Infection stages of charcoal rot fungus Macrophomina phaseolina in sesame revealed for the first time a transition from biotrophy via BNS (biotrophy-to-necrotrophy switch) to necrotrophy as confirmed by transcriptional studies. Microscopy using normal and GFP-expressing pathogen showed typical constricted thick intercellular bitrophic hyphae which gave rise to thin intracellular necrotrophic hyphae during BNS and this stage was delayed in a resistant host. Results also show that as the pathogen switched its strategy of infection, the host tailored its defense strategy to meet the changing situation. Less ROS accumulation, upregulation of ROS signaling genes and higher antioxidant enzyme activities post BNS resulted in resistance. There was greater accumulation of secondary metabolites and upregulation of secondary metabolite-related genes after BNS. A total of twenty genes functioning in different aspects of plant defense that were monitored over a time course during the changing infection phases showed a coordinated response. Experiments using phytohormone priming and phytohormone inhibitors showed that resistance resulted from activation of JA-ET signaling pathway. Most importantly this defense response was more prompt in the resistant than the susceptible host indicating that a resistant host makes different choices from a susceptible host during infection which ultimately influences the severity of the disease.
Fungal plant pathogens can be classified as biotrophs, necrotrophs or hemibiotrophs based on their life-style and interaction with the host. Hemibiotrophic fungi represent the most interesting group of pathogens since they use sequential biotrophic and necrotrophic infection strategies to invade and colonize host plants1. Transition from the asymptomatic biotrophic phase, characterized by intercellular thick primary hyphae, to the destructive necrotrophic phase, characterized by thin filamentous secondary hyphae, is referred to as the biotrophy-necrotrophy switch (BNS). BNS is characteristic of typical hemibiotrophic fungi like Colletotrichum sp 2, Phytopthora capsici 3 and Moniliophthora roreri 3,4,5,6,7,8,9,10.
The BNS and modulation of plant defense in response to BNS is not well understood4. One important strategy for studying these dynamic but highly regulated host defenses is to observe gene expression patterns in the host5. There are only a handful of studies in hemibiotrophic fungi-host interaction5 most of these being the overall transcriptome analysis of the pathogen and/or the host2,3,4,6,7,8 without going into details of individual gene expression before, during and after BNS in the pathogen. The few existing studies at the transcriptional level do show that the host can tailor the defense response according to the changing phases of the pathogen9,10,11. There are only two preliminary studies that involve susceptible and resistant host during interaction with hemibiotrophic pathogens12,13.
Phytohormone signaling involving JA, ET or SA is an integral component of multilayered host-defense system against plethora of fungal pathogens. The lifestyle of a pathogen often dictates the host’s defense strategy and the pathogen may even manipulate hormonal cross-talk for successful colonization14. On the counter side plants adopt timely activation of suitable phytohormone signaling depending on the pathogen’s lifestyle so as to restrict the infection process12.
Sesame (Sesamum indicum L.), one of the most important oilseed crop is cultivated throughout the world in tropical and subtropical regions. Yet there is an absolute lack of any transcriptional study regarding molecular defense response of sesame against any biotic/abiotic stress. One of the major threats of global sesame production is the charcoal rot disease caused by Macrophomina phaseolina (Tassi) Goid15,16. With the recent availability genome sequence of sesame17, it has opened up an enormous scope for studying defense related gene regulation in response to stresses. Moreover, M. phaseolina has thus far been classified as a necrotrophic pathogen. In spite of our earlier report on M. phaseolina infection in sesame15, whether a brief biotrophic phase exists for the pathogen during initial infection stage was never investigated.
In the present study, during the early infection stages of M. phaseolina in sesame, we detected a lifestyle transition from biotrophy to necrotrophy which has been supported by microscopic and transcriptional data. We attempted to understand if the host defense response is tailored specifically to meet the changing strategies of the pathogen i.e. as the pathogen moves from a biotrophic phase through the BNS and finally to a necrotrophic phase. Along with microscopic and biochemical studies, in order to get an insight into the defense signaling against a hemibiotrophic fungi, we have investigated whether priming with different phytohormones evokes resistance. Moreover we attempted to investigate for the first time whether this dynamic molecular response of the host against a hemibiotrophic pathogen, is different in a resistant versus a susceptible host. The transcript levels of a total of 20 genes functioning in the different arms of defense signaling and changes in phytohormone levels have been monitored over a time course to get an insight into the different choices a resistant host makes to combat the infection which a susceptible host cannot.
A distinct biotrophic phase is followed by necrotrophic phase in Macrophomina phaseolina during infection of sesame
Observation of M. phaseolina infection in sesame roots revealed a short yet distinct biotrophic phase followed by transition from biotrophy to necrotrophy (BNS phase) and then a prominent necrotrophic phase. The duration of each phase and its transition to next one varied considerably between the susceptible (VRI-1) and resistant (Nirmala) variety. The infection stages were studied using normal and transformed M. phaseolina expressing GFP.
At early biotrophic phase (3–4 hpi), typical aggregates of swollen vesicles consistent with biotrophic phase of other hemibiotrophic fungi18, were found in the root cortical tissues of both resistant variety (Fig. 1a) and susceptible variety (Fig. 1c). Associated with infection pegs, hyphopodia-like penetrating structure were visible at infection sites in both susceptible and resistant roots (Fig. 1b,d). Infection with GFP-expressing transformed M. phaseolina followed by confocal microscopy revealed root surface colonization by typical biotrophic runner hyphae18 at 9–12 hpi. (Fig. 1e,g). After penetration, the fungi produce typically constricted intracellular biotrophic primary hyphae in both varieties (Fig. 1f,h,i,k). Following penetration, the hyphae remained mostly intercellular, avoiding direct penetration of host cells in the root epidermis and cortical tissue at 16–24 hpi (Fig. 1j,l). Even in places where the hyphae did penetrate the host cells, the hyphal extension invaginated into the host plasma membrane thereby covering itself with the host membrane which is a typical strategy of host defense avoidance in biotrophic fungi (Fig. 1m,o). Development of double membrane intercellular primary hyphae took place during late hours of biotrophy, 32–34 hpi for Nirmala, 20–22 hpi in VRI-1. The biotrophic phase was also characterized by typical thick, biotrophic primary hyphae confined initially to infected epidermal cells (Fig. 1n,p).
During biotrophic phase, roots of both varieties appeared externally symptomless (Fig. 1q,s). The internal tissues also remained symptom-free with cross-sections of root showing no evidence of tissue necrosis up to 24 hpi in VRI-I and 36 hpi in Nirmala (Fig. 1r,t). The biotrophic infection phase was completed within 24 hrs in VRI-1 roots, but it continued up to 36–38 hrs in Nirmala.
Timing of transition from biotrophy to necrotrophic phase (BNS phase) of M. phaseolina was delayed considerably in the resistant variety compared to the susceptible one, being 36–38 hpi for Nirmala and 24 hpi for VRI-1. During BNS, majority of biotrophy-associated thick primary hyphae gave rise to thinner necrotrophy-associated secondary hyphae (Fig. 1u). Still no prominent symptoms were visible in stems and roots of the two varieties up to this particular phase (Fig. 1v,w,x,y).
The onset of necrotrophic phase was characterized by extensive growth of thin, secondary hyphae which necrosed the host tissues (Fig. 2a,c). The growth of the thin necrotrophic hyphae was intra- and inter-cellular in both varieties (Fig. 2b,d,e,h). The extent of GFP expressing hyphal growth over the root surface was visibly less in Nirmala roots (Fig. 2f) than VRI-1 where the mycelia formed a mantle covering the susceptible root (Fig. 2i). Formation of dark microsclerotia appearing as black spots was visibly less in the resistant variety (Fig. 2g) than the susceptible one (Fig. 2j). This resulted in less external symptoms in Nirmala roots (Fig. 2k) than VRI-1 (Fig. 2m). Cross sections revealed that VRI-1 roots were heavily colonized with fungal hyphae which induced more tissue necrosis (Fig. 2n), compared to Nirmala (Fig. 2l).
After root infection, M. phaseolina colonized the lower stem, which externally appeared ashy black (Fig. 2o). Confocal microscopy revealed that the fluorescent hyphae colonized the stem cortical tissue in both varieties (Fig. 2p). Ultimately hyphae clogging the xylem vessels was visible in longitudinal sections (Fig. 2q) and cross sections (Fig. 2r), blocking the water supply, causing plants to collapse in the necrotrophic phase in both varieties.
Transition from biotrophy to necrotrophy in M. phaseolina is confirmed by changes in fungal biomass and expression of fungal biotrophy and necrotrophy marker genes
Our results show that delayed disease progression in Nirmala correlates withless fungal biomass. At 12 hpi, during biotrophic phase in both varieties, no significant differences in the amounts of fungal DNA were detected (Fig. 2s). At later time points, during BNS and necrotrophic phase, fungal proliferation was less in Nirmala compared to VRI-1.
The expression of M. phaseolina biotrophy marker gene BAS3 (Table 1) was consistently higher in Nirmala compared to VRI-1 (Fig. 2t). With the onset of BNS (24 hpi for VRI-1 and 36 hpi for Nirmala), there was a sharp decrease in its expression. The M. phaseolina necrotrophy marker gene NIP (Table 1) showed gradual increase in expression in VRI-1 during late hours of biotrophy and it was predominantly expressed throughout necrotrophic phase in greater amounts compared to Nirmala (Fig. 2u), correlating with greater necrosis.
Less ROS accumulation, upregulation of ROS signaling genes and better antioxidant enzyme activities post BNS correlate with resistance
Production of ROS is known to be one of the earliest events in response to microbe recognition. At early biotrophic infection phase, no difference was detected in H2O2 accumulation in the roots of VRI-1 and Nirmala (Fig. 3a). However, with the onset of BNS, after 24 hpi, there was higher accumulation of H2O2 in VRI-1 roots compared to Nirmala and remained higher until end of experiment (72 hpi) (Fig. 3a). This observation was supported by DAB staining of roots for H2O2 accumulation (Fig. 3b). During biotrophic phase up to 12 hpi, malonedialdehyde (MDA) content, a measure of lipid peroxidation, was not much different in the two varieties. From 24 hpi onwards which coincided with the BNS phase, there was consistently higher lipid peroxidation in VRI-1 compared to Nirmala (Fig. 3c). In the necrotrophic phase, much less lipid peroxidation was found in Nirmala, owing to successful ROS detoxification, contributing to less necrotrophy-induced tissue damage.
Consistent with the high H2O2 accumulation, antioxidant activity of SOD was less in Nirmala throughout biotrophic phase compared to VRI-1 (Fig. 3d). An interesting observation was that after 36 hpi i.e. during the necrotrophic phase, antioxidant activity of SOD became higher in Nirmala compared to VRI-1. For APX enzyme, until 12 hpi there was no significant difference in activity in the two varieties after which there was a steady increase in activity in Nirmala which peaked at 48 hpi (Fig. 3e). Catalase showed changes in activity similar to that of SOD during biotrophic to necrotrophic phase shift in the two varieties (Fig. 3f).
Expression analyses of four genes associated with ROS signaling pathway, SiRbOH, SiSOD, SiCysPI and SiGST 19,20,21,22 (Tables 2,3) was done over a time course to get an insight into the regulation of these genes during different phases of infection. SiRbOH, a ROS signaling gene, showed steady increase in its expression from late biotrophy to necrotrophic phase, with greater accumulation of transcripts in VRI-1 compared to Nirmala, indicating greater ROS accumulation in susceptible variety (Fig. 3g). In spite of early spiking of ROS scavenging gene SiSOD in VRI-1, from 12 hpi onwards Nirmala maintained a constant higher expression, indicating better ROS scavenging (Fig. 3h). Expression of SiGST, SiCysPI remained similar up to 12 hpi in the two varieties, after which there was gradual increase in the rate of transcript accumulation in Nirmala compared to VRI-1, reaching a peak at 48 hpi (Fig. 4i,j).
Greater accumulation of secondary metabolites and upregulation of secondary metabolite-related genes after BNS correlate with resistance
Production of antimicrobial secondary metabolites constituted one of the earliest defense responses in sesame against M. phaseolina. Up to 6 hpi, the accumulation of phenolics was similar in the two varieties with in fact more accumulation in VRI-1 at 12 hpi. But at the onset of necrotrophic phase in Nirmala (36 hpi) there was a sudden increase in the rate of accumulation of phenolics (Fig. 4a). This was supported by the detection of stronger autofluorescence of cell wall-bound phenolics in infected Nirmala root cortical cells compared to VRI-1 at 36 hpi (Fig. 4b). Accumulation of phenolics correlated with high PAL activity, the key enzyme in biosynthesis of p-hydroxycinnamic acid and derivative phenolic compounds, in Nirmala throughout biotrophic and necrotrophic phase with a wider gap between Nirmala and VRI-1 after 36 hpi (Fig. 4c). Similar results were obtained for flavonoids (Fig. 4d).
Callose deposition along the cell-wall, which is known to impede hyphal growth, initiated as early as 12 hpi in Nirmala. Time course detection of callose by fluorescent microscopy showed visibly higher amount of callose deposition in Nirmala roots than VRI-1 throughout biotrophic and necrotrophic phase (Fig. 4e). Differential accumulation of secondary metabolites during different phases of infection in the two varieties in mediating better tolerance against M. phaseolina in the resistant variety was further confirmed by transcriptional activation of SiIFR, SiFLM (involved in Isoflavone and Dihydroflavonol biosynthesis respectively) and SiPCHY (involved in lignin biosynthesis and structural barrier defense)23,24. Expression of SiIFR was higher in Nirmala compared to VRI-1throughout biotrophic and necrotrophic phase but a distinct jump in the expression level occurred at BNS in Nirmala (Fig. 4f, Tables 2 and 3). Expression of SiFLM was higher in VRI-1 compared to Nirmala during the biotrophic phase but during BNS there was a sudden increase in expression in Nirmala becoming three to four times higher than VRI-1 in the subsequent time points (Fig. 4g). SiPCHY transcript accumulation on the other hand was constantly higher in Nirmala throughout the infection phases (Fig. 4h).
Differential expression of defense signaling genes with respect to changing phases of the pathogen results in coordinated defense response
A total of 13 different genes were selected from four signaling cascades to observe if the host can alter its defense strategy with changing the phases of the pathogen and whether the tolerant host makes more prompt alterations compared to the susceptible host. The acronyms of the genes from different pathways and primers are given in Tables 2, 3.
Upregulation of SA-inducible genes, as consequence of SA buildup contributes to early defense response after pathogen recognition during biotrophic phase. Early peaking and consistent greater transcript accumulation of SA regulated genes (SiEDS1, SiNPR1) in Nirmala compared to VRI-1 contributes to early immune response (Fig. 5a,b). Again, SA-regulated PR genes SiTLP (PR-5), SiChi (PR-3) showed higher expression in the late biotrophic phase and BNS for defense against biotrophic phase and then extending into the necrotrophic phase likely for inducing SAR (Fig. 5c,d).
SA levels were directly quantified to see if SA levels increased with activation of SA-regulated genes. SA levels peaked at 6 hpi and showed greater accumulation in the biotrophic phase and thereafter decreased in the necrotrophic phase (Fig. 5g). SA accumulation was overall greater in Nirmala. Under mock inoculation there was no significant difference in SA level between two varieties (Fig. 5h).
Sesame Calmodulin homolog, SiCaM (regulator of Ca+2 signal transduction) expression was higher during the BNS phase in Nirmala. In VRI1 SiCaM expression remained at constant low level compared to Nirmala (Fig. 5e). SiCDPK (which sense intracellular Ca+2 levels and translates signal to phosphorylation events) also showed a peak just prior to BNS in Nirmala but in VRI-1 the level was constant (Fig. 5f). Participation of SiCaM and SiCDPK in early response to pathogen infection indicates role of intracellular Ca+2 signaling in activation of defense in sesame just prior to BNS of pathogen.
With approach of the necrotrophic phase the activation of JA-ET signaling was evident (Fig. 6a–h, Tables 2 and 3). Early peaking of SiAOS (JA biosynthesis gene) at 6 hpi enabled the plant to promptly upregulate the downstream genes in the JA pathway. Upregulation of SiSAM (Ethylene biosynthesis gene) during BNS (36 hpi) in Nirmala indicated activation of JA-ET biosynthesis pathway as consequence of BNS in pathogen. Higher accumulation of marker genes for JA signaling (SiPDF1.2, SiAP2) and ET signaling (SiERF) around BNS and necrotrophic phase distinctly indicates change in defense strategy with respect to changing phases of the pathogen. SiDef, another JA regulated gene, peaked at 24 hpi in Nirmala which has a late BNS but at 12 hpi in VRI-1 correlating with earlier BNS in VRI1. SiJAZ gene, negative regulator of JA signaling, behaved in opposite way, i.e. showing higher expression in biotrophic phase, with sharp decrease during necrotrophy. JAZ expression trend was similar in Nirmala and VRI-1 but the level was much less in VRI1 (Fig. 6g).
JA buildup was confirmed by quantitative estimation (Fig. 6h). Higher accumulation of endogenous JA in Nirmala around the time of BNS and during necrotrophic correlate with expression pattern of JA-ET regulated genes with respect to the infection stages of the pathogen. Under mock inoculation there was no significant difference in JA content between the two varieties (Fig. 6i).
Tolerance of sesame against charcoal rot results from activation of JA-ET signaling studied through priming with phytohormones and their inhibitors
Given the observed activation of phytohormone regulated defense genes upon fungal infection, we investigated the effect of priming with JA/ET/SA and their inhibitors on resistance of sesame (using resistant variety Nirmala) against M. phaseolina (Fig. 7a–i). Priming studies showed that in comparison to control (69.93%), no significant difference in Disease index (DI) was observed for SA treated seedlings (65.53%) (Fig. 7j). But for either JA or ET treated seedlings, DI was significantly reduced to 50 and 53.3% respectively (Fig. 7j). When JA and ET were applied together, DI reduced to 39% indicating strong induction of basal defense against M. phaseolina. Application of Ibuprofen (JA biosynthesis inhibitor), DIECA (JA pathway inhibitor) or STS (ET pathway inhibitor) alone increases DI to 79.23%, 80% and 77.8% respectively. Combined application of DIECA and STS resulted in high DI (91.11%) indicating intact JA/ET signalling pathway is required for tolerance against charcoal rot (Fig. 7j). This hypothesis has been further confirmed by microscopic study of infected roots of treated plants and control. In plants pre-treated with JA + ET, less hyphal growth was seen on roots compared to control (Fig. 7k,l). In DIECA + STS treated plants, compromised plant defense was correlated with overgrowth of M. phaseolina hyphae in roots, resulting in necrosis (Fig. 7m).
Functional activation of JA-ET signaling in imparting charcoal rot tolerance was confirmed by transcriptional analysis of genes involved in the pathway. Activation of JA and ET biosynthetic pathway genes (SiAOS and SiSAM respectively) under phytohormone treatment at early biotrophic phase is congruent with that in the control set (plants infected with M. phaseolina only) thereby indicating involvement of JA-ET signaling pathway to boost early defense responses (Fig. 7n,o). Positive regulation of SiAOS and SiSAM by JA + ET and suppression of their responses via potent inhibitor of the pathways (DIECA, IBU for JA, STS for ET, DIECA + STS for JA + ET signaling) further supports this notion. Gradual upregulation of SiAP2 by M. phaseolina in control set followed similar expression profile as that observed after application of JA + ET. Either JA or ET al.one only slightly increased SiAP2, but in much less amount compared control. Application of STS + DIECA (inhibitor of JA, ET pathway) progressively downregulated SiAP2 expression, thereby further indicating possible regulation of the gene by combined JA-ET signaling (Fig. 7p). Thus it can be inferred that SiAP2 likely acts downstream of SiAOS and SiSAM by integrating signals from both pathways (Fig. 7q).
Similar observations were made with priming experiments using VRI1 but as expected the DI was higher (Fig S1 a–j). The expression of SiAOS, SiSAM and SiAP2 remained constant up to 24 hrs after mock inoculation (Fig. S1 k,l,m).
The general perception is that the successful establishment of all necrotrophic fungi in a host entails rapid pathogen-mediated host-cell death as the primary step. Recent study with archetypal necrotrophic fungus Botrytis has revealed its versatility to switch from symptomless, biotrophic lifestyle to obligate necrotrophy under appropriate conditions25. Other studies on previously designated necrotroph such as Sclerotinia sclerotiorum, show that the fungus has a brief 24 hrs. biotrophic phase prior to the necrotrophic phase entailing the fungus to be repositioned as a hemibiotroph25,26. Therefore, it is possible some of the necrotrophs may have a short biotrophic phase. Thus far M. phaseolina has been considered as a broad host-range necrotroph infecting most species of dicot plants15. In the present study, a previously undocumented biotrophic phase lasting for a significant period of up to 36 hours in the resistant variety and the transitional phase to necrotrophy has been confirmed in M. phaseolina. Along with microscopic observation, time wise transcriptional activation of BAS3 and NIP (stage specific proteins of M. phaseolina) distinctly marks the onset of biotrophic and necrotrophic infection phase, similar to other hemibiotroph like Phytopthora 4. In hemibiotroph Septoria tritici, phase transition from symptomless biotrophy to destructive necrotrophy has been directly correlated with increase in fungal biomass10 which is in congruence with transcriptional data from current study, indicating the hemibiotrophic nature of M. phaseolina. The symptomless biotrophic phase of the charcoal rot fungus is a cause for concern under field conditions as this could make the disease virtually undetectable during early stages of infection. Since physiological switching in lifestyle of a pathogen entails an ecologically flexible outcome in terms of disease progression27, it is important that based on our findings M. phaseolina be repositioned among hemibiotrophs rather than necrotrophs.
Accumulation of ROS, such as H2O2, may also have contrasting defense functions depending on a pathogen’s lifestyle. While the level of ROS accumulation acts as virulence factor for disease development in necrotrophs like B. cinerea, Alternaria solani 28 on other hand the production of ROS, at the penetration site is one of the earliest defense reactions to resist fungal growth and is particularly useful against biotroph9. For hemibiotroph S. sclerotiorum, in the early stage, pathogen creates a reducing environment that suppresses the oxidative burst, but later it utilizes ROS induced cell death for successful infection29. In hemibiotroph Septoria tritici, Verticillium dahliae, infection is characterized by massive H2O2 accumulation during necrotrophy. RbOH (Respiratory burst oxidase homologs) in plants are directly involved in ROS accumulation and plant susceptibility against necrotrophic fungi30. Disease tolerance against hemibiotrophic F. oxysporum has been co-related in resistant banana with reduced expression of an RbOH homolog compared to susceptible one31. Earlier reports show that higher activities of ROS scavenging enzymes from 24 hpi onwards in the necrotrophic phases confer better ROS homeostasis in resistant varieties32,33. In present study, less H2O2 accumulation in Nirmala through reduced expression of RbOH and higher activity of ROS scavenging enzymes corresponds to delayed disease progression and tolerance, which is in line to a recent study in Medicago truncatula, where reduced ROS accumulation in roots show enhanced resistance to root-rot pathogen Aphanomyces euteiches 28.
Isoflavonoids, flavonoids or phenylpropanoid derivatives are some of the widely used secondary metabolites employed in plant immunity24,34. Activation of phenylpropanoid pathway as part of defense response in sesame against M. phaseolina was evidenced earlier by polyphenol accumulation and increased PAL activity35. The significantly higher PAL activity in resistant Nirmala from 12 hpi onwards as basal immune response, led to the accumulation of both free and cell wall-bound phenolics similar to that reported during the hemibiotroph Colletotrichum infection in maize9. Activation of phenylpropanoid pathway led to flavonoid biosynthesis, as estimated by higher SiIFR and SiFLM expression, similar to defense response in wheat against hemibiotroph Fusarium graminearum 12. Defense response also included lignin biosynthesis, as indicated by SiPCHY peaking at necrotrophic phase in both varieties of sesame. Consistent higher callose deposition in Nirmala led to less necrosis-induced tissue damage compared to VRI-1 by increased cell wall reinforcement, consistent with earlier report on wheat36 Overall the higher activity of secondary metabolite pathway in resistant variety is one of the key factors behind its tolerance against M. phaseolina.
For hemibiotrophic pathogen, plant defense is dependent on coordinated and orderly expression of SA, JA signaling37,38 although response is differential between susceptible and resistant genotype39. RNA seq analysis in Brassica showed activation of SA signaling during biotrophic infection of Leptosphaeria, which shifts to JA signaling during necrotrophy40. In this study we found we found significant increase in SA level during biotrophy and JA during necrotrophy which correlates with transcript accumulation. Such results are in accordance to recent study in tomato infected with hemibiotroph Phytopthora 41, thereby directly indicating involvement of both phytohormones during different infection stage. Similarly, Ca2+ signaling is critical for transcriptional reprogramming in plant’s innate immunity42. In response to M. phaseolina infection, SiCaM and SiCDPK were rapidly but coordinately induced in Nirmala during early hours of biotrophic infection phase with gradual reduction after 24 hpi. This is consistent with that observed in other plants that there is transient Ca2+ accumulation in the cytoplasm during the initial plant-pathogen interaction43.
For long lasting activation of induced resistance in plants, modulation of immunogenic memory with a low, non-effective concentration of a phytohormone gives better, faster and stronger immune response than that in non-primed plants44. Upon priming plants are capable of enhancing their basal resistance against future pathogenic attack by either improving perception of pathogen signals or by systemic activation of defense related pathways45. Following microbe perception, plants produce a complex blend of JA, ET and SA with specific combination seemingly depending on the infection strategy and lifestyle of the invading pathogen. Our study showed priming using combined JA and ET resulted in enhanced tolerance in sesame against M. phaseolina which is similar to an earlier study in Medicago where JA + ET application induced partial tolerance against M. phaseolina 46.As exogenous MeJA application in wheat provides resistance against hemibiotroph Fusarium by activation of JA signaling47, our results suggests combined JA-ET application prior inoculation is likely contributing to plant immunity by synergistic activation of JA-ET signaling in advance to fungal infection48,49.
Synergism between the defense activation pathways controlled by JA and ET is mainly characterized by the induction of PDF1.2 via ERF1 and ORA59, which acts as integrator of two signaling pathway49,50. Pharmacological inhibitor and transcriptional study showed SiAP2 (member of ERF family), downstream of both SiAOS and SiSAM, showed highest expression under combined JA/ET treatment followed similar pattern as induced by M. phaseolina. Our results suggest probable involvement of SiAP2 as integrator of both JA, ET signaling which supposedly activates upon M. phaseolina infection as evident by transcriptional upregulation of JA, ET biosynthesis genes. JA and ET independently activate not just separate sets of genes, they also synergistically activate defensins like PDF1.2 and PR genes49. Activation of SiPDF1.2, SiTLP and SiChi during necrotrophic indicates SiAP2 effectively upregulate downstream defense signaling genes, thereby leading to tolerance in sesame against charcoal rot.
In this article we present a comprehensive study of the host pathogen interaction between the hemibiotrophic pathogen M. phaseolina with a resistant and a susceptible variety of sesame. For successful infection, the hemibiotrophic fungi utilize biotrophy to necrotrophy switch so as to trick the host into applying PCD during the initial biotrophic phase. This adaptation enables the fungus to take full advantage of defense-related cell death during the subsequent necrotrophic stage, as seen in some recent studies11. Following pathogen perception, plants are known to produce complex and layered defense response seemingly depending on the infection strategy and lifestyle of the invading pathogen37. Here, just as the pathogen changed its strategy of infection, switching from biotrophic to necrotrophic lifestyle, the host could tailor its defense strategy to meet the changing situation. Most importantly this defense response was more prompt in the resistant host compared to the susceptible host, signifying that a resistant variety makes different choices from a susceptible host during the changing infection stages which influences the outcome in terms of disease progression. Our findings uncover new areas of research that will allow a better understanding of hemibiotrophic interactions and hosts responses.
Materials and Methods
Plant maintenance, fungus inoculation and molecular characterization of disease development
Susceptible (VRI-1) and resistant (Nirmala) varieties of sesame15 were grown aseptically in Hoagland’s agar medium. Pure culture of M. phaseolina was maintained according to our publication15. For fluorescence microscopy, M. phaseolina was transformed with GFP constructs via Agrobacterium-mediated method according to our protocol51. For infection studies, PDA discs of the fungalculture were placed in Hoagland’s agar medium and allowed to grow. At the edge of actively growing hyphae, roots of six week old sesame seedlings were placed, allowing fungus to infect. Root infection was periodically monitored at different time points (hours post inoculations, hpi) by bright field microscopy, epifluorescence microscopy (Leica DMLS, Germany) and confocal microscopy (Olympus, Singapore). To define the infection phases of M. phaseolina within host, expression analysis of marker genes for biotrophy (BAS3, Biotrophy associated secreted protein-EKG18082.1) and necrotrophy (NIP, Necrosis inducing protein-EKG16185.1) were analyzed by q-RT-PCR. M.phaseolina β-tubulin gene (KF952242.1) was used as an internal control for normalization of expression. List of primers for these genes are in Table 2. Fungal biomass was quantified by determination of fungal DNA in plant extract by q-PCR using primers mp(f) 5′-CCGAAGAATATCCACCTCCA-3′ and mp(r) 5′-GCAAAGGGTGGAAAGGAAGT-3′ spanning internal transcribed sequences of rRNA gene (JN241996.1)52. For normalization, the sesame eIF4A was amplified with primers eIF4A(f) 5′-AGCCCGTCCGCATTCT-3′ and eIF4A(r) 5′-AAGCCAGTCAACCTTTCTCC-3′
Calculation of Disease index
Disease index was calculated according to our earlier publication15, Chowdhury et al., 2014.
Analysis of gene transcript level by reverse transcription-quantitative real time PCR (RT-qPCR)
Isolation of RNA and cDNA synthesis was performed according to our published protocol53. RT-qPCR reactions were carried out in 20 µl volume, 96-well blocks, (Applied Biosystems 7500 Real-Time PCR System, USA) and the Power SYBR Green mastermix (Applied Biosystems). The sesame genome sequence17 was used to identify candidate genes, known to act in different signaling pathway in other plants and were ascribed with acronyms which were maintained throughout the study (Table 1). Primers for the selected genes were designed using Primer-3plus-software (http://www.bioinformatics.nl/cgi-bin/primer3plus/primer3plus.cgi) and IDT-oligo-analyzer 471 (http://www.idtdna.com/analyzer/Applications/OligoAnalyzer/). Amplified genes were sequenced to confirm their identity (Table 2). According to our publication54 Sesame eIF4A gene was used as an internal control to normalize the variations in the cDNA amounts used for RT-qPCR. All RT-qPCR reactions were performed in biological triplicates using RNA samples extracted from three independent plants grown under identical conditions. The comparative method (ΔΔCt) was employed to evaluate the relative quantity of each amplified product in the samples. The specificity of the PCR reactions was determined based on a melting curve analysis of the amplified products using the standard method installed with the system.
Analysis of ROS, lipid peroxidation and antioxidative enzyme activities
Hydrogen peroxide (H2O2) was quantified using Amplex red according to Chakraborty55 and histochemical detection in roots was visualized by DAB staining. Lipid peroxidation was estimated according to Chowdhury56. Antioxidant enzyme assays were done accordingly.
Enzyme extract was prepared by homogenizing tissue in 0.1 M Sodium Phosphate buffer (pH = 7). After centrifugation, supernatant was used for enzyme assay. The reaction mixture was prepared by mixing 1.110 ml of 50 mM phosphate buffer (pH 7.4), 0.075 ml of 20 mM L-methionine, 0.040 ml of 1% (v/v) Triton X-100, 0.075 ml of 10 mM hydroxylamine hydrochloride and 0.1 ml of 50 µM EDTA. To this mixture 100 µl of enzyme extract and 80 µl of riboflavin (50 µM) were added. The reaction mixture was mixed and then illuminated for 10 min under two 20 W-Philips fluorescent lamps (60 µmol m−2 s−1). After 10 min exposure, 1 ml of Greiss reagent (prepared freshly by mixing equal volume of 1% sulphanilamide in 5% phosphoric acid and 0.1% N-1-napthyl ethylene diamine) was added and the absorbance was measured at 543 nm. The activity was calculated as nkat/mg protein
Enzyme extract was prepared by homogenizing tissues in 50 mM potassium phosphate buffer (pH 7.8) containing 1.0 mM EDTA, 1% PVP, 1 mM ascorbic acid, and 1 mM phenylmethylsulfonyl fluoride at 4 °C. Reaction mixture in a final volume of 3 ml contained 50 mM potassium phosphate buffer (pH 7.0), 0.2 mM EDTA, 0.5 mM AsA, 0.2 mM H2O2, and the enzyme at 25 °C. H2O2 was the last component to be added and the rate of ascorbate oxidation was monitored by the decrease in absorbance at 290 nm (extinction coefficient of 2.8 mM−1 cm−1) up to 5 min. Specific activity of enzyme was expressed as μmol ascorbate oxidized min−1 mg−1 protein.
Enzyme extract was prepared by crushing infected roots in 50 mM Tris–NaOH buffer (pH 8.0) containing 0.5 mM EDTA, 2% (w/v) polyvinyl pyrrolidone (PVP), and 0.5% (v/v) Triton X-100 and after centrifugation supernatant was used for enzyme assay. The assay mixture contained 100 mM potassium phosphate buffer (pH 7.0), 50 mM H2O2, and 200 μl enzyme extract in a final volume of 3 ml. The decomposition of H2O2 was followed at 240 nm (extinction coefficient of 0.036 mM−1 cm−1) by decrease in absorbance for 5 min at 25 °C. Catalase activity was expressed as μmol of H2O2 oxidized min−1 mg−1 protein.
Determination of phenolics, flavonoids, Phenylalanine ammonium lyase (PAL) activity and callose deposition
Phenolics and flavonoids from infected root tissue were estimated according to our published paper33. Cell wall bound phenolics were detected as bright autofluorescence under epifluorescence microscope (excitation at 436 nm, emission 470 nm)9. PAL activity was estimated according to Jogaiah57 using trans-cinnamic acid as a standard. The enzyme activity was expressed as µg trans-cinnamic acid/g FW. Fungus-induced callose deposition in infected root tissues were visualized as bluish-green fluorescence by aniline blue staining under epifluorescence microscope (Leica DMLS, excitation maximum 330–385 nm, dichroic mirror DM 400, barrier filter >420 nm). For each time point four roots were examined and in each root, 10 microscopic fields were studied for callose deposition.
Quantification of phytohormones SA and JA
Quantification of SA, JA from infected root tissues was done by gas chromatography following modified vapor phase extraction method according to Mishina and Zeier58. 200 mg of infected root tissue were homogenized with 600 mL of extraction buffer (water:1-propanole:HCl 51:2:0.005), followed by addition of internal standards (D4-SA, dihydrojasmonic acid- 100 ng each) and 1 ml of methylene chloride. The phase separation was done by centrifugation and lower organic phase was dried over Na2SO4, treated with 2 ml of 2 M trimethyl silyldiazomethane in hexane (Sigma-Aldrich) for 5 min at room temperature to convert carboxylic acids into their corresponding methyl esters. Methylation was terminated with 2 M acetic acid in hexane and the sample was subjected to a vapor-phase extraction using a volatile collector trap packed with Super-Q absorbent (VCT-1/4 × 3-SPQ; Analytical Research Systems). The final evaporation temperature was set to 200 °C, and samples were eluted from the collector trap with 1 ml methylene chloride. Finally, the sample mixture was separated on a gas chromatograph (GC 6890N; Agilent Technologies) equipped with a fused silica capillary column combined with a 5975 mass spectrometric detector (Agilent Technologies). For quantitative determination of metabolites, peaks originating from selected ion chromatograms were integrated. The area of a substance peak was related to the peak area of the corresponding internal standard (SA/D4-SA; JA/dihydro jasmonic acid).
Priming sesame plants with exogenous phytohormones and chemicals
Priming experiments were done using both susceptible (VRI-1) and resistant (Nirmala) plants. For tolerance assays, 6 week old seedlings were pre-treated with chemicals and at 1 day after treatment were inoculated with M. phaseolina by infected soil method according to Kamalkannan59. For priming experiments following chemicals were used: MeJA (Sigma-Aldrich), Ethepon (Sigma-Aldrich), salicylic acid (Himedia, India) Silver thiosulphate (STS, inhibitor of ET signaling), Ibuprofen (IBU, Sigma- inhibitor of JA signaling), diethyldithiocarbamic acid (DIECA, SRL-inhibitor of JA signaling). STS was prepared fresh by mixing 100 mM AgNO3 and Na2S2O3. Different chemicals were used at following concentrations: MeJA (100 µM), Ethepon (500 µM), Salicylic acid (200 µM), STS (20 mM), DIECA (100 µM), Ibuprofen (20 µM). 15 ml of chemicals (single/combination) were added to plant roots in soilrite (mixture of horticulture-grade expanded perlite, Irish Moss Peat, and exfoliated vermiculite in the ratio 1:1:1) and pots were kept in convirons (28 ± 1 °C, 16/8 hrs photoperiod, light intensity 50 μmol m−2 s−1 using cool-white fluorescent tubes) for 24 hrs prior to infection. The experiment was done thrice with identical results, using 6 plants of same age for each chemical treatment. Disease development assessment and disease index was calculated according to our earlier published work15 after two weeks of inoculation. For transcriptional studies, roots of six week old seedlings were treated with chemicals and after specific time point, tissue was collected for RNA analysis. Roots infected with M. phaseolina served as control.
All data are mean of three independent experiments ± S.E.M. Each experiment was done in a completely randomized design (CRD) with three replicates60. The data were subjected to one-way analysis of variance (ANOVA) and different letters indicate significant differences between treatments at p < 0.05, according to Duncan’s multiple range test (DMRT) using software package for statistical analysis (SPSS version 16, 2007). Data represented are means ± standard error of mean (S.E.M) of three independent experiments with three replicates.
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This work was partially supported by Department of Biotechnology, Ministry of Science and Technology (DBT), Government of India. S. Chowdhury and A. Basu received UGC-NET and CSIR-NET fellowships, respectively. The infrastructure provided by DST-FIST and UGC-CAS of the department were utilized. We thank Bose Institute, for qRT-PCR facility and Calcutta University for CLSM facility of DBT, IPLS for some instruments.
The authors declare that they have no competing interests.
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Chowdhury, S., Basu, A. & Kundu, S. Biotrophy-necrotrophy switch in pathogen evoke differential response in resistant and susceptible sesame involving multiple signaling pathways at different phases. Sci Rep 7, 17251 (2017). https://doi.org/10.1038/s41598-017-17248-7
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