- Research article
- Open Access
Genome analyses of the sunflower pathogen Plasmopara halstedii provide insights into effector evolution in downy mildews and Phytophthora
BMC Genomicsvolume 16, Article number: 741 (2015)
Downy mildews are the most speciose group of oomycetes and affect crops of great economic importance. So far, there is only a single deeply-sequenced downy mildew genome available, from Hyaloperonospora arabidopsidis. Further genomic resources for downy mildews are required to study their evolution, including pathogenicity effector proteins, such as RxLR effectors. Plasmopara halstedii is a devastating pathogen of sunflower and a potential pathosystem model to study downy mildews, as several Avr-genes and R-genes have been predicted and unlike Arabidopsis downy mildew, large quantities of almost contamination-free material can be obtained easily.
Here a high-quality draft genome of Plasmopara halstedii is reported and analysed with respect to various aspects, including genome organisation, secondary metabolism, effector proteins and comparative genomics with other sequenced oomycetes. Interestingly, the present analyses revealed further variation of the RxLR motif, suggesting an important role of the conservation of the dEER-motif. Orthology analyses revealed the conservation of 28 RxLR-like core effectors among Phytophthora species. Only six putative RxLR-like effectors were shared by the two sequenced downy mildews, highlighting the fast and largely independent evolution of two of the three major downy mildew lineages. This is seemingly supported by phylogenomic results, in which downy mildews did not appear to be monophyletic.
The genome resource will be useful for developing markers for monitoring the pathogen population and might provide the basis for new approaches to fight Phytophthora and downy mildew pathogens by targeting core pathogenicity effectors.
Oomycetes include devastating pathogens of plants and animals that can be found in almost all ecosystems and show a variety of different lifestyles [1–3]. They often cause serious infections on their hosts and are responsible for huge economic losses . Understanding the evolution of these pathogens and their virulence mechanisms is key to developing strategies towards the sustainable control of the diseases that they cause.
The oomycete Plasmopara halstedii is an obligate biotroph that causes the economically important downy mildew disease of sunflower . The life cycle of Pl. halstedii, described in earlier studies , is typical for a downy mildew pathogen. Disease symptoms include stunting and chlorosis, alteration of the secondary metabolism of the infected plant, reduced biomass production, damping off, and reduced seed yield, leading to reduced oil yield [4, 5]. Considering the devastating effects on the sunflower crop, it is crucial to develop genomic resources for Pl. halstedii to achieve a better understanding of its infection biology and reveal new strategies for avoiding the loss of sunflower crop to this pathogen.
Like all downy mildews, Pl. halstedii is an obligate biotrophic pathogen and thus cannot be grown apart from its living host. Other sequenced obligate biotrophic oomycetes include the downy mildew Hyaloperonospora arabidopsidis  and the white rusts Albugo candida  and Albugo laibachii , which are all pathogens of Brassicaceae, including Arabidopsis thaliana. Apart from downy mildews the order Peronosporales also includes cultivable pathogens, such as the well-studied hemibiotrophic pathogen Phytophthora infestans, the causative agent of potato late blight, which triggered the Irish potato famine in the mid-19th century [8–10]. Genome sequences have been published for several Phytophthora species, e.g. Ph. ramorum , Ph. sojae , Ph. infestans , Ph. lateralis  and Ph. capsici . In addition, the necrotrophic phytopathogen Pythium ultimum  and the fish pathogen Saprolegnia parasitica  have been sequenced. These genome sequences have provided interesting insights into the evolution of oomycete pathogens with reference to their lifestyles, particularly the loss or gain of pathways or genes responsible for a certain lifestyle [3, 6, 15, 17], e.g. in the evolution of biotrophy . In this study, the assembled genome sequence of Pl. halstedii was analysed and compared to eight deeply sequenced oomycete genomes (Al. laibachii, Hy. arabidopsidis, Ph. capsici, Ph. infestans, Ph. ramorum, Ph. sojae, Py. ultimum, and Sa. parasitica). The genome of Pseudoperonospora cubensis, which causes downy mildew of cucurbit, has also been reported in the past , but the quality of its assembly, while sufficient for general aspects regarding cucurbit downy mildew pathogenicity, does not allow for in-depth comparative analyses, leaving only one downy mildew genome, from Hy. arabidopsidis, available for such studies.
The obligate biotrophic downy mildews constitute the most species-rich group within the oomycetes , and are derived from Phytophthora-like ancestors [19–22]. So far, their monophyly could not be ascertained, even though Runge et al.  obtained high support for a grouping of the two major lineages of the downy mildews included in their study. Based on phylogenomic investigations with limited taxon sampling, downy mildews were inferred to be the sister-group to Phytophthora [23, 24], contradicting earlier reports in which downy mildews were proposed to be nested within Phytophthora [19, 20, 22].
A hallmark of downy mildews, Phytophthora species, and other oomycetes is the presence of a distinct core set of around 60 phospholipid modifying and signalling enzymes (PMSE), which might be important for pathogenic interaction [6, 11, 12, 15, 16, 25–27]. With the exception of Sa. parasitica, the previously sequenced oomycetes lack the classical phospholipase C (PLC). The role of the PSME in plant pathogenicity has not been fully explored, and currently, most plant-pathogen interaction studies in oomycetes focus on effector proteins [6, 28–30].
During infection, plant pathogenic oomycetes secrete an arsenal of effector proteins that target intracellular or extracellular host processes and enable sustained colonisation . A range of Nep1-like proteins (NLPs) was identified, which seem to be typical for the Peronosporales, and are either inducing cell death during the switch from biotrophy to necrotrophy, or, in case of downy mildews are thought to be involved in other processes . Protease inhibitors are secreted in the extracellular space (apoplast) where they interact with and inhibit plant proteases to repress or induce defence reactions . The production of protease inhibitors in oomycetes was first described in the potato late blight pathogen Ph. infestans with two major structural classes: (1) Kazal-like serine protease inhibitors (EPIs) [31, 32] and (2) cystatin-like cysteine protease inhibitors (EPICs) . Further transcriptome sequencing revealed the presence of both structural classes in other oomycetes [34, 35]. Preliminary transcriptome analysis in Pl. halstedii reported one Kazal-like EPI effector and one cystatin-like EPIC effector .
A common feature of both the downy mildews and Phytophthora is the presence of RxLR effector proteins [6, 11, 12]. Studies on the evolution of oomycetes revealed a high degree of positive selection in putative secreted effector proteins [28, 30]. Of the RxLR effectors identified in oomycetes, 44 % contain a conserved 3D structural motif based on the WY-fold . The WY-fold is reported to be restricted to the proteomes of peronosporalean oomycetes .
A few studies have reported pathogenicity related genes in the genome of other downy mildew pathogens apart from Hy. arabidopsidis and Ps. cubensis, e.g. in grape downy mildew, Plasmopara viticola  and sunflower downy mildew, Plasmopara halstedii [4, 36, 40]. Thus, more genomic resources for downy mildews are required for performing comparative genomic analyses with the aim to elucidate the evolution of this group of pathogens, especially in terms of pathogenicity effectors. But also some other aspects of oomycete genomics, such as secondary metabolism and hormone synthesis, have previously been neglected, despite their potential roles in pathogenicity. To contribute towards filling this knowledge gap, the genome and transcriptome of Pl. halstedii were sequenced and analysed.
The aims of this study include: (i) Conducting comparative genomic analyses with deeply-sequenced oomycete genomes for elucidating evolutionary patterns of these pathogens, (ii) In-silico prediction and annotation of the gene space and promoters of Pl. halstedii, with a focus on pathogenicity-related genes, and those involved in secondary metabolism and hormone production, (iii) Expression-profiling of the candidate pathogenicity related genes with respect to certain stages of infection, (iv) Elucidation of effector evolution, in particular the evolution of RxLR-like effectors and their canonical motifs in downy mildews and Phytophthora species.
General genome features
The genome assembly of Pl. halstedii was performed using small-insert libraries with insert sizes of 300 bp and 800 bp and large-insert mate-pair libraries with insert sizes of 8 kbp and 20 kbp. Illumina sequencing of the four libraries with insert sizes of 300 bp, 800 bp, 8 kbp, and 20 kbp generated 42.92, 36.13, 73.89 and 70.56 millions of paired-end reads, respectively. Illumina standard adapter and primer sequences were removed from these reads and further quality control (QC) trimming was performed using an average phred quality score cut-off of 20 and a minimum length threshold of 72 bp. Using these filters, 72.03 %, 57.20 %, 44.71 % and 50.57 % paired-end reads were retained for the libraries with insert sizes of 300 bp, 800 bp, 8kbp and 20 kbp, respectively. All reads were assembled using the Velvet  genome assembler v1.2.09 and the resulting scaffolds were compared to the NCBI nt (nucleotide) database using Blast to check for bacterial and host plant contamination (Additional file 1). A local database of genomes of possible contaminants was created and a mapping of the QC filtered reads on this database was performed. Contamination filters filtered around one per cent of the raw reads, which mapped mostly to bacterial genomes and the genome of the host plant, sunflower. All reads which mapped to the contaminant genomes were not used in the genome assembly.
Filtered reads were used to generate the final genome assembly, with a total length of 75.3 Mb, with an N50 scaffold length of 1.54 Mb. This assembly consisted of 3162 scaffolds, comprising 7857 contigs in total. The longest contig was 297.2 kb and the N50 contig length was 58.1 kb. To assess the quality of this genome assembly, the number of scaffolds and the length of the shortest scaffold of the respective class from N10 to N100 were plotted (Fig. 1). 95 % of the nuclear genome was assembled in only 95 scaffolds, indicating a highly contiguous genome assembly.
The completeness of the genome assembly was assessed using the CEGMA pipeline . This confirmed the presence of 98.41 % of the core conserved genes by partial mapping and 97.18 % by complete mapping. Similar analyses on other sequenced oomycete genomes (Table 1) revealed that the assembled genome of Pl. halstedii is slightly more complete than those of Al. laibachii and Hy. arabidopsidis, while it is similar in completeness to the assembled genomes of Phytophthora spp., Py. ultimum and Sa. parasitica (Fig. 2). In addition, genome comparisons revealed that the genomes of the obligate biotrophic oomycetes (Hy. arabidopsidis, Pl. halstedii and Al. laibachii) are more AT-rich than the other species (Table 1).
Gene prediction was performed using both ab-initio (without using RNA-seq data support) and evidence-based (RNA-Seq transcript mapping) approaches. This combined approach (Additional file 2: Figure S1) resulted in the prediction of a total of 15,469 protein encoding genes. Standalone Panther  protein class information and InterPro  protein family and domain information considering all protein encoding genes, revealed a plethora of pathogenicity related proteins, as given in Table 2. The Pl. halstedii genome was predicted to encode 631 secreted putative pathogenicity effectors, comparable to other biotrophic oomycete genomes screened in the same way (Table 1).
The rate of heterozygosity in the sequenced isolate of Pl. halstedii is very low, which is consistent with multiple generations of inbreeding (‘selfing’) through homothallism . Only 120 sites per Mb have a major allele frequency between 0.45 and 0.55 (Additional file 2: Figure S2). Although the global rate of heterozygosity is very low for the whole genome, we found two regions with apparently high rates of heterozygosity that correspond to predicted gene models, namely PHALS_03871 on “Scaffold_2386” [ENA accession: CCYD01002371] (Additional file 2: Figure S3) and PHALS_09122 on “Scaffold_350” [ENA accession: CCYD01000349] (Additional file 2: Figure S4). Each aligned sequence read-pair supports one of two apparent haplotypes (Additional file 2: Figure S5). However, it is possible that these loci represent paralogs sharing almost identical sequences that erroneously assembled into single gene models. This may also explain the increased depth of coverage in this region. The extremely low levels of heterozygosity precluded an assessment of ploidy levels throughout the genome.
The sequences of core housekeeping genes identified by the CEGMA pipeline were used to infer phylogenetic relationships among these sequenced oomycete genomes. A total of 393 such core genes were found in the nine oomycete genomes. A phylogenetic tree, generated using RAxML (Fig. 3), revealed that Pl. halstedii is nested within the Phytophthora spp. with maximum bootstrap support, while Hy. arabidopsidis was placed as a sister-group of Phytophthora and Pl. halstedii, thus refuting monophyly of the downy mildews. It should be noted, however, that the sparse taxon sampling renders it possible that the phylogenetic position of the different species is an artefact resulting from highly divergent mutation rates. The nexus file containing the tree and alignment has been submitted to Dryad Digital Repository (doi:10.5061/dryad.qg3ft) and a local server (dx.doi.org/10.12761/SGN.2015.7).
Repeat elements and microsatellite markers
Both ab-initio and reference-based repeat element prediction approaches were used to reveal that repeat elements make up 38.93 % of the genome of Pl. halstedii. Further characterization using computational methods resulted in the prediction of 7643 gypsy elements, 2183 TY1_Copia elements and 230 LINE elements. A total of 112 simple sequence repeat (SSR) markers (109 nuclear and three mitochondrial) of potential use in population genetic studies were identified (Additional file 3). Dinucleotide motifs were the most abundant type of repeats (89.36 %), followed by tri- (8.16 %), penta- (1.05 %), and tetra-nucleotide motifs (0.6 %) (Additional file 4). None of the most frequent nucleotide motifs represented more than 1 % of the total SSRs (Additional file 5).
Orthology analysis was performed using the protein sequences of two obligate biotrophic members of the Peronosporaceae (Hy. arabidopsidis and Pl. halstedii) and three hemibiotrophic Phytophthora species. A total of 5384 orthologs were detected in the five genomes. Out of these 4062 were 1:1 orthologs (Fig. 4a). A similar analysis was performed considering the nine deeply sequenced oomycete genomes. These analyses revealed 3316 shared orthologs, of which 1737 were 1:1 orthologs.
A total of 631 putative secreted effector protein (PSEP)-encoding genes were predicted in the genome of Pl. halstedii. By applying these methods to the other available downy mildew genome, we could predict 649 PSEP-encoding genes in Hy. arabidopsidis. This suggests that both of these downy mildew pathogens require an almost identical amount of PSEP-encoding genes for biotrophic colonization of their phylogenetically divergent hosts. Orthology analyses revealed that the nine deeply sequenced oomycete genomes share five orthologs of PSEP-encoding genes (Additional file 6). Orthology searches considering the PSEPs in the plant parasitic Peronosporaceae (Hy. arabidopsidis, Ph. capsici, Ph. infestans, Ph. sojae, and Pl. halstedii) resulted in 77 PSEP orthologs (Fig. 4b) shared by the five genomes (Additional file 7). Our analyses suggest that there are in total 65 (Additional file 8) orthologs of PSEP-encoding genes among the four Phytophthora spp. and two downy mildew pathogen genomes. These orthologs code for 3, 1, 2 and 26 proteins classified as serine protease, Nep1-like proteins (NLPs), proteinase inhibitors and RxLR-like, respectively (Additional file 8). No secreted CRN was found conserved among the Peronosporaceae. However, orthology analyses of 49 CRNs of Pl. halstedii derived from protein encoding genes supported by gene predictions revealed the presence of orthologs of 32 CRNs of Pl. halstedii not predicted to be secreted in at least one of the eight other deeply sequenced oomycetes. Out of these 32 orthologs, six were present in Pl. halstedii and the four Phytophthora genomes and four were shared by Pl. halstedii and Hy. arabidopsidis. Only two orthologs were found among the two downy mildews and four Phytophthora genomes.
Notably, 183 PSEP-encoding gene orthologs were found in three deeply sequenced Phytophthora genomes but in none of the downy mildew genomes (Fig. 4b). Only 11 PSEPs were unique for the downy mildews and absent from the Phytophthora genomes (Additional file 9).
The lengths of gene flanking regions were calculated to estimate gene density in the Pl. halstedii genome. This revealed that the overall means of 5′ and 3′ flanking distances are 3.1 kb and 3.7 kb, respectively (Fig. 5a). The core ortholog genes of Pl. halstedii had mean 5′ and 3′ flanking distances of 1.9 kb and 3.0 kb (Fig. 5b). Similar analyses were specifically performed for all genes that encode PSEP, RxLR-like, and Crinkler (CRN)-like protein encoding genes (Fig. 5). The majority of such genes are localized in regions sparser in genes (3′ or 5′ gene flanking distance more than 4 kb) in comparison to non-effector protein-encoding genes.
The intergenic regions upstream of Pl. halstedii start codons span a wide size range, which is consistent with organization of the genome into gene dense region (GDR) and gene-sparse region (GSR). About 51 % of such regions are < 2 kb, with a median size of 418 nt (Additional file 2: Figure S6), suggesting that the typical Pl. halstedii promoter is compact. This value is based on scaffolds containing at least 100 genes, 13,349 genes in total, to avoid bias due to gaps in the assembly. The fraction of closely spaced (<2 kb) genes in Pl. halstedii is smaller than that of Ph. infestans (51 % versus 67 %), despite the much larger genome of the latter .
Both coding and promoter regions in Pl. halstedii are more AT-rich than those of most other sequenced oomycetes (Fig. 6a). The A + T content within promoters peaks at nearly 60 % about 75 nt upstream of the translation start, the region in which the transcription start site would be expected.
Prior studies of Phytophthora spp. identified core promoter elements  with a fair degree of conservation in other oomycetes . These include the 7-nt Initiator (INR), 7-nt FPR, and 7-nt DPEP elements. Frequently, the INR and FPR elements  co-occur in a 16-nt INR + FPR supra-motif. All of these elements were present in Pl. halstedii (Fig. 6b and c). However, the motifs were less frequently detected in Pl. halstedii compared to Ph. infestans. For instance, the INR + FPR supra-motif was detected two times less in the downy mildew. A similar reduction in the frequency of this element was observed in Hy. arabidopsidis.
About 2/3 of Pl. halstedii promoters lacked any recognizable core promoter motif. Attempts to identify additional core promoter motifs using maximum expectation methods (e.g. the MEME program ), using motif sizes between 6 and 12 nucleotides, were unsuccessful.
Few of the regulatory sites identified in Phytophthora were found conserved in Pl. halstedii. Two recent studies predicted general and stage-specific transcription factor binding sites (TFBSs) in Ph. infestans, with a total of 113 motifs identified with high confidence [47, 49]. Approximately 47 of the motifs appeared to be over-represented in Pl. halstedii promoters compared to shuffled promoter sequences (P < 0.01 by Fisher’s Exact Test). Furthermore, most of the hits in Pl. halstedii lacked the positional or orientational biases seen for most TFBSs in Ph. infestans. Most of such motifs may not be functionally conserved in Ph. infestans and Pl. halstedii, however, since 35 also appeared to be over-represented in promoters from Drosophila.
One TFBS that did appear to be conserved between the species was the CCAAT box. This binds an evolutionarily conserved transcription factor that influences initiation and core motif recognition . On average, the CCAAT motif in Pl. halstedii resides slightly upstream of motifs such as INR + FPR (Fig. 6c) or the INR alone. Even though attempts to identify additional Pl. halstedii TFBSs using MEME with total promoters were unsuccessful, it may be possible to identify such motifs in future studies by evaluating the promoters of co-regulated genes.
Pathways related to phospholipid signalling
Screening the genome for homologs of genes encoding phospholipid modifying and signaling enzymes (PMSEs) showed that nearly all PMSE genes as identified from other oomycetes have an ortholog in Pl. halstedii (Additional files 10 and 11) with the exception of two phosphatidylinositol kinase (PIK) genes (one type C and one type E) that are absent. In addition, there is a significant reduction in the number of phospholipase D (PLD) genes compared to Ph. infestans, 6 versus 18 . Also, Pl. halstedii is the first oomycete to be sequenced in which the oomycete-specific trans-membrane domains-PLD (TM-PLD) class is absent. The second largest group of PMSEs is made up by the G-protein coupled receptor (GPCR)-phosphatidylinositol phosphate kinases (PIPKs), known as GPCR-PIPKs (GKs), with 12 members in most oomycetes. This group is highly conserved as illustrated in Additional file 2: Figure S7 for GK9. As in most oomycetes, there are no gene predictions supporting the presence of a phospholipase C (Additional file 11).
An antiSMASH  analysis of genes and gene clusters involved in the biosynthesis of secondary metabolites detected the presence of four loci encoding nonribosomal peptide synthetases (NRPS) . PhalNRPS_1 and PhalNRPS_4 show a two-domain structure with an adenylation (A) domain with unknown amino or 2-ketocarboxylic acid specificity and a thiolation (T) domain (Additional file 2: Figure S8). BlastP searches revealed that NRPS_1 and NRPS_4 are widespread in fungi and oomycetes. The PhalNRPS_2 operon encodes an A-T didomain NRPS and has a flanking gene encoding a PQQ binding protein, which might be involved in the reductive release of the T domain-bound thioester (Additional file 2: Figure S8) .
PhalNRPS_3 is an unusual monomodular NRPS with a four-domain composition: An N-terminal thioesterase (TE) domain followed by an A and a T domain and a C-terminal reductase (Red) domain potentially involved in reductive release of the bound thioester (Additional file 2: Figure S8) . The coexistence here of the TE and Red domains is uncommon as both usually act on the C-terminus of the NRPS-build peptide chain. Interestingly, NRPS_3 homologs are also present in other oomycete genomes including Ph. infestans and Ph. sojae. Although the function of the N-terminal TE domain is unknown it might be involved in precursor supply for the A domain.
Phytohormones are a group of metabolites that are also potential virulence determinants. The close coevolution of downy mildews with their hosts renders it possible that the former have acquired the ability to produce hormones to manipulate their host plants in addition to secreting effector proteins. Thus pathways leading to the production of plant hormones were investigated in detail. One of the crucial pathways that can lead to the production of salicylate and auxin originates from the shikimate pathway that catalyses the stepwise conversion of erythrose-4-phosphate and phosphoenolpyruvate to chorismate. Comparable to other oomycetes and plants, in Pl. halstedii all steps are catalysed by the pentafunctional AROM complex. Examination of genes involved in the salicylate biosynthesis pathway that branches from chorismate via isochorismate to salicylate neither identified an isochorismate synthase nor an isochorismate pyruvate lyase, rendering it unlikely that salicylate is synthesized by Pl. halstedii. Even though all enzymes are present in the genome to enable synthesis of L-tryptophan from chorismate, an important precursor of auxin production (Additional file 2: Figure S9), none of the enzymes involved in indole-3-acetic acid biosynthesis was found. It thus seems highly unlikely that auxin derivatives are synthesized by Pl. halstedii.
We could further identify all enzymes needed for the biosynthesis of geranyl-gernayl-PP from acetyl-CoA but no key enzymes for diterpenoid biosynthesis (Additional file 2: Figure S10). Therefore the biosynthesis of gibberellins by Pl. halstedii is unlikely. The pathogen has the potential to synthesize phytoene from geranyl-geranyl-PP via phytoene synthase but none of the genes encoding the downstream enzymes such as phytoene desaturase was identified. It is therefore unlikely that Pl. halstedii is able to synthesize complex carotenoids, abscisic acid derivatives or strigolactones (Additional file 2: Figure S10).
Despite the absence of most genes encoding proteins involved in the production of phytohormones, candidates encoding all key steps of cytokinin production were present in the genome of Pl. halstedii (Additional file 2: Figure S10). We can therefore speculate that Pl. halstedii produces cytokinins. In addition, all the enzymes required to produce brassinolide from campesterol (Additional file 2: Figure S11) seem to be present. Based on the identification of two potential cholesterol transporters we hypothesize that sterols are obtained from the plant and converted into campesterol. Brassinolide together with cytokinins might be important virulence factors and contribute to the dwarfing and stunting of infected sunflower plants. The potential capacity of plant hormone biosynthesis in Pl. halstedii has been summarised in Additional file 12.
Necrosis and ethylene-inducing peptide 1 (Nep1)-like proteins (NLPs)
Plasmopara halstedii has 19 NLP genes (Additional file 13) and one NLP pseudogene (Additional file 14). Of these 19 genes, there are two type 1 NLPs and 17 type 1a NLPs, which are distinguished based on substitutions in the cation binding pocket that is required for induction of necrosis by cytotoxic NLPs . Features of these NLPs have been listed in Additional file 15. Remarkably, one of its type 1 NLPs (PHALS_06084) is very closely related to the non-cytotoxic Hy. arabidopsidis HaNLP3 protein , including the presence of the N-terminal Q-rich region and a second disulphide bridge (Additional file 2: Figure S12). Multiple sequence alignments and sequence features of all NLPs are given in Additional file 2: Figure S13.
Plasmopara halstedii-specific expansion of type 1a NLPs, similar to that observed in Hy. arabidopsidis , is depicted in Additional file 2: Figure S14, which shows two expanded groups of Pl. halstedii NLPs. Group 1 clusters with Phytophthora NLPs, while group 2 clusters with several NLPs of Bremia lactucae , the lettuce downy mildew pathogen, representing a potential apomorphy of the group of downy mildews with pyriform haustoria. Three NLPs (PHALS_01213, PHALS_05247, and PHALS_13274) group together with HaNLP5 and type 1a NLPs of other Peronosporaceae. PHALS_01213 is most closely related to Br. lactucae NLP6 (Additional file 2: Figure S14). While the expanded HaNLPs group in one clade, the PhalNLPs display two divergent species–specific expansions (Additional file 2: Figure S14).
The low number of PhalNLP pseudogenes is remarkable compared to the situation in the Hy. arabidopsidis genome where 14 HaNLP genes and 15 HaNLP pseudogenes were identified , and in the Phytophthora sojae genome where 33 PsNLP genes and 37 PsNLP pseudogenes were identified . In Pl. halstedii 19 PhalNLP genes were identified, yet only one PhalNLP pseudogene (Additional file 2: Figure S15); the latter has a premature stop codon when compared to its most closely related PhalNLP gene PHALS_14423 (Additional file 2: Figure S16).
In total, 15 PhalNLPs showed induced expression during infection. In particular, members of group 2 are up-regulated during infection, compared to their expression in spores, suggesting the identified PhalNLP proteins in Pl. halstedii play a role during the infection process (Additional file 2: Figure S17).
Protease-inhibiting proteins are virulence factors that impair the function of plant proteinases targeted against pathogenicity effectors. The genome of Pl. halstedii has a total of 19 genes encoding putative Kazal-like EPI effectors and 4 putative cystatin-like EPIC effectors (Table 3; Additional file 15). Sequence alignments of the Pl. halstedii Kazal-like inhibitor domains and 139 Kazal-like domains from six other oomycete pathogens show that these sequences contain the six conserved cysteines with the consensus pattern C-X3,4-C-X7-C-X6-Y-X3-C-X6-C-X9,12,13,14-C (Additional file 2: Figure S18). Some of the serine-like inhibitor effectors in Ph. infestans exhibit atypical Kazal-like domains that lack cysteines C3 and C6. We identified an independent deletion of cysteines C2 and C4 in serine-like inhibitor effectors from Pl. halstedii that also results in atypical Kazal-like domains (e.g. in PHALS_09920).
The N-terminal Trunk (G), the Loop1 (QxVxG) and Loop2 (W) motifs representative of cystatin-like cysteine inhibitors are conserved in four of the predicted cystatin-like proteins from Pl. halstedii (Additional file 2: Figure S19). All Kazal-like and cystatin-like sequences are listed in Additional file 16 and Additional file 17, respectively.
Crinkler (CRN)-like proteins
The genome of Pl. halstedii was searched for CRN protein-coding genes. For predicting CRNs, both regular expression and Hidden Markov Model (HMM) methods were used . A total of 49 CRNs were predicted from the protein-coding genes (Additional file 18). Out of these 49 CRNs, 4 had both the canonical LFLAK and HVLVVVP motifs.
In a second approach a total of 200 and 139 sequences were derived from open reading frames (ORFs) using full length and LFLAK HMMs, respectively, which were similar by Blast and HMM alignments to previously known CRNs. A total of 125 CRN-like proteins matched both HMMs (Additional file 2: Figure S20). Manual curation based on high-confidence motifs known from previous studies reduced this number to 55. In total, 28 CRN motifs encoded in ORFs (genome stretches with an ATG followed by at least 30 codons before a stop codon) and were not predicted as protein-coding genes (Additional file 19). A total of 77 putative CRNs were identified in the genome of Pl. halstedii by merging the outputs from both translated ORFs containing high-confidence CRN signatures and iterative HMM predictions from translated predicted genes (Additional file 2: Figure S20). Consistent with previous studies [15, 40], only a handful of putative CRNs were predicted to be secreted. Out of the 77 putative CRNs, only 2 bore classical secretion signals based on our secretome prediction pipeline (Additional file 1). However, in total 11 CRNs were having a signal peptide probability (SignalP v2) greater than 0.5. All 15 CRNs of Pl. halstedii reported in a previous study  were also present in this set of 77 CRNs.
Candidate secreted proteins with RxLR-dEER-like domains were predicted using both regular expression and HMM-based methods (Additional file 2: Figure S21, S22A-B). A total of 260 candidate RxLR-like proteins were predicted from PSEP-en coding genes (Additional file 20). Out of these 260 RxLR-like proteins, 21 sequences had the exact RxLR-dEER motif. Features and occurrences of the RxLR-dEER like proteins were further analysed (Fig. 7a) and revealed an overrepresentation of some RxLR-dEER variants, e.g. KxLR-dEER and RxLK-dEER (Fig. 7b).
Fourteen RxLR-like proteins (Additional file 21) were found in ORFs that were not predicted as protein coding genes, as these resided in highly repetitive regions. These 14 putative RxLR-like effectors represent high conservation of RxLR-dEER motifs (Additional file 2: Figure S22C). Out of these 14, 7 were masked as repeat elements by the repeat element masking pipeline. The other 7 RxLR-like protein-coding ORFs were surrounded by repeat-rich regions and their start codon positions were not well supported. By combining both predictions from protein sequences and translated ORFs from repetitive regions, a total of 274 RxLR-like proteins were predicted. Out of these 274, 34 had both the canonical RxLR and dEER motifs.
To determine whether the Pl. halstedii genome encodes RxLR-like proteins with WY-folds, HMMER was used to search the predicted proteome using the WY-fold HMM. In total 132 proteins out of the 15,469 protein sequences were predicted to have at least one WY-fold (Additional file 22). Among these, 16 proteins were predicted to be secreted, of which 8 contained RxLR-like motifs. The number of WY-folds present in each protein ranged from 1 to 7. In the predicted secretome, all WY-fold containing proteins had no known functional annotations except PHALS_02683, which was annotated as similar to a reverse transcriptase.
Conservation of RxLR-like effectors within Phytophthora species and downy mildew pathogens
To look for orthologs of RxLR-like proteins among oomycete genomes, a subset of high-confidence RxLR-like proteins (categories AAA, AA and A in Additional file 20; the categorisation method is explained in Additional file 1) was generated for Pl. halstedii as for the four Phytophthora spp. and Hy. arabidopsidis. Orthology predictions generated 28 orthologs (Table 4; multiple sequence alignments are shown in Additional file 2: Figure S23) of RxLR-like proteins that were found in the four Phytophthora spp. genomes (Fig. 8a). Multiple sequence alignments of these 28 orthologs revealed high sequence conservation (Additional file 2: Figure S23). However, only six such orthologs (Additional file 23) were found in Hy. arabidopsidis and Pl. halstedii (Fig. 8b). Interestingly, only three high confidence RxLR-like proteins had orthologs in each of the six genomes (Additional file 24). Their multiple sequence alignments revealed a high degree of conservation (Fig. 8c; Additional file 2: Figure S24-S26), and all were predicted to be targeted to the cytoplasm after secretion and signal peptide cleavage. InterProScan searches revealed that Pl. halstedii protein sequences of Ortholog1 (PHALS_05912), Ortholog2 (PHALS_03692) and Ortholog3 (PHALS_07128) (Fig. 8c) contain a tetratricopeptide-like helical domain (IPR019734), a pectate lyase catalytic domain (IPR004898) and a DnaJ domain (IPR001623), respectively. Only one of the three orthologous genes (represented by PHALS_05912) had previously been annotated as a putative RxLR-effector (Additional file 24).
Expression profiling of genes encoding RxLR and CRN-like proteins
In order to obtain insight into effector expression during infection, RNA-Seq analysis of samples corresponding to newly formed spores, and early and late stages of infection on cotyledons was performed. Genes encoding CRNs and RxLR effectors were expressed at all three stages. Some genes were up-regulated during the early stage of infection (102 putative RxLR effectors and 15 CRNs; Additional file 2: Figure S27A and S27C, Additional file 25), while others were up-regulated in spores and late stages (181 putative RxLR effectors and 34 CRNs; Additional file 2: Figure S27b and S27D, Additional file 26). Taken together, these results suggest that stage-specific sets of CRN and RxLR effector candidates are expressed during the infection of sunflower by Pl. halstedii.
The assembled genome Pl. halstedii has a size of 75.3 Mb. This size is similar to that of the other sequenced downy mildew pathogen, Hy. arabidopsidis, which has an assembled genome size of 78.9 Mb. According to a recent study , the estimated genome size of Pl. halstedii is 100 Mb, which is comparable to that of Hy. arabidopsidis . Phytophthora spp. assemblies range from 64 Mb for Ph. capsici to more than 200 Mb for Ph. infestans and other clade 1c species . The significantly bigger genome of Ph. infestans compared to other oomycetes is due to repeat-driven genome expansion, with a repeat element content of 74 % . In contrast only 39 % of the Pl. halstedii genome was comprised of repeat elements, comparable to the 43 % reported for Hy. arabidopsidis . The N50 scaffold size for the genome assembly of Pl. halstedii is 1.54 Mb, which reflects its high quality of genome. Genome completeness with respect to 248 core eukaryotic genes is similar in the eight deeply sequenced oomycete genomes, reflecting an adequate coverage of the gene space.
To study the genome architecture of Pl. halstedii, 5′ and 3′ flanking distances of all genes were calculated. These studies revealed that CRN, RxLR and other PSEP-encoding genes were localized in more gene-sparse regions than non-PSEP-encoding genes, particularly than the core housekeeping genes. This situation is similar to other genomes of other oomycete pathogens [3, 12].
Unexpectedly, the two downy mildew species included in the analysis, Pl. halstedii and Hy. Arabidopsidis, did not show a sister group relationship (Fig. 3). While Hy. arabidopsidis was placed outside of the clade containing Phytophthora species, as inferred by some earlier studies [23, 59], Pl. halstedii was found to be nested within Phytophthora, rendering the genus paraphyletic. Reasons for the disjunction of the downy mildew species could be either that downy mildews are a polyphyletic assemblage or that the limited taxon sampling, in conjunction with the comparatively high mutation rates in downy mildews, leads to an incorrect estimate of phylogenetic relationships. Both multigene analyses with a larger taxon sampling  and morphological data  suggest the nesting of a potentially monophyletic downy mildew clade within a paraphyletic genus Phytophthora. It seems likely that the question of downy mildew monophyly cannot be resolved until representatives from all major clades of downy mildews and Phytophthora, especially of Phytophthora clades inferred to be closely related to downy mildews , have been sequenced.
Within both downy mildews and Phytophthora spp., homothalism has evolved several times , and might be an adaptation towards ensuring sexual reproduction and the formation of durable resting spores even when hosts plants are sparsely distributed. As a consequence of homothalism of Pl. halstedii , rates of sexual recombination between two independent strains are expected to be very low, resulting in pathogen strains with extremely low heterozygosity, similar to the situation in Ph. lateralis . This is supported by the present study, which reports only 0.0012 % of sites with a major allele frequency of 0.45 to 0.55. As only a few sunflower genotypes are grown commercially, selfing after rare events of outcrossing or parasexual recombination  might lead to abundant pathogen genotypes adapted to a variety of sunflower genotypes lacking the R-genes that would match their effector complement [62, 63].
How effectors and other genes are regulated in oomycetes is still very unclear and motif identification apart from a few basic patterns proved to be difficult. Some motifs have been described with respect to general oomycete promoter structure [47, 49], and only a few stage-specific transcription factor binding sites have been identified , so far.
Pl. halstedii harbours a set of PMSEs that is well conserved in respect to the ones identified in other oomycetes. A slight reduction in numbers is observed in PIKs whereas a large reduction is found in the number of PLDs. The latter resulted in the absence of one class of oomycete specific PLDs, the TM-PLD. Among the strongly conserved PMSE are the GKs. In Phytophthora spp. Twelve GKs are encoded, suggestive of a unique signaling pathway that bypasses G-protein mediated signaling by direct PIPK activation . So far it is unclear, which role these receptors play in pathogenicity, but it has been speculated that they are important for sensing the host environment . However, experimental support is necessary for testing this hypothesis.
Secondary metabolites and phytohormones
Secondary metabolites, and phytohormones in particular, are important virulence determinants in several bacterial and fungal pathogens, e.g. in Xenorhabdus spp. , Ustilago maydis  and Fusarium oxysporum . However, while some studies have examined the primary metabolites of oomycetes, in particular fatty acids [69, 70], little is currently known about the capability of oomycetes to produce secondary metabolites. The identification of few NRPS and PKS genes in Pl. halstedii and other oomycetes is suggestive of the production of only few secondary metabolites; however, it has been reported that some fungal PKS can produce a variety of different compounds . Monomodular NRPS composed of A-T-TE or A-T-Red domains are responsible for the biosynthesis of quinone  or pyrazine structures  composed of two amino or 2-ketocarboxylic acids. As these compounds often show biological activity , compounds derived from these enzymes in Pl. halstedii might act as virulence factors or protect the host environment against competitors and might thus be promising targets for future research.
Plasmopara halstedii seems to lack the capacity to produce most phytohormone classes, with the exception of cytokines and brassinolides. Even though these two classes of phytohormones might contribute to the disease phenotype, it has been shown in previous studies that the stunting effects in systemically-infected sunflowers are likely to be mostly auxin-mediated  Depletion of IAA by IAA oxidase activity  is a hallmark of this process, but it remains unclear how the pathogen interferes with the host to incite this remarkable disturbance of phytohormone signaling.
All pathogenic and endosymbiotic oomycete and fungal species secrete a plethora of proteins into their hosts to manipulate host defence reactions and to enable the formation of an interface for plant-microbe interaction in (hemi-) biotrophic species. Most genes encoding secreted effectors are fast-evolving and show limited sequence conservation, even though some effectors have been reported to be conserved among species within a certain pathogen group [6, 13, 76]. Positive selection studies in both oomycete and fungal plant pathogens have shown that effector-encoding genes are under higher selection pressure than non-effector genes [3, 28, 30, 58, 76].
High numbers of NLP genes have been found in the genomes of Phytophthora species [11, 12, 77]. The members of this family that induce host cell death have been suggested to function during their switch from biotrophy to necrotrophy [78, 79]. It was thus unexpected that while most branches of the NLP family were not present one clade of NLPs was expanded in Hy. arabidopsidis . However, no evidence could be found with respect to an induction of necrosis by any downy mildew NLP tested, suggesting an alternative role during disease development . Similar to the genome of Hy. arabidopsidis, most branches of the NLP family were absent in Pl. halstedii, but twice as many branches of NLPs were retained. Two of these have expanded into small protein subfamilies independent from Hy. arabidopsidis. Several of these NLPs were found upregulated during infection as compared to spores, highlighting their potential importance for pathogenicity in this biotrophic pathogen.
CRN proteins are an ancient class of proteins that has been reported to contain effectors targeted to the nucleus of the host cell . Genes encoding CRNs have been found in the genomes of all sequenced oomycete plant pathogens and are especially abundant in Phytophthora species . In the genome of Pl. halstedii 77 CRN-like proteins were predicted, an amount similar to Hy. arabidopsidis. Surprisingly, 75 out of 77 proteins with a CRN signature in Pl. halstedii were not predicted to contain a classical secretion signal, and the function of these proteins remains enigmatic. It is also noteworthy that while a few other pathogenicity-related genes, such as three proteases, an NLP, two proteinase inhibitors, and 26 RxLR-like proteins had orthologs in all Peronosporaceae, no universally conserved secreted CRN-like gene was identified. However, orthology of 32 CRNs of Pl. halstedii with at least one oomycete species was revealed. The function of these conserved CRNs in pathogenicity or cellular processes within the pathogen remains to be tested.
A hallmark of a large fraction of cytoplasmic effectors in downy mildew and Phytophthora species is the presence of a N-terminal RxLR-dEER motif [81–83]. While these effectors seem to be abundant in the crown lineages of Peronosporaceae, canonical RxLR effectors are apparently absent in the genomes of two necrotrophic pathogens, Py. ultimum of the Pythiaceae and the oomycete fish pathogen Sa. Parasitica of the Saprolegniaceae. However, the presence of possibly convergently evolved RxLR-like effectors in the genome of Sa. parasitica and their translocation into the fish cells has been demonstrated . Even though Albugo species seem to contain a few secreted proteins with RxLR-like motifs [3, 7], their function is currently unclear. It seems possible that they have evolved independently in the Albuginaceae, which represent an ancient biotrophic lineage [1, 85]. In the genome of Pl. halstedii a total of 274 RxLR-like proteins coding genes were predicted, out of which only 34 were having the RxLR-dEER motif typical for Phytophthora species. Interestingly, the genome of Pl. halstedii also encodes many variants of RxLR-like effectors (Fig. 7b), including putative KxLR-dEER and RxLK-dEER effectors. A few proteins with a QxLR motif, previously reported from Pseudoperonospora cubensis , were also observed, but none of these had a predicted dEER motif. This highlights that while in Phytophthora species the majority of cytoplasmic effectors of the RxLR-type seem to have a highly conserved RxLR-motif, conservation is much lower in downy mildews, which seem to have evolved a huge variety of motifs, rendering their identification less straightforward. However, the dEER motif seems to be of much higher conservation. In Pl. halstedii a significant number of secreted, dEER-motif containing proteins were predicted, which showed variant RxLR motifs, or which, similar to the effector ATR5 from Hy. arabidopsidis  did not show any recognisable RxLR-motif. This raises doubts regarding the importance of the biochemical features of the RxLR-motif for protein translocation into host cells, in line with recent findings of Yaeno and Shirasu , and might be suggestive of a combined action of RxLR-like and dEER-like motif, either host-independent  or involving additional proteins.
Conservation of PSEPs within downy mildews and Phytophthora species
Orthology analyses were conducted for the PSEPs of Phytophthora and downy mildew pathogens. In total there were 65 orthologs predicted among Phytophthora and downy mildew genomes, in terms of PSEP-encoding genes. Functional annotations of these orthologs suggest that they contain peptide bond-degrading enzymes, NLPs, proteinase inhibitors and RxLR-like proteins. These genes might represent a core set of effectors which is required for infection. No secreted CRN was found in the set of 65 PSEP orthologs, which was expected, as these analyses were conducted only on the PSEP-encoding genes. However, we could identify six orthologs of high confidence RxLR-like protein encoding genes shared by the downy mildew pathogens Hy. arabidopsidis and Pl. halstedii. Similarly, 28 orthologs of such candidate RxLR-like proteins were predicted among the four Phytophthora species. This suggests the presence of a conserved core set of candidate RxLR-like effectors, which potentially target basic hubs in plant defence pathways, similar to the PEP1 effector, which remained conserved in smut genomes [76, 89] and acts as an inhibitor of conserved plant peroxidases. It is notable that only the RxL part of the RxLR seems to be highly conserved within potential core effectors of Phytophthora and downy mildews, similar to the situation in Plasmodium , in which the same residues seem to play a vital role for delivering its effectors to the host cytoplasm [90–92].
Overall it was found that the assembled genome of Pl. halstedii is extremely low in heterozygosity, presumably due to its homothallism, and shows a similar amount of genome completeness in terms of CEGMA genes like other deeply-sequenced oomycete genomes. It is noteworthy that the genomes of obligate biotrophic oomycetes are apparently more AT-rich than those of related species with other lifestyles. Interestingly, phylogenomic analyses seem to refute downy mildew monophyly, although it cannot be ruled out at present that this is an artefact from low taxon sampling. However, the high degree of distinctiveness and independent evolution is supported by orthology analyses, which revealed a higher degree of gene conservation among Phytophthora species than downy mildews. Core promoter structures in oomycetes remain obscure, as apart from the CCAAT-box, no additional conserved motifs could be identified. Notably Pl. halstedii seems to have the capacity to produce phytohormones of the classes brassinolids and cytokines. However, it remains to be tested in future studies, whether the production of phytohormones by Pl. halstedii is important for its pathogenicity. Its genome codes for some secondary metabolite clusters, including an unusual NRPS with both TE and Red domains, but their products and their role in pathogenicity have yet to be identified. Conservation of candidate effector protein encoding genes in the genome of Phytophthora and downy mildew pathogens was observed, suggesting a core set of effector proteins that might play a key role in the pathogenicity of these pathogens. However, while 183 PSEP-encoding orthologs were present in Phytophthora spp. genomes but absent from downy mildews, only 11 PSEPs were present in downy mildews but absent from Phytophthora. Functional annotations of the predicted gene models revealed several variants of the RxLR motif, while the RxL part of RxLR motif within Phytophthora and downy mildew pathogen genomes was mostly conserved. In addition, several proteins in which only the dEER motif is conserved were identified. Taking into consideration the additional variation of the RxLR-motif found in this study, this is suggestive of a major role of the dEER motif in the function of the RxLR-dEER-like effectors.
Genome assemblies, repeat elements masking and gene predictions
In total four genomic DNA libraries were sequenced from the DNA extracted from Plasmopara halstedii zoosporocysts (methods used for DNA isolation and extraction have been described in Additional file 1). Adapter and primer sequences from reads were removed using Trimmomatic . Filtering parameters estimation and filtering was done using the FastQFS tool . All genomic reads were filtered using an average read quality threshold of 26 phred score and a length cut-off of 72 bp. Bacterial or other contamination in the sequenced reads were removed from the raw reads prior to the analyses (Additional file 1). Genome assemblies were performed using the Velvet v1.2.10  genome assembler. The best assembly was determined by comparing the N50 scaffold size, the largest scaffold size, the number of scaffolds, the percentage of reads mapped to the assembled genome and CEGMA  genome completeness analysis. A k-mer of length 59 generated the best genome assembly considering above mentioned assembly quality parameters. The resulting set of assembled scaffolds were scanned for repeat elements (Additional file 1). Gene predictions on the masked genome were performed by both transcript mapping based and ab-initio based methods (Additional file 1) as described before . The resulting consensus gene set was subjected to expression profiling by using the three RNA-Seq libraries (Additional file 1). A plot representing the length distribution of protein sequences (Additional file 2: Figure S28) was generated using the hist() function of R . Methods used for the investigation of heterozygosity levels and for the development of SSR markers have been described in the Additional file 1.
Functional annotations of the predicted genes were performed by using the Blast2GO software  (Additional file 1). Putative secreted effector protein (PSEP)-encoding genes were predicted using SignalP  along with other tools (Additional file 1). Methods used for the functional annotation of secondary metabolite synthase producing genes, genes involved in certain pathways, phospholipid modifying and signaling enzymes (PMSE)-encoding genes, NLPs, protease inhibitors, CRNs and RxLR-like protein encoding genes have been described in Additional file 1.
Orthology analyses were done using the OrthoMCL  software, using an e-value cut-off of e−5 and a 50 % identity cut-off to define orthologous proteins among nine oomycete genomes. Subsequently perl and shell scripts were used to extract the 1:1 orthologs. Orthologs in terms of PSEPs were identified by running OrthoMCL on all predicted PSEPs encoded by the nine genomes using same input parameters.
A phylogenetic analysis was conducted on the core ortholog genes predicted using the CEGMA pipeline . Multiple sequence alignments were performed using MAFFT  and subsequently concatenated. Maximum likelihood phylogenetic analysis was done with RAxML , with 1000 bootstrap replicates and default settings.
To study the promoter architecture of Pl. halstedii, intergenic regions were extracted from the scaffolds. Only scaffolds which contained at least 100 genes were used, to avoid bias due to gaps in the assembly. Sequences upstream of genes were extracted and A + T contents were calculated. To measure the frequency of incidence of the 7-nt Initiator (INR), 7-nt FPR, 7-nt DPEP and 16-nt INR + FPR supra-motif elements in Pl. halstedii, position-specific probability matrices (PSPMs) corresponding to the motifs in Ph. infestans were used to scan 400 nucleotides of DNA upstream of 5000 Pl. halstedii genes, and then PSPMs corresponding to the Pl. halstedii matches were used to rescan the Pl. halstedii promoters. Control searches were performed against databases of twice-shuffled promoter DNA. The genome of Pl. halstedii was also searched for other known Phytophthora TFBSs, using Fisher’s Exact Test with a P < 0.01 threshold to test the significance of any hits, compared to searches of shuffled promoter sequences. MEME  was used to search for novel motifs in the Pl. halstedii promoter sequences.
Genomic data files have been uploaded to a local server dx.doi.org/10.12761/SGN.2015.7. The study has been registered in the ENA database under the study accession number PRJEB6932. Raw genomic reads and RNA-Seq reads have been uploaded to the ENA database and are available via the same study accession numbers. Genomic sequence reads from all four sequenced libraries are available via accession numbers ERR583679 to ERR583682 and the three RNA-seq libraries are deposited under the accession numbers ERR583683 to ERR583685. Genome assembly scaffolds and annotation were deposited under the accessions CCYD01000001-CCYD01003162.
Core eukaryotic gene mapping approach
Downstream promoter element
Cystatin-like cysteine protease inhibitors
Kazal-like serine protease inhibitors
Flanking promoter region
G-protein coupled receptor (GPCR)-phosphatidylinositol phosphate kinase (PIPK)
G-protein coupled receptor
Hidden markov model
Long interspersed elements
National center for biotechnology information
Necrosis and ethylene-inducing peptide 1(Nep1)-like proteins
Nonribosomal peptide synthetases
Necrosis and ethylene-inducing peptide 1
Open reading frame
Phosphatidylinositol phosphate kinase
Phospholipid modifying and signalling enzymes
Putative secreted effector protein
Randomized axelerated maximum likelihood
Simple sequence repeats
Transcription factor binding sites
Thines M. Phylogeny and evolution of plant pathogenic oomycetes—a global overview. Eur J Plant Pathol. 2014;138(3):431–47.
Kemen AC, Agler MT, Kemen E. Host–microbe and microbe–microbe interactions in the evolution of obligate plant parasitism. New Phytologist. 2015;206(4):1207–28.
Kemen E, Gardiner A, Schultz-Larsen T, Kemen AC, Balmuth AL, Robert-Seilaniantz A, et al. Gene gain and loss during evolution of obligate parasitism in the white rust pathogen of Arabidopsis thaliana. PLoS Biol. 2011;9(7):e1001094.
Gascuel Q, Martinez Y, Boniface MC, Vear F, Pichon M, Godiard L. The sunflower downy mildew pathogen Plasmopara halstedii. Mol Plant Pathol. 2015;16(2):109–22.
Sackston WE. Downy mildew of sunflower. London: Academic; 1981.
Baxter L, Tripathy S, Ishaque N, Boot N, Cabral A, Kemen E, et al. Signatures of adaptation to obligate biotrophy in the Hyaloperonospora arabidopsidis genome. Science. 2010;330(6010):1549–51.
Links MG, Holub E, Jiang RH, Sharpe AG, Hegedus D, Beynon E, et al. De novo sequence assembly of Albugo candida reveals a small genome relative to other biotrophic oomycetes. BMC Genomics. 2011;12:503.
van West P, and Vleeshouwers, V.G.A.A. The Phytophthora infestans -host interaction, vol. Chapter 9. Hoboken, New Jersey: Blackwell Scientific Publishers; 2004.
Yoshida K, Burbano HA, Krause J, Thines M, Weigel D, Kamoun S. Mining herbaria for plant pathogen genomes: back to the future. PLoS Pathog. 2014;10(4):e1004028.
Yoshida K, Schuenemann VJ, Cano LM, Pais M, Mishra B, Sharma R, et al. The rise and fall of the Phytophthora infestans lineage that triggered the Irish potato famine. eLife. 2013;2:e00731.
Tyler BM, Tripathy S, Zhang X, Dehal P, Jiang RH, Aerts A, et al. Phytophthora genome sequences uncover evolutionary origins and mechanisms of pathogenesis. Science. 2006;313(5791):1261–6.
Haas BJ, Kamoun S, Zody MC, Jiang RH, Handsaker RE, Cano LM, et al. Genome sequence and analysis of the Irish potato famine pathogen Phytophthora infestans. Nature. 2009;461(7262):393–8.
Quinn L, O’Neill PA, Harrison J, Paskiewicz KH, McCracken AR, Cooke LR, et al. Genome-wide sequencing of Phytophthora lateralis reveals genetic variation among isolates from Lawson cypress (Chamaecyparis lawsoniana) in Northern Ireland. FEMS Microbiol Lett. 2013;344(2):179–85.
Lamour KH, Mudge J, Gobena D, Hurtado-Gonzales OP, Schmutz J, Kuo A, et al. Genome sequencing and mapping reveal loss of heterozygosity as a mechanism for rapid adaptation in the vegetable pathogen Phytophthora capsici. Mol Plant Microbe Interact. 2012;25(10):1350–60.
Levesque CA, Brouwer H, Cano L, Hamilton JP, Holt C, Huitema E, et al. Genome sequence of the necrotrophic plant pathogen Pythium ultimum reveals original pathogenicity mechanisms and effector repertoire. Genome Biol. 2010;11(7):R73.
Jiang RH, de Bruijn I, Haas BJ, Belmonte R, Lobach L, Christie J, et al. Distinctive expansion of potential virulence genes in the genome of the oomycete fish pathogen Saprolegnia parasitica. PLoS Genet. 2013;9(6):e1003272.
Spanu PD, Abbott JC, Amselem J, Burgis TA, Soanes DM, Stuber K, et al. Genome expansion and gene loss in powdery mildew fungi reveal tradeoffs in extreme parasitism. Science. 2010;330(6010):1543–6.
Tian M, Win J, Savory E, Burkhardt A, Held M, Brandizzi F, et al. 454 Genome sequencing of Pseudoperonospora cubensis reveals effector proteins with a QXLR translocation motif. Mol Plant Microbe Interact. 2011;24(5):543–53.
Cooke DE, Drenth A, Duncan JM, Wagels G, Brasier CM. A molecular phylogeny of Phytophthora and related oomycetes. Fungal Genet Biol. 2000;30(1):17–32.
Goker M, Voglmayr H, Riethmuller A, Oberwinkler F. How do obligate parasites evolve? A multi-gene phylogenetic analysis of downy mildews. Fungal Genet Biol. 2007;44(2):105–22.
Thines M, Choi YJ, Kemen E, Ploch S, Holub EB, Shin HD, et al. A new species of Albugo parasitic to Arabidopsis thaliana reveals new evolutionary patterns in white blister rusts (Albuginaceae). Persoonia. 2009;22:123–8.
Runge F, Telle S, Ploch S, Savory E, Day B, Sharma R, et al. The inclusion of downy mildews in a multi-locus-dataset and its reanalysis reveals a high degree of paraphyly in Phytophthora. IMA Fungus. 2011;2(2):163–71.
Pais M, Win J, Yoshida K, Etherington GJ, Cano LM, Raffaele S, et al. From pathogen genomes to host plant processes: the power of plant parasitic oomycetes. Genome Biol. 2013;14(6):211.
Seidl MF, Van den Ackerveken G, Govers F, Snel B. Reconstruction of oomycete genome evolution identifies differences in evolutionary trajectories leading to present-day large gene families. Genome Biol Evol. 2012;4(3):199–211.
Meijer HJG, Hassen HH, Govers F. Phytophthora infestans has a plethora of phospholipase D enzymes including a subclass that has extracellular activity. PLoS One. 2011;6(3):e17767.
Meijer HJG, Govers F. Genomewide analysis of phospholipid signaling genes in Phytophthora spp.: novelties and a missing link. Mol Plant-Microbe Interact. 2006;19(12):1337–47.
Hua C, Meijer HJG, de Keijzer J, Zhao W, Wang Y, Govers F. GK4, a G-protein-coupled receptor with a phosphatidylinositol phosphate kinase domain in Phytophthora infestans, is involved in sporangia development and virulence. Mol Microbiol. 2013;88(2):352–70.
Kamoun S. A catalogue of the effector secretome of plant pathogenic oomycetes. Annu Rev Phytopathol. 2006;44:41–60.
Song J, Win J, Tian M, Schornack S, Kaschani F, Ilyas M, et al. Apoplastic effectors secreted by two unrelated eukaryotic plant pathogens target the tomato defense protease Rcr3. Proc Natl Acad Sci U S A. 2009;106(5):1654–9.
Soanes DM, Talbot NJ. Moving targets: rapid evolution of oomycete effectors. Trends Microbiol. 2008;16(11):507–10.
Tian M, Huitema E, Da Cunha L, Torto-Alalibo T, Kamoun S. A Kazal-like extracellular serine protease inhibitor from Phytophthora infestans targets the tomato pathogenesis-related protease P69B. J Biol Chem. 2004;279(25):26370–7.
Tian M, Benedetti B, Kamoun S. A Second Kazal-like protease inhibitor from Phytophthora infestans inhibits and interacts with the apoplastic pathogenesis-related protease P69B of tomato. Plant Physiol. 2005;138(3):1785–93.
Tian M, Win J, Song J, van der Hoorn R, van der Knaap E, Kamoun S. A Phytophthora infestans cystatin-like protein targets a novel tomato papain-like apoplastic protease. Plant Physiol. 2007;143(1):364–77.
Torto-Alalibo T, Tian M, Gajendran K, Waugh ME, van West P, Kamoun S. Expressed sequence tags from the oomycete fish pathogen Saprolegnia parasitica reveal putative virulence factors. BMC Microbiol. 2005;5:46.
Cheung F, Win J, Lang JM, Hamilton J, Vuong H, Leach JE, et al. Analysis of the Pythium ultimum transcriptome using Sanger and Pyrosequencing approaches. BMC Genomics. 2008;9:542.
Bouzidi MF, Parlange F, Nicolas P, Mouzeyar S. Expressed Sequence Tags from the oomycete Plasmopara halstedii, an obligate parasite of the sunflower. BMC Microbiol. 2007;7:110.
Boutemy LS, King SR, Win J, Hughes RK, Clarke TA, Blumenschein TM, et al. Structures of Phytophthora RXLR effector proteins: a conserved but adaptable fold underpins functional diversity. J Biol Chem. 2011;286(41):35834–42.
Win J, Krasileva KV, Kamoun S, Shirasu K, Staskawicz BJ, Banfield MJ. Sequence divergent RXLR effectors share a structural fold conserved across plant pathogenic oomycete species. PLoS Pathog. 2012;8(1):e1002400.
Mestre P, Piron MC, Merdinoglu D. Identification of effector genes from the phytopathogenic Oomycete Plasmopara viticola through the analysis of gene expression in germinated zoospores. Fungal Biol. 2012;116(7):825–35.
As-sadi F, Carrere S, Gascuel Q, Hourlier T, Rengel D, Le Paslier MC, et al. Transcriptomic analysis of the interaction between Helianthus annuus and its obligate parasite Plasmopara halstedii shows single nucleotide polymorphisms in CRN sequences. BMC Genomics. 2011;12:498.
Zerbino DR, Birney E. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res. 2008;18(5):821–9.
Parra G, Bradnam K, Korf I. CEGMA: a pipeline to accurately annotate core genes in eukaryotic genomes. Bioinformatics. 2007;23(9):1061–7.
Mi H, Lazareva-Ulitsky B, Loo R, Kejariwal A, Vandergriff J, Rabkin S, et al. The PANTHER database of protein families, subfamilies, functions and pathways. Nucleic Acids Res. 2005;33(Database issue):D284–288.
Hunter S, Apweiler R, Attwood TK, Bairoch A, Bateman A, Binns D, et al. InterPro: the integrative protein signature database. Nucleic Acids Res. 2009;37(Database issue):D211–215.
Spring O. Homothallic sexual reproduction in Plasmopara halstedii, the downy mildew of sunflower. Helia. 2000;23(32):19–26.
Roy S, Kagda M, Judelson HS. Genome-wide prediction and functional validation of promoter motifs regulating gene expression in spore and infection stages of Phytophthora infestans. PLoS Pathog. 2013;9(3):e1003182.
Roy S, Poidevin L, Jiang T, Judelson HS. Novel core promoter elements in the oomycete pathogen Phytophthora infestans and their influence on expression detected by genome-wide analysis. BMC Genomics. 2013;14:106.
Bailey TL, Boden M, Buske FA, Frith M, Grant CE, Clementi L, et al. MEME SUITE: tools for motif discovery and searching. Nucleic Acids Res. 2009;37(Web Server issue):W202–208.
Seidl MF, Wang R-P, Van den Ackerveken G, Govers F, Snel B. Bioinformatic Inference of Specific and General Transcription Factor Binding Sites in the Plant Pathogen Phytophthora infestans. PLoS One. 2013;7:e51295.
Dolfini D, Zambelli F, Pavesi G, Mantovani R. A perspective of promoter architecture from the CCAAT box. Cell Cycle. 2009;8(24):4127–37.
Blin K, Medema MH, Kazempour D, Fischbach MA, Breitling R, Takano E, et al. antiSMASH 2.0--a versatile platform for genome mining of secondary metabolite producers. Nucleic Acids Res. 2013;41(Web Server issue):W204–212.
Sieber SA, Marahiel MA. Molecular mechanisms underlying nonribosomal peptide synthesis: approaches to new antibiotics. Chem Rev. 2005;105(2):715–38.
Du L, Lou L. PKS and NRPS release mechanisms. Nat Prod Rep. 2010;27(2):255–78.
Oome S, Van den Ackerveken G. Comparative and functional analysis of the widely occurring family of Nep1-like proteins. Mol Plant Microbe Interact. 2014;27(10):1081–94.
Cabral A, Oome S, Sander N, Kufner I, Nurnberger T, Van den Ackerveken G. Nontoxic Nep1-like proteins of the downy mildew pathogen Hyaloperonospora arabidopsidis: repression of necrosis-inducing activity by a surface-exposed region. Mol Plant Microbe Interact. 2012;25(5):697–708.
Stassen JH, Seidl MF, Vergeer PW, Nijman IJ, Snel B, Cuppen E, et al. Effector identification in the lettuce downy mildew Bremia lactucae by massively parallel transcriptome sequencing. Mol Plant Pathol. 2012;13(7):719–31.
Dong S, Kong G, Qutob D, Yu X, Tang J, Kang J, et al. The NLP toxin family in Phytophthora sojae includes rapidly evolving groups that lack necrosis-inducing activity. Mol Plant Microbe Interact. 2012;25(7):896–909.
Raffaele S, Farrer RA, Cano LM, Studholme DJ, MacLean D, Thines M, et al. Genome evolution following host jumps in the Irish potato famine pathogen lineage. Science. 2010;330(6010):1540–3.
Raffaele S, Kamoun S. Genome evolution in filamentous plant pathogens: why bigger can be better. Nat Rev Microbiol. 2012;10(6):417–30.
Judelson HS. Sexual Reproduction in Oomycetes: Biology, Diversity, and Contributions to Fitness. Inc. Hoboken: John Wiley & Sons; 2009.
Spring O, Zipper R. Evidence for asexual genetic recombination in sunflower downy mildew, Plasmopara halstedii. Mycol Res. 2006;110(Pt 6):657–63.
Rozynek B, Spring O. Pathotypes of sunflower downy mildew in southern parts of Germany. HELIA. 2000;23(32):27–34.
Spring O, Bachofer M, Thines M, Riethmüller A, Göker M, Oberwinkler F. Intraspecific Relationship of Plasmopara halstedii Isolates Differing in Pathogenicity and Geographic Origin Based on ITS Sequence Data. Eur J Plant Pathol. 2006;114(3):309–15.
Xiang Q, Judelson HS. Myb transcription factors in the oomycete Phytophthora with novel diversified DNA-binding domains and developmental stage-specific expression. Gene. 2010;453(1–2):1–8.
Bakthavatsalam D, Meijer HJG, Noegel AA, Govers F. Novel phosphatidylinositol phosphate kinases with a G-protein coupled receptor signature are shared by Dictyostelium and Phytophthora. Trends Microbiol. 2006;14(9):378–82.
Bode HB. Entomopathogenic bacteria as a source of secondary metabolites. Curr Opin Chem Biol. 2009;13(2):224–30.
Bolker M, Basse CW, Schirawski J. Ustilago maydis secondary metabolism-from genomics to biochemistry. Fungal Genet Biol. 2008;45 Suppl 1:S88–93.
Waskiewicz A, Golinski P, Karolewski Z, Irzykowska L, Bocianowski J, Kostecki M, et al. Formation of fumonisins and other secondary metabolites by Fusarium oxysporum and F. proliferatum: a comparative study. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2010;27(5):608–15.
Spring O, Haas K. The fatty acid composition of Plasmopara halstedii and its taxonomic significance. Eur J Plant Pathol. 2002;108:263–7.
Yousef LF, Wojno M, Dick WA, Dick RP. Lipid profiling of the soybean pathogen Phytophthora sojae using Fatty Acid Methyl Esters (FAMEs). Fungal Biol. 2012;116(5):613–9.
Keller NP, Turner G, Bennett JW. Fungal secondary metabolism - from biochemistry to genomics. Nat Rev Microbiol. 2005;3(12):937–47.
Schneider P, Weber M, Rosenberger K, Hoffmeister D. A one-pot chemoenzymatic synthesis for the universal precursor of antidiabetes and antiviral bis-indolylquinones. Chem Biol. 2007;14(6):635–44.
Forseth RR, Amaike S, Schwenk D, Affeldt KJ, Hoffmeister D, Schroeder FC, et al. Homologous NRPS-like gene clusters mediate redundant small-molecule biosynthesis in Aspergillus flavus. Angewandte Chemie. 2013;52(5):1590–4.
Cohen Y, Sackston WE. Disappearance of IAA in the presence of tissues of sunflowers infected by Plasmopara halstedii. Can J Bot. 1974;52(4):861–6.
Benz A, Spring O. Identification and characterization of an auxin-degrading enzyme in downy mildew infected sunflower. Physiol Mol Plant Pathol. 1995;46(3):163–75.
Sharma R, Mishra B, Runge F, Thines M. Gene loss rather than gene gain is associated with a host jump from Monocots to Dicots in the Smut Fungus Melanopsichium pennsylvanicum. Genome Biol Evol. 2014;6(8):2034–49.
Feng BZ, Zhu XP, Fu L, Lv RF, Storey D, Tooley P, et al. Characterization of necrosis-inducing NLP proteins in Phytophthora capsici. BMC Plant Biol. 2014;14:126.
Lee SJ, Rose JK. Mediation of the transition from biotrophy to necrotrophy in hemibiotrophic plant pathogens by secreted effector proteins. Plant Signal Behav. 2010;5(6):769–72.
Qutob D, Kamoun S, Gijzen M. Expression of a Phytophthora sojae necrosis-inducing protein occurs during transition from biotrophy to necrotrophy. Plant J. 2002;32(3):361–73.
Schornack S, van Damme M, Bozkurt TO, Cano LM, Smoker M, Thines M, et al. Ancient class of translocated oomycete effectors targets the host nucleus. Proc Natl Acad Sci U S A. 2010;107(40):17421–6.
Win J, Morgan W, Bos J, Krasileva KV, Cano LM, Chaparro-Garcia A, et al. Adaptive evolution has targeted the C-terminal domain of the RXLR effectors of plant pathogenic oomycetes. Plant Cell. 2007;19(8):2349–69.
Thines M, Kamoun S. Oomycete-plant coevolution: recent advances and future prospects. Curr Opin Plant Biol. 2010;13(4):427–33.
Whisson SC, Boevink PC, Moleleki L, Avrova AO, Morales JG, Gilroy EM, et al. A translocation signal for delivery of oomycete effector proteins into host plant cells. Nature. 2007;450(7166):115–8.
van West P, de Bruijn I, Minor KL, Phillips AJ, Robertson EJ, Wawra S, et al. The putative RxLR effector protein SpHtp1 from the fish pathogenic oomycete Saprolegnia parasitica is translocated into fish cells. FEMS Microbiol Lett. 2010;310(2):127–37.
Thines M, Voglmayr H. An Introduction to the White Blister Rusts (Albuginales). In: Lamour K, Kamoun S, editors. Oomycete Genetics and Genomics: Diversity, Interactions, and Research Tools. Hoboken: John Wiley & Sons; 2008.
Bailey H, Dagenbach D, Jennings JM. The locus of the benefits of repetition-lag memory training. Neuropsychol Dev Cogn B Aging Neuropsychol Cogn. 2011;18(5):577–93.
Yaeno T, Shirasu K. The RXLR motif of oomycete effectors is not a sufficient element for binding to phosphatidylinositol monophosphates. Plant Signal Behav. 2013;8(4):e23865.
Dou D, Kale SD, Wang X, Jiang RH, Bruce NA, Arredondo FD, et al. RXLR-mediated entry of Phytophthora sojae effector Avr1b into soybean cells does not require pathogen-encoded machinery. Plant Cell. 2008;20(7):1930–47.
Hemetsberger C, Mueller AN, Matei A, Herrberger C, Hensel G, Kumlehn J, et al. The fungal core effector Pep1 is conserved across smuts of dicots and monocots. New Phytol. 2015;206(3):1116–26.
Hiller NL, Bhattacharjee S, van Ooij C, Liolios K, Harrison T, Lopez-Estrano C, et al. A host-targeting signal in virulence proteins reveals a secretome in malarial infection. Science. 2004;306(5703):1934–7.
Bhattacharjee S, Hiller NL, Liolios K, Win J, Kanneganti TD, Young C, et al. The malarial host-targeting signal is conserved in the Irish potato famine pathogen. PLoS Pathog. 2006;2(5):e50.
Marti M, Good RT, Rug M, Knuepfer E, Cowman AF. Targeting malaria virulence and remodeling proteins to the host erythrocyte. Science. 2004;306(5703):1930–3.
Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014;30(15):2114–20.
Sharma R, Thines M. FastQFS – A tool for evaluating and filtering paired-end sequencing data generated from high throughput sequencing. Mycological Progress. 2015;14:60.
Sharma R, Gassel S, Steiger S, Xia X, Bauer R, Sandmann G, et al. The genome of the basal agaricomycete Xanthophyllomyces dendrorhous provides insights into the organization of its acetyl-CoA derived pathways and the evolution of Agaricomycotina. BMC Genomics. 2015;16(1):233.
team RDc. R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing; 2008.
Conesa A, Gotz S, Garcia-Gomez JM, Terol J, Talon M, Robles M. Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics. 2005;21(18):3674–6.
Nielsen H, Engelbrecht J, Brunak S, von Heijne G. Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites. Protein Eng. 1997;10(1):1–6.
Li L, Stoeckert Jr CJ, Roos DS. OrthoMCL: identification of ortholog groups for eukaryotic genomes. Genome Res. 2003;13(9):2178–89.
Katoh K, Standley DM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol. 2013;30(4):772–80.
Stamatakis A. RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics. 2006;22(21):2688–90.
Gaulin E, Madoui MA, Bottin A, Jacquet C, Mathe C, Couloux A, et al. Transcriptome of Aphanomyces euteiches: new oomycete putative pathogenicity factors and metabolic pathways. Plos One. 2008;3:e1723.
We thank Claus Weiland and Eva-Maria Gerstner for support with respect to cluster access and setting up DOI for Pl. halstedii data files. This work was funded by the research funding program LOEWE “Landes-Offensive zur Entwicklung Wissenschaftlich-ökonomischer Exzellenz” of Hesse’s Ministry of Higher Education, Research, and the Arts in the framework of IPF. MT is grateful to WE, who helped to tidy up the final version of the draft, with help from DV, OK and LS.
The sequence data have been deposited at the European Nucleotide Archive (ENA) under the BioProject accession number PRJEB6932 and at our local server: dx.doi.org/10.12761/SGN.2015.7.
The authors declare that they have no competing interests.
MT designed and led the sequencing effort, DS, FG, GA, HJ, MK, MT, RS, SK, and SS conceived analyses; RS performed genome assemblies, gene predictions, orthology analyses including conserved effectors and phylogenetic analyses; OS and RZ isolated the single zoospore strain OS-Ph8-99-BlA4, XX handled the pathogen, conducted infection experiments, and isolated DNA and RNA for sequencing; LMC performed protease inhibitor predictions; EE has done expression profiling studies; EK and HBB performed secondary metabolite analyses; HJ investigated promoter sequences; RS, CS and JW performed RxLR and CRN predictions; SO and JK performed NLP analyses; CS and DS investigated the heterozygosity levels; JW looked for WY motifs in RxLR effectors; DJH and HM performed phospholipid predictions, MK performed SSR marker predictions. HJ and DS helped MT in proofreading the manuscript. All authors contributed to writing the manuscript. All authors read and approved the final manuscript.
Additional Material and Methods section. (DOCX 128 kb)
Supplementary figures. (PDF 34119 kb)
Simple sequence repeats within the genome of Plasmophara halstedii . (XLSX 26 kb)
Statistics of repetitive motifs in Pl. halstedii genome. (DOCX 38 kb)
Repeat motifs and their frequencies. (DOCX 57 kb)
Five candidate orthologs among the nine genomes. (XLSX 40 kb)
77 candidate orthologs among the five genomes. (XLSX 36 kb)
65 candidate orthologs among the six genomes. (XLSX 42 kb)
11 orthologs among the downy mildew genomes. (XLSX 40 kb)
PMSE genes among the oomycete genomes. (DOCX 50 kb)
PMSE gene ids of Pl. halstedii. (XLSX 12 kb)
Potential capacity of biosynthesis of plant hormones in Pl. halstedii. (DOCX 40 kb)
19 candidate NLPs of Pl. halstedii. (XLSX 58 kb)
Properties of candidate NLPs of Pl. halstedii. (DOCX 72 kb)
Protease inhibitors effector families predicted in the genome of Plasmopara halstedii. (DOCX 95 kb)
Kazal-like domain features among the different genomes. (XLSX 47 kb)
Cystatin-like domain features among the different genomes. (XLSX 44 kb)
Candidate CRNs of Pl. halstedii, predictions based on gene models. (XLSX 46 kb)
Candidate CRNs of Pl. halstedii, predictions based on ORFs generated from the un-masked genome. (XLSX 38 kb)
Candidate RxLR-like effectors of Pl. halstedii, predictions based on gene models. (XLSX 98 kb)
Candidate RxLR-like effectors of Pl. halstedii, predictions based on ORFs generated from the un-masked genome. (XLSX 11 kb)
Proteins with positive score for WY-fold hidden Markov model. (XLSX 13 kb)
Six orthologs of candidate RxLR-like proteins among the downy mildew genomes. (XLSX 34 kb)
Three orthologs of candidate RxLR-like proteins among the downy mildew and Phytophthora spp. genomes. (XLSX 32 kb)
Gene expression values of up-regulated candidate RxLR-like proteins and CRNs of Pl. halstedii. (XLSX 14 kb)
Gene expression values of down-regulated candidate RxLR-like proteins and CRNs of Pl. halstedii. (XLSX 65 kb)
About this article
- Comparative genomics
- Core effectors
- Downy mildew
- Obligate biotroph
- Plant pathogen
- RxLR effectors