A Virulence Essential CRN Effector of Phytophthora capsici Suppresses Host Defense and Induces Cell Death in Plant Nucleus

Phytophthora capsici is a soil-borne plant pathogen with a wide range of hosts. The pathogen secretes a large array of effectors during infection of host plants, including Crinkler (CRN) effectors. However, it remains largely unknown on the roles of these effectors in virulence especially in P. capsici. In this study, we identified a cell death-inducing CRN effector PcCRN4 using agroinfiltration approach. Transient expression of PcCRN4 gene induced cell death in N. benthamiana, N. tabacum and Solanum lycopersicum. Overexpression of the gene in N. benthamiana enhanced susceptibility to P. capsici. Subcellular localization results showed that PcCRN4 localized to the plant nucleus, and the localization was required for both of its cell death-inducing activity and virulent function. Silencing PcCRN4 gene in P. capsici significantly reduced pathogen virulence. The expression of the pathogenesis-related gene PR1b in N. benthamiana was significantly induced when plants were inoculated with PcCRN4-silenced P. capsici transformant compared to the wilt-type. Callose deposits were also abundant at sites inoculated with PcCRN4-silenced transformant, indicating that silencing of PcCRN4 in P. capsici reduced the ability of the pathogen to suppress plant defenses. Transcriptions of cell death-related genes were affected when PcCRN4-silenced line were inoculated on Arabidopsis thaliana, suggesting that PcCRN4 may induce cell death by manipulating cell death-related genes. Overall, our results demonstrate that PcCRN4 is a virulence essential effector and it needs target to the plant nucleus to suppress plant immune responses.


Introduction
During plant-pathogen interactions, pathogens secrete an array of effector proteins to aid infection and establishment of parasitic lifestyles by modulating host cell defenses [1][2][3]. At the same time plants defend themselves through several mechanisms of local immune system of each cell and systemic acquired resistance (SAR) of the whole plant [1,2]. The plant immune system and its interplay with pathogen effectors are widely illustrated as a four-stage zigzag model. When plants are attacked by microbes, they recognize microbe or pathogen-associated molecular patterns (PAMPS) which elicits PAMP-triggered immunity (PTI). Effective microbes have evolved a huge and diverse effector repertoires to counter PTI by suppression and subsequently enhance susceptibility (Effector-triggered susceptibility, ETS) [1,4]. A dynamic interaction between host immune responses and pathogen effectors has been widely reported in different pathosystems [5,6]; and identifying pathogen effectors and discovering their functions have become as essential routes to understand pathogen establishment.
Phytophthora pathogens encode a large number of effectors to interfere with host plant cell physiology and function. They belong to the fungus-like oomycetes, which are evolutionarily closely to algae in the kingdom Stramenopila [7,8]. Phytophthora species are arguably the most destructive pathogens of many dicotyledonous plants and contain many well-known pathogens including P. capsici [9,10]. P. capsici is a broad-host-range pathogen, and may cause damage to many economically important vegetables including all cucurbits, pepper, tomato and eggplant. The disease occurrence and acuteness have significantly increased in recent decades worldwide [10]. However, its pathogenesis mechanisms are still largely unknown. Similar to other wellstudied Phytophthora pathogens, such as P. infestans and P. sojae, P. capsici also encodes a large number of host cytoplasmic effectors, including 357 putative RXLR (Arg-any amino acid-Leu-Arg) and 84 CRN (Crinkler, Crinkling and necrosis inducing protein) effectors [11]. The RXLR effectors contain a conserved N-terminal motif that is involved in translocation inside host cells [12,13] and C-terminal domains that may manipulate plant immunity responses [5,14].
CRN effectors are another group of pathogen proteins presumed to enter the host cytoplasm [15,16]. Interestingly, CRN effectors are also modular proteins. Their N-termini contain the predicted signal peptide and a conserved motif, FLAK (F, Phe; L, Leu; A, Ala; and K, Lys), which is essential for effector translocation to host cells [17]. The C-terminal effector domains have various functions, such as inducing cell death (CD) and suppressing host immunity [15,[18][19][20]. They usually target host cell nucleus to efficiently exert their biological functions [17,20]. Analyses of three necrosis-inducing CRN effector domains (DN17, D2, and DXZ) revealed differences in the timing and occurrence of cell death in N. benthamiana [21]. Several CRN effectors studied so far have shown that they enhance pathogen virulence. For example, CRN8 with a functional RD kinase enhanced virulence of P. infestans when it was expressed in planta. In contrast, its dominant-negative CRN8 R469A;D470A resulted in reduced virulence [22]. Liu et al. have demonstrated that silencing of PsCRN63 and PsCRN115 jointly in P. sojae led to a reduction of virulence on soybean [18]. In a recent study, N. benthamiana expressing PsCRN70 gene increased its vulnerability to P. parasitica [23]. However, the virulence mechanisms of P. capsici CRN effectors are mostly unknown.
In this report, a P. capsici CRN effector PcCRN4 was identified by cell death-inducing assay in planta. It can induce CD on the tested plants and the encoding gene was dramatically induced at the infectious stages. Silencing the genes in a stable transformant leads to a significant reduction of virulence on plants and its transient expression in planta enhances plant susceptibility. Furthermore, ROS accumulation, callose deposition and expressions of PR1b and CD-related genes were altered in plants inoculated with the PcCRN4-silenced transformant. Collectively, we propose a role for CRN effectors in P. capsici virulence.

Plasmid construction
The oligonucleotides used for the following plasmid constructs are documented in S1 Table. For PVX recombinant constructs, 47 genes encoding CRN effectors were amplified and inserted into the modified PVX vector [6] using the Sma I and Not I restriction sites. For GFP fusion constructs, PcCRN4, PcCRN4:NES and PcCRN4:nes were amplified using combinations of oligonucleotide primers PcCRN4-F and PcCRN4-R, PcCRN4-F and PcCRN4-NES-R, and PcCRN4-F and CRN4-nes-R, respectively. PCR products were digested with Sma I and Xba I restriction enzymes, and then inserted into the expression vector pBinGFP2 [24]. To make the construct for gene silencing in P. capsici, partial sequence of PcCRN4 was amplified using Pri-meSTAR HS DNA Polymerase (Takara code DR010A) and subsequently inserted into pTOR [13,25]. All the generated plasmids were validated by sequencing by GenScript Corporation Company (Nanjing, China).

Agrobacterium tumefaciens infiltration assays
The A. tumefaciens infiltration assays were performed as previously described methods [26], except that an A. tumefaciens strain GV3101 [27] was used. For infiltration, each recombinant strain was cultured in Luria-Bertani broth supplemented with 50 μg ml -1 kanamycin at 28°C to 30°C and 220 rpm for 48 h. The bacterial cells were collected by centrifugation (3,000g, 5 min), washed three times with 10 mM MgCl 2 , and then resuspended in 10 mM MgCl 2 to an optical density at 600 nm of 0.4. Infiltrations were performed on 6-8 week-old Nicotiana benthamiana, N. tabacum and Solanum lycopersicum plants. Plants were grown and maintained all through the experiments in a greenhouse with favorable temperature of 22-25°C and high light intensity under a 16-h/8-h light/dark photoperiod. For CD triggering assays, A. tumefaciens cells loaded with the respective constructs were infiltrated into the leaves by pressure infiltration by placing a small nick on each leaf with a needle, then 30-50 ml of cell suspension was infiltrated through the nick using a syringe without a needle. Symptoms were monitored from 4 to 8 days after infiltration, and photographs were taken after 5 days for N. benthamiana, 8 days for N. tabacum and 15 days for S. lycopersicum. These experiments were repeated at least three times.

Pathogenicity assay
Phytophthora capsici infection assays were performed by droplet inoculations of zoospore solutions of the P. capsici isolate LT263 (10 x 100 of zoospores μl -1 ) on detached N. benthamiana and Arabidopsis thaliana leaves. At least ten independent N. benthamiana leaves (4 weeks old) and A. thaliana leaves (6-8 weeks old) were tested per construct combination. Agrobacteria cells containing GFP:PcCRN4, PcCRN4:NES, PcCRN4:nes or GFP (control) were infiltrated into N. benthamiana leaves, and 24 h later the leaves were detached and inoculated with P. capsici zoospores on the abaxial side. Diseased plant tissues (36 hpi) were stained by Trypan blue as described methods [28]. The diameters of the diseased lesions were measured at 24, 36 and 48 hpi, and photographed at 36 hpi. The assay was repeated at least three times. Dunnett's test was used for statistical analysis.

Phytophthora capsici inoculation and in vitro samples
Phytophthora capsici wild-type strain LT263 was grown in petri dishes on V8 agar medium in a dark climate chamber at 25°C for 4 days and under standard light at 22°C for 3 days. To induce zoospore release, the cultures were washed twice with sterilized distilled water and released in 10 ml of sterile distilled water per plate by placing at 4°C for 0.5 h followed by incubation at 25°C for about 1 h. Release of zoospores was monitored; their numbers counted with a hemocytometer under a microscope, and adjusted to 100 zoospores μl -1 . The detached leaves were inoculated with 20 μl droplets of the zoospore solution and samples were collected after 3 h, 6 h, 12 h, 24 h, 36 h and 48 h then frozen in liquid nitrogen and stored at -80°C. In addition to samples to be taken during the infectious stages, zoospores (ZO), germinating cysts (GC), and mycelia (MY) grown in vitro were also prepared. ZO were collected in 50 ml centrifuge tube, shaken vigorously, then observed under the microscope. For GC, an equal volume of V8 broth was added to the zoospore suspension, mixed and allowed to stand for 1 h at 25°C. The mixture was centrifuged at 2000 rpm for 5 minutes and pellets collected. The mycelia were grown in 1 ml pea broth, infected with 20 μl of inoculum at 22°C, and harvested 48 hpi by collecting the mycelial mat into 10 ml tubes. The samples were placed in the controlled incubator with the same conditions as the leaf samples, and then harvested with 5 minutes centrifugation at 1,200 g. The pellets were collected and frozen in liquid nitrogen after the supernatant was removed.

RNA extraction and real time quantitative RT-PCR
Total RNA was isolated from frozen leaf tissue (RNAsimple Total RNA kit, Tiangen) according to the manufacture's protocols. Its quality was confirmed by agarose gel electrophoresis, then the quantity was measured with a spectrophotometer (Nanodrop ND-1000). The total RNA was treated with DNase to remove genomic DNA contamination and cDNA was synthesized using 1000 ng of total RNA using a commercial kit (PrimeScript reagent Kit, TaKaRa) following the recommended instructions.
All the specific primers for quantitative RT-PCR (qRT-PCR) were designed for each gene (S1 Table). The experiments of qRT-PCR were performed in 20 μl reactions, including 20 ng cDNA, 0.2 μM gene-specific primers, 0.4 ul ROX Reference Dye, 10 μl of SYBR Premix ExTaq (TaKaRa), and 6.8 μl of deionized water. An ABI Prism 7500 Fast Real-Time PCR System (Applied Biosystems) was used under the following conditions: 95°C for 30 s and 40 cycles at 95°C for 5 s, 60°C for 34 s, followed by a dissociation step of 95°C for 15 s, 60°C for 1 min, and 95°C for 15 s. The relative expression levels of the tested genes were normalized to the P. capsici Actin gene.

Protein extraction and Western blot
The experiments were performed as previously described methods [24]. Briefly, the N. benthamiana leaves were infiltrated with GFP:PcCRN4, GFP:PcCRN4:NES, GFP:PcCRN4:nes and GFP harvested at 2 dpi. Protein extractions were done using GTEN buffer (10% Glycerol, 25 mM Tris, 1 mM EDTA, 150 mM NaCl) that is supplemented with 2% PVP, 10 mM DTT and 1X Complete protease inhibitor cocktail (Roche). Samples were separated on 12% SDS PAGE gels and then transferred to PVDF membranes. The membranes were blocked for 30 minutes with 5% milk in PBS-T (0.1% tween) and probed with GFP antibody (Genscript). The treated membranes were washed 3 times in PBS-T for 5 minutes and then incubated in PBS-T with a goat anti-mouse IRDye 800CW (Li-Cor) for 40 min. After three times wash with PBS-T, the membranes were visualized using a LI-COR Odyssey scanner with excitation 700 and 800 nm to obtain images.

Confocal microscopy
All localization studies were done on N. benthamiana leaves that were infiltrated with GFPtagged PcCRN4, PcCRN4:NES and CRN4:nes two days earlier. The leaves were infiltrated with water to maintain cell structure after detachment and then mounted on a microscope slide. The controls were leaves infiltrated with GFP. Leaf samples were imaged using a Zeiss 710 CLSM with the excitation wavelength at 488 nm.
Stable silencing of PcCRN4 in P. capsici A partial sense sequence of PcCRN4 was cloned into the pTOR vector and transformed into wild-type isolate LT263 as described previously [26]. The transformants were maintained on V8 agar plates supplemented with 50 μg ml -1 of G418 and gene expression levels from the mycelium were determined by qRT-PCR as described previously.

Oxygen burst detection and callose deposition assay
Oxygen burst was observed based on H 2 O 2 accumulation after staining N. benthamiana leaves with diaminobenzidine (DAB) [28]. Briefly, the leaves were infiltrated with PcCRN4 constructs adjusted to OD 0.2 then 24 hpi, they were inoculated with P. capsici zoospores (10 x 100 zoospores μl -1 ). The leaves were then soaked in DAB at 1 mg ml -1 12 hpi thereafter maintained at 25°C for 8 h. Leaf sections were cleared by boiling in 95% ethanol for 15 min and incubated in bleaching solution until all the chlorophyll was completely bleached. The experiments were repeated at least three times.
Callose deposition assays for Arabidopsis were modified as follows from previously described procedures [29]. Briefly, leaves of 8-week-old Arabidopsis ecotype Columbia-0 plants, were inoculated with 3-day-old P. capsici mycelium (5 mm). After 6 and 24 h, leaf disks from inoculated areas were excised with a cork borer from Arabidopsis (5 mm in diameter), and then incubated in bleaching solution of 1:1:1:1:8 (phenol: glycerol: lactic acid: water: ethanol) at 60°C until the leaf disks were cleared of chlorophyll. The cleared leaf disks were washed three times with distilled water, and then immersed in 0.01% aniline blue in 150 mM K 2 HPO4 (pH 9.5) and incubated in the dark for 4 hours. The stained leaf disks were mounted with 60% glycerol on glass slides and observed from the adaxial surface of the disk by epifluorescence microscopy using ultraviolet light.

Identification of PcCRN4 homologs and cell death inducing activities in three plants
To investigate the roles of CRN effectors from P. capsici, we screened CRN effectors that can trigger cell death (CD) using the potato virus X (PVX)-mediated transient expression in N. benthamiana and N. tabacum [30]. In total 47 PcCRN genes (S2 Table), three genes (PcCRN4, PcCRN23 and PcCRN42) exhibit CD-inducing activities in N. benthamiana and PcCRN4 induced CD in both plants while no CD activities were observed in all other genes (S1 Fig). The PcCRN4 gene has been reported as PcCRN83_152 and induced CD in N. benthamiana [20]. We named the genes depending on their relative expression levels in P. capsici hyphae, determined by RNA-seq analysis (S2 Table), implying that PcCRN4 was the 4 th highest in terms of relative expression among the 47 PcCRN effectors. We selected PcCRN4 gene for further analysis based on the following reasons. It exhibited strong CD in the tested plants at 4 dpi (days post infiltration) while the other two genes (PcCRN23 and PcCRN42) induced weak cell death in N. benthamiana only at 5 dpi (S1 Fig). On the phylogenetic tree, the 22 CRNs were categorized into three clades according to origin (Fig 1A). Clade 1 include 9 members from P. sojae and 2 from P. rumorum. All 7 P. infestans genes belong to Clade 2 while clade 3 contains 4 members from P. capsici, suggestive of a specie-specific expansion of this orthologous gene group. Its homologs PsCRN63 from P. sojae and PiCRN2 from P. infestans have been shown to elicit cell death in N. benthamiana [16,18].
Furthermore, we confirmed PcCRN4 CD-inducing activities using plant infiltration experiments by Agrobacterium tumefaciens-mediated transient expression (GFP gene fusion with the mature PcCRN4 gene without the predicted signal peptides) in N. benthamiana, N. tabacum and S. lycopersicum. A known elicitor of cell death, the P. infestans INF1 [31] and GFP were used as a positive and negative controls respectively. Strong necrosis phenotype was observed in N. benthamiana at 5 dpi (Fig 1B), N. tabacum at 8 dpi ( Fig 1C) and S. lycopersicum at 15 dpi ( Fig 1D). The results were similar for each repeat and demonstrated that PcCRN4 can trigger cell death in a variety of the tested plants.
PcCRN4 is expressed at infection stages Nextly, we determined its expression levels at different stages using quantitative RT-PCR on N. benthamiana leaves inoculated with motile zoospores of P. capsici. PcCRN4 transcripts were detectable in the mycelium (MY), zoospores (ZO) and germinating cysts (GC) at low levels; and increased during the early biotrophic phase (3 hours post-inoculation; hpi) and reached the peak at 12 hpi (Fig 2). The amount of PcCRN4 transcripts declined in late biotrophy (24 hpi) and became barely detectable during the necrotrophic phase of the infection (36 and 48 hpi). These results suggested that the PcCRN4 transcripts accumulate at the early stages of infection.

PcCRN4 requires nuclear localization to trigger cell death
Previous reports have shown that PiCRN8 [22] and PsCRN63 [18] target the plant nucleus to trigger cell death. To determine whether PcCRN4 also targets the nucleus, we searched the potential nuclear localization signal (NLS) using cNLS Mapper [32] and found that PcCRN4 contained a predicted NLS amino acid region at 363-388 (LAEPVKRRKLNQMLPFEPVKRRKLNQ). We hypothesized that the nuclear localization is required for CD induction and then tested this by fusing a nuclear exclusion signal (NES) [33] to the C terminus of PcCRN4. The fused protein was ectopically expressed by agroinfiltration. PcCRN4:NES consistently failed to elicit cell death 5 dpi (Fig 3A). To exclude the possibility that the NES may interfere with the activity, its mutated counterpart (nes) was fused to the C terminus of PcCRN4. In the nonfunctional nes, the second and third Leu residues and the first Ile residue were all substituted with Ala residues [33]. This construct robustly induced cell death as the wild-type (Fig 3A). NES constructs prevented nuclear accumulation of PcCRN4 inferred from the localization experiments, whereas PcCRN4 fused to the mutated NES domain retained in the nucleus (Fig 3B). We used Western blot analysis to confirm that these protein fusions were correctly expressed and the resultant proteins were largely stable in plant cells as only low levels of free GFP was observed (Fig 3C). Thus, we inferred that PcCRN4 requires nuclear accumulation to induce plant cell death.

PcCRN4 enhances Phytophthora virulence on N. benthamiana and decreases ROS accumulation
Many oomycete effectors can suppress plant immunity responses [12,[34][35][36]. Thus, we determined whether PcCRN4 interferes with plant immunity using plant transformation experiments by Agrobacterium tumefaciens-mediated transient expression of PcCRN4, PcCRN4:NES and PcCRN4:nes in N. benthamiana, whereas GFP was used as a control. Following agroinfiltration with the constructs (24 h later), we inoculated the infiltrated regions with P. capsici zoospores (10 x 100 zoospores μl -1 ) and evaluated disease development at the indicated times following inoculation (Fig 4A). On leaves infiltrated with strains carrying control gene (GFP), the diameter of the diseased lesion was approximately 1.2-1.5 cm at 36 hpi, which was similar to PcCRN4:NES at 1.3-1.7 cm; however, the lesion diameter expanded to 1.9-2.5 cm and 1.8-2.4 cm on leaves with strains carrying PcCRN4 and PcCRN4:nes, respectively (Fig 4B).
To explore mechanisms behind the increased Phytophthora susceptibility of PcCRN4, diaminobenzidine (DAB) was used to examine infected plant tissues for H 2 O 2 production [28]. Less DAB staining was observed (12 hpi) in infected regions of PcCRN4 and PcCRN4:nes compared to the PcCRN4:NES and GFP control (Fig 4C), indicating that PcCRN4 needs to target the plant nucleus to suppress H 2 O 2 accumulation. Taken together, we showed that PcCRN4 needs to target plant nucleus to suppress plant defenses and promote colonization of the pathogen.

PcCRN4 is required for full virulence
To directly test the contribution of PcCRN4 to P. capsici virulence, stable silencing of PcCRN4 gene in P. capsici was carried out by polyethylene glycol (PEG)-mediated transformation method with the sense construct PcCRN4 gene [18,26]. One silenced transformant (T4) was identified from 10 putative transformants that could grow on selective medium containing 50 μg ml -1 G418 and PCR screening. This transformant (T4) had the expression level of PcCRN4 reduced to <40% of the wild-type according to qPCR results (Fig 5A). The T4 transformant showed significantly reduced virulence on N. benthamiana at 36 hpi and A. thaliana at 24 hpi leaves as compared to the wild type (P<0.01) (Fig 5B-5D). To measure virulence of the transformant more precisely, we quantified the host and pathogen DNA by qPCR 12 h after inoculation [37,38]. The relative virulence was significantly reduced in T4 as compared to WT and another transformant in which PcCRN4 gene was not silenced (Fig 5E). To investigate the effect PcCRN4 on host resistance, transcript accumulation of pathogenesis-related gene  PR1b was examined. When the N. benthamiana leaves were inoculated with T4, rapid and increased levels of the transcriptions were observed at early stages of infection more than the non-silenced lines (Fig 5F). These results together with the virulence data indicated that PcCRN4 plays an important virulent role during infection.
To determine the effect of PcCRN4 on T4 growth in planta, we infiltrated N. benthamiana leaves with PcCRN4, and 24 h later inoculated the leaves with T4 and WT zoospores. The lesion diameter of T4 increased from 1.3 cm when inoculated with GFP to 2.7 cm with PcCRN4 at 36 hpi (Fig 6A and 6B). Collectively, the results suggested that in planta expression of PcCRN4 can complement the PcCRN4 silencing line based on the virulence tests.
To analyze pathogen development in the host, we used an inverted microscope to visualize hyphae in infected tissue. At 24 hpi the transformant T4 and WT on infected A. thaliana leaves were stained with trypan blue. Abundant P. capsici hyphae were observed in tissues of WT but few hyphae were present in the tissues of silenced line T4 (Fig 7A). This result suggested that PcCRN4 is required for full development of P. capsici.
DAB staining was performed on A. thaliana leaves, strong staining was observed in the silenced line T4 as compared to the WT at 12 hpi (Fig 7B). This result indicated that PcCRN4 may promote Phytophthora infection by suppressing the H 2 O 2 accumulation. Callose deposition was performed on the silenced line T4 and WT on A. thaliana leaves as described methods [29]. At 6 hpi, the callose deposits were almost undetectable and the same in T4 and WT. However, a strong signal of callose deposition was only found at 24 hpi in A. thaliana cells inoculated with WT ( Fig 7C). This result indicated that a reduction in expression of the PcCRN4 in P. capsici resulted in loss of abilities to suppress PTI in host cells. PcCRN4 may manipulate cell death by regulating expression of cell death-related genes Since PcCRN4 must enter plant cell nucleus to induce cell death, it is likely to affect the transcriptional levels of plant genes involved in cell death. Therefore, we tested expression levels of four well-known cell death-related genes (AtMC1, AtLSD1, AtBI-1 and AtPAD4) in Arabidopsis after inoculation with wild-type and PcCRN4-silenced line. Transcripts of AtMC1 and AtLSD1 genes, which are positive regulators of cell death [39,40], were down-regulated in Arabidopsis leaves inoculated with PcCRN4-silenced line compared to that infected with wild-type (Fig 8). However, expression of another positive cell death regulator AtPAD4 [41] was not significantly affected (Fig 8). These results suggested that PcCRN4 triggers cell death via a pathway dependent on AtMC1/AtLSD1 but independent on AtPAD4. Interestingly, transcripts of the broad-spectrum cell-death suppressor AtBI-1 [41,42] were significantly higher in the PcCRN4-silenced line, compared to wild-type-infected plant tissues, suggesting that PcCRN4 promotes cell death partially by suppressing expression of the cell death inhibitor AtBI-1. Taken together, these results suggested that PcCRN4 promotes cell death by regulating expression of cell death-related genes.

Discussion
Oomycete CRN proteins were initially identified through their ability to induce crinkling and necrosis when expressed in plant tissue, consequently this protein family is generally considered as a class of CD-triggering effectors [16]. However, recent studies suggested that the majority of CRNs could suppress CD triggered by PAMPs or other elicitors [15,19,23]. A recent study revealed that some CRN domains in P. capsici induce necrosis when expressed in planta [20]. Our study showed that PcCRN4 induced cell death in N. benthamiana, N. tabacum and S. lycopersicum, suggesting that PcCRN4 may target conserved and critical host proteins or signaling pathways.
We previously identified P. sojae effectors PsCRN63 and PsCRN115 and determined their expression patterns. PsCRN63 was found to be induced during the late infection stages (12 and 24 hpi), whereas the highest levels of PsCRN115 RNA were found at the mycelium stage [18]. We analyzed the expression pattern of the PcCRN4 gene during infection. PcCRN4 transcripts were low in the mycelium, motile zoospores and geminating cysts before infection. The transcripts accumulated during infection stage and reached maximum at 12 hpi, and their abundance dropped rapidly in late infection stages. Earlier studies on gene expression during pre-infection stages indicated that the greatest changes in P. capsici occurred during cyst germination compared with mycelium and zoospores [43]. Nevertheless, another study found evidence of a distinct biotrophic phase followed by a transition to necrotrophy after 24 hpi and sporulation at 72 hpi on susceptible tomato by P. capsici [44]. The gene expression pattern of PcCRN4 suggests that it is involved in the initial manipulation of host cell death and defenses. Emerging evidence has shown that oomycete and fungal pathogen effectors can enter inside plant cells to promote virulence [5,6]. Our results showed that PcCRN4 was required for the full virulence, and can induce cell death and enhance susceptibility when it was overexpressed in N. benthamiana. Its functions in plant cells are similar to its homologues effector PsCRN63 from P. sojae [18], but contrary to other effectors. For example, other cell-death-inducing CRN effectors could not enhance virulence [20]. Plant cell death is not only a major consequence of pathogen infection, but also prevent pathogen growth [39]. P. capsici, as a hemibiotrophic and wide-host-range pathogen, is assumed to evade host CD during the biotrophic phase but promote it during the necrotrophic phase. Since this gene is mostly expressed at the biotrophic phase, it is still unclear how CD-inducing activity of PcCRN4 contributes to its virulence. Considering that PcCRN4 may suppress plant ROS accumulation, PR1b gene expression and callose deposits, we speculate that this effector can suppress plant immunity when other effectors that can block PcCRN4-induced-CD are present. This is consistent with that two P. sojae RXLR effectors (Avh172 and Avh238) that can regulate host CD and play a positive role in infection [38].
Many Phytophthora CRN proteins are nuclear effectors [15,18,20]. We demonstrated that PcCRN4 need plant nuclear localization for its virulent and CD-inducing activities, although its biochemical mechanisms are unknown. The nucleus is the heart of plant cells and is also important for plant immunity. It has been shown that some bacterial effectors enter the host nucleus to interfere with transcription, chromatin-remodelling, RNA splicing or DNA replication and repair. These effectors are called 'nucleomodulins' or 'nuclear attacks' [45]. Thus, PcCRN4 belongs to a group of oomycete 'nucleomodulins' which might have permanent genetic or epigenetic effects on the hosts. Our results suggest that PcCRN4 promotes cell death by regulating transcription of cell death-related genes. However, it is still unknown whether PcCRN4 regulates expression of these cell death-related genes by direct binding to their promoter regions to promote/suppress transcription. Future identification of its host targets, including DNA and nuclear proteins, might lead to a better understanding or its functions in the nucleus.