Plants have co-evolved with a diverse array of pathogens and insect herbivores and so have evolved an extensive repertoire of constitutive and induced defence mechanisms activated through complex signalling pathways. OXI1 kinase is required for activation of mitogen-activated protein kinases (MAPKs) and is an essential part of the signal transduction pathway linking oxidative burst signals to diverse downstream responses. Furthermore, changes in the levels of OXI1 appear to be crucial for appropriate signalling. Callose deposition also plays a key role in defence. Here we demonstrate, for the first time, that OXI1 plays an important role in defence against aphids. The Arabidopsis mutant, oxi1-2, showed significant resistance both in terms of population build-up (p < 0.001) and the rate of build-up (p < 0.001). Arabidopsis mutants for β-1,3-glucanase, gns2 and gns3, showed partial aphid resistance, significantly delaying developmental rate, taking two-fold longer to reach adulthood. Whilst β-1,3-glucanase genes GNS1, GNS2, GNS3 and GNS5 were not induced in oxi1-2 in response to aphid feeding, GNS2 was expressed to high levels in the corresponding WT (Col-0) in response to aphid feeding. Callose synthase GSL5 was up-regulated in oxi1-2 in response to aphids. The results suggest that resistance in oxi1-2 mutants is through induction of callose deposition via MAPKs resulting in ROS induction as an early response. Furthermore, the results suggest that the β-1,3-glucanase genes, especially GNS2, play an important role in host plant susceptibility to aphids. Better understanding of signalling cascades underpinning tolerance to biotic stress will help inform future breeding programmes for enhancing crop resilience.
Aphids are economically important pests globally causing extensive crop damage both as a result of nutrient abstraction, but, more importantly as disease vectors. The plant–aphid interaction is complex and highly dynamic, subject to continual change (Mello and Silva-Filho 2002). Recently, studies have shown that aphids secrete effectors that modulate plant defence responses (Bos et al. 2010; Atamian et al. 2013; Pitino and Hogenhout 2013) pointing to parallels between plant-pathogen and plant–insect interactions (Jaouannet et al. 2014). It has been suggested that two different processes are involved in the elicitation of plant defence. One involves a gene-for-gene recognition of aphid-derived elicitors by plant resistance genes, followed by the activation of aphid resistance and defence responses. The other involves recognition of aphid-damaged tissue leading to changes in plant chemistry, followed by the production of signalling molecules that trigger a general stress response, similar to the basal plant defence to pathogens (Smith and Boyko 2007). The activation of signalling pathways in response to phloem-feeding aphids alters gene expression, which in turn leads to changes in the molecular composition within the cell. Transcriptional and proteomic analyses have indicated that encoded proteins of these differentially regulated genes function in direct defence, defence signalling, oxidative burst, secondary metabolism, cell maintenance and photosynthesis (Zhu-Salzman et al. 2004; Ferry et al. 2011; Guan et al. 2015). There is also evidence of crosstalk between different plant signalling pathways resulting in plants subjected to abiotic stress being more resistant to biotic stress. For instance, the phytohormone abscisic acid (ABA), an important regulator of plant responses to osmotic stress imposed by drought and salt, interacts in a complex, but well understood way with SA, JA and ET (Pineda et al. 2013). Cytokinins (CKs) play important roles in plant biotic interactions and in the regulation of complex source–sink relationships structuring plant-based food webs (Giron et al. 2013).
Active oxygen species (AOS) can function as signalling molecules leading to specific downstream events, playing key roles in plants in response to stress e.g. pathogen attack (Levine et al. 1994) and wounding (Orozco-Cárdenas et al. 2001). Oxidative signal inducible 1 (OXI1) is a serine/threonine kinase related to the protein kinase family (AGC) (Alessi 2001; Bogre et al. 2003) required for the partial activation of mitogen-activating protein kinases 3 and 6 (MPK3 and MPK6) (Rentel et al. 2004) and has been shown to be an essential component of the signal transduction pathway linking oxidative burst signals to diverse downstream processes. This is supported by the findings that Arabidopsis null oxi1 mutants were more susceptible than WT plants to the bacterial pathogen Pseudomonas syringae so confirming its role in plant immunity. The level of OXI1 expression appears to be critical in mounting an appropriate defence response since these authors also showed that OXI1 overexpressing lines also display increased susceptibility to biotrophic pathogens; the induction of OXI1 following P. syringae infection was found to be correlated with the oxidative burst and that ROS produced through NADPH oxidases drives OXI1 expression during the plant–pathogen interaction (Petersen et al. 2009). The endophytic fungus Piriformospora indica is known to promote plant growth and enhance resistance to certain plant pathogens and there is now evidence that this is mediated via the OXI1 kinase pathway and that H2O2 formation is reduced (Camehl et al. 2011).
Not only is OXI1 responsive to pathogen attack but also to other external stimuli such as H2O2 (Rentel et al. 2004). Interestingly, Pei et al. (2000) showed that ABA-induced H2O2 production and the H2O2-activated Ca2+ channels are important mechanisms for ABA-induced stomatal closing thus enabling the plants to respond to drought. Thus stomatal opening and closure is controlled by the concentration of cytosolic Ca2+. Cytosolic Ca2+ also stimulates the synthesis and deposition of callose (β-1,3-glucan), an important component of the plant defence system both in response to biotic and abiotic stress (Verma and Hong 2001), including both pathogen infection and insect attack (Aidemark et al. 2009) where its deposition at the sieve plates (McNairn and Currier 1967) regulates intercellular transport of molecules by controlling the size exclusion limit of plasmodesmata as a response to developmental signals or environmental signals, e.g. wounding and pathogen attack (Kauss 1996; Köhle et al. 1985). Not only does callose deposition strengthen the cell wall at the site of attack (Aist 1976; Bell 1981), but in resistant carnation cultivars it has been found in plasmodesmata in non-infected cells bordering the infected site so preventing the spread of fungal infection in resistant cultivars (Trillas et al. 2000). Callose deposition can also be synthesized in response to ABA, and other physiological stresses (Stone and Clarke 1992). Recent studies have reported that callose synthase 7 (CSL7 or GSL7) is responsible for callose deposition in the sieve plates and that Arabidopsis gsl7 mutants were unable to produce callose in the sieve pores in response to stresses (Xie and Hong 2011; Barratt et al. 2011; Xie et al. 2011).
β-1,3-Glucanases are a class of hydrolytic enzymes that hydrolyse the 1,3-β-d-glucosidic linkages in β-1,3-glucans (callose) and are recognised as one of the commonly known pathogenesis-related (PR) proteins, belonging to the PR2 group; they are rapidly induced by pathogenic infections but also by salicylic acid (SA), Jasmonic acid (JA) and ethylene (ET). Not only are β-1,3-glucanases induced by pathogen infection, but they exhibit antifungal activity, hydrolysing the fungal β-1,3-glucans, a major cell wall structural component of both fungi and plants (Leubner-Metzger and Meins 1999; Van Loon et al. 2006). In Arabidopsis the expression of PR1 and β-1,3-glucanase 2 (GNS2) genes increases in response to aphid (Myzus persicae) feeding; furthermore, following exposure to the signalling molecule salicylic acid (SA), transcription of PR1 and GNS2 was increased 10- and 23-fold respectively (Moran and Thompson 2001).
The present study demonstrates the involvement of OXI1, GNS1, GNS2 and GNS3 in the interaction between a model plant-aphid system at both the phenotypic and molecular levels. Aphid survival is reported using a number of Arabidopsis mutants (oxi1-2, oxi1-1, gns1, gns2, and gns3) in comparison to their wild type backgrounds and correlated with transcript levels for selected callose synthase and β-1,3-glucanase genes in these mutant lines. The results suggest that resistance in oxi1 mutants is through induction of callose deposition via MAPKs resulting in ROS induction as an early response. Furthermore, that β-1, 3-glucanase genes, especially GNS2, play an important role in host plant susceptibility to aphids.
Materials and methods
Plant materials and growth conditions
Arabidopsis thaliana mutants Two different ecotypes were used, Columbia (Col-0) and Wassilewskija (Ws). Two mutant lines for the OXI1 gene were investigated; oxi1-1, background Ws, is a null mutant with an insertion in the beginning of the coding region, from the Salk collection, whilst oxi1-2 (in Col-0), from the Wisconsin collection, has an insertion in the promoter and exhibits severely reduced function (about 5% transcript level compared to WT) (Rentel et al. 2004; Petersen et al. 2009). Arabidopsis β-1,3-glucanase mutants (gns1, gns2 and gns3 (Salk) in Col-0; stock numbers N633409; N587824; N609800; N60000, respectively) were obtained from the Arabidopsis Biological Resource Centre (Nottingham Arabidopsis Stock Centre). Plants were grown in John Innes compost number 2 in controlled environment chambers under a 16:8 h light/dark cycles at 23 °C, 55% relative humidity.
Prior to the start of the bioassays, aphids (peach-potato aphid Myzus persicae) were reared either on Arabidopsis Col-0 or Ws. All bioassays were carried out on plants that were between 25 to 30 days old (i.e. rosette stage 5–10 leaves) maintained under growing conditions described above. Aphid performance was investigated by measuring the intrinsic rate (Rm) of population build-up on the following Arabidopsis mutants together with their respective WTs as controls: oxi1-1, oxi1-2, gns1, gns2, gns3. Two adult females were placed on each plant (at 5–10 leaf stage; all plants were isolated from each other) and allowed to produce nymphs. On the onset of nymph production, with the exception of two nymphs, all aphids including the original adults were removed and population build-up from the two remaining nymphs was monitored every 2 days for the duration of the study; zero time point (day 1) started when the two nymphs became adults. All bioassays were conducted concurrently and 15 plants were used for each line; n = 15).
Gene expression studies in Arabidopsis mutants in response to aphid feeding over time
For gene expression studies all Arabidopsis plants, using the same lines as described for the aphid bioassays above, were between 25 to 30 days old (i.e. rosette stage 5–10 leaves). Each plant was infested with 10 aphids for a range of different times (3, 6, 12, 24 and 48 h) after which the aphids were removed and leaves immediately harvested and flash frozen; three time points (0, 3 and 48 h) for non-infested plants were used as controls. Relative expression was measured for: (1) callose synthases genes GSL1, GSL5 both in oxi1-1, oxi1-2 and their respective WT, Ws and Col-0; and (2) β-1,3-glucanase gene GNS2 in oxi1-1, oxi1-2 and their respective WT, Ws and Col-0; three Arabidopsis plants were used per line giving three individual biological replicates/line/gene.
Reverse transcription quantitative PCR (RT-qPCR)
Total RNA was isolated from ca. 200 mg of frozen leaf tissue using Trizol Reagent (Invitrogen), according to the manufacturer’s protocols. The concentration and purity of the RNA samples was determined using a Nanodrop (ND-1000 Spectrophotometer; Nanodrop Technologies). All samples had an absorbance ratio (absorbance at A260/A280 nm) of between 1.9 and 2.2. Following quantification, all RNA samples were normalized to 100 ng μl−1. To ensure maximum specificity and efficiency during qPCR amplification under a standard set of reaction conditions, Allele ID 7.7 software was used to design RT-qPCR primers (Table 1). One-step brilliant ll sybr green master mix was used for RT-qPCR. Gradient PCR was used to identify the annealing temperature. A 25-μl reaction volume PCR was employed using 1 μl RNA at 100 ng μl−1, 12.5 μl of one step Master Mix (Agilent), 2 pmol each gene-specific primer, and UltraPure DNase/RNase-free distilled water (Qiagen) to 25 μl. Amplification of RNA employed the following conditions: 30 min incubation at (50–60 °C) to allow the reverse transcription, initial 10 min of denaturation at 94 °C; followed by 39 cycles of denaturation 94 °C for 30 s, annealing at (50–60 °C) for 30 s, and extension at 72 °C for 45 s; followed by a final extension for 5 min at 72 °C. For normalisation the elongation factor (EF) gene was used as an endogenous control as it gave consistent expression levels. Three independent biological repeats and three independent technical repeats were performed for each gene/time point and threshold cycle reactions determined using Opticon Monitor software. Relative expression was calculated according to Pfaffl (2001).
Repeated measures ANOVA were conducted for aphid bioassays. Two-way ANOVA with replication was used to test the p value of qRT-PCR results followed by Tukey test. *p < 0.05, **p < 0.01 and ***p < 0.001.
Arabidopsis mutants show enhanced resistance to aphids
Aphid population build-up was measured on two Arabidopsis mutant lines and compared to wild type control plants (Col-0). On control plants nymph production was seen to increase over the course of the bioassay reaching a population maximum of 120 at day 17, thereafter nymph production declined. In contrast, on oxi1-2, nymph production was significantly lower although the duration was longer (p < 0.001). Moreover there was a shift in the reproductive peak, this being delayed by 4 days on the mutant line (Fig. 1). In comparison, the number of adults on Col-0 peaked at day 19 with 114 adult aphids, with no survivors after 37 days. However, on oxi1-2, the number of adult aphids was significantly lower after 19 days with 80 adults (p < 0.001). Interestingly, as with nymph production there was a shift in the developmental peak to adulthood by 4 days. (Fig. 1). The population dynamics of the adults thus followed those exhibited by the nymphs demonstrating that the oxi1-2 mutant exhibited enhanced resistance to aphid infestation.
Aphid performance on the wild type was also compared to that on the gns mutant lines. Whilst there were no significant differences in terms of the number of nymphs produced on gns1, there was a shift in the reproduction peak by 4 days, as seen with oxi1-2, with no aphids in the nymphal stages after 47 days (Fig. 2a). Again, as seen on oxi1-2, the mean number of adults was significantly lower on gns1 after 19 days with 84 adult aphids (p < 0.001). However, in contrast to either the WT or oxi1-2 the maximum population density (116 adults) was not reached for a further 10 days, thus demonstrating a very large shift in the developmental peak; thereafter the number of adults rapidly decreased (Fig. 2a). For gns2 (Fig. 2b) and gns3 (Fig. 2c) the delay in the reproductive peaks were even greater, with an approximate doubling of the time taken, compared to their WT controls. However, the numbers of nymphs produced were greater, particularly for gns3.
Relative expression of callose synthase genes GSL1 and GSL5 in oxi1-2 and the WT (Col-0) in response to aphid feeding
Expression levels for GSL1 in non-infested WT and oxi1-2 plants remained low over the duration of the assay (48 h), with relative expression levels being 1.2-fold and 2.5-fold, respectively, at both 3 h and 48 h compared, to 0 h. However, expression was significantly enhanced in both lines in response to aphid feeding and at 3 h post feeding was significantly greater in oxi1-2 compared to WT, being 14.6-fold and 8.4-fold greater than in the absence of aphid feeding (Fig. 3a). Irrespective of the line, maximal expression occurred 6 h post feeding, but at this stage was significantly (p < 0.01) greater in the control compared to the mutant line, with relative expression being 27.2-fold and 14.3-fold, respectively. After 24 h, relative expression levels declined rapidly.
Expression levels for GSL5 were far more consistent than for GSL1, and although expression for this gene were increased in both the WT and mutant line in response to aphid feeding, expression was always significantly greater in oxi1-2 compared to WT, with maximal expression 12 h post infestation where relative expression levels were 6.6-fold and 1.8-fold respectively (Fig. 3b). As for GSL1, expression levels of GSL5 in non-infested WT and oxi1-2 mutant plants remained low over the duration of the assay (48 h).
Relative expression of callose synthase genes GSL1 and GSL5 in oxi1-1 and the WT (Ws) in response to aphid feeding
Background levels for both GSL1 and GSL5 expression in oxi1-1and its WT in the absence of aphid feeding remained low and moderately constant throughout the 48 h time period of the trial (Figs. 3b, 4a). As with expression of GSL1 in the oxi1-2 mutant, expression of this gene in oxi1-1, representing a different genetic background, resulted in increased expression in response to aphid feeding, with maximal expression occurring 12 h post feeding, and relative expression levels being 11.2-fold higher; however, in contrast to oxi1-2, expression levels for this particular gene remained high, even after 48 h (7.1-fold higher). Surprisingly, the relative expression of GSL1 in the WT Ws behaved differently to WT Col-0 in that aphid feeding overall caused down regulation of this gene (Fig. 4a). In both the Ws and the null mutant oxi1-1, aphid feeding caused highly significant (p < 0.001) down regulation of expression of GSL5 over the 48 h time period, and was greatest in oxi1-1 48 h post infestation (Fig. 4b).
Relative expression of β-1,3-glucanase genes GNS1, GNS2, GNS3, and GNS5 in oxi1-2 and its WT (Col-0) in response to aphid feeding
β-1,3-Glucanase genes (GNS1, GNS2, GNS3 and GNS5) did not appear to be expressed in oxi1-2, irrespective of whether the plants had been infested with aphids or not (Fig. 5a). Furthermore, in the WT (Col-0), GNS1, GNS3 and GNS5 were expressed at such low levels making it difficult to quantify gene expression accurately and reliably. However, expression of GNS2 was readily detected in Col-0, and whilst the expression levels remained low and constant throughout the 48 h time course in non-infested plants, relative expression significantly increased at 6 h post feeding, with maximal expression at 12 h (26.4-fold; p < 0.001), before rapidly falling back to basal levels (Fig. 5a).
Relative expression of β-1,3-glucanase genes GNS1, GNS2, GNS3 and GNS5 in oxi1-1 and its WT (Ws) in response to aphid feeding
As with oxi1-2 and its WT (Col-0), expression of genes encoding GNS1, GNS3 and GNS5 genes were not detected in oxi1-1 in response to aphid feeding, neither were they detected in the WT. In contrast, GNS2 was detected at low levels in both oxi1-1 and the WT (Ws), remaining low throughout the 48 h time course in the absence of aphid feeding. Whilst GNS2 expression remained low in the WT plants in response to aphid feeding, expression was significantly enhanced in the null mutant, with maximal expression (14.2-fold) occurring 6 h post feeding, thereafter showing a decline with relative expression levels of 2.9-fold at 48 h (Fig. 5b). Interestingly, at this same time point, expression was down-regulated in the corresponding WT, in response to aphid feeding (Fig. 5b). These results suggest that for β-1,3-glucanase GNS2, the genetic background may have an effect on subsequent gene expression in that it is not expressed in oxi1-2 in response to aphid feeding but is in oxi1-1.
The potential roles of oxidative signal inducible 1 (OXI1) kinases, β-1,3-glucanase (GNS) and callose synthase (GSL), and their interaction in enhancing resistance to aphids, was investigated in the present study using a range of Arabidopsis mutants. Bioassay results showed that oxi1-2 significantly (p < 0.001) reduced the numbers of aphids produced, delaying both the developmental period and reproductive peak, thus reducing population build-up compared to the corresponding wild type (Col-0; Fig. 1a). Similar effects were also observed for the three different mutants of β-1,3-glucanase (Fig. 2) in that there was a delay in the rate of development, particularly for gns2 and gns3, accompanied by a significant shift in the reproductive peak but, in contrast to oxi1-2, aphid numbers were either the same as for their respective wild types (Col-0; gns1), or significantly (p < 0.001) greater (gns2, gns3). Notably, despite the gns mutants being able to support similar, or greater aphid densities compared to their wild types, the plants were able to tolerate this, remaining healthier and surviving much longer than the control plants (Fig. 2b, c), presumably as a result of these genes not being expressed in the mutant in response to aphid feeding.
Callose synthase is a key enzyme involved in the synthesis of β-1,3-glucan (callose), whilst β-1,3-glucanase is involved in the breakdown of this compound. Their roles in plant defence are not surprising and have been well documented, particularly in pathogen defence. For example, GSL5, which is required for wound and papillary callose formation (Jacobs et al. 2003) at sites of pathogen attack, has been shown to increase resistance of Arabidopsis to powdery mildew (Jacobs et al. 2003; Nishimura et al. 2003; Kim et al. 2005). Studies using pathogen elicitors have resulted in similar effects. Treatment of Arabidopsis leaves with chitosan, an elicitor allied with fungal pathogens, showed callose deposition in gsl5 disruption mutants (El Hadrami et al. 2010), whilst application of flagellin (flg22), derived from a bacterial pathogen, resulted in GSL5 callose deposition (Gomez-Gomez et al. 1999; Luna et al. 2011). More recent studies using GSL5-overexpressing Arabidopsis lines demonstrated that callose synthase activity was four-fold higher than in wild-type plants 6 h post inoculation with the virulent powdery mildew Golovinomyces cichoracearum. This increase in activity was correlated with enlarged callose deposits at the sites of attempted fungal penetration (Ellinger et al. 2013). Furthermore, haustoria formation was prevented in these resistant transgenic lines during infection, and neither the salicylic acid-dependent nor jasmonate-dependent pathways were induced. Subsequently this group also reported the exposition of a callose layer on the surface of the pre-existing cellulosic cell wall facing the invading pathogen and suggested that the importance of this previously unknown polymeric defence network was to prevent cell wall hydrolysis and penetration by the fungus (Eggert et al. 2014). Will and Van Bel (2006) have also reported the involvement of callose synthase in response to pathogen attack and wounding. In the present study the oxi1-2 mutant was shown to be significantly more resistant to aphid infestation compared to wild type plants. Interestingly, expression of GSL5 in these plants was significantly up-regulated in response to aphid feeding, with maximal expression 24 h post infestation (Fig. 3b). This would suggest that callose synthase is playing a major role in the observed resistance and is in agreement with pathogen studies where this same gene, GSL5, has been over-expressed. These findings are also in agreement with Lu et al. (2011) who reported the role of glucan synthase in callose deposition and aphid resistance, again implicating the role of GSL5 in host-plant resistance. Whilst a direct link between expression of GSL5 and callose deposition was not investigated in the present study, numerous other studies have demonstrated a direct correlation between the expression of this gene and callose accumulation.
OXI1 is a serine/threonine kinase induced in response to a wide range of Reactive Oxygen Species (ROS), especially hydrogen peroxide (Rentel et al. 2004), and is required for full activation of MAPKs genes, especially MAPK3 and MAPK6. These genes are involved in plant defence against bacterial and fungal pathogens. Full activation of MAPK cascades trigger the calcium pathway (Asai et al. 2002), which in turn stimulates callose synthase activity followed by callose production, leading to enhanced resistance to biotic stress. OXI1 plays an essential role in the signal transduction pathway connecting oxidative burst signals to different downstream responses (Petersen et al. 2009); it thus facilitates signal transduction of ROS (Kwak et al. 2003). The oxi1 mutant has unique features including continuous induction of MAPK kinase genes, early response ROS accumulation and signal transduction, and increased callose synthase and catalase activity (Petersen et al. 2009). These features not only enable oxi1-2 to tolerate moderately high aphid populations, but, importantly confer greater resistance than the wild types by decreasing aphid numbers, and delaying the rate of development so shifting the reproductive peak, as seen in the present study. In contrast the wild type (Col-0), which was susceptible to aphid infestation supporting a rapid population increase in the short term, was unable to survive such high levels of aphid infestation and died. These wild type plants showed significant upregulation of β-1,3-glucanase gene GNS2 in response to aphid feeding (Fig. 5a), but low expression of GSL5 (Fig. 3b) post aphid feeding, again consistent with their proposed roles in plant defence. However, the oxi1-1 null mutant (Ws) showed significant up-regulation of β-1,3-glucanase GNS2 and down-regulation of callose synthase GSL5 which may result in plant susceptibility in response to aphid feeding. Previous studies have shown that this oxi1-1 (Ws) null mutant exhibits enhanced susceptibility when challenged with virulent Hyaloperonospora parasitica (Rentel et al. 2004). These findings are consistent with the hypothesis that callose synthase is involved in enhancing plant defence through production of callose deposits whilst β-1,3-glucanases, responsible for callose degradation, are involved in susceptibility since they enable sap-sucking insect such as aphids, to abstract nutrients from the phloem cells. Furthermore, Hao et al. (2008) demonstrated that the brown planthopper Nilaparvata lugens is able to unplug callose deposition in the sieve pores by activating β-1,3-glucanases in rice plants.Whether aphids also stimulate filament formation of sieve element occlusion (SEO) proteins (Batailler et al. 2012) or cause callose degradation, is currently unknown.
In Arabidopsis, PR1 and β-1,3-glucanase GNS2, both associated with the salicylic acid dependent response to pathogens, have been shown to be induced in response to aphid (M. persicae) feeding with increased transcript levels of 10 and 23 fold, respectively (Moran and Thompson 2001). Arabidopsis plants challenged with both virulent and avirulent strains of the pathogen Pseudomonas syringae pv. tomato DC3000 induced the expression of OXI1; furthermore, PR1 has been induced in response to a diverse range of P. syringae isolates and linked to the observed resistance to this bacterial pathogen (Dempsey et al. 1999). Interestingly, Arabidopsis ascorbate-deficient mutants showed microlesions, constitutive PR gene expression in response to P. syringae infection, and although these mutants were deficient in induction of H2O2 sensitive genes, they exhibited increased pathogen resistance (Pavet et al. 2005). Results from the present study suggest that β-1,3-glucanases are involved in host plant susceptibility to aphids since the Arabidopsis mutants (gns1, gns2 and gns3) all showed enhanced tolerance in terms of delaying aphid development but also being able to withstand greater aphid densities, surviving much longer than the control plants. These findings are in keeping with Anderson et al. (2014) who suggest a role for (1,3;1,4)-β-glucanase in susceptibility of wheat to Russian wheat aphid. This hypothesis could be tested using RNAi.
The role of OXI1 in plant defence is clearly very complex. For example, Petersen et al. (2009) have shown that both reduced expression and overexpression led to enhanced susceptibility to biotrophic pathogens using the same mutants as in the present study. Since it is unlikely that a single kinase plays both a negative and positive role during the same defence, these authors proposed that it was the actual level of OXI1 protein that was crucial for the appropriate signalling, and that modulation of these levels (either higher or lower) disrupts OXI1 function.
The present study demonstrates that resistance in oxi1 mutants is through MAPK induction of callose deposition resulting in ROS induction as an early response. In addition, it demonstrates the involvement of OXI1, GNS1, GNS2 and GNS3 in the interaction between a model plant-aphid system at both the phenotypic and molecular levels. Furthermore, it demonstrates that β-1,3-glucanase genes, especially GNS2, play an important role in host plant susceptibility to aphids. The data presented have important implications for future crop breeding programmes in terms of increasing host plant resistance, particularly with respect to enhanced resistance to sap-sucking insect pests.
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Shoala, T., Edwards, M.G., Knight, M.R. et al. OXI1 kinase plays a key role in resistance of Arabidopsis towards aphids (Myzus persicae). Transgenic Res 27, 355–366 (2018). https://doi.org/10.1007/s11248-018-0078-x
- Aphid resistance/susceptibility
- Oxidative burst
- Oxidative signal inducible 1 (OXI1) kinases
- Callose synthase (GSL)
- β-1,3-Glucanase (GNS)
- Arabidopsis mutants
- Differential gene expression