Abstract
Background
Trypanosoma equiperdum causes dourine via sexual transmission in Equidae. T. equiperdum is classified under the subgenus Trypanozoon along with the T. brucei sspp. and T. evansi; however, the species classification of Trypanozoon remains a controversial topic due to the limited number of T. equiperdum reference strains. In addition, it is possible that some were misclassified T. evansi strains. Thus, there is a strong need for a new T. equiperdum strain directly isolated from the genital mucosa of a horse with a clinically- and parasitologically-confirmed dourine infection.
Methods
Trypanosomes isolated from the urethral tract of a stallion with suspected dourine, were directly cultivated using soft agarose media at 37 °C in 5 % CO2. For molecular characterization, 18S ribosomal RNA (rRNA) gene, the internal transcribed spacer (ITS) and 8 maxicircle DNA regions were amplified by a PCR and their sequences were determined. To analyze the ratio of the kinetoplastic/akinetoplastic population, the kinetoplasts and the nuclei of trypanosomes were subjected to Hoechst staining and observed by fluorescence microscopy.
Results
In addition to the clinical symptoms and the molecular diagnosis, this stallion was definitively diagnosed with dourine by the detection of trypanosomes in the urethral mucosa. These results strongly suggested that the isolated trypanosome was true T. equiperdum. T. equiperdum isolated from the urethral tract was adapted in vitro using soft agarose media. Based on the results of a phylogenetic analysis of 18S rRNA and ITS, this T. equiperdum isolate was classified into the Trypanozoon clade. In a PCR of the maxicircle DNA region, only NADH-dehydrogenase subunits 4 and 5 was amplified. Clear kinetoplasts were observed in most of the T. equiperdum isolates. In contrast, most culture-adapted T. equiperdum were of the akinetoplastic form.
Conclusion
We concluded that our isolated trypanosome was the first confirmed case of T. equiperdum in Mongolia and named it “T. equiperdum IVM-t1”. T. equiperdum IVM-t1 was well adapted and propagated in soft agarose media, which indicates that this culture method is useful for isolation of T. equiperdum from horses with dourine.
Electronic supplementary material
The online version of this article (doi:10.1186/s13071-016-1755-3) contains supplementary material, which is available to authorized users.
Keywords: Dourine, In vitro culture, Maxicircle DNA, Mongolia, Soft agarose media, Trypanosoma equiperdum
Background
Dourine is caused by Trypanosoma equiperdum of the subgenus Trypanozoon. Unlike other trypanosomes, dourine is not transmitted by insect vectors; rather, it is transmitted by the infected horse via coitus. Thus, dourine has previously been distributed worldwide [1].
Subgenus Trypanozoon includes three subspecies of T. brucei. (T. brucei brucei, T. b. gambiense and T. b. rhodesiense), T. evansi and T. equiperdum. T. brucei, T. evansi and T. equiperdum have been classified based on their kinetoplast DNA (kDNA) components: T. brucei contains complete maxicircle kDNA, T. evansi completely lacks maxicircle kDNA, while the integrity of the maxicircle kDNA of T. equiperdum varies in each strain. Nevertheless, its classification within the subgenus Trypanozoon remains a controversial topic because it has been hypothesized that a very close evolutionary relationship exists among the trypanosome species of Trypanozoon [2, 3]. Moreover, many of T. equiperdum strains were isolated over 50 years ago, and it was hypothesized that some of the isolates were misclassified T. evansi strains [3]. Some of the new T. equiperdum strains were recently isolated in Italy and Ethiopia from horses with suspected dourine infections [4, 5]. However, these T. equiperdum strains were not directly isolated from the genital mucosa (the primary site of infectious lesions of T. equiperdum). Instead, they were isolated from udder secretion samples or jugular venous blood. Thus, new T. equiperdum strains that are directly isolated from the infectious lesions of horses with clinically- and parasitologically-confirmed dourine have long been needed for further studies on T. equiperdum and dourine.
Previous reports have shown the prevalence of equine trypanosomosis in Mongolia and Kazakhstan to be 6–8 % and 16.8 %, respectively [6, 7]. However, these reports did not identify the causative species because it is very difficult to distinguish T. equiperdum from T. evansi using serological diagnostic techniques. On the other hand, the re-emergence of dourine was reported in Italy in May 2011 when the characteristic symptoms of dourine (e.g. paralysis of the lip, edema of the vulva and cutaneous wheals) were observed in a number of horses [8]. A serological test revealed that approximately 0.5 % of the equine population was diagnosed as dourine-positive by CFT, moreover, dourine positivity (based on the case definition) has been confirmed in 0.03 % of all horses [9]. Moreover, trypanosomes were observed in the skin lesions and were isolated from infected horses by intrascrotal inoculation [5].
Our ongoing epidemiological research suggests high prevalence of trypanosomoses in horses in Mongolia. In the present study, dourine was diagnosed parasitologically via the detection of T. equiperdum in the urethral tract of a stallion with the characteristic clinical symptoms. Moreover, we established a new true T. equiperdum strain that was isolated from the urethral tract of a dourine-infected stallion. Furthermore, we used a PCR to molecularly characterize this new strain of T. equiperdum.
Methods
The identification of the stallion with suspected dourine
The brown-colored 7-year-old stallion was bred in an equestrian farm in Töv aimag in Mongolia. It was suspected of being infected with dourine based on the presence of slight paraphimosis and edema in the genital organ (Fig. 1a and b). The blood parameters (white blood cell [WBC], red blood cell [RBC], hemoglobin [HGB], hematocrit [HCT], mean corpuscular volume [MCV], mean corpuscular hematocrit [MCH], mean corpuscular hemoglobin concentration [MCHC], and platelet [PLT] count) were measured using a Celltac α (Nihon Khoden, Tokyo, Japan); while the measurement of the blood chemistry parameters (alkaline phosphatase [ALP], alanine transaminase [ALT], aspartate aminotransferase [AST], albumin, total protein, total cholesterol, bilirubin, blood urea nitrogen [BUN], creatinine, and amylase) was outsourced (Table 1). Molecular diagnoses were then performed using DNA extracted from the blood and serum of the stallion by a KIN-PCR, a complement fixation test (CFT), a recombinant T. evansi GM6-4r antigen-based immunochromatographic test (ICT) and an enzyme-linked immunosorbent assay (ELISA) [10–13]. The collected cerebrospinal fluid (CSF) was centrifuged to concentrate the trypanosomes. Trypanosomes in the sediment of the CSF and in the blood were observed by the wet blood film method. Parasitemia in the blood was estimated using Herbert & Lumsden’s method [14].
Fig. 1.
The swelling of the genital organ of the dourine-infected stallion and sampling of trypanosomes from the urethral tract. a and b The swelling of the genital organ of the dourine-infected stallion. c HMI-9 was injected into the urethral tract using a transfer pipette to detach adherent T. equiperdum from the urethral tract mucosa. d Sampling of T. equiperdum from the urethral tract mucosa using a cotton swab
Table 1.
The clinical symptoms, blood parameters and blood chemistry of the dourine-infected stallion
| Clinical symptoms | Slight edema in the genital organ |
| Slight paraphimosis | |
| A large amount of smegma around the penis | |
| Small skin lesion | |
| Slight anemia | |
| Blood parameters | WBC: 12.9 ×103 cells/μl (slightly high) |
| RBC: 6.32 ×106 cells/μl (slightly low) | |
| HGB: 10.6 g/dl (slightly low) | |
| HCT: 30.9 % (slightly low) | |
| Other parameters: normal (MCV, MCH, MCHC, PLT) | |
| Blood chemistry parameters | Normal (ALP, ALT, AST, albumin, total protein, total cholesterol, bilirubin, BUN, creatinine, amylase) |
| Parasitemia | Swab of the urethral tract mucosa: a lot of trypanosomes |
| Blood: < 2.5 × 105 cells/mla (1 trypanosome per 500 fields; magnification 400×) | |
| Cerebrospinal fluid: relatively a lot of trypanosomes in sediment |
aParasitemia was estimated using Herbert & Lumsden's method [14]
Isolation and cultivation of T. equiperdum in vitro
To isolate T. equiperdum from the urethral tract of the stallion, Hirumi’s modified Iscove’s medium-9 supplemented with 20 % heat-inactivated adult horse serum (HMI-9) [15] was injected into the urethral tract of the stallion with a suspected dourine infection to detach T. equiperdum from the urethral tract mucosa (Fig. 1c). Subsequently, T. equiperdum was sampled from the urethral tract mucosa using a cotton swab (Fig. 1d). The T. equiperdum specimens from the urethral tract mucosa were smeared on slide glasses, fixed with 100 % methanol and stained with Giemsa for microscopic observation. The major axis of isolated T. equiperdum was measured using a Nikon Eclipse Ci microscope and the Nice D software program (Nikon Corporation, Tokyo, Japan).
The T. equiperdum isolates from the urethral tract were centrifuged with HMI-9 media at 3000× g for 10 min at room temperature. The pellets containing T. equiperdum and urethral mucosa cells were washed twice with HMI-9. Finally, T. equiperdum suspended in HMI-9 was spread on soft agarose media (HMI-9 with 0.8 % low gelling agarose [Type VII, Sigma-Aldrich Japan, Tokyo, Japan]) at 37 °C in 5 % CO2. Culture-adapted T. equiperdum specimens were cryopreserved in horse serum supplemented with 10 % dimethyl sulfoxide at -80 °C.
DNA extraction
Total DNA of T. equiperdum was extracted and purified using TE-saturated phenol (Sigma-Aldrich, Japan) and phenol-chloroform-isoamyl alcohol solution (Sigma-Aldrich, Japan) [16]. Purified DNA was kept at -30 °C until use.
PCR amplification and phylogenetic analysis of 18S rRNA gene and ITS
The 18S ribosomal RNA (18S rRNA) gene and the internal transcribed spacer (ITS) region of the Mongolian isolate and the reference strains of T. equiperdum (the total DNA of the STIB818, STIB841, STIB842 and BoTat1.1 strains were all kindly provided by Dr. Zhao-Rong Lun of Sun Yat-Sen University in the People’s Republic of China) were amplified and cloned into the pCR 2.1 cloning vector (Thermo Fisher Scientific K.K., Tokyo, Japan), and the sequences were analyzed using an ABI3100 genomic analyzer (Thermo Fisher Scientific K.K.) [17]. In addition to these T. equiperdum sequence data, the reference sequences from the NCBI database (T. brucei [Accession No. AC012647.18], T. b. rhodesiense [AJ009142], T. b. gambiense [FN554966.1 and AJ009141] and T. evansi [AB551922.1, AY912277, AY912279 and D89527.1]) were included in the phylogenetic analyses. The phylogenetic analyses of the 18S rDNA and ITS regions were performed using the neighbor-joining method using the MEGA 7 software program.
Maxicircle kDNA characterization
The target loci on the maxicircle genes were amplified from the total DNA of the Mongolian T. equiperdum isolate. In addition, the total DNA from T. b. brucei GUTat3.1, T. evansi IL3960 and T. equiperdum STIB818, STIB841, STIB842 and BoTat1.1 were used for maxicircle gene amplification in order to compare the maxicircle kinetoplast DNA (kDNA) sequences among the trypanosome species. The primer sequences for each of the target loci on the maxicircle gene have been described previously (Additional file 1: Table S1) [18]. The amplicons were cloned into pCR 2.1 cloning vector (Thermo Fisher Scientific K.K.), and the sequences were analyzed using an ABI3100 genomic analyzer (Thermo Fisher Scientific K.K.).
The measurement of kinetoplastic and akinetoplastic T. equiperdum population
Culture-adapted T. equiperdum and T. equiperdum that were directly obtained from the urethral tract and CSF of an infected stallion were spread over glass slides printed with highly water-repellent marking (Matsunami Glass Ind., Ltd., Tokyo, Japan), air-dried, and fixed with 100 % methanol for 10 min at room temperature. The specimens were blocked with 5 % skim milk in TBS supplemented with 0.05 % tween for 1 h at room temperature. The specimens were then incubated with a primary antibody (anti-recombinant T. congolense α-tubulin serum) [19]. Next, the slides were incubated with a secondary antibody (Alexa Fluor 488 goat anti-rabbit IgG [H + L], Thermo Fisher Scientific K.K.) with Hoechst 33342 (Dojindo, Co. Ltd., Kumamoto, Japan). The specimens were observed by confocal laser scanning microscopy (Leica TCS SP5, Leica Microsystems, Wetzlar, Germany).
Results
T. equiperdum isolated from the urethral tract of the dourine-infected stallion
Dourine was suspected based on the swelling of the genital organ, slight paraphimosis, a large amount of smegma and a small skin lesion on the stallion (Fig. 1a and b). In addition, slight anemia was suggested based on a hematological examination (Table 1). Moreover, the CFT, ICT and ELISA results strongly suggested a trypanosome infection (data not shown). However, these molecular diagnostic methods were not capable of differentiating between T. equiperdum and T. evansi. Thus, we could not eliminate the possibility of a T. evansi infection (Surra) based on these results. In addition to suspecting dourine based on the clinical symptoms and the molecular diagnostic results, actively moving trypanosomes were detected from the mucosa of the urethral tract by microscopy. Moreover, the parasitemia in the blood was very low, while that in the sediment of the CSF was relatively high (Table 1). We therefore concluded that this stallion was infected with T. equiperdum. The microscopic observation of Giemsa-stained trypanosomes was used for the morphological characterization of the T. equiperdum isolate of the naturally infected stallion. Kinetoplasts were clearly stained and observed in all of the trypanosomes. Single-form and dividing-form (2K1N and 2K2N) trypanosomes with a free flagellum were observed (Fig. 2). The major axis of the trypanosomes was 26.4 ± 3.1 μm (mean ± standard deviation, n = 27).
Fig. 2.
Giemsa-stained T. equiperdum isolated from the urethral tract of the dourine-infected stallion. a and b (1K1N) show the single form of T. equiperdum. c (2K1N) and d (2K2N) show the dividing form of T. equiperdum. Arrow: nucleus; arrowhead: kinetoplast
Culture adaptation of the T. equiperdum isolate
T. equiperdum isolated from urethral tract of the dourine-infected stallion was directly transferred into an in vitro culture. They were adapted in a soft agarose media culture system. Unlike the culturing of other bloodstream-form trypanosomes, the primary culture of isolated T. equiperdum could not be successfully propagated in HMI-9 liquid media. The parasites were found to be attached and actively moving on the surface of soft agarose media (Additional file 2: Movie 1). Some of them invaded the soft agarose and propagate under the surface of soft agarose during cultivation. Unlike T. brucei, they could not form colonies on the surface of soft agar [20]. This new culture-adapted T. equiperdum strain was named, “IVM-t1 (T. equiperdum isolated in the Institute of Veterinary Medicine from Töv aimag dourine horse no. 1), 2015.”
Phylogenetic analyses
The phylogenetic relationships were inferred from a comparison of the 18S rRNA and ITS sequences of T. equiperdum and other Trypanozoon. Like the other T. equiperdum strains, the newly isolated T. equiperdum IVM-t1 strain belonged to the Trypanozoon clade (Additional file 3: Figure S1).
T. equiperdum IVM-t1 strain lacks maxicircle integrity
Eight PCRs targeting the maxicircle genes were performed to compare the maxicircle integrity among the Trypanozoon parasites. The maxicircle PCR of T. evansi IL3960, T. brucei GUTat3.1 and T. equiperdum STIB818, STIB841, STIB842 and BoTat1.1 strains (as the reference strains) showed the same results as previous reports (Table 2) [18]. On the other hand, only NADH-dehydrogenase subunits 4 and 5 (ND4-ND5) was amplified in T. equiperdum IVM-t1 strain (Table 2, Fig. 3 and Additional file 3: Figure S2). The PCR signal of ND4-ND5 in the T. equiperdum IVM-t1 strain was somewhat weaker than the ND4-ND5 signals of the other trypanosomes. Sequence analyses showed that the other bright PCR bands (e.g. around the 1.5 kbp band in lane 3 of Additional file 3: Figure S2-A) were not the maxicircle target genes.
Table 2.
Summary of the maxicircle PCR results
| Target locusa | T. b. brucei | T. evansi | T. equiperdum | ||||
|---|---|---|---|---|---|---|---|
| GUTat3.1 | IL3960 | IVM-t1 | STIB818 | STIB841 | STIB842 | BoTat1.1 | |
| NAD7 | P | N | N | N | P | P | P |
| Cox2 | P | N | N | N | P | P | P |
| A6 | P | N | N | N | P | P | P |
| 12S rRNA | P | N | N | P | P | P | P |
| ND7-CyB | P | N | N | N | P | P | P |
| MURF1-ND1 | P | N | N | N | P | P | P |
| MURF2-Cox1 | P | N | N | N | P | P | P |
| ND4-ND5 | P | N | P | P | P | P | P |
All of the PCR product sequences were confirmed by a sequence analysis and the NCBI BlastN software program
Abbreviations: P Positive, N Negative
aNAD7, NADH-dehydrogenase subunit 7; Cox2, Cytochrome oxidase subunit 2; A6, ATPase subunit 6; 12S rRNA, 12S ribosomal RNA; ND7-CyB, NADH-dehydrogenase subunit 7-cytochrome b; MURF-ND1, Maxicircle unknown reading frame-NADH dehydrogenase subunit 1; MURF2-Cox1, Maxicircle unknown reading frame 2-cytochrome oxidase subunit 1 and ND4-ND5, NADH-dehydrogenase subunits 4–5
Fig. 3.
The PCR to detect NADH-dehydrogenase subunits 4 and 5 (ND4-ND5). A gel electrophoresis image of the PCR products of NADH-dehydrogenase subunits 4 and 5 (ND4-ND5). The arrowhead at 1515 bp indicates the amplicon of ND4-ND5 in lanes 1 and 3 to 7. M: 100 bp and 1 kbp DNA ladders, Lanes 1 to 8 are T. b. brucei GUTat3.1, T. evansi IL3960, T. equiperdum IVM-t1, STIB818, STIB841, STIB842, BoTat1.1 strains and a negative control (distilled water), respectively
The majority of the culture-adapted T. equiperdum IVM-t1 strain population was akinetoplastic after long-term in vitro cultivation
Kinetoplasts were clearly observed in almost all of the T. equiperdum specimens from the urethral tract by Giemsa and DNA staining (1 out of 160 [0.63 %] trypanosomes were akinetoplastic) (Figs. 2 and 4a). In addition, akinetoplastic T. equiperdum accounted for a minor part of the trypanosome population in the CSF (6 out of 326 [1.84 %] of the trypanosomes were akinetoplastic). On the other hand, kinetoplasts were not observed in most of the culture-adapted from T. equiperdum IVM-t1 strain (480 out of 500 [96.0 %] trypanosomes were akinetoplastic) (Fig. 4b).
Fig. 4.
Akinetoplastic and kinetoplastic T. equiperdum in wild-type and in vitro culture. a T. equiperdum isolated from the urethral tract. Upper panel, akinetoplastic form; middle and lower panels, kinetoplastic form. b Kinetoplastic and akinetoplastic T. equiperdum in vitro culture. Arrow: nucleus; arrowhead: kinetoplast
Discussion
T. equiperdum is a cosmopolitan trypanosome that causes dourine via sexual transmission in the Equidae. The phylogenetic relationships of the subgenus Trypanozoon (T. brucei sspp., T. evansi and T. equiperdum) have been unclear, and serological methods for differentially diagnosing the various Trypanozoon trypanosomes have not been established due to the lack of information about the T. equiperdum genome. Many of the T. equiperdum strains were isolated more than 50 years ago [3]. Recently new T. equiperdum strains were isolated from horses with suspected dourine in Italy and Ethiopia [4, 5]. However, these T. equiperdum strains were not directly isolated from the genital mucosa (infectious lesion of T. equiperdum). In the present study, we isolated T. equiperdum from the urethral tract of a dourine-infected stallion and established a new culture-adapted T. equiperdum strain. Moreover, we conducted the molecular characterization of this T. equiperdum strain based on the 18S rRNA, ITS and maxicircle gene sequences.
In addition to the clinical symptoms that led us to suspect dourine and the results of the molecular diagnosis, live trypanosomes were observed on a wet smear from the urethral tract mucosa of one stallion in Mongolia (Table 1). Moreover, trypanosomes were detected in the blood (< 2.5 × 105 cells/ml) and CSF (relatively high parasitemia was observed in the sediment) (Table 1). Although T. equiperdum mainly parasitizes in the tissue, it is rarely observed in the bloodstream of horses with chronic infection [1]. We therefore concluded that this stallion was infected with T. equiperdum. Since the dividing-form and actively moving trypanosomes were observed, it was concluded that T. equiperdum parasites were propagating in the urethral tract mucosa and that they caused dourine in this stallion (Fig. 2). Our ongoing surveillance project in Mongolia also revealed Surra epidemics in other domestic animals (data not shown). Previous reports showed that Tabanus spp. were trapped in Hustai National Park, Mongolia [21]. These results indicated that the Tabanus spp. that can transmit T. evansi can be found in Mongolia. Although the parasitemia was very low, T. equiperdum parasitized the bloodstream in this infected stallion. We therefore could not completely exclude the possibility of the mechanical transmission of T. equiperdum due to blood sacking by the Tabanus spp.
Isolated T. equiperdum parasites were adapted and proliferated well using HMI-9 soft agarose media as a primary trypanosome culture (Additional file 2: Movie 1). While isolated, T. equiperdum could not be propagated in HMI-9 liquid media in primary trypanosome cultures. Furthermore, unlike T. brucei, to proliferate on the surface of the soft agarose media, T. equiperdum invaded the surface of soft agarose media but could not form colonies [20]. After the infection of the genital mucosa via coitus, T. equiperdum invade the tissue and parasitize in the blood, lymph, CSF and sub-cutaneous lesions [5]. These results suggest that the soft agarose media mimics the natural environment of the host genital mucosa. Thus, the isolated T. equiperdum were well adapted and proliferated using soft agarose media but did not adapt in liquid media. This culture system will be useful for the future isolation of T. equiperdum from dourine-infected horses in the field.
A phylogenetic analysis using 18S rRNA and the ITS region revealed that, along with the other T. equiperdum strains, the T. equiperdum IVM-t1 strain was a member of the Trypanozoon clade (Additional file 3: Figure S1). T. equiperdum and T. evansi were hypothesized to have independently evolved from ancestral T. brucei at least four times [22, 23]. Thus, T. equiperdum is a polyphyletic group and, based on the results of a previous gnomic analysis, is considered to be a subspecies of T. brucei. However, Desquesnes et al. [24] suggested that T. equiperdum and T. evansi should keep their current species status based on the significant biological and parasitical differences between these species. A RoTat 1.2 VSG PCR, which was performed to analyze the sequence of the amplicon, was negative (data not shown). Moreover, only NADH-dehydrogenase subunit 4 and 5 (ND4-ND5) was amplified in the maxicircle of this strain of T. equiperdum (Table 2 and Fig. 3). The majority of the culture-adapted T. equiperdum IVM-t1 strain population was composed of akinetoplastic-form parasites; thus, the weak ND4-ND5 signal was caused by the small amount of maxicircle template DNA because of the small population in kinetoplastic culture-adapted T. equiperdum IVM-t1. The results of this molecular analysis also supported that this isolated trypanosome was T. equiperdum.
Many of the akinetoplastic Trypanozoon trypanosome strains have been established from a parental kinetoplastic strain by the supplementation of DNA binding drugs or RNA interference during in vitro culture [25]. The predominance of the akinetoplastic T. evansi and T. equiperdum population was also induced from a kinetoplastic parental trypanosome by long-term aseptic cultivation [26]. In the present study, the T. equiperdum IVM-t1 strain was cultivated without any drug supplementation based on the intention to remove kinetoplasts from the kinetoplastic parental T. equiperdum over a one-year cultivation period. However, the majority of the population (96.0 %) in culture-adapted T. equiperdum IVM-t1 strain was akinetoplastic-form, despite akinetoplastic T. equiperdum being a minority population in the parental T. equiperdum population (0.63 %) (Fig. 4). We cannot conclude that the predominance of akinetoplastic forms in the culture-adapted T. equiperdum IVM-t1 strain were simply selected from parental akinetoplastic T. equiperdum, which was the minority population in the urethral tract, or induced rapid kinetoplast loss from the parental kinetoplastic T. equiperdum during long-term in vitro cultivation without any drug supplementation. The rapid loss of kinetoplasts in culture-adapted T. equiperdum IVM-t1 strain might be due to the acquisition of a rapid proliferative potential in the culture, similarly to the proliferation of unregulated cancer cells in the host [27]. T. equiperdum is usually distinguished from T. evansi by an analysis of the kDNA (by a PCR); however, it was not possible to detect dyskinetoplastic T. equiperdum strains (such as the culture-adapted T. equiperdum IVM-t1 strain) by an analysis of the kDNA. Other species-specific markers are therefore expected to be useful for the definitive diagnosis of Trypanozoon infections. We performed a further comparative whole genomic analysis and transcriptome analysis using a next generation sequencing technique to compare the T. equiperdum IVM-t1 strain with other Trypanozoon species. Based on these results, we intend to develop T. equiperdum-specific PCR methods and serodiagnostic methods that can be used to definitively diagnose Trypanozoon infections and reveal the evolution, origin and pathogenic effects of Trypanozoon.
Conclusions
In conclusion, we successfully isolated T. equiperdum from the urethral tract mucosa of a dourine-infected stallion with characteristic clinical symptoms using soft agarose media. We therefore propose that this T. equiperdum IVM-t1 strain is a new T. equiperdum reference strain. Whole genome and transcriptome analyses using this new reference T. equiperdum strain are expected to reveal the phylogenetic relationship between Trypanozoon and to be useful in the development of novel methods for diagnosing dourine.
Acknowledgments
We thank Ms. Noriko Endo and Ms. Bat-Uyanga Lhagva for their project management in Mongolia. We thank all of the Mongolian SATREPS project researchers for supporting this study. We also thank Ms. Yoko Matsushita for her excellent technical assistance. This study was financially supported by the Japan Society for the Promotion of Science (JSPS), Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), and the AMED/JICA SATREPS.
Funding
This study was financially supported by the Japan Society for the Promotion of Science (JSPS), Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), and the AMED/JICA SATREPS.
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional files
Authors’ contributions
KS and SN helped to conceive the study and participated in its design and the laboratory experiments. B Battur, B Battsetseg and NI helped to conceive the study, participated in its design, analyzed data and helped to draft and edit the manuscript and obtain funding. SY, DO, SPM and BD helped to conceive the study, participated in its design and analyzed the data. All of the authors read and approved the final manuscript.
Competing interests
The authors declare that they have no competing interests.
Consent for publication
Not applicable.
Ethics approval and consent to participate
Not applicable.
Abbreviations
- 18S rRNA
18S ribosomal RNA
- ALP
Alkaline phosphatase
- ALT
Alanine transaminase
- AST
Aspartate aminotransferase
- BUN
Blood urea nitrogen
- CFT
Complement fixation test
- CSF
Cerebrospinal fluid
- ELISA
Enzyme-linked immunosorbent assay
- HCT
Hematocrit
- HGB
Hemoglobin
- HMI-9
Hirumi’s modified Isocove’s medium-9
- ICT
Immunochromatographic test
- ITS
Internal transcribed spacer
- kDNA
Kinetoplast DNA
- MCH
Mean corpuscular hematocrit
- MCHC
Mean corpuscular hemoglobin concentration
- MCV
Mean corpuscular volume
- ND4-ND5
NADH-dehydrogenase subunits 4 and 5
- PLT
Platelet
- RBC
Red blood cell
- WBC
White blood cell
Additional files
The PCR primers used in the present study. (DOCX 25 kb)
Additional file 2:
Movie 1. Culture-adapted T. equiperdum IVM-t1 were proliferated on the surface of soft agarose media. (M4V 8770KB)
The phylogenetic tree of the 18S rRNA and ITS region. A phylogenetic analysis was performed using the T. equiperdum IVM-t1, SITB818, STIB841, STIB842, BoTat1.1, T. evansi Tansui (Accession No. D89527.1), Cairo (AB551922.1), KAI.2 (AY912277), Sam.2 (AY912279.1), T. brucei TREU927 (AC012647), T. b. gambiense DAL972 (FN554966.1), T. b. gambiense Tsuua (AJ009141) and T. b. rhodesiense Utro (AJ009142) sequences. A: A phylogenetic tree based on the 18S rRNA sequence. B: A phylogenetic tree based on the ITS sequence. Figure S2. The maxicircle PCR of the Trypanozoon species. Gel electrophoresis images of the PCR products are shown in A to G, NADH-dehydrogenase subunit 7 (NAD7; 383 bp), Cytochrome oxidase subunit 2 (Cox2; 1747 bp), ATOas subunit 6 (A6; 299 bp), 12S ribosomal RNA (12S rRNA; 1597 bp in T. b. brucei GUTat3.1 strain and T. equiperdum STIB818 strain, 1415 bp in T. equiperdum STIB841, STIB842, BoTat1.1 strains, respectively), NADH-dehydrogenase subunit 7-cytochromeB (ND7-CyB; 1450 bp), Maxicircle unknown reading frame-NADH dehydrogenase subunit 1 (MURF-ND1; 1779 bp) and Maxicircle unknown reading frame 2-cytochrome oxidase subunit 1 (MURF2-Cox1; 1551 bp), respectively. M: the 100 bp and 1 kbp DNA ladders; Lanes 1 to 8 show T. b. brucei GUTat3.1, T. evansi IL3960, T. equiperdum IVM-t1, STIB818, STIB841, STIB842, BoTat1.1 strains and negative control (distilled water), respectively. (PPTX 164 kb)
Contributor Information
Keisuke Suganuma, Email: k.suganuma@obihiro.ac.jp.
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Data Availability Statement
The datasets supporting the conclusions of this article are included within the article and its additional files