev-arplant-042811-105518
Segarra, G., Van Der Ent, S., Trillas, I., and Pieterse, C. M. J. (2009). MYB72, a node of convergence in induced systemic resistance triggered by a fungal and a bacterial beneficial microbe. Plant Biol. 11, 90–96. doi: 10.1111/j.1438-8677.2008.00162.x
Shah, J., Chaturvedi, R., Chowdhury, Z., Venables, B., and Petros, R. A. (2014). Signaling by small metabolites in systemic acquired resistance. Plant J. 79, 645–658. doi: 10.1111/tpj.12464
Shimono, M., Sugano, S., Nakayama, A., Jiang, C.-J., Ono, K., Toki, S., et al. (2007). Rice WRKY45 plays a crucial role in benzothiadiazole-inducible blast resistance. Plant Cell 19, 2064–2076. doi: 10.1105/tpc.106.046250
Silverman, F. P., Petracek, P. D., Heiman, D. F., Fledderman, C. M., and Warrior, P. (2005). Salicylate activity. 3. Structure relationship to systemic acquired resistance. J. Agric. Food Chem. 53, 9775–9780. doi: 10.1021/jf051383t
Slaughter, A., Daniel, X., Flors, V., Luna, E., Hohn, B., and Mauch-Mani, B. (2012). Descendants of primed Arabidopsis plants exhibit resistance to biotic stress. Plant Physiol. 158, 835–843. doi: 10.1104/pp.111.191593
Soylu, S., Baysal,Ö, and Soylu, E. M. (2003). Induction of disease resistance by the plant activator, acibenzolar-S-methyl (ASM), against bacterial canker (Clavibacter michiganensis subsp. michiganensis) in tomato seedlings. Plant Sci. 165, 1069–1075. doi: 10.1016/S0168-9452(03)00302-9
Spoel, S. H., and Dong, X. (2012). How do plants achieve immunity? Defence without specialized immune cells. Nat. Rev. Immunol. 12, 89–100. doi: 10.1038/nri3141
Spoel, S. H., Mou, Z. L., Tada, Y., Spivey, N. W., Genschik, P., and Dong, X. N. A. (2009). Proteasome-mediated turnover of the transcription coactivator NPR1 plays dual roles in regulating plant immunity. Cell 137, 860–872. doi: 10.1016/j.cell.2009.03.038
Stein, E., Molitor, A., Kogel, K. H., and Waller, F. (2008). Systemic resistance in Arabidopsis conferred by the mycorrhizal fungus Piriformospora indica requires jasmonic acid signaling and the cytoplasmic Function of NPR1. Plant Cell Physiol. 49, 1747–1751. doi: 10.1093/pcp/pcn147
Svoboda, J., and Boland, W. (2010). Plant defense elicitors: analogues of jasmonoyl-isoleucine conjugate. Phytochemistry 71, 1445–1449. doi: 10.1016/j.phytochem.2010.04.027
Tada, Y., Spoel, S. H., Pajerowska-Mukhtar, K., Mou, Z., Song, J., Wang, C., et al. (2008). Plant immunity requires conformational changes [corrected] of NPR1 via S-nitrosylation and thioredoxins. Science 321, 952–956. doi: 10.1126/science.1156970
Takaoka, Y., Iwahashi, M., Chini, A., Saito, H., Ishimaru, Y., Egoshi, S., et al. (2018). A rationally designed JAZ subtype-selective agonist of jasmonate perception. Nat. Commun. 9:3654. doi: 10.1038/s41467-018-06135-y
Thevenet, D., Pastor, V., Baccelli, I., Balmer, A., Vallat, A., Neier, R., et al. (2017). The priming molecule β-aminobutyric acid is naturally present in plants and is induced by stress. New Phytol. 213, 552–559. doi: 10.1111/nph.14298
Ton, J., Jakab, G., Toquin, V., Flors, V., Iavicoli, A., Maeder, M. N., et al. (2005). Dissecting the beta-aminobutyric acid-induced priming phenomenon in Arabidopsis. Plant Cell 17, 987–999. doi: 10.1105/tpc.104.029728
Ton, J., Van Pelt, J. A., Van Loon, L. C., and Pieterse, C. M. J. (2002). Differential effectiveness of salicylate-dependent and jasmonate/ethylene-dependent induced resistance in Arabidopsis. Mol. Plant Microbe Interact. 15, 27–34. doi: 10.1094/MPMI.2002.15.1.27
Tripathi, D., Jiang, Y. L., and Kumar, D. (2010). SABP2, a methyl salicylate esterase is required for the systemic acquired resistance induced by acibenzolar-S-methyl in plants. FEBS Lett. 584, 3458–3463. doi: 10.1016/j.febslet.2010.06.046
Truman, W., Bennett, M. H., Kubigsteltig, I., Turnbull, C., and Grant, M. (2007). Arabidopsis systemic immunity uses conserved defense signaling pathways and is mediated by jasmonates. Proc. Natl. Acad. Sci. U.S.A. 104, 1075–1080. doi: 10.1073/pnas.0605423104
Truman, W. M., Bennett, M. H., Turnbull, C. G., and Grant, M. R. (2010). Arabidopsis auxin mutants are compromised in systemic acquired resistance and exhibit aberrant accumulation of various indolic compounds. Plant Physiol. 152, 1562–1573. doi: 10.1104/pp.109.152173
Uknes, S., Mauch-Mani, B., Moyer, M., Potter, S., Williams, S., Dincher, S., et al. (1992). Acquired resistance in Arabidopsis. Plant Cell 4, 645–656. doi: 10.1105/tpc.4.6.645
van Hulten, M., Pelser, M., Van Loon, L. C., Pieterse, C. M. J., and Ton, J. (2006). Costs and benefits of priming for defense in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 103, 5602–5607. doi: 10.1073/pnas.0510213103
Vernooij, B. (1995). 2,6-Dichloroisonicotinic acidinduced resistance to pathogen without the accumulation of salicylic acid. Mol. Plant Microbe Interact. 8, 228–234. doi: 10.1094/MPMI-8-0228
Vernooij, B., Friedrich, L., Morse, A., Reist, R., Kolditz-Jawhar, R., Ward, E., et al. (1994). Salicylic acid is not the translocated signal responsible for inducing systemic acquired resistance but is required in signal transduction. Plant Cell 6, 959–965. doi: 10.1105/tpc.6.7.959
Veselinoviæ, J. B., Nikoliæ, G. M., Trutiæ, N. V., Živkoviæ, J. V., and Veselinoviæ, A. M. (2015). Monte Carlo QSAR models for predicting organophosphate inhibition of acetycholinesterase. SAR QSAR Environ. Res. 26, 449–460. doi: 10.1080/1062936X.2015.1049665
Vos, I. A., Pieterse, C. M. J., and Van Wees, S. C. M. (2013). Costs and benefits of hormone-regulated plant defences. Plant Pathol. 62, 43–55. doi: 10.1111/ppa.12105
Walters, D. R., Paterson, L., Walsh, D. J., and Havis, N. D. (2008). Priming for plant defense in barley provides benefits only under high disease pressure. Physiol. Mol. Plant Pathol. 73, 95–100. doi: 10.1016/j.pmpp.2009.03.002
Wang, C., El-Shetehy, M., Shine, M. B., Yu, K., Navarre, D., Wendehenne, D., et al. (2014). Free radicals mediate systemic acquired resistance. Cell Rep. 7, 348–355. doi: 10.1016/j.celrep.2014.03.032
Wang, D., Amornsiripanitch, N., and Dong, X. N. (2006). A genomic approach to identify regulatory nodes in the transcriptional network of systemic acquired resistance in plants. PLoS Pathog. 2:e123. doi: 10.1371/journal.ppat.0020123
Wang, D., Weaver, N. D., Kesarwani, M., and Dong, X. (2005). Induction of protein secretory pathway is required for systemic acquired resistance. Science 308, 1036–1040. doi: 10.1126/science.1108791
Ward, E. R., Uknes, S. J., Williams, S. C., Dincher, S. S., Wiederhold, D. L., Alexander, D. C., et al. (1991). Coordinate gene activity in response to agents that induce systemic acquired-resistance. Plant Cell 3, 1085–1094. doi: 10.1105/tpc.3.10.1085
Weiler, E. W., Kutchan, T. M., Gorba, T., Brodschelm, W., Niesel, U., and Bublitz, F. (1994). The Pseudomonas phytotoxin coronatine mimics octadecanoid signalling molecules of higher plants. FEBS Lett. 345, 9–13. doi: 10.1016/0014-5793(94)00411-0
Weller, D. M., Mavrodi, D. V., Van Pelt, J. A., Pieterse, C. M. J., Van Loon, L. C., and Bakker, P. A. H. M. (2012). Induced systemic resistance in Arabidopsis thaliana against Pseudomonas syringae pv. tomato by 2,4-diacetylphloroglucinol-producing Pseudomonas fluorescens. Phytopathology 102, 403–412. doi: 10.1094/PHYTO-08-11-0222
Wendehenne, D., Gao, Q. M., Kachroo, A., and Kachroo, P. (2014). Free radical-mediated systemic immunity in plants. Curr. Opin. Plant Biol. 20, 127–134. doi: 10.1016/j.pbi.2014.05.012
White, R. F. (1979). Acetylsalicylic acid (aspirin) induces resistance to tobacco mosaic virus in tobacco. Virology 99, 410–412. doi: 10.1016/0042-6822(79)90019-9
Wu, Y., Zhang, D., Chu, J. Y., Boyle, P., Wang, Y., Brindle, I. D., et al. (2012). The Arabidopsis NPR1 protein is a receptor for the plant defense hormone salicylic acid. Cell Rep. 1, 639–647. doi: 10.1016/j.celrep.2012.05.008
Xia, S., Feng, Y., Cheng, J.-G., Luo, H.-B., Li, Z., and Li, Z.-M. (2014). QAAR exploration on pesticides with high solubility: an investigation on sulfonylurea herbicide dimers formed through π–π stacking interactions. Chin. Chem. Lett. 25, 973–977. doi: 10.1016/j.cclet.2014.05.046
Xia, Y., Gao, Q. M., Yu, K., Lapchyk, L., Navarre, D., Hildebrand, D., et al. (2009). An intact cuticle in distal tissues is essential for the induction of systemic acquired resistance in plants. Cell Host Microbe 5, 151–165. doi: 10.1016/j.chom.2009.01.001
Yan, J., Li, H., Li, S., Yao, R., Deng, H., Xie, Q., et al. (2013). The Arabidopsis F-Box protein coronatine insensitive1 is stabilized by SCF COI1 and degraded via the 26S proteasome pathway. Plant Cell 25, 486–498. doi: 10.1105/tpc.112.105486
Yan, J., Li, S., Gu, M., Yao, R., Li, Y., Chen, J., et al. (2016). Endogenous bioactive jasmonate is composed of a set of (+)-7-iso-JA-Amino Acid conjugates. Plant Physiol. 172, 2154–2164. doi: 10.1104/pp.16.00906
Yan, J., Yao, R., Chen, L., Li, S., Gu, M., Nan, F., et al. (2018). Dynamic perception of jasmonates by the F-Box protein COI1. Mol. Plant 11, 1237–1247. doi: 10.1016/j.molp.2018.07.007
Yasuda, M. (2007). Regulation mechanisms of systemic acquired resistance induced by plant activators(Society Awards 2007(on high prospectiveness)). J. Pestic. Sci. 32, 281–282. doi: 10.1584/jpestics.32.281
Yasuda, M., Nakashita, H., Hasegawa, S., Nishioka, M., Arai, Y., Uramoto, M., et al. (2003). N-Cyanomethyl-2-chloroisonicotinamide induces systemic acquired resistance in Arabidopsis without salicylic acid accumulation. J. Agric. Chem. Soc. Japan 67, 322–328.
Yoshida, H., Konishi, K., Koike, K., Nakagawa, T., Sekido, S., and Yamaguchi, I. (1990a). Effect of N-cyanomethyl-2-chloroisonicotinamide for control of rice blast. J. Pestic. Sci. 15, 413–417. doi: 10.1584/jpestics.15.413
Yoshida, H., Konishi, K., Nakagawa, T., Sekido, S., and Yamaguchi, I. (1990b). Characteristics of N-phenylsulfonyl-2-chloroisonicotinamide as an anti-rice blast agent. J. Pestic. Sci. 15, 199–203. doi: 10.1584/jpestics.15.199
Zhou, J. M., Trifa, Y., Silva, H., Pontier, D., Lam, E., Shah, J., et al. (2000). NPR1 differentially interacts with members of the TGA/OBF family of transcription factors that bind an element of the PR-1 gene required for induction by salicylic acid. Mol. Plant Microbe Interact. 13, 191–202. doi: 10.1094/MPMI.2000.13.2.191
Zimmerli, L., Jakab, G., Metraux, J. P., and Mauch-Mani, B. (2000). Potentiation of pathogen-specific defense mechanisms in Arabidopsis by beta -aminobutyric acid. Proc. Natl. Acad. Sci. U.S.A. 97, 12920–12925. doi: 10.1073/pnas.230416897
Keywords: plant immunity, plant immune inducers, chemical derivation, ionic liquids, diversity-oriented synthesis, computer-aided design
Citation: Zhou M and Wang W (2018) Recent Advances in Synthetic Chemical Inducers of Plant Immunity. Front. Plant Sci. 9:1613. doi: 10.3389/fpls.2018.01613
Received: 15 September 2018; Accepted: 17 October 2018;
Published: 06 November 2018.
Edited by:
Shui Wang, Shanghai Normal University, ChinaReviewed by:
Wenli Chen, South China Normal University, ChinaSusheng Song, Capital Normal University, China
Copyright © 2018 Zhou and Wang. 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) and the copyright owner(s) 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: Mian Zhou, zhoumian1986@aliyun.com Wei Wang, oneway1985@pku.edu.cn