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Article

Cysteine Proteinase C1A Paralog Profiles Correspond with Phylogenetic Lineages of Pathogenic Piroplasmids

by
Mariano E. Ascencio
1,2,
Monica Florin-Christensen
1,2,
Choukri B. Mamoun
3,
William Weir
4,
Brian Shiels
4 and
Leonhard Schnittger
1,2,*
1
Instituto de Patobiología, Centro de Investigaciones en Ciencias Veterinarias y Agronómicas (CICVyA), INTA-Castelar, Los Reseros y Nicolas Repetto s/n, Hurlingham 1686, Argentina
2
National Council of Scientific and Technological Research (CONICET), Ciudad Autónoma de Buenos Aires C1033AAJ, Argentina
3
Department of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, CT 06520, USA
4
Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary & Life Sciences, University of Glasgow, 464 Bearsden Road, Glasgow G61 1QH, UK
*
Author to whom correspondence should be addressed.
Vet. Sci. 2018, 5(2), 41; https://doi.org/10.3390/vetsci5020041
Submission received: 16 February 2018 / Revised: 6 April 2018 / Accepted: 11 April 2018 / Published: 17 April 2018

Abstract

:
Piroplasmid parasites comprising of Babesia, Theileria, and Cytauxzoon are transmitted by ticks to farm and pet animals and have a significant impact on livestock industries and animal health in tropical and subtropical regions worldwide. In addition, diverse Babesia spp. infect humans as opportunistic hosts. Molecular phylogeny has demonstrated at least six piroplasmid lineages exemplified by B. microti, B. duncani, C. felis, T. equi, Theileria sensu stricto (T. annulata, T. parva, and T. orientalis) and Babesia sensu stricto (B. bovis, B. bigemina, and B. ovis). C1A cysteine-proteinases (C1A-Cp) are papain-like enzymes implicated in pathogenic and vital steps of the parasite life cycle such as nutrition and host cell egress. An expansion of C1A-Cp of T. annulata and T. parva with respect to B. bovis and B. ovis was previously described. In the present work, C1A-Cp paralogs were identified in available genomes of species pertaining to each piroplasmid lineage. Phylogenetic analysis revealed eight C1A-Cp groups. The profile of C1A-Cp paralogs across these groups corroborates and defines the existence of six piroplasmid lineages. C. felis, T. equi and Theileria s.s. each showed characteristic expansions into extensive families of C1A-Cp paralogs in two of the eight groups. Underlying gene duplications have occurred as independent unique evolutionary events that allow distinguishing these three piroplasmid lineages. We hypothesize that C1A-Cp paralog families may be associated with the advent of the schizont stage. Differences in the invertebrate tick host specificity and/or mode of transmission in piroplasmid lineages might also be associated with the observed C1A-Cp paralog profiles.

1. Introduction

Piroplasmids are tick-transmitted obligatory hemoprotozoan parasites including species of the genus Babesia, Theileria, and Cytauxzoon. Many species are of veterinary significance, either due to their negative economic impact on livestock industries or due to the diseases they cause in pets and occasionally in wild life [1,2,3]. Examples of the former group include Babesia bovis and/or B. bigemina causing bovine babesiosis of cattle; Theileria annulata, Theileria parva, and Theileria orientalis that cause tropical theileriosis, East Coast Fever, and oriental theileriosis of cattle, respectively; and Babesia ovis causing ovine babesiosis of sheep [4,5,6,7,8]. Piroplasmids that infect companion animals include Cytauxzoon felis, the causative agent of feline cytauxzoonosis, and Theileria equi and Babesia caballi causing equine piroplasmosis [9,10,11,12]. In addition, a third group of piroplasmid species has been reported as pathogens of human babesiosis including B. microti, B. duncani, and B. venatorum, while B. divergens infects both cattle and humans [2,13,14,15,16].
Classical taxonomy distinguishes four piroplasmid genera based on morphology and/or biological characteristics of their life cycle history. (i) Babesia sensu stricto (s.s.) shows typically a transovarial transmission by Rhipicephalus or Hyalomma ticks; (ii) Theileria sensu stricto (s.s.) and (iii) Cytauxzoon spp. are typically transstadially transmitted, the former by Haemaphysalis and Hyalomma ticks and the latter by Dermacentor and Amblyomma ticks. In addition, Theileria and Cytauxzoon are characterized by the presence of an additional intraleukocytic schizont stage, which in Theileria is present in macrophages and T and B lymphocytes whereas in Cytauxzoon in mononuclear phagocytes. Finally, a fourth piroplasmid group is referred to as (iv) Babesia sensu lato (s.l.) which are commonly transmitted transstadially by ticks of the genus Ixodes but cannot be classified as Theileria (s.s.) since schizonts are absent [17,18,19].
Importantly, molecular phylogenetic analysis based on the 18S rRNA gene has been able to largely confirm the above outlined classical taxonomic units, yet could further refine and improve their relationship resulting in the definition of six piroplasmid genera [2,20]. Nearly complete agreement between classical taxonomy and molecular phylogeny has been shown for the Babesia s.s. and Theileria s.s. groups (Clades VI and V, respectively, as defined by Schnittger et al. [2]). It is however noteworthy that it could be shown that Theileria equi does not belong to Theileria s.s. but represents with B. bicornis a separate monophyletic group (Clade IV as defined by Schnittger et al. [2]), a finding that was subsequently confirmed by whole genome and mitochondrial gene analysis [21,22]. Furthermore, findings based on 18S rRNA phylogenetic analysis strongly suggests that the genus Cytauxzoon represents a monophyletic group that can be clearly delineated from Theileria s.s. (Clade IIIb as defined by Schnittger et al. [2]). However, using mitochondrial genes, Schreeg et al. [22] could integrate C. felis as sister group of Theileria s.s. into a single taxon with good support. By molecular phylogeny it was possible to show that Babesia s.l. parasites represent a paraphyletic group which is distantly related to Babesia s.s. and more closely related to Theileria and Cytauxzoon parasites. Furthermore, the Babesia s.l. group can be distinguished into at least two genera (Clade I and Clade II as defined by Schnittger et al. [2], Lack et al. [20], Schreeg et al. [22]). Meanwhile, it is worth noting that additional piroplasmid genera have been identified that are not considered in the present study as no genome sequences are available from species pertaining to these groups [23,24].
Cysteine proteinases (Cps) are involved in vital steps of the apicomplexan life cycle such as host cell invasion, egress, and parasite nutrition [25,26,27]. Papain-like cysteine peptidases designated as C1A family (C1 family of the Clan CA) attracted particular interest because of their involvement in pathogenic processes such as intracellular hemoglobin degradation and cytoskeletal rupture during host cell egress, as described for falcipain of Plasmodium falciparum [28,29,30].
C1A falcipain-homologs bovipain, ovipain, and babesipain of B. bovis, B. ovis, and B. bigemina, respectively, have been characterized [31,32,33,34]. Interestingly, whereas only a single bovipain and ovipain encoding gene is present in the B. bovis and B. ovis-genome, this gene has expanded in a gene family encoding six and seven paralogs in T. parva and T. annulata, respectively [31,35,36]. It has been suggested that the augmented copy number of falcipain-orthologs in T. annulata and T. parva reflects the biological differences of this piroplasmid lineage compared to B. bovis such as the distinct tick host specificity, transstadial vs. transovarial transmission, and presence vs. absence of the schizont parasite stage [36,37,38].
In this study, all C1A cysteine proteinases (C1A-Cp) were mined from available genomes of pathogenic Babesia, Theileria, and Cytauxzoon piroplasmids appertaining to Clades I to VI as defined by Schnittger et al. [2]. A phylogenetic tree was constructed to allocate C1A-Cp paralogs into different evolutionary groups (C1A-Cp Groups 1–8). We hypothesized that the profile of C1A-Cp paralogs across revealed evolutionary group is specific and corresponds with the phylogenetic classification of piroplasmids into Clades I to VI, as previously suggested.

2. Materials and Methods

The amino acid sequence of C1A family holotype, Peptidase_C1 (PF00112, Pfam), was used in a BLASTp search adjusting parameter settings to piroplasmid sequences (taxid:5863) and refseq database in order to identify homologs in completely sequenced genomes of piroplasmid species from B. bigemina strain BOND [39], B. bovis strain T2Bo [40], B. microti strain RI [41], T. annulata strain Ankara [42], T. equi strain WA [21], T. orientalis strain Shintoku [43], and T. parva strain Muguga, [44]. Since the C. felis genome is not available in the GenBank, corresponding C1A-Cp have been retrieved using a similar approach from the PiroplasmaDB database (C. felis strain Winnie [45]). In addition, C1A-Cp sequences of B. duncani and B. ovis have been retrieved by courtesy from as yet public unavailable genomes (B. duncani strain WA1: Choukri Ben Mamoun, Yale School of Medicine, New Haven, CT, USA; B. ovis strain Israel: William Weir, University of Glasgow, Glasgow, UK). Following the above described procedure, all sequence hits with an E-value < 0.05 were subsequently included in the study. The C1A-Cp proteinase domain of each sequence was determined either by MEROPS (http://merops.sanger.ac.uk) and/or Pfam (http://pfam.xfam.org) and then aligned using the MUSCLE algorithm. To eliminate end gaps, the alignment was finally truncated at its C and N terminal to a length of 315 aa. The phylogenetic tree was constructed using maximum likelihood based on the model LG [46]. Briefly, initial tree(s) for the heuristic search were obtained by applying the Neighbor-Joining method to a matrix of pairwise distances estimated using a JTT model. Then, the best evolutionary model, determined based on Akaike Information Criteria (AIC) as LG + G (G = 1.4880, estimated over five categories) was applied to infer the tree. The analysis involved eighty-three amino acid sequences, of which eighty-two belong to C1A-Cp of Babesia, Theileria, and Cytauxzoon spp., and falcipain-2 of P. falciparum was used as an outgroup. Altogether 1000 bootstrap replicates were carried out. Bootstrap values ≥80 were considered as highly significant. Alignment, model search, and tree construction was carried out using MEGA 6 [47]. Orthology was inferred by bidirectional best hits (BBH) in pairwise genome comparisons using pBLAST. However, as the C. felis, B. ovis and B. duncani genomes are not available in GenBank, BBH could not be carried out for these species.

3. Results and Discussion

3.1. Molecular Phylogeny Allows Subgrouping of Piroplasmid C1A Cysteine Proteinases

The aim of this work was to compare C1A-Cp homologs across genomes of well-defined and evolutionary diverse piroplasmid species to assess whether paralog numbers and variant profiles support current piroplasmid taxonomy.
A total of eighty-two cysteine proteinase-homologs (including orthologs and paralogs) of the subfamily C1A were identified in the ten studied piroplasmid genomes appertaining to six different evolutionary lineages (Table 1). Sixty-six of the eighty-two C1A-Cp displayed the conserved functional amino acids glutamine, cysteine, histidine, and asparagine at catalytic active sites, whereas fourteen showed substitutions and/or gaps at these positions representing enzymatically non-functional proteinase homologs. Based on the inferred phylogenetic tree, C1A-Cp could be divided in altogether eight groups designated, Groups 1–8 (Figure 1). In addition to the displayed maximum likelihood tree, a neighbor joining tree was also inferred resulting in similar groupings. Noteworthy these groupings are neither recognized by MEROPS nor by Pfam evidencing the sensitivity of our approach.

3.2. Molecular Phylogeny Provides Evidence for Independent Duplication Events of C1A-Cp in Different Piroplasmid Lineages

In the phylogenetic tree, at least four monophyletic lineages of CpA-Cp homologs are strongly supported that precede piroplasmid speciation (Figure 1). Group 1 consists of a single C1A-Cp of B. microti which segregates as sister to Group 2, although with a non-significant support. An analogous situation is observed for each B. microti C1A-Cp of Groups 4 and 6 which place as sisters in relation to Groups 5 and 7, respectively, likewise with a non-significant bootstrap. We consider each of the B. microti-C1A-Cp of Groups 1, 4, and 6 a group of their own, since they neither show a significant relation to each other nor to any other of the remaining groups. We consider that this observation reflects a loss of phylogenetic signal in these sequences supporting the ancient evolutionary relationship of B. microti (Clade I) to all other piroplasmid species of Clade II to VI, as has been reported previously [2,20,49]. As B. microti sequences were not included in the phylogenetic analysis of Martins et al. [36], corresponding groups do not appear in their study.
Interestingly, in Group 2, the C1A-Cp proteinase of C. felis (Clade IIIb) places with strong support as sister to T. annulata and T. orientalis (Theileria s.s., Clade V) sequences. A truncated C1A-Cp of T. parva has not been included in the tree analysis, while C1A-Cp of other piroplasmid species might have gone lost in this group. This group is related with the SERA Cp-family from P. falciparum of which some members have serine instead cysteine in the active site [50].
Except for B. microti, Group 3 includes C1A-Cp of all studied piroplasmid species and is very well supported. C1A-Cps of this group represent orthologs as confirmed by BBH and should be thus suitable to verify the phylogenetic relationship between these species. Importantly, C1A-Cps of B. duncani (Clade II), C. felis (Clade IIIb), T. equi (Clade IV), and Theileria s.s. parasites (Clade V) endorse the phylogenetic relation as established by Schnittger et al. [2] with strong support. However, the placement of Babesia s.s. proteinases (Group 3a, Clade VI) as sister group with respect to C. felis (Clade IIIb), T. equi (Clade IV), and Theileria s.s. parasites (Clade V) (Group 3b) seems to be incidental and is not supported. Interestingly, C1A-Cp of T. annulata (XP952571) and T. parva (XP764709) show serine instead of cysteine in their active site as has been also reported for some SERA proteins of P. falciparum [36,50]. The proteinases of this subgroup belong to the cathepsin L-like Cps.
Group 5 C1A-Cp are of the cathepsin C type and segregate with a strong bootstrap support. Subgroup 5a includes C1A-Cp of all studied species but B. microti. As expected, cysteine proteinases of Theileria s.s. parasites (Clade V) place as sister taxon with regard to Babesia s.s. (Clade VI) group, whereas the placement of C. felis (Clade IIIb) and T. equi (Clade IV) is unsupported.
Exclusively, Subgroup 5b includes C1A-Cp orthologs of all ten studied piroplasmids. The tree placement of C1A-Cp of B. microti (Clade I), C. felis (Clade IIIb), T. equi (Clade IV), and Theileria s.s. parasites (Clade V) agrees with the phylogenetic relation as proposed by Schnittger et al. [2]. However, the position of T. equi (Clade IV) and B. duncani (Clade II) are not supported. Thus, not surprisingly, the segregation of B. duncani as sister to Babesia s.s. (Clade VI) disagrees with the commonly accepted placement of this species. C1A-Cp proteinases of Subgroups 5a and 5b represent out-paralogs with regard to each other as duplication has preceded speciation (Table 2).
C1A-Cp of Group 7 include families of eight, two, three, and five paralogs in T. equi (Clade IV), T. annulata, T. parva, and T. orientalis (Theileria s.s., Clade V) genomes, respectively, whereas C1A-Cp members of B. bovis, B. ovis, and B. duncani have been lost. Possibly due to multiple events of gene duplication and loss in this sequence group, current evolutionary lineages of some single sequences such as B. bigemina (XP_012766037), T. equi (XP004828646), and C. felis (CF003226) are difficult to interpret based on their tree segregation and low support (Group 7). C1A-Cp within Subgroup 7a and T. orientalis XP_009690114, T. annulata XP_952609, and T. parva XP_764667 within Subgroup 7c represent co-orthologs. Remarkably, after speciation into T. equi multiple duplication events have resulted in an extensive in-paralog group of altogether seven C1A-Cp (Subgroup 7b). This gene amplification seems to have occurred as a single unique event in this piroplasmid species which strongly supports its classification separate from Theileria s.s. Likewise, multiple duplication events in T. orientalis resulted in a group of at least four paralogs (Subgroup 7c). Most likely, T. orientalis proteinases XP_009692826 and the lineage resulting in XP_009690114/XP_009690115 have arisen prior to speciation and resulted therefore in the generation of three out-paralogs in T. orientalis with respect to orthologs XP_952609 of T. annulata, XP_764667 of T. parva, and XP_009690114 of T. orientalis. In contrast, C1A-Cp pairs of T. parva (XP_764667/XP_764668) and of T. orientalis (XP_009690114/XP_009690115) represent in-paralogs that have generated after speciation. In addition, C1A-Cps of Group 7, similar to those of Groups 3 and 8 discussed in the following, are of the cathepsin L-like type.
Group 8 is well supported and consists of three monophyletic C1A-Cp lineages. Contrary to the expected, the well supported Babesia s.s. (Clade VI) sequences (Subgroup 8a), which include ovipain-2 of B. ovis and bovipain-2 of B. bovis, place as a sister with respect to the remaining proteinases of Group 8 (Subgroup 8a). Notably, however, the position of the C1A-Cp of B. duncani as a sister of this grouping is not supported. Three paralogs of C. felis (Subgroup 8b) represent a sister group to T. equi (Clade IV) and Theileria s.s. (Clade V) sequences (Subgroup 8c). Most likely, C1A proteinases of C. felis (Clade IIIb) have expanded to a family of three in-paralogs after the split of this lineage from T. equi (Clade IV) and Theileria s.s. (Clade V). C1A cysteine proteinases of T. equi (Clade IV) but in particular those of Theileria s.s. (Clade V) species T. annulata, T. parva, and T. orientalis have greatly expanded into three, seven, six, and six C1A paralog families, respectively (Subgroup 8c). The C1A proteinase family of T. equi represent in-paralogs that have generated after the split of this species from Theileria s.s. (Subgroup 8c). Based on the observed segregation pattern of T. annulata, T. parva, and T. orientalis C1A-Cp, the underlying gene duplication events most likely happened before speciation in their most recent common ancestor (MRCA). This strongly suggests that the respective C1A-Cp-encoding gene family has been inherited by the descendants of all Theileria s.s. parasites and presents a common feature of this group. Thus, in accordance with genome homology nomenclature, each member of a protein family of a given species (e.g., T. annulata) represents an out-paralog to any of the other protein family members of the remaining two species (e.g., T. parva and T. orientalis). The above interpretation is also supported by synteny studies of the respective T. annulata, T. parva, and T. orientalis genome regions [31,35,37,38]. The unique evolution of the C1A-Cp family of Theileria s.s. seems to be a characteristic hallmark of this parasite genus that might have been crucial for their evolutionary radiation [51]. In summary, independent and characteristic C1A proteinase duplication events distinguish and define the T. equi and the C. felis groups from each other but also from Theileria s.s., supporting their classification into three evolutionary lineages and taxonomic entities. Furthermore, altogether eight subgroups of C1A-Cp proteinase paralogs could be distinguished, of which the five Groups 2, 3, 5, 7, and 8, were highly significantly supported. Group 2 comprises cysteine proteinases of the SERA-like family, whereas Groups 3, 7, and 8 and Group 5 comprise cysteine proteinases of the cathepsin L and cathepsin C-like family, respectively. In addition, Groups 1, 4, and 6 correspond to three C1A-Cp proteinases of B. microti whose assignment to other groups could not be supported reflecting the relatively distant evolutionary relation of B. microti with respect to the other piroplasmid lineages included in the study.
Recently, a molecular phylogenetic analysis using concatenated mitochondrial genes cytb, cox1, and cox3 and the 18S rRNA gene could integrate C. felis with Theileria s.s. into a single monophyletic group. In addition, synteny of mitochondrial genomes of C. felis corresponded with those of Theileria s.s. and Babesia s.s. Furthermore, in the inferred tree, T. equi represents a sister group with respect to a clade comprised of C. felis and Theileria s.s. and a clade of Babesia s.s. [22]. This is in contrast to the present phylogenetic analysis in which C. felis-C1A-Cp segregate commonly with a high bootstrap support as a sister taxon with regard to sequences of T. equi and Theileria s.s. (see Group 2 and Subgroups 3b, 5b, 7b, and 8b), and, whenever other placements are observed, they remain unsupported (Groups 5a). Furthermore, T. equi commonly places as sister with regard to Theileria s.s. (Subgroups 3b, 5a, 5b, 7b/c, and 8c), although this position is only supported in a single case (Subgroup 3b). All in all, our findings strongly support C. felis as a sister group of T. equi and Theileria s.s., rather than T. equi as a sister group of C. felis and Theileria s.s., corresponding with previous studies [2]. This analysis also suggests that cysteine proteinase sequences may aid in the phylogenetic inference particularly of more closely related piroplasmid species and/or groups.

3.3. C1A Cysteine Proteinase Profiles Characterize Piroplasmid Lineages

A synopsis of the allocation of identified C1A cysteine-proteinases to C1A groups and piroplasmids is shown in Table 2. By far, the highest number of C1A-Cp paralogs was found in T. equi (n = 13), T. annulata (n = 13), T. parva (n = 13), and T. orientalis (n = 15), followed by C. felis, which also presents a relatively high number of C1A-Cp paralogs (n = 8). In contrast, the analyzed Babesia parasites account for a lower number of 3–5 paralogs. Characteristic C1A-Cp group profiles allow distinguishing between the different piroplasmid Clades I to VI. In the case of B. microti (Clade I), three of four C1A-Cp are unique and have no orthologs in any other piroplasmid species. B. duncani (Clade II) exhibits only a single C1A-Cp in Groups 3, 5, and 8. C. felis (Clade IIIb) displays, together with T. equi (Clade IV) and Theileria s.s. (Clade V), C1A-Cps in Groups 3, 5, 7, and 8, while a C1A-Cp in Group 2 is exclusively found in C. felis and Theileria s.s. In Group 8 of C. felis (Clade IIIb) and T. equi (Clade IV), a moderate expansion into three paralogs is observed. In addition, T. equi (Clade IV) presents a conspicuously increased number of eight paralogs in Group 7. All studied Theileria s.s exhibit characteristic C1A expansions of 2–5 paralogs in Group 7, and of 6–7 paralogs in Group 8. Finally, exclusively in Babesia s.s. a single C1A-Cp is found in Group 3 and 8, and a C1A paralog pair in Group 5. The observation that similar C1A paralog profiles repeat in T. annulata, T. parva, and T. orientalis of Theileria s.s. (Clade V) and in B. ovis, B. bovis, and B. bigemina of Babesia s.s. (Clade VI) suggests that they constitute suitable taxonomic genome markers for the respective groups.
It is noticeable that C. felis, T. equi, and Theileria s.s., which are all characterized by the possession of a schizont stage, jointly exhibit a moderate (C. felis) to extreme (T. equi and Theileria s.s.) expansion of C1A-Cp paralogs. We cautiously suggest that this might be functionally associated with the evolution of the schizont stage. Alternatively, different tick host specificity and/or mode of transmission might also be associated with the observed C1A-Cp paralog profiles. Future investigations including gene knockout studies might be able to shed light on the hypothesized functional associations.

Acknowledgments

Financial support from the National Research Council (CONICET), the National Institute of Technological Agriculture (INTA, PNBIO 1131034) and the Ministerio de Ciencia, Tecnologia y Innovación Productiva (MinCyT, PICT-2013-1249), Argentina, are gratefully acknowledged.

Author Contributions

Leonhard Schnittger conceived and designed the experiments; Mariano E. Ascencio performed the experiments; Leonhard Schnittger and Mariano E. Ascencio analyzed the data; Choukri B. Mamoun William Weir and Brian Shiels contributed reagents/materials/analysis tools; and Leonhard Schnittger, Mariano E. Ascencio and Monica Florin-Christensen wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Rodriguez, A.E.; Schnittger, L.; Tomazic, M.L.; Florin-Christensen, M. Current and prospective tools for the control of cattle-infecting Babesia parasites. In Protozoa: Biology, Classification and Role in Disease; Castillo, V., Harris, R., Eds.; Nova Publishers: Hauppauge, NY, USA, 2013; pp. 1–44. ISBN 9781624170720. [Google Scholar]
  2. Schnittger, L.; Rodriguez, A.E.; Florin-Christensen, M.; Morrison, D.A. Babesia: A world emerging. Infect. Genet. Evol. 2012, 12, 1788–1809. [Google Scholar] [CrossRef] [PubMed]
  3. Florin-Christensen, M.; Suarez, C.E.; Rodriguez, A.E.; Flores, D.A.; Schnittger, L. Vaccines against bovine babesiosis: Where we are now and possible roads ahead. Parasitology 2014, 28, 1–30. [Google Scholar] [CrossRef] [PubMed]
  4. Weber, G.; Friedhoff, K. Lichtmikroskopische Untersuchungen ueber die Entwicklung yon Babesia ovis (Piroplasmidea) in Rhipicephalus bursa (Ixodoidea). Z. Parasitenk 1971, 35, 218–233. [Google Scholar] [CrossRef] [PubMed]
  5. Bock, R.; Jackson, L.; De Vos, A.; Jorgensen, W. Babesiosis of cattle. Parasitology 2004, 129, S247–S269. [Google Scholar] [CrossRef] [PubMed]
  6. Mans, B.J.; Pienaar, R.; Latif, A.A. A Review of Theileria diagnostics and epidemiology. Int. J. Parasitol. 2014, 4, 104–118. [Google Scholar] [CrossRef] [PubMed]
  7. Ganzinelli, S.; Rodriguez, A.; Schnittger, L.; Florin-Christensen, M. Babesia in Domestic Ruminants. In Parasitic Protozoa of Farm Animals and Pets, 1st ed.; Florin-Christensen, M., Schnittger, L., Eds.; Springer: Heidelberg, Germany, 2018; ISBN 3319701312. [Google Scholar]
  8. Kiara, H.; Steinaa, L.; Vishvanath, N.; Svitek, N. Theileria in ruminants. In Parasitic Protozoa of Farm Animals and Pets, 1st ed.; Florin-Christensen, M., Schnittger, L., Eds.; Springer: Heidelberg, Germany, 2018; ISBN 3319701312. [Google Scholar]
  9. Mehlhorn, H.; Schein, E. Redescription of Babesia equi Laveran, 1901 as Theileria equi Mehlhorn, Schein 1998. Parasitol. Res. 1998, 84, 467–475. [Google Scholar] [CrossRef] [PubMed]
  10. Nietfeld, J.C.; Pollock, C. Fatal cytauxzoonosis in a free-ranging Bobcat (Lynx rufus). J. Wildl. Dis. 2002, 38, 607–610. [Google Scholar] [CrossRef] [PubMed]
  11. Wang, J.L.; Li, T.T.; Liu, G.H.; Zhu, X.Q.; Yao, C. Two tales of Cytauxzoon felis infections in domestic cats. Clin. Microbiol. Rev. 2017, 30, 861–885. [Google Scholar] [CrossRef] [PubMed]
  12. Ueti, M.W.; Knowles, D.P. Equine Piroplasmids. In Parasitic Protozoa of Farm Animals and Pets, 1st ed.; Florin-Christensen, M., Schnittger, L., Eds.; Springer: Heidelberg, Germany, 2018; ISBN 3319701312. [Google Scholar]
  13. Dammin, G.J.; Spielman, A. The rising incidence of clinical Babesia microti infection. Hum. Pathol. 1981, 12, 1979–1981. [Google Scholar] [CrossRef]
  14. Conrad, P.A.; Kjemtrup, A.M.; Carreno, R.A.; Thomford, J.; Wainwright, K.; Eberhard, M.; Quick, R.; Telford, S.R.; Herwaldt, B.L. Description of Babesia duncani sp. nov. (Apicomplexa: Babesiidae) from humans and its differentiation from other piroplasms. Int. J. Parasitol. 2006, 36, 779–789. [Google Scholar] [CrossRef] [PubMed]
  15. Yabsley, M.J.; Shock, B.C. Natural history of zoonotic Babesia: Role of wildlife reservoirs. Int. J. Parasitol. Parasites Wildl. 2013, 2, 18–31. [Google Scholar] [CrossRef] [PubMed]
  16. Baneth, G.; Florin-Christensen, M.; Cardoso, L.; Schnittger, L. Reclassification of Theileria annae as Babesia vulpes sp. nov. Parasite Vector 2015, 8, 207. [Google Scholar] [CrossRef] [PubMed]
  17. Mehlhorn, H.; Schein, E.; Ahmed, J.S. Theileria. In Parasitic Protozoa; Kreier, J.P., Ed.; Academic Press: San Diego, CA, USA, 1994; pp. 217–304. ISBN 0123960339. [Google Scholar]
  18. Reichard, M.V.; Van Den Bussche, R.A.; Meinkoth, J.H.; Hoover, J.P.; Kocan, A.A. A New species of Cytauxzoon from Pallas’ Cats caught in Mongolia and comments on the systematics and taxonomy of piroplasmids. J. Parasitol. 2005, 91, 420–426. [Google Scholar] [CrossRef] [PubMed]
  19. Uilenberg, G. Babesia-a historical overview. Vet. Parasitol. 2006, 138, 3–10. [Google Scholar] [CrossRef] [PubMed]
  20. Lack, J.B.; Reichard, M.V.; Van Den Bussche, R.A. Phylogeny and evolution of the piroplasmida as inferred from 18S rRNA sequences. Int. J. Parasitol. 2012, 42, 353–363. [Google Scholar] [CrossRef] [PubMed]
  21. Kappmeyer, L.S.; Thiagarajan, M.; Herndon, D.R.; Ramsay, J.D.; Caler, E.; Djikeng, A.; Gillespie, J.J.; Lau, A.O.; Roalson, E.H.; Silva, J.C.; et al. Comparative genomic analysis and phylogenetic position of Theileria equi. BMC Genom. 2012, 13, 603. [Google Scholar] [CrossRef] [PubMed]
  22. Schreeg, M.E.; Marr, H.S.; Tarigo, J.L.; Cohn, L.A.; Bird, D.M.; Scholl, E.H.; Levy, M.G.; Wiegmann, B.M.; Birkenheuer, A.J. Mitochondrial genome sequences and structures aid in the resolution of piroplasmida phylogeny. PLoS ONE 2016, 11, e0165702. [Google Scholar] [CrossRef] [PubMed]
  23. Paparini, A.; Macgregor, J.; Ryan, U.M.; Irwin, P.J. First molecular characterization of Theileria ornithorhynchi Mackerras, 1959: Yet another challenge to the systematics of the piroplasms. Protist 2015, 166, 609–620. [Google Scholar] [CrossRef] [PubMed]
  24. Yabsley, M.J.; Vanstreels, R.E.T.; Shock, B.C.; Purdee, M.; Horne, E.C.; Peirce, M.A.; Parsons, N.J. Molecular characterization of Babesia peircei and Babesia ugwidiensis provides insight into the evolution and host specificity of avian piroplasmids. Int. J. Parasitol. Parasites Wildl. 2017, 24, 257–264. [Google Scholar] [CrossRef] [PubMed]
  25. Klemba, M.; Goldberg, D.E. Biological roles of proteases in parasitic protozoa. Annu. Rev. Biochem. 2002, 71, 275–305. [Google Scholar] [CrossRef] [PubMed]
  26. Kim, K. Role of proteases in host cell invasion by Toxoplasma gondii and other Apicomplexa. Acta Trop. 2004, 91, 69–81. [Google Scholar] [CrossRef] [PubMed]
  27. Cowman, A.F.; Crabb, B.S. Invasion of red blood cells by malaria parasites. Cell 2006, 124, 755–766. [Google Scholar] [CrossRef] [PubMed]
  28. Hanspal, M.; Dua, M.; Takakuwa, Y.; Chishti, A.H.; Mizuno, A. Plasmodium falciparum cysteine protease falcipain-2 cleaves erythrocyte membrane skeletal proteins at late dtages of parasite fevelopment. Blood 2002, 100, 1048–1054. [Google Scholar] [CrossRef] [PubMed]
  29. Sijwali, P.S.; Rosenthal, P.J. Gene disruption confirms a critical role for the cysteine protease falcipain-2 in hemoglobin hydrolysis by Plasmodium falciparum. Proc. Natl. Acad. Sci. USA 2004, 101, 4384–4389. [Google Scholar] [CrossRef] [PubMed]
  30. Li, H.; Child, M.A.; Bogyo, M. Proteases as regulators of pathogenesis: Examples from the Apicomplexa. Biochim. Biophys. Acta (BBA)-Proteins Proteom. 2012, 1824, 177–185. [Google Scholar] [CrossRef] [PubMed]
  31. Mesplet, M.; Echaide, I.; Dominguez, M.; Mosqueda, J.J.; Suarez, C.E.; Schnittger, L.; Florin-Christensen, M. Bovipain-2, the falcipain-2 ortholog, is expressed in intraerythrocytic stages of the tick-transmitted hemoparasite Babesia bovis. Parasite Vector 2010, 3, 113. [Google Scholar] [CrossRef] [PubMed]
  32. Carletti, T.; Barreto, C.; Mesplet, M.; Mira, A.; Weir, W.; Shiels, B.; Gonzalez Oliva, A.; Schnittger, L.; Florin-Christensen, M. Characterization of a papain-like cysteine protease essential for the survival of Babesia ovis merozoites. Ticks Tick-Borne Dis. 2016, 7, 85–93. [Google Scholar] [CrossRef] [PubMed]
  33. Martins, T.M.; Gonçalves, L.M.; Capela, R.; Moreira, R.; do Rosário, V.E.; Domingos, A. Effect of synthesized inhibitors on babesipain-1, a new cysteine protease from the bovine piroplasm Babesia bigemina. Transbound. Emerg. Dis. 2010, 57, 68–69. [Google Scholar] [CrossRef] [PubMed]
  34. Martins, T.M.; do Rosário, V.E.; Domingos, A. Expression and characterization of the Babesia bigemina cysteine protease BbiCPL1. Acta Trop. 2012, 121, 1–5. [Google Scholar] [CrossRef] [PubMed]
  35. Sajid, M.; Blackman, M.J.; Doyle, P.; He, C.; Land, K.M.; Lobo, C.; Mackey, Z.; Ndao, M.; Reed, S.L.; Shiels, B.; et al. Proteases of Parasitic Protozoa–Current Status and Validation. In Antiparasitic and Antibacterial Drug Discovery: From Molecular Targets to Drug Candidates, 1st ed.; Selzer, P.M., Ed.; Wiley-VCH: Weinheim, Germany, 2009; pp. 190–197. ISBN 3527323279. [Google Scholar]
  36. Martins, T.M.; do Rosário, V.E.; Domingos, A. Identification of papain-like cysteine proteases from the bovine piroplasm Babesia bigemina and evolutionary relationship of piroplasms C1 family of cysteine proteases. Exp. Parasitol. 2011, 127, 184–194. [Google Scholar] [CrossRef] [PubMed]
  37. Schnittger, L.; Mesplet, M.; Florin-Christensen, M. Proteinases of piroplasmid bovine pathogens: Comparative genomic analysis of Babesia bovis and Theileria annulata. In Proceedings of the International Conference of International Congress of Parasitology (ICOPA), Mexico City, Mexico, 10–15 August 2014. [Google Scholar]
  38. Poklepovich, T.J.; Mesplet, M.; Florin-Christensen, M.; Schnittger, L. Comparative degradome analysis of the bovine piroplasmid pathogens Babesia bovis and Theileria annulata. 2018; (unpublished data). [Google Scholar]
  39. Jackson, A.P.; Otto, T.D.; Darby, A.; Ramaprasad, A.; Xia, D.; Echaide, I.E.; Farber, M.; Gahlot, S.; Gamble, J.; Gupta, D.; et al. The evolutionary dynamics of variant antigen genes in Babesia reveal a history of genomic innovation underlying host-parasite interaction. Nucleic Acids Res. 2014, 42, 7113–7131. [Google Scholar] [CrossRef] [PubMed]
  40. Brayton, K.A.; Lau, A.O.; Herndon, D.R.; Hannick, L.; Kappmeyer, L.S.; Berens, S.J.; Bidwell, S.L.; Brown, W.C.; Crabtree, J.; Fadrosh, D.; et al. Genome sequence of Babesia bovis and comparative analysis of apicomplexan hemoprotozoa. PLoS Pathog. 2007, 3, 1401–1413. [Google Scholar] [CrossRef] [PubMed]
  41. Silva, J.C.; Cornillot, E.; McCracken, C.; Usmani-Brown, S.; Dwivedi, A.; Ifeonu, O.O.; Crabtree, J.; Gotia, H.T.; Virji, A.Z.; Reynes, C.; et al. Genome-wide diversity and gene expression profiling of Babesia microti isolates identify polymorphic genes that mediate host-pathogen interactions. Sci. Rep. 2016, 6, 352–384. [Google Scholar] [CrossRef] [PubMed]
  42. Pain, A.; Renauld, H.; Berriman, M.; Murphy, L.; Yeats, C.A.; Weir, W.; Kerhornou, A.; Aslett, M.; Bishop, R.; Bouchier, C.; et al. Genome of the host-cell transforming parasite Theileria annulata compared with T. parva. Science 2005, 309, 131–133. [Google Scholar] [CrossRef] [PubMed]
  43. Hayashida, K.; Hara, Y.; Abe, T.; Yamasaki, C.; Toyoda, A.; Kosuge, T.; Suzuki, Y.; Sato, Y.; Kawashima, S.; Katayama, T.; et al. Comparative genome analysis of three eukaryotic parasites with differing abilities to transform leukocytes reveals key mediators of Theileria-induced leukocyte transformation. MBio 2012, 3, e00204-12. [Google Scholar] [CrossRef] [PubMed]
  44. Gardner, M.J.; Bishop, R.; Shah, T.; de Villiers, E.P.; Carlton, J.M.; Hall, N.; Ren, Q.; Paulsen, I.T.; Pain, A.; Berriman, M.; et al. Genome sequence of Theileria parva, a bovine pathogen that transforms lymphocytes. Science 2005, 309, 134–137. [Google Scholar] [CrossRef] [PubMed]
  45. Tarigo, J.L.; Scholl, E.H.; McK Bird, D.; Brown, C.C.; Cohn, L.A.; Dean, G.A.; Levy, M.G.; Doolan, D.L.; Trieu, A.; Nordone, S.K.; et al. A novel candidate vaccine for cytauxzoonosis inferred from comparative apicomplexan genomics. PLoS ONE 2013, 8, e71233. [Google Scholar] [CrossRef]
  46. Le, S.Q.; Gascuel, O. An Improved General Amino Acid Replacement Matrix. Mol. Biol. Evol. 2008, 25, 1307–1320. [Google Scholar] [CrossRef] [PubMed]
  47. Tamura, K.; Stecher, G.; Peterson, D.; Filipski, A.; Kumar, S. MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0. Mol. Biol. Evol. 2013, 30, 2725–2729. [Google Scholar] [CrossRef] [PubMed]
  48. Bajer, A.; Alsarraf, M.; Bednarska, M.; Mohallal, E.M.; Mierzejewska, E.J.; Behnke-Borowczyk, J.; Zalat, S.; Gilbert, F.; Welc-Falęciak, R. Babesia behnkei sp. nov.; a novel Babesia species infecting isolated populations of Wagner’s gerbil, Dipodillus dasyurus, from the Sinai Mountains, Egypt. Parasite Vector 2014, 7, 572. [Google Scholar] [CrossRef] [PubMed]
  49. Criado-Fornelio, A.; Martinez-Marcos, A.; Buling-Saraña, A.; Barba-Carretero, J.C. Molecular Studies on Babesia, Theileria and Hepatozoon in Southern Europe: Part II. Phylogenetic Analysis and Evolutionary History. Vet. Parasitol. 2003, 114, 173–194. [Google Scholar] [CrossRef]
  50. Hodder, A.N.; Drew, D.R.; Epa, V.C.; Delorenzi, M.; Bourgon, R.; Miller, S.K.; Moritz, R.L.; Frecklington, D.F.; Simpson, R.J.; Speed, T.P.; et al. Enzymic, phylogenetic, and structural characterization of the unusual papain-like protease domain of Plasmodium falciparum SERA5. J. Biol. Chem. 2003, 278, 48169–48177. [Google Scholar] [CrossRef] [PubMed]
  51. Schnittger, L.; Yin, H.; Gubbels, M.J.; Beyer, D.; Niemann, S.; Jongejan, F.; Ahmed, J.S. Phylogeny of sheep and goat Theileria and Babesia parasites. Parasitol. Res. 2003, 91, 398–406. [Google Scholar] [PubMed]
Figure 1. Maximum likelihood tree of C1A proteinase amino acid domains of Babesia, Theileria, and Cytauxzoon parasites. Each C1A cysteine proteinase sequence is designated with the corresponding piroplasmid species and accession number. Numbers 1–8 designate revealed C1A cysteine proteinase Groups 1–8. OG, outgroup. Bootstrap values based on 1000 replicates are displayed next to the branches.
Figure 1. Maximum likelihood tree of C1A proteinase amino acid domains of Babesia, Theileria, and Cytauxzoon parasites. Each C1A cysteine proteinase sequence is designated with the corresponding piroplasmid species and accession number. Numbers 1–8 designate revealed C1A cysteine proteinase Groups 1–8. OG, outgroup. Bootstrap values based on 1000 replicates are displayed next to the branches.
Vetsci 05 00041 g001
Table 1. Babesia, Theileria, and Cytauxzoon parasites included in this study and their classical taxonomy, molecular phylogeny, common designation, diseases, and geographic distribution.
Table 1. Babesia, Theileria, and Cytauxzoon parasites included in this study and their classical taxonomy, molecular phylogeny, common designation, diseases, and geographic distribution.
SpeciesClassic Taxonomy3 Phylogenetic CladeCommon DesignationDiseasesGeographic Distribution
B. microtiBabesia s.l.IB. microti-grouphuman babesiosisUSA, Europe, Japan,
B. duncani II4 western cladehuman babesiosisUSA
1T. bicornis IIIaTheileria s.l.n.d.Africa
C. felisCytauxzoonIIIbCytauxzoonfeline cytauxzoonosisUSA
T. equi2Theileria s.s.IV5T. equi6 equine piroplasmosistropical and subtropical regions worldwide
T. annulata
T. parva
T. orientalis
Theileria s.s.Vtrue Theileriatropical theileriosis
East Coast Fever
oriental theileriosis
tropical and subtropical regions of the old world
East Africa
Asia
B. bovis
B. bigemina
B. ovis
Babesia s.s.VItrue Babesia7 bovine babesiosis
ovine babesiosis
tropical and subtropical regions worldwide
1 No sequenced genome is available for any species of Clade IIIa but for the sake of completeness T. bicornis has been included in this table; 2 T. equi has been described by classical taxonomy as Theileria s.s. [9]; 3 Clades are designated as defined by Schnittger et al. [2]; 4 Piroplasmid species that place in this clade have now also been described in other geographic regions besides the US western states Washington and California [48]; 5 T. equi segregates with B. bicornis in a single Clade IV; 6 The disease referred to as equine piroplasmosis is caused by infection with T. equi and/or B. caballi; 7 bovine babesiosis is caused by infection with B. bovis and/or B. bigemina. n.d., no data available.
Table 2. Assignment of C1A cysteine proteinase sequences to Babesia, Theileria, and Cytauxzoon species and clades.
Table 2. Assignment of C1A cysteine proteinase sequences to Babesia, Theileria, and Cytauxzoon species and clades.
2 C1A-Cp Group1 Piroplasmid Clade
IIIIIIbIVVVI
B. microtiB. duncaniC. felisT. equiT. annulataT. parvaT. orientalisB. ovisB. bovisB. bigemina
1XP_012650559
2 CF000928 XP_9532433 XP_764233XP_009692255
3 BdWA1_II1487CF001943XP_004828689XP_952571XP_764709XP_009690157ALJ75577XP_001612131XP_012766088
4XP_012647584
5XP_021338611BdWA1_III2972CF001234XP_004832347XP_955044XP_763377XP_009691533ALJ75578XP_001609546XP_012768370
CF003813XP_004832939XP_951829XP_765451XP_009690911ALJ75579XP_001608716XP_012768246
6XP_012647628
7 CF003226XP_004828646XP_952610XP_764666XP_009690112
XP_004828875XP_952609XP_764667XP_009690113 XP_012766037
XP_004830320 XP_764668XP_009690114
XP_004831551 XP_009690115
XP_004831655 XP_009692826
XP_004831668
XP_004833425
XP_004833462
8 BdWA1_III3014CF002922XP_004830368XP_954970XP_763298XP_009691605ALJ75576XP_001610695XP_012769730
CF003554XP_004832412XP_954972XP_763299XP_009691603
CF000752XP_004833381XP_954973XP_763300XP_009691602
XP_954974XP_763301XP_009691601
XP_954976XP_763303XP_009691599
XP_954975XP 763302XP_009691600
XP_954971
∑ 8343813131315445
1 Piroplasmid lineages are designated as defined by Schnittger et al. [2] by roman numbers. 2 C1A proteinase groups are designated according to those identified in the phylogenetic tree of Figure 1. 3 This C1A proteinase has not been included in the phylogenetic tree since it is truncated but could be confirmed by BBH. C1A proteinases framed blue and green represent in- and out-paralogs, respectively. C1A proteinases designated by an underlined accession numbers within a line represent orthologs as identified either by BBH or by tree analysis with respect to C1A proteinases designated with a bold accession number. C1A proteinases in italics represent non-functional proteinase homologs that exhibit incomplete or exchanged amino acids at active sites.

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Ascencio, M.E.; Florin-Christensen, M.; Mamoun, C.B.; Weir, W.; Shiels, B.; Schnittger, L. Cysteine Proteinase C1A Paralog Profiles Correspond with Phylogenetic Lineages of Pathogenic Piroplasmids. Vet. Sci. 2018, 5, 41. https://doi.org/10.3390/vetsci5020041

AMA Style

Ascencio ME, Florin-Christensen M, Mamoun CB, Weir W, Shiels B, Schnittger L. Cysteine Proteinase C1A Paralog Profiles Correspond with Phylogenetic Lineages of Pathogenic Piroplasmids. Veterinary Sciences. 2018; 5(2):41. https://doi.org/10.3390/vetsci5020041

Chicago/Turabian Style

Ascencio, Mariano E., Monica Florin-Christensen, Choukri B. Mamoun, William Weir, Brian Shiels, and Leonhard Schnittger. 2018. "Cysteine Proteinase C1A Paralog Profiles Correspond with Phylogenetic Lineages of Pathogenic Piroplasmids" Veterinary Sciences 5, no. 2: 41. https://doi.org/10.3390/vetsci5020041

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