Biotrophic eukaryotic plant pathogens require a living host for their growth and form an intimate haustorial interface with parasitized cells. Evolution to biotrophy occurred independently in fungal rusts and powdery mildews, and in oomycete white rusts and downy mildews. Biotroph evolution and molecular mechanisms of biotrophy are poorly understood. It has been proposed, but not shown, that obligate biotrophy results from (i) reduced selection for maintenance of biosynthetic pathways and (ii) gain of mechanisms to evade host recognition or suppress host defence. Here we use Illumina sequencing to define the genome, transcriptome, and gene models for the obligate biotroph oomycete and Arabidopsis parasite, Albugo laibachii. A. laibachii is a member of the Chromalveolata, which incorporates Heterokonts (containing the oomycetes), Apicomplexa (which includes human parasites like Plasmodium falciparum and Toxoplasma gondii), and four other taxa. From comparisons with other oomycete plant pathogens and other chromalveolates, we reveal independent loss of molybdenum-cofactor-requiring enzymes in downy mildews, white rusts, and the malaria parasite P. falciparum. Biotrophy also requires “effectors” to suppress host defence; we reveal RXLR and Crinkler effectors shared with other oomycetes, and also discover and verify a novel class of effectors, the “CHXCs”, by showing effector delivery and effector functionality. Our findings suggest that evolution to progressively more intimate association between host and parasite results in reduced selection for retention of certain biosynthetic pathways, and particularly reduced selection for retention of molybdopterin-requiring biosynthetic pathways. These mechanisms are not only relevant to plant pathogenic oomycetes but also to human pathogens within the Chromalveolata.
Plant pathogens that cannot grow except on their hosts are called obligate biotrophs. How such biotrophy evolves is poorly understood. In this study, we sequenced the genome of the obligate biotroph white rust pathogen (Albugo laibachii, Oomycota) of Arabidopsis. From comparisons with other oomycete plant pathogens, diatoms, and the human pathogen Plasmodium falciparum, we reveal a loss of important metabolic enzymes. We also reveal the appearance of defence-suppressing “effectors”, some carrying motifs known from other oomycete effectors, and discover and experimentally verify a novel class of effectors that share a CHXC motif within 50 amino acids of the signal peptide cleavage site. Obligate biotrophy involves an intimate association within host cells at the haustorial interface (where the parasite penetrates the host cell's cell wall), where nutrients are acquired from the host and effectors are delivered to the host. We found that A. laibachii, like Hyaloperonospora arabidopsidis and Plasmodium falciparum, lacks molybdopterin-requiring biosynthetic pathways, suggesting relaxed selection for retention of, or even selection against, this pathway. We propose that when defence suppression becomes sufficiently effective, hosts become such a reliable source of nutrients that a free-living phase can be lost. These mechanisms leading to obligate biotrophy and host specificity are relevant not only to plant pathogenic oomycetes but also to human pathogens.
Citation: Kemen E, Gardiner A, Schultz-Larsen T, Kemen AC, Balmuth AL, Robert-Seilaniantz A, et al. (2011) Gene Gain and Loss during Evolution of Obligate Parasitism in the White Rust Pathogen of Arabidopsis thaliana. PLoS Biol 9(7): e1001094. doi:10.1371/journal.pbio.1001094
Academic Editor: Frederick M. Ausubel, Massachusetts General Hospital, Harvard Medical School, United States of America
Received: October 27, 2010; Accepted: May 10, 2011; Published: July 5, 2011
Copyright: © 2011 Kemen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors thank European Research Council Advanced Investigator grant 233376 (ALBUGON), Gatsby Foundation, BBSRC, DFG (KE 1509/1-1), DASTI (Danish Agency for Science, Technology and Innovation) for funding. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: KOG, core eukaryotic orthologous group; LTR, long terminal repeat; Nc14, Norwich 14; Pst, Pseudomonas syringae pv. tomato; TM, transmembrane
For more than 150 years, attempts to culture downy mildews, powdery mildews, and rusts on artificial nutrient media have been unsuccessful. The terms obligate parasitism and obligate biotrophy are used to denote organisms that live in such an obligatory association with living hosts ,. Recent research on the obligate biotroph powdery mildew fungus Blumeria graminis or downy mildew oomycete Hyaloperonospora arabidopsidis reveals a close correlation between the biotrophic life style and massive gene losses in primary and secondary metabolism ,. Obligate biotrophs form an intimate haustorial interface with parasitized cells. Haustoria are differentiated intercellular hyphae, but little is known about their functionality and evolution beyond their involvement in nutrient uptake ,.
The obligate biotroph oomycete Albugo laibachii is a member of the Chromalveolata, which incorporates Dinophyta, Ciliophora, Heterokonts (containing the oomycetes), Haptophyta, Cryptophyta, and Apicomplexa (which includes human parasites like Plasmodium falciparum and Toxoplasma gondii ,).
Within the oomycetes, A. laibachii belongs to a lineage known as peronosporalean, which includes the hemibiotrophic pathogen of potato Phytophthora infestans  and the necrotroph pathogen Pythium ultimum . Within this lineage, obligate biotrophy evolved twice independently in white blister rusts (Albuginales) and downy mildews (part of the Peronosporaceae) . The downy mildew pathogen H. arabidopsidis and A. laibachii are both pathogens of the model plant Arabidopsis thaliana . While both show similar infection structures within the host ,, A. laibachii releases motile zoospores from asexual spores and sexual oospores, while H. arabidopsidis lacks all motile stages ,. Both pathogens are regularly found to co-infect plants and sporulate on the same leaf .
A remarkable consequence of infection by Albugo sp. is enhanced host plant susceptibility to other parasites to which the host is resistant in the absence of Albugo infection, and also impairment of cell death mechanisms . Albugo sp. infect 63 genera and 241 species , including economically important Brassica rapa (canola), B. juncea (oilseed mustard), and B. oleracea (cabbage family vegetables) ,. Recent analysis of oomycete evolutionary history  suggest that Albugo is more closely related to necrotrophs such as Pythium than to downy mildews, and thus provides a unique system to study the evolution and consequences of biotrophy, and to identify new defence-suppressing effectors and their host targets.
A. laibachii Isolates
Since prolonged culture of pathogen strains can result in genetic changes , we sequenced a fresh highly virulent field isolate of A. laibachii. The strain was selected from a heavily infected Ar. thaliana field plot (Norwich, United Kingdom) , and strains were single zoospore purified. Isolate Norwich 14 (Nc14) was determined as A. laibachii  and used for further analyses. In contrast to Nc14, A. laibachii isolate Em1 (formerly Acem1, A. candida East Malling 1 ) is an established Albugo strain that was collected 15 y ago ,,, and we resequenced this strain. Both strains show identical ITS (internal transcribed spacer of ribosomal RNAs) and COX2 (cytochrome C oxidase subunit II) sequences. To ensure that sequence differences observed between these strains are of biological relevance not just the result of background mutations, we tested the host range for both isolates on 126 Ar. thaliana accessions and identified 12 that show resistance to only one of the A. laibachii isolates (Table S1). Nc14 is virulent on more accessions than the Em1 isolate is (Table 1).
Illumina Genome Sequencing, Assembly, and Quality Assessment
The A. laibachii Nc14 genome was sequenced using Illumina 76-bp paired reads with ~240-fold coverage (Figure 1). In order to assemble the diploid heterozygous genome, an assembly pipeline was developed using Velvet  as primary assembler and Minimus  as meta-assembler (Figure S1). Short read assembly programs are sensitive to heterozygous positions depending on read depth and kmer-length. Reads not aligning to bacterial or plant sequence in public databases were used to estimate the genome size as ~37 Mbp. Using the estimated genome size, 50% of the resulting assembly is contained in 164 contigs with an N50 of 56.5 kbp. A comparative analysis of contig size classes versus frequency indicates that 90% of the assembled genome shows a high degree of continuity in only 585 contigs, while 10% of the genome is fragmented in 3,231 contigs (Figure 2A). Read depth indicates that this 10% of the genome shows elevated levels of nucleotide coverage that are likely to comprise unresolved repeats (Figure 2B). Aligning Illumina cDNA reads from different stages of infection to reveal transcriptionally active regions in the assembly shows that few transcripts arise from the unresolved repetitive regions of the genome (Figure 2D), suggesting that the gene space of a genome can be reliably defined using Illumina-only approaches. A CEGMA  analysis revealed a high degree of completeness of assembly of core eukaryotic genes, as well as a continuity within the core genes comparable to high-quality Sanger read assemblies (Figure S2; Table S2). We designed 32 primer pairs for regions between 0.6 and 5 kb based on our assembly (Table S3). Thirty-one genomic regions could be amplified and were Sanger sequenced from both ends. All PCR products had the predicted size, and sequences showed 100% identity to the genome assembly.
(A) Reads generated for A. laibachii Nc14 using Illumina genome analyzer version 1 (GA1) or version 2 (GA2). (B) Distribution of genomic coverage. Grey fields indicate the total amount of sequence represented by the 100-bp windows with corresponding coverage. (C) Reads generated for A. laibachii Em1. (D) Distribution of genomic coverage showing Em1 reads aligned to the Nc14 genome using MAQ aligner. Nc14 and Em1 show a major peak at 226× and 43× coverage, respectively. A second peak is detected at 112× or 22×, showing half the coverage of the main peak, indicating highly heterozygous regions that were not merged in the assembly or hemizygous regions.
(A) Genomic distribution of contig length (N length) versus contig number (N number). N lengths were calculated by ordering all sequences according to their length and then adding the length from longest to shortest until the summed length exceeded 10% (N10), 20% (N20), etc., up to 100% (N100) of the assembled contigs (32.7 Mbp). Blotting the N length versus the N number (number of contigs in each N category) indicates that 90% of the assembled genome show high continuity, while the last 10% are highly fragmented. (B) Average coverage for each category for Nc14 (red) and Em1 (green). In all, 90% of the genome shows low variation, consistent with 210–240× coverage for Nc14 and 40–50× for Em1. The last 10% show highly elevated coverage, indicating unresolved highly repetitive regions present in Nc14 and Em1. (C) Distribution of heterozygosity in each N category shows elevated levels in the set of short contigs. Heterozygous positions were accepted only if coverage was >180× and <350× for Nc14 (red) or >27× and <80× for Em1 (green). SNPs between Nc14 and Em1 were calculated ignoring heterozygous positions (lilac). (D) Alignment of Nc14 cDNA and summing up all regions showing >2× coverage indicate that the more continuous part of the genome contains more transcribed regions than the highly repetitive regions of the genome (in the histogram, N length and N number are cumulative while read depth, SNP frequency, and cDNA coverage are presented as binned data).
The mitochondrial draft genome was assembled in a separate attempt because of its high repeat content and therefore higher coverage compared to the core genome. The assembled genome comprises 26.7 kb in 11 contigs and shows a high degree of synteny to the P. infestans mitochondrion Ia  and the Py. ultimum mitochondrion  (Figure S3). Considering the node coverage of the Velvet primary assembly (~150×), 15.6 kb of the mitochondrial genome have >300× node coverage and seem to be duplicated. This might indicate, comparable to the Py. ultimum mitochondrion genome , that ~50% of the genome is duplicated, leading to an estimated genome size of ~43 kb. While the highly repetitive tRNAs are not resolved within the A. laibachii mitochondrial genome, regions of high synteny between the Py. ultimum and the P. infestans mitochondrial genome are found in ribosomal proteins and subunits of the NADH dehydrogenase as well as cytochrome C oxidase.
Features of the A. laibachii Nuclear Genome
Approximately 22% of the A. laibachii Nc14 genome assembly consists of repetitive regions (Figure 3; Tables S4 and S5). The majority of repeats are represented by transposable elements (96%), while 4% of all repeats are A. laibachii-specific (Table S5). Compared to other obligate biotrophs, the number of repeats is low. H. arabidopsidis, for example, with an estimated genome size of 100 Mb, contains ~43.3% repeats , while transposable elements account for 64% of the ~120-Mb Bl. graminis (powdery mildew) genome . We identified 45 contigs carrying telomeric repeats; amongst these, 25 contigs have telomeric repeats located at one end of a contig. We therefore postulate that the A. laibachii Nc14 genome is distributed over 12 or 13 chromosomes (Table S6). tRNA genes are difficult to resolve because of their high copy number . Within our Illumina assembly, 153 tRNA genes were detected with 48 distinct anticodons (Figure S4; Table S7). Our ability to resolve all these repeats within the Illumina short read assembly illustrates its quality.
Initial run of RepeatScout produced a library of 1,252 consensus repetitive sequences that include transposable elements, recently duplicated paralogous genes, and other dispersed duplicated regions. (A) Inset: The distribution of lengths of the identified repeats versus their frequency in the genome is shown. The majority of repeats fell into the category of short and rare in the assembly. The primary plot in (A) shows that the majority of the longest and most frequent repeats in the genome are transposon elements (shown in green and Table 1), while Albugo-specific repetitive sequences are mostly short (shown in red). (B) Summary of the proportion of the repetitive sequences (percent) in the A. laibachii Nc14 genome.
Based on read depth, both Nc14 and Em1 isolates possess ~6 Mbp of hemizygous or highly heterozygous regions (6.2 and 5.6 Mbp for Nc14 and Em1, respectively) (Figure 1B and 1D) as well as ~13,000 heterozygous loci (13,116 and 13,523 for Nc14 and Em1, respectively) (Figure 2C). Remarkably, most of the hemizygous/highly heterozygous regions are shared between Nc14 and Em1.
Compared to other sequenced oomycetes like P. infestans (240 Mbp), H. arabidopsidis (100 Mbp), or even Py. ultimum (42.8 Mbp), A. laibachii has a highly compact genome structure (Figure 4A). Approximately 50% of the A. laibachii genome assembly matched cDNA reads, and transcriptionally active regions are further clustered, resulting in transcriptional hot spots and silent genomic regions (Figure 4B).
(A) Synteny between A. laibachii, Py. ultimum, H. arabidopsidis, and P. infestans. The region shown is an example of the dense clustering of genes in the pentafunctional AROM polypeptide and a P-type ATPase. The AROM polypeptide comprises five enzymes of the shikimate pathway in one enzyme. With increasing genome size the distance between both genes increases and re-organisations occur (red, synteny without inversion; blue, inverted regions). (B) Plotting the distance between transcriptional islands based on the 5′ to 3′ orientation of the forward strand reveals that transcriptional regions are clustered close together. The maximum peak reflects the average intron size. Regions with no 3′ but with 5′ distance and vice versa reflect overlapping 3′ and 5′ non-coding regions of genes. Analysing the distance distribution between transcriptional units reveals a median distance between genes of 45 bp, showing that within transcribed regions, nearly all the DNA sequence corresponds to genes. (C) Plotting the 5′–3′ distance for all genes from ATG to stop to the next gene confirms the gene clustering. Only 10.8% of all genes have a distance to the next gene or the end of the contig greater than 3 kb. Summing the distance between these genes contributes to only 10.9 Mbp of the genome because of the close packaging, while summing the distance of the few genes that are not in clusters contributes to 8.4 Mbp of the genome.
Annotation and Validation of Protein Coding Genes
A reference set of 13,032 gene models was generated incorporating cDNA reads from different stages of infection (Figure S5A). From extensive cDNA sequencing of infected Arabidopsis leaves, approximately 20 M (~1.5 Gbp) unique Illumina reads match the Nc14 genome assembly but not Ar. thaliana TAIR 9.0, and these were used to generate training sets for ab initio gene predictions and as evidence sets for consensus gene prediction. In all, 88.3% of all gene models are supported by at least three cDNA hits.
For validation of these gene models, a set of 860 annotated core eukaryotic orthologous groups (KOGs)  was compiled and tested. In all, 75% of these groups are present in the current annotation. For comparison, 78% of KOGs were present in P. infestans, 73% in H. arabidopsidis, 42% in Pl. falciparum, and 85% in Ar. thaliana (Figure S5B). In addition, 49.9% of all gene models show Pfam support, resulting in 2,505 Pfam domains, and 803 genes were functionally assigned to pathways using ASGARD  and manual annotation. Transcriptional units show an even more compact, clustered occurrence than P. sojae or P. ramorum and an occurrence pattern clearly different from that of P. infestans  (Figure 4C).
From our annotations using ASGARD we identified major enzymes of the lipopolysaccharide biosynthesis pathway, as have been described for P. infestans . These analyses revealed, in addition, the possibility that A. laibachii is able to synthesize brassinosteroids. We identified potential homologues to the Ar. thaliana brassinosteroid biosynthesis genes Dwf4 and DET2 (Table S8). Although ASGARD identified homologues of Br6ox, D2, and CPD, manual annotation revealed that assigning function to members of the superfamily of cytochrome P450 enzymes in A. laibachii is difficult based on homology alone (Table S8). It has been hypothesized that the frequency of functionally redundant genes is reduced in obligate biotrophs, as reported for Bl. graminis . Combining ASGARD and manual annotation we identified the absence of the whole steroid biosynthesis pathway, and, like other oomycetes, A. laibachii probably relies on the host as a source of sterols. We hypothesize that A. laibachii would need to take up campesterol from the plant as a precursor for brassinosteroid synthesis.
Ancestral Red and Green Algae Genes in the A. laibachii Genome
During evolution, plastids of both red algae and green algae were transferred to other lineages by secondary endosymbiosis. How often and when secondary endosymbiosis occurred is difficult to address but of importance to clarify the origin of chromalveolates and their gain and loss of endosymbionts. There are two distinct hypotheses for what took place. The monophyletic hypothesis posits that a red alga was taken up only once, followed by repeated losses of this algal genome, giving rise to the highly divergent group of chromalveolates . An alternative and more common view hypothesizes polyphyletic origins of the Chromalveolata, with in some cases multiple events of secondary endosymbiosis –.
Molecular divergence of A. laibachii from other species within the Chromalveolata was assessed by examining the percentage of amino acid identity between orthologous gene pairs (Figure 5). These analyses demonstrate that the green alga Chlamydomonas reinhardtii, the brown alga Ectocarpus siliculosus, and the diatom Phaeodactylum tricornutum show the same distribution of percentage amino acid identity to A. laibachii Nc14 regarding the cumulative frequency of orthologous pairs. In contrast, previous systematic analyses suggested that brown algae and diatoms are the closest relatives of oomycetes and that secondary endosymbiosis occurred with a red alga , although there are suggestions that oomycetes diverged before this event . Using a set of >1,700 genes that are of “green” origin (from green algae) or “red” origin (from red algae) and that have been integrated into the diatom nuclear genome , we found more oomycete genes that show significant BLAST hits to green algae than to red algae (34 “green” compared to five “red”) (Figure S6; Table S9). These findings are consistent with the results published by Moustafa et al.  for diatoms. In a separate approach we identified genes showing high similarity between oomycetes, green algae, and red algae that are absent from diatoms (32 “green”; 11 “red”) (Tables S10 and S11). This result might indicate the presence of all these genes in a common ancestor, followed by loss or expansion of the gene family depending on adopted live style. To address this question, we further analysed genes absent from A. laibachii Nc14 and studied their presence/absence in three other oomycetes, Pl. falciparum, and the brown alga E. siliculosus (Table S12). The majority of genes absent from A. laibachii Nc14 are absent from other oomycetes and from Pl. falciparum but are present in the brown alga. These genes are involved in the photoautotrophic, aquatic life style of diatoms and algae, such as a sodium/bile acid cotransporter, a haloacid dehalogenase-like hydrolase, fatty acid biosynthesis genes, a zeaxanthin epoxidase and a fucoxanthin chlorophyll a/c binding protein. In contrast to the genes lost, we found that certain gene families like aspartic proteases or proteases containing MORN (membrane occupation and recognition nexus) repeats  show expansion in A. laibachii Nc14 compared to in diatoms. Although our results fit the hypothesis of a common ancestor, we cannot exclude horizontal gene transfer and uptake of an endosymbiont after the divergence between a brown algal ancestor and an oomycete ancestor, given the low number of diagnosed genes that we could analyse.
(A) Molecular divergence based on all pairwise comparisons of the one-to-one orthologues. In the figure, the cumulative frequencies of amino acid identity across each set of potential orthologous pairs is presented, indicating that although H. arabidopsidis and A. laibachii are both biotrophs, H. arabidopsidis is less diverged from P. infestans than it is from A. laibachii (e.g., in the H. arabidopsidis–A. laibachii comparison, ~22% of all orthologues show an amino acid identity of <50%, while only ~14% in a Py. ultimum–A. laibachii comparison show an amino acid identity of <50%). A. laibachii shows the highest amino acid identity to Py. ultimum. (B) Molecular divergence between A. laibachii and other species based on the subset of core eukaryotic genes to show stability of the test. Results are consistent with the one-to-one orthologue analyses although differences between A. laibachii, P. infestans, H. arabidopsidis, and Py. ultimum are less obvious, indicating the lack of selection pressure on the core eukaryotic genes . For comparative reasons, a tree using ITS2 sequences is added. The represented tree is a maximum likelihood tree produced with PhyML.
Potentially green-algae-derived proteins carrying MORN repeat domains (Figure S7) are involved in the complex process of internal budding in apicomplexans , which may be similar to the zoospore formation of oomycetes within oospores or zoosporangia or gamete formation in diatoms . While oomycetes with a motile zoospore stage like A. laibachii and P. infestans carry the MORN repeat proteins, these proteins are absent in the non-motile H. arabidopsidis and absent in the non-motile red alga Cyanidioschyzon merolae . We therefore hypothesize that loss of this gene of hypothetical green algal origin could have led to the evolutionary loss of the whole flagellum apparatus in H. arabidopsidis . However, we cannot rule out that depletion of any major flagellar protein could have caused evolutionary loss of the whole flagellum apparatus. Inspection of the flagellar inner arm dynein 1 heavy chain alpha, which is absolutely necessary for flagellum function, reveals that genomic regions carrying flagellar inner arm dynein 1 heavy chain alpha genes show a high degree of synteny between oomycetes like Py. ultimum and A. laibachii. In contrast, a syntenic region in H. arabidopsidis shows replacement of the flagellar dynein by Mariner- or Gypsy-like transposable elements (Figure S8).
Comparative Genomics to Identify Genes Implicated in Biotrophy
Since within the peronosporalean lineage, biotrophy evolved twice independently , we compared A. laibachii with the other obligate biotroph H. arabidopsidis , hemibiotroph P. infestans , and necrotroph Py. ultimum  (Figure 5; Tables S13 and S14). We found that H. arabidopsidis is the most diverged from A. laibachii. H. arabidopsidis shares the fewest (4,826) orthologous genes with A. laibachii, versus the average of 5,722 in A. laibachii/P. infestans and A. laibachii/Py. ultimum comparisons. Meanwhile, H. arabidopsidis genes show the highest amino acid identity with the genes of P. infestans, on average 73% of amino acid identity between all single copy orthologous pairs.
Py. ultimum shares the highest number of orthologous genes with A. laibachii (5,910 pairs). P. ultimum proteins also have a slightly higher percentage of amino acid identity with A. laibachii proteins than with other oomycetes (Figure 5). Yet, Py. ultimum itself is closer to H. arabidopsidis and P. infestans than to A. laibachii, sharing with them more orthologous genes with higher mean amino acid identity.
These analyses support the hypothesis that A. laibachii and H. arabidopsidis evolved biotrophy independently; genes missing in one or the other genome compared to the necrotroph Py. ultimum or hemibiotroph P. infestans may be correlated with biotrophy (Table S15). One of these genes is that for molybdenum-cofactor-dependent nitrate reductase. Nitrate reductase catalyzes pyridine-nucleotide-dependent nitrate reduction for nitrogen acquisition . Both biotroph pathogens have a set of transporters showing homology to amino acid transporters, but other uptake mechanisms or sources could also enable nitrogen acquisition from their hosts . While H. arabidopsidis lost only the nitrate reductase, A. laibachii also lost the sulphite oxidase and the whole molybdopterin (a cofactor required for nitrate reductase and sulphite oxidase function) biosynthesis pathway. In Pl. falciparum, which shows a high degree of adaptation to parasitism, nitrate reductase, sulphite oxidase, and the whole molybdopterin biosynthesis pathway are also missing. Most likely the loss of the two Mo-containing enzymes and the Mo-cofactor biosynthesis is the outcome of biotrophy and not the reason for biotrophy, though conceivably there may have been selection against this pathway if other nitrogen or sulphate sources are less energy-consuming and therefore enhance fitness during parasitism. Molybdenum has been reported to interfere with function of chaperones like Hsp90 ,. Avoiding the uptake of molybdenum might prevent this Hsp90 inhibition and increase fitness on Ar. thaliana accessions with high molybdenum levels like Col-0 . H. arabidopsidis therefore could be in a less advanced stage of host adaptation compared to A. laibachii and Pl. falciparum.
Besides biotrophy, the formation of haustoria and haustorium-like structures evolved several times in peronosporalean biotroph and hemibiotroph pathogens. Haustoria in fungi are sites of enhanced nutrient uptake  and metabolism, such as thiamine biosynthesis . In the oomycetes, all haustorium-forming species have lost the thiamine biosynthetic pathway. We infer that haustorial oomycetes obtain thiamine from the host.
We therefore hypothesize that evolution to biotrophy is initiated not by gene loss, but rather from the ability to build a haustorium and therefore differentiate a sophisticated interface with a host. The critical step to adopting biotrophy is likely to be efficient defence suppression to enable persistence of functioning haustoria; subsequent loss of biosynthetic pathways is likely to be secondary.
The A. laibachii Secretome
Well-adapted human pathogens like Pl. falciparum and plant pathogenic fungi like Ustilago maydis have small secretomes (320  and 426  proteins, respectively) compared to necrotrophic fungi like Aspergillus fumigatus (up to 881 proteins ). We found that the same is true for oomycetes. Using SignalP  to predict potential secretion signal peptides and MEMSAT  to predict transmembrane (TM) domains, we identified 2,473 (2,136 without TM domains) potentially secreted proteins in the hemibiotroph P. infestans and 1,636 (1,222 without TM domains) in the necrotroph Py. ultimum. For H. arabidopsidis only 1,350 (1,054 without TM domains) and for A. laibachii 949 (672 without TM domains) were identified. Analysing the secretome for pathogenicity-related proteins like proteases, glucosyl hydrolases, and potential elicitins or lectins reveals a significant reduction in the H. arabidopsidis and A. laibachii secretome (Tables 2 and S16). We postulate that biotrophs reduce their activation of host defence by reducing their inventory of secreted proteins, particularly cell wall hydrolyzing enzymes.
The A. laibachii Effector Complement
The ability to establish a sophisticated zone of interaction like the parasitophorous vacuole in Pl. falciparum or the haustorium in oomycetes and fungi requires sophisticated host defence suppression , which is predominantly achieved via secreted proteins delivered into the host cell ,. The A. laibachii secretome comprises 672 secreted proteins without TM domains. Genetically identified oomycete avirulence (Avr) proteins are secreted proteins that have signal peptide and RXLR motifs ,. In many oomycete genomes the RXLR motif is over-represented and positionally constrained within the secreted protein . We identified 25 RXLR and 24 RXLQ effector candidates in the A. laibachii secretome. To determine the likelihood that RXLR or RXLQ motifs occur merely by chance in the A. laibachii secretome based on amino acid content, we performed in silico permutation of the motifs (Figure 6A and 6B). We concluded that the RXLR and RXLQ motifs were not likely to occur merely by chance, and that the likelihood of occurrence by chance is higher in the proteome as a whole than among secreted proteins. It was shown for P. infestans that effectors are often located in gene-depleted repetitive regions of the genome . We therefore investigated RXLR candidate proteins in highly repetitive regions of the genome. We identified two RXLRs, one in a highly conserved repeat region with ~10 repeats in Nc14 and one in a more diverged repeat region with >80 repeats within the genome. The first region also exists in A. laibachii isolate Em1; the diverged repeat of the second identified region exists but without the RXLR gene-containing region (Figure S9). There are 563 RXLR effector candidates identified in P. infestans , so RXLR effectors are less likely to be relevant for A. laibachii virulence.
To identify potential effector delivery motifs we analysed RXLR (A), RXLQ (B), and the new CHXC (C) effector candidates for enrichment in the secretome. Motif shuffling was used to identify background levels. Calculating the cumulative hypergeometric probability to analyse the enrichment of secreted proteins (red) over non-secreted proteins (blue) for each of the permutated motifs reveals a significant enrichment of CHXCs in the secretome (p[X≥x] = 2.19×10−22). None of the RXLR or RXLQ motifs or permutations shows significant enrichment. There is also enrichment for CXHC proteins in the secretome. Except for one CHHC protein, there is no overlap between the two motif classes. The logo blot (D) clearly indicates that RXLR-containing proteins are conserved only within the selected amino acids, while for CHXCs it is not only the motif but also sequences C-terminal to it are conserved, including conserved glycine, leucines, and a tyrosine.
Similar conclusions can be drawn for the CRN protein family, which shows expansion in P. infestans , but not A. laibachii, where only three members of the CRN family could be identified with signal peptides. Eight additional CRN-like proteins were identified where no signal peptide has been predicted.
To identify new classes of effectors in the Albuginales clade, the secretome of A. laibachii was computationally screened for genes either showing heterozygosity or showing nucleotide polymorphisms between Nc14 and Em1. We identified a new class carrying a “CHXC” motif by inspection of the first 80 amino acids after the signal peptide cleavage site. CHXC candidates are significantly enriched within the secretome (Figure 6C). Comparisons of the N-terminal part of the CHXC proteins revealed additional conserved amino acids, particularly a glycin at +6 to the CHXC motif (Figure 6D).
Intraspecies Comparison between A. laibachii Nc14 and A. laibachii Em1
In host–pathogen interactions, intraspecies comparisons enable the search for virulence alleles that undergo positive selection and fixation within the population ,. Secreted proteins with close contact to the host cell, such as effector proteins, often show enhanced levels of positive selection ,. By comparing the two A. laibachii isolates Nc14 and Em1, we identified a significantly higher frequency of non-synonymous to synonymous mutations within the predicted secretome compared to the rest of the proteome. Our analyses showed that this was particularly true for heterozygous positions and less convincing for homozygous SNPs (Table S17). Genes that are highly conserved between species, like KOGs, showed comparable non-synonymous and synonymous substitution rates, with a slight excess of synonymous mutations. There are significantly more genes within the KOGs showing a non-synonymous/synonymous ratio less than 1 than genes with values greater than 1. Comparing this to candidate effector classes like RXLRs, RXLQs, and CHXCs reveals that in particular the CHXCs show significantly higher frequencies of non-synonymous to synonymous mutations. This supports the idea that the CHXC sub-class of secreted proteins is under positive selection, similar to other described oomycete effectors like ATR1 or ATR13 from H. arabidopsidis ,.
Further to this we identified Nc14 genes absent or highly diverged from the Em1 complement. We defined a gene as absent or highly diverged if >10 bp showed 0 coverage in the Em1 alignment. Out of the 672 secreted proteins without TM domains, we identified seven as absent from Em1 (1.04%). We also detected two with a predicted TM domain (0.73%) that are absent from Em1. Regarding all gene models, 96 were absent (0.74%). This finding is a further indication for a greater selection pressure on secreted than on non-secreted proteins, as has been found in species or interspecies comparisons in Phytophthora sp.  and Ustilago/Sporisorium .
Validation of Effector Delivery
We tested A. laibachii effector candidates (one CHXC, one RXLR, and one CRN effector candidate) for their host delivery efficiency using a P. capsici–Nicotiana benthamiana translocation assay . Briefly, N-terminal domains of candidate effectors were fused to the P. infestans Avr3a effector domain, transformed into P. capsici, and tested for whether they confer translocation of Avr3a into N. benthamiana carrying R3a, resulting in avirulence. Statistical analyses of the delivery efficiency (Figure 7) clearly indicate that the A. laibachii CRN3 N-terminus and CHXC9 N-terminus are as efficient as the Avr3a N-terminus in Avr3a translocation, while the RXLR1 N-terminal domain is less efficient. An alanine replacement construct of the CHXC motif supports the importance of this motif for delivery efficiency. The Avr3a C-terminus alone confers a low basal delivery level without the need for the N-terminal enhancer. These findings reveal the potential of the CHXC proteins to be delivered into the host cell, similar to RXLRs and CRNs, though the delivery mechanism for all these effector classes requires further investigation.
To identify known and new classes of transfer motifs in A. laibachii, the P. capsici–N. benthamiana translocation assay was used. This test system is based on Avr3a-mediated avirulence in plants carrying R3a . (A) virulence assay to show that transgenic P. capsici is not impaired in growth; (B) Hypersensitive response (HR) assay on R3a-carrying plants for delivery assay. The Avr3a RxLR translocation domain is replaced by the N-terminus of different A. laibachii effector candidates. For the assay, RXLR1, CRN3, and CHXC9 carrying the newly identified CHXC motif were used. Our results validate that known motifs like the CRN motif are functional while the selected RXLR shows low delivery efficiency. CHXC9 shows the same efficiency as Avr3a does, and dependency of the CHXC motif could be identified (statistical analyses using the Tukey test; means with the same letter are not significantly different; error bars denote standard error of the mean). wt, wild type.
Validation of Virulence-Conferring Function of A. laibachii Effector Candidates
To assay the effectors for virulence function, we used Pseudomonas syringae pv. tomato (Pst) DC3000 luciferase  carrying “effector detector vector” (EDV) constructs to deliver effectors into the plant cytoplasm via type III secretion  (Figure 8). Tests on Ar. thaliana Nd-0 plants revealed that several selected A. laibachii RXLRs, CRNs, and CHXCs enhance virulence compared to a non-functional AvrRps4 (AvrRps4[AAAA]). On Ar. thaliana Col-0, in contrast, the CRN and one RXLR (RXLR1) do not enhance virulence while RXLR2 and CHXCs still do. These tests indicate that CHXCs carry the capacity to enhance virulence in phytopathogenic bacteria, perhaps by suppression of host resistance mechanisms ,. These virulence assays together suggest that A. laibachii uses at least three different major effector classes.
(A) Arabidopsis plants (4- to 5-wk-old) were spray inoculated with 5×108 CFU Pst DC3000 lux harbouring candidate effectors cloned in pEDV6. Bacterial growth was measured as an increase in luciferase photon emission per gram fresh weight per second (photon/g[fw]/sec). The histogram represents the log median of photon emission of three independent experiments, each with four technical replicates. Error bars denote standard error of the mean. Two-way ANOVA: #, p<0.001; **, p<0.01; *, p<0.05 from AvrRps4(AAAA). (B) Plants 4- to 5-wk-old were infected with 5×108 CFU of Pst DC3000 ΔAvrPto/ΔAvrPtoB harbouring candidate effector cloned in pEDV6. Bacterial populations were sampled 4 d post-inoculation. The histogram represents the median colony count of two independent experiments, each with more than four technical replicates. Error bars denote standard error of the mean.
Evolutionary Origin of CHXC Effectors
To try to identify the evolutionary source of CHXCs, we investigated enrichment of CHXC-motif-containing proteins in the secretomes of P. infestans, Py. ultimum, H. arabidopsidis, Saprolegnia parasitica, Thalassiosira pseudonana (diatom), Pl. falciparum (Apicomplexa), E. siliculosus (brown alga), C. merolae (red alga), Ch. reinhardtii (green alga), Volvox carteri (green alga), and Ar. thaliana. Only A. laibachii contained a significant enrichment of CHXCs in its secretome. Although not significantly enriched, both the fish pathogen S. parasitica and the land plant Ar. thaliana contained more than ten CHXC proteins carrying potential secretion signals (14 and 11, respectively) (Figure S10). In contrast to CHXC-containing proteins, almost all inspected organisms show a high number of CXHC-containing potentially secreted proteins; a common CXHC protein is protein disulphide isomerase (Table S18).
Given that A. laibachii CHXCs show the closest clustering with S. parasitica, V. carteri, Ch. reinhardtii, and Ar. thaliana CHXCs (Figure 9), conceivably this candidate effector class evolved from an ancestral green-alga-derived gene.
The outer ring summarises clades with N-termini predominantly carrying CHXC or CXHC motif or mixed clades (CXHC/CHXC) into classes. A. laibachii CHXCs are mainly clustered in the CHXC class (green), containing besides A. laibachii distantly related CHXCs from S. parasitica, V. carteri, Ch. reinhardtii, and Ar. thaliana. CHXCs are distant from endoplasmic reticulum proteins like disulphide isomerases that predominantly carry the CXHC motif and are grouped within the CXHC class (red). Between the CHXC class and the CXHC class, mixed clades contain protease and defensin homologues (orange) or Ar. thaliana cystein-rich proteins (violet). (Names in green indicate A. laibachii CHXCs and in yellow, A. laibachii CXHCs. Blue indicates CHXCs from other species; magenta indicates CXHCs from other species; 16 amino acids before and 45 amino acids after the CHXC or CXHC motif in the N-terminus were used. The tree is midpoint rooted. All bootstrap counts refer to 1,000 replications.). Ath, Ar. thaliana; Cla, Ch. reinhardtii; Cme, C. merolae; Ect, E. siliculosus; Hpa, H. arabidopsidis; Pfa, Pl. falciparum; Pin, P. infestans; Pul, Py. ultimum; Spr, S. parasitica (Spr); Tps, T. pseudonana; Vca, V. carteri.
Whatever their origin, we conclude that CHXC proteins are present in all organisms analysed but evolved effector function only in Albuginales and possibly Saprolegniales. In Albuginales, one N-terminal sub-class of CHXCs (CHxCLx(4)Gx(5–6)L) shows significant expansion, with 23 members, while other CHXCs are distinct from this clade. S. parasitica CHXCs are distinct from this major A. laibachii clade and therefore remain to be tested in future experiments.
The A. laibachii genome assembly sheds light on the evolution of biotrophy since it allows the first comparison, to our knowledge, of two oomycete obligate biotroph pathogens (A. laibachii and H. arabidopsidis) that evolved biotrophy independently. In addition, A. laibachii shows the highest overall amino acid identity to the necrotroph pathogen Py. ultimum and the hemibiotroph P. infestans. One of the striking results of this comparison is that all organisms able to build haustoria have lost their thiamine biosynthesis pathway, presumably because thiamine is easily obtained from hosts via the haustorial interface. A closer interface requires effective host defence suppression. We therefore hypothesize that the evolution of biotrophy involves a series of steps: step 1, involving progressively more effective effectors to suppress defence, step 2, attenuated activation of defence by reduction in the inventory of cell wall hydrolyzing enzymes, resulting in, step 3, weak selection to maintain certain biosynthetic pathways if the products of the pathways can be directly obtained from the host. This results in progressively more comprehensive auxotrophy and culminates in irreversible biotrophy (Figure 10).
It was hypothesized that the last common ancestor of Chromalveolata was a brown-alga-like organism with genes from green and red algae integrated into the nuclear genome after primary and secondary endosymbiosis ,. While some heterokonts kept their secondary endosymbiont and, in the case of diatoms, acquired a silicated bipartite cell wall , others lost their secondary endosymbiont. We postulate that after the loss of the endosymbiont, convergent evolution led to effector proteins like PEXEL , and RXLR precursors. PEXEL effectors might have enabled Pl. falciparum to achieve more complex interactions with its host and establish intercellular growth. In addition to the RXLR effector proteins, oomycetes acquired or evolved another class of effectors, the CRNs  and a secreted invertase that allows use of sucrose from host plants . Oomycetes that are biotrophs or hemibiotrophs today lost their thiamine biosynthesis pathway and, in the case of A. laibachii, evolved a new “CHXC” effector class. After taking up the biotroph lifestyle, the genomes of Pl. falciparum, H. arabidopsidis, and A. laibachii started a gene reduction that is exemplified by looking at enzymes that require molybdenum cofactors and the molybdopterin biosynthesis pathway. Hemibiotroph P. infestans instead shows a strong genome expansion . In this context, H. arabidopsidis showed a genome expansion and acquired biotrophy late, based on the loss of only one molybdenum-dependent enzyme.
Materials and Methods
An infected leaf was harvested from an Ar. thaliana plant grown in a heavy infected field plot in Norwich (UK; 52.6236,1.2182)  in December 2007. Zoosporangia were washed off the leaf surface and used to infect Ar. thaliana Ws-0-eds1 plants. After 1 wk one pustule was punched out, and spores were placed on ice for 30 min to release zoospores. Unhatched zoosporangia were removed by filtration, and zoospores were diluted to ~10 zoospores/ml and sprayed on Ar. thaliana Ws-0 plants (~100 µl/plant). This procedure was repeated 4× until spores were bulked up on Ar. thaliana Ws-0 plants. Zoosporangia were harvested using a home-made cyclone spore collector .
Zoospores were suspended in water (105 spores/ml) and incubated on ice for 30 min. The spore suspension was then sprayed on plants using a spray gun (~700 µl/plant), and plants were incubated in a cold room in the dark over night. Infected plants were kept under 10-h light and 14-h dark cycles with a 20°C day and 16°C night temperature.
DNA Extraction and Sequencing
High molecular weight DNA was extracted from zoosporangia using a phenol/chloroform-based purification method after grinding in liquid nitrogen, adapted from . Library preparation for Illumina sequencing was performed as described . All data were generated using paired-end reads. 800 bp and 400 bp paired-end sequencing libraries were constructed, and 8.8 Gbp of usable data were generated (for read and insert length, see Figure 1A).
Calculation of Expected Nc14 Genome Size
Figure 1A lists all reads after purification from plant and bacterial contamination as well as all reads aligned to the assembly. In summary, 91.6% of all reads can be aligned to the contigs, suggesting 2.8 Mbp missing from the assembly. Since 32.7 Mbp are in the assembly, the genome can be estimated to 35.5 Mbp. In another approach considering all reads and their read length, 8.8 Gbp (~7% correction for lower quality of second read pair) were generated, which would lead to an expected coverage of the 32.7 Mbp genome of ~270×. The mean coverage using single copy genes (glycolysis and TCA) is 240×. Considering the 2.5 Mbp of repeats (Figure 1B, right side, coverage underestimated) with an average coverage of 1,086×, which is ~4.4 times more than the mean coverage of the contigs, this repeat region corresponds to 10.9 Mbp. In contrast to this, the genome contains ~6.2 Mbp of hemizygous regions (Figure 1B, left side, coverage overestimated). These calculations suggest a genome size of ~43 Mbp, given all repeats resolved, or an effective genome size of ~37 Mbp.
cDNA Preparation and Sequencing
A. laibachii–infected Ar. thaliana Ws-0 plants were harvested 0 (after cold room, see plant inoculation), 2, 4, 6, 8 and 10 d after infection. Total RNA was extracted using TRI Reagent RNA Isolation Reagent (Sigma), and Dynabeads (Invitrogen) were used to enrich for mRNA. First and second strand cDNA synthesis was performed according to manufacturer's instructions using the SMART cDNA Library Construction Kit (Clontech), and cDNA was normalized using the Trimmer kit from Evrogen. cDNA samples were mixed in equal amounts and fragmented using a Covaris sonicator (Covaris). Illumina libraries were prepared as described for fragmented genomic DNA .
Data for comparative genomics were downloaded from the sources listed in Table 3.
First Velvet  was used, running different kmer-lengths and different sequencing library subsets (kmer-length: 23, 31, 41, 45, 49, 55, 61, 67, and 73; subsets: 400-bp insert only, 800-bp insert only). N50 number and length were determined for each of the assemblies, and the best assembly was selected as the matrix to be used with the Minimus2 genome merge pipeline . For the current assembly the 400-bp only subset with kmer-length 61 was used as matrix, and for kmer-lengths 49, 55, 61, 67 and 73, all 400- and 800-bp assemblies were added (Minimus parameters: consensus error <0.001; minimum identity >99%; 20-bp maximum trimming). A set of genes showing high heterozygosity was used to ensure that contigs were properly joined. Parameters were changed through several rounds, and minimum overlap, in particular, was lowered from 100 bp to 15 bp. An overlap of 15 bp was found to be the optimum for difficult heterozygous regions. After each Minimus assembly, all reads were back aligned to the contigs using MAQ aligner . Regions showing less than 3× average coverage were removed, and redundant fragments were removed using BLASTN with an e-value cut-off of 1e−20 and 99.9% identity. After this step a next round of Minimus was started, with changing minimum overlap in steps of 20 bp down from 100 bp. Below 20 bp steps were changed by 5 bp (See Figure S1 for work flow).
Since it is impossible to cultivate obligate biotrophs under sterile conditions, plant and bacterial contaminations were removed by using BLAST against genome sequences of the host plant Ar. thaliana (TAIR 9.0), fungal genomes (Neurospora crassa), oomycetes (H. arabidopsidis), and diverse bacterial genomes (Xanthomonas sp. and Pseudomonas sp.).
Prediction of Heterozygous Loci
To identify heterozygous loci, Illumina reads were aligned using MAQ, and the SNP detection pipeline was used according to the manual, with default parameters and minimum coverage greater than 180× for the Nc14 alignment and greater than 20× for the Em1 alignment. From the MAQ SNP file, positions were selected where two bases are possible and maximum coverage was less than 350×.
Assembled repetitive elements were identified using the RepeatScout program (http://bix.ucsd.edu/repeatscout/) with a seed size of 14. The frequency of elements and their location in the assembly were estimated with RepeatMasker using a library of repetitive elements built up by RepeatScout. A sequence was considered to be repetitive if it occurred in the genome assembly on at least three different contigs. The resulting library was searched for the sequences homologous to the known transposon elements using TBLASTX (e-value cut-off of 1e−5) and a database of transposons, RepBase . Consensus repeats that matched predicted Nc14 protein coding genes were filtered out. The remaining consensus repeats that do not match any sequences deposited in the NCBI database or any known transposon element and that do not overlap with Nc14 protein coding genes represent either Albugo-specific repeats or simple repeats.
tRNA genes were predicted with the program ARAGORN  using first default parameters and second options allowing introns in the gene sequences.
Genome Quality Using CEGMA
CEGMA was used according to the manual  with a local installation.
For the combined ABySS  and Oases  assembly, adaptor sequences from the SMART kit cDNA synthesis were removed for the ABySS assembly, and the ABySS program was used according to the manual. Different kmer-lengths were tested, and a length of 61 used for the final assembly.
Untrimmed cDNA sequences were assembled using Velvet and a kmer-length of 51, 57, 61, and 71. Oases was used for the final assembly of the contigs according to the manual, using default parameters.
MUMmer in maxmatch mode was used to combine all ABySS and Velvet assemblies. Redundant contigs were removed using BLAST.
Since the assembled cDNA is not strand specific but orientation is needed for gene prediction, cDNA 5′ tags were generated by Illumina sequencing (E. Kemen, A. Balmuth, J. D. Jones, unpublished data). Using Bowtie aligner , cDNA 5′ tags were aligned onto the assembled cDNA and, based on tag counts, orientated in the 5′ to 3′ direction.
Illumina reads were directly mapped to the genome using the Bowtie aligner, in “best” mode and with strand correction (strandfix mode). Pileup files were generated using bowtie-maqconvert and maq pileup allowing four mismatches per 76-bp read. To incorporate this data as hints files for gene prediction, regions with greater than 3× coverage were extracted.
Gene Prediction and Annotation
To generate a reliable gene set to train further programs, GeneMark  was used for ab initio gene prediction. ORFs plus 50 bp on the 3′ end and 50 bp on the 5′ end were extracted, and Illumina-sequenced cDNA was aligned to the ORFs using Bowtie. Gene models were selected if the coverage within the ORF didn't drop below three. This dataset with more than 2,000 genes was used as “traingenes” for the automated training program provided with the Augustus package (autoAug.pl). The trained Augustus program was then used for gene prediction including the combined Oases/ABySS-assembled cDNA (mapped using BLAT) as evidence. Default parameters (extrinsic.ME.cfg) were used for all predictions.
For consensus gene predictions with P. infestans, SGP2 was used according to the manual .
ASGARD  alignments were converted into GFF files to be used for consensus predictions.
Consensus gene models were generated using Evigan . cDNA from assemblies and alignments was converted into GFF files and combined with Augustus, GeneMark, SGP2, and ASGARD predictions. The genome was than screened for gene-free regions, and Augustus gene predictions were added if available. In a third round, regions that did not contain consensus gene models or Augustus gene models were extracted, and GeneMark annotations were added if available.
A set of genes was further tested by 5′ and 3′ RACE to validate start and stop sites.
Orthologous Genes and Divergence Level
Molecular divergence of A. laibachii from other species was assessed by examining the percentage of amino acid identity between orthologous gene pairs .
Amino acid identity was calculated only for the single copy genes by either excluding alignment gaps from calculations or taking gaps into account. The results show similar trends, so we present only results for the calculations when alignment gaps were excluded.
The total number of orthologous groups identified between species and the number of one-to-one orthologous pairs, as well as a mean amino acid identity, are shown in Table S7. In the comparison of T. gondii and A. laibachii, we found few orthologous pairs represented by the single copy genes (23 pairs); therefore, we excluded this pair of species from the analyses of sequence divergence.
We also estimated the levels of amino acid identity for the core eukaryotic genes (orthologous genes shared by all examined species); these data are presented in Table S8.
Green- and Red-Alga-Derived Genes
To identify A. laibachii genes with sequence similarity to green- or red-algal-derived diatom genes, a set published by Moustafa et al.  was used. All A. laibachii proteins showing homology to genes identified by Moustafa et al.  were further blasted (BLASTP) against the Ch. reinhardtii gene set, the E. siliculosus gene set, the U. maydis gene set, and the Fusarium oxysporum gene set with an e-value cut-off of 1e−20. Genes were considered to be green-alga-derived only if the protein was absent from U. maydis and F. oxysporum but present in Ch. reinhardtii, and was considered red-alga-derived if not in U. maydis or F. oxysporum but in E. siliculosus. The same analyses were performed on the Saccharomyces cerevisiae, Pl. falciparum, H. arabidopsidis, P. infestans, Py. ultimum, V. carteri, Ch. reinhardtii, C. merolae, C. merolae, Th. pseudonana, and Ph. tricornutum gene sets.
A. laibachii candidate genes with significant sequence similarity to green or red algae and other oomycetes (e-value cut-off of 1e−20) but not to fungi, brown algae, or diatoms were identified using the criteria in Table 4. Representative organisms for each group are as follows: green algae: V. carteri, Ch. reinhardtii; red algae: C. merolae, Galdieria sulphuraria; fungi: F. oxysporum; brown algae: E. siliculosus; diatoms: Ph. tricornutum, Th. pseudonana; oomycetes: P. sojae, Py. ultimum, H. arabidopsidis.
Homologues between oomycetes, fungi, brown algae, and diatoms were identified using OrthoMCL (e-value cut-off of 1e−20 or 1e−5) .
Synteny between multiple species was analysed using the Artemis Comparison Tool . Alignments between genomic sequences were performed using TBLASTX with a score cut-off of 210. Annotations of P. infestans, Py. ultimum, and H. arabidopsidis were transferred using TBLASTN with an e-value cut-off of 1e−30. LTR_FINDER  was used to annotate long terminal repeats (LTRs) within the genomic sequences, and coordinates were manually added. Regions between LTRs were blasted against RepBase  to identify the presence and/or type of transposon.
Defining the Secretome
Secreted proteins were predicted using a local installation of SignalP 3.0 . Proteins were considered to be secreted if both the neural networks and hidden Markov model methods predicted the protein to have a signal peptide. Predictions of TM domains were performed after removing the predicted secretion signal. TM domains were identified using MEMSAT3 . Proteins were considered to be without a TM domain with pnon-TM>0.0004 or, for high stringency, pnon-TM>0.01.
To identify new motifs, subsets of secreted proteins were selected and analysed using MEME  with default parameters. Identified motifs were tested against the whole gene set and the Swiss-Prot database using MOTIF Search. In a second step, motifs were selected only if they were positioned within 50 amino acids after the secretion signal.
Tests for over-representation of an identified motif were done using motif and sequence shuffling. Secreted proteins were predicted  as described in the previous section, and the signal peptide was removed prior to further analyses.
Each of the sequences without secretion signal was randomly shuffled 30 times. After each shuffling the sequences were screened for the motif in question. If the motif was identified after shuffling, the sequence was excluded from the next round. If the motif was never identified within the 30 times shuffling, the motif in the original protein was counted as “unique empirical”. All possible combinations of the amino acid sequence within the motif were calculated. For each of these permutations, the “unique empirical” proteins were calculated.
The 30 times shuffling was repeated 1,000 times to calculate background levels. Background levels were defined as how often a sequence was found again having the motif or the permutated motif. This was called “background (mean)”. Motifs that were above this background were considered for further analyses.
The second criterion was if a motif was significantly enriched in the secretome compared to all non-secreted proteins. For statistical validations we calculated the cumulative hypergeometric probability.
Selection of Candidates for Further Experiments
Candidates for further experiments were evaluated according to a ranking list. Maximum possible score was nine points, and the following scores were given: one point for being on a shorter, repetitive contig (≤3,000 bp) or end of contig, since we assumed that effector candidates might be in repetitive regions as shown for P. infestans effectors ; one point for having cDNA support; two points for being a short protein (≤400 amino acids); two points for carrying one of the identified motifs (RXLR, RXLQ, CHXC, CRN); one point for being expressed before day 10 after infection; one point for being expressed before day 4 after infection; and one point for showing SNPs in the Em1 comparison.
P. capsici Tests
Plant and bacterial growth procedures and P. capsici culturing.
N. benthamiana plant genotypes and P. capsici strain LT1534 were grown and cultured as described by Schornack et al. . P. capsici transformation was performed as described by Schornack et al. .
Plasmid construction and preparation.
Phytophthora transformation constructs SP_AVR3aC, RXLR1_AVR3aC, CRN3_AVR3aC, CHXC9_AVR3aC, CHXC9AAAA_AVR3aC, CHXC7_AVR3aC, and CHXC7AAAA_AVR3aC were synthesized and cloned into pTOR by Genscript. Fusion genes were flanked by ClaI (5′) and SacII (3′), and internal AscI sites were inserted between the N-terminal effector domain and AVR3aC coding domain. N-terminal domains used are listed in Table 5.
Phytophthora infection assays.
Phytophthora infection assays were performed according to Schornack et al.  with slight modifications.
Vector pTOR::Avr3a and pTOR::Avr3a (AAAA-AAA) were obtained from Dr. Steve Whisson . The control construct SP_Avr3aP was synthesized using the signal peptide of P. infestans Avr3a, fusing the signal peptide directly to the Avr3a C-terminus (GenBank accession number ACX46530.1). Translocation fusion constructs were synthesized using N-terminal coding sequences of Albugo RXLR1 (Gene name: AlNc14C278G10072, GI: 325190660), CRN3 (Gene name: AlNc14C196G8578, GI: 325188975), CHXC9 (Gene name: AlNc14C832G12555, GI: 325193652), and CHXC7 (Gene name: AlNc14C191G8449, GI: 325188831), and the AVR3a C-terminus (GenBank accession number ACX46530.1, GI: 260594559). CHXC9_AAAA_AVR3aC and CHXC7_AAAA_AVR3aC fusion constructs were synthesized by replacing the CHXC motif with a quadA motif. All plasmid suspensions used for P. capsici transformation were prepared using the Qiagen Midi Prep kit (Qiagen). For a summary of constructs see Table 5.
Effector Detector Vector Assays
Candidate RXLR effectors were cloned from RXLR to stop; all other candidate effectors were cloned from SP cleavage site to stop into pENTR D-TOPO (Invitrogen) and mobilized into pEDV6 . The resulting effector:pEDV6 constructs were conjugated into Pst DC3000 luxCDABE  and Pst DC3000 ΔAvrPto/ΔAvrPtoB . The contribution of an individual effector was assessed by spray inoculating 4- to 5-wk-old short day grown plants as previously described .
Growth of Pst DC3000 luxCDABE effector:pEDV6 was calculated by measuring whole plant luminescence using a Photek camera system and normalizing this to plant fresh weight .
To assess the virulence of Pst DC3000 ΔAvrPto/ΔAvrPtoB effector:pEDV6, bacterial colony counts were performed as previously described .
All Illumina sequence reads generated during this study have been submitted to the Sequence Read Archive at EBI and are accessible under the accession number ERA015557. Individual studies are available with accession numbers ERP000440 (Alias: albugo_laibachii_nc14_dna_sequencing, http://www.ebi.ac.uk/ena/data/view/ERP000440), ERP000441 (Alias: albugo_laibachii_nc14_cdna_sequencing, http://www.ebi.ac.uk/ena/data/view/ERP000441), and ERP000442 (Alias: albugo_laibachii_em1_dna_resequencing, http://www.ebi.ac.uk/ena/data/view/ERP000442).
All contigs and annotations are available through EBI or NCBI. The accession range is from FR824046 to FR827861 (3,816 contigs including annotations) and can be accessed through the ENA browser (http://www.ebi.ac.uk/ena/).
Assembly pipeline using Velvet and Minimus. Blue boxes with white filling indicate the different Velvet assemblies used. For the Minimus assembler the best contig was used as a seed leading to supercontigs v1. Mis-assemblies in this version were identified and corrected by back aligning all reads (Figure 1A) using MAQ  and Bowtie . A self-BLAST was used to avoid redundancy in the contigs. This pipeline was retrained using RACE data of highly heterozygous regions using contig-spanning genes.
The continuity and quality of the assembled contigs were assessed using CEGMA. In terms of core eukaryotic genes, 93.6% of a selected set of 248 genes could be detected. While 98.4% and 100%, respectively, of the highly conserved classes 3 and 4 were detected, 86.4% and 89.3%, respectively, of the more divergent classes 1 and 2 were found. Since CEGMA distinguishes between partial and full-length predicted genes, it allows studying the continuity of the genome as well. For the A. laibachii Nc14 genome only poorly conserved proteins show an elevated number in partial compared to full-length genes. For groups 2, 3, and 4, all genes predicted were present in full length, indicating that none of the genes was split over contigs. The Illumina-assembled Panda genome and the Sanger/Illumina combined genome of H. arabidopsidis were compared (dotted lines). The Panda genome shows high fragmentation of genes, indicated by the distance between partial and complete annotations. The H. arabidopsidis genome shows high continuity and a high detection level, although some genes are fragmented in the highly conserved class 4.
Synteny between the A. laibachii Nc14 draft, the P. infestans Ia, and the Py. ultimum mitochondrial sequence. The much bigger size of the Py. ultimum mitochondrial genome is due to a ~22-kb inverted repeat . Several regions within the A. laibachii mitochondrion show direct synteny (red) and inverted synteny (blue), reflecting regions within the Py. ultimum inverted repeats. The same region is not inverted in comparison to the P. infestans mitochondrion (far left and far right contigs of the A. laibachii assembly). Gene annotation in the P. infestans genome (annotated by BLAST from the protein sequences) shows that some genes don't show synteny in the A. laibachii Nc14 sequence, which is due to unresolved tRNA sequences. Genes in regions with synteny are in particular genes coding for ribosomal proteins, NADH dehydrogenase, and cytochrome C oxidase.
Annotation of tRNA genes. The trend shows that copy number correlates with possible codons and amino acid usage in the proteome. Exceptions are the tRNA for the start codon that encodes Met and for the codons that encode Val and Pro.
Gene prediction pipeline and quality control. (A) To ensure the best possible gene calls, we combined trained (Augustus), ab initio (GeneMark), and consensus (SGP2) gene predictions. Consensus gene calls were made using Evigan based on cDNA evidence. Evidence was generated either by direct alignment of cDNA reads from different stages of infection using Bowtie or by assembling the cDNA using Velvet in combination with Oases or/and using ABySS. (B) For validation of these gene models, a set of 860 annotated KOGs was compiled and tested. Results indicate that 75% of these groups are present in the current annotation. For comparison, 78% of KOGs were present in P. infestans, 73% in H. arabidopsidis, 42% in Pl. falciparum, and 85% in Ar. thaliana.
Genes of “green” or “red” origin present in diatoms and a set of other chromalveolates. Diagram showing the fraction of genes that are in common between the diatom Ph. tricornutum and the tested species that are integrated into the nuclear genome but are of green alga or red alga origin . Bars show the percent of genes present in Ph. tricornutum; lines show absolute numbers. Coloured bar below the diagram indicates systematic groups (yellow: fungi; light blue: Apicomplexa; blue: Oomycota; green: green algae; red: red algae; brown: brown algae; lilac: diatoms). The diagram shows that oomycetes still carry about 20% of the green-alga-derived genes that diatoms do. The brown alga E. siliculosus carries ~60% of the green alga genes the diatoms do. This might indicate that the ancestral brown algae contained far more green alga genes but these genes were replaced by red alga genes.
Maximum likelihood trees inferred from comparisons of ITS2 (A) or MORN repeat proteins (B). A comparison between both trees indicates incongruence between the ITS2 tree and the MORN repeat tree. The ITS2 tree reflects current systematics and indicates that brown algae and diatoms are closer to oomycetes than green algae are. Green algae build an isolated clade from brown algae and chromalveolates. The MORN repeat analyses indicate closer clustering of green algae to brown algae and oomycetes than to diatoms and apicomplexans. These analyses might support a hypothesis that brown-alga-like ancestors accumulated green alga genes. (All bootstrap counts were calculated from 100 replications. Both trees are midpoint rooted.)
Synteny of a region in A. laibachii containing the flagellar inner arm dynein 1 heavy chain alpha (essential for flagellar function) to Py. ultimum and H. arabidopsidis. Py. ultimum is able to form mobile zoospores while H. arabidopsidis isn't. Compared to A. laibachii the region is expanded in Py. ultimum and H. arabidopsidis, but while Py. ultimum maintains the flagellar dynein, H. arabidopsidis shows a region with synteny but an insertion with homology to transposable elements. LTR sites were annotated using LTR_Finder (labelled in red).
Gbrowse view of two repetitive regions in the A. laibachii Nc14 and A. laibachii Em1 genome. Both regions contain RXLR effector candidates. (A) A highly conserved repeat region with ~10 repeats in Nc14 and ~6 repeats in Em1. (B) A more diverged repeat region with >80 repeats within the Nc14 genome but deletion of the gene-containing region within the Em1 repeats.
Representation analyses of permutated CHXC motifs in the proteome of selected chromalveolates, red and green algae, and Ar. thaliana. The analyses reveal that only A. laibachii and S. parasitica contain a significant number of CHXC-motif-containing proteins in the secretome. Only for A. laibachii is there a significant enrichment of secreted CHXCs over non-secreted CHXCs. All organisms show a significant number of CXHC proteins, with a high proportion of secreted proteins. CXHC proteins are conserved between genomes and are predominantly enzymes like disulphide isomerase.
Host range of A. laibachii Nc14 and A. laibachii Em1 tested on 126 Ar. thaliana ecotypes. Twelve ecotypes could be identified that show resistance to only one of the A. laibachii isolates, indicating a difference in host range (red: Ar. thaliana ecotypes resistant to both A. laibachii isolates; orange: ecotypes resistant to one; green: ecotypes susceptible to both).
Genes missing from the CEGMA prediction. Genes not detected by CEGMA in the A. laibachii Nc14 assembly were further analysed and compared to the P. infestans genome and H. arabidopsidis Emoy2 genome. In all, 12 out of 28 core eukaryotic genes not predicted in A. laibachii Nc14 were not predicted in the other two oomycete genomes as well (light grey shading). In addition, three were present in only one of the tested genomes. To rule out the possibility that genes were not predicted because of unusual gene models that cannot be predicted by CEGMA, a BLAST and manual curation was performed on all missing candidates. Eleven could not be identified in the genome as well, while some genes gave multiple results (e.g., ATB binding domains) and were therefore ignored (labelled with “?”). The blast cut-off value was 1e−20. (Asterisk indicates partial genes.)
Primer pairs used to validate genome continuity and accuracy. Genomic regions were selected and PCR amplified. The first column gives the primer name and orientation, the second column, primer sequence, the third column, expected length of the PCR product, and the last column indicates if the region could be amplified or not.
Repetitive elements in the A. laibachii assembly. After a search of the library generated with RepeatScout for sequences homologous to transposons, we identified 270 consensus elements showing significant similarity to known transposons. The most abundant in the genome were mariner (DNA transposon) and copia (LTR retrotransposon) elements. Consensus repeats that do not match any deposited in the NCBI database and do not overlap with Nc14 protein coding genes are either Albugo-specific repeats (light grey background) or simple repeats. We identified 191 such consensus sequences that compose about 1% of the assembly.
Distribution of repetitive elements relative to contig length. Out of the total 3,816 contigs in the assembly, 2,211 contigs have regions with similarity to transposons or other repetitive sequences. Most of these contigs (1,528 contigs) are less than 5,000 bp long.
Distribution of repeats matching telomeric consensus sequences. Forward and reverse telomeric consensus sequences were identified with RepeatScout. A total of 45 contigs have repeats matching telomeric consensus sequences; amongst these, 25 contigs have telomeric repeats located either at the beginning or at the end of a contig. In all, 5,925 bp of telomeric repeats was assembled.
Characterisation of tRNA genes in the assembled A. laibachii contigs. Type of tRNA gene, number of genes (without and with introns), number of anticodons, type of anticodon, and frequency of usage as a number of stars; 15 tRNA genes were predicted with introns.
Annotations for the brassinosteroid biosynthesis pathway. The first column gives the enzyme commission numbers (EC numbers) of possible genes. The second column indicates gene names in Ar. thaliana. Question marks indicate genes that are difficult to annotate for a certain function (genes that belong to the superfamily of cytochrome P450s). The third column indicates genes identified using the ASGARD annotation pipeline, and the fourth column indicates manual annotation. (GI numbers in brackets.)
Potentially green-alga-derived genes that were identified based on results of a set of green- and red-alga-derived genes present in the diatom Ph. tricornutum. Genes listed here had to be present in the green alga Ch. reinhardtii (chloroplast or nuclear genome) but had to be absent from the red alga C. merolae and from the fungi F. oxysporum and U. maydis. (Orange: in A. laibachii, P. infestans, Py. ultimum, Ph. tricornutum, Th. pseudonana, Ch. reinhardtii, and Pl. falciparum but not in H. arabidopsidis and E. siliculosus. Brown: as before but in E. siliculosus. Green: shared at least between Pl. falciparum and oomycetes. Annotations for identified genes were taken from the list published by Moustafa et al. .)
Green alga genes showing homology to A. laibachii genes but not to diatome, red alga, brown alga, or fungal genes. Genes listed here had to be present in the green algae Ch. reinhardtii (chloroplast or nuclear genome) and V. carteri but had to be absent from the red alga C. merolae, the fungi F. oxysporum and U. maydis, and the brown alga E. siliculosus (for the BLAST analyses, an e-value cut-off of 1e−20 was used; proteins retained by repeating the analyses using an e-value cut-off of 1e−5 are indicated in blue).
Red alga genes showing homology to A. laibachii genes but not to diatom, green algae, brown alga, or fungal genes. Genes listed here had to be present in the red algae C. merolae and G. sulphuraria but had to be absent from the green algae Ch. reinhardtii (chloroplast or nuclear genome) and V. carteri, the fungi F. oxysporum and U. maydis, and the brown alga E. siliculosus (for the BLAST analyses, an e-value cut-off of 1e−20 was used; proteins retained by repeating the analyses using an e-value cut-off of 1e−5 are indicated in blue).
Potentially green-alga-derived genes that are present in the diatoms Ph. tricornutum and Th. pseudonana but not in A. laibachii Nc14. Genes listed here had to be present in the green alga Ch. reinhardtii (chloroplast or nuclear genome) but had to be absent from A. laibachii Nc14, the red alga C. merolae, and the fungi F. oxysporum and U. maydis. Columns 3–7 show presence/absence in Py. ultimum, P. infestans, H. arabidopsidis, Pl. falciparum, and E. siliculosus using the same criteria. (a, absent; p, present. Annotations for identified genes were taken from the list published by Moustafa et al. .)
Molecular divergence of A. laibachii based on all orthologous genes.
Molecular divergence of A. laibachii based on core eukaryotic gene pairs.
Presence and absence of important metabolic enzymes. Red indicates absence and green indicates presence of genes. Genes present were annotated or validated in each organism. Remarkable is the absence of all molybdopterin biosynthesis genes, and enzymes using the cofactor, in A. laibachii and Pl. falciparum. P. infestans and H. arabidopsidis each lack one of the molybdopterin biosynthesis enzymes but contain molybdopterin-dependent enzymes, which might indicate that other enzymes can compensate for the missing step; in case of B73, the missing enzyme might be replaced by a multifunctional Cnx1 or by high concentrations of Mo inside the cell .
List of all annotated proteins of A. laibachii that might be associated with pathogenicity. Annotation and identification were done using Pfam and BLASTP against the NCBI database. Localisation was predicted using a local installation of WoLF PSORT . SignalP 3.0 was used for secretion prediction.
Intraspecies comparison between Nc14 and Em1. All genes, genes with a predicted secretion signal peptide and without a TM domain, genes representing KOGs, or genes carrying a CHXC, RXLR, or RXLQ motif were compared. The second column in the table indicates heterozygosity (het) within Nc14; the third column indicates heterozygous positions within Em1 (green) or homozygous (hom) SNPs between Nc14 and Em1 (blue). The fourth column shows Em1-specific heterozygous positions or SNPs corrected against Nc14 heterozygous positions carrying the same nucleotide in one of the haplotypes. Frequencies of non-synonymous and synonymous mutations (darker coloured fields, mutations per 100 bp) are almost balanced in the all-gene and KOG gene comparisons, while a comparison of all secreted proteins indicates a 3:1 ratio (non-synonymous:synonymous). RXLRs and, particularly, RXLQs show an imbalance (~2:1), with high variation due to the small sample size. CHXCs, with a ratio of ~5:1, show a significant imbalance in the comparison between Nc14 and Em1. Considering total number and percentage of genes with a ratio of non-synonymous/synonymous <1 or >1 (light-coloured fields), only KOG genes show a significantly higher number of genes with a value <1, while all other classes show more genes with a value >1.
CHXC and CXHC candidate genes. This table gives an overview of all predicted CHXC (white background) and CXHC (grey background) candidates from various species. The first column of the table indicates name of CHXC or CXHC candidates used for the phylogenetic analyses (Figure 9). The second column indicates the species name, and the third column indicates the locus tag within the corresponding genome. The fourth column shows the best BLAST hit against the NCBI nr database with an e-value<10−50. The last column indicates the accession number of the best hit.
The authors thank S. Whisson for the pTOR and pTOR::Avr3a constructs; Caroline Dean and colleagues for access to their Arabidopsis field plots; Jonathan Urbach for his critical comments and suggestions on the manuscript; Jodie Pike and Matthew Smoker for technical assistance; Michael Burrell for computational assistance; Richard Gibson (European Bioinformatics Institute) for his help in making our data publicly available; and Brett Tyler, Sophien Kamoun, and Marco Thines for discussions.
The author(s) have made the following declarations about their contributions: Conceived and designed the experiments: EK JDGJ. Performed the experiments: EK TSL ACK ALB ARS KB. Analyzed the data: EK AG. Contributed reagents/materials/analysis tools: EH DJS DM. Wrote the paper: EK JDGJ. Prepared data for submission to databases and did the submission: DM.
- 1. Yarwood C. E (1956) Obligate parasitism. Ann Rev Plant Physiol 7: 115–142.
- 2. Goker M, Voglmayr H, Riethmuller A, Oberwinkler F (2007) How do obligate parasites evolve? A multi-gene phylogenetic analysis of downy mildews. Fungal Genet Biol 44: 105–122.
- 3. Spanu P. D, Abbott J. C, Amselem J, Burgis T. A, Soanes D. M, et al. (2010) Genome expansion and gene loss in powdery mildew fungi reveal tradeoffs in extreme parasitism. Science 330: 1543–1546.
- 4. Baxter L, Tripathy S, Ishaque N, Boot N, Cabral A, et al. (2010) Signatures of adaptation to obligate biotrophy in the Hyaloperonospora arabidopsidis genome. Science 330: 1549–1551.
- 5. Friml J, Wisniewska J, Benkova E, Mendgen K, Palme K (2002) Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis. Nature 415: 806–809.
- 6. Spanu P, Kamper J (2010) Genomics of biotrophy in fungi and oomycetes—emerging patterns. Curr Opin Plant Biol 13: 409–414.
- 7. Parfrey L. W, Barbero E, Lasser E, Dunthorn M, Bhattacharya D, et al. (2006) Evaluating support for the current classification of eukaryotic diversity. PLoS Genet 2: e220. doi:10.1371/journal.pgen.0020220.
- 8. Cavalier-Smith T (1999) Principles of protein and lipid targeting in secondary symbiogenesis: euglenoid, dinoflagellate, and sporozoan plastid origins and the eukaryote family tree. J Eukaryot Microbiol 46: 347–366.
- 9. Haas B. J, Kamoun S, Zody M. C, Jiang R. H, Handsaker R. E, et al. (2009) Genome sequence and analysis of the Irish potato famine pathogen Phytophthora infestans. Nature 461: 393–398.
- 10. Levesque C. A, Brouwer H, Cano L, Hamilton J. P, Holt C, et al. (2010) Genome sequence of the necrotrophic plant pathogen, Pythium ultimum, reveals original pathogenicity mechanisms and effector repertoire. Genome Biol 11: R73.
- 11. Thines M, Kamoun S (2010) Oomycete-plant coevolution: recent advances and future prospects. Curr Opin Plant Biol 13: 427–433.
- 12. Holub E. B, Beynon J. L (1997) Symbiology of mouse-ear cress (Arabidopsis thaliana) and oomycetes. Adv Bot Res24: 227–273.
- 13. Soylu S (2004) Ultrastructural characterisation of the host-pathogen interface in white blister-infected Arabidopsis leaves. Mycopathologia 158: 457–464.
- 14. Mims C. W, Richardson E. A, Holt B. F 3rd, Dangl J. L (2004) Ultrastructure of the host-pathogen interface in Arabidopsis thaliana leaves infected by the downy mildew Hyaloperonospora parasitica. Can J Bot 82: 1545–1545.
- 15. Coates M. E, Beynon J. L (2010) Hyaloperonospora arabidopsidis as a pathogen model. Annu Rev Phytopathol 48: 329–345.
- 16. Cooper A. J, Latunde-Dada A. O, Woods-Tor A, Lynn J, Lucas J. A, et al. (2008) Basic compatibility of Albugo candida in Arabidopsis thaliana and Brassica juncea causes broad-spectrum suppression of innate immunity. Mol Plant Microbe Interact 21: 745–756.
- 17. Saharan G. S, Verma P. R (1992) White rusts: a review of economically important species. Rugby (United Kingdom): ITDG Publishing. 380 p.
- 18. Petkowskia J. E, Cunningtona J. H, Minchintona E. J, Cahillb D. M (2010) Molecular phylogenetic relationships between Albugo candida collections on the Brassicaceae in Australas. Plant Pathol 59: 6.
- 19. Thines M, Choi Y. J, Kemen E, Ploch S, Holub E. B, et al. (2009) A new species of Albugo parasitic to Arabidopsis thaliana reveals new evolutionary patterns in white blister rusts (Albuginaceae). Persoonia 22: 123–128.
- 20. Elena S. F, Lenski R. E (2003) Evolution experiments with microorganisms: the dynamics and genetic bases of adaptation. Nat Rev Genet 4: 457–469.
- 21. Wilczek A. M, Roe J. L, Knapp M. C, Cooper M. D, Lopez-Gallego C, et al. (2009) Effects of genetic perturbation on seasonal life history plasticity. Science 323: 930–934.
- 22. Holub E. B, Brose E, Tor M, Clay C, Crute I. R, et al. (1995) Phenotypic and genotypic variation in the interaction between Arabidopsis thaliana and Albugo candida. Mol Plant Microbe Interact 8: 916–928.
- 23. Borhan M. H, Holub E. B, Beynon J. L, Rozwadowski K, Rimmer S. R (2004) The arabidopsis TIR-NB-LRR gene RAC1 confers resistance to Albugo candida (white rust) and is dependent on EDS1 but not PAD4. Mol Plant Microbe Interact 17: 711–719.
- 24. Zerbino D. R, Birney E (2008) Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18: 821–829.
- 25. Sommer D. D, Delcher A. L, Salzberg S. L, Pop M (2007) Minimus: a fast, lightweight genome assembler. BMC Bioinformatics 8: 64.
- 26. Parra G, Bradnam K, Korf I (2007) CEGMA: a pipeline to accurately annotate core genes in eukaryotic genomes. Bioinformatics 23: 1061–1067.
- 27. Avila-Adame C, Gomez-Alpizar L, Zismann V, Jones K. M, Buell C. R, et al. (2006) Mitochondrial genome sequences and molecular evolution of the Irish potato famine pathogen, Phytophthora infestans. Curr Genet 49: 39–46.
- 28. Farrer R. A, Kemen E, Jones J. D, Studholme D. J (2009) De novo assembly of the Pseudomonas syringae pv. syringae B728a genome using Illumina/Solexa short sequence reads. FEMS Microbiol Lett 291: 103–111.
- 29. Tatusov R. L, Fedorova N. D, Jackson J. D, Jacobs A. R, Kiryutin B, et al. (2003) The COG database: an updated version includes eukaryotes. BMC Bioinformatics 4: 41.
- 30. Alves J. M, Buck G. A (2007) Automated system for gene annotation and metabolic pathway reconstruction using general sequence databases. Chem Biodivers 4: 2593–2602.
- 31. Whitaker J. W, McConkey G. A, Westhead D. R (2009) The transferome of metabolic genes explored: analysis of the horizontal transfer of enzyme encoding genes in unicellular eukaryotes. Genome Biol 10: R36.
- 32. Keeling P. J (2010) The endosymbiotic origin, diversification and fate of plastids. Philos Trans R Soc Lond B Biol Sci 365: 729–748.
- 33. Bodyl A, Stiller J. W, Mackiewicz P (2009) Chromalveolate plastids: direct descent or multiple endosymbioses? Trends Ecol Evol 24: 119–121; author reply 121-112.
- 34. Parfrey L. W, Grant J, Tekle Y. I, Lasek-Nesselquist E, Morrison H. G, et al. (2010) Broadly sampled multigene analyses yield a well-resolved eukaryotic tree of life. Syst Biol 59: 518–533.
- 35. Riisberg I, Orr R. J, Kluge R, Shalchian-Tabrizi K, Bowers H. A, et al. (2009) Seven gene phylogeny of heterokonts. Protist 160: 191–204.
- 36. Stiller J. W, Huang J, Ding Q, Tian J, Goodwillie C (2009) Are algal genes in nonphotosynthetic protists evidence of historical plastid endosymbioses? BMC Genomics 10: 484.
- 37. Moustafa A, Beszteri B, Maier U. G, Bowler C, Valentin K, et al. (2009) Genomic footprints of a cryptic plastid endosymbiosis in diatoms. Science 324: 1724–1726.
- 38. Takeshima H, Komazaki S, Nishi M, Iino M, Kangawa K (2000) Junctophilins: a novel family of junctional membrane complex proteins. Mol Cell 6: 11–22.
- 39. Gubbels M. J, Vaishnava S, Boot N, Dubremetz J. F, Striepen B (2006) A MORN-repeat protein is a dynamic component of the Toxoplasma gondii cell division apparatus. J Cell Sci 119: 2236–2245.
- 40. Round F. E, Crawford R. M (1990) The diatoms. Biology and morphology of the genera. Cambridge: Cambridge University Press.
- 41. Misumi O, Matsuzaki M, Nozaki H, Miyagishima S. Y, Mori T, et al. (2005) Cyanidioschyzon merolae genome. A tool for facilitating comparable studies on organelle biogenesis in photosynthetic eukaryotes. Plant Physiol 137: 567–585.
- 42. Campbell W. H (1999) Nitrate reductase structure, function and regulation: bridging the gap between biochemistry and physiology. Annu Rev Plant Physiol Plant Mol Biol 50: 277–303.
- 43. Divon H. H, Fluhr R (2007) Nutrition acquisition strategies during fungal infection of plants. FEMS Microbiol Lett 266: 65–74.
- 44. Hartson S. D, Thulasiraman V, Huang W, Whitesell L, Matts R. L (1999) Molybdate inhibits hsp90, induces structural changes in its C-terminal domain, and alters its interactions with substrates. Biochemistry 38: 3837–3849.
- 45. Millson S. H, Nuttall J. M, Mollapour M, Piper P. W (2009) The Hsp90/Cdc37p chaperone system is a determinant of molybdate resistance in Saccharomyces cerevisiae. Yeast 26: 339–347.
- 46. Baxter I, Muthukumar B, Park H. C, Buchner P, Lahner B, et al. (2008) Variation in molybdenum content across broadly distributed populations of Arabidopsis thaliana is controlled by a mitochondrial molybdenum transporter (MOT1). PLoS Genet 4: e1000004. doi:10.1371/journal.pgen.1000004.
- 47. Latijnhouwers M, de Wit P. J, Govers F (2003) Oomycetes and fungi: similar weaponry to attack plants. Trends Microbiol 11: 462–469.
- 48. Sohn J, Voegele R. T, Mendgen K, Hahn M (2000) High level activation of vitamin B1 biosynthesis genes in haustoria of the rust fungus Uromyces fabae. Mol Plant Microbe Interact 13: 629–636.
- 49. Hiller N. L, Bhattacharjee S, van Ooij C, Liolios K, Harrison T, et al. (2004) A host-targeting signal in virulence proteins reveals a secretome in malarial infection. Science 306: 1934–1937.
- 50. Kämper J, Kahmann R, Bolker M, Ma L. J, Brefort T, et al. (2006) Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis. Nature 444: 97–101.
- 51. Tsang A, Butler G, Powlowski J, Panisko E. A, Baker S. E (2009) Analytical and computational approaches to define the Aspergillus niger secretome. Fungal Genet Biol 46: Suppl 1S153–S160.
- 52. Nielsen H, Engelbrecht J, Brunak S, von Heijne G (1997) Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites. Protein Eng 10: 1–6.
- 53. Jones D. T, Taylor W. R, Thornton J. M (1994) A model recognition approach to the prediction of all-helical membrane protein structure and topology. Biochemistry 33: 3038–3049.
- 54. Dodds P. N, Rathjen J. P (2010) Plant immunity: towards an integrated view of plant-pathogen interactions. Nat Rev Genet 11: 539–548.
- 55. Bos J. I, Armstrong M. R, Gilroy E. M, Boevink P. C, Hein I, et al. (2010) Phytophthora infestans effector AVR3a is essential for virulence and manipulates plant immunity by stabilizing host E3 ligase CMPG1. Proc Natl Acad Sci U S A 107: 9909–9914.
- 56. Kelley B. S, Lee S. J, Damasceno C. M, Chakravarthy S, Kim B. D, et al. (2010) A secreted effector protein (SNE1) from Phytophthora infestans is a broadly acting suppressor of programmed cell death. Plant J 62: 357–366.
- 57. Rehmany A. P, Gordon A, Rose L. E, Allen R. L, Armstrong M. R, et al. (2005) Differential recognition of highly divergent downy mildew avirulence gene alleles by RPP1 resistance genes from two Arabidopsis lines. Plant Cell 17: 1839–1850.
- 58. Armstrong M. R, Whisson S. C, Pritchard L, Bos J. I, Venter E, et al. (2005) An ancestral oomycete locus contains late blight avirulence gene Avr3a, encoding a protein that is recognized in the host cytoplasm. Proc Natl Acad Sci U S A 102: 7766–7771.
- 59. Win J, Kanneganti T. D, Torto-Alalibo T, Kamoun S (2006) Computational and comparative analyses of 150 full-length cDNA sequences from the oomycete plant pathogen Phytophthora infestans. Fungal Genet Biol 43: 20–33.
- 60. Torto T. A, Li S, Styer A, Huitema E, Testa A, et al. (2003) EST mining and functional expression assays identify extracellular effector proteins from the plant pathogen Phytophthora. Genome Res 13: 1675–1685.
- 61. Oleksyk T. K, Smith M. W, O'Brien S. J (2010) Genome-wide scans for footprints of natural selection. Philos Trans R Soc Lond B Biol Sci 365: 185–205.
- 62. Aguileta G, Refregier G, Yockteng R, Fournier E, Giraud T (2009) Rapidly evolving genes in pathogens: methods for detecting positive selection and examples among fungi, bacteria, viruses and protists. Infect Genet Evol 9: 656–670.
- 63. Kamoun S (2006) A catalogue of the effector secretome of plant pathogenic Oomycetes. Annu Rev Phytopathol 44: 41–60.
- 64. Soanes D. M, Talbot N. J (2008) Moving targets: rapid evolution of oomycete effectors. Trends Microbiol 16: 507–510.
- 65. Allen R. L, Bittner-Eddy P. D, Grenville-Briggs L. J, Meitz J. C, Rehmany A. P, et al. (2004) Host-parasite coevolutionary conflict between Arabidopsis and downy mildew. Science 306: 1957–1960.
- 66. Raffaele S, Farrer R. A, Cano L. M, Studholme D. J, MacLean D, et al. (2010) Genome evolution following host jumps in the Irish potato famine pathogen lineage. Science 330: 1540–1543.
- 67. Schirawski J, Mannhaupt G, Munch K, Brefort T, Schipper K, et al. (2010) Pathogenicity determinants in smut fungi revealed by genome comparison. Science 330: 1546–1548.
- 68. Schornack S, van Damme M, Bozkurt T. O, Cano L. M, Smoker M, et al. (2010) Ancient class of translocated oomycete effectors targets the host nucleus. Proc Natl Acad Sci U S A 107: 17421–17426.
- 69. Fan J, Crooks C, Lamb C (2008) High-throughput quantitative luminescence assay of the growth in planta of Pseudomonas syringae chromosomally tagged with Photorhabdus luminescens luxCDABE. Plant J 53: 393–399.
- 70. Sohn K. H, Lei R, Nemri A, Jones J. D (2007) The downy mildew effector proteins ATR1 and ATR13 promote disease susceptibility in Arabidopsis thaliana. Plant Cell 19: 4077–4090.
- 71. Mehta Y. R, Zadoks J. C (1971) Note on the efficiency of a miniaturized cyclone spore collector. Eur J Plant Pathol 77: 60–63.
- 72. McKinney E. C, Ali N, Traut A, Feldmann K. A, Belostotsky D. A, et al. (1995) Sequence-based identification of T-DNA insertion mutations in Arabidopsis: actin mutants act2-1 and act4-1. Plant J 8: 613–622.
- 73. Li H, Ruan J, Durbin R (2008) Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res 18: 1851–1858.
- 74. Jurka J, Kapitonov V. V, Pavlicek A, Klonowski P, Kohany O, et al. (2005) Repbase Update, a database of eukaryotic repetitive elements. Cytogenet Genome Res 110: 462–467.
- 75. Laslett D, Canback B (2004) ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences. Nucleic Acids Res 32: 11–16.
- 76. Simpson J. T, Wong K, Jackman S. D, Schein J. E, Jones S. J, et al. (2009) ABySS: a parallel assembler for short read sequence data. Genome Res 19: 1117–1123.
- 77. Schulz M, Zerbino D. R (2010) Oases: De novo transcriptome assembler for very short reads. Published online: http://www.ebi.ac.uk/~zerbino/oases/.
- 78. Langmead B, Trapnell C, Pop M, Salzberg S. L (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol 10: R25.
- 79. Kent W. J (2002) BLAT—the BLAST-like alignment tool. Genome Res 12: 656–664.
- 80. Haas B. J, Delcher A. L, Mount S. M, Wortman J. R, Smith R. K Jr, et al. (2003) Improving the Arabidopsis genome annotation using maximal transcript alignment assemblies. Nucleic Acids Res 31: 5654–5666.
- 81. Ter-Hovhannisyan V, Lomsadze A, Chernoff Y. O, Borodovsky M (2008) Gene prediction in novel fungal genomes using an ab initio algorithm with unsupervised training. Genome Res 18: 1979–1990.
- 82. Parra G, Agarwal P, Abril J. F, Wiehe T, Fickett J. W, et al. (2003) Comparative gene prediction in human and mouse. Genome Res 13: 108–117.
- 83. Liu Q, Mackey A. J, Roos D. S, Pereira F. C (2008) Evigan: a hidden variable model for integrating gene evidence for eukaryotic gene prediction. Bioinformatics 24: 597–605.
- 84. Li L, Stoeckert C. J Jr, Roos D. S (2003) OrthoMCL: identification of ortholog groups for eukaryotic genomes. Genome Res 13: 2178–2189.
- 85. Edgar R. C (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 32: 1792–1797.
- 86. Carver T. J, Rutherford K. M, Berriman M, Rajandream M. A, Barrell B. G, et al. (2005) ACT: the Artemis Comparison Tool. Bioinformatics 21: 3422–3423.
- 87. Xu Z, Wang H (2007) LTR_FINDER: an efficient tool for the prediction of full-length LTR retrotransposons. Nucleic Acids Res 35: W265–W268.
- 88. Emanuelsson O, Brunak S, von Heijne G, Nielsen H (2007) Locating proteins in the cell using TargetP, SignalP and related tools. Nat Protoc 2: 953–971.
- 89. Jones D. T (2007) Improving the accuracy of transmembrane protein topology prediction using evolutionary information. Bioinformatics 23: 538–544.
- 90. Bailey T. L, Elkan C (1994) Fitting a mixture model by expectation maximization to discover motifs in biopolymers. Proc Int Conf Intell Syst Mol Biol 2: 28–36.
- 91. Whisson S. C, Boevink P. C, Moleleki L, Avrova A. O, Morales J. G, et al. (2007) A translocation signal for delivery of oomycete effector proteins into host plant cells. Nature 450: 115–118.
- 92. Lin N. C, Martin G. B (2005) An avrPto/avrPtoB mutant of Pseudomonas syringae pv. tomato DC3000 does not elicit Pto-mediated resistance and is less virulent on tomato. Mol Plant Microbe Interact 18: 43–51.
- 93. Zipfel C, Robatzek S, Navarro L, Oakeley E. J, Jones J. D, et al. (2004) Bacterial disease resistance in Arabidopsis through flagellin perception. Nature 428: 764–767.
- 94. Whalen M. C, Innes R. W, Bent A. F, Staskawicz B. J (1991) Identification of Pseudomonas syringae pathogens of Arabidopsis and a bacterial locus determining avirulence on both Arabidopsis and soybean. Plant Cell 3: 49–59.
- 95. Schwarz G, Schulze J, Bittner F, Eilers T, Kuper J, et al. (2000) The molybdenum cofactor biosynthetic protein Cnx1 complements molybdate-repairable mutants, transfers molybdenum to the metal binding pterin, and is associated with the cytoskeleton. Plant Cell 12: 2455–2472.
- 96. Horton P, Park K. J, Obayashi T, Fujita N, Harada H, et al. (2007) WoLF PSORT: protein localization predictor. Nucleic Acids Res 35: W585–W587.
- 97. Raven J. A, Waite A. M (2004) The evolution of silicification in diatoms: inescapable sinking and sinking as escape? New Phytol 162: 45–61.
- 98. Marti M, Good R. T, Rug M, Knuepfer E, Cowman A. F (2004) Targeting malaria virulence and remodeling proteins to the host erythrocyte. Science 306: 1930–1933.
- 99. Voegele R. T, Wirsel S, Möll U, Lechner M, Mendgen K (2006) Cloning and characterization of a novel invertase from the obligate biotroph Uromyces fabae and analysis of expression patterns of host and pathogen invertases in the course of infection. Mol Plant Microbe Interact 19: 625–634.
- 100. Merchant S. S, Prochnik S. E, Vallon O, Harris E. H, Karpowicz S. J, et al. (2007) The Chlamydomonas genome reveals the evolution of key animal and plant functions. Science 318: 245–250.
- 101. Cock J. M, Sterck L, Rouze P, Scornet D, Allen A. E, et al. (2010) The Ectocarpus genome and the independent evolution of multicellularity in brown algae. Nature 465: 617–621.
- 102. Bowler C, Allen A. E, Badger J. H, Grimwood J, Jabbari K, et al. (2008) The Phaeodactylum genome reveals the evolutionary history of diatom genomes. Nature 456: 239–244.
- 103. Armbrust E. V, Berges J. A, Bowler C, Green B. R, Martinez D, et al. (2004) The genome of the diatom Thalassiosira pseudonana: ecology, evolution, and metabolism. Science 306: 79–86.
- 104. Goffeau A, Barrell B. G, Bussey H, Davis R. W, Dujon B, et al. (1996) Life with 6000 genes. Science 274: 546.563–547
- 105. Dujon B, Sherman D, Fischer G, Durrens P, Casaregola S, et al. (2004) Genome evolution in yeasts. Nature 430: 35–44.
- 106. Kissinger J. C, Gajria B, Li L, Paulsen I. T, Roos D. S (2003) ToxoDB: accessing the Toxoplasma gondii genome. Nucleic Acids Res 31: 234–236.
- 107. Gardner M. J, Hall N, Fung E, White O, Berriman M, et al. (2002) Genome sequence of the human malaria parasite Plasmodium falciparum. Nature 419: 498–511.
- 108. Lander E. S, Linton L. M, Birren B, Nusbaum C, Zody M. C, et al. (2001) Initial sequencing and analysis of the human genome. Nature 409: 860–921.
- 109. Aparicio S, Chapman J, Stupka E, Putnam N, Chia J. M, et al. (2002) Whole-genome shotgun assembly and analysis of the genome of Fugu rubripes. Science 297: 1301–1310.
- 110. Tyler B. M, Tripathy S, Zhang X, Dehal P, Jiang R. H, et al. (2006) Phytophthora genome sequences uncover evolutionary origins and mechanisms of pathogenesis. Science 313: 1261–1266.
- 111. Thoquet P, Gherardi M, Journet E. P, Kereszt A, Ane J. M, et al. (2002) The molecular genetic linkage map of the model legume Medicago truncatula: an essential tool for comparative legume genomics and the isolation of agronomically important genes. BMC Plant Biol 2: 1.
- 112. Ma L. J, van der Does H. C, Borkovich K. A, Coleman J. J, Daboussi M. J, et al. (2010) Comparative genomics reveals mobile pathogenicity chromosomes in Fusarium. Nature 464: 367–373.
- 113. Prochnik S. E, Umen J, Nedelcu A. M, Hallmann A, Miller S. M, et al. (2010) Genomic analysis of organismal complexity in the multicellular green alga Volvox carteri. Science 329: 223–226.
- 114. Matsuzaki M, Misumi O, Shin I. T, Maruyama S, Takahara M, et al. (2004) Genome sequence of the ultrasmall unicellular red alga Cyanidioschyzon merolae 10D. Nature 428: 653–657.