Defensins are cysteine-rich cationic antimicrobial peptides contributing to the innate immunity in plants. A unique gene encoding a highly cationic bi-domain defensin MtDef5 has been identified in a model legume Medicago truncatula. MtDef5 consists of two defensin domains of 50 amino acids each linked by a 7-amino acid peptide. It exhibits broad-spectrum antifungal activity against filamentous fungi at submicromolar concentrations. It rapidly permeabilizes the plasma membrane of the ascomycete fungi Fusarium graminearum and Neurospora crassa and induces accumulation of reactive oxygen species. It is internalized by these fungi, but uses spatially distinct modes of entry into these fungi. It co-localizes with cellular membranes, travels to nucleus and becomes dispersed in other subcellular locations. It binds to several membrane-resident phospholipids with preference for phosphatidylinositol monophosphates and forms oligomers. Mutations of the cationic amino acids present in the two γ-core motifs of this defensin that eliminate oligomerization also knockout its ability to induce membrane permeabilization and fungal growth arrest. MtDef5 is the first bi-domain plant defensin that exhibits potent broad-spectrum antifungal activity, recruits multiple membrane phospholipids and forms oligomers in their presence. These findings raise the possibility that MtDef5 might be useful as a novel antifungal agent in transgenic crops.
Plants have evolved an innate immune system for defense against pathogenic microorganisms. This ancient defense system provides nonspecific broad-spectrum resistance against microbial invasion. The innate immunity of plants comprises fortification of cell wall, hypersensitive response and production of antimicrobial compounds and antimicrobial peptides (AMPs). AMPs serve as one of the first lines of defense against pathogen invasion and are one of the key contributors to innate immunity in plants1.
Defensins represent a major class of AMPs found in almost all eukaryotes. These cysteine-rich peptides are diverse members of one of several AMP families in plants2. They are 45–54 amino acids in length and their constitutive, regulated or induced expression confers durable resistance to fungal pathogens3,4. In the oxidized form, they contain an invariant tetradisulfide array and share a cysteine-stabilized αβ backbone in which one α-helix is stabilized through disulfide bonding to three antiparallel β strands. Despite their structural similarity, plant defensins vary greatly in their amino acid sequences revealing a rich diversity of variants5. This variation in their primary amino acid sequences likely confers diverse physiological functions to members of the plant defensin family6,7.
The best known property of the cationic plant defensins is their ability to inhibit the growth of fungal pathogens in vitro and in planta. However, their mechanisms of action (MOA) are not yet fully understood. It is now recognized that plant defensins vary in their MOA3,8,9. Interaction of some plant defensins with specific cell wall/plasma membrane resident sphingolipids results in the induction of cell wall stress, accumulation of ceramides and reactive oxygen species (ROS), and ultimately cell death2,3. During the last few years, antifungal plant defensins have been discovered that gain entry into fungal cells and bind to bioactive plasma membrane resident phospholipids10,11,12,13,14. The vacuole-localized defensins NaD1 and TPP3 from Nicotiana alata and Solanum lycopersicum, respectively, bind to plasma membrane localized phosphoinositides, in particular, phosphatidylinositol 4, 5-bisphosphate (PIP2), and form PIP2-dependent oligomeric complexes13,15. Medicago truncatula defensin MtDef4 and N. suaveolens defensin NsD7 target phosphatidic acid (PA) and this interaction is important for their antifungal activity14,16. NsD7 forms PA-dependent oligomeric complexes and disrupts the fungal plasma membrane16. These findings suggest that plant defensins recruit one or more bioactive phospholipids to oligomerize, induce membrane disruption and trigger fungal cell death.
The genome of the model legume M. truncatula is predicted to encode 63 defensins with a tetradisulfide array17. Here, we report characterization of a novel bi-domain defensin MtDef5 encoded by a single gene in the genome of this plant. This defensin consists of two 50-amino acid defensin domains that are linked by a 7-amino acid peptide. We show that it inhibits the growth of fungal pathogens tested at submicromolar concentrations. It disrupts the plasma membrane of fungal cells and induces accumulation of ROS. MtDef5 also binds to several membrane-resident phospholipids with strong preference for phosphatidylinositol monophosphates (PIP). We provide further evidence that this interaction with phospholipids leads to oligomerization of MtDef5 regardless of its affinity for them. Using site-directed mutagenesis, we demonstrate that the cationic amino acid residues present in each of the two γ-core motifs of this defensin are required for its oligomerization and antifungal activity.
MtDef5 is a bi-domain defensin from Medicago truncatula
Previously, our search of the M. truncatula GeneIndex (MtGI 4.0) revealed the expression of a bi-domain defensin gene identified as a Tentative Consensus 8727318. The genomic locus (MTR_8g012775) representing TC87273 encodes a signal peptide of 29 amino acids and a mature protein of 107 amino acids (Fig. 1). The sequence of the predicted mature protein revealed the presence of two defensin domains, designated MtDef5A and MtDef5B, each 50 amino acids in length, that are connected by a 7-amino acid linker sequence APKKVEP. MtDef5 contains a net charge of +16 and 39% amino acids with hydrophobic side chains. The two domains share 84% amino acid identity (Fig. 1). The tertiary protein structure of MtDef5 predicted by Raptorx web portal (http://raptorx.uchicago.edu/) indicates each domain to fold independently into a cysteine-stabilized alpha-beta (CSαβ) configuration consisting of three antiparallel β strands and one α-helix stabilized by four disulfide bridges. Each domain contains a γ-core motif GACHRQG(F/I)GFAC which connects the two anti-parallel β2 and β3 strands and carries a net positive charge of +2 and 4 hydrophobic amino acids. This nearly identical motif present in each domain differs in sequence from that of all previously characterized single domain plant defensins.
MtDef5 exhibits potent broad-spectrum antifungal activity
Plant defensins exhibit inhibitory activity against filamentous fungi in vitro at micromolar concentrations. Since MtDef5 consists of two domains and is highly cationic, we determined its in vitro antifungal activity against several filamentous fungi. MtDef5 expressed in Pichia pastoris was determined to have the molecular mass of 12915.35 Da, ~1025 Da higher than the calculated mass of 11887.74 Da (Supplementary Figure S1). The α-factor signal peptide was incorrectly processed adding EEGVSLEKR at the N-terminus of the mature MtDef5 peptide sequence. However, this additional sequence of 9 amino acids has minor effect on the overall net charge and hydrophobicity of MtDef5 (Supplementary Table S1) and exhibits no antifungal activity against F. graminearum (Figure S2). Therefore, we decided to proceed with testing the antifungal activity of MtDef5 with the observed mass of 12915.35 Da. MtDef5 inhibited the growth of F. graminearum and N. crassa with an IC50 value of 0.25–0.3 µM and minimal inhibitory concentration (MIC) of 0.70–0.75 µM (Fig. 2A,B). It also inhibited the growth in vitro of several other filamentous plant fungal pathogens including F. verticilloides, F. thapsinum, Alternaria brassicicola, Colletotrichum higginsianum and Botrytis cinerea (Fig. 2C). C. higginsianum was the least sensitive pathogen among this group of fungal pathogens with an IC50 value of 1.75 µM and MIC of 3.0 µM. The antifungal activity of MtDef5 against F. graminearum was also compared with that of each of its two domains. From the data presented in Supplementary Table S2, it is clear that MtDef5 has more potent antifungal activity than its two domains, MtDef5A and MtDef5B. In addition, the in vitro antifungal activity of MtDef5A and MtDef5B, when used in combination, did not equal to that of MtDef5 suggesting the linker peptide APKKVEP contributes to the potent antifungal activity of the bi-domain MtDef5.
MtDef5 permeabilizes fungal plasma membrane and induces accumulation of ROS
Cationic antimicrobial peptides are known to permeabilize the plasma membrane of their target microbes. Thus, plant defensins have been previously shown to permeabilize the plasma membrane of their target fungi12,19,20. The SYTOX Green (SG) uptake assay was used to test if MtDef5 permeabilizes the plasma membrane of F. graminearum and N. crassa. SG is a dye which is only taken up by cells with a compromised plasma membrane and its fluorescence increases >500-fold upon binding to nucleic acids thus allowing quantitative analysis and fluorescence microscopy. The uptake of SG was assessed using confocal microscopy in fungal hyphae treated with 0.75 µM MtDef5. SG uptake was visible in the hyphal cells of both fungi after 2 h of treatment with MtDef5 (Fig. 3A). This result suggests that membrane disruption likely contributes to the antifungal action of MtDef5.
Antifungal defensins with different MOA are known to converge on a vital cellular hub representing the production of ROS to achieve fungal killing10,21,22. Therefore, we examined if the fungal plasma membrane permeabilization induced by MtDef5 is paired with a commensurate rise in the production of ROS in the cells of F. graminearum and N. crassa. The production of ROS was monitored by confocal microscopy using the cell permeant ROS indicator 2′,7′-dichlorodihydrofluorescein diacetate (H2DCF-DA) following treatment of fungal hyphae with MtDef5. Upon production of ROS, the nonfluorescent H2DCF-DA is converted to highly fluorescent 2′,7′-dichlorofluorescein (DCF). Accumulation of intracellular ROS was observed in both F. graminearum and N. crassa hyphae following exposure to MtDef5 (Fig. 3B) indicating ROS-mediated apoptosis- or necrosis-like process involved in fungal cell killing by this defensin.
Internalization and subcellular localization of MtDef5
In order to determine if MtDef5 acts via the extracellular side or gains entry into fungal cells, it was labeled with the fluorophore DyLight550 and its uptake was monitored using the live-cell imaging of conidia and conidial germlings of F. graminearum and N. crassa. DyLight550 labeled MtDef5 exhibited reduced antifungal activity with an MIC of 1.5 µM compared with an MIC of 0.75 µM for the unlabeled MtDef5. At MIC, entry of DyLight550 labeled MtDef5 within conidial germlings was monitored by confocal microscopy and time-lapse imaging. In F. graminearum, within 10 min of treatment, MtDef5 readily bound to the conidial surface uniformly and a considerable increase in binding was evident over the next 60 min. After approximately 60 min, MtDef5 started entering into the growing hyphal tip first and, in 90 to 120 min, it was internalized by most of the fungal cell (Fig. 4A and Supplementary Video S1). In sharp contrast, MtDef5 did not bind to the conidial surface uniformly in N. crassa. Instead, it entered into the cell by making random entry sites (Fig. 4B and Supplementary Video S2). Within 10 min, MtDef5 bound to specific sites of the cell surface and accumulated there before entering the cell. After ~30 min, MtDef5 started entering the cell from the entry sites. The membrane selective dye FM4-64 is also co-localized at the entry sites indicating perhaps endosomal uptake of the defensin (see below). Accumulation of MtDef5 inside the N. crassa cells continued to increase over time until it was almost completely internalized by the cells after 2 h of treatment (Fig. 4B). Thus, the uptake process of MtDef5 in N. crassa is strikingly different from that in F. graminearum.
Intracellular localization of MtDef5 was further investigated by examining co-localization of DyLight550 labeled MtDef5 with the membrane selective dye FM4-6423, membrane permeant dye SG which binds to nucleic acid and DNA specific stain 4′,6-diamidino-2-phenylindole (DAPI) in germlings of F. graminearum and N. crassa. MtDef5 is uniformly dispersed in the cells of both fungi. Dual labeling with FM4-64 showed that MtDef5 is co-localized with cellular membranes in cells of both fungi (Fig. 4). As shown in Fig. 5, MtDef5 accumulates first in the nucleus of F.graminearum cells (red) as revealed by its co-localization with a blue fluorescent DNA stain DAPI. The subcellular localization of MtDef5 in the nucleus and subsequent degeneration of this organelle was further confirmed by demonstrating co-localization of DyLight550-labeled defensin with DNA-complexed SG (green) as shown in the Supplementary Fig. S3 and Supplementary Video S3 and S4.Following entry of this defensin into fungal cells, we also observed a gradual increase in the size of the vacuole and ultimately its burst. The cell lysis was also observed within the timeframe of live cell imaging in both fungi (Supplementary Video S3 and S4). We conclude that MtDef5 is targeted to the nucleus, intracellular membranes and other subcellular locations following its entry into fungal cells suggesting the involvement of perhaps multiple targets contributing to fungal cell killing.
MtDef5 binds to multiple phospholipids with strong preference for PIP
Plant defensins target membrane phospholipids as part of their modus operandi. The characterization of defensin-phospholipid interactions can provide novel information regarding the functions of defensins relevant to their subcellular targeting and their potential effects on fungal signaling and vesicle trafficking. To assess the ability of MtDef5 to bind to membrane phospholipids, a protein-lipid overlay assay was performed with various biologically active phospholipids immobilized on a lipid strip (Echelon Bioscience, UT). We found that MtDef5 strongly binds to PI3P, PI4P and PI5P. However, it also shows somewhat weaker binding to PI3,5P2, PI4,5P2, PA and phosphatidylserine (PS) (Fig. 6A). Based on this lipid binding profile, we selected a more specific lipid array spotted with PI and PIPs at different concentrations. This experiment again confirmed higher affinity of MtDef5 to the monophosphorylated forms of PI with lower affinity for PIP2 and lack of affinity for nonphosphorylated PI. Consistent with the initial results obtained using PIP strips, we observed binding of MtDef5 to all three PIPs even at 12.5 pmoles per spot indicating high affinity of this defensin to these bioactive phospholipids (Fig. 6B).
To further validate the binding of MtDef5 to PIP, a liposome binding assay was performed using the commercially available PIP containing liposomes (Echelon Bioscience, UT). As shown in Fig. 6C, MtDef5 showed a preference for binding to PI3P and PI4P, but not for PI5P. Some MtDef5 was also detected in the pellet of liposomes containing PC/PE or PI, indicating PIP-independent binding (Fig. 6C). In summary, MtDef5 binds promiscuously to multiple membrane phospholipids but has a preference for PI3P and PI4P.
MtDef5 forms oligomers in presence of PIP, PA and PI
The ability of defensins to self-assemble into oligomers is important for their antimicrobial activity. We tested the ability of MtDef5 to oligomerize by treating MtDef5 with the biochemical cross-linker BS3 in absence and presence of PI3P, PI4P, PI5P, PI and PA. Separation of cross-linked protein complexes by a gradient SDS-PAGE indicated that MtDef5 formed covalently linked higher-order oligomers in presence of all three PIP (Fig. 7A). Surprisingly, it also formed oligomers in presence of PI and PA with whom it shows weak binding (Fig. 7B). This ability of MtDef5 to form oligomers in presence of multiple phospholipids is striking and may account for its potent antifungal activity against a broad range of fungi.
The γ-core motif mediated oligomerization, but not phospholipid binding, is important for the antifungal activity of MtDef5
The γ-core motif has been shown to be important for phospholipid binding and antifungal activity of plant defensins14. A four-membered MtDef5 variant family was designed and prepared to identify amino acid residues mediating phospholipid binding, oligomerization and antifungal activity in the γ-core motif of this defensin. Since the amino acid sequence of this motif is nearly identical in both domains, we used alanine scanning mutagenesis to substitute two adjacent amino acids of each motif simultaneously for alanine generating four variants (Fig. 8A). These variants were each expressed in P. pastoris and purified by ion exchange chromatography. They were subsequently tested for phospholipid binding, plasma membrane permeabilization, oligomerization and antifungal activity. The antifungal activity of MtDef5 variants was tested against F. graminearum. As shown in Fig. 8B, MtDef5F40A, G41A/I97A, G98A (MtDef5_V3) and MtDef5F42A/F99A (MtDef5_V4) retained wild-type (WT) antifungal activity. However, MtDef5H36A, R37A/H93A, R94A (MtDef5_V1) almost completely lost its antifungal activity and MtDef5Q38A, G39A/Q95A, G96A (MtDef5_V2) showed 2-fold reduction in its antifungal activity against F. graminearum relative to that of the WT MtDef5. These variants were also tested for their ability to permeabilize the plasma membrane of F. graminearum using the SG uptake quantification assay. As shown in Fig. 8C, WT MtDef5 and MtDef5 F42A/F99A (MtDef5_V4) exhibited faster and higher uptake of SG than the MtDef5 Q38A, G39A/Q95A, G96A (MtDef5_V2) and MtDef5 F40A, G41A/I97A, G98A (MtDef5_V3). In contrast, MtDef5 H36A, R37A/H93A, R94A (MtDef5_V1) lost its ability to permeabilize the fungal plasma membrane almost completely (Fig. 8C).
The ability of each variant to interact with PIPs was examined by performing a protein-lipid overlay assay. Surprisingly, the protein-lipid overlay assay revealed that MtDef5 γ-core motif variants did not significantly alter their lipid binding profiles and retained the WT MtDef5 PIP binding affinity and specificity (Fig. 8D). Some non-specific binding to phospholipids on PIP strips is known to occur by the presence of small amount of misfolded peptide and the non-specific binding can be blocked by adding sub-stoichiometric amounts of DnaK24. To eliminate non-specific binding, the WT and variant peptides were each incubated with DnaK and subsequently used on PIP strips. However, no non-specific binding to any of the phospholipids was observed indicating there was little or no misfolded peptide (data not shown) in the WT or γ-core motif variants used in the assay. By contrast, in the liposome binding assay, all γ-core motif variants exhibited somewhat reduced binding to all three PIPs. In particular, MtDef5 H36A, R37A/H93A, R94A (MtDef5_V1) showed a much weaker binding affinity for all three PIPs as compared to that of the WT MtDef5 and the other three MtDef5 γ-core motif variants (Fig. 8E). Like MtDef5, each γ-core motif variant was also detected in the pellet of liposomes containing PC/PE or PI, indicating PIP-independent binding (Fig. 8E). MtDef5 γ-core motif variants were further investigated for their capacity to form PIP-dependent oligomer formation by protein cross-linking. The oligomer formation by MtDef5_V2 and MtDef5_V3 variants in presence of PIP was similar to that of the WT MtDef5. MtDef5_V4 variant consistently showed less higher-order oligomer formation than the WT MtDef5. However, MtDef5_V1 variant containing the H36A, R37A, H93A and R94A substitutions showed complete loss of oligomer formation in presence of PI3P. It also did not form any oligomers in presence of either PI or PA (data not shown). We conclude that histidine and arginine residues present in the γ-core motif of each domain are critical for oligomerization and antifungal activity of MtDef5; however, the antifungal activity of this defensin does not appear to correlate tightly with its ability to bind phospholipids.
In the present study, we report the presence of a single gene in the genome of M. truncatula encoding a novel bi-domain antifungal defensin MtDef5 in which two domains, 50 amino acids each, are linked by a 7-amino acid peptide APKKVEP. The genome of M. truncatula is predicted to encode 63 defensins17; however, MtDef5 is the only bi-domain defensin encoded by a single gene in this model legume plant. A homolog of MtDef5 sharing high sequence homology is also present in a crop legume M. sativa. It is likely that this bi-domain defensin arose through a fusion of two recently duplicated genes encoding single domain defensins in the genomes of these two legumes. The biological function of this defensin in Medicago spp. remains to be determined.
Consistent with its high cationicity and hydrophobicity, we find that MtDef5 exhibits potent antifungal activity in vitro against several filamentous fungal pathogens at submicromolar concentrations. Its IC50 value below 500 nM against several fungi has been rarely reported for other antifungal plant defensins. N. alata defensin NaD1 inhibits the growth of filamentous fungi with an IC50 value ranging from 0.75 to 1.0 µM10. An IC50 value of 80 nM was reported for antifungal activity of RsAFP2 against Pyricularia oryzae 25 and 100 nM for HsAFP1 and AhAMP1 against Septoria tritici and Leptosphaeria maculans 26, respectively. It should be noted here that MIC values of different defensins depend upon the ionic strength of the fungal growth media used. Based on its MIC value of 750 nM for antifungal activity against F. graminearum, MtDef5 is 8- and 32-fold more potent than MtDef4 and MsDef1, respectively, when assayed for antifungal activity under the same conditions27. Thus, MtDef5 is one of the most potent broad-spectrum antifungal plant defensins expressed in M. truncatula.
In the present study, we have conducted several experiments that shed light on the mechanisms governing the highly potent antifungal activity of MtDef5. Plant defensins exert their broad-spectrum antifungal activity using multiple mechanisms including cell membrane permeabilization13,14,15,20,28. At MIC, MtDef5 rapidly permeabilizes the plasma membrane of F. graminearum and N. crassa as shown by the uptake of SG dye within minutes. In sharp contrast, MtDef4 permeabilizes the plasma membrane of F. graminearum, but not of N. crassa 29. It is likely that, the antifungal action of MtDef5, unlike that of MtDef4, involves plasma membrane permeabilization of all its target fungi. MtDef5 challenge also induces accumulation of ROS in fungal cells. ROS has been reported to cause membrane damage and loss of organelle integrity. Its accumulation has been also reported as part of the antifungal action of plant defensins NaD110 and RsAFP230. We propose that plant defensins including MtDef5 that exhibit different MOA converge on ROS accumulation as a central hub for initiating cell death in their target fungi.
Plant defensins, NaD1, TPP2, Psd1 and MtDef4, are internalized and accumulate intracellularly in their target fungi10,11,12,13,14. The confocal microscopy of F. graminearum and N. crassa cells treated with the fluorescently labeled MtDef5 has revealed that this defensin is also internalized into the cells of both fungi. Interestingly, we have observed key spatial differences in the entry routes of this defensin in these fungi. In N. crassa, MtDef5 induces one or more entry points on the cell surface where membrane dye FM4-64 is also co-localized. Thus, the formation of membrane-rich spatially restricted sites on cell surface causes initial injury to N. crassa and offers a mechanism for its internalization into the cytoplasm. By contrast, in F. graminearum, MtDef5 binds uniformly to the conidial cell wall before entering its cells. Thus, mechanism for entry of MtDef5 in N. crassa is different from that in F. graminearum. As shown previously for Pisum sativum defensin 111, MtDef5 also travels first to the nucleus and then becomes dispersed in the cytosol. Rapid expansion of the vacuole is observed in both F. graminearum and N. crassa culminating in its burst just before cell lysis. It is worth noting that MtDef5 and MtDef4 use different mechanisms for gaining entry into conidial cells of N. crassa as observed by live cell imaging. The mechanism of entry of MtDef5 as observed by live cell imaging of N. crassa is also very different from that of MtDef429. To what extent does translocation of this defensin into fungal cells mediates cell death remains to be determined. However, its MOA likely involves interference with metabolic processes, such as protein synthesis or DNA replication. It could also interact directly with specific membrane components.
The molecular mechanism by which MtDef5 permeabilizes the plasma membrane of fungal cells is unknown. It has been previously reported that direct interaction with plasma membrane resident phospholipids and subsequent formation of oligomeric complexes play a major role in mediating membrane permeabilization by plant defensins, NaD1, TPP3 and NsD713,15,16. The phospholipid binding assays used in our study have revealed that MtDef5 binds with high affinity to PI3P and PI4P indicating that phosphorylation on the third and fourth positions on the inositol ring are critical for lipid head group binding. Some binding to PI5P, PIP2, PI, PA and PS is also evident. MtDef5 is the first plant defensin that targets preferentially PIP. Based on the protein-lipid overlay assays, the phospholipid binding profiles of the single domain MtDef5A and MtDef5B are similar to that of the bi-domain MtDef5 (data not shown). However, determination of the quantitative differences in the binding specificity of MtDef5A and MtDef5B to specific phospholipids will require further studies. Thus, the phospholipid binding profile of MtDef5 is different from those of MtDef4 and NsD7 which bind to PA, and also different from those of NaD1and TPP3 which bind preferentially to PIP2. Plant defensins evidently utilize a broad “phospholipid code” to identify and attack fungal membranes as part of the first line of defense16.
PIP is present in tiny amounts in all eukaryotic cells. It is required for endocytic processes such as protein sorting and membrane trafficking31. In filamentous fungi, several phospholipids are found including PA, PI3P, PI4P, PI4,5P2 and PI3,5P2. Fungal hyphae are highly polarized cells and cellular morphogenesis is driven through PIP2-dependent organization at the plasma membrane of the growing tip of hypha32. As substrates for synthesis of PI4,5P2 and PI3,5P2, PIP contributes to the polar tip growth in filamentous fungi. Different roles for PIP binding by MtDef5 can be proposed: that binding of PIP present on the inner leaflet of the plasma membrane leads to oligomerization of MtDef5 and subsequent disruption of plasma membrane and that intracellular PIP may enhance the stability and antifungal activity of MtDef5 upon entry into fungal cells.
It is becoming increasingly clear that oligomerization is a critical mechanistic step underlying the antimicrobial action of defensins. The oligomerization of plant defensins, NaD1, TPP3 and NsD7, is mediated by their interaction with specific phospholipids13,15,16. Like NaD1, TPP3 and NsD7, MtDef5 also forms oligomers in presence of PI3P, PI4P and PI5P. Surprisingly, MtDef5 also forms oligomers in presence of PA and PI to which it shows very weak but detectable binding in lipid-protein interaction assays. This ability of MtDef5 to form oligomers by recognizing a broad range of phospholipids is indeed intriguing and may explain its potent broad-spectrum antifungal activity at submicromolar concentrations. NaD1 and TPP3 have been reported to oligomerize in presence of PIP2 13,15, whereas NsD7 has been reported to oligomerize in presence of PA16. Recently, both NaD1 and NsD7 have also been reported to oligomerize in presence of PA and PIP2 33. Our findings raise important questions regarding the mechanism of phospholipid-dependent oligomerization of MtDef5. It seems likely that interaction of MtDef5 with a negatively charged phospho group is perhaps sufficient to initiate the oligomerization process. MtDef5 forms nanonet-like structures in presence of PI3P (data not shown). Human α-defensin HD6 and more recently human β-defensin 1 has been reported to form self-assembled nanonets that trap bacteria and restrict their motility34,35. However, the biological significance of the PIP-dependent nanonet formation by MtDef5 remains to be determined. As reported earlier for NaD1, TPP3 and NsD713,15,16, the X-ray crystal structural analysis of the MtDef5-PIP complex will help understand the assembly process and molecular structure of nanonets. In particular, it will reveal if MtDef5 binds to PIP in a highly cooperative manner to facilitate oligomerization as reported earlier for NaD1- and TPP3-PIP2 complex formation13,15.
A major issue surrounding the functional consequences of PIP recognition and oligomer formation by antifungal plant defensins remains unresolved. To test the requirement of PIP binding and oligomerization for membrane permeabilization and antifungal activity, a 2-point site-directed mutagenesis of the γ-core motif [GACHRQG(F/I)GFAC] present in each domain of MtDef5 has been carried out. The cationic amino acids H36 and R37 in MtDef5A and H93 and R94 in MtDef5B are critical for oligomerization of MtDef5. Mutations of these amino acids to alanine completely abolished the ability of MtDef5 to induce membrane permeabilization and inhibit fungal growth. Amino acids Q38, G39, F40, G41, F42, A43 in the γ-core motif of MtDef5A and Q95, G96, I97, G98, F99, A100 in γ-core motif of MtDef5B apparently play a more minor role in mediating oligomerization of MtDef5 and consequently have relatively small but significant effect on its antifungal activity. In future, it will be important to directly identify all PIP-binding residues by performing nuclear magnetic resonance titration of MtDef5 with PIP head group or by structural analysis of the MtDef5-PIP complex using X-ray crystallography. The site-directed mutagenesis of these residues should provide further insight into mechanisms underlying the antifungal activity of MtDef5.
Based on the data presented here, we propose a multistep mechanism for antifungal action of MtDef5. This involves (1) initial interaction of MtDef5 with the fungal cell envelope, (2) binding to plasma membrane resident phospholipids, oligomerization and membrane disruption, (3) internalization into cells, induction of ROS and interaction with as yet unknown intracellular targets, and (4) cell killing. It remains to be determined if all steps are essential for antifungal activity of this defensin. Better understanding of each individual step will help elucidate its MOA in detail.
Growth of Fungal Cultures
F. graminearum PH-1 was routinely cultured on complete medium (CM)36. For production of conidia, the fungus was inoculated into carboxymethyl cellulose medium (CMC) and cultured for 2–5 days at 28 °C with shaking at 180 rpm. N. crassa was routinely cultured on Vogel’s agar media. Fusarium verticilloides, Fusarium thapsinum, Botrytis cinerea, Alternaria brassicicola and Colletotrichum higginsianum were cultured on potato dextrose agar.
Expression and Purification of MtDef5 and Its Variants
The chemically synthesized MtDef5A with four disulfide bonds was obtained from JPT Peptide Technologies (Berlin, Germany). MtDef5 and MtDef5B were generated by recombinant expression in Pichia pastoris. The codon-optimized synthetic genes encoding MtDef5 and MtDef5B were obtained from GenScript Corporation (Piscataway, NJ) and subsequently cloned into pPICZαA, as described below. MtDef5 and MtDef5B genes were cloned into the EcoRV site of pUC57. A sequence encoding the XhoI restriction endonuclease and the KEX2 protease site (CTCGAGAAAAGA) was added upstream of the mature coding sequence of each defensin. Two stop codons, along with an XbaI restriction enzyme site (TAGTAATCTAGA) were added downstream of the mature coding sequence. Synthetic genes encoding the MtDef5 γ-core motif variants were custom synthesized by GenScript (Piscataway, NJ). The synthetic genes encoding MtDef5H36A,R37A/H93A,R94A (MtDef5_V1), MtDef5Q38A, G39A/Q95A, G96A (MtDef5_V2), MtDef5F40A,G41A/I97A,G98A (MtDef5_V3) and MtDef5F42A/F99A (MtDef5_V4) were thus generated.
For expression in Pichia pastoris, the codon-optimized DNA sequences encoding the mature defensin sequence of MtDef5 and its variants and MtDef5B were cloned between the XhoI and XbaI sites of pPICZαA vector in frame with the α-factor secretion signal sequence without the Glu-Ala repeats at the Kex2 signal cleavage site. The resulting recombinant plasmid containing each defensin sequence was then linearized by digestion with SacI restriction enzyme and transformed into P. pastoris × 33 by electroporation. Transformants were initially selected on YPD (10 g/L yeast extract, 20 g/L peptone, 20 g/L glucose and 20 g/L agar) plates containing 150 µg/mL of zeocin, followed by restreaking the transformants on YPD plates containing 500 µg/mL of zeocin. Finally, transformants that survived at higher zeocin concentration were used for production of MtDef5 protein and its variants. The P. pastoris transformants were grown in liquid medium containing methanol for induction of each defensin. MtDef5, its variants and MtDef5B secreted into the medium were purified using the CM-Sephadex C-25 cation-exchange chromatography as described previously27. Fractions containing defensin were dialyzed against 50 mM Tris, pH 7.6 and subsequently lyophilized. Each lyophilized defensin was re-suspended in nuclease-free water and the protein concentration was determined by NanoDrop spectrophotometry. Purity and size of each defensin were assessed by electrophoresis on a 15% SDS-PAGE gel. From one liter of P. pastoris culture expressing each defensin, yield of approximately 3 mg of purified protein was obtained. Mass Spectrophotometry analysis of each protein sample was performed by the Proteomics and Mass Spectrophotometry Facility at the Danforth Center.
In vitro antifungal assays were performed using a synthetic fungal medium (SFM) without calcium as described previously37. Antifungal activity of MtDef5 and its variants, MtDef5A and MtDef5B was observed by taking bright-field images using the transmitted light channel in a Leica SP8-X confocal microscope. The quantitative fungal growth inhibition was estimated by measuring the absorbance at 595 nm using a Tecan Infinite M200 Pro (Tecan Systems Inc., San Jose, CA) microplate reader at different time points. Statistical data analysis was performed using Microsoft Excel (2010).
SYTOX Green (SG) Uptake Assay
SG uptake assays were conducted as described20. N. crassa and F. graminearum conidia (50 µL of 5 × 104 / mL) were allowed to germinate overnight at room temperature in Vogel’s liquid and 2X SFM media, respectively, in a 10 mm microwell of 35 mm glass bottom microwell dish with a No. 1.5 cover glass. Wet filter papers were placed in the container to prevent drying of the conidial suspension. After 16 hours, MtDef5 (50 µL, at concentrations of 0.375 µM and 0.75 µM) and 1 µL of 0.5 µM SG (Thermo-Fisher Scientific, NY) were added to fungal hyphae. Samples were incubated with gentle agitation for 2 hours in dark and mounted on a microscope for imaging. SG was excited at 488 nm and detected at 510–530 nm. A Leica SP8-X confocal microscope was used for all confocal imaging. Control plates with SG, and without MtDef5, were used as negative controls. SG uptake quantification assays of MtDef5 and its variants were performed as described previously20. Statistical data analysis was done using Microsoft Excel (2010).
Intracellular Detection of ROS
Intracellular ROS were detected on 16 h-old germinating conidia after exposure to 0.75 µM MtDef5 for 2 h. After treatment, the incubation mixtures were mixed with 2′,7′-dichlorodihydrofluorescein diacetate (H2DCF-DA, Invitogen) at 10 μM final concentration and observations were performed under a confocal microscope (Leica SP8) with the 480 and 527 nm excitation and emission wavelengths.
To test the binding properties of MtDef5 and its γ-core motif variants, a protein-lipid overlay experiment was performed using PIP StripsTM (2 × 6 cm nitrocellulose membranes) that are spotted with 100 pmol of various biologically active lipids, respectively (Echelon Biosciences, Salt Lake City, UT). To determine relative degree of the binding of MtDef5, PIP Array (P-6001, Echelon Biosciences, UT) pre-spotted with the concentration gradient of various phosphoinositides was used. The MtDef5-phospholipid interactions were detected using the affinity-purified MtDef5-derived peptide (CQKRSTTWSGP) polyclonal antibody (GenScript, Piscataway, NJ) and HRP-conjugated Goat Anti-Rabbit IgG secondary antibody following the manufacturer’s protocol with minor modifications as described previously14. The binding of the peptide polyclonal antibody to MtDef5 was confirmed by Western blot analysis (Supplemental Figure S7). The specificity of the binding of polyclonal antibody used here to MtDef5 was confirmed by Western blot analysis (Figure S8).
PolyPIPosome Binding Assay
Preferential binding of the MtDef5 and its γ-core motif variants to PIP was further validated by a liposome binding assay. PolyPIPosome binding assays were performed in 200 µL of binding buffer (20 mM HEPES pH 7.4, 120 mM NaCl, 1 mM EGTA, 1 mM MgCl2, 1 mg/mL BSA, 0.2 mM CaCl2, 5 mM KCl) containing 10 µL each of control PolyPIPosome, PI PolyPIPosome, PI3P PolyPIPosome, PI4P PolyPIPosomes and PI5P PolyPIPosome (Echelon Biosciences). Subsequently, a total of 1.25 µg each of MtDef5 and its γ-core motif variants was added and incubated for 1 h at room temperature. Liposomes were collected by centrifugation at 16, 000 × g for 20 min, and supernatant saved and the pellet was washed three times in 1 mL of binding buffer. Following three washes, pellet was resuspended in 40 µL of 2x Laemmli sample buffer and an aliquot of 20 µL of the supernatant was mixed with 20 µL of sample buffer. Both samples were reduced with 100 mM dithiothreitol (DTT) and separated on a 4–20% (Bio-Rad, TGX Stain-Free™ precast gels) SDS-PAGE gel. The proteins were visualized using a Bio-Rad ChemiDoc XRS + system. Stain-free gels contain a special Trihalo compound, which, when activated, reacts with tryptophan residues in the protein sample to emit a fluorescence signal. For SDS-PAGE, Precision Plus Dual Xtra Protein Standards (2–250 kD) from Bio-Rad (Hercules, CA) were used.
Defensin Oligomerization Assays
To determine the oligomeric status of MtDef5 and its γ-core motif variants, protein cross-linking experiments were performed in the presence or absence of PIP, PA and PI cross-linked with bis[sulfosuccinimidyl] suberate (BS3) substrate15. Briefly, MtDef5 and its γ-core motif variants, prepared in 1X PBS buffer, at 1.5 mg/ml (5 µL) were incubated with 2.73 mM PI3P, PI4P or PI5P (1.5 µL) at room temperature for 30 min. The cross-linking reaction was initiated by addition of freshly dissolved water soluble 12.5 mM BS3 (0.5 μL) and incubated for 30 min at room temperature. After crosslinking, samples were reduced with 100 mM dithiothreitol (DTT) and separated on a 4–20% (Bio-Rad, TGX Stain-Free™ precast gels) SDS-PAGE. The oligomerization pattern was visualized using a Bio-Rad ChemiDoc XRS + system. For SDS-PAGE, Precision Plus Dual Xtra Protein Standards (2–250 kD) from Bio-Rad (Hercules, CA) were used.
Live Cell Imaging
MtDef5 defensin was labeled with DyLight550 amine-reactive dye following the protocol provided by the manufacturer (Thermo Scientific, USA). Time-lapse confocal laser scanning microscopy was performed to monitor internalization and subcellular localizations of fluorescently labeled MtDef5 into N. crassa and F. graminearum cells. For time lapse imaging, N. crassa and F. graminearum conidia (50 µL of 105/mL) and germlings (4 h old) were placed in 10 mm microwell of 35 mm glass bottom microwell dishes (MatTek Corporation, Ashland, MA). Fungal conidia or germlings were treated with Dylight550-MtDef5 (50 µL of 3 µM) and labeled with either nucleic acid selective dye SG (final concentration: 0.5 µM) or membrane selective dye FM4-64 (final concentration: 5 µM) before mounting on the microscope for time-lapse imaging. Wet filter papers were placed in petri dishes to prevent drying of the conidial suspension. A Leica SP8-X confocal microscope was used for confocal imaging at room temperature in a dark room. DyLight550-MtDef5 was excited at 550 nm and fluorescence detected at 560–600 nm, SG was excited at 488 nm and detected at 510–530 nm, and FM4–64 dye was excited at 550 nm and fluorescence detected at 690–800 nm. Bright-field images were also taken with a transmitted light detector simultaneously. The laser intensity and laser exposure of the cells was kept to a minimum to reduce photobleaching and fungal cell damage. Images were analyzed using ImageJ and Bitplane Imaris softwares.
DAPI staining of MtDef5-treated F. graminearum
F. graminearum conidia germlings (50 µL of 105/mL) were incubated with Dylight550-MtDef5 (50 µL of 3 µM) for 1 h or 2 h at room temperature in 10 mm microwell of 35 mm glass bottom microwell dishes (MatTek Corporation, Ashland, MA). Fungal germlings were fixed in 4% paraformaldehyde and washed twice with PBS. DAPI stain solution was prepared by diluting 300 µM DAPI intermediate in PBS (dilution 1:1,000) to make final concentration 300 nM. Nuclear staining was performed by the addition of 100 µL of 300 nM DAPI for 15 min followed by three washes with PBS and culture dish was mounted immediately on the confocal microscope for imaging. DyLight550-MtDef5 was excited at 550 nm and fluorescence was detected at 560–600 nm and DAPI was excited at 405 nm and fluorescence was detected at 430–461 nm.
All data generated or analyzed during this study are included in this published article
(Supplementary Information files).
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We thank Drs. Shin-Cheng Tzeng and Bradley Evans of the Mass Spec and Proteomic Facility for conducting mass spec analysis of MtDef5 and its variants. We are grateful to Monsanto Company for her generous support of this work.