|Identification of defensin-encoding genes of Picea glauca: characterization of PgD5, a conserved spruce defensin with strong antifungal activity.|
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|PMID: 23035776 Owner: NLM Status: MEDLINE|
|BACKGROUND: Plant defensins represent a major innate immune protein superfamily that displays strong inhibitory effects on filamentous fungi. The total number of plant defensins in a conifer species is unknown since there are no sequenced conifer genomes published, however the genomes of several angiosperm species provide an insight on the diversity of plant defensins. Here we report the identification of five new defensin-encoding genes from the Picea glauca genome and the characterization of two of their gene products, named PgD5 and endopiceasin.
RESULTS: Screening of a P. glauca EST database with sequences of known plant defensins identified four genes with homology to the known P. glauca defensin PgD1, which were designated PgD2-5. Whereas in the mature PgD2-4 only 7-9 amino acids differed from PgD1, PgD5 had only 64% sequence identity. PgD5 was amplified from P. glauca genomic DNA by PCR. It codes for a precursor of 77-amino acid that is fully conserved within the Picea genus and has similarity to plant defensins. Recombinant PgD5, produced in Escherichia coli, had a molecular mass of 5.721 kDa, as determined by mass spectrometry. The PgD5 peptide exhibited strong antifungal activity against several phytopathogens without any effect on the morphology of the treated fungal hyphae, but strongly inhibited hyphal elongation. A SYTOX uptake assay suggested that the inhibitory activity of PgD5 could be associated with altering the permeability of the fungal membranes. Another completely unrelated defensin gene was identified in the EST library and named endopiceasin. Its gene codes for a 6-cysteine peptide that shares high similarity with the fungal defensin plectasin.
CONCLUSIONS: Screening of a P. glauca EST database resulted in the identification of five new defensin-encoding genes. PgD5 codes for a plant defensin that displays non-morphogenic antifungal activity against the phytopathogens tested, probably by altering membrane permeability. PgD5 has potential for application in the plant biotechnology sector. Endopiceasin appears to derive from an endo- or epiphytic fungal strain rather than from the plant itself.
|Pere Picart; Anna Maria Pirttilä; Dora Raventos; Hans-Henrik Kristensen; Hans-Georg Sahl|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2012-10-05|
|Title: BMC plant biology Volume: 12 ISSN: 1471-2229 ISO Abbreviation: BMC Plant Biol. Publication Date: 2012|
|Created Date: 2012-11-20 Completed Date: 2013-04-30 Revised Date: 2013-07-11|
Medline Journal Info:
|Nlm Unique ID: 100967807 Medline TA: BMC Plant Biol Country: England|
|Languages: eng Pagination: 180 Citation Subset: IM|
|Institut für Mikrobiologie und Biotechnologie, der Universität Bonn, Meckenheimer, Allee, Bonn, 167, 53115, Germany. firstname.lastname@example.org|
|APA/MLA Format Download EndNote Download BibTex|
Amino Acid Sequence
Antifungal Agents / pharmacology*
Cations / pharmacology
Cell Membrane Permeability / drug effects
Defensins / chemistry, genetics*, pharmacology*
Fungi / drug effects
Genes, Plant / genetics*
Microbial Sensitivity Tests
Molecular Sequence Data
Open Reading Frames / genetics
Organic Chemicals / metabolism
Peptides / genetics
Picea / cytology, drug effects, genetics*
Protein Stability / drug effects
Recombinant Proteins / biosynthesis, isolation & purification
|0/Antifungal Agents; 0/Cations; 0/Defensins; 0/Organic Chemicals; 0/Peptides; 0/Recombinant Proteins; 0/SYTOX Green|
Journal ID (nlm-ta): BMC Plant Biol
Journal ID (iso-abbrev): BMC Plant Biol
Publisher: BioMed Central
Copyright ©2012 Picart et al.; licensee BioMed Central Ltd.
Received Day: 22 Month: 6 Year: 2012
Accepted Day: 28 Month: 9 Year: 2012
collection publication date: Year: 2012
Electronic publication date: Day: 5 Month: 10 Year: 2012
Volume: 12First Page: 180 Last Page: 180
PubMed Id: 23035776
Publisher Id: 1471-2229-12-180
|Identification of defensin-encoding genes of Picea glauca: characterization of PgD5, a conserved spruce defensin with strong antifungal activity|
|Pere Picart1||Email: email@example.com|
|Anna Maria Pirttilä2||Email: firstname.lastname@example.org|
|Dora Raventos3||Email: DRAV@novozymes.com|
|Hans-Henrik Kristensen3||Email: HAHK@novozymes.com|
|Hans-Georg Sahl1||Email: email@example.com|
1Institut für Mikrobiologie und Biotechnologie, der Universität Bonn, Meckenheimer, Allee, Bonn, 167, 53115, Germany
2Department of Biology, University of Oulu, Linnanmaa, Oulu, PO Box 3000 A6, FIN-90014, Finland
3Novozymes A/S, Krogshoejvej, Bagsvaerd, 36, DK-2880, Denmark
Plants are exposed to a diverse array of pathogens and pests and their survival depends on different mechanisms for self-defense. Such defenses include physical cell wall barriers , as well as the production of a diverse range of molecules which can inhibit the growth of microbial pathogens [2-6]. Among the latter, cationic antimicrobial peptides such as defensins, are a most relevant and large family of defense compounds [7-9].
Plant defensins are characterized as small globular, basic, cysteine-rich proteins (45–54 amino acids), containing a triple-stranded antiparallel β-sheet and one α-helix that are stabilized into a compact shape by four disulfide bridges [10-14]. These bridges form a cysteine-stabilized α-helix β-sheet motif (CSα/β) that is well conserved in peptides with antimicrobial activity. Two additional structural motifs have been described in the plant defensin structure, namely the α-core, encompassing the loop connecting the first β-strand and the α-helix, and the γ-core containing the hairpin loop connecting β-strands 2 and 3 (Lβ2β3) [15,16]. Despite the tertiary structure being strongly conserved in plant defensins, the similarity on the primary sequence level is limited to eight cysteine residues, two glycines, one aromatic residue and a glutamic acid in the defined positions . Variations in the amino acid sequences are reflected by small changes in the spatial display of the loops that contribute to the wide range of biological activities observed in these peptides, as a single amino acid substitution can change the spectrum of activity.
Unlike the insect and mammalian defensins, which are mainly active against bacteria [2,8,18,19], plant defensins, with a few exceptions, do not exhibit antibacterial activity . They inhibit the growth of a broad spectrum of fungal plant pathogens, such as Fusarium oxysporum, Verticillium dahliae and Botrytis cinerea, but also of Saccharomyces cerevisiae and human pathogenic fungi such as Candida albicans at very low concentrations in vitro. The precise mode of action of plant defensins is still unclear, and for most plant defensins the molecular components involved in signaling and putative intracellular targets remain unknown [21,22]. Only for the defensin Rs-AFP2 from Raphanus sativus and the defensin Dm-AMP1 from Dahlia merckii, a putative target in the fungal membrane has been identified [23,24]. More recently, it was demonstrated that plant defensins can be internalized into the cytoplasm and interact with specific intracellular targets [25,26]. Moreover, some members of the plant defensins family were found to have additional activities in vitro. These include the inhibition of α-amylase [27-29], protein translation [30,31] and proteases , as well as zinc tolerance mediators in plant , ion channel blockers [34,35], enzymatic activity involved in ascorbic acid redox state [36,37] and activity towards mammalian cells [38-40].
Plant defensins and their antimicrobial effects have been reported from many angiosperm plants, including monocots and dicots. The genome of Arabidopsis thaliana contains 14 different defensin genes that respond to various stresses . However, polypeptides with similar properties have not been well studied in gymnosperms. The availability of a substantial expressed sequence tag (over 300 000 ESTs) resource developed for Picea glauca[41,42] has resulted in the identification of only one expressed defensin gene, PgD1, and one antifungal protein . This prompted us to perform a wide bioinformatics analysis to screen for novel spruce defensins.
Here, we describe the identification of new Picea defensin genes, and the characterization of one of the defensin peptides, PgD5. The identification of new defensins from P. glauca expands our knowledge on conifer genomics and raises interest to study the potential of spruce defensins as fungicidal agents.
The P. glauca EST database was first screened with the amino acid sequence of Picea glauca defensin 1 (PgD1, GenBank:AAR84643) by the TBLASTN program. TBLASTN is especially suitable for the discovery of distant homologues with a conserved sequence motif . This initial screening yielded four different EST hits, GQ03918_C16, GQ02811_I12, GQ03707_G02 and GQ01307_A13, which shared similarity to PgD1. The complete coding sequences of the isolated ESTs were then named P. glauca defensin 2 to 5 (PgD2-5), respectively. When the deduced coding sequences of the new PgDs were compared to PgD1, high similarity was observed for PgD2-4 with 83-86% sequence identity (Figure 1A). In contrast, only 60% identity was observed when PgD1 was compared with PgD5.
Alignment analysis of the deduced amino acid sequences of PgD2-5 revealed that PgD2 codes for a precursor of 83 amino acid with the highest similarity to defensin 3 from Pinus sylvestris [GenBank:JN980401] at the 93% similarity level (data not shown). PgD3 and PgD4 code for 83 amino acid peptides sharing 100% and 99% identities with an unknown protein from Picea sitchensis [GenBank:ABK21016], respectively (data not shown). The deduced amino acid sequences of PgD3 and PgD4 were identical, except for a substitution of Ser for Gly in position 73 (numbering according to PgD1 from P. glauca) (Figure 1A). PgD5 codes for a precursor of 77-amino acids. Alignment of the deduced amino acid sequence revealed that the mature region of PgD5 shares high similarity with members of the gymnosperms, displaying 64% homology to both the Scots pine defensin 2 [Swiss-Prot:A4L7R8.1]  and the defensin 1 from Picea glauca [GenBank:CAA62761.1] , respectively, as well as to unrelated plant defensins from different families (Figure 1B). For instance, it displays 62% similarity to defensin vv-AMP1 from Vitis vinifera and 62% similarity to putative defensin 1 from Olea europaea. PgD5 shares 12 conserved amino acids, including eight cysteine and two glycine residues, as well as one glutamic acid and one aromatic residue at conserved positions. These amino acids are common to all plant defensins . Disulphide-bridge analysis done with DIpro confirmed that the eight cysteine residues of PgD5 are connected by four disulfide bridges (Figure 1B).
When the P. glauca EST database was further screened with the amino acid sequences of several other gymnosperm defensins, no additional new defensins were identified. Surprisingly, screening of the P. glauca EST database with the amino acid sequence of plectasin [Swiss-Prot:Q53I06.1]  yielded one EST hit, GQ0132.B7_K03, which shared 58% similarity to plectasin ( Additional file 1). The complete coding sequence of EST GQ0132.B7_K03 was 273 bp in size and codes for a predicted 90-amino acid peptide. SignalP results showed that the first 20 amino acids code for a signal peptide followed by a 30-amino acid pro-peptide and a mature peptide of 40 amino acids ( Additional file 2). Comparative analysis of the deduced amino acid sequence of mature peptide with other members of the defensin family revealed that the peptide shares a disulphide bridge pattern common to defensins of fungi, insects and other invertebrates [50,51]. It contains three disulphide bridges in contrast to all plant defensins that typically have four disulphide bridges ( Additional file 3).
The most distantly related PgD5 and the gene encoded within EST GQ0132.B7_K03 were selected for further analysis. In both cases, the cDNA library containing the corresponding genes was exclusively isolated from actively elongating roots tips free of mycorrhiza.
Primers were designed based on the EST GQ01307_A13 sequence and PCR was carried out to amplify the complete coding sequence of PgD5 using genomic DNA of P. glauca. Genomic amplification of the sample resulted in a product of about 330 bp and a comparative analysis with the EST GQ01307_A13 revealed that a 96 bp-intron interrupts the predicted signal peptide (Figure 2A). SignalP analysis showed that the first 27 amino acids code for a signal peptide followed by a 50-amino acid mature peptide (Figure 2B). PA-SUB predicted that the signal peptide of PgD5 directs its product to the extracellular space of plant cells. The peptide parameters obtained from the Expasy-Compute pI/Mw tool showed that PgD5 has a predicted mono-isotopic mass of 5721.56 Da and is highly basic with a net charge of +5 and an isoelectric point above 8.9. Seven different spruce species, namely P. glauca and P. mariana (native to North America), P. smithiana, P. wilsonii and P. orientalis (native to Asia), and P. abies and P. omorika (native to Europe) were selected to isolate the corresponding putative defensins from genomic DNA. PCR reactions resulted in amplification of seven genomic copies of PgD5, which were sequenced. Alignment analysis of these genomic sequences revealed a very high level of similarity (99%) between the sequences at nucleotide level where the majority of mismatches occurred in the intron region ( Additional file 4). The sequences at the deduced amino acid level were 100% identical, indicating that the peptide is fully conserved within the genus Picea.
In the case of endopiceasin, primers were designed based on the EST GQ0132.B7_K03 sequence and PCR was carried out to amplify the complete coding sequence of the mature peptide using genomic DNA of P. glauca. Genomic amplification was unsuccessful as no product was obtained. These results suggest that the defensin is not encoded by the plant genome itself and we suggest to designate this defensin as endopiceasin.
Comparative modeling of the deduced amino acid sequence suggested that the tertiary structure of PgD5 closely resembles that of NaD1, a floral defensin from Nicotiana tabacum (UniProtKB:P32026). These defensins contain an invariant tetradisulfide array and have the common cysteine-stabilized α/β structure (CSα/β) composed of three antiparallel β-strands and one α-helix which are organized in a βαββ configuration (Figure 3A). Analysis of the PgD5 primary sequence identified γ-core and α-core motifs , as shown in Figure 3B.
The His6-SUMO-PgD5 fusion was successfully expressed in E. coli BL21 (Origami pLys S) DE3. The recombinant fusion protein of 18 kDa was efficiently produced in soluble form and purified to > 90% purity by Ni-NTA column chromatography in a single step (Figure 4A). The SUMO-tag was removed by the Sumo protease. The resulting protein products were further purified using a C18 reversed phase chromatography column and a TFA/acetonitrile gradient. Recombinant PgD5 eluted at 23.6 min (at 38% solvent B) while the digested SUMO-tag eluted at 38.2 min (at 52% solvent B) (Figure 4B). SDS-PAGE analysis confirmed that PgD5 was successfully separated from the cleaved tag and purified to homogeneity (Figure 4A). The purified peptide was further characterized by MALDI-TOF-MS. MALDI-TOF-MS analysis yielded a mass of 5721.56 Da for the purified peptide, which is 8 Da less than the theoretical mass calculated with the Expasy-Compute pI/Mw tool of 5729.66 Da (Figure 4C). These data indicate that the four disulphide bridges which are common to all plant defensins were correctly formed. Incubation of the peptide in 2 mM DTT reduced the disulphide bridges and completely inactivated the peptide.
Antifungal activity of PgD5 was assayed by microspectrophotometry using a dose–response growth inhibition assay. PgD5 significantly inhibited the fungal growth over time in all fungal isolates tested even at very low concentrations. PgD5 was most active against V. dahliae (Figure 5A) and B. cinerea (Figure 5B), with IC50 values of 2 μg/mL and 4 μg/mL, respectively. However, PgD5 was less effective against F. oxysporum with an IC50 value of 11 μg/mL (Figure 5C). Treatment of V. dahliae spores, the causal agent of wilting disease, with a peptide concentration of 3 μg/mL resulted in > 90% growth inhibition, and a concentration of 8 μg/mL completely arrested spore germination (data not shown). The antifungal activity of PgD5 was also determined in vitro with a plate assay on Rhizoctonia solani. As illustrated in Figure 5D, there are inhibition zones of R. solani in areas containing sterile discs of filter paper on which various concentrations of purified PgD5 were applied. Distilled water served as the negative control.
One characteristic feature of many cationic antimicrobial peptides is their ability to permeabilize the plasma membrane of target organisms. We examined membrane permeabilization using the fluorometric SYTOX Green dye, which is taken up only by cells with compromised plasma membrane. Microscopical analyses of fungal hyphae treated with PgD5 did not reveal increased hyphal branching and morphologically altered hyphae that are typically induced by some plant defensins [7,50,52] (Figure 6). However, PgD5 strongly inhibited elongation of fungal hyphae. By measuring the SYTOX green uptake by fluorescence microscopy we observed that PgD5 induced membrane permeabilization in the three fungi tested. Hyphae of Pgd5-treated B. cinerea, F. oxysporum and V. dahliae had strong fluorescence in the cytosol (Figure 6M-O), especially in the nuclei, when compared to the untreated fungi that showed no fluorescence (Figure 6E-G). The ability of PgD5 to permeabilize the plasma membrane was also tested in S. cerevisiae. By fluorescence microscopy, Pgd5-treated S. cerevisiae cells showed strong SYTOX Green fluorescence in the cytosol (Figure 6P) as compared to negative controls (cells grown without peptide) (Figure 6H), indicating that PgD5 also induced membrane permeabilization in the yeast cells. In contrast to these findings, PgD5 was not active against Candida albicans at the concentration of 50 μg/mL (data not shown).
PgD5 was tested for its stability at various temperatures using the antifungal growth assay against V. dahliae. PgD5 was remarkably stable at temperatures of up to 100°C. Seventy one percent of its antifungal activity was retained after 30 min of treatment at 75°C and 61% at 100°C (Figure 7A). Analysis of the effect of monovalent and divalent cations on antifungal activity of PgD5 showed that the divalent cation Ca2+ diminished about 50% the antifungal activity of the peptide at the concentration of 5 mM. The monovalent cation K+ had no effect on the antifungal activity of PgD5 at the concentration of 50 mM (Figure 7B).
Plant defensins are a prominent family of cationic peptides that are ubiquitous among the plant kingdom and represent an important part of the plant innate immune system. Previously, only two antifungal proteins have been described in P. glauca. The first PgD1 (Picea glauca Defensin 1), is a plant defensin of 50 amino acids that displays antifungal activity against Cylindrocladium floridanum, Fusarium oxysporum, and Nectria galligena at 14 μg/mL . The second is an embryo-abundant protein of 109 amino acids that shares 85% similarity with an antifungal protein of Ginkgo biloba but lacks the characteristic features of plant defensins.
In the present work, the screening of the P. glauca EST database using the TBLASTN algorithm resulted in identification of five new defensin-encoding genes (Figure 1 and Additional file 1). In addition to expanding the list of existing spruce defensins, our research on P. glauca defensins and their encoding genes gives insight into conifer biology and genomics. Our results show that the habitual family of defensins found in angiosperms  is also present in gymnosperms, giving another example of the high diversity of plant defensins.
Defensins are expressed in different plant tissues including leaves, pods, tubers, fruits, roots, bark and floral organs [2,8,19]. They provide specific defensive capacity to the plant. The cDNA library containing the EST GQ01307_A13 and EST GQ0132.B7_K03 was constructed from mRNA exclusively isolated from actively elongating roots tips free of mycorrhiza, indicating that PgD5 and endopiceasin genes might be expressed in a tissue-specific manner, only in the roots. To the best of our knowledge, these peptides are, along with defensin SPI1 from Norway spruce (Picea abies) , the only reported plant defensins that are expressed exclusively in the plant root system.
Endopiceasin resembles the structure of classical defensins of fungi, insects and invertebrates with 6 cysteine residues connected by three disulphide-bridges that stabilize the CSαβ motif [2,8,55-57]. PCR for isolation of endopiceasin did not result in a product and efforts to amplify the gene by changing the PCR conditions were unsuccessful. DNA isolated from higher plants may originate from symbiotic microbes called endophytes occupying plant tissues at surprisingly high frequencies. Accordingly, few reports have described DNA sequences attributed to gymnosperms and angiosperms, which actually belong to specific endophytes [58,59]. We believe that EST GQ0132.B7_K03 present in P. glauca cDNA library originates from an endophyte or epiphytic fungal strain colonizing the root system of P. glauca. Experiments are in progress to further identify the origin of the endopiceasin peptide. In this context, the high degree of similarity between endopiceasin and plectasin might be of special interest because plectasin is a potent peptide antibiotic with strong therapeutic potential [49,51]. We also confirmed the similarity of endopiceasin to plectasin by analysing its mode of action. Endopiceasin was only active against gram-positive bacteria and its activity was based on inhibition of cell wall biosynthesis and lipid II binding (manuscript in preparation). In fact, endophytes that colonize internal plant tissues as mutualists have a role in protection of the plant against pathogens , and our report indicates that antibacterial defensins from endophytes might play a significant role in such protection.
PgD5 showed high similarity at amino acid level with related and unrelated plant defensins of the Gymnospermae family (Figure 1B), which supports the idea of a common origin of plant defensins. The presence of a typical secretion signal peptide is one of the characteristic features of plant defensins . Based on the precursor protein structure, PgD5 groups with Class I of the defensin family , containing an N-terminal signal peptide followed by the mature defensin domain. This is in contrast to Class II defensin peptides which have an additional C-terminal prodomain.
PgD5 appears completely conserved within the genus Picea. There are many reports of plant defensins showing more than 96% identity within the same genus and differing only by one or two amino acids [62-64], which turns into different antimicrobial activities. However, to our best knowledge, this is the first report on a plant defensin being fully conserved within a genus or, at least, within the seven different Picea sp. analyzed in this work. This suggests a very specific role for the PgD5 gene being highly conserved during evolution of the genus Picea.
PgD5 exhibited strong antifungal activity inhibiting growth of hyphae of four agronomically important pathogens: B. cinerea, an airbone pathogen of broadleaved and coniferous trees; R. solani, a soilborne pathogen of economically important agricultural plants and F. oxysporum and V. dahliae, which are the leading causes of wilting disease (Figure 5). Based on the structural and functional similarity, PgD5 was included into the ‘’non-morphogenic” group of plant defensins, which slow down hyphal elongation but do not induce marked morphological distortions [8,18,47]. The activity exerted by PgD5 against the phytopathogenic fungi and S. cerevisiae was linked to alteration of fungal membrane permeability. The nuclei of these permeabilized hyphae appeared intact and the cytoplasm unaltered with no signs of granulation of the hyphal cytoplasm, which is observed in some defensins. However, PgD5 was not active against C. albicans at concentration of 50 μg/mL. Probably PgD5 interacts with essential plasma membrane structures of S. cerevisiae that are not present in C. albicans, causing a structural disruption and alteration of the membrane permeability. However, more studies are necessary to discern whether the permeabilization itself is a result of the interaction of the plant defensins with components of the membrane, or with an intracellular target or signaling pathway triggered by the peptide .
The antifungal potency of a peptide in the presence of cations is of particular importance for evaluation of defense capacity against microorganisms in plants. Most plant defensins show little or no antifungal activity in the presence of monovalent and divalent cations in the growth medium at concentrations above 50 or 5 mM, respectively [20,64,65]. In these conditions, the interaction of plant defensins with their binding site dictates the specificity of the antifungal activity observed [21,22,66]. In the present study, PgD5 was shown to be highly heat stable and the antifungal activity against V. dahliae was unaffected in the presence of monovalent cation K+ and moderately affected in the presence of divalent cation Ca++ (Figure 7). This makes PgD5 an attractive candidate in the fields of agricultural biotechnology and therapeutic drug design, with possible application as a transferable resistance trait for molecular breeding of crop plants.
Screening of a EST database of P. glauca resulted in the identification of four homologues of PgD1, designated PgD2-5, and endopiceasin which is probably of fungal origin. PgD5 codes for a defensin that is fully conserved within the genus Picea. Recombinant PgD5 displayed non-morphogenic antifungal activity, possibly associated with membrane permeabilization, at low concentrations against several fungal plant pathogens. The strong antifungal activity of PgD5 against V. dahliae even in high-ionic-strength medium is of special interest, making PgD5 an attractive candidate for engineering pathogen-resistant crops.
Leaves from Picea glauca were collected from the botanical garden of the University of Oulu, Oulu (Finland). Escherichia coli DH5α (maintained in our laboratory) was used for cloning and plasmid amplification. E. coli BL21 (origami pLys S) DE3 (Novagen, USA) was used as the expression host. Candida utilis and Saccharomyces cerevisiae were obtained from our collection in the Pharmazeutische Mikrobiologie des Universitatsklinikums, Bonn, Germany. Yeasts were maintained on potato dextrose agar (PDA). Rizoctonia solani (CBS 340.58), Fusarium oxysporum (CBS 619.87), Botrytis cinerea (CBS 125.58) and Verticillium dahliae (CBS 110272) were purchased from the CBS-KNAW Fungal Biodiversity Center in Utrecht, Netherlands. Fungi were also maintained in PDA at 25°C until sporulation. Spores were harvested in dH2O and spore concentration was determined using a Thoma chamber.
Plant defensin-encoding sequences were discovered by screening the P. glauca EST database of the National Centre for Biotechnological Information (NCBI) using TBLASTN. This database was screened using the amino acid sequences of Picea glauca defensin 1 [GenBank:AAR84643], Ginkgo biloba defensin 1 [GenBank:AY695796.1], Pinus sylvestris defensin 1 [GenBank:EF455616.1], Pinus sylvestris defensin 2 [GenBank:EF455617.1], Pinus sylvestris defensin 3 [GenBank:JN980401.1] and Pseudoplectania nigrella defensin [plectasin, Swiss-Prot:Q53I06.1]. Primers were designed based on the EST clones GQ01307_A13 and GQ0132.B7_K03 to identify the complete coding sequences encoded within the ESTs.
Genomic DNA was isolated from P. glauca leaves. Leaf tissue was collected, frozen in liquid nitrogen and ground to a fine powder using mortar and pestle. The DNA was extracted by the CTAB method .
The genomic DNA isolated from P. glauca was used as the template in PCR to isolate the complete coding sequences of PgD5 and endopiceasin. The two primer sets used were forward primer PgD5F (5’-ATGGAGAAGAGAATGGGCAG-3’) and reverse primer PgD5rev (5'-TTAACAGGGTTTCTCGCAGA-3') for PgD5, and EST_K03F (5’- ATGAAG TTCACCATCTCCATC-3’) together with reverse primer EST_K03rev (5’-CTAGTAGCACTTGCAAGTGGT-3’) for endopiceasin. Amplification conditions were 95°C for 3 minutes, 30 cycles: 95°C for 1 min, 58°C for 45 s, 72°C for 45 s and final extension at 72°C for 7 minutes. The gel-eluted (QIAquick PCR Purification Kit, Qiagen) amplification products were ligated into the pGEM®-T vector (PROMEGA Corporation, Madison, USA) and submitted for sequencing to Eurofins MWG Operon. Nucleotide and deduced amino acid sequence comparisons were made using the BLAST algorithm.
Leaves from several Picea species (P. abies, P. smithiana, P. mariana, P. orientalis, P. omorika and P. wilsonii) were collected from the botanical garden of the University of Bonn, Bonn (Germany) and genomic DNA was isolated as described above. Gene homologues of PgD5 were isolated from the different Picea species as described above. Genomic sequences obtained for the different Picea species were analyzed and aligned using ClustalX .
The deduced amino acid sequence of PgD5 was produced in VectorNTi and analyzed using the BLASTP algorithm. Homologous sequences identified were further aligned using ClustalX . The deduced PgD5 sequence was also subjected to disulfide bridge analyses using DiANNA ; secondary structure analysis as well as homology modeling was done using the I-TASSER server [70,71]. The peptide structure of PgD5 was evaluated for the presence of a signal peptide sequence with SignalP  and sub-cellular localization directed by signal peptide was predicted on the Proteome Analyst Specialized Sub-cellular Localization Server (PA-SUB) . The peptide mass prediction was done with the Expasy tool, PEPTIDE-MASS .
The Champion™ pET SUMO Expression System was purchased from Invitrogen and used for the recombinant production of PgD5 in E. coli BL21 (Origami pLys S) DE3. This system allows for the production of a His6-tag at the N-terminus of the SUMO protein followed by mature PgD5 at the C-terminus (His6-SUMO-PgD5). pGEM-T-PgD5 served as the template to prepare the mature PgD5 sequence by PCR. The expected 153-bp fragment encoding the mature form of PgD5 was amplified with the primer set mPgD5FWD (5’-CGGATGTGTGAGTCGCAGA-3’) and mPGD5rev (5’-TTAACAGGGTTTCTCGCAGA-3’). The gel-eluted amplification product was ligated into the linearized pET-SUMO T/A vector and termed pET-SUMO/PgD5. pET-SUMO/PgD5 was transformed into E. coli DH5α and the identity and the correct orientation of the sequence was confirmed by sequencing.
The pET-SUMO/PgD5 plasmid that had been constructed was transformed into E. coli (Origami pLys S) DE3 expression strain and bacterial colonies were selected by plating onto Luria-Bertani (LB) agar with 25 μg/mL kanamycin, 34 μg/mL chloramphenicol and 12.5 μg/mL tetracycline. A single colony was inoculated to 10-mL LB medium containing antibiotics and grown overnight at 37°C. The overnight cultures were diluted 1:50 (v/v) in 1L of the same medium without antibiotics and grown in the shaking incubator at 37°C and 200 rpm until an optical density (OD600) of 0.6. Protein expression was induced by adding 0.4 mM IPTG and subsequent culturing at 25°C overnight with shaking. Cells were harvested by centrifugation at 10,000xg for 15 min at 4°C and the pellets were stored at −80°C until protein extraction.
Each gram of pelleted cells (wet weight) expressing His6-SUMO-PgD5 was resuspended in 10 mL BugBuster Protein Extraction Reagent (Novagen) according to the manual, complemented with 1 mM PSMF. The suspensions were gently mixed to facilitate cell lysis and centrifuged at 10,000xg for 20 min at 4°C. The supernatant was applied to the pre-equilibrated Ni-NTA column with binding buffer (50 mM NaH2PO4, 500 mM NaCl, 20 mM imidazole, pH 7). After extensive washing with binding buffer, the fusion protein was eluted with eluting buffer (50 mM NaH2PO4, 500 mM NaCl, 250 mM imidazole, pH 8). The eluted fractions containing the fusion protein were pooled and dialyzed overnight at 4°C against 10 mM Tris–HCl containing 150 mM NaCl, pH 8, and concentrated to a final 1–5 mL volume. The recombinant PgD5 was digested with 1U SUMO protease per 50 μg fusion protein in the presence of 0.5 mM DTT for 1h at 30°C.
Reverse phase-HPLC was used for the final PgD5 purification step using a reverse-phase C18 column (0.46 cm × 25 cm). The chromatography was performed at a flow rate of 1 mL/min and elution was carried out with a linear gradient from 100% solvent A (TFA 0.1%) to 60% of solvent B (100% acetonitrile containing 0.1 % TFA) over 40 min. The eluate was monitored by on-line measurement of the absorbance at 220 nm. Eluted peptide was freeze-dried, dissolved in distilled water at a final concentration of 100 μg/mL and stored at −20°C.
The purity of eluted PgD5 was evaluated by separating 1 μg peptide on a 15% [w/v] Tris-Tricine gel ; after separation the peptide band was visualized by staining with SimplyBlue™ SafeStain (Invitrogen). The molecular mass of purified peptide was analyzed on a MALDI-TOF-MS system (BIFLEX III, Bruker Daltonics GmbH). Aliquots of 1 μL were mixed with 2 μL of α-cyano-4-hydroxycinnamic acid and spotted onto a ground-steel MALDI target plate (Bruker Daltonics GmbH) and air dried at room temperature. Spectra were recorded in the linear mode at a laser frequency of 20 Hz within a mass range of 1000–6000 Da and further analyzed using FlexAnalysis (version 2.0) software (Bruker Daltonics, GmbH). The spectra were externally calibrated using peptide standards. The mass obtained for the peptide was compared to the predicted mono-isotopic mass of the peptide generated with the Expasy-Compute pI/Mw tool.
The activity of PgD5 against the yeasts S. cerevisiae and C. albicans was determined using the microbroth dilution method in a 96-well microtiter plate (Nunc U96 microtiter plates) . Briefly, wells were filled with 50 μl of serial dilutions of the peptide and mixed with 50 mL of Potato Dextrose Broth (PDB) containing 2x106 colony forming units (CFU/mL). The 20 mM Tris solution (pH 8.0) was added as the negative control. Experiments were performed at least in three replicates. Microbial growth was assessed by measuring the optical density at 600 nm after 16 h incubation at 30°C without shaking. The minimal inhibitory concentration (MIC) was defined as the lowest concentration of peptide that induced no change in optical density.
Quantitative antifungal activity of PgD5 was assessed using a microspectrophotometric assay in a 96-well microtiter plate (Nunc F96 microtiter plates)  with the following fungal pathogens: F. oxysporum, B. cinerea and V. dahliae. Each well contained 1000 fungal spores in 100 μl half-strength Potato Dextrose Broth (PDB) and purified PgD5 at concentrations ranging from 1 to 50 μg/mL. Control reactions contained no peptide. Plates were incubated in the dark at 23°C for 3 days, with microspectrophotometric readings taken every 24 hours at A595. PgD5 defensin activity was scored after 48 h in the case of the fungi F. oxysporum and B. cinerea and after 72 h in the case of V. dahliae, and was expressed as a percentage of growth inhibition. Growth inhibition percentage is defined as 100 × the ratio of the A595 of the control minus the A595 of the sample over the A595 of the control . IC50 is defined as the protein concentration at which 50% inhibitions was reached.
Antifungal activity was also tested in vitro against the fungus R. solani. Fungal discs of uniform size were inoculated at the center of the Petri dish containing about 15 mL PDB and incubated at 25°C. When the mycelia reached 6 cm in diameter, sterile Whatman no.1 filter paper discs (1 cm diameter) were placed on the plate at equal distances from the center. Various quantities of purified PgD5 were added to each disk. The plates were incubated at 25°C and observed periodically until the mycelial growth had enveloped control discs containing sterile distilled water growth inhibition zones had formed around the discs containing active preparations of PgD5.
The ability of PgD5 to cause plasma membrane permeabilization was measured by SYTOX GREEN (Molecular Probes; Invitrogen Corp, Carlsbad, CA, USA) uptake as described previously  on F. oxysporum, B. cinerea and V. dahliae. The permeabilization assay consisted of 200 mL half-strength PDB containing fungal spores (2 × 104 spores/mL) and PgD5 peptide at concentrations of 11 μg/mL for F. oxysporum, 4 μg/mL for B. cinerea and 2 μg/mL for the V. dahliae isolate. Fungal strains were incubated at 25°C in the presence of PgD5 for 48 hours. Control samples contained no PgD5. After incubation the samples were washed with 0.1M Tris–HCl, pH 8 and stained with 0.2 μM SYTOX Green in 96-well microplates for 30 min at 25°C with periodic agitation, followed by observation in a phase-contrast microscope (Axiophoto Zeiss) equipped with a fluorescence filter set for fluorescein detection (excitation wavelengths, 450 to 490 nm; emission wavelength, 500 nm). Intracellular fluorescence is indicative of a compromised fungal membrane. SYTOX Green uptake in S. cerevisiae was measured similarly, except the cell density was approximately 2x108 cells per mL, and incubation was 1h at 30°C in the presence of PgD5 at a concentration of 11 μg/mL.
The stability of the purified PgD5 peptide was assessed by an antifungal assay as described above. The heat stability of the peptide was assessed at the final peptide concentration of 2 μg/mL against V. dahliae spores, with the peptide being pretreated at 25°C, 50°C, 75°C and 100°C for 30 min, before starting with the antifungal assay. The activity of PgD5 was scored against the control reaction conducted at 25°C. In a similar assay, the effect of the presence of cations on the antifungal activity of PgD5 was also tested. The cations were added to the medium at concentrations of 10 mM and 50 mM for KCl, and 1 mM and 5 mM for CaCl2. The effect of monovalent and divalent cations on PgD5 activity was scored against the control reaction conducted without cations.
HGS and HHK supervised the work and helped with conceptual design and manuscript preparation as well as final data analysis. PP, AMP and DR performed conceptual and experimental design and PP was responsible for all the research procedures, data analysis and writing the paper. The authors declare no conflicts of interest. All authors read and approved the final manuscript.
Alignment analysis of the deduced amino acid sequence ofendopiceasindiscovered by database searches. EST GQ0132.B7_K03 (endopiceasin) was found by screening the P. glauca EST database using the amino acid sequence of plectasin. The percentage similarity compared to plectasin is indicated in the last column.
Additional file 2
The complete coding sequence and the deduced amino acid sequence ofendopiceasinencoded within the EST GQ0132.B7_K03. The underlined amino acids represent the signal peptide, the amino acids in red indicate the pro-peptide while blue amino acids indicate the mature peptide.
Additional file 3
Alignment of the mature region of endopiceasin with other members of the defensins family. Alignment analysis of endopiceasin. The percentage similarity compared to endopiceasin is indicated in the last column. [Swiss-Prot:Q53I06.1] plectasin from fungi Pseudoplectania nigrella; [GenBank:BAB41027.1] defenisn A from arthropod Ornithodoros moubata; [GenBank:ABI52817.1] defensin B from arthropod Argas monolakensis. The six-cysteine residues are indicated by yellow and the disulphide bridge pattern is shown below.
Additional file 4
Alignment analysis ofPgD5genomic copies isolated from differentPiceasp. The differences between the sequences are indicated by yellow. The intron sequences are indicated in lowercase.
We would like to thank the following members of the Institut für Mikrobiologie und Biotechnologie der Universität Bonn, M Josten for the LC-MS analysis, Dr P Saas for the live cell imaging microscopy and I Stock for revising the manuscript. The work was financially supported by the Marie Curie Industry-Academia Partnership and Pathways (IAPP) funded by the EU 7th Framework Programme for Research and Technological Development, New Antimicrobials (NAM) Project Project (PIAP-GA-2008-218191).
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Keywords: Spruce defensins, Endophyte, Antifungal activity, Membrane permeabilization.
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