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. 2016 Sep 22;7:12845. doi: 10.1038/ncomms12845

Comparative genomics reveals adaptive evolution of Asian tapeworm in switching to a new intermediate host

Shuai Wang 1,*, Sen Wang 2,3,*, Yingfeng Luo 2, Lihua Xiao 4, Xuenong Luo 1, Shenghan Gao 2, Yongxi Dou 1, Huangkai Zhang 2,3, Aijiang Guo 1, Qingshu Meng 2, Junling Hou 1, Bing Zhang 5, Shaohua Zhang 1, Meng Yang 2, Xuelian Meng 1, Hailiang Mei 2, Hui Li 1, Zilong He 2, Xueliang Zhu 1, Xinyu Tan 2, Xing-quan Zhu 1, Jun Yu 2, Jianping Cai 1, Guan Zhu 6,a, Songnian Hu 2,a, Xuepeng Cai 1,a
PMCID: PMC5036155  PMID: 27653464

Abstract

Taenia saginata, Taenia solium and Taenia asiatica (beef, pork and Asian tapeworms, respectively) are parasitic flatworms of major public health and food safety importance. Among them, T. asiatica is a newly recognized species that split from T. saginata via an intermediate host switch ∼1.14 Myr ago. Here we report the 169- and 168-Mb draft genomes of T. saginata and T. asiatica. Comparative analysis reveals that high rates of gene duplications and functional diversifications might have partially driven the divergence between T. asiatica and T. saginata. We observe accelerated evolutionary rates, adaptive evolutions in homeostasis regulation, tegument maintenance and lipid uptakes, and differential/specialized gene family expansions in T. asiatica that may favour its hepatotropism in the new intermediate host. We also identify potential targets for developing diagnostic or intervention tools against human tapeworms. These data provide new insights into the evolution of Taenia parasites, particularly the recent speciation of T. asiatica.

Inline graphicOnly one of the three Taenia species causing taeniasis in humans was previously sequenced. Here the authors provide draft genomes of Taenia saginata and Taenia asiatica, analyse genome evolution of all three species, and identify potential targets for developing diagnostic markers or intervention tools.

Tapeworms (cestodes) infect all major groups of animals, including humans and many economically important species. Among them, Taenia solium (pork), Taenia saginata (beef) and Taenia asiatica (Asian) tapeworms cause taeniasis in humans (definitive host)1. Pork and beef tapeworms are globally distributed, each infecting ∼50–60 million people around the world2,3. Their larvae infect swine and cattle (intermediate hosts), respectively, leading to considerable economic losses and significant burdens in global food trade1. Asian tapeworm is confined to only Asian endemics, and was previously confused with beef tapeworm due to their morphological similarity in adult stage until the mid-1980s when pigs were found to be the major intermediate host. It was recognized as a new species in 1993 (refs 4, 5).

Asian and beef tapeworms differ in several morphological details and predilection sites in intermediate hosts. Like T. solium, the cysticerci of T. saginata (∼10 mm in diameter) are mainly established in the bovine striated muscles, whereas those of T. asiatica (∼2 mm) mainly infect pig livers6,7. For T. asiatica, fully mature cysticerci are developed in 4 weeks (versus ∼10–12 weeks for T. saginata)5. The hepatotropic feature is considered the major reason that T. asiatica has been documented only in Asian countries where some populations consume raw or undercooked pork livers8. However, the global impact is probably underappreciated because adult Asian tapeworm can only be distinguished from beef tapeworm by molecular techniques that are not routinely used in some regions of the world, and its ability to cause human cysticercosis has not been ruled out5,8. Besides morphological similarity, earlier studies indicated that Asian and beef tapeworms share a recent common ancestor that infected hominids and bovids (resembling T. saginata) at the Pleistocene period in Africa, suggesting a switch of the preferred intermediate host from bovids to suids during the speciation of T. asiatica9,10,11. Their divergence date were estimated between 0.78 and 1.71 Myr ago9, or ∼1 Myr ago (0.24–1.64)12, based on substitution rates of the mitochondrial COI gene. However, it is unclear how T. asiatica became adapted to a new intermediate host and infection site, and evolved into a new species in a relatively short evolutionary time.

Among human intestinal tapeworms, only the pork tapeworm genome was recently reported13. Here we present the genomes of beef and Asian tapeworms, making the genomes of all three human taeniasis parasites available for comparative analysis to gain insights into their biological features and genome evolutions, and adaptation of T. asiatica to a new intermediate host. Our genome-scale analyses reveal that the divergence time between beef and Asian tapeworms coincided with the migration of Homo erectus from Africa to Asia. The frequent gene duplications may have contributed significantly to the speciation processes. We observe higher genome variability and more accelerated adaptive evolution in T. asiatica, particularly in genes involved in host–parasite interactions, physiological homeostasis and nutrient uptake. The two genomes also provide an urgently needed resource for identifying molecular targets shared by human tapeworms for developing new therapeutics, as well as species-specific genes for developing molecular diagnostic tools as described below.

Results

Genome features and comparison

We sequenced the T. saginata and T. asiatica genomes derived from single adult worms to ∼95-fold coverage using the Illumina platform, and assembled them into 3,626 (N50=583 kb, total size=169.1 Mb) and 6,904 (N50=342 kb, size=168.0 Mb) scaffolds with lengths >0.5 kb, respectively. (Note: for clarity, parameters will be described in order of T. saginata and T. asiatica whenever appropriate hereafter.) The draft assemblies are larger than that of T. solium (122.3 Mb)13. Both genomes have an identical 42.3% GC content, similar to those of T. solium, Echinococcus multilocularis and E. granulosus (41.9–43.5%)13,14, but higher than Schistosoma spp.15 and Caenorhabditis spp. (34.1–37.9%; Table 1; Supplementary Table 1). The completeness of the two sequenced genomes are similar, at 89.52% and 90.32%, respectively, as estimated using the Core Eukaryotic Genes Mapping Approach16, which are comparable with those of the two well-assembled Echinococcus genomes (89.11–92.74%; Supplementary Fig. 1). The two tapeworm genomes contain 10.38 and 10.90% repeated sequences, similar to other tapeworms, but lower than flukes, and all major non-coding RNA species, including conserved microRNA and transfer RNA genes (Table 1; Supplementary Tables 2 and 3).

Table 1. Genomic features of T. saginata and T. asiatica in comparison with other worms.

  T. saginata T. asiatica T. solium* E. multilocularis H. microstoma S. mansoni C. elegans
Assembly size (Mb) 169 168 131 114 141 365 100
GC content (%) 43.2 43.2 43.5 42.2 36.0 35.2 35.4
Coding genes number 13,161 13,323 11,902 10,506 10,141 10,772 20,469
Average gene length (Kb) 6.0 5.9 4.6 5.4 6.1 15.4 3.1
Protein length (aa) 464 466 444 505 490 477 453
Gene density (genes per Mb) 77.9 79.3 90.9 92.2 71.9 29.5 201.0
Number of exons per gene 6.2 6.2 6.6 6.8 6.4 6.5 6.4
Mean length of exons (bp) 237 244 237 220 229 226 212
Number of introns per gene 5.2 5.2 5.6 5.8 5.4 5.5 5.4
Mean length of introns (bp) 864 831 775 684 862 2,460 354
GC content of exon (%) 49.7 49.6 50.2 50.0 44.3 36.0 42.6
GC content of intron (%) 41.5 41.2 40.8 39.9 34.6 34.7 32.5
Repeat content (%) 10.4 10.9 18.1 10.9 7.6 40.0 17.0
tRNA number 339 353 162 856 44 153 966
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*T. solium v2 genome (China isolate) properties and gene models.

We predicted 13,161 and 13,323 protein-coding genes in the two genomes, 77.2 and 75.7% of which were supported by RNA sequencing (RNA-seq; Supplementary Methods). More than half of these genes were mappable to the gene ontology (GO) terms (1,472 and 1,461 terms), KO identifiers in the Kyoto Encyclopedia of Genes and Genomes database (3,039 and 3,033) and Pfam domains (3,123 and 3,111). Among the predicted proteins, 2,361 (17.93%) and 2,365 (17.75%) contained transmembrane (TM) domains, and 1,094 (8.21%) and 1,048 (7.87%) possessed signal peptide sequences. These genes constitute metabolic pathways that are virtually identical to those in other tapeworms, including the loss of ability to de novo synthesize certain nutrients such as most amino acids, steroid hormones and lipids13,14 (Supplementary Fig. 2).

Introns are present in 81.0 and 80.9% of the genes in the two tapeworms. The lengths of short introns follow a bimodal distribution pattern with two major peaks at ∼36 bp (peak-1 introns) and ∼73 bp (peak-2; Fig. 1a). This feature was also observed in other tapeworms13 and the monogenean Gyrodactylus salaris17, but not in the flukes and Schmidtea mediterranea (peak-1 only), suggesting the presence of this feature predating the expansion of cestodes (or before the divergence of parasitic flatworms, but lost in the fluke lineage). These peak-1 and 2 introns are located preferentially in the 3′-end and middle regions of genes, respectively (Fig. 1b). Genes containing peak-2 introns tend to possess more introns than those containing peak-1 introns (for example, average 10.52 and 14.80 introns per gene in peak-1 and 2 intron-containing sequences in T. saginata (P<0.01 by two-sided Wilcoxon-rank sum test) (Supplementary Fig. 3). Interestingly, peak-2 intron-containing genes are significantly enriched to certain functional groups (for example, pyrophosphatase activity, hydrolase activity and nucleoside binding) and cellular components (for example, cytoskeletal motor proteins and membrane proteins; Fig. 1c; Supplementary Data 1). A striking but previously unreported feature in the tapeworms is the apparent preference of the mean lengths of neighbouring introns flanking small exons. The minimal mean lengths of introns flanking small exons (<400 bp) are 502 and 370 bp long in T. saginata and T. asiatica, respectively. This feature also occurs in some other invertebrate species, for example, S. mansoni, Caenorhabditis elegans and Drosophila melanogaster (Fig. 1d; Supplementary Figs 4 and 5). However, the extensiveness of this feature among eukaryotes and the mechanism behind it remains to be elucidated. Introns in tapeworms are biased towards A/T bases (26.8/31.1% in T. saginata; 26.6/31.1% in T. asiatica), but not as obvious as in S. mansoni (31.3/33.6%) and G. salaris (33.8/35.3%; Supplementary Fig. 6). However, no A/T-bias in exons was observed in tapeworms, although it was found in the flukes (that is, 25.2/25.0% in T. saginata and 25.3/25.1% in T. asiatica, versus 31.5/33.2% in S. mansoni; Supplementary Fig. 7).

Figure 1. Unique intron features in the tapeworm genomes.

Figure 1

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(a) Bimodal length distributions of short introns in tapeworms (T. asiatica, T. saginata, T. solium and E. multilocularis) and monogenean G. salaris in comparison with the unimodal distributions in the fluke S. mansoni and the free-living flatworm S. mediterranea. (b) Preferential distributions of peak-1 and peak-2 introns toward 3′-end and middle regions of genes, respectively. The curves show the relationship between intron densities and relative positions from the 5′-ends of genes. (c) Peak-2 intron-containing genes are highly enriched to certain functional groups (shown for T. asiatica, by two-sided Fisher's exact test). (d) Length preference of introns flanking small exons (<400 bp; shown for T. asiatica). The minimal mean length of (5′ or 3′) introns flanking small exons that have a specific length (<400 bp) is 370 bp in T. asiatica.

We compared homologous genes among human tapeworms, and observed that 12,984 (97.5%) and 11,888 T. asiatica genes (90.3%) had homologues in T. saginata and T. solium (BLASTP cutoff: 1e−4; Fig. 2a). Pair-wise collinearity analysis of orthologous blocks on scaffolds revealed a higher degree of similarity between T. saginata and T. asiatica (n1=7,201, n2=7,212, 292 blocks) than between the two species and T. solium (n1=6,055, n2=6,058, 303 blocks; Fig. 2b). Similarly, a higher nucleotide identity (92.26%) with larger alignable blocks (total 138 Mb, mean length=5.4 kb) was observed between T. saginata and T. asiatica (versus ∼88.53% identity, ∼108 Mb total and 3.8 kb mean lengths between beef/Asian and pork tapeworms). These data agree with their taxonomic affiliations.

Figure 2. Homologues and synteny between T. asiatica and related tapeworms.

Figure 2

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(a) Homologous genes shared between T. asiatica and other tapeworms (that is, T. saginata, T. solium, E. multicularis and H. microstoma). (b) Gene block linkages between T. asiatica and T. saginata. The collinear gene blocks determined by MCScan between genome scaffolds (>1 Mb) represent 7,212 and 7,201 genes for T. asiatica and T. saginata, respectively.

Gene duplications during divergence of tapeworms

Gene duplication (GD) is known as a primary source of materials for evolutionary innovations and adaptations18,19, in which the age of a GD event is proportional to the number of synonymous substitutions per synonymous site (Ks) of paralogous genes. In the genomes of T. saginata, T. asiatica and other related parasitic flatworms, the Ks distributions are typically quasi-exponentially L shaped (Fig. 3a,b; Supplementary Fig. 8), which agrees well with the notions that most duplications are young (for example, 4.36 and 4.98% GDs with Ks<0.01 in the T. saginata and T. asiatica genomes) because of the continuous loss of duplicated genes over the time. These events are mostly derived from small-scale gene duplications (SSGDs), predominated by dispersed duplications (for example, 71.95% in T. saginata, 74.14% in T. asiatica and 69.94% in E. multilocularis), followed by tandem (16.69, 15.69 and 15.08%) and proximal duplications (10.75, 8.90 and 11.29%; Supplementary Table 4) in the current assemblies.

Figure 3. Gene duplications revealed by Ks analysis.

Figure 3

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(a) The percentage of paralogous gene pairs of duplicated genes along with Ks values are typically L shaped in the T. saginata (Tsa) and T. asiatica (Tas) genomes, indicating the occurrence of continuous gene duplication events and the losses of duplicated genes over the time. (b) Distribution of Ks values in orthologous genes with peaks indicating the splits between various flatworms T. asiatica (Tas), T. saginata (Tsa), T. solium (Tso), E. granulosus (Egr), E. multilocularis (Emu), S. mansoni (Sma) and S. japanicum (Sja). The grey bar indicates the divergence point between the Taenia and Echinococcus lineages. (c) Extensive duplications of diagnostic antigen gp50 genes in the tapeworm lineage (Taenia, Echinococcus and Hymenolepis). (d) Sequence logo shows the conserved and distinct sequence characteristics of the gp50 sequences from the tapeworms. The sequence logo was generated from 183 sequences aligned at the conserved blocks selected by Gblocks with a less stringent selection (http://molevol.cmima.csic.es/castresana/Gblocks_server.html).

Although retrotransposons are the major elements subjected to GDs in the T. saginata and T. asiatica genomes, several functional homologous groups (including surface antigens, HSP70, ubiquitin conjugating enzyme, ryanodine receptor 44f, cyclin-dependent kinase, puromycin-sensitive aminopeptidase and zinc-finger proteins) appear to have also experienced continuous and extensive SSGDs during the evolution history of the tapeworm lineage (Fig. 3c; Supplementary Figs 9 and 10; Supplementary Table 5). These SSGD events resulted in many overrepresented super-families with high sequence diversities accompanying the diversification of their biological functions. Among them, the frequent duplications and retentions of tapeworm-specific surface antigens (for example, Taeniidae antigens and diagnostic antigen gp50) are indicative of their importance in the parasite survival and/or adaptations to new environments. Indeed, Taeniidae antigens are known to play important roles in the evasion of host immunity20, while the diagnostic antigen gp50 proteins are glycosyl phosphatidylinositol-anchored membrane glycoproteins also heavily involved in interacting with the host immune system21. The gp50 gene family appears to have duplicated more extensively, driven mostly by duplicative transpositions and tandem duplications along the Taeniidae and Taenia-specific evolution history (Fig. 3c). These duplicated genes have been differentially retained in different tapeworms, and might have carried out multiple functions through neo-/sub-functionalization with greatly divergent sequences (Fig. 3d), although their precise biological roles remain to be illustrated.

As a major force in evolution, species-specific GDs can lead to the differentiation of gene functions, thus facilitating the species-specific adaptation and divergence18. Both T. saginata and T. asiatica genomes possess a large number of recently duplicated genes (involving 866 and 1,075 in-paralogs after their divergence, respectively) that were derived from 481 and 614 duplicate events along each lineage, respectively. The duplicate genes appear to arise at a high average rate in their genomes (0.0321 and 0.0404 duplicates per gene per Myr for T. saginata and T. asiatica, respectively), similar to those in estimated in E. multilocularis (0.0304) and C. elegans (0.0208)22, suggesting a probable high degree of plasticity of their genomes (Supplementary Methods, section 8.9). Species-specific GDs were also shown by gene enrichment analysis, in which differential distributions of significantly enriched gene categories in biological processes (P<0.05 by two-sided Fisher's exact test) were observed between T. asiatica (mostly enriched in nucleosome assembly, cilium movement and ribosome localization) and T. saginata (mostly enriched in protein glycosylation; Supplementary Table 6), indicative of nonrandom processes of gene retentions in each genome. These observations suggest that the high rate of origin of GDs and preferential retentions of duplicated gene families might have contributed, at least partially, to the divergence of the two closely related tapeworms.

Duplicated genes in the process of acquiring new functions at the time of species separation are likely to contribute to species differentiation19. Using out-paralogous genes from T. solium as outgroups, we compared the evolutionary rate for each pair of the in-paralogous genes arising after the divergence of T. saginata and T. asiatica, and identified a number of newly duplicated genes that evolved significantly asymmetrically between paralogous pairs (88/592 in T. saginata, 72/804 in T. asiatica; P<0.05 by Tajima's relative rate test), implying that they were prone to diverge functions. Particularly, the cytoskeleton components (for example, actin, dynein heavy chain and kinesin), tegument surface antigens (for example, EG95 and gp50), ion transporters/channels (for example, ryanodine receptors 44f, solute carrier family 12 and multidrug resistance protein) and growth/development-related proteins (for example, fibroblast growth factor receptor 4, round spermatid basic protein 1 and segment polarity protein disheveled) appear to not reach at a stable rate yet in T. asiatica (Supplementary Data 2). These proteins are probably important in the speciation of T. asiatica, considering their roles in the tegument maintenance, homeostasis regulation and growth/reproduction. The galactosyltransferase gene family may play a particularly important but yet undefined biological role in T. saginata because of its continuous duplications along tapeworm evolution. In addition, the evolutionary divergence of recently duplicated gene pairs is echoed by the divergences in their expression patterns (R2=0.2462 in T. saginata; 0.0114 in T. asiatica) (Supplementary Fig. 11) and gene structures (accounting for 23.82 and 15.05% in-paralogous pairs in T. saginata and T. asiatica), indicative of their possible functional divergences.

Speciation history and accelerated evolution in T. asiatica

We collected 102 single-copy genes conserved in 10 flatworms and related species for estimating the divergence dates of tapeworms using a relaxed-clock Bayesian approach23. The genome-based analysis suggested that beef and Asian tapeworms diverged at 1.142 Myr (0.55–1.43, 95% highest probability density) in the early Pleistocene period (Supplementary Fig. 12), which was close to previously estimated date (∼1.0 Myr ago) based on mitochondrial genes11,12. This split predated the domestication of pigs and cattle (∼10,000 years ago)24, and the migration out of Africa of Homo sapiens (∼100,000 years ago)25, but fell within the periods of population expansion and migration of H. erectus from Africa to Asia (from ∼1.8 to 0.4 Myr ago)26. Currently, the closest relatives of T. saginata and T. asiatica (for example, T. simbae) are only found in Africa or adjacent regions10,11. If the ‘minimum number of host shifts' theory was assumed, our finding agrees with an earlier speculation9,10,11 that the common ancestor of beef and Asian tapeworms (T. saginata like) first colonized humans at or before early Pleistocene, and the hominid ancestor H. erectus acquired this tapeworm from bovids in Africa and then transmitted it to suids in Asia. We further speculate that the persistent hunting activity in H. erectus permitted long and consistent interactions among three host species, thus mediating the transfer of T. saginata-like ancestor from bovids to suids, giving rise to T. asiatica.

Despite high molecular and morphological similarities between Asian and beef tapeworms, the nucleotide substitution rate (branch-length) in protein-encoding genes of T. asiatica (0.00467 mutation per site) is 1.27-fold higher than that of T. saginata (0.00379 mutation per site) (Supplementary Fig. 13; Tajima's relative rate test, P<0.01). In addition, the nucleotide mutation rate in the T. asiatica genome is at 4.09 × 10−9 (3.27–8.52 × 10−9) mutations per site per year (versus ∼3.32 × 10−9 in T. saginata and ∼2.82 × 10−9 in T. solium), which is ∼10-fold higher than that of humans (0.33–0.47 × 10−9)27. The higher mutation rate provided a greater genome variation for selection and adaptation needed for the divergence/speciation of T. asiatica from T. saginata. However, the mechanism leading to the accelerated evolution rate in the T. asiatica genome is unclear.

By mapping useful sequence reads of short paired-end libraries to the assembled genomes, we detected substantial numbers of heterozygous single-nucleotide variations (SNVs). The overall SNV rate in T. asiatica is 2.97-fold higher than in T. saginata (Supplementary Table 7). The genomes of T. asiatica and T. saginata contained 60,734 (362 sites per Mb) and 20,700 (122 sites per Mb) high-quality heterozygous SNVs, respectively. Among them, 6.90% (T. asiatica) and 5.96% (T. saginata) were located in protein-coding genes, in which the most significantly enriched genes were transporters in T. asiatica, including those for ions (n=32), organic anions (n=11), amino acids (n=5) and sulfates (n=2; Supplementary Data 3). These proteins are mostly involved in maintaining cellular homeostasis and nutrients absorption (Supplementary Fig. 14). In addition, we observed more small indels (size=1–5 bp) in the T. asiatica genome (2,359 indels) than in T. saginata (1,014 indels; Supplementary Table 7). Both natural mutations over the time and genetic exchanges between individuals might contribute to heterozygosity, but their individual contributions in T. asiatica could not be established here due to the lack of intra-species genetic diversity data.

The T. asiatica genome also experienced more gene family gain (n=231) and expansion (n=408) than T. saginata (n=182 and 308; Fig. 4a). The gained gene families are mainly novel domains of unknown functions, possibly related to certain specialized adaptations, while the gene copy-number variations are related to functional extension. Intriguingly, significant expansions (branch-specific P values<0.05) of low-density lipoprotein receptor (LDLR) and fatty acid desaturase (FADS) genes were noticed in T. asiatica (n=9 and 4 versus n=7 and 1 in T. saginata or T. solium; Fig. 4b,c). We speculate that this expansion played an important role in the switch of the intermediate host from cattle to swine by promoting the establishment of cysterici of Asian tapeworm in the lipid-rich liver.

Figure 4. Evolution of gene families in the flatworms and roundworms.

Figure 4

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(a) The dynamics of gene family sizes in the genomes of T. saginata, T. asiatica, T. solium, E. granulosus, E. multilocularis, H. microstoma, S. japonicum and S. mansoni. Numbers above and below the branches indicate gene family gains/losses (red) and the expansions/contractions (blue), respectively. (b) Phylogenetic reconstruction clustered low-density lipoprotein receptor (LDLR) genes from T. saginata, T. asiatica and T. solium into four groups, in which group-4 LDLR genes were expanded only in the T. asiatica genome (Supplementary Methods, section 8.8). (c) The expansion of fatty acid desaturases (FADS) in the T. asiatica genome, compared with that in the T. saginata genome (Supplementary Methods, section 8.8).

Adaptive selection in the T. asiatica genome

Positive selection is an important source of evolutionary innovation and one of the major forces driving species divergence. To evaluate the role of positive selection in the evolution of T. asiatica, we selected 1:1 orthologous genes from six tapeworms for branch-site model analysis by Phylogenetic Analysis by Maximum Likelihood (PAML)28, and identified 134 and 102 positively selected genes (PSGs) in the T. asiatica and T. saginata genomes (likelihood ratio test, P<0.05; Supplementary Data 4). We analysed the PSGs in T. asiatica to examine whether these rapidly evolving genes were enriched for specific functions after the divergence from T. saginata. We observed evolutionary pressures on some essential genes in cellular processes, including those involved in transcription, translation and regulating protein degradation (for example, various ribosomal proteins, tRNA guanine N7 methyltransferase, bifunctional aminoacyl-tRNA synthetase, small subunit processome component 20, transcription factors and ubiquitination-associated proteins; Supplementary Data 4).

Adaptive selection signals were also observed in some genes associated with specialized survival environment for T. asiatica, but not in T. saginata. For instance, selection was detected in genes involved in pH maintenance and ion homeostasis (for example, carbonic anhydrase, glutamate receptor ionotropic kainite and amiloride-sensitive cation channel 4), implying adaptation to the new host internal environment. In addition to LDLR and FADS genes, we observed PSGs involved in lipid scavenge (for example, Niemann Pick C1 protein, fatty acid-binding protein and glycolipid transfer protein) and glycolysis (for example, pyruvate kinase and fructose-2,6-bisphosphatase) that were probably beneficial to T. asiatica in establishing infection in the lipid/sugar-rich liver in pigs. The tegument is essential for protecting parasitic flatworms from attacks by host defence systems29,30,31. We observed strong selection signals in genes responsible for maintaining body surface integrity in Asian tapeworm, including cytoskeleton-associated proteins32,33 (for example, myotubularin protein, myosin heavy chain, dynein heavy and light chains, kinesin-related proteins, intraflagellar transport protein, calponin, katanin and 4.1 protein, ezrin, radixin, moesin (FERM) domain-containing protein), cell adhesion/junction (for example, tight junction protein, β-catenin protein, protocadherin gamma and FRAS1-related extracellular matrix protein), and a glycosyltransferase gene probably involved in forming the thick glycocalyx layer on the tegumental surface13,34.

Proteins involved in host–parasite interactions

We analysed proteases, protease inhibitors (PIs) and excretory/secretory (E/S) proteins that are commonly involved in interacting with hosts and modulating host immune responses35,36. Particularly, secreted proteases can modulate host Th2 immune responses against helminths37. We predicted 157 and 161 proteases, plus 142 and 155 non-protease homologues, in the T. saginata and T. asiatica gnomes, which were comparable to those in E. multilocularis13 (Supplementary Data 5 and 6). They belong to five major classes (aspartic, cysteine, metallo, serine and threonine), predominated by metallo- (n=46–48), cysteine (n=41–44) and serine proteases (n=27–30; Supplementary Fig. 15). In addition, 23 and 26 proteases are encoded by the top 10% highly transcribed genes in larval T. saginata and adult T. asiatica (Supplementary Table 8). The two genomes encode 70–71 PIs that are all serine, cysteine and metalloprotease inhibitors, including I39 family PIs that interact with endopeptidases regardless of the catalytic type (Supplementary Data 7). The largest PI family is I02 (n=22, 14.0% in T. saginata and n=20, 12.4% in T. asiatica), which are serine PIs (aka Kunitz inhibitors; Supplementary Table 9). Several families of proteases and PIs were among the most enriched E/S proteins (Supplementary Tables 10 and 11). By comparison with PIs in S. mansoni, we identified several tapeworm-specific inhibitor families (for example, I87, I21 and I93), suggesting that tapeworms and flukes employ lineage-specific mechanisms to regulate protease activities.

The secretomes are large in T. asiatica (n=824, 6.18%) and T. saginata (n=885, 6.72%; Supplementary Tables 10 and 11; Supplementary Fig. 16). Many of them are proteases and PIs as described above. The two genomes also encode a large set of other classes of E/S proteins that may be involved in modulating host immune responses. For instance, some ‘Taeniidae antigens' (n=24 in T. asiatica and n=39 in T. saginata) could impair neutrophil chemotaxis and/or modulate Th2 polarization38. Another large E/S family is venom allergen-like proteins, which are known to modulate host immune function and regulate sexual development of parasites in the host39.

Molecular targets for intervention and diagnosis

Together with the previously reported T. solium and Echinococcus genomes, the availability of T. saginata and T. asiatica genome sequences allowed us to identify potential targets shared by all human tapeworms but divergent or absent in hosts for developing therapeutics. We identified 75–78 G-protein-coupled receptors (GPCRs) and 353–355 protein kinases in T. asiatica and T. saginata that are well-known classic drug targets (Supplementary Data 8 and 9). Most GPCRs are rhodopsin family proteins (n=63), while protein kinases cover ∼10 major classes, in which 180 kinase groups (Supplementary Data 9) could not be clustered with those from the reference species (that is, human, D. melanogaster and C. elegans), thus may serve as potential ideal drug or vaccine targets against the parasitic helminthes. Ligand-gated ion channels (LGICs) are validated targets for many current antihelminthic drugs. We identified at least 33 members of three major LGIC families (glutamate-activated cationic channels, cys-loop LGIC and ATP-gated ion channels), and ∼20 members of related families (that is, cyclic-nucleotide-gated cation channel and amiloride-sensitive sodium channel related; Supplementary Data 10). Most of these drug targets are conserved among tapeworm genomes, thus might potentially serve as broad-spectrum drug targets.

We further searched for parasite-specific sequences from the potential drug targets and host–parasite interaction-associated proteins, and identified 34 sequences (T. saginata) and 45 sequences (T. asiatica) with no homologues in mammals (Supplementary Data 11 and 12). Most of these sequences were supported by transcription data, including several homologues of known drug targets. Among them, cystatin and phytochelatin synthase are the top drug target candidates because they are present in all tapeworms and critical in interacting with hosts and heavy-metal detoxification, respectively13,40.

The tapeworm genomes were searched for species-specific genes potentially valuable in developing molecular and/or immunological diagnostic tools, particularly those for specific detection of Asian tapeworm. We collected all single-copy genes in the T. saginata and T. asiatica genomes, and ranked them by nucleotide sequence divergence as a community resource for developing molecular detection tools (Supplementary Data 13). We also recovered 15 (versus T. saginata) and 110 (versus T. solium) high-confidence species-specific protein-coding genes in the T. asiatica genome (Supplementary Table 12). However, the feasibility of these genes in developing immunological assays needs experimental evaluations.

Discussion

T. asiatica is morphologically indistinguishable from T. saginata in adult stage, but shares the same intermediate host with T. solium. Its speciation and switch of the intermediate host are intriguing evolutionary questions. Our comparative analysis revealed that the three human taeniasis parasites share many common genomic features but differ from each other in the evolutions and diversifications of certain specialized gene families, and reaffirmed the sister relationship between T. asiatica and T. saginata. Genome-based analysis suggests that Asian and beef tapeworms diverged ∼1.14 Myr ago, which coincides the migration of H. erectus to Asia, rather than the more recent migration of H. sapiens9,11. Thus, the speciation of T. asiatica predated that of H. sapiens. The divergence between the Asian and beef tapeworms might have been driven by the differential GDs in their genomes that display typically L-shaped distribution patterns. The high rates of extensive and continuous duplications, differential retentions and subsequent functional diversifications of gene families in the two tapeworm genome (for example, families associated with the cytoskeleton components, tegument surface antigens, ion transporters/channels in T. asiatica and glycosylation in T. saginata) might have significantly contributed to the speciation of T. asiatica.

We observed accelerated evolution in T. asiatica in mutation rate, heterozygosity and gene family gain/expansion that are all at higher rates than in T. saginata, suggesting that this parasite is of high evolution vigour in adaptation to new host environments. These observations challenge the hypothesis that T. asiatica species is at risk of extinction due to its minimal genetic diversity and limited geographical distribution41,42,43. Given that those studies were only based on analyses of a limited number of mitochondrial or nuclear genes, the real intra-species diversity within the T. asiatica populations may still need further large-scale investigations.

The PSGs in T. asiatica are more concentrated to gene families involved in internal homeostasis (for example, carbonic anhydrase), tegumental development (for example, cytoskeletal proteins, cell junction proteins and glycosyltransferases) and lipid uptake (for example, LDLR and fatty acid-binding protein), which are probably associated with the establishment of new immune-evasion and nutrient uptake strategies at the lipid-rich infection site (liver) in a new intermediate host (pigs). Our analysis indicates that tegument and membrane proteins in tapeworms are under particularly high evolutionary pressure in adaptation to new hosts, as evidenced by the rapidly evolved new genes/adaptive evolution/gene expansion associated with the recent host switch or speciation in T. asiatica. The tegument surface antigens (for example, Taeniidae antigens and diagnostic antigen gp50) may be of particular importance in tapeworm's survival and/or adaptations to new environments due to their critical roles in interacting with the host immune systems.

We identified several sets of proteins that might serve as broad-spectrum drug targets in tapeworms, including kinases, GPCRs and ion channels, as well as two proteins (cystatin and phytochelatin synthase) that could serve as potentially ideal targets in T. saginata and T. asiatica. Due to the morphological similarities, misdiagnosis between T. saginata and T. asiatica is not uncommon. Recently, several molecular approaches using sequence-specific DNA probes, PCR-based RFLP and multiplex PCR based on mitochondrial sequences were explored for differential diagnosis of the two Taenia tapeworms44,45,46. We also provide here a list of nuclear genes based on sequence divergence between the two closely related tapeworms for development of new molecular diagnostic tools.

Methods

Samples and preparations

Adult worms of T. saginata and T. asiatica were isolated from two patients (one worm per patient) in Yunnan Province, China. The study was approved by the ethics committee of Affiliated Hospital of Dali University (Yunnan, China) and patients have given written consent to publication of this study with the exclusion of any personal identifiers. Larvae (cysticerci) of T. saginata were obtained from the skeletal muscle of an experimentally infected calf 7 weeks after infection. The animal was cared in accordance with good animal practice according to the Animal Ethics Procedures and Guidelines of the People's Republic of China, and the study was approved by the Institutional Committee for the Care and Use of Experimental Animals of Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences (no. LVRIAEC2010-002). Genomic DNA was extracted from freshly collected middle proglottids for constructing two paired-end libraries (300 and 500 bp inserts) and three mate-pair libraries (1, 5 and 10 kb) for T. saginata, and two paired-end libraries (500 bp) and seven mate-pair libraries (2, 2, 3.5, 5, 5, 7 and 10 kb) for T. asiatica (Supplementary Methods, section 1). Messenger RNA was isolated from T. saginata larvae and the middle proglotids of T. asiatica for the construction of paired-end cDNA libraries (300 bp). For each worm, the clonality was confirmed by the distribution of minor allele frequencies of the heterozygous sites (Supplementary Fig. 17).

High-throughput sequencing and assembly

Paired-end and mate-pair sequencing was performed using the Illumina Sequencing Systems. Adaptor sequences, PCR duplicates, contaminants and low-quality sequences were removed, and high-quality sequences were assembled into contigs using ABySS (v1.3.5)47 and SOAPde novo (v1.05)48. Scaffolds were constructed from contigs using SSPACE (v-PREMIUM-2.3)49. Gaps in the scaffolds were closed using GapFiller (v1.10)50. Assembly completeness and redundancy were assessed with Core Eukaryotic Genes Mapping Approach16 and RNA-seq data (Supplementary Methods, section 2). Genome sizes were estimated by the k-mer-based method (Supplementary Fig. 18). For transcriptome analysis, high-quality RNA-seq reads were mapped to the genomes using TopHat (v2.0.12)51. Transcripts were built by Cufflinks (v2.0.2)52 with default settings. De novo assembly of RNA-seq reads was performed using Trinity (v2.0.3)53. Expression levels were evaluated by fragments per kilobase of transcript per million fragments of mapped genes, using Cufflinks (v2.0.2) (-G parameter) referenced to the final EVM integrated GFF files (Supplementary Methods, section 4).

Gene prediction and annotation

We combined several approaches to predict protein-encoding genes, including homology-based searches, ab initio prediction and transcriptome-based prediction methods. Individual predictions were merged by EvidenceModeler (v1.1.1)54. Untranslated regions were added with PASA (v2.0.0)55. Predicted proteins were searched by BLAST algorithms for homologues in the National Center for Biotechnology Information non-redundant protein databases and Uniprot database. InterproScan5 (ref. 56) was used for identifying domains, mapping GO terms and assigning functional classifications. KO terms were assigned and pathway mapping was performed using the annotation tools at the Kyoto Encyclopedia of Genes and Genomes server (http://www.genome.jp/tools/kaas/) (see Supplementary Methods, section 5). Non-coding RNA and repeat elements were also predicted (Supplementary Methods, section 3.2).

Comparative genomics and SNV analysis

Protein similarities were determined by all-against-all BLASTP searches (1e−4) using predicted proteome sequences of T. asiatica as queries against those of T. saginata and T. solium. The T. solium genome assembles (version 2) available at http://taenia.big.ac.cn/taenia/index.html were used in all analyses or otherwise as specified. The resulting T. asiatica-specific genes were further searched by BLASTP (1e−3, 80% length coverage) against genome assemblies of T. saginata and T. solium to identify high-confident-specific genes. The assemblies of the three human tapeworms were aligned using MUMmer (v3.22)57 to identify genome syntenic blocks. The collinearity analysis for orthologous genes on scaffolds was conducted using MCscanX58 (Supplementary Methods, section 6). High-quality reads were mapped to the reference assemblies using Bowtie2 (v2.2.3)59. Reads corresponding to PCR duplicates were removed by MarkDuplicates from PICARD (v1.119) (http://picard.sourceforge.net), followed by base quality recalibration and indel realignment by GATK (v3.5)60. SNVs and indels in the T. asiatica and T. saginata genomes were detected by HaplotypeCaller from GATK and filtered by the coverage, mapping quality score, FisherStrand (FS) value (Phred-scaled P value using Fisher's exact test) and other filters. To make the result comparable, a similar coverage (∼65 × ) of reads for each genome was used to calculate the proportion of variants removed by each filter (Supplementary Methods, section 3.3).

Gene family construction and phylogeny analysis

Gene families were identified using protein sequences of T. saginata, T. asiatica and 8 other worms (that is., T. solium, E. granulosus, E. multilocularis, Hymenolepis microstoma, Schistosoma japonicum, S. mansoni, Ascaris suum and C. elegans; Supplementary Table 13) by OrthoMCL (v2.0.9)61 (Supplementary Figs 19 and 20). A maximum likelihood phylogenetic tree was inferred from a concatenated nucleotide data set containing 747 single-copy orthologous genes shared by all 10 species by RAxML (v8.0.24)62 with the best fit model (GTR+I+4-rate Γ for CDS; Supplementary Methods, section 7). The divergence dates were estimated with the relaxed-clock model using BEAST2 (v2.1.3)23 (Supplementary Methods, section 8).

Gene family analysis

Gene family expansion and contraction were determined using the CAFÉ (v3.0)63 based on the phylogenetic tree constructed by RAxML (v8.0.24). The minimum ancestral gene families were determined using DOLLOP program included in the PHYLIP package (v3.695)64 to estimate gain/loss evolutions of gene families.

Paralogous gene groups and GDs

An all-against-all protein sequence similarity search was performed using BLASTP (e value≤1e−10), followed by clustering the paralogous groups within each genome using Markov Clustering (MCL) (mclblastline pipeline)65. For each gene family, a protein alignment was constructed using MAFFT (v7.147b)66. This alignment was used as a guide for aligning the DNA sequences of gene family pairs, using ParaAT (v1.0)67. Paralogous gene pairs were retained if the two sequences were alignable over a length of >150 amino acids with an identity score of at least 30%. Ks value was calculated with the maximum likelihood estimation method using the program codeml (CodonFreq=2, runmodel=−2) in the PAML package (v4.8). Only Ks values ≤5 were retained for further analysis. An average linkage clustering approach was used to correct the redundancy of Ks values that correspond to GD events. The GD modes of each genome were estimated by MSCANX. Recently, duplicated genes (in-paralogs) along T. asiatica and T. saginata that arise after their divergence were determined by Inparanoid (v4.1)68. The Tajima's relative rate test for in-paralogous gene pairs was performed, using orthologous genes of T. solium as outgroup (supplementary Methods, section 8).

Likelihood ratio tests for PSGs

A total of 6,581 one-to-one orthologous gene groups were extracted from genomes of the six tapeworms (T. asiatica, T. saginata, T. solium, E. granulosus, E. multilocularis and H. microstoma) to identify PSGs. Multiple protein-coding DNA sequence alignments were generated using ParaAT (v1.0)67 and MAFFT (v7.147b)66. All gaps in the alignments were removed, and likelihood ratio tests for selection (P<0.05) on each branch of the phylogenetic tree were performed using Codeml implemented in the PAML package (v4.8)28 with a modified branch-site model A (model=2, NSsites=2; Supplementary Methods, section 9).

Identification of potential drug targets

Putative proteases and PIs were detected using the MEROPS batch BLAST server (http://merops.sanger.ac.uk/cgi-bin/batch_blast) (E value<1e−4). LGIC genes were identified by searching tapeworm homologues against the LGIC database (http://www.ebi.ac.uk/compneur-srv/LGICdb/) and annotated LGIC proteins from E. multilocularis and S. mansoni13,15. The resulting hits were used as BLASTP queries against the National Center for Biotechnology Information non-redundant database. Sequences homologous to LGIC-related proteins or having no hits in the non-redundant database were retained as putative LGICs. Protein kinase domain-containing proteins were extracted from InterProScan5 domain annotations. The corresponding domains were clustered with a reference domain data set (Human, fly and C. elegans; KINBASE; http://kinase.com/kinbase/FastaFiles/) using OrthoMCL. The non-assignable domains during the clustering were searched against other tapeworm kinases for classification. TM domains were first predicted by Phobius algorithm69 (length >250 aa). The resulting proteins with ≥3 and ≤15 TM domains were retained and searched by HMMER (v3.1b1)70 with HMMs against annotated GPCR sequences from Pfam database and from other tapeworms. Hits were further filtered by BLAST search against the non-redundant protein database (Supplementary Methods, section 11). Several bioinformatics tools were employed to identify classic and non-classic E/S proteins in the T. asiatica and T. saginata genomes (Supplementary Methods, section 10).

Data availability

All sequence data that support the findings of this study have been deposited in GenBank with the following accession numbers: LWMK00000000 and LWMJ00000000 for Whole Genome Shotgun projects of T. saginata and T. asiatica under BioProject accession PRJNA71493 and PRJNA299871, respectively; SRR2890401, SRR2890402, SRR2890403, SRR2890404 and SRR2890405 for the T. saginata genome sequencing data; SRR2890205, SRR2890207, SRR2890209, SRR2890210, SRR2890211, SRR2890213, SRR2890214, SRR2890215 and SRR2890216 for the T. asiatica genome sequencing data; SRR2895139 and SRR2895068 for the transcriptome data of T. saginata and T. asiatica, respectively. The genome assemblies and annotations used in this study are also available at http://taenia.big.ac.cn/taenia/index.html. All other data supporting the findings of this study are available within the article and its Supplementary Information files, or from the corresponding authors on request.

Additional information

How to cite this article: Wang, S. et al. Comparative genomics reveals adaptive evolution of Asian tapeworm in switching to a new intermediate host. Nat. Commun. 7:12845 doi: 10.1038/ncomms12845 (2016).

Supplementary Material

Supplementary Information

Supplementary Figures 1-20, Supplementary Tables 1-13, Supplementary Methods and Supplementary References.

ncomms12845-s1.pdf (13.9MB, pdf)
Supplementary Data 1

GO enrichment analysis of the genes containing peak-2 introns in the T. asiatica and T. saginata genomes.

ncomms12845-s2.xlsx (35.7KB, xlsx)
Supplementary Data 2

The in-paralog pairs showing differential evolution rates in the T. asiatica and T. saginata genomes.

ncomms12845-s3.xlsx (19.5KB, xlsx)
Supplementary Data 3

GO enrichment analysis of heterozygous genes in the T. asiatica and T. saginata genomes.

ncomms12845-s4.xlsx (21.3KB, xlsx)
Supplementary Data 4

Positively selected genes identified from T. asiatica and T. saginata lineage.

ncomms12845-s5.xlsx (40.9KB, xlsx)
Supplementary Data 5

Proteases identified from the T. asiatica and T. saginata genomes.

ncomms12845-s6.xlsx (18.7KB, xlsx)
Supplementary Data 6

Non-protease homologues in the T. asiatica and T. saginata genomes.

ncomms12845-s7.xlsx (20.2KB, xlsx)
Supplementary Data 7

Protease inhibitors identified from the T. saginata and T. asiatica genomes.

ncomms12845-s8.xlsx (12.3KB, xlsx)
Supplementary Data 8

GPCRs in the T. asiatica and T. saginata genomes.

ncomms12845-s9.xlsx (13.1KB, xlsx)
Supplementary Data 9

Protein Kinases in the T. asiatica and T. saginata genomes.

ncomms12845-s10.xlsx (35.8KB, xlsx)
Supplementary Data 10

Ligand-gated ion channels.

ncomms12845-s11.xlsx (15.4KB, xlsx)
Supplementary Data 11

Potential drug targets specific to tapeworms compared with human.

ncomms12845-s12.xlsx (14.5KB, xlsx)
Supplementary Data 12

Potential drug targets with homologs in drug target databases.

ncomms12845-s13.xlsx (58.3KB, xlsx)
Supplementary Data 13

Potential nuclear molecular markers to differentiate T. saginata (TSA) and T. asiatica (TAS).

ncomms12845-s14.xlsx (18.6KB, xlsx)

Acknowledgments

We thank H. Li from Dali University for providing parasite material; Y. Liu, M. Sun, W. Li, J. Yang and S. Li from Beijing Institute of Genomics, Chinese Academy of Sciences for preparing genomic DNA, constructing libraries and generating raw sequencing reads; and Y. Zheng for helpful discussions. This work was funded by the ‘National Key Basic Research Program (973 Program) of China' (grant no. 2015CB150300), ‘International Science & Technology Cooperation Program of China' (grant no. 2013DFA31840) and State Key Laboratory of Veterinary Etiological Biology of Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences.

Author contributions Sh.W., J.H., S.Z., X.L., H.L., Y.D., X.Z. and X.M. collected, cultivated and prepared parasite material for sequencing. B.Z., X.T., Q.M. and J.Y. purified nucleic acids and coordinated sequencing. Se.W., Sh.W., G.Z., S.H. and X.C. planed and undertook the assembly, annotation and comparative analyses of genomic and transcriptomic data. Y.L. and S.G. improved the genome assemblies and curated genes. Sh.W., Se.W. and G.Z. performed the phylogenetic and adaptive evolution analyses. H.Z., S.G., H.M., Z.H. and M.Y. created the Taenia genome database. Sh.W., A.G., J.C. and X-Q.Z. analysed drug targets. Sh.W., Se.W., G.Z. and L.X. wrote the manuscript. X.C., G.Z. and S.H. directed the project.

11/03/2016

A correction has been published and is appended to both the HTML and PDF versions of this paper. The error has not been fixed in the paper.

References

  1. Food and Agriculture Organization of the United Nations & World Health Organization. Multicriteria-based Ranking for Risk Management of Food-borne Parasites. Available at http://www.who.int/foodsafety/publications/mra_23/en/ (2014).
  2. Hawk M. W., Shahlaie K., Kim K. D. & Theis J. H. Neurocysticercosis: a review. Surg. Neurol. 63, 123–132 (2005). [DOI] [PubMed] [Google Scholar]
  3. Craig P. & Ito A. Intestinal cestodes. Curr. Opin. Infect. Dis. 20, 524–532 (2007). [DOI] [PubMed] [Google Scholar]
  4. Jeon H. K., Kim K. H. & Eom K. S. Complete sequence of the mitochondrial genome of Taenia saginata: comparison with T. solium and T. asiatica. Parasitol. Int. 56, 243–246 (2007). [DOI] [PubMed] [Google Scholar]
  5. Galán-Puchades M. T. & Fuentes M. V. Lights and shadows of the Taenia asiatica life cycle and pathogenicity. Trop. Parasitol. 3, 114–119 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Flisser A. et al. Portrait of human tapeworms. J. Parasitol. 90, 914–916 (2004). [DOI] [PubMed] [Google Scholar]
  7. Eom K. S. & Rim H.-J. Natural infections of Asian Taem'a saginata metacestodes in the livers of Korean domestic pigs. Korean J. Parasitol. 30, 15–20 (1992). [DOI] [PubMed] [Google Scholar]
  8. Galan-Puchades M. T. & Fuentes M. V. Taenia asiatica: the most neglected human Taenia and the possibility of cysticercosis. Korean J. Parasitol. 51, 51–54 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hoberg E. P., Alkire N. L., de Queiroz A. & Jones A. Out of Africa: origins of the Taenia tapeworms in humans. Proc. Biol. Sci. 268, 781–787 (2001). [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hoberg E. P. Phylogeny of Taenia: species definitions and origins of human parasites. Parasitol. Int. 55, S23–S30 (2006). [DOI] [PubMed] [Google Scholar]
  11. Michelet L. & Dauga C. Molecular evidence of host influences on the evolution and spread of human tapeworms. Biol. Rev. 87, 731–741 (2012). [DOI] [PubMed] [Google Scholar]
  12. Michelet L. et al. The pig tapeworm Taenia solium, the cause of cysticercosis: biogeographic (temporal and spacial) origins in Madagascar. Mol. Phylogenet. Evol. 55, 744–750 (2010). [DOI] [PubMed] [Google Scholar]
  13. Tsai I. J. et al. The genomes of four tapeworm species reveal adaptations to parasitism. Nature 496, 57–63 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Zheng H. J. et al. The genome of the hydatid tapeworm Echinococcus granulosus. Nat. Genet. 45, 1168–1302 (2013). [DOI] [PubMed] [Google Scholar]
  15. Berriman M. et al. The genome of the blood fluke Schistosoma mansoni. Nature 460, 352–358 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Parra G., Bradnam K. & Korf I. CEGMA: a pipeline to accurately annotate core genes in eukaryotic genomes. Bioinformatics 23, 1061–1067 (2007). [DOI] [PubMed] [Google Scholar]
  17. Hahn C., Fromm B. & Bachmann L. Comparative genomics of flatworms (platyhelminthes) reveals shared genomic features of ecto- and endoparastic neodermata. Genome Biol. Evol. 6, 1105–1117 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Zhang J. Z. Evolution by gene duplication: an update. Trends Ecol. Evol. 18, 292–298 (2003). [Google Scholar]
  19. Ting C. T. et al. Gene duplication and speciation in Drosophila: evidence from the Odysseus locus. Proc. Natl Acad. Sci. USA 101, 12232–12235 (2004). [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Rigano R. et al. Modulation of human immune response by Echinococcus granulosus antigen B and its possible role in evading host defenses. Infect. Immun. 69, 288–296 (2001). [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Hancock K. et al. Characterization and cloning of GP50, a Taenia solium antigen diagnostic for cysticercosis. Mol. Biochem. Parasitol. 133, 115–124 (2004). [DOI] [PubMed] [Google Scholar]
  22. Lynch M. & Conery J. S. The evolutionary fate and consequences of duplicate genes. Science 290, 1151–1155 (2000). [DOI] [PubMed] [Google Scholar]
  23. Bouckaert R. et al. BEAST 2: a software platform for bayesian evolutionary analysis. PLoS Comput. Biol. 10, e1003537 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Bradley D. G., MacHugh D. E., Cunningham P. & Loftus R. T. Mitochondrial diversity and the origins of African and European cattle. Proc. Natl Acad. Sci. USA 93, 5131–5135 (1996). [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Stringer C. B. & Andrews P. Genetic and fossil evidence for the origin of modern humans. Science 239, 1263–1268 (1988). [DOI] [PubMed] [Google Scholar]
  26. Klein R. G. Darwin and the recent African origin of modern humans. Proc. Natl Acad. Sci. USA 106, 16007–16009 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Langergraber K. E. et al. Generation times in wild chimpanzees and gorillas suggest earlier divergence times in great ape and human evolution. Proc. Natl Acad. Sci. USA 109, 15716–15721 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Yang Z. H. PAML 4: phylogenetic analysis by maximum likelihood. Mol. Biol. Evol. 24, 1586–1591 (2007). [DOI] [PubMed] [Google Scholar]
  29. Van Hellemond J. J. et al. Functions of the tegument of schistosomes: clues from the proteome and lipidome. Int. J. Parasitol. 36, 691–699 (2006). [DOI] [PubMed] [Google Scholar]
  30. Smyth J. D. & McManus D. P. The Physiology and Biochemistry of Cestodes Cambridge Univ. Press (1989). [Google Scholar]
  31. Lumsden R. D. The tapeworm tegument: a model system for studies on membrane structure and function in host-parasite relationships. Trans. Am. Microsc. Soc. 94, 501–507 (1975). [PubMed] [Google Scholar]
  32. Jones M. K., Gobert G. N., Zhang L. H., Sunderland P. & McManus D. P. The cytoskeleton and motor proteins of human schistosomes and their roles in surface maintenance and host-parasite interactions. Bioessays 26, 752–765 (2004). [DOI] [PubMed] [Google Scholar]
  33. Poddubnaya L. G., Scholz T., Kuchta R., Levron C. & Brunanska M. Ultrastructure of the proglottid tegument (neodermis) of the cestode Echinophallus wageneri (Pseudophyllidea: Echinophallidae), a parasite of the bathypelagic fish Centrolophus niger. Parasitol. Res. 101, 373–383 (2007). [DOI] [PubMed] [Google Scholar]
  34. Diaz A., Casaravilla C., Allen J. E., Sim R. B. & Ferreira A. M. Understanding the laminated layer of larval Echinococcus II: immunology. Trends Parasitol. 27, 263–272 (2011). [DOI] [PubMed] [Google Scholar]
  35. Jex A. R. et al. Ascaris suum draft genome. Nature 479, 529–533 (2011). [DOI] [PubMed] [Google Scholar]
  36. McKerrow J. H., Caffrey C., Kelly B., Loke P. & Sajid M. Proteases in parasitic diseases. Annu. Rev. Pathol. 1, 497–536 (2006). [DOI] [PubMed] [Google Scholar]
  37. McSorley H. J., Hewitson J. P. & Maizels R. M. Immunomodulation by helminth parasites: defining mechanisms and mediators. Int. J. Parasitol. 43, 301–310 (2013). [DOI] [PubMed] [Google Scholar]
  38. Rott M. B. et al. Comparative analysis of two different subunits of antigen B from Echinococcus granulosus: gene sequences, expression in Escherichia coli and serological evaluation. Acta Trop. 75, 331–340 (2000). [DOI] [PubMed] [Google Scholar]
  39. Chalmers I. W. & Hoffmann K. F. Platyhelminth venom allergen-like (VAL) proteins: revealing structural diversity, class-specific features and biological associations across the phylum. Parasitology 139, 1231–1245 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Gregory W. F. & Maizels R. M. Cystatins from filarial parasites: evolution, adaptation and function in the host-parasite relationship. Int. J. Biochem. Cell Biol. 40, 1389–1398 (2008). [DOI] [PubMed] [Google Scholar]
  41. Ale A. et al. Epidemiology and genetic diversity of Taenia asiatica: a systematic review. Parasite Vector 7, 45 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Jeon H. K. & Eom K. S. Taenia asiatica and Taenia saginata: genetic divergence estimated from their mitochondrial genomes. Exp. Parasitol. 113, 58–61 (2006). [DOI] [PubMed] [Google Scholar]
  43. Gonzalez L. M. et al. Genetic variability of the 18 kDa/HP6 protective antigen in Taenia saginata and Taenia asiatica: implications for vaccine development. Mol. Biochem. Parasitol. 176, 131–134 (2011). [DOI] [PubMed] [Google Scholar]
  44. Bowles J. & McManus D. Genetic characterization of the Asian Taenia, a newly described taeniid cestode of humans. Am. J. Trop. Med. Hyg. 50, 33–44 (1994). [PubMed] [Google Scholar]
  45. Yamasaki H. et al. DNA differential diagnosis of human taeniid cestodes by base excision sequence scanning thymine-base reader analysis with mitochondrial genes. J. Clin. Microbiol. 40, 3818–3821 (2002). [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. McManus D. P. Molecular discrimination of taeniid cestodes. Parasitol. Int. 55, S31–S37 (2006). [DOI] [PubMed] [Google Scholar]
  47. Simpson J. T. et al. ABySS: a parallel assembler for short read sequence data. Genome Res. 19, 1117–1123 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Li R. Q. et al. De novo assembly of human genomes with massively parallel short read sequencing. Genome Res. 20, 265–272 (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Boetzer M., Henkel C. V., Jansen H. J., Butler D. & Pirovano W. Scaffolding pre-assembled contigs using SSPACE. Bioinformatics 27, 578–579 (2011). [DOI] [PubMed] [Google Scholar]
  50. Boetzer M. & Pirovano W. Toward almost closed genomes with GapFiller. Genome Biol. 13, R56 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Kim D. et al. TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biol. 14, R36 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Trapnell C. et al. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. Nat. Protoc. 7, 562–578 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Grabherr M. G. et al. Full-length transcriptome assembly from RNA-Seq data without a reference genome. Nat. Biotechnol. 29, 644–652 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Haas B. J. et al. Automated eukaryotic gene structure annotation using EVidenceModeler and the program to assemble spliced alignments. Genome Biol. 9, R7 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Haas B. J. et al. Improving the Arabidopsis genome annotation using maximal transcript alignment assemblies. Nucleic Acids Res. 31, 5654–5666 (2003). [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Zdobnov E. M. & Apweiler R. InterProScan—an integration platform for the signature-recognition methods in InterPro. Bioinformatics 17, 847–848 (2001). [DOI] [PubMed] [Google Scholar]
  57. Kurtz S. et al. Versatile and open software for comparing large genomes. Genome Biol. 5, R12 (2004). [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Wang Y. P. et al. MCScanX: a toolkit for detection and evolutionary analysis of gene synteny and collinearity. Nucleic Acids Res. 40, e49 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Langmead B. & Salzberg S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods. 9, 357–359 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. DePristo M. A. et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet. 43, 491–498 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Li L., Stoeckert C. J. & Roos D. S. OrthoMCL: identification of ortholog groups for eukaryotic genomes. Genome Res. 13, 2178–2189 (2003). [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Stamatakis A. RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics 22, 2688–2690 (2006). [DOI] [PubMed] [Google Scholar]
  63. De Bie T., Cristianini N., Demuth J. P. & Hahn M. W. CAFE: a computational tool for the study of gene family evolution. Bioinformatics 22, 1269–1271 (2006). [DOI] [PubMed] [Google Scholar]
  64. Felsenstein J. PHYLIP: Phylogenetic Inference Program, Version 3.6 Univ. of Washington (2005). [Google Scholar]
  65. Enright A. J., Van Dongen S. & Ouzounis C. A. An efficient algorithm for large-scale detection of protein families. Nucleic Acids Res. 30, 1575–1584 (2002). [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Katoh K. & Standley D. M. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol. Biol. Evol. 30, 772–780 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Zhang Z. et al. ParaAT: a parallel tool for constructing multiple protein-coding DNA alignments. Biochem. Biophs. Res. Commun. 419, 779–781 (2012). [DOI] [PubMed] [Google Scholar]
  68. O'Brien K. P., Remm M. & Sonnhammer E. L. L. Inparanoid: a comprehensive database of eukaryotic orthologs. Nucleic Acids Res. 33, D476–D480 (2005). [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Kall L., Krogh A. & Sonnhammer E. L. L. Advantages of combined transmembrane topology and signal peptide prediction—the Phobius web server. Nucleic Acids Res. 35, W429–W432 (2007). [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. Mistry J., Finn R. D., Eddy S. R., Bateman A. & Punta M. Challenges in homology search: HMMER3 and convergent evolution of coiled-coil regions. Nucleic Acids Res. 41, e121 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Information

Supplementary Figures 1-20, Supplementary Tables 1-13, Supplementary Methods and Supplementary References.

ncomms12845-s1.pdf (13.9MB, pdf)
Supplementary Data 1

GO enrichment analysis of the genes containing peak-2 introns in the T. asiatica and T. saginata genomes.

ncomms12845-s2.xlsx (35.7KB, xlsx)
Supplementary Data 2

The in-paralog pairs showing differential evolution rates in the T. asiatica and T. saginata genomes.

ncomms12845-s3.xlsx (19.5KB, xlsx)
Supplementary Data 3

GO enrichment analysis of heterozygous genes in the T. asiatica and T. saginata genomes.

ncomms12845-s4.xlsx (21.3KB, xlsx)
Supplementary Data 4

Positively selected genes identified from T. asiatica and T. saginata lineage.

ncomms12845-s5.xlsx (40.9KB, xlsx)
Supplementary Data 5

Proteases identified from the T. asiatica and T. saginata genomes.

ncomms12845-s6.xlsx (18.7KB, xlsx)
Supplementary Data 6

Non-protease homologues in the T. asiatica and T. saginata genomes.

ncomms12845-s7.xlsx (20.2KB, xlsx)
Supplementary Data 7

Protease inhibitors identified from the T. saginata and T. asiatica genomes.

ncomms12845-s8.xlsx (12.3KB, xlsx)
Supplementary Data 8

GPCRs in the T. asiatica and T. saginata genomes.

ncomms12845-s9.xlsx (13.1KB, xlsx)
Supplementary Data 9

Protein Kinases in the T. asiatica and T. saginata genomes.

ncomms12845-s10.xlsx (35.8KB, xlsx)
Supplementary Data 10

Ligand-gated ion channels.

ncomms12845-s11.xlsx (15.4KB, xlsx)
Supplementary Data 11

Potential drug targets specific to tapeworms compared with human.

ncomms12845-s12.xlsx (14.5KB, xlsx)
Supplementary Data 12

Potential drug targets with homologs in drug target databases.

ncomms12845-s13.xlsx (58.3KB, xlsx)
Supplementary Data 13

Potential nuclear molecular markers to differentiate T. saginata (TSA) and T. asiatica (TAS).

ncomms12845-s14.xlsx (18.6KB, xlsx)

Data Availability Statement

All sequence data that support the findings of this study have been deposited in GenBank with the following accession numbers: LWMK00000000 and LWMJ00000000 for Whole Genome Shotgun projects of T. saginata and T. asiatica under BioProject accession PRJNA71493 and PRJNA299871, respectively; SRR2890401, SRR2890402, SRR2890403, SRR2890404 and SRR2890405 for the T. saginata genome sequencing data; SRR2890205, SRR2890207, SRR2890209, SRR2890210, SRR2890211, SRR2890213, SRR2890214, SRR2890215 and SRR2890216 for the T. asiatica genome sequencing data; SRR2895139 and SRR2895068 for the transcriptome data of T. saginata and T. asiatica, respectively. The genome assemblies and annotations used in this study are also available at http://taenia.big.ac.cn/taenia/index.html. All other data supporting the findings of this study are available within the article and its Supplementary Information files, or from the corresponding authors on request.

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