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Transcriptomic and Proteomic Analyses of a Wolbachia-Free Filarial Parasite Provide Evidence of Trans-Kingdom Horizontal Gene Transfer

  • Samantha N. McNulty ,

    smcnulty@wustl.edu

    Affiliation Infectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America

  • Sahar Abubucker,

    Affiliation The Genome Institute, Washington University School of Medicine, St. Louis, Missouri, United States of America

  • Gabriel M. Simon,

    Affiliation Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, Missouri, United States of America

  • Makedonka Mitreva,

    Affiliations The Genome Institute, Washington University School of Medicine, St. Louis, Missouri, United States of America, Department of Genetics, Washington University School of Medicine, St. Louis, Missouri, United States of America

  • Nathan P. McNulty,

    Affiliation Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, Missouri, United States of America

  • Kerstin Fischer,

    Affiliation Infectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America

  • Kurt C. Curtis,

    Affiliation Infectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America

  • Norbert W. Brattig,

    Affiliation Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany

  • Gary J. Weil,

    Affiliation Infectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America

  • Peter U. Fischer

    Affiliation Infectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America

Transcriptomic and Proteomic Analyses of a Wolbachia-Free Filarial Parasite Provide Evidence of Trans-Kingdom Horizontal Gene Transfer

  • Samantha N. McNulty, 
  • Sahar Abubucker, 
  • Gabriel M. Simon, 
  • Makedonka Mitreva, 
  • Nathan P. McNulty, 
  • Kerstin Fischer, 
  • Kurt C. Curtis, 
  • Norbert W. Brattig, 
  • Gary J. Weil, 
  • Peter U. Fischer
PLOS
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Abstract

Most filarial parasites in the subfamilies Onchocercinae and Dirofilariinae depend on Wolbachia endobacteria to successfully carry out their life cycle. Recently published data indicate that the few Wolbachia-free species in these subfamilies were infected in the distant past and have subsequently shed their endosymbionts. We used an integrated transcriptomic and proteomic analysis of Onchocerca flexuosa to explore the molecular mechanisms that allow worms of this species to survive without a bacterial partner. Roche/454 sequencing of the adult transcriptome produced 16,814 isogroup and 47,252 singleton sequences that are estimated to represent approximately 41% of the complete gene set. Sequences similar to 97 Wolbachia genes were identified from the transcriptome, some of which appear on the same transcripts as sequences similar to nematode genes. Computationally predicted peptides, including those with similarity to Wolbachia proteins, were classified at the domain and pathway levels in order to assess the metabolic capabilities of O. flexuosa and compare against the Wolbachia-dependent model filaria, Brugia malayi. Transcript data further facilitated a shotgun proteomic analysis of O. flexuosa adult worm lysate, resulting in the identification of 1,803 proteins. Three of the peptides detected by mass spectroscopy map to two ABC transport-related proteins from Wolbachia. Antibodies raised to one of the Wolbachia-like peptides labeled a single 38 kDa band on Western blots of O. flexuosa lysate and stained specific worm tissues by immunohistology. Future studies will be required to determine the exact functions of Wolbachia-like peptides and proteins in O. flexuosa and to assess their roles in worm biology.

Introduction

Filarial nematodes are a family of medically and economically significant parasites that infect all classes of vertebrates except fish [1]. Eight filarial species parasitize humans, but most morbidity is caused by Wuchereria bancrofti, Brugia malayi, and Onchocerca volvulus. Global efforts are underway to eliminate transmission of these three organisms because of their significant impact on human health [2], [3]. Unfortunately, the drugs employed in these efforts have limited activity against adult filarial worms [4]. More effective therapies would significantly strengthen disease elimination efforts and improve prospects for a world without disabling filarial diseases like elephantiasis and river blindness.

Most filarial parasites of humans and domestic animals contain a bacterial endosymbiont (Wolbachia pipientis) that is required for development and reproduction [5]. Antibiotic treatments that clear Wolbachia cause stunted growth, infertility, and eventual death of adult filarial worms [6], [7]. This suggests that the Wolbachia-mediated biochemical pathways or processes required by filarial nematodes could serve as drug targets [8]. Although several hypotheses have been suggested regarding bacterial contributions to filarial biology [9], the molecular mechanisms that underlie this fascinating relationship are poorly understood. Therefore, the best pathways or processes to target have not been identified.

Most medically and economically significant filarial nematodes belong to two subfamilies, the Onchocercinae and the Dirofilariinae [10]. Surveys suggest that the majority of these species are Wolbachia-dependent [11], [12], [13]. General agreement between the phylogenies of Wolbachia and filarial nematodes implies that the initial infection occurred in an ancestor of the Onchocercinae and Dirofilariinae and that the worms and bacteria co-evolved thereafter [12]. The Wolbachia-free species in these subfamilies, which are scattered throughout the lineage, most likely arose through secondary loss of the endosymbiont [12]. Our recent genomic surveys of two distantly related Wolbachia-free species, Acanthocheilonema viteae and Onchocerca flexuosa, revealed evidence of horizontal gene transfer (HGT) from Wolbachia, supporting the secondary loss hypothesis [14].

Clearly, Wolbachia-independent worms must possess some “enhanced” biochemistry in relation to their Wolbachia-dependent counterparts. They must have developed a mechanism of synthesizing or scavenging critical resources that Wolbachia-dependent species obtain from their endobacterial partner. In some cases, Wolbachia-free worms may have evolved their own compensatory mechanisms. However, it is also possible that they acquired essential Wolbachia genes or biochemical pathways from a former endosymbiont via HGT given that they were associated with Wolbachia in the past. Evidence for either possibility should be present in the genomes of Wolbachia-free filarial species. The identification of compensatory or Wolbachia-like genes/pathways may provide clues as to the nature of the interactions between Wolbachia and filarial nematodes and suggest targets for drugs aimed at disrupting this critical relationship in Wolbachia-dependent human and animal pathogens.

In this study, we used an integrated transcriptomic and proteomic approach to facilitate gene discovery in O. flexuosa (subfamily Onchocercinae), a Wolbachia-free parasite of European red deer [15]. Sequencing the adult transcriptome allowed us to assess this organism’s biochemical capabilities and gather a more complete inventory of transcribed Wolbachia-like sequences. This work confirmed and expanded our prior finding that many Wolbachia-like sequences are transcribed in O. flexuosa. A mass spectrometry analysis extended the work a step further by demonstrating the presence of Wolbachia-like peptides. Western blot and immunohistology results corroborated this finding and indicated that a peptide matching to a Wolbachia LolC protein was expressed in a tissue- and stage-specific manner in O. flexuosa. This suggests that Wolbachia-like sequences could have biological functions in Wolbachia-free worms and may not be merely inactive, fossilized remains of past infections.

Results

Transcriptome Sequencing, Assembly, and Quality Assessment

Sequencing and assembly results are outlined in Table 1. O. flexuosa nodules (typically containing one or a few large female worms, the developing embryos and microfilaria within the females, and potentially a smaller male worm) [15]) were collected from wild European red deer. Worm fragments were removed from nodules, and RNA was isolated, reverse transcribed and subjected to Roche/454 sequencing. Reads were assembled with publically available ESTs using a cDNA specific protocol to accommodate alternative splicing and allelic variation. Our assembly produced 16,814 isogroups (unique loci) containing 25,222 isotigs (unique transcripts or spliced variants), leaving 47,252 unassembled singletons (Table 1). 23.5% of the isogroups contained more than one isotig (mean 3.1 isotigs per isogroup for this subset), which suggests the possibility of alternate splicing (AS). For comparison, nearly 25% of C. elegans genes are thought to undergo some form of AS (e.g., tissue, sex or stage-specific) with an average of two isoforms per AS gene [16].

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Table 1. Results of sequencing, assembly, and translation of the O. flexuosa transcriptome.

https://doi.org/10.1371/journal.pone.0045777.t001

The conserved eukaryotic gene (CEG) mapping approach was used to estimate the completeness of our dataset [17], [18]. 101 of the 248 CEGs were identified, suggesting that 41% of all O. flexuosa genes are represented in our transcriptome. The O. flexuosa genome is expected to be similar to that of B. malayi, a closely related filarial nematode encoding some 14,500 to 17,800 genes [19]. Since our 16,814 isogroups only represent 41% of the complete gene set, it is highly unlikely that the 16,814 isogroups correspond to 16,814 unique genes. This is suggestive of fragmentation. Fragmentation, defined as non-overlapping isogroups derived from the same gene, was estimated to be 32%, 25% or 7%, by comparison with B. malayi, C. elegans, and the CEG dataset, respectively.

BLAST Analyses of the O. flexuosa Transcriptome

59.6% of the isogroups (67.2% of isotigs) and 34.6% of the singletons were matched to known sequences in BLAST searches against various databases (Table 2). More than 95% of the isogroups and singletons had a top hit to a B. malayi or C. elegans protein in BLAST searches against the non-redundant protein database (nr). 32.0% percent of B. malayi protein sequences and 11.0% of C. elegans protein sequences had putative orthologs in the O. flexuosa transcriptome (Table 2), with top-hit high scoring segment pairs (HSPs) sharing an average of 80.7% and 70.0% sequence identity between O. flexuosa and B. malayi or C. elegans, respectively.

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Table 2. Results of BLAST searches comparing O. flexuosa transcripts to various databases.

https://doi.org/10.1371/journal.pone.0045777.t002

Regions of 62 isogroups (73 isotigs) and 36 singletons had top ranking hits to Wolbachia proteins in BLAST searches against nr (Table 2 and Table S1, see Methods for cutoff values). Altogether, these Wolbachia-like sequence fragments represent a total of 97 different Wolbachia genes (43 from filarial Wolbachia strains and 54 from insect Wolbachia strains) with diverse functions. BLAST HSPs ranged in size from 62 to 308 bp and shared an average of 70.6% sequence identity with Wolbachia proteins at the amino acid level. In some instances, Wolbachia-like sequences were present on the same transcript as nematode-like sequences (Table 2, Fig. 1). These “hybrid” transcripts were verified by PCR amplification from genomic DNA and re-sequencing in order to ensure that they did not arise from assembly errors.

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Figure 1. Onchocerca flexuosa transcripts sharing sequence identity with Wolbachia and nematode genes.

17 “hybrid” isogroups (23 isotigs) and four “hybrid” singletons were identified as sharing sequence identity with Wolbachia (red) and nematode (blue) genes in a BLAST search against the non-redundant protein database. One representative isotig from each of the 17 “hybrid” isogroups was chosen for display. Arrows indicate predicted directionality of high-scoring segment pairs, and isotigs and singletons with Wolbachia-like and nematode-like sequences in the same reading frame are marked with an asterisk. Color intensity was used to indicate the degree of similarity shared between a given sequence and its top BLAST hit (see key in image).

https://doi.org/10.1371/journal.pone.0045777.g001

O. volvulus is a Wolbachia-dependent filarial nematode species in the same genus as O. flexuosa. Its genome has been sequenced, and it is currently being assembled and annotated. Preliminary data are publicly available, but the sequences have not yet been added to nr. The O. flexuosa isotigs and singletons containing Wolbachia-like sequences were compared against the latest version of the O. volvulus genome assembly. Eighteen isogroups (24 isotigs) and eight singletons matched (with greater than 80% sequence identity shared over more than 80% of the length of the O. flexuosa transcript) O. volvulus genomic sequences that contained similar Wolbachia-like inserts (Table S2, Fig. 2A). Nine other O. flexuosa isogroups (nine isotigs) and one singleton that contained Wolbachia-like inserts flanked by Onchocerca sequences matched O. volvulus genomic sequences that did not contain Wolbachia-like inserts (Table S2, Fig. 2B).

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Figure 2. Sequence conservation between Onchocerca flexuosa and O. volvulus.

O. flexuosa transcripts containing Wolbachia-like sequences were compared with the latest version of the O. volvulus genome assembly. Eighteen O. flexuosa isogroups (24 isotigs) and eight singletons with Wolbachia-like sequences shared at least 80% sequence identity with sequences from O. volvulus over 80% of the length of the O. flexuosa transcript. For example, O. flexuosa isotig05747 shares 90% sequence identity with a 1344 bp portion of O. volvulus scaffold245.1; both of these sequences contain a similar Wolbachia-like insert (A). Another nine O. flexuosa isogroups (9 isotigs) and one singleton matched O. volvulus sequences, except the latter did not contain Wolbachia-like inserts. For example, the sequences before and after the Wolbachia-like insert in O. flexuosa isotig09655 share 84% and 89% sequence identity with corresponding regions of O. volvulus scaffold14.1, respectively; however, the Wolbachia-like sequence present in O. flexuosa is not present in O. volvulus (B). Regions sharing sequence identity with Wolbachia are indicated in red while regions similar to nematode genes are indicated in blue. Arrows indicate directionality of high-scoring segment pairs. The grey dashed line represents a gap in the sequence alignment between the two species.

https://doi.org/10.1371/journal.pone.0045777.g002

Translation and Functional Annotation of the Transcriptome

68,402 unique peptide translations were produced from the O. flexuosa isotigs and singletons (Table 1). Sixty-two of these, ranging in size from 38 to 216 aa (mean 65.8±37.3 aa), had top hits to Wolbachia proteins by BLAST against nr. Predicted peptide sequences (including those from Wolbachia-like peptides), were compared to InterPro domains and KEGG orthologous (KO) groups. Collagen triple helix repeats, kinase domains and WD40 related domains were among the most commonly occurring protein domains (Table S3), while “folding, sorting and degradation”, “transcription, replication and repair”, and “signal transduction” were among the most abundantly represented pathway categories (Tables S4).

O. flexuosa peptide translations and B. malayi proteins assigned to KO groups were binned into pathway modules to provide a means of comparing the metabolic capabilities of these two organisms (Table S5). Genes related to the de novo synthesis of riboflavin, heme and nucleotides are missing from the nuclear genome of B. malayi but present in the genome of its Wolbachia endosymbiont, suggesting that B. malayi may rely on Wolbachia as a source of these substances [9], [19]. Table 3 highlights these four pathway modules. More sequences related to inosine monophosphate and uridine monophosphate biosynthesis (required for the de novo synthesis of purines and pyrimidines, respectively) were identified from O. flexuosa transcripts than from the nearly-complete genome of B. malayi (Table 3, Fig. 3), but key enzymatic steps in both pathways remain unaccounted for in O. flexuosa. Interestingly, some of the sequences binned into these modules are similar to enzymes from Wolbachia rather than enzymes from nematodes or other metazoans (Fig. 3). Wolbachia-like sequences could be assigned to 41 unique KO groups which were further binned into 26 pathway modules, all of which were sparsely populated (Table S6).

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Figure 3. Onchocerca flexuosa sequences related to de novo purine and pyrimidine biosynthesis.

KEGG pathway modules are outlined for inosine monophosphate (A) and uridine monophosphate (B) biosynthesis (module entries M00048 and M00051, respectively). Boxes representing enzymes present in nematodes (e.g., C. elegans), Wolbachia, or both are colored blue, red and purple, respectively. Enzymes sharing sequence identity with O. flexuosa peptide translations are highlighted in yellow. Enzymes identified from B. malayi are marked with an asterisk.

https://doi.org/10.1371/journal.pone.0045777.g003

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Table 3. Selected KEGG pathway modules in B. malayi and O. flexuosa. Table lists the number of module enzymes represented in each dataset.

https://doi.org/10.1371/journal.pone.0045777.t003

Analysis of the O. flexuosa Proteome

Adult worm lysate was subjected to a shotgun proteomic analysis in order to characterize the O. flexuosa proteome. Using this method, proteins are identified by matching experimentally obtained mass spectra to amino acid sequences predicted from the organism’s genome. Because the O. flexuosa genome has not been fully sequenced, we compiled a custom comparative database for analysis of MS results. This database contained peptide translations from the O. flexuosa transcriptome and sequences from the phylum Nematoda and the genus Wolbachia (see methods). Interrogation of this database resulted in the successful characterization of 8,537 unique peptides that mapped to 2,685 database entries. Matches were further grouped into 1,803 potential proteins (Table S7). Of the 1,803 proteins, 673 matched O. flexuosa peptide translations, 1,077 matched sequences from other organisms, and 53 matched to both. Database entries identified by MS (available from Nematode.net [20]) were annotated in the same manner as the transcriptome. Thioredoxin folds, concanavalin A-like lectin/glucanase domains and immunoglobulin fold domains were among the most abundant protein domains (Table S3), while “Folding, sorting and degradation”, “translation”, “energy metabolism” and “carbohydrate metabolism” were among the most heavily represented KEGG pathway categories (Table S4).

Although none of the Wolbachia-like peptides predicted from the O. flexuosa transcriptome were identified by MS, three MS peptides matched to two Wolbachia proteins (see MS proteins 1591 and 1637, Table S7). A 23aa peptide present in two separate charge states mapped to a lipoprotein releasing system transmembrane protein, LolC, that is present in several insect Wolbachia strains (Fig. 4A). A sequence similar to the Wolbachia LolC gene was previously identified in the O. flexuosa genome (see genomic fragment wOf3, [14]); however, this sequence has diverged to an extent that it would not be capable of producing the exact peptide detected by MS (Fig. 4A). Two more peptides (17 aa and 9 aa) mapped to an HlyD family secretion protein from the Wolbachia endosymbiont of Culex quinquefasciatus (Fig. 4B). Several PCR primer sets corresponding to different regions of HlyD were used in unsuccessful attempts to amplify sequences from O. flexuosa. Thus far, we have not identified any genomic or transcriptomic sequence capable of producing these Wolbachia-like peptides.

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Figure 4. Wolbachia-like peptides identified by mass spectroscopy (MS).

Wolbachia genes are shown in red with MS peptides highlighted in blue and peptide sequences shown in black text. One peptide with two charge states was mapped to a LolC protein found in several insect Wolbachia strains, including the Wolbachia endosymbiont of Drosophila simulans (wRi) (A), and two unique peptides were mapped to a HlyD family protein from the Wolbachia endosymbiont of Culex quinquefasciatus (wCq) (B). A region with sequence identity to the LolC gene was identified in the O. flexuosa genome [14], but this locus would not be capable of producing the exact peptide identified in our MS experiment (consensus shown in blue text). Polyclonal antibodies were raised against the underlined portion of the LolC peptide.

https://doi.org/10.1371/journal.pone.0045777.g004

Detection of Wolbachia-like Peptides in O. flexuosa Using Anti-peptide Antibodies

Polyclonal antibodies raised against the peptide mapping to Wolbachia LolC (see Fig. 4A) detected a single band at approximately 38 kDa in O. flexuosa adult worm lysate by Western blot (Fig. 5). Similar bands were not detected by IgG from pre-immune serum or antibodies against the keyhole limpit hemocyanin (KLH) carrier protein used in antibody synthesis. For comparison, the LolC protein from the Wolbachia endosymbiont of Drosophila simulans (accession ACN95889) is 44.9 kDa while its homolog in the Wolbachia endosymbiont of B. malayi (accession YP_198313) is 42.5 kDa.

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Figure 5. Western blots detecting the putative LolC peptide in Onchocerca flexuosa adult worm lysate.

Affinity-purified rabbit antibodies raised against a peptide from MS protein 1591, a putative LolC homolog, bound a 38 kDa band in Western blots of O. flexuosa adult worm lysate (lane 1). Purified IgG from pre-immune serum (lane 2) and antibodies against the keyhole limpit hemocyanin carrier (lane 3) did not bind to proteins in this size range.

https://doi.org/10.1371/journal.pone.0045777.g005

The same antibodies were used to localize the target peptide in O. flexuosa worms (Fig. 6). Control antibodies to KLH did not label O. flexuosa (Fig. 6A), and total IgG from pre-immune serum produced the same result (not shown). In contrast, antibody to the putative LolC peptide strongly labeled fibrillar portions of the somatic muscles of adult male (Fig. 6B) and young female (Fig. 6C, D) worms. Older females have less pronounced somatic musculature and showed weaker labeling; however, the antibody labeled uterine muscles and coiled and stretched microfilariae in these worms (Figs. 6F, G). Distinct staining was also seen in the membrane of the excretory cell (Fig. 6D, E). Sequences homologous to LolC were identified from the genome of the Wolbachia endosymbiont of B. malayi and used to make RNA probes for in situ hybridization since corresponding sequences have not yet been identified from O. flexuosa. In situ hybridization studies indicated that the target RNA was produced in the lateral chords (Fig. 6I, J, K), the hypodermis (Fig. 6K), developing sperm (Fig. 6I), uteri (Fig. 6K) and intestine (Fig. 6K).

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Figure 6. Localization of the putative LolC peptide by immunohistology and in situ hybridization in Onchocerca flexuosa.

The putative LolC peptide and transcript were localized in adult worm tissues via immunohistology (A-G) and in situ hybridization (H-K), respectively. Negative control antibodies against keyhole limpit hemocyanin (carrier protein) showed no specific staining in O. flexuosa (A). Antibodies against a peptide from MS protein 1591, a putative homolog of Wolbachia LolC, stained the fibrillar portions of the somatic muscles (arrow) in a cross section of an adult male worm (B). The somatic muscles (solid arrows) and excretory cell (dashed arrow) are stained in cross sections of young adult females (C, D). Magnification of the excretory cell shows intense staining of the cell membrane (dashed arrow) and more diffuse staining in adjacent muscles (solid arrow) (E). The uterine muscles of an older female (arrow) are clearly stained (F), as are the intrauterine stretched microfilaria (F, G). The LolC sense RNA probe produced no signal in in situ hybridizations (H), while the antisense RNA probe labeled the lateral chords (arrows) and developing sperm within the male testes (I, J). The antisense RNA probe also labeled the lateral chords (arrow), intestine, and uteri of a young adult female (K). Abbreviations: m, muscle; lc, lateral chords; i, intestine; ut, uterus; mf, microfilariae; hy, hypodermis; t, testes; vd, vas deferens. Scale bars = 25 µm.

https://doi.org/10.1371/journal.pone.0045777.g006

Discussion

The relationship between Wolbachia and Wolbachia-dependent filarial nematodes has been a topic of keen interest in recent years since Wolbachia was identified as a potential anti-filarial drug target. Most research on this relationship has focused on Wolbachia-dependent filarial parasites of humans and domestic animals. Wolbachia-free species have been overlooked since most are animal parasites with no economic or medical importance. Therefore, the mechanisms allowing these species to survive without an endosymbiont remain unknown. We believe that the genetic characterization of Wolbachia-free filarial parasites like O. flexuosa may lead to a better understanding of filarial biology and the mechanisms responsible for Wolbachia dependence in important filarial pathogens such as W. bancrofti, Dirofilaria immitis, and O. volvulus.

In this study, we focused on the transcriptome rather than the genome of O. flexuosa as an efficient and cost-effective method for gene discovery in a Wolbachia-free filarial parasite. Estimates of completeness suggest that our dataset represents approximately 41% of the genes encoded in the O. flexuosa genome. This result was not unexpected, since RNA from nodules does not contain transcripts from all parasite stages. O. flexuosa nodules, and the cDNA libraries derived from them, are biased towards adult females due to the size and relative abundance of the female worms within. However, 41% is on par with the number of genes represented by unambiguously-mapped reads derived from adult female transcripts in a recent analysis of the B. malayi transcriptome [21]. It will be difficult to discover more genes for this species through transcriptome sequencing since these parasites are only found in wild deer and the life cycle cannot be maintained in the laboratory; therefore, it is not possible to collect material representing life cycle stages that are not well represented in nodules.

One major motivation for studying the O. flexuosa transcriptome was to develop a more complete inventory of transcribed Wolbachia-like sequences. Our previous genomic surveys indicated that O. flexuosa had incorporated fragments of at least 92 Wolbachia genes in its nuclear genome through HGT [14]. An additional 86 Wolbachia genes were represented in our partial transcriptome, increasing the total number of Wolbachia genes represented by Wolbachia-like sequence fragments in O. flexuosa to 178. Interestingly, only 11 Wolbachia genes were represented in both the genomic and transcriptomic datasets despite the fact that a majority of the Wolbachia-like sequences identified in the genome were shown to be expressed at the RNA level using qRT-PCR [14]. This disparity could be due to variation in the wild-caught samples, differences in sequencing coverage between the two studies, differences in cDNA preparation (total RNA in the previous study versus poly(A) selected RNA in the present study), or differences in sensitivity between qRT-PCR used in the prior study versus 454/Roche sequencing used in this study. No effort was made in either study to quantify the relative expression of Wolbachia-like gene sequences since no criteria exist to define “biologically relevant” expression levels. However, some of the isogroups found to contain Wolbachia-like sequences were constructed from many reads, suggesting a reasonably abundant transcript population.

It is possible that O. flexuosa contains many more Wolbachia-like sequences than those uncovered by our genomic and transcriptomic surveys, as nearly complete Wolbachia gene sets have been discovered in other species (e.g., Drosophila ananassae [22] and Callosobruchus chinensis [23]). Once comprehensive inventories of HGT sequences have been obtained from many species, it would be interesting to compare and contrast the Wolbachia genes represented in various insect and filarial genomes, especially between Wolbachia-dependent and independent filaria. Cataloging transferred sequences shared between Wolbachia-independent species but absent from Wolbachia-dependent species could provide clues as to which sequences, if any, could have facilitated endosymbiont loss. As one might expect, preliminarily comparisons between the Wolbachia-like sequences found in O. flexuosa and the preliminary draft of the nuclear genome of the Wolbachia-dependent species Onchocerca volvulus indicate that some Wolbachia-like inserts are unique to O. flexuosa while others are shared between the two species. Shared inserts were presumably transferred prior to separation of the two Onchocerca species whereas O. flexuosa specific inserts were presumably transferred afterwards. However, it must be noted that the O. volvulus genome assembly is not fully complete, and the putative transfers have not been experimentally verified. The catalogs of shared versus unique fragments will certainly grow and change as the available datasets evolve.

Despite our extensive catalog of Wolbachia-like sequences, we have yet to identify a full-length, uninterrupted Wolbachia-like gene in O. flexuosa. This may be due to technical issues (e.g., insufficient coverage, fragmentation, etc.). It may also be that complete genes were transferred but decayed over time in the absence of selective pressure. However, it is possible that transfers took place on the level of domains rather than complete genes. Many proteins are made up of multiple domains that each contribute to overall function, and studies have suggested that domains, rather than complete genes, might be common units of genetic transfer [24]. For example, transfers of mitochondrial DNA to the nuclear genome have generated “hybrid” proteins containing both “nuclear” and “organellar” exons [25]. In support of this hypothesis, we identified 17 isogroups and four singletons containing separate regions of similarity to Wolbachia and nematode genes. Most of the “hybrid” transcripts seem incapable of producing a functional product (i.e., nematode-like and Wolbachia-like sequences code in opposing directions or different reading frames), but some have the potential to yield a “hybrid” protein with nematode-like and Wolbachia-like subunits. Of course, whether the inserted Wolbachia domains disrupt protein function, impart novel capabilities, or have no effect at all remains to be seen.

Given that we have only sampled some 41% of the complete genome and that the transcripts are still heavily fragmented, it is difficult to make definitive statements regarding the biochemical capabilities of O. flexuosa. Many important biochemical pathways appear incomplete, presumably due to insufficient sequence coverage (Table S5). However, more sequences related to de novo purine and pyrimidine synthesis were identified from the partial transcriptome of O. flexuosa than the nearly complete genome of B. malayi. While missing from B. malayi, purine and pyrimidine synthesis pathways are present in other nematodes (i.e., Caenorhabditis species) and in the Wolbachia endosymbiont [9], [19], raising the possibility that B. malayi relies on Wolbachia as a source of nucleotides, particularly during times of intense demand (e.g., growth and for reproduction). Further testing will be required to determine whether the O. flexuosa sequences binned into these two pathway modules belong to full-length, intact, functional genes and, if so, whether nematode-like and Wolbachia-like enzymes could act in concert in a functional biochemical pathway. De novo nucleotide synthesis could contribute to O. flexuosa’s ability to survive without an endosymbiont, so this is an interesting possibility that deserves closer examination.

Our transcriptome data facilitated a parallel proteomic analysis of O. flexuosa adult worm lysate. Shotgun proteomic studies are generally restricted to organisms with sequenced genomes, as MS data are only informative if sequences from the organism of interest are available for comparison. Information from closely related species can be used when genomic data are unavailable, but only very highly conserved proteins will be identified since matches between experimentally collected mass spectra and database sequences must be exact [26], [27], [28]. Our approach of adding transcript sequences to a database of orthologous proteins from Wolbachia and other nematodes led to identification of 1,803 proteins in adult worm lysate. Sequence conservation between O. flexuosa and better-studied filarial species like B. malayi allowed for a high rate of cross-species matches (∼60% of matches) and greatly increased the number of proteins that we were able to identify.

The present study identified Wolbachia-like peptides in a Wolbachia-free filarial worm (O. flexuosa), an important step beyond what we had previously reported. Peptides mapping to Wolbachia HlyD and LolC were identified in adult worm lysate by MS, and the putative LolC peptide was identified by Western blot and by immunohistology using polyclonal antibodies to the peptide. Neither of these proteins has been studied in Wolbachia, but both LolC and HlyD are related to ABC transport in Escherichia coli and other bacteria [29], [30]. ABC transporters are common in both prokaryotes and eukaryotes. They interact with a diverse array of substrates, and they may play a role in drug resistance in filarial nematodes [31], [32], [33], [34]. We do not know whether the peptides mapping to LolC and HlyD exist as small inserts in larger nematode proteins or whether they represent fragments of complete Wolbachia-like proteins. The fact that the two peptides that mapped to HlyD are separated by 99 amino acids supports the latter hypothesis (see Fig. 4B). In any case, it is fair to say that the function(s), if any, of the putative HlyD and LolC sequences in O. flexuosa are unknown at this time.

Our immunohistological and in situ hybridization studies revealed interesting, tissue-specific patterns of expression for the putative LolC gene and peptide. To date, three Wolbachia like transcripts (homologs of 2-methylthioadenine synthase and DNA polymerase I previously described in [14] and LolC described in Fig. 6 of this paper) have been localized, and all three exhibit similar expression patterns. While various tissues appear to be capable of producing Wolbachia-like transcripts, strong transcription signals were observed in tissues that harbor Wolbachia in infected species (e.g., lateral chords and reproductive organs) (see [35] for localization of Wolbachia in B. malayi; see [14] and Fig. 6 in this paper for localization of Wolbachia-like transcripts in O. flexuosa). However, immunohistology studies showed that the putative LolC peptide was mainly present in fibrillar portions of muscle. This does not correspond to the in situ hybridization results. mRNAs and their corresponding proteins are generally found in the same tissues, but there are precedents for disparate localization of transcripts and proteins derived from the same gene. For example, the filarial gene shp-1 is expressed in the uterine epithelium of female worms, while the protein localized to the sheath of microfilariae [36], [37]. Our results suggest that tissues known to harbor Wolbachia in infected worms are at least partially responsible for the production of Wolbachia-like products in Wolbachia-free worms, and that these proteins are transported to other tissues after they are produced.

We hypothesize that technical issues limited our ability to detect more Wolbachia-like proteins. These hindrances include the suboptimal comparative database (discussed previously), the complexity of our analyzed sample, and the relative paucity of Wolbachia-like proteins compared to other proteins in the sample. Detection of Wolbachia proteins from both infected and uninfected filarial species might benefit from a more directed approach, as certain tissues (i.e. lateral chords, ovaries, developing sperm) or lifecycle stages (i.e. adolescent worms) may express these genes to a higher degree than others (see [14], [35] and Fig. 6). Analyses of isolated tissues might lead to a higher identification rates for Wolbachia-like proteins and peptides in tissues from both infected and uninfected filarial species.

Thus far, our studies have provided compelling evidence that Wolbachia-like sequences are present in the genome of O. flexuosa, and that they are expressed at the RNA and protein levels in a tissue- and stage-specific manner. Although the preservation, expression, and regulation of these sequences suggest that they may play important roles in filarial biology, expression does not guarantee utility. It is possible that Wolbachia sequences could insert themselves into existing O. flexuosa proteins without imparting new functions, and it is possible that even full-length, abundantly expressed Wolbachia-like proteins could be useless in the context of the worm interactome. Clearly, additional studies will be needed to determine the significance of Wolbachia-like sequences in Wolbachia-free filarial nematodes and to determine whether they are capable of supporting the independent, Wolbachia-free lifestyle of these species.

Materials and Methods

Parasite Material

Nodules containing O. flexuosa worms were taken from the skins of freshly-shot European red deer (Cervus elaphus) in northern Germany (Schleswig-Holstein) as previously described [15]. Several nodules were dissected immediately after excision from the deer, and the worm fragments pooled and stored in TRIzol (Invitrogen, Carlsbad, CA, USA) at −80°C prior to RNA isolation. Some nodules were frozen whole at −80°C and dissected at a later time to obtain worms for the proteomic study while others were fixed in 4% buffered formalin, embedded in paraffin and sectioned according to standard histological technique for use in in situ hybridization or immunohistology.

Adult B. malayi were obtained from experimentally infected Mongolian gerbils as previously described [38]. Animals were handled in accordance with guidelines defined by the Animal Welfare Act, the Guide for the Care and Use of Laboratory Animals, and the Division of Comparative Medicine, Washington University School of Medicine. Animal work was approved under WUSM Institutional Animal Care and Use Protocol 20110292. Worms were stored at −80°C prior to use.

RNA Isolation, Library Construction and 454 Sequencing

Total RNA was isolated from O. flexuosa worm fragments, DNase treated and tested for DNA contamination as previously described [14]. RNA yield and integrity were assessed using a NanoDrop ND-1000 UV-VIS spectrophotometer (NanoDrop Technologies, Wilmington, DE) and a Bioanalyzer 2100 (Agilent Technologies, Cedar Creek, TX), respectively. Full-length cDNA was generated from 1.0 µg total RNA using an optimized 27-cycle protocol with the Accuscript HF Reverse Transcriptase Kit (Agilent) and SMART primers (Invitrogen). The resulting cDNA library was normalized with the Trimmer kit (Evrogen, San Diego, CA) and amplified over 14 cycles using SMART primers (Invitrogen) and Clontech Advantage-HF 2 polymerase (Clontech/Takara Bio, CA). 300–800 bp fragments were selected using AMPure paramagnetic beads (Agencourt, Beckman Coulter Genomics, Beverly, MA) following removal of 3′ and 5′ adaptors by restriction digest and processed using the Titanium General Library Kit (Roche, Branford, CT). Sequencing was performed on the Genome Sequencer 454 Titanium instrument using the GS FLX Titanium Sequencing Kit (Roche) according to standard protocol [39].

Assembly and Translation of Transcript Sequences

Raw 454 reads were trimmed for adapters and low complexity regions using SeqClean (http://www.tigr.org/tdb/tgi/software) and screened against UniVec (http://www.ncbi.nlm.nih.gov/VecScreen/UniVec.html) and genome sequences from Bos taurus (the closest sequenced relative of the deer host) and Homo sapiens. The Newbler v2.5 assembler (Roche) was used to assemble clean reads and 2,124 Genbank ESTs (September 2010) using the following parameters “-cdna –ml 100–mi 95–icl –het”. According to this protocol, contiguous sequences (contigs) are clustered into “isogroups” that encompass all of the sequences related to a given locus. Within each isogroup, the contigs are tiled into “isotigs” meant to represent individual transcripts or splice variants. Following assembly, any isotig or singleton less than 200 bp, with more than 10% ambiguous bases, or with a top BLAST hit to a human or ruminant nucleotide or protein sequence was excluded from analysis. Isotig sequences were deposited in the GenBank transcriptome shotgun assembly database under BioProject number 62565 (accession numbers JI459010-JI484230). All sequences used in subsequent analyses, including singletons, are available at Nematode.net [20].

Peptide translations were obtained from isotigs and singletons using Prot4EST [40], [41].

Core Eukaryotic Gene Mapping and Assessment of Fragmentation

The coverage of the O. flexuosa transcriptome was estimated by profile searching isotigs and singletons against core eukaryotic genes [17], [18] using HMMer [42]. A custom perl script was used to calculate the fragmentation rate based on WU-BLAST (http://blast.wustl.edu) BLASTX alignments to B. malayi proteins (brugpep.WS225.fa), C. elegans proteins (wormpep.WS21.fa), and the core eukaryotic gene set since the O. flexuosa genome is unavailable. The presence of multiple, non-overlapping matches to a given B. malayi or C. elegans protein was taken as evidence for fragmentation.

BLAST Analyses

All BLAST searches were performed using blastall version 2.2.22 with the following cutoff values: e-values less than 1e-05, bit scores greater than 35 bits, and percent identity greater than 55%. Databases queried included: non-redundant protein and non-redundant nucleotide databases (downloaded 5/27/2010), all Genbank ESTs related to the Nematoda (downloaded 1/6/2011), WormBase B. malayi genome assembly (b_malayi.WS221.dna.fa), WormBase B. malayi predicted proteins (brugpep.WS221.fa), WormBase C. elegans predicted proteins (wormpep.WS215.fa), the O. volvulus genome assembly (available from The Wellcome Trust Sanger Institute, ftp://ftp.sanger.ac.uk/pub/pathogens/Onchocerca/volvulus/, last modified 2/27/2012), and the KEGG protein database (version 57). A custom perl script was used to extract the top hit from each region of the query before parsing BLAST results.

Mass Spectroscopy

O. flexuosa worms were dissected from frozen nodules, pulverized in liquid nitrogen, dissolved in 50 mM Tris pH 8.0 with cOmplete protease inhibitor cocktail (Roche), and sonicated on ice. Two nodules were prepared in this manner to provide biological replicates. Half of each sonicated sample was pooled and subjected to centrifugation at 20,000 g for 90 minutes to separate soluble from insoluble proteins. This resulted in four separate samples (nodule 1, nodule 2, mixed soluble fraction, and mixed insoluble fraction) that were treated in the same manner. Protein concentration was determined by the DC Protein Assay (Bio Rad, Hercules, CA). Proteins were denatured with 8 M urea, reduced with 5 mM tris (2-carboxyethyl) phosphine (TCEP), and alkylated with iodoacetamide, prior to digestion with sequencing-grade trypsin (1∶50 trypsin:protein ratio).

Peptides from the four samples were separated using multidimensional chromatography (MudPIT) and analyzed by tandem MS as previously described [43]. Briefly, 50 µg of peptides were pressure-loaded onto a biphasic capillary column packed with strong cation exchange (SCX) and C18 resins, and fractionated by a combination of ion exchange and reverse phase chromatography. Peptides were eluted from SCX resin with six injections of increasing concentrations of ammonium acetate, followed by 120 minute organic gradients to elute peptides from the C18 resin directly into an LTQ Orbitrap Discovery hybrid mass spectrometer (Thermo Scientific, West Palm Beach, FL). MS1 spectra were acquired in the orbitrap (FTMS) with a resolution of 30,000 followed by seven data-dependent MS2 spectra in the ion trap (ITMS) at low resolution. Data were stored in Thermo RAW format, and converted to MS2 format using RawXtract 1.9.9.2 [44].

MS2 spectra were searched using the ProLuCID algorithm [45] against a combined database containing 238,403 sequences derived from O. flexuosa peptide translations, all GenBank protein entries from the phylum Nematoda and genus Wolbachia (downloaded February 2010), WormBase protein sequences from B. malayi (brugpep.WS221.fa) and C. elegans (wormpep.WS215.fa). Reversed “decoy” versions of each entry were also included to allow for estimation of false-discovery rates [46]. Peptide spectral matches were filtered using DTASelect 2.0 [47] resulting in a peptide false-positive rate of 1.2%.

Functional Annotation of Predicted and Experimentally Verified Proteins

InterProScan version 4.5 was used to identify conserved domains from peptide translations and database protein sequences with matches to MS peptides [48]. Sequences were assigned to KEGG orthologous groups by comparison with the KEGG protein database [49]. Custom perl scripts were used to bin orthologous groups into broad categories and KEGG modules.

Antibody Production

A 15 amino acid portion of MS protein 1591 (see Table S7, Fig. 4A) was selected based on inferred immunogenic properties (i.e. predicted secondary structure and hydrophobicity). Polyclonal antisera were raised against the synthetic peptide coupled to KLH in two rabbits (LifeTein LLC, South Plainfield, NJ). Antibodies were affinity purified with the original peptide and tested by ELISA prior to use (LifeTein LLC). Polyclonal antisera against the KHL carrier protein were raised, purified, and tested in the same manner. Total IgG were purified from rabbit pre-immune sera using the Protein A Agarose Kit (KPL, Gaithersburg, MD) for use as negative controls.

Western Blots

Adult O. flexuosa were dissected from nodules and homogenized on ice in RIPA buffer (G Biosciences, Maryland Heights, MO) and ProteaseArrest (G Biosciences) in a one mL mini homogenizer (GPE Scientific Limited, Leighton Buzzard, UK). Homogenate was spun at 19,000 g for 15 minutes to pellet debris, and the protein concentration of the supernatant was determined using the BCA method (Pierce, Rockford, IL). O. flexuosa protein was subjected to SDS-PAGE using a 4–12% reducing gel (NuPAGE BisTris Mini Gel, Invitrogen) according to the manufacturer’s suggested protocol. Separated proteins were transferred to a nitrocellulose membrane (Invitrogen). The membrane was blocked overnight at 4°C in blocking buffer (0.5% Tween, 5% nonfat dry milk in 1×PBS), washed in 1×PBS with 0.5% Tween (PBS/T), and cut into strips for blotting. Antibodies were diluted in PBS/T to final concentrations of 4.4 µg/mL, 15 µg/mL and 50 µg/mL for anti-MS1591, purified pre-immune IgG and anti-KLH, respectively. Blot strips were incubated with primary antibody dilutions overnight at 4°C and washed with PBS/T at room temperature. Strips were then incubated with anti-rabbit IgG(Fc) AP conjugate (1∶3,500 in PBS/T) (Promega, Sunnyvale, CA) for 1 h at 37°C, washed with PBS/T at room temperature and developed using NBT/BCIP substrate (Promega). Substrate reaction was stopped using 20 mM Tris-HCl pH 7.4 with 5 mM EDTA.

In situ Hybridization and Immunohistochemistry

DNA was isolated from adult B. malayi as previously described [14] using the DNeasy Blood and Tissue Kit (Qiagen). A 369 bp portion of the LolC gene from the Wolbachia endosymbiont of B. malayi (locus Wbm0483) was amplified from B. malayi genomic DNA using the following primers: 5′- TCTTTCATTCTCGGCACCTCA-3′ and 5′- TGGCATTGATGGCCATATCA-3′. Biotinylated RNA probes were constructed from PCR products by in vitro transcription as previously described [14].

Immunohistological stainings and in situ hybridizations were carried out as previously described [35]. In situ hybridizations were performed overnight at 60°C using 1 µg/mL of RNA probe in hybridization buffer. Antibodies against MS protein 1591 (LolC) were used at 0.88 µg/mL while anti-KLH antibodies were used at 1.4 µg/mL. A total of twelve nodules were examined.

Supporting Information

Table S1.

Onchocerca flexuosa transcripts with similarity to Wolbachia genes. O. flexuosa isotigs and singletons were compared against the non-redundant protein database. The accession numbers, descriptions and coordinates of each BLAST hit are given for isotigs and singletons that share sequence similarity to Wolbachia. Note that every other isotigs was highlighted in yellow to aid in distinguishing separate isotigs from separate BLAST hits.

https://doi.org/10.1371/journal.pone.0045777.s001

(XLSX)

Table S2.

Sequence conservation between Onchocerca flexuosa and O. volvulus. Sequences are designated as conserved between the transcriptome of O. flexuosa and genome of O. volvulus if they share at least 80% ID at the nucleotide level over at least 80% of the length of the O. flexuosa transcript. Gaps were allowed in the alignments to account for potential introns in O. volvulus genomic sequences. The relevant portions of the O. volvulus genomic scaffolds are included in this table for convenience.

https://doi.org/10.1371/journal.pone.0045777.s002

(XLSX)

Table S3.

Top 25 InterPro protein domains identified from Onchocerca flexuosa peptide translations and proteins identified by mass spectrometry (MS). O. flexuosa peptide translations and protein database entries with matches to MS peptides (termed MS proteins in this table) were compared to InterPro protein domains. Translations from 3,853 isogroups and 2,121 singletons share sequence similarity with 2,804 unique InterPro domains, while 1,573 of the 1,803 protein groups identified by MS share sequence similarity with 1,516 InterPro domains.

https://doi.org/10.1371/journal.pone.0045777.s003

(DOC)

Table S4.

KEGG pathway category mappings for Onchocerca flexuosa peptide translations and proteins identified by mass spectroscopy (MS). Peptide translations from 5,159 isogroups and singletons were assigned to 2,049 unique KEGG orthologous (KO) groups, while 608 protein database entries with matches to MS peptides (termed MS proteins) were associated with 446 unique KO groups. The sequences were binned into broad pathway categories based on their association with these KO groups.

https://doi.org/10.1371/journal.pone.0045777.s004

(DOC)

Table S5.

KEGG pathway modules represented in Onchocerca flexuosa and Brugia malayi. After being assigned to KEGG orthologous groups, sequences from O. flexuosa (both peptide translations derived from the adult transcriptome and protein database entries with matches to mass spectroscopy peptides) and B. malalyi predicted proteins (WormBase brugpep.WS221.fa) were binned in to KEGG pathway modules in order to compare the metabolic capabilities of the two filarial species.

https://doi.org/10.1371/journal.pone.0045777.s005

(DOC)

Table S6.

KEGG pathways represented by Wolbachia-like sequences in O. flexuosa. Peptide translations sharing sequence identity with Wolbachia genes were assigned to KEGG orthologous groups and binned into KEGG pathway modules in order to determine what pathways/processes these sequences might be related to.

https://doi.org/10.1371/journal.pone.0045777.s006

(DOCX)

Table S7.

Results of mass spectrometry analysis of O. flexuosa adult worm lysate. Experimentally detected mass spectra were compared to a protein database containing peptide translations derived from the adult transcriptome of O. flexuosa and known protein sequences related to the phylum Nematoda and the genus Wolbachia (see methods for details).

https://doi.org/10.1371/journal.pone.0045777.s007

(XLSX)

Acknowledgments

We would like to thank Jeffrey I. Gordon (Center for Genome Sciences and Systems Biology, Washington University) for access to the mass spectrometer and related reagents and Katherine Mann for technical assistance.

Author Contributions

Conceived and designed the experiments: SNM GMS MM GJW PUF. Performed the experiments: SNM GMS KF KCC. Analyzed the data: SNM SA GMS MM NPM GJW PUF. Contributed reagents/materials/analysis tools: MM NWB. Wrote the paper: SNM GJW PUF.

References

  1. 1. Anderson RC, Bain O (1976) Keys to genera of the order Spirurida. Part 3. Diplotriaenoidea, Aproctoidea and Filarioidea. In: Anderson RC, Chabaud AG, Willmott S, editors. CIH keys to the nematode parasites of vertebrates. Farnham Royal, UK: Commonwealth Agricultural Bureau. 59–116.
  2. 2. WHO (2011) Global programme to eliminate lymphatic filariasis: progress report on mass drug administration, 2010. Wkly Epidemiol Rec 86: 377–388.
  3. 3. WHO (2011) African programme for onchocerciasis control: meeting of national task forces, September 2011. Wkly Epidemiol Rec 86: 541–549.
  4. 4. Taylor MJ, Hoerauf A, Bockarie M (2010) Lymphatic filariasis and onchocerciasis. Lancet 376: 1175–1185.
  5. 5. Taylor MJ, Bandi C, Hoerauf A (2005) Wolbachia bacterial endosymbionts of filarial nematodes. Adv Parasitol 60: 245–284.
  6. 6. Hoerauf A, Mand S, Fischer K, Kruppa T, Marfo-Debrekyei Y, et al. (2003) Doxycycline as a novel strategy against bancroftian filariasis-depletion of Wolbachia endosymbionts from Wuchereria bancrofti and stop of microfilaria production. Med Microbiol Immunol 192: 211–216.
  7. 7. Hoerauf A, Nissen-Pahle K, Schmetz C, Henkle-Duhrsen K, Blaxter ML, et al. (1999) Tetracycline therapy targets intracellular bacteria in the filarial nematode Litomosoides sigmodontis and results in filarial infertility. J Clin Invest 103: 11–18.
  8. 8. Slatko BE, Taylor MJ, Foster JM (2010) The Wolbachia endosymbiont as an anti-filarial nematode target. Symbiosis 51: 55–65.
  9. 9. Foster J, Ganatra M, Kamal I, Ware J, Makarova K, et al. (2005) The Wolbachia genome of Brugia malayi: endosymbiont evolution within a human pathogenic nematode. PLoS Biol 3: e121.
  10. 10. Anderson RC (2000) Nematode parasites of vertebrates: their development and transmission. New York, New York, USA: CABI Publishing.
  11. 11. Bandi C, Anderson TJ, Genchi C, Blaxter ML (1998) Phylogeny of Wolbachia in filarial nematodes. Proc Biol Sci 265: 2407–2413.
  12. 12. Casiraghi M, Bain O, Guerrero R, Martin C, Pocacqua V, et al. (2004) Mapping the presence of Wolbachia pipientis on the phylogeny of filarial nematodes: evidence for symbiont loss during evolution. Int J Parasitol 34: 191–203.
  13. 13. Ferri E, Bain O, Barbuto M, Martin C, Lo N, et al. (2011) New insights into the evolution of Wolbachia infections in filarial nematodes inferred from a large range of screened species. PLoS One 6: e20843.
  14. 14. McNulty SN, Foster JM, Mitreva M, Dunning Hotopp JC, Martin J, et al. (2010) Endosymbiont DNA in endobacteria-free filarial nematodes indicates ancient horizontal genetic transfer. PLoS One 5: e11029.
  15. 15. Plenge-Bonig A, Kromer M, Buttner DW (1995) Light and electron microscopy studies on Onchocerca jakutensis and O. flexuosa of red deer show different host-parasite interactions. Parasitol Res 81: 66–73.
  16. 16. Ramani AK, Calarco JA, Pan Q, Mavandadi S, Wang Y, et al. (2011) Genome-wide analysis of alternative splicing in Caenorhabditis elegans. Genome Res.
  17. 17. Parra G, Bradnam K, Korf I (2007) CEGMA: a pipeline to accurately annotate core genes in eukaryotic genomes. Bioinformatics 23: 1061–1067.
  18. 18. Parra G, Bradnam K, Ning Z, Keane T, Korf I (2009) Assessing the gene space in draft genomes. Nucleic Acids Res 37: 289–297.
  19. 19. Ghedin E, Wang S, Spiro D, Caler E, Zhao Q, et al. (2007) Draft genome of the filarial nematode parasite Brugia malayi. Science 317: 1756–1760.
  20. 20. Martin J, Abubucker S, Heizer E, Taylor CM, Mitreva M (2012) Nematode.net update 2011: addition of data sets and tools featuring next-generation sequencing data. Nucleic Acids Res 40: D720–728.
  21. 21. Choi YJ, Ghedin E, Berriman M, McQuillan J, Holroyd N, et al. (2011) A deep sequencing approach to comparatively analyze the transcriptome of lifecycle stages of the filarial worm, Brugia malayi. PLoS Negl Trop Dis 5: e1409.
  22. 22. Hotopp JC, Clark ME, Oliveira DC, Foster JM, Fischer P, et al. (2007) Widespread lateral gene transfer from intracellular bacteria to multicellular eukaryotes. Science 317: 1753–1756.
  23. 23. Nikoh N, Tanaka K, Shibata F, Kondo N, Hizume M, et al. (2008) Wolbachia genome integrated in an insect chromosome: evolution and fate of laterally transferred endosymbiont genes. Genome Res 18: 272–280.
  24. 24. Chan CX, Darling AE, Beiko RG, Ragan MA (2009) Are protein domains modules of lateral genetic transfer? PLoS One 4: e4524.
  25. 25. Noutsos C, Kleine T, Armbruster U, DalCorso G, Leister D (2007) Nuclear insertions of organellar DNA can create novel patches of functional exon sequences. Trends Genet 23: 597–601.
  26. 26. Carpentier SC, Panis B, Vertommen A, Swennen R, Sergeant K, et al. (2008) Proteome analysis of non-model plants: a challenging but powerful approach. Mass Spectrom Rev 27: 354–377.
  27. 27. Moreno Y, Gros PP, Tam M, Segura M, Valanparambil R, et al. (2011) Proteomic analysis of excretory-secretory products of Heligmosomoides polygyrus assessed with next-generation sequencing transcriptomic information. PLoS Negl Trop Dis 5: e1370.
  28. 28. Buggiotti L, Primmer CR, Kouvonen P, Bures S, Corthals GL, et al. (2008) Identification of differentially expressed proteins in Ficedula flycatchers. Proteomics 8: 2150–2153.
  29. 29. Fath MJ, Kolter R (1993) ABC transporters: bacterial exporters. Microbiol Rev 57: 995–1017.
  30. 30. Yakushi T, Masuda K, Narita S, Matsuyama S, Tokuda H (2000) A new ABC transporter mediating the detachment of lipid-modified proteins from membranes. Nat Cell Biol 2: 212–218.
  31. 31. Ardelli BF, Prichard RK (2004) Identification of variant ABC-transporter genes among Onchocerca volvulus collected from ivermectin-treated and untreated patients in Ghana, West Africa. Ann Trop Med Parasitol 98: 371–384.
  32. 32. Ardelli BF, Prichard RK (2007) Reduced genetic variation of an Onchocerca volvulus ABC transporter gene following treatment with ivermectin. Trans R Soc Trop Med Hyg 101: 1223–1232.
  33. 33. Bourguinat C, Ardelli BF, Pion SD, Kamgno J, Gardon J, et al. (2008) P-glycoprotein-like protein, a possible genetic marker for ivermectin resistance selection in Onchocerca volvulus. Mol Biochem Parasitol 158: 101–111.
  34. 34. Tompkins JB, Stitt LE, Morrissette AM, Ardelli BF (2011) The role of Brugia malayi ATP-binding cassette (ABC) transporters in potentiating drug sensitivity. Parasitol Res 109: 1311–1322.
  35. 35. Fischer K, Beatty WL, Jiang D, Weil GJ, Fischer PU (2011) Tissue and stage-specific distribution of Wolbachia in Brugia malayi. PLoS Negl Trop Dis 5: e1174.
  36. 36. Jiang D, Li BW, Fischer PU, Weil GJ (2008) Localization of gender-regulated gene expression in the filarial nematode Brugia malayi. Int J Parasitol 38: 503–512.
  37. 37. Dafa’alla TH, Taubert A, Hobom G, Beck E, Zahner H (2000) Molecular characterization of a Litomosoides sigmodontis protein involved in the development of the microfilarial sheath during embryogenesis. Mol Biochem Parasitol 106: 37–50.
  38. 38. Ash LR, Riley JM (1970) Development of subperiodic Brugia malayi in the jird, Meriones unguiculatus, with notes on infections in other rodents. J Parasitol 56: 969–973.
  39. 39. Margulies M, Egholm M, Altman WE, Attiya S, Bader JS, et al. (2005) Genome sequencing in microfabricated high-density picolitre reactors. Nature 437: 376–380.
  40. 40. Wasmuth J, Blaxter M (2009) Obtaining accurate translations from expressed sequence tags. Methods Mol Biol 533: 221–239.
  41. 41. Wasmuth JD, Blaxter ML (2004) prot4EST: translating expressed sequence tags from neglected genomes. BMC Bioinformatics 5: 187.
  42. 42. Eddy SR (1998) Profile hidden Markov models. Bioinformatics 14: 755–763.
  43. 43. Washburn MP, Wolters D, Yates JR 3rd (2001) Large-scale analysis of the yeast proteome by multidimensional protein identification technology. Nat Biotechnol 19: 242–247.
  44. 44. McDonald WH, Tabb DL, Sadygov RG, MacCoss MJ, Venable J, et al. (2004) MS1, MS2, and SQT-three unified, compact, and easily parsed file formats for the storage of shotgun proteomic spectra and identifications. Rapid Commun Mass Spectrom 18: 2162–2168.
  45. 45. Xu T, Venable JD, Park SK, Cociorva D, Lu B, et al. (2006) ProLuCID, a fast and sensitive tandem mass spectra-based protein identification program. Mol Cell Proteomics 5: S174.
  46. 46. Elias JE, Gygi SP (2007) Target-decoy search strategy for increased confidence in large-scale protein identifications by mass spectrometry. Nat Methods 4: 207–214.
  47. 47. Tabb DL, McDonald WH, Yates JR 3rd (2002) DTASelect and Contrast: tools for assembling and comparing protein identifications from shotgun proteomics. J Proteome Res 1: 21–26.
  48. 48. Zdobnov EM, Apweiler R (2001) InterProScan–an integration platform for the signature-recognition methods in InterPro. Bioinformatics 17: 847–848.
  49. 49. Kanehisa M, Goto S (2000) KEGG: kyoto encyclopedia of genes and genomes. Nucleic Acids Res 28: 27–30.