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S. No. | Plant | Type of elicitor used | Effects | References |
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1 | Brassica napus | Methyl jasmonate | Accumulation of indolyl glucosinolates in the leaves. The predominant components of the response were 3-indolylmethyl- and 1-methoxy-3-indolylmethylglucosinolates, which together comprised 90% of the total glucosinolates in treated leaves. | [23] |
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2 | Oryza sativa | Benzothiadiazole | BTH protected wheat systemically against powdery mildew infection by affecting multiple steps in the life cycle of the pathogen. The onset of resistance was accompanied by the induction of a number of wheat chemically induced (WCI) genes, including genes encoding a lipoxygenase and a sulfur-rich protein. | [24] |
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3 | Lycopersicon esculentum | Salicylic acid | Diminished susceptibleness to pathogens harm and abiotic stress. | [25] |
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4 | Beta vulgaris | Benzothiadiazole | Induced synthesis of chitinase and β-1,3-glucanase isozymes providing resistance against tobacco necrosis virus. | [26] |
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5 | Brassica oleracea (var. Botrytis) | Benzothiadiazole | BTH induced downy mildew (caused by P. parasitica) resistance in both cauliflower seedlings and 30-day old plants. | [27] |
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6 | Lycopersicon esculentum, Commelina communis | Oligogalacturonic acid (OGA) and chitosan | These elicitors reduced the size of the stomatal aperture. OGA not only inhibited light-induced stomatal opening, but also accelerated stomatal closing in both species; chitosan inhibited light-induced stomatal opening in tomato epidermis. | [28] |
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7 | Musa acuminata | Salicylic acid | Delayed ripening of banana fruit. | [29] |
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8 | Lycopersicon esculentum | Salicylic acid | Induced the synthesis of some stress proteins, such as PR proteins, which leads to increased chilling tolerance and resistance to pathogens, thereby decreasing the incidence of decay. | [30] |
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9 | Lilium | Benzoic acid | Modified the growth, stress tolerance, anatomy and morphology of eatable and ornamental species. | [31] |
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10 | Helianthus annuus | Benzothiadiazole | Prevented infestation by the parasitic weed Orobanche cumana. Root exudates revealed synthesis of the phytoalexin scopoletin, PR-protein chitinase and H2O2. | [32] |
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11 | Avena sativa, Oryza sativa, Raphanus sativus, Arachis hypogea, Nicotiana tabacum, Pisum sativum | Chitosan | Act as a stress tolerance inductor when directly applied to plant tissues, unchaining a hypersensitive reaction and lignifications, and promoting the activation of defenses against pathogens. | [33] |
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12 | Lycopersicum esculentum | Chitosan | Produced a higher resistance against Fusarium oxysporum and Phytophthora capsici. | [34] |
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13 | Lycopersicon esculentum (var. Castlemart) | Salicylic acid | Upregulation of transcription of PR1 and BGL2 genes (marker genes of SA pathway), increased endogenous H2O2 level involved in resistance against Helicoverpa armigera. | [35] |
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14 | Pisum sativum | Salicylic acid and 4-aminobutyric acid | Increased activity of phenol metabolizing enzymes viz., POD, PPO, PAL providing resistance against Erysiphe. polygony in pea. | [36] |
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15 | Brassica juncea | Benzothiadiazole | Increased phenolics and extracellular proteins act as markers of induced resistance. | [37] |
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16 | Lycopersicon esculentum | Chitosan and salicylic acid | Increased level of catalase and peroxidase enzymes activity. | [38] |
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17 | Citrus sinensis | β-amino butyric acid | Inhibited Penicillium italicum spore germination and germ tube elongation in vitro. Involved in the induced resistance against Penicillium italicum. | [39] |
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18 | Glycine max | Benzothiadiazole | Decreased incidence of soybean stem vascular discoloration, increased germination, photosynthetic pigments, lignin, phenolics, and flavonoids. Increased activities of phenylalanine ammonia lyase, peroxidase, and polyphenoloxidase. Decreased catalase activity was observed. | [40] |
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19 | Bhendi | Salicylic acid | Accumulation of phenolics and increased activity of enzyme PAL leading to resistance against Erysiphe cichoracearum. | [41] |
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20 | Brassica species | Salicylic acid | Recovery from heat stress, increased seedling length, reduced electrolyte leakage, and enhanced membrane protection. Increased level of total soluble sugars, fresh/dry weight, and enzymatic activities of invertase, catalase, and peroxidase conferred thermotolerance. Enhanced expression of some new proteins including heat shock proteins (HSPs) was also observed. | [42] |
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21 | Brassica napus | Salicylic acid and nitric oxide | Increased the activities of the antioxidant enzymes in leaves of Ni-stressed plants, improved the chlorophyll content and decreased the level of lipid peroxidation, and H2O2 and proline accumulation in leaves. | [43] |
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22 | Solanum melongena | Salicylic acid, chitosan, methyl salicylate, and methyl jasmonate | Increased lignin deposition in cell walls of roots, accumulation of phenolics, increase in the activity of enzymes PAL, POD, polyphenol oxidase, cinnamyl alcohol dehydrogenase, and catalase. Provided resistance against Ralstonia solanacearum. | [44] |
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23 | Brassica juncea (var. Rlm619) | Benzothiadiazole and salicylic acid | Induction of defense related enzymes, namely, peroxidase, phenylalanine ammonia lyase, and superoxide dismutase; increase in oil content and yield. Prevention of invasion of Alternaria brassicae. | [45] |
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24 | Phaseolus vulgaris | Salicylic acid and Methyl jasmonate | Controlled spider mite infestation, improved plant growth and bean yield. | [46] |
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25 | Brassica oleracea (var. Italica) | Methionine, tryptophan, chitosan, salicylic acid, and methyl jasmonate | Salicylic acid and chitosan induced increase in vitamin C content. Flavonoid concentration increased after MeJA and SA treatments. Methionine or tryptophan solutions did not positively affect the vitamin C or the phenolic compounds. Methionine increased the levels of aliphatic glucosinolates. However, indole glucosinolates presented a significant response to the induction with tryptophan, SA, or MeJA treatments. | [47] |
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26 | Glycine max | Benzothiadiazole and humic acid | Reduced damping-off and wilt diseases and increased growth parameters. BTH and HA in combination showed the highest activities of oxidative enzymes followed by BTH and HA alone. | [48] |
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27 | Soybean, rice, and wheat | β-glucans and chitin oligomers from Phytophthora and Pythium | Produced phytoalexins in soybean and rice plants. Lignification in wheat leaves. | [49] |
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28 | Arabidopsis, tomato | Oligogalacturonides from bacteria and fungi | Synthesis of protein inhibitors and activation of defense genes. | [50] |
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29 | Tobacco, tomato | Viral coat protein harpin from TMV | Activation of hypersensitive response. | [49] |
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30 | Tomato | Avr gene products, for example, AVR4 and AVR9 from Cladosporium fulvum | Activation of hypersensitive response. | [51] |
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31 | Arabidopsis | Flagellin, flg 15 from gram negative bacteria | Deposition of callose and activation of defense genes in Arabidopsis. | [52] |
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32 | Oat | Protein or peptide toxin, victorin from Helminthosporium victoriae (rust) | Programmed cell death in oat. | [53] |
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33 | Parsley | Glycoprotein from Phytophthora sojae | Synthesis of phytoalexin and activation of defense genes in parsley. | [49] |
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34 | Soybean | Syringolids from Pseudomonas syringae | Activation of hypersensitive response. | [49] |
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35 | Tobacco | Fatty acid amino acid conjugates from Lepidopterans | Synthesis of monoterpenes leading to activation of indirect defense in tobacco. | [49] |
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36 | Arabidopsis | Bacterial toxin, for example, coronatine from Pseudomonas syringae | Acivation of defense genes in Arabidopsis. | [54] |
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37 | Arabidopsis, tomato | Sphinganine analogue mycotoxins from Fusarium moniliforme | Programmed cell death and activation of defense genes in Arabidopsis and tomato. | [49] |
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