Identification and characterization of the Non-race specific Disease Resistance 1 (NDR1) orthologous protein in coffee
© Cacas et al; licensee BioMed Central Ltd. 2011
Received: 14 March 2011
Accepted: 24 October 2011
Published: 24 October 2011
Leaf rust, which is caused by the fungus Hemileia vastatrix (Pucciniales), is a devastating disease that affects coffee plants (Coffea arabica L.). Disadvantages that are associated with currently developed phytoprotection approaches have recently led to the search for alternative strategies. These include genetic manipulations that constitutively activate disease resistance signaling pathways. However, molecular actors of such pathways still remain unknown in C. arabica. In this study, we have isolated and characterized the coffee NDR1 gene, whose Arabidopsis ortholog is a well-known master regulator of the hypersensitive response that is dependent on coiled-coil type R-proteins.
Two highly homologous cDNAs coding for putative NDR1 proteins were identified and cloned from leaves of coffee plants. One of the candidate coding sequences was then expressed in the Arabidopsis knock-out null mutant ndr1-1. Upon a challenge with a specific strain of the bacterium Pseudomonas syringae (DC3000::AvrRpt2), analysis of both macroscopic symptoms and in planta microbial growth showed that the coffee cDNA was able to restore the resistance phenotype in the mutant genetic background. Thus, the cDNA was dubbed CaNDR1a (standing for Coffea arabica Non-race specific Disease Resistance 1a). Finally, biochemical and microscopy data were obtained that strongly suggest the mechanistic conservation of the NDR1-driven function within coffee and Arabidopsis plants. Using a transient expression system, it was indeed shown that the CaNDR1a protein, like its Arabidopsis counterpart, is localized to the plasma membrane, where it is possibly tethered by means of a GPI anchor.
Our data provide molecular and genetic evidence for the identification of a novel functional NDR1 homolog in plants. As a key regulator initiating hypersensitive signalling pathways, CaNDR1 gene(s) might be target(s) of choice for manipulating the coffee innate immune system and achieving broad spectrum resistance to pathogens. Given the potential conservation of NDR1-dependent defense mechanisms between Arabidopsis and coffee plants, our work also suggests new ways to isolate the as-yet-unidentified R-gene(s) responsible for resistance to H. vastatrix.
The genus Coffea includes about 120 species of subtropical/tropical woody perennial trees and shrubs (family Rubiaceae), of which at least two species are of worldwide agro-economic interest. Nearly 75% of world coffee production originates from Coffea arabica L., while about 20% comes from C. canephora Pierre ex A. Froehner (= C. robusta). Orange coffee leaf rust is considered to be one of the major plagues affecting C. arabica . The fungus responsible for the disease, Hemileia vastatrix Berkeley & Broome, is widely spread throughout coffee-growing countries and can cause severe defoliation, resulting in substantial berry yield losses [1, 2]. Furthermore, the two current approaches for restricting pathogen infection offer limited advantages. First, fungicide application, although cost-effective, does not always result in adequate disease control and, moreover, it has a negative environmental impact. Second, even though several varieties of coffee that are resistant to H. vastatrix have been used for introgression purposes [3, 4], such alternatives are time-consuming and do not provide durable resistance due to the rapid co-evolution of races of the fungus that harbor new virulence genes . Therefore, additional methods to control leaf rust in the fields are required.
H. vastatrix is an obligate biotrophic parasite belonging to the division Basidiomycetes, order Pucciniales . Following urediospore germination on the abaxial leaf surface, hyphae grow and penetrate intercellular spaces of the mesophyll tissue through stomatal openings before differentiating intra-cellular feeding structures, or haustoria. In susceptible coffee plants, the successful pathogen can complete its dikaryotic cycle within three weeks following infection and reach the ultimate stage, which is characterized by the formation of a sporulating sorus. In resistant plants, hyphal invasion is rapidly sensed and arrested within 2-3 days [7, 8]. Based on quantitative and Mendelian genetic studies [3, 4], the occurrence of at least nine dominant resistance (R) genes in Coffea spp., and a similar number of fungal virulence genes, have been inferred. It is thus commonly accepted that the outcome of coffee/rust interactions, whether the plant resists pathogen attack (incompatibility) or develops disease (compatibility), relies on the gene-for-gene model , which has been recently amended . Once delivered into coffee cells, H. vastatrix effector proteins, and the intracellular perturbations that they trigger, are supposed to be perceived by specific R-proteins. The recognition step promotes the launching of signaling defense pathway(s) and subsequent resistance. Alternatively, virulent rust races are believed to secrete effectors that escape or even counteract the host surveillance system, which allow for the highjacking of coffee cell metabolism and tissue colonization .
During incompatible interactions with biotrophic pathogens, the plant resistance phenotype results from the onset of a complex and multilayered-defense response, which is the so-called hypersensitive response or HR [12, 13]. Although little is still known about the molecular mechanisms that govern resistance to H. vastatrix, several studies have advanced the case for the existence of a HR-like phenomenon in coffee plants. Resistant varieties that were inoculated with avirulent fungal strains displayed a morphotype that exhibits many HR characteristics. These include rapid host cell death, which is localized at the infection site and that is associated with fungal hyphae collapse [7, 8], callose encasement of haustoria and subsequent cell wall lignification , early oxidative burst [14, 15], and the activation of typical defense-related genes [16–18].
In previous work, we performed a suppression subtractive hybridization-based screening in C. arabica that had been challenged with H. vastatrix and identified a series of Expressed Sequence Tags (ESTs) that were regulated during compatible or incompatible interactions [16, 19]. One of these ESTs shared a significant identity with the coding sequence of the NON-RACE-SPECIFIC DISEASE RESISTANCE 1 (NDR1) gene. Originally isolated in Arabidopsis thaliana, NDR1 encodes a small plasma membrane-resident protein, the deficiency of which was found to abolish HR and confer susceptibility to some fungal and bacterial pathogens carrying specific effector genes [20–22]. Notably, it has been established that NDR1-driven resistance is dependent on a specific subset of R-proteins (such as RPM1, RPS2 and RPS5) that are defined by the presence of a coiled-coil (CC) structure within their N-terminal parts . From a mechanistic perspective, the best characterized example illustrating NDR1 function is the pathosystem involving strain DC3000::AvrRpt2 of the plant pathogenic bacterium Pseudomonas syringae pv. tomato (Pst). In this model, under resting conditions, AtNDR1 indirectly retains the RPS2 protein on the cytosolic side of the plasma membrane through its interaction with the RPM1-INTERACTING PROTEIN 4 (RIN4), thereby preventing HR activation . Upon infection with Pst, the bacterial protease AvrRpt2 is secreted into the cytoplasm where it can cleave RIN4, releasing RPS2 and initiating a disease resistance signaling pathway .
In this study, we cloned two C. arabica candidate cDNAs for NDR1 and analyzed the deduced primary amino-acid sequences. Domain conservation and the high degree of homology between the coffee proteins and AtNDR1 led us to undertake a genetic complementation approach. Using the Arabidopsis ndr1-1 null mutant, we obtained genetic and molecular evidence that at least one of our candidate genes is a functional NDR1 ortholog. Both laser-confocal microscopy and biochemical analyses further suggested that the protein is likely to be attached to the plasma membrane via a glycosylphosphatidylinositol-anchor. Based on these data, the possibility that a NDR1-contingent mechanism could be invoked in R-gene-mediated resistance to H. vastatrix is discussed. The impact this result could have in the context of resistance improvement is also outlined.
Cloning and analysis of a novel NDR1 sequence homolog fromCoffea arabica
In previous work , we used a subtractive hybridization approach to identify genes involved in defense/resistance of coffee plants (C. arabica L.) to the orange rust fungus H. vastatrix. Of the 9 ESTs which were significantly up-regulated during HR, one displayed 43% identity with the canonical NDR1 coding sequence from A. thaliana. In this study, we focused our efforts on the coffee candidate for NDR1 gene and isolated two distinct full-length transcripts by nested RACE-PCR. The corresponding cDNAs were cloned as described in the 'Methods' section (CaNDR1a [GenBank:DQ335596], CaNDR1b [GenBank:DQ335597]). Open reading frames differed from one another by only 3 single nucleotide positions with one of the substitutions being non-silent (F69L). Both sequences were predicted to encode proteins that were 214 amino acids long, which shared a calculated molecular weight of 23.8 kDa and an isoelectric point of 9.58.
Ectopic expression of CaNDR1a in Arabidopsis ndr1-1 null mutant restores specific resistance to Pseudomonas syringae pv. tomato (DC3000::AvrRpt2)
From our in silico analysis, the question arises as to whether the two identified coffee genes are functional homologs of AtNDR1 or code for distinct NHL counterparts. To answer this question, a genetic complementation approach was undertaken. Given the high degree of identity between the two predicted CaNDR1 amino-acid sequences, we decided to study CaNDR1a and expressed the corresponding ORF under the control of the CaMV35S promoter in the Arabidopsis ndr1-1 null mutant. Segregation analysis on a selective medium allowed for the isolation of single-locus, homozygous insertion lines (see additional file 2 for segregation results). T3 lines were then screened by RT-qPCR for high steady-state levels of transgene transcripts and three of them were selected for further experiments. The expression level of CaNDR1a in these lines, designated T3-1, T3-2 and T3-3, was respectively 92-, 190-, and 714-fold higher than that of the endogenous AtNDR1 gene, when compared to WT Col-0 plants grown under the exact same conditions.
The mature CaNDR1a protein is C-terminally processed
Two to three days post-infiltration with an Agrobacterium strain, which was dedicated to the expression of the HA-CaNDR1a-His construct, protein extracts prepared from fresh tissues were resolved by SDS-PAGE and immunoblotted using either HA- or His-specific antisera as described in the 'Methods' section. Immunoblot conditions were tested using a N-terminally HA-tagged CaNDR1a (HA-CaNDR1; Figure 5a) and C-terminally His-tagged Bax Inhibitor 1 (BI1-His) versions as controls. Six independent experiments including independent Agrobacterium infiltrations and protein extractions were carried out. Using anti-HA antibody, only one major band was detectable in lanes loaded with NDR1 samples (Figure 5b, lanes 3-6), whereas no specific signal was visualized in lanes loaded with negative control samples (Figure 5b, lanes 1, 2 & 7). Although the nucleotide sequences of HA-CaNDR1a and HA-CaNDR1a-His code for proteins with predicted molecular weights averaging 25-26 kDa, the detected proteins migrated to approximately 45 kDa under denaturating conditions. Such an apparent discrepancy is not surprising based on previous work. Coppinger and coworkers , indeed, showed that the native AtNDR1 protein resolved by SDS-PAGE displays a mass of about 48 kDa instead of the predicted 24.6 kDa. These authors further demonstrated that the protein regains its theoretical size when translated in vitro without the machinery dedicated to glycosylation, indicating that the latter post-translational modification could account for the migration shift of the mature proteins on polyacrylamide gels. Consistently, the CaNDR1a protein, like its Arabidopsis ortholog, exhibits a significant number of putative glycosylation sites (Figure 4). Hence, one can assume that our protein extracts (Figure 5b, lanes 3-6) are likely to contain glycosylated forms of CaNDR1a, the migration behavior of which is altered on polyacrylamide gels.
Finally, using the same set of samples and anti-His antibody, we were unable to detect HA-NDR1-His protein (Figure 5b, lanes 4-6), whereas BI1-His protein (31 kDa) was clearly identified (Figure 5b, lane 7). The latter data indicate that CaNDR1a is C-terminally processed in tobacco leaves, which strongly suggests that the protein is modified by addition of a GPI moiety. Further experiments are nevertheless needed to confirm this assumption.
CaNDR1a is localized to the plasma membrane
Identification of a potential homologous RIN4 protein from coffee plants
The Arabidopsis ndr1 locus was identified in the late 1990's using a forward genetic screen based on the loss of resistance to the Pst strain DC3000::AvrRpt2 [20, 21]. Since then, NDR1 homologous genes have been found by sequence comparison in other plant species such as Brassica napus  and Vitis vinifera . Many sequence homologs (around 19 non-redundant hits within 11 plant species) can also be retrieved from the GenBank database by means of the BLAST P algorithm (data not shown). However, to our knowledge, our data constitute a novel report on the identification and characterization of a functional NDR1 homolog, despite the plethora of orthologous candidates.
In this study, several lines of evidence indeed demonstrated that ectopic expression of CaNDR1a coding sequence was able to rescue the phenotype of the Arabidopsis ndr1-1 null mutant. Upon infection with DC3000::AvrRpt2, the three mutant lines expressing the coffee transgene were found to develop hypersensitive cell death symptoms that were absent in mutant plants (Figure 3a). This macroscopic study was further corroborated by two independent in planta bacterial growth assays showing that leaf populations of the bacterial pathogen in our transgenic lines were low and comparable to those of WT plants (Figure 3b). In addition, high overexpression level of the coffee CaNDR1a gene in the Col-0 genetic background was also found to confer enhanced disease resistance to the DC3000 strain, as previously reported when the AtNDR1 gene was overexpressed in A. thaliana .
Importantly, NDR1-driven resistance in A. thaliana is not restricted to bacterial pathogen attacks. Two reports have demonstrated that the ndr1 mutation renders plants susceptible to infection by the oomycete Hyaloperonospora arabidopsidis  and the fungus Verticillium longisporum . Therefore, given that (i) CaNDR1a is a functional homolog of the Arabidopsis NDR1 gene, and (ii) transcripts of the former accumulate in coffee leaves undergoing HR in response to the fungus H. vastatrix [16, 19], it would not be surprising if NDR1 proteins could regulate the defense signaling pathway(s) leading to coffee rust resistance. This hypothesis is currently under investigation in our laboratory using a functional approach. Recently, we also showed that A. thaliana Col-0 plants display a rapid non-host response to H. vastatrix. This response is reminiscent of HR in that it prevents haustorium formation and hyphal spread in plant tissues . This work raises the possibility of testing the role of NDR1 in response to the coffee leaf rust in the A. thaliana heterologous system.
As predicted by our bioinformatic analysis, imaging of GFP6-tagged CaNDR1a protein by confocal microscopy revealed a fluorescent pattern that was consistent with a plasma membrane localization (Figure 6b, (i)). Colocalization experiments with a PM fluorescent protein marker also supported this observation (Figure 6b, (iv-vi)). Furthermore, the need of an anionic detergent like sodium dodecyl-sulfate for the HA-tagged CaNDR1a proteins to be extracted from tobacco leaves (Additional file 4) indicated an association with membranes. Finally, our biochemical approach based on the purification of PM by two-phase PEG/dextran partitioning (Figure 7b,c) clearly demonstrated the presence of HA-CaNDR1a proteins in tobacco PM fractions. Therefore, it is likely that the mature CaNDR1a protein resides in the plasma membrane of coffee cells.
No fluorescent labeling of the organelle corresponding to a GFP6 spectrum was observed in chloroplasts, although it had been reported previously for a tagged version of AtNDR1 . Instead, internal reticulated labeling reminiscent of the ER network (Figure 6b, (iii)) was observed in a few cases and may correspond to cells overloaded with the ectopic fluorescent proteins. This observation is consistent with our results, suggesting that the CaNDR1a protein could be modified by addition of a GPI moiety to its C-terminal part (Figure 5b). It has been well-described that proteins tethered to the cell surface by means of a GPI anchor undergo this sort of post-translational modification in the ER before being sorted via the secretory pathway to their final destination, i.e., the plasma membrane.
Usually, GPI-anchored-proteins are also thought to locate on the apoplasm side of the plasma membrane . In A. thaliana, it has been clearly established that NDR1 is attached to the plasma membrane through a C-terminal GPI anchor . It has also been inferred that the N-terminal portion of NDR1 lies within the cytoplasm because it was found to interact with the cytosolic protein RIN4 in planta . Since the C-terminal anchor of AtNDR1 is resistant to cleavage by phospholipase C, these data further led to the hypothesis that the protein possesses a transmembrane-spanning domain as a second anchor site. This was recently corroborated by a modelling study  and, in fact, the coffee protein, like its Arabidopsis relative, was predicted to present a single transmembrane domain (Figure 4), suggesting a similar, but atypical topology of the two counterparts (Figure 8b).
Recently, a new mode of action of NDR1 was revealed by Knepper et al. . Based on structural homology with mammalian integrins and the Arabidopsis late embryogenesis abundant (LEA) protein 14, known to be involved in abiotic stress response , the aforementioned authors investigated the possibility that AtNDR1 may control cell integrity through PM-cell wall adhesions. Besides its well-characterized role as a key signaling component during pathogen attack, a broader function for NDR1 is strongly suggested by the data in mediating primary cellular functions in Arabidospsis through maintenance of PM-cell wall connections . From these unexpected results, the question arises as to whether or not CaNDR1a could perform a similar function in C. arabica.
Interestingly, upon inoculation with DC3000::AvrRpt2, successful activation of HR required NDR1-RIN4 physical interaction. Further examination using an alanine-scanning mutagenesis strategy revealed that two amino acid residues within the N-terminal part of NDR1 were necessary for the interaction . Despite the apparent lack of conservation of these two amino acid determinants within the CaNDR1a end (Figure 8c), our results showing that the coffee gene was able to restore RPS2-mediated resistance in the ndr1-1 mutant tend to prove that CaNDR1a does interact with AtRIN4 in our transgenic lines. Thus, this raises the possibility that mechanism(s) whereby NDR1 proteins exert their function could be conserved in Arabidopsis and coffee plants.
Consistent with this idea, searching for RIN4 sequence homologs in the HarvEST© Coffea database resulted in the identification of a candidate contig from Coffea canephora. The deduced protein shows, within its N-terminal portion, a highly conserved region with the members of the RIN4 family, as well as a putative conserved canonical AvrRpt2 cleavage site (Figure 8a). Nonetheless, further experiments are needed to answer the question as to whether or not CaNDR1a, like its Arabidopsis ortholog, could serve as a PM anchor that indirectly recruits R-protein(s) via its interaction with RIN4-like intermediates (Figure 8b) [24, 46]. Split-ubiquitin and yeast two-hybrid systems, combined with bimolecular fluorescence complementation (BiFC), would be useful tools for tackling this question. This might also be a faster and more convenient strategy, as opposed to classical genetic approaches, for the isolation of R-gene(s) conferring resistance to H. vastatrix. To date, no coffee R-gene(s) have been isolated despite the efforts of the coffee research community [3, 4]. The reproductive barriers affecting genetic exchanges between diploid coffee species and the allopolyploid C. arabica have thus far prevented the successful isolation of the loci responsible for resistance to H. vastatrix through a map-based cloning strategy .
The functional and biochemical characterization of the orthologous NDR1 protein from C. arabica that we have carried out represents a crucial step towards the elucidation of the molecular events underpinning resistance to coffee rust. It should help identify new players in the coffee NDR1-dependent signaling pathway(s) in the near future, and might thus be crucial for the engineering of transgenic coffee plants with broad spectrum resistance to H. vastatrix races. The development of efficient techniques to transform and propagate coffee varieties renders these biotechnological approaches feasible [47, 48].
Plants and growth conditions
Tobacco plants (Nicotiana benthamiana) that were used for transient expression experiments were grown in a greenhouse, at 150 μmol/m2/s light radiance, with a 14/10 h, 23/20°C light-dark cycle, and 60% relative humidity.
Wild-type Arabidopsis thaliana ecotype Columbia (Col-0), ndr1-1 null mutants , and transgenic lines expressing CaNDR1a were all grown in a growth chamber under short-day conditions (10 h photoperiod, 100 μmol/m2/s light fluency), at 22/20°C day/night with 80% relative humidity. Pathogen challenge conditions are described hereafter.
Isolation and cloning of CaNDR1a/b cDNA
As previously described , the 5' end of the CaNDR1 cDNA that is referred to as DSS12 had already been sequenced (Genbank:CO773976). 3'-RACE PCR was thus conducted to determine the sequence of the full-length cDNA. Total RNA (1 μg) isolated from C. arabica cv. caturra leaves that had been challenged with H. vastatrix for 18 hours were first reverse-transcribed using the Smart CDS primer and a combination of the Omniscript RT (Qiagen, Courtaboeuf, France) and SMART PCR cDNA synthesis kits (Clontech, Mountain View, CA, USA). RACE assays were then performed using specific oligonucleotides designed in the 5' non-coding region (3R-NDR1, 5'-CTACTTTGTTCACTGGTAGTCCCTC-3'; n3R-NDR1, 5'-CATAATACTTCACCGGAGAACCACC-3') and the 5'PCR Smart primer (Clontech). The resulting 1-kb PCR product was cloned into the pGEM-Teasy vector (Promega, Charbonnières-les-bains, France) and finally sequenced (Genome Express, Grenoble, France).
To assess the complementation of the Arabidopsis null mutant ndr1-1 , the open reading frame of CaNDR1a was cloned into the binary vector pCAMBIA 1305.1 (Cambia, Brisbane, Australia) downstream of the strong and constitutive 35S promoter of the cauliflower mosaic virus. For this purpose, the iud gene was removed from the vector by restriction digestion with BglII and BstEII enzymes. The coding sequence of CaNDR1a was amplified by PCR (DAP Goldstar DNA polymerase, Eurogentec, Seraing, Belgium) using the corresponding pGEM-T clone (GenBank:DQ335596) as a template and the following primers: CaNDR1-BglII 5'-TCAGATCTTATGGACAAAGGATGGGGC-3', and CaNDR1-BstEII 5'-TAGGTCACCAAATTAATTCCCAGGAAA-3'. Digested PCR products were then ligated into the binary vector to get the final construct.
To test the hypothesis that the C-terminal part of CaNDR1a is removed from the mature protein, single- and double-tag constructs were created (Figure 5). CaNDR1a was amplified by PCR using a high fidelity DNA polymerase according to the manufacturer's instructions (PfuTurbo, Stratagene, La Jolla, CA, USA). The following primer couple was used for directly adding haemaglutinin (HA) and poly-histidine (His) sequences to the 5'- and 3'-ends of the PCR products, respectively: CaNDR1-Forward 4, 5'-CACC ATG TAT CCC TAC GAC GTA CCA GAT TAT ATG TC AGA CCC CAG CAG CAG TGC-3' and CaNDR1-Reverse 3, 5'-CTA ATG GTG ATG GTG ATG GTG CAA CAG CAG AAC CAA GAA A-3'. The primers used for obtaining the single HA-tagged version were CaNDR1-Forward 4 and CaNDR1-Reverse 2 (5'-CTA CAA CAG CAG AAC CAA GA-3'). PCR fragments were then subcloned into the pENTR-D/TOPO vector (Invitrogen, Cergy Pontoise, France) and sequenced. To get directional cloning, the underlined nucleotide sequence was added to the forward primers. Selected clones were digested with Mlu-I restriction enzyme (R0198L, NEB, OZYME, Saint Quentin Yvelines, France) before overnight recombination with the binary vector pMDC32  using the LR Clonase II kit (Invitrogen).
The N-terminally GFP6-tagged version was produced to examine the subcellular localization of CaNDR1a. PCR products were amplified, subcloned, sequenced and recombined with the binary vector pMDC43  as described above. Primers used for the initial PCR step were as follows: CaNDR1-Forward 1, 5'-CACC ATG TCA GAC CCC AGC AGC AGT-3' and CaNDR1-Reverse 2. The vector used for in planta expression of the plasma membrane fluorescent marker (mCherry-tagged protein) was purchased from the Arabidopsis Biological Resource Center (ABRC) at Ohio State University (Stock # CD3-1008) .
Final binary constructs were all sequenced (Genome Express) prior to transformation into Agrobacterium tumefaciens by heat shock or electroporation methods. Bacterial strain GV3101 was used for transformation of Arabidopsis plants by floral dipping according to . Strain LBA1119 was used for transient expression experiments in tobacco plants.
Pathogen challenge and growth curve assays
The Pseudomonas syringae pv. tomato (Pst ) strain DC3000 and the isogenic strains expressing the bacterial effector proteins AvrRpt2 or AvrRps4 were provided by Dr. Jane Glazebrook (University of Minnesota) . For pathogen challenges, bacteria were grown overnight at 28°C under mild shaking in liquid King B medium. Pst DC3000 bacteria were selected with rifampicin (50 μg mL-1); DC3000::AvrRpt2 and Pst DC3000::AvrRps4 with rifampicin and tetracycline (10 μg mL-1). Bacteria were collected by centrifugation and resuspended at 2 × 105 CFU mL-1 in physiological water (9 g NaCl/L) prior to inoculation.
Progeny of Arabidopsis ndr1-1 T0 plants (ndr1-1::CaNDR1a) were screened on half-strength Murashige and Skoog medium supplemented with 30 μg mL-1 hygromycin. Transformation of individual resistant seedlings was confirmed by PCR using genomic DNA as the template and CaNDR1a-specific primers (CaNDR1-BglII and CaNDR1-BstEII). Homozygous single locus insertion lines were then isolated by following segregation of hygromycin-resistant plants in T2/T3 generations (Additional file 2). To assess ndr1-1 complementation, three independent T3 lines displaying distinct expression levels for CaNDR1a (designated T3-1, T3-2 and T3-3) were challenged with Pst and in planta bacterial growth was followed over a four-day period (0, 2 and 4 dpi). Wild type (Columbia, Col-0) and ndr1-1 plants were also inoculated for comparison. Negative controls were infiltrated with physiological water. Half-leaves (6 to 7-week-old plants) were hand-infiltrated with a 1-mL needleless syringe. Two independent experiments that gave similar results were carried out. Each experiment comprised four replicates that were each performed by different individuals. In one replicate, each plant genotype (5 plants/genotype) was infiltrated with water or suspensions of Pst DC3000, Pst DC3000::AvrRpt2 or Pst DC3000::AvrRps4. Upon infiltration, plants were immediately placed in a tray covered with a plastic dome that was removed at 24 hours post-inoculation. Bacterial growth was monitored as follows. At each time point, two leaves (per plant) were harvested and ground with a mortar and pestle. The resulting mixture was serially diluted in sterile physiological water and plated onto solid King B medium supplemented with the appropriate antibiotics. The bacterial population was scored two days upon plating. Inoculation data were square-root transformed prior to ANOVA and subsequently subjected to the Student-Newman-Keuls multiple comparison test. When transformation failed to satisfy assumptions of normality and homoscedasticity, the non-parametric Kruskal-Wallis test was used.
Hypersensitive and disease symptoms were also visually assessed in an independent experiment using higher concentrations of bacterial suspension (2 × 107 CFU mL-1) for infiltration. Samples from this experiment were also harvested for RT-qPCR analysis.
RNA extraction, reverse transcription and real time quantitative-polymerase chain reaction
Expression of AtNDR1 and CaNDR1a was measured as previously described  with the specific primers (Additional file 5) that were previously used . Each assay was conducted in duplicate and included a negative control without template. The strong and constitutive actin gene (At3g18780) was chosen as internal control for normalization. Specificity of amplification was estimated by analyzing melting-temperature curves. Calculations for gene expression quantification were carried out using the comparative cycle-threshold method, as described previously .
Agrobacterium tumefaciens-mediated transient expression
Ten mL Agrobacterium cultures were grown overnight under mild shaking at 30°C in regular Luria-Bertani medium containing 25 μg mL-1 rifampicin, and 50 μg mL-1 kanamycin when necessary. Bacteria were collected the following day by centrifugation. Pellets were resuspended in induction buffer (20 mM MES pH5.5, 10 mM MgSO4, 200 μM acetosyringone) so that OD600 nm of the solution reaches 0.5-0.6. Upon incubation at room temperature for 3 hours, the bacterial suspension was infiltrated onto the abaxial side of Nicotiana benthamiana leaves (4 to 6-week-old plants) using a needleless syringe. Samples for western blot analysis and microscopy studies were harvested 2-3 dpi. Each experiment included a transformation control that was carried out by infiltrating a bacterial clone containing a 35S::uidA intron construct . Histochemical beta-glucuronidase (GUS) staining was performed according to  using X-Gluc (5-bromo-4-chloro-3-indolyl-beta-D-glucuronic acid) as substrate.
Protein colocalization by confocal microscopy
Subcellular localization of CaNDR1a was assessed by means of a transient expression system as described in the above sections. Overnight grown bacterial suspensions (GFP6-fused CaNDR1a and mCherry-fused marker) were individually induced and then mixed at 1:1 ratio before infiltration into tobacco leaves. Induction buffer and individual bacterial suspensions were also infiltrated as controls. Two to three days post infiltration, leaf disks (1.2 cm diameter) were punched from the infiltrated area and directly observed with a LSM 510 Meta Zeiss upright laser scanning confocal microscope (Objective C-Apochromat 40X/1,2 water, 488 nm laser and 505-530 band-pass filter to GFP, 543 nm laser and 585-615 band-pass filter to mCherry). Spectral imaging was obtained with a 488 nm laser on the Meta detector. After Lambda stack acquisition between 500 and 640 nm, the Linear Unmixing Function of confocal microscope discriminates between the fluorescence of GFP and mCherry in cells from reference spectra of these molecules obtained on leaves from GFP or mCherry plants (method of Emission Fingerprinting from Zeiss). The autofluorescence of chlorophyll was detected via a 650-nm long pass filter. The images were coded green (GFP) or red (mCherry). The experiment was repeated five times (each replicate included at least two infiltrated leaves per plant and three independent plants).
Plasma membrane purification
To unambigously determine the subcellular localization of CaNDR1a proteins, the HA-tagged version of CaNDR1a was ectopically expressed in N. benthamiana leaves under conditions described above. Plasma membrane was prepared from infiltrated leaves at 2 dpi and purified by two-phase PEG/dextran partitioning, as previously described . The purity of PM fractions was checked by assessing the enrichment of the endogenous PM-resident protein PMA2. Western blotting conditions for PMA2 are described in the next section.
Protein extraction, SDS-PAGE and immunoblotting
Protein samples were isolated by a two-step extraction protocol. Briefly, frozen leaf tissues (1 g fresh weight) were ground in ice-cold buffer 100 mM, pH 8.0, Tris buffer (50 mL) containing 1 mM ethylenediamine tetraacetic acid, 1 mM dithiothreitol and a protease inhibitor cocktail (1 tablet for 100 mL of buffer, Complete Mini, Roche Diagnostics, Meylan, France). Mixtures were centrifuged for 40 min at 12,000 × g at 4°C. Protein concentration of supernatants was determined according to  using BSA as a standard. Overnight acetone precipitation was performed in order to concentrate samples. Upon western blot analysis, these crude extracts comprising the main soluble proteins appeared to contain neither of the two HA-tagged CaNDR1 versions. Mono- and polytopic membrane proteins were then extracted by resuspending the pellet in 400 μL of extraction buffer in the presence of 2% (w/v) sodium dodecyl sulphate (SDS) (Additional file 4). Mixtures were warmed in a water bath at 70°C for 15 min and centrifuged for 25 min at 18,000 × g at room temperature. Pellets were discarded. Concentration of supernatant proteins was determined using the bicinchoninic acid assay (B-9643/C-2284, Sigma-Aldrich, Saint-Quentin-Fallavier, France) according to the manufacturer's instructions. Protein samples were loaded onto 12.5% polyacrylamide gels to be separated by SDS-PAGE. Proteins were transferred for immunoblot analysis by electroblotting onto nitrocellulose membranes (0.45 μm, Hybond, GE Healthcare, Saclay, France) using X Cell II™ Blot Modules (Invitrogen). Successful transfer of proteins was checked by staining with a Ponceau S solution. Membranes were then incubated overnight at 4°C under mild shaking in a Tris-buffered saline solution containing 4% (w/v) dry milk (Cat. # 170-6404, Bio-Rad, Marnes-la-Coquette, France) and 0.2% (v/v) Tween 20. They were probed with anti-HA-HRP (Cat.# A00169, GenScript Corporation, Paris, France) or anti-(His)5-HRP (Cat.# 34460, Qiagen) antibodies to detect epitope-tagged proteins. Both antibodies were used at a 1:2000 dilution.
Protein samples used as positive controls for His blots were prepared from Arabidopsis transgenic lines constitutively overexpressing a C-terminally His-tagged version of AtBI1 . Seeds were kindly provided by Dr. Eric Lam (Biotechnology Center for Agriculture and the Environment, Rutgers University, USA). Proteins were extracted as described by the authors . Freshly harvested leaves were directly ground in Laemmli buffer , warmed at 95°C for 5 min and centrifuged. The resulting supernatant was resolved by SDS-PAGE and blotted like other protein samples. The expected size of epitope-tagged AtBI1 is about 31 kDa.
Microsomal and plasma membrane samples were resolved by SDS-PAGE and transferred onto PVDF membranes for immunoblotting under the exact same conditions as other protein samples. HA-CaNDR1a detection was carried out as described above. When membranes were probed with antibodies raised against PMA2 (1:16.000 dilution) , a goat anti-rabbit antibody coupled to HRP (Cat.# 656120, Invitrogen) was used as secondary antibody at a 1:2000 dilution. To test for the presence of HA-CaNDR1a, membranes probed with the PMA2-specific antiserum were then stripped off in the electrophoresis SDS-PAGE migration buffer in the presence of β-mercaptoethanol (28 mM final concentration) at 50°C for 30 minutes. Membranes were then blocked and reprobed with anti-HA-HRP antibodies.
Searches for CaNDR1 sequence homologs in the GenBank database were performed by means of Basic Local Alignment Search Tools, or BLAST , available online at the National Center for Biotechnology Information (http://ncbi.nlm.nih.gov/). Sequences were aligned using the ClustalX algorithm (version 2.0.10)  and further processed online at the BoxShade server (http://www.ch.embnet.org/software/BOX_form.html). The phylogenetic tree was built using Phylowin freeware using the neighbor-joining method . Putative GPI-anchor attachment sites were identified using the Big-Pi Plant Predictor (http://mendel.imp.univie.ac.at/sat/gpi/plant_server.html) [30, 31]. The occurence of signal peptides and transmembrane domains within primary amino-acid sequences was assessed using SignalP-3.0 (http://www.cbs.dtu.dk/services/SignalP/) [32, 33]; that of glycosylation sites was predicted using NetNGlyc 1.0 (http://www.cbs.dtu.dk/services/NetNGlyc/). The freeware Mwcalc was used for calculations of the theoretical protein molecular weight and isoelectric point (http://sourceforge.net/search/?q=mwcalc). Subcellular localization of proteins was predicted using the PSORTII program . ChloroP1.1  was also used for checking for the absence of putative chloroplast-targeting sequences in our proteins of interest. HarvEST© software that was used to identify the coffee RIN4-like protein is available online at http://harvest.ucr.edu/.
List of abbreviations
bimolecular fluorescence complementation
expressed sequence tag
Harpin-induced gene 1
Non-race specific Disease Resistance 1
polymerase chain reaction
Pseudomonas syringae pv. tomato
- R-gene Resistance:
Rapid Amplification of cDNA ends
RPM1-interacting protein 4.
The Arabidopsis null mutant ndr1-1 was a generous gift from Dr. Brian J. Staskawicz (University of California, Berkeley, CA, USA). Arabidopsis His-tagged Bax Inhibitor 1 lines were kindly provided by Dr. Eric Lam (Biotechnology Center for Agriculture and the Environment, Rutgers University, New Brunswick, NJ, USA). Construct CD3-1008 (mCherry plasma membrane marker) was purchased from the Arabidopsis Biological Resource Center (Ohio State University, Columbus, OH, USA). We wish to thank Dr. Jane Glazebrook (University of Minnesota, St. Paul, MN, USA) for providing the virulent and avirulent strains of Pseudomonas syringae pv. tomato used in this study (DC3000, DC3000::AvrRpt2 and DC3000::AvrRps4). We are grateful to Drs. Patrick Moreau and Su Melser for their contributions to the microscopy study. We also thank the Bordeaux Imaging Center (BIC, Université Bordeaux 2, UMS 3420 CNRS-US4 INSERM, Bordeaux, France). We also wish to warmly thank Drs Mark Diamond, and Jean-Luc Montillet for critically reading the manuscript, as well as Drs. Alison D Munson, Mark Diamond and William FJ Parsons for English editing. This work was partially supported through a bilateral cooperative agreement between France and Brazil (CAPES-COFECUB n° Sv 555/07). We declare no conflicts of interest with any work cited in this study.
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