Defence priming by organismal and non-organismal stimulants can reduce effects of biotic stress in plants. Thus, it could help efforts to enhance the sustainability of agricultural production by reducing use of agrochemicals in protection of crops from pests and diseases. We have explored effects of applying this approach to both Arabidopsis plants and seeds of various crops in meta-analyses. The results show that its effects on Arabidopsis plants depend on both the priming agent and antagonist. Fungi and vitamins can have strong priming effects, and priming is usually more effective against bacterial pathogens than against herbivores. Moreover, application of bio-stimulants (particularly vitamins and plant defence elicitors) to seeds can have promising defence priming effects. However, the published evidence is scattered, does not include Arabidopsis, and additional studies are required before we can draw general conclusions and understand the molecular mechanisms involved in priming of seeds’ defences. In conclusion, defence priming of plants has clear potential and application of bio-stimulants to seeds may protect plants from an early age, promises to be both labour- and resource-efficient, poses very little environmental risk, and is thus both economically and ecologically promising.
Pesticides are used by farmers globally to protect crops from pests and diseases1, and they played important roles in “the green revolution” that brought huge benefits for agriculture and mankind2. However, conventional uses of pesticides also have serious drawbacks as they contaminate the environment3, cause fatalities1, and may foster a false sense of security regarding risks of pest outbreaks4. Hence, both national and international authorities, e.g., FAO5 and EU6 advocate development of alternative strategies.
Current approaches include biotechnological enhancement of plant resistance7 and optimization of integrated management efforts8. In addition, organismal interactions can be used to promote natural plant resistance interactions and mechanisms9,10,11,12,13. There is increasing evidence14,15 that plant-associated microorganisms can bolster plants’ resistance to biotic stresses. Inter alia, authors including16,17 have shown that manipulations of single microorganisms or entire microbiomes can enhance plant health. Plant resistance to biotic stressors can also be strengthened by activating plant defences through innovative uses of non-toxic internal or environmental bio-stimulants18,19,20.
Such stimulants can “prime” plants’ defences, i.e. enhance their responsiveness to biotic stressors21,22,23, thereby potentially offering a sustainable alternative to use of conventional plant protection chemicals24,25,26,27. Priming initially triggers a minor part of a defence response that increases the plant’s ability to defend itself against future antagonists (for example herbivores or pathogens). Once a plant has been primed, it will defend itself more rapidly, strongly and/or enduringly against subsequent threats. Priming agents may be live organisms (e.g. microorganisms or arthropods), chemicals (e.g. vitamins or plant hormones) or components thereof, and priming can be applied to various tissues and at diverse developmental stages (for example to foliage or roots of mature plants, or to seeds).
Molecular mechanisms underlying priming are far from completely understood, but there is a consensus that primed plants conserve a memory. Two potential mechanisms have been suggested. One involves accumulation of mitogen-activated protein kinases (MPKs). For example, Beckers et al.28 found that two MPKs (MPK3 and MPK6) accumulate during induction of systemic acquired resistance (SAR) by benzothiadiazole (BTH). Gene expression studies of knockout mutants showed that the kinases remain dormant until the plant is under attack, which initiates accumulation of defence enzymes (Ibid.). The other suggested mechanism is that epigenetic changes in DNA methylation and histone modifications may be carriers of stress memories and triggers of immune responses29,30,31. Reversible histone acetylation may be involved, at least in some cases, according to suggestions by Chen and Tian32 and observations of Arabidopsis plants’ responses to BTH31. Similarly, Lopez Sanchez, et al.33 found that hypomethylated Arabidopsis mutants were resistant to the biotrophic pathogen Hyaloperonospora arabidopsidis, whereas hypermethylated mutants were susceptible.
Numerous studies of plants’ defences have provided detailed information about how plants recognise attackers, the resulting modulation of hormonal pathways, and effects at multiple metabolic and physiological levels34,35,36. Diverse priming agents and biotic stresses have been applied to diverse plant taxa in various developmental stages. Clearly, it would be helpful to identify general patterns in responses, and their relationships (if any) with priming agents or antagonists. Therefore, we have sought such patterns and relationships through review of seed priming documented for various crops and meta-analyses of studies of priming of Arabidopsis plants. As effects of dosage and priming agent may be plant-species dependent, we focused our meta-analysis on one species and used Arabidopsis as a model. This is the first meta-analysis of defence priming in any plant species.
Seed priming in Arabidopsis
Evidence of enhanced resistance to biotic stresses has been found in several plant systems after priming seeds’ defences using biological organisms or chemical biostimuli (see Table 1). Defence priming appears to generally enhance plants’ health, either by reducing effects of herbivore damage or disease symptoms, or by impairing the growth of populations or replication of pests or pathogens.
More than 200 studies identified through the Web of Science searches investigated effects of priming seeds on the subsequent growth and development of Arabidopsis plants, but far fewer (11) reported effects of defence priming on biotic stress resistance, and none included the model plant Arabidopsis. With the diverse experimental backgrounds meta-analyses could not be performed on this dataset. However, a general conclusion is that priming with (for instance) vitamins and plant hormones has reportedly enhanced the resistance of many crops to a wide array of antagonists. In addition, increases in expression of defence genes recorded in the 11 studies were generally interpreted as increases in resistance, although neither general nor specific metabolomic responses were necessarily considered.
Of the 835 papers initially identified by Web of Science searches, 77 (describing 296 experiments) met the inclusion criteria. Of the excluded studies, 52% lacked information about the priming agent or biotic stress or the study was irrelevant, ca. 38% did not include experiments with wild-type Arabidopsis thaliana plants, ca. 3% were not peer-reviewed research articles, and 2% did not include data on performance of the antagonist. The remaining ca. 6% lacked information about sample sizes or errors, had poor figure resolution, included retracted or un-available parts or were studies of transgenerational priming.
The 296 studies (all included in the meta-analyses) documented results of applying defence priming treatments to foliage or root tissue, but not seed priming, except for a few studies of priming via soil enrichment by bacterial or fungal agents37,38,39,40.
Plant priming increases resistance to biotic stress
To meet our objective of identifying patterns in priming responses we focused on experiments involving application of priming treatments to the model plant Arabidopsis (in vegetative stages), to exploit the large pool of relevant available information41. We used data drawn from 267 independent Arabidopsis defence priming experiments, reported in 77 papers, in our meta-analyses. In all of these experiments whole plants were exposed to either selected bio-stimuli or live organisms in the priming treatments. In almost all of the experiments priming enhanced resistance to biotic stress, on average (Fig. 1, Hedge’s g < 0). Ca. 7% (19 of 267 studies) suggested that it had no or negative effects on plant resistance (Hedge’s g > 0). Vitamins and microorganisms proved to be stronger primers, providing better general protection, than herbivores (Dunn’s test, P < 0.05). In addition, fungi primed Arabidopsis plants more strongly than bacteria (Dunn’s test, P = 0.002)). When ranking individual priming agents across all categories, priming with riboflavin and BABA yielded the highest improvement of plant resistance to biotic stresses, whereas aphids, caterpillars and ologigalacturonides (OGs) performed as the worst priming agents (Fig. S1).
No general advantage of self-priming
As several organisms had been used to prime the plants, we investigated their relative efficacy and dependence of their effectiveness on the antagonist used in the tests (Fig. 2). The meta-analyses suggested that priming with organisms is more likely to protect plants against bacterial and fungal antagonists than against herbivores (Dunn’s test, P < 0.05). In addition, there was no significant indication that “self” priming (i.e. priming by an organism that is later used as a stressor) was either more or less advantageous than priming by another organism. For example, Kruskal-Wallis rank sum tests detected no significant differences (P > 0.05) in effects of priming with fungal and non-fungal agents on fungal infections (N = 53), or effects of priming with herbivore and non-herbivore agents on herbivore damage (N = 33). However, bacterial “self” priming (Hedge’s g = −3.7 ± 0.6, N = 44) provided weaker protection than fungal priming against bacteria (Hedge’s g = −5.5 ± 0.7, N = 11, Dunn’s test, P < 0.05; Fig. S2). Note, throughout the paper, data in x ± y format are means ± standard errors.
Evidence of organismal-specific priming effects
We also assessed variations in reported effects of defence priming among sub-groups of organisms (Fig. 3). Pathogenic bacteria reportedly induced significantly stronger resistance (Hedge’s g = −3.6 ± 0.5, N = 23) than non-pathogenic bacteria (Hedge’s g = −2.4 ± 0.6, N = 42; Wilcoxon rank sum test, P < 0.001; Fig. 3a). This result appears, however, to be highly affected by the difference in antagonist composition between the groups. Herbivores for example make up ca. 43% of the antagonists in the non-pathogenic bacteria dataset whereas pathogenic bacteria have 9% herbivores. When excluding herbivores, non-pathogenic bacteria appears to induce slightly stronger resistance (Hedge’s g = −3.7 ± 1.0, N = 24) compared to pathogenic bacteria (Hedge’s g = −3.6 ± 0.5, N = 21; Wilcoxon rank sum test, P = 0.04). In addition, as shown in Fig. 3b, Trichoderma induced somewhat higher resistance (Hedge’s g = −5.4 ± 0.4, N = 3) than Penicillium (Hedge’s g = −5.0 ± 1.2, N = 7), which induced stronger priming than “Other” fungi (including Phoma sp. and baker’s yeast; Hedge’s g = −4.0 ± 0.6, N = 10). However, these differences were not significant according to the Kruskal-Wallis rank sum test, possibly because the sample numbers did not provide sufficient statistical power. Herbivores used as priming agents were divided into two classes: aphids (Hedge’s g = −0.7 ± 0.3, N = 5) and caterpillars (Hedge’s g = −1.5 ± 0.2, N = 8). Caterpillars had significantly stronger priming effects than aphids according to Student’s t-test (P = 0.048, Fig. 3c).
Evidence of priming effects of plant-related elicitors
Chemical priming was included in many experiments (N = 139) and effects of diverse biotic stressors were tested. The tested chemical compounds included two classes of phytohormones, jasmonic acid compounds (JA and MeJA; Hedge’s g = −2.8 ± 1.1, N = 9) and salicylic acids (Hedge’s g = −2.5 ± 0.4, N = 10), which did not apparently differ in priming strength (Wilcoxon rank sum, P > 0.05). There was also no significant difference between effects of the B vitamins thiamine (Hedge’s g = −4.7 ± 1.5, N = 7) and riboflavin (Hedge’s g = −7.4 ± 1.6, N = 4; Wilcoxon rank sum, P > 0.05). To further investigate priming compounds’ effects, we tested differences in priming effects of four kinds of elicitors —BABA, BTH, selected bacterial and fungal compounds (B/F), and “Other” — on bacterial antagonists. The results indicated that, generally, chemical priming protects Arabidopsis against bacterial antagonists (Fig. 4a). Moreover, BABA provides the strongest protection (Hedge’s g = −8.6 ± 1.4, N = 13), followed by BTH (Hedge’s g = −6.0 ± 1.7, N = 12), “Other” (Hedge’s g = −2.9 ± 0.4, N = 50), and B/F (Hedge’s g = −2.7 ± 0.5, N = 23). Differences between chemical priming agents on bacterial antagonists were confirmed statistically (Dunn’s test, P < 0.05). In addition, several chemicals reportedly primed Arabidopsis against fungal infections (Fig. 4b), including BABA (Hedge’s g = −3.2 ± 1.2, N = 6), volatiles (Hedge’s g = −4.4 ± 1.0, N = 8), oligogalacturonides (OGs, Hedge’s g = −1.1 ± 0.1, N = 7) and “Other” compounds (Hedge’s g = −2.5 ± 0.8, N = 13). However, we found no significant differences between effects of those compounds (Kruskal-Wallis rank sum, P > 0.05).
Quality control of the database
Publication biases were evaluated with funnel plots, which were either symmetric suggesting that data were unbiased (for example, for herbivore priming effects and resistance), or slightly asymmetric, suggesting that data were slightly biased (Fig. S3). However, Fail-safe numbers indicating the number of non-significant findings required to reject the outcome of a meta-analysis suggested that our database was highly representative (Table S4).
Fungi and vitamins prime Arabidopsis plants’ defences most strongly
There is ample evidence that seed defence priming with diverse agents can protect various plant species against diverse antagonists (Table 1). Curiously, we found no published studies that assessed effects of priming defences of Arabidopsis seeds, apart a few indicating that enrichment of soil by bacterial or fungal agents may have indirect priming effects40,42,43,44. Regarding priming at the plant stage, we found 835 Arabidopsis studies of which 77, describing 267 experiments, fulfilled our requirements. More specifically, they provide information on effects of priming by organisms or plant-derived elicitors on defences against bio-stresses, including quantifiable details about antagonist responses (Supplementary Material List S5). Meta-analysis of this information confirmed that such priming generally enhances pest or pathogen resistance in Arabidopsis, and that fungi and vitamins have stronger effects than other tested agents, inducing stronger resistance to bacterial and fungal antagonists than to herbivores. The meta-analyses summarize indications of priming strength and antagonist specificity in previous studies, which may support future efforts to study and understand defence priming in Arabidopsis and other plants.
Priming agents and their generality
Organismal priming: microorganisms
An increasing number of studies suggest that plant resistance may be orchestrated interactively with associated organisms45 and those interactions could potentially be commercially manipulated46. Below-ground relationships with mycorrhizal fungi and bacteria, for example, not only promote growth, but also reduce damage to above-ground parts47, pre-inoculation of fungal endophytes modulates later plant disease development47,48,49, and spread of Heterobasidion (stem rot) to healthy spruce trees may be avoided by applying Phlebiopsis gigantean fungal spores to stumps50. Spontaneous associations between microbiomes and plants further suggest that cross-kingdom associations may provide overlooked promotion of plant growth and development16,17. Generally positive effects of priming by bacteria and fungi have been reported in Arabidopsis (Figs 1–4), confirming the potential to use microorganisms commercially for priming plants’ defences, as knowledge of the specificity and strength of various organisms’ effects increases.
Our meta-analyses suggest that defence priming by certain groups of organisms may provide better general protection than others. Fungi appear as the stronger of the tested organismal priming agents in Arabidopsis (Figs 1 and 3b), and bacteria follow closely (Fig. 3a). Organismal priming may offer some advantages over use of chemicals. For example, cold season tall fescue grasses that host defensive endophytic symbionts (Neotyphodium) have selective advantages in the presence of herbivores51, illustrating the potential importance of associated organisms for mutual protection. There is increasing awareness that the microbiota associated with plants is constantly filtered by the taxa, organs, and developing tissues present16. Moreover, plants and associated organisms share both semiochemical signals17,19,52 and evolutionary histories53,54,55. Unravelling such relationships and exploiting them for plant production may offer environmentally sound agricultural strategies. The diversity of natural interactions and associations is vast but increasing knowledge of the patterns involved is enhancing our ability to recognize and apply them8,10,56.
Organismal priming: Herbivores
As evidenced by meta-analyses, herbivores appear as generally weak priming agents (Figs 1 and 3c). Higher organisms induce defences in plants, as they give rise to immediate activation of defensive pathways and upregulated pools of specialised defence products57,58. Long-lasting trans-generational resistance shaped by herbivory has also been documented in Arabidopsis and tomato by Rasmann, et al.12. Our meta-analyses indicate that herbivores are generally weak priming agents (Figs 1 and 3c), although they induce immediate activation of defensive pathways and upregulation of pools of specialised defence products57,58. Internal herbivore feeders (e.g. miners and gallers) have more intimate associations with their hosts, but maintaining them in culture for experimental purposes is demanding, which may explain the scarcity of mechanistic and detailed studies of their impact on defence priming in the literature.
In addition, any reported priming of Arabidopsis plants included in our meta-analyses had weak anti-herbivory effects. In contrast, several studies found that seed priming effectively prevented herbivory in various crop systems (Table 1 and references herein, also see Rasmann, et al.12). Thus, we cannot exclude the possibility that the success of priming treatments against herbivore attacks may depend on the developmental stage at which they are applied to plants.
Non-organismal chemical priming: Vitamins
Vitamins are strong chemical priming agents according to our meta-analyses (Fig. 1). Moreover, they are essential, natural organic substances and many have additional defensive functions in planta. Hence, they have commercially appealing properties for priming purposes, including non-phytotoxicity and potentially growth-stimulating properties (Table 1), and B vitamins in particular are widely used as priming agents59,60,61,62.
Thiamine (vitamin B1) is an antioxidant produced by plants, bacteria, and fungi60,63. It naturally functions as a coenzyme in several metabolic pathways, including the Krebs cycle, glycolysis, and pentose phosphate pathway63,64. In Arabidopsis, Tunc-Ozdemir, et al.64 found that various stress treatments (cold, salt and paraquat) led to accumulation of thiamine, accompanied following paraquat treatment with reduced production of reactive oxygen species (ROS). Observations of enhanced defence responses to infection by Pseudomonas syringae pv tomato bacteria in various plants following foliar applications of thiamine confirmed that it has diverse, species- and genotype-specific priming effects24,65. When applied to seeds, thiamine also enhances resistance of several crops (including pea, barley, oat, wheat, and millet) against aphid pests27,66 and fungal infections62.
Vitamin-B2 (riboflavin) is also produced naturally in plants, but its effects as a priming agent have not been frequently tested. However, Azami-Sardooei, et al.67 reported that priming with B2 enhanced resistance to the pathogen B. cinerea in bean but not tomato plants. The authors cited argue that the latter may have been insensitive to B2 priming because the tomato plants already had sufficient endogenous levels of B2, lacked riboflavin receptors, or were unable to absorb it adequately.
Vitamin B3 is another natural metabolite in plants, niacin, that has frequently been used to prime plants. More strictly, niacin refers to nicotinamide and the closely related nicotinic acid (also with B3 activity). Nicotinamide is released by the enzyme poly (ADP-ribose) polymerase (PARP) in response to oxidative stress causing single-strand breaks in DNA68,69. Thus, as it is formed during oxidative stress, it putatively functions as a general signal and stress response59. Plants primed with B3, in either nicotinic acid or nicotinamide forms70, reportedly have enhanced resistance to both subsequent biotic26,61 and abiotic26,71 stressors.
Vitamins B1 and B3 have also been used as priming agents for a range of crops (including barley, wheat, and pea) without causing detectable phenotypic changes. Hamada, et al.27 and Hamada and Jonsson66 found that vitamin B1 protected several crops against aphid attacks, while Berglund, et al.26 found that B3 protected spruce against pine weevils. The lack of detected phenotypic responses to treatment with these agents is very promising as the ideal defence priming agent would have no or minimal performance penalties for the host, compared to unprimed controls22. In our meta-analyses there were too few studies to distinguish between effects of specific vitamins. However, our results confirm that vitamins may be attractive agents for priming plants of various species, applied either in vegetative stages (as in Arabidopsis studies) or seeds (as in studies with assorted non-model crop species).
Non-organismal chemical priming: Defence elicitors
Another potentially strong priming agent is the signalling compound aminobutyric acid isomer BABA (Fig. 4a)20. This is usually present at levels so low that it was only recently proven to be synthesised in highly diverse plant species in response to several kinds of pathogens72. Our meta-analyses show that BABA-priming of Arabidopsis plants has provided strong protection against bacterial diseases and, to a lesser degree, fungal diseases (Fig. 4a,b). Wilkinson, et al.73 also detected strong long-lasting effects of BABA against Botrytis cinerea post-harvest infections in tomatoes with no yield penalty. Elucidation of mechanisms behind these diverse effects may provide highly interesting insights and opportunities.
In contrast to BABA, oligogalacturonides (OGs) appear to have weak priming efficiency against fungal diseases (Fig. 4b). OGs comprise a diverse group of defence signalling molecules that are degradation products of pectin in plants’ cell walls. When disrupted they break into fragments, or so-called Damage Associated Molecular Patterns (DAMPs) that induce plant immune responses via an MPK-dependent pathway74,75,76. Thus, the finding that OGs did not score highly as priming agents in our analyses was surprising, but may be due to their diversity, and OG specificity may warrant further attention in future studies. Only general effects of OGs have been tested in seven Arabidopsis studies as yet, so it is too early to draw robust conclusions about their potential utility as priming agents.
Priming of plants with jasmonates is highly efficient, and even deters relatively large insects such as pine weevils from de-barking coniferous plants26. Martinez-Medina et al.22 argue that priming may come at an initial cost, that is outweighed by later benefits, but methyl-jasmonate (MeJA) appears to come with fairly high cost because it stunts growth, and causes plants to reallocate resources towards specialized metabolism e.g. terpenoid production in spruce77. Li, et al.78 found that MeJA applications may also cause changes in cuticle thickness and composition, and increases in densities of trichomes and stomata, as well as reductions in height and biomass, in various species (e.g., tomato, sunflower and soybean). Thus, although application of MeJA efficiently enhances herbivore resistance its value as a priming agent is questionable due to its undesirable phenotypic effects.
Previous meta-analyses have shown that green leaf volatiles (GLV) may protect plants against bacterial, fungal and herbivorous antagonists57,79. Despite the evidence of shared cross-kingdom chemical signalling, volatiles (and compounds derived from bacteria and fungi) did not collectively score high as priming agents in our meta-analyses. However, they are also highly heterogenous groups of compounds. Diverse expression-level responses to these compounds have been examined, and they have usually included responses of defence-associated pathways (for example JA or SA pathways) or pathways leading to specialised defence compounds (e.g., phenylpropanoids or glucosinolates, Table 1). Organisms secrete chemicals. Bacteria, for example, produce signaling molecules to regulate transcription and cell population density80 that may affect plant performance. Therefore, the mechanisms behind any organismal or chemical treatments may have shared mechanisms, which motivated a general illustration of efficiency order of all biostimulants included in this study (Fig. S1).
The increasing abundance of information about plants’ responses to stress conditions is rapidly increasing knowledge of the sophisticated metabolic and signalling networks involved in finetuning their defence responses. Understanding these responses and plants’ interactions with associated organisms may undoubtedly facilitate discovery of alternative strategies to protect plants, as noted by various authors10,16,17,53,81. However, the mechanisms involved in diverse responses must be elucidated to enable any generalisations.
Potential bias and sources of error
The quality of the database used in any meta-analysis is a major concern, mainly because publications on any topic may be subject to biases that exaggerate evidence, as significant effects or relationships are more attractive for publication than non-significant effects or relationships82. In our case, a risk of overestimating effects was weakly suggested in the funnel plots (Fig. S3). However, that concern was strongly contradicted by Fail-safe numbers (Table S4), which indicate the number of conflicting studies needed to reject findings of a meta-analysis.
Another potential source of error in meta-analyses lies in the way parameters are chosen. There are endless ways to measure priming effects, due to the diversity of both potential experimental systems (e.g. between non-pathogenic and pathogenic bacteria) and biological settings of priming treatments. There is also often no general agreement between responses that may be dynamic, non-linear and dependent on both spatial and temporal parameters (e.g. when evaluating relationships between gene expression, enzyme activity, and metabolomic changes). Currently we have no general mechanistic understanding of priming, although potential MPK accumulation and epigenetic alterations have been suggested. Any measurable general mechanistic understanding of plant memory would be a huge step forward in assessing and documenting plant priming.
Arabidopsis and general insights
The meta-analyses presented here are based on studies of the model species Arabidopsis thaliana. This is advantageous as it avoids potentially confounding variation in responses due to variations in the host plant, thereby assisting inter-study comparisons. The Col-0 accession, the first model plant to be sequenced was used in more than 85% of the studies included in our database and meta-analyses. Thus, the findings may not be relevant for all plant systems, but Arabidopsis provides a convenient model of higher plants generally, and the Brassicaceae specifically, offering high potential for molecular follow-up studies to unravel mechanisms underlying defence priming41.
Curiously, although diverse plant systems may be primed at the seed stage (Table 1), we identified no studies of defence priming Arabidopsis seeds, so we could only consider aspects of priming this species at the plant stage. Moreover, we identified relatively few studies on priming of seeds of other species, although priming at the seed stage appears to be commercially attractive. This could be due to biased knowledge in this field of research, which is often driven by private seed companies83, so knowledge of seed-priming mechanisms could be protected by commercial interests.
Despite advances in knowledge of priming, several challenges must be addressed before priming may be commercially viable84. Reliable priming methods must be established with detailed knowledge about priming strength for relevant crop species, and detailed information about priming stability and reliability will be expected by the customers. Successful priming increases plants’ overall performance under stress21,22,85, and to evaluate priming strength in any experimental test, it is desirable to include both physiological costs and performance benefits. This is not straightforward. Positive effects on yield and negative effects on an antagonist are convincing indications of successful priming, but bioassays are costly and elaborate to perform, and demanding to standardize86. A mechanistic understanding of priming might indicate convenient and cost-effective ways to assess priming. Assessments of MPK accumulation and epigenetic responses (DNA methylation/demethylation and histone modifications) are promising possibilities. However, they cannot stand alone and must be calibrated according to plant and antagonist performance.
A priming agent can be applied in diverse ways, e.g. by spraying or submerging seeds, foliage or roots. Seeds have obvious advantages, as they can be treated evenly and precisely with little if any environmental impact or non-target ramifications87. Moreover, in contrast to plant priming, seed priming will also protect plants from the earliest stages of germination and throughout their development. Thus, seed treatment promises to be less labour intensive and more cost-efficient than treatment of plants88. However, the development of robust seed priming procedures will involve several optimization steps, including choices of plant system and priming agents, test conditions, stresses, and responses of both plants and antagonists (Fig. 5).
Ugena et al.89 developed a multi-trait high throughput screening method of biostimulants on Arabidopsis seeds to assess effects on growth and germination in response to subsequent salt stress. This work provides a rare resource for characterization of biostimulants towards plant health promotion.
There is an urgent need for sustainable crop protection techniques and seed defence priming appears to be an attractive strategy. However, before it can be commercially applied several aspects, starting with the priming mechanism(s), must be elucidated. Assessments of priming treatments’ persistence (duration of priming effects) and the range of biotic stresses they may protect against are also warranted. The meta-analyses presented here convincingly show that priming has general potential for raising crop productivity. This is increasingly important as our agricultural systems are facing severe challenges including increasing demands, higher costs, and a changing climate.
Material and Methods
Literature covering priming of seeds to enhance germination and growth extends back to the 1970s, but relatively few published studies have focused on the priming of seeds’ defences against biotic stress. Strategic searches of databases like Web-of Science detected few relevant papers, which address diverse systems. A much larger body of literature covers defence priming in the plant stage, and we used Web-of-Science to compile a database of these studies in Arabidopsis thaliana (hereafter Arabidopsis) that provides a model for studies of plant biology, and is a suitable study system to understand mechanistic responses in plants at the molecular scale41.
Seed defence priming
As already mentioned, Web of Science searches identified relatively few studies on defence priming in seeds. For example, a search for papers on the Topics seed priming AND biotic stress on 27 July 2018 resulted in 31 papers, published from 2009–2018 including 20 published in 2012–2018 that addressed seed priming. Of the latter, 15 covered enhancement of resistance to abiotic stress and just four documented defence priming against pathogens. Host plants considered in those 20 studies were mainly crops such as rice, barley, wheat, maize, tomato, onion, corn and Brassica species, and only four included defence priming with use of a specific compound (beta-aminobutyric acid, BABA) or pathogen (Trichoderma or a hemibiotrophic pathogen). The search also listed a few reviews on, for example, uses of macro-algal compounds as agricultural bio-stimulants90. Back-tracing through such reviews, as described for example by18,60, was a more rewarding search strategy, resulting in identification of most of the studies on defence priming in seeds listed in Table 1 (see List S6 for references).
Plant defence priming
To cover defence priming of Arabidopsis plants, we searched the Web of Science for documents of Article type in the Category Plant Sciences on the Topics Arabidopsis AND priming. This resulted in 509 hits (collected on the 17th and 18th of April 2018). An additional search for Articles in the Category Plant Sciences with Arabidopsis in the title on the Topics treatm* AND resistance AND plant defen?e resulted in 326 more hits (collected on the 2nd and 3rd of May 2018). Thus, the resulting database included 835 articles.
Papers that mentioned Arabidopsis as a main study organism in the title, abstract or author keywords were then selected. Fifty of the discarded papers were randomly chosen for quality checking, and scrutinised to verify that they did not include data on responses of Arabidopsis that should have been included according to the data selection criteria. Thus, although a few studies may have been overlooked by chance, we judge that the database is rich enough to fulfil the purpose of this study.
Next, in order to extract usable information from the identified papers, each reported study was examined and retained if:
It included experiments with a priming agent and a wild-type population of any specified ecotype of Arabidopsis thaliana. Priming and tests with any kinds of organs or tissues (e.g. seeds, plants, or roots) were allowed.
The priming agent was organismal (e.g., a herbivore, bacterium, fungus, or pathogen effector), or plant-related elicitor, e.g., beta aminobutyric acid (BABA), or flagellin (flg22), a plant hormone related to biotic stress, e.g., jasmonic acid (JA, or its methyl derivative, MeJA) or salicylic acid (SA), or any vitamin.
Experiments were detailed and information about the priming agent (its kind, concentration, treatment duration etc) was included.
Responses to any kinds of biotic stresses (e.g. any herbivore, bacterium, fungus or virus) were detailed, but not responses to un-groupable stress agents (e.g. singletons, oomycota or transgenic stresses).
The study provided information about both primed and unprimed plants, statistical data about their responses (averages and standard deviations, standard errors or confidence intervals), and sample sizes, as well as resistance effects in terms of quantified pest/pathogen performance. Experiments that solely quantified Arabidopsis defence responses (e.g. gene expression, metabolite accumulation, etc.) were excluded. Papers indicating pathogen performance based solely on use of RT-PCR and ELISA were also excluded (ca. eight papers were excluded on these grounds). Studies providing information on behavioural responses of herbivores, for example, data on feeding responses of aphids obtained using electrical penetration graphs showing durations and frequencies of phloem phase were included.
Experiments were not included if:
The authors had not specified treatments of the primed or control plants (regarding, for example, concentrations/amounts of primer used), or information about types of errors was incomplete.
Effects of an abiotic stress such as salt stress or drought, or the highly specific agents ethylene, abscisic acid (ABA), coroatine, catechol, silicon, quinolinate, mycotoxins, transgenic bacterial strains, and volatiles or exudates produced by transgenic plants were defined or regarded as priming agents.
Priming treatments included use of NADPH oxidase inhibitors (e.g. DPI), H2O2 scavengers (e.g. catalase), a mETC uncoupler (e.g. antimycin or rotenone), nitric oxide inhibitors (e.g. cPTIO, L-NAME and OA) or BABA-inhibitors (e.g. L-Glutamine).
Several priming agents, for instance two compounds, were combined.
They were intended to determine active components or sizes of the priming agent (e.g. via use of proteases or deacetylases).
Transgenerational priming was tested.
Mean values and variances of resistance data were extracted from tables and figures in the remaining studies and listed according to priming agent and antagonist. The plugin “Figure Calibration” in ImageJ, available at: http://www.astro.physik.uni-goettingen.de/hessman/ImageJ/, was used to obtain data from plots when numbers were not available. If sample sizes were given as a range (e.g. 20–25 replicates), the lowest number was listed. If the resolution of a figure was too low to extract data, the study was excluded.
If a primer’s effects at several concentrations and/or time points were tested in an experiment, data pertaining to the strongest effect (positive or negative) were included. Bacterial growth assays presented at log-scale were log-transformed after data extraction. Repeated experiments were included if they were independent of each other. Effect size (Hedge’s g) was calculated using Rstudio as described by Del Re91.
If several parameters (e.g. bacterial growth and disease severity) of individuals were measured, the effect sizes obtained were aggregated into a single effect size according to the “BHHR” procedure91. After aggregation, 267 experiments described in 77 papers remained and were included in the database, and subsequent meta-analyses. Responses quantified in these experiments included lesion area, feeding damage, bacterial growth, infection, disease severity, spore production, feeding duration, population increase, herbivore weight, time to pupation and/or reproduction rate. The studies reporting these experiments are listed in the Supplementary Information (List S5). Funnel plots and Fail-safe numbers, indicating how many conflicting studies would be needed to reject the outcome of a meta-analysis, are also reported in the Supplementary Information (Fig. S3 and Table S4) in agreement with use of Funnel plots and Fail-safe numbers92,93.
After calculating the effect sizes, the experiments were divided into classes depending on the type of priming (Bacteria, Fungi, Herbivores, Chemicals, Hormones or Vitamins, with further division into sub-classes such as JA, SA, or B1) and biotic stressor (bacterial, fungal, herbivore, or viral) applied.
QQ-plot and Shapiro tests were used to assess the normality of data distributions. The variance of the data was assessed with F- or Levene’s tests. When comparing two groups, statistical analyses were performed using the parametric Student’s t-test (with equal or unequal variance settings depending on the outcome from the variance test) and nonparametric Wilcoxon rank sum and Kolmogorov-Smirnov tests (for datasets with sufficiently equal and unequal variance, respectively). If more than two groups were compared, statistical analysis were performed using One-way ANOVA for normally distributed data and Kruskal Wallis tests for non-normally distributed data. Pairwise comparison after the Kruskal Wallis test was performed using post-hoc Dunn’s tests (with Benjamini-Hochberg methodology for P-value adjustment). A significance threshold of 0.05 was applied in all tests. R version 3.4.2 was used for all analyses and generating all plots.
Ethical and third parts issues do not apply to this submission as no experiments were performed and no copying of any material included.
The data of this study is based on extracts from published papers available through scientific citation data bases, and it is available as open access on-line data https://springernature.figshare.com/s/19070f9acfb5182cce0b. Lists of references that were included to compile the data base are available in the up-loaded supplemental material document included in the submission.
Alavanja, M. C. R. Pesticides Use and Exposure Extensive Worldwide. Reviews on environmental health 24, 303–309 (2009).
Borlaug, N. E. Ending world hunger. The promise of biotechnology and the threat of antiscience zealotry. Plant Physiol 124, 487–490 (2000).
Aktar, M. W. et al. Impact assessment of pesticide residues in fish of Ganga river around Kolkata in West Bengal. Environ Monit Assess 157, 97–104, https://doi.org/10.1007/s10661-008-0518-9 (2009).
Oerke, E. C. Crop losses to pests. J Agr Sci 144, 31–43, https://doi.org/10.1017/S0021859605005708 (2006).
FAO. International Code of Conduct on the Distribution and Use of Pesticides. (Food and Agriculture Organization of the United Nations, 2010).
EC-Directive. In Official Journal of the European Union (ed the European Parliament), (https://doi.org/10.3000/17252555.L_2009.309.eng, 2009/128/EC).
Montesinos, E. Development, registration and commercialization of microbial pesticides for plant protection. Int Microbiol 6, 245–252, https://doi.org/10.1007/s10123-003-0144-x (2003).
Barzman, M. et al. Eight principles of integrated pest management. Agron Sustain Dev 35, 1199–1215, https://doi.org/10.1007/s13593-015-0327-9 (2015).
Albrectsen, B. R. & Witzell, J. In Fungi: Types, Environmental Impact and Role in Disease (ed Maria Sol Adolfo Paz Silva) 235–246 (Nova Science Publishers, 2012).
Biere, A. & Bennett, A. E. Three-way interactions between plants, microbes and insects. Funct Ecol 27, 567–573, https://doi.org/10.1111/1365-2435.12100 (2013).
Bruce, T. J. A., Matthes, M. C., Napier, J. A. & Pickett, J. A. Stressful “memories” of plants: Evidence and possible mechanisms. Plant Sci 173, 603–608, https://doi.org/10.1016/j.plantsci.2007.09.002 (2007).
Rasmann, S. et al. Herbivory in the Previous Generation Primes Plants for Enhanced Insect Resistance. Plant Physiol 158, 854–863, https://doi.org/10.1104/pp.111.187831 (2012).
Schulz, B. & Boyle, C. The endophytic continuum. Mycol Res 109, 661–686, https://doi.org/10.1017/S095375620500273x (2005).
Innerebner, G., Knief, C. & Vorholt, J. A. Protection of Arabidopsis thaliana against Leaf-Pathogenic Pseudomonas syringae by Sphingomonas Strains in a Controlled Model System. Appl Environ Microb 77, 3202–3210, https://doi.org/10.1128/Aem.00133-11 (2011).
Jogaiah, S., Abdelrahman, M., Tran, L. S. P. & Shin-ichi, I. Characterization of rhizosphere fungi that mediate resistance in tomato against bacterial wilt disease. J Exp Bot 64, 3829–3842, https://doi.org/10.1093/jxb/ert212 (2013).
Bai, Y. et al. Functional overlap of the Arabidopsis leaf and root microbiota. Nature 528, 364–369, https://doi.org/10.1038/nature16192 (2015).
Zhang, Y. X., Ruyter-Spira, C. & Bouwmeester, H. J. Engineering the plant rhizosphere. Curr Opin Biotech 32, 136–142, https://doi.org/10.1016/j.copbio.2014.12.006 (2015).
Song, G. C., Choi, H. K., Kim, Y. S., Choi, J. S. & Ryu, C. M. Seed defense biopriming with bacterial cyclodipeptides triggers immunity in cucumber and pepper. Sci Rep-Uk 7, https://doi.org/10.1038/s41598-017-14155-9 (2017).
Song, L. X. et al. Brassinosteroids act as a positive regulator for resistance against root-knot nematode involving RESPIRATORY BURST OXIDASE HOMOLOG-dependent activation of MAPKs in tomato. Plant Cell Environ 41, 1113–1125, https://doi.org/10.1111/pce.12952 (2018).
Worrall, D. et al. Treating seeds with activators of plant defence generates long-lasting priming of resistance to pests and pathogens. New Phytol 193, 770–778, https://doi.org/10.1111/j.1469-8137.2011.03987.x (2012).
Hilker, M. et al. Priming and memory of stress responses in organisms lacking a nervous system. Biol Rev 91, 1118–1133, https://doi.org/10.1111/brv.12215 (2016).
Martinez-Medina, A. et al. Recognizing Plant Defense Priming. Trends Plant Sci 21, 818–822, https://doi.org/10.1016/j.tplants.2016.07.009 (2016).
Mauch-Mani, B., Baccelli, I., Luna, E. & Flors, V. Defense Priming: An Adaptive Part of Induced Resistance. Annu Rev Plant Biol 68, 485–512, https://doi.org/10.1146/annurev-arplant-042916-041132 (2017).
Ahn, I. P., Kim, S. & Lee, Y. H. Vitamin B-1 functions as an activator of plant disease resistance. Plant Physiol 138, 1505–1515, https://doi.org/10.1104/pp.104.058693 (2005).
Beckers, G. J. & Conrath, U. Priming for stress resistance: from the lab to the field. Curr Opin Plant Biol 10, 425–431, https://doi.org/10.1016/j.pbi.2007.06.002 (2007).
Berglund, T., Lindstrom, A., Aghelpasand, H., Stattin, E. & Ohlsson, A. B. Protection of spruce seedlings against pine weevil attacks by treatment of seeds or seedlings with nicotinamide, nicotinic acid and jasmonic acid. Forestry 89, 127–135, https://doi.org/10.1093/forestry/cpv040 (2016).
Hamada, A. M., Fatehi, J. & Jonsson, L. M. V. Seed treatments with thiamine reduce the performance of generalist and specialist aphids on crop plants. Bull Entomol Res 108, 84–92, https://doi.org/10.1017/S0007485317000529 (2018).
Beckers, G. J. M. et al. Mitogen-Activated Protein Kinases 3 and 6 Are Required for Full Priming of Stress Responses in Arabidopsis thaliana. Plant Cell 21, 944–953, https://doi.org/10.1105/tpc.108.062158 (2009).
Conrath, U. Molecular aspects of defence priming. Trends Plant Sci 16, 524–531, https://doi.org/10.1016/j.tplants.2011.06.004 (2011).
Espinas, N. A., Saze, H. & Saijo, Y. Epigenetic Control of Defense Signaling and Priming in Plants. Front Plant Sci 7, https://doi.org/10.3389/fpls.2016.01201 (2016).
Jaskiewicz, M., Conrath, U. & Peterhansel, C. Chromatin modification acts as a memory for systemic acquired resistance in the plant stress response. Embo Rep 12, 50–55, https://doi.org/10.1038/embor.2010.186 (2011).
Chen, Z. J. & Tian, L. Roles of dynamic and reversible histone acetylation in plant development and polyploidy. Bba-Gene Struct Expr 1769, 295–307, https://doi.org/10.1016/j.bbaexp.2007.04.007 (2007).
Lopez Sanchez, A., Stassen, J. H., Furci, L., Smith, L. M. & Ton, J. The role of DNA (de)methylation in immune responsiveness of Arabidopsis. Plant J 88, 361–374, https://doi.org/10.1111/tpj.13252 (2016).
Jones, J. D. G. & Dangl, J. L. The plant immune system. Nature 444, 323–329, https://doi.org/10.1038/nature05286 (2006).
Macel, M., van Dam, N. M. & Keurentjes, J. J. B. Metabolomics: the chemistry between ecology and genetics. Mol Ecol Resour 10, 583–593, https://doi.org/10.1111/j.1755-0998.2010.02854.x (2010).
Pieterse, C. M. J., der Does, V., Zamioudis, D., Leon-Reyes, C. & Van Wees, A. S. C. M. Hormonal Modulation of Plant Immunity. Annu Rev Cell Dev Bi 28, 489–521, https://doi.org/10.1146/annurev-cellbio-092910-154055 (2012).
Aziz, M. et al. Augmenting Sulfur Metabolism and Herbivore Defense in Arabidopsis by Bacterial Volatile Signaling. Front Plant Sci 7, https://doi.org/10.3389/fpls.2016.00458 (2016).
Elsharkawy, M. M., Shimizu, M., Takahashi, H. & Hyakumachi, M. Induction of systemic resistance against Cucumber mosaic virus by Penicillium simplicissimum GP17-2 in Arabidopsis and tobacco. Plant Pathol 61, 964–976, https://doi.org/10.1111/j.1365-3059.2011.02573.x (2012).
Hossain, M. M., Sultana, F. & Hyakumachi, M. Role of ethylene signalling in growth and systemic resistance induction by the plant growth-promoting fungus Penicillium viridicatum in Arabidopsis. J Phytopathol 165, 432–441, https://doi.org/10.1111/jph.12577 (2017).
Hossain, M. M., Sultana, F., Kubota, M. & Hyakumachi, M. 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 (2008).
Koornneef, M. & Meinke, D. The development of Arabidopsis as a model plant. Plant J 61, 909–921, https://doi.org/10.1111/j.1365-313X.2009.04086.x (2010).
Aziz, A. et al. Effectiveness of beneficial bacteria to promote systemic resistance of grapevine to gray mold as related to phytoalexin production in vineyards. Plant Soil 405, 141–153, https://doi.org/10.1007/s11104-015-2783-z (2016).
Elsharkawy, M. M., Shimizu, M., Takahashi, H. & Hyakumachi, M. The plant growth-promoting fungus Fusarium equiseti and the arbuscular mycorrhizal fungus Glomus mosseae induce systemic resistance against Cucumber mosaic virus in cucumber plants. Plant Soil 361, 397–409, https://doi.org/10.1007/s11104-012-1255-y (2012).
Hossain, M. D. et al. Differential enzymatic defense mechanisms in leaves and roots of two true mangrove species under long- term salt stress. Aquat Bot 142, 32–40 (2017).
Barbosa, P. et al. Associational Resistance and Associational Susceptibility: Having Right or Wrong Neighbors. Annu Rev Ecol Evol S 40, 1–20, https://doi.org/10.1146/annurev.ecolsys.110308.120242 (2009).
Friesen, M. L. et al. Microbially Mediated Plant Functional Traits. Annual Review of Ecology, Evolution, and Systematics 42, 23–46, https://doi.org/10.1146/annurev-ecolsys-102710-145039 (2011).
Jung, S. C., Martinez-Medina, A., Lopez-Raez, J. A. & Pozo, M. J. Mycorrhiza-Induced Resistance and Priming of Plant Defenses. J Chem Ecol 38, 651–664, https://doi.org/10.1007/s10886-012-0134-6 (2012).
Busby, P. E. et al. Genetics-based interactions among plants, pathogens, and herbivores define arthropod community structure. Ecology 96, 1974–1984, https://doi.org/10.1890/13-2031.1 (2015).
Busby, P. E., Peay, K. G. & Newcombe, G. Common foliar fungi of Populus trichocarpa modify Melampsora rust disease severity. New Phytol 209, 1681–1692, https://doi.org/10.1111/nph.13742 (2016).
Kenigsvalde, K. et al. Evaluation of the biological control agent Rotstop in controlling the infection of spruce and pine stumps by Heterobasidion in Latvia. Scand J Forest Res 31, 254–261, https://doi.org/10.1080/02827581.2015.1085081 (2016).
Clay, K., Holah, J. & Rudgers, J. A. Herbivores cause a rapid increase in hereditary symbiosis and alter plant community composition. P Natl Acad Sci USA 102, 12465–12470, https://doi.org/10.1073/pnas.0503059102 (2005).
Jelenska, J., Davern, S. M., Standaert, R. F., Mirzadeh, S. & Greenberg, J. T. Flagellin peptide flg22 gains access to long-distance trafficking in Arabidopsis via its receptor, FLS2. J Exp Bot 68, 1769–1783 (2017).
Gourbal, B. et al. Innate immune memory: An evolutionary perspective. Immunol Rev 283, 21–40, https://doi.org/10.1111/imr.12647 (2018).
Kohler, A. et al. Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists. Nat Genet 47, 410–415, https://doi.org/10.1038/ng.3223 (2015).
Tisserant, E. et al. Genome of an arbuscular mycorrhizal fungus provides insight into the oldest plant symbiosis. P Natl Acad Sci USA 110, 20117–20122, https://doi.org/10.1073/pnas.1313452110 (2013).
Kumar, S., Kumari, R. & Sharma, V. Transgenerational Inheritance in Plants of Acquired Defence Against Biotic and Abiotic Stresses: Implications and Applications. Agr Res 4, 109–120, https://doi.org/10.1007/s40003-015-0170-x (2015).
Ameye, M. et al. Priming of Wheat with the Green Leaf Volatile Z-3-Hexenyl Acetate Enhances Defense against Fusarium graminearum But Boosts Deoxynivalenol Production. Plant Physiol 167, 1671–1684, https://doi.org/10.1104/pp.15.00107 (2015).
Karban, R., Agrawal, A. A., Thaler, J. S. & Adler, L. S. Induced plant responses and information content about risk of herbivory. Trends Ecol Evol 14, 443–447, https://doi.org/10.1016/S0169-5347(99)01678-X (1999).
Berglund, T. Nicotinamide, a Missing Link in the Early Stress-Response in Eukaryotic Cells - a Hypothesis with Special Reference to Oxidative Stress in Plants. Febs Lett 351, 145–149, https://doi.org/10.1016/0014-5793(94)00850-7 (1994).
Boubakri, H. et al. Vitamins for enhancing plant resistance. Planta 244, 529–543, https://doi.org/10.1007/s00425-016-2552-0 (2016).
Pushpalatha, H. G. et al. Ability of vitamins to induce downy mildew disease resistance and growth promotion in pearl millet. Crop Prot 26, 1674–1681, https://doi.org/10.1016/j.cropro.2007.02.012 (2007).
Pushpalatha, H. G., Sudisha, J., Geetha, N. P., Amruthesh, K. N. & Shetty, H. S. Thiamine seed treatment enhances LOX expression, promotes growth and induces downy mildew disease resistance in pearl millet. Biol Plantarum 55, 522–527, https://doi.org/10.1007/s10535-011-0118-3 (2011).
Goyer, A. Thiamine in plants: Aspects of its metabolism and functions. Phytochemistry 71, 1615–1624, https://doi.org/10.1016/j.phytochem.2010.06.022 (2010).
Tunc-Ozdemir, M. et al. Thiamin Confers Enhanced Tolerance to Oxidative Stress in Arabidopsis. Plant Physiol 151, 421–432, https://doi.org/10.1104/pp.109.140046 (2009).
Ahn, I. P., Kim, S., Lee, Y. H. & Suh, S. C. Vitamin B-1-induced priming is dependent on hydrogen peroxide and the NPR1 gene in Arabidopsis. Plant Physiol 143, 838–848, https://doi.org/10.1104/pp.106.092627 (2007).
Hamada, A. M. & Jonsson, L. M. V. Thiamine treatments alleviate aphid infestations in barley and pea. Phytochemistry 94, 135–141, https://doi.org/10.1016/j.phytochem.2013.05.012 (2013).
Azami-Sardooei, Z., Franca, S. C., De Vleesschauwer, D. & Hofte, M. Riboflavin induces resistance against Botrytis cinerea in bean, but not in tomato, by priming for a hydrogen peroxide-fueled resistance response. Physiol Mol Plant P 75, 23–29, https://doi.org/10.1016/j.pmpp.2010.08.001 (2010).
Briggs, A. G. et al. A transcriptomics approach uncovers novel roles for poly(ADP-ribosyl) ation in the basal defense response in Arabidopsis thaliana. Plos One 12, https://doi.org/10.1371/journal.pone.0190268 (2017).
Vriet, C., Hennig, L. & Laloi, C. Stress-induced chromatin changes in plants: of memories, metabolites and crop improvement. Cell Mol Life Sci 72, 1261–1273, https://doi.org/10.1007/s00018-014-1792-z (2015).
Sasamoto, H. & Ashihara, H. Effect of nicotinic acid, nicotinamide and trigonelline on the proliferation of lettuce cells derived from protoplasts. Phytochem Lett 7, 38–41 (2014).
Ohlsson, A. B., Landberg, T., Berglund, T. & Greger, M. Increased metal tolerance in Salix by nicotinamide and nicotinic acid. Plant Physiol Bioch 46, 655–664, https://doi.org/10.1016/j.plaphy.2008.04.004 (2008).
Thevenet, D. et al. The priming molecule beta-aminobutyric acid is naturally present in plants and is induced by stress. New Phytol 213, 552–559, https://doi.org/10.1111/nph.14298 (2017).
Wilkinson, S. W., Pastor, V., Paplauskas, S., Petriacq, P. & Luna, E. Long-lasting -aminobutyric acid-induced resistance protects tomato fruit against Botrytis cinerea. Plant Pathol 67, 30–41, https://doi.org/10.1111/ppa.12725 (2018).
Ferrari, S. et al. Oligogalacturonides: plant damage-associated molecular patterns and regulators of growth and development. Front Plant Sci 4, https://doi.org/10.3389/fpls.2013.00049 (2013).
Galletti, R., Ferrari, S. & De Lorenzo, G. Arabidopsis MPK3 and MPK6 Play Different Roles in Basal and Oligogalacturonide- or Flagellin-Induced Resistance against Botrytis cinerea. Plant Physiol 157, 804–814 (2011).
Vorwerk, S., Somerville, S. & Somerville, C. The role of plant cell wall polysaccharide composition in disease resistance. Trends Plant Sci 9, 203–209, https://doi.org/10.1016/j.tplants.2004.02.005 (2004).
Sampedro, L., Moreira, X. & Zas, R. Resistance and response of Pinus pinaster seedlings to Hylobius abietis after induction with methyl jasmonate. Plant Ecol 212, 397–401, https://doi.org/10.1007/s11258-010-9830-x (2011).
Li, C., Wang, P., Menzies, N. W., Lombi, E. & Kopittke, P. M. Effects of methyl jasmonate on plant growth and leaf properties. J Plant Nutr Soil Sc 181, 409–418, https://doi.org/10.1002/jpln.201700373 (2018).
Ameye, M. et al. Green leaf volatile production by plants: a meta-analysis. New Phytol, https://doi.org/10.1111/nph.14671 (2017).
Whiteley, M., Diggle, S. P. & Greenberg, E. P. Progress in and promise of bacterial quorum sensing research. Nature 551, 313–320 (2017).
Tugizimana, F., Mhlongo, M. I., Piater, L. A. & Dubery, I. A. Metabolomics in Plant Priming Research: The Way Forward? Int J Mol Sci 19 (2018).
Peters, J. L. et al. Assessing publication bias in meta-analyses in the presence of between-study heterogeneity. J R Stat Soc a Stat 173, 575–591, https://doi.org/10.1111/j.1467-985X.2009.00629.x (2010).
Pedrini, S., Merritt, D. J., Stevens, J. & Dixon, K. Seed Coating: Science or Marketing Spin? Trends Plant Sci 22, 106–116, https://doi.org/10.1016/j.tplants.2016.11.002 (2017).
Paparella, S. et al. Seed priming: state of the art and new perspectives. Plant Cell Rep 34, 1281–1293, https://doi.org/10.1007/s00299-015-1784-y (2015).
van Hulten, M., Pelser, M., van Loon, L. C., Pieterse, C. M. J. & Ton, J. Costs and benefits of priming for defense in Arabidopsis. P Natl Acad Sci USA 103, 5602–5607, https://doi.org/10.1073/pnas.0510213103 (2006).
Schmidt, L., Schurr, U. & Rose, U. S. R. Local and systemic effects of two herbivores with different feeding mechanisms on primary metabolism of cotton leaves. Plant Cell Environ 32, 893–903, https://doi.org/10.1111/j.1365-3040.2009.01969.x (2009).
Chen, K. & Arora, R. Priming memory invokes seed stress-tolerance. Environ Exp Bot 94, 33–45, https://doi.org/10.1016/j.envexpbot.2012.03.005 (2013).
Sharma, K. K., Singh, U. S., Sharma, P., Kumar, A. & Sharma, L. Seed treatments for sustainable agriculture-A review. Journal of Applied and Natural Science 7, 521–539 (2015).
Ugena, L. et al. Characterization of Biostimulant Mode of Action Using Novel Multi-Trait High-Throughput Screening of Arabidopsis Germination and Rosette Growth. Front Plant Sci 9 (2018).
Sharma, H. S. S., Fleming, C., Selby, C., Rao, J. R. & Martin, T. Plant biostimulants: a review on the processing of macroalgae and use of extracts for crop management to reduce abiotic and biotic stresses. J Appl Phycol 26, 465–490, https://doi.org/10.1007/s10811-013-0101-9 (2014).
Del Re, A. C. A Practical Tutorial on Conducting Meta-Analysis in R. Quant Meth Psychol 11, 37–50, https://doi.org/10.20982/tqmp.11.1.p037 (2015).
Rowen, E. & Kaplan, I. Eco-evolutionary factors drive induced plant volatiles: a meta-analysis. New Phytol 210, 284–294, https://doi.org/10.1111/nph.13804 (2016).
Viechtbauer, W. Conducting Meta-Analyses in R with the metafor Package. J Stat Softw 36, 1–48 (2010).
The present paper was the result of the masters’ thesis by Sara M. Westman. We thank two anonymous reviewers for valuable comments. The authors associated with the Umeå Plant Science Centre were supported by the UPSC Centre for Forest Biotechnology and BRA was supported by the TC4F (Trees and Crops for the Future) both with financial support by the Swedish Governmental Agency for Innovation Systems – VINNOVA. Open access funding provided by Umea University.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Westman, S.M., Kloth, K.J., Hanson, J. et al. Defence priming in Arabidopsis – a Meta-Analysis. Sci Rep 9, 13309 (2019). https://doi.org/10.1038/s41598-019-49811-9
Nature Ecology & Evolution (2020)