An enhanced understanding of the hookworm genome and its resident mobile genetic elements should facilitate understanding of the genome evolution, genome organization, possibly host-parasite co-evolution and horizontal gene transfer, and from a practical perspective, development of transposon-based transgenesis for hookworms and other parasitic nematodes.
A novel mariner-like element (MLE) was characterized from the genome of the dog hookworm, Ancylostoma caninum, and termed bandit. The consensus sequence of the bandit transposon was 1,285 base pairs (bp) in length. The new transposon was flanked by perfect terminal inverted repeats of 32 nucleotides in length with a common target site duplication TA, and it encoded an open reading frame (ORF) of 342 deduced amino acid residues. Phylogenetic comparisons confirmed that the ORF encoded a mariner-like transposase, which included conserved catalytic domains, and that the bandit transposon belonged to the cecropia subfamily of MLEs. The phylogenetic analysis also indicated that the Hsmar1 transposon from humans was the closest known relative of bandit, and that bandit and Hsmar1 constituted a clade discrete from the Tc1 subfamily of MLEs from the nematode Caenorhabditis elegans. Moreover, homology models based on the crystal structure of Mos1 from Drosophila mauritiana revealed closer identity in active site residues of the catalytic domain including Ser281, Lys289 and Asp293 between bandit and Hsmar1 than between Mos1 and either bandit or Hsmar1. The entire bandit ORF was amplified from genomic DNA and a fragment of the bandit ORF was amplified from RNA, indicating that this transposon is actively transcribed in hookworms.
A mariner-like transposon termed bandit has colonized the genome of the hookworm A. caninum. Although MLEs exhibit a broad host range, and are identified in other nematodes, the closest phylogenetic relative of bandit is the Hsmar1 element of humans. This surprising finding suggests that bandit was transferred horizontally between hookworm parasites and their mammalian hosts.
Because of its importance to public health, the hookworm parasite has become the focus of increased research over the past decade—research that will ultimately decipher its genetic code. We now report a gene from hookworm chromosomes known as a transposon. Transposons are genes that can move around in the genome and even between genomes of different species. We named the hookworm transposon bandit because hookworms are “thieves” that steal the blood of their hosts, leading to protein deficiency anemia. The bandit transposon is a close relative of a well studied assemblage of transposons, the mariner-like elements, known from the chromosomes of many other organisms. The founding member of this group—the mariner transposon—was isolated originally from a fruit fly; mariner has been harnessed in the laboratory as a valuable gene therapy tool. Likewise, it may be feasible to employ the bandit transposon for genetic manipulation of hookworms and functional genomics to investigate the importance of hookworm genes as new intervention targets. Finally, bandit may have transferred horizontally from primates to hookworm or vice versa in the relatively recent evolutionary history of the hookworm–human host–parasite relationship.
Citation: Laha T, Loukas A, Wattanasatitarpa S, Somprakhon J, Kewgrai N, et al. (2007) The bandit, a New DNA Transposon from a Hookworm—Possible Horizontal Genetic Transfer between Host and Parasite. PLoS Negl Trop Dis 1(1): e35. doi:10.1371/journal.pntd.0000035
Academic Editor: John Dalton, University of Technology, Sydney, Australia
Received: April 10, 2007; Accepted: June 1, 2007; Published: September 27, 2007
Copyright: © 2007 Laha 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: This investigation received financial support from the Thailand-Tropical Diseases Research Programme, T2 (BIOTEC, NSTDA, TRF and TDR/WHO) project ID 02-2-HEL-05-013. PJB is a recipient of a Burroughs Wellcome Fund scholar award in Molecular Parasitology, AL is a recipient of an R. Douglas Wright Biomedical Career Development Award from the National Health and Medical Research Council of Australia, and MM is supported by NIH-NIAID research grant AI 46593. 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.
Almost one billion people throughout tropical and sub-tropical latitudes are infected with hookworms. In the countries affected, hookworm infection is often the major contributor to iron-deficiency anemia, a direct consequence of the parasite's blood-feeding activities . Comparatively little is known about the genome or population genetics of hookworms. The karyotype of only one hookworm species, the dog hookworm, Ancylostoma caninum, is known where the haploid chromosome number n = 6 . Hookworms are dioecious and sex determination is by an XX-XO mechanism as in their free-living relative, the model nematode Caenorhabditis elegans . Although the genome size of hookworms has not been reported, it may be of similar dimensions and complexity to that of C. elegans-around 100 megabase pairs (Mb) and containing about 20,000 protein-encoding genes (see ). By contrast, flow cytometric based techniques have shown that the haploid genome size of two trichostrongyle nematodes, Haemonchus contortus and Teladorsagia circumcincta, is ~50 Mb in length . Trichostrongyle nematodes are more closely related to hookworms than is the free-living nematode, C. elegans .
Over 20,000 expressed sequence tags (ESTs) from A. caninum and the related parasite, A. ceylanicum, have been characterized to some degree [6–8], including transcripts from the gut of adult worms. Interestingly, most of the genes share homologues in C. elegans, highlighting the suitability of this free-living nematode as a model for hookworm developmental biology . Moreover, the Genome Survey Sequences (GSS) Database at GenBank contains nearly 100,000 genome survey sequences from A. caninum (http://www.ncbi.nlm.nih.gov/dbGSS/dbGSS_summary.html), which when assembled provide a 57.6 Mb unique sequence, establishing a tractable framework for an eventual genome sequence. It can be anticipated that an enhanced understanding of the hookworm genome will aid in the control of hookworm disease and hookworm-associated anemia, including the development of new anti-parasite interventions .
A substantial proportion of the genome of most metazoans is composed of repetitive sequences, including various types of mobile genetic elements (MGEs). MGEs are drivers of genome evolution . In addition to this role, from a practical perspective MGEs offer potential as transgenesis and gene silencing vectors [12–14], technologies that have yet to be reliably established for the study of parasitic nematodes. Problematically, however, their interspersed, repetitive nature can impede progress during genome sequencing using shotgun sequencing approaches through the confounding effects of their repetitions on sequence assembly algorithms [15,16]. For these and other reasons, knowledge of hookworm MGEs is of theoretical and practical value. Recently we reported the presence of a family of non-long terminal repeat (LTR) retrotransposons, the dingo retrotransposons, from the genome of A. caninum . Here we report the presence of a mariner like transposon, termed bandit, within the genome of A. caninum. Bandit is a DD(34)D family mariner-like transposon  which, intriguingly, is much more closely related to the human mariner-like element Hsmar1 than to any other MLE so far reported from other species of the phylum Nematoda.
Genomic DNA of the hookworm Ancylostoma caninum
Adult A. caninum hookworms were collected from naturally infected dogs from Ta Rae district, Sakonnakorn province, Thailand, as described previously . After removal from the canine small intestines, the hookworms were identified microscopically as A. caninum, and the living worms were snap frozen and stored at −80°C. Subsequently, genomic DNA (gDNA) of adult mixed sexes of A. caninum was isolated from the parasites using a Qiagen genomic tip-100/G column and genomic buffer set kit (Qiagen, Germany) according to the manufacturer's instructions. Briefly, worms (50–100 mg) were lysed in DNase-free lysis buffer supplemented with RNase (Qiagen) using a DNase-free glass homogenizer. Proteinase K was added to the extracts and incubated at 50°C for 2 hours. The homogenate was clarified by centrifugation, the supernatant applied to a Qiagen genomic-tip column (Qiagen), the eluted A. caninum gDNA recovered by ethanol precipitation, dissolved in TE buffer, and its concentration and purity determined using a spectrophotomer.
Construction and screening of hookworm genomic DNA libraries; bioinformatics
Size selected plasmid libraries of gDNA from adult A. caninum were constructed as described . Briefly, gDNA was digested with the endonuclease Hind III and Xba I (Fermentas, Sweden) and size separated through 0.8% agarose gel. Fragments ranging in size from 2–7 kilobase pairs (kb) were excised, eluted from the gel, and ligated into plasmid pBluescript SK (+/−) (Stratagene). Bacterial E. coli strain XL-1 blue cells were transformed with the ligation products and recombinant colonies selected by blue-white screen on LB agar supplemented with ampicillin. White colonies were transferred to wells of 96-well microtitre plates and cryopreserved in 20% glycerol at −80°C.
Mobile genetic element (MGE)-like gene fragments were identified from dbEST using text and blast searches. MGE fragments were amplified by polymerase chain reaction (PCR) from gDNA and used to probe gDNA libraries (see below). At the outset, a gene probe was obtained by PCR using primers AcCR1F (5′-CAATTCTCCGATAAGGCAATG) and AcCR1R (5′-CGCGTATCCCATAGAATGTCA) specific for an A. caninum transcript annotated in GenBank to have identity to reverse transcriptase (GenBank AW700339), with PCR cycling conditions of 35 cycles of 94°C for 1 min, 55°C for 1 min and 72°C for 1.5 mins, and a final elongation step at 72°C for 10 mins. An amplicon encoding a retrotransposon-like gene was sequenced to confirm its identity, and the probe was named AcCR1 (not shown). Subsequently, a transposon-like gene probe (genomic DNA clone H118; GenBank DQ377715) was obtained by library screening with AcCR1. Nucleotides 118–416 of the insert of H118 were PCR amplified, and after labeling with digoxygenin (DIG), the PCR product was employed to screen ~500 clones from the size selected, Hind III and Xba I libraries of A. caninum gDNA. The inserts of positive clones were sequenced and the sequences used to search the non-redundant database of GenBank using the Blastn, Blastx and tBlastx algorithms . Genomic DNA and cDNA of A. caninum were amplified with the aim of obtaining longer fragments of the A. caninum transposon, using specific primers, AcMarinerF; 5′-GCTCACTCTTGGCTTGGTTC and AcMarinerR; 5′-TAATCGATTGGCGAAAGGTC, spanning nucleotide residues 154 to 1,033 of the consensus sequence of the full-length bandit transposon (Figure 1). PCR conditions were 94°C for 1 min, 55°C for 1 min and 72°C for 3 min, 35 cycles after which PCR products were ligated into plasmid pTOPO (Stratagene) and sequenced.
Figure 1. Schematic diagram representing clones and genomic survey sequences (GSS) from public databases which were used to assemble the consensus sequence of the bandit transposon from the genome of Ancylostoma caninum.
Numbers on clones represent the nucleotide positions within the consensus, full length bandit sequence. GenBank accession numbers of contributing GSS clones are provided. The sequences of the terminal inverted repeats are presented in the top panel. In clone H118, the black colored region is bandit sequence whereas the white region on non-bandit encoding DNA.doi:10.1371/journal.pntd.0000035.g001
A consensus sequence of a new transposon was assembled from the positive clones and also from A. caninum GSS sequences in GenBank with assistance from the contig assembly program of BioEdit version 126.96.36.199  (Figure 1). To identify bandit-like sequences in related hookworm species, the bandit transposase (342 amino acids) was queried against 4,953 polypeptides from A. ceylanicum  and 2,328 polypeptides from N. americanus . Only the best homologous sequence is reported, including the identity and similarity values for the longest high-scoring segment pair (HSP) in each subject.
Southern hybridization analysis
Thirty μg of A. caninum gDNA were cleaved with the restriction enzymes, Xho I and Xba I. The bandit probe sequence did not include recognition sites for either of these enzymes. Digested gDNA was fractionated by electrophoresis through 0.8% agarose gel, after which the fragments were transferred to nylon membrane (Hybond-N+, Amersham Biosciences) by capillary action. The bandit-specific probe was obtained by PCR using specific primer AcMarinerF; 5′-GCTCACTCTTGGCTTGGTTC and AcMarinerR; 5′-TAATCGATTGGCGAAAGGTC, spanning nucleotide residues 154 to 1,033 of the consensus sequence of the full-length bandit transposon (Figure 1). Southern hybridization analysis was performed using DIG labelled probes and detection system (Roche, USA). The membranes were incubated in hybridization medium under high stringency conditions. High stringency washing conditions were performed as recommended by the manufacturer. Signal was detected by exposure to X-ray film (Fuji).
Total RNA of A. caninum mixed sex adult worms was extracted using the Nucleospin RNA II kit (Machery-Nagel, Germany) according to the manufacturer's procedures. RT-PCR was performed using the RobusT II RT-PCR Kit (FINNZYMES, Finland), primers P118F (5′-CTTCTAACGGATAGCTGCGGA and P118R (5′-GGGCGCTCTCTGATCCATCTT) specific for the bandit transposase based on the sequence of genomic clone H118 (GenBank accession number DQ377715) spanning nt. 118–417 (Figure 1), and the following PCR cycling conditions: 42°C for 30 mins and 94°C for 2 mins for the first cycle, 94°C for 1 min, 55°C for 1 min and 72°C for 1.5 mins, for 40 cycles, and finally an elongation step at 72°C for 10 mins. RT-PCR products were sized by electrophoresis through a 1% agarose gel. To confirm the identity of the RT-PCR products, they were transferred to nylon membranes , and probed with a DIG-labelled bandit probe (residues 152 to 1031 of bandit, shown in Figure 1). Southern hybridization analysis was performed using DIG labelled probes and the DIG detection system from Roche. Signals were detected by exposure to X-ray film (Fuji).
The entire transposase ORFs of bandit and other related elements were employed for construction of the phylogenetic tree. Alignments of amino acid sequences of functional domains were accomplished with ClustalW  and edited with Bioedit version 5.0.9 . Sequence alignments for phylogenetic analysis comparing the conserved transposase domains were adjusted as described previously [24,25]. A phylogenetic analysis was performed on this sequence alignment using PROTDIST in PHYLIP packages and a tree was constructed using the neighbor joining method (PHYLIP, version 3.6 software) . A distance matrix analysis was also carried out using maximum parsimony. The resulting phylogenetic trees were displayed using TreeView . Statistical significance of branching points was evaluated with 1,000 repetitions in a bootstrap analysis (SEQBOOT). The predicted protein sequences were obtained directly from the GenBank entries where provided, otherwise ORFs were predicted by translating the nucleotide sequences provided in GenBank.
The transposase ORFs of bandit and Hsmar1 were used as a query for the Swiss-Model comparative protein modeling server (http://swissmodel.expasy.org). Homologues of known structure were sought from the Research Collaboratory for Structural Bioinformatics (RCSB) Protein Data Bank (http://www.rcsb.org./pdb/home/home.do). Models were viewed and manipulated in first approach mode using Swiss-PdbViewer (http://swissmodel.expasy.org/spdbv).
A mariner-like transposon present in the genome of A. caninum
A positive clone was identified from an A. caninum genomic DNA library that was screened with a reverse transcriptase-like gene probe, clone H118 (GenBank accession number DQ377715). The clone showed sequence identity with mariner-like transposons from many eukaryotes including mariner from Homo sapiens and mariner from Bos taurus. Sequence analysis revealed that clone H118 contained sequence that encoded part of a transposase protein (Figure 1). The consensus full length transposon was constructed using clone H118 and multiple GSSs identified by homology searches from the GenBank database (GenBank accession numbers CW709686, CZ213904 and CZ241797) (Figure 1). We termed the new transposon bandit, in keeping with the informal convention of naming mobile genetic elements with terms suggestive of a peripatetic lifestyle (e.g. mariner, hobo and fugitive)[28–30]. Given the present results, the name bandit seemed appropriate since a bandit is often difficult to apprehend, and in this present context, it appears that bandit has moved furtively between hookworms and their mammalian hosts (see below). The consensus sequence of bandit was 1,285 bp flanked by 32 nt perfect terminal inverted repeats at each extremity with a common target site duplication TA (Figure 1 and Figure S1). bandit has one ORF of 342 amino acid residues encoding for a transposase enzyme. The bandit transposase contained the conserved DD34D motif that is found in the active site of the catalytic C-terminal domain of mariner-like transposons as opposed to the DDE motif found in the Tc1-like elements  (Figure 2). The ORF of the bandit showed highest similarities to Hsmar1 from human (55% identity, 70% similarity), Bos taurus (54% identity, 70% similarity) and Tc1 of C. elegans (41% identity, 58% similarity), HcTc1 of Haemonchus contortus (22% identity, 42% similarity). On the other hand, no bandit-like sequences were identified in the National Center for Biotechnology Information (NCBI) catalogue of dog sequences (not shown), indicating that bandit is not of canine origin.
Figure 2. Multiple sequence alignment of the transposases of bandit with those from related transposons.
The position of the catalytic triad domain DD(34)D/E is indicated. The conserved motifs of mariner-like elements were overlined. Conservation of residues is indicated by the shading of boxes. The GenBank accession numbers of these aligned transposons are human (Hsmar1, AAC52010), Rhesus monkey (XP_001099426), G. tigrina (CAA50801), Atlas moth (BAA21826), C. elegans (T23086), Meloidogyne chitwoodi (CAD26968), MOS-1 (AAC16609), Tc1 (P03939), HcTc1 (AAD34306).doi:10.1371/journal.pntd.0000035.g002
The perfect inverted repeats of 32 bp are the standard length for mariner-like elements  compared with 54 bp for Tc1 from C. elegans  and 55 bp for HcTc1 from H. contortus . In addition to the catalytic triad, bandit contains most of the additional canonical features of mariner-like elements (MLEs); the WVPHEL motif (RVPHEL in bandit) and YSPDLAP (CSPDLSP in bandit) . However, bandit did not contain the conserved FLHDNARPH motif that overlaps the second D of catalytic triad in most MLE transposases. In bandit, this motif is replaced by a LLHDNARSH motif [35,36] (Figure S1).
Numerous copies of bandit interspersed throughout the A. caninum genome
Smeared bands of hybridization were evident when a Southern blot of A. caninum genomic DNA (gDNA) was probed with the labeled bandit-specific sequence. Xba I and Xho I were used to cleave the gDNA, and hybridization of each restriction digest to a bandit-specific probe revealed a smear-like pattern of numerous bands of hybridization ranging in size from >5-<0.5 kb (Figure 3), confirming the presence of numerous copies of the bandit transposon in the genome of natural populations of A. caninum from north-eastern Thailand. This also suggests that the bandit element is widely dispersed in the hookworm genome rather than being localized at just one or a few isolated sites. To more specifically address the copy number, we queried the A. caninum GSS in NCBI with the bandit sequence using blastn and tblastx algorithms. Using blastn, we identified 23 GSS with 87–98% identity over at least 250 bp. Using tblastx, we identified >200 GSS with >90% identity over at least 50 amino acids (not shown). The A. caninum GSS are predicted to cover about 15% of the genome (M. Mitreva, unpublished). Extrapolating from these numbers there may be between 150–1,500 copies of bandit dispersed throughout the genome.
Figure 3. Southern hybridization analysis of Ancylostoma caninum genomic DNA to a probe specific for the bandit transposon.
The genomic DNAs were cleaved with endonucleases Xba I (lane 1) and Xho I (lane 2). Molecular size standards in kilobase pairs (kb) are shown at the left.doi:10.1371/journal.pntd.0000035.g003
bandit is a novel mariner-like transposon of the cecropia subfamily
A phylogenetic tree was constructed based on the sequence alignment of the entire transposase ORFs of bandit and 37 other transposon sequences available in public databases. A neighbor-joining tree with 1,000 replicates revealed that bandit is most closely related to Hsmar1 from Homo sapiens (Figure 4). Mariner-like transposons can be classified into six subfamilies [24,25]. Bandit formed a clade with elements from the cecropia subfamily with solid bootstrap support (564), and this diphyletic clade included a branch containing bandit and three primate-originated MLEs, and a branch with Funmar1 from the coral Fungia sp., Aamar1 from the atlas moth, Attacus atlas and Dtmar1 from the planarian, Girardia tigrina. The appearance of the branches of the cecropia clade was the same when either neighbor joining or maximum parsimony (not shown) methods were employed in tree construction. Indeed, bootstrap support for the clade that included bandit and the primate elements was even stronger in the maximum parsimony analysis (982) than that obtained using the neighbor joining method (723). The phylogenetic distance between human and hookworm is far greater than that reflected in the phylogenetic analysis of these transposons, suggesting to us that bandit is only distantly related to MLEs from nematodes that are closely related to A. caninum, and is much more similar to transposons from the hookworm's mammalian hosts. For example, the MLE HcTc1 from the trichostrongyle parasite, H. contortus (a close relative of A. caninum) belongs to the mori clade of MLEs (Figure 4). The remarkable identity between bandit and the primate MLEs, Hsmar1 and SETMAR, strongly suggests horizontal transmission of this element from host to parasite (or vice versa).
Figure 4. Phylogram constructed using the neighbor-joining method to compare the relationships among transposases of the bandit transposon and of representative mariner-like elements belonging to the Tc1/mariner superfamily of transposons from a range of host genomes.
Representatives of six clades of mariner-like elements including the mori, irritans, mauritiana, and cecropia were included in the analysis. The elements used in the tree includes Tc1-like (AAD12818) and Tc1 (P03934), T19261, T23086 and AF003149 from C. elegans, HcTc1 (AAD34306) from Haemonchus contortus, TCb1 (CAA30681) from C. briggsae, Bmmar1 (U47917) and BmMar6 (AAN06610) from Bombyx mori, Crmar1 (AAK61417) from Ceratitis rosa, Himar1 (ABB59013) mutagenesis vector pFNLTP16H3, Cpmar1 (AAC46945) from Chrysoperla plorabunda, Damar1 (DAU11648) from Drosophila ananassae, Bytmar1-8 (CAD45868) and Bytmar1-11 (CAD45369) from Bythogreae thermydron, Dtesmar1 (AAC28261) from D. teissieri, Dsecmar1 (AAC16609) from D. sechellia, Mbmar1 (AAL69970) from Mamesta brassicae, Mudmar1 (AK54758) from Musca domestica, Mos1 (pdb2F7T) from D. mauritiana, XP_001099426 from Macaca mulatta, SETMAR (ABC72092) from Cercopithecus aethiops, Hsmar1 (AAC52010) from Homo sapiens, Aamar1 (BAA21826) from Attacus atlas, Funmar1 (BAB32436) from Fungia sp., Dtmar1 (CAA50801) from Girardia tigrina, Mcmar1 (CAD26968) from Meloidogyne chitwoodi, Famar1 (AAO12863) from Forficula auricularia, Ammar1 (AAO12861) from Apis mellifera, Ccmar2 (AAO12864) from Ceratitis capitata, Camar1 (AAO12862) from Chymomyza amoena, Acmar1 (BAB86288) from Apis cerana, Ccmar1 (AAB17945) from Ceratitis capitata. The outgroup included transposases from gram positive and negative bacteria including Bacillus halodurans (BAA75315), Escherichia coli (AAB28848) and Klebsiella pneumoniae (CAB82575). Bootstrap values, where 500 or greater from a maximum of 1,000 replicates, are presented at the nodes.doi:10.1371/journal.pntd.0000035.g004
Homology models confirm close identity of hookworm bandit and human Hsmar1 transposons
The catalytic C-terminal domain of the predicted transpose ORF of bandit was modeled on the crystal structure of the C-terminal catalytic domain (residues 126–345) of mos1 transposase from Drosophila mauritiana (pdb accession number 2f7tA). The structural alignment spanned residues 158–345 of mos1 and 178–342 of bandit. The general fold of the bandit catalytic domain was highly conserved with that of mos1 (Figure 5A). The first alpha helix and beta sheet of the catalytic domain of bandit (including the first catalytic Asp residue) were too dissimilar to mos1 to be included in the model; however, the rest of the domain revealed similar active site architecture. Because bandit is most similar to human Hsmar1 at the primary sequence level (Figure 4), we also modeled the catalytic domain of Hsmar1 transposase on the crystal structure of mos1. The sequence conservation between mos1 and Hsmar1 also was high (Figure 2). Surprisingly, when the key active site residues of the catalytic domains  of bandit and Hsmar1 were compared with those of mos1, we observed that bandit and Hsmar1 had identical active site residues but, by contrast, three of these residues had non-conservative substitutions in mos1 (Figure 5B, C and D).
Figure 5. Homology models of bandit from Ancylostoma caninum and Hsmar1 from Homo sapiens based on the crystal structure of the mos1 element from Drosophila mauritiana.
Ribbon diagram showing the predicted structure of the catalytic domains of bandit and mos1 (A). s1 and h1 refer to β sheet number 1 and α helix number 1 of the mos1 catalytic domain–homologous regions were present in bandit but were not included in the model. Superimposition of the catalytic active sites of bandit (B) and Hsmar1 (C) on the crystal structure of mos1 highlighting the residues involved in catalysis. Conserved active site residues are labeled in red font; where bandit or Hsmar1 active site residues differ from mos1, the substitution is denoted in green font. Yellow arrows denote the three catalytic Asp residues. Numbering of side chains is based on the mos1 sequence. Comparison of the residues predicted to be involved in catalysis from bandit, Hsmar1 and mos1 (D). Residues selected were based on the crystal structure of mos1.doi:10.1371/journal.pntd.0000035.g005
bandit is transcribed in the parasitic stages of A. caninum
Transcripts encoding the transposase of bandit were amplified by PCR from cDNA from mixed sex adult hookworms. Products of the expected size, 300 bp, were amplified (Figure 6), and the identity of the amplicons was confirmed by sequence analysis and Southern hybridization using a bandit-specific probe (not shown). Together with the presence of relatively intact inverted repeats, this approach indicated that functional domains of the element are transcribed in the adult hookworm, and suggests that copies of bandit are active and mobile within the genome of A. caninum.
Figure 6. Reverse transcription PCR targeting the bandit transposon.
Transcripts encoding the transposase of bandit were amplified by PCR from cDNA of the adult mixed sex of A. caninum. Products of the expected size, 300 bp are indicated with the arrow; lane 1, negative control where reverse transcriptase was omitted from the reaction; lane 2, empty lane; lane 3, plasmid DNA of clone H118 (positive control); lane 4, cDNA of mixed sex adult hookworms. Molecular size standards (lane M) are shown at the left.doi:10.1371/journal.pntd.0000035.g006
bandit integrates into non-coding regions of the A. caninum genome
Sequences flanking the different individual copies of bandit (from the GSS dataset) were aligned (Figure 7). Blast search analysis of the 5′ and 3′ flanking regions of bandit did not show homology to sequences in the public database. The flanking DNA was however generally AT-rich and appeared to be of non-coding origin.
Figure 7. Multiple sequence alignment of the nucleotide sequences flanking the insertion sites of copies of the bandit transposons within the genome of Ancylostoma caninum.
Alignments of nucleotide sequences flanking the 5′- (A) and 3′- (B) termini of bandit. Conservation of residues is indicated by the shading of boxes. Target sequences, with GenBank accession numbers as indicated on the left, were identified among entries in the GSS database of A. caninum sequences at GenBank. The target site TA duplications are indicated with asterisks.doi:10.1371/journal.pntd.0000035.g007
bandit in related hookworm species
Available transcriptomic data of related hookworm species, A. ceylanicum  and N. americanus  was explored to identify putative bandit-like transposons. The similarity search (BlastX) resulted in identification of a homologous sequence from A. ceylanicum (contig id AE04671, 44% identity, 64% similarity over 185 amino acids) and from Necator americanus (contig id NAC01255, 45% identity, 58% similarity over 91 amino acids) (data not shown). Based on these interspecific partial matches the conservation is lower compared to A. caninum bandit and Hsmar 1 (55% identity, 70% similarity), but higher between the A. caninum bandit and other hookworm bandit-like sequences than with the HcTc1 from the ruminant blood-feeder H. contortus (22% identity, 42% similarity) or the Tc1 from C. elegans (41% identity, 58% similarity). Unavailability of the full length ORF of the bandit from these two related hookworm species contributed to their exclusion from the above described analysis.
A new member of the Tc1/mariner superfamily of DNA transposons has been characterized from the genome of a parasitic nematode, and termed bandit. Sequence identity, structure, and phylogenetic relationships demonstrated that the bandit transposon belonged to the cecropia sub-family of mariner-like elements (MLEs). The cecropia clade is populated by transposons from diverse animal taxa including the cecropia moth , a coral , primates including the African green monkey and humans  and now from a hookworm. Earlier reports dealing with members of this clade have suggested that horizontal transmission has likely been involved in the present disposition of its members (e.g., ). In like fashion, given that the closest relatives of bandit are Hsmar1 and SETMAR from humans and monkeys, bandit may have been transmitted to or from hookworms and their primate hosts.
The bandit transposon displayed the structural hallmarks of the Tc1/mariner superfamily of transposons including an overall length of ~1.3 kb, a single ORF encoding a transposase of 342 amino acid residues in length, a DD(34)D catalytic motif, duplication of TA dinucleotide pairs upon insertion and inverted terminal repeats of 32 bp in length . The DD(34)D motif indicated that bandit was a mariner-rather than a Tc1-family member. Phylogenetic analysis confirmed that bandit was indeed mariner-like and, remarkably, indicated that its closest relative was the primate Hsmar1 transposon. Moreover, homology models established using the crystal structure coordinates of mos1 transposase (from D. mauritiana) revealed closer identity between bandit and Hsmar1 than between bandit or Hsmar1 and Mos1 in active site architecture and catalytic domain residues.
The hookworm, A. caninum, is a parasite of dogs but is frequently found in the human small intestine. Although it does not generally reach sexual maturity in humans, it may now be evolving this capacity . Moreover, A. caninum larvae commonly infect human skin resulting in pruritic dermatitis termed cutaneous larva migrans . A. caninum is closely related to the anthropophilic hookworm, Ancylostoma duodenale, and another close relative, A. ceylanicum, parasitizes both humans and dogs. (The human hookworms A. duodenale and N. americanus infect more than 700 million people, causing widespread morbidity–primarily iron deficiency anemia– and mortality ). The intimacy of host-parasite relationships is known to facilitate horizontal transmission of genetic material , and parasitism is known to facilitate horizontal transmission of transposons. For example, P elements have been transferred among Drosophila species by a parasitic mite , as have mariner-like elements between parasitic wasps and their lepidopteran hosts . Since the closest known relative of bandit is Hsmar1 from humans, and given the parasitic association between hookworms and primates–the hosts of bandit and Hsmar1, respectively–it is likely that the presence of bandit and Hsmar1 in both parasite and host genomes reflects parasitism-facilitated horizontal transmission.
After entry into a naïve lineage, an active autonomous MLE undergoes unrestrained spread through transposition and sexual exchange for a time until regulatory and/or mutational inactivation dampens transposition activity and associated deleterious mutations [46,47]. Given that transcription of bandit was detected by RT-PCR analysis, and given that the intact integration footprint of bandit within the hookworm genome remains readily apparent, it appears that bandit is transpositionally active within the A. caninum genome. If so, the hypothesized horizontal transmission of Hsmar1/bandit elements between host and parasite may be a recent event, and since Hsmar1 is now inactive , the direction of the horizontal transfer may have been from host to parasite.
Eukaryotic genomes generally include substantial amounts of sequences derived from MGEs, primarily retrotransposons and transposons. These mobile sequences are drivers of genome evolution . A number of MGEs have been characterized from nematode genomes including Tas, a LTR retrotransposon, and R4, a non-LTR retrotransposon, both from Ascaris lumbricoides [49,50], mariner-like elements (MLEs) from Trichostrongylus colubriformis  and the RTE1, NeSL, and Cer retrotransposons from C. elegans. Recently, it was reported that the A. caninum genome includes elements with identity to the Transib superfamily of transposons. In vertebrates, the Transib transposon has mutated to form the RAG1 protein and recombination signal sequences involved in catalyzing B and T cell receptor gene V(D)J recombination . Also, recently we described the dingo non-LTR retrotransposons from the genome of A. caninum  and numerous transcripts encoding reverse transcriptase are evident in the EST database of A. caninum, A. ceylanicum and N. americanus hookworms (http://nematode.net), indicating the presence of endogenous retroviruses or retrotransposons. Based on the genomes of C. elegans  and several parasitic helminths including schistosomes , it is apparent that that the hookworm genome has been colonized not only by the bandit transposon, but also by numerous other waves of MGEs. From a practical perspective, understanding of MGE complexity, diversity and copy numbers can be expected to facilitate the assembly and annotation of the hookworm genome sequence (a focus of current genome sequencing effort, http://nematode.net). Finally, as with other MGEs, an endogenous hookworm mariner-like transposon such as bandit holds potential as a transgenesis vector for manipulation of the hookworm genome, given the ability of other Tc1/mariner superfamily members such as mos1 to transpose within the genomes of C. elegans, planarians and other species (e.g., [55–57]).
Consensus nucleotide and deduced amino acid sequence of the entire bandit element. Sequence features of the bandit are indicated within duplicated TA dinucleotides. The inverted repeats at both ends are highlighted with green. The ORF starts at the Met encoded at nt. 189 and terminates at the stop codon at nt. 117, encoding an enzyme of 342 amino acid residues. Two conserved hallmark motifs of mariner-like elements  are highlighted with grey and the catalytic triad DD34D residues are indicated by red colored font.
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Conceived and designed the experiments: AL PB TL. Performed the experiments: AL PB TL SW JS NK. Analyzed the data: MM AL PB TL SW JS NK. Contributed reagents/materials/analysis tools: AL PB SK PS TL. Wrote the paper: MM AL PB TL. Carried out the molecular genetic experiments: TL. Carried out parasitological and molecular analyses including cloning and sequencing genomic fragments: SW JS NK. Participated in parasitological analyses including identification of the parasites as A. caninum: SK PS. Performed the homology modeling: AL TL. Participated in analysis of hookworm databases for bandit-like sequences and in the assembly of the contigs: MM.
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